5056 NP_705833 S439R not found in SNVbox database
5323 NP_109597 L176M not found in SNVbox database
8722 NP_109597 P308R not found in SNVbox database
8874 NP_002531 R611C not found in SNVbox database
9665 NP_705833 I1021L not found in SNVbox database
73 NP_705833 H159L not found in SNVbox database
286 NP_705833 S174Y not found in SNVbox database
2556 NP_705833 V626F not found in SNVbox database
2815 NP_705833 P87T not found in SNVbox database
3683 NP_001070868 S340P not found in SNVbox database
4034 NP_001070868 S690P not found in SNVbox database
4311 NP_001070868 Q67H not found in SNVbox database
4371 NP_705833 L13I not found in SNVbox database
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:8844284 G>T maps to NM_001127448.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:8844284 G>T maps to NM_001127448.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:8407758 C>A maps to NM_003501.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:8407758 C>A maps to NM_003501.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:114709123 T>A maps to NM_005721.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:114709123 T>A maps to NM_005721.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:43860486 G>A maps to ENST00000389420 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:43860486 G>A maps to ENST00000389420 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:110825554 G>A maps to NM_016238.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:110825554 G>A maps to NM_016238.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:114275530 C>A maps to NM_001148.4 S1919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:114275530 C>A maps to NM_001148.4 S1919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:36123063 C>T maps to NM_030642.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:36123063 C>T maps to NM_030642.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:78426858 G>T maps to NM_001713.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:78426858 G>T maps to NM_001713.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:59939766 T>C maps to NM_144581.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:59939766 T>C maps to NM_144581.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:36991510 G>A maps to NM_001080465.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:36991510 G>A maps to NM_001080465.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:41160436 G>T maps to NM_001115131.1 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:41160436 G>T maps to NM_001115131.1 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:201028376 C>A maps to NM_000069.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:201028376 C>A maps to NM_000069.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:87795509 C>T maps to NM_000735.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:87795509 C>T maps to NM_000735.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:240070931 G>T maps to NM_000740.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:240070931 G>T maps to NM_000740.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:189871099 T>A maps to NM_000090.3 G1041G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:189871099 T>A maps to NM_000090.3 G1041G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:83215262 A>T maps to ENST00000261723 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:83215262 A>T maps to ENST00000261723 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:2776023 C>A maps to NM_019609.4 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:2776023 C>A maps to NM_019609.4 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15989715 C>T maps to NM_001082.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15989715 C>T maps to NM_001082.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:532471 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:532471 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:5789412 G>A maps to NM_020175.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:5789412 G>A maps to NM_020175.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:50667199 G>A maps to NM_000124.2 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:50667199 G>A maps to NM_000124.2 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:23718373 C>T maps to NM_033266.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:23718373 C>T maps to NM_033266.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:131521153 C>A maps to NM_001105195.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:131521153 C>A maps to NM_001105195.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:190203535 C>A maps to NM_199051.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:190203535 C>A maps to NM_199051.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:84607298 C>T maps to NM_001001670.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:84607298 C>T maps to NM_001001670.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:150171184 C>T maps to NM_175571.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:150171184 C>T maps to NM_175571.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:9791284 G>T maps to NM_004246.1 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:9791284 G>T maps to NM_004246.1 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:42169749 C>A maps to NM_001015053.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:42169749 C>A maps to NM_001015053.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:44222904 G>A maps to NM_019612.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:44222904 G>A maps to NM_019612.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:52858332 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:52858332 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:63483637 C>A maps to NM_139318.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:63483637 C>A maps to NM_139318.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:53230769 G>A maps to NM_004187.3 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:53230769 G>A maps to NM_004187.3 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:143676235 T>G maps to NM_003937.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:143676235 T>G maps to NM_003937.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:1943778 C>T maps to NM_001163926.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:1943778 C>T maps to NM_001163926.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:129902900 G>A maps to NM_002417.4 N2401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:129902900 G>A maps to NM_002417.4 N2401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:152426723 G>T maps to NM_001164507.1 I5767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:152426723 G>T maps to NM_001164507.1 I5767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:248512354 G>C maps to NM_001001918.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:248512354 G>C maps to NM_001001918.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:143826246 G>A maps to NM_001001659.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:143826246 G>A maps to NM_001001659.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:120263890 T>A maps to NM_006623.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:120263890 T>A maps to NM_006623.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:52878239 G>T maps to NM_032864.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:52878239 G>T maps to NM_032864.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43258470 T>G maps to NM_182707.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43258470 T>G maps to NM_182707.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:112141904 G>C maps to NM_002829.3 Y891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:112141904 G>C maps to NM_002829.3 Y891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:23960892 T>A maps to NM_002948.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:23960892 T>A maps to NM_002948.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:60074058 G>A maps to NM_021136.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:60074058 G>A maps to NM_021136.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:67801778 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:67801778 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:95090003 C>T maps to ENST00000393080 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:95090003 C>T maps to ENST00000393080 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:174936181 A>T maps to NM_022754.5 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:174936181 A>T maps to NM_022754.5 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15061008 A>T maps to NM_005071.1 *565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15061008 A>T maps to NM_005071.1 *565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:21391918 C>A maps to NM_006446.4 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:21391918 C>A maps to NM_006446.4 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:35445091 G>T maps to ENST00000357281 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:35445091 G>T maps to ENST00000357281 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:98188476 G>T maps to NM_012465.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:98188476 G>T maps to NM_012465.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:92033632 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:92033632 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:31329912 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:31329912 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:219603496 C>T maps to NM_014640.4 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:219603496 C>T maps to NM_014640.4 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:90039405 C>A maps to NM_016021.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:90039405 C>A maps to NM_016021.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:89819578 G>T maps to NM_001143975.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:89819578 G>T maps to NM_001143975.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:70361225 T>A maps to NM_021139.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:70361225 T>A maps to NM_021139.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:8988971 C>T maps to NM_003470.2 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:8988971 C>T maps to NM_003470.2 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:62239392 A>G maps to NM_020821.2 H1625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:62239392 A>G maps to NM_020821.2 H1625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:50280789 G>A maps to NM_014838.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:50280789 G>A maps to NM_014838.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:77763195 G>T maps to NM_024721.4 E1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:77763195 G>T maps to NM_024721.4 E1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:30409830 G>T maps to ENST00000495929 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:30409830 G>T maps to ENST00000495929 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:58858920 G>T maps to NM_130786.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:58858920 G>T maps to NM_130786.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:127724717 G>T maps to NM_003474.4 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:127724717 G>T maps to NM_003474.4 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:33683975 G>T maps to NM_030955.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:33683975 G>T maps to NM_030955.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:39445555 C>G maps to NM_145298.5 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:39445555 C>G maps to NM_145298.5 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:46245319 G>T maps to NM_152641.2 G1138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:46245319 G>T maps to NM_152641.2 G1138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:23270391 C>A maps to NM_173081.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:23270391 C>A maps to NM_173081.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31476155 T>C maps to ENST00000408912 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31476155 T>C maps to ENST00000408912 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:232141471 C>G maps to ENST00000359743 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:232141471 C>G maps to ENST00000359743 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:101170137 C>T maps to NM_198243.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:101170137 C>T maps to NM_198243.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:1458248 G>T maps to NM_018188.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:1458248 G>T maps to NM_018188.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:26148944 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:26148944 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:69348713 T>A maps to NM_001704.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:69348713 T>A maps to NM_001704.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:59445832 G>T maps to ENST00000407086 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:59445832 G>T maps to ENST00000407086 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:81320985 G>A maps to NM_017429.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:81320985 G>A maps to NM_017429.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:40966603 A>G maps to NM_003766.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:40966603 A>G maps to NM_003766.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10608453 C>T maps to NM_020233.4 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10608453 C>T maps to NM_020233.4 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:8141518 C>A maps to NM_025099.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:8141518 C>A maps to NM_025099.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:36181805 G>C maps to NM_152374.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:36181805 G>C maps to NM_152374.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:10555359 G>T maps to NM_001040032.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:10555359 G>T maps to NM_001040032.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:90576191 A>G maps to NM_012115.3 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:90576191 A>G maps to NM_012115.3 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:91779573 C>G maps to NM_001080414.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:91779573 C>G maps to NM_001080414.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:34340788 A>C maps to NM_005064.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:34340788 A>C maps to NM_005064.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:17072375 C>G maps to NM_014406.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:17072375 C>G maps to NM_014406.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:214791960 A>T maps to NM_016343.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:214791960 A>T maps to NM_016343.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:24201555 T>A maps to NM_001841.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:24201555 T>A maps to NM_001841.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:47542429 C>G maps to NM_001849.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:47542429 C>G maps to NM_001849.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:20031145 C>A maps to NM_016652.4 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:20031145 C>A maps to NM_016652.4 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:225376299 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:225376299 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:17805365 C>A maps to NM_017741.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:17805365 C>A maps to NM_017741.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:140301876 C>T maps to NM_015689.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:140301876 C>T maps to NM_015689.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:60582752 T>A maps to NM_001042517.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:60582752 T>A maps to NM_001042517.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:117395562 G>A maps to NM_020693.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:117395562 G>A maps to NM_020693.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:7150663 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:7150663 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:454085 G>T maps to ENST00000315013 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:454085 G>T maps to ENST00000315013 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:177226495 C>A maps to NM_021165.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:177226495 C>A maps to NM_021165.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:87498775 A>T maps to NM_016033.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:87498775 A>T maps to NM_016033.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:52778791 C>A maps to NM_013409.1 C56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:52778791 C>A maps to NM_013409.1 C56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:29574724 G>A maps to NM_001470.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:29574724 G>A maps to NM_001470.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:79118028 G>T maps to NM_001097636.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:79118028 G>T maps to NM_001097636.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:72631269 C>A maps to ENST00000504199 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:72631269 C>A maps to ENST00000504199 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:150389569 G>T maps to NM_015660.2 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:150389569 G>T maps to NM_015660.2 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:94482404 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:94482404 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:41004552 A>G maps to ENST00000296803 C1364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:41004552 A>G maps to ENST00000296803 C1364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:38137444 A>G maps to NM_000411.5 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:38137444 A>G maps to NM_000411.5 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:86593298 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:86593298 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:100963142 C>A maps to NM_016247.2 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:100963142 C>A maps to NM_016247.2 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:156810733 G>T maps to NM_014215.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:156810733 G>T maps to NM_014215.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:39278774 G>A maps to NM_031460.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:39278774 G>A maps to NM_031460.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:94088408 A>G maps to ENST00000393153 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:94088408 A>G maps to ENST00000393153 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:152733140 G>A maps to NM_001025231.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:152733140 G>A maps to NM_001025231.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:151773297 T>A maps to NM_006726.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:151773297 T>A maps to NM_006726.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:141812829 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:141812829 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:47504502 T>A maps to NM_001113498.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:47504502 T>A maps to NM_001113498.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:18301670 C>A maps to NM_015241.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:18301670 C>A maps to NM_015241.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10403990 G>A maps to NM_005963.3 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10403990 G>A maps to NM_005963.3 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18023557 C>T maps to ENST00000205890 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18023557 C>T maps to ENST00000205890 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:24771755 C>A maps to NM_005382.2 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:24771755 C>A maps to NM_005382.2 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:75573381 C>A maps to NM_033116.4 G451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:75573381 C>A maps to NM_033116.4 G451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:7317980 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:7317980 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:162313766 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:162313766 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:70774415 C>G maps to NM_181672.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:70774415 C>G maps to NM_181672.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:4661751 G>T maps to NM_001004751.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:4661751 G>T maps to NM_001004751.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:195953989 G>A maps to NM_152672.5 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:195953989 G>A maps to NM_152672.5 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44527412 C>T maps to NM_001003828.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44527412 C>T maps to NM_001003828.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:19062358 C>A maps to NM_002584.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:19062358 C>A maps to NM_002584.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:31144128 G>T maps to NM_001173523.1 G1142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:31144128 G>T maps to NM_001173523.1 G1142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:140256795 T>A maps to NM_018903.2 L580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:140256795 T>A maps to NM_018903.2 L580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:140564341 G>T maps to NM_020957.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:140564341 G>T maps to NM_020957.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:82764744 C>T maps to NM_033026.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:82764744 C>T maps to NM_033026.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:95791384 C>T maps to ENST00000371380 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:95791384 C>T maps to ENST00000371380 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161135877 C>A maps to NM_000301.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161135877 C>A maps to NM_000301.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:4511379 G>C maps to NM_001080400.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:4511379 G>C maps to NM_001080400.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:131888168 C>A maps to NM_020911.1 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:131888168 C>A maps to NM_020911.1 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:38172803 G>A maps to NM_006475.2 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:38172803 G>A maps to NM_006475.2 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:157414081 G>T maps to NM_002847.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:157414081 G>T maps to NM_002847.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:141327426 C>T maps to ENST00000452898 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:141327426 C>T maps to ENST00000452898 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:103126852 G>T maps to ENST00000428762 C3258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:103126852 G>T maps to ENST00000428762 C3258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21052267 G>T maps to NM_145250.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21052267 G>T maps to NM_145250.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:77612381 G>T maps to ENST00000332191 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:77612381 G>T maps to ENST00000332191 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:10470213 G>T maps to NM_178857.5 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:10470213 G>T maps to NM_178857.5 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52034720 C>A maps to NM_001245.5 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52034720 C>A maps to NM_001245.5 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:84454288 G>A maps to NM_052910.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:84454288 G>A maps to NM_052910.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:167656176 C>T maps to NM_016950.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:167656176 C>T maps to NM_016950.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:158615030 C>A maps to NM_003126.2 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:158615030 C>A maps to NM_003126.2 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:31374708 T>A maps to NM_001083893.1 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:31374708 T>A maps to NM_001083893.1 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:27011937 A>T maps to NM_003170.3 K816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:27011937 A>T maps to NM_003170.3 K816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:75427938 G>T maps to NM_014979.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:75427938 G>T maps to NM_014979.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:159888697 A>G maps to ENST00000368096 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:159888697 A>G maps to ENST00000368096 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:12901385 G>A maps to NM_021961.5 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:12901385 G>A maps to NM_021961.5 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:169648859 C>A maps to NM_003247.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:169648859 C>A maps to NM_003247.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:79375017 G>A maps to NM_003248.4 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:79375017 G>A maps to NM_003248.4 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:98273370 C>A maps to NM_012465.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:98273370 C>A maps to NM_012465.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:12938518 C>T maps to ENST00000311912 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:12938518 C>T maps to ENST00000311912 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:43181006 C>T maps to NM_003701.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:43181006 C>T maps to NM_003701.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:1426847 C>A maps to NM_000547.5 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:1426847 C>A maps to NM_000547.5 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:6750570 G>A maps to ENST00000313244 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:6750570 G>A maps to ENST00000313244 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:72984006 A>T maps to NM_007332.2 Y69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:72984006 A>T maps to NM_007332.2 Y69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:73218373 C>A maps to ENST00000419692 G848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:73218373 C>A maps to ENST00000419692 G848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:24676507 T>A maps to NM_001184739.1 C209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:24676507 T>A maps to NM_001184739.1 C209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:167753912 C>A maps to NM_031949.4 Y175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:167753912 C>A maps to NM_031949.4 Y175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:179610733 G>T maps to ENST00000375038 R5467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:179610733 G>T maps to ENST00000375038 R5467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:1192479 C>A maps to NM_194315.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:1192479 C>A maps to NM_194315.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:101185436 G>T maps to NM_001078.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:101185436 G>T maps to NM_001078.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:48546469 C>A maps to NM_000377.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:48546469 C>A maps to NM_000377.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:69256989 C>A maps to NM_004926.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:69256989 C>A maps to NM_004926.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31092790 C>T maps to NM_014699.3 L1716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31092790 C>T maps to NM_014699.3 L1716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:8808679 G>T maps to NM_178525.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:8808679 G>T maps to NM_178525.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:9666320 C>A maps to NM_003183.4 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:9666320 C>A maps to NM_003183.4 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:39666958 T>G maps to NM_001464.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:39666958 T>G maps to NM_001464.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:957681 C>T maps to NM_198576.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:957681 C>T maps to NM_198576.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:247063502 T>A maps to ENST00000428671 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:247063502 T>A maps to ENST00000428671 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:142437234 T>A maps to NM_015071.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:142437234 T>A maps to NM_015071.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:32563252 A>G maps to NM_001030055.1 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:32563252 A>G maps to NM_001030055.1 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:1808321 C>T maps to ENST00000398564 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:1808321 C>T maps to ENST00000398564 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:31323006 G>T maps to NM_030632.1 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:31323006 G>T maps to NM_030632.1 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:128118365 G>A maps to NM_001004298.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:128118365 G>A maps to NM_001004298.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34648155 C>A maps to ENST00000438749 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34648155 C>A maps to ENST00000438749 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:172558559 C>A maps to ENST00000367723 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:172558559 C>A maps to ENST00000367723 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:146617752 G>A maps to NM_001080531.1 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:146617752 G>A maps to NM_001080531.1 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:78162252 G>C maps to NM_024110.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:78162252 G>C maps to NM_024110.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:54429306 A>G maps to NM_001170402.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:54429306 A>G maps to NM_001170402.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:139866269 G>A maps to NM_004065.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:139866269 G>A maps to NM_004065.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:184104848 T>C maps to NM_003741.2 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:184104848 T>C maps to NM_003741.2 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:78921764 G>A maps to NM_000750.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:78921764 G>A maps to NM_000750.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:152487954 G>T maps to NM_019060.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:152487954 G>T maps to NM_019060.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:149449493 C>T maps to NM_005211.3 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:149449493 C>T maps to NM_005211.3 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:2830667 G>T maps to NM_033225.5 S2965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:2830667 G>T maps to NM_033225.5 S2965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:20944577 G>A maps to NM_017539.1 G4083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:20944577 G>A maps to NM_017539.1 G4083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:129152930 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:129152930 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:105405182 G>A maps to NM_001385.2 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:105405182 G>A maps to NM_001385.2 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:13702490 G>T maps to NM_018027.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:13702490 G>T maps to NM_018027.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:128200778 G>A maps to NM_032638.4 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:128200778 G>A maps to NM_032638.4 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153789862 G>A maps to NM_020699.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153789862 G>A maps to NM_020699.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:35260117 C>A maps to NM_002060.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:35260117 C>A maps to NM_002060.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:45476309 C>A maps to NM_024602.5 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:45476309 C>A maps to NM_024602.5 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:27100921 C>G maps to NM_021064.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:27100921 C>G maps to NM_021064.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:67795268 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:67795268 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:31336930 G>T maps to NM_001145808.1 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:31336930 G>T maps to NM_001145808.1 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:6042383 G>A maps to NM_001099433.1 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:6042383 G>A maps to NM_001099433.1 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:63416869 C>G maps to NM_139318.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:63416869 C>G maps to NM_139318.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:88658610 C>A maps to NM_138318.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:88658610 C>A maps to NM_138318.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:36611947 G>C maps to NM_014657.1 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:36611947 G>C maps to NM_014657.1 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:5463460 G>A maps to NM_015325.1 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:5463460 G>A maps to NM_015325.1 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:93962755 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:93962755 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:43005457 C>A maps to ENST00000438933 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:43005457 C>A maps to ENST00000438933 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:18809214 G>T maps to NM_152375.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:18809214 G>T maps to NM_152375.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:239056487 C>T maps to NM_198582.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:239056487 C>T maps to NM_198582.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:52910539 C>T maps to NM_000424.3 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:52910539 C>T maps to NM_000424.3 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:31797798 G>T maps to NM_181622.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:31797798 G>T maps to NM_181622.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:35773815 G>T maps to NM_182548.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:35773815 G>T maps to NM_182548.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:25755957 G>A maps to NM_001135772.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:25755957 G>A maps to NM_001135772.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:129902309 C>A maps to NM_002417.4 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:129902309 C>A maps to NM_002417.4 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:36228978 C>T maps to NM_014727.1 R2587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:36228978 C>T maps to NM_014727.1 R2587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:31222753 C>T maps to NM_014967.4 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:31222753 C>T maps to NM_014967.4 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1102475 C>A maps to ENST00000441003 A2620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1102475 C>A maps to ENST00000441003 A2620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:23894912 G>A maps to NM_000257.2 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:23894912 G>A maps to NM_000257.2 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:145362114 G>A maps to NM_001039703.4 L3141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:145362114 G>A maps to NM_001039703.4 L3141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:19338711 C>T maps to NM_004386.2 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:19338711 C>T maps to NM_004386.2 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:94171717 C>T maps to NM_005384.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:94171717 C>T maps to NM_005384.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:236176843 G>T maps to NM_002508.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:236176843 G>T maps to NM_002508.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:56565063 G>A maps to NM_153447.4 R1063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:56565063 G>A maps to NM_153447.4 R1063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:183594201 G>T maps to NM_001080477.1 G386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:183594201 G>T maps to NM_001080477.1 G386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:53624884 T>A maps to NM_006418.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:53624884 T>A maps to NM_006418.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15918598 G>A maps to NM_013940.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15918598 G>A maps to NM_013940.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15839101 C>T maps to NM_013939.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15839101 C>T maps to NM_013939.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:125273574 G>A maps to ENST00000444856 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:125273574 G>A maps to ENST00000444856 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:55371294 A>T maps to NM_001004700.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:55371294 A>T maps to NM_001004700.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:5443759 C>T maps to NM_001004757.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:5443759 C>T maps to NM_001004757.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:56344618 A>T maps to NM_001004741.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:56344618 A>T maps to NM_001004741.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:127251681 G>A maps to NM_006193.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:127251681 G>A maps to NM_006193.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:91873722 C>A maps to NM_032968.3 V1276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:91873722 C>A maps to NM_032968.3 V1276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:140175811 T>C maps to NM_018905.2 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:140175811 T>C maps to NM_018905.2 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:56138619 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:56138619 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:71542903 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:71542903 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:527725 G>T maps to NM_001127178.1 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:527725 G>T maps to NM_001127178.1 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:98363771 G>A maps to NM_152309.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:98363771 G>A maps to NM_152309.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:81187864 G>T maps to NM_052892.3 R1402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:81187864 G>T maps to NM_052892.3 R1402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:67319225 G>T maps to NM_001129729.1 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:67319225 G>T maps to NM_001129729.1 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:22890695 A>G maps to NM_206954.1 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:22890695 A>G maps to NM_206954.1 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:48777167 G>A maps to NM_006904.6 F1839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:48777167 G>A maps to NM_006904.6 F1839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:50102992 C>T maps to NM_020719.1 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:50102992 C>T maps to NM_020719.1 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43430162 G>C maps to NM_002783.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43430162 G>C maps to NM_002783.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:110852593 G>A maps to NM_015480.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:110852593 G>A maps to NM_015480.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:241262062 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:241262062 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:107209054 G>C maps to ENST00000392837 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:107209054 G>C maps to ENST00000392837 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34102735 C>G maps to NM_001036.3 S3361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34102735 C>G maps to NM_001036.3 S3361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:92763289 T>C maps to NM_152703.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:92763289 T>C maps to NM_152703.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:76994154 G>A maps to ENST00000324767 Q818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:76994154 G>A maps to ENST00000324767 Q818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:196612171 G>T maps to NM_152699.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:196612171 G>T maps to NM_152699.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:30974842 A>T maps to NM_014712.1 K203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:30974842 A>T maps to NM_014712.1 K203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:26706650 C>T maps to NM_021115.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:26706650 C>T maps to NM_021115.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:162372582 A>G maps to NM_053282.4 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:162372582 A>G maps to NM_053282.4 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:92922950 G>A maps to NM_153646.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:92922950 G>A maps to NM_153646.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79219673 C>T maps to NM_001037984.1 Q1014Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79219673 C>T maps to NM_001037984.1 Q1014Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79249933 G>T maps to NM_001037984.1 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79249933 G>T maps to NM_001037984.1 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:57258836 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:57258836 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:70634944 C>A maps to NM_183002.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:70634944 C>A maps to NM_183002.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:144469214 T>C maps to NM_003601.2 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:144469214 T>C maps to NM_003601.2 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:90743426 A>T maps to NM_001146055.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:90743426 A>T maps to NM_001146055.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:53722568 C>G maps to NM_001173467.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:53722568 C>G maps to NM_001173467.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:158596790 G>A maps to NM_003126.2 Q1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:158596790 G>A maps to NM_003126.2 Q1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:41019338 C>T maps to NM_020971.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:41019338 C>T maps to NM_020971.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:62174735 C>T maps to NM_080823.2 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:62174735 C>T maps to NM_080823.2 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:53045645 G>T maps to NM_014682.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:53045645 G>T maps to NM_014682.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229738447 G>A maps to NM_014409.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229738447 G>A maps to NM_014409.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:150477144 C>T maps to NM_025150.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:150477144 C>T maps to NM_025150.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:97870216 G>T maps to ENST00000379795 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:97870216 G>T maps to ENST00000379795 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:20850849 C>A maps to NM_007110.4 E1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:20850849 C>A maps to NM_007110.4 E1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56679775 C>G maps to ENST00000240361 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56679775 C>G maps to ENST00000240361 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:120476466 G>A maps to NM_138554.3 W687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:120476466 G>A maps to NM_138554.3 W687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:41162311 G>T maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:41162311 G>T maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:14498687 C>A maps to NM_007118.2 Y2757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:14498687 C>A maps to NM_007118.2 Y2757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:38266166 G>T maps to NM_003306.1 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:38266166 G>T maps to NM_003306.1 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:215847653 T>C maps to ENST00000366943 S4533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:215847653 T>C maps to ENST00000366943 S4533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:55598340 G>A maps to NM_015306.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:55598340 G>A maps to NM_015306.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:95645843 A>G maps to NM_017599.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:95645843 A>G maps to NM_017599.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:108604017 G>C maps to ENST00000261400 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:108604017 G>C maps to ENST00000261400 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:75248654 G>T maps to NM_019589.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:75248654 G>T maps to NM_019589.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:112878168 C>G maps to NM_022828.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:112878168 C>G maps to NM_022828.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:77618057 C>A maps to NM_024721.4 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:77618057 C>A maps to NM_024721.4 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:42729558 T>G maps to NM_022473.1 P1516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:42729558 T>G maps to NM_022473.1 P1516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:57647095 T>C maps to NM_052882.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:57647095 T>C maps to NM_052882.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:30935347 C>T maps to NM_014717.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:30935347 C>T maps to NM_014717.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:59390 C>A maps to NM_182524.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:59390 C>A maps to NM_182524.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:52856948 C>T maps to NM_001161425.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:52856948 C>T maps to NM_001161425.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:5456194 G>T maps to NM_181710.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:5456194 G>T maps to NM_181710.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:12785390 C>T maps to NM_001103170.1 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:12785390 C>T maps to NM_001103170.1 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:66980198 C>A maps to NM_080283.3 L1499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:66980198 C>A maps to NM_080283.3 L1499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:48162468 G>T maps to NM_033226.2 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:48162468 G>T maps to NM_033226.2 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:135628550 C>G maps to NM_138326.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:135628550 C>G maps to NM_138326.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:8418140 C>T maps to NM_003501.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:8418140 C>T maps to NM_003501.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20448430 C>A maps to NM_017888.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20448430 C>A maps to NM_017888.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8807929 G>T maps to NM_178525.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8807929 G>T maps to NM_178525.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:114699824 G>T maps to NM_005721.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:114699824 G>T maps to NM_005721.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:127185555 G>T maps to NM_138289.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:127185555 G>T maps to NM_138289.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:26721658 G>T maps to ENST00000356368 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:26721658 G>T maps to ENST00000356368 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:76202118 C>T maps to NM_001145526.1 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:76202118 C>T maps to NM_001145526.1 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:45402210 G>T maps to NM_001037553.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:45402210 G>T maps to NM_001037553.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:186338718 G>T maps to ENST00000273784 *369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:186338718 G>T maps to ENST00000273784 *369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15483985 C>T maps to NM_005858.2 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15483985 C>T maps to NM_005858.2 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:125877312 C>A maps to ENST00000273450 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:125877312 C>A maps to ENST00000273450 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:29416584 G>T maps to NM_004304.3 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:29416584 G>T maps to NM_004304.3 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:85677429 C>A maps to NM_006982.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:85677429 C>A maps to NM_006982.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:71384524 C>T maps to NM_212557.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:71384524 C>T maps to NM_212557.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41543691 G>T maps to ENST00000415018 I1456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41543691 G>T maps to ENST00000415018 I1456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:16666730 C>A maps to NM_020319.2 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:16666730 C>A maps to NM_020319.2 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:145563068 C>A maps to NM_144698.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:145563068 C>A maps to NM_144698.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:101552506 C>T maps to ENST00000375018 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:101552506 C>T maps to ENST00000375018 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:5724380 G>T maps to ENST00000356134 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:5724380 G>T maps to ENST00000356134 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:22296137 A>T maps to NM_213599.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:22296137 A>T maps to NM_213599.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:165118374 C>A maps to NM_012403.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:165118374 C>A maps to NM_012403.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:90347592 C>T maps to NM_001150.2 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:90347592 C>T maps to NM_001150.2 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:40997102 G>T maps to NM_009590.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:40997102 G>T maps to NM_009590.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:41001304 C>G maps to NM_009590.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:41001304 C>G maps to NM_009590.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:16338501 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:16338501 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:21238275 G>T maps to NM_000384.2 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:21238275 G>T maps to NM_000384.2 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:27105666 G>T maps to NM_006015.4 E1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:27105666 G>T maps to NM_006015.4 E1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:35723371 G>A maps to ENST00000458225 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:35723371 G>A maps to ENST00000458225 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3682644 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3682644 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:132400146 G>C maps to NM_017873.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:132400146 G>C maps to NM_017873.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:197072367 T>G maps to NM_018136.4 R2005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:197072367 T>G maps to NM_018136.4 R2005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:31325262 A>T maps to NM_030632.1 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:31325262 A>T maps to NM_030632.1 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:175986269 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:175986269 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:10574811 T>C maps to NM_024997.2 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:10574811 T>C maps to NM_024997.2 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:108153532 C>T maps to NM_000051.3 Q1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:108153532 C>T maps to NM_000051.3 Q1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:182605387 C>T maps to NM_014616.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:182605387 C>T maps to NM_014616.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36050769 G>A maps to NM_000704.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36050769 G>A maps to NM_000704.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:90661410 A>G maps to NM_001170794.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:90661410 A>G maps to NM_001170794.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:40751730 G>T maps to NM_014952.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:40751730 G>T maps to NM_014952.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31599435 G>T maps to NM_080686.2 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31599435 G>T maps to NM_080686.2 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:76742008 C>A maps to NM_024685.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:76742008 C>A maps to NM_024685.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:6929780 G>T maps to NM_181844.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:6929780 G>T maps to NM_181844.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:32740257 A>T maps to NM_016252.3 S3590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:32740257 A>T maps to NM_016252.3 S3590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:34182961 G>A maps to NM_133468.3 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:34182961 G>A maps to NM_133468.3 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:43288496 G>T maps to NM_014753.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:43288496 G>T maps to NM_014753.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:112991431 G>A maps to ENST00000273395 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:112991431 G>A maps to ENST00000273395 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:59820496 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:59820496 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:21784771 C>A maps to NM_001010911.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:21784771 C>A maps to NM_001010911.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:124457440 C>A maps to NM_001010912.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:124457440 C>A maps to NM_001010912.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:557580 G>A maps to NM_173573.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:557580 G>A maps to NM_173573.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:103338685 G>A maps to NM_001010977.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:103338685 G>A maps to NM_001010977.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:50550443 G>A maps to NM_001014830.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:50550443 G>A maps to NM_001014830.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:40678593 C>A maps to NM_033286.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:40678593 C>A maps to NM_033286.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:37578326 C>A maps to NM_182486.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:37578326 C>A maps to NM_182486.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:32546304 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:32546304 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:24406433 C>T maps to NM_001040710.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:24406433 C>T maps to NM_001040710.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:47543342 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:47543342 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:100458875 T>A maps to NM_032149.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:100458875 T>A maps to NM_032149.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:175716847 G>C maps to ENST00000443967 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:175716847 G>C maps to ENST00000443967 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:41181562 C>A maps to NM_001115131.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:41181562 C>A maps to NM_001115131.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:165711482 G>T maps to NM_144980.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:165711482 G>T maps to NM_144980.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:104238431 C>A maps to NM_032342.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:104238431 C>A maps to NM_032342.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:116191476 C>A maps to ENST00000451722 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:116191476 C>A maps to ENST00000451722 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87921827 C>T maps to NM_001739.1 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87921827 C>T maps to NM_001739.1 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:181705561 C>T maps to ENST00000357570 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:181705561 C>T maps to ENST00000357570 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:62751547 C>A maps to ENST00000383709 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:62751547 C>A maps to ENST00000383709 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:30975917 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:30975917 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:26526437 C>A maps to NM_198137.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:26526437 C>A maps to NM_198137.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:219893020 G>T maps to NM_194302.2 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:219893020 G>T maps to NM_194302.2 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:219894145 C>T maps to NM_194302.2 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:219894145 C>T maps to NM_194302.2 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31592659 G>T maps to NM_194300.2 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31592659 G>T maps to NM_194300.2 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31617852 A>G maps to NM_194300.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31617852 A>G maps to NM_194300.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:3669281 G>T maps to NM_152492.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:3669281 G>T maps to NM_152492.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:43111811 A>T maps to NM_001080850.2 K633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:43111811 A>T maps to NM_001080850.2 K633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:180366129 C>A maps to NM_181426.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:180366129 C>A maps to NM_181426.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:23066262 C>T maps to NM_012072.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:23066262 C>T maps to NM_012072.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:23066265 G>T maps to NM_012072.3 C188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:23066265 G>T maps to NM_012072.3 C188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:59206353 C>A maps to NM_031891.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:59206353 C>A maps to NM_031891.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:80638383 C>T maps to NM_152342.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:80638383 C>T maps to NM_152342.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:27016113 G>T maps to NM_001809.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:27016113 G>T maps to NM_001809.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:196654311 G>T maps to NM_000186.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:196654311 G>T maps to NM_000186.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:87796105 C>A maps to NM_000735.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:87796105 C>A maps to NM_000735.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:6196656 C>G maps to NM_015557.2 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:6196656 C>G maps to NM_015557.2 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120146112 C>A maps to ENST00000392521 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120146112 C>A maps to ENST00000392521 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120221782 C>A maps to ENST00000392521 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120221782 C>A maps to ENST00000392521 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:130941552 G>A maps to NM_012127.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:130941552 G>A maps to NM_012127.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:170140989 C>A maps to NM_005602.5 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:170140989 C>A maps to NM_005602.5 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10226011 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10226011 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:157233055 C>A maps to NM_001195555.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:157233055 C>A maps to NM_001195555.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:70713109 G>T maps to NM_014515.5 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:70713109 G>T maps to NM_014515.5 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:99715817 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:99715817 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46888411 G>T maps to ENST00000359759 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46888411 G>T maps to ENST00000359759 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:61951686 C>A maps to ENST00000326996 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:61951686 C>A maps to ENST00000326996 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:55924960 C>A maps to NM_030820.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:55924960 C>A maps to NM_030820.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:111121562 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:111121562 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137664634 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137664634 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:238303367 C>A maps to NM_004369.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:238303367 C>A maps to NM_004369.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:130282041 T>C maps to NM_001102608.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:130282041 T>C maps to NM_001102608.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:3691446 C>T maps to ENST00000418971 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:3691446 C>T maps to ENST00000418971 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:197396582 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:197396582 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:43910879 C>A maps to NM_001145146.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:43910879 C>A maps to NM_001145146.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:26995454 C>T maps to NM_001887.3 *253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:26995454 C>T maps to NM_001887.3 *253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:27008145 G>A maps to NM_001887.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:27008145 G>A maps to NM_001887.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:104390388 T>A maps to NM_138455.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:104390388 T>A maps to NM_138455.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:49032884 C>A maps to NM_025087.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:49032884 C>A maps to NM_025087.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:45051244 C>T maps to NM_176819.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:45051244 C>T maps to NM_176819.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:36122804 A>T maps to NM_173695.2 K348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:36122804 A>T maps to NM_173695.2 K348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32006973 C>T maps to NM_000500.5 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32006973 C>T maps to NM_000500.5 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:65537044 C>A maps to NM_004820.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:65537044 C>A maps to NM_004820.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:242707189 G>T maps to NM_152783.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:242707189 G>T maps to NM_152783.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:136501726 G>T maps to NM_000787.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:136501726 G>T maps to NM_000787.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:125685885 C>A maps to NM_178470.4 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:125685885 C>A maps to NM_178470.4 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:50936981 A>C maps to NM_005215.3 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:50936981 A>C maps to NM_005215.3 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:6662547 C>A maps to NM_003737.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:6662547 C>A maps to NM_003737.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49239370 G>A maps to NM_004818.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49239370 G>A maps to NM_004818.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:134703356 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:134703356 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:74116136 C>A maps to NM_018665.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:74116136 C>A maps to NM_018665.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:29847347 G>T maps to NM_001037730.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:29847347 G>T maps to NM_001037730.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:31566470 C>T maps to NM_144973.3 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:31566470 C>T maps to NM_144973.3 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47987385 G>T maps to ENST00000318711 E1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47987385 G>T maps to ENST00000318711 E1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:96637037 C>G maps to NM_005222.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:96637037 C>G maps to NM_005222.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:78350087 C>A maps to NM_013391.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:78350087 C>A maps to NM_013391.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:847034 G>T maps to NM_021951.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:847034 G>T maps to NM_021951.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:38980321 T>A maps to ENST00000327475 T4529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:38980321 T>A maps to ENST00000327475 T4529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30021411 C>T maps to NM_003586.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30021411 C>T maps to NM_003586.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:73219971 C>A maps to NM_012074.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:73219971 C>A maps to NM_012074.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:28662235 T>A maps to ENST00000438199 K424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:28662235 T>A maps to ENST00000438199 K424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:56371470 T>A maps to ENST00000361203 I6241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:56371470 T>A maps to ENST00000361203 I6241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:45400284 G>T maps to NM_014080.4 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:45400284 G>T maps to NM_014080.4 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:102446175 C>T maps to NM_001376.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:102446175 C>T maps to NM_001376.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:102992158 A>T maps to NM_001080463.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:102992158 A>T maps to NM_001080463.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:131755542 G>C maps to ENST00000355311 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:131755542 G>C maps to ENST00000355311 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:43637202 G>A maps to NM_001159936.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:43637202 G>A maps to NM_001159936.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:127611310 G>C maps to NM_001139510.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:127611310 G>C maps to NM_001139510.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:71497576 C>A maps to NM_031889.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:71497576 C>A maps to NM_031889.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:66280038 G>T maps to NM_004439.5 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:66280038 G>T maps to NM_004439.5 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:134898708 A>T maps to NM_004441.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:134898708 A>T maps to NM_004441.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:134920488 C>G maps to NM_004441.4 Y768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:134920488 C>G maps to NM_004441.4 Y768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:43462493 G>T maps to NM_001002264.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:43462493 G>T maps to NM_001002264.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50736570 C>A maps to ENST00000515869 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50736570 C>A maps to ENST00000515869 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:72184100 G>T maps to NM_000503.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:72184100 G>T maps to NM_000503.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:131520420 C>A maps to NM_001105195.1 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:131520420 C>A maps to NM_001105195.1 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:37028189 T>C maps to NM_001013736.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:37028189 T>C maps to NM_001013736.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45943049 C>A maps to ENST00000348697 Y469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45943049 C>A maps to ENST00000348697 Y469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8196579 C>A maps to NM_032447.3 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8196579 C>A maps to NM_032447.3 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:48059589 C>A maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:48059589 C>A maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137801874 G>T maps to NM_002003.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137801874 G>T maps to NM_002003.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137809690 G>T maps to NM_002003.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137809690 G>T maps to NM_002003.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157555976 C>G maps to NM_031282.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157555976 C>G maps to NM_031282.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:155487753 C>T maps to NM_005141.4 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:155487753 C>T maps to NM_005141.4 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:152279054 C>T maps to NM_002016.1 Q2769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:152279054 C>T maps to NM_002016.1 Q2769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:28959103 G>T maps to NM_002019.4 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:28959103 G>T maps to NM_002019.4 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:109270512 G>T maps to NM_001144937.1 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:109270512 G>T maps to NM_001144937.1 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:89403611 G>A maps to NM_153696.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:89403611 G>A maps to NM_153696.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:52272798 C>A maps to NM_001005738.1 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:52272798 C>A maps to NM_001005738.1 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:14868958 C>T maps to ENST00000380880 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:14868958 C>T maps to ENST00000380880 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:39435605 G>T maps to NM_207361.4 E2520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:39435605 G>T maps to NM_207361.4 E2520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:100183081 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:100183081 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32783212 G>T maps to NM_023037.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32783212 G>T maps to NM_023037.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:49190599 C>A maps to NM_000145.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:49190599 C>A maps to NM_000145.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:31168709 C>A maps to NM_024572.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:31168709 C>A maps to NM_024572.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:11314628 C>A maps to NM_198516.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:11314628 C>A maps to NM_198516.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:128061358 C>A maps to NM_015635.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:128061358 C>A maps to NM_015635.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9830017 G>T maps to NM_201433.1 C318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9830017 G>T maps to NM_201433.1 C318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:35738835 C>T maps to NM_020944.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:35738835 C>T maps to NM_020944.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31014633 G>T maps to NM_000823.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31014633 G>T maps to NM_000823.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:150416162 G>T maps to NM_130759.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:150416162 G>T maps to NM_130759.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:121744023 G>C maps to NM_005270.4 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:121744023 G>C maps to NM_005270.4 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:56388844 C>A maps to NM_020988.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:56388844 C>A maps to NM_020988.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57430251 G>A maps to NM_080425.2 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57430251 G>A maps to NM_080425.2 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:38034453 G>A maps to NM_013285.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:38034453 G>A maps to NM_013285.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:34884874 G>T maps to NM_000175.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:34884874 G>T maps to NM_000175.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:236341795 G>T maps to NM_003272.3 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:236341795 G>T maps to NM_003272.3 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20043323 G>T maps to NM_001002911.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20043323 G>T maps to NM_001002911.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51274315 C>T maps to NM_001506.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51274315 C>T maps to NM_001506.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51274423 G>T maps to NM_001506.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51274423 G>T maps to NM_001506.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:41586497 C>T maps to NM_080817.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:41586497 C>T maps to NM_080817.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:90012411 C>A maps to NM_032119.3 R3105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:90012411 C>A maps to NM_032119.3 R3105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:47000058 G>T maps to NM_014696.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:47000058 G>T maps to NM_014696.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54456890 C>T maps to NM_001008397.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54456890 C>T maps to NM_001008397.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:153182037 C>T maps to NM_001114183.1 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:153182037 C>T maps to NM_001114183.1 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:37267484 G>T maps to NM_000831.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:37267484 G>T maps to NM_000831.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:37291208 G>A maps to NM_000831.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:37291208 G>A maps to NM_000831.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:13719973 G>T maps to NM_000834.3 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:13719973 G>T maps to NM_000834.3 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:14547154 C>T maps to ENST00000507975 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:14547154 C>T maps to ENST00000507975 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:33996101 C>G maps to NM_000841.1 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:33996101 C>G maps to NM_000841.1 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:88330420 T>C maps to NM_001143831.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:88330420 T>C maps to NM_001143831.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:13243461 G>A maps to NM_001080555.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:13243461 G>A maps to NM_001080555.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:27476637 G>A maps to NM_001520.3 F1766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:27476637 G>A maps to NM_001520.3 F1766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:14778849 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:14778849 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:5290848 C>A maps to NM_005330.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:5290848 C>A maps to NM_005330.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30659584 G>A maps to NM_002110.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30659584 G>A maps to NM_002110.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36394805 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36394805 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:43484003 G>A maps to NM_015052.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:43484003 G>A maps to NM_015052.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:91818089 C>T maps to NM_001017975.3 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:91818089 C>T maps to NM_001017975.3 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:139416275 C>G maps to NM_022740.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:139416275 C>G maps to NM_022740.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:1748975 A>T maps to ENST00000382711 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:1748975 A>T maps to ENST00000382711 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:60328549 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:60328549 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:54405719 C>A maps to NM_016126.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:54405719 C>A maps to NM_016126.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:87725345 G>A maps to NM_000865.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:87725345 G>A maps to NM_000865.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:113860403 G>T maps to NM_213621.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:113860403 G>T maps to NM_213621.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:8307700 C>A maps to NM_053044.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:8307700 C>A maps to NM_053044.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:47118739 G>C maps to NM_006546.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:47118739 G>C maps to NM_006546.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:151163171 T>A maps to NM_178822.4 K1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:151163171 T>A maps to NM_178822.4 K1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67816659 C>T maps to NM_001559.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67816659 C>T maps to NM_001559.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:103013213 G>A maps to NM_003855.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:103013213 G>A maps to NM_003855.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67705956 C>A maps to NM_144701.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67705956 C>A maps to NM_144701.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:27373905 C>T maps to NM_000418.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:27373905 C>T maps to NM_000418.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:62582841 C>G maps to NM_176877.2 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:62582841 C>G maps to NM_176877.2 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:99169338 C>T maps to NM_001134224.1 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:99169338 C>T maps to NM_001134224.1 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:44429989 A>C maps to NM_014652.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:44429989 A>C maps to NM_014652.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:227663166 C>A maps to NM_005544.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:227663166 C>A maps to NM_005544.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:107977663 G>T maps to NM_003604.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:107977663 G>T maps to NM_003604.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:145539089 C>T maps to NM_003637.3 N1010N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:145539089 C>T maps to NM_003637.3 N1010N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:52816057 C>A maps to NM_002215.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:52816057 C>A maps to NM_002215.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:7786919 C>T maps to NM_002216.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:7786919 C>T maps to NM_002216.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:35199147 G>T maps to NM_003024.2 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:35199147 G>T maps to NM_003024.2 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:17937596 G>A maps to NM_000215.3 F1110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:17937596 G>A maps to NM_000215.3 F1110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87677996 C>T maps to NM_020655.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87677996 C>T maps to NM_020655.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87678561 G>T maps to NM_020655.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87678561 G>T maps to NM_020655.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:111060305 C>T maps to NM_005549.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:111060305 C>T maps to NM_005549.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:5021977 C>A maps to NM_000217.2 C478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:5021977 C>A maps to NM_000217.2 C478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:170145846 C>T maps to NM_001034837.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:170145846 C>T maps to NM_001034837.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:215259912 G>A maps to NM_001017425.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:215259912 G>A maps to NM_001017425.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:202715448 T>A maps to ENST00000367264 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:202715448 T>A maps to ENST00000367264 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:22624353 C>A maps to ENST00000446597 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:22624353 C>A maps to ENST00000446597 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:2604049 C>A maps to NM_015229.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:2604049 C>A maps to NM_015229.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:8824924 G>T maps to ENST00000456698 G1458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:8824924 G>T maps to ENST00000456698 G1458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:95508629 C>A maps to NM_015496.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:95508629 C>A maps to NM_015496.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138536985 C>A maps to NM_001164665.1 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138536985 C>A maps to NM_001164665.1 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1920389 C>G maps to ENST00000434971 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1920389 C>G maps to ENST00000434971 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:36841716 A>T maps to NM_001029864.1 P1110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:36841716 A>T maps to NM_001029864.1 P1110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:28058002 T>A maps to NM_031217.3 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:28058002 T>A maps to NM_031217.3 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36350478 C>A maps to NM_199180.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36350478 C>A maps to NM_199180.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36352121 G>T maps to NM_199180.2 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36352121 G>T maps to NM_199180.2 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:202878153 C>T maps to NM_021633.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:202878153 C>T maps to NM_021633.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:32626213 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:32626213 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:38953455 C>A maps to NM_181535.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:38953455 C>A maps to NM_181535.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52911460 C>A maps to NM_000424.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52911460 C>A maps to NM_000424.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52845378 C>A maps to NM_005555.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52845378 C>A maps to NM_005555.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52992866 C>A maps to NM_080747.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52992866 C>A maps to NM_080747.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:39316799 G>A maps to NM_032524.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:39316799 G>A maps to NM_032524.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:155145211 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:155145211 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153130871 G>T maps to NM_000425.3 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153130871 G>T maps to NM_000425.3 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:6961755 G>T maps to NM_005559.2 P2485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:6961755 G>T maps to NM_005559.2 P2485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:7079971 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:7079971 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:60892795 C>A maps to NM_005560.3 L2426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:60892795 C>A maps to NM_005560.3 L2426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:50529759 G>A maps to NM_147190.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:50529759 G>A maps to NM_147190.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:18436750 C>G maps to NM_017448.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:18436750 C>G maps to NM_017448.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49491725 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49491725 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:82456309 C>G maps to ENST00000370717 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:82456309 C>G maps to ENST00000370717 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:85985201 C>A maps to NM_001017924.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:85985201 C>A maps to NM_001017924.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141299534 T>A maps to NM_018557.2 I2400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141299534 T>A maps to NM_018557.2 I2400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141473548 C>A maps to NM_018557.2 E2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141473548 C>A maps to NM_018557.2 E2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:133644984 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:133644984 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:77746568 G>T maps to NM_001134745.1 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:77746568 G>T maps to NM_001134745.1 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:34263781 G>A maps to NM_020426.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:34263781 G>A maps to NM_020426.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:39888556 G>A maps to ENST00000361689 Q3316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:39888556 G>A maps to ENST00000361689 Q3316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:26213126 A>T maps to NM_173523.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:26213126 A>T maps to NM_173523.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:140967166 C>A maps to NM_138702.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:140967166 C>A maps to NM_138702.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:20062498 C>A maps to NM_001168465.1 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:20062498 C>A maps to NM_001168465.1 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:217124199 G>T maps to NM_020814.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:217124199 G>T maps to NM_020814.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:10423936 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:10423936 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:220791839 C>T maps to NM_018650.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:220791839 C>T maps to NM_018650.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:74778253 C>A maps to NM_001025101.1 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:74778253 C>A maps to NM_001025101.1 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:127336222 G>C maps to NM_004526.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:127336222 G>C maps to NM_004526.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:94248657 T>A maps to NM_024717.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:94248657 T>A maps to NM_024717.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:37620024 G>A maps to ENST00000297153 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:37620024 G>A maps to ENST00000297153 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:116428864 C>A maps to NM_015335.4 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:116428864 C>A maps to NM_015335.4 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:126674905 C>A maps to NM_032446.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:126674905 C>A maps to NM_032446.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:55525858 G>T maps to NM_004530.4 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:55525858 G>T maps to NM_004530.4 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:55530858 G>A maps to NM_004530.4 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:55530858 G>A maps to NM_004530.4 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:90857617 A>G maps to NM_007351.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:90857617 A>G maps to NM_007351.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:30602882 T>C maps to ENST00000358107 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:30602882 T>C maps to ENST00000358107 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:9065902 T>A maps to NM_024690.2 T7181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:9065902 T>A maps to NM_024690.2 T7181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:10547772 C>T maps to NM_002470.2 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:10547772 C>T maps to NM_002470.2 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:101256814 G>A maps to NM_138403.4 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:101256814 G>A maps to NM_138403.4 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:2749381 A>G maps to NM_001012418.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:2749381 A>G maps to NM_001012418.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:123452993 C>A maps to NM_053025.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:123452993 C>A maps to NM_053025.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:192194696 A>T maps to NM_001130158.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:192194696 A>T maps to NM_001130158.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:59494606 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:59494606 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:89907011 G>T maps to NM_005467.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:89907011 G>T maps to NM_005467.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101717914 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101717914 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101944673 G>C maps to NM_052867.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101944673 G>C maps to NM_052867.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:10548348 A>G maps to NM_003826.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:10548348 A>G maps to NM_003826.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:78513203 T>A maps to NM_014903.4 S1076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:78513203 T>A maps to NM_014903.4 S1076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:22370901 C>T maps to NM_004540.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:22370901 C>T maps to NM_004540.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:158482645 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:158482645 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:183902767 G>A maps to NM_205842.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:183902767 G>A maps to NM_205842.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15790759 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15790759 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:58541756 C>A maps to NM_001130487.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:58541756 C>A maps to NM_001130487.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:233898902 G>T maps to NM_005383.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:233898902 G>T maps to NM_005383.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:204951080 C>T maps to ENST00000367172 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:204951080 C>T maps to ENST00000367172 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:7982525 C>A maps to NM_176821.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:7982525 C>A maps to NM_176821.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:56369119 C>T maps to NM_134444.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:56369119 C>T maps to NM_134444.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:120478158 C>T maps to NM_024408.2 Q1197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:120478158 C>T maps to NM_024408.2 Q1197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:5967249 C>A maps to NM_015102.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:5967249 C>A maps to NM_015102.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:11918460 G>A maps to NM_002521.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:11918460 G>A maps to NM_002521.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:24324909 C>T maps to NM_000905.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:24324909 C>T maps to NM_000905.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:84733611 C>A maps to ENST00000404547 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:84733611 C>A maps to ENST00000404547 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:79270161 C>T maps to NM_004796.4 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:79270161 C>T maps to NM_004796.4 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:18745190 G>A maps to ENST00000455492 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:18745190 G>A maps to ENST00000455492 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:229588381 C>A maps to NM_018230.2 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:229588381 C>A maps to NM_018230.2 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:50412419 G>T maps to NM_012346.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:50412419 G>T maps to NM_012346.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:120097703 A>G maps to NM_178507.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:120097703 A>G maps to NM_178507.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:13785313 C>T maps to NM_003611.2 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:13785313 C>T maps to NM_003611.2 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:123886967 C>A maps to NM_001004462.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:123886967 C>A maps to NM_001004462.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:159283597 A>G maps to NM_001004467.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:159283597 A>G maps to NM_001004467.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20666363 C>A maps to NM_001005503.1 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20666363 C>A maps to NM_001005503.1 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:247751879 C>A maps to NM_001001915.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:247751879 C>A maps to NM_001001915.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:29079940 G>T maps to NM_001005216.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:29079940 G>T maps to NM_001005216.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55136381 G>A maps to NM_001005275.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55136381 G>A maps to NM_001005275.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:102358679 T>A maps to NM_001001674.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:102358679 T>A maps to NM_001001674.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20404274 G>A maps to NM_001004063.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20404274 G>A maps to NM_001004063.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20344995 G>C maps to NM_001005501.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20344995 G>C maps to NM_001005501.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20248993 C>A maps to NM_001005500.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:20248993 C>A maps to NM_001005500.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55541278 T>C maps to NM_001001967.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55541278 T>C maps to NM_001001967.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:97887788 G>A maps to NM_001005515.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:97887788 G>A maps to NM_001005515.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55944329 C>A maps to NM_001005492.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55944329 C>A maps to NM_001005492.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55944911 G>T maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55944911 G>T maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158669884 C>G maps to NM_001005279.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158669884 C>G maps to NM_001005279.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:21109499 C>T maps to NM_001001968.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:21109499 C>T maps to NM_001001968.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158517592 G>T maps to NM_001005189.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158517592 G>T maps to NM_001005189.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:124413355 G>C maps to NM_001005195.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:124413355 G>C maps to NM_001005195.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:124095876 A>G maps to NM_001007249.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:124095876 A>G maps to NM_001007249.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:83992863 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:83992863 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:109571950 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:109571950 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21726421 C>A maps to ENST00000286149 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21726421 C>A maps to ENST00000286149 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17593245 C>A maps to NM_016233.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17593245 C>A maps to NM_016233.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:102361024 A>C maps to NM_000919.3 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:102361024 A>C maps to NM_000919.3 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:34690797 T>C maps to NM_019619.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:34690797 T>C maps to NM_019619.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:31812321 G>T maps to NM_001604.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:31812321 G>T maps to NM_001604.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:61985942 C>A maps to NM_022843.3 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:61985942 C>A maps to NM_022843.3 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140222066 C>A maps to NM_018911.2 C387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140222066 C>A maps to NM_018911.2 C387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140347670 A>T maps to NM_018899.5 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140347670 A>T maps to NM_018899.5 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140627194 C>A maps to NM_018935.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140627194 C>A maps to NM_018935.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140740130 C>G maps to NM_018923.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140740130 C>G maps to NM_018923.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:82579982 C>A maps to NM_033026.5 L3307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:82579982 C>A maps to NM_033026.5 L3307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47754561 A>T maps to NM_006031.5 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47754561 A>T maps to NM_006031.5 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47851462 G>A maps to NM_006031.5 E2695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47851462 G>A maps to NM_006031.5 E2695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:165801828 G>T maps to NM_001130690.1 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:165801828 G>T maps to NM_001130690.1 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:20766630 A>T maps to NM_000921.3 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:20766630 A>T maps to NM_000921.3 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:149264108 G>A maps to NM_000440.2 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:149264108 G>A maps to NM_000440.2 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:55139721 C>G maps to NM_006206.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:55139721 C>G maps to NM_006206.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:55140698 C>T maps to NM_006206.4 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:55140698 C>T maps to NM_006206.4 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:32089568 C>A maps to NM_178140.2 V2005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:32089568 C>A maps to NM_178140.2 V2005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:119043129 G>A maps to NM_173791.3 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:119043129 G>A maps to NM_173791.3 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:216914081 G>A maps to NM_018441.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:216914081 G>A maps to NM_018441.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57328675 A>G maps to NM_006210.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57328675 A>G maps to NM_006210.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57333090 C>A maps to NM_006210.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57333090 C>A maps to NM_006210.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60506076 C>T maps to NM_194449.2 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60506076 C>T maps to NM_194449.2 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:71697943 C>A maps to NM_015020.2 G615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:71697943 C>A maps to NM_015020.2 G615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:21157609 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:21157609 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:207111096 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:207111096 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:142836647 G>T maps to NM_002652.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:142836647 G>T maps to NM_002652.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:22210597 C>T maps to NM_001135721.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:22210597 C>T maps to NM_001135721.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:2168791 T>A maps to NM_001009944.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:2168791 T>A maps to NM_001009944.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:113822700 G>T maps to NM_173542.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:113822700 G>T maps to NM_173542.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145003951 G>A maps to NM_201380.2 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145003951 G>A maps to NM_201380.2 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:30092444 C>T maps to ENST00000440706 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:30092444 C>T maps to ENST00000440706 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:65209850 G>T maps to ENST00000394691 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:65209850 G>T maps to ENST00000394691 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:131913152 C>A maps to NM_020911.1 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:131913152 C>A maps to NM_020911.1 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:190660674 G>T maps to NM_000534.4 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:190660674 G>T maps to NM_000534.4 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:53103525 C>G maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:53103525 C>G maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:134394318 C>T maps to NM_007171.3 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:134394318 C>T maps to NM_007171.3 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:124532323 T>A maps to NM_015450.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:124532323 T>A maps to NM_015450.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:104357037 G>T maps to NM_147180.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:104357037 G>T maps to NM_147180.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:12837327 T>G maps to NM_001080830.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:12837327 T>G maps to NM_001080830.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:22890545 C>A maps to NM_206954.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:22890545 C>A maps to NM_206954.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:22892503 C>T maps to NM_206954.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:22892503 C>T maps to NM_206954.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:22899245 G>A maps to NM_206954.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:22899245 G>A maps to NM_206954.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186266033 C>G maps to NM_005807.3 Y9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186266033 C>G maps to NM_005807.3 Y9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:20429515 G>T maps to NM_005788.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:20429515 G>T maps to NM_005788.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:5294853 G>A maps to NM_144773.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:5294853 G>A maps to NM_144773.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:75330423 G>T maps to ENST00000445876 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:75330423 G>T maps to ENST00000445876 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:138724342 C>A maps to NM_001134659.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:138724342 C>A maps to NM_001134659.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:138762811 C>A maps to NM_001134657.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:138762811 C>A maps to NM_001134657.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:87076622 G>T maps to ENST00000276616 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:87076622 G>T maps to ENST00000276616 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:23512072 C>A maps to NM_001099780.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:23512072 C>A maps to NM_001099780.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:54125015 T>A maps to NM_014614.2 V1199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:54125015 T>A maps to NM_014614.2 V1199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:87679885 C>T maps to NM_080685.2 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:87679885 C>T maps to NM_080685.2 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:8376608 T>A maps to NM_002839.3 K1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:8376608 T>A maps to NM_002839.3 K1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:8524976 G>T maps to NM_002839.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:8524976 G>T maps to NM_002839.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55697268 C>G maps to NM_002842.3 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55697268 C>G maps to NM_002842.3 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:121651805 G>T maps to NM_002851.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:121651805 G>T maps to NM_002851.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:36614950 G>T maps to NM_000536.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:36614950 G>T maps to NM_000536.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:85799895 C>A maps to NM_001100391.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:85799895 C>A maps to NM_001100391.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:109352660 G>T maps to NM_006267.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:109352660 G>T maps to NM_006267.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48134465 G>C maps to NM_001098531.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48134465 G>C maps to NM_001098531.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65351718 C>T maps to NM_016563.2 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65351718 C>T maps to NM_016563.2 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:74447532 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:74447532 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65041693 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65041693 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:103138648 C>T maps to ENST00000428762 W2906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:103138648 C>T maps to ENST00000428762 W2906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:8425870 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:8425870 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53137993 T>A maps to NM_052859.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53137993 T>A maps to NM_052859.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:86007431 G>T maps to ENST00000358110 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:86007431 G>T maps to ENST00000358110 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:163122408 G>T maps to NM_003617.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:163122408 G>T maps to NM_003617.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:75517555 G>A maps to NM_001040456.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:75517555 G>A maps to NM_001040456.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:122217460 G>C maps to NM_019034.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:122217460 G>C maps to NM_019034.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:8132301 G>A maps to ENST00000309737 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:8132301 G>A maps to ENST00000309737 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10465813 C>A maps to NM_178857.5 E1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10465813 C>A maps to NM_178857.5 E1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:77402526 C>G maps to NM_198467.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:77402526 C>G maps to NM_198467.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:33937207 C>A maps to NM_016568.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:33937207 C>A maps to NM_016568.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:76757282 G>T maps to NM_171999.2 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:76757282 G>T maps to NM_171999.2 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:200173680 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:200173680 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:62025294 C>A maps to NM_000334.4 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:62025294 C>A maps to NM_000334.4 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:30857303 G>A maps to NM_174975.4 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:30857303 G>A maps to NM_174975.4 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:9337871 C>A maps to NM_003966.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:9337871 C>A maps to NM_003966.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:94772488 C>T maps to NM_001756.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:94772488 C>T maps to NM_001756.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:173883689 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:173883689 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:26688678 C>G maps to NM_021115.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:26688678 C>G maps to NM_021115.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:201448174 G>A maps to NM_152524.5 K1262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:201448174 G>A maps to NM_152524.5 K1262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:235950022 G>T maps to NM_014521.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:235950022 G>T maps to NM_014521.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:232596805 C>A maps to NM_020808.3 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:232596805 C>A maps to NM_020808.3 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160719713 G>T maps to NM_021181.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160719713 G>T maps to NM_021181.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:87770120 C>A maps to NM_197965.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:87770120 C>A maps to NM_197965.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51385986 G>A maps to NM_001174125.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51385986 G>A maps to NM_001174125.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51390649 C>A maps to NM_001174125.1 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51390649 C>A maps to NM_001174125.1 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:66267478 G>T maps to NM_004694.4 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:66267478 G>T maps to NM_004694.4 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:22397613 G>T maps to NM_020346.2 G421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:22397613 G>T maps to NM_020346.2 G421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:128302063 C>T maps to NM_001017372.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:128302063 C>T maps to NM_001017372.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:162757506 C>A maps to NM_001178015.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:162757506 C>A maps to NM_001178015.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:108618377 C>A maps to NM_021815.2 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:108618377 C>A maps to NM_021815.2 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:30110069 C>A maps to NM_003045.4 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:30110069 C>A maps to NM_003045.4 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:98820416 C>A maps to NM_003061.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:98820416 C>A maps to NM_003061.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:45368311 C>A maps to NM_001003652.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:45368311 C>A maps to NM_001003652.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:16502316 T>A maps to ENST00000396652 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:16502316 T>A maps to ENST00000396652 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:95364146 C>A maps to NM_007084.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:95364146 C>A maps to NM_007084.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:228973592 G>T maps to NM_001142644.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:228973592 G>T maps to NM_001142644.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:29675183 C>A maps to NM_003123.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:29675183 C>A maps to NM_003123.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:14282210 C>A maps to NM_006108.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:14282210 C>A maps to NM_006108.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30724539 G>A maps to NM_006662.2 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30724539 G>A maps to NM_006662.2 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:44260274 G>T maps to NM_013305.4 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:44260274 G>T maps to NM_013305.4 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:113208288 C>A maps to ENST00000374463 E1431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:113208288 C>A maps to ENST00000374463 E1431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:113234498 G>T maps to ENST00000374463 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:113234498 G>T maps to ENST00000374463 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:64635687 A>C maps to NM_182914.2 R5667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:64635687 A>C maps to NM_182914.2 R5667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:19166908 A>T maps to NM_152232.2 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:19166908 A>T maps to NM_152232.2 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:122635592 C>A maps to NM_016945.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:122635592 C>A maps to NM_016945.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:27827144 G>T maps to ENST00000409980 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:27827144 G>T maps to ENST00000409980 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:101655069 G>T maps to NM_001102426.1 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:101655069 G>T maps to NM_001102426.1 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:35090036 G>T maps to NM_001093728.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:35090036 G>T maps to NM_001093728.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:179631267 G>T maps to ENST00000444136 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:179631267 G>T maps to ENST00000444136 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:74328906 C>A maps to ENST00000409262 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:74328906 C>A maps to ENST00000409262 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:218607768 G>T maps to NM_001135599.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:218607768 G>T maps to NM_001135599.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:120474736 G>T maps to NM_138554.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:120474736 G>T maps to NM_138554.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:120476442 C>A maps to NM_138554.3 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:120476442 C>A maps to NM_138554.3 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:86802402 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:86802402 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:142983813 G>A maps to NM_153345.1 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:142983813 G>A maps to NM_153345.1 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:87494825 C>T maps to NM_153354.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:87494825 C>T maps to NM_153354.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:130761605 C>A maps to NM_052913.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:130761605 C>A maps to NM_052913.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:27263286 G>A maps to NM_017727.4 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:27263286 G>A maps to NM_017727.4 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18731226 C>T maps to NM_012109.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18731226 C>T maps to NM_012109.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:702963 A>G maps to ENST00000449452 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:702963 A>G maps to ENST00000449452 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:42529729 C>G maps to ENST00000389834 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:42529729 C>G maps to ENST00000389834 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:111780675 G>T maps to ENST00000443106 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:111780675 G>T maps to ENST00000443106 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:92480595 T>A maps to NM_004239.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:92480595 T>A maps to NM_004239.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:72958753 G>T maps to NM_007332.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:72958753 G>T maps to NM_007332.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:31355408 C>A maps to NM_002420.4 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:31355408 C>A maps to NM_002420.4 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:234835271 G>T maps to NM_024080.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:234835271 G>T maps to NM_024080.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:51870275 G>T maps to NM_173485.5 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:51870275 G>T maps to NM_173485.5 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:31769067 C>T maps to NM_020856.2 W544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:31769067 C>T maps to NM_020856.2 W544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:67861259 C>A maps to ENST00000339830 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:67861259 C>A maps to ENST00000339830 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:166737204 C>A maps to NM_024753.3 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:166737204 C>A maps to NM_024753.3 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179403315 C>T maps to NM_133378.4 G30512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179403315 C>T maps to NM_133378.4 G30512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179435495 G>T maps to NM_133378.4 I22553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179435495 G>T maps to NM_133378.4 I22553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179479055 A>T maps to NM_133378.4 A13788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179479055 A>T maps to NM_133378.4 A13788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179590275 G>T maps to NM_133378.4 V5641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179590275 G>T maps to NM_133378.4 V5641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179633571 G>T maps to NM_133378.4 I2997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179633571 G>T maps to NM_133378.4 I2997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49521754 C>A maps to NM_006082.2 G448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49521754 C>A maps to NM_006082.2 G448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:34951383 G>T maps to NM_005499.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:34951383 G>T maps to NM_005499.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:34957911 C>G maps to NM_005499.2 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:34957911 C>G maps to NM_005499.2 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1190768 G>A maps to NM_194315.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1190768 G>A maps to NM_194315.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:103317409 T>C maps to NM_015902.4 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:103317409 T>C maps to NM_015902.4 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165877059 A>T maps to NM_012474.4 *262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165877059 A>T maps to NM_012474.4 *262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:128873836 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:128873836 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20362002 G>A maps to ENST00000424589 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20362002 G>A maps to ENST00000424589 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:47103905 G>T maps to NM_004651.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:47103905 G>T maps to NM_004651.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:9004655 T>A maps to NM_003470.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:9004655 T>A maps to NM_003470.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:144758882 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:144758882 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160389246 G>T maps to NM_020335.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160389246 G>T maps to NM_020335.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:177608674 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:177608674 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:6125811 G>A maps to NM_000552.3 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:6125811 G>A maps to NM_000552.3 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:74976634 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:74976634 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:78584956 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:78584956 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:994340 A>C maps to NM_001184985.1 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:994340 A>C maps to NM_001184985.1 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:44950056 C>G maps to NM_003396.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:44950056 C>G maps to NM_003396.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:168101336 A>T maps to NM_152381.5 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:168101336 A>T maps to NM_152381.5 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30584557 G>A maps to NM_001011718.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30584557 G>A maps to NM_001011718.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:44058903 G>C maps to NM_006297.2 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:44058903 G>C maps to NM_006297.2 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60241758 A>G maps to NM_017742.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60241758 A>G maps to NM_017742.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:32355982 C>G maps to NM_016107.3 P1036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:32355982 C>G maps to NM_016107.3 P1036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44588901 G>C maps to NM_022095.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44588901 G>C maps to NM_022095.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57802136 C>T maps to NM_006635.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57802136 C>T maps to NM_006635.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:109692039 G>A maps to NM_021224.4 R1949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:109692039 G>A maps to NM_021224.4 R1949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:20308559 G>A maps to ENST00000428290 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:20308559 G>A maps to ENST00000428290 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:22807007 C>A maps to NM_015461.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:22807007 C>A maps to NM_015461.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:30935447 G>T maps to NM_014717.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:30935447 G>T maps to NM_014717.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:52394292 T>A maps to NM_023074.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:52394292 T>A maps to NM_023074.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:124497155 C>T maps to NM_152437.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:124497155 C>T maps to NM_152437.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57769380 C>T maps to NM_178457.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57769380 C>T maps to NM_178457.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:22939969 T>A maps to ENST00000397104 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:22939969 T>A maps to ENST00000397104 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:89382101 C>A maps to NM_013227.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:89382101 C>A maps to NM_013227.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:122774155 C>T maps to NM_176824.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:122774155 C>T maps to NM_176824.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:23517503 G>C maps to NM_022478.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:23517503 G>C maps to NM_022478.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:143029824 C>A maps to NM_000083.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:143029824 C>A maps to NM_000083.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:34006260 C>T maps to ENST00000373381 G3125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:34006260 C>T maps to ENST00000373381 G3125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:28650691 C>A maps to ENST00000438199 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:28650691 C>A maps to ENST00000438199 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:139135692 A>G maps to NM_001195037.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:139135692 A>G maps to NM_001195037.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:37876037 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:37876037 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:203630352 C>T maps to NM_173511.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:203630352 C>T maps to NM_173511.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:37028495 C>T maps to NM_001013736.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:37028495 C>T maps to NM_001013736.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:177249933 G>A maps to NM_021165.2 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:177249933 G>A maps to NM_021165.2 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:125047561 C>A maps to NM_001039112.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:125047561 C>A maps to NM_001039112.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:74980578 A>G maps to NM_001480.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:74980578 A>G maps to NM_001480.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:74980857 A>C maps to NM_001480.3 *350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:74980857 A>C maps to NM_001480.3 *350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:95152246 C>A maps to NM_002064.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:95152246 C>A maps to NM_002064.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:102250222 C>G maps to NM_021956.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:102250222 C>G maps to NM_021956.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:94731099 G>C maps to NM_018039.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:94731099 G>C maps to NM_018039.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:142641807 C>A maps to NM_000420.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:142641807 C>A maps to NM_000420.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:32307276 G>C maps to NM_004521.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:32307276 G>C maps to NM_004521.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:196386666 G>T maps to NM_198565.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:196386666 G>T maps to NM_198565.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:3107614 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:3107614 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:60531431 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:60531431 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:3240768 G>C maps to NM_015419.3 S986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:3240768 G>C maps to NM_015419.3 S986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:128347794 G>A maps to ENST00000389524 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:128347794 G>A maps to ENST00000389524 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:117726018 C>A maps to ENST00000338101 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:117726018 C>A maps to ENST00000338101 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248512807 G>T maps to NM_001001918.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248512807 G>T maps to NM_001001918.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:247695441 G>A maps to NM_198074.4 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:247695441 G>A maps to NM_198074.4 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248550950 C>T maps to NM_001005471.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248550950 C>T maps to NM_001005471.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:59376079 T>A maps to NM_002556.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:59376079 T>A maps to NM_002556.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:34400443 G>A maps to NM_019619.3 Q1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:34400443 G>A maps to NM_019619.3 Q1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:105166429 A>G maps to NM_014976.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:105166429 A>G maps to NM_014976.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:55156541 T>A maps to ENST00000507166 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:55156541 T>A maps to ENST00000507166 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:55611454 A>C maps to ENST00000164305 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:55611454 A>C maps to ENST00000164305 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:146639437 C>T maps to NM_005399.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:146639437 C>T maps to NM_005399.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:44148625 G>A maps to NM_031292.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:44148625 G>A maps to NM_031292.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:33962734 G>A maps to NM_001036.3 T1946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:33962734 G>A maps to NM_001036.3 T1946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:44087737 C>T maps to ENST00000319327 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:44087737 C>T maps to ENST00000319327 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:31930284 G>C maps to NM_006929.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:31930284 G>C maps to NM_006929.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:79689916 C>A maps to NM_005639.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:79689916 C>A maps to NM_005639.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:114680332 C>A maps to ENST00000369545 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:114680332 C>A maps to ENST00000369545 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:102191955 G>A maps to NM_078474.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:102191955 G>A maps to NM_078474.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:72698970 T>C maps to NM_001080462.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:72698970 T>C maps to NM_001080462.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:217724643 C>T maps to NM_003284.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:217724643 C>T maps to NM_003284.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:64066554 G>A maps to NM_080666.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:64066554 G>A maps to NM_080666.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:7687538 C>A maps to NM_020196.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:7687538 C>A maps to NM_020196.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:77763344 G>A maps to NM_024721.4 K1396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:77763344 G>A maps to NM_024721.4 K1396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:77776173 C>A maps to NM_024721.4 C3408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:77776173 C>A maps to NM_024721.4 C3408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:57066565 G>A maps to NM_020828.1 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:57066565 G>A maps to NM_020828.1 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:185802718 G>T maps to NM_194250.1 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:185802718 G>T maps to NM_194250.1 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:88964341 C>A maps to NM_181646.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:88964341 C>A maps to NM_181646.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:277225 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:277225 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:141006209 C>T maps to NM_001037172.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:141006209 C>T maps to NM_001037172.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:105415205 C>T maps to NM_138420.2 G2194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:105415205 C>T maps to NM_138420.2 G2194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:105417680 C>T maps to NM_138420.2 G1369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:105417680 C>T maps to NM_138420.2 G1369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:62300196 G>A maps to NM_001620.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:62300196 G>A maps to NM_001620.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:27936420 G>A maps to NM_152345.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:27936420 G>A maps to NM_152345.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:27303584 G>T maps to NM_014915.2 S1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:27303584 G>T maps to NM_014915.2 S1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:30963177 C>T maps to ENST00000509504 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:30963177 C>T maps to ENST00000509504 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:68112720 G>A maps to NM_006421.3 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:68112720 G>A maps to NM_006421.3 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:155448828 G>A maps to ENST00000368346 Q1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:155448828 G>A maps to ENST00000368346 Q1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:70188283 G>A maps to NM_152792.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:70188283 G>A maps to NM_152792.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:28914368 C>A maps to NM_173201.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:28914368 C>A maps to NM_173201.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:45496130 G>T maps to NM_001039380.2 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:45496130 G>T maps to NM_001039380.2 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:121098633 T>A maps to NM_001033677.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:121098633 T>A maps to NM_001033677.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:2614018 C>G maps to NM_199460.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:2614018 C>G maps to NM_199460.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:227441854 A>G maps to ENST00000366766 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:227441854 A>G maps to ENST00000366766 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:202736999 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:202736999 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:639205 G>A maps to NM_018140.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:639205 G>A maps to NM_018140.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:240071332 C>A maps to NM_000740.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:240071332 C>A maps to NM_000740.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:201718133 G>C maps to NM_001162407.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:201718133 G>C maps to NM_001162407.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:72238503 C>T maps to NM_032649.5 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:72238503 C>T maps to NM_032649.5 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:49231354 C>T maps to NM_004818.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:49231354 C>T maps to NM_004818.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:9684873 C>T maps to ENST00000330255 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:9684873 C>T maps to ENST00000330255 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:7640476 C>T maps to NM_020877.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:7640476 C>T maps to NM_020877.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:7644210 G>A maps to NM_020877.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:7644210 G>A maps to NM_020877.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:11597207 C>T maps to NM_001372.3 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:11597207 C>T maps to NM_001372.3 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:111634225 T>C maps to ENST00000428084 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:111634225 T>C maps to ENST00000428084 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:117647509 G>A maps to NM_020693.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:117647509 G>A maps to NM_020693.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:43933317 C>G maps to NM_022785.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:43933317 C>G maps to NM_022785.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:10821640 G>C maps to ENST00000429377 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:10821640 G>C maps to ENST00000429377 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:77073538 C>G maps to NM_001042573.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:77073538 C>G maps to NM_001042573.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:128018851 G>A maps to NM_000122.1 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:128018851 G>A maps to NM_000122.1 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:49116500 C>T maps to NM_017708.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:49116500 C>T maps to NM_017708.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:187627768 G>A maps to ENST00000260147 Y1071Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:187627768 G>A maps to ENST00000260147 Y1071Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:126240610 C>T maps to NM_024582.4 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:126240610 C>T maps to NM_024582.4 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:41743229 G>T maps to NM_006653.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:41743229 G>T maps to NM_006653.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:4382450 C>G maps to NM_032575.2 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:4382450 C>G maps to NM_032575.2 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:52418242 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:52418242 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:34868424 C>T maps to NM_000175.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:34868424 C>T maps to NM_000175.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:175301047 C>G maps to NM_152529.5 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:175301047 C>G maps to NM_152529.5 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:101909098 A>C maps to NM_001184727.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:101909098 A>C maps to NM_001184727.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:93225764 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:93225764 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:126173584 T>C maps to NM_001127323.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:126173584 T>C maps to NM_001127323.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:89334305 C>T maps to NM_017912.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:89334305 C>T maps to NM_017912.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:3726566 G>T maps to NM_052970.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:3726566 G>T maps to NM_052970.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:111099151 G>A maps to NM_001040107.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:111099151 G>A maps to NM_001040107.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:28654151 G>C maps to NM_018250.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:28654151 G>C maps to NM_018250.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:7755191 G>A maps to NM_002216.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:7755191 G>A maps to NM_002216.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:119915636 G>A maps to NM_012281.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:119915636 G>A maps to NM_012281.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:62073779 C>T maps to NM_172107.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:62073779 C>T maps to NM_172107.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:36641891 G>A maps to NM_014657.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:36641891 G>A maps to NM_014657.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:39512385 T>C maps to NM_145027.4 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:39512385 T>C maps to NM_145027.4 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:38926017 G>A maps to NM_181539.4 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:38926017 G>A maps to NM_181539.4 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:53202128 G>A maps to NM_002272.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:53202128 G>A maps to NM_002272.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:53012170 C>G maps to NM_175068.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:53012170 C>G maps to NM_175068.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:129762060 C>T maps to NM_000426.3 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:129762060 C>T maps to NM_000426.3 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:18497988 T>C maps to NM_144972.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:18497988 T>C maps to NM_144972.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:3699301 C>A maps to NM_020710.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:3699301 C>A maps to NM_020710.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:210557841 C>T maps to NM_002374.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:210557841 C>T maps to NM_002374.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:84025048 G>A maps to NM_002395.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:84025048 G>A maps to NM_002395.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:1273699 G>A maps to ENST00000447027 P5000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:1273699 G>A maps to ENST00000447027 P5000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:10298620 C>A maps to NM_002472.2 V1597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:10298620 C>A maps to NM_002472.2 V1597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:33462470 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:33462470 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:73012877 C>G maps to NM_004885.2 Y306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:73012877 C>G maps to NM_004885.2 Y306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:29080182 T>A maps to NM_001005216.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:29080182 T>A maps to NM_001005216.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:56230487 A>G maps to NM_001004743.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:56230487 A>G maps to NM_001004743.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:150932032 G>T maps to NM_014879.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:150932032 G>T maps to NM_014879.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:140589828 C>T maps to NM_018932.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:140589828 C>T maps to NM_018932.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:140777699 G>T maps to NM_018925.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:140777699 G>T maps to NM_018925.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:72290424 G>A maps to NM_002599.3 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:72290424 G>A maps to NM_002599.3 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:45289360 G>T maps to NM_138415.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:45289360 G>T maps to NM_138415.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:19501349 C>G maps to ENST00000429027 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:19501349 C>G maps to ENST00000429027 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:67314354 G>A maps to NM_001129729.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:67314354 G>A maps to NM_001129729.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:127358109 G>T maps to NM_015720.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:127358109 G>T maps to NM_015720.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:45244879 C>T maps to ENST00000352766 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:45244879 C>T maps to ENST00000352766 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:73653562 C>T maps to NM_000021.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:73653562 C>T maps to NM_000021.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:1652005 T>A maps to NM_012293.1 A1182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:1652005 T>A maps to NM_012293.1 A1182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:68670477 G>A maps to NM_133339.1 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:68670477 G>A maps to NM_133339.1 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:114358413 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:114358413 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:67697256 C>T maps to NM_173630.3 L1912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:67697256 C>T maps to NM_173630.3 L1912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153598846 G>A maps to NM_001024210.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153598846 G>A maps to NM_001024210.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:54823476 G>A maps to NM_014302.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:54823476 G>A maps to NM_014302.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:42088435 G>C maps to NM_006275.5 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:42088435 G>C maps to NM_006275.5 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:42977284 A>G maps to NM_032237.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:42977284 A>G maps to NM_032237.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:25917310 G>A maps to NM_005835.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:25917310 G>A maps to NM_005835.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:31486830 G>T maps to ENST00000454496 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:31486830 G>T maps to ENST00000454496 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:48523253 C>T maps to NM_006038.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:48523253 C>T maps to NM_006038.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:158584067 G>A maps to NM_003126.2 L2273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:158584067 G>A maps to NM_003126.2 L2273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:74570504 G>C maps to NM_006456.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:74570504 G>C maps to NM_006456.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:150464138 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:150464138 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:120996138 C>T maps to NM_005422.2 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:120996138 C>T maps to NM_005422.2 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175360439 C>A maps to NM_003285.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175360439 C>A maps to NM_003285.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:158924615 G>A maps to NM_020245.3 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:158924615 G>A maps to NM_020245.3 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:78458909 C>G maps to NM_016373.1 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:78458909 C>G maps to NM_016373.1 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:146156369 G>A maps to NM_006958.2 Y601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:146156369 G>A maps to NM_006958.2 Y601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:3381327 C>A maps to NM_001130520.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:3381327 C>A maps to NM_001130520.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:57188722 A>T maps to NM_033273.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:57188722 A>T maps to NM_033273.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:95815559 G>T maps to NM_032788.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:95815559 G>T maps to NM_032788.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:247265289 T>C maps to NM_024804.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:247265289 T>C maps to NM_024804.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:99581986 G>A maps to NM_001001662.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:99581986 G>A maps to NM_001001662.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:48248818 G>T maps to NM_032583.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:48248818 G>T maps to NM_032583.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:77317891 G>T maps to NM_199355.2 Y1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:77317891 G>T maps to NM_199355.2 Y1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:64672543 C>T maps to NM_182920.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:64672543 C>T maps to NM_182920.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:49510038 C>T maps to NM_181442.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:49510038 C>T maps to NM_181442.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:21233988 G>C maps to NM_000384.2 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:21233988 G>C maps to NM_000384.2 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:62550536 A>G maps to NM_004318.3 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:62550536 A>G maps to NM_004318.3 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:176903320 G>A maps to ENST00000281881 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:176903320 G>A maps to ENST00000281881 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:31323006 G>T maps to NM_030632.1 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:31323006 G>T maps to NM_030632.1 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:51087336 A>T maps to ENST00000358385 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:51087336 A>T maps to ENST00000358385 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108183153 G>T maps to NM_000051.3 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108183153 G>T maps to NM_000051.3 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:117001386 C>A maps to NM_207303.2 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:117001386 C>A maps to NM_207303.2 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:104125072 A>C maps to NM_001701.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:104125072 A>C maps to NM_001701.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:147092303 C>A maps to NM_004326.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:147092303 C>A maps to NM_004326.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:93776186 A>T maps to NM_003972.2 K1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:93776186 A>T maps to NM_003972.2 K1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:100626676 C>A maps to NM_000061.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:100626676 C>A maps to NM_000061.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:42232033 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:42232033 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:165715540 G>T maps to NM_144980.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:165715540 G>T maps to NM_144980.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:2016648 C>T maps to NM_172364.4 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:2016648 C>T maps to NM_172364.4 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:121973134 C>A maps to NM_001178065.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:121973134 C>A maps to NM_001178065.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:50053544 G>A maps to NM_033031.2 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:50053544 G>A maps to NM_033031.2 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:204599580 C>G maps to NM_006139.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:204599580 C>G maps to NM_006139.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:35618282 G>T maps to NM_001782.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:35618282 G>T maps to NM_001782.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:59195339 C>A maps to NM_031891.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:59195339 C>A maps to NM_031891.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:106171517 C>A maps to NM_001171095.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:106171517 C>A maps to NM_001171095.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:140277557 C>A maps to NM_022131.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:140277557 C>A maps to NM_022131.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:94054960 C>T maps to NM_000089.3 Q941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:94054960 C>T maps to NM_000089.3 Q941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:113293553 G>A maps to NM_198123.1 T3119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:113293553 G>A maps to NM_198123.1 T3119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:79878762 G>T maps to ENST00000402739 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:79878762 G>T maps to ENST00000402739 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:119694175 G>T maps to NM_003588.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:119694175 G>T maps to NM_003588.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:111729243 G>A maps to NM_015267.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:111729243 G>A maps to NM_015267.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:59112600 G>A maps to NM_016651.5 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:59112600 G>A maps to NM_016651.5 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:31576609 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:31576609 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:234370996 C>A maps to NM_152879.2 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:234370996 C>A maps to NM_152879.2 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:71146588 C>A maps to NM_001360.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:71146588 C>A maps to NM_001360.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:21788209 C>T maps to NM_003777.3 S2848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:21788209 C>T maps to NM_003777.3 S2848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7638001 T>C maps to NM_020877.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7638001 T>C maps to NM_020877.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:196913023 G>A maps to NM_018897.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:196913023 G>A maps to NM_018897.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11837220 C>T maps to NM_001372.3 L4108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11837220 C>T maps to NM_001372.3 L4108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169469015 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169469015 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113890578 T>A maps to NM_000796.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113890578 T>A maps to NM_000796.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:152914961 C>A maps to NM_001395.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:152914961 C>A maps to NM_001395.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:48386708 G>A maps to NM_006579.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:48386708 G>A maps to NM_006579.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:66535310 G>T maps to NM_004439.5 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:66535310 G>T maps to NM_004439.5 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:103495019 C>G maps to NM_153448.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:103495019 C>G maps to NM_153448.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100042083 C>A maps to NM_153364.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100042083 C>A maps to NM_153364.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:127666357 G>A maps to NM_001999.3 Q1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:127666357 G>A maps to NM_001999.3 Q1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:6690698 G>T maps to NM_153230.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:6690698 G>T maps to NM_153230.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:14861825 G>A maps to NM_152536.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:14861825 G>A maps to NM_152536.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:137939713 C>A maps to NM_001139500.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:137939713 C>A maps to NM_001139500.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:135438788 C>T maps to ENST00000443774 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:135438788 C>T maps to ENST00000443774 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:14627194 G>T maps to NM_002063.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:14627194 G>T maps to NM_002063.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:155632278 C>A maps to NM_003875.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:155632278 C>A maps to NM_003875.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:27333097 G>T maps to NM_005288.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:27333097 G>T maps to NM_005288.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:48956134 C>T maps to NM_031485.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:48956134 C>T maps to NM_031485.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153217334 C>A maps to ENST00000369984 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153217334 C>A maps to ENST00000369984 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153222984 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153222984 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:120301894 T>A maps to NM_005518.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:120301894 T>A maps to NM_005518.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:124909092 C>A maps to NM_005519.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:124909092 C>A maps to NM_005519.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:176982208 G>A maps to NM_002148.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:176982208 G>A maps to NM_002148.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:119985604 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:119985604 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:119985678 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:119985678 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:203644315 C>T maps to NM_138468.4 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:203644315 C>T maps to NM_138468.4 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:2641598 C>A maps to NM_006899.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:2641598 C>A maps to NM_006899.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:94568238 A>T maps to NM_206949.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:94568238 A>T maps to NM_206949.2 A47A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4390-01A-02D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4390-01A-02D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:67804385 G>A maps to NM_001559.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:67804385 G>A maps to NM_001559.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:15197460 G>T maps to NM_001031853.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:15197460 G>T maps to NM_001031853.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:107979481 G>T maps to NM_003604.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:107979481 G>T maps to NM_003604.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:20441684 G>T maps to NM_002214.2 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:20441684 G>T maps to NM_002214.2 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:128252491 C>A maps to NM_017969.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:128252491 C>A maps to NM_017969.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:150690184 C>T maps to NM_203395.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:150690184 C>T maps to NM_203395.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:75227184 T>G maps to NM_020647.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:75227184 T>G maps to NM_020647.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:8503630 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:8503630 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:154548816 C>T maps to NM_001131007.1 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:154548816 C>T maps to NM_001131007.1 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113724428 T>A maps to NM_020817.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113724428 T>A maps to NM_020817.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:5968613 C>T maps to NM_001017969.2 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:5968613 C>T maps to NM_001017969.2 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:154395644 A>T maps to NM_001099293.1 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:154395644 A>T maps to NM_001099293.1 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:70456618 T>A maps to NM_020866.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:70456618 T>A maps to NM_020866.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:9997029 G>T maps to NM_016523.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:9997029 G>T maps to NM_016523.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:33635063 G>A maps to NM_004795.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:33635063 G>A maps to NM_004795.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:38955965 G>A maps to NM_181535.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:38955965 G>A maps to NM_181535.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:7008578 T>A maps to NM_005559.2 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:7008578 T>A maps to NM_005559.2 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:21508617 A>C maps to ENST00000416669 G2777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:21508617 A>C maps to ENST00000416669 G2777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:47108729 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:47108729 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:110763691 G>A maps to NM_018334.4 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:110763691 G>A maps to NM_018334.4 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:33585789 C>A maps to ENST00000354476 S1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:33585789 C>A maps to ENST00000354476 S1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:24927593 G>T maps to NM_001009909.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:24927593 G>T maps to NM_001009909.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:40710445 C>T maps to NM_002446.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:40710445 C>T maps to NM_002446.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:12963014 C>A maps to NM_014975.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:12963014 C>A maps to NM_014975.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:182947467 G>T maps to NM_015078.2 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:182947467 G>T maps to NM_015078.2 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:90468062 C>A maps to NM_014611.1 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:90468062 C>A maps to NM_014611.1 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:20937231 A>T maps to NM_001003891.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:20937231 A>T maps to NM_001003891.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:149905221 G>C maps to NM_003828.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:149905221 G>C maps to NM_003828.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:100685328 C>A maps to NM_001040105.1 S3544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:100685328 C>A maps to NM_001040105.1 S3544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10397670 C>T maps to NM_005963.3 A1889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10397670 C>T maps to NM_005963.3 A1889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:5811256 C>T maps to ENST00000381093 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:5811256 C>T maps to ENST00000381093 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:57111714 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:57111714 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:56410251 G>T maps to NM_176810.2 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:56410251 G>T maps to NM_176810.2 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:56424607 C>T maps to NM_176810.2 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:56424607 C>T maps to NM_176810.2 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:128699805 G>A maps to NM_000276.3 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:128699805 G>A maps to NM_000276.3 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:247614729 C>A maps to NM_001004492.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:247614729 C>A maps to NM_001004492.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:29054920 G>A maps to NM_001005226.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:29054920 G>A maps to NM_001005226.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:4843367 C>A maps to NM_001004753.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:4843367 C>A maps to NM_001004753.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:5444218 T>A maps to NM_001004757.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:5444218 T>A maps to NM_001004757.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:9525047 C>A maps to NM_177990.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:9525047 C>A maps to NM_177990.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:169632954 C>T maps to NM_001166108.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:169632954 C>T maps to NM_001166108.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:242066562 C>A maps to ENST00000358649 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:242066562 C>A maps to ENST00000358649 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:58207804 G>T maps to NM_001040429.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:58207804 G>T maps to NM_001040429.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:82582432 A>G maps to NM_033026.5 D2612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:82582432 A>G maps to NM_033026.5 D2612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119044377 C>A maps to NM_173791.3 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119044377 C>A maps to NM_173791.3 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:27117368 G>T maps to NM_017837.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:27117368 G>T maps to NM_017837.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:106508038 G>C maps to NM_002649.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:106508038 G>C maps to NM_002649.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:68381542 G>A maps to NM_145119.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:68381542 G>A maps to NM_145119.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:125255500 C>A maps to NM_022062.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:125255500 C>A maps to NM_022062.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:44171829 C>A maps to NM_002659.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:44171829 C>A maps to NM_002659.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:16287714 G>T maps to NM_001136213.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:16287714 G>T maps to NM_001136213.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:49376607 G>T maps to NM_014330.3 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:49376607 G>T maps to NM_014330.3 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:49142648 A>T maps to NM_033215.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:49142648 A>T maps to NM_033215.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:22891031 T>A maps to NM_206954.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:22891031 T>A maps to NM_206954.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:5283096 C>A maps to NM_144773.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:5283096 C>A maps to NM_144773.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:70974891 G>A maps to NM_001109754.1 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:70974891 G>A maps to NM_001109754.1 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:70983909 G>T maps to NM_001109754.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:70983909 G>T maps to NM_001109754.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:129318488 C>A maps to NM_004794.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:129318488 C>A maps to NM_004794.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:51679121 C>T maps to NM_015106.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:51679121 C>T maps to NM_015106.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:36597179 C>A maps to NM_000448.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:36597179 C>A maps to NM_000448.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:85619414 G>A maps to NM_152573.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:85619414 G>A maps to NM_152573.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:53156536 G>T maps to NM_052859.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:53156536 G>T maps to NM_052859.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:84563491 G>T maps to NM_001009994.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:84563491 G>T maps to NM_001009994.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:38995660 G>A maps to NM_000540.2 K2750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:38995660 G>A maps to NM_000540.2 K2750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:55243226 C>G maps to NM_015589.4 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:55243226 C>G maps to NM_015589.4 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55753603 C>A maps to ENST00000443936 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55753603 C>A maps to ENST00000443936 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:84751059 T>A maps to NM_152754.2 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:84751059 T>A maps to NM_152754.2 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:61460396 A>T maps to NM_001040147.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:61460396 A>T maps to NM_001040147.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:96318268 T>C maps to NM_006304.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:96318268 T>C maps to NM_006304.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:52023449 G>T maps to NM_001245.5 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:52023449 G>T maps to NM_001245.5 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160709144 A>T maps to NM_021181.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160709144 A>T maps to NM_021181.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153716928 G>T maps to ENST00000440701 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153716928 G>T maps to ENST00000440701 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:43247834 C>A maps to NM_007163.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:43247834 C>A maps to NM_007163.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119017344 G>T maps to NM_003054.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119017344 G>T maps to NM_003054.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:64366302 G>A maps to NM_144585.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:64366302 G>A maps to NM_144585.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:33947360 C>A maps to NM_016180.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:33947360 C>A maps to NM_016180.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:84455263 G>A maps to NM_052910.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:84455263 G>A maps to NM_052910.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164906716 C>A maps to NM_014926.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164906716 C>A maps to NM_014926.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:53514664 C>A maps to NM_003578.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:53514664 C>A maps to NM_003578.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:106907475 G>A maps to NM_014978.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:106907475 G>A maps to NM_014978.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:153085167 T>C maps to NM_001014450.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:153085167 T>C maps to NM_001014450.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:109315284 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:109315284 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:29813490 C>A maps to NM_021738.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:29813490 C>A maps to NM_021738.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:7866335 G>T maps to NM_031923.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:7866335 G>T maps to NM_031923.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:30695123 C>T maps to NM_031271.3 S2509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:30695123 C>T maps to NM_031271.3 S2509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:11676129 G>T maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:11676129 G>T maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:32537341 G>A maps to NM_003253.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:32537341 G>A maps to NM_003253.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:120476379 G>T maps to NM_138554.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:120476379 G>T maps to NM_138554.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:103310024 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:103310024 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159174648 A>G maps to NM_018342.4 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159174648 A>G maps to NM_018342.4 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:150488657 C>A maps to NM_014020.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:150488657 C>A maps to NM_014020.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:39931219 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:39931219 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:29904682 C>T maps to NM_001193451.1 W285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:29904682 C>T maps to NM_001193451.1 W285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:175375583 C>T maps to NM_003285.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:175375583 C>T maps to NM_003285.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:32011607 G>A maps to ENST00000375244 I3816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:32011607 G>A maps to ENST00000375244 I3816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:25665828 G>C maps to ENST00000264331 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:25665828 G>C maps to ENST00000264331 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:54950179 C>A maps to NM_001039705.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:54950179 C>A maps to NM_001039705.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:128801518 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:128801518 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:179459154 C>A maps to NM_133378.4 E16788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:179459154 C>A maps to NM_133378.4 E16788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:54817796 T>C maps to ENST00000260323 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:54817796 T>C maps to ENST00000260323 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:35608281 C>A maps to ENST00000416672 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:35608281 C>A maps to ENST00000416672 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:33999770 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:33999770 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:216262469 C>T maps to ENST00000366943 V1590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:216262469 C>T maps to ENST00000366943 V1590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:76831479 G>A maps to NM_025090.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:76831479 G>A maps to NM_025090.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:101689352 C>A maps to NM_014503.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:101689352 C>A maps to NM_014503.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:85724620 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:85724620 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113084978 C>A maps to NM_001164496.1 V874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113084978 C>A maps to NM_001164496.1 V874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:85547061 A>T maps to NM_145172.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:85547061 A>T maps to NM_145172.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:705381 C>T maps to NM_145294.4 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:705381 C>T maps to NM_145294.4 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:54337610 T>C maps to NM_020922.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:54337610 T>C maps to NM_020922.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:197169210 T>A maps to NM_194314.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:197169210 T>A maps to NM_194314.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:72993846 C>A maps to NM_006885.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:72993846 C>A maps to NM_006885.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:106801084 G>C maps to NM_012082.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:106801084 G>C maps to NM_012082.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:47272882 G>T maps to NM_003446.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:47272882 G>T maps to NM_003446.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:7022735 C>A maps to NM_013249.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:7022735 C>A maps to NM_013249.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:44570524 G>T maps to NM_013361.4 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:44570524 G>T maps to NM_013361.4 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:130206725 C>A maps to NM_007135.2 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:130206725 C>A maps to NM_007135.2 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:149561357 C>T maps to NM_001099220.1 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:149561357 C>T maps to NM_001099220.1 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66811349 G>T maps to NM_017975.3 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66811349 G>T maps to NM_017975.3 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:57618741 C>A maps to NM_007157.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:57618741 C>A maps to NM_007157.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:7703844 C>A maps to NM_145891.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:7703844 C>A maps to NM_145891.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:2347903 G>A maps to NM_001089.2 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:2347903 G>A maps to NM_001089.2 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100490352 G>A maps to NM_000665.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100490352 G>A maps to NM_000665.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20788794 A>G maps to NM_005622.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20788794 A>G maps to NM_005622.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:133995666 A>T maps to NM_001185095.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:133995666 A>T maps to NM_001185095.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:39441196 G>A maps to NM_145298.5 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:39441196 G>A maps to NM_145298.5 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:21235077 G>T maps to NM_000384.2 I1554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:21235077 G>T maps to NM_000384.2 I1554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:45411924 G>T maps to NM_000041.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:45411924 G>T maps to NM_000041.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197101453 C>G maps to NM_018136.4 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197101453 C>G maps to NM_018136.4 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:31325018 C>A maps to NM_030632.1 S1736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:31325018 C>A maps to NM_030632.1 S1736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:292926 C>T maps to ENST00000409479 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:292926 C>T maps to ENST00000409479 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:33397599 C>A maps to NM_198428.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:33397599 C>A maps to NM_198428.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:60588569 C>T maps to NM_001080512.1 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:60588569 C>T maps to NM_001080512.1 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:112622800 G>T maps to NM_001109662.2 S3151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:112622800 G>T maps to NM_001109662.2 S3151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:11766417 C>A maps to NM_198545.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:11766417 C>A maps to NM_198545.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:190027980 G>A maps to NM_021101.4 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:190027980 G>A maps to NM_021101.4 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:71043248 G>A maps to NM_173535.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:71043248 G>A maps to NM_173535.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:130290237 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:130290237 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197446915 G>A maps to NM_201253.2 Q1376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197446915 G>A maps to NM_201253.2 Q1376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:26995495 G>A maps to NM_001887.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:26995495 G>A maps to NM_001887.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67645893 G>C maps to NM_006565.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67645893 G>C maps to NM_006565.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:176885525 C>A maps to ENST00000393565 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:176885525 C>A maps to ENST00000393565 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:100660778 G>A maps to ENST00000422147 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:100660778 G>A maps to ENST00000422147 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:11725837 C>A maps to NM_001372.3 I2978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:11725837 C>A maps to NM_001372.3 I2978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:45394041 C>A maps to NM_014080.4 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:45394041 C>A maps to NM_014080.4 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:109547431 G>T maps to ENST00000376651 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:109547431 G>T maps to ENST00000376651 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67911273 C>T maps to NM_014329.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67911273 C>T maps to NM_014329.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:184681005 C>A maps to NM_025191.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:184681005 C>A maps to NM_025191.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:140611348 C>G maps to NM_024757.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:140611348 C>G maps to NM_024757.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197021762 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197021762 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:200182759 C>T maps to NM_001105517.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:200182759 C>T maps to NM_001105517.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:92534617 C>G maps to ENST00000298047 V2813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:92534617 C>G maps to ENST00000298047 V2813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:121943804 G>T maps to NM_001024613.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:121943804 G>T maps to NM_001024613.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:38958888 T>A maps to NM_138801.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:38958888 T>A maps to NM_138801.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:125426264 C>A maps to NM_153442.3 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:125426264 C>A maps to NM_153442.3 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:228333278 G>A maps to ENST00000366720 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:228333278 G>A maps to ENST00000366720 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:91727808 T>C maps to NM_001017975.3 E1409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:91727808 T>C maps to NM_001017975.3 E1409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:152187997 G>C maps to NM_001009931.1 S2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:152187997 G>C maps to NM_001009931.1 S2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:997366 C>T maps to NM_000203.3 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:997366 C>T maps to NM_000203.3 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:6658969 G>A maps to NM_001193457.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:6658969 G>A maps to NM_001193457.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:65622918 T>C maps to NM_004884.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:65622918 T>C maps to NM_004884.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:13280018 C>A maps to NM_080826.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:13280018 C>A maps to NM_080826.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:126091003 C>G maps to ENST00000377985 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:126091003 C>G maps to ENST00000377985 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:169547563 G>C maps to ENST00000392687 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:169547563 G>C maps to ENST00000392687 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:136594655 G>A maps to NM_002299.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:136594655 G>A maps to NM_002299.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:71978258 C>T maps to NM_003667.2 F823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:71978258 C>T maps to NM_003667.2 F823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:74763215 C>T maps to NM_032603.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:74763215 C>T maps to NM_032603.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:160953583 G>A maps to NM_005577.2 A1980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:160953583 G>A maps to NM_005577.2 A1980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:42356778 A>T maps to NM_152447.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:42356778 A>T maps to NM_152447.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:39844178 A>G maps to ENST00000361689 G2358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:39844178 A>G maps to ENST00000361689 G2358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:30268768 T>A maps to NM_177404.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:30268768 T>A maps to NM_177404.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:30254709 C>A maps to NM_002365.4 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:30254709 C>A maps to NM_002365.4 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:47957469 G>C maps to ENST00000426837 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:47957469 G>C maps to ENST00000426837 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:164449920 G>T maps to ENST00000514618 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:164449920 G>T maps to ENST00000514618 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:10535643 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:10535643 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:154861314 G>A maps to NM_007289.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:154861314 G>A maps to NM_007289.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:41958158 C>A maps to NM_005374.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:41958158 C>A maps to NM_005374.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:10419598 C>A maps to NM_005963.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:10419598 C>A maps to NM_005963.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23883230 G>C maps to NM_000257.2 R1880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23883230 G>C maps to NM_000257.2 R1880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:18023154 G>A maps to ENST00000205890 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:18023154 G>A maps to ENST00000205890 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:109853403 G>T maps to NM_001101421.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:109853403 G>T maps to NM_001101421.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:46254146 T>C maps to NM_181659.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:46254146 T>C maps to NM_181659.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:33330705 C>T maps to NM_014071.2 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:33330705 C>T maps to NM_014071.2 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:24884149 G>T maps to NM_025081.2 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:24884149 G>T maps to NM_025081.2 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:15107657 G>T maps to NM_018324.2 G213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:15107657 G>T maps to NM_018324.2 G213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:48596694 G>A maps to NM_001004134.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:48596694 G>A maps to NM_001004134.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:158389726 G>A maps to NM_001004476.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:158389726 G>A maps to NM_001004476.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20692095 C>A maps to NM_001004480.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20692095 C>A maps to NM_001004480.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:248004694 G>A maps to NM_001001959.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:248004694 G>A maps to NM_001001959.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:6048373 G>T maps to NM_001001917.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:6048373 G>T maps to NM_001001917.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:97887573 G>T maps to NM_001005515.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:97887573 G>T maps to NM_001005515.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:56230565 G>T maps to NM_001004743.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:56230565 G>T maps to NM_001004743.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:9361886 G>A maps to NM_001079935.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:9361886 G>A maps to NM_001079935.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:38919156 C>T maps to NM_003999.2 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:38919156 C>T maps to NM_003999.2 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:120387531 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:120387531 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20380966 A>T maps to NM_174924.1 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20380966 A>T maps to NM_174924.1 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:66918315 C>T maps to NM_020786.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:66918315 C>T maps to NM_020786.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:108704448 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:108704448 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:17476411 G>T maps to NM_031310.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:17476411 G>T maps to NM_031310.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:118360713 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:118360713 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:129814845 C>G maps to NM_020228.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:129814845 C>G maps to NM_020228.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:64299088 C>A maps to NM_002737.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:64299088 C>A maps to NM_002737.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:121275046 G>A maps to NM_001005339.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:121275046 G>A maps to NM_001005339.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:33292038 C>G maps to NM_022753.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:33292038 C>G maps to NM_022753.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:167141097 C>T maps to ENST00000303354 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:167141097 C>T maps to ENST00000303354 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:30391339 C>T maps to NM_052838.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:30391339 C>T maps to NM_052838.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:8220036 C>T maps to NM_018986.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:8220036 C>T maps to NM_018986.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:73121983 C>T maps to NM_018344.5 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:73121983 C>T maps to NM_018344.5 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:234454682 T>C maps to NM_173508.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:234454682 T>C maps to NM_173508.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:69908951 G>A maps to NM_018375.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:69908951 G>A maps to NM_018375.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:33947449 C>A maps to NM_016180.3 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:33947449 C>A maps to NM_016180.3 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:20568940 A>T maps to ENST00000273739 K932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:20568940 A>T maps to ENST00000273739 K932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:34918599 C>T maps to NM_138927.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:34918599 C>T maps to NM_138927.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:158618418 C>T maps to NM_003126.2 Q1198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:158618418 C>T maps to NM_003126.2 Q1198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:91827440 C>G maps to NM_014848.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:91827440 C>G maps to NM_014848.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:155465908 C>T maps to ENST00000456144 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:155465908 C>T maps to ENST00000456144 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:51561378 C>T maps to ENST00000338969 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:51561378 C>T maps to ENST00000338969 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:81610057 C>T maps to NM_000369.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:81610057 C>T maps to NM_000369.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:31768901 C>T maps to NM_020856.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:31768901 C>T maps to NM_020856.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:52936817 T>A maps to NM_020784.2 K519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:52936817 T>A maps to NM_020784.2 K519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:215802230 G>A maps to ENST00000366943 L5172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:215802230 G>A maps to ENST00000366943 L5172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:101702084 G>A maps to NM_014503.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:101702084 G>A maps to NM_014503.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:116937674 G>T maps to NM_003391.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:116937674 G>T maps to NM_003391.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:52901104 G>A maps to NM_001009881.2 Q1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:52901104 G>A maps to NM_001009881.2 Q1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:35477542 G>C maps to NM_007167.3 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:35477542 G>C maps to NM_007167.3 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:44605072 C>T maps to NM_013398.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:44605072 C>T maps to NM_013398.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:44578471 C>T maps to NM_022095.3 Q1212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:44578471 C>T maps to NM_022095.3 Q1212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:53668505 G>A maps to NM_024733.3 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:53668505 G>A maps to NM_024733.3 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:9004879 C>A maps to NM_144670.3 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:9004879 C>A maps to NM_144670.3 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:9010601 C>A maps to NM_144670.3 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:9010601 C>A maps to NM_144670.3 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125587223 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125587223 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125612780 C>A maps to NM_023928.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125612780 C>A maps to NM_023928.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125613941 C>A maps to NM_023928.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125613941 C>A maps to NM_023928.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151458601 C>A maps to NM_207365.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151458601 C>A maps to NM_207365.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151463408 C>A maps to NM_207365.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151463408 C>A maps to NM_207365.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70316555 G>T maps to ENST00000418685 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70316555 G>T maps to ENST00000418685 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57209024 G>T maps to NM_181806.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57209024 G>T maps to NM_181806.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121717922 G>C maps to NM_005763.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121717922 G>C maps to NM_005763.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121756989 C>A maps to NM_005763.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121756989 C>A maps to NM_005763.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:215876354 G>T maps to NM_173076.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:215876354 G>T maps to NM_173076.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48318374 G>T maps to NM_152701.3 L2528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48318374 G>T maps to NM_152701.3 L2528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48318389 G>T maps to NM_152701.3 S2533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48318389 G>T maps to NM_152701.3 S2533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48335439 G>T maps to NM_152701.3 T3033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48335439 G>T maps to NM_152701.3 T3033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48349647 G>T maps to NM_152701.3 A3142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:48349647 G>T maps to NM_152701.3 A3142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107549223 G>T maps to NM_005502.3 R2080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107549223 G>T maps to NM_005502.3 R2080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107578465 C>G maps to NM_005502.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107578465 C>G maps to NM_005502.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107582280 C>A maps to NM_005502.3 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107582280 C>A maps to NM_005502.3 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94471031 G>T maps to NM_000350.2 R2038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94471031 G>T maps to NM_000350.2 R2038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94473281 C>A maps to NM_000350.2 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94473281 C>A maps to NM_000350.2 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94476878 C>A maps to NM_000350.2 L1841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94476878 C>A maps to NM_000350.2 L1841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94490565 C>A maps to NM_000350.2 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94490565 C>A maps to NM_000350.2 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94502296 C>A maps to NM_000350.2 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94502296 C>A maps to NM_000350.2 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94502326 C>A maps to NM_000350.2 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94502326 C>A maps to NM_000350.2 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94528753 G>T maps to NM_000350.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94528753 G>T maps to NM_000350.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169847417 C>A maps to NM_003742.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169847417 C>A maps to NM_003742.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169847426 G>T maps to NM_003742.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169847426 G>T maps to NM_003742.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169869837 G>T maps to NM_003742.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169869837 G>T maps to NM_003742.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169869884 C>A maps to NM_003742.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169869884 C>A maps to NM_003742.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87145839 C>A maps to NM_000927.3 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87145839 C>A maps to NM_000927.3 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87032524 G>T maps to NM_018849.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87032524 G>T maps to NM_018849.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87082320 G>A maps to NM_018849.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87082320 G>A maps to NM_018849.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48232116 C>A maps to NM_032583.3 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48232116 C>A maps to NM_032583.3 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48242377 C>A maps to NM_032583.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48242377 C>A maps to NM_032583.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48180329 C>A maps to NM_033226.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48180329 C>A maps to NM_033226.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:95860157 C>A maps to NM_005845.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:95860157 C>A maps to NM_005845.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183663721 C>A maps to NM_005688.2 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183663721 C>A maps to NM_005688.2 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:16272671 C>A maps to NM_001171.5 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:16272671 C>A maps to NM_001171.5 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21981954 C>A maps to NM_005691.2 T1202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21981954 C>A maps to NM_005691.2 T1202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94946084 C>A maps to ENST00000454898 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94946084 C>A maps to ENST00000454898 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74766250 C>A maps to NM_005050.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74766250 C>A maps to NM_005050.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146038492 C>A maps to NM_002940.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146038492 C>A maps to NM_002940.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146044237 C>A maps to NM_002940.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146044237 C>A maps to NM_002940.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30558469 C>A maps to NM_001025091.1 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30558469 C>A maps to NM_001025091.1 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119027347 C>A maps to NM_001142505.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119027347 C>A maps to NM_001142505.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119028948 G>T maps to NM_001142505.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119028948 G>T maps to NM_001142505.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119028954 C>A maps to NM_001142505.1 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119028954 C>A maps to NM_001142505.1 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119029026 C>A maps to NM_001142505.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119029026 C>A maps to NM_001142505.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44041633 C>A maps to NM_022436.2 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44041633 C>A maps to NM_022436.2 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44051153 G>T maps to NM_022436.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44051153 G>T maps to NM_022436.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111710466 C>A maps to NM_018394.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111710466 C>A maps to NM_018394.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89695060 C>A maps to NM_152924.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89695060 C>A maps to NM_152924.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58256777 C>A maps to NM_020676.5 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58256777 C>A maps to NM_020676.5 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116247755 G>T maps to ENST00000277895 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116247755 G>T maps to ENST00000277895 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:148617060 C>A maps to NM_014945.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:148617060 C>A maps to NM_014945.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26598525 G>T maps to NM_013375.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26598525 G>T maps to NM_013375.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34176291 C>A maps to NM_145804.2 G908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34176291 C>A maps to NM_145804.2 G908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38175461 G>T maps to NM_001607.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38175461 G>T maps to NM_001607.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47329178 C>A maps to NM_006111.2 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47329178 C>A maps to NM_006111.2 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35583301 G>T maps to NM_198834.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35583301 G>T maps to NM_198834.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109629451 C>A maps to NM_001093.3 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109629451 C>A maps to NM_001093.3 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109629471 C>A maps to NM_001093.3 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109629471 C>A maps to NM_001093.3 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109661702 C>A maps to NM_001093.3 S1292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109661702 C>A maps to NM_001093.3 S1292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109679028 G>T maps to NM_001093.3 S1655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109679028 G>T maps to NM_001093.3 S1655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109690857 G>C maps to NM_001093.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109690857 G>C maps to NM_001093.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112150444 G>T maps to NM_001136538.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112150444 G>T maps to NM_001136538.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112193525 C>A maps to NM_001136538.1 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112193525 C>A maps to NM_001136538.1 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134126503 C>A maps to NM_014384.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134126503 C>A maps to NM_014384.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128623317 C>A maps to NM_014049.4 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128623317 C>A maps to NM_014049.4 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128627065 G>T maps to NM_014049.4 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128627065 G>T maps to NM_014049.4 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226346976 C>A maps to NM_022735.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226346976 C>A maps to NM_022735.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135619537 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135619537 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74036037 C>A maps to NM_006821.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74036037 C>A maps to NM_006821.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74040290 C>A maps to NM_006821.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74040290 C>A maps to NM_006821.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:271917 C>A maps to NM_004300.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:271917 C>A maps to NM_004300.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:277078 C>G maps to NM_004300.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:277078 C>G maps to NM_004300.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:277249 G>T maps to NM_004300.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:277249 G>T maps to NM_004300.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141011845 C>A maps to NM_001037172.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141011845 C>A maps to NM_001037172.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141011861 C>A maps to NM_001037172.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141011861 C>A maps to NM_001037172.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141011932 C>A maps to NM_001037172.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141011932 C>A maps to NM_001037172.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823573 C>A maps to NM_052957.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823573 C>A maps to NM_052957.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823741 C>A maps to NM_052957.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823741 C>A maps to NM_052957.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823831 C>A maps to NM_052957.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823831 C>A maps to NM_052957.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823861 C>A maps to NM_052957.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70823861 C>A maps to NM_052957.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70824041 C>A maps to NM_052957.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70824041 C>A maps to NM_052957.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70824071 C>A maps to NM_052957.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70824071 C>A maps to NM_052957.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70824101 C>A maps to NM_052957.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70824101 C>A maps to NM_052957.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89178570 C>A maps to NM_174917.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89178570 C>A maps to NM_174917.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:185705104 G>T maps to NM_001995.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:185705104 G>T maps to NM_001995.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:223773625 G>T maps to NM_203372.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:223773625 G>T maps to NM_203372.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20491902 C>A maps to NM_001010845.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20491902 C>A maps to NM_001010845.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20429418 C>G maps to NM_017888.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20429418 C>G maps to NM_017888.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:24989989 C>A maps to NM_032501.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:24989989 C>A maps to NM_032501.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:24993545 G>T maps to NM_032501.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:24993545 G>T maps to NM_032501.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:81647159 C>A maps to NM_024560.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:81647159 C>A maps to NM_024560.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:111625336 G>T maps to NM_006687.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:111625336 G>T maps to NM_006687.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66330356 C>A maps to NM_001104.1 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66330356 C>A maps to NM_001104.1 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104245400 G>T maps to NM_005736.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104245400 G>T maps to NM_005736.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104245417 C>A maps to NM_005736.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104245417 C>A maps to NM_005736.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:152520512 G>T maps to NM_020445.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:152520512 G>T maps to NM_020445.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37394882 C>A maps to NM_024855.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37394882 C>A maps to NM_024855.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158395160 G>T maps to NM_145259.2 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158395160 G>T maps to NM_145259.2 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158443750 G>T maps to NM_145259.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158443750 G>T maps to NM_145259.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158443768 G>T maps to NM_145259.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158443768 G>T maps to NM_145259.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52309837 C>A maps to NM_001077401.1 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52309837 C>A maps to NM_001077401.1 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67413314 G>T maps to NM_080658.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67413314 G>T maps to NM_080658.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42854296 C>A maps to NM_002390.4 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42854296 C>A maps to NM_002390.4 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:9637278 C>A maps to NM_003183.4 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:9637278 C>A maps to NM_003183.4 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207310189 C>A maps to NM_003812.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207310189 C>A maps to NM_003812.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120437807 C>A maps to NM_021794.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120437807 C>A maps to NM_021794.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:24321433 C>A maps to ENST00000380789 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:24321433 C>A maps to ENST00000380789 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33527361 G>T maps to NM_030955.2 P1572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33527361 G>T maps to NM_030955.2 P1572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33576341 C>A maps to NM_030955.2 T1263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33576341 C>A maps to NM_030955.2 T1263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33577067 G>T maps to NM_030955.2 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33577067 G>T maps to NM_030955.2 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33658332 C>A maps to NM_030955.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33658332 C>A maps to NM_030955.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33881537 G>T maps to NM_030955.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33881537 G>T maps to NM_030955.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72462069 G>T maps to NM_139155.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72462069 G>T maps to NM_139155.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:43826171 G>T maps to ENST00000389420 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:43826171 G>T maps to ENST00000389420 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178540959 G>T maps to NM_014244.4 R1182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178540959 G>T maps to NM_014244.4 R1182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73205279 C>A maps to NM_014243.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73205279 C>A maps to NM_014243.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:28306955 G>T maps to NM_007038.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:28306955 G>T maps to NM_007038.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64769443 C>A maps to NM_197941.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64769443 C>A maps to NM_197941.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79058001 C>A maps to ENST00000258883 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79058001 C>A maps to ENST00000258883 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:64527078 C>A maps to NM_182920.1 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:64527078 C>A maps to NM_182920.1 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:18622303 G>T maps to NM_001040272.4 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:18622303 G>T maps to NM_001040272.4 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136403491 C>A maps to ENST00000393061 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136403491 C>A maps to ENST00000393061 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136409658 C>A maps to ENST00000393061 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136409658 C>A maps to ENST00000393061 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136412217 C>A maps to ENST00000393061 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136412217 C>A maps to ENST00000393061 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:84373178 C>A maps to NM_207517.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:84373178 C>A maps to NM_207517.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:84690267 G>T maps to NM_207517.2 V1460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:84690267 G>T maps to NM_207517.2 V1460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154557499 G>T maps to ENST00000292205 R1198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154557499 G>T maps to ENST00000292205 R1198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154574010 C>A maps to ENST00000292205 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154574010 C>A maps to ENST00000292205 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154574345 C>A maps to ENST00000292205 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154574345 C>A maps to ENST00000292205 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167865929 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167865929 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7707947 C>A maps to NM_020546.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7707947 C>A maps to NM_020546.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7773085 C>A maps to NM_020546.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7773085 C>A maps to NM_020546.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7789867 C>A maps to NM_020546.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7789867 C>A maps to NM_020546.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131793033 G>T maps to NM_001115.2 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131793033 G>T maps to NM_001115.2 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131916029 C>A maps to NM_001115.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131916029 C>A maps to NM_001115.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2929907 G>T maps to NM_014189.2 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2929907 G>T maps to NM_014189.2 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70890609 G>T maps to NM_001185054.1 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70890609 G>T maps to NM_001185054.1 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:111872650 G>T maps to NM_016824.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:111872650 G>T maps to NM_016824.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100203664 C>A maps to NM_000667.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100203664 C>A maps to NM_000667.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:99993812 G>T maps to NM_000671.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:99993812 G>T maps to NM_000671.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100349051 C>A maps to NM_000673.4 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100349051 C>A maps to NM_000673.4 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67356974 G>T maps to NM_144650.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67356974 G>T maps to NM_144650.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67361124 C>A maps to NM_144650.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67361124 C>A maps to NM_144650.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67361170 C>A maps to NM_144650.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67361170 C>A maps to NM_144650.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67366308 C>A maps to NM_144650.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67366308 C>A maps to NM_144650.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202914123 G>T maps to NM_015999.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202914123 G>T maps to NM_015999.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1889638 G>T maps to NM_024551.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1889638 G>T maps to NM_024551.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77896028 C>A maps to NM_014913.3 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77896028 C>A maps to NM_014913.3 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:26627893 C>A maps to ENST00000356368 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:26627893 C>A maps to ENST00000356368 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:26627998 C>A maps to ENST00000356368 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:26627998 C>A maps to ENST00000356368 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159344562 G>T maps to NM_000679.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159344562 G>T maps to NM_000679.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67047339 C>A maps to NM_001619.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67047339 C>A maps to NM_001619.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116060058 C>A maps to NM_001001936.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116060058 C>A maps to NM_001001936.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7780582 G>T maps to NM_001134647.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7780582 G>T maps to NM_001134647.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7795499 C>A maps to NM_001134647.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7795499 C>A maps to NM_001134647.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7873682 G>T maps to NM_001134647.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7873682 G>T maps to NM_001134647.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88055673 C>A maps to NM_001166693.1 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88055673 C>A maps to NM_001166693.1 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:100170775 G>T maps to NM_001025108.1 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:100170775 G>T maps to NM_001025108.1 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:100210180 C>A maps to NM_001025108.1 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:100210180 C>A maps to NM_001025108.1 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:74351739 C>A maps to NM_001133.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:74351739 C>A maps to NM_001133.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64796764 G>T maps to ENST00000422803 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64796764 G>T maps to ENST00000422803 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88764111 G>T maps to NM_133447.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88764111 G>T maps to NM_133447.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88768374 C>A maps to NM_133447.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88768374 C>A maps to NM_133447.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58124278 C>A maps to NM_001122772.1 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58124278 C>A maps to NM_001122772.1 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51768751 C>A maps to NM_001077665.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51768751 C>A maps to NM_001077665.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51768811 C>A maps to NM_001077665.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51768811 C>A maps to NM_001077665.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27278870 G>T maps to NM_021831.5 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27278870 G>T maps to NM_021831.5 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32151346 G>T maps to ENST00000375070 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32151346 G>T maps to ENST00000375070 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100327110 C>A maps to ENST00000311030 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100327110 C>A maps to ENST00000311030 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100327851 C>A maps to ENST00000311030 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100327851 C>A maps to ENST00000311030 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100346234 C>A maps to ENST00000311030 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100346234 C>A maps to ENST00000311030 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100346260 C>A maps to ENST00000311030 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100346260 C>A maps to ENST00000311030 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100347200 C>A maps to ENST00000311030 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100347200 C>A maps to ENST00000311030 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100366212 G>T maps to ENST00000311030 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100366212 G>T maps to ENST00000311030 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100366248 G>T maps to ENST00000311030 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100366248 G>T maps to ENST00000311030 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100368301 C>A maps to ENST00000311030 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100368301 C>A maps to ENST00000311030 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161575273 G>T maps to NM_020133.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161575273 G>T maps to NM_020133.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178386077 C>A maps to NM_003659.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178386077 C>A maps to NM_003659.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178402889 C>A maps to NM_003659.3 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178402889 C>A maps to NM_003659.3 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88257807 C>A maps to ENST00000395847 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88257807 C>A maps to ENST00000395847 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35037070 G>T maps to NM_031900.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35037070 G>T maps to NM_031900.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:247059154 G>T maps to ENST00000428671 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:247059154 G>T maps to ENST00000428671 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:135679325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:135679325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:135754218 G>T maps to NM_017651.4 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:135754218 G>T maps to NM_017651.4 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:135778731 G>T maps to NM_017651.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:135778731 G>T maps to NM_017651.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105408731 G>T maps to NM_138420.2 S4352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105408731 G>T maps to NM_138420.2 S4352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105409322 G>T maps to NM_138420.2 S4155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105409322 G>T maps to NM_138420.2 S4155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105409805 G>T maps to NM_138420.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105409805 G>T maps to NM_138420.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105418379 C>A maps to NM_138420.2 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105418379 C>A maps to NM_138420.2 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105419036 G>T maps to NM_138420.2 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105419036 G>T maps to NM_138420.2 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62284251 G>T maps to NM_001620.1 P5879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62284251 G>T maps to NM_001620.1 P5879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62287440 C>A maps to NM_001620.1 V4816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62287440 C>A maps to NM_001620.1 V4816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62287914 G>T maps to NM_001620.1 P4658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62287914 G>T maps to NM_001620.1 P4658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62287986 C>A maps to NM_001620.1 V4634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62287986 C>A maps to NM_001620.1 V4634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62288574 C>A maps to NM_001620.1 P4438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62288574 C>A maps to NM_001620.1 P4438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62289321 G>T maps to NM_001620.1 P4189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62289321 G>T maps to NM_001620.1 P4189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62289606 G>T maps to NM_001620.1 P4094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62289606 G>T maps to NM_001620.1 P4094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62290401 G>T maps to NM_001620.1 P3829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62290401 G>T maps to NM_001620.1 P3829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62290806 G>T maps to NM_001620.1 P3694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62290806 G>T maps to NM_001620.1 P3694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62295084 G>T maps to NM_001620.1 P2268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62295084 G>T maps to NM_001620.1 P2268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62295543 G>T maps to NM_001620.1 P2115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62295543 G>T maps to NM_001620.1 P2115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62295777 C>A maps to NM_001620.1 V2037V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62295777 C>A maps to NM_001620.1 V2037V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62296893 G>T maps to NM_001620.1 P1665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62296893 G>T maps to NM_001620.1 P1665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62298186 G>T maps to NM_001620.1 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62298186 G>T maps to NM_001620.1 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62298267 G>T maps to NM_001620.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62298267 G>T maps to NM_001620.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62299623 G>T maps to NM_001620.1 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62299623 G>T maps to NM_001620.1 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62299718 C>A maps to NM_001620.1 G724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62299718 C>A maps to NM_001620.1 G724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62299839 G>T maps to NM_001620.1 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62299839 G>T maps to NM_001620.1 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:353908 G>T maps to NM_020731.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:353908 G>T maps to NM_020731.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71883245 G>T maps to NM_032797.5 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71883245 G>T maps to NM_032797.5 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:106973162 C>A maps to NM_001624.2 P1030P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:106973162 C>A maps to NM_001624.2 P1030P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:106999774 G>T maps to NM_001624.2 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:106999774 G>T maps to NM_001624.2 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42874015 C>A maps to NM_016248.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42874015 C>A maps to NM_016248.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42875230 C>A maps to NM_016248.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42875230 C>A maps to NM_016248.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151670546 G>T maps to NM_005100.3 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151670546 G>T maps to NM_005100.3 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151671919 C>G maps to NM_005100.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151671919 C>G maps to NM_005100.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151672141 C>A maps to NM_005100.3 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151672141 C>A maps to NM_005100.3 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:86124091 G>T maps to NM_006738.4 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:86124091 G>T maps to NM_006738.4 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119048780 C>A maps to NM_178813.5 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119048780 C>A maps to NM_178813.5 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:4737316 C>A maps to NM_006422.2 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:4737316 C>A maps to NM_006422.2 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:64935786 G>T maps to NM_004857.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:64935786 G>T maps to NM_004857.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5242254 C>A maps to NM_001818.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5242254 C>A maps to NM_001818.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:105250888 C>A maps to NM_001627.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:105250888 C>A maps to NM_001627.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97371129 G>T maps to NM_002860.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97371129 G>T maps to NM_002860.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97385173 C>A maps to NM_002860.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97385173 C>A maps to NM_002860.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97413098 G>T maps to NM_002860.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97413098 G>T maps to NM_002860.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75533639 G>T maps to NM_000689.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75533639 G>T maps to NM_000689.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101427778 C>A maps to NM_000693.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101427778 C>A maps to NM_000693.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101447396 C>A maps to NM_000693.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101447396 C>A maps to NM_000693.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:125876337 C>A maps to ENST00000273450 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:125876337 C>A maps to ENST00000273450 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105420355 C>A maps to NM_001034173.3 G895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105420355 C>A maps to NM_001034173.3 G895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:38712166 C>A maps to NM_001013620.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:38712166 C>A maps to NM_001013620.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:34176934 G>T maps to NM_032834.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:34176934 G>T maps to NM_032834.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:34179207 G>T maps to NM_032834.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:34179207 G>T maps to NM_032834.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50298117 C>A maps to NM_024105.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50298117 C>A maps to NM_024105.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101980241 G>T maps to NM_033087.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101980241 G>T maps to NM_033087.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101980763 C>A maps to NM_033087.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101980763 C>A maps to NM_033087.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77820535 G>T maps to NM_024079.4 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77820535 G>T maps to NM_024079.4 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77832144 T>C maps to NM_024079.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77832144 T>C maps to NM_024079.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:78146284 G>T maps to NM_006020.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:78146284 G>T maps to NM_006020.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:78170751 G>T maps to NM_006020.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:78170751 G>T maps to NM_006020.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109526160 C>A maps to NM_001145375.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109526160 C>A maps to NM_001145375.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109526247 G>T maps to NM_001145375.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109526247 G>T maps to NM_001145375.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:29416299 C>A maps to NM_004304.3 P1551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:29416299 C>A maps to NM_004304.3 P1551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:29917880 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:29917880 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73677087 C>A maps to NM_015120.4 S1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73677087 C>A maps to NM_015120.4 S1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73786219 C>A maps to NM_015120.4 P3444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73786219 C>A maps to NM_015120.4 P3444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7990712 C>A maps to NM_001139.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7990712 C>A maps to NM_001139.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:6903714 C>A maps to NM_000697.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:6903714 C>A maps to NM_000697.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:45941108 C>A maps to NM_000698.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:45941108 C>A maps to NM_000698.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56202338 G>T maps to NM_052947.3 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56202338 G>T maps to NM_052947.3 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56247215 G>T maps to NM_052947.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56247215 G>T maps to NM_052947.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56247542 C>A maps to NM_052947.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56247542 C>A maps to NM_052947.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233243696 G>T maps to NM_001632.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233243696 G>T maps to NM_001632.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202436668 G>T maps to NM_001168221.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202436668 G>T maps to NM_001168221.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202469414 C>A maps to NM_001168221.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202469414 C>A maps to NM_001168221.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203839188 G>T maps to NM_024744.14 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203839188 G>T maps to NM_024744.14 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203848280 C>A maps to NM_024744.14 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203848280 C>A maps to NM_024744.14 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202580486 C>A maps to NM_020919.3 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202580486 C>A maps to NM_020919.3 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202593774 C>A maps to NM_020919.3 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202593774 C>A maps to NM_020919.3 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:85677429 C>A maps to NM_006982.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:85677429 C>A maps to NM_006982.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:85695099 C>A maps to NM_006982.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:85695099 C>A maps to NM_006982.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11189346 C>A maps to NM_054028.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11189346 C>A maps to NM_054028.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116836384 C>A maps to NM_001633.3 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116836384 C>A maps to NM_001633.3 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46439469 G>T maps to ENST00000458649 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46439469 G>T maps to ENST00000458649 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96360233 G>T maps to NM_152435.2 G381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96360233 G>T maps to NM_152435.2 G381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115223034 C>A maps to NM_000036.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115223034 C>A maps to NM_000036.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10483153 C>A maps to NM_000480.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10483153 C>A maps to NM_000480.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38424432 G>T maps to NM_001635.3 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38424432 G>T maps to NM_001635.3 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38502706 C>A maps to NM_001635.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38502706 C>A maps to NM_001635.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104163171 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104163171 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104116967 C>A maps to NM_020978.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104116967 C>A maps to NM_020978.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104121993 G>T maps to NM_020978.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104121993 G>T maps to NM_020978.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2749347 G>A maps to NM_133463.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2749347 G>A maps to NM_133463.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121746378 C>A maps to NM_016237.4 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121746378 C>A maps to NM_016237.4 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121746476 C>A maps to NM_016237.4 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121746476 C>A maps to NM_016237.4 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:6420227 C>A maps to NM_001147.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:6420227 C>A maps to NM_001147.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129851306 C>A maps to NM_012098.2 G465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129851306 C>A maps to NM_012098.2 G465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114277304 C>A maps to NM_001148.4 R2511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114277304 C>A maps to NM_001148.4 R2511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114280036 C>A maps to NM_001148.4 A3421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114280036 C>A maps to NM_001148.4 A3421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61828511 G>T maps to NM_020987.2 R4043R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61828511 G>T maps to NM_020987.2 R4043R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61829196 G>T maps to NM_020987.2 P3814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61829196 G>T maps to NM_020987.2 P3814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61829490 G>T maps to NM_020987.2 P3716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61829490 G>T maps to NM_020987.2 P3716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61831755 G>T maps to NM_020987.2 P2961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61831755 G>T maps to NM_020987.2 P2961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61832367 G>T maps to NM_020987.2 P2757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61832367 G>T maps to NM_020987.2 P2757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61844464 G>T maps to NM_020987.2 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61844464 G>T maps to NM_020987.2 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190606122 C>G maps to NM_144708.3 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190606122 C>G maps to NM_144708.3 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190611116 C>A maps to NM_144708.3 R1357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190611116 C>A maps to NM_144708.3 R1357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14749312 G>T maps to NM_054027.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14749312 G>T maps to NM_054027.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:91948777 C>A maps to NM_019004.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:91948777 C>A maps to NM_019004.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17396261 C>A maps to NM_152363.4 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17396261 C>A maps to NM_152363.4 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133304628 C>A maps to NM_015114.1 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133304628 C>A maps to NM_015114.1 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89348020 C>A maps to NM_013275.4 P1643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89348020 C>A maps to NM_013275.4 P1643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89350233 G>T maps to NM_013275.4 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89350233 G>T maps to NM_013275.4 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89351986 G>T maps to NM_013275.4 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89351986 G>T maps to NM_013275.4 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89352569 C>A maps to NM_013275.4 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89352569 C>A maps to NM_013275.4 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5920164 C>A maps to NM_001009941.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5920164 C>A maps to NM_001009941.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73956585 G>T maps to NM_032217.3 P2253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73956585 G>T maps to NM_032217.3 P2253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73956900 C>A maps to NM_032217.3 A2148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73956900 C>A maps to NM_032217.3 A2148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73959811 G>T maps to NM_032217.3 R1771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73959811 G>T maps to NM_032217.3 R1771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27301927 C>A maps to NM_014915.2 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27301927 C>A maps to NM_014915.2 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:33140668 C>A maps to NM_032139.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:33140668 C>A maps to NM_032139.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:15762579 C>A maps to NM_015199.3 G250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:15762579 C>A maps to NM_015199.3 G250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:14850278 C>A maps to NM_001145029.1 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:14850278 C>A maps to NM_001145029.1 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145561839 C>A maps to NM_144698.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145561839 C>A maps to NM_144698.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:82922341 C>G maps to ENST00000260047 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:82922341 C>G maps to ENST00000260047 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101540108 G>T maps to NM_198401.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101540108 G>T maps to NM_198401.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:125590708 G>T maps to NM_020337.2 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:125590708 G>T maps to NM_020337.2 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:55407425 G>T maps to NM_024669.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:55407425 G>T maps to NM_024669.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:55466528 G>T maps to NM_024669.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:55466528 G>T maps to NM_024669.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35051201 G>T maps to NM_015245.2 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35051201 G>T maps to NM_015245.2 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:99222980 G>T maps to NM_152788.3 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:99222980 G>T maps to NM_152788.3 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36462404 G>T maps to NM_018685.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36462404 G>T maps to NM_018685.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:43591307 C>A maps to NM_018075.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:43591307 C>A maps to NM_018075.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6055340 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6055340 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:22261113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:22261113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:45782032 C>A maps to NM_001142679.1 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:45782032 C>A maps to NM_001142679.1 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242149905 G>T maps to NM_001001891.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242149905 G>T maps to NM_001001891.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:418544 G>T maps to NM_001012302.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:418544 G>T maps to NM_001012302.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:165118481 C>A maps to NM_012403.1 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:165118481 C>A maps to NM_012403.1 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48866497 C>A maps to NM_012404.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48866497 C>A maps to NM_012404.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69271910 C>A maps to NM_032208.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69271910 C>A maps to NM_032208.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69330008 C>A maps to NM_032208.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69330008 C>A maps to NM_032208.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69408958 G>T maps to NM_032208.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69408958 G>T maps to NM_032208.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75139866 G>T maps to NM_004034.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75139866 G>T maps to NM_004034.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75147541 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75147541 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36588261 G>T maps to NM_001177506.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36588261 G>T maps to NM_001177506.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41002310 C>A maps to NM_009590.2 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41002310 C>A maps to NM_009590.2 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201469486 C>A maps to NM_001159.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201469486 C>A maps to NM_001159.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201476208 C>A maps to NM_001159.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201476208 C>A maps to NM_001159.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201485875 C>A maps to NM_001159.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201485875 C>A maps to NM_001159.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:29759006 G>T maps to NM_001127.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:29759006 G>T maps to NM_001127.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71768553 C>A maps to ENST00000423132 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71768553 C>A maps to ENST00000423132 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71823330 G>T maps to ENST00000423132 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71823330 G>T maps to ENST00000423132 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42019811 G>T maps to NM_006803.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42019811 G>T maps to NM_006803.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:99042131 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:99042131 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:99119293 G>T maps to NM_181861.1 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:99119293 G>T maps to NM_181861.1 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:40895371 G>T maps to NM_004307.1 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:40895371 G>T maps to NM_004307.1 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41015876 C>A maps to NM_004307.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41015876 C>A maps to NM_004307.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68740265 C>A maps to NM_173545.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68740265 C>A maps to NM_173545.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68740346 C>A maps to NM_173545.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68740346 C>A maps to NM_173545.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68804994 C>A maps to NM_173545.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68804994 C>A maps to NM_173545.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116707736 G>T maps to NM_000039.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116707736 G>T maps to NM_000039.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116691774 C>A maps to NM_000482.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116691774 C>A maps to NM_000482.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21224685 C>A maps to NM_000384.2 T4536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21224685 C>A maps to NM_000384.2 T4536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21226169 C>A maps to NM_000384.2 E4042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21226169 C>A maps to NM_000384.2 E4042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21228063 G>T maps to NM_000384.2 P3892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21228063 G>T maps to NM_000384.2 P3892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21231228 C>A maps to NM_000384.2 T2837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:21231228 C>A maps to NM_000384.2 T2837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27369689 G>T maps to NM_000484.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27369689 G>T maps to NM_000484.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27372471 C>A maps to NM_000484.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27372471 C>A maps to NM_000484.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154295569 G>T maps to NM_080429.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154295569 G>T maps to NM_080429.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30962225 C>A maps to ENST00000509504 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30962225 C>A maps to ENST00000509504 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:24436279 C>A maps to NM_001650.4 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:24436279 C>A maps to NM_001650.4 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50369315 C>A maps to NM_001652.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50369315 C>A maps to NM_001652.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:58465384 C>A maps to NM_020980.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:58465384 C>A maps to NM_020980.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:36212251 G>T maps to NM_015230.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:36212251 G>T maps to NM_015230.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118452032 C>A maps to ENST00000359415 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118452032 C>A maps to ENST00000359415 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49333511 G>T maps to NM_001659.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49333511 G>T maps to NM_001659.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47196622 G>T maps to NM_032389.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47196622 G>T maps to NM_032389.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68170029 C>A maps to NM_006421.3 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68170029 C>A maps to NM_006421.3 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121289589 C>A maps to NM_001012659.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121289589 C>A maps to NM_001012659.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:107211833 G>T maps to NM_018011.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:107211833 G>T maps to NM_018011.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:148802987 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:148802987 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24874876 C>A maps to NM_020824.3 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24874876 C>A maps to NM_020824.3 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:86898749 G>T maps to NM_001025616.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:86898749 G>T maps to NM_001025616.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:142513548 C>A maps to NM_015071.4 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:142513548 C>A maps to NM_015071.4 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94639424 C>A maps to NM_004815.3 *1262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94639424 C>A maps to NM_004815.3 *1262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94639838 G>T maps to NM_004815.3 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94639838 G>T maps to NM_004815.3 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94643638 G>T maps to NM_004815.3 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94643638 G>T maps to NM_004815.3 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119132834 G>T maps to NM_020754.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119132834 G>T maps to NM_020754.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:128840946 G>T maps to NM_001142685.1 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:128840946 G>T maps to NM_001142685.1 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:128842500 G>T maps to NM_001142685.1 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:128842500 G>T maps to NM_001142685.1 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79827225 G>T maps to NM_004309.4 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79827225 G>T maps to NM_004309.4 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:1824844 C>A maps to ENST00000398564 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:1824844 C>A maps to ENST00000398564 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156925513 G>T maps to NM_198236.1 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156925513 G>T maps to NM_198236.1 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8219165 G>T maps to NM_173728.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8219165 G>T maps to NM_173728.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111862250 C>A maps to NM_001113511.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111862250 C>A maps to NM_001113511.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111862310 C>A maps to NM_001113511.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111862310 C>A maps to NM_001113511.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111919900 C>A maps to NM_001113511.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111919900 C>A maps to NM_001113511.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157527755 C>A maps to ENST00000367148 T1867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157527755 C>A maps to ENST00000367148 T1867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157528495 C>A maps to ENST00000367148 S2114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157528495 C>A maps to ENST00000367148 S2114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235338607 G>T maps to NM_016374.5 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235338607 G>T maps to NM_016374.5 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235345470 G>T maps to NM_016374.5 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235345470 G>T maps to NM_016374.5 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235345739 C>A maps to NM_016374.5 E832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235345739 C>A maps to NM_016374.5 E832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235345863 G>T maps to NM_016374.5 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235345863 G>T maps to NM_016374.5 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:63852098 C>A maps to NM_032199.2 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:63852098 C>A maps to NM_032199.2 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72874455 C>A maps to NM_005744.3 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72874455 C>A maps to NM_005744.3 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49019148 C>A maps to NM_006321.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49019148 C>A maps to NM_006321.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93722606 C>A maps to NM_182896.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93722606 C>A maps to NM_182896.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202104621 C>A maps to NM_138795.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202104621 C>A maps to NM_138795.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:5213858 C>A maps to ENST00000438743 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:5213858 C>A maps to ENST00000438743 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:66539585 C>A maps to NM_018120.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:66539585 C>A maps to NM_018120.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109225448 G>T maps to NM_032131.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109225448 G>T maps to NM_032131.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109233742 G>T maps to NM_032131.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109233742 G>T maps to NM_032131.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109249364 C>A maps to NM_032131.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109249364 C>A maps to NM_032131.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:23295820 C>A maps to NM_173081.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:23295820 C>A maps to NM_173081.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:28233891 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:28233891 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138003298 G>T maps to ENST00000469044 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138003298 G>T maps to ENST00000469044 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101857707 C>A maps to NM_022838.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101857707 C>A maps to NM_022838.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:13402758 G>T maps to ENST00000403290 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:13402758 G>T maps to ENST00000403290 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150814940 C>A maps to NM_001668.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150814940 C>A maps to NM_001668.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127636015 C>A maps to NM_030978.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127636015 C>A maps to NM_030978.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52844214 C>A maps to NM_006628.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52844214 C>A maps to NM_006628.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:35729352 C>A maps to ENST00000458225 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:35729352 C>A maps to ENST00000458225 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74988429 C>A maps to NM_004041.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74988429 C>A maps to NM_004041.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4902705 G>T maps to NM_001080523.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4902705 G>T maps to NM_001080523.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114823986 G>T maps to NM_024590.3 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114823986 G>T maps to NM_024590.3 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76997050 G>T maps to NM_001130016.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76997050 G>T maps to NM_001130016.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77025121 G>T maps to NM_001130016.1 G324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77025121 G>T maps to NM_001130016.1 G324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3660009 C>A maps to NM_001079536.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3660009 C>A maps to NM_001079536.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:52005004 C>A maps to NM_019893.2 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:52005004 C>A maps to NM_019893.2 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:9498928 G>T maps to NM_003887.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:9498928 G>T maps to NM_003887.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5683810 G>T maps to NM_024701.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5683810 G>T maps to NM_024701.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94419737 C>A maps to ENST00000434324 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94419737 C>A maps to ENST00000434324 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:100964150 C>A maps to NM_006828.2 E1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:100964150 C>A maps to NM_006828.2 E1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155307976 G>T maps to ENST00000368346 P2907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155307976 G>T maps to ENST00000368346 P2907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155330189 C>A maps to ENST00000368346 G2238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155330189 C>A maps to ENST00000368346 G2238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155449597 C>A maps to ENST00000368346 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155449597 C>A maps to ENST00000368346 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1540694 C>A maps to NM_004192.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1540694 C>A maps to NM_004192.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3402279 C>A maps to NM_000049.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3402279 C>A maps to NM_000049.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62430617 G>T maps to NM_004318.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62430617 G>T maps to NM_004318.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62465679 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62465679 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62475353 C>A maps to NM_004318.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62475353 C>A maps to NM_004318.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197072530 C>A maps to NM_018136.4 A1950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197072530 C>A maps to NM_018136.4 A1950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197087023 G>T maps to NM_018136.4 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197087023 G>T maps to NM_018136.4 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197108948 G>T maps to NM_018136.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197108948 G>T maps to NM_018136.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176918391 C>T maps to ENST00000281881 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176918391 C>T maps to ENST00000281881 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119737506 C>A maps to ENST00000313400 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119737506 C>A maps to ENST00000313400 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119770370 C>A maps to ENST00000313400 G531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119770370 C>A maps to ENST00000313400 G531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31319521 G>A maps to NM_030632.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31319521 G>A maps to NM_030632.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31319635 C>A maps to NM_030632.1 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31319635 C>A maps to NM_030632.1 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31326297 G>T maps to NM_030632.1 T2162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31326297 G>T maps to NM_030632.1 T2162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123670628 C>A maps to NM_001001976.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123670628 C>A maps to NM_001001976.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161761277 G>T maps to NM_007348.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161761277 G>T maps to NM_007348.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14613501 G>T maps to NM_018179.3 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14613501 G>T maps to NM_018179.3 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81354414 C>A maps to NM_031482.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81354414 C>A maps to NM_031482.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11389502 C>A maps to NM_006395.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11389502 C>A maps to NM_006395.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11421483 C>A maps to NM_006395.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11421483 C>A maps to NM_006395.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:293175 C>A maps to ENST00000409479 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:293175 C>A maps to ENST00000409479 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216214332 G>T maps to NM_004044.6 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216214332 G>T maps to NM_004044.6 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81078124 G>T maps to NM_015251.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81078124 G>T maps to NM_015251.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108170468 G>T maps to NM_000051.3 V1678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108170468 G>T maps to NM_000051.3 V1678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:160061381 C>A maps to NM_025153.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:160061381 C>A maps to NM_025153.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:160114831 G>T maps to NM_025153.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:160114831 G>T maps to NM_025153.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113478673 G>T maps to NM_032189.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113478673 G>T maps to NM_032189.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182554240 G>T maps to NM_014616.1 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182554240 G>T maps to NM_014616.1 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25262563 G>T maps to NM_001185085.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25262563 G>T maps to NM_001185085.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25281478 G>T maps to NM_001185085.1 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25281478 G>T maps to NM_001185085.1 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19756736 G>T maps to NM_020410.2 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19756736 G>T maps to NM_020410.2 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193201746 C>A maps to NM_032279.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193201746 C>A maps to NM_032279.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116927461 C>A maps to NM_000701.7 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116927461 C>A maps to NM_000701.7 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116930760 G>T maps to NM_000701.7 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116930760 G>T maps to NM_000701.7 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116932064 C>A maps to NM_000701.7 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116932064 C>A maps to NM_000701.7 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116935594 C>A maps to NM_000701.7 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116935594 C>A maps to NM_000701.7 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116941343 C>A maps to NM_000701.7 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116941343 C>A maps to NM_000701.7 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116941594 C>A maps to NM_000701.7 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116941594 C>A maps to NM_000701.7 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116943568 C>A maps to NM_000701.7 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116943568 C>A maps to NM_000701.7 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116944174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116944174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160093196 C>A maps to NM_000702.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160093196 C>A maps to NM_000702.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160099147 C>A maps to NM_000702.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160099147 C>A maps to NM_000702.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160099177 C>A maps to NM_000702.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160099177 C>A maps to NM_000702.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160109743 C>A maps to NM_000702.3 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160109743 C>A maps to NM_000702.3 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160141496 C>A maps to NM_144699.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160141496 C>A maps to NM_144699.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160143472 C>A maps to NM_144699.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160143472 C>A maps to NM_144699.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:90021478 C>A maps to ENST00000428670 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:90021478 C>A maps to ENST00000428670 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10452317 G>T maps to NM_001001331.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10452317 G>T maps to NM_001001331.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10452491 C>A maps to NM_001001331.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10452491 C>A maps to NM_001001331.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:152821584 C>A maps to NM_001001344.2 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:152821584 C>A maps to NM_001001344.2 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203691727 C>A maps to NM_001001396.1 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203691727 C>A maps to NM_001001396.1 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84476117 G>T maps to ENST00000416219 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84476117 G>T maps to ENST00000416219 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84485635 C>A maps to ENST00000416219 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84485635 C>A maps to ENST00000416219 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84492884 C>A maps to ENST00000416219 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84492884 C>A maps to ENST00000416219 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111999319 G>T maps to NM_001688.4 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111999319 G>T maps to NM_001688.4 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81608484 C>A maps to NM_001017971.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81608484 C>A maps to NM_001017971.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:40450541 C>A maps to NM_005765.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:40450541 C>A maps to NM_005765.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124209217 C>A maps to NM_012463.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124209217 C>A maps to NM_012463.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124232212 C>A maps to NM_012463.3 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124232212 C>A maps to NM_012463.3 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10923316 G>T maps to NM_001039362.1 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10923316 G>T maps to NM_001039362.1 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:46739190 G>T maps to NM_080653.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:46739190 G>T maps to NM_080653.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:46739391 G>T maps to NM_080653.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:46739391 G>T maps to NM_080653.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:54754205 G>T maps to NM_015941.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:54754205 G>T maps to NM_015941.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52513225 C>A maps to NM_000053.2 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52513225 C>A maps to NM_000053.2 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52548698 C>G maps to NM_000053.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52548698 C>G maps to NM_000053.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52548707 G>T maps to NM_000053.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52548707 G>T maps to NM_000053.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:55355591 C>A maps to NM_005603.4 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:55355591 C>A maps to NM_005603.4 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154306604 C>A maps to NM_020452.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154306604 C>A maps to NM_020452.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154318753 G>T maps to NM_020452.3 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154318753 G>T maps to NM_020452.3 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154319121 G>T maps to NM_020452.3 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154319121 G>T maps to NM_020452.3 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:50271830 G>T maps to NM_024837.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:50271830 G>T maps to NM_024837.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50273569 G>T maps to NM_006045.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50273569 G>T maps to NM_006045.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50305653 C>A maps to NM_006045.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50305653 C>A maps to NM_006045.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50342399 G>T maps to NM_006045.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50342399 G>T maps to NM_006045.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48493214 C>A maps to NM_130384.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48493214 C>A maps to NM_130384.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:76939502 G>T maps to NM_000489.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:76939502 G>T maps to NM_000489.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:76939727 G>T maps to NM_000489.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:76939727 G>T maps to NM_000489.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142180800 G>T maps to NM_001184.3 T2391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142180800 G>T maps to NM_001184.3 T2391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142277589 C>A maps to NM_001184.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142277589 C>A maps to NM_001184.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16326846 C>A maps to NM_000332.3 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16326846 C>A maps to NM_000332.3 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:13337299 C>A maps to NM_001135995.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:13337299 C>A maps to NM_001135995.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:63973799 C>A maps to NM_001177387.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:63973799 C>A maps to NM_001177387.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:63973886 C>A maps to NM_001177387.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:63973886 C>A maps to NM_001177387.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:70236563 G>T maps to NM_015570.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:70236563 G>T maps to NM_015570.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58191673 C>G maps to NM_006576.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58191673 C>G maps to NM_006576.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99566014 C>A maps to NM_001185.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99566014 C>A maps to NM_001185.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31897959 C>A maps to NM_194318.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31897959 C>A maps to NM_194318.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62449570 C>A maps to NM_006577.5 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62449570 C>A maps to NM_006577.5 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62449597 G>T maps to NM_006577.5 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62449597 G>T maps to NM_006577.5 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62449606 G>T maps to NM_006577.5 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62449606 G>T maps to NM_006577.5 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:118943050 C>A maps to NM_212543.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:118943050 C>A maps to NM_212543.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48252856 C>A maps to NM_004776.3 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48252856 C>A maps to NM_004776.3 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104133565 C>A maps to NM_001701.3 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104133565 C>A maps to NM_001701.3 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117161762 C>A maps to NM_012104.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117161762 C>A maps to NM_012104.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90718488 C>A maps to NM_001170794.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90718488 C>A maps to NM_001170794.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64051813 C>A maps to NM_032989.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64051813 C>A maps to NM_032989.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:104026972 C>A maps to NM_001015049.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:104026972 C>A maps to NM_001015049.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79411730 C>A maps to ENST00000436173 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79411730 C>A maps to ENST00000436173 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40750704 G>T maps to NM_014952.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40750704 G>T maps to NM_014952.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143561114 G>T maps to NM_001702.2 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143561114 G>T maps to NM_001702.2 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143623434 G>T maps to NM_001702.2 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143623434 G>T maps to NM_001702.2 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:102951370 C>A maps to NM_017935.4 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:102951370 C>A maps to NM_017935.4 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91180281 C>A maps to NM_020063.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91180281 C>A maps to NM_020063.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129246115 G>T maps to NM_003658.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129246115 G>T maps to NM_003658.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31608253 G>T maps to ENST00000404765 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31608253 G>T maps to ENST00000404765 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31609585 C>A maps to ENST00000404765 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31609585 C>A maps to ENST00000404765 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31616461 G>T maps to ENST00000404765 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31616461 G>T maps to ENST00000404765 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72877253 G>T maps to NM_032408.3 R1083R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72877253 G>T maps to NM_032408.3 R1083R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72892518 G>T maps to NM_032408.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72892518 G>T maps to NM_032408.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56995524 C>A maps to NM_013449.3 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56995524 C>A maps to NM_013449.3 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160205686 C>A maps to NM_013450.2 S1656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160205686 C>A maps to NM_013450.2 S1656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66288760 C>A maps to NM_024649.4 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66288760 C>A maps to NM_024649.4 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45314566 G>T maps to NM_005581.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45314566 G>T maps to NM_005581.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94037349 C>A maps to NM_003567.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94037349 C>A maps to NM_003567.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94047988 C>A maps to NM_003567.2 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94047988 C>A maps to NM_003567.2 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94048439 C>A maps to NM_003567.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94048439 C>A maps to NM_003567.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94049650 G>T maps to NM_003567.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94049650 G>T maps to NM_003567.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115110764 G>T maps to NM_005872.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115110764 G>T maps to NM_005872.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41930425 C>A maps to NM_000709.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41930425 C>A maps to NM_000709.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:60773196 G>T maps to NM_022893.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:60773196 G>T maps to NM_022893.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30899186 C>A maps to NM_004765.2 *218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30899186 C>A maps to NM_004765.2 *218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30899236 C>A maps to NM_004765.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30899236 C>A maps to NM_004765.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:147091361 C>A maps to NM_004326.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:147091361 C>A maps to NM_004326.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:147096117 G>T maps to NM_004326.2 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:147096117 G>T maps to NM_004326.2 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81295770 C>A maps to NM_017429.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81295770 C>A maps to NM_017429.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81295810 G>T maps to NM_017429.2 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81295810 G>T maps to NM_017429.2 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129147581 G>T maps to ENST00000303743 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129147581 G>T maps to ENST00000303743 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129149309 C>A maps to ENST00000303743 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129149309 C>A maps to ENST00000303743 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18222008 C>A maps to NM_153346.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18222008 C>A maps to NM_153346.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56857307 C>A maps to NM_152731.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56857307 C>A maps to NM_152731.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:102318028 G>T maps to NM_018476.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:102318028 G>T maps to NM_018476.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:26276668 C>A maps to NM_030762.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:26276668 C>A maps to NM_030762.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51693449 G>T maps to NM_016293.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51693449 G>T maps to NM_016293.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22487990 C>A maps to NM_018688.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22487990 C>A maps to NM_018688.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102220755 C>A maps to NM_001166.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102220755 C>A maps to NM_001166.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32602827 C>A maps to NM_016252.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32602827 C>A maps to NM_016252.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32626341 G>T maps to NM_016252.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32626341 G>T maps to NM_016252.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32694652 G>T maps to NM_016252.3 S2106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32694652 G>T maps to NM_016252.3 S2106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32724788 G>T maps to NM_016252.3 G2882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32724788 G>T maps to NM_016252.3 G2882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69092780 G>T maps to NM_014482.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69092780 G>T maps to NM_014482.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:55739372 C>A maps to NM_021073.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:55739372 C>A maps to NM_021073.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:96035877 G>T maps to ENST00000440890 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:96035877 G>T maps to ENST00000440890 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203420625 C>A maps to NM_001204.6 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203420625 C>A maps to NM_001204.6 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43288420 C>A maps to NM_014753.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43288420 C>A maps to NM_014753.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172590779 G>T maps to NM_013979.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172590779 G>T maps to NM_013979.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151018350 C>A maps to NM_138278.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151018350 C>A maps to NM_138278.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:112997024 C>A maps to ENST00000273395 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:112997024 C>A maps to ENST00000273395 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:13605301 C>T maps to NM_148894.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:13605301 C>T maps to NM_148894.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134346783 C>A maps to NM_001724.4 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134346783 C>A maps to NM_001724.4 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31622018 C>A maps to NM_174897.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31622018 C>A maps to NM_174897.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36946846 C>A maps to NM_001725.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36946846 C>A maps to NM_001725.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220233031 C>A maps to NM_006085.4 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220233031 C>A maps to NM_006085.4 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220242729 G>T maps to NM_006085.4 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220242729 G>T maps to NM_006085.4 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220247343 G>T maps to NM_006085.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220247343 G>T maps to NM_006085.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32911269 C>A maps to NM_000059.3 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32911269 C>A maps to NM_000059.3 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32915262 C>A maps to NM_000059.3 P2257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32915262 C>A maps to NM_000059.3 P2257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32929039 C>A maps to NM_000059.3 T2350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32929039 C>A maps to NM_000059.3 T2350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50192286 C>A maps to ENST00000342989 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50192286 C>A maps to ENST00000342989 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:15355538 G>T maps to NM_058243.2 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:15355538 G>T maps to NM_058243.2 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50402141 C>A maps to NM_001173984.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50402141 C>A maps to NM_001173984.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:889144 C>A maps to NM_001009877.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:889144 C>A maps to NM_001009877.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92428463 C>A maps to ENST00000347608 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92428463 C>A maps to ENST00000347608 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92470044 C>A maps to ENST00000347608 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92470044 C>A maps to ENST00000347608 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92470786 C>A maps to ENST00000347608 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92470786 C>A maps to ENST00000347608 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37702613 G>T maps to NM_018310.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37702613 G>T maps to NM_018310.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:59861785 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:59861785 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9781177 G>T maps to NM_001003694.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9781177 G>T maps to NM_001003694.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36181663 C>A maps to NM_015695.2 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36181663 C>A maps to NM_015695.2 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32834140 C>A maps to NM_001143888.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32834140 C>A maps to NM_001143888.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116132364 G>T maps to NM_017688.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116132364 G>T maps to NM_017688.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:13438767 G>T maps to NM_032320.5 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:13438767 G>T maps to NM_032320.5 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:3639203 G>T maps to NM_032444.2 R1479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:3639203 G>T maps to NM_032444.2 R1479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:11898958 C>A maps to NM_014962.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:11898958 C>A maps to NM_014962.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:11904100 C>A maps to NM_014962.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:11904100 C>A maps to NM_014962.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92612793 G>T maps to NM_183242.3 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92612793 G>T maps to NM_183242.3 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:75675909 C>A maps to NM_001729.2 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:75675909 C>A maps to NM_001729.2 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:112198616 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:112198616 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26508762 C>A maps to NM_001732.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26508762 C>A maps to NM_001732.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26459844 C>A maps to NM_007049.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26459844 C>A maps to NM_007049.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26385324 C>A maps to NM_001197237.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26385324 C>A maps to NM_001197237.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26390287 C>A maps to NM_001197237.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26390287 C>A maps to NM_001197237.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180338411 G>T maps to NM_001040462.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180338411 G>T maps to NM_001040462.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180486690 G>C maps to NM_152547.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180486690 G>C maps to NM_152547.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115891029 G>T maps to NM_018017.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115891029 G>T maps to NM_018017.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121612601 G>T maps to NM_024834.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121612601 G>T maps to NM_024834.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124457983 G>T maps to NM_001010912.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124457983 G>T maps to NM_001010912.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98744138 C>A maps to NM_015652.2 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98744138 C>A maps to NM_015652.2 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127434402 G>T maps to ENST00000356792 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127434402 G>T maps to ENST00000356792 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:21804623 C>A maps to NM_207371.3 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:21804623 C>A maps to NM_207371.3 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5784165 C>A maps to NM_017782.4 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5784165 C>A maps to NM_017782.4 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748051 C>A maps to NM_021830.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748051 C>A maps to NM_021830.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748444 C>A maps to NM_021830.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748444 C>A maps to NM_021830.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748794 G>T maps to NM_021830.4 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748794 G>T maps to NM_021830.4 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748819 C>A maps to NM_021830.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102748819 C>A maps to NM_021830.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33134883 C>A maps to ENST00000375025 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33134883 C>A maps to ENST00000375025 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50256538 G>T maps to NM_001031746.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50256538 G>T maps to NM_001031746.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103784912 G>T maps to NM_024541.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103784912 G>T maps to NM_024541.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115536931 G>T maps to NM_182601.1 G361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115536931 G>T maps to NM_182601.1 G361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120070743 G>T maps to NM_022063.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120070743 G>T maps to NM_022063.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128153268 G>T maps to NM_001004298.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128153268 G>T maps to NM_001004298.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118084573 G>T maps to NM_198515.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118084573 G>T maps to NM_198515.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76171052 G>T maps to ENST00000393457 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76171052 G>T maps to ENST00000393457 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124637340 G>T maps to ENST00000374979 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124637340 G>T maps to ENST00000374979 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122756769 C>A maps to NM_024806.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122756769 C>A maps to NM_024806.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65685121 C>A maps to NM_001135635.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65685121 C>A maps to NM_001135635.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:114270941 C>A maps to NM_019021.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:114270941 C>A maps to NM_019021.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53696883 G>T maps to NM_021640.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53696883 G>T maps to NM_021640.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110924438 G>T maps to NM_013300.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110924438 G>T maps to NM_013300.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110924453 C>A maps to NM_013300.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110924453 C>A maps to NM_013300.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32137852 C>A maps to NM_018169.3 R1322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32137852 C>A maps to NM_018169.3 R1322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:103699776 G>T maps to NM_001099336.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:103699776 G>T maps to NM_001099336.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117158240 C>A maps to NM_024738.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117158240 C>A maps to NM_024738.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112620944 G>T maps to NM_001109662.2 T3463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112620944 G>T maps to NM_001109662.2 T3463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112654664 C>A maps to NM_001109662.2 G2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112654664 C>A maps to NM_001109662.2 G2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112691951 C>A maps to NM_001109662.2 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112691951 C>A maps to NM_001109662.2 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112694198 C>A maps to NM_001109662.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112694198 C>A maps to NM_001109662.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112708042 G>T maps to NM_001109662.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112708042 G>T maps to NM_001109662.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112708168 G>T maps to NM_001109662.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112708168 G>T maps to NM_001109662.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112717073 G>T maps to NM_001109662.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112717073 G>T maps to NM_001109662.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:73319245 C>A maps to ENST00000377815 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:73319245 C>A maps to ENST00000377815 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103346731 C>A maps to NM_001010977.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103346731 C>A maps to NM_001010977.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:90770446 G>T maps to NM_017970.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:90770446 G>T maps to NM_017970.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:90782986 G>T maps to NM_017970.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:90782986 G>T maps to NM_017970.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:60903648 C>A maps to NM_174978.2 G560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:60903648 C>A maps to NM_174978.2 G560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34393959 G>T maps to NM_020154.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34393959 G>T maps to NM_020154.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45723233 G>T maps to NM_197955.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45723233 G>T maps to NM_197955.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40631056 G>T maps to NM_207380.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40631056 G>T maps to NM_207380.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15977963 G>T maps to NM_144600.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15977963 G>T maps to NM_144600.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:5106074 G>T maps to ENST00000350219 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:5106074 G>T maps to ENST00000350219 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30768823 C>A maps to NM_001014979.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30768823 C>A maps to NM_001014979.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:54892244 G>T maps to NM_001085430.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:54892244 G>T maps to NM_001085430.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:57290205 G>T maps to NM_018149.6 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:57290205 G>T maps to NM_018149.6 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7329105 C>A maps to NM_175734.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7329105 C>A maps to NM_175734.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7161977 C>A maps to NM_203414.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7161977 C>A maps to NM_203414.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34387846 G>T maps to NM_015476.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34387846 G>T maps to NM_015476.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43796178 C>A maps to NM_145055.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43796178 C>A maps to NM_145055.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:20889648 C>A maps to NM_032933.4 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:20889648 C>A maps to NM_032933.4 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:51892103 C>A maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:51892103 C>A maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11486218 C>A maps to NM_175871.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11486218 C>A maps to NM_175871.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44237569 C>A maps to NM_019108.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44237569 C>A maps to NM_019108.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159776219 C>A maps to NM_031908.4 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159776219 C>A maps to NM_031908.4 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24895617 G>T maps to NM_178540.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24895617 G>T maps to NM_178540.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7172504 C>A maps to NM_001734.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7172504 C>A maps to NM_001734.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7173849 C>A maps to NM_001734.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7173849 C>A maps to NM_001734.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7177213 C>A maps to NM_001734.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7177213 C>A maps to NM_001734.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172437641 G>T maps to NM_139240.3 G154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172437641 G>T maps to NM_139240.3 G154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200880655 G>T maps to NM_018265.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200880655 G>T maps to NM_018265.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162824745 C>A maps to NM_178550.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162824745 C>A maps to NM_178550.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207196213 G>T maps to NM_023938.5 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207196213 G>T maps to NM_023938.5 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116663587 G>T maps to NM_152367.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116663587 G>T maps to NM_152367.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116670103 G>T maps to NM_152367.2 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116670103 G>T maps to NM_152367.2 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116670171 C>A maps to NM_152367.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116670171 C>A maps to NM_152367.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27278385 G>T maps to NM_152365.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27278385 G>T maps to NM_152365.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:3807168 G>T maps to NM_207356.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:3807168 G>T maps to NM_207356.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109650545 G>T maps to NM_001122961.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109650545 G>T maps to NM_001122961.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184588668 G>T maps to NM_030806.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184588668 G>T maps to NM_030806.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185191084 G>T maps to NM_001105518.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185191084 G>T maps to NM_001105518.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185191105 C>A maps to NM_001105518.1 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185191105 C>A maps to NM_001105518.1 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226180156 G>T maps to NM_152608.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226180156 G>T maps to NM_152608.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226183011 C>A maps to NM_152608.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226183011 C>A maps to NM_152608.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223568359 C>A maps to NM_152610.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223568359 C>A maps to NM_152610.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153615730 C>A maps to NM_015607.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153615730 C>A maps to NM_015607.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60506760 C>A maps to NM_152377.2 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60506760 C>A maps to NM_152377.2 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111891265 C>A maps to NM_181643.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111891265 C>A maps to NM_181643.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229462682 G>T maps to NM_145257.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229462682 G>T maps to NM_145257.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172538211 C>A maps to ENST00000367723 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172538211 C>A maps to ENST00000367723 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55100930 C>A maps to NM_001012971.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55100930 C>A maps to NM_001012971.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:54941159 C>A maps to NM_080821.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:54941159 C>A maps to NM_080821.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31891813 C>A maps to NM_033197.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31891813 C>A maps to NM_033197.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35422878 G>T maps to NM_080627.2 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35422878 G>T maps to NM_080627.2 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18379270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18379270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35783516 C>A maps to ENST00000343811 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35783516 C>A maps to ENST00000343811 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34560628 C>A maps to ENST00000373973 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34560628 C>A maps to ENST00000373973 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30602816 C>A maps to ENST00000300415 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30602816 C>A maps to ENST00000300415 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31661398 C>A maps to NM_182658.1 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31661398 C>A maps to NM_182658.1 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31682940 G>T maps to NM_182519.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31682940 G>T maps to NM_182519.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58645021 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58645021 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:20271004 C>A maps to ENST00000389655 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:20271004 C>A maps to ENST00000389655 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3802817 G>T maps to NM_018347.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3802817 G>T maps to NM_018347.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34827760 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34827760 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:271289 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:271289 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:32546407 C>A maps to NM_001010859.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:32546407 C>A maps to NM_001010859.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220040313 G>T maps to NM_015680.4 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220040313 G>T maps to NM_015680.4 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:75933754 G>T maps to NM_003203.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:75933754 G>T maps to NM_003203.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:200820955 C>A maps to NM_024520.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:200820955 C>A maps to NM_024520.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10282395 G>T maps to NM_182626.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10282395 G>T maps to NM_182626.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99413824 G>T maps to NM_207362.2 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99413824 G>T maps to NM_207362.2 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37475456 C>A maps to NM_144736.4 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37475456 C>A maps to NM_144736.4 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:200797876 G>T maps to NM_001039693.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:200797876 G>T maps to NM_001039693.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209036792 G>T maps to NM_001099334.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209036792 G>T maps to NM_001099334.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209045486 G>T maps to NM_001099334.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209045486 G>T maps to NM_001099334.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6718134 G>T maps to NM_000064.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6718134 G>T maps to NM_000064.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14703202 C>A maps to NM_016474.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14703202 C>A maps to NM_016474.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14745963 G>T maps to NM_032137.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14745963 G>T maps to NM_032137.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10146113 G>T maps to NM_001164839.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10146113 G>T maps to NM_001164839.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99895255 C>A maps to NM_032359.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99895255 C>A maps to NM_032359.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:8667333 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:8667333 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57830593 G>T maps to NM_032313.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57830593 G>T maps to NM_032313.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113479456 C>A maps to NM_018392.4 G1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113479456 C>A maps to NM_018392.4 G1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113527235 C>A maps to NM_018392.4 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113527235 C>A maps to NM_018392.4 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:8477698 C>A maps to NM_152544.2 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:8477698 C>A maps to NM_152544.2 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184585208 C>A maps to NM_021942.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184585208 C>A maps to NM_021942.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184598622 C>A maps to NM_021942.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184598622 C>A maps to NM_021942.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184614147 G>T maps to NM_021942.4 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184614147 G>T maps to NM_021942.4 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47823715 C>A maps to ENST00000355085 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47823715 C>A maps to ENST00000355085 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36211947 G>T maps to NM_001085411.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36211947 G>T maps to NM_001085411.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43494655 C>A maps to NM_198566.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43494655 C>A maps to NM_198566.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43039866 C>A maps to NM_001014279.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43039866 C>A maps to NM_001014279.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172517394 G>T maps to NM_153607.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172517394 G>T maps to NM_153607.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179268991 C>A maps to NM_016175.3 G122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179268991 C>A maps to NM_016175.3 G122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:131796341 C>A maps to NM_001013717.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:131796341 C>A maps to NM_001013717.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11778901 C>A maps to NM_001143948.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11778901 C>A maps to NM_001143948.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34622441 C>A maps to NM_024294.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34622441 C>A maps to NM_024294.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32317580 C>A maps to ENST00000447241 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32317580 C>A maps to ENST00000447241 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32334073 G>T maps to ENST00000447241 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32334073 G>T maps to ENST00000447241 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30619189 C>A maps to NM_001161376.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30619189 C>A maps to NM_001161376.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127796662 C>A maps to NM_001012279.2 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127796662 C>A maps to NM_001012279.2 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127797414 C>A maps to NM_001012279.2 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127797414 C>A maps to NM_001012279.2 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:112420501 G>T maps to NM_001033564.1 G6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:112420501 G>T maps to NM_001033564.1 G6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31735434 C>A maps to NM_025258.2 G534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31735434 C>A maps to NM_025258.2 G534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:40234622 G>T maps to NM_001193311.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:40234622 G>T maps to NM_001193311.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23340597 C>A maps to NM_138446.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23340597 C>A maps to NM_138446.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66410181 G>T maps to NM_017994.4 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66410181 G>T maps to NM_017994.4 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66418349 C>A maps to NM_017994.4 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66418349 C>A maps to NM_017994.4 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43684939 G>T maps to NM_018224.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43684939 G>T maps to NM_018224.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129856217 C>A maps to NM_145268.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129856217 C>A maps to NM_145268.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:120737810 G>T maps to NM_024913.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:120737810 G>T maps to NM_024913.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:117950577 C>A maps to NM_001025357.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:117950577 C>A maps to NM_001025357.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39288923 C>A maps to NM_001737.3 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39288923 C>A maps to NM_001737.3 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39306790 G>T maps to NM_001737.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39306790 G>T maps to NM_001737.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39331812 G>T maps to NM_001737.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39331812 G>T maps to NM_001737.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130469469 C>A maps to NM_001012502.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130469469 C>A maps to NM_001012502.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35043105 C>A maps to NM_203299.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35043105 C>A maps to NM_203299.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139960770 G>C maps to NM_178448.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139960770 G>C maps to NM_178448.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34402389 C>A maps to NM_001184940.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34402389 C>A maps to NM_001184940.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:97555110 G>T maps to NM_001193329.1 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:97555110 G>T maps to NM_001193329.1 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135698649 C>A maps to NM_152572.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135698649 C>A maps to NM_152572.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135702295 G>T maps to NM_152572.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135702295 G>T maps to NM_152572.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135702352 C>A maps to NM_152572.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135702352 C>A maps to NM_152572.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135742311 G>T maps to NM_152572.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135742311 G>T maps to NM_152572.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150234600 C>A maps to NM_012113.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150234600 C>A maps to NM_012113.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:20817115 G>T maps to NM_001100619.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:20817115 G>T maps to NM_001100619.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121098637 C>A maps to NM_001033677.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121098637 C>A maps to NM_001033677.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2229574 C>A maps to NM_199460.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2229574 C>A maps to NM_199460.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53774311 G>T maps to NM_001128840.1 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53774311 G>T maps to NM_001128840.1 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53785828 C>A maps to NM_001128840.1 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53785828 C>A maps to NM_001128840.1 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181453050 C>A maps to ENST00000357570 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181453050 C>A maps to ENST00000357570 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181453071 C>A maps to ENST00000357570 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181453071 C>A maps to ENST00000357570 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181453096 G>T maps to ENST00000357570 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181453096 G>T maps to ENST00000357570 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:81599995 G>T maps to NM_000722.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:81599995 G>T maps to NM_000722.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18816563 C>A maps to NM_201596.2 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18816563 C>A maps to NM_201596.2 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18828190 C>A maps to NM_201596.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18828190 C>A maps to NM_201596.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:64876750 G>T maps to NM_014404.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:64876750 G>T maps to NM_014404.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:115049427 C>A maps to NM_014333.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:115049427 C>A maps to NM_014333.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:122130293 C>A maps to NM_001167940.1 G565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:122130293 C>A maps to NM_001167940.1 G565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:62451041 G>T maps to ENST00000383709 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:62451041 G>T maps to ENST00000383709 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91072436 C>A maps to NM_004929.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91072436 C>A maps to NM_004929.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91072918 C>A maps to NM_004929.2 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91072918 C>A maps to NM_004929.2 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71417926 C>A maps to NM_001740.4 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71417926 C>A maps to NM_001740.4 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54115389 G>T maps to NM_020898.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54115389 G>T maps to NM_020898.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:188223789 C>A maps to NM_005795.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:188223789 C>A maps to NM_005795.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:188243690 G>T maps to NM_005795.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:188243690 G>T maps to NM_005795.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:90866422 C>A maps to NM_006888.4 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:90866422 C>A maps to NM_006888.4 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12595235 C>A maps to NM_153498.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12595235 C>A maps to NM_153498.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209782357 G>T maps to NM_020439.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209782357 G>T maps to NM_020439.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75632749 G>T maps to ENST00000423381 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75632749 G>T maps to ENST00000423381 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48266805 G>T maps to NM_004345.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48266805 G>T maps to NM_004345.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200816825 C>A maps to ENST00000236925 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200816825 C>A maps to ENST00000236925 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7724952 C>A maps to NM_015215.2 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7724952 C>A maps to NM_015215.2 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7811312 C>A maps to NM_015215.2 R1582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7811312 C>A maps to NM_015215.2 R1582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:67703957 G>T maps to NM_018448.3 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:67703957 G>T maps to NM_018448.3 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12858941 G>T maps to NM_001162499.1 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12858941 G>T maps to NM_001162499.1 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179136957 C>A maps to ENST00000415618 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179136957 C>A maps to ENST00000415618 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40527408 G>T maps to NM_001105530.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40527408 G>T maps to NM_001105530.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241533327 C>A maps to NM_023083.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241533327 C>A maps to NM_023083.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241555908 C>A maps to ENST00000270364 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241555908 C>A maps to ENST00000270364 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:30966292 C>A maps to ENST00000295055 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:30966292 C>A maps to ENST00000295055 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42652165 G>T maps to NM_000070.2 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42652165 G>T maps to NM_000070.2 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42695959 C>A maps to NM_000070.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42695959 C>A maps to NM_000070.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76825350 G>T maps to ENST00000360841 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76825350 G>T maps to ENST00000360841 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:110494237 C>A maps to NM_014289.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:110494237 C>A maps to NM_014289.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230916452 C>A maps to NM_006615.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230916452 C>A maps to NM_006615.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230921726 G>T maps to NM_006615.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230921726 G>T maps to NM_006615.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2987350 C>A maps to NM_032415.4 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2987350 C>A maps to NM_032415.4 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104915212 G>T maps to NM_001017534.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104915212 G>T maps to NM_001017534.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40853648 G>T maps to NM_032587.3 G739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40853648 G>T maps to NM_032587.3 G739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48714990 G>T maps to NM_001184900.1 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48714990 G>T maps to NM_001184900.1 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139266347 C>A maps to NM_052813.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139266347 C>A maps to NM_052813.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3023268 G>T maps to NM_001014437.2 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3023268 G>T maps to NM_001014437.2 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3059393 G>T maps to NM_001014437.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3059393 G>T maps to NM_001014437.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:41390309 G>T maps to ENST00000378163 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:41390309 G>T maps to ENST00000378163 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142989400 G>T maps to NM_032982.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142989400 G>T maps to NM_032982.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115486107 G>T maps to NM_033338.4 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115486107 G>T maps to NM_033338.4 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90576887 C>A maps to NM_012115.3 T1293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90576887 C>A maps to NM_012115.3 T1293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116280938 C>A maps to NM_001232.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116280938 C>A maps to NM_001232.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121976008 C>A maps to NM_001178065.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121976008 C>A maps to NM_001178065.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43940219 G>T maps to NM_172095.1 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43940219 G>T maps to NM_172095.1 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26524784 C>A maps to NM_198137.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26524784 C>A maps to NM_198137.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34472637 C>A maps to NM_001752.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34472637 C>A maps to NM_001752.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119170425 G>T maps to NM_005188.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119170425 G>T maps to NM_005188.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:77768511 C>G maps to NM_020649.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:77768511 C>G maps to NM_020649.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97791581 G>T maps to NM_001159747.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97791581 G>T maps to NM_001159747.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70520835 C>A maps to NM_018237.2 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70520835 C>A maps to NM_018237.2 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35660826 G>T maps to NM_174923.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35660826 G>T maps to NM_174923.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186379865 C>A maps to NM_152775.3 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186379865 C>A maps to NM_152775.3 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47777207 C>A maps to NM_145020.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47777207 C>A maps to NM_145020.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47778002 G>T maps to NM_145020.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47778002 G>T maps to NM_145020.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27850587 G>T maps to ENST00000435516 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27850587 G>T maps to ENST00000435516 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27850660 C>A maps to ENST00000435516 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27850660 C>A maps to ENST00000435516 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92869177 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92869177 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92905526 C>A maps to NM_017667.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92905526 C>A maps to NM_017667.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92905553 G>T maps to NM_017667.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92905553 G>T maps to NM_017667.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57752275 G>T maps to NM_032269.5 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57752275 G>T maps to NM_032269.5 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109408219 C>A maps to NM_144978.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109408219 C>A maps to NM_144978.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109421373 C>A maps to NM_144978.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109421373 C>A maps to NM_144978.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93646318 G>T maps to NM_206886.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93646318 G>T maps to NM_206886.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93687224 C>A maps to NM_206886.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93687224 C>A maps to NM_206886.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93687287 G>T maps to NM_206886.2 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93687287 G>T maps to NM_206886.2 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27610104 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27610104 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43011224 C>A maps to NM_001080850.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43011224 C>A maps to NM_001080850.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49294625 G>T maps to NM_178173.3 G566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49294625 G>T maps to NM_178173.3 G566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94806179 C>A maps to NM_001042399.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94806179 C>A maps to NM_001042399.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61829436 G>T maps to NM_020198.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61829436 G>T maps to NM_020198.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113166907 G>T maps to NM_144718.3 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113166907 G>T maps to NM_144718.3 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122090587 C>A maps to NM_001017928.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122090587 C>A maps to NM_001017928.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119773054 C>A maps to NM_178499.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119773054 C>A maps to NM_178499.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119943007 G>T maps to NM_178499.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119943007 G>T maps to NM_178499.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123270331 C>A maps to NM_201435.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123270331 C>A maps to NM_201435.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93118682 C>A maps to NM_181645.3 C303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93118682 C>A maps to NM_181645.3 C303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:538003 C>A maps to NM_032358.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:538003 C>A maps to NM_032358.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:542374 C>A maps to NM_032358.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:542374 C>A maps to NM_032358.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:549866 C>A maps to NM_032358.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:549866 C>A maps to NM_032358.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:86123497 C>A maps to NM_001156474.1 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:86123497 C>A maps to NM_001156474.1 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:96092201 C>A maps to NM_024725.3 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:96092201 C>A maps to NM_024725.3 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66358100 C>A maps to NM_018219.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66358100 C>A maps to NM_018219.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:55528357 C>A maps to ENST00000436346 T1576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:55528357 C>A maps to ENST00000436346 T1576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64108391 C>A maps to NM_032251.5 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64108391 C>A maps to NM_032251.5 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31122337 G>T maps to NM_001105564.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31122337 G>T maps to NM_001105564.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:100009498 C>A maps to NM_005190.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:100009498 C>A maps to NM_005190.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49087775 C>A maps to NM_001240.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49087775 C>A maps to NM_001240.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55652470 G>T maps to ENST00000442196 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55652470 G>T maps to ENST00000442196 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55652649 C>A maps to ENST00000442196 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55652649 C>A maps to ENST00000442196 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46415037 G>T maps to NM_001100168.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46415037 G>T maps to NM_001100168.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46415065 C>A maps to NM_001100168.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46415065 C>A maps to NM_001100168.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46415388 C>A maps to NM_001100168.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46415388 C>A maps to NM_001100168.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69980088 G>T maps to NM_006431.2 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69980088 G>T maps to NM_006431.2 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156287301 G>T maps to NM_005998.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156287301 G>T maps to NM_005998.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62099288 G>T maps to NM_006430.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:62099288 G>T maps to NM_006430.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10256094 G>T maps to NM_012073.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10256094 G>T maps to NM_012073.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10261736 G>T maps to NM_012073.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10261736 G>T maps to NM_012073.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117552512 G>T maps to NM_004258.3 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117552512 G>T maps to NM_004258.3 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7528341 C>A maps to ENST00000416109 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7528341 C>A maps to ENST00000416109 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7651598 C>A maps to NM_004244.4 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7651598 C>A maps to NM_004244.4 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109690145 C>A maps to NM_006016.4 G168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109690145 C>A maps to NM_006016.4 G168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7808095 G>T maps to NM_021155.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7808095 G>T maps to NM_021155.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67563012 C>A maps to NM_006566.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67563012 C>A maps to NM_006566.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47563612 G>T maps to NM_012120.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47563612 G>T maps to NM_012120.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135741228 C>A maps to NM_000074.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135741228 C>A maps to NM_000074.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:35208418 C>A maps to NM_000610.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:35208418 C>A maps to NM_000610.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207925578 G>T maps to NM_172359.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207925578 G>T maps to NM_172359.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160520782 G>T maps to NM_001184879.1 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160520782 G>T maps to NM_001184879.1 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121825276 G>T maps to NM_175862.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121825276 G>T maps to NM_175862.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111296362 G>T maps to NM_198196.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111296362 G>T maps to NM_198196.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12240745 C>A maps to NM_006023.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12240745 C>A maps to NM_006023.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100933519 G>T maps to NM_033312.2 G283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100933519 G>T maps to NM_033312.2 G283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100933542 C>A maps to NM_033312.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100933542 C>A maps to NM_033312.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100963712 G>T maps to NM_033312.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100963712 G>T maps to NM_033312.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43826223 C>A maps to NM_001255.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43826223 C>A maps to NM_001255.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43828679 C>A maps to NM_001255.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43828679 C>A maps to NM_001255.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3778379 C>A maps to NM_021873.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3778379 C>A maps to NM_021873.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10505731 G>T maps to NM_007065.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10505731 G>T maps to NM_007065.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10506198 G>T maps to NM_007065.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10506198 G>T maps to NM_007065.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227203783 G>T maps to ENST00000366766 P1618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227203783 G>T maps to ENST00000366766 P1618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227216601 C>A maps to ENST00000366766 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227216601 C>A maps to ENST00000366766 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227300460 G>T maps to ENST00000366766 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227300460 G>T maps to ENST00000366766 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22413337 G>T maps to NM_001039802.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22413337 G>T maps to NM_001039802.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44390497 C>A maps to NM_001253.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44390497 C>A maps to NM_001253.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91967323 C>G maps to NM_001134420.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91967323 C>G maps to NM_001134420.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91989685 C>A maps to NM_001134420.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91989685 C>A maps to NM_001134420.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25365236 G>T maps to ENST00000434814 G1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25365236 G>T maps to ENST00000434814 G1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45127528 C>G maps to NM_022842.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45127528 C>G maps to NM_022842.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45152318 C>A maps to NM_022842.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45152318 C>A maps to NM_022842.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24509909 G>T maps to NM_006727.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24509909 G>T maps to NM_006727.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24511473 C>A maps to NM_006727.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24511473 C>A maps to NM_006727.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24537504 G>T maps to NM_006727.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24537504 G>T maps to NM_006727.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:21842273 G>T maps to NM_004061.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:21842273 G>T maps to NM_004061.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:21842303 G>T maps to NM_004061.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:21842303 G>T maps to NM_004061.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:83636072 C>A maps to ENST00000268613 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:83636072 C>A maps to ENST00000268613 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:83711883 C>A maps to ENST00000268613 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:83711883 C>A maps to ENST00000268613 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95143208 G>T maps to NM_001144663.1 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95143208 G>T maps to NM_001144663.1 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68835639 G>T maps to NM_004360.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68835639 G>T maps to NM_004360.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68867245 C>A maps to NM_004360.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68867245 C>A maps to NM_004360.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73461870 G>T maps to ENST00000398860 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73461870 G>T maps to ENST00000398860 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73498293 C>A maps to ENST00000398860 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73498293 C>A maps to ENST00000398860 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73498331 C>A maps to ENST00000398860 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73498331 C>A maps to ENST00000398860 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73569628 C>A maps to ENST00000398860 P2930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73569628 C>A maps to ENST00000398860 P2930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58571791 G>T maps to NM_177980.2 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58571791 G>T maps to NM_177980.2 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66434743 C>A maps to NM_001795.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66434743 C>A maps to NM_001795.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31294253 C>A maps to NM_004932.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31294253 C>A maps to NM_004932.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31294262 C>A maps to NM_004932.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31294262 C>A maps to NM_004932.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31323123 C>A maps to NM_004932.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31323123 C>A maps to NM_004932.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:63476971 C>A maps to NM_004361.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:63476971 C>A maps to NM_004361.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26881252 G>T maps to NM_016279.3 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26881252 G>T maps to NM_016279.3 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26886149 G>T maps to NM_016279.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26886149 G>T maps to NM_016279.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26903853 C>A maps to NM_016279.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26903853 C>A maps to NM_016279.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26906071 G>T maps to NM_016279.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26906071 G>T maps to NM_016279.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176004672 C>A maps to NM_001171976.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176004672 C>A maps to NM_001171976.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:621850 G>T maps to NM_021924.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:621850 G>T maps to NM_021924.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37665991 C>A maps to NM_016507.2 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37665991 C>A maps to NM_016507.2 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:40134287 C>A maps to NM_003718.4 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:40134287 C>A maps to NM_003718.4 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96674616 C>A maps to NM_002595.4 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96674616 C>A maps to NM_002595.4 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58142313 C>A maps to NM_000075.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58142313 C>A maps to NM_000075.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58142982 C>A maps to NM_000075.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58142982 C>A maps to NM_000075.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123210191 G>T maps to NM_018249.4 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123210191 G>T maps to NM_018249.4 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:26978118 C>A maps to NM_001260.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:26978118 C>A maps to NM_001260.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39417578 C>A maps to ENST00000395035 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39417578 C>A maps to ENST00000395035 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18606109 G>T maps to NM_001037343.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18606109 G>T maps to NM_001037343.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18668710 C>A maps to NM_001037343.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18668710 C>A maps to NM_001037343.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85564175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85564175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149562370 C>A maps to NM_001804.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149562370 C>A maps to NM_001804.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:80667071 C>A maps to NM_152342.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:80667071 C>A maps to NM_152342.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:42190904 G>T maps to NM_006890.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:42190904 G>T maps to NM_006890.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37455612 C>A maps to NM_005760.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37455612 C>A maps to NM_005760.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47510506 C>A maps to NM_001172639.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47510506 C>A maps to NM_001172639.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72580679 C>A maps to NM_052840.4 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72580679 C>A maps to NM_052840.4 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104044084 G>T maps to NM_001813.2 T2362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104044084 G>T maps to NM_001813.2 T2362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104059540 C>A maps to NM_001813.2 T2090T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104059540 C>A maps to NM_001813.2 T2090T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104101491 G>T maps to NM_001813.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104101491 G>T maps to NM_001813.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25457410 G>T maps to NM_018451.3 T1307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25457410 G>T maps to NM_018451.3 T1307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95375350 C>A maps to NM_001012267.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95375350 C>A maps to NM_001012267.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67863788 G>T maps to NM_025082.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67863788 G>T maps to NM_025082.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:126667415 G>T maps to ENST00000368325 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:126667415 G>T maps to ENST00000368325 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123936006 C>A maps to NM_007018.4 R2247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123936006 C>A maps to NM_007018.4 R2247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123937304 C>A maps to NM_007018.4 R2253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123937304 C>A maps to NM_007018.4 R2253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49031276 C>A maps to NM_001194998.1 V1434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49031276 C>A maps to NM_001194998.1 V1434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117280346 G>T maps to NM_014956.4 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117280346 G>T maps to NM_014956.4 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13068179 C>A maps to NM_032142.3 R1568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13068179 C>A maps to NM_032142.3 R1568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13068920 C>A maps to NM_032142.3 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13068920 C>A maps to NM_032142.3 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13114127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13114127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138219315 G>T maps to NM_024491.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138219315 G>T maps to NM_024491.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138219409 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138219409 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:640628 C>G maps to NM_018140.3 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:640628 C>G maps to NM_018140.3 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101477063 C>G maps to ENST00000327230 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101477063 C>G maps to ENST00000327230 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67006352 C>A maps to NM_024922.5 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67006352 C>A maps to NM_024922.5 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57005958 C>A maps to NM_000078.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57005958 C>A maps to NM_000078.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31917119 G>T maps to ENST00000437789 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31917119 G>T maps to ENST00000437789 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31919726 C>A maps to ENST00000437789 R1241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31919726 C>A maps to ENST00000437789 R1241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:196799636 G>T maps to NM_002113.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:196799636 G>T maps to NM_002113.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110670477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110670477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:132709319 G>T maps to ENST00000448878 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:132709319 G>T maps to ENST00000448878 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146747899 C>A maps to NM_004284.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146747899 C>A maps to NM_004284.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146756157 C>A maps to NM_004284.3 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146756157 C>A maps to NM_004284.3 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:93521583 C>A maps to NM_001271.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:93521583 C>A maps to NM_001271.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6690213 G>T maps to ENST00000309577 P1663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6690213 G>T maps to ENST00000309577 P1663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6707094 G>T maps to ENST00000309577 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6707094 G>T maps to ENST00000309577 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6709097 G>T maps to ENST00000309577 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6709097 G>T maps to ENST00000309577 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40043834 C>A maps to NM_032221.3 A2310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40043834 C>A maps to NM_032221.3 A2310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40052213 C>A maps to NM_032221.3 S1491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40052213 C>A maps to NM_032221.3 S1491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40141487 C>A maps to NM_032221.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40141487 C>A maps to NM_032221.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40141556 C>A maps to NM_032221.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40141556 C>A maps to NM_032221.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40161771 G>T maps to NM_032221.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40161771 G>T maps to NM_032221.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61655235 G>T maps to NM_017780.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61655235 G>T maps to NM_017780.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61735209 C>A maps to NM_017780.2 R1036R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61735209 C>A maps to NM_017780.2 R1036R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61736559 C>A maps to NM_017780.2 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61736559 C>A maps to NM_017780.2 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61743012 C>A maps to NM_017780.2 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61743012 C>A maps to NM_017780.2 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61761697 G>T maps to NM_017780.2 G1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61761697 G>T maps to NM_017780.2 G1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53190321 C>A maps to ENST00000219084 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53190321 C>A maps to ENST00000219084 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53283891 C>A maps to ENST00000219084 R1259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53283891 C>A maps to ENST00000219084 R1259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53301917 C>A maps to ENST00000219084 R1533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53301917 C>A maps to ENST00000219084 R1533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133433142 G>T maps to NM_001161344.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133433142 G>T maps to NM_001161344.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111778325 G>T maps to NM_004000.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111778325 G>T maps to NM_004000.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:29407578 C>A maps to NM_004067.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:29407578 C>A maps to NM_004067.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34355490 C>A maps to NM_012125.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34355490 C>A maps to NM_012125.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34355569 C>A maps to NM_012125.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34355569 C>A maps to NM_012125.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233396324 C>A maps to NM_000751.1 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233396324 C>A maps to NM_000751.1 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4805621 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4805621 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71570699 C>A maps to NM_001166395.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71570699 C>A maps to NM_001166395.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57473150 G>T maps to NM_020313.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57473150 G>T maps to NM_020313.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12274141 G>T maps to ENST00000342845 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12274141 G>T maps to ENST00000342845 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:11002978 C>T maps to NM_000246.3 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:11002978 C>T maps to NM_000246.3 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:11012338 C>A maps to NM_000246.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:11012338 C>A maps to NM_000246.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120150099 G>T maps to ENST00000392521 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120150099 G>T maps to ENST00000392521 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120198753 C>A maps to ENST00000392521 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120198753 C>A maps to ENST00000392521 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120204980 G>T maps to ENST00000392521 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120204980 G>T maps to ENST00000392521 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120210696 C>A maps to ENST00000392521 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120210696 C>A maps to ENST00000392521 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130931414 C>A maps to NM_012127.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130931414 C>A maps to NM_012127.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53035977 C>A maps to NM_001098525.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53035977 C>A maps to NM_001098525.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106632919 G>T maps to NM_006825.3 S564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106632919 G>T maps to NM_006825.3 S564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66592175 C>A maps to NM_016951.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66592175 C>A maps to NM_016951.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:122216417 G>T maps to NM_015282.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:122216417 G>T maps to NM_015282.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33614669 G>T maps to ENST00000359576 S886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33614669 G>T maps to ENST00000359576 S886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33614708 C>A maps to ENST00000359576 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33614708 C>A maps to ENST00000359576 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170613411 G>T maps to NM_173872.2 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170613411 G>T maps to NM_173872.2 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170618602 C>A maps to NM_173872.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170618602 C>A maps to NM_173872.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74447478 G>T maps to NM_001011880.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74447478 G>T maps to NM_001011880.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10147756 G>T maps to NM_016509.3 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10147756 G>T maps to NM_016509.3 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10151642 G>T maps to NM_016509.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10151642 G>T maps to NM_016509.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10151672 G>T maps to NM_016509.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10151672 G>T maps to NM_016509.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:25167380 G>T maps to NM_013943.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:25167380 G>T maps to NM_013943.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:157214695 G>T maps to NM_001195555.1 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:157214695 G>T maps to NM_001195555.1 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:157218740 C>A maps to NM_001195555.1 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:157218740 C>A maps to NM_001195555.1 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122763597 C>A maps to ENST00000302528 E1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122763597 C>A maps to ENST00000302528 E1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122812813 C>A maps to ENST00000302528 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122812813 C>A maps to ENST00000302528 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122825791 C>A maps to ENST00000302528 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122825791 C>A maps to ENST00000302528 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122826012 G>T maps to ENST00000302528 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122826012 G>T maps to ENST00000302528 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:29366687 G>T maps to ENST00000379543 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:29366687 G>T maps to ENST00000379543 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155234030 G>T maps to ENST00000368361 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155234030 G>T maps to ENST00000368361 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:68504050 C>A maps to NM_017882.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:68504050 C>A maps to NM_017882.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72012924 G>T maps to NM_030813.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72012924 G>T maps to NM_030813.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45494599 C>A maps to NM_001294.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45494599 C>A maps to NM_001294.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45495626 C>A maps to NM_001294.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45495626 C>A maps to NM_001294.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36209117 C>A maps to NM_022111.3 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36209117 C>A maps to NM_022111.3 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:175819938 C>A maps to NM_007097.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:175819938 C>A maps to NM_007097.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62370976 C>A maps to NM_173519.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62370976 C>A maps to NM_173519.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:123369844 C>A maps to NM_001010852.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:123369844 C>A maps to NM_001010852.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100518534 C>A maps to NM_206808.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100518534 C>A maps to NM_206808.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10290760 G>T maps to NM_138809.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10290760 G>T maps to NM_138809.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10290792 C>A maps to NM_138809.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10290792 C>A maps to NM_138809.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66612819 G>T maps to NM_052999.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66612819 G>T maps to NM_052999.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6261341 G>T maps to NM_001037329.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6261341 G>T maps to NM_001037329.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87623851 G>T maps to NM_019098.4 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87623851 G>T maps to NM_019098.4 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87680294 C>A maps to NM_019098.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87680294 C>A maps to NM_019098.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87683190 G>T maps to NM_019098.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87683190 G>T maps to NM_019098.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:21450880 C>A maps to NM_014927.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:21450880 C>A maps to NM_014927.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97427929 G>T maps to NM_020184.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97427929 G>T maps to NM_020184.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97428031 C>A maps to NM_020184.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97428031 C>A maps to NM_020184.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32801042 C>A maps to NM_015442.1 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32801042 C>A maps to NM_015442.1 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58581157 C>A maps to NM_016284.3 G1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58581157 C>A maps to NM_016284.3 G1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179977087 C>A maps to NM_015455.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179977087 C>A maps to NM_015455.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179992869 C>A maps to NM_015455.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179992869 C>A maps to NM_015455.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17102567 G>T maps to NM_013354.5 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17102567 G>T maps to NM_013354.5 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42903386 C>A maps to NM_006586.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42903386 C>A maps to NM_006586.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:17330767 C>A maps to NM_017738.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:17330767 C>A maps to NM_017738.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:17416150 C>A maps to NM_017738.2 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:17416150 C>A maps to NM_017738.2 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:41327261 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:41327261 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:74413645 A>C maps to NM_020872.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:74413645 A>C maps to NM_020872.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:74414845 G>T maps to NM_020872.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:74414845 G>T maps to NM_020872.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:2967386 G>T maps to NM_175607.1 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:2967386 G>T maps to NM_175607.1 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:1424777 C>A maps to NM_014461.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:1424777 C>A maps to NM_014461.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:147869451 G>T maps to NM_014141.5 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:147869451 G>T maps to NM_014141.5 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:76555115 G>T maps to NM_033401.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:76555115 G>T maps to NM_033401.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:76556002 C>A maps to NM_033401.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:76556002 C>A maps to NM_033401.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125261891 C>A maps to NM_130773.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125261891 C>A maps to NM_130773.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125671721 C>A maps to NM_130773.2 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125671721 C>A maps to NM_130773.2 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165551684 G>T maps to ENST00000392717 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165551684 G>T maps to ENST00000392717 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70543220 G>T maps to NM_015386.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70543220 G>T maps to NM_015386.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103352407 G>T maps to NM_080629.2 R1617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103352407 G>T maps to NM_080629.2 R1617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103471420 C>A maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103471420 C>A maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491774 C>A maps to NM_001854.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491774 C>A maps to NM_001854.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103548460 C>A maps to NM_080629.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103548460 C>A maps to NM_080629.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103573680 G>T maps to NM_080629.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103573680 G>T maps to NM_080629.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33133722 G>T maps to NM_080680.2 G1489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33133722 G>T maps to NM_080680.2 G1489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75811719 G>T maps to ENST00000322507 R2822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75811719 G>T maps to ENST00000322507 R2822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75843057 G>T maps to ENST00000322507 P1915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75843057 G>T maps to ENST00000322507 P1915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75861681 G>T maps to ENST00000322507 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75861681 G>T maps to ENST00000322507 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75865510 G>T maps to ENST00000322507 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75865510 G>T maps to ENST00000322507 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75890661 G>T maps to ENST00000322507 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75890661 G>T maps to ENST00000322507 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75904547 C>A maps to ENST00000322507 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75904547 C>A maps to ENST00000322507 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:121256197 C>A maps to NM_021110.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:121256197 C>A maps to NM_021110.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:121383410 G>T maps to NM_021110.1 E1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:121383410 G>T maps to NM_021110.1 E1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101810111 C>A maps to NM_001855.3 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101810111 C>A maps to NM_001855.3 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101817635 C>A maps to NM_001855.3 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101817635 C>A maps to NM_001855.3 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105823570 C>A maps to NM_000494.3 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105823570 C>A maps to NM_000494.3 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139649037 C>A maps to NM_152888.1 G1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139649037 C>A maps to NM_152888.1 G1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139727960 C>A maps to NM_152888.1 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139727960 C>A maps to NM_152888.1 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139833644 G>T maps to NM_152888.1 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139833644 G>T maps to NM_152888.1 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139856393 G>T maps to NM_152888.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139856393 G>T maps to NM_152888.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:109783701 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:109783701 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116931124 G>T maps to NM_032888.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116931124 G>T maps to NM_032888.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116999976 C>A maps to NM_032888.2 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116999976 C>A maps to NM_032888.2 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117071592 C>A maps to NM_032888.2 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117071592 C>A maps to NM_032888.2 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7480432 G>T maps to NM_001037763.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7480432 G>T maps to NM_001037763.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7493097 G>T maps to NM_001037763.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7493097 G>T maps to NM_001037763.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189873897 C>A maps to NM_000090.3 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189873897 C>A maps to NM_000090.3 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110827078 C>A maps to NM_001845.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110827078 C>A maps to NM_001845.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110830474 C>A maps to NM_001845.4 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110830474 C>A maps to NM_001845.4 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110850912 G>T maps to NM_001845.4 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110850912 G>T maps to NM_001845.4 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110864215 G>T maps to NM_001845.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110864215 G>T maps to NM_001845.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111145564 G>T maps to NM_001846.2 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111145564 G>T maps to NM_001846.2 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228102682 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228102682 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228172520 C>A maps to NM_000091.4 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228172520 C>A maps to NM_000091.4 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227946903 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227946903 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107814668 C>A maps to ENST00000328300 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107814668 C>A maps to ENST00000328300 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107930826 G>T maps to ENST00000328300 T1477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107930826 G>T maps to ENST00000328300 T1477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137623496 C>A maps to NM_000093.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137623496 C>A maps to NM_000093.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189916924 C>A maps to NM_000393.3 A914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189916924 C>A maps to NM_000393.3 A914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189932951 C>A maps to NM_000393.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189932951 C>A maps to NM_000393.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189945769 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189945769 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10108800 C>A maps to NM_015719.3 G379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10108800 C>A maps to NM_015719.3 G379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10114749 G>T maps to NM_015719.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10114749 G>T maps to NM_015719.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238249671 G>T maps to NM_004369.3 T2629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238249671 G>T maps to NM_004369.3 T2629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238266525 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238266525 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238268022 C>A maps to NM_004369.3 R2097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238268022 C>A maps to NM_004369.3 R2097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238274445 G>T maps to NM_004369.3 L1911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238274445 G>T maps to NM_004369.3 L1911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130300612 C>A maps to NM_001102608.1 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130300612 C>A maps to NM_001102608.1 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130311931 G>T maps to NM_001102608.1 G1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130311931 G>T maps to NM_001102608.1 G1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48618703 G>T maps to NM_000094.3 R1630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48618703 G>T maps to NM_000094.3 R1630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48619355 G>T maps to NM_000094.3 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48619355 G>T maps to NM_000094.3 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99514796 C>A maps to ENST00000429802 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99514796 C>A maps to ENST00000429802 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:76100730 C>A maps to NM_203497.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:76100730 C>A maps to NM_203497.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160261680 C>A maps to NM_001098398.1 V1071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160261680 C>A maps to NM_001098398.1 V1071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160275257 G>T maps to NM_001098398.1 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160275257 G>T maps to NM_001098398.1 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19030139 G>T maps to NM_007263.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19030139 G>T maps to NM_007263.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:130295860 G>T maps to NM_012133.4 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:130295860 G>T maps to NM_012133.4 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54743402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54743402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99817669 C>A maps to NM_017421.3 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99817669 C>A maps to NM_017421.3 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120954391 G>T maps to NM_032314.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120954391 G>T maps to NM_032314.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57490420 G>T maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57490420 G>T maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109095012 G>T maps to ENST00000420959 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109095012 G>T maps to ENST00000420959 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69011755 C>A maps to NM_006091.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69011755 C>A maps to NM_006091.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:85915249 C>A maps to NM_001867.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:85915249 C>A maps to NM_001867.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:19562516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:19562516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46627853 C>A maps to NM_001872.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46627853 C>A maps to NM_001872.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15060879 C>A maps to NM_001177382.1 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15060879 C>A maps to NM_001177382.1 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15067856 C>A maps to NM_001177382.1 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15067856 C>A maps to NM_001177382.1 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69265642 G>T maps to NM_001874.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69265642 G>T maps to NM_001874.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101816853 C>A maps to NM_001308.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101816853 C>A maps to NM_001308.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57147237 C>A maps to NM_152727.5 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57147237 C>A maps to NM_152727.5 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57155643 C>A maps to NM_152727.5 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57155643 C>A maps to NM_152727.5 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87556969 G>T maps to NM_003909.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87556969 G>T maps to NM_003909.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9747678 G>T maps to ENST00000383832 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9747678 G>T maps to ENST00000383832 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207833929 C>A maps to NM_173077.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207833929 C>A maps to NM_173077.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:211464172 G>T maps to NM_001122633.1 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:211464172 G>T maps to NM_001122633.1 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145625814 G>T maps to NM_013291.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145625814 G>T maps to NM_013291.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:9582074 G>T maps to NM_016207.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:9582074 G>T maps to NM_016207.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99045870 C>A maps to NM_006693.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99045870 C>A maps to NM_006693.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207867875 G>T maps to NM_175710.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207867875 G>T maps to NM_175710.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207870944 C>A maps to NM_175710.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207870944 C>A maps to NM_175710.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207871137 G>T maps to NM_175710.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207871137 G>T maps to NM_175710.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207785368 C>A maps to NM_000651.4 S2186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207785368 C>A maps to NM_000651.4 S2186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207639869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207639869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78640310 C>A maps to NM_004378.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78640310 C>A maps to NM_004378.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3209446 G>T maps to NM_016302.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3209446 G>T maps to NM_016302.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35500641 C>A maps to ENST00000429130 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35500641 C>A maps to ENST00000429130 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1388829 C>A maps to NM_175918.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1388829 C>A maps to NM_175918.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49803097 C>A maps to NM_001131.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49803097 C>A maps to NM_001131.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49665619 G>T maps to ENST00000211238 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49665619 G>T maps to ENST00000211238 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49698884 C>A maps to NM_001190986.1 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49698884 C>A maps to NM_001190986.1 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21304127 G>T maps to NM_005207.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21304127 G>T maps to NM_005207.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29119513 C>A maps to NM_015986.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29119513 C>A maps to NM_015986.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29130951 C>A maps to NM_015986.3 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29130951 C>A maps to NM_015986.3 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87022264 G>T maps to NM_001143935.1 G562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87022264 G>T maps to NM_001143935.1 G562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:25597386 C>A maps to NM_004076.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:25597386 C>A maps to NM_004076.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115267907 C>A maps to NM_001130523.1 E578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115267907 C>A maps to NM_001130523.1 E578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115272947 C>A maps to NM_001130523.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115272947 C>A maps to NM_001130523.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1409341 G>T maps to NM_001161530.1 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1409341 G>T maps to NM_001161530.1 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1413248 C>A maps to NM_001161530.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1413248 C>A maps to NM_001161530.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36941125 G>T maps to NM_156039.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36941125 G>T maps to NM_156039.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19316144 G>T maps to NM_018371.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19316144 G>T maps to NM_018371.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19363305 G>T maps to NM_018371.4 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19363305 G>T maps to NM_018371.4 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43654263 G>T maps to NM_018590.3 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43654263 G>T maps to NM_018590.3 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43678848 C>G maps to NM_018590.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43678848 C>G maps to NM_018590.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:34286101 G>T maps to ENST00000373381 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:34286101 G>T maps to ENST00000373381 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113237029 G>T maps to NM_198123.1 P3698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113237029 G>T maps to NM_198123.1 P3698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113253964 G>C maps to NM_198123.1 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113253964 G>C maps to NM_198123.1 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113253973 C>A maps to NM_198123.1 L3481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113253973 C>A maps to NM_198123.1 L3481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:114448921 C>A maps to NM_198123.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:114448921 C>A maps to NM_198123.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:37678990 G>T maps to NM_145203.5 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:37678990 G>T maps to NM_145203.5 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47614201 C>A maps to ENST00000383738 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47614201 C>A maps to ENST00000383738 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68107672 G>T maps to ENST00000389042 G1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68107672 G>T maps to ENST00000389042 G1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166536238 C>A maps to ENST00000409420 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166536238 C>A maps to ENST00000409420 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18163859 C>A maps to NM_020536.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18163859 C>A maps to NM_020536.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:23860126 C>A maps to NM_001900.4 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:23860126 C>A maps to NM_001900.4 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122060338 C>A maps to NM_005213.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122060338 C>A maps to NM_005213.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:54974177 C>A maps to NM_001033522.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:54974177 C>A maps to NM_001033522.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:120008753 G>T maps to NM_001145718.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:120008753 G>T maps to NM_001145718.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19995824 G>T maps to NM_172241.2 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19995824 G>T maps to NM_172241.2 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19996570 G>T maps to NM_172241.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19996570 G>T maps to NM_172241.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19997363 C>A maps to NM_172241.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19997363 C>A maps to NM_172241.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:56099204 G>T maps to ENST00000423479 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:56099204 G>T maps to ENST00000423479 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77470424 G>T maps to NM_004715.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77470424 G>T maps to NM_004715.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:138266341 C>A maps to ENST00000355078 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:138266341 C>A maps to ENST00000355078 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:80874836 C>A maps to ENST00000402739 S901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:80874836 C>A maps to ENST00000402739 S901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57569559 G>T maps to NM_001085458.1 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57569559 G>T maps to NM_001085458.1 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10988264 C>A maps to NM_001332.2 G1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10988264 C>A maps to NM_001332.2 G1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:11159791 C>A maps to NM_001332.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:11159791 C>A maps to NM_001332.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:11397160 C>A maps to NM_001332.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:11397160 C>A maps to NM_001332.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:41471762 C>A maps to NM_001905.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:41471762 C>A maps to NM_001905.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10789519 C>A maps to NM_014633.3 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10789519 C>A maps to NM_014633.3 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88027535 C>A maps to NM_001814.4 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88027535 C>A maps to NM_001814.4 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88045626 G>T maps to NM_001814.4 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88045626 G>T maps to NM_001814.4 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1778747 G>A maps to NM_001909.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1778747 G>A maps to NM_001909.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79223845 C>A maps to NM_004390.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79223845 C>A maps to NM_004390.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117407202 C>A maps to NM_033427.2 G936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117407202 C>A maps to NM_033427.2 G936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117450854 G>T maps to NM_033427.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117450854 G>T maps to NM_033427.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70256054 C>A maps to NM_001184740.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70256054 C>A maps to NM_001184740.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70267615 G>T maps to NM_005231.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70267615 G>T maps to NM_005231.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88773582 C>A maps to ENST00000378384 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88773582 C>A maps to ENST00000378384 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16911698 C>A maps to NM_001081.3 L3130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16911698 C>A maps to NM_001081.3 L3130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16948288 C>A maps to NM_001081.3 G2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16948288 C>A maps to NM_001081.3 G2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16960654 G>T maps to NM_001081.3 P2322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16960654 G>T maps to NM_001081.3 P2322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16982055 C>A maps to NM_001081.3 T1841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16982055 C>A maps to NM_001081.3 T1841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17147545 C>A maps to NM_001081.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17147545 C>A maps to NM_001081.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35333561 C>A maps to NM_001198778.1 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35333561 C>A maps to NM_001198778.1 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:107965134 G>T maps to NM_003478.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:107965134 G>T maps to NM_003478.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33385319 C>A maps to NM_001014433.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33385319 C>A maps to NM_001014433.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33385343 C>A maps to NM_001014433.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33385343 C>A maps to NM_001014433.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39307460 G>T maps to NM_001171174.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39307460 G>T maps to NM_001171174.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:44876320 G>T maps to NM_001178134.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:44876320 G>T maps to NM_001178134.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136873278 C>A maps to NM_001008540.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136873278 C>A maps to NM_001008540.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118764417 C>A maps to NM_001716.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118764417 C>A maps to NM_001716.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:237489662 C>A maps to NM_020311.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:237489662 C>A maps to NM_020311.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:105393492 G>T maps to NM_025212.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:105393492 G>T maps to NM_025212.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19971146 C>A maps to ENST00000379682 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19971146 C>A maps to ENST00000379682 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19984670 G>T maps to ENST00000379682 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19984670 G>T maps to ENST00000379682 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:105868477 C>A maps to NM_018015.5 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:105868477 C>A maps to NM_018015.5 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143961141 G>T maps to ENST00000377675 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143961141 G>T maps to ENST00000377675 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104594685 C>A maps to NM_000102.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104594685 C>A maps to NM_000102.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75042178 C>A maps to NM_000761.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75042178 C>A maps to NM_000761.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75042694 G>T maps to NM_000761.3 G206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75042694 G>T maps to NM_000761.3 G206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75047179 C>A maps to NM_000761.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75047179 C>A maps to NM_000761.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204111558 G>T maps to ENST00000429815 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204111558 G>T maps to ENST00000429815 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219677416 C>A maps to NM_000784.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219677416 C>A maps to NM_000784.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58158180 C>A maps to NM_000785.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58158180 C>A maps to NM_000785.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41351981 C>A maps to NM_000762.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41351981 C>A maps to NM_000762.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60359483 C>A maps to NM_000775.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60359483 C>A maps to NM_000775.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108866315 C>A maps to NM_183075.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108866315 C>A maps to NM_183075.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108866750 C>A maps to NM_183075.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108866750 C>A maps to NM_183075.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99355770 G>T maps to NM_017460.3 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99355770 G>T maps to NM_017460.3 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99308360 G>T maps to ENST00000292414 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99308360 G>T maps to ENST00000292414 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59404264 G>T maps to NM_000780.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59404264 G>T maps to NM_000780.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59409337 C>A maps to NM_000780.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59409337 C>A maps to NM_000780.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6227298 G>T maps to ENST00000396741 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6227298 G>T maps to ENST00000396741 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:20108084 C>A maps to NM_001033553.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:20108084 C>A maps to NM_001033553.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:59830499 G>T maps to NM_014992.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:59830499 G>T maps to NM_014992.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:57480706 G>T maps to ENST00000371231 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:57480706 G>T maps to ENST00000371231 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124329475 C>A maps to NM_032552.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124329475 C>A maps to NM_032552.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39381673 G>T maps to NM_001343.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39381673 G>T maps to NM_001343.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39394380 G>T maps to NM_001343.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39394380 G>T maps to NM_001343.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49568596 C>A maps to NM_004393.4 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49568596 C>A maps to NM_004393.4 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109281225 G>T maps to NM_001917.4 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109281225 G>T maps to NM_001917.4 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136670055 G>T maps to NM_001349.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136670055 G>T maps to NM_001349.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16633628 C>A maps to NM_001190811.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16633628 C>A maps to NM_001190811.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:121929406 C>A maps to NM_014618.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:121929406 C>A maps to NM_014618.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87536697 C>A maps to NM_006716.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87536697 C>A maps to NM_006716.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176887472 C>A maps to ENST00000393565 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176887472 C>A maps to ENST00000393565 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37854944 C>A maps to NM_024345.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37854944 C>A maps to NM_024345.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172305279 G>T maps to NM_025000.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172305279 G>T maps to NM_025000.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172314572 C>A maps to NM_025000.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172314572 C>A maps to NM_025000.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41984453 G>T maps to NM_001029955.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41984453 G>T maps to NM_001029955.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167935925 C>A maps to ENST00000367840 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167935925 C>A maps to ENST00000367840 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:27997831 C>A maps to NM_001017930.1 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:27997831 C>A maps to NM_001017930.1 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160201109 C>G maps to NM_015726.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160201109 C>G maps to NM_015726.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117862162 C>A maps to ENST00000338728 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117862162 C>A maps to ENST00000338728 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117864302 G>T maps to ENST00000338728 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117864302 G>T maps to ENST00000338728 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:50734107 T>A maps to NM_005215.3 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:50734107 T>A maps to NM_005215.3 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:50734143 G>C maps to NM_005215.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:50734143 G>C maps to NM_005215.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:31327198 C>A maps to NM_181807.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:31327198 C>A maps to NM_181807.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6661248 C>A maps to NM_003737.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6661248 C>A maps to NM_003737.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155254410 C>A maps to NM_017639.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155254410 C>A maps to NM_017639.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115602116 C>A maps to NM_014881.3 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115602116 C>A maps to NM_014881.3 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976470 G>T maps to NM_001033855.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976470 G>T maps to NM_001033855.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976485 G>T maps to NM_001033855.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976485 G>T maps to NM_001033855.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:91550873 G>T maps to NM_133503.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:91550873 G>T maps to NM_133503.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74597181 C>A maps to NM_004082.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74597181 C>A maps to NM_004082.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85787215 G>T maps to NM_012137.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85787215 G>T maps to NM_012137.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61091489 G>T maps to NM_001923.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61091489 G>T maps to NM_001923.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38109667 C>A maps to NM_001164232.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38109667 C>A maps to NM_001164232.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30857032 C>A maps to NM_013994.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30857032 C>A maps to NM_013994.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:118575203 C>A maps to NM_006773.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:118575203 C>A maps to NM_006773.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:15757390 G>T maps to NM_004939.1 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:15757390 G>T maps to NM_004939.1 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70741315 C>A maps to NM_004728.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70741315 C>A maps to NM_004728.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49224335 G>T maps to NM_004818.2 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49224335 G>T maps to NM_004818.2 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49224449 C>A maps to NM_004818.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49224449 C>A maps to NM_004818.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49237774 G>T maps to NM_004818.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49237774 G>T maps to NM_004818.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94521371 G>T maps to NM_020414.3 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94521371 G>T maps to NM_020414.3 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47839937 C>A maps to NM_017895.7 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47839937 C>A maps to NM_017895.7 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47858706 C>A maps to NM_017895.7 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47858706 C>A maps to NM_017895.7 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135487540 C>A maps to NM_022779.7 G748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135487540 C>A maps to NM_022779.7 G748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135505691 C>A maps to NM_022779.7 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135505691 C>A maps to NM_022779.7 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12967063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12967063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124104072 C>G maps to NM_020936.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124104072 C>G maps to NM_020936.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91031160 C>A maps to NM_001359.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91031160 C>A maps to NM_001359.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:126371753 G>T maps to NM_020946.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:126371753 G>T maps to NM_020946.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197479766 G>T maps to NM_001195215.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197479766 G>T maps to NM_001195215.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197564418 C>A maps to NM_001195215.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197564418 C>A maps to NM_001195215.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111741262 G>T maps to NM_024901.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111741262 G>T maps to NM_024901.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142173430 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142173430 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142195313 C>A maps to NM_014957.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142195313 C>A maps to NM_014957.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142204208 C>A maps to NM_014957.2 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142204208 C>A maps to NM_014957.2 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65988715 C>A maps to ENST00000443035 G1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65988715 C>A maps to ENST00000443035 G1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9200461 G>T maps to NM_015213.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9200461 G>T maps to NM_015213.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31605332 C>A maps to NM_144973.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31605332 C>A maps to NM_144973.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:33054488 G>T maps to NM_001077242.1 G440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:33054488 G>T maps to NM_001077242.1 G440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89074818 G>T maps to NM_017996.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89074818 G>T maps to NM_017996.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117169019 C>A maps to NM_015404.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117169019 C>A maps to NM_015404.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185978268 G>T maps to NM_001346.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185978268 G>T maps to NM_001346.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42773991 C>A maps to NM_178009.2 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42773991 C>A maps to NM_178009.2 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26769332 C>A maps to NM_024887.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26769332 C>A maps to NM_024887.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52373768 G>T maps to NM_001031719.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52373768 G>T maps to NM_001031719.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24761869 C>A maps to NM_001136050.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24761869 C>A maps to NM_001136050.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169939947 C>A maps to NM_001142271.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169939947 C>A maps to NM_001142271.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2343307 C>A maps to NM_145177.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2343307 C>A maps to NM_145177.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47888782 C>A maps to NM_138615.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47888782 C>A maps to NM_138615.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127527655 C>A maps to NM_018180.2 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127527655 C>A maps to NM_018180.2 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37634872 C>A maps to NM_021931.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37634872 C>A maps to NM_021931.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154024078 C>A maps to NM_020865.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154024078 C>A maps to NM_020865.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125432386 G>T maps to NM_032656.3 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125432386 G>T maps to NM_032656.3 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125467127 G>T maps to NM_032656.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125467127 G>T maps to NM_032656.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39081287 C>A maps to NM_198963.1 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39081287 C>A maps to NM_198963.1 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41577430 C>A maps to NM_004941.1 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41577430 C>A maps to NM_004941.1 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182848415 C>A maps to NM_001357.4 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182848415 C>A maps to NM_001357.4 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182856251 C>A maps to NM_001357.4 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182856251 C>A maps to NM_001357.4 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:60407249 G>T maps to NM_001042517.1 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:60407249 G>T maps to NM_001042517.1 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:95556875 G>T maps to NM_177438.2 R1910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:95556875 G>T maps to NM_177438.2 R1910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:327171 C>A maps to NM_014974.2 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:327171 C>A maps to NM_014974.2 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:415566 C>A maps to NM_014974.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:415566 C>A maps to NM_014974.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:436256 G>T maps to NM_014974.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:436256 G>T maps to NM_014974.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:454886 G>T maps to NM_014974.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:454886 G>T maps to NM_014974.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:465052 G>T maps to NM_014974.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:465052 G>T maps to NM_014974.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122545787 G>T maps to NM_032839.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122545787 G>T maps to NM_032839.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122578975 G>T maps to NM_032839.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122578975 G>T maps to NM_032839.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122591289 G>T maps to NM_032839.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122591289 G>T maps to NM_032839.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122598209 G>T maps to NM_032839.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122598209 G>T maps to NM_032839.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232894774 C>A maps to NM_152383.4 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232894774 C>A maps to NM_152383.4 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233075072 C>A maps to NM_152383.4 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233075072 C>A maps to NM_152383.4 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233194675 C>A maps to NM_152383.4 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233194675 C>A maps to NM_152383.4 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66612995 G>T maps to NM_001143688.1 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66612995 G>T maps to NM_001143688.1 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223176988 C>A maps to NM_032890.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223176988 C>A maps to NM_032890.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40657868 G>T maps to NM_033510.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40657868 G>T maps to NM_033510.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111922034 C>A maps to NM_001931.4 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111922034 C>A maps to NM_001931.4 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:12952304 C>A maps to NM_182643.2 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:12952304 C>A maps to NM_182643.2 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107557361 C>A maps to NM_000108.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107557361 C>A maps to NM_000108.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38101311 C>A maps to NM_007335.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38101311 C>A maps to NM_007335.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:83641498 C>A maps to NM_001142699.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:83641498 C>A maps to NM_001142699.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3502619 G>T maps to NM_004746.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3502619 G>T maps to NM_004746.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3534198 G>T maps to NM_004746.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3534198 G>T maps to NM_004746.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35333202 C>A maps to NM_001080418.1 V837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35333202 C>A maps to NM_001080418.1 V837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071135 G>T maps to ENST00000339266 G455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071135 G>T maps to ENST00000339266 G455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170592123 C>A maps to NM_005618.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170592123 C>A maps to NM_005618.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41227130 G>T maps to NM_019074.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41227130 G>T maps to NM_019074.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44680065 C>A maps to NM_019100.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44680065 C>A maps to NM_019100.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124339298 C>G maps to ENST00000368915 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124339298 C>G maps to ENST00000368915 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124345757 C>A maps to ENST00000368915 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124345757 C>A maps to ENST00000368915 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124348641 C>A maps to ENST00000368915 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124348641 C>A maps to ENST00000368915 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124351843 C>A maps to ENST00000368915 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124351843 C>A maps to ENST00000368915 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124351861 C>A maps to ENST00000368915 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124351861 C>A maps to ENST00000368915 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124358380 C>A maps to ENST00000368915 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124358380 C>A maps to ENST00000368915 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124380663 C>A maps to ENST00000368915 T1792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124380663 C>A maps to ENST00000368915 T1792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:31854903 C>A maps to ENST00000357033 P2377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:31854903 C>A maps to ENST00000357033 P2377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:32459325 C>A maps to ENST00000357033 G1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:32459325 C>A maps to ENST00000357033 G1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:1056234 G>T maps to NM_181872.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:1056234 G>T maps to NM_181872.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:42354384 C>A maps to ENST00000427618 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:42354384 C>A maps to ENST00000427618 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51755688 G>T maps to NM_001174116.1 R2605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51755688 G>T maps to NM_001174116.1 R2605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51791168 G>T maps to NM_001174116.1 R1418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51791168 G>T maps to NM_001174116.1 R1418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51791579 C>A maps to NM_001174116.1 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51791579 C>A maps to NM_001174116.1 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124265733 C>A maps to NM_207437.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124265733 C>A maps to NM_207437.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124293476 C>A maps to NM_207437.3 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124293476 C>A maps to NM_207437.3 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124325930 C>A maps to NM_207437.3 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124325930 C>A maps to NM_207437.3 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:21640511 C>A maps to NM_003777.3 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:21640511 C>A maps to NM_003777.3 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:21723446 C>A maps to NM_003777.3 R1843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:21723446 C>A maps to NM_003777.3 R1843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76455259 G>T maps to ENST00000389840 P3214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76455259 G>T maps to ENST00000389840 P3214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52397024 C>A maps to ENST00000273600 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52397024 C>A maps to ENST00000273600 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52427015 G>T maps to ENST00000273600 S3547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52427015 G>T maps to ENST00000273600 S3547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20976496 G>T maps to NM_017539.1 P2903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20976496 G>T maps to NM_017539.1 P2903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21071677 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21071677 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21098183 G>T maps to NM_017539.1 R955R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21098183 G>T maps to NM_017539.1 R955R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21098346 C>A maps to NM_017539.1 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21098346 C>A maps to NM_017539.1 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13737439 G>T maps to NM_001369.2 A3792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13737439 G>T maps to NM_001369.2 A3792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13776598 C>A maps to NM_001369.2 G3108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13776598 C>A maps to NM_001369.2 G3108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13841890 G>T maps to NM_001369.2 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13841890 G>T maps to NM_001369.2 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196689020 G>T maps to NM_018897.2 T3083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196689020 G>T maps to NM_018897.2 T3083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196865544 G>T maps to NM_018897.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196865544 G>T maps to NM_018897.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:38950159 C>A maps to ENST00000327475 P4279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:38950159 C>A maps to ENST00000327475 P4279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:72287262 G>T maps to NM_023036.4 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:72287262 G>T maps to NM_023036.4 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:183616511 C>A maps to NM_018981.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:183616511 C>A maps to NM_018981.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:6705986 G>T maps to NM_018198.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:6705986 G>T maps to NM_018198.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34936259 G>T maps to NM_194283.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34936259 G>T maps to NM_194283.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114415378 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114415378 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27500693 C>A maps to NM_173650.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27500693 C>A maps to NM_173650.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:65845179 C>A maps to ENST00000371069 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:65845179 C>A maps to ENST00000371069 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28527817 C>A maps to NM_014280.2 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28527817 C>A maps to NM_014280.2 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12986959 C>A maps to NM_001375.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12986959 C>A maps to NM_001375.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230272007 C>A maps to NM_139072.3 G555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230272007 C>A maps to NM_139072.3 G555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130980508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130980508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172017883 C>A maps to ENST00000359070 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172017883 C>A maps to ENST00000359070 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101639927 C>A maps to ENST00000342239 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101639927 C>A maps to ENST00000342239 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101715754 G>T maps to ENST00000342239 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101715754 G>T maps to ENST00000342239 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25462009 G>T maps to NM_175629.1 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25462009 G>T maps to NM_175629.1 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25469062 G>T maps to NM_175629.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25469062 G>T maps to NM_175629.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31379477 C>A maps to NM_006892.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31379477 C>A maps to NM_006892.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31390241 C>A maps to NM_006892.3 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31390241 C>A maps to NM_006892.3 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98087321 G>T maps to NM_004088.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98087321 G>T maps to NM_004088.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:225657700 G>T maps to NM_014689.2 P1767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:225657700 G>T maps to NM_014689.2 P1767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:225659715 G>T maps to NM_014689.2 P1678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:225659715 G>T maps to NM_014689.2 P1678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117676917 G>T maps to ENST00000276204 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117676917 G>T maps to ENST00000276204 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117764344 C>A maps to ENST00000276204 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117764344 C>A maps to ENST00000276204 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117777497 G>T maps to ENST00000276204 G1447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117777497 G>T maps to ENST00000276204 G1447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128821551 G>T maps to ENST00000398025 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128821551 G>T maps to ENST00000398025 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169127117 G>T maps to NM_004946.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169127117 G>T maps to NM_004946.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51196728 C>A maps to NM_004947.4 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51196728 C>A maps to NM_004947.4 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:111400267 G>T maps to ENST00000428084 P1377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:111400267 G>T maps to ENST00000428084 P1377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62940938 G>T maps to ENST00000371140 P2015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62940938 G>T maps to ENST00000371140 P2015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941500 G>T maps to ENST00000371140 P1946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941500 G>T maps to ENST00000371140 P1946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941805 C>A maps to ENST00000371140 G1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941805 C>A maps to ENST00000371140 G1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62958410 C>A maps to ENST00000371140 V1775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62958410 C>A maps to ENST00000371140 V1775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62958485 C>A maps to ENST00000371140 A1750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62958485 C>A maps to ENST00000371140 A1750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62970389 G>T maps to ENST00000371140 R1559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62970389 G>T maps to ENST00000371140 R1559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99489849 C>A maps to ENST00000428223 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99489849 C>A maps to ENST00000428223 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99505746 G>T maps to ENST00000428223 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99505746 G>T maps to ENST00000428223 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131708573 G>T maps to NM_014908.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131708573 G>T maps to NM_014908.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131849063 C>A maps to NM_020438.4 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131849063 C>A maps to NM_020438.4 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31938817 G>T maps to NM_005510.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31938817 G>T maps to NM_005510.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83838811 C>G maps to NM_015018.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83838811 C>G maps to NM_015018.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:1937115 C>A maps to NM_001383.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:1937115 C>A maps to NM_001383.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44437602 G>C maps to NM_001384.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44437602 G>C maps to NM_001384.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101458296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101458296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:162865132 C>A maps to NM_001935.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:162865132 C>A maps to NM_001935.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:162929930 G>T maps to NM_001935.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:162929930 G>T maps to NM_001935.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:154172102 C>A maps to NM_130797.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:154172102 C>A maps to NM_130797.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65793044 C>A maps to NM_197960.2 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65793044 C>A maps to NM_197960.2 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:109026990 C>A maps to NM_138815.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:109026990 C>A maps to NM_138815.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:109028037 G>T maps to NM_138815.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:109028037 G>T maps to NM_138815.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:63991612 G>T maps to NM_173812.4 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:63991612 G>T maps to NM_173812.4 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95789953 C>A maps to NM_181787.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95789953 C>A maps to NM_181787.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97564172 C>A maps to NM_000110.3 G880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97564172 C>A maps to NM_000110.3 G880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:98060654 G>T maps to NM_000110.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:98060654 G>T maps to NM_000110.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:98293682 G>T maps to NM_000110.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:98293682 G>T maps to NM_000110.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:105440228 G>T maps to NM_001385.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:105440228 G>T maps to NM_001385.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74750441 G>T maps to NM_133637.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74750441 G>T maps to NM_133637.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102291646 G>T maps to NM_018370.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102291646 G>T maps to NM_018370.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65687876 C>A maps to ENST00000376991 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65687876 C>A maps to ENST00000376991 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113847600 C>A maps to NM_000796.3 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113847600 C>A maps to NM_000796.3 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:9784720 C>A maps to NM_000798.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:9784720 C>A maps to NM_000798.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:28574239 C>A maps to NM_001941.3 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:28574239 C>A maps to NM_001941.3 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117391914 G>T maps to NM_020693.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117391914 G>T maps to NM_020693.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:65180987 G>T maps to NM_032160.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:65180987 G>T maps to NM_032160.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116757917 C>A maps to NM_013352.2 R763R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116757917 C>A maps to NM_013352.2 R763R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29111050 C>A maps to NM_001943.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29111050 C>A maps to NM_001943.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29046499 G>T maps to NM_001944.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29046499 G>T maps to NM_001944.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29055625 G>T maps to NM_001944.2 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29055625 G>T maps to NM_001944.2 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29056126 C>A maps to NM_001944.2 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29056126 C>A maps to NM_001944.2 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:28979308 C>A maps to NM_001134453.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:28979308 C>A maps to NM_001134453.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7579759 C>A maps to NM_004415.2 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7579759 C>A maps to NM_004415.2 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7585021 G>T maps to NM_004415.2 T2509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7585021 G>T maps to NM_004415.2 T2509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56342199 G>T maps to ENST00000361203 P6995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56342199 G>T maps to ENST00000361203 P6995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56342220 G>T maps to ENST00000361203 T6988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56342220 G>T maps to ENST00000361203 T6988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56417650 G>T maps to ENST00000361203 T5102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56417650 G>T maps to ENST00000361203 T5102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56417827 C>A maps to ENST00000361203 V5043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56417827 C>A maps to ENST00000361203 V5043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56499056 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56499056 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56819223 C>A maps to ENST00000370754 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56819223 C>A maps to ENST00000370754 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:212273603 G>T maps to NM_016448.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:212273603 G>T maps to NM_016448.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:118264245 G>T maps to NM_173666.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:118264245 G>T maps to NM_173666.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113532921 G>T maps to NM_004416.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113532921 G>T maps to NM_004416.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76112321 C>A maps to NM_020892.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76112321 C>A maps to NM_020892.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58000717 C>A maps to NM_178502.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58000717 C>A maps to NM_178502.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58949674 A>C maps to NM_015177.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58949674 A>C maps to NM_015177.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242625222 G>T maps to NM_012145.3 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242625222 G>T maps to NM_012145.3 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:221912317 C>A maps to NM_007207.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:221912317 C>A maps to NM_007207.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35872649 C>A maps to NM_007026.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35872649 C>A maps to NM_007026.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12640046 G>T maps to NM_030640.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12640046 G>T maps to NM_030640.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:304635 C>A maps to ENST00000457386 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:304635 C>A maps to ENST00000457386 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:89744620 C>A maps to NM_001946.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:89744620 C>A maps to NM_001946.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7133722 G>T maps to NM_004422.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7133722 G>T maps to NM_004422.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102442091 C>A maps to NM_001376.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102442091 C>A maps to NM_001376.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102478402 C>A maps to NM_001376.4 P2270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102478402 C>A maps to NM_001376.4 P2270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95657551 G>T maps to NM_004411.4 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95657551 G>T maps to NM_004411.4 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95661983 C>A maps to NM_004411.4 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95661983 C>A maps to NM_004411.4 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95664995 G>T maps to NM_004411.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95664995 G>T maps to NM_004411.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206821097 C>A maps to NM_003582.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206821097 C>A maps to NM_003582.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71791283 C>A maps to NM_001130987.1 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71791283 C>A maps to NM_001130987.1 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71827840 G>T maps to NM_001130987.1 E1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71827840 G>T maps to NM_001130987.1 E1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:137796415 G>T maps to NM_173543.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:137796415 G>T maps to NM_173543.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96239796 G>T maps to NM_198968.2 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96239796 G>T maps to NM_198968.2 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:131646679 C>A maps to ENST00000355311 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:131646679 C>A maps to ENST00000355311 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74899398 G>T maps to NM_001135752.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74899398 G>T maps to NM_001135752.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:21563330 C>A maps to NM_001397.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:21563330 C>A maps to NM_001397.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184008452 C>A maps to NM_014693.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184008452 C>A maps to NM_014693.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95279975 G>T maps to NM_001393.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95279975 G>T maps to NM_001393.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33703295 G>T maps to NM_018217.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33703295 G>T maps to NM_018217.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:12296197 G>T maps to NM_001955.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:12296197 G>T maps to NM_001955.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57876774 C>A maps to NM_207034.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57876774 C>A maps to NM_207034.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78477670 C>A maps to ENST00000377211 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78477670 C>A maps to ENST00000377211 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:85989030 C>A maps to ENST00000351625 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:85989030 C>A maps to ENST00000351625 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36336698 C>A maps to NM_030636.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36336698 C>A maps to NM_030636.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:56149515 G>T maps to NM_001039349.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:56149515 G>T maps to NM_001039349.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:19959804 C>A maps to NM_144715.3 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:19959804 C>A maps to NM_144715.3 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:107145741 C>A maps to NM_004093.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:107145741 C>A maps to NM_004093.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:82422814 G>T maps to NM_024580.5 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:82422814 G>T maps to NM_024580.5 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:82512470 G>T maps to NM_024580.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:82512470 G>T maps to NM_024580.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38352349 G>T maps to ENST00000354891 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38352349 G>T maps to ENST00000354891 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38352385 G>T maps to ENST00000354891 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38352385 G>T maps to ENST00000354891 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38427288 C>A maps to ENST00000354891 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38427288 C>A maps to ENST00000354891 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38435283 G>T maps to ENST00000354891 G738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38435283 G>T maps to ENST00000354891 G738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38458479 C>A maps to ENST00000354891 R927R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38458479 C>A maps to ENST00000354891 R927R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:55220269 C>A maps to NM_005228.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:55220269 C>A maps to NM_005228.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:55268076 C>A maps to NM_005228.3 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:55268076 C>A maps to NM_005228.3 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:55273027 C>A maps to NM_005228.3 P1117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:55273027 C>A maps to NM_005228.3 P1117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110884341 C>A maps to NM_001963.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110884341 C>A maps to NM_001963.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110902007 G>T maps to NM_001963.4 G750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110902007 G>T maps to NM_001963.4 G750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125447446 G>T maps to ENST00000278903 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125447446 G>T maps to ENST00000278903 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125447456 C>A maps to ENST00000278903 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125447456 C>A maps to ENST00000278903 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88857310 C>A maps to NM_004836.5 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88857310 C>A maps to NM_004836.5 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40241381 C>A maps to NM_001013703.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40241381 C>A maps to NM_001013703.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40265884 C>A maps to NM_001013703.2 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40265884 C>A maps to NM_001013703.2 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45347334 C>A maps to NM_020365.3 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45347334 C>A maps to NM_020365.3 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36315795 G>T maps to NM_017629.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36315795 G>T maps to NM_017629.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120802219 G>T maps to NM_003750.2 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120802219 G>T maps to NM_003750.2 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120820278 G>T maps to NM_003750.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120820278 G>T maps to NM_003750.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8014491 C>A maps to ENST00000449102 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8014491 C>A maps to ENST00000449102 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:99823085 C>A maps to NM_001130679.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:99823085 C>A maps to NM_001130679.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184039493 G>T maps to NM_001194947.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184039493 G>T maps to NM_001194947.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184041272 C>A maps to NM_001194947.1 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184041272 C>A maps to NM_001194947.1 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184042719 C>A maps to NM_001194947.1 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184042719 C>A maps to NM_001194947.1 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41515193 G>T maps to NM_172373.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41515193 G>T maps to NM_172373.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41523978 C>A maps to NM_172373.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41523978 C>A maps to NM_172373.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96641343 G>T maps to NM_005230.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96641343 G>T maps to NM_005230.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44066806 G>T maps to NM_025165.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44066806 G>T maps to NM_025165.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36910048 C>A maps to NM_014800.9 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36910048 C>A maps to NM_014800.9 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37298913 C>A maps to NM_014800.9 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37298913 C>A maps to NM_014800.9 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73470664 C>A maps to ENST00000358929 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73470664 C>A maps to ENST00000358929 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103988323 C>A maps to NM_152310.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103988323 C>A maps to NM_152310.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62375741 C>A maps to ENST00000278845 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62375741 C>A maps to ENST00000278845 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:89093301 C>A maps to ENST00000380664 V1540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:89093301 C>A maps to ENST00000380664 V1540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6926396 G>T maps to ENST00000381407 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6926396 G>T maps to ENST00000381407 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43788191 C>A maps to NM_001127615.1 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43788191 C>A maps to NM_001127615.1 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129801510 G>T maps to NM_182314.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129801510 G>T maps to NM_182314.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:111436531 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:111436531 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132201161 C>A maps to NM_006208.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132201161 C>A maps to NM_006208.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120594732 G>T maps to NM_006209.3 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120594732 G>T maps to NM_006209.3 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23294506 G>T maps to NM_004901.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23294506 G>T maps to NM_004901.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23301973 G>T maps to NM_004901.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23301973 G>T maps to NM_004901.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25203540 G>T maps to NM_001247.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25203540 G>T maps to NM_001247.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101460752 G>T maps to NM_020354.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101460752 G>T maps to NM_020354.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132539559 C>A maps to ENST00000333577 P2626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132539559 C>A maps to ENST00000333577 P2626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:131186747 C>A maps to NM_001431.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:131186747 C>A maps to NM_001431.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:131277418 C>A maps to NM_001431.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:131277418 C>A maps to NM_001431.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5395092 C>A maps to NM_012307.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5395092 C>A maps to NM_012307.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5397407 C>A maps to NM_012307.2 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5397407 C>A maps to NM_012307.2 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:111506679 G>T maps to NM_022140.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:111506679 G>T maps to NM_022140.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120848032 C>A maps to NM_020909.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120848032 C>A maps to NM_020909.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:29319858 C>A maps to NM_001166005.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:29319858 C>A maps to NM_001166005.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43507463 G>T maps to NM_000119.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43507463 G>T maps to NM_000119.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:222347368 C>A maps to NM_004438.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:222347368 C>A maps to NM_004438.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:222436887 G>T maps to NM_004438.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:222436887 G>T maps to NM_004438.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134898763 C>A maps to NM_004441.4 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134898763 C>A maps to NM_004441.4 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:23111543 C>A maps to ENST00000400191 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:23111543 C>A maps to ENST00000400191 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100411605 C>G maps to NM_004444.4 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100411605 C>G maps to NM_004444.4 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142561765 C>A maps to NM_004445.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142561765 C>A maps to NM_004445.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37033599 C>A maps to NM_014805.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37033599 C>A maps to NM_014805.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37034165 C>A maps to NM_014805.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37034165 C>A maps to NM_014805.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100319586 G>T maps to NM_000799.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100319586 G>T maps to NM_000799.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100320645 C>A maps to NM_000799.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100320645 C>A maps to NM_000799.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100320692 C>A maps to NM_000799.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100320692 C>A maps to NM_000799.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940386 C>G maps to NM_031308.1 T2345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940386 C>G maps to NM_031308.1 T2345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940815 C>A maps to NM_031308.1 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940815 C>A maps to NM_031308.1 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940962 C>A maps to NM_031308.1 T2153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940962 C>A maps to NM_031308.1 T2153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16487936 G>C maps to ENST00000455140 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16487936 G>C maps to ENST00000455140 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:15834228 C>A maps to NM_004447.5 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:15834228 C>A maps to NM_004447.5 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27182315 C>A maps to NM_005702.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27182315 C>A maps to NM_005702.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:96139362 G>T maps to NM_016442.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:96139362 G>T maps to NM_016442.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:96228090 C>A maps to NM_001130140.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:96228090 C>A maps to NM_001130140.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56490381 G>T maps to NM_001982.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56490381 G>T maps to NM_001982.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56491619 C>A maps to NM_001982.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56491619 C>A maps to NM_001982.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1599350 C>A maps to NM_178040.2 P1102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1599350 C>A maps to NM_178040.2 P1102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:55922487 G>T maps to ENST00000460849 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:55922487 G>T maps to ENST00000460849 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:56044617 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:56044617 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:56330219 G>T maps to ENST00000460849 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:56330219 G>T maps to ENST00000460849 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128044381 C>A maps to NM_000122.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128044381 C>A maps to NM_000122.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103459829 G>T maps to NM_017693.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103459829 G>T maps to NM_017693.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103513970 C>A maps to NM_000123.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103513970 C>A maps to NM_000123.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50680450 C>A maps to NM_000124.2 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50680450 C>A maps to NM_000124.2 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:60199526 G>T maps to NM_000082.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:60199526 G>T maps to NM_000082.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:8887403 C>A maps to NM_153332.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:8887403 C>A maps to NM_153332.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11105333 C>A maps to NM_207582.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11105333 C>A maps to NM_207582.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:54275189 G>T maps to NM_007036.4 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:54275189 G>T maps to NM_007036.4 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95677233 C>A maps to NM_017697.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95677233 C>A maps to NM_017697.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:76928909 G>T maps to NM_004452.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:76928909 G>T maps to NM_004452.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216824330 C>G maps to NM_001438.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216824330 C>G maps to NM_001438.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56525295 C>A maps to NM_001184796.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56525295 C>A maps to NM_001184796.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159627979 C>A maps to NM_004453.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159627979 C>A maps to NM_004453.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:128354928 C>A maps to NM_001143820.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:128354928 C>A maps to NM_001143820.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36353395 G>T maps to NM_016135.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36353395 G>T maps to NM_016135.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29646022 C>A maps to NM_001003927.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29646022 C>A maps to NM_001003927.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93101826 G>T maps to NM_005665.4 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93101826 G>T maps to NM_005665.4 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74003729 G>T maps to NM_001988.2 P1852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74003729 G>T maps to NM_001988.2 P1852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:69695766 C>A maps to NM_001193363.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:69695766 C>A maps to NM_001193363.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:486757 C>G maps to NM_018303.4 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:486757 C>G maps to NM_018303.4 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:491132 G>T maps to NM_018303.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:491132 G>T maps to NM_018303.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:497489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:497489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:133314870 C>A maps to NM_021807.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:133314870 C>A maps to NM_021807.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:57675340 G>T maps to ENST00000340918 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:57675340 G>T maps to ENST00000340918 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:72968483 C>A maps to NM_015189.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:72968483 C>A maps to NM_015189.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94594490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94594490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11151169 G>T maps to NM_001001998.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11151169 G>T maps to NM_001001998.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99203014 C>G maps to NM_016046.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99203014 C>G maps to NM_016046.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108409841 G>T maps to NM_015065.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108409841 G>T maps to NM_015065.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:119122559 G>T maps to NM_000127.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:119122559 G>T maps to NM_000127.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:44148403 G>T maps to NM_000401.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:44148403 G>T maps to NM_000401.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101339566 G>T maps to NM_001439.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101339566 G>T maps to NM_001439.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101342382 G>T maps to NM_001439.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101342382 G>T maps to NM_001439.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28575162 C>A maps to NM_001440.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28575162 C>A maps to NM_001440.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45725779 G>T maps to ENST00000360649 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45725779 G>T maps to ENST00000360649 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133777758 G>T maps to ENST00000452339 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133777758 G>T maps to ENST00000452339 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133849873 C>A maps to ENST00000452339 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133849873 C>A maps to ENST00000452339 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148511154 G>T maps to NM_004456.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148511154 G>T maps to NM_004456.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148511212 C>A maps to NM_004456.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148511212 C>A maps to NM_004456.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113803342 C>A maps to NM_000504.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113803342 C>A maps to NM_000504.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187209614 G>T maps to NM_000128.3 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187209614 G>T maps to NM_000128.3 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6318846 G>T maps to NM_000129.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6318846 G>T maps to NM_000129.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6318876 G>T maps to NM_000129.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6318876 G>T maps to NM_000129.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94998815 C>A maps to NM_001993.4 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94998815 C>A maps to NM_001993.4 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95001587 C>A maps to NM_001993.4 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95001587 C>A maps to NM_001993.4 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154157147 G>T maps to NM_000132.3 P1639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154157147 G>T maps to NM_000132.3 P1639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88425775 G>T maps to NM_001443.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88425775 G>T maps to NM_001443.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80460615 C>A maps to NM_000137.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80460615 C>A maps to NM_000137.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207087296 G>T maps to NM_005449.4 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207087296 G>T maps to NM_005449.4 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14607517 C>A maps to NM_019018.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14607517 C>A maps to NM_019018.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74485057 C>A maps to NM_016014.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74485057 C>A maps to NM_016014.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59059604 G>T maps to NM_147189.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59059604 G>T maps to NM_147189.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:41612 G>T maps to NM_001077710.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:41612 G>T maps to NM_001077710.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58919561 G>T maps to NM_198847.2 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58919561 G>T maps to NM_198847.2 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58892632 C>A maps to NM_198947.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58892632 C>A maps to NM_198947.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96212837 C>A maps to NM_198841.2 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96212837 C>A maps to NM_198841.2 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96294435 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96294435 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96318681 C>A maps to ENST00000333936 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96318681 C>A maps to ENST00000333936 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170627503 C>A maps to NM_032448.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170627503 C>A maps to NM_032448.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:63411677 G>T maps to NM_152424.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:63411677 G>T maps to NM_152424.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22985687 C>A maps to NM_032581.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22985687 C>A maps to NM_032581.3 S362S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22999874 C>A maps to NM_032581.3 G331*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22999874 C>A maps to NM_032581.3 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184787865 G>T maps to NM_052966.2 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184787865 G>T maps to NM_052966.2 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184868314 G>T maps to NM_052966.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184868314 G>T maps to NM_052966.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130279192 G>T maps to NM_022833.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130279192 G>T maps to NM_022833.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184062464 C>A maps to NM_144635.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184062464 C>A maps to NM_144635.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143053777 C>A maps to NM_001031690.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143053777 C>A maps to NM_001031690.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220046460 C>A maps to NM_024293.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220046460 C>A maps to NM_024293.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139153536 G>T maps to NM_015912.3 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139153536 G>T maps to NM_015912.3 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139209857 G>T maps to NM_015912.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139209857 G>T maps to NM_015912.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89950665 G>T maps to NM_014883.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89950665 G>T maps to NM_014883.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61007406 G>T maps to ENST00000442566 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61007406 G>T maps to ENST00000442566 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116595303 G>T maps to NM_020940.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116595303 G>T maps to NM_020940.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116620579 G>T maps to NM_020940.3 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116620579 G>T maps to NM_020940.3 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:93410360 G>T maps to NM_032042.5 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:93410360 G>T maps to NM_032042.5 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84390216 G>T maps to NM_139076.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84390216 G>T maps to NM_139076.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:126523500 C>A maps to NM_032182.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:126523500 C>A maps to NM_032182.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:45432407 C>A maps to ENST00000361462 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:45432407 C>A maps to ENST00000361462 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:119281284 G>T maps to NM_024581.4 R1136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:119281284 G>T maps to NM_024581.4 R1136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15885238 C>A maps to NM_024948.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15885238 C>A maps to NM_024948.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155223961 C>A maps to ENST00000368370 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155223961 C>A maps to ENST00000368370 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2641565 C>A maps to ENST00000324666 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2641565 C>A maps to ENST00000324666 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2664891 G>T maps to ENST00000324666 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2664891 G>T maps to ENST00000324666 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150416578 C>A maps to NM_152394.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150416578 C>A maps to NM_152394.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128936126 C>A maps to NM_001039762.2 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128936126 C>A maps to NM_001039762.2 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128936160 G>T maps to NM_001039762.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128936160 G>T maps to NM_001039762.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128974428 G>T maps to NM_001039762.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128974428 G>T maps to NM_001039762.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159048603 G>T maps to NM_001128424.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159048603 G>T maps to NM_001128424.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:68802080 C>A maps to NM_182522.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:68802080 C>A maps to NM_182522.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51829378 G>T maps to NM_001005751.1 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51829378 G>T maps to NM_001005751.1 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116878992 G>T maps to ENST00000368596 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116878992 G>T maps to ENST00000368596 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116784508 C>A maps to NM_001010919.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116784508 C>A maps to NM_001010919.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58625896 C>A maps to NM_138805.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58625896 C>A maps to NM_138805.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129120721 C>A maps to ENST00000450266 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129120721 C>A maps to ENST00000450266 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118166116 C>A maps to NM_017709.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118166116 C>A maps to NM_017709.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:114441949 G>T maps to NM_001077639.1 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:114441949 G>T maps to NM_001077639.1 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:177199203 C>T maps to NM_021165.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:177199203 C>T maps to NM_021165.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:190067936 C>A maps to NM_199051.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:190067936 C>A maps to NM_199051.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150970623 G>T maps to NM_001163258.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150970623 G>T maps to NM_001163258.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150973085 C>A maps to NM_001163258.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150973085 C>A maps to NM_001163258.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24843407 C>T maps to NM_014722.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24843407 C>T maps to NM_014722.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156589499 G>T maps to NM_130899.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156589499 G>T maps to NM_130899.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:78332045 G>T maps to NM_198549.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:78332045 G>T maps to NM_198549.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43625065 C>A maps to NM_001145196.1 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43625065 C>A maps to NM_001145196.1 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43625350 G>T maps to NM_001145196.1 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43625350 G>T maps to NM_001145196.1 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43627134 C>A maps to NM_001145196.1 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43627134 C>A maps to NM_001145196.1 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43627702 C>A maps to NM_001145196.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:43627702 C>A maps to NM_001145196.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:90536663 C>A maps to NM_001145124.1 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:90536663 C>A maps to NM_001145124.1 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134136547 G>T maps to NM_033387.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134136547 G>T maps to NM_033387.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:94764399 C>A maps to NM_152548.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:94764399 C>A maps to NM_152548.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87519299 G>T maps to NM_016033.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87519299 G>T maps to NM_016033.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144811237 C>A maps to NM_198488.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144811237 C>A maps to NM_198488.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8375152 G>T maps to NM_018088.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8375152 G>T maps to NM_018088.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8376754 G>T maps to NM_018088.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8376754 G>T maps to NM_018088.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85143900 G>T maps to ENST00000393246 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85143900 G>T maps to ENST00000393246 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89806458 C>A maps to NM_000135.2 E1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89806458 C>A maps to NM_000135.2 E1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89809306 C>A maps to NM_000135.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89809306 C>A maps to NM_000135.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89877375 C>A maps to NM_000135.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89877375 C>A maps to NM_000135.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10076216 C>A maps to NM_033084.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10076216 C>A maps to NM_033084.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:22646885 G>T maps to NM_022725.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:22646885 G>T maps to NM_022725.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:45658453 C>A maps to NM_020937.2 S1743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:45658453 C>A maps to NM_020937.2 S1743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163070501 C>A maps to NM_004460.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163070501 C>A maps to NM_004460.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163074570 C>A maps to NM_004460.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163074570 C>A maps to NM_004460.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:29460734 C>A maps to NM_018099.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:29460734 C>A maps to NM_018099.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:29462117 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:29462117 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:98865555 G>T maps to NM_005766.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:98865555 G>T maps to NM_005766.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99042338 C>A maps to NM_005766.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99042338 C>A maps to NM_005766.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207655349 C>A maps to NM_014929.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207655349 C>A maps to NM_014929.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7863110 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7863110 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187510039 G>T maps to ENST00000260147 P4494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187510039 G>T maps to ENST00000260147 P4494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187510246 C>A maps to ENST00000260147 T4425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187510246 C>A maps to ENST00000260147 T4425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187539563 G>T maps to ENST00000260147 R2729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187539563 G>T maps to ENST00000260147 R2729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187540188 C>A maps to ENST00000260147 T2520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187540188 C>A maps to ENST00000260147 T2520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187541781 C>A maps to ENST00000260147 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187541781 C>A maps to ENST00000260147 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187557824 C>A maps to ENST00000260147 E1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187557824 C>A maps to ENST00000260147 E1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187627885 G>T maps to ENST00000260147 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187627885 G>T maps to ENST00000260147 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187630528 G>T maps to ENST00000260147 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187630528 G>T maps to ENST00000260147 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150921974 G>T maps to NM_001447.2 R2905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150921974 G>T maps to NM_001447.2 R2905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:92577302 G>T maps to ENST00000298047 S3590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:92577302 G>T maps to ENST00000298047 S3590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126241564 C>A maps to NM_024582.4 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126241564 C>A maps to NM_024582.4 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126242309 G>T maps to NM_024582.4 G1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126242309 G>T maps to NM_024582.4 G1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126336204 C>A maps to NM_024582.4 S2029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126336204 C>A maps to NM_024582.4 S2029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126371284 G>T maps to NM_024582.4 T3038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126371284 G>T maps to NM_024582.4 T3038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126411152 C>A maps to NM_024582.4 P4392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:126411152 C>A maps to NM_024582.4 P4392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:45938098 C>A maps to ENST00000348697 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:45938098 C>A maps to ENST00000348697 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48707881 G>T maps to NM_000138.4 P2634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48707881 G>T maps to NM_000138.4 P2634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48725102 G>T maps to NM_000138.4 P2233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48725102 G>T maps to NM_000138.4 P2233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48726812 G>T maps to NM_000138.4 P2198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48726812 G>T maps to NM_000138.4 P2198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48826376 G>T maps to NM_000138.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48826376 G>T maps to NM_000138.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127595290 G>T maps to NM_001999.3 P2865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127595290 G>T maps to NM_001999.3 P2865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127597501 C>A maps to NM_001999.3 E2764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127597501 C>A maps to NM_001999.3 E2764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:97349720 C>A maps to NM_003837.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:97349720 C>A maps to NM_003837.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30680872 G>T maps to ENST00000356166 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30680872 G>T maps to ENST00000356166 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:77592778 C>A maps to NM_012158.2 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:77592778 C>A maps to NM_012158.2 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117595733 G>T maps to NM_033624.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117595733 G>T maps to NM_033624.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:18675790 C>A maps to ENST00000395665 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:18675790 C>A maps to ENST00000395665 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123526905 C>A maps to NM_012164.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123526905 C>A maps to NM_012164.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72695251 G>T maps to ENST00000409314 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72695251 G>T maps to ENST00000409314 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137801877 C>A maps to NM_002003.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137801877 C>A maps to NM_002003.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:157668218 G>T maps to NM_052939.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:157668218 G>T maps to NM_052939.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155279984 C>A maps to NM_001135821.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155279984 C>A maps to NM_001135821.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111746442 C>A maps to NM_138378.1 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111746442 C>A maps to NM_138378.1 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111747260 C>A maps to ENST00000428306 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111747260 C>A maps to ENST00000428306 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61563075 C>A maps to NM_004111.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61563075 C>A maps to NM_004111.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63987722 C>A maps to NM_178443.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63987722 C>A maps to NM_178443.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:36805745 G>T maps to NM_001042548.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:36805745 G>T maps to NM_001042548.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121942915 G>T maps to NM_001024613.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121942915 G>T maps to NM_001024613.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121943753 C>A maps to NM_001024613.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121943753 C>A maps to NM_001024613.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155506819 C>A maps to NM_000508.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155506819 C>A maps to NM_000508.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95773520 C>A maps to NM_033086.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95773520 C>A maps to NM_033086.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14862791 G>T maps to NM_152536.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14862791 G>T maps to NM_152536.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:191888334 C>A maps to NM_021032.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:191888334 C>A maps to NM_021032.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:191888348 G>T maps to NM_021032.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:191888348 G>T maps to NM_021032.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:102521130 C>A maps to NM_175929.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:102521130 C>A maps to NM_175929.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170863158 G>C maps to NM_003862.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170863158 G>C maps to NM_003862.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:69631174 C>A maps to NM_005247.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:69631174 C>A maps to NM_005247.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:69588172 G>T maps to NM_002007.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:69588172 G>T maps to NM_002007.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27110592 C>A maps to NM_015633.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27110592 C>A maps to NM_015633.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167438313 C>A maps to NM_007045.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167438313 C>A maps to NM_007045.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123239507 C>A maps to ENST00000351936 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123239507 C>A maps to ENST00000351936 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123256051 G>T maps to ENST00000351936 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123256051 G>T maps to ENST00000351936 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:59844449 G>T maps to NM_001113411.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:59844449 G>T maps to NM_001113411.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60133043 C>A maps to NM_001113411.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60133043 C>A maps to NM_001113411.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60133064 G>T maps to NM_001113411.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60133064 G>T maps to NM_001113411.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155526086 C>A maps to ENST00000407946 G429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155526086 C>A maps to ENST00000407946 G429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155526146 G>T maps to ENST00000407946 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155526146 G>T maps to ENST00000407946 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76828744 C>A maps to NM_006682.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76828744 C>A maps to NM_006682.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34349267 C>A maps to NM_025135.2 P1372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34349267 C>A maps to NM_025135.2 P1372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:164468083 G>T maps to NM_018086.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:164468083 G>T maps to NM_018086.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99567248 G>T maps to NM_001042459.1 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99567248 G>T maps to NM_001042459.1 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99567726 C>A maps to NM_001042459.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:99567726 C>A maps to NM_001042459.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:76023009 G>T maps to NM_015687.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:76023009 G>T maps to NM_015687.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:76124436 G>T maps to NM_015687.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:76124436 G>T maps to NM_015687.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39976615 C>A maps to NM_021939.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39976615 C>A maps to NM_021939.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:115931682 G>T maps to ENST00000446284 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:115931682 G>T maps to ENST00000446284 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35544940 C>A maps to NM_001145775.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35544940 C>A maps to NM_001145775.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35554822 G>T maps to NM_001145775.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35554822 G>T maps to NM_001145775.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72743371 C>A maps to NM_003602.3 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72743371 C>A maps to NM_003602.3 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72755304 C>A maps to NM_003602.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72755304 C>A maps to NM_003602.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179343130 G>T maps to ENST00000350591 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179343130 G>T maps to ENST00000350591 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:108397481 C>A maps to NM_006731.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:108397481 C>A maps to NM_006731.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152323751 G>C maps to NM_001014342.2 S2170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152323751 G>C maps to NM_001014342.2 S2170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152324441 G>T maps to NM_001014342.2 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152324441 G>T maps to NM_001014342.2 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152325048 G>T maps to NM_001014342.2 S1738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152325048 G>T maps to NM_001014342.2 S1738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152325803 G>T maps to NM_001014342.2 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152325803 G>T maps to NM_001014342.2 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327078 G>T maps to NM_001014342.2 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327078 G>T maps to NM_001014342.2 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327309 G>T maps to NM_001014342.2 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327309 G>T maps to NM_001014342.2 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152328227 G>T maps to NM_001014342.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152328227 G>T maps to NM_001014342.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152328506 C>A maps to NM_001014342.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152328506 C>A maps to NM_001014342.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152275826 G>T maps to NM_002016.1 S3845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152275826 G>T maps to NM_002016.1 S3845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152275978 C>A maps to NM_002016.1 G3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152275978 C>A maps to NM_002016.1 G3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152281685 G>T maps to NM_002016.1 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152281685 G>T maps to NM_002016.1 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152282662 G>T maps to NM_002016.1 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152282662 G>T maps to NM_002016.1 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152283199 G>T maps to NM_002016.1 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152283199 G>T maps to NM_002016.1 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152283512 G>T maps to NM_002016.1 S1283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152283512 G>T maps to NM_002016.1 S1283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152285756 C>A maps to NM_002016.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152285756 C>A maps to NM_002016.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152285801 C>A maps to NM_002016.1 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152285801 C>A maps to NM_002016.1 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152286118 G>T maps to NM_002016.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152286118 G>T maps to NM_002016.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152286623 G>T maps to NM_002016.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152286623 G>T maps to NM_002016.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:21553004 G>T maps to NM_018071.3 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:21553004 G>T maps to NM_018071.3 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:84608327 C>A maps to NM_001001670.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:84608327 C>A maps to NM_001001670.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:84608622 C>A maps to NM_001001670.2 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:84608622 C>A maps to NM_001001670.2 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153595179 C>A maps to NM_001110556.1 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153595179 C>A maps to NM_001110556.1 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58090836 G>T maps to NM_001164317.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58090836 G>T maps to NM_001164317.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58095768 C>A maps to NM_001164317.1 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58095768 C>A maps to NM_001164317.1 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58106998 C>A maps to NM_001164317.1 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58106998 C>A maps to NM_001164317.1 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58109058 C>A maps to NM_001164317.1 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58109058 C>A maps to NM_001164317.1 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58109109 G>T maps to NM_001164317.1 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58109109 G>T maps to NM_001164317.1 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58111446 C>A maps to NM_001164317.1 P1346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58111446 C>A maps to NM_001164317.1 P1346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58111458 C>A maps to NM_001164317.1 T1350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58111458 C>A maps to NM_001164317.1 T1350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58124189 G>T maps to NM_001164317.1 P1712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58124189 G>T maps to NM_001164317.1 P1712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58145285 G>T maps to NM_001164317.1 S2329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58145285 G>T maps to NM_001164317.1 S2329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128489559 C>A maps to NM_001458.4 P1709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128489559 C>A maps to NM_001458.4 P1709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27210234 C>A maps to ENST00000394906 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27210234 C>A maps to ENST00000394906 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:86089313 C>A maps to NM_013231.4 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:86089313 C>A maps to NM_013231.4 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:14306970 G>T maps to NM_198391.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:14306970 G>T maps to NM_198391.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28959073 G>T maps to NM_002019.4 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28959073 G>T maps to NM_002019.4 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:33261456 G>T maps to NM_001103184.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:33261456 G>T maps to NM_001103184.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:240341333 C>A maps to ENST00000406993 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:240341333 C>A maps to ENST00000406993 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50050678 C>A maps to NM_175736.4 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50050678 C>A maps to NM_175736.4 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146696506 C>A maps to NM_001461.2 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146696506 C>A maps to NM_001461.2 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216257654 C>A maps to NM_212482.1 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216257654 C>A maps to NM_212482.1 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132757141 G>T maps to NM_015033.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132757141 G>T maps to NM_015033.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47786900 C>A maps to NM_015308.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47786900 C>A maps to NM_015308.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159682278 G>T maps to NM_032532.2 S1744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159682278 G>T maps to NM_032532.2 S1744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:49705436 C>A maps to NM_001079673.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:49705436 C>A maps to NM_001079673.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172052792 G>T maps to NM_022763.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172052792 G>T maps to NM_022763.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159782926 G>T maps to ENST00000379346 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159782926 G>T maps to ENST00000379346 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159789299 C>A maps to ENST00000379346 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159789299 C>A maps to ENST00000379346 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8196335 C>A maps to NM_018416.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8196335 C>A maps to NM_018416.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2981279 C>A maps to NM_202002.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2981279 C>A maps to NM_202002.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26862013 G>T maps to NM_003593.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26862013 G>T maps to NM_003593.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:71037144 G>T maps to NM_032682.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:71037144 G>T maps to NM_032682.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41533671 C>A maps to NM_001012426.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41533671 C>A maps to NM_001012426.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:74671074 C>A maps to NM_003838.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:74671074 C>A maps to NM_003838.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:79434557 G>T maps to NM_025074.6 S3342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:79434557 G>T maps to NM_025074.6 S3342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:14807977 C>A maps to ENST00000380880 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:14807977 C>A maps to ENST00000380880 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39266382 G>T maps to NM_207361.4 T1634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39266382 G>T maps to NM_207361.4 T1634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44198147 C>A maps to NM_032892.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44198147 C>A maps to NM_032892.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:131216452 C>A maps to NM_194277.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:131216452 C>A maps to NM_194277.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37692722 C>A maps to NM_014907.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37692722 C>A maps to NM_014907.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37733512 C>A maps to NM_014907.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37733512 C>A maps to NM_014907.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:49381010 C>A maps to NM_001018071.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:49381010 C>A maps to NM_001018071.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:12708372 C>A maps to ENST00000429478 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:12708372 C>A maps to ENST00000429478 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:12736646 C>A maps to ENST00000429478 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:12736646 C>A maps to ENST00000429478 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100183024 G>T maps to NM_001013660.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100183024 G>T maps to NM_001013660.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100203710 C>A maps to NM_001013660.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100203710 C>A maps to NM_001013660.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100206369 G>T maps to NM_001013660.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100206369 G>T maps to NM_001013660.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48514611 G>T maps to NM_015030.1 P2677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48514611 G>T maps to NM_015030.1 P2677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48559637 C>A maps to NM_015030.1 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48559637 C>A maps to NM_015030.1 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32776545 G>T maps to NM_023037.2 P1300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32776545 G>T maps to NM_023037.2 P1300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32783724 G>T maps to NM_023037.2 G1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32783724 G>T maps to NM_023037.2 G1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32800028 C>A maps to NM_023037.2 S1708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32800028 C>A maps to NM_023037.2 S1708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32849121 C>A maps to NM_023037.2 A2760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32849121 C>A maps to NM_023037.2 A2760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:49247264 C>A maps to NM_000145.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:49247264 C>A maps to NM_000145.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40062636 C>A maps to NM_152597.4 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40062636 C>A maps to NM_152597.4 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:54145753 C>A maps to NM_001080432.2 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:54145753 C>A maps to NM_001080432.2 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61898802 C>A maps to NM_017647.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61898802 C>A maps to NM_017647.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61901532 G>T maps to NM_017647.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61901532 G>T maps to NM_017647.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37446265 C>A maps to NM_015050.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37446265 C>A maps to NM_015050.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133470944 G>T maps to NM_003934.1 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133470944 G>T maps to NM_003934.1 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31200486 G>T maps to NM_004960.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31200486 G>T maps to NM_004960.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49206903 C>A maps to NM_001097638.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49206903 C>A maps to NM_001097638.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139925476 C>A maps to NM_004479.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139925476 C>A maps to NM_004479.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180675706 C>A maps to NM_005087.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180675706 C>A maps to NM_005087.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39153706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39153706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39202015 G>T maps to ENST00000263405 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39202015 G>T maps to ENST00000263405 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39202474 G>T maps to ENST00000263405 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39202474 G>T maps to ENST00000263405 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39202753 G>T maps to ENST00000263405 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39202753 G>T maps to ENST00000263405 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45977986 G>T maps to NM_024513.2 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45977986 G>T maps to NM_024513.2 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46008649 G>T maps to NM_024513.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46008649 G>T maps to NM_024513.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:112015656 C>A maps to NM_153047.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:112015656 C>A maps to NM_153047.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:90894632 G>T maps to NM_003505.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:90894632 G>T maps to NM_003505.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28384775 C>A maps to NM_017412.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28384775 C>A maps to NM_017412.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28409238 C>A maps to NM_017412.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28409238 C>A maps to NM_017412.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:86663407 G>T maps to NM_012193.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:86663407 G>T maps to NM_012193.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:104343631 C>A maps to NM_003506.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:104343631 C>A maps to NM_003506.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72849053 G>T maps to NM_003508.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72849053 G>T maps to NM_003508.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31066642 G>T maps to NM_017769.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31066642 G>T maps to NM_017769.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76582198 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76582198 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41052970 C>T maps to NM_000151.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41052970 C>T maps to NM_000151.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7144690 G>T maps to NM_007278.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7144690 G>T maps to NM_007278.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29572317 G>T maps to NM_001470.2 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29572317 G>T maps to NM_001470.2 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46252492 G>T maps to ENST00000507069 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46252492 G>T maps to ENST00000507069 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46252525 G>T maps to ENST00000507069 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46252525 G>T maps to ENST00000507069 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:151393300 C>A maps to NM_000808.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:151393300 C>A maps to NM_000808.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:151532928 C>A maps to NM_000808.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:151532928 C>A maps to NM_000808.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161119077 G>T maps to NM_000811.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161119077 G>T maps to NM_000811.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46099286 C>A maps to NM_173536.3 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46099286 C>A maps to NM_173536.3 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46099326 C>A maps to NM_173536.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46099326 C>A maps to NM_173536.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161495048 C>A maps to NM_198903.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161495048 C>A maps to NM_198903.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161524721 C>A maps to NM_198903.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161524721 C>A maps to NM_198903.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161528318 C>A maps to NM_198903.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:161528318 C>A maps to NM_198903.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90009487 G>T maps to NM_002043.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90009487 G>T maps to NM_002043.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49528120 G>T maps to NM_002044.2 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49528120 G>T maps to NM_002044.2 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:38903156 C>A maps to NM_138801.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:38903156 C>A maps to NM_138801.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:153765878 C>A maps to NM_198321.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:153765878 C>A maps to NM_198321.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151810390 C>A maps to NM_022087.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151810390 C>A maps to NM_022087.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101611280 G>T maps to NM_024642.3 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101611280 G>T maps to NM_024642.3 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:31133844 G>T maps to NM_024572.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:31133844 G>T maps to NM_024572.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:31147091 G>T maps to NM_024572.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:31147091 G>T maps to NM_024572.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230410289 C>A maps to NM_004481.3 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230410289 C>A maps to NM_004481.3 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51759270 G>T maps to NM_007210.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51759270 G>T maps to NM_007210.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51773262 G>T maps to NM_007210.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51773262 G>T maps to NM_007210.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:69813780 C>A maps to NM_020692.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:69813780 C>A maps to NM_020692.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11314704 C>A maps to NM_198516.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11314704 C>A maps to NM_198516.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34649058 C>A maps to NM_000155.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34649058 C>A maps to NM_000155.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68452456 G>T maps to NM_015973.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68452456 G>T maps to NM_015973.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81390560 C>A maps to NM_022041.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81390560 C>A maps to NM_022041.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81410859 C>A maps to NM_022041.3 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81410859 C>A maps to NM_022041.3 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81410881 G>T maps to NM_022041.3 G521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81410881 G>T maps to NM_022041.3 G521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130152941 C>A maps to NM_032293.4 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130152941 C>A maps to NM_032293.4 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101016130 C>A maps to NM_174942.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101016130 C>A maps to NM_174942.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39871735 C>A maps to NM_000805.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39871735 C>A maps to NM_000805.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11614582 C>A maps to NM_002052.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11614582 C>A maps to NM_002052.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11615893 C>A maps to NM_002052.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11615893 C>A maps to NM_002052.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19761499 C>A maps to NM_005257.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19761499 C>A maps to NM_005257.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19780620 G>T maps to NM_005257.3 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19780620 G>T maps to NM_005257.3 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19780644 G>T maps to NM_005257.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:19780644 G>T maps to NM_005257.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92083964 C>A maps to NM_021167.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92083964 C>A maps to NM_021167.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22749333 C>A maps to NM_020973.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22749333 C>A maps to NM_020973.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104140315 G>T maps to NM_004193.2 A1681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104140315 G>T maps to NM_004193.2 A1681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:89583305 G>T maps to NM_004120.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:89583305 G>T maps to NM_004120.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:89654279 G>T maps to NM_052941.4 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:89654279 G>T maps to NM_052941.4 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:237074648 G>T maps to NM_001485.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:237074648 G>T maps to NM_001485.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109111927 C>A maps to NM_181453.3 P1543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109111927 C>A maps to NM_181453.3 P1543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:34133417 G>T maps to NM_016631.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:34133417 G>T maps to NM_016631.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163002129 G>T maps to ENST00000233604 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163002129 G>T maps to ENST00000233604 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44187259 G>T maps to NM_000162.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44187259 G>T maps to NM_000162.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:53385675 C>A maps to NM_001498.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:53385675 C>A maps to NM_001498.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10876730 C>A maps to NM_004752.3 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10876730 C>A maps to NM_004752.3 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120578770 G>T maps to NM_006836.1 P1962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120578770 G>T maps to NM_006836.1 P1962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120582537 G>T maps to NM_006836.1 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120582537 G>T maps to NM_006836.1 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79118028 G>T maps to NM_001097636.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79118028 G>T maps to NM_001097636.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10530031 C>A maps to NM_145649.4 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10530031 C>A maps to NM_145649.4 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:74325640 C>A maps to NM_016591.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:74325640 C>A maps to NM_016591.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42891891 G>T maps to NM_024034.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42891891 G>T maps to NM_024034.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118455254 G>T maps to NM_017686.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118455254 G>T maps to NM_017686.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74860133 C>A maps to ENST00000238018 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74860133 C>A maps to ENST00000238018 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:48426671 G>T maps to NM_004962.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:48426671 G>T maps to NM_004962.2 P445P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75146601 G>T maps to NM_030792.6 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75146601 G>T maps to NM_030792.6 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:649452 G>T maps to NM_015721.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:649452 G>T maps to NM_015721.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:154278870 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:154278870 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69569309 C>A maps to ENST00000357308 G393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69569309 C>A maps to ENST00000357308 G393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179731846 G>T maps to NM_005110.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179731846 G>T maps to NM_005110.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30544313 C>A maps to NM_024051.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30544313 C>A maps to NM_024051.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34943635 C>A maps to NM_024835.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34943635 C>A maps to NM_024835.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34945742 C>A maps to NM_024835.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34945742 C>A maps to NM_024835.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61959189 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61959189 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42711355 G>T maps to NM_000163.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42711355 G>T maps to NM_000163.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42718610 C>A maps to NM_000163.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42718610 C>A maps to NM_000163.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233659542 C>A maps to ENST00000373566 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233659542 C>A maps to ENST00000373566 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233671240 G>T maps to ENST00000373566 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233671240 G>T maps to ENST00000373566 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233681730 C>A maps to ENST00000373566 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233681730 C>A maps to ENST00000373566 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150417158 C>A maps to NM_130759.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150417158 C>A maps to NM_130759.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150325220 C>A maps to ENST00000438845 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150325220 C>A maps to ENST00000438845 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150164052 C>A maps to NM_175571.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150164052 C>A maps to NM_175571.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110376267 G>T maps to NM_057169.3 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110376267 G>T maps to NM_057169.3 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110390968 G>T maps to NM_057169.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110390968 G>T maps to NM_057169.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110421191 G>T maps to NM_057169.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110421191 G>T maps to NM_057169.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99527069 C>A maps to NM_181538.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99527069 C>A maps to NM_181538.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141923630 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141923630 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69172541 C>A maps to NM_182536.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:69172541 C>A maps to NM_182536.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134234253 G>T maps to NM_138342.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134234253 G>T maps to NM_138342.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:8125840 G>T maps to NM_138426.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:8125840 G>T maps to NM_138426.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:8125892 G>T maps to NM_138426.2 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:8125892 G>T maps to NM_138426.2 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:6553472 G>T maps to NM_000170.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:6553472 G>T maps to NM_000170.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74490600 G>T maps to NM_012201.5 P1106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74490600 G>T maps to NM_012201.5 P1106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74542784 G>T maps to NM_012201.5 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74542784 G>T maps to NM_012201.5 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57865367 G>T maps to NM_005269.2 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57865367 G>T maps to NM_005269.2 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:75763886 G>T maps to ENST00000378695 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:75763886 G>T maps to ENST00000378695 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:175565034 G>T maps to NM_006529.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:175565034 G>T maps to NM_006529.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56872886 C>A maps to NM_013267.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56872886 C>A maps to NM_013267.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191766710 C>A maps to NM_014905.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191766710 C>A maps to NM_014905.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88820794 C>A maps to NM_005271.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88820794 C>A maps to NM_005271.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88854252 G>T maps to NM_005271.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88854252 G>T maps to NM_005271.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182354924 C>A maps to NM_002065.5 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182354924 C>A maps to NM_002065.5 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4873893 C>A maps to NM_032569.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4873893 C>A maps to NM_032569.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19745899 C>A maps to NM_016573.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19745899 C>A maps to NM_016573.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220366686 C>A maps to ENST00000373917 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220366686 C>A maps to ENST00000373917 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:80144050 G>T maps to NM_004297.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:80144050 G>T maps to NM_004297.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:11876644 C>A maps to NM_182978.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:11876644 C>A maps to NM_182978.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68606377 C>A maps to NM_000406.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68606377 C>A maps to NM_000406.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131028580 C>A maps to NM_004486.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131028580 C>A maps to NM_004486.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133363282 G>T maps to NM_005895.3 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133363282 G>T maps to NM_005895.3 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133384913 G>T maps to NM_005895.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133384913 G>T maps to NM_005895.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133384924 G>T maps to NM_005895.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133384924 G>T maps to NM_005895.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37368005 C>A maps to NM_001172713.1 S1565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37368005 C>A maps to NM_001172713.1 S1565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167745544 G>T maps to NM_014498.3 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167745544 G>T maps to NM_014498.3 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204170924 C>A maps to NM_198447.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204170924 C>A maps to NM_198447.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37791957 G>T maps to NM_152413.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37791957 G>T maps to NM_152413.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101180551 C>A maps to NM_002079.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101180551 C>A maps to NM_002079.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58743365 G>T maps to NM_002080.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58743365 G>T maps to NM_002080.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194117403 G>T maps to NM_004488.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194117403 G>T maps to NM_004488.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194117475 C>G maps to NM_004488.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194117475 C>G maps to NM_004488.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:217783725 G>T maps to NM_018040.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:217783725 G>T maps to NM_018040.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27219261 G>T maps to NM_022078.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27219261 G>T maps to NM_022078.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27223995 G>T maps to NM_022078.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27223995 G>T maps to NM_022078.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42478442 G>T maps to NM_001002909.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42478442 G>T maps to NM_001002909.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42478802 G>T maps to NM_001002909.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42478802 G>T maps to NM_001002909.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:132439844 G>T maps to NM_001448.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:132439844 G>T maps to NM_001448.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:92346023 G>T maps to NM_004466.4 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:92346023 G>T maps to NM_004466.4 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27862968 C>A maps to NM_007266.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27862968 C>A maps to NM_007266.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132890959 G>T maps to NM_001136557.1 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132890959 G>T maps to NM_001136557.1 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123187766 G>T maps to NM_177551.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123187766 G>T maps to NM_177551.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123201220 G>T maps to NM_006018.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123201220 G>T maps to NM_006018.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47649692 C>A maps to NM_153839.6 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47649692 C>A maps to NM_153839.6 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57597803 C>A maps to ENST00000349457 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57597803 C>A maps to ENST00000349457 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47680329 C>A maps to NM_153838.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47680329 C>A maps to NM_153838.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47682279 G>T maps to NM_153838.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47682279 G>T maps to NM_153838.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47682517 C>A maps to NM_153838.3 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47682517 C>A maps to NM_153838.3 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46851310 G>T maps to NM_015234.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46851310 G>T maps to NM_015234.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22389552 G>T maps to NM_145290.2 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22389552 G>T maps to NM_145290.2 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22404413 C>A maps to NM_145290.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22404413 C>A maps to NM_145290.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22414867 G>T maps to NM_145290.2 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22414867 G>T maps to NM_145290.2 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22414905 C>A maps to NM_145290.2 G711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22414905 C>A maps to NM_145290.2 G711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22422601 C>A maps to NM_145290.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22422601 C>A maps to NM_145290.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22422658 C>A maps to NM_145290.2 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22422658 C>A maps to NM_145290.2 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22422703 G>T maps to NM_145290.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22422703 G>T maps to NM_145290.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37780136 C>A maps to NM_181791.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37780136 C>A maps to NM_181791.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:9711638 G>T maps to ENST00000380929 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:9711638 G>T maps to ENST00000380929 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154146723 G>T maps to NM_001038705.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154146723 G>T maps to NM_001038705.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:175311382 G>T maps to NM_152529.5 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:175311382 G>T maps to NM_152529.5 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150916483 C>A maps to NM_013308.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150916483 C>A maps to NM_013308.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145583397 G>T maps to NM_024531.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145583397 G>T maps to NM_024531.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40093785 C>A maps to NM_007223.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40093785 C>A maps to NM_007223.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:95271402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:95271402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99907180 G>T maps to NM_005292.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99907180 G>T maps to NM_005292.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99907619 G>T maps to NM_005292.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99907619 G>T maps to NM_005292.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207041782 C>A maps to NM_005279.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207041782 C>A maps to NM_005279.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:124386653 C>A maps to NM_005302.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:124386653 C>A maps to NM_005302.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:105859166 C>A maps to NM_007227.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:105859166 C>A maps to NM_007227.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:174417704 G>T maps to NM_005684.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:174417704 G>T maps to NM_005684.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57689352 C>A maps to NM_005682.5 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57689352 C>A maps to NM_005682.5 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110300440 G>T maps to ENST00000414000 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110300440 G>T maps to ENST00000414000 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145811901 G>T maps to NM_001097612.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145811901 G>T maps to NM_001097612.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13061794 G>T maps to NM_003979.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13061794 G>T maps to NM_003979.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:90170922 C>A maps to NM_198281.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:90170922 C>A maps to NM_198281.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113659165 C>A maps to NM_017577.4 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113659165 C>A maps to NM_017577.4 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:50694567 C>A maps to NM_005311.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:50694567 C>A maps to NM_005311.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73316466 G>C maps to NM_002086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73316466 G>C maps to NM_002086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11778849 G>T maps to NM_014668.3 S1867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11778849 G>T maps to NM_014668.3 S1867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10136076 C>A maps to NM_198182.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10136076 C>A maps to NM_198182.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:102555523 C>A maps to NM_024915.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:102555523 C>A maps to NM_024915.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:158224719 G>T maps to NM_000826.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:158224719 G>T maps to NM_000826.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:158254054 C>A maps to NM_000826.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:158254054 C>A maps to NM_000826.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:120732720 G>T maps to NM_014619.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:120732720 G>T maps to NM_014619.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140052897 C>A maps to ENST00000371546 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140052897 C>A maps to ENST00000371546 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:9858736 C>A maps to NM_000833.3 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:9858736 C>A maps to NM_000833.3 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13717381 G>T maps to NM_000834.3 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13717381 G>T maps to NM_000834.3 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14018943 G>T maps to NM_000834.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14018943 G>T maps to NM_000834.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104433277 G>C maps to NM_133445.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104433277 G>C maps to NM_133445.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66909525 G>T maps to ENST00000359742 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66909525 G>T maps to ENST00000359742 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14564582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14564582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3021471 C>A maps to NM_182982.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3021471 C>A maps to NM_182982.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146719914 C>A maps to NM_000838.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146719914 C>A maps to NM_000838.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146755625 C>A maps to NM_000838.3 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146755625 C>A maps to NM_000838.3 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:7620494 G>T maps to NM_181874.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:7620494 G>T maps to NM_181874.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:7620935 C>G maps to NM_181874.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:7620935 C>G maps to NM_181874.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:42965067 G>T maps to NM_001080476.2 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:42965067 G>T maps to NM_001080476.2 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:130777972 C>A maps to NM_031415.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:130777972 C>A maps to NM_031415.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119720955 G>T maps to NM_002093.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119720955 G>T maps to NM_002093.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52697686 C>A maps to NM_153699.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52697686 C>A maps to NM_153699.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30464631 G>T maps to NM_002095.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30464631 G>T maps to NM_002095.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73961457 C>A maps to NM_016328.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73961457 C>A maps to NM_016328.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73961544 C>A maps to NM_016328.2 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73961544 C>A maps to NM_016328.2 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:74211800 G>T maps to NM_173537.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:74211800 G>T maps to NM_173537.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27552130 C>A maps to NM_001521.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27552130 C>A maps to NM_001521.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135554802 C>A maps to NM_012204.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135554802 C>A maps to NM_012204.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135562695 C>A maps to NM_012204.2 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135562695 C>A maps to NM_012204.2 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:1046795 C>A maps to NM_012341.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:1046795 C>A maps to NM_012341.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14772154 G>T maps to NM_004963.3 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14772154 G>T maps to NM_004963.3 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:44687990 G>T maps to NM_021927.2 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:44687990 G>T maps to NM_021927.2 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65426033 C>G maps to NM_000181.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65426033 C>G maps to NM_000181.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:73024208 G>T maps to NM_001080393.1 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:73024208 G>T maps to NM_001080393.1 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115340365 G>T maps to NM_004132.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115340365 G>T maps to NM_004132.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:105192039 C>A maps to NM_020771.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:105192039 C>A maps to NM_020771.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26426931 C>A maps to NM_000182.4 G407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26426931 C>A maps to NM_000182.4 G407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26426955 G>T maps to NM_000182.4 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26426955 G>T maps to NM_000182.4 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26427010 G>T maps to NM_000182.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26427010 G>T maps to NM_000182.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108954417 G>T maps to ENST00000351726 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108954417 G>T maps to ENST00000351726 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119923713 C>A maps to ENST00000361035 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119923713 C>A maps to ENST00000361035 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39881201 G>T maps to ENST00000310778 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39881201 G>T maps to ENST00000310778 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:122626660 G>T maps to NM_005328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:122626660 G>T maps to NM_005328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172844218 C>A maps to NM_003642.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172844218 C>A maps to NM_003642.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156464342 C>A maps to NM_001173393.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156464342 C>A maps to NM_001173393.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156469679 G>T maps to NM_001173393.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156469679 G>T maps to NM_001173393.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156479462 C>A maps to NM_001173393.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156479462 C>A maps to NM_001173393.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156479606 C>A maps to NM_001173393.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156479606 C>A maps to NM_001173393.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154247928 C>A maps to NM_006118.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154247928 C>A maps to NM_006118.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:114274491 C>A maps to ENST00000398283 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:114274491 C>A maps to ENST00000398283 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48191964 C>A maps to NM_015401.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48191964 C>A maps to NM_015401.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:18624985 C>A maps to NM_178425.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:18624985 C>A maps to NM_178425.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236760258 C>A maps to NM_018072.5 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236760258 C>A maps to NM_018072.5 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:794326 C>A maps to NM_017802.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:794326 C>A maps to NM_017802.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50118048 C>A maps to NM_182922.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50118048 C>A maps to NM_182922.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50128646 C>A maps to NM_182922.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50128646 C>A maps to NM_182922.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31778284 C>A maps to ENST00000389961 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31778284 C>A maps to ENST00000389961 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31855748 G>T maps to ENST00000389961 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31855748 G>T maps to ENST00000389961 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37287780 G>T maps to NM_019024.1 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37287780 G>T maps to NM_019024.1 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31637571 G>T maps to NM_015382.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31637571 G>T maps to NM_015382.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93221009 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93221009 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66704291 G>T maps to NM_033647.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66704291 G>T maps to NM_033647.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66717830 C>A maps to NM_033647.2 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66717830 C>A maps to NM_033647.2 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:65074658 C>A maps to NM_014877.3 S1846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:65074658 C>A maps to NM_014877.3 S1846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92848753 C>A maps to ENST00000453812 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92848753 C>A maps to ENST00000453812 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93844969 G>T maps to NM_001098672.1 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93844969 G>T maps to NM_001098672.1 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93845044 C>A maps to NM_001098672.1 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93845044 C>A maps to NM_001098672.1 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63904656 G>T maps to ENST00000261887 P4732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63904656 G>T maps to ENST00000261887 P4732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63928198 G>T maps to ENST00000261887 P4125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63928198 G>T maps to ENST00000261887 P4125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63978586 C>A maps to ENST00000261887 G2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63978586 C>A maps to ENST00000261887 G2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64048665 G>T maps to ENST00000261887 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64048665 G>T maps to ENST00000261887 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28386697 G>T maps to NM_004667.4 L3965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28386697 G>T maps to NM_004667.4 L3965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28443578 G>T maps to NM_004667.4 T2652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28443578 G>T maps to NM_004667.4 T2652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28443912 C>A maps to NM_004667.4 V2573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28443912 C>A maps to NM_004667.4 V2573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28446679 C>A maps to NM_004667.4 T2546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28446679 C>A maps to NM_004667.4 T2546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28478873 G>T maps to NM_004667.4 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28478873 G>T maps to NM_004667.4 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28499550 C>A maps to NM_004667.4 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28499550 C>A maps to NM_004667.4 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89571147 C>A maps to NM_014606.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89571147 C>A maps to NM_014606.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69692461 C>A maps to NM_022079.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69692461 C>A maps to NM_022079.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69716655 G>T maps to NM_022079.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69716655 G>T maps to NM_022079.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:80393626 G>T maps to NM_173620.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:80393626 G>T maps to NM_173620.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26091202 C>A maps to NM_000410.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26091202 C>A maps to NM_000410.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91728124 C>A maps to NM_001017975.3 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91728124 C>A maps to NM_001017975.3 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91843968 G>T maps to NM_001017975.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91843968 G>T maps to NM_001017975.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43033357 C>A maps to ENST00000458501 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43033357 C>A maps to ENST00000458501 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:145580845 C>A maps to NM_022475.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:145580845 C>A maps to NM_022475.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108076863 C>A maps to NM_007072.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108076863 C>A maps to NM_007072.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100525432 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100525432 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100525513 G>T maps to NM_033055.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100525513 G>T maps to NM_033055.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191125959 C>A maps to NM_014362.3 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191125959 C>A maps to NM_014362.3 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119003667 C>A maps to NM_198971.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119003667 C>A maps to NM_198971.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123332618 C>A maps to NM_003959.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123332618 C>A maps to NM_003959.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123335398 G>T maps to NM_003959.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123335398 G>T maps to NM_003959.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75177092 G>T maps to NM_005338.4 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75177092 G>T maps to NM_005338.4 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114483107 G>T maps to ENST00000426820 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114483107 G>T maps to ENST00000426820 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114506076 G>T maps to ENST00000426820 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114506076 G>T maps to ENST00000426820 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139281497 C>A maps to NM_022740.4 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139281497 C>A maps to NM_022740.4 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30004780 C>A maps to NM_003609.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30004780 C>A maps to NM_003609.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27834902 C>A maps to NM_005322.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27834902 C>A maps to NM_005322.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27835190 C>A maps to NM_005322.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27835190 C>A maps to NM_005322.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26033595 C>A maps to NM_003513.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26033595 C>A maps to NM_003513.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26043732 G>T maps to NM_021062.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26043732 G>T maps to NM_021062.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26123979 G>T maps to NM_003526.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26123979 G>T maps to NM_003526.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26184175 C>A maps to NM_003523.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26184175 C>A maps to NM_003523.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26199938 C>A maps to NM_003522.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26199938 C>A maps to NM_003522.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26216718 G>T maps to NM_003518.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26216718 G>T maps to NM_003518.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26273319 C>A maps to NM_003525.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26273319 C>A maps to NM_003525.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27775531 G>T maps to NM_003519.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27775531 G>T maps to NM_003519.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27775567 G>T maps to NM_003519.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27775567 G>T maps to NM_003519.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27806591 C>A maps to NM_003520.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27806591 C>A maps to NM_003520.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149858023 G>T maps to NM_003528.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149858023 G>T maps to NM_003528.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149783725 G>T maps to ENST00000427880 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149783725 G>T maps to ENST00000427880 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228645982 C>A maps to NM_175055.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228645982 C>A maps to NM_175055.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228646162 C>A maps to NM_175055.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228646162 C>A maps to NM_175055.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:12120300 G>T maps to NM_002114.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:12120300 G>T maps to NM_002114.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143093844 G>T maps to NM_006734.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143093844 G>T maps to NM_006734.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234749295 C>A maps to NM_018410.3 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234749295 C>A maps to NM_018410.3 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234750282 G>T maps to NM_018410.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234750282 G>T maps to NM_018410.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71144625 G>T maps to ENST00000439900 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71144625 G>T maps to ENST00000439900 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71007160 G>T maps to NM_025130.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71007160 G>T maps to NM_025130.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71018665 C>A maps to NM_025130.3 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71018665 C>A maps to NM_025130.3 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32918419 G>T maps to NM_006120.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32918419 G>T maps to NM_006120.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30136874 G>T maps to NM_178581.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30136874 G>T maps to NM_178581.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118959361 G>T maps to NM_000190.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118959361 G>T maps to NM_000190.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185932947 C>A maps to NM_031935.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185932947 C>A maps to NM_031935.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185959423 G>T maps to NM_031935.2 G1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185959423 G>T maps to NM_031935.2 G1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185959467 C>A maps to NM_031935.2 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185959467 C>A maps to NM_031935.2 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186024577 C>A maps to NM_031935.2 R2306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186024577 C>A maps to NM_031935.2 R2306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186106020 C>A maps to NM_031935.2 R4512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186106020 C>A maps to NM_031935.2 R4512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186120774 C>A maps to NM_031935.2 P4932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186120774 C>A maps to NM_031935.2 P4932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186158994 C>A maps to NM_031935.2 S5631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186158994 C>A maps to NM_031935.2 S5631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34208667 C>A maps to NM_145899.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34208667 C>A maps to NM_145899.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:34329999 C>A maps to NM_145205.4 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:34329999 C>A maps to NM_145205.4 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43882348 C>A maps to NM_001098204.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43882348 C>A maps to NM_001098204.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179046349 C>A maps to NM_005520.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179046349 C>A maps to NM_005520.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:23640159 C>A maps to ENST00000414299 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:23640159 C>A maps to ENST00000414299 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62488795 G>T maps to NM_001079559.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62488795 G>T maps to NM_001079559.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83544129 C>T maps to NM_199330.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83544129 C>T maps to NM_199330.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60299129 C>A maps to NM_015888.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60299129 C>A maps to NM_015888.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27140422 G>T maps to NM_006735.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27140422 G>T maps to NM_006735.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27196116 C>A maps to NM_006896.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27196116 C>A maps to NM_006896.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27203328 C>A maps to NM_152739.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27203328 C>A maps to NM_152739.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:46673804 G>T maps to NM_018952.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:46673804 G>T maps to NM_018952.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54367426 C>A maps to NM_014212.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54367426 C>A maps to NM_014212.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54428081 C>A maps to NM_018953.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54428081 C>A maps to NM_018953.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:177034270 C>A maps to NM_006898.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:177034270 C>A maps to NM_006898.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:176996252 C>A maps to NM_019558.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:176996252 C>A maps to NM_019558.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122285059 C>A maps to NM_002150.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122285059 C>A maps to NM_002150.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:100904022 G>T maps to NM_021828.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:100904022 G>T maps to NM_021828.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84231891 C>A maps to NM_006665.5 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84231891 C>A maps to NM_006665.5 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63257749 C>A maps to NM_054108.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63257749 C>A maps to NM_054108.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:192988447 C>A maps to NM_020386.3 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:192988447 C>A maps to NM_020386.3 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186387732 G>T maps to NM_000412.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186387732 G>T maps to NM_000412.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22048810 G>T maps to NM_021624.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22048810 G>T maps to NM_021624.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152187656 C>A maps to NM_001009931.1 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152187656 C>A maps to NM_001009931.1 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188023 C>A maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188023 C>A maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188152 G>T maps to NM_001009931.1 S1984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188152 G>T maps to NM_001009931.1 S1984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188419 G>T maps to NM_001009931.1 S1895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188419 G>T maps to NM_001009931.1 S1895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20845120 G>T maps to NM_022460.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20845120 G>T maps to NM_022460.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120054210 G>T maps to ENST00000235547 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120054210 G>T maps to ENST00000235547 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102550183 C>A maps to NM_001017963.2 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102550183 C>A maps to NM_001017963.2 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44216431 C>A maps to NM_007355.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44216431 C>A maps to NM_007355.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104336949 C>A maps to NM_003299.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104336949 C>A maps to NM_003299.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128715247 G>T maps to ENST00000438626 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128715247 G>T maps to ENST00000438626 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:132424229 C>A maps to NM_002154.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:132424229 C>A maps to NM_002154.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:137895663 C>A maps to NM_004134.6 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:137895663 C>A maps to NM_004134.6 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64682527 G>T maps to NM_014181.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64682527 G>T maps to NM_014181.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31722575 G>T maps to NM_006644.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31722575 G>T maps to NM_006644.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:88040052 C>A maps to NM_000866.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:88040052 C>A maps to NM_000866.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183823110 C>A maps to NM_182589.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183823110 C>A maps to NM_182589.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124273754 C>A maps to NM_002775.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124273754 C>A maps to NM_002775.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124273763 C>A maps to NM_002775.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124273763 C>A maps to NM_002775.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3109062 C>A maps to NM_002111.6 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3109062 C>A maps to NM_002111.6 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70841817 C>A maps to NM_032821.2 G5010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70841817 C>A maps to NM_032821.2 G5010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71127814 G>T maps to NM_032821.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71127814 G>T maps to NM_032821.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:82937016 C>A maps to NM_015525.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:82937016 C>A maps to NM_015525.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94267920 G>T maps to NM_004969.3 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94267920 G>T maps to NM_004969.3 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90631629 G>T maps to NM_002168.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90631629 G>T maps to NM_002168.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78458638 G>T maps to NM_005530.2 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78458638 G>T maps to NM_005530.2 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:1068644 C>A maps to NM_033261.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:1068644 C>A maps to NM_033261.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6650691 G>C maps to NM_001193457.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6650691 G>C maps to NM_001193457.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6657245 G>T maps to NM_001193457.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6657245 G>T maps to NM_001193457.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41165099 C>A maps to NM_005533.4 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41165099 C>A maps to NM_005533.4 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163174366 G>T maps to NM_022168.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163174366 G>T maps to NM_022168.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:21202031 C>A maps to NM_021057.2 G45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:21202031 C>A maps to NM_021057.2 G45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137524779 C>A maps to NM_000416.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137524779 C>A maps to NM_000416.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129211007 C>A maps to NM_052985.2 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129211007 C>A maps to NM_052985.2 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27682694 C>A maps to NM_015662.1 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27682694 C>A maps to NM_015662.1 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99459226 G>T maps to NM_000875.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99459226 G>T maps to NM_000875.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99467840 C>A maps to NM_000875.3 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99467840 C>A maps to NM_000875.3 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151155402 G>T maps to NM_178822.4 R2316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151155402 G>T maps to NM_178822.4 R2316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151163418 G>T maps to NM_178822.4 T1450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151163418 G>T maps to NM_178822.4 T1450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18736084 C>A maps to NM_173588.3 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18736084 C>A maps to NM_173588.3 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18738386 G>T maps to NM_173588.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18738386 G>T maps to NM_173588.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18741361 G>T maps to NM_173588.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18741361 G>T maps to NM_173588.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117146465 G>T maps to NM_001542.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117146465 G>T maps to NM_001542.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117156620 G>T maps to NM_001542.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117156620 G>T maps to NM_001542.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:159901275 G>T maps to NM_001135050.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:159901275 G>T maps to NM_001135050.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206649578 G>T maps to NM_014002.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206649578 G>T maps to NM_014002.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37988354 G>T maps to NM_012481.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37988354 G>T maps to NM_012481.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117870292 G>T maps to NM_001558.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117870292 G>T maps to NM_001558.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:18179253 G>T maps to NM_005535.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:18179253 G>T maps to NM_005535.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:18180463 G>T maps to NM_005535.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:18180463 G>T maps to NM_005535.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117875055 C>A maps to NM_001560.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:117875055 C>A maps to NM_001560.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81593774 C>A maps to NM_172217.3 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81593774 C>A maps to NM_172217.3 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52052499 C>A maps to NM_002190.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52052499 C>A maps to NM_002190.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9969872 C>A maps to NM_153461.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9969872 C>A maps to NM_153461.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57143567 G>T maps to NM_017563.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57143567 G>T maps to NM_017563.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113535635 G>T maps to NM_000575.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113535635 G>T maps to NM_000575.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113588883 G>T maps to NM_000576.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113588883 G>T maps to NM_000576.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113820136 G>T maps to NM_173170.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113820136 G>T maps to NM_173170.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113742448 C>A maps to NM_019618.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113742448 C>A maps to NM_019618.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102851420 C>A maps to NM_003854.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102851420 C>A maps to NM_003854.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113890378 C>A maps to NM_173841.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113890378 C>A maps to NM_173841.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137325835 G>T maps to NM_014432.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137325835 G>T maps to NM_014432.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1464287 C>A maps to NM_002183.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1464287 C>A maps to NM_002183.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1467350 G>T maps to NM_002183.2 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1467350 G>T maps to NM_002183.2 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1484093 C>A maps to NM_002183.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1484093 C>A maps to NM_002183.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27357824 C>A maps to NM_000418.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27357824 C>A maps to NM_000418.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3111974 C>A maps to NM_000564.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3111974 C>A maps to NM_000564.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86400875 C>A maps to NM_006839.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86400875 C>A maps to NM_006839.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:43924074 C>A maps to NM_175882.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:43924074 C>A maps to NM_175882.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100949925 G>T maps to NM_016247.2 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100949925 G>T maps to NM_016247.2 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62545165 C>A maps to NM_176877.2 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62545165 C>A maps to NM_176877.2 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62550217 C>A maps to NM_176877.2 P1425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62550217 C>A maps to NM_176877.2 P1425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62550316 C>A maps to NM_176877.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62550316 C>A maps to NM_176877.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62586851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62586851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62593708 C>A maps to NM_176877.2 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62593708 C>A maps to NM_176877.2 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62614032 C>A maps to NM_176877.2 P1783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62614032 C>A maps to NM_176877.2 P1783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57850381 C>A maps to NM_031479.3 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57850381 C>A maps to NM_031479.3 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33060527 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33060527 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41371978 C>A maps to NM_017553.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41371978 C>A maps to NM_017553.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191233956 G>T maps to NM_002194.3 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191233956 G>T maps to NM_002194.3 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191235677 C>A maps to NM_002194.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191235677 C>A maps to NM_002194.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99182489 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99182489 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99204040 C>A maps to NM_001134224.1 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99204040 C>A maps to NM_001134224.1 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:143226657 C>A maps to NM_003866.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:143226657 C>A maps to NM_003866.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:143324090 G>T maps to NM_003866.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:143324090 G>T maps to NM_003866.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234104057 G>T maps to ENST00000359570 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234104057 G>T maps to ENST00000359570 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:155093297 C>A maps to ENST00000344756 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:155093297 C>A maps to ENST00000344756 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156811571 G>T maps to NM_014215.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156811571 G>T maps to NM_014215.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62415085 G>T maps to NM_030628.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62415085 G>T maps to NM_030628.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95853775 C>A maps to NM_017864.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95853775 C>A maps to NM_017864.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28717004 C>A maps to NM_018250.3 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28717004 C>A maps to NM_018250.3 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128564855 C>A maps to NM_015693.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128564855 C>A maps to NM_015693.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128626744 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128626744 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:103014601 C>A maps to NM_014425.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:103014601 C>A maps to NM_014425.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:154489077 G>T maps to NM_001130700.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:154489077 G>T maps to NM_001130700.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9459747 G>T maps to NM_006391.2 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9459747 G>T maps to NM_006391.2 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201845112 C>A maps to NM_018085.4 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201845112 C>A maps to NM_018085.4 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121508958 G>T maps to NM_001023570.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121508958 G>T maps to NM_001023570.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197670837 G>T maps to NM_001134435.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197670837 G>T maps to NM_001134435.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197670867 C>A maps to NM_001134435.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197670867 C>A maps to NM_001134435.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:75886290 C>A maps to NM_006633.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:75886290 C>A maps to NM_006633.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10280467 C>A maps to NM_001570.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10280467 C>A maps to NM_001570.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66641827 C>A maps to NM_007199.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66641827 C>A maps to NM_007199.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209964095 G>T maps to NM_006147.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209964095 G>T maps to NM_006147.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227663189 G>T maps to NM_005544.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227663189 G>T maps to NM_005544.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107977986 G>T maps to NM_003604.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107977986 G>T maps to NM_003604.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1880921 C>A maps to NM_016358.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1880921 C>A maps to NM_016358.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156696822 C>A maps to NM_030980.1 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156696822 C>A maps to NM_030980.1 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33033181 C>A maps to ENST00000262650 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33033181 C>A maps to ENST00000262650 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33057859 G>T maps to ENST00000262650 G519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33057859 G>T maps to ENST00000262650 G519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145532150 C>A maps to NM_003637.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145532150 C>A maps to NM_003637.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182347320 C>G maps to NM_000885.4 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182347320 C>G maps to NM_000885.4 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182387034 C>A maps to NM_000885.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182387034 C>A maps to NM_000885.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54798233 C>A maps to NM_002205.2 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54798233 C>A maps to NM_002205.2 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173344372 C>A maps to ENST00000264106 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173344372 C>A maps to ENST00000264106 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15561329 C>A maps to NM_003638.1 G1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15561329 C>A maps to NM_003638.1 G1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37523051 C>A maps to NM_002207.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37523051 C>A maps to NM_002207.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37818884 G>T maps to NM_002207.2 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37818884 G>T maps to NM_002207.2 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31427904 G>T maps to ENST00000444228 G829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31427904 G>T maps to ENST00000444228 G829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30495498 G>T maps to NM_002209.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30495498 G>T maps to NM_002209.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30495502 G>T maps to NM_002209.2 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30495502 G>T maps to NM_002209.2 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30521770 C>A maps to NM_002209.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30521770 C>A maps to NM_002209.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30528331 C>A maps to NM_002209.2 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30528331 C>A maps to NM_002209.2 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:187455127 G>T maps to NM_002210.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:187455127 G>T maps to NM_002210.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:187500857 C>A maps to NM_002210.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:187500857 C>A maps to NM_002210.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31393206 C>A maps to NM_000887.3 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31393206 C>A maps to NM_000887.3 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33200557 G>T maps to ENST00000374956 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33200557 G>T maps to ENST00000374956 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160994584 C>A maps to NM_000888.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160994584 C>A maps to NM_000888.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20421417 C>A maps to NM_002214.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20421417 C>A maps to NM_002214.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7762868 C>A maps to NM_002216.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7762868 C>A maps to NM_002216.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52848354 C>A maps to ENST00000485816 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52848354 C>A maps to ENST00000485816 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52850901 G>T maps to ENST00000485816 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52850901 G>T maps to ENST00000485816 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156665171 C>A maps to NM_005546.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156665171 C>A maps to NM_005546.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226829738 G>T maps to NM_002221.3 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226829738 G>T maps to NM_002221.3 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:26639108 G>T maps to NM_002223.2 P1913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:26639108 G>T maps to NM_002223.2 P1913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:26810647 G>T maps to NM_002223.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:26810647 G>T maps to NM_002223.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35183304 C>A maps to NM_003024.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35183304 C>A maps to NM_003024.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35190569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35190569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35201955 C>A maps to NM_003024.2 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35201955 C>A maps to NM_003024.2 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24431136 G>T maps to NM_006277.2 T1549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24431136 G>T maps to NM_006277.2 T1549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185269591 G>T maps to NM_006469.4 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185269591 G>T maps to NM_006469.4 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:10620165 G>T maps to NM_000214.2 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:10620165 G>T maps to NM_000214.2 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:10625624 G>T maps to NM_000214.2 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:10625624 G>T maps to NM_000214.2 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:10627605 C>A maps to NM_000214.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:10627605 C>A maps to NM_000214.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:15512521 G>T maps to NM_004973.2 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:15512521 G>T maps to NM_004973.2 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139791670 C>A maps to NM_030647.1 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139791670 C>A maps to NM_030647.1 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139797359 G>T maps to NM_030647.1 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139797359 G>T maps to NM_030647.1 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64973852 G>T maps to NM_032776.1 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64973852 G>T maps to NM_032776.1 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:78610360 C>A maps to NM_152405.4 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:78610360 C>A maps to NM_152405.4 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153949719 C>A maps to NM_006694.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153949719 C>A maps to NM_006694.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124174061 C>A maps to NM_001024660.3 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124174061 C>A maps to NM_001024660.3 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124379768 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124379768 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124413200 C>A maps to NM_001024660.3 P2476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124413200 C>A maps to NM_001024660.3 P2476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62718837 G>T maps to NM_181712.4 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62718837 G>T maps to NM_181712.4 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62734157 C>A maps to NM_181712.4 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62734157 C>A maps to NM_181712.4 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62739326 G>T maps to NM_181712.4 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62739326 G>T maps to NM_181712.4 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62739545 C>A maps to NM_181712.4 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62739545 C>A maps to NM_181712.4 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62740564 G>T maps to NM_181712.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62740564 G>T maps to NM_181712.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62747252 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62747252 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40269067 C>A maps to NM_021078.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40269067 C>A maps to NM_021078.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65484373 G>T maps to NM_182710.1 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65484373 G>T maps to NM_182710.1 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44584674 G>T maps to ENST00000356157 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44584674 G>T maps to ENST00000356157 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57778385 G>T maps to NM_005886.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57778385 G>T maps to NM_005886.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57785629 C>A maps to NM_005886.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57785629 C>A maps to NM_005886.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170367247 G>T maps to NM_006063.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170367247 G>T maps to NM_006063.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41766649 G>T maps to NM_032138.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41766649 G>T maps to NM_032138.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:67049523 G>T maps to NM_032505.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:67049523 G>T maps to NM_032505.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5021284 G>T maps to NM_000217.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5021284 G>T maps to NM_000217.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5021707 G>T maps to NM_000217.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5021707 G>T maps to NM_000217.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5022022 C>A maps to NM_000217.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5022022 C>A maps to NM_000217.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:30033265 G>T maps to NM_002233.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:30033265 G>T maps to NM_002233.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155838412 C>A maps to NM_172160.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155838412 C>A maps to NM_172160.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47989732 C>A maps to NM_004975.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47989732 C>A maps to NM_004975.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47990467 G>T maps to NM_004975.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47990467 G>T maps to NM_004975.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:119914694 G>T maps to NM_012281.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:119914694 G>T maps to NM_012281.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42671625 G>T maps to NM_133329.5 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42671625 G>T maps to NM_133329.5 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210857003 G>T maps to NM_172362.2 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210857003 G>T maps to NM_172362.2 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163279986 C>A maps to NM_033272.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163279986 C>A maps to NM_033272.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:19295237 C>A maps to NM_144633.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:19295237 C>A maps to NM_144633.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233633070 G>T maps to NM_002242.4 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233633070 G>T maps to NM_002242.4 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118969092 C>A maps to NM_181840.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118969092 C>A maps to NM_181840.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:215368405 C>A maps to NM_001017425.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:215368405 C>A maps to NM_001017425.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:215408220 C>A maps to NM_001017425.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:215408220 C>A maps to NM_001017425.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:78870023 G>T maps to NM_001161352.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:78870023 G>T maps to NM_001161352.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:78870098 C>A maps to NM_001161352.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:78870098 C>A maps to NM_001161352.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73751714 G>T maps to NM_001160133.1 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73751714 G>T maps to NM_001160133.1 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73815017 C>A maps to NM_001160133.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73815017 C>A maps to NM_001160133.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73815029 G>T maps to NM_001160133.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73815029 G>T maps to NM_001160133.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:143586847 C>A maps to NM_020768.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:143586847 C>A maps to NM_020768.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36438023 C>A maps to NM_173562.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36438023 C>A maps to NM_173562.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25293809 G>T maps to NM_017634.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25293809 G>T maps to NM_017634.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108345649 G>T maps to NM_153705.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108345649 G>T maps to NM_153705.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:23409763 G>T maps to NM_001009999.2 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:23409763 G>T maps to NM_001009999.2 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86678284 G>T maps to NM_001146688.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86678284 G>T maps to NM_001146688.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86709167 C>A maps to NM_001146688.1 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86709167 C>A maps to NM_001146688.1 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44156682 C>A maps to NM_014663.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44156682 C>A maps to NM_014663.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:53227963 C>A maps to NM_004187.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:53227963 C>A maps to NM_004187.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55972047 C>A maps to NM_002253.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55972047 C>A maps to NM_002253.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55976687 C>A maps to NM_002253.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55976687 C>A maps to NM_002253.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142641426 G>T maps to NM_000420.2 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142641426 G>T maps to NM_000420.2 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142658032 G>T maps to NM_000420.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142658032 G>T maps to NM_000420.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:136561008 A>C maps to NM_006558.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:136561008 A>C maps to NM_006558.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26942152 G>T maps to NM_014680.2 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26942152 G>T maps to NM_014680.2 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:48586374 G>T maps to NM_001080394.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:48586374 G>T maps to NM_001080394.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:48612970 G>T maps to NM_001080394.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:48612970 G>T maps to NM_001080394.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71961683 C>A maps to NM_014761.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71961683 C>A maps to NM_014761.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126044540 C>A maps to ENST00000377985 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126044540 C>A maps to ENST00000377985 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42797388 G>T maps to NM_015349.1 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42797388 G>T maps to NM_015349.1 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42823607 G>T maps to NM_015349.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42823607 G>T maps to NM_015349.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42830319 C>A maps to NM_015349.1 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42830319 C>A maps to NM_015349.1 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35906653 G>T maps to NM_024874.4 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35906653 G>T maps to NM_024874.4 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24576805 C>A maps to NM_014809.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24576805 C>A maps to NM_014809.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114133956 C>A maps to NM_001080398.1 G1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114133956 C>A maps to NM_001080398.1 G1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114173377 C>A maps to NM_001080398.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114173377 C>A maps to NM_001080398.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36624802 G>T maps to NM_014657.1 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36624802 G>T maps to NM_014657.1 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36631152 C>A maps to NM_014657.1 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36631152 C>A maps to NM_014657.1 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36641612 C>A maps to NM_014657.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36641612 C>A maps to NM_014657.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4820841 C>A maps to ENST00000450194 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4820841 C>A maps to ENST00000450194 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:46284697 C>A maps to NM_001142397.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:46284697 C>A maps to NM_001142397.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:46343716 C>A maps to NM_001142397.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:46343716 C>A maps to NM_001142397.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15729973 C>A maps to NM_014647.3 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15729973 C>A maps to NM_014647.3 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43893036 C>A maps to NM_015284.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43893036 C>A maps to NM_015284.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43895382 C>A maps to NM_015284.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43895382 C>A maps to NM_015284.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43914302 G>T maps to NM_015284.2 T2431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43914302 G>T maps to NM_015284.2 T2431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85106541 C>A maps to NM_014732.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85106541 C>A maps to NM_014732.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:22666313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:22666313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:22670926 G>T maps to ENST00000446597 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:22670926 G>T maps to ENST00000446597 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27751861 C>G maps to NM_015202.2 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27751861 C>G maps to NM_015202.2 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42439949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42439949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46686436 G>C maps to NM_001142673.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46686436 G>C maps to NM_001142673.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:96976506 C>A maps to NM_015323.4 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:96976506 C>A maps to NM_015323.4 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:96984145 G>T maps to NM_015323.4 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:96984145 G>T maps to NM_015323.4 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8818981 C>A maps to ENST00000456698 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8818981 C>A maps to ENST00000456698 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:55848787 C>A maps to NM_014924.3 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:55848787 C>A maps to NM_014924.3 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155885720 C>A maps to NM_014949.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155885720 C>A maps to NM_014949.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155891405 G>T maps to NM_014949.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155891405 G>T maps to NM_014949.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154502015 G>T maps to NM_001131007.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154502015 G>T maps to NM_001131007.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154544185 C>A maps to NM_001131007.1 S1332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154544185 C>A maps to NM_001131007.1 S1332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154557592 G>T maps to NM_001131007.1 A1566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154557592 G>T maps to NM_001131007.1 A1566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5460962 C>A maps to NM_015325.1 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5460962 C>A maps to NM_015325.1 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5461096 C>A maps to NM_015325.1 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5461096 C>A maps to NM_015325.1 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5464411 G>T maps to NM_015325.1 S1655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5464411 G>T maps to NM_015325.1 S1655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5464766 C>T maps to NM_015325.1 Q1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5464766 C>T maps to NM_015325.1 Q1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79748656 C>A maps to NM_015206.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79748656 C>A maps to NM_015206.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123150352 C>A maps to NM_015312.3 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123150352 C>A maps to NM_015312.3 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123188003 C>A maps to NM_015312.3 R2462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123188003 C>A maps to NM_015312.3 R2462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123264571 G>T maps to NM_015312.3 S4120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123264571 G>T maps to NM_015312.3 S4120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34372821 G>T maps to NM_020702.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34372821 G>T maps to NM_020702.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81176578 C>A maps to NM_018689.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81176578 C>A maps to NM_018689.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118220869 G>T maps to NM_020721.1 S1441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118220869 G>T maps to NM_020721.1 S1441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24508700 C>A maps to NM_019590.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24508700 C>A maps to NM_019590.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:138584485 G>T maps to NM_020340.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:138584485 G>T maps to NM_020340.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:138640891 C>A maps to NM_020340.4 S1509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:138640891 C>A maps to NM_020340.4 S1509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44248240 G>T maps to NM_015443.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44248240 G>T maps to NM_015443.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44249148 G>T maps to NM_015443.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44249148 G>T maps to NM_015443.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86522332 C>A maps to NM_001142749.2 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86522332 C>A maps to NM_001142749.2 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86522341 G>T maps to NM_001142749.2 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86522341 G>T maps to NM_001142749.2 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86541450 G>T maps to NM_001142749.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86541450 G>T maps to NM_001142749.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109714583 C>A maps to NM_020775.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109714583 C>A maps to NM_020775.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52901597 G>T maps to NM_019600.2 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52901597 G>T maps to NM_019600.2 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:101828967 C>A maps to NM_020802.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:101828967 C>A maps to NM_020802.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113729824 G>T maps to NM_020817.1 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113729824 G>T maps to NM_020817.1 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94044189 G>T maps to ENST00000393153 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94044189 G>T maps to ENST00000393153 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94120099 C>A maps to ENST00000393153 P2093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94120099 C>A maps to ENST00000393153 P2093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95503983 C>A maps to NM_015496.3 V1654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95503983 C>A maps to NM_015496.3 V1654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:226446819 C>A maps to NM_020864.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:226446819 C>A maps to NM_020864.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:226446837 G>T maps to NM_020864.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:226446837 G>T maps to NM_020864.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1360196 C>A maps to NM_020894.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1360196 C>A maps to NM_020894.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138556054 C>A maps to NM_001164665.1 E1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138556054 C>A maps to NM_001164665.1 E1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138603741 C>A maps to NM_001164665.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138603741 C>A maps to NM_001164665.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118646022 G>T maps to NM_001127211.1 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118646022 G>T maps to NM_001127211.1 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118674915 G>T maps to NM_001127211.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118674915 G>T maps to NM_001127211.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43505802 C>A maps to NM_020964.2 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43505802 C>A maps to NM_020964.2 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36851965 T>A maps to NM_001029864.1 K748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36851965 T>A maps to NM_001029864.1 K748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30652688 G>T maps to NM_133471.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30652688 G>T maps to NM_133471.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30652977 G>T maps to NM_133471.3 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30652977 G>T maps to NM_133471.3 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30653242 G>T maps to NM_133471.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30653242 G>T maps to NM_133471.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:5921330 C>A maps to NM_001017969.2 V1555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:5921330 C>A maps to NM_001017969.2 V1555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94410162 G>T maps to NM_004523.3 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94410162 G>T maps to NM_004523.3 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:17800205 G>T maps to NM_022113.4 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:17800205 G>T maps to NM_022113.4 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28984775 G>T maps to NM_015254.3 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28984775 G>T maps to NM_015254.3 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28989888 G>T maps to NM_015254.3 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28989888 G>T maps to NM_015254.3 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200534576 A>G maps to NM_014875.2 D1294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200534576 A>G maps to NM_014875.2 D1294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:16492084 G>T maps to NM_024704.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:16492084 G>T maps to NM_024704.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:28080557 G>T maps to NM_031217.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:28080557 G>T maps to NM_031217.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:10394610 C>A maps to ENST00000377086 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:10394610 C>A maps to ENST00000377086 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:39695355 C>A maps to ENST00000395670 V1620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:39695355 C>A maps to ENST00000395670 V1620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200943957 C>A maps to NM_017596.2 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200943957 C>A maps to NM_017596.2 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200948811 C>A maps to NM_017596.2 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200948811 C>A maps to NM_017596.2 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29808316 G>T maps to NM_007317.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29808316 G>T maps to NM_007317.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69738346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69738346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:245849587 C>A maps to NM_018012.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:245849587 C>A maps to NM_018012.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86518670 C>A maps to NM_017576.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86518670 C>A maps to NM_017576.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205617 C>A maps to NM_006845.3 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205617 C>A maps to NM_006845.3 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205642 C>A maps to NM_006845.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205642 C>A maps to NM_006845.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45220457 C>A maps to NM_006845.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45220457 C>A maps to NM_006845.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:69625731 C>A maps to NM_012310.4 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:69625731 C>A maps to NM_012310.4 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32327107 G>T maps to NM_004521.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32327107 G>T maps to NM_004521.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:149799275 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:149799275 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33366081 G>T maps to NM_002263.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33366081 G>T maps to NM_002263.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126318967 G>T maps to NM_032531.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126318967 G>T maps to NM_032531.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:88926232 G>T maps to NM_000899.4 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:88926232 G>T maps to NM_000899.4 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103662530 C>A maps to NM_005655.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103662530 C>A maps to NM_005655.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:74420057 C>A maps to NM_007249.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:74420057 C>A maps to NM_007249.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129756484 C>A maps to NM_014997.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129756484 C>A maps to NM_014997.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129767257 C>A maps to NM_014997.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129767257 C>A maps to NM_014997.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42985613 C>A maps to NM_057161.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42985613 C>A maps to NM_057161.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42985884 G>T maps to NM_057161.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42985884 G>T maps to NM_057161.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87743093 C>A maps to NM_017566.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87743093 C>A maps to NM_017566.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87764231 C>A maps to NM_017566.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87764231 C>A maps to NM_017566.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87782348 C>A maps to NM_017566.3 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87782348 C>A maps to NM_017566.3 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27933610 C>T maps to NM_020782.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27933610 C>T maps to NM_020782.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27944724 C>A maps to NM_020782.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27944724 C>A maps to NM_020782.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39114810 C>A maps to NM_015990.4 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39114810 C>A maps to NM_015990.4 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183211937 C>A maps to NM_130446.2 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183211937 C>A maps to NM_130446.2 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187172711 G>T maps to ENST00000511608 G361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187172711 G>T maps to ENST00000511608 G361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48687003 C>A maps to NM_001135629.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48687003 C>A maps to NM_001135629.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117050810 G>T maps to NM_002269.2 G447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117050810 G>T maps to NM_002269.2 G447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32628011 G>T maps to NM_012316.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32628011 G>T maps to NM_012316.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47984057 G>T maps to NM_007059.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47984057 G>T maps to NM_007059.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47986419 C>A maps to NM_007059.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47986419 C>A maps to NM_007059.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88327464 G>T maps to NM_016618.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88327464 G>T maps to NM_016618.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39081633 G>T maps to NM_015515.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39081633 G>T maps to NM_015515.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53039158 C>A maps to NM_000423.2 G522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53039158 C>A maps to NM_000423.2 G522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39118443 C>A maps to NM_213656.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39118443 C>A maps to NM_213656.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52884508 G>T maps to NM_005554.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52884508 G>T maps to NM_005554.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52943931 G>T maps to NM_033448.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52943931 G>T maps to NM_033448.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52979801 C>A maps to NM_080747.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52979801 C>A maps to NM_080747.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52711713 C>A maps to NM_002282.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52711713 C>A maps to NM_002282.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52757155 C>A maps to NM_002283.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52757155 C>A maps to NM_002283.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:31852476 C>A maps to NM_181607.1 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:31852476 C>A maps to NM_181607.1 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1605666 G>T maps to NM_001005922.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1605666 G>T maps to NM_001005922.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1606344 G>T maps to NM_001005922.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1606344 G>T maps to NM_001005922.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1651759 C>A maps to NM_001001480.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1651759 C>A maps to NM_001001480.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1718567 C>A maps to NM_001012416.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1718567 C>A maps to NM_001012416.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71238366 C>A maps to ENST00000422553 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71238366 C>A maps to ENST00000422553 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71238459 C>A maps to NM_001012503.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71238459 C>A maps to NM_001012503.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71238477 C>A maps to NM_001012503.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71238477 C>A maps to NM_001012503.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71259816 C>A maps to NM_005553.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71259816 C>A maps to NM_005553.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71260059 G>T maps to NM_005553.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71260059 G>T maps to NM_005553.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118198915 G>T maps to ENST00000339824 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118198915 G>T maps to ENST00000339824 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118198979 C>A maps to ENST00000339824 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118198979 C>A maps to ENST00000339824 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62675591 C>A maps to NM_019079.4 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62675591 C>A maps to NM_019079.4 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62676068 C>A maps to NM_019079.4 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62676068 C>A maps to NM_019079.4 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108843568 C>A maps to NM_145315.3 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108843568 C>A maps to NM_145315.3 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6964737 C>A maps to NM_005559.2 P2420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6964737 C>A maps to NM_005559.2 P2420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129475821 C>A maps to NM_000426.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129475821 C>A maps to NM_000426.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129637233 C>A maps to NM_000426.3 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129637233 C>A maps to NM_000426.3 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129799921 C>A maps to NM_000426.3 P2512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129799921 C>A maps to NM_000426.3 P2512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129837375 C>A maps to NM_000426.3 R3085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:129837375 C>A maps to NM_000426.3 R3085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21413848 G>T maps to ENST00000416669 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21413848 G>T maps to ENST00000416669 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21422393 G>T maps to ENST00000416669 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21422393 G>T maps to ENST00000416669 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21496553 G>T maps to ENST00000416669 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21496553 G>T maps to ENST00000416669 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107569508 C>A maps to NM_002291.2 S1629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107569508 C>A maps to NM_002291.2 S1629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107580480 G>T maps to NM_002291.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107580480 G>T maps to NM_002291.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107580684 C>A maps to NM_002291.2 S1170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107580684 C>A maps to NM_002291.2 S1170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107605017 C>A maps to NM_002291.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107605017 C>A maps to NM_002291.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49168415 G>C maps to NM_002292.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49168415 G>C maps to NM_002292.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107688549 C>A maps to NM_007356.2 G1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107688549 C>A maps to NM_007356.2 G1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183094583 C>A maps to NM_002293.3 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183094583 C>A maps to NM_002293.3 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183102539 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183102539 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183177131 G>T maps to NM_005562.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183177131 G>T maps to NM_005562.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183177199 C>A maps to NM_005562.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183177199 C>A maps to NM_005562.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183194833 C>A maps to NM_005562.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183194833 C>A maps to NM_005562.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182870221 G>T maps to NM_014398.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182870221 G>T maps to NM_014398.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:17585106 G>T maps to NM_015907.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:17585106 G>T maps to NM_015907.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:33673114 C>A maps to NM_133642.3 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:33673114 C>A maps to NM_133642.3 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:129012229 C>A maps to NM_018078.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:129012229 C>A maps to NM_018078.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150939314 C>A maps to NM_181746.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150939314 C>A maps to NM_181746.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50532378 G>T maps to NM_147190.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50532378 G>T maps to NM_147190.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169487531 G>T maps to ENST00000392687 G149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169487531 G>T maps to ENST00000392687 G149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169571585 C>A maps to ENST00000392687 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:169571585 C>A maps to ENST00000392687 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150004504 C>A maps to NM_004690.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150004504 C>A maps to NM_004690.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21562181 G>T maps to NM_014572.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21562181 G>T maps to NM_014572.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21562187 G>T maps to NM_014572.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21562187 G>T maps to NM_014572.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21620051 G>T maps to NM_014572.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21620051 G>T maps to NM_014572.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203740528 C>A maps to NM_017773.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203740528 C>A maps to NM_017773.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139650992 C>A maps to ENST00000371689 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139650992 C>A maps to ENST00000371689 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46701838 G>T maps to NM_002298.4 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46701838 G>T maps to NM_002298.4 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66845510 G>T maps to NM_207338.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66845510 G>T maps to NM_207338.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103869249 G>T maps to NM_001113407.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103869249 G>T maps to NM_001113407.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16504355 G>T maps to NM_001290.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16504355 G>T maps to NM_001290.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21790022 G>T maps to NM_002300.6 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21790022 G>T maps to NM_002300.6 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226127290 G>T maps to NM_003240.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226127290 G>T maps to NM_003240.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:65639639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:65639639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40197970 C>A maps to NM_203471.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40197970 C>A maps to NM_203471.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:25969280 C>A maps to NM_009587.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:25969280 C>A maps to NM_009587.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:93171048 C>A maps to NM_005606.6 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:93171048 C>A maps to NM_005606.6 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206769144 G>T maps to NM_006893.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206769144 G>T maps to NM_006893.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:40175178 G>T maps to NM_005780.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:40175178 G>T maps to NM_005780.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:126777532 G>T maps to NM_004789.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:126777532 G>T maps to NM_004789.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:180240543 C>A maps to NM_033343.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:180240543 C>A maps to NM_033343.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:180243656 C>A maps to NM_033343.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:180243656 C>A maps to NM_033343.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197889163 G>T maps to NM_020204.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197889163 G>T maps to NM_020204.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197889247 C>A maps to NM_020204.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197889247 C>A maps to NM_020204.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38481794 G>T maps to NM_002310.5 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38481794 G>T maps to NM_002310.5 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38481912 C>A maps to NM_002310.5 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38481912 C>A maps to NM_002310.5 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50642474 G>T maps to NM_001113546.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50642474 G>T maps to NM_001113546.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41601004 G>T maps to NM_014988.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41601004 G>T maps to NM_014988.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:83891596 G>T maps to NM_194282.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:83891596 G>T maps to NM_194282.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101114084 C>A maps to NM_001040616.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101114084 C>A maps to NM_001040616.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185252858 C>A maps to NM_139248.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185252858 C>A maps to NM_139248.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:76415877 C>A maps to ENST00000357063 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:76415877 C>A maps to ENST00000357063 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201869150 G>T maps to NM_012134.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201869150 G>T maps to NM_012134.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69168365 C>A maps to NM_198271.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69168365 C>A maps to NM_198271.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97821751 G>T maps to NM_014916.3 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97821751 G>T maps to NM_014916.3 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129455828 G>T maps to NM_001174147.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129455828 G>T maps to NM_001174147.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12908010 C>A maps to NM_001013631.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12908010 C>A maps to NM_001013631.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12514233 C>A maps to NM_058169.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12514233 C>A maps to NM_058169.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48290625 C>A maps to NM_031490.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48290625 C>A maps to NM_031490.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48382084 G>T maps to NM_031490.2 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:48382084 G>T maps to NM_031490.2 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161026110 G>T maps to NM_005577.2 S971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161026110 G>T maps to NM_005577.2 S971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1489937 G>T maps to NM_024830.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1489937 G>T maps to NM_024830.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34657241 G>T maps to NM_153613.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34657241 G>T maps to NM_153613.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:62812686 G>T maps to ENST00000506720 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:62812686 G>T maps to ENST00000506720 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:62845291 G>T maps to ENST00000506720 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:62845291 G>T maps to ENST00000506720 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:2951126 G>T maps to NM_014646.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:2951126 G>T maps to NM_014646.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19809438 C>A maps to NM_000237.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19809438 C>A maps to NM_000237.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99753705 G>T maps to NM_014839.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99753705 G>T maps to NM_014839.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99767302 G>T maps to NM_014839.4 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99767302 G>T maps to NM_014839.4 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99771803 C>A maps to NM_014839.4 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99771803 C>A maps to NM_014839.4 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58317505 G>T maps to NM_004811.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58317505 G>T maps to NM_004811.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151749354 G>T maps to NM_006726.3 P1716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151749354 G>T maps to NM_006726.3 P1716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100173369 C>A maps to NM_002319.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100173369 C>A maps to NM_002319.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:133881802 C>A maps to NM_144648.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:133881802 C>A maps to NM_144648.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:66433622 C>A maps to NM_015541.2 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:66433622 C>A maps to NM_015541.2 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113638891 G>T maps to NM_014813.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113638891 G>T maps to NM_014813.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110791017 G>T maps to NM_198506.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110791017 G>T maps to NM_198506.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:141215113 C>A maps to NM_018557.2 S3244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:141215113 C>A maps to NM_018557.2 S3244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57599257 C>A maps to NM_002332.2 P3820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57599257 C>A maps to NM_002332.2 P3820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186288381 G>T maps to ENST00000362004 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186288381 G>T maps to ENST00000362004 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186299341 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186299341 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170009406 G>T maps to NM_004525.2 P4121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170009406 G>T maps to NM_004525.2 P4121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170030441 G>T maps to NM_004525.2 P3667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170030441 G>T maps to NM_004525.2 P3667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170034316 G>T maps to NM_004525.2 P3463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170034316 G>T maps to NM_004525.2 P3463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170034393 C>A maps to NM_004525.2 G3438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170034393 C>A maps to NM_004525.2 G3438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170139460 G>T maps to NM_004525.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170139460 G>T maps to NM_004525.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170147448 C>A maps to NM_004525.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170147448 C>A maps to NM_004525.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68201157 C>A maps to NM_002335.2 P1284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68201157 C>A maps to NM_002335.2 P1284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12301918 C>A maps to NM_002336.2 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12301918 C>A maps to NM_002336.2 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12302069 C>A maps to NM_002336.2 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12302069 C>A maps to NM_002336.2 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12334004 G>T maps to NM_002336.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12334004 G>T maps to NM_002336.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:53728133 G>T maps to NM_004631.3 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:53728133 G>T maps to NM_004631.3 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3520694 G>T maps to NM_002337.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3520694 G>T maps to NM_002337.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3526709 G>T maps to NM_002337.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3526709 G>T maps to NM_002337.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44200946 G>T maps to NM_133259.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44200946 G>T maps to NM_133259.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44201357 G>T maps to NM_133259.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44201357 G>T maps to NM_133259.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194081273 C>A maps to NM_001135057.2 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194081273 C>A maps to NM_001135057.2 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25488752 C>A maps to NM_017640.5 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25488752 C>A maps to NM_017640.5 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:53787570 C>A maps to NM_018214.4 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:53787570 C>A maps to NM_018214.4 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:134165143 C>A maps to NM_030626.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:134165143 C>A maps to NM_030626.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99901639 G>T maps to NM_144598.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99901639 G>T maps to NM_144598.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99926300 G>T maps to NM_144598.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99926300 G>T maps to NM_144598.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169558084 C>A maps to NM_024727.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169558084 C>A maps to NM_024727.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67401127 C>A maps to NM_018296.5 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67401127 C>A maps to NM_018296.5 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44626461 C>A maps to NM_001006607.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44626461 C>A maps to NM_001006607.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30348371 G>T maps to ENST00000327564 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30348371 G>T maps to ENST00000327564 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30349743 G>T maps to ENST00000327564 G554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30349743 G>T maps to ENST00000327564 G554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122674679 C>A maps to NM_001098519.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122674679 C>A maps to NM_001098519.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71185241 C>A maps to NM_017691.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71185241 C>A maps to NM_017691.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71256165 G>T maps to NM_017691.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71256165 G>T maps to NM_017691.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:133622438 C>A maps to ENST00000250173 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:133622438 C>A maps to ENST00000250173 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238662049 C>A maps to NM_001137552.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238662049 C>A maps to NM_001137552.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238671987 C>A maps to NM_001137552.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238671987 C>A maps to NM_001137552.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:74648379 C>A maps to NM_001105659.1 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:74648379 C>A maps to NM_001105659.1 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:40702472 C>A maps to NM_198578.3 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:40702472 C>A maps to NM_198578.3 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:40753147 G>T maps to NM_198578.3 T2310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:40753147 G>T maps to NM_198578.3 T2310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3887938 C>A maps to NM_020873.5 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3887938 C>A maps to NM_020873.5 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204587971 C>A maps to NM_201630.1 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204587971 C>A maps to NM_201630.1 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130217305 C>A maps to NM_001005374.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130217305 C>A maps to NM_001005374.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21205113 C>A maps to ENST00000381541 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21205113 C>A maps to ENST00000381541 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96394808 G>T maps to NM_000895.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96394808 G>T maps to NM_000895.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33413863 C>A maps to ENST00000354476 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33413863 C>A maps to ENST00000354476 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33447183 G>T maps to ENST00000354476 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33447183 G>T maps to ENST00000354476 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144179005 C>A maps to NM_032860.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144179005 C>A maps to NM_032860.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31639663 C>A maps to ENST00000375873 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31639663 C>A maps to ENST00000375873 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31644828 G>T maps to NM_025262.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31644828 G>T maps to NM_025262.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160636684 C>A maps to NM_001198759.1 A1741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160636684 C>A maps to NM_001198759.1 A1741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160731975 G>T maps to NM_001198759.1 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160731975 G>T maps to NM_001198759.1 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160783651 C>A maps to ENST00000263285 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160783651 C>A maps to ENST00000263285 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:150069635 G>T maps to NM_177964.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:150069635 G>T maps to NM_177964.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:150327195 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:150327195 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:219384930 C>A maps to NM_138794.3 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:219384930 C>A maps to NM_138794.3 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235827306 G>T maps to NM_000081.2 P3748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235827306 G>T maps to NM_000081.2 P3748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235840463 C>A maps to NM_000081.2 A3655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235840463 C>A maps to NM_000081.2 A3655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235866075 G>T maps to NM_000081.2 R3449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235866075 G>T maps to NM_000081.2 R3449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235884057 G>T maps to NM_000081.2 R3155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235884057 G>T maps to NM_000081.2 R3155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:36049788 G>T maps to NM_005584.4 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:36049788 G>T maps to NM_005584.4 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:15843466 C>A maps to ENST00000310348 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:15843466 C>A maps to ENST00000310348 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47350683 C>A maps to NM_003682.3 R1643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47350683 C>A maps to NM_003682.3 R1643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:152482461 C>A maps to NM_004988.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:152482461 C>A maps to NM_004988.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:75003689 G>T maps to NM_138703.4 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:75003689 G>T maps to NM_138703.4 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:65433718 G>T maps to NM_001033057.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:65433718 G>T maps to NM_001033057.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:65479297 G>T maps to NM_001033057.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:65479297 G>T maps to NM_001033057.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114215326 C>A maps to NM_001142782.1 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114215326 C>A maps to NM_001142782.1 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114225852 G>T maps to NM_001142782.1 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114225852 G>T maps to NM_001142782.1 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:77130977 G>T maps to NM_032121.5 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:77130977 G>T maps to NM_032121.5 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179195972 C>A maps to NM_014757.4 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179195972 C>A maps to NM_014757.4 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:140811004 C>A maps to ENST00000509479 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:140811004 C>A maps to ENST00000509479 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117948212 G>T maps to NM_006699.3 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117948212 G>T maps to NM_006699.3 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140001841 C>A maps to NM_016219.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140001841 C>A maps to NM_016219.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75651473 C>A maps to NM_006715.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75651473 C>A maps to NM_006715.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35929815 G>T maps to NM_022077.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35929815 G>T maps to NM_022077.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:71482467 C>A maps to NM_005909.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:71482467 C>A maps to NM_005909.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:71494434 C>A maps to NM_005909.3 S1751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:71494434 C>A maps to NM_005909.3 S1751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:71494449 C>A maps to NM_005909.3 P1756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:71494449 C>A maps to NM_005909.3 P1756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66779570 G>T maps to NM_002755.3 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66779570 G>T maps to NM_002755.3 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:67879203 C>A maps to NM_145160.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:67879203 C>A maps to NM_145160.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210559080 C>A maps to NM_002374.3 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210559080 C>A maps to NM_002374.3 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210565028 C>A maps to NM_002374.3 P1517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210565028 C>A maps to NM_002374.3 P1517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53877696 G>T maps to NM_001193511.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53877696 G>T maps to NM_001193511.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161532907 G>C maps to NM_005922.2 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161532907 G>C maps to NM_005922.2 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161536201 G>T maps to NM_005922.2 V1558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161536201 G>T maps to NM_005922.2 V1558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:91246114 C>A maps to NM_145331.1 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:91246114 C>A maps to NM_145331.1 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48040236 C>A maps to ENST00000426837 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48040236 C>A maps to ENST00000426837 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75299015 C>A maps to NM_033063.1 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75299015 C>A maps to NM_033063.1 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75319345 C>A maps to NM_033063.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75319345 C>A maps to NM_033063.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:20031232 C>A maps to NM_001168465.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:20031232 C>A maps to NM_001168465.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136677897 C>A maps to NM_001198609.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136677897 C>A maps to NM_001198609.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36068010 C>A maps to NM_001315.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36068010 C>A maps to NM_001315.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:49628328 C>A maps to NM_139049.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:49628328 C>A maps to NM_139049.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112308953 C>A maps to NM_139078.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112308953 C>A maps to NM_139078.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112321432 G>T maps to NM_139078.1 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112321432 G>T maps to NM_139078.1 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42092082 C>A maps to NM_001128608.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42092082 C>A maps to NM_001128608.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42111545 C>A maps to NM_001128608.1 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42111545 C>A maps to NM_001128608.1 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44061021 C>A maps to NM_001123066.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44061021 C>A maps to NM_001123066.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44101479 C>A maps to NM_001123066.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:44101479 C>A maps to NM_001123066.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94109426 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94109426 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10402661 G>T maps to NM_005885.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10402661 G>T maps to NM_005885.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10405768 C>A maps to NM_005885.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10405768 C>A maps to NM_005885.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10415633 G>T maps to NM_005885.2 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10415633 G>T maps to NM_005885.2 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10417404 G>T maps to NM_005885.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10417404 G>T maps to NM_005885.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10426563 C>A maps to NM_005885.2 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10426563 C>A maps to NM_005885.2 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:119739939 C>A maps to NM_006770.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:119739939 C>A maps to NM_006770.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63667549 G>T maps to NM_001039469.2 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63667549 G>T maps to NM_001039469.2 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160328340 G>T maps to NM_002377.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160328340 G>T maps to NM_002377.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160328836 G>T maps to NM_002377.2 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160328836 G>T maps to NM_002377.2 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186970995 C>A maps to NM_139125.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186970995 C>A maps to NM_139125.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46493514 C>A maps to NM_015112.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46493514 C>A maps to NM_015112.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27462117 C>A maps to NM_001172303.1 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27462117 C>A maps to NM_001172303.1 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27469888 G>T maps to NM_001172303.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27469888 G>T maps to NM_001172303.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99030220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99030220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:138658544 C>A maps to ENST00000394800 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:138658544 C>A maps to ENST00000394800 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47799196 G>T maps to ENST00000424334 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47799196 G>T maps to ENST00000424334 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:149247082 G>T maps to ENST00000404807 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:149247082 G>T maps to ENST00000404807 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:54528148 G>T maps to NM_000242.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:54528148 G>T maps to NM_000242.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:152150564 C>A maps to NM_021038.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:152150564 C>A maps to NM_021038.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:98017388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:98017388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:98017411 C>A maps to ENST00000376673 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:98017411 C>A maps to ENST00000376673 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:74692426 C>A maps to NM_001025101.1 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:74692426 C>A maps to NM_001025101.1 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:54823952 G>T maps to ENST00000371389 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:54823952 G>T maps to ENST00000371389 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13826432 C>G maps to NM_005913.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13826432 C>G maps to NM_005913.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182735092 C>A maps to NM_020166.3 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182735092 C>A maps to NM_020166.3 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182751816 G>T maps to NM_020166.3 S548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182751816 G>T maps to NM_020166.3 S548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183041078 G>T maps to NM_015078.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183041078 G>T maps to NM_015078.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13213030 C>A maps to NM_182751.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13213030 C>A maps to NM_182751.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127318250 C>A maps to NM_004526.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127318250 C>A maps to NM_004526.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47681279 C>A maps to NM_003906.3 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47681279 C>A maps to NM_003906.3 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7594579 G>T maps to NM_020533.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7594579 G>T maps to NM_020533.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85403684 C>A maps to NM_153259.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85403684 C>A maps to NM_153259.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49959344 C>A maps to NM_001012300.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49959344 C>A maps to NM_001012300.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:94928753 C>A maps to NM_018349.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:94928753 C>A maps to NM_018349.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:94943179 C>A maps to NM_018349.3 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:94943179 C>A maps to NM_018349.3 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37622576 C>A maps to ENST00000297153 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37622576 C>A maps to ENST00000297153 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204499930 C>A maps to NM_002393.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204499930 C>A maps to NM_002393.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90362752 G>T maps to NM_014611.1 T5261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90362752 G>T maps to NM_014611.1 T5261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90366513 C>A maps to NM_014611.1 G5064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90366513 C>A maps to NM_014611.1 G5064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90424276 G>T maps to NM_014611.1 R2352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90424276 G>T maps to NM_014611.1 R2352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90428500 C>A maps to NM_014611.1 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90428500 C>A maps to NM_014611.1 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90432691 G>T maps to NM_014611.1 T1983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90432691 G>T maps to NM_014611.1 T1983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90434944 G>T maps to NM_014611.1 P1881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90434944 G>T maps to NM_014611.1 P1881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153295964 G>T maps to NM_001110792.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153295964 G>T maps to NM_001110792.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150877809 C>A maps to NM_053002.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150877809 C>A maps to NM_053002.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:116446461 C>A maps to NM_015335.4 G586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:116446461 C>A maps to NM_015335.4 G586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:60024338 C>A maps to NM_005121.2 E2111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:60024338 C>A maps to NM_005121.2 E2111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:100214665 C>A maps to ENST00000338042 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:100214665 C>A maps to ENST00000338042 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156452276 C>A maps to NM_005920.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156452276 C>A maps to NM_005920.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:3424407 C>A maps to ENST00000452816 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:3424407 C>A maps to ENST00000452816 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123367616 C>A maps to ENST00000426959 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123367616 C>A maps to ENST00000426959 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:66667100 C>A maps to ENST00000407092 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:66667100 C>A maps to ENST00000407092 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:66795806 G>T maps to ENST00000407092 G345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:66795806 G>T maps to ENST00000407092 G345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64571923 G>T maps to NM_130804.2 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64571923 G>T maps to NM_130804.2 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46806746 G>T maps to NM_005588.2 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46806746 G>T maps to NM_005588.2 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29788088 C>A maps to NM_005925.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29788088 C>A maps to NM_005925.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29788105 C>A maps to NM_005925.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29788105 C>A maps to NM_005925.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100028721 C>A maps to NM_019606.5 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100028721 C>A maps to NM_019606.5 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:95879718 C>A maps to NM_006838.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:95879718 C>A maps to NM_006838.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:28232634 G>T maps to NM_001113528.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:28232634 G>T maps to NM_001113528.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119609094 C>A maps to NM_020961.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119609094 C>A maps to NM_020961.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58163434 G>T maps to ENST00000408972 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58163434 G>T maps to ENST00000408972 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116339605 G>T maps to NM_001127500.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116339605 G>T maps to NM_001127500.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116417441 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116417441 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170912696 G>T maps to NM_021647.6 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170912696 G>T maps to NM_021647.6 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:8749163 G>T maps to NM_004225.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:8749163 G>T maps to NM_004225.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40432295 G>T maps to NM_001136493.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40432295 G>T maps to NM_001136493.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145736531 C>A maps to NM_138431.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145736531 C>A maps to NM_138431.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128871002 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128871002 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42042399 G>T maps to ENST00000219905 E2248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42042399 G>T maps to ENST00000219905 E2248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:88423977 G>T maps to NM_152706.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:88423977 G>T maps to NM_152706.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43277258 C>A maps to NM_153361.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43277258 C>A maps to NM_153361.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:16516800 C>A maps to NM_145764.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:16516800 C>A maps to NM_145764.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:165620270 G>T maps to ENST00000367886 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:165620270 G>T maps to ENST00000367886 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222800921 G>T maps to NM_198551.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222800921 G>T maps to NM_198551.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222802181 C>A maps to NM_198551.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222802181 C>A maps to NM_198551.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109773533 G>T maps to NM_022765.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109773533 G>T maps to NM_022765.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:12247765 C>A maps to NM_014632.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:12247765 C>A maps to NM_014632.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:18301202 G>T maps to NM_015241.2 S1408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:18301202 G>T maps to NM_015241.2 S1408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1488345 C>A maps to NM_182924.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1488345 C>A maps to NM_182924.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:10450524 G>T maps to NM_001193277.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:10450524 G>T maps to NM_001193277.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:97669698 C>A maps to NM_153182.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:97669698 C>A maps to NM_153182.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50926403 G>T maps to NM_017584.5 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50926403 G>T maps to NM_017584.5 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24460635 C>A maps to NM_005932.3 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24460635 C>A maps to NM_005932.3 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56848037 C>A maps to NM_012064.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56848037 C>A maps to NM_012064.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:70014095 C>A maps to ENST00000448226 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:70014095 C>A maps to ENST00000448226 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129900858 G>T maps to NM_002417.4 S3082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129900858 G>T maps to NM_002417.4 S3082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129902669 G>T maps to NM_002417.4 S2478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129902669 G>T maps to NM_002417.4 S2478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129904187 G>T maps to NM_002417.4 T1972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129904187 G>T maps to NM_002417.4 T1972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129904502 C>A maps to NM_002417.4 A1867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129904502 C>A maps to NM_002417.4 A1867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129904748 G>T maps to NM_002417.4 P1785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129904748 G>T maps to NM_002417.4 P1785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129905549 C>A maps to NM_002417.4 V1518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129905549 C>A maps to NM_002417.4 V1518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129905570 G>T maps to NM_002417.4 S1511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129905570 G>T maps to NM_002417.4 S1511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:158317880 C>A maps to NM_001195432.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:158317880 C>A maps to NM_001195432.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37070323 C>A maps to NM_000249.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37070323 C>A maps to NM_000249.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74725238 C>A maps to NM_152649.2 G220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74725238 C>A maps to NM_152649.2 G220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49416437 C>A maps to NM_003482.3 E5425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49416437 C>A maps to NM_003482.3 E5425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49424969 G>T maps to NM_003482.3 P4506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49424969 G>T maps to NM_003482.3 P4506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49427974 G>T maps to NM_003482.3 R3539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49427974 G>T maps to NM_003482.3 R3539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49446798 C>A maps to NM_003482.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49446798 C>A maps to NM_003482.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49446825 C>A maps to NM_003482.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49446825 C>A maps to NM_003482.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151845607 C>A maps to ENST00000355193 T4525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151845607 C>A maps to ENST00000355193 T4525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151856046 C>A maps to ENST00000355193 T3857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151856046 C>A maps to ENST00000355193 T3857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151860305 G>T maps to ENST00000355193 P3452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151860305 G>T maps to ENST00000355193 P3452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151877124 G>T maps to ENST00000355193 P2412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151877124 G>T maps to ENST00000355193 P2412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151960208 C>A maps to ENST00000355193 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151960208 C>A maps to ENST00000355193 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151962184 C>A maps to ENST00000355193 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151962184 C>A maps to ENST00000355193 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:104748303 G>T maps to NM_182931.2 G1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:104748303 G>T maps to NM_182931.2 G1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:21962474 C>A maps to NM_004641.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:21962474 C>A maps to NM_004641.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6227098 G>T maps to NM_005934.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6227098 G>T maps to NM_005934.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168265352 G>T maps to ENST00000400822 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168265352 G>T maps to ENST00000400822 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168276072 C>A maps to ENST00000400822 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168276072 C>A maps to ENST00000400822 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168347570 C>A maps to ENST00000400822 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168347570 C>A maps to ENST00000400822 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:36865472 G>T maps to NM_005937.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:36865472 G>T maps to NM_005937.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118342930 C>A maps to NM_001197104.1 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118342930 C>A maps to NM_001197104.1 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118368740 G>T maps to NM_001197104.1 G1919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118368740 G>T maps to NM_001197104.1 G1919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122614648 C>T maps to NM_014938.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122614648 C>T maps to NM_014938.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:83948642 C>A maps to NM_012213.2 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:83948642 C>A maps to NM_012213.2 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146560354 C>A maps to NM_172250.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146560354 C>A maps to NM_172250.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102815074 C>A maps to NM_002427.3 G446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102815074 C>A maps to NM_002427.3 G446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102826183 C>A maps to NM_002427.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102826183 C>A maps to NM_002427.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:89198810 G>T maps to NM_005941.4 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:89198810 G>T maps to NM_005941.4 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56231133 C>A maps to NM_002429.4 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56231133 C>A maps to NM_002429.4 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56231726 C>A maps to NM_002429.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56231726 C>A maps to NM_002429.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102661497 G>T maps to NM_002421.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102661497 G>T maps to NM_002421.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102479667 C>A maps to NM_004771.3 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102479667 C>A maps to NM_004771.3 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102487571 G>T maps to NM_004771.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102487571 G>T maps to NM_004771.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102573830 C>A maps to NM_022122.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102573830 C>A maps to NM_022122.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102593281 C>A maps to NM_002424.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:102593281 C>A maps to NM_002424.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44640853 C>A maps to NM_004994.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44640853 C>A maps to NM_004994.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:90816376 C>A maps to NM_007351.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:90816376 C>A maps to NM_007351.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88696622 C>A maps to NM_024756.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88696622 C>A maps to NM_024756.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75431106 G>T maps to NM_025098.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75431106 G>T maps to NM_025098.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75431208 C>A maps to NM_025098.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75431208 C>A maps to NM_025098.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:31328970 C>A maps to ENST00000397641 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:31328970 C>A maps to ENST00000397641 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:37711141 G>T maps to ENST00000290384 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:37711141 G>T maps to ENST00000290384 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:174537308 G>T maps to NM_006792.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:174537308 G>T maps to NM_006792.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220971268 G>T maps to NM_022746.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220971268 G>T maps to NM_022746.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50547181 C>A maps to NM_018995.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50547181 C>A maps to NM_018995.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:13188782 G>T maps to ENST00000319217 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:13188782 G>T maps to ENST00000319217 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58979246 C>A maps to NM_001039396.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58979246 C>A maps to NM_001039396.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58979893 G>T maps to NM_001039396.1 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58979893 G>T maps to NM_001039396.1 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:20221184 C>A maps to ENST00000414242 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:20221184 C>A maps to ENST00000414242 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123646665 C>A maps to NM_022782.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123646665 C>A maps to NM_022782.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154009877 G>T maps to NM_002436.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154009877 G>T maps to NM_002436.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:24720138 C>A maps to ENST00000409253 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:24720138 C>A maps to ENST00000409253 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:24727157 C>A maps to ENST00000409253 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:24727157 C>A maps to ENST00000409253 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167742506 G>T maps to NM_003953.5 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167742506 G>T maps to NM_003953.5 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118130800 G>T maps to NM_144765.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118130800 G>T maps to NM_144765.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:94170371 G>T maps to NM_005591.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:94170371 G>T maps to NM_005591.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:1342360 C>A maps to NM_017971.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:1342360 C>A maps to NM_017971.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68664111 C>A maps to NM_181514.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68664111 C>A maps to NM_181514.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68668016 C>A maps to NM_181514.1 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68668016 C>A maps to NM_181514.1 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:54681839 C>A maps to NM_016491.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:54681839 C>A maps to NM_016491.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6601546 G>T maps to NM_016497.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6601546 G>T maps to NM_016497.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151735505 G>T maps to NM_031420.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151735505 G>T maps to NM_031420.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:56020893 C>A maps to ENST00000426595 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:56020893 C>A maps to ENST00000426595 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:56020908 C>A maps to ENST00000426595 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:56020908 C>A maps to ENST00000426595 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30585699 C>A maps to NM_014046.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30585699 C>A maps to NM_014046.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30587377 G>T maps to NM_014046.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30587377 G>T maps to NM_014046.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84377316 C>A maps to NM_016067.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84377316 C>A maps to NM_016067.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59860922 G>T maps to NM_000139.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59860922 G>T maps to NM_000139.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60198307 G>T maps to NM_023945.2 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60198307 G>T maps to NM_023945.2 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:72754928 G>T maps to NM_005098.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:72754928 G>T maps to NM_005098.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47672685 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47672685 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:80150077 G>T maps to NM_002439.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:80150077 G>T maps to NM_002439.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:55335714 G>T maps to NM_138962.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:55335714 G>T maps to NM_138962.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:64949376 C>A maps to NM_002444.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:64949376 C>A maps to NM_002444.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49939932 G>T maps to NM_002447.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49939932 G>T maps to NM_002447.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155582979 C>A maps to NM_018116.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155582979 C>A maps to NM_018116.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:174156490 G>T maps to NM_002449.4 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:174156490 G>T maps to NM_002449.4 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:98703285 C>A maps to NM_178812.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:98703285 C>A maps to NM_178812.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:91503699 G>T maps to NM_006980.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:91503699 G>T maps to NM_006980.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65297260 C>A maps to NM_139242.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65297260 C>A maps to NM_139242.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151247377 C>A maps to NM_015440.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151247377 C>A maps to NM_015440.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31234125 C>A maps to NM_017762.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31234125 C>A maps to NM_017762.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31234146 G>T maps to NM_017762.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31234146 G>T maps to NM_017762.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32248878 C>A maps to NM_001040446.1 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32248878 C>A maps to NM_001040446.1 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9695403 C>A maps to NM_001077525.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9695403 C>A maps to NM_001077525.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9703962 C>A maps to NM_001077525.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9703962 C>A maps to NM_001077525.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:95582866 G>T maps to NM_016156.5 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:95582866 G>T maps to NM_016156.5 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:30412617 C>A maps to NM_021090.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:30412617 C>A maps to NM_021090.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56573279 C>A maps to NM_004687.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56573279 C>A maps to NM_004687.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17169071 G>T maps to NM_004686.4 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17169071 G>T maps to NM_004686.4 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30625790 C>A maps to ENST00000358107 G371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30625790 C>A maps to ENST00000358107 G371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30625824 G>T maps to ENST00000358107 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30625824 G>T maps to ENST00000358107 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41800704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41800704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41834736 G>T maps to NM_004294.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41834736 G>T maps to NM_004294.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7875447 C>A maps to NM_024010.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7875447 C>A maps to NM_024010.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7900090 G>T maps to NM_024010.2 G700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7900090 G>T maps to NM_024010.2 G700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236998969 G>T maps to NM_000254.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236998969 G>T maps to NM_000254.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237060369 C>A maps to NM_000254.2 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237060369 C>A maps to NM_000254.2 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100540241 C>A maps to ENST00000511045 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100540241 C>A maps to ENST00000511045 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17611878 C>A maps to NM_001001924.2 G480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17611878 C>A maps to NM_001001924.2 G480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17612410 G>T maps to NM_001001924.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17612410 G>T maps to NM_001001924.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9000462 C>A maps to NM_024690.2 T13507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9000462 C>A maps to NM_024690.2 T13507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9049227 C>A maps to NM_024690.2 A10801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9049227 C>A maps to NM_024690.2 A10801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9071236 C>A maps to NM_024690.2 P5403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9071236 C>A maps to NM_024690.2 P5403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9080466 C>A maps to NM_024690.2 T3188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9080466 C>A maps to NM_024690.2 T3188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100677623 C>A maps to NM_001040105.1 S976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100677623 C>A maps to NM_001040105.1 S976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100682097 G>T maps to NM_001040105.1 P2467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100682097 G>T maps to NM_001040105.1 P2467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100682370 C>A maps to NM_001040105.1 S2558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100682370 C>A maps to NM_001040105.1 S2558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100683336 G>T maps to NM_001040105.1 P2880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100683336 G>T maps to NM_001040105.1 P2880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30954866 C>A maps to NM_001010909.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30954866 C>A maps to NM_001010909.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195516674 C>A maps to NM_018406.5 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195516674 C>A maps to NM_018406.5 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1267049 G>T maps to ENST00000447027 T2983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1267049 G>T maps to ENST00000447027 T2983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1267637 C>A maps to ENST00000447027 P3179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1267637 C>A maps to ENST00000447027 P3179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1270338 G>T maps to ENST00000447027 E4080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1270338 G>T maps to ENST00000447027 E4080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1015930 C>A maps to NM_005961.2 S2290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1015930 C>A maps to NM_005961.2 S2290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1017646 G>T maps to NM_005961.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1017646 G>T maps to NM_005961.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1017736 G>T maps to NM_005961.2 A1688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1017736 G>T maps to NM_005961.2 A1688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1018564 C>A maps to NM_005961.2 A1412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1018564 C>A maps to NM_005961.2 A1412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113509956 C>A maps to ENST00000189978 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113509956 C>A maps to ENST00000189978 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49412358 G>T maps to NM_000255.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49412358 G>T maps to NM_000255.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49412397 C>A maps to NM_000255.3 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49412397 C>A maps to NM_000255.3 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49416552 G>T maps to NM_000255.3 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49416552 G>T maps to NM_000255.3 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:3229208 G>T maps to NM_015419.3 P2345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:3229208 G>T maps to NM_015419.3 P2345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:3238657 G>T maps to NM_015419.3 R1690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:3238657 G>T maps to NM_015419.3 R1690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42343868 C>A maps to NM_002466.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42343868 C>A maps to NM_002466.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:77636769 C>A maps to NM_015057.4 S4245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:77636769 C>A maps to NM_015057.4 S4245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:128753098 C>A maps to NM_002467.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:128753098 C>A maps to NM_002467.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8449929 G>T maps to ENST00000360416 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8449929 G>T maps to ENST00000360416 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8452040 C>A maps to ENST00000360416 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8452040 C>A maps to ENST00000360416 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15808793 C>A maps to NM_001040114.1 E1927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15808793 C>A maps to NM_001040114.1 E1927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15872667 C>A maps to NM_001040114.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15872667 C>A maps to NM_001040114.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10243709 C>A maps to NM_003802.2 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10243709 C>A maps to NM_003802.2 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10406204 C>A maps to NM_005963.3 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10406204 C>A maps to NM_005963.3 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10415206 G>T maps to NM_005963.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10415206 G>T maps to NM_005963.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10442631 C>A maps to NM_017534.5 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10442631 C>A maps to NM_017534.5 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10535908 G>T maps to NM_002470.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10535908 G>T maps to NM_002470.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10357036 C>A maps to NM_017533.2 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10357036 C>A maps to NM_017533.2 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10368906 C>A maps to NM_017533.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10368906 C>A maps to NM_017533.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23876243 G>T maps to NM_002471.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23876243 G>T maps to NM_002471.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23876312 G>T maps to NM_002471.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23876312 G>T maps to NM_002471.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10314102 G>T maps to NM_002472.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10314102 G>T maps to NM_002472.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10323355 G>T maps to NM_002472.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10323355 G>T maps to NM_002472.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3272901 G>T maps to NM_033546.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3272901 G>T maps to NM_033546.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16145413 C>A maps to NM_013262.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16145413 C>A maps to NM_013262.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30418899 C>A maps to NM_033118.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30418899 C>A maps to NM_033118.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:123339177 C>A maps to NM_053025.3 T1748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:123339177 C>A maps to NM_053025.3 T1748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30387813 C>A maps to NM_013292.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30387813 C>A maps to NM_013292.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16673900 G>T maps to NM_012334.2 R1688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16673900 G>T maps to NM_012334.2 R1688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16673972 C>A maps to NM_012334.2 E1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16673972 C>A maps to NM_012334.2 E1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16682118 G>T maps to NM_012334.2 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16682118 G>T maps to NM_012334.2 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:109379876 C>A maps to NM_015011.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:109379876 C>A maps to NM_015011.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:109475608 C>A maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:109475608 C>A maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:109817309 C>A maps to NM_015011.1 S1720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:109817309 C>A maps to NM_015011.1 S1720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27417836 G>T maps to NM_078471.3 A1765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27417836 G>T maps to NM_078471.3 A1765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27425224 C>A maps to NM_078471.3 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27425224 C>A maps to NM_078471.3 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192252059 C>A maps to NM_001130158.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192252059 C>A maps to NM_001130158.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192261186 C>A maps to NM_001130158.1 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192261186 C>A maps to NM_001130158.1 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:31039073 G>T maps to NM_015194.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:31039073 G>T maps to NM_015194.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:59510112 G>T maps to NM_004998.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:59510112 G>T maps to NM_004998.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109870794 C>A maps to NM_001101421.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109870794 C>A maps to NM_001101421.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:26455079 C>A maps to NM_017433.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:26455079 C>A maps to NM_017433.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:171260791 C>A maps to NM_138995.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:171260791 C>A maps to NM_138995.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52622645 G>T maps to ENST00000358212 R1487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52622645 G>T maps to ENST00000358212 R1487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47398599 C>A maps to NM_001080467.2 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47398599 C>A maps to NM_001080467.2 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47406768 G>T maps to NM_001080467.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47406768 G>T maps to NM_001080467.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47479668 C>A maps to NM_001080467.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47479668 C>A maps to NM_001080467.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76909585 G>T maps to NM_000260.3 T1496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76909585 G>T maps to NM_000260.3 T1496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128317302 G>T maps to ENST00000389524 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128317302 G>T maps to ENST00000389524 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72146846 G>T maps to ENST00000424560 R2144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72146846 G>T maps to ENST00000424560 R2144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72195370 G>T maps to ENST00000424560 R971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72195370 G>T maps to ENST00000424560 R971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72302704 G>T maps to ENST00000424560 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72302704 G>T maps to ENST00000424560 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171607790 G>T maps to NM_000261.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171607790 G>T maps to NM_000261.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171621186 G>T maps to NM_000261.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171621186 G>T maps to NM_000261.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171621480 G>T maps to NM_000261.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171621480 G>T maps to NM_000261.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95115478 G>T maps to NM_013451.3 T1103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95115478 G>T maps to NM_013451.3 T1103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95121286 C>A maps to NM_013451.3 E966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95121286 C>A maps to NM_013451.3 E966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95148825 C>A maps to NM_013451.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95148825 C>A maps to NM_013451.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3134661 G>T maps to NM_003803.3 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:3134661 G>T maps to NM_003803.3 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2040208 C>A maps to NM_003970.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2040208 C>A maps to NM_003970.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2092628 C>A maps to NM_003970.2 P1374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2092628 C>A maps to NM_003970.2 P1374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2092877 C>A maps to NM_003970.2 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2092877 C>A maps to NM_003970.2 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24392407 C>A maps to ENST00000330966 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24392407 C>A maps to ENST00000330966 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24394770 G>T maps to ENST00000330966 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24394770 G>T maps to ENST00000330966 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69970182 C>A maps to NM_032578.2 R1312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69970182 C>A maps to NM_032578.2 R1312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:41790016 G>T maps to NM_006766.3 P1907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:41790016 G>T maps to NM_006766.3 P1907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:41845078 C>A maps to NM_006766.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:41845078 C>A maps to NM_006766.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1926118 G>T maps to ENST00000399161 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1926118 G>T maps to ENST00000399161 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30250642 C>A maps to NM_013240.3 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30250642 C>A maps to NM_013240.3 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112528532 G>T maps to NM_024953.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112528532 G>T maps to NM_024953.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88574706 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88574706 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63719974 C>A maps to NM_024771.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63719974 C>A maps to NM_024771.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89880632 C>A maps to NM_005467.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89880632 C>A maps to NM_005467.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89891356 C>A maps to NM_005467.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89891356 C>A maps to NM_005467.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89896569 C>A maps to NM_005467.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89896569 C>A maps to NM_005467.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:175184903 C>A maps to NM_207015.2 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:175184903 C>A maps to NM_207015.2 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57485186 C>A maps to NM_005967.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57485186 C>A maps to NM_005967.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71300654 C>A maps to NM_017567.4 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71300654 C>A maps to NM_017567.4 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42082135 G>A maps to NM_153006.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42082135 G>A maps to NM_153006.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130825763 G>T maps to NM_197956.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130825763 G>T maps to NM_197956.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101890168 G>T maps to NM_052867.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101890168 G>T maps to NM_052867.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:102760247 G>T maps to ENST00000455523 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:102760247 G>T maps to ENST00000455523 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:60742021 C>A maps to NM_024611.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:60742021 C>A maps to NM_024611.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78152159 C>A maps to NM_024678.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78152159 C>A maps to NM_024678.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201751445 G>T maps to ENST00000367296 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201751445 G>T maps to ENST00000367296 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201752563 C>A maps to ENST00000367296 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201752563 C>A maps to ENST00000367296 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201752677 G>T maps to ENST00000367296 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201752677 G>T maps to ENST00000367296 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201755628 C>A maps to ENST00000367296 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201755628 C>A maps to ENST00000367296 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201763700 C>A maps to ENST00000367296 P1171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201763700 C>A maps to ENST00000367296 P1171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201777145 G>T maps to ENST00000367296 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201777145 G>T maps to ENST00000367296 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201777193 C>A maps to ENST00000367296 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201777193 C>A maps to ENST00000367296 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:19954752 C>A maps to ENST00000396087 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:19954752 C>A maps to ENST00000396087 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:19970480 C>A maps to ENST00000396087 R857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:19970480 C>A maps to ENST00000396087 R857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:36229773 C>A maps to ENST00000400445 S2729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:36229773 C>A maps to ENST00000400445 S2729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:36229809 C>A maps to ENST00000400445 S2741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:36229809 C>A maps to ENST00000400445 S2741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:90993657 G>T maps to NM_002485.4 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:90993657 G>T maps to NM_002485.4 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145301727 G>T maps to NM_001039703.4 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145301727 G>T maps to NM_001039703.4 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16891303 G>T maps to NM_017940.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16891303 G>T maps to NM_017940.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16893744 G>T maps to NM_017940.3 S923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16893744 G>T maps to NM_017940.3 S923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16918356 G>T maps to NM_017940.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16918356 G>T maps to NM_017940.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120382881 G>T maps to NM_001047980.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120382881 G>T maps to NM_001047980.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6640147 C>A maps to NM_014865.3 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6640147 C>A maps to NM_014865.3 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134054812 G>T maps to NM_015261.2 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134054812 G>T maps to NM_015261.2 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134054882 G>T maps to NM_015261.2 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134054882 G>T maps to NM_015261.2 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172363464 C>A maps to NM_001146276.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172363464 C>A maps to NM_001146276.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183543660 G>T maps to NM_001127651.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183543660 G>T maps to NM_001127651.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183559352 G>T maps to NM_001127651.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183559352 G>T maps to NM_001127651.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54903673 C>A maps to NM_005337.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54903673 C>A maps to NM_005337.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50189230 C>G maps to NM_001037806.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50189230 C>G maps to NM_001037806.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:133541011 G>T maps to NM_207363.2 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:133541011 G>T maps to NM_207363.2 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:133541926 G>T maps to NM_207363.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:133541926 G>T maps to NM_207363.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:133542364 C>A maps to NM_207363.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:133542364 C>A maps to NM_207363.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232322420 G>T maps to NM_005381.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232322420 G>T maps to NM_005381.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:46266486 G>T maps to NM_181659.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:46266486 G>T maps to NM_181659.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51580695 G>T maps to NM_001145260.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51580695 G>T maps to NM_001145260.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44699041 G>T maps to NM_020967.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44699041 G>T maps to NM_020967.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33329373 G>T maps to NM_014071.2 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33329373 G>T maps to NM_014071.2 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33338251 G>T maps to NM_014071.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33338251 G>T maps to NM_014071.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:15964780 G>T maps to ENST00000395857 R1954R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:15964780 G>T maps to ENST00000395857 R1954R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:15978925 C>A maps to ENST00000395857 E1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:15978925 C>A maps to ENST00000395857 E1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55420751 C>A maps to NM_004829.5 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55420751 C>A maps to NM_004829.5 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160321592 C>A maps to NM_015331.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160321592 C>A maps to NM_015331.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160322738 C>A maps to NM_015331.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160322738 C>A maps to NM_015331.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160327955 G>T maps to NM_015331.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160327955 G>T maps to NM_015331.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:2589218 G>T maps to NM_006101.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:2589218 G>T maps to NM_006101.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:29561180 G>T maps to NM_138704.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:29561180 G>T maps to NM_138704.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:23931902 G>A maps to NM_002487.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:23931902 G>A maps to NM_002487.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140100698 G>T maps to NM_001144026.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140100698 G>T maps to NM_001144026.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149932777 C>A maps to NM_001543.4 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149932777 C>A maps to NM_001543.4 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75566884 C>A maps to NM_003635.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75566884 C>A maps to NM_003635.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119059258 G>T maps to NM_004784.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119059258 G>T maps to NM_004784.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124906594 C>A maps to NM_014222.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124906594 C>A maps to NM_014222.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41688722 G>T maps to NM_016013.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41688722 G>T maps to NM_016013.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49060157 C>A maps to NM_199069.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49060157 C>A maps to NM_199069.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49060194 C>A maps to NM_199069.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49060194 C>A maps to NM_199069.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140402741 G>T maps to NM_004546.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140402741 G>T maps to NM_004546.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179336273 C>A maps to NM_002492.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179336273 C>A maps to NM_002492.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207008819 G>T maps to ENST00000455934 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207008819 G>T maps to ENST00000455934 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67376085 C>A maps to NM_007103.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67376085 C>A maps to NM_007103.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67376148 C>A maps to NM_007103.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67376148 C>A maps to NM_007103.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:21157652 G>T maps to ENST00000430741 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:21157652 G>T maps to ENST00000430741 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152346520 C>A maps to NM_001164507.1 T8456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152346520 C>A maps to NM_001164507.1 T8456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152348680 G>T maps to NM_001164507.1 R8330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152348680 G>T maps to NM_001164507.1 R8330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152362732 C>A maps to NM_001164507.1 G7866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152362732 C>A maps to NM_001164507.1 G7866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152374882 G>T maps to NM_001164507.1 P7583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152374882 G>T maps to NM_001164507.1 P7583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152394710 C>A maps to NM_001164507.1 T6980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152394710 C>A maps to NM_001164507.1 T6980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152410392 G>T maps to NM_001164507.1 P6525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152410392 G>T maps to NM_001164507.1 P6525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152418665 G>T maps to NM_001164507.1 P6318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152418665 G>T maps to NM_001164507.1 P6318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152474839 C>A maps to NM_001164507.1 T3675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152474839 C>A maps to NM_001164507.1 T3675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152484296 G>T maps to NM_001164507.1 R3295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152484296 G>T maps to NM_001164507.1 R3295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152496997 C>A maps to NM_001164507.1 V2852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152496997 C>A maps to NM_001164507.1 V2852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152500382 G>T maps to NM_001164507.1 P2635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152500382 G>T maps to NM_001164507.1 P2635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152500591 G>T maps to NM_001164507.1 R2566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152500591 G>T maps to NM_001164507.1 R2566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11192625 C>A maps to NM_006403.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11192625 C>A maps to NM_006403.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11213668 G>T maps to NM_006403.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11213668 G>T maps to NM_006403.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11643526 C>A maps to NM_145043.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11643526 C>A maps to NM_145043.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130828741 G>C maps to NM_024800.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130828741 G>C maps to NM_024800.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130871300 C>A maps to NM_024800.4 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130871300 C>A maps to NM_024800.4 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170327832 G>T maps to ENST00000507142 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170327832 G>T maps to ENST00000507142 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170458971 G>T maps to ENST00000507142 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170458971 G>T maps to ENST00000507142 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170458976 G>T maps to ENST00000507142 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170458976 G>T maps to ENST00000507142 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127089650 G>T maps to NM_001166171.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127089650 G>T maps to NM_001166171.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:198247180 C>A maps to NM_133494.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:198247180 C>A maps to NM_133494.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27066103 C>A maps to NM_178170.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27066103 C>A maps to NM_178170.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27068099 G>T maps to NM_178170.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27068099 G>T maps to NM_178170.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73547109 C>A maps to NM_002499.3 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73547109 C>A maps to NM_002499.3 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156641483 C>A maps to NM_006617.1 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156641483 C>A maps to NM_006617.1 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:47165916 C>A maps to NM_018092.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:47165916 C>A maps to NM_018092.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74717462 C>A maps to NM_006656.5 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74717462 C>A maps to NM_006656.5 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31378806 C>A maps to NM_022728.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31378806 C>A maps to NM_022728.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69689610 G>T maps to NM_138713.2 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69689610 G>T maps to NM_138713.2 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77170925 C>A maps to NM_172387.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77170925 C>A maps to NM_172387.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77210989 C>A maps to NM_172387.1 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77210989 C>A maps to NM_172387.1 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50049276 C>A maps to NM_012340.3 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50049276 C>A maps to NM_012340.3 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50071207 C>A maps to NM_012340.3 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50071207 C>A maps to NM_012340.3 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50092014 G>T maps to NM_012340.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50092014 G>T maps to NM_012340.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:26224286 C>A maps to NM_004289.6 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:26224286 C>A maps to NM_004289.6 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61553819 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61553819 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61553898 C>A maps to NM_001145512.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61553898 C>A maps to NM_001145512.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61554047 C>A maps to NM_001145512.1 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61554047 C>A maps to NM_001145512.1 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61848939 G>T maps to NM_001145512.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61848939 G>T maps to NM_001145512.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61849012 C>A maps to NM_001145512.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61849012 C>A maps to NM_001145512.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61849032 C>A maps to NM_001145512.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61849032 C>A maps to NM_001145512.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94172692 C>A maps to NM_005384.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94172692 C>A maps to NM_005384.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129756336 C>A maps to NM_006165.3 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129756336 C>A maps to NM_006165.3 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:25773829 G>T maps to NM_018297.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:25773829 G>T maps to NM_018297.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90814527 C>A maps to NM_001033088.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90814527 C>A maps to NM_001033088.1 P128P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:103822371 C>A maps to NM_139173.3 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:103822371 C>A maps to NM_139173.3 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115661598 C>A maps to NM_198514.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115661598 C>A maps to NM_198514.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:71360535 C>A maps to NM_001013627.2 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:71360535 C>A maps to NM_001013627.2 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:52477706 C>A maps to NM_007361.3 T1203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:52477706 C>A maps to NM_007361.3 T1203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25450679 C>A maps to NM_025176.4 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25450679 C>A maps to NM_025176.4 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25507085 G>T maps to NM_025176.4 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25507085 G>T maps to NM_025176.4 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48037615 C>A maps to NM_207330.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48037615 C>A maps to NM_207330.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156899487 G>T maps to NM_001099287.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156899487 G>T maps to NM_001099287.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36976220 C>A maps to NM_133433.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36976220 C>A maps to NM_133433.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36984865 G>T maps to NM_133433.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36984865 G>T maps to NM_133433.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37020894 G>T maps to NM_133433.3 V1748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37020894 G>T maps to NM_133433.3 V1748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37045638 C>A maps to NM_133433.3 T2146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37045638 C>A maps to NM_133433.3 T2146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37045642 G>T maps to NM_133433.3 G2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37045642 G>T maps to NM_133433.3 G2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37048688 C>A maps to NM_133433.3 S2225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37048688 C>A maps to NM_133433.3 S2225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37064663 G>T maps to NM_133433.3 T2695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37064663 G>T maps to NM_133433.3 T2695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37064969 C>A maps to NM_133433.3 A2797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37064969 C>A maps to NM_133433.3 A2797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23538819 G>T maps to NM_006167.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23538819 G>T maps to NM_006167.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85414594 C>A maps to NM_006168.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85414594 C>A maps to NM_006168.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:65108104 G>T maps to NM_020726.4 G623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:65108104 G>T maps to NM_020726.4 G623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7064513 C>A maps to NM_176822.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7064513 C>A maps to NM_176822.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55494709 C>A maps to NM_017852.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55494709 C>A maps to NM_017852.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:247586559 C>A maps to NM_004895.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:247586559 C>A maps to NM_004895.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:142409473 C>A maps to NM_002511.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:142409473 C>A maps to NM_002511.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169256556 G>T maps to NM_013330.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169256556 G>T maps to NM_013330.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:139279950 G>T maps to ENST00000296202 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:139279950 G>T maps to ENST00000296202 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15172175 C>G maps to ENST00000378143 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15172175 C>G maps to ENST00000378143 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43613142 G>T maps to NM_182977.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43613142 G>T maps to NM_182977.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43624205 C>A maps to NM_182977.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43624205 C>A maps to NM_182977.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96094399 G>T maps to NM_022451.9 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96094399 G>T maps to NM_022451.9 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30485797 G>T maps to NM_006092.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30485797 G>T maps to NM_006092.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:6610485 G>T maps to NM_024654.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:6610485 G>T maps to NM_024654.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156754915 C>A maps to NM_138400.1 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156754915 C>A maps to NM_138400.1 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:14970238 G>T maps to ENST00000456867 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:14970238 G>T maps to ENST00000456867 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2940650 C>A maps to NM_003703.1 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2940650 C>A maps to NM_003703.1 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2951765 C>A maps to NM_003703.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2951765 C>A maps to NM_003703.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2959371 G>T maps to NM_003703.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2959371 G>T maps to NM_003703.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203160433 C>A maps to NM_015934.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203160433 C>A maps to NM_015934.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117655855 G>T maps to ENST00000338101 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117655855 G>T maps to ENST00000338101 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150696367 C>A maps to NM_000603.4 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150696367 C>A maps to NM_000603.4 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120458345 C>A maps to NM_024408.2 A2333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120458345 C>A maps to NM_024408.2 A2333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120460307 G>T maps to NM_024408.2 R2003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120460307 G>T maps to NM_024408.2 R2003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120467980 C>A maps to NM_024408.2 T1486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120467980 C>A maps to NM_024408.2 T1486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120506320 G>T maps to NM_024408.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120506320 G>T maps to NM_024408.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120510200 C>A maps to NM_024408.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120510200 C>A maps to NM_024408.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69331297 C>A maps to NM_024505.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69331297 C>A maps to NM_024505.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2030384 G>T maps to NM_172168.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2030384 G>T maps to NM_172168.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101584857 C>A maps to NM_002518.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101584857 C>A maps to NM_002518.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101591323 G>T maps to NM_002518.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101591323 G>T maps to NM_002518.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66192487 C>A maps to NM_178864.3 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66192487 C>A maps to NM_178864.3 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108044558 G>T maps to NM_002519.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108044558 G>T maps to NM_002519.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108058838 G>T maps to NM_002519.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:108058838 G>T maps to NM_002519.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21136257 C>A maps to NM_000271.4 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21136257 C>A maps to NM_000271.4 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110917823 C>A maps to NM_000272.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110917823 C>A maps to NM_000272.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110922261 C>A maps to NM_000272.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110922261 C>A maps to NM_000272.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132407555 C>A maps to ENST00000393156 A1021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132407555 C>A maps to ENST00000393156 A1021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179520400 G>T maps to NM_014625.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179520400 G>T maps to NM_014625.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179530457 C>A maps to NM_014625.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179530457 C>A maps to NM_014625.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170818427 G>T maps to NM_002520.6 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170818427 G>T maps to NM_002520.6 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35792770 G>T maps to NM_003995.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35792770 G>T maps to NM_003995.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35799692 C>A maps to NM_003995.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35799692 C>A maps to NM_003995.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35800102 C>A maps to NM_003995.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35800102 C>A maps to NM_003995.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35800423 C>A maps to NM_003995.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35800423 C>A maps to NM_003995.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32739026 C>A maps to ENST00000265074 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32739026 C>A maps to ENST00000265074 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:25266261 G>T maps to NM_022150.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:25266261 G>T maps to NM_022150.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69745102 G>T maps to NM_000903.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69745102 G>T maps to NM_000903.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108492707 G>T maps to ENST00000368983 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108492707 G>T maps to ENST00000368983 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:96877563 C>A maps to NM_021005.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:96877563 C>A maps to NM_021005.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115381678 G>T maps to ENST00000369358 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115381678 G>T maps to ENST00000369358 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115384610 G>T maps to ENST00000369358 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115384610 G>T maps to ENST00000369358 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115410238 G>T maps to ENST00000369358 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115410238 G>T maps to ENST00000369358 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115251226 G>T maps to NM_002524.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115251226 G>T maps to NM_002524.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107880466 C>A maps to ENST00000379032 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107880466 C>A maps to ENST00000379032 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129297289 C>A maps to ENST00000393231 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129297289 C>A maps to ENST00000393231 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129351376 C>A maps to ENST00000393231 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129351376 C>A maps to ENST00000393231 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:32617901 C>A maps to NM_013956.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:32617901 C>A maps to NM_013956.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2939956 G>T maps to NM_031474.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2939956 G>T maps to NM_031474.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:105168961 C>A maps to NM_198465.2 S1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:105168961 C>A maps to NM_198465.2 S1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33502355 C>A maps to NM_003873.5 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33502355 C>A maps to NM_003873.5 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33542985 G>T maps to NM_003873.5 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33542985 G>T maps to NM_003873.5 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206562278 G>T maps to NM_201266.1 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206562278 G>T maps to NM_201266.1 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:50149312 C>G maps to ENST00000404971 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:50149312 C>G maps to ENST00000404971 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64419600 C>A maps to NM_015080.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64419600 C>A maps to NM_015080.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64453131 G>T maps to NM_015080.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64453131 G>T maps to NM_015080.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:74065188 G>T maps to NM_014886.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:74065188 G>T maps to NM_014886.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6600059 C>A maps to NM_017755.5 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6600059 C>A maps to NM_017755.5 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:33057164 G>T maps to NM_001002010.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:33057164 G>T maps to NM_001002010.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104179175 C>A maps to NM_001031701.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104179175 C>A maps to NM_001031701.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104187043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104187043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15141760 C>A maps to NM_173474.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15141760 C>A maps to NM_173474.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:131240754 G>T maps to NM_001048209.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:131240754 G>T maps to NM_001048209.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61386080 G>T maps to NM_002531.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61386080 G>T maps to NM_002531.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151046280 G>T maps to ENST00000355851 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151046280 G>T maps to ENST00000355851 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:10851749 C>A maps to NM_002484.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:10851749 C>A maps to NM_002484.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205687461 G>T maps to NM_022731.4 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205687461 G>T maps to NM_022731.4 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205687572 C>A maps to NM_022731.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205687572 C>A maps to NM_022731.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110255472 G>T maps to NM_032869.3 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110255472 G>T maps to NM_032869.3 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2290518 C>A maps to NM_198954.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2290518 C>A maps to NM_198954.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93793046 G>T maps to NM_199040.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93793046 G>T maps to NM_199040.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12215729 G>T maps to ENST00000378937 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12215729 G>T maps to ENST00000378937 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88379140 G>T maps to NM_024047.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88379140 G>T maps to NM_024047.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27614177 G>T maps to NM_020772.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27614177 G>T maps to NM_020772.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41173726 G>T maps to NM_004756.3 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41173726 G>T maps to NM_004756.3 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69084484 C>A maps to NM_020401.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69084484 C>A maps to NM_020401.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229631743 C>A maps to NM_018230.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229631743 C>A maps to NM_018230.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37310731 G>T maps to NM_153485.1 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37310731 G>T maps to NM_153485.1 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47808042 G>T maps to NM_015231.1 A1270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47808042 G>T maps to NM_015231.1 A1270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131750388 C>A maps to NM_015354.1 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131750388 C>A maps to NM_015354.1 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135282769 C>A maps to NM_015135.2 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135282769 C>A maps to NM_015135.2 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135330312 G>T maps to NM_015135.2 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135330312 G>T maps to NM_015135.2 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154042757 G>T maps to NM_207308.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154042757 G>T maps to NM_207308.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154090238 G>T maps to NM_207308.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154090238 G>T maps to NM_207308.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154112354 C>A maps to NM_207308.2 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154112354 C>A maps to NM_207308.2 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13363297 C>A maps to NM_024923.2 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13363297 C>A maps to NM_024923.2 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13419062 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13419062 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134002981 G>T maps to ENST00000451030 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134002981 G>T maps to ENST00000451030 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134021653 C>A maps to ENST00000451030 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134021653 C>A maps to ENST00000451030 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134039331 C>A maps to ENST00000451030 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134039331 C>A maps to ENST00000451030 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56865888 G>T maps to NM_014669.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56865888 G>T maps to NM_014669.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25889499 G>T maps to NM_014089.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25889499 G>T maps to NM_014089.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25893473 G>T maps to NM_014089.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25893473 G>T maps to NM_014089.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:118015230 G>T maps to NM_138459.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:118015230 G>T maps to NM_138459.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224437964 C>A maps to NM_002533.2 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224437964 C>A maps to NM_002533.2 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224491523 C>A maps to NM_002533.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224491523 C>A maps to NM_002533.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16861220 C>A maps to ENST00000438489 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16861220 C>A maps to ENST00000438489 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16918733 G>T maps to ENST00000438489 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16918733 G>T maps to ENST00000438489 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62571273 G>T maps to NM_006362.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62571273 G>T maps to NM_006362.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113440874 C>A maps to NM_016817.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113440874 C>A maps to NM_016817.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228432054 G>T maps to NM_001098623.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228432054 G>T maps to NM_001098623.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228467092 C>A maps to NM_001098623.1 P2448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228467092 C>A maps to NM_001098623.1 P2448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28202869 C>A maps to NM_000275.2 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28202869 C>A maps to NM_000275.2 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28231759 C>A maps to NM_000275.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28231759 C>A maps to NM_000275.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10580954 G>T maps to NM_002539.1 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10580954 G>T maps to NM_002539.1 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10582147 C>A maps to NM_002539.1 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10582147 C>A maps to NM_002539.1 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:123515065 G>T maps to NM_001163278.1 R2507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:123515065 G>T maps to NM_001163278.1 R2507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:123517928 G>T maps to NM_001163278.1 P2284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:123517928 G>T maps to NM_001163278.1 P2284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167517754 C>A maps to NM_001122679.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167517754 C>A maps to NM_001122679.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167675152 C>A maps to NM_001122679.1 P2394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167675152 C>A maps to NM_001122679.1 P2394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:183672997 G>T maps to NM_001080477.1 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:183672997 G>T maps to NM_001080477.1 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78369119 C>A maps to NM_001098816.2 E2765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78369119 C>A maps to NM_001098816.2 E2765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50959891 G>T maps to NM_018245.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50959891 G>T maps to NM_018245.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44715687 C>A maps to ENST00000444676 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44715687 C>A maps to ENST00000444676 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44721422 C>A maps to ENST00000444676 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44721422 C>A maps to ENST00000444676 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56501148 C>A maps to NM_018233.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56501148 C>A maps to NM_018233.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74684300 C>A maps to NM_152635.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74684300 C>A maps to NM_152635.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74690313 G>T maps to NM_152635.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74690313 G>T maps to NM_152635.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15107713 C>A maps to NM_018324.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15107713 C>A maps to NM_018324.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:102290759 G>T maps to ENST00000338858 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:102290759 G>T maps to ENST00000338858 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53603066 C>A maps to NM_006418.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53603066 C>A maps to NM_006418.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53608562 C>A maps to NM_006418.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53608562 C>A maps to NM_006418.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161953674 C>A maps to ENST00000451379 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161953674 C>A maps to ENST00000451379 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161968049 G>T maps to ENST00000451379 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161968049 G>T maps to ENST00000451379 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114523755 C>A maps to NM_020190.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114523755 C>A maps to NM_020190.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95179686 C>A maps to NM_005014.2 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95179686 C>A maps to NM_005014.2 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193333491 G>T maps to NM_130837.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193333491 G>T maps to NM_130837.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:154412195 C>A maps to NM_001145279.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:154412195 C>A maps to NM_001145279.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:123909380 C>A maps to NM_001004463.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:123909380 C>A maps to NM_001004463.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158449756 C>A maps to NM_001004472.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158449756 C>A maps to NM_001004472.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29395094 T>A maps to NM_013937.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29395094 T>A maps to NM_013937.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29364508 C>A maps to NM_013936.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29364508 C>A maps to NM_013936.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29364694 G>T maps to NM_013936.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29364694 G>T maps to NM_013936.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107367098 C>A maps to NM_001004481.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107367098 C>A maps to NM_001004481.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107288801 G>T maps to NM_001001919.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107288801 G>T maps to NM_001001919.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107266629 G>T maps to NM_001004485.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107266629 G>T maps to NM_001004485.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:15198160 G>T maps to NM_001004713.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:15198160 G>T maps to NM_001004713.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125239356 G>T maps to NM_001004451.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125239356 G>T maps to NM_001004451.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125512413 G>T maps to ENST00000373684 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125512413 G>T maps to ENST00000373684 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125315735 C>A maps to NM_001004457.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125315735 C>A maps to NM_001004457.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143771878 G>T maps to NM_001004488.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143771878 G>T maps to NM_001004488.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6789273 C>A maps to NM_001004490.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6789273 C>A maps to NM_001004490.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:247614369 C>A maps to NM_001004492.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:247614369 C>A maps to NM_001004492.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6912918 C>A maps to NM_003700.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6912918 C>A maps to NM_003700.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6942393 C>A maps to NM_001004684.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6942393 C>A maps to NM_001004684.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29429698 C>A maps to NM_030883.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29429698 C>A maps to NM_030883.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29141762 G>C maps to NM_030905.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29141762 G>C maps to NM_030905.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29142263 G>T maps to NM_030905.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29142263 G>T maps to NM_030905.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248344135 C>A maps to NM_001004688.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248344135 C>A maps to NM_001004688.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248366641 C>A maps to NM_001004689.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248366641 C>A maps to NM_001004689.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248308679 C>A maps to NM_001004690.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248308679 C>A maps to NM_001004690.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248308685 C>A maps to NM_001004690.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248308685 C>A maps to NM_001004690.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:49974639 C>A maps to NM_001001955.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:49974639 C>A maps to NM_001001955.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:51515596 G>T maps to NM_001004703.1 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:51515596 G>T maps to NM_001004703.1 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56247867 C>A maps to NM_001004707.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56247867 C>A maps to NM_001004707.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59224933 C>A maps to NM_001004708.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59224933 C>A maps to NM_001004708.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59225260 G>T maps to NM_001004708.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59225260 G>T maps to NM_001004708.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:69536 G>T maps to NM_001005484.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:69536 G>T maps to NM_001005484.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20585639 G>T maps to NM_001004715.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20585639 G>T maps to NM_001004715.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20404664 C>A maps to NM_001004063.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20404664 C>A maps to NM_001004063.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20344566 C>A maps to NM_001005501.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20344566 C>A maps to NM_001005501.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20345010 G>T maps to NM_001005501.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20345010 G>T maps to NM_001005501.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20528233 G>T maps to NM_001004717.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20528233 G>T maps to NM_001004717.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20295795 G>T maps to NM_001004723.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20295795 G>T maps to NM_001004723.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20612130 C>A maps to NM_001004724.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20612130 C>A maps to NM_001004724.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5372944 G>T maps to NM_001004750.1 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5372944 G>T maps to NM_001004750.1 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4790739 G>T maps to ENST00000380383 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4790739 G>T maps to ENST00000380383 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5020691 C>A maps to NM_001004755.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5020691 C>A maps to NM_001004755.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5411114 C>A maps to NM_001004756.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5411114 C>A maps to NM_001004756.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5510500 C>A maps to NM_001005163.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5510500 C>A maps to NM_001005163.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5862710 G>C maps to ENST00000379946 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5862710 G>C maps to ENST00000379946 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4615516 C>A maps to ENST00000450052 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4615516 C>A maps to ENST00000450052 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4608707 C>A maps to NM_001005170.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4608707 C>A maps to NM_001005170.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5809245 C>A maps to NM_001001913.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5809245 C>A maps to NM_001001913.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59189574 G>T maps to NM_001001954.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59189574 G>T maps to NM_001001954.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59190192 G>T maps to NM_001001954.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59190192 G>T maps to NM_001001954.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:56756799 C>A maps to NM_001005323.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:56756799 C>A maps to NM_001005323.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58207585 C>A maps to NM_001004733.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58207585 C>A maps to NM_001004733.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98188539 G>T maps to NM_001004736.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98188539 G>T maps to NM_001004736.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98217072 C>A maps to NM_001004737.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98217072 C>A maps to NM_001004737.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98109628 G>T maps to NM_001005516.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98109628 G>T maps to NM_001005516.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55999683 G>T maps to NM_001004746.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55999683 G>T maps to NM_001004746.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143701743 G>T maps to NM_001005281.1 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143701743 G>T maps to NM_001005281.1 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143701775 C>A maps to NM_001005281.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143701775 C>A maps to NM_001005281.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158687490 G>T maps to ENST00000368146 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158687490 G>T maps to ENST00000368146 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158735917 C>A maps to NM_001005185.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158735917 C>A maps to NM_001005185.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142749751 G>T maps to NM_001001667.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142749751 G>T maps to NM_001001667.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14938336 G>T maps to NM_017506.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14938336 G>T maps to NM_017506.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14938678 G>A maps to NM_017506.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14938678 G>A maps to NM_017506.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14910186 C>A maps to NM_198944.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14910186 C>A maps to NM_198944.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124310852 C>A maps to NM_012378.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124310852 C>A maps to NM_012378.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124095789 G>T maps to NM_001007249.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124095789 G>T maps to NM_001007249.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124095873 G>T maps to NM_001007249.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124095873 G>T maps to NM_001007249.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55872694 C>A maps to NM_001005200.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55872694 C>A maps to NM_001005200.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55873102 C>A maps to NM_001005200.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55873102 C>A maps to NM_001005200.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55889970 G>T maps to NM_001005201.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55889970 G>T maps to NM_001005201.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55890132 G>T maps to NM_001005201.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55890132 G>T maps to NM_001005201.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48921774 C>A maps to NM_001005203.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48921774 C>A maps to NM_001005203.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56213148 G>T maps to NM_014182.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56213148 G>T maps to NM_014182.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:31774892 C>A maps to NM_017784.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:31774892 C>A maps to NM_017784.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:125250831 G>T maps to NM_022776.4 S684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:125250831 G>T maps to NM_022776.4 S684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21913014 C>A maps to NM_080597.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21913014 C>A maps to NM_080597.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:60835091 G>T maps to NM_144498.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:60835091 G>T maps to NM_144498.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3141803 C>A maps to NM_020896.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3141803 C>A maps to NM_020896.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179259109 C>A maps to ENST00000392505 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179259109 C>A maps to ENST00000392505 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76783468 C>A maps to NM_020841.4 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76783468 C>A maps to NM_020841.4 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59345682 G>T maps to NM_002556.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59345682 G>T maps to NM_002556.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36886090 G>T maps to ENST00000356637 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36886090 G>T maps to ENST00000356637 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38921837 C>A maps to NM_003999.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38921837 C>A maps to NM_003999.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38933257 G>T maps to NM_003999.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38933257 G>T maps to NM_003999.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:16729075 G>T maps to NM_020157.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:16729075 G>T maps to NM_020157.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63764601 C>A maps to ENST00000422031 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63764601 C>A maps to ENST00000422031 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:29630369 C>A maps to NM_183378.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:29630369 C>A maps to NM_183378.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41807518 C>A maps to NM_000436.3 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41807518 C>A maps to NM_000436.3 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16336422 C>A maps to NM_138381.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16336422 C>A maps to NM_138381.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:107696512 G>T maps to NM_001198533.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:107696512 G>T maps to NM_001198533.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:107726068 C>A maps to NM_001198533.1 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:107726068 C>A maps to NM_001198533.1 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57106131 C>A maps to NM_002559.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57106131 C>A maps to NM_002559.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121655062 G>T maps to NM_002560.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121655062 G>T maps to NM_002560.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121670804 C>A maps to NM_002560.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121670804 C>A maps to NM_002560.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21377641 C>A maps to NM_005446.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21377641 C>A maps to NM_005446.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121593946 C>A maps to NM_002562.5 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121593946 C>A maps to NM_002562.5 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121598737 C>A maps to NM_002562.5 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121598737 C>A maps to NM_002562.5 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74774017 C>A maps to NM_000917.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74774017 C>A maps to NM_000917.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74810842 C>A maps to NM_000917.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:74810842 C>A maps to NM_000917.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74015317 G>T maps to NM_182904.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74015317 G>T maps to NM_182904.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:43545420 C>A maps to NM_001124756.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:43545420 C>A maps to NM_001124756.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101724630 G>T maps to NM_002568.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101724630 G>T maps to NM_002568.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20714409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20714409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20728951 C>A maps to ENST00000503585 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20728951 C>A maps to ENST00000503585 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:163235228 C>A maps to NM_152410.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:163235228 C>A maps to NM_152410.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:43273000 C>A maps to NM_001184970.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:43273000 C>A maps to NM_001184970.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10695280 C>A maps to NM_017906.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10695280 C>A maps to NM_017906.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10697603 C>A maps to NM_017906.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10697603 C>A maps to NM_017906.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:9561352 G>T maps to NM_177990.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:9561352 G>T maps to NM_177990.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:112924408 C>A maps to NM_007203.4 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:112924408 C>A maps to NM_007203.4 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100127902 C>A maps to NM_017734.4 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100127902 C>A maps to NM_017734.4 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100154803 C>A maps to NM_017734.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100154803 C>A maps to NM_017734.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56713244 C>G maps to NM_001127460.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56713244 C>G maps to NM_001127460.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:91353618 C>A maps to NM_148977.1 G480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:91353618 C>A maps to NM_148977.1 G480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167993177 C>A maps to NM_024594.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167993177 C>A maps to NM_024594.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93913088 C>A maps to NM_015368.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93913088 C>A maps to NM_015368.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135202489 C>A maps to NM_152911.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135202489 C>A maps to NM_152911.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135204832 G>T maps to NM_152911.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135204832 G>T maps to NM_152911.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:78936974 C>A maps to NM_173797.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:78936974 C>A maps to NM_173797.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176661389 G>T maps to NM_020318.2 G854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176661389 G>T maps to NM_020318.2 G854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176708829 C>A maps to NM_020318.2 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176708829 C>A maps to NM_020318.2 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:89474813 C>A maps to NM_001015880.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:89474813 C>A maps to NM_001015880.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:205989105 C>A maps to ENST00000406610 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:205989105 C>A maps to ENST00000406610 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206364631 G>T maps to ENST00000406610 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206364631 G>T maps to ENST00000406610 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206480188 C>A maps to ENST00000406610 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206480188 C>A maps to ENST00000406610 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:34400396 G>T maps to NM_019619.3 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:34400396 G>T maps to NM_019619.3 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:34690767 G>T maps to NM_019619.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:34690767 G>T maps to NM_019619.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226564844 G>T maps to NM_001618.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226564844 G>T maps to NM_001618.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51981892 C>A maps to NM_001003931.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51981892 C>A maps to NM_001003931.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25023905 C>A maps to NM_006437.3 G1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25023905 C>A maps to NM_006437.3 G1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72549733 C>G maps to NM_020214.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72549733 C>G maps to NM_020214.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59420423 G>T maps to NM_152716.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59420423 G>T maps to NM_152716.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114002023 G>C maps to NM_003466.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114002023 G>C maps to NM_003466.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114002070 G>T maps to NM_003466.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114002070 G>T maps to NM_003466.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70048387 C>A maps to NM_022129.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70048387 C>A maps to NM_022129.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52637668 C>A maps to ENST00000296302 G883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52637668 C>A maps to ENST00000296302 G883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52677280 G>T maps to ENST00000296302 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52677280 G>T maps to ENST00000296302 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:128691995 C>A maps to ENST00000373487 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:128691995 C>A maps to ENST00000373487 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51994907 C>A maps to NM_033010.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51994907 C>A maps to NM_033010.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100982899 C>A maps to NM_000282.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100982899 C>A maps to NM_000282.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:134071465 C>A maps to NM_032961.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:134071465 C>A maps to NM_032961.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:134072569 G>T maps to NM_032961.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:134072569 G>T maps to NM_032961.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:55566608 C>A maps to ENST00000373965 L1595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:55566608 C>A maps to ENST00000373965 L1595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:55839180 C>A maps to NM_001142763.1 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:55839180 C>A maps to NM_001142763.1 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:58208650 C>A maps to NM_001040429.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:58208650 C>A maps to NM_001040429.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:58208701 C>A maps to NM_001040429.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:58208701 C>A maps to NM_001040429.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:30725713 G>T maps to NM_001173523.1 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:30725713 G>T maps to NM_001173523.1 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:67801462 G>T maps to NM_203487.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:67801462 G>T maps to NM_203487.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140250067 C>A maps to NM_018902.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140250067 C>A maps to NM_018902.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140255857 C>A maps to NM_018903.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140255857 C>A maps to NM_018903.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140261960 C>A maps to NM_018904.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140261960 C>A maps to NM_018904.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140166267 C>A maps to NM_018900.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140166267 C>A maps to NM_018900.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140209559 G>T maps to NM_018909.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140209559 G>T maps to NM_018909.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140307445 C>A maps to NM_018898.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140307445 C>A maps to NM_018898.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140516258 G>T maps to NM_015669.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140516258 G>T maps to NM_015669.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140794434 G>T maps to NM_018913.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140794434 G>T maps to NM_018913.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140812020 C>A maps to NM_003735.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140812020 C>A maps to NM_003735.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140812290 C>A maps to NM_003735.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140812290 C>A maps to NM_003735.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140755329 C>A maps to NM_018919.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140755329 C>A maps to NM_018919.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140751310 C>A maps to NM_018924.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140751310 C>A maps to NM_018924.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140769755 G>T maps to NM_003736.2 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140769755 G>T maps to NM_003736.2 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140779763 G>T maps to NM_018925.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140779763 G>T maps to NM_018925.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140890718 G>T maps to NM_018915.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140890718 G>T maps to NM_018915.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113832529 G>T maps to ENST00000246505 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113832529 G>T maps to ENST00000246505 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113834491 C>A maps to ENST00000246505 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113834491 C>A maps to ENST00000246505 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82579025 G>T maps to NM_033026.5 P3626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82579025 G>T maps to NM_033026.5 P3626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82580167 G>T maps to NM_033026.5 R3246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82580167 G>T maps to NM_033026.5 R3246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82581607 G>T maps to NM_033026.5 T2887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82581607 G>T maps to NM_033026.5 T2887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82583254 G>T maps to NM_033026.5 T2338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82583254 G>T maps to NM_033026.5 T2338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82583284 G>T maps to NM_033026.5 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82583284 G>T maps to NM_033026.5 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82584993 G>T maps to NM_033026.5 R1759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82584993 G>T maps to NM_033026.5 R1759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82585385 G>T maps to NM_033026.5 S1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82585385 G>T maps to NM_033026.5 S1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82585431 G>T maps to NM_033026.5 R1613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82585431 G>T maps to NM_033026.5 R1613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82764321 G>T maps to NM_033026.5 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:82764321 G>T maps to NM_033026.5 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150111158 G>T maps to NM_005389.2 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150111158 G>T maps to NM_005389.2 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62891390 C>A maps to NM_018257.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62891390 C>A maps to NM_018257.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62891527 G>T maps to NM_018257.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62891527 G>T maps to NM_018257.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47805796 C>A maps to NM_006031.5 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47805796 C>A maps to NM_006031.5 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47860063 C>A maps to NM_006031.5 P3114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47860063 C>A maps to NM_006031.5 P3114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:233388418 G>T maps to NM_014801.3 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:233388418 G>T maps to NM_014801.3 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:233394269 G>T maps to NM_014801.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:233394269 G>T maps to NM_014801.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142542410 C>A maps to NM_013363.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142542410 C>A maps to NM_013363.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100201055 C>A maps to NM_002593.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100201055 C>A maps to NM_002593.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17437054 C>G maps to NM_002594.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17437054 C>G maps to NM_002594.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78547358 C>A maps to NM_001190482.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78547358 C>A maps to NM_001190482.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78638724 G>T maps to NM_001190482.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78638724 G>T maps to NM_001190482.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78686741 G>T maps to NM_001190482.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78686741 G>T maps to NM_001190482.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78772037 C>A maps to NM_001190482.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78772037 C>A maps to NM_001190482.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101933521 G>T maps to NM_002570.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101933521 G>T maps to NM_002570.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105162948 C>A maps to NM_014976.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105162948 C>A maps to NM_014976.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105165755 C>A maps to NM_014976.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105165755 C>A maps to NM_014976.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:112649295 G>T maps to NM_014456.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:112649295 G>T maps to NM_014456.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:112649343 C>A maps to NM_014456.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:112649343 C>A maps to NM_014456.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57542675 C>A maps to NM_177966.5 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57542675 C>A maps to NM_177966.5 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:183053787 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:183053787 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54966413 G>T maps to NM_000924.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54966413 G>T maps to NM_000924.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31862735 C>A maps to NM_001191057.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31862735 C>A maps to NM_001191057.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31918657 G>T maps to NM_001191057.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31918657 G>T maps to NM_001191057.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144854617 G>T maps to NM_014644.4 T2284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144854617 G>T maps to NM_014644.4 T2284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144854656 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144854656 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144864154 G>T maps to NM_014644.4 S1980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144864154 G>T maps to NM_014644.4 S1980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144865924 G>T maps to NM_014644.4 S1885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144865924 G>T maps to NM_014644.4 S1885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144867924 G>T maps to NM_014644.4 P1838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144867924 G>T maps to NM_014644.4 P1838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144867930 G>T maps to NM_014644.4 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144867930 G>T maps to NM_014644.4 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144874690 G>T maps to NM_014644.4 P1639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144874690 G>T maps to NM_014644.4 P1639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144877239 G>T maps to NM_014644.4 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144877239 G>T maps to NM_014644.4 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144879456 G>T maps to NM_014644.4 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144879456 G>T maps to NM_014644.4 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144882847 C>A maps to NM_014644.4 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144882847 C>A maps to NM_014644.4 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144886113 G>T maps to NM_014644.4 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144886113 G>T maps to NM_014644.4 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144892566 G>T maps to NM_014644.4 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144892566 G>T maps to NM_014644.4 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144903190 G>T maps to NM_014644.4 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144903190 G>T maps to NM_014644.4 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144923770 G>T maps to NM_014644.4 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144923770 G>T maps to NM_014644.4 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145021124 C>A maps to NM_001198832.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145021124 C>A maps to NM_001198832.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:58273130 C>A maps to NM_001104631.1 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:58273130 C>A maps to NM_001104631.1 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120460114 C>A maps to NM_001083.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120460114 C>A maps to NM_001083.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17447160 C>A maps to NM_006207.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17447160 C>A maps to NM_006207.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44055348 C>A maps to NM_005313.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44055348 C>A maps to NM_005313.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44061819 C>G maps to NM_005313.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44061819 C>G maps to NM_005313.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148701245 G>T maps to NM_004911.4 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148701245 G>T maps to NM_004911.4 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148716216 G>T maps to NM_004911.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148716216 G>T maps to NM_004911.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10924446 G>T maps to ENST00000381611 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10924446 G>T maps to ENST00000381611 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10929924 G>T maps to ENST00000381611 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10929924 G>T maps to ENST00000381611 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26448528 C>A maps to NM_152835.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26448528 C>A maps to NM_152835.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:26998605 G>T maps to NM_014317.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:26998605 G>T maps to NM_014317.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:26998665 C>A maps to NM_014317.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:26998665 C>A maps to NM_014317.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32000346 G>T maps to NM_178140.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32000346 G>T maps to NM_178140.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32010443 C>A maps to NM_178140.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32010443 C>A maps to NM_178140.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32052796 C>A maps to NM_178140.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32052796 C>A maps to NM_178140.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32053873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32053873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32088185 G>T maps to NM_178140.2 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32088185 G>T maps to NM_178140.2 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32090174 G>T maps to NM_178140.2 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32090174 G>T maps to NM_178140.2 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:119043327 G>T maps to NM_173791.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:119043327 G>T maps to NM_173791.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:41946514 C>A maps to NM_001164595.1 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:41946514 C>A maps to NM_001164595.1 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156880143 C>A maps to NM_001080471.1 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156880143 C>A maps to NM_001080471.1 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118577321 C>A maps to NM_002567.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118577321 C>A maps to NM_002567.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:4125501 G>T maps to NM_206836.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:4125501 G>T maps to NM_206836.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:4131003 G>T maps to NM_206836.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:4131003 G>T maps to NM_206836.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216914012 G>T maps to NM_018441.5 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216914012 G>T maps to NM_018441.5 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216930059 C>A maps to NM_018441.5 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216930059 C>A maps to NM_018441.5 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57333026 G>T maps to NM_006210.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57333026 G>T maps to NM_006210.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66239884 C>A maps to NM_145065.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66239884 C>A maps to NM_145065.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:239157732 C>A maps to NM_022817.2 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:239157732 C>A maps to NM_022817.2 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:239185824 G>T maps to NM_022817.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:239185824 G>T maps to NM_022817.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:152640660 C>A maps to NM_004564.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:152640660 C>A maps to NM_004564.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92120644 G>T maps to NM_000466.2 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92120644 G>T maps to NM_000466.2 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92123851 G>T maps to NM_000466.2 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92123851 G>T maps to NM_000466.2 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137191047 G>T maps to NM_000288.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137191047 G>T maps to NM_000288.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207237134 C>A maps to NM_006212.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207237134 C>A maps to NM_006212.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48577179 G>T maps to NM_004567.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48577179 G>T maps to NM_004567.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45745065 G>T maps to NM_002626.4 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45745065 G>T maps to NM_002626.4 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:3175424 C>A maps to NM_002627.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:3175424 C>A maps to NM_002627.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:3176764 C>A maps to NM_002627.3 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:3176764 C>A maps to NM_002627.3 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:197784828 C>A maps to NM_024989.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:197784828 C>A maps to NM_024989.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28268648 C>A maps to NM_032507.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28268648 C>A maps to NM_032507.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:249211397 C>A maps to NM_170725.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:249211397 C>A maps to NM_170725.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:249212556 C>A maps to NM_170725.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:249212556 C>A maps to NM_170725.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50724749 G>T maps to ENST00000515869 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50724749 G>T maps to ENST00000515869 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:64095712 G>T maps to NM_002633.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:64095712 G>T maps to NM_002633.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118377202 C>A maps to NM_006667.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118377202 C>A maps to NM_006667.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144033157 G>T maps to NM_001100164.1 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144033157 G>T maps to NM_001100164.1 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144033195 C>A maps to NM_001100164.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144033195 C>A maps to NM_001100164.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58381175 C>A maps to NM_080672.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58381175 C>A maps to NM_080672.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28807114 C>A maps to NM_023923.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28807114 C>A maps to NM_023923.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33832978 C>A maps to ENST00000419414 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33832978 C>A maps to ENST00000419414 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169896574 G>T maps to NM_024947.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169896574 G>T maps to NM_024947.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:22095660 C>A maps to NM_000444.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:22095660 C>A maps to NM_000444.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:129767660 G>T maps to NM_199320.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:129767660 G>T maps to NM_199320.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33383372 C>A maps to NM_024165.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33383372 C>A maps to NM_024165.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34515763 C>A maps to NM_016436.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34515763 C>A maps to NM_016436.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:45309779 G>T maps to NM_138415.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:45309779 G>T maps to NM_138415.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96439897 C>A maps to NM_005392.3 T1077T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96439897 C>A maps to NM_005392.3 T1077T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:64394351 G>T maps to NM_015153.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:64394351 G>T maps to NM_015153.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120263833 C>A maps to NM_006623.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120263833 C>A maps to NM_006623.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18958166 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18958166 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30762912 G>T maps to NM_000294.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30762912 G>T maps to NM_000294.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118486843 G>T maps to NM_015157.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118486843 G>T maps to NM_015157.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111603694 C>A maps to NM_001134438.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111603694 C>A maps to NM_001134438.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111637978 C>A maps to NM_001134438.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111637978 C>A maps to NM_001134438.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111685540 C>A maps to NM_001134438.1 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111685540 C>A maps to NM_001134438.1 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:60563127 C>A maps to NM_194449.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:60563127 C>A maps to NM_194449.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71689260 G>T maps to NM_015020.2 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71689260 G>T maps to NM_015020.2 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71703182 G>T maps to NM_015020.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71703182 G>T maps to NM_015020.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71715676 G>T maps to NM_015020.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71715676 G>T maps to NM_015020.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:77558439 G>T maps to ENST00000427986 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:77558439 G>T maps to ENST00000427986 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61005083 G>T maps to NM_032439.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:61005083 G>T maps to NM_032439.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36930831 G>T maps to NM_153370.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36930831 G>T maps to NM_153370.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36931674 G>T maps to NM_153370.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36931674 G>T maps to NM_153370.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21188861 G>T maps to NM_058004.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21188861 G>T maps to NM_058004.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145578220 C>A maps to NM_006099.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145578220 C>A maps to NM_006099.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172411766 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172411766 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:509795 G>T maps to NM_001127178.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:509795 G>T maps to NM_001127178.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:517252 C>A maps to NM_001127178.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:517252 C>A maps to NM_001127178.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207104856 G>T maps to NM_002644.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207104856 G>T maps to NM_002644.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207107966 C>A maps to NM_002644.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207107966 C>A maps to NM_002644.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49950316 G>T maps to NM_017916.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49950316 G>T maps to NM_017916.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98355345 G>T maps to NM_152309.2 P802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98355345 G>T maps to NM_152309.2 P802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98376434 G>T maps to NM_152309.2 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98376434 G>T maps to NM_152309.2 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204401450 C>A maps to NM_002646.3 T1344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204401450 C>A maps to NM_002646.3 T1344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204438111 G>T maps to NM_002646.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204438111 G>T maps to NM_002646.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:39575889 C>A maps to ENST00000398870 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:39575889 C>A maps to ENST00000398870 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:178917542 C>A maps to NM_006218.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:178917542 C>A maps to NM_006218.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:67569287 C>A maps to ENST00000396611 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:67569287 C>A maps to ENST00000396611 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130452743 G>T maps to NM_014602.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130452743 G>T maps to NM_014602.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209185026 G>T maps to NM_015040.3 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209185026 G>T maps to NM_015040.3 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209190486 G>T maps to NM_015040.3 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209190486 G>T maps to NM_015040.3 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209215631 C>A maps to NM_015040.3 R1858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209215631 C>A maps to NM_015040.3 R1858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57992901 C>A maps to NM_024779.4 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57992901 C>A maps to NM_024779.4 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151171528 C>A maps to NM_001135638.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151171528 C>A maps to NM_001135638.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:71555565 G>T maps to NM_003558.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:71555565 G>T maps to NM_003558.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123489907 C>A maps to NM_020845.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123489907 C>A maps to NM_020845.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:111554124 C>A maps to NM_153426.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:111554124 C>A maps to NM_153426.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:130839523 G>T maps to NM_004764.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:130839523 G>T maps to NM_004764.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88957412 C>A maps to NM_000297.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88957412 C>A maps to NM_000297.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88959449 C>A maps to NM_000297.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88959449 C>A maps to NM_000297.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88996608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88996608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110445368 G>T maps to ENST00000426474 V1088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110445368 G>T maps to ENST00000426474 V1088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110453070 C>A maps to ENST00000426474 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110453070 C>A maps to ENST00000426474 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110476965 G>T maps to ENST00000426474 T2635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110476965 G>T maps to ENST00000426474 T2635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110477009 C>A maps to ENST00000426474 S2650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110477009 C>A maps to ENST00000426474 S2650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72502118 C>A maps to ENST00000419739 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72502118 C>A maps to ENST00000419739 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:89273441 C>A maps to NM_006256.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:89273441 C>A maps to NM_006256.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201297955 C>A maps to NM_000299.3 R746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201297955 C>A maps to NM_000299.3 R746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32955363 G>T maps to NM_004572.3 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32955363 G>T maps to NM_004572.3 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32994065 C>A maps to NM_004572.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32994065 C>A maps to NM_004572.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119327615 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119327615 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120763749 C>A maps to NM_000928.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120763749 C>A maps to NM_000928.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48578087 G>T maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48578087 G>T maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59814542 C>A maps to NM_173801.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59814542 C>A maps to NM_173801.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28764629 C>A maps to NM_153021.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28764629 C>A maps to NM_153021.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28812873 G>C maps to NM_153021.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28812873 G>C maps to NM_153021.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64021951 G>T maps to NM_000932.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64021951 G>T maps to NM_000932.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38052735 G>T maps to NM_001130964.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38052735 G>T maps to NM_001130964.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96084128 C>A maps to ENST00000371380 S2175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96084128 C>A maps to ENST00000371380 S2175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155199944 C>A maps to ENST00000340059 A1298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155199944 C>A maps to ENST00000340059 A1298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155210567 C>A maps to ENST00000340059 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155210567 C>A maps to ENST00000340059 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198948756 G>T maps to NM_006226.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198948756 G>T maps to NM_006226.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:17056328 G>T maps to NM_001144382.1 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:17056328 G>T maps to NM_001144382.1 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:205461 C>A maps to NM_018390.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:205461 C>A maps to NM_018390.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111432756 C>A maps to ENST00000312791 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111432756 C>A maps to ENST00000312791 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41381986 G>T maps to NM_001005473.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41381986 G>T maps to NM_001005473.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:171404501 C>A maps to NM_002662.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:171404501 C>A maps to NM_002662.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144991277 C>A maps to NM_201380.2 S4374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144991277 C>A maps to NM_201380.2 S4374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124159890 G>T maps to NM_021622.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124159890 G>T maps to NM_021622.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204218322 G>T maps to ENST00000367191 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204218322 G>T maps to ENST00000367191 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204237353 C>A maps to ENST00000367191 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204237353 C>A maps to ENST00000367191 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16838769 C>A maps to ENST00000448080 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16838769 C>A maps to ENST00000448080 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16877352 G>T maps to ENST00000448080 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16877352 G>T maps to ENST00000448080 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151054843 C>A maps to NM_001029884.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151054843 C>A maps to NM_001029884.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:143261 C>A maps to NM_052909.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:143261 C>A maps to NM_052909.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93135355 C>A maps to NM_001004330.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93135355 C>A maps to NM_001004330.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93163949 C>A maps to NM_001004330.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93163949 C>A maps to NM_001004330.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:68052796 C>A maps to NM_020715.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:68052796 C>A maps to NM_020715.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68622933 C>A maps to NM_002664.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:68622933 C>A maps to NM_002664.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4511907 C>A maps to NM_001080400.1 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4511907 C>A maps to NM_001080400.1 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45270366 C>A maps to NM_004073.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45270366 C>A maps to NM_004073.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45271230 C>A maps to NM_004073.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45271230 C>A maps to NM_004073.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12030750 G>T maps to ENST00000376369 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12030750 G>T maps to ENST00000376369 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:49029743 C>A maps to NM_002668.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:49029743 C>A maps to NM_002668.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:114883776 G>T maps to NM_001136025.3 G597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:114883776 G>T maps to NM_001136025.3 G597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:146251311 C>A maps to NM_021105.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:146251311 C>A maps to NM_021105.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:20466284 C>A maps to NM_032812.7 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:20466284 C>A maps to NM_032812.7 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126708342 G>T maps to NM_032242.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126708342 G>T maps to NM_032242.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126736641 G>T maps to NM_032242.3 T1189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126736641 G>T maps to NM_032242.3 T1189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208201377 G>T maps to NM_025179.3 S1855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208201377 G>T maps to NM_025179.3 S1855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208269408 G>T maps to NM_025179.3 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208269408 G>T maps to NM_025179.3 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208390487 G>T maps to NM_025179.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208390487 G>T maps to NM_025179.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131844253 G>T maps to NM_020911.1 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131844253 G>T maps to NM_020911.1 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131864551 C>A maps to NM_020911.1 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131864551 C>A maps to NM_020911.1 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131872278 C>A maps to NM_020911.1 G982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131872278 C>A maps to NM_020911.1 G982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:132192498 C>A maps to NM_020911.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:132192498 C>A maps to NM_020911.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94641722 C>A maps to NM_005761.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94641722 C>A maps to NM_005761.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94658863 G>T maps to NM_005761.1 G1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94658863 G>T maps to NM_005761.1 G1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129278491 G>T maps to NM_015103.2 P1756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129278491 G>T maps to NM_015103.2 P1756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129289909 G>T maps to NM_015103.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129289909 G>T maps to NM_015103.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102590449 G>T maps to NM_002674.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102590449 G>T maps to NM_002674.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:82357158 C>A maps to NM_002677.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:82357158 C>A maps to NM_002677.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:102939026 G>T maps to NM_004279.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:102939026 G>T maps to NM_004279.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190728663 C>A maps to NM_000534.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190728663 C>A maps to NM_000534.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6026415 G>T maps to NM_000535.5 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6026415 G>T maps to NM_000535.5 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6045571 C>A maps to NM_000535.5 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6045571 C>A maps to NM_000535.5 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118351990 C>A maps to NM_006229.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118351990 C>A maps to NM_006229.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118359628 C>A maps to NM_006229.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118359628 C>A maps to NM_006229.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:26365707 G>T maps to NM_007257.5 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:26365707 G>T maps to NM_007257.5 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:108119727 C>A maps to NM_015723.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:108119727 C>A maps to NM_015723.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131195680 C>A maps to NM_001018111.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131195680 C>A maps to NM_001018111.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:46698080 G>T maps to NM_133635.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:46698080 G>T maps to NM_133635.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151377879 G>T maps to NM_015100.3 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151377879 G>T maps to NM_015100.3 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151378840 C>A maps to NM_015100.3 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151378840 C>A maps to NM_015100.3 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151381202 G>T maps to NM_015100.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151381202 G>T maps to NM_015100.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65061707 C>A maps to NM_002689.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65061707 C>A maps to NM_002689.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50906781 C>A maps to ENST00000391817 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50906781 C>A maps to ENST00000391817 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133234519 C>A maps to ENST00000455752 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133234519 C>A maps to ENST00000455752 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2172441 C>A maps to NM_181808.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2172441 C>A maps to NM_181808.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121212467 C>A maps to ENST00000393672 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121212467 C>A maps to ENST00000393672 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121238732 C>A maps to ENST00000393672 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121238732 C>A maps to ENST00000393672 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86258545 G>T maps to NM_015425.3 P1495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86258545 G>T maps to NM_015425.3 P1495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86266539 G>C maps to NM_015425.3 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86266539 G>C maps to NM_015425.3 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113306888 C>A maps to NM_019014.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113306888 C>A maps to NM_019014.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57861527 C>A maps to NM_000938.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57861527 C>A maps to NM_000938.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57883388 C>A maps to NM_000938.1 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57883388 C>A maps to NM_000938.1 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57504901 G>T maps to NM_032940.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57504901 G>T maps to NM_032940.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62532698 C>A maps to NM_002696.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62532698 C>A maps to NM_002696.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184082993 C>A maps to NM_006232.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184082993 C>A maps to NM_006232.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:840406 C>A maps to NM_021128.4 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:840406 C>A maps to NM_021128.4 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:79744964 G>T maps to NM_007055.3 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:79744964 G>T maps to NM_007055.3 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:79760813 C>A maps to NM_007055.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:79760813 C>A maps to NM_007055.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145592704 G>T maps to NM_006468.6 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145592704 G>T maps to NM_006468.6 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145595144 G>T maps to NM_006468.6 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145595144 G>T maps to NM_006468.6 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95035508 C>A maps to NM_000305.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95035508 C>A maps to NM_000305.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99170453 C>A maps to NM_015029.2 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99170453 C>A maps to NM_015029.2 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:30099606 C>A maps to NM_006627.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:30099606 C>A maps to NM_006627.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:105609468 G>T maps to NM_022361.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:105609468 G>T maps to NM_022361.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38153364 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38153364 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:130832625 C>A maps to NM_001099771.2 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:130832625 C>A maps to NM_001099771.2 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:122334703 C>A maps to NM_001030059.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:122334703 C>A maps to NM_001030059.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:122348824 G>T maps to NM_001030059.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:122348824 G>T maps to NM_001030059.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57265548 C>A maps to NM_002703.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57265548 C>A maps to NM_002703.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70171011 C>A maps to NM_003626.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70171011 C>A maps to NM_003626.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70208222 C>A maps to NM_003626.2 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70208222 C>A maps to NM_003626.2 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7650712 G>T maps to NM_003621.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7650712 G>T maps to NM_003621.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7652162 G>T maps to NM_003621.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7652162 G>T maps to NM_003621.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:143767731 C>A maps to NM_001123068.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:143767731 C>A maps to NM_001123068.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170487392 C>A maps to NM_004792.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170487392 C>A maps to NM_004792.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:149855897 C>A maps to NM_139126.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:149855897 C>A maps to NM_139126.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:102472454 G>T maps to ENST00000451606 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:102472454 G>T maps to ENST00000451606 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27609146 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27609146 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:160474164 C>A maps to NM_139245.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:160474164 C>A maps to NM_139245.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:111160001 C>A maps to NM_002710.2 G274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:111160001 C>A maps to NM_002710.2 G274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30571942 C>A maps to NM_002714.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30571942 C>A maps to NM_002714.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30572488 C>A maps to NM_002714.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30572488 C>A maps to NM_002714.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:80199974 C>A maps to NM_001143885.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:80199974 C>A maps to NM_001143885.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:113519423 G>T maps to NM_002711.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:113519423 G>T maps to NM_002711.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:113519997 G>T maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:113519997 G>T maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48216820 G>T maps to NM_032595.3 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48216820 G>T maps to NM_032595.3 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111625730 G>T maps to NM_181699.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111625730 G>T maps to NM_181699.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111625770 G>T maps to NM_181699.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111625770 G>T maps to NM_181699.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111636104 G>T maps to NM_181699.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111636104 G>T maps to NM_181699.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30096340 G>T maps to NM_002720.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30096340 G>T maps to NM_002720.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103899381 C>A maps to NM_015062.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103899381 C>A maps to NM_015062.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12884886 G>T maps to NM_001146344.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12884886 G>T maps to NM_001146344.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11461355 G>T maps to NM_002723.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11461355 G>T maps to NM_002723.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11461396 G>T maps to NM_002723.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11461396 G>T maps to NM_002723.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91527304 G>T maps to NM_003981.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91527304 G>T maps to NM_003981.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43222982 C>G maps to NM_022115.3 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43222982 C>G maps to NM_022115.3 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43259869 G>T maps to NM_022115.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43259869 G>T maps to NM_022115.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:14107076 G>T maps to NM_012231.4 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:14107076 G>T maps to NM_012231.4 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23509577 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23509577 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23509616 C>A maps to NM_020227.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23509616 C>A maps to NM_020227.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27356071 G>T maps to NM_013388.4 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27356071 G>T maps to NM_013388.4 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203452761 C>A maps to NM_201348.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203452761 C>A maps to NM_201348.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44549894 C>A maps to NM_001171603.1 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44549894 C>A maps to NM_001171603.1 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:105781309 C>A maps to NM_002726.4 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:105781309 C>A maps to NM_002726.4 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47317358 C>A maps to NM_020820.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47317358 C>A maps to NM_020820.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47324917 G>T maps to NM_020820.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47324917 G>T maps to NM_020820.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57146263 C>A maps to NM_006093.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57146263 C>A maps to NM_006093.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40763077 C>A maps to NM_206907.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40763077 C>A maps to NM_206907.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219694796 G>T maps to NM_017431.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219694796 G>T maps to NM_017431.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:66521095 G>T maps to NM_212472.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:66521095 G>T maps to NM_212472.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:645867 C>A maps to NM_002735.2 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:645867 C>A maps to NM_002735.2 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:24196863 G>A maps to NM_002738.6 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:24196863 G>A maps to NM_002738.6 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:54406343 C>A maps to NM_002739.3 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:54406343 C>A maps to NM_002739.3 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6506332 C>A maps to NM_006257.2 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6506332 C>A maps to NM_006257.2 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6527123 C>A maps to NM_006257.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6527123 C>A maps to NM_006257.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6539184 G>T maps to NM_006257.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6539184 G>T maps to NM_006257.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35065831 C>A maps to NM_000949.4 G410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35065831 C>A maps to NM_000949.4 G410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35072697 G>T maps to NM_000949.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35072697 G>T maps to NM_000949.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:148594114 G>T maps to NM_138364.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:148594114 G>T maps to NM_138364.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20413770 G>T maps to NM_005788.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20413770 G>T maps to NM_005788.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27031385 C>A maps to ENST00000415329 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27031385 C>A maps to ENST00000415329 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27031410 C>A maps to ENST00000415329 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27031410 C>A maps to ENST00000415329 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186120 G>T maps to ENST00000409048 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186120 G>T maps to ENST00000409048 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186155 G>T maps to ENST00000409048 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186155 G>T maps to ENST00000409048 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186233 C>A maps to ENST00000409048 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186233 C>A maps to ENST00000409048 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186443 C>A maps to ENST00000409048 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128186443 C>A maps to ENST00000409048 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93595864 G>T maps to NM_000313.3 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93595864 G>T maps to NM_000313.3 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214171296 G>T maps to NM_002763.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214171296 G>T maps to NM_002763.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116038959 G>T maps to NM_004697.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116038959 G>T maps to NM_004697.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30666517 C>A maps to NM_024031.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30666517 C>A maps to NM_024031.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30667517 C>A maps to NM_024031.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30667517 C>A maps to NM_024031.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10999780 G>T maps to NM_007244.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10999780 G>T maps to NM_007244.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:45218337 C>A maps to ENST00000352766 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:45218337 C>A maps to ENST00000352766 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119204016 G>T maps to NM_003619.3 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119204016 G>T maps to NM_003619.3 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:84233436 C>A maps to NM_153362.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:84233436 C>A maps to NM_153362.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141537010 G>T maps to NM_001008270.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141537010 G>T maps to NM_001008270.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:10387197 C>A maps to NM_198464.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:10387197 C>A maps to NM_198464.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79320640 G>T maps to NM_015225.2 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79320640 G>T maps to NM_015225.2 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79323876 G>T maps to NM_015225.2 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79323876 G>T maps to NM_015225.2 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150990293 C>A maps to NM_021222.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150990293 C>A maps to NM_021222.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150998031 G>T maps to NM_021222.1 G188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150998031 G>T maps to NM_021222.1 G188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:80921329 C>A maps to ENST00000421149 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:80921329 C>A maps to ENST00000421149 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:80943902 G>T maps to ENST00000421149 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:80943902 G>T maps to ENST00000421149 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43233293 G>T maps to NM_021016.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43233293 G>T maps to NM_021016.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43702332 G>T maps to NM_002780.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43702332 G>T maps to NM_002780.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43674281 C>A maps to ENST00000270059 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43674281 C>A maps to ENST00000270059 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43680256 G>T maps to ENST00000270059 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43680256 G>T maps to ENST00000270059 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43415008 C>A maps to NM_002782.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43415008 C>A maps to NM_002782.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43420484 C>A maps to NM_002782.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43420484 C>A maps to NM_002782.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43439579 C>A maps to NM_002783.2 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43439579 C>A maps to NM_002783.2 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43772146 C>A maps to NM_002784.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43772146 C>A maps to NM_002784.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:15486851 G>T maps to NM_001128217.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:15486851 G>T maps to NM_001128217.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87060836 G>T maps to ENST00000276616 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87060836 G>T maps to ENST00000276616 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:35761735 C>A maps to NM_002791.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:35761735 C>A maps to NM_002791.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170844369 G>T maps to NM_002793.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170844369 G>T maps to NM_002793.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151373006 C>A maps to NM_002796.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151373006 C>A maps to NM_002796.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32809449 C>A maps to NM_148919.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32809449 C>A maps to NM_148919.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32823968 C>A maps to NM_002800.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32823968 C>A maps to NM_002800.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47444403 G>T maps to NM_002804.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47444403 G>T maps to NM_002804.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:251915 C>A maps to NM_002817.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:251915 C>A maps to NM_002817.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184026292 C>A maps to NM_002808.3 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184026292 C>A maps to NM_002808.3 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151239680 C>A maps to ENST00000368881 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151239680 C>A maps to ENST00000368881 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:54147373 G>T maps to NM_014614.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:54147373 G>T maps to NM_014614.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:20304443 G>T maps to NM_001042414.1 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:20304443 G>T maps to NM_001042414.1 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43577752 G>T maps to NM_024430.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43577752 G>T maps to NM_024430.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28476560 C>A maps to NM_001164721.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28476560 C>A maps to NM_001164721.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97216979 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97216979 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99027402 C>A maps to NM_001198879.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99027402 C>A maps to NM_001198879.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45292589 C>A maps to NM_003738.4 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45292589 C>A maps to NM_003738.4 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27702138 G>T maps to NM_001034842.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27702138 G>T maps to NM_001034842.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16528529 G>A maps to NM_030664.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16528529 G>A maps to NM_030664.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40681106 C>A maps to NM_000958.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40681106 C>A maps to NM_000958.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40681502 G>T maps to NM_000958.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40681502 G>T maps to NM_000958.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57065610 C>A maps to NM_006601.5 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57065610 C>A maps to NM_006601.5 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117491893 C>A maps to NM_020440.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117491893 C>A maps to NM_020440.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117509536 C>A maps to NM_020440.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117509536 C>A maps to NM_020440.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117527515 C>A maps to NM_020440.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117527515 C>A maps to NM_020440.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125140265 G>T maps to NM_000962.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125140265 G>T maps to NM_000962.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209353826 C>T maps to NM_005048.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209353826 C>T maps to NM_005048.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:28116414 G>T maps to ENST00000354417 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:28116414 G>T maps to ENST00000354417 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141810557 C>A maps to NM_005607.4 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141810557 C>A maps to NM_005607.4 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141889715 C>A maps to NM_005607.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141889715 C>A maps to NM_005607.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142437070 C>A maps to NM_032611.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:142437070 C>A maps to NM_032611.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17636293 C>A maps to NM_014241.3 G232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17636293 C>A maps to NM_014241.3 G232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:87724934 G>T maps to NM_080685.2 T2198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:87724934 G>T maps to NM_080685.2 T2198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214542998 G>T maps to NM_005401.4 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214542998 G>T maps to NM_005401.4 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:49195730 C>A maps to NM_002827.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:49195730 C>A maps to NM_002827.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:112225660 C>A maps to NM_002829.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:112225660 C>A maps to NM_002829.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7064608 C>A maps to ENST00000416215 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7064608 C>A maps to ENST00000416215 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:70974879 G>T maps to NM_001109754.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:70974879 G>T maps to NM_001109754.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:70983831 C>A maps to NM_001109754.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:70983831 C>A maps to NM_001109754.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:8341728 C>A maps to NM_002839.3 T1637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:8341728 C>A maps to NM_002839.3 T1637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:8636818 G>T maps to NM_002839.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:8636818 G>T maps to NM_002839.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:62153673 G>T maps to NM_002841.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:62153673 G>T maps to NM_002841.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55711726 G>T maps to NM_002842.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55711726 G>T maps to NM_002842.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55718095 C>A maps to NM_002842.3 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55718095 C>A maps to NM_002842.3 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:48145327 G>T maps to NM_002843.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:48145327 G>T maps to NM_002843.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:48186003 C>A maps to NM_002843.3 T1264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:48186003 C>A maps to NM_002843.3 T1264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:15704549 G>T maps to NM_030667.1 G835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:15704549 G>T maps to NM_030667.1 G835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:71286757 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:71286757 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:157160201 G>T maps to NM_002852.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:157160201 G>T maps to NM_002852.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:31440089 C>A maps to ENST00000373741 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:31440089 C>A maps to ENST00000373741 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20463218 C>A maps to ENST00000361078 G654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20463218 C>A maps to ENST00000361078 G654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61194729 C>A maps to NM_144709.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61194729 C>A maps to NM_144709.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:44142332 C>A maps to NM_031292.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:44142332 C>A maps to NM_031292.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:110852527 C>A maps to NM_015480.1 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:110852527 C>A maps to NM_015480.1 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108104180 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108104180 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159520765 G>T maps to NM_001130864.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159520765 G>T maps to NM_001130864.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1653121 G>T maps to NM_012293.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1653121 G>T maps to NM_012293.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58382894 C>A maps to NM_017771.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58382894 C>A maps to NM_017771.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58383447 G>T maps to NM_017771.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58383447 G>T maps to NM_017771.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25277052 G>T maps to NM_002862.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25277052 G>T maps to NM_002862.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:163899895 C>A maps to ENST00000361752 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:163899895 C>A maps to ENST00000361752 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29706198 C>A maps to NM_014298.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29706198 C>A maps to NM_014298.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49070103 C>A maps to NM_198880.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49070103 C>A maps to NM_198880.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49114404 G>T maps to NM_198880.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49114404 G>T maps to NM_198880.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74272769 G>T maps to NM_032134.1 R1616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74272769 G>T maps to NM_032134.1 R1616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74286114 G>T maps to NM_032134.1 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74286114 G>T maps to NM_032134.1 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32975562 C>A maps to NM_001076786.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32975562 C>A maps to NM_001076786.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113798788 C>A maps to ENST00000485050 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113798788 C>A maps to ENST00000485050 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136396537 G>T maps to ENST00000409606 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136396537 G>T maps to ENST00000409606 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42979315 G>T maps to NM_178491.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42979315 G>T maps to NM_178491.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37729384 C>A maps to NM_001002814.2 G979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37729384 C>A maps to NM_001002814.2 G979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37730363 C>A maps to NM_001002814.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37730363 C>A maps to NM_001002814.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37732223 C>A maps to NM_001002814.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37732223 C>A maps to NM_001002814.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37732817 C>A maps to NM_001002814.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37732817 C>A maps to NM_001002814.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:119799847 G>T maps to ENST00000369199 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:119799847 G>T maps to ENST00000369199 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73303310 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73303310 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:57055315 G>T maps to NM_016277.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:57055315 G>T maps to NM_016277.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55497749 C>A maps to NM_183235.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55497749 C>A maps to NM_183235.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:87882995 G>T maps to NM_022337.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:87882995 G>T maps to NM_022337.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:87883084 G>T maps to NM_022337.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:87883084 G>T maps to NM_022337.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154490408 G>T maps to NM_171998.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154490408 G>T maps to NM_171998.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11447910 C>A maps to NM_004283.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11447910 C>A maps to NM_004283.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135911338 C>A maps to NM_001172435.1 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135911338 C>A maps to NM_001172435.1 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135920603 C>A maps to NM_001172435.1 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135920603 C>A maps to NM_001172435.1 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220383744 G>T maps to ENST00000358951 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220383744 G>T maps to ENST00000358951 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61665793 C>A maps to NM_013401.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61665793 C>A maps to NM_013401.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128878015 G>T maps to ENST00000418265 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128878015 G>T maps to ENST00000418265 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40282427 C>A maps to NM_201434.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40282427 C>A maps to NM_201434.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:103080348 C>A maps to NM_016370.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:103080348 C>A maps to NM_016370.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125759581 G>T maps to NM_012197.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125759581 G>T maps to NM_012197.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125827653 C>A maps to NM_012197.3 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125827653 C>A maps to NM_012197.3 R608R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1039017 C>A maps to NM_134424.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1039017 C>A maps to NM_134424.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1042196 C>A maps to NM_134424.2 G10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1042196 C>A maps to NM_134424.2 G10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95405992 G>T maps to NM_012415.2 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95405992 G>T maps to NM_012415.2 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67163736 C>A maps to NM_004584.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67163736 C>A maps to NM_004584.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55949709 G>T maps to NM_001015885.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55949709 G>T maps to NM_001015885.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150210738 C>A maps to NM_139165.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150210738 C>A maps to NM_139165.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150240692 G>T maps to NM_001001788.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150240692 G>T maps to NM_001001788.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102700053 G>T maps to NM_014226.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102700053 G>T maps to NM_014226.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34796130 C>A maps to NM_001145521.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34796130 C>A maps to NM_001145521.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34811205 C>A maps to NM_001145521.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34811205 C>A maps to NM_001145521.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34823080 G>T maps to NM_001145521.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34823080 G>T maps to NM_001145521.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:20592070 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:20592070 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37121623 G>T maps to NM_020336.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37121623 G>T maps to NM_020336.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37137767 C>A maps to NM_020336.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37137767 C>A maps to NM_020336.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37146162 C>A maps to NM_020336.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37146162 C>A maps to NM_020336.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129931000 C>A maps to NM_014636.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129931000 C>A maps to NM_014636.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67778299 C>A maps to NM_020850.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67778299 C>A maps to NM_020850.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109368449 G>T maps to NM_006267.4 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109368449 G>T maps to NM_006267.4 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109374931 G>T maps to NM_006267.4 E844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109374931 G>T maps to NM_006267.4 E844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109384800 G>T maps to NM_006267.4 T2602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109384800 G>T maps to NM_006267.4 T2602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109388229 C>A maps to NM_006267.4 T2641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109388229 C>A maps to NM_006267.4 T2641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109389017 C>A maps to NM_006267.4 P2698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109389017 C>A maps to NM_006267.4 P2698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5928029 G>T maps to NM_007322.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5928029 G>T maps to NM_007322.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:99300252 C>A maps to NM_001100426.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:99300252 C>A maps to NM_001100426.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:160252865 C>A maps to NM_014247.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:160252865 C>A maps to NM_014247.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204304257 C>A maps to ENST00000374493 G1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204304257 C>A maps to ENST00000374493 G1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:25638004 C>A maps to NM_000965.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:25638004 C>A maps to NM_000965.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63312102 C>A maps to NM_004585.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63312102 C>A maps to NM_004585.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:88239335 C>A maps to NM_020320.3 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:88239335 C>A maps to NM_020320.3 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141295905 C>A maps to ENST00000452898 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141295905 C>A maps to ENST00000452898 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114781695 C>A maps to ENST00000389544 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114781695 C>A maps to ENST00000389544 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114782757 C>A maps to ENST00000389544 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114782757 C>A maps to ENST00000389544 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:178427490 C>A maps to ENST00000263528 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:178427490 C>A maps to ENST00000263528 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79284082 C>A maps to NM_002891.4 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79284082 C>A maps to NM_002891.4 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205069065 C>A maps to NM_005057.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205069065 C>A maps to NM_005057.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205073002 C>A maps to NM_005057.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205073002 C>A maps to NM_005057.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:402851 G>T maps to NM_031229.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:402851 G>T maps to NM_031229.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:94747621 G>T maps to NM_203390.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:94747621 G>T maps to NM_203390.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34242518 C>A maps to NM_001198838.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34242518 C>A maps to NM_001198838.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:155153496 G>T maps to NM_014892.3 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:155153496 G>T maps to NM_014892.3 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114386800 G>T maps to NM_016196.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114386800 G>T maps to NM_016196.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23378756 G>T maps to NM_001077351.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23378756 G>T maps to NM_001077351.1 T38T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127964699 C>A maps to NM_018077.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127964699 C>A maps to NM_018077.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50004929 C>A maps to NM_005777.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50004929 C>A maps to NM_005777.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50091791 C>A maps to NM_005777.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50091791 C>A maps to NM_005777.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:139173576 C>A maps to NM_004164.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:139173576 C>A maps to NM_004164.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173930918 C>A maps to NM_172071.2 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173930918 C>A maps to NM_172071.2 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:50134212 C>A maps to NM_018191.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:50134212 C>A maps to NM_018191.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50040425 C>A maps to NM_020650.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50040425 C>A maps to NM_020650.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:110104000 G>T maps to ENST00000405097 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:110104000 G>T maps to ENST00000405097 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24647852 G>T maps to NM_005132.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24647852 G>T maps to NM_005132.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73624384 G>T maps to NM_004259.5 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73624384 G>T maps to NM_004259.5 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120337248 G>T maps to NM_032044.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120337248 G>T maps to NM_032044.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65425947 C>A maps to NM_021975.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65425947 C>A maps to NM_021975.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:103214569 G>T maps to ENST00000428762 R1494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:103214569 G>T maps to ENST00000428762 R1494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:139237102 C>A maps to ENST00000367663 G538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:139237102 C>A maps to ENST00000367663 G538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:139266667 C>A maps to ENST00000367663 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:139266667 C>A maps to ENST00000367663 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:15262378 G>T maps to NM_032918.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:15262378 G>T maps to NM_032918.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111694769 G>T maps to NM_002912.3 P1596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111694769 G>T maps to NM_002912.3 P1596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111695258 C>A maps to NM_002912.3 A1433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111695258 C>A maps to NM_002912.3 A1433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:114320613 C>A maps to NM_015523.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:114320613 C>A maps to NM_015523.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136277473 G>T maps to NM_020385.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136277473 G>T maps to NM_020385.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136280010 C>A maps to NM_020385.2 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136280010 C>A maps to NM_020385.2 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39291551 C>A maps to ENST00000381897 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39291551 C>A maps to ENST00000381897 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39306548 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39306548 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33343424 G>T maps to NM_001017368.1 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33343424 G>T maps to NM_001017368.1 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53145849 T>C maps to NM_052859.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53145849 T>C maps to NM_052859.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16358349 C>A maps to NM_015150.1 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16358349 C>A maps to NM_015150.1 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176132950 G>T maps to NM_022457.5 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176132950 G>T maps to NM_022457.5 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74678305 G>T maps to NM_018124.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74678305 G>T maps to NM_018124.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106977124 C>A maps to NM_213594.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106977124 C>A maps to NM_213594.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:107075818 C>A maps to ENST00000357881 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:107075818 C>A maps to ENST00000357881 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:107144483 C>A maps to ENST00000357881 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:107144483 C>A maps to ENST00000357881 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33263861 C>A maps to NM_004761.3 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33263861 C>A maps to NM_004761.3 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33263912 G>T maps to NM_004761.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33263912 G>T maps to NM_004761.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:73072452 G>T maps to NM_001080479.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:73072452 G>T maps to NM_001080479.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:107041638 C>A maps to ENST00000304514 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:107041638 C>A maps to ENST00000304514 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108479412 C>A maps to NM_182588.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108479412 C>A maps to NM_182588.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108487243 G>T maps to NM_182588.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108487243 G>T maps to NM_182588.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:86012637 C>A maps to ENST00000358110 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:86012637 C>A maps to ENST00000358110 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3429820 C>A maps to NM_198229.2 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3429820 C>A maps to NM_198229.2 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:153347641 C>A maps to NM_012419.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:153347641 C>A maps to NM_012419.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:192316469 G>T maps to NM_001039152.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:192316469 G>T maps to NM_001039152.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101020676 C>A maps to NM_015668.3 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101020676 C>A maps to NM_015668.3 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101092400 G>T maps to NM_015668.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101092400 G>T maps to NM_015668.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75513109 C>A maps to NM_001040456.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75513109 C>A maps to NM_001040456.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:39384719 G>T maps to ENST00000372985 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:39384719 G>T maps to ENST00000372985 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49460259 G>T maps to NM_144593.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49460259 G>T maps to NM_144593.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:95087965 C>A maps to NM_014899.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:95087965 C>A maps to NM_014899.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:63749924 C>A maps to NM_020663.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:63749924 C>A maps to NM_020663.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:209513 G>C maps to NM_021932.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:209513 G>C maps to NM_021932.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:107237686 C>A maps to ENST00000392837 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:107237686 C>A maps to ENST00000392837 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38945090 C>A maps to ENST00000296782 S1595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38945090 C>A maps to ENST00000296782 S1595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38960544 C>A maps to ENST00000296782 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38960544 C>A maps to ENST00000296782 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38982000 G>T maps to ENST00000296782 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38982000 G>T maps to ENST00000296782 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38996958 C>A maps to ENST00000296782 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38996958 C>A maps to ENST00000296782 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152273180 C>A maps to NM_018151.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152273180 C>A maps to NM_018151.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152285371 C>A maps to NM_018151.4 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152285371 C>A maps to NM_018151.4 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152318979 G>T maps to NM_018151.4 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152318979 G>T maps to NM_018151.4 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:130929780 G>T maps to NM_015347.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:130929780 G>T maps to NM_015347.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:72968752 C>A maps to NM_014989.4 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:72968752 C>A maps to NM_014989.4 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:93022098 G>T maps to NM_024832.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:93022098 G>T maps to NM_024832.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:3596656 C>A maps to NM_002936.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:3596656 C>A maps to NM_002936.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31401630 C>A maps to NM_013235.4 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31401630 C>A maps to NM_013235.4 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31515208 G>T maps to NM_013235.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31515208 G>T maps to NM_013235.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121013670 C>A maps to ENST00000458409 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121013670 C>A maps to ENST00000458409 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:59381910 G>T maps to ENST00000434298 G875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:59381910 G>T maps to ENST00000434298 G875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119004571 G>T maps to NM_006978.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119004571 G>T maps to NM_006978.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29617090 C>A maps to NM_017831.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29617090 C>A maps to NM_017831.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29645890 C>A maps to NM_017831.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29645890 C>A maps to NM_017831.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18457455 G>T maps to NM_182757.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18457455 G>T maps to NM_182757.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:122342307 G>T maps to NM_198085.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:122342307 G>T maps to NM_198085.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101898360 G>T maps to NM_173647.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101898360 G>T maps to NM_173647.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:141358244 G>T maps to NM_183399.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:141358244 G>T maps to NM_183399.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:141359783 C>A maps to NM_183399.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:141359783 C>A maps to NM_183399.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30324530 G>T maps to NM_015565.2 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30324530 G>T maps to NM_015565.2 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30339393 C>A maps to NM_015565.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30339393 C>A maps to NM_015565.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74528741 C>A maps to NM_001098638.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74528741 C>A maps to NM_001098638.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25399894 C>A maps to ENST00000381927 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25399894 C>A maps to ENST00000381927 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101271373 G>T maps to NM_183419.1 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101271373 G>T maps to NM_183419.1 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101300023 C>A maps to NM_183419.1 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101300023 C>A maps to NM_183419.1 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104319664 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104319664 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117109605 C>A maps to NM_207343.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117109605 C>A maps to NM_207343.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117152351 G>T maps to NM_207343.2 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117152351 G>T maps to NM_207343.2 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219532838 G>T maps to NM_022453.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219532838 G>T maps to NM_022453.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121868027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121868027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121868061 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121868061 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30774765 C>A maps to NM_014771.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30774765 C>A maps to NM_014771.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30780613 C>A maps to NM_014771.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30780613 C>A maps to NM_014771.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201958048 C>A maps to NM_020216.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201958048 C>A maps to NM_020216.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:78655976 G>T maps to NM_002941.3 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:78655976 G>T maps to NM_002941.3 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:77572049 C>A maps to ENST00000332191 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:77572049 C>A maps to ENST00000332191 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:18619438 G>T maps to NM_005406.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:18619438 G>T maps to NM_005406.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94486315 G>T maps to NM_004560.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94486315 G>T maps to NM_004560.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94519682 G>T maps to NM_004560.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94519682 G>T maps to NM_004560.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:60794977 G>T maps to NM_134260.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:60794977 G>T maps to NM_134260.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151785723 G>T maps to ENST00000392697 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151785723 G>T maps to ENST00000392697 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117658377 C>A maps to NM_002944.2 T1735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117658377 C>A maps to NM_002944.2 T1735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117718232 G>T maps to NM_002944.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117718232 G>T maps to NM_002944.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:10467278 G>T maps to NM_178857.5 P1443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:10467278 G>T maps to NM_178857.5 P1443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:46713092 C>A maps to NM_006915.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:46713092 C>A maps to NM_006915.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:33136942 C>A maps to NM_203288.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:33136942 C>A maps to NM_203288.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7678700 G>T maps to NM_002947.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7678700 G>T maps to NM_002947.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41819637 G>T maps to NM_015540.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41819637 G>T maps to NM_015540.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41823346 C>A maps to NM_015540.2 G273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41823346 C>A maps to NM_015540.2 G273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92789670 C>A maps to NM_024813.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92789670 C>A maps to NM_024813.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92798982 C>A maps to NM_024813.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92798982 C>A maps to NM_024813.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48084336 G>T maps to NM_024604.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48084336 G>T maps to NM_024604.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113327858 C>A maps to NM_001143854.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113327858 C>A maps to NM_001143854.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101399998 G>T maps to NM_000986.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101399998 G>T maps to NM_000986.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12880957 G>T maps to ENST00000273223 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12880957 G>T maps to ENST00000273223 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120635151 C>A maps to NM_053275.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120635151 C>A maps to NM_053275.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150444025 G>T maps to NM_015203.3 E868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150444025 G>T maps to NM_015203.3 E868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150444216 G>T maps to NM_015203.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150444216 G>T maps to NM_015203.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150444378 G>T maps to NM_015203.3 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150444378 G>T maps to NM_015203.3 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167184356 G>T maps to ENST00000510118 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167184356 G>T maps to ENST00000510118 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:20194425 C>A maps to NM_004586.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:20194425 C>A maps to NM_004586.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:3624123 C>A maps to NM_001011.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:3624123 C>A maps to NM_001011.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152128760 C>A maps to NM_001122965.1 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152128760 C>A maps to NM_001122965.1 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40863921 C>A maps to NM_152260.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40863921 C>A maps to NM_152260.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126081392 C>A maps to NM_032795.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126081392 C>A maps to NM_032795.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90097268 C>A maps to NM_021244.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90097268 C>A maps to NM_021244.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17600949 C>A maps to ENST00000377813 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17600949 C>A maps to ENST00000377813 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7182161 C>A maps to NM_001003699.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7182161 C>A maps to NM_001003699.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7231085 C>A maps to NM_001003699.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7231085 C>A maps to NM_001003699.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99126518 G>T maps to NM_015179.3 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99126518 G>T maps to NM_015179.3 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:15986488 C>A maps to NM_006511.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:15986488 C>A maps to NM_006511.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77412035 G>T maps to NM_016578.3 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77412035 G>T maps to NM_016578.3 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77412677 G>T maps to NM_016578.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77412677 G>T maps to NM_016578.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6820485 G>T maps to NM_173565.3 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6820485 G>T maps to NM_173565.3 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159401898 G>T maps to NM_031924.4 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159401898 G>T maps to NM_031924.4 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57238602 G>T maps to NM_133368.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57238602 G>T maps to NM_133368.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57238638 C>A maps to NM_133368.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57238638 C>A maps to NM_133368.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57241984 C>A maps to NM_133368.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57241984 C>A maps to NM_133368.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57243092 C>A maps to NM_133368.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57243092 C>A maps to NM_133368.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41770783 C>A maps to NM_015138.4 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41770783 C>A maps to NM_015138.4 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186917806 G>T maps to NM_153708.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186917806 G>T maps to NM_153708.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67687922 C>A maps to NM_173630.3 T2027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67687922 C>A maps to NM_173630.3 T2027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67817852 G>T maps to NM_173630.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67817852 G>T maps to NM_173630.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178996383 C>A maps to NM_025158.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178996383 C>A maps to NM_025158.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71628284 C>A maps to NM_001037442.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71628284 C>A maps to NM_001037442.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71629285 G>T maps to NM_001037442.2 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71629285 G>T maps to NM_001037442.2 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92972687 G>T maps to NM_175634.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92972687 G>T maps to NM_175634.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92998376 G>T maps to NM_175634.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92998376 G>T maps to NM_175634.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92998432 C>A maps to NM_175634.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92998432 C>A maps to NM_175634.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:45399611 G>T maps to ENST00000359524 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:45399611 G>T maps to ENST00000359524 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155291629 G>T maps to NM_001105203.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155291629 G>T maps to NM_001105203.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155296473 G>T maps to NM_001105203.1 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155296473 G>T maps to NM_001105203.1 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155296890 C>A maps to NM_001105203.1 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155296890 C>A maps to NM_001105203.1 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127820407 G>T maps to NM_003707.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127820407 G>T maps to NM_003707.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95709821 G>T maps to NM_015485.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95709821 G>T maps to NM_015485.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32332480 C>A maps to NM_130806.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:32332480 C>A maps to NM_130806.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:39062837 C>A maps to NM_000540.2 P4642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:39062837 C>A maps to NM_000540.2 P4642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237604755 C>A maps to NM_001035.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237604755 C>A maps to NM_001035.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237608778 C>A maps to NM_001035.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237608778 C>A maps to NM_001035.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237664009 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237664009 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237729972 G>T maps to NM_001035.2 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237729972 G>T maps to NM_001035.2 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237777846 C>A maps to NM_001035.2 R1807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237777846 C>A maps to NM_001035.2 R1807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237972269 C>A maps to NM_001035.2 R4790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237972269 C>A maps to NM_001035.2 R4790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:33928639 G>T maps to NM_001036.3 G1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:33928639 G>T maps to NM_001036.3 G1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151955701 C>G maps to NM_002966.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151955701 C>G maps to NM_002966.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153390680 C>A maps to NM_176823.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153390680 C>A maps to NM_176823.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153409565 C>A maps to NM_001045479.1 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153409565 C>A maps to NM_001045479.1 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101704635 G>T maps to NM_001400.4 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101704635 G>T maps to NM_001400.4 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101704881 C>A maps to NM_001400.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101704881 C>A maps to NM_001400.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101705418 G>T maps to NM_001400.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101705418 G>T maps to NM_001400.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101705568 C>A maps to NM_001400.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101705568 C>A maps to NM_001400.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91616729 G>T maps to NM_005226.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91616729 G>T maps to NM_005226.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18288448 G>T maps to NM_199161.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18288448 G>T maps to NM_199161.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:23904858 G>T maps to NM_014363.4 R4386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:23904858 G>T maps to NM_014363.4 R4386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:23910525 C>A maps to NM_014363.4 G2497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:23910525 C>A maps to NM_014363.4 G2497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5621404 C>G maps to NM_014649.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5621404 C>G maps to NM_014649.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234243658 C>A maps to NM_000541.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234243658 C>A maps to NM_000541.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51171081 C>A maps to ENST00000251020 G1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51171081 C>A maps to ENST00000251020 G1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51174932 C>A maps to ENST00000251020 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51174932 C>A maps to ENST00000251020 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51176033 C>A maps to ENST00000251020 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51176033 C>A maps to ENST00000251020 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50407326 G>T maps to NM_020436.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50407326 G>T maps to NM_020436.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50408574 C>A maps to NM_020436.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50408574 C>A maps to NM_020436.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50408640 G>T maps to NM_020436.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50408640 G>T maps to NM_020436.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:84791386 C>A maps to NM_001010971.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:84791386 C>A maps to NM_001010971.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92762757 G>T maps to NM_152703.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92762757 G>T maps to NM_152703.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92765023 C>A maps to NM_152703.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92765023 C>A maps to NM_152703.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92734749 G>T maps to NM_017654.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92734749 G>T maps to NM_017654.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21715084 G>T maps to NM_005870.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21715084 G>T maps to NM_005870.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108919884 G>T maps to NM_014706.3 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108919884 G>T maps to NM_014706.3 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108920247 G>T maps to NM_014706.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108920247 G>T maps to NM_014706.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:148840794 C>A maps to NM_015278.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:148840794 C>A maps to NM_015278.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:200137047 G>T maps to NM_001172509.1 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:200137047 G>T maps to NM_001172509.1 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10051398 G>T maps to NM_030962.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10051398 G>T maps to NM_030962.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9861094 G>T maps to NM_030962.3 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9861094 G>T maps to NM_030962.3 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123780520 C>A maps to NM_001167856.1 A1372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123780520 C>A maps to NM_001167856.1 A1372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76696941 G>T maps to ENST00000324767 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76696941 G>T maps to ENST00000324767 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77087447 C>A maps to NM_005506.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77087447 C>A maps to NM_005506.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:246929381 C>A maps to NM_016002.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:246929381 C>A maps to NM_016002.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78188066 C>A maps to NM_144777.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78188066 C>A maps to NM_144777.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38739975 G>T maps to NM_006514.2 R1579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38739975 G>T maps to NM_006514.2 R1579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166848333 G>T maps to NM_001165963.1 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166848333 G>T maps to NM_001165963.1 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166848567 G>T maps to NM_001165963.1 P1739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166848567 G>T maps to NM_001165963.1 P1739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166901795 G>T maps to NM_001165963.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166901795 G>T maps to NM_001165963.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166229796 C>A maps to NM_001040142.1 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:166229796 C>A maps to NM_001040142.1 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165947490 G>T maps to NM_006922.3 P1724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165947490 G>T maps to NM_006922.3 P1724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165986734 C>A maps to NM_006922.3 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165986734 C>A maps to NM_006922.3 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52156342 C>A maps to NM_014191.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52156342 C>A maps to NM_014191.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167055511 G>T maps to ENST00000303354 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167055511 G>T maps to ENST00000303354 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167055775 G>T maps to ENST00000303354 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167055775 G>T maps to ENST00000303354 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167085347 G>T maps to ENST00000303354 T1354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167085347 G>T maps to ENST00000303354 T1354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:29963593 C>A maps to NM_001145514.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:29963593 C>A maps to NM_001145514.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9042665 G>T maps to ENST00000457346 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9042665 G>T maps to ENST00000457346 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9055313 C>A maps to ENST00000457346 G678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9055313 C>A maps to ENST00000457346 G678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9072177 G>T maps to ENST00000457346 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9072177 G>T maps to ENST00000457346 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9077451 C>A maps to ENST00000457346 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9077451 C>A maps to ENST00000457346 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65303494 G>T maps to NM_020680.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65303494 G>T maps to NM_020680.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169847900 C>A maps to NM_181093.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169847900 C>A maps to NM_181093.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139299542 G>T maps to NM_001039707.1 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139299542 G>T maps to NM_001039707.1 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:243456391 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:243456391 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:223623 C>A maps to NM_004168.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:223623 C>A maps to NM_004168.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:233749 C>A maps to NM_004168.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:233749 C>A maps to NM_004168.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:240566 G>T maps to NM_004168.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:240566 G>T maps to NM_004168.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4008917 C>A maps to NM_152744.3 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4008917 C>A maps to NM_152744.3 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4008967 C>A maps to NM_152744.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4008967 C>A maps to NM_152744.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4152975 C>A maps to NM_152744.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4152975 C>A maps to NM_152744.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:71427710 C>A maps to NM_001144952.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:71427710 C>A maps to NM_001144952.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10342986 G>T maps to ENST00000343726 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10342986 G>T maps to ENST00000343726 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145112436 C>A maps to NM_004892.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145112436 C>A maps to NM_004892.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18523776 C>A maps to NM_001172745.1 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18523776 C>A maps to NM_001172745.1 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:133997029 C>A maps to NM_021982.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:133997029 C>A maps to NM_021982.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110384558 C>A maps to NM_006323.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110384558 C>A maps to NM_006323.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110448544 G>T maps to NM_006323.2 A1011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110448544 G>T maps to NM_006323.2 A1011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75529704 C>A maps to NM_198597.1 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75529704 C>A maps to NM_198597.1 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75530048 C>A maps to NM_198597.1 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75530048 C>A maps to NM_198597.1 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102265200 C>A maps to NM_015490.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102265200 C>A maps to NM_015490.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127786346 C>A maps to ENST00000464451 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127786346 C>A maps to ENST00000464451 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169710571 C>A maps to NM_003262.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169710571 C>A maps to NM_003262.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108214799 G>T maps to NM_007214.4 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108214799 G>T maps to NM_007214.4 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108225844 G>T maps to NM_007214.4 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108225844 G>T maps to NM_007214.4 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108234611 G>T maps to NM_007214.4 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108234611 G>T maps to NM_007214.4 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108234624 C>A maps to NM_007214.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108234624 C>A maps to NM_007214.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49285001 G>T maps to NM_001193489.1 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49285001 G>T maps to NM_001193489.1 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49288756 G>T maps to NM_001193489.1 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49288756 G>T maps to NM_001193489.1 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:13868478 C>A maps to NM_025229.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:13868478 C>A maps to NM_025229.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151338253 G>T maps to ENST00000435071 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151338253 G>T maps to ENST00000435071 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169697208 G>T maps to NM_000450.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169697208 G>T maps to NM_000450.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169572366 G>T maps to NM_003005.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169572366 G>T maps to NM_003005.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:80418627 C>A maps to NM_006379.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:80418627 C>A maps to NM_006379.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:83029467 G>T maps to NM_012431.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:83029467 G>T maps to NM_012431.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50220182 C>A maps to NM_004186.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50220182 C>A maps to NM_004186.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156144969 C>A maps to NM_022367.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156144969 C>A maps to NM_022367.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97526380 G>T maps to NM_017789.4 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97526380 G>T maps to NM_017789.4 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97526392 G>T maps to NM_017789.4 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97526392 G>T maps to NM_017789.4 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91994251 G>T maps to NM_006378.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91994251 G>T maps to NM_006378.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:92008486 G>T maps to NM_006378.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:92008486 G>T maps to NM_006378.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74883758 C>A maps to NM_004263.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74883758 C>A maps to NM_004263.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122642508 G>T maps to NM_001031702.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122642508 G>T maps to NM_001031702.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48063879 G>T maps to NM_153618.1 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48063879 G>T maps to NM_153618.1 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48477523 C>A maps to ENST00000004980 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48477523 C>A maps to ENST00000004980 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185318608 C>A maps to ENST00000427465 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185318608 C>A maps to ENST00000427465 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101177835 G>T maps to NM_020654.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101177835 G>T maps to NM_020654.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72431972 C>A maps to NM_145204.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72431972 C>A maps to NM_145204.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392489 C>A maps to NM_052838.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392489 C>A maps to NM_052838.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392524 C>A maps to NM_052838.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392524 C>A maps to NM_052838.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392702 G>T maps to NM_052838.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392702 G>T maps to NM_052838.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118797554 C>A maps to ENST00000394612 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118797554 C>A maps to ENST00000394612 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:35872433 G>T maps to NM_001788.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:35872433 G>T maps to NM_001788.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:67895689 G>T maps to NM_001018067.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:67895689 G>T maps to NM_001018067.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94964445 C>A maps to NM_173850.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94964445 C>A maps to NM_173850.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:105277499 C>A maps to NM_000354.5 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:105277499 C>A maps to NM_000354.5 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:61600358 G>T maps to NM_005024.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:61600358 G>T maps to NM_005024.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:61264279 C>A maps to NM_012397.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:61264279 C>A maps to NM_012397.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:2953409 C>A maps to ENST00000316782 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:2953409 C>A maps to ENST00000316782 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210415127 C>A maps to NM_019605.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210415127 C>A maps to NM_019605.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:42529889 G>T maps to NM_015559.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:42529889 G>T maps to NM_015559.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:42530297 G>T maps to NM_015559.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:42530297 G>T maps to NM_015559.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:42532010 G>T maps to NM_015559.2 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:42532010 G>T maps to NM_015559.2 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30974817 C>A maps to NM_014712.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30974817 C>A maps to NM_014712.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47163424 C>A maps to NM_014159.6 G901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47163424 C>A maps to NM_014159.6 G901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123880969 C>A maps to NM_020382.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123880969 C>A maps to NM_020382.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150916443 G>T maps to NM_001145415.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150916443 G>T maps to NM_001145415.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150936040 C>A maps to NM_001145415.1 R1165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150936040 C>A maps to NM_001145415.1 R1165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135147173 C>A maps to ENST00000372169 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135147173 C>A maps to ENST00000372169 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135163660 G>T maps to ENST00000372169 R2096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135163660 G>T maps to ENST00000372169 R2096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135203333 C>A maps to ENST00000372169 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135203333 C>A maps to ENST00000372169 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135218183 C>A maps to ENST00000372169 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135218183 C>A maps to ENST00000372169 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198267376 C>A maps to NM_012433.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198267376 C>A maps to NM_012433.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198274506 G>T maps to NM_012433.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198274506 G>T maps to NM_012433.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198281494 G>T maps to NM_012433.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198281494 G>T maps to NM_012433.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65820562 C>A maps to NM_006842.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65820562 C>A maps to NM_006842.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70564700 C>A maps to NM_012426.4 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70564700 C>A maps to NM_012426.4 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70573044 C>A maps to NM_012426.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70573044 C>A maps to NM_012426.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70595651 C>A maps to NM_012426.4 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70595651 C>A maps to NM_012426.4 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70599116 C>A maps to NM_012426.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70599116 C>A maps to NM_012426.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:70687375 C>A maps to NM_004768.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:70687375 C>A maps to NM_004768.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19119142 G>T maps to NM_001017392.3 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19119142 G>T maps to NM_001017392.3 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:33043929 G>T maps to NM_020706.2 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:33043929 G>T maps to NM_020706.2 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1712432 C>A maps to NM_005088.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1712432 C>A maps to NM_005088.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99848426 G>T maps to NM_032870.2 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99848426 G>T maps to NM_032870.2 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99856121 G>T maps to NM_032870.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99856121 G>T maps to NM_032870.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46316731 G>T maps to NM_004719.2 S1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46316731 G>T maps to NM_004719.2 S1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46321194 C>A maps to NM_004719.2 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46321194 C>A maps to NM_004719.2 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36569548 C>A maps to NM_003017.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36569548 C>A maps to NM_003017.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:174940564 C>A maps to NM_022754.5 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:174940564 C>A maps to NM_022754.5 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120914656 G>T maps to NM_213649.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120914656 G>T maps to NM_213649.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120920466 G>T maps to NM_213649.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120920466 G>T maps to NM_213649.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77471817 G>T maps to NM_024776.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77471817 G>T maps to NM_024776.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77472416 G>T maps to NM_024776.2 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77472416 G>T maps to NM_024776.2 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77472528 G>T maps to NM_024776.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77472528 G>T maps to NM_024776.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77474094 C>A maps to NM_024776.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:77474094 C>A maps to NM_024776.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6755125 C>A maps to NM_005490.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6755125 C>A maps to NM_005490.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6755288 C>A maps to NM_005490.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6755288 C>A maps to NM_005490.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19190550 C>A maps to NM_022071.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:19190550 C>A maps to NM_022071.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80383461 C>A maps to NM_031469.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80383461 C>A maps to NM_031469.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:235950156 G>T maps to NM_014521.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:235950156 G>T maps to NM_014521.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105362235 G>T maps to ENST00000369774 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105362235 G>T maps to ENST00000369774 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105372879 G>T maps to ENST00000369774 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105372879 G>T maps to ENST00000369774 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170190189 C>G maps to NM_020870.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170190189 C>G maps to NM_020870.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70332366 G>T maps to ENST00000338508 S1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70332366 G>T maps to ENST00000338508 S1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70332563 C>A maps to ENST00000338508 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70332563 C>A maps to ENST00000338508 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70507758 C>A maps to ENST00000338508 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70507758 C>A maps to ENST00000338508 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7535242 G>T maps to NM_001040.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7535242 G>T maps to NM_001040.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91652961 C>A maps to NM_016848.5 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91652961 C>A maps to NM_016848.5 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91661881 C>A maps to NM_016848.5 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91661881 C>A maps to NM_016848.5 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:155604659 C>A maps to NM_000193.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:155604659 C>A maps to NM_000193.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:18257052 G>T maps to NM_004169.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:18257052 G>T maps to NM_004169.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146234630 G>T maps to ENST00000367503 R1441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146234630 G>T maps to ENST00000367503 R1441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146234667 C>A maps to ENST00000367503 S1428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:146234667 C>A maps to ENST00000367503 S1428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111594418 G>T maps to NM_015191.1 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111594418 G>T maps to NM_015191.1 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116718255 C>A maps to ENST00000445177 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116718255 C>A maps to ENST00000445177 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75705331 G>T maps to NM_001145357.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75705331 G>T maps to NM_001145357.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16973747 C>A maps to NM_015260.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16973747 C>A maps to NM_015260.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:72054517 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:72054517 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232600948 G>T maps to NM_020808.3 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232600948 G>T maps to NM_020808.3 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232600966 C>A maps to NM_020808.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232600966 C>A maps to NM_020808.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232601083 G>T maps to NM_020808.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232601083 G>T maps to NM_020808.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232649717 G>T maps to NM_020808.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232649717 G>T maps to NM_020808.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65417515 C>A maps to NM_153253.29 R948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65417515 C>A maps to NM_153253.29 R948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1532390 C>A maps to ENST00000381621 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1532390 C>A maps to ENST00000381621 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1638297 C>A maps to NM_018556.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1638297 C>A maps to NM_018556.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164712181 G>T maps to NM_001041.3 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164712181 G>T maps to NM_001041.3 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47911642 C>A maps to NM_145060.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47911642 C>A maps to NM_145060.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170078421 G>T maps to NM_005414.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170078421 G>T maps to NM_005414.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31931695 G>T maps to NM_006929.4 G552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31931695 G>T maps to NM_006929.4 G552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78320766 G>T maps to ENST00000389459 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78320766 G>T maps to ENST00000389459 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48381849 C>A maps to NM_020846.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48381849 C>A maps to NM_020846.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48541772 G>T maps to NM_000338.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48541772 G>T maps to NM_000338.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127469904 G>T maps to NM_001046.2 G413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127469904 G>T maps to NM_001046.2 G413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56926001 C>A maps to NM_000339.2 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56926001 C>A maps to NM_000339.2 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44671918 C>A maps to NM_001134771.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44671918 C>A maps to NM_001134771.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1079552 G>T maps to NM_006598.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1079552 G>T maps to NM_006598.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1079600 C>A maps to NM_006598.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1079600 C>A maps to NM_006598.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45194969 G>T maps to NM_022829.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45194969 G>T maps to NM_022829.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45224839 G>T maps to NM_022829.5 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45224839 G>T maps to NM_022829.5 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135376038 G>T maps to NM_012450.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135376038 G>T maps to NM_012450.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43311052 C>A maps to NM_001146037.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43311052 C>A maps to NM_001146037.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43204712 G>T maps to NM_007163.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43204712 G>T maps to NM_007163.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43249372 G>T maps to NM_007163.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43249372 G>T maps to NM_007163.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43262286 G>T maps to NM_007163.3 G856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43262286 G>T maps to NM_007163.3 G856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121643879 C>A maps to NM_021082.3 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121643879 C>A maps to NM_021082.3 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60709506 C>A maps to NM_016582.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60709506 C>A maps to NM_016582.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113464669 A>T maps to NM_003051.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113464669 A>T maps to NM_003051.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:66268903 C>A maps to NM_004694.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:66268903 C>A maps to NM_004694.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25913552 G>T maps to NM_005835.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25913552 G>T maps to NM_005835.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:100774700 C>A maps to NM_139319.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:100774700 C>A maps to NM_139319.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:119012936 G>T maps to NM_003054.4 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:119012936 G>T maps to NM_003054.4 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228564079 G>T maps to NM_025243.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228564079 G>T maps to NM_025243.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:4583121 G>T maps to NM_004170.5 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:4583121 G>T maps to NM_004170.5 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36608611 C>A maps to NM_004172.4 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36608611 C>A maps to NM_004172.4 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36679740 G>T maps to NM_004172.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36679740 G>T maps to NM_004172.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36679821 C>A maps to NM_004172.4 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36679821 C>A maps to NM_004172.4 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36680577 C>A maps to NM_004172.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36680577 C>A maps to NM_004172.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36684085 G>T maps to NM_004172.4 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36684085 G>T maps to NM_004172.4 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:65228623 G>T maps to NM_003038.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:65228623 G>T maps to NM_003038.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47278925 C>A maps to NM_005628.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47278925 C>A maps to NM_005628.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42294976 C>A maps to NM_006749.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42294976 C>A maps to NM_006749.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42329659 C>A maps to NM_006749.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42329659 C>A maps to NM_006749.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42329731 G>T maps to NM_006749.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42329731 G>T maps to NM_006749.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116563486 C>A maps to NM_018420.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116563486 C>A maps to NM_018420.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116577849 G>T maps to NM_018420.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116577849 G>T maps to NM_018420.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116605401 G>T maps to NM_018420.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116605401 G>T maps to NM_018420.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116607090 C>A maps to NM_018420.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116607090 C>A maps to NM_018420.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110763546 G>T maps to NM_033125.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110763546 G>T maps to NM_033125.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110777772 C>A maps to NM_033125.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110777772 C>A maps to NM_033125.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110777783 C>A maps to NM_033125.2 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110777783 C>A maps to NM_033125.2 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160553314 G>T maps to NM_003057.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160553314 G>T maps to NM_003057.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160553338 C>A maps to NM_003057.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160553338 C>A maps to NM_003057.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63149710 C>A maps to NM_080866.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63149710 C>A maps to NM_080866.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:4865409 G>T maps to NM_203327.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:4865409 G>T maps to NM_203327.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65917986 G>T maps to NM_004727.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65917986 G>T maps to NM_004727.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65946326 G>T maps to NM_004727.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65946326 G>T maps to NM_004727.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:19701765 C>A maps to NM_020689.3 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:19701765 C>A maps to NM_020689.3 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48426734 G>T maps to NM_205850.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48426734 G>T maps to NM_205850.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113742145 G>T maps to NM_024959.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113742145 G>T maps to NM_024959.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95926263 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95926263 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130860893 G>T maps to NM_052901.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130860893 G>T maps to NM_052901.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:66428155 G>T maps to NM_173471.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:66428155 G>T maps to NM_173471.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46623751 C>A maps to NM_004277.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46623751 C>A maps to NM_004277.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45970134 C>A maps to NM_001010875.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45970134 C>A maps to NM_001010875.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45983063 C>A maps to NM_001010875.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45983063 C>A maps to NM_001010875.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118604073 C>A maps to NM_001152.4 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118604073 C>A maps to NM_001152.4 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58016355 C>A maps to NM_133489.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58016355 C>A maps to NM_133489.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92365182 C>A maps to NM_134266.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92365182 C>A maps to NM_134266.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45556875 G>T maps to NM_004212.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45556875 G>T maps to NM_004212.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73104000 C>A maps to NM_018344.5 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73104000 C>A maps to NM_018344.5 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211748813 G>T maps to NM_021194.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211748813 G>T maps to NM_021194.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45803402 G>T maps to NM_013309.4 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45803402 G>T maps to NM_013309.4 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32396436 C>A maps to NM_001193513.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32396436 C>A maps to NM_001193513.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:25673284 G>T maps to NM_006424.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:25673284 G>T maps to NM_006424.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:25677926 G>T maps to NM_006424.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:25677926 G>T maps to NM_006424.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140126159 G>T maps to NM_080877.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140126159 G>T maps to NM_080877.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69158526 G>T maps to NM_018656.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69158526 G>T maps to NM_018656.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:118588162 G>T maps to NM_001029858.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:118588162 G>T maps to NM_001029858.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140048471 C>A maps to NM_207113.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140048471 C>A maps to NM_207113.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46758303 C>G maps to NM_018976.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46758303 C>G maps to NM_018976.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:47170762 C>A maps to NM_018018.4 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:47170762 C>A maps to NM_018018.4 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48319136 C>A maps to NM_033518.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48319136 C>A maps to NM_033518.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196545123 G>T maps to NM_001127257.1 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196545123 G>T maps to NM_001127257.1 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33706228 G>T maps to NM_012319.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33706228 G>T maps to NM_012319.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33169652 G>T maps to NM_006979.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33169652 G>T maps to NM_006979.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44531323 C>A maps to NM_000341.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44531323 C>A maps to NM_000341.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62655906 C>A maps to NM_001012661.1 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62655906 C>A maps to NM_001012661.1 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190439932 C>G maps to NM_014585.5 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190439932 C>G maps to NM_014585.5 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95290146 C>A maps to NM_001114106.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95290146 C>A maps to NM_001114106.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95303386 G>T maps to NM_001114106.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95303386 G>T maps to NM_001114106.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75684359 C>T maps to NM_152697.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75684359 C>T maps to NM_152697.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:115652673 C>A maps to NM_033051.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:115652673 C>A maps to NM_033051.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3210899 C>A maps to NM_001174090.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3210899 C>A maps to NM_001174090.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3211234 C>A maps to NM_001174090.1 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3211234 C>A maps to NM_001174090.1 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:72338619 C>A maps to NM_001098484.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:72338619 C>A maps to NM_001098484.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:72420898 G>T maps to NM_001098484.2 G913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:72420898 G>T maps to NM_001098484.2 G913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27463237 C>A maps to ENST00000454389 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27463237 C>A maps to ENST00000454389 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51853820 C>A maps to NM_001039960.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51853820 C>A maps to NM_001039960.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51888799 G>C maps to NM_001039960.1 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51888799 G>C maps to NM_001039960.1 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26725493 C>A maps to NM_178498.3 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26725493 C>A maps to NM_178498.3 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26734187 C>A maps to NM_178498.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26734187 C>A maps to NM_178498.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31499408 G>T maps to ENST00000431354 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31499408 G>T maps to ENST00000431354 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10967723 G>T maps to NM_014229.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10967723 G>T maps to NM_014229.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1239674 C>A maps to NM_182632.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1239674 C>A maps to NM_182632.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1217002 C>A maps to NM_001003841.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1217002 C>A maps to NM_001003841.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:55732379 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:55732379 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:28537637 C>A maps to ENST00000394821 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:28537637 C>A maps to ENST00000394821 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20636285 C>A maps to NM_004211.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20636285 C>A maps to NM_004211.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20660030 G>T maps to NM_004211.3 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20660030 G>T maps to NM_004211.3 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14489105 C>A maps to NM_001134367.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14489105 C>A maps to NM_001134367.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14509594 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14509594 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14520641 C>A maps to NM_001134367.1 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14520641 C>A maps to NM_001134367.1 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44468547 G>T maps to NM_201649.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44468547 G>T maps to NM_201649.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170198531 G>T maps to NM_020949.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170198531 G>T maps to NM_020949.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:30096466 C>A maps to NM_003045.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:30096466 C>A maps to NM_003045.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17406253 C>A maps to NM_001164771.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17406253 C>A maps to NM_001164771.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:40656843 C>A maps to NM_021097.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:40656843 C>A maps to NM_021097.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173486699 G>T maps to NM_178527.3 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173486699 G>T maps to NM_178527.3 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173526508 G>T maps to NM_178527.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173526508 G>T maps to NM_178527.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103274254 G>T maps to NM_003048.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103274254 G>T maps to NM_003048.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103300755 G>T maps to NM_003048.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103300755 G>T maps to NM_003048.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135076987 G>T maps to NM_001042537.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135076987 G>T maps to NM_001042537.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135084289 G>T maps to NM_001042537.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135084289 G>T maps to NM_001042537.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48472052 C>A maps to ENST00000417961 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48472052 C>A maps to ENST00000417961 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74876962 G>T maps to NM_007256.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74876962 G>T maps to NM_007256.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61297855 G>T maps to NM_016354.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61297855 G>T maps to NM_016354.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33690616 G>T maps to NM_152270.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33690616 G>T maps to NM_152270.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98923185 C>A maps to NM_003061.2 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98923185 C>A maps to NM_003061.2 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20544187 C>A maps to ENST00000273739 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20544187 C>A maps to ENST00000273739 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20555426 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20555426 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20620476 C>A maps to ENST00000273739 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20620476 C>A maps to ENST00000273739 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:84454324 G>T maps to NM_052910.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:84454324 G>T maps to NM_052910.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164907850 C>A maps to NM_014926.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164907850 C>A maps to NM_014926.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:142717031 C>A maps to NM_001184749.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:142717031 C>A maps to NM_001184749.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:88328551 G>T maps to NM_015567.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:88328551 G>T maps to NM_015567.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:86368864 C>A maps to NM_032229.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:86368864 C>A maps to NM_032229.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105762141 C>A maps to NM_014720.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105762141 C>A maps to NM_014720.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:48573608 G>T maps to NM_005359.5 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:48573608 G>T maps to NM_005359.5 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:135496749 C>A maps to NM_001001419.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:135496749 C>A maps to NM_001001419.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:37453778 G>T maps to NM_001127217.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:37453778 G>T maps to NM_001127217.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:71562282 G>T maps to NM_001044305.1 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:71562282 G>T maps to NM_001044305.1 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128645905 G>T maps to NM_003069.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128645905 G>T maps to NM_003069.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217279540 G>T maps to NM_014140.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217279540 G>T maps to NM_014140.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217343003 C>A maps to NM_014140.3 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217343003 C>A maps to NM_014140.3 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47702802 G>T maps to NM_003074.3 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47702802 G>T maps to NM_003074.3 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56579997 C>A maps to NM_003075.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56579997 C>A maps to NM_003075.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:106891987 C>A maps to NM_001042550.1 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:106891987 C>A maps to NM_001042550.1 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:112337177 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:112337177 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:72912932 C>A maps to NM_015110.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:72912932 C>A maps to NM_015110.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:17846824 C>A maps to ENST00000381272 G1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:17846824 C>A maps to ENST00000381272 G1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156230271 C>A maps to NM_015327.2 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156230271 C>A maps to NM_015327.2 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156235862 G>T maps to NM_015327.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156235862 G>T maps to NM_015327.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156236359 G>T maps to NM_015327.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156236359 G>T maps to NM_015327.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33071821 G>T maps to NM_018225.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33071821 G>T maps to NM_018225.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48604410 G>T maps to NM_005985.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48604410 G>T maps to NM_005985.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127347658 C>A maps to NM_014390.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127347658 C>A maps to NM_014390.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127569338 C>A maps to NM_014390.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127569338 C>A maps to NM_014390.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:38006337 G>T maps to NM_024700.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:38006337 G>T maps to NM_024700.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:38018280 G>T maps to NM_024700.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:38018280 G>T maps to NM_024700.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96964041 C>A maps to NM_014014.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96964041 C>A maps to NM_014014.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96969004 C>A maps to NM_014014.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96969004 C>A maps to NM_014014.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70122239 C>A maps to NM_006857.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70122239 C>A maps to NM_006857.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123950654 C>A maps to NM_180699.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123950654 C>A maps to NM_180699.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:31742055 G>T maps to ENST00000446633 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:31742055 G>T maps to ENST00000446633 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49589806 C>A maps to NM_003089.4 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49589806 C>A maps to NM_003089.4 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101832172 C>A maps to NM_003090.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101832172 C>A maps to NM_003090.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:25223433 G>T maps to NM_022805.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:25223433 G>T maps to NM_022805.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32026689 C>A maps to NM_003098.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32026689 C>A maps to NM_003098.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69318049 C>A maps to NM_006750.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69318049 C>A maps to NM_006750.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69333664 C>A maps to NM_006750.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69333664 C>A maps to NM_006750.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:51442809 C>A maps to NM_018967.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:51442809 C>A maps to NM_018967.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:86243448 G>T maps to NM_153816.3 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:86243448 G>T maps to NM_153816.3 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130784210 G>T maps to NM_014758.2 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130784210 G>T maps to NM_014758.2 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:122343389 G>T maps to ENST00000395451 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:122343389 G>T maps to ENST00000395451 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101601189 C>A maps to NM_152628.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101601189 C>A maps to NM_152628.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:125216719 G>T maps to NM_003794.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:125216719 G>T maps to NM_003794.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17928219 G>T maps to NM_152227.1 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17928219 G>T maps to NM_152227.1 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179271824 G>T maps to NM_003101.4 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179271824 G>T maps to NM_003101.4 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179310361 G>T maps to NM_003101.4 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179310361 G>T maps to NM_003101.4 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179310421 C>A maps to NM_003101.4 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179310421 C>A maps to NM_003101.4 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:107908379 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:107908379 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:34925403 C>A maps to NM_138927.1 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:34925403 C>A maps to NM_138927.1 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186544263 G>T maps to ENST00000355634 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186544263 G>T maps to ENST00000355634 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186544971 G>T maps to ENST00000355634 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186544971 G>T maps to ENST00000355634 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:108447982 C>A maps to NM_001013031.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:108447982 C>A maps to NM_001013031.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121457025 G>T maps to NM_003105.5 E1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121457025 G>T maps to NM_003105.5 E1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121476245 C>A maps to NM_003105.5 T1638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121476245 C>A maps to NM_003105.5 T1638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121490565 G>T maps to NM_003105.5 T1943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121490565 G>T maps to NM_003105.5 T1943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121490577 C>A maps to NM_003105.5 S1947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121490577 C>A maps to NM_003105.5 S1947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39224536 C>A maps to NM_005633.3 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39224536 C>A maps to NM_005633.3 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:23687260 G>T maps to NM_006940.4 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:23687260 G>T maps to NM_006940.4 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:23818465 G>T maps to NM_006940.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:23818465 G>T maps to NM_006940.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16010576 G>T maps to NM_001145819.1 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16010576 G>T maps to NM_001145819.1 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16340052 G>T maps to NM_001145819.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16340052 G>T maps to NM_001145819.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16362659 G>T maps to NM_001145819.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:16362659 G>T maps to NM_001145819.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231309026 C>A maps to NM_001080391.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231309026 C>A maps to NM_001080391.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231331883 C>A maps to NM_001080391.1 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231331883 C>A maps to NM_001080391.1 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231380144 C>A maps to NM_003113.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231380144 C>A maps to NM_003113.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231042391 G>T maps to NM_080424.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231042391 G>T maps to NM_080424.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231101959 C>A maps to NM_007237.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231101959 C>A maps to NM_007237.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:174820359 C>A maps to NM_003111.4 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:174820359 C>A maps to NM_003111.4 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:174820399 C>A maps to NM_003111.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:174820399 C>A maps to NM_003111.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20824766 G>A maps to NM_182700.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20824766 G>A maps to NM_182700.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118516125 C>A maps to NM_206996.2 A2021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118516125 C>A maps to NM_206996.2 A2021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118574428 C>A maps to NM_206996.2 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118574428 C>A maps to NM_206996.2 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118581915 C>A maps to NM_206996.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118581915 C>A maps to NM_206996.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26919346 G>T maps to NM_006461.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26919346 G>T maps to NM_006461.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26919808 G>T maps to NM_006461.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26919808 G>T maps to NM_006461.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26919966 C>A maps to NM_006461.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26919966 C>A maps to NM_006461.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:22700090 C>A maps to ENST00000376603 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:22700090 C>A maps to ENST00000376603 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35811952 C>A maps to NM_001039592.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35811952 C>A maps to NM_001039592.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:49048170 C>A maps to ENST00000376407 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:49048170 C>A maps to ENST00000376407 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:140335726 G>T maps to ENST00000452778 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:140335726 G>T maps to ENST00000452778 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:140785698 G>T maps to NM_145665.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:140785698 G>T maps to NM_145665.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:52825544 C>A maps to NM_001009616.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:52825544 C>A maps to NM_001009616.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:52928469 C>A maps to NM_145263.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:52928469 C>A maps to NM_145263.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:133715329 C>A maps to NM_174927.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:133715329 C>A maps to NM_174927.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:48865183 C>A maps to NM_019073.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:48865183 C>A maps to NM_019073.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35646869 C>A maps to NM_024867.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35646869 C>A maps to NM_024867.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35753775 G>T maps to NM_024867.3 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35753775 G>T maps to NM_024867.3 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35759768 C>A maps to NM_024867.3 R1190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35759768 C>A maps to NM_024867.3 R1190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16256527 C>A maps to NM_015001.2 R1265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16256527 C>A maps to NM_015001.2 R1265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16257948 C>G maps to NM_015001.2 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16257948 C>G maps to NM_015001.2 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69238505 C>A maps to NM_145658.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69238505 C>A maps to NM_145658.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44865018 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44865018 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228883493 G>T maps to NM_001142644.1 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228883493 G>T maps to NM_001142644.1 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228886505 G>T maps to NM_001142644.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228886505 G>T maps to NM_001142644.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101876649 C>A maps to ENST00000299272 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101876649 C>A maps to ENST00000299272 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41149133 G>T maps to NM_181642.2 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41149133 G>T maps to NM_181642.2 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1165715 C>A maps to NM_012445.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1165715 C>A maps to NM_012445.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:139326646 C>A maps to NM_001001664.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:139326646 C>A maps to NM_001001664.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88903969 C>A maps to NM_001040058.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88903969 C>A maps to NM_001040058.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:65540820 G>T maps to NM_181784.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:65540820 G>T maps to NM_181784.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155003544 G>C maps to NM_005840.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155003544 G>C maps to NM_005840.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53461480 G>T maps to NM_032840.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53461480 G>T maps to NM_032840.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158592859 G>T maps to NM_003126.2 A2011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158592859 G>T maps to NM_003126.2 A2011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158592973 C>A maps to NM_003126.2 L1973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158592973 C>A maps to NM_003126.2 L1973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158644195 G>T maps to NM_003126.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158644195 G>T maps to NM_003126.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131351101 C>A maps to NM_001130438.2 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131351101 C>A maps to NM_001130438.2 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131356573 C>A maps to NM_001130438.2 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131356573 C>A maps to NM_001130438.2 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131370473 C>A maps to NM_001130438.2 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131370473 C>A maps to NM_001130438.2 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131388755 C>A maps to NM_001130438.2 P2122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131388755 C>A maps to NM_001130438.2 P2122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:54853284 C>A maps to NM_003128.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:54853284 C>A maps to NM_003128.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66463960 C>A maps to NM_006946.2 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66463960 C>A maps to NM_006946.2 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42166530 C>A maps to ENST00000320955 E1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42166530 C>A maps to ENST00000320955 E1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:65239357 G>T maps to ENST00000389723 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:65239357 G>T maps to ENST00000389723 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18637061 G>T maps to NM_194285.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18637061 G>T maps to NM_194285.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18637136 G>T maps to NM_194285.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18637136 G>T maps to NM_194285.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18637459 G>T maps to NM_194285.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18637459 G>T maps to NM_194285.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126015632 G>T maps to NM_003129.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126015632 G>T maps to NM_003129.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30727452 G>T maps to NM_006662.2 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30727452 G>T maps to NM_006662.2 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30731533 C>A maps to NM_006662.2 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30731533 C>A maps to NM_006662.2 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30731560 C>A maps to NM_006662.2 R966R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30731560 C>A maps to NM_006662.2 R966R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30735148 G>T maps to NM_006662.2 S1468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30735148 G>T maps to NM_006662.2 S1468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30735517 G>T maps to NM_006662.2 A1591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30735517 G>T maps to NM_006662.2 A1591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30744680 C>A maps to NM_006662.2 R2070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30744680 C>A maps to NM_006662.2 R2070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30747679 C>A maps to NM_006662.2 R2297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30747679 C>A maps to NM_006662.2 R2297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30748533 G>T maps to NM_006662.2 P2391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30748533 G>T maps to NM_006662.2 P2391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:42263192 G>T maps to NM_004599.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:42263192 G>T maps to NM_004599.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64377851 C>A maps to NM_020762.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64377851 C>A maps to NM_020762.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9068672 C>A maps to NM_014850.2 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9068672 C>A maps to NM_014850.2 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62172236 G>T maps to NM_080823.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62172236 G>T maps to NM_080823.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:35478010 C>A maps to NM_003136.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:35478010 C>A maps to NM_003136.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74060169 G>T maps to NM_014230.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74060169 G>T maps to NM_014230.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57350948 C>A maps to NM_006947.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57350948 C>A maps to NM_006947.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126136474 G>T maps to NM_003139.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126136474 G>T maps to NM_003139.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24975465 G>T maps to NM_005839.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24975465 G>T maps to NM_005839.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24979111 C>A maps to NM_005839.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24979111 C>A maps to NM_005839.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2816007 C>A maps to NM_016333.3 R1827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2816007 C>A maps to NM_016333.3 R1827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:23632774 G>T maps to ENST00000415083 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:23632774 G>T maps to ENST00000415083 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:54693962 C>A maps to NM_145716.2 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:54693962 C>A maps to NM_145716.2 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:149481948 G>T maps to NM_198455.2 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:149481948 G>T maps to NM_198455.2 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57097812 G>T maps to NM_003146.2 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57097812 G>T maps to NM_003146.2 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65338412 C>A maps to NM_006396.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65338412 C>A maps to NM_006396.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65338439 C>A maps to NM_006396.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65338439 C>A maps to NM_006396.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:23016380 C>A maps to NM_001052.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:23016380 C>A maps to NM_001052.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:187386908 G>T maps to NM_001048.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:187386908 G>T maps to NM_001048.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:187387014 C>A maps to NM_001048.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:187387014 C>A maps to NM_001048.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85124124 G>A maps to NM_001166417.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85124124 G>A maps to NM_001166417.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:52682515 C>A maps to NM_173358.2 G3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:52682515 C>A maps to NM_173358.2 G3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:53045833 C>A maps to NM_014682.2 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:53045833 C>A maps to NM_014682.2 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:53092774 G>T maps to NM_014682.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:53092774 G>T maps to NM_014682.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44386083 G>T maps to NM_174963.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44386083 G>T maps to NM_174963.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98492809 C>A maps to ENST00000493584 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98492809 C>A maps to ENST00000493584 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:107459974 G>T maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:107459974 G>T maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:92987896 C>A maps to NM_006011.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:92987896 C>A maps to NM_006011.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44260148 C>A maps to NM_013305.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44260148 C>A maps to NM_013305.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17432585 C>A maps to NM_001004470.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17432585 C>A maps to NM_001004470.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52547913 C>A maps to NM_015136.2 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52547913 C>A maps to NM_015136.2 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104054131 C>A maps to NM_017564.9 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104054131 C>A maps to NM_017564.9 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104121125 C>A maps to NM_017564.9 R1645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104121125 C>A maps to NM_017564.9 R1645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104155079 G>T maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104155079 G>T maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104156134 C>A maps to NM_017564.9 S2481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104156134 C>A maps to NM_017564.9 S2481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104157271 G>T maps to NM_017564.9 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104157271 G>T maps to NM_017564.9 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57642521 G>T maps to NM_145064.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57642521 G>T maps to NM_145064.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136059388 G>T maps to NM_005862.2 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136059388 G>T maps to NM_005862.2 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99786114 C>A maps to NM_012447.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99786114 C>A maps to NM_012447.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99786439 G>T maps to NM_012447.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99786439 G>T maps to NM_012447.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99802727 C>A maps to NM_012447.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99802727 C>A maps to NM_012447.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152989774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152989774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90673007 C>A maps to NM_020799.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90673007 C>A maps to NM_020799.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33692286 C>A maps to NM_178007.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33692286 C>A maps to NM_178007.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33700283 C>A maps to NM_178007.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33700283 C>A maps to NM_178007.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96858199 C>A maps to NM_020151.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96858199 C>A maps to NM_020151.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191895739 C>A maps to NM_003151.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191895739 C>A maps to NM_003151.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191895760 G>T maps to NM_003151.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191895760 G>T maps to NM_003151.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191905874 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191905874 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191927612 C>A maps to NM_003151.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191927612 C>A maps to NM_003151.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57492805 G>T maps to NM_003153.4 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57492805 G>T maps to NM_003153.4 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63965413 C>A maps to ENST00000358794 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63965413 C>A maps to ENST00000358794 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31940166 C>A maps to NM_032454.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31940166 C>A maps to NM_032454.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99116018 G>T maps to NM_003576.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99116018 G>T maps to NM_003576.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219561889 C>A maps to NM_015690.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219561889 C>A maps to NM_015690.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27098708 C>A maps to NM_030795.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27098708 C>A maps to NM_030795.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39542596 G>T maps to NM_145286.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39542596 G>T maps to NM_145286.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48808770 C>A maps to NM_172311.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48808770 C>A maps to NM_172311.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:81744601 C>A maps to NM_033104.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:81744601 C>A maps to NM_033104.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202337726 C>A maps to NM_018571.5 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202337726 C>A maps to NM_018571.5 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125909235 G>T maps to NM_018387.4 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125909235 G>T maps to NM_018387.4 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125941287 G>T maps to NM_018387.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125941287 G>T maps to NM_018387.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125475522 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125475522 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125479347 G>T maps to NM_152713.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125479347 G>T maps to NM_152713.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125484265 C>A maps to NM_152713.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125484265 C>A maps to NM_152713.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31004539 C>A maps to NM_052874.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31004539 C>A maps to NM_052874.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31012478 C>A maps to NM_052874.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31012478 C>A maps to NM_052874.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59540715 G>T maps to NM_004177.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59540715 G>T maps to NM_004177.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31045558 C>A maps to NM_004604.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31045558 C>A maps to NM_004604.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132824636 G>T maps to NM_003569.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132824636 G>T maps to NM_003569.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132824653 C>A maps to NM_003569.2 G6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132824653 C>A maps to NM_003569.2 G6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130423418 C>A maps to NM_003165.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130423418 C>A maps to NM_003165.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120673815 C>A maps to NM_014980.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120673815 C>A maps to NM_014980.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:67659947 C>A maps to NM_003848.3 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:67659947 C>A maps to NM_003848.3 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108998865 C>A maps to NM_006588.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108998865 C>A maps to NM_006588.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108998895 C>A maps to NM_006588.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:108998895 C>A maps to NM_006588.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37410570 G>T maps to NM_001032377.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37410570 G>T maps to NM_001032377.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203072041 C>A maps to ENST00000409368 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:203072041 C>A maps to ENST00000409368 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:883113 C>A maps to ENST00000456758 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:883113 C>A maps to ENST00000456758 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:892492 C>A maps to ENST00000456758 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:892492 C>A maps to ENST00000456758 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31583483 G>T maps to NM_080675.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31583483 G>T maps to NM_080675.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:21820894 C>A maps to NM_007192.3 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:21820894 C>A maps to NM_007192.3 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27014203 C>A maps to NM_003170.3 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27014203 C>A maps to NM_003170.3 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27026858 C>A maps to NM_003170.3 T1503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27026858 C>A maps to NM_003170.3 T1503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136227981 C>A maps to NM_017503.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136227981 C>A maps to NM_017503.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223465897 G>T maps to NM_017982.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223465897 G>T maps to NM_017982.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67926093 G>T maps to NM_017635.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67926093 G>T maps to NM_017635.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67957438 C>A maps to NM_017635.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67957438 C>A maps to NM_017635.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149877448 G>T maps to NM_014849.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149877448 G>T maps to NM_014849.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91827395 C>A maps to NM_014848.4 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91827395 C>A maps to NM_014848.4 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113141701 C>A maps to ENST00000374463 G3448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113141701 C>A maps to ENST00000374463 G3448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113148214 G>T maps to ENST00000374463 P3403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113148214 G>T maps to ENST00000374463 P3403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113166720 C>A maps to ENST00000374463 P3187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113166720 C>A maps to ENST00000374463 P3187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113168522 G>T maps to ENST00000374463 P3122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113168522 G>T maps to ENST00000374463 P3122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113169470 G>T maps to ENST00000374463 P2806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113169470 G>T maps to ENST00000374463 P2806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110587458 G>T maps to NM_001099744.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110587458 G>T maps to NM_001099744.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110592122 C>T maps to NM_001099744.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110592122 C>T maps to NM_001099744.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10926642 C>A maps to NM_001040274.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10926642 C>A maps to NM_001040274.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10955409 G>T maps to NM_001040274.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10955409 G>T maps to NM_001040274.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:93629423 G>T maps to NM_003177.5 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:93629423 G>T maps to NM_003177.5 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:93639903 C>A maps to NM_003177.5 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:93639903 C>A maps to NM_003177.5 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33149647 G>T maps to NM_030786.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33149647 G>T maps to NM_030786.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152462353 G>T maps to NM_182961.2 T8410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152462353 G>T maps to NM_182961.2 T8410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152542604 G>T maps to NM_182961.2 P7204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152542604 G>T maps to NM_182961.2 P7204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152650918 G>T maps to NM_182961.2 L4967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152650918 G>T maps to NM_182961.2 L4967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152737673 C>A maps to NM_182961.2 L1966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152737673 C>A maps to NM_182961.2 L1966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33393630 G>T maps to NM_006772.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33393630 G>T maps to NM_006772.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99669599 C>A maps to ENST00000336292 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99669599 C>A maps to ENST00000336292 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99669680 G>T maps to ENST00000336292 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99669680 G>T maps to ENST00000336292 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99669722 G>T maps to ENST00000336292 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99669722 G>T maps to ENST00000336292 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99672797 G>T maps to ENST00000336292 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99672797 G>T maps to ENST00000336292 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75407459 G>T maps to NM_001114133.1 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75407459 G>T maps to NM_001114133.1 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75407492 C>A maps to NM_001114133.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75407492 C>A maps to NM_001114133.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150028928 G>T maps to NM_001166209.1 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150028928 G>T maps to NM_001166209.1 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:110022031 C>A maps to NM_001040709.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:110022031 C>A maps to NM_001040709.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155851134 G>T maps to NM_152280.4 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155851134 G>T maps to NM_152280.4 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210273727 G>A maps to NM_001146261.1 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210273727 G>A maps to NM_001146261.1 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46968679 G>T maps to NM_031912.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46968679 G>T maps to NM_031912.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:79689967 C>A maps to NM_005639.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:79689967 C>A maps to NM_005639.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7439308 C>A maps to NM_175733.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7439308 C>A maps to NM_175733.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:85445573 C>A maps to NM_001162953.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:85445573 C>A maps to NM_001162953.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132910732 C>A maps to NM_003967.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132910732 C>A maps to NM_003967.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132891858 G>T maps to NM_175067.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132891858 G>T maps to NM_175067.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132874262 C>A maps to NM_053278.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132874262 C>A maps to NM_053278.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132874274 G>T maps to NM_053278.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:132874274 G>T maps to NM_053278.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123970284 G>T maps to NM_206862.2 T2115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:123970284 G>T maps to NM_206862.2 T2115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124008245 C>A maps to NM_206862.2 S2827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124008245 C>A maps to NM_206862.2 S2827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124008606 C>A maps to NM_206862.2 R2866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124008606 C>A maps to NM_206862.2 R2866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1729455 G>T maps to NM_006342.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1729455 G>T maps to NM_006342.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7056043 G>T maps to NM_152293.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7056043 G>T maps to NM_152293.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222750876 G>T maps to NM_005681.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222750876 G>T maps to NM_005681.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93471380 G>T maps to NM_024116.3 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93471380 G>T maps to NM_024116.3 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32634452 G>T maps to NM_153809.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32634452 G>T maps to NM_153809.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32635433 C>A maps to NM_153809.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32635433 C>A maps to NM_153809.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70678119 C>A maps to ENST00000449580 S1655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:70678119 C>A maps to ENST00000449580 S1655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120805634 G>T maps to NM_003184.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120805634 G>T maps to NM_003184.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120816185 G>T maps to NM_003184.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120816185 G>T maps to NM_003184.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105147033 G>T maps to NM_006951.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105147033 G>T maps to NM_006951.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:77388874 C>A maps to NM_015975.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:77388874 C>A maps to NM_015975.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117075048 G>T maps to NM_003186.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117075048 G>T maps to NM_003186.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160085356 C>A maps to NM_033394.2 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160085356 C>A maps to NM_033394.2 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29994970 C>A maps to NM_016151.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29994970 C>A maps to NM_016151.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11082644 G>T maps to NM_007375.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11082644 G>T maps to NM_007375.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38301799 G>T maps to ENST00000443402 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38301799 G>T maps to ENST00000443402 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38313209 G>T maps to ENST00000390338 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38313209 G>T maps to ENST00000390338 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150471413 C>A maps to NM_025150.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150471413 C>A maps to NM_025150.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33459873 G>T maps to ENST00000455217 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33459873 G>T maps to ENST00000455217 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33461115 C>A maps to ENST00000455217 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33461115 C>A maps to ENST00000455217 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11149831 C>A maps to NM_176889.2 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11149831 C>A maps to NM_176889.2 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11183027 C>A maps to NM_176885.2 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11183027 C>A maps to NM_176885.2 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11183778 C>A maps to NM_176885.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11183778 C>A maps to NM_176885.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141673284 C>A maps to NM_176817.4 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141673284 C>A maps to NM_176817.4 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141464392 C>A maps to NM_016943.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141464392 C>A maps to NM_016943.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11139297 G>T maps to NM_176890.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11139297 G>T maps to NM_176890.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11139401 C>A maps to NM_176890.2 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11139401 C>A maps to NM_176890.2 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10320028 G>T maps to NM_014760.3 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10320028 G>T maps to NM_014760.3 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27827103 T>A maps to ENST00000409980 L307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27827103 T>A maps to ENST00000409980 L307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72288554 C>A maps to NM_022771.4 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72288554 C>A maps to NM_022771.4 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:38016161 G>T maps to NM_015173.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:38016161 G>T maps to NM_015173.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:38022225 G>T maps to NM_015173.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:38022225 G>T maps to NM_015173.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:38119672 C>A maps to NM_015173.2 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:38119672 C>A maps to NM_015173.2 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:75861014 G>T maps to ENST00000431480 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:75861014 G>T maps to ENST00000431480 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:75876483 G>T maps to ENST00000431480 R937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:75876483 G>T maps to ENST00000431480 R937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13316855 G>T maps to NM_016495.4 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13316855 G>T maps to NM_016495.4 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101650074 C>A maps to NM_001102426.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101650074 C>A maps to NM_001102426.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141578865 G>T maps to NM_015130.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141578865 G>T maps to NM_015130.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141592038 G>T maps to NM_015130.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141592038 G>T maps to NM_015130.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141600139 G>T maps to NM_015130.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141600139 G>T maps to NM_015130.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235602091 C>A maps to NM_003193.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235602091 C>A maps to NM_003193.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72988805 C>A maps to NM_012453.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72988805 C>A maps to NM_012453.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119427369 G>T maps to ENST00000369429 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119427369 G>T maps to ENST00000369429 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:168260481 G>T maps to NM_005149.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:168260481 G>T maps to NM_005149.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37821713 C>G maps to NM_003673.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37821713 C>G maps to NM_003673.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101396015 G>T maps to NM_001006938.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101396015 G>T maps to NM_001006938.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44560087 C>A maps to NM_016427.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44560087 C>A maps to NM_016427.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:57574763 C>A maps to NM_207036.1 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:57574763 C>A maps to NM_207036.1 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31129414 C>A maps to NM_007109.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31129414 C>A maps to NM_007109.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:53018134 G>T maps to ENST00000398339 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:53018134 G>T maps to ENST00000398339 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:53018221 C>A maps to ENST00000398339 G230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:53018221 C>A maps to ENST00000398339 G230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:114912183 C>A maps to NM_030756.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:114912183 C>A maps to NM_030756.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152084219 G>T maps to NM_007113.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152084219 G>T maps to NM_007113.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110354401 G>T maps to NM_032300.4 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110354401 G>T maps to NM_032300.4 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67815244 C>A maps to NM_006019.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67815244 C>A maps to NM_006019.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97423877 G>T maps to ENST00000371217 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97423877 G>T maps to ENST00000371217 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104374684 G>T maps to NM_003211.4 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104374684 G>T maps to NM_003211.4 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104379454 G>T maps to NM_003211.4 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104379454 G>T maps to NM_003211.4 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154517325 G>T maps to NM_001098475.1 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154517325 G>T maps to NM_001098475.1 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154517336 C>A maps to NM_001098475.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154517336 C>A maps to NM_001098475.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179609036 G>T maps to ENST00000444136 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179609036 G>T maps to ENST00000444136 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46659899 C>A maps to NM_001010870.2 P1345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46659899 C>A maps to NM_001010870.2 P1345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46660100 G>T maps to NM_001010870.2 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46660100 G>T maps to NM_001010870.2 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46665799 C>A maps to NM_001010870.2 P2079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46665799 C>A maps to NM_001010870.2 P2079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:12904648 G>T maps to NM_021961.5 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:12904648 G>T maps to NM_021961.5 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49850499 G>T maps to NM_003598.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49850499 G>T maps to NM_003598.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49862705 G>T maps to NM_003598.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49862705 G>T maps to NM_003598.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97870520 G>T maps to ENST00000379795 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97870520 G>T maps to ENST00000379795 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97873978 G>T maps to ENST00000379795 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97873978 G>T maps to ENST00000379795 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:120996174 C>A maps to NM_005422.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:120996174 C>A maps to NM_005422.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121016298 G>T maps to NM_005422.2 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121016298 G>T maps to NM_005422.2 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:114057835 G>T maps to NM_058222.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:114057835 G>T maps to NM_058222.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48152959 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48152959 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48169844 G>T maps to NM_003215.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48169844 G>T maps to NM_003215.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:10769851 C>A maps to NM_144674.1 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:10769851 C>A maps to NM_144674.1 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53451609 G>T maps to NM_170754.2 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53451609 G>T maps to NM_170754.2 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75690398 C>A maps to NM_018975.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75690398 C>A maps to NM_018975.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1278863 C>A maps to NM_198253.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1278863 C>A maps to NM_198253.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1282620 C>A maps to NM_198253.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1282620 C>A maps to NM_198253.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45813597 G>T maps to NM_007170.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45813597 G>T maps to NM_007170.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107224618 G>T maps to NM_031273.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107224618 G>T maps to NM_031273.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:62291280 G>T maps to NM_018469.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:62291280 G>T maps to NM_018469.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10398697 C>A maps to ENST00000379613 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10398697 C>A maps to ENST00000379613 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4312593 C>A maps to NM_003223.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4312593 C>A maps to NM_003223.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51501030 G>T maps to NM_005653.4 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51501030 G>T maps to NM_005653.4 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51502992 G>T maps to NM_005653.4 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51502992 G>T maps to NM_005653.4 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:115582011 G>T maps to NM_012252.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:115582011 G>T maps to NM_012252.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195802077 C>A maps to NM_001128148.1 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195802077 C>A maps to NM_001128148.1 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:218578538 C>A maps to NM_001135599.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:218578538 C>A maps to NM_001135599.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92182162 C>A maps to NM_003243.4 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92182162 C>A maps to NM_003243.4 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92185006 C>A maps to NM_003243.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92185006 C>A maps to NM_003243.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36758679 C>A maps to NM_004613.2 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36758679 C>A maps to NM_004613.2 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2376048 G>T maps to NM_198994.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2376048 G>T maps to NM_198994.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85554434 C>A maps to ENST00000409015 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85554434 C>A maps to ENST00000409015 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85554680 C>A maps to ENST00000409015 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85554680 C>A maps to ENST00000409015 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134125824 C>A maps to NM_003235.4 R2578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134125824 C>A maps to NM_003235.4 R2578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:43755034 G>T maps to ENST00000330266 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:43755034 G>T maps to ENST00000330266 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42694454 G>T maps to NM_018105.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42694454 G>T maps to NM_018105.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:39883471 C>A maps to NM_003246.2 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:39883471 C>A maps to NM_003246.2 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169629675 G>T maps to NM_003247.2 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169629675 G>T maps to NM_003247.2 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:122758459 C>A maps to NM_001081550.1 G1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:122758459 C>A maps to NM_001081550.1 G1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:122765538 C>A maps to NM_001081550.1 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:122765538 C>A maps to NM_001081550.1 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36755183 C>A maps to NM_005119.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36755183 C>A maps to NM_005119.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:24188313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:24188313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52952319 G>T maps to NM_018676.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52952319 G>T maps to NM_018676.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:11464332 G>T maps to ENST00000423059 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:11464332 G>T maps to ENST00000423059 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9416265 C>A maps to NM_015453.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9416265 C>A maps to NM_015453.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134119784 C>A maps to NM_199298.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134119784 C>A maps to NM_199298.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134121140 C>A maps to NM_199298.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134121140 C>A maps to NM_199298.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4817219 C>A maps to NM_182919.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4817219 C>A maps to NM_182919.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43778156 T>A maps to NM_005424.2 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43778156 T>A maps to NM_005424.2 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113199487 C>A maps to NM_052864.2 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113199487 C>A maps to NM_052864.2 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56811936 C>A maps to NM_003920.3 A1145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56811936 C>A maps to NM_003920.3 A1145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56815565 C>A maps to NM_003920.3 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56815565 C>A maps to NM_003920.3 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30001003 G>T maps to NM_003257.3 R1537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30001003 G>T maps to NM_003257.3 R1537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30011131 G>T maps to NM_003257.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30011131 G>T maps to NM_003257.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30011144 C>A maps to NM_003257.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30011144 C>A maps to NM_003257.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30058480 G>T maps to NM_003257.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30058480 G>T maps to NM_003257.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:71840266 C>A maps to NM_004817.3 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:71840266 C>A maps to NM_004817.3 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66570911 C>A maps to ENST00000299697 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:66570911 C>A maps to ENST00000299697 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153537731 C>A maps to NM_012253.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153537731 C>A maps to NM_012253.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98154989 G>T maps to NM_012465.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98154989 G>T maps to NM_012465.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98155082 C>A maps to NM_012465.3 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98155082 C>A maps to NM_012465.3 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154626275 C>A maps to NM_003264.3 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154626275 C>A maps to NM_003264.3 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187005224 G>T maps to NM_003265.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:187005224 G>T maps to NM_003265.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:120476547 C>A maps to NM_138554.3 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:120476547 C>A maps to NM_138554.3 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149093466 C>A maps to ENST00000383054 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149093466 C>A maps to ENST00000383054 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64881050 C>A maps to NM_003273.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64881050 C>A maps to NM_003273.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50152019 G>T maps to NM_001098576.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50152019 G>T maps to NM_001098576.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75366818 G>T maps to NM_138691.2 G197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75366818 G>T maps to NM_138691.2 G197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75387345 C>A maps to NM_138691.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75387345 C>A maps to NM_138691.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:19451842 G>T maps to NM_001105248.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:19451842 G>T maps to NM_001105248.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129373821 G>T maps to NM_001017395.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129373821 G>T maps to NM_001017395.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129547209 C>A maps to NM_001017395.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129547209 C>A maps to NM_001017395.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114188467 C>A maps to NM_017905.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114188467 C>A maps to NM_017905.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68894268 C>A maps to NM_024562.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68894268 C>A maps to NM_024562.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68901098 C>A maps to NM_024562.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68901098 C>A maps to NM_024562.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68912102 C>G maps to NM_024562.1 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68912102 C>G maps to NM_024562.1 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:72832378 G>T maps to NM_017728.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:72832378 G>T maps to NM_017728.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41367879 C>A maps to NM_145041.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41367879 C>A maps to NM_145041.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:133109036 G>T maps to NM_001136469.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:133109036 G>T maps to NM_001136469.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96920571 C>A maps to NM_017849.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:96920571 C>A maps to NM_017849.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:98375499 G>T maps to NM_015348.1 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:98375499 G>T maps to NM_015348.1 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60703949 C>A maps to NM_017870.3 P882P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60703949 C>A maps to NM_017870.3 P882P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10749853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10749853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:109416555 G>T maps to NM_032227.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:109416555 G>T maps to NM_032227.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82360852 G>C maps to NM_174909.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82360852 G>C maps to NM_174909.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:112423842 G>T maps to NM_022484.4 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:112423842 G>T maps to NM_022484.4 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11575781 C>A maps to NM_001100829.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11575781 C>A maps to NM_001100829.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:952103 G>T maps to NM_032326.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:952103 G>T maps to NM_032326.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159046212 C>A maps to NM_020823.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159046212 C>A maps to NM_020823.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202989964 C>A maps to NM_001079809.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202989964 C>A maps to NM_001079809.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1594943 C>A maps to NM_001097620.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1594943 C>A maps to NM_001097620.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48699328 G>T maps to NM_199203.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48699328 G>T maps to NM_199203.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72091105 C>A maps to NM_018279.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72091105 C>A maps to NM_018279.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129813712 C>A maps to NM_032842.3 G471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129813712 C>A maps to NM_032842.3 G471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27262684 C>A maps to NM_017727.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27262684 C>A maps to NM_017727.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136573358 C>A maps to NM_025246.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136573358 C>A maps to NM_025246.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136573605 C>A maps to NM_025246.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136573605 C>A maps to NM_025246.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136574393 C>A maps to NM_025246.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136574393 C>A maps to NM_025246.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41940647 G>T maps to NM_018126.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41940647 G>T maps to NM_018126.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16791231 G>T maps to NM_024074.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16791231 G>T maps to NM_024074.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129727242 C>A maps to NM_138788.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129727242 C>A maps to NM_138788.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95657234 C>A maps to NM_152487.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95657234 C>A maps to NM_152487.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95657252 C>A maps to NM_152487.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95657252 C>A maps to NM_152487.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64174805 C>A maps to NM_014254.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64174805 C>A maps to NM_014254.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46158898 G>T maps to NM_016486.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46158898 G>T maps to NM_016486.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:74891083 C>A maps to NM_017866.5 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:74891083 C>A maps to NM_017866.5 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:109797042 C>A maps to NM_153015.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:109797042 C>A maps to NM_153015.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42553155 G>T maps to ENST00000389834 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42553155 G>T maps to ENST00000389834 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7259360 C>A maps to NM_198154.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7259360 C>A maps to NM_198154.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69084263 C>A maps to NM_007114.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69084263 C>A maps to NM_007114.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:28651864 C>A maps to NM_206832.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:28651864 C>A maps to NM_206832.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4292844 C>A maps to NM_144615.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4292844 C>A maps to NM_144615.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100308586 C>A maps to NM_003275.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100308586 C>A maps to NM_003275.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52192419 G>T maps to NM_014547.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52192419 G>T maps to NM_014547.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151143009 G>T maps to NM_013353.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151143009 G>T maps to NM_013353.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:98938064 G>T maps to NM_001032283.2 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:98938064 G>T maps to NM_001032283.2 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68780427 G>T maps to NM_182606.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68780427 G>T maps to NM_182606.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111782382 G>T maps to ENST00000443106 G475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111782382 G>T maps to ENST00000443106 G475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:91760173 G>T maps to NM_183049.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:91760173 G>T maps to NM_183049.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:83289718 C>A maps to NM_152588.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:83289718 C>A maps to NM_152588.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101278337 G>T maps to NM_032813.2 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101278337 G>T maps to NM_032813.2 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:7963022 G>T maps to NM_021156.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:7963022 G>T maps to NM_021156.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117791707 C>A maps to NM_002160.2 E2034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117791707 C>A maps to NM_002160.2 E2034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117827016 C>A maps to NM_002160.2 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117827016 C>A maps to NM_002160.2 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26668431 C>A maps to NM_021137.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26668431 C>A maps to NM_021137.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:138196884 C>A maps to NM_006290.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:138196884 C>A maps to NM_006290.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23003289 G>T maps to NM_003840.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:23003289 G>T maps to NM_003840.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:119945314 G>C maps to NM_002546.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:119945314 G>C maps to NM_002546.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170819245 G>T maps to NM_015028.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170819245 G>T maps to NM_015028.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150418701 G>T maps to NM_006058.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150418701 G>T maps to NM_006058.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57075875 C>A maps to NM_033396.2 G1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57075875 C>A maps to NM_033396.2 G1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93600409 C>A maps to NM_025235.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93600409 C>A maps to NM_025235.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175048793 G>C maps to NM_022093.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175048793 G>C maps to NM_022093.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12813667 G>T maps to NM_001136196.1 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12813667 G>T maps to NM_001136196.1 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175331943 C>A maps to NM_003285.2 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175331943 C>A maps to NM_003285.2 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38548921 G>T maps to ENST00000357601 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38548921 G>T maps to ENST00000357601 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:133358854 C>A maps to NM_007027.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:133358854 C>A maps to NM_007027.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32541935 G>T maps to NM_005802.4 R863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32541935 G>T maps to NM_005802.4 R863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179886867 C>A maps to ENST00000398836 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179886867 C>A maps to ENST00000398836 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132569592 G>T maps to NM_014506.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132569592 G>T maps to NM_014506.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59739410 G>T maps to NM_014729.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59739410 G>T maps to NM_014729.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223986193 C>A maps to NM_001031685.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223986193 C>A maps to NM_001031685.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:44956542 C>A maps to NM_006034.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:44956542 C>A maps to NM_006034.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24303823 G>T maps to NM_147184.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24303823 G>T maps to NM_147184.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24303848 C>A maps to NM_147184.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24303848 C>A maps to NM_147184.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83075904 C>A maps to NM_006670.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83075904 C>A maps to NM_006670.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113710496 C>A maps to NM_001143819.1 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113710496 C>A maps to NM_001143819.1 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:80950386 C>A maps to NM_001025252.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:80950386 C>A maps to NM_001025252.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72366469 C>A maps to ENST00000389376 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72366469 C>A maps to ENST00000389376 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:144320354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:144320354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154142912 C>A maps to NM_001043351.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154142912 C>A maps to NM_001043351.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154164409 C>A maps to ENST00000271850 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154164409 C>A maps to ENST00000271850 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18149317 G>T maps to NM_000367.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18149317 G>T maps to NM_000367.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103275271 C>A maps to ENST00000376052 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103275271 C>A maps to ENST00000376052 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103275340 C>A maps to ENST00000376052 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103275340 C>A maps to ENST00000376052 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103297266 G>T maps to ENST00000376052 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103297266 G>T maps to ENST00000376052 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73961618 C>A maps to ENST00000409716 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73961618 C>A maps to ENST00000409716 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186316441 G>T maps to NM_003292.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186316441 G>T maps to NM_003292.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30385265 C>A maps to ENST00000340513 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30385265 C>A maps to ENST00000340513 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23561429 C>A maps to NM_013293.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23561429 C>A maps to NM_013293.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185643391 G>T maps to NM_004593.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185643391 G>T maps to NM_004593.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209953827 C>A maps to NM_025228.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209953827 C>A maps to NM_025228.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:36522876 G>T maps to NM_145803.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:36522876 G>T maps to NM_145803.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112578718 C>A maps to NM_006700.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112578718 C>A maps to NM_006700.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:118005504 C>A maps to NM_152402.2 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:118005504 C>A maps to NM_152402.2 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36873249 G>T maps to NM_014831.2 P2564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36873249 G>T maps to NM_014831.2 P2564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36896823 C>A maps to NM_014831.2 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36896823 C>A maps to NM_014831.2 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36897276 C>A maps to NM_014831.2 T1268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36897276 C>A maps to NM_014831.2 T1268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88925065 G>T maps to NM_016209.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88925065 G>T maps to NM_016209.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:140922434 G>T maps to NM_031466.5 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:140922434 G>T maps to NM_031466.5 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141294106 C>A maps to NM_031466.5 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141294106 C>A maps to NM_031466.5 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41166017 G>T maps to ENST00000373108 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41166017 G>T maps to ENST00000373108 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196271 G>T maps to NM_033502.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196271 G>T maps to NM_033502.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196277 C>A maps to NM_033502.2 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196277 C>A maps to NM_033502.2 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196319 C>A maps to NM_033502.2 A1122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196319 C>A maps to NM_033502.2 A1122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72680607 C>A maps to NM_013381.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72680607 C>A maps to NM_013381.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72969289 G>T maps to NM_013381.2 A718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72969289 G>T maps to NM_013381.2 A718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:372007 C>A maps to ENST00000422053 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:372007 C>A maps to ENST00000422053 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100857227 G>T maps to NM_033219.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100857227 G>T maps to NM_033219.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119998087 G>T maps to NM_012101.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119998087 G>T maps to NM_012101.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154197119 C>A maps to NM_015271.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:154197119 C>A maps to NM_015271.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:57109389 G>T maps to NM_015294.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:57109389 G>T maps to NM_015294.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117660695 G>T maps to NM_025188.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117660695 G>T maps to NM_025188.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99514345 G>T maps to NM_033017.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99514345 G>T maps to NM_033017.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:160156356 C>A maps to ENST00000483754 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:160156356 C>A maps to ENST00000483754 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5656044 C>A maps to NM_001003819.3 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5656044 C>A maps to NM_001003819.3 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104414480 C>A maps to NM_030912.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104414480 C>A maps to NM_030912.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:189068015 C>A maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:189068015 C>A maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:189068072 C>A maps to NM_178556.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:189068072 C>A maps to NM_178556.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:189068225 C>A maps to NM_178556.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:189068225 C>A maps to NM_178556.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14336715 C>A maps to NM_007118.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14336715 C>A maps to NM_007118.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14399014 G>T maps to NM_007118.2 G1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14399014 G>T maps to NM_007118.2 G1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230654475 C>A maps to ENST00000389044 G1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230654475 C>A maps to ENST00000389044 G1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64717778 G>T maps to NM_016213.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64717778 G>T maps to NM_016213.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49722972 C>A maps to NM_005480.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49722972 C>A maps to NM_005480.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38213191 G>T maps to NM_003306.1 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38213191 G>T maps to NM_003306.1 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38320253 C>A maps to NM_003306.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38320253 C>A maps to NM_003306.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:101342018 C>A maps to NM_004621.5 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:101342018 C>A maps to NM_004621.5 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31294432 C>A maps to NM_002420.4 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31294432 C>A maps to NM_002420.4 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31295094 G>T maps to NM_002420.4 R1248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31295094 G>T maps to NM_002420.4 R1248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31341633 C>A maps to NM_002420.4 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31341633 C>A maps to NM_002420.4 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:73235269 G>T maps to ENST00000419692 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:73235269 G>T maps to ENST00000419692 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:73296488 C>A maps to ENST00000419692 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:73296488 C>A maps to ENST00000419692 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77397657 G>T maps to NM_017662.4 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77397657 G>T maps to NM_017662.4 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:50886635 G>T maps to NM_017672.4 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:50886635 G>T maps to NM_017672.4 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234854498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234854498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234879015 C>A maps to NM_024080.4 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234879015 C>A maps to NM_024080.4 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:116430557 C>A maps to NM_014112.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:116430557 C>A maps to NM_014112.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:116616109 G>T maps to NM_014112.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:116616109 G>T maps to NM_014112.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:116616611 G>T maps to NM_014112.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:116616611 G>T maps to NM_014112.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98547696 G>T maps to ENST00000359863 G1709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98547696 G>T maps to ENST00000359863 G1709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98606004 C>A maps to ENST00000359863 R3573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98606004 C>A maps to ENST00000359863 R3573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116702489 C>A maps to NM_139169.4 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116702489 C>A maps to NM_139169.4 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45149844 G>T maps to NM_183422.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45149844 G>T maps to NM_183422.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2105442 G>T maps to NM_000548.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2105442 G>T maps to NM_000548.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2129134 G>T maps to NM_000548.3 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2129134 G>T maps to NM_000548.3 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73513705 C>A maps to NM_207346.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73513705 C>A maps to NM_207346.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18505560 C>A maps to NM_006292.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18505560 C>A maps to NM_006292.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:130038847 C>A maps to NM_018718.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:130038847 C>A maps to NM_018718.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115576619 C>A maps to NM_000549.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115576619 C>A maps to NM_000549.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115576709 C>A maps to NM_000549.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115576709 C>A maps to NM_000549.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72998822 C>A maps to NM_005786.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72998822 C>A maps to NM_005786.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:73000553 C>A maps to NM_005786.4 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:73000553 C>A maps to NM_005786.4 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:51870468 C>A maps to NM_173485.5 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:51870468 C>A maps to NM_173485.5 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:31768235 C>A maps to NM_020856.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:31768235 C>A maps to NM_020856.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:31769557 G>T maps to NM_020856.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:31769557 G>T maps to NM_020856.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31131539 G>T maps to NM_001080509.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31131539 G>T maps to NM_001080509.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31135552 C>A maps to NM_001080509.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31135552 C>A maps to NM_001080509.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176078804 C>A maps to NM_012171.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176078804 C>A maps to NM_012171.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115600201 C>A maps to NM_005725.4 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115600201 C>A maps to NM_005725.4 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58140868 C>A maps to NM_005981.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58140868 C>A maps to NM_005981.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116600165 C>A maps to NM_003309.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116600165 C>A maps to NM_003309.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:98288991 C>A maps to NM_033512.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:98288991 C>A maps to NM_033512.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100389745 G>T maps to NM_139246.4 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100389745 G>T maps to NM_139246.4 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43075697 C>A maps to ENST00000263802 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43075697 C>A maps to ENST00000263802 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231044741 C>A maps to NM_024525.4 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231044741 C>A maps to NM_024525.4 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231059657 G>T maps to NM_024525.4 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231059657 G>T maps to NM_024525.4 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231081142 C>A maps to NM_024525.4 G191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231081142 C>A maps to NM_024525.4 G191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180327787 G>T maps to NM_133462.3 G591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180327787 G>T maps to NM_133462.3 G591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43411311 C>A maps to NM_018259.5 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43411311 C>A maps to NM_018259.5 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43515376 G>T maps to NM_018259.5 E1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43515376 G>T maps to NM_018259.5 E1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39169873 C>A maps to ENST00000301819 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39169873 C>A maps to ENST00000301819 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39180218 C>A maps to ENST00000301819 P1302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39180218 C>A maps to ENST00000301819 P1302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99759175 C>A maps to NM_022905.4 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99759175 C>A maps to NM_022905.4 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138874133 C>A maps to NM_024926.2 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138874133 C>A maps to NM_024926.2 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178481580 C>A maps to NM_152275.3 G617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178481580 C>A maps to NM_152275.3 G617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178416491 C>A maps to NM_152517.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178416491 C>A maps to NM_152517.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40716251 G>T maps to NM_012382.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40716251 G>T maps to NM_012382.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20768861 G>T maps to NM_138376.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20768861 G>T maps to NM_138376.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:91077092 G>T maps to NM_001010854.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:91077092 G>T maps to NM_001010854.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135266182 G>T maps to NM_007344.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135266182 G>T maps to NM_007344.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117618442 C>A maps to NM_003594.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117618442 C>A maps to NM_003594.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117639996 G>T maps to NM_003594.3 G1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117639996 G>T maps to NM_003594.3 G1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644103 C>A maps to NM_003594.3 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644103 C>A maps to NM_003594.3 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90799111 C>A maps to ENST00000438251 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90799111 C>A maps to ENST00000438251 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113243503 C>A maps to NM_153712.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113243503 C>A maps to NM_153712.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179395885 G>T maps to NM_133378.4 T32584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179395885 G>T maps to NM_133378.4 T32584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179404291 C>A maps to NM_133378.4 E30266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179404291 C>A maps to NM_133378.4 E30266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179407817 G>T maps to NM_133378.4 A29726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179407817 G>T maps to NM_133378.4 A29726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179409009 G>T maps to NM_133378.4 S29414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179409009 G>T maps to NM_133378.4 S29414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179414793 G>T maps to NM_133378.4 R28023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179414793 G>T maps to NM_133378.4 R28023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179427743 G>T maps to NM_133378.4 P25137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179427743 G>T maps to NM_133378.4 P25137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179428253 G>T maps to NM_133378.4 T24967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179428253 G>T maps to NM_133378.4 T24967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179430005 G>T maps to NM_133378.4 T24383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179430005 G>T maps to NM_133378.4 T24383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179434061 C>A maps to NM_133378.4 L23031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179434061 C>A maps to NM_133378.4 L23031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179435608 G>T maps to NM_133378.4 R22516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179435608 G>T maps to NM_133378.4 R22516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179441794 C>A maps to NM_133378.4 V20521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179441794 C>A maps to NM_133378.4 V20521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179449452 G>T maps to NM_133378.4 R19071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179449452 G>T maps to NM_133378.4 R19071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179454956 G>T maps to NM_133378.4 R17931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179454956 G>T maps to NM_133378.4 R17931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179456109 G>T maps to NM_133378.4 T17546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179456109 G>T maps to NM_133378.4 T17546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179469836 G>T maps to NM_133378.4 R15455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179469836 G>T maps to NM_133378.4 R15455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179474289 G>T maps to NM_133378.4 P14681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179474289 G>T maps to NM_133378.4 P14681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179542438 G>T maps to NM_133378.4 P10156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179542438 G>T maps to NM_133378.4 P10156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179565880 G>T maps to NM_133378.4 P8972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179565880 G>T maps to NM_133378.4 P8972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179571292 G>T maps to NM_133378.4 R8526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179571292 G>T maps to NM_133378.4 R8526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179575969 G>T maps to NM_133378.4 S8087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179575969 G>T maps to NM_133378.4 S8087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179584293 G>T maps to NM_133378.4 S6731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179584293 G>T maps to NM_133378.4 S6731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179596041 G>T maps to NM_133378.4 L4573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179596041 G>T maps to NM_133378.4 L4573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179596080 G>T maps to NM_133378.4 A4560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179596080 G>T maps to NM_133378.4 A4560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179598188 G>T maps to NM_133378.4 P4033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179598188 G>T maps to NM_133378.4 P4033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179605725 G>T maps to NM_133437.3 T3907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179605725 G>T maps to NM_133437.3 T3907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179610899 G>T maps to ENST00000375038 P5411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179610899 G>T maps to ENST00000375038 P5411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179640848 C>A maps to NM_133378.4 A1914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179640848 C>A maps to NM_133378.4 A1914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179641949 C>A maps to NM_133378.4 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179641949 C>A maps to NM_133378.4 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179659891 G>T maps to NM_133378.4 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179659891 G>T maps to NM_133378.4 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179664562 G>T maps to NM_133378.4 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179664562 G>T maps to NM_133378.4 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49580106 G>T maps to NM_006009.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49580106 G>T maps to NM_006009.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:19751456 G>T maps to NM_006001.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:19751456 G>T maps to NM_006001.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:132235768 G>T maps to NM_080386.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:132235768 G>T maps to NM_080386.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:132240384 C>G maps to NM_080386.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:132240384 C>G maps to NM_080386.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:130953851 G>T maps to NM_207312.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:130953851 G>T maps to NM_207312.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5437397 G>T maps to NM_024803.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:5437397 G>T maps to NM_024803.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57598638 C>A maps to NM_030773.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57598638 C>A maps to NM_030773.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57599036 G>T maps to NM_030773.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57599036 G>T maps to NM_030773.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89986469 C>A maps to ENST00000304984 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89986469 C>A maps to ENST00000304984 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6495276 G>T maps to NM_006087.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6495276 G>T maps to NM_006087.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6495282 G>T maps to NM_006087.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6495282 G>T maps to NM_006087.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6495312 C>A maps to NM_006087.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6495312 C>A maps to NM_006087.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12325072 G>T maps to NM_032525.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12325072 G>T maps to NM_032525.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93293 G>T maps to NM_177987.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93293 G>T maps to NM_177987.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113210369 C>A maps to NM_006322.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113210369 C>A maps to NM_006322.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:22851019 C>A maps to NM_052903.4 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:22851019 C>A maps to NM_052903.4 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:22863003 G>T maps to NM_052903.4 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:22863003 G>T maps to NM_052903.4 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35478680 G>T maps to NM_003322.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35478680 G>T maps to NM_003322.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:3047296 C>A maps to NM_001160408.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:3047296 C>A maps to NM_001160408.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158850871 C>A maps to NM_020245.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158850871 C>A maps to NM_020245.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158873217 C>A maps to NM_020245.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158873217 C>A maps to NM_020245.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:15605950 C>A maps to NM_006765.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:15605950 C>A maps to NM_006765.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:44189498 G>T maps to NM_002822.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:44189498 G>T maps to NM_002822.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104682766 C>A maps to NM_001093771.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104682766 C>A maps to NM_001093771.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104714898 G>T maps to NM_001093771.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104714898 G>T maps to NM_001093771.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:19865924 C>A maps to NM_006440.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:19865924 C>A maps to NM_006440.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:19870925 G>T maps to NM_006440.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:19870925 G>T maps to NM_006440.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41862462 C>A maps to NM_006293.3 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41862462 C>A maps to NM_006293.3 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88961018 G>T maps to NM_000372.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88961018 G>T maps to NM_000372.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75229634 C>A maps to NM_138467.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75229634 C>A maps to NM_138467.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:166580130 G>T maps to NM_003181.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:166580130 G>T maps to NM_003181.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:70961405 G>T maps to NM_018003.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:70961405 G>T maps to NM_018003.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139973521 G>T maps to NM_207309.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139973521 G>T maps to NM_207309.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139974583 C>A maps to NM_207309.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139974583 C>A maps to NM_207309.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162557297 G>T maps to ENST00000367925 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162557297 G>T maps to ENST00000367925 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69105053 C>A maps to NM_003968.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69105053 C>A maps to NM_003968.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68506918 C>A maps to NM_018227.5 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68506918 C>A maps to NM_018227.5 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99890738 C>A maps to NM_001144072.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99890738 C>A maps to NM_001144072.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154239018 C>A maps to NM_014847.3 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154239018 C>A maps to NM_014847.3 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33944407 G>T maps to NM_018449.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33944407 G>T maps to NM_018449.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33948492 C>A maps to NM_018449.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33948492 C>A maps to NM_018449.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33986797 C>A maps to NM_018449.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33986797 C>A maps to NM_018449.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122653912 C>A maps to NM_032873.4 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122653912 C>A maps to NM_032873.4 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125396427 G>T maps to NM_021009.5 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125396427 G>T maps to NM_021009.5 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4200056 G>T maps to NM_003342.4 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4200056 G>T maps to NM_003342.4 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129519467 C>A maps to NM_003344.2 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129519467 C>A maps to NM_003344.2 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129592356 C>A maps to NM_003344.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129592356 C>A maps to NM_003344.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74392593 G>C maps to NM_022066.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74392593 G>C maps to NM_022066.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76168526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76168526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109926397 C>A maps to NM_183415.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109926397 C>A maps to NM_183415.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109939182 G>T maps to NM_183415.1 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109939182 G>T maps to NM_183415.1 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:157060370 C>A maps to NM_014671.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:157060370 C>A maps to NM_014671.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118239373 G>T maps to NM_004788.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118239373 G>T maps to NM_004788.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118260524 C>A maps to NM_004788.2 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118260524 C>A maps to NM_004788.2 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3090940 C>A maps to NM_014948.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3090940 C>A maps to NM_014948.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33450742 G>T maps to NM_001128161.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33450742 G>T maps to NM_001128161.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86293456 G>T maps to NM_013438.4 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86293456 G>T maps to NM_013438.4 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42574341 C>A maps to NM_015255.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42574341 C>A maps to NM_015255.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42637934 C>A maps to NM_015255.2 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42637934 C>A maps to NM_015255.2 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103301734 G>T maps to NM_015902.4 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103301734 G>T maps to NM_015902.4 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103316392 C>A maps to NM_015902.4 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103316392 C>A maps to NM_015902.4 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103372396 C>A maps to NM_015902.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103372396 C>A maps to NM_015902.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42290592 G>T maps to NM_014233.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42290592 G>T maps to NM_014233.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42293937 C>A maps to NM_014233.2 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42293937 C>A maps to NM_014233.2 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24194265 C>A maps to NM_181713.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24194265 C>A maps to NM_181713.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4445527 G>T maps to NM_025241.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4445527 G>T maps to NM_025241.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4446168 C>A maps to NM_025241.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4446168 C>A maps to NM_025241.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196134246 C>A maps to NM_015562.1 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196134246 C>A maps to NM_015562.1 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:165865553 C>A maps to NM_012474.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:165865553 C>A maps to NM_012474.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73689041 G>T maps to NM_003355.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73689041 G>T maps to NM_003355.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161123853 C>A maps to NM_016406.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:161123853 C>A maps to NM_016406.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:19438195 G>T maps to ENST00000399525 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:19438195 G>T maps to ENST00000399525 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234545429 C>A maps to NM_019075.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234545429 C>A maps to NM_019075.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234545932 G>T maps to NM_019075.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234545932 G>T maps to NM_019075.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234545968 C>A maps to NM_019075.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234545968 C>A maps to NM_019075.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234628224 C>A maps to NM_007120.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234628224 C>A maps to NM_007120.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234622345 G>T maps to NM_019078.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234622345 G>T maps to NM_019078.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234622408 C>A maps to NM_019078.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234622408 C>A maps to NM_019078.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234591302 G>T maps to ENST00000373460 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234591302 G>T maps to ENST00000373460 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234527144 C>A maps to NM_019076.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234527144 C>A maps to NM_019076.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234581344 G>T maps to NM_021027.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234581344 G>T maps to NM_021027.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69796271 G>T maps to NM_024743.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69796271 G>T maps to NM_024743.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69519966 G>T maps to NM_001076.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69519966 G>T maps to NM_001076.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:70146439 C>A maps to NM_053039.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:70146439 C>A maps to NM_053039.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69962447 C>A maps to NM_001074.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69962447 C>A maps to NM_001074.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36039681 G>T maps to NM_174914.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36039681 G>T maps to NM_174914.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34804115 C>A maps to NM_017754.3 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34804115 C>A maps to NM_017754.3 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34824130 G>T maps to NM_017754.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34824130 G>T maps to NM_017754.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41841683 G>T maps to NM_017886.2 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41841683 G>T maps to NM_017886.2 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41942234 G>T maps to NM_017886.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41942234 G>T maps to NM_017886.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41942258 C>A maps to NM_017886.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41942258 C>A maps to NM_017886.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41996220 C>A maps to NM_017886.2 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41996220 C>A maps to NM_017886.2 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43522324 G>T maps to NM_173568.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43522324 G>T maps to NM_173568.3 T412T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124461052 C>A maps to NM_000373.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124461052 C>A maps to NM_000373.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35400425 C>A maps to ENST00000396787 S1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35400425 C>A maps to ENST00000396787 S1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:54919113 G>T maps to ENST00000260323 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:54919113 G>T maps to ENST00000260323 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73832181 C>A maps to ENST00000412096 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73832181 C>A maps to ENST00000412096 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91482980 G>T maps to NM_018671.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91482980 G>T maps to NM_018671.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73050693 G>T maps to NM_170744.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73050693 G>T maps to NM_170744.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:96140339 G>T maps to NM_003728.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:96140339 G>T maps to NM_003728.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167709627 G>T maps to NM_018974.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167709627 G>T maps to NM_018974.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109547696 G>T maps to NM_080911.2 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109547696 G>T maps to NM_080911.2 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12001175 G>T maps to NM_015542.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12001175 G>T maps to NM_015542.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158977979 C>A maps to NM_001135098.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:158977979 C>A maps to NM_001135098.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229772942 C>A maps to NM_014777.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229772942 C>A maps to NM_014777.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229773044 G>T maps to NM_014777.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229773044 G>T maps to NM_014777.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229773134 C>A maps to NM_014777.2 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:229773134 C>A maps to NM_014777.2 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43921520 C>A maps to NM_001077663.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43921520 C>A maps to NM_001077663.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216052409 C>A maps to ENST00000366943 G2752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216052409 C>A maps to ENST00000366943 G2752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216258076 G>T maps to ENST00000366943 P1710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216258076 G>T maps to ENST00000366943 P1710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62910807 C>A maps to NM_003368.4 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62910807 C>A maps to NM_003368.4 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113683141 G>T maps to NM_020886.2 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113683141 G>T maps to NM_020886.2 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113704161 G>T maps to NM_020886.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113704161 G>T maps to NM_020886.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113711321 G>A maps to NM_020886.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113711321 G>A maps to NM_020886.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113725030 C>A maps to NM_020886.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113725030 C>A maps to NM_020886.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:58267962 G>T maps to NM_032582.3 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:58267962 G>T maps to NM_032582.3 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:58348782 G>T maps to NM_032582.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:58348782 G>T maps to NM_032582.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61441511 C>A maps to NM_014709.3 E2789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61441511 C>A maps to NM_014709.3 E2789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61605508 C>A maps to NM_014709.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61605508 C>A maps to NM_014709.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61610447 G>T maps to NM_014709.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61610447 G>T maps to NM_014709.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76795039 G>T maps to NM_025090.3 R1064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76795039 G>T maps to NM_025090.3 R1064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219339353 C>A maps to NM_020935.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219339353 C>A maps to NM_020935.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6185200 G>T maps to ENST00000404835 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6185200 G>T maps to ENST00000404835 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11963880 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11963880 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41774538 C>A maps to ENST00000373009 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41774538 C>A maps to ENST00000373009 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49322010 C>A maps to NM_003363.3 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49322010 C>A maps to NM_003363.3 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49363182 C>A maps to NM_003363.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49363182 C>A maps to NM_003363.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120169946 C>A maps to NM_019050.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120169946 C>A maps to NM_019050.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6972467 C>A maps to NM_001098536.1 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6972467 C>A maps to NM_001098536.1 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:11505471 G>T maps to NM_001080491.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:11505471 G>T maps to NM_001080491.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:9014235 C>A maps to NM_003470.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:9014235 C>A maps to NM_003470.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52603606 C>A maps to NM_021645.5 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52603606 C>A maps to NM_021645.5 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:72868389 C>A maps to NM_032175.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:72868389 C>A maps to NM_032175.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71555306 C>A maps to NM_020368.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71555306 C>A maps to NM_020368.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:145160397 C>A maps to NM_007124.2 S3385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:145160397 C>A maps to NM_007124.2 S3385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:190999924 G>T maps to NM_198152.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:190999924 G>T maps to NM_198152.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75562960 C>A maps to NM_003369.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75562960 C>A maps to NM_003369.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75590942 C>A maps to NM_003369.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75590942 C>A maps to NM_003369.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75727940 C>G maps to NM_003369.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75727940 C>G maps to NM_003369.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155169400 C>A maps to NM_005638.5 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155169400 C>A maps to NM_005638.5 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116206325 G>T maps to NM_001172412.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116206325 G>T maps to NM_001172412.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116233993 C>A maps to NM_001172412.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116233993 C>A maps to NM_001172412.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30884928 G>T maps to NM_001167734.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30884928 G>T maps to NM_001167734.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6829914 C>A maps to NM_005428.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:6829914 C>A maps to NM_005428.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:108315356 G>T maps to NM_006113.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:108315356 G>T maps to NM_006113.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101197992 C>A maps to NM_001078.3 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101197992 C>A maps to NM_001078.3 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101203710 G>T maps to NM_001078.3 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101203710 G>T maps to NM_001078.3 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101203718 C>A maps to NM_001078.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101203718 C>A maps to NM_001078.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75855495 C>A maps to NM_014000.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75855495 C>A maps to NM_014000.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177608594 C>A maps to NM_005429.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177608594 C>A maps to NM_005429.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177632711 C>A maps to NM_005429.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177632711 C>A maps to NM_005429.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:157081332 C>A maps to NM_001167912.1 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:157081332 C>A maps to NM_001167912.1 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219301235 C>A maps to NM_007127.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219301235 C>A maps to NM_007127.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219313956 C>A maps to NM_007127.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219313956 C>A maps to NM_007127.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38048476 C>A maps to NM_015873.3 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38048476 C>A maps to NM_015873.3 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118951914 C>A maps to NM_021729.4 S850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118951914 C>A maps to NM_021729.4 S850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79954787 C>A maps to ENST00000376646 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79954787 C>A maps to ENST00000376646 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100479780 G>T maps to NM_017890.3 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100479780 G>T maps to NM_017890.3 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100654403 C>A maps to NM_017890.3 P1887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100654403 C>A maps to NM_017890.3 P1887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100791177 C>A maps to NM_017890.3 T2591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100791177 C>A maps to NM_017890.3 T2591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100836190 C>A maps to NM_017890.3 P3130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100836190 C>A maps to NM_017890.3 P3130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100866129 C>A maps to NM_017890.3 R3530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100866129 C>A maps to NM_017890.3 R3530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:62283952 C>A maps to NM_020821.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:62283952 C>A maps to NM_020821.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12429616 C>A maps to NM_015378.2 P3556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12429616 C>A maps to NM_015378.2 P3556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70931006 C>A maps to NM_004896.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:70931006 C>A maps to NM_004896.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122720401 C>A maps to NM_022916.4 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122720401 C>A maps to NM_022916.4 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122723230 G>T maps to NM_022916.4 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122723230 G>T maps to NM_022916.4 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46712914 C>A maps to NM_018206.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46712914 C>A maps to NM_018206.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17132451 G>T maps to NM_152415.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17132451 G>T maps to NM_152415.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33238057 C>A maps to NM_022553.4 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33238057 C>A maps to NM_022553.4 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184632825 C>A maps to ENST00000437079 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184632825 C>A maps to ENST00000437079 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:58315575 C>A maps to NM_001130480.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:58315575 C>A maps to NM_001130480.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124618383 C>A maps to NM_014312.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124618383 C>A maps to NM_014312.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:17830721 C>A maps to NM_003385.4 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:17830721 C>A maps to NM_003385.4 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:54610467 C>A maps to ENST00000404951 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:54610467 C>A maps to ENST00000404951 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25059479 G>T maps to NM_014588.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25059479 G>T maps to NM_014588.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25059511 G>T maps to NM_014588.4 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25059511 G>T maps to NM_014588.4 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117690399 C>A maps to NM_024626.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117690399 C>A maps to NM_024626.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116014800 C>A maps to NM_198496.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116014800 C>A maps to NM_198496.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119575731 C>A maps to NM_015836.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119575731 C>A maps to NM_015836.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27739100 G>T maps to NM_006990.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27739100 G>T maps to NM_006990.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123329147 C>A maps to NM_003941.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123329147 C>A maps to NM_003941.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73851355 G>T maps to NM_012478.3 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73851355 G>T maps to NM_012478.3 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73098117 C>A maps to ENST00000423497 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73098117 C>A maps to ENST00000423497 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73101040 C>A maps to ENST00000423497 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73101040 C>A maps to ENST00000423497 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85654534 C>A maps to NM_014991.4 A2407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85654534 C>A maps to NM_014991.4 A2407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177069286 C>A maps to NM_170710.4 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177069286 C>A maps to NM_170710.4 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39278645 C>A maps to NM_025132.3 P1241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39278645 C>A maps to NM_025132.3 P1241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224607246 G>T maps to NM_025160.6 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224607246 G>T maps to NM_025160.6 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131403137 C>T maps to NM_052844.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131403137 C>T maps to NM_052844.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20145668 C>A maps to NM_001006657.1 G586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20145668 C>A maps to NM_001006657.1 G586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:110446901 C>A maps to NM_139281.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:110446901 C>A maps to NM_139281.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:110454737 G>T maps to NM_139281.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:110454737 G>T maps to NM_139281.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127616564 C>A maps to NM_001045476.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127616564 C>A maps to NM_001045476.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118483475 C>A maps to NM_006784.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118483475 C>A maps to NM_006784.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118492636 C>A maps to NM_006784.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118492636 C>A maps to NM_006784.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118492683 C>A maps to NM_006784.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118492683 C>A maps to NM_006784.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118494624 C>A maps to NM_006784.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118494624 C>A maps to NM_006784.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118496662 C>A maps to NM_006784.2 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118496662 C>A maps to NM_006784.2 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167293814 G>T maps to NM_178824.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167293814 G>T maps to NM_178824.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113084888 G>T maps to NM_001164496.1 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113084888 G>T maps to NM_001164496.1 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113118757 G>T maps to NM_001164496.1 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113118757 G>T maps to NM_001164496.1 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196281650 G>T maps to NM_182627.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196281650 G>T maps to NM_182627.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85559269 C>A maps to NM_145172.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85559269 C>A maps to NM_145172.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43650906 C>A maps to NM_001195831.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43650906 C>A maps to NM_001195831.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124146418 C>A maps to NM_145647.3 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124146418 C>A maps to NM_145647.3 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37381750 C>A maps to NM_018034.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37381750 C>A maps to NM_018034.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37516653 C>A maps to NM_018034.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37516653 C>A maps to NM_018034.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37697793 C>A maps to NM_018034.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37697793 C>A maps to NM_018034.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190316542 G>T maps to NM_032168.1 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190316542 G>T maps to NM_032168.1 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44143305 G>T maps to NM_024908.3 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44143305 G>T maps to NM_024908.3 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54353208 G>T maps to NM_015285.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54353208 G>T maps to NM_015285.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54446753 C>A maps to NM_015285.2 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54446753 C>A maps to NM_015285.2 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134873211 G>T maps to NM_014149.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134873211 G>T maps to NM_014149.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134894384 G>T maps to NM_014149.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134894384 G>T maps to NM_014149.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141424842 C>A maps to NM_001105558.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141424842 C>A maps to NM_001105558.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6303384 G>T maps to NM_006005.3 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6303384 G>T maps to NM_006005.3 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83499371 C>A maps to NM_001080435.1 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83499371 C>A maps to NM_001080435.1 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38173456 G>T maps to NM_023034.1 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38173456 G>T maps to NM_023034.1 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38187102 C>A maps to NM_023034.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38187102 C>A maps to NM_023034.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1961301 G>T maps to NM_133335.3 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1961301 G>T maps to NM_133335.3 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38433432 C>A maps to NM_133264.4 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38433432 C>A maps to NM_133264.4 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:990029 C>A maps to NM_001184985.1 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:990029 C>A maps to NM_001184985.1 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96062339 G>T maps to ENST00000297954 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96062339 G>T maps to ENST00000297954 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96062414 C>A maps to ENST00000297954 P2103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96062414 C>A maps to ENST00000297954 P2103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113057613 C>A maps to NM_024494.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113057613 C>A maps to NM_024494.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:31012183 G>T maps to NM_000553.4 T1244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:31012183 G>T maps to NM_000553.4 T1244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118474228 G>T maps to ENST00000441406 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118474228 G>T maps to ENST00000441406 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:5998450 C>A maps to NM_015253.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:5998450 C>A maps to NM_015253.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32413565 G>T maps to NM_024426.4 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32413565 G>T maps to NM_024426.4 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167850579 C>A maps to NM_001161661.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167850579 C>A maps to NM_001161661.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184190204 C>A maps to ENST00000448232 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184190204 C>A maps to ENST00000448232 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:10094186 G>T maps to NM_015691.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:10094186 G>T maps to NM_015691.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:78143685 G>T maps to NM_016373.1 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:78143685 G>T maps to NM_016373.1 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69959337 G>T maps to NM_007014.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69959337 G>T maps to NM_007014.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69969784 G>T maps to NM_007014.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69969784 G>T maps to NM_007014.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149238680 C>A maps to NM_001168278.1 G372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149238680 C>A maps to NM_001168278.1 G372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149245657 G>T maps to NM_001168278.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149245657 G>T maps to NM_001168278.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7685450 G>T maps to NM_020196.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7685450 G>T maps to NM_020196.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:31590877 C>A maps to NM_000379.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:31590877 C>A maps to NM_000379.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:168067273 G>T maps to NM_152381.5 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:168067273 G>T maps to NM_152381.5 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:168107039 C>A maps to NM_152381.5 P3046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:168107039 C>A maps to NM_152381.5 P3046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:111628452 C>A maps to NM_020383.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:111628452 C>A maps to NM_020383.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43495392 G>T maps to NM_020750.2 R967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43495392 G>T maps to NM_020750.2 R967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43533404 G>T maps to NM_020750.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43533404 G>T maps to NM_020750.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:21827748 G>T maps to ENST00000434536 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:21827748 G>T maps to ENST00000434536 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64816975 C>A maps to NM_007235.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64816975 C>A maps to NM_007235.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217012885 C>G maps to NM_021141.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217012885 C>G maps to NM_021141.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142054342 C>A maps to NM_019001.3 E1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142054342 C>A maps to NM_019001.3 E1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183454550 C>A maps to NM_018023.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183454550 C>A maps to NM_018023.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183469922 G>T maps to NM_018023.4 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183469922 G>T maps to NM_018023.4 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27437843 G>C maps to NM_139312.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27437843 G>C maps to NM_139312.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135763041 G>T maps to NM_025052.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135763041 G>T maps to NM_025052.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61834499 G>T maps to NM_017798.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61834499 G>T maps to NM_017798.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61835008 C>A maps to NM_017798.3 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61835008 C>A maps to NM_017798.3 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101960910 C>A maps to NM_003406.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:101960910 C>A maps to NM_003406.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72913949 C>A maps to NM_175907.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72913949 C>A maps to NM_175907.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72913991 C>A maps to NM_175907.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72913991 C>A maps to NM_175907.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72914027 G>T maps to NM_175907.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72914027 G>T maps to NM_175907.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72914060 G>T maps to NM_175907.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72914060 G>T maps to NM_175907.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2407371 G>T maps to NM_004729.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2407371 G>T maps to NM_004729.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50278735 G>T maps to NM_014838.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50278735 G>T maps to NM_014838.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101384029 G>T maps to NM_014415.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101384029 G>T maps to NM_014415.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101390911 C>A maps to NM_014415.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101390911 C>A maps to NM_014415.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16268517 G>T maps to ENST00000375733 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16268517 G>T maps to ENST00000375733 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109802500 G>T maps to NM_014797.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109802500 G>T maps to NM_014797.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125680968 G>T maps to NM_020924.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125680968 G>T maps to NM_020924.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151687972 G>T maps to NM_020861.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151687972 G>T maps to NM_020861.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173840008 C>A maps to NM_001122770.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173840008 C>A maps to NM_001122770.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141162762 G>T maps to NM_001080412.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141162762 G>T maps to NM_001080412.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141164412 G>T maps to NM_001080412.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141164412 G>T maps to NM_001080412.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141164650 G>T maps to NM_001080412.2 G1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141164650 G>T maps to NM_001080412.2 G1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129596035 G>T maps to NM_014007.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129596035 G>T maps to NM_014007.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130130951 C>A maps to ENST00000397753 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130130951 C>A maps to ENST00000397753 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:4317665 G>T maps to NM_145291.3 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:4317665 G>T maps to NM_145291.3 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7365426 C>A maps to NM_020899.3 A958A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7365426 C>A maps to NM_020899.3 A958A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:37948794 G>T maps to NM_025079.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:37948794 G>T maps to NM_025079.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:64718934 C>A maps to NM_001010888.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:64718934 C>A maps to NM_001010888.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46541740 G>T maps to ENST00000242848 R1407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46541740 G>T maps to ENST00000242848 R1407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46619578 G>T maps to ENST00000242848 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46619578 G>T maps to ENST00000242848 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88697532 C>A maps to ENST00000452588 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88697532 C>A maps to ENST00000452588 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47588353 C>A maps to NM_015168.1 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47588353 C>A maps to NM_015168.1 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113060834 G>T maps to NM_198581.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113060834 G>T maps to NM_198581.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87445898 G>T maps to NM_015144.2 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87445898 G>T maps to NM_015144.2 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88967735 G>T maps to NM_024617.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88967735 G>T maps to NM_024617.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122958544 G>T maps to NM_017612.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122958544 G>T maps to NM_017612.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207171912 C>A maps to NM_020923.1 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207171912 C>A maps to NM_020923.1 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207172902 C>A maps to NM_020923.1 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207172902 C>A maps to NM_020923.1 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:840676 G>T maps to NM_024786.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:840676 G>T maps to NM_024786.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:74670639 C>A maps to NM_144969.2 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:74670639 C>A maps to NM_144969.2 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99212231 C>A maps to NM_198046.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99212231 C>A maps to NM_198046.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45000622 G>T maps to NM_016598.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45000622 G>T maps to NM_016598.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6621823 C>A maps to NM_018106.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6621823 C>A maps to NM_018106.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:135622752 G>T maps to NM_020863.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:135622752 G>T maps to NM_020863.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72004320 C>A maps to NM_144982.4 G1953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72004320 C>A maps to NM_144982.4 G1953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72017979 G>T maps to NM_144982.4 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72017979 G>T maps to NM_144982.4 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72827367 G>T maps to NM_006885.3 T3071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72827367 G>T maps to NM_006885.3 T3071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72828578 G>T maps to NM_006885.3 R2668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72828578 G>T maps to NM_006885.3 R2668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72832029 C>A maps to NM_006885.3 S1517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72832029 C>A maps to NM_006885.3 S1517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72832062 C>A maps to NM_006885.3 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72832062 C>A maps to NM_006885.3 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:77763159 G>T maps to NM_024721.4 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:77763159 G>T maps to NM_024721.4 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42731443 G>T maps to NM_022473.1 S1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42731443 G>T maps to NM_022473.1 S1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42742465 G>T maps to NM_022473.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42742465 G>T maps to NM_022473.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42744078 G>T maps to NM_022473.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42744078 G>T maps to NM_022473.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:69256915 C>A maps to NM_004926.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:69256915 C>A maps to NM_004926.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:188924603 C>A maps to NM_174900.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:188924603 C>A maps to NM_174900.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64853933 C>A maps to NM_006782.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64853933 C>A maps to NM_006782.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:106813920 C>A maps to NM_012082.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:106813920 C>A maps to NM_012082.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:106814100 C>A maps to NM_012082.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:106814100 C>A maps to NM_012082.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32397395 C>A maps to NM_016107.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32397395 C>A maps to NM_016107.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32415287 G>T maps to NM_016107.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32415287 G>T maps to NM_016107.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:24197510 G>T maps to NM_003410.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:24197510 G>T maps to NM_003410.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:73445585 G>T maps to NM_021260.2 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:73445585 G>T maps to NM_021260.2 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52769578 C>A maps to NM_004799.2 P1140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52769578 C>A maps to NM_004799.2 P1140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28327467 C>A maps to NM_024493.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28327467 C>A maps to NM_024493.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28213079 G>T maps to NM_019110.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28213079 G>T maps to NM_019110.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:80961428 C>A maps to NM_020338.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:80961428 C>A maps to NM_020338.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:81056251 G>T maps to NM_020338.3 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:81056251 G>T maps to NM_020338.3 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:20660061 C>A maps to NM_001190965.1 R1348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:20660061 C>A maps to NM_001190965.1 R1348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35862195 C>A maps to NM_005095.2 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35862195 C>A maps to NM_005095.2 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:294322 C>A maps to NM_006624.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:294322 C>A maps to NM_006624.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140477532 G>T maps to NM_138462.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140477532 G>T maps to NM_138462.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140482271 G>T maps to NM_138462.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140482271 G>T maps to NM_138462.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45875138 C>A maps to ENST00000471951 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45875138 C>A maps to ENST00000471951 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45875244 C>A maps to ENST00000471951 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45875244 C>A maps to ENST00000471951 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45905373 G>T maps to ENST00000471951 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45905373 G>T maps to ENST00000471951 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48789960 C>A maps to NM_153608.1 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48789960 C>A maps to NM_153608.1 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:64441804 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:64441804 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:367155 C>A maps to NM_003441.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:367155 C>A maps to NM_003441.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36727546 G>T maps to NM_007145.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36727546 G>T maps to NM_007145.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146156720 C>A maps to NM_006958.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146156720 C>A maps to NM_006958.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:47836294 C>A maps to NM_006962.1 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:47836294 C>A maps to NM_006962.1 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27419414 G>T maps to NM_007149.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27419414 G>T maps to NM_007149.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28116380 C>A maps to NM_006298.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28116380 C>A maps to NM_006298.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6953613 C>A maps to NM_013250.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6953613 C>A maps to NM_013250.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:52193298 C>A maps to NM_006526.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:52193298 C>A maps to NM_006526.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:52198528 C>A maps to NM_006526.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:52198528 C>A maps to NM_006526.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44469100 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44469100 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44622424 C>A maps to NM_013362.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44622424 C>A maps to NM_013362.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44680029 C>A maps to NM_001032372.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44680029 C>A maps to NM_001032372.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44740715 G>T maps to NM_182490.1 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44740715 G>T maps to NM_182490.1 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:244218593 G>T maps to NM_205768.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:244218593 G>T maps to NM_205768.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71483579 G>T maps to NM_145911.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71483579 G>T maps to NM_145911.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145947301 G>T maps to NM_138367.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145947301 G>T maps to NM_138367.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116656258 G>T maps to NM_003904.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116656258 G>T maps to NM_003904.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44351958 C>A maps to NM_181845.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44351958 C>A maps to NM_181845.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43411924 G>T maps to NM_020727.4 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43411924 G>T maps to NM_020727.4 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57869166 G>T maps to ENST00000391705 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57869166 G>T maps to ENST00000391705 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43325503 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43325503 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58031554 G>T maps to NM_020807.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58031554 G>T maps to NM_020807.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28294052 G>T maps to NM_030899.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28294052 G>T maps to NM_030899.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28297300 G>T maps to NM_030899.4 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28297300 G>T maps to NM_030899.4 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44590800 C>A maps to NM_022095.3 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44590800 C>A maps to NM_022095.3 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25656222 C>A maps to NM_015655.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25656222 C>A maps to NM_015655.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:38344719 C>A maps to NM_006954.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:38344719 C>A maps to NM_006954.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43088669 C>A maps to NM_006955.1 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43088669 C>A maps to NM_006955.1 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32344994 C>A maps to ENST00000375200 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32344994 C>A maps to ENST00000375200 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53652554 G>T maps to NM_001172674.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53652554 G>T maps to NM_001172674.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178140301 C>A maps to NM_005649.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178140301 C>A maps to NM_005649.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64159307 G>T maps to NM_014951.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64159307 G>T maps to NM_014951.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99160538 C>A maps to NM_153695.3 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99160538 C>A maps to NM_153695.3 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:37118175 G>T maps to NM_032825.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:37118175 G>T maps to NM_032825.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28210124 C>A maps to NM_018660.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28210124 C>A maps to NM_018660.2 V295V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4396-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72589227 G>T maps to NM_017757.2 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:72589227 G>T maps to NM_017757.2 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46722647 C>A maps to NM_024741.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46722647 C>A maps to NM_024741.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:49672018 G>T maps to NM_015069.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:49672018 G>T maps to NM_015069.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:134494577 C>A maps to NM_152695.5 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:134494577 C>A maps to NM_152695.5 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12384778 G>T maps to NM_001164276.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12384778 G>T maps to NM_001164276.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178373364 G>T maps to NM_182594.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178373364 G>T maps to NM_182594.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109688100 C>A maps to NM_021224.4 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109688100 C>A maps to NM_021224.4 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109688259 C>A maps to NM_021224.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109688259 C>A maps to NM_021224.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109689871 C>A maps to NM_021224.4 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109689871 C>A maps to NM_021224.4 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109690017 C>A maps to NM_021224.4 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109690017 C>A maps to NM_021224.4 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109690611 G>T maps to NM_021224.4 T1473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109690611 G>T maps to NM_021224.4 T1473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109701236 C>A maps to NM_021224.4 T2092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109701236 C>A maps to NM_021224.4 T2092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:121487918 G>T maps to NM_207317.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:121487918 G>T maps to NM_207317.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:121488515 G>T maps to NM_207317.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:121488515 G>T maps to NM_207317.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114296626 C>A maps to NM_133464.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114296626 C>A maps to NM_133464.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30408681 G>T maps to ENST00000495929 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30408681 G>T maps to ENST00000495929 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12691301 G>T maps to NM_020714.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12691301 G>T maps to NM_020714.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99521944 C>A maps to NM_014930.1 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99521944 C>A maps to NM_014930.1 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135125372 C>A maps to ENST00000359035 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135125372 C>A maps to ENST00000359035 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62595188 G>T maps to NM_020713.1 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62595188 G>T maps to NM_020713.1 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597696 C>A maps to NM_020713.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597696 C>A maps to NM_020713.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597720 G>T maps to NM_020713.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597720 G>T maps to NM_020713.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597732 C>A maps to NM_020713.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597732 C>A maps to NM_020713.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597786 G>T maps to NM_020713.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62597786 G>T maps to NM_020713.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27844168 C>A maps to NM_032434.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27844168 C>A maps to NM_032434.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97919438 C>A maps to NM_014803.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97919438 C>A maps to NM_014803.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804314 C>A maps to NM_015461.2 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804314 C>A maps to NM_015461.2 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804394 C>A maps to NM_015461.2 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804394 C>A maps to NM_015461.2 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804548 G>T maps to NM_015461.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804548 G>T maps to NM_015461.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805058 G>T maps to NM_015461.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805058 G>T maps to NM_015461.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805337 G>T maps to NM_015461.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805337 G>T maps to NM_015461.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805421 C>A maps to NM_015461.2 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805421 C>A maps to NM_015461.2 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805763 C>A maps to NM_015461.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805763 C>A maps to NM_015461.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805829 G>T maps to NM_015461.2 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805829 G>T maps to NM_015461.2 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22806254 G>T maps to NM_015461.2 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22806254 G>T maps to NM_015461.2 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22806690 C>A maps to NM_015461.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22806690 C>A maps to NM_015461.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22807071 G>T maps to NM_015461.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22807071 G>T maps to NM_015461.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22902146 G>T maps to NM_015461.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22902146 G>T maps to NM_015461.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:31040366 G>T maps to NM_014717.1 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:31040366 G>T maps to NM_014717.1 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:38103902 G>T maps to NM_152606.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:38103902 G>T maps to NM_152606.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57909930 C>A maps to NM_001172773.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57909930 C>A maps to NM_001172773.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36674429 G>T maps to ENST00000355114 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36674429 G>T maps to ENST00000355114 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:125989166 C>A maps to NM_152412.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:125989166 C>A maps to NM_152412.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:86540 C>A maps to NM_182524.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:86540 C>A maps to NM_182524.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:35251099 C>A maps to NM_001007248.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:35251099 C>A maps to NM_001007248.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58489717 G>T maps to NM_025027.3 S777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58489717 G>T maps to NM_025027.3 S777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58490274 C>A maps to NM_025027.3 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58490274 C>A maps to NM_025027.3 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:52447672 C>A maps to NM_001031721.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:52447672 C>A maps to NM_001031721.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16465239 G>T maps to NM_033414.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16465239 G>T maps to NM_033414.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16465527 C>A maps to NM_033414.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16465527 C>A maps to NM_033414.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144732179 C>A maps to NM_014789.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144732179 C>A maps to NM_014789.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30793149 G>T maps to NM_001080417.1 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30793149 G>T maps to NM_001080417.1 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30793254 G>T maps to NM_001080417.1 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30793254 G>T maps to NM_001080417.1 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30793359 C>A maps to NM_001080417.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30793359 C>A maps to NM_001080417.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30794181 G>T maps to NM_001080417.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30794181 G>T maps to NM_001080417.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91403420 G>T maps to NM_201269.1 P1103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91403420 G>T maps to NM_201269.1 P1103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91405095 C>A maps to NM_201269.1 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91405095 C>A maps to NM_201269.1 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91406747 C>A maps to NM_201269.1 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91406747 C>A maps to NM_201269.1 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:52393987 G>T maps to NM_023074.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:52393987 G>T maps to NM_023074.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:52394113 C>A maps to NM_023074.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:52394113 C>A maps to NM_023074.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30616672 G>T maps to NM_138447.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30616672 G>T maps to NM_138447.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:81577127 C>A maps to NM_001033723.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:81577127 C>A maps to NM_001033723.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57133473 C>A maps to NM_021216.4 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57133473 C>A maps to NM_021216.4 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:80789466 C>A maps to NM_024702.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:80789466 C>A maps to NM_024702.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12089094 C>A maps to NM_001012753.1 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12089094 C>A maps to NM_001012753.1 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30536020 C>A maps to NM_024671.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30536020 C>A maps to NM_024671.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30536893 G>T maps to NM_024671.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30536893 G>T maps to NM_024671.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30536920 G>T maps to NM_024671.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30536920 G>T maps to NM_024671.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35258143 C>A maps to NM_003427.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35258143 C>A maps to NM_003427.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:149129361 G>T maps to ENST00000440594 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:149129361 G>T maps to ENST00000440594 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89293490 C>A maps to NM_182531.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89293490 C>A maps to NM_182531.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40542066 G>T maps to NM_001005851.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40542066 G>T maps to NM_001005851.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146066908 C>A maps to ENST00000446747 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146066908 C>A maps to ENST00000446747 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146067310 G>T maps to ENST00000446747 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146067310 G>T maps to ENST00000446747 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:185802627 C>A maps to NM_194250.1 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:185802627 C>A maps to NM_194250.1 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53058550 G>T maps to NM_001039886.3 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53058550 G>T maps to NM_001039886.3 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53459324 G>T maps to NM_001031665.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53459324 G>T maps to NM_001031665.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71894289 G>T maps to ENST00000425432 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71894289 G>T maps to ENST00000425432 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11832934 C>A maps to NM_001080493.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11832934 C>A maps to NM_001080493.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146686192 G>T maps to ENST00000508784 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:146686192 G>T maps to ENST00000508784 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53856406 G>T maps to NM_138374.1 G827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53856406 G>T maps to NM_138374.1 G827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9868447 C>A maps to NM_001077624.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:9868447 C>A maps to NM_001077624.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33960637 G>T maps to NM_145238.3 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33960637 G>T maps to NM_145238.3 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44511558 C>A maps to NM_080603.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44511558 C>A maps to NM_080603.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116967013 G>T maps to NM_145062.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116967013 G>T maps to NM_145062.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113618377 C>A maps to NM_004724.2 G383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113618377 C>A maps to NM_004724.2 G383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:57620751 G>C maps to NM_007157.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:57620751 G>C maps to NM_007157.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126178508 C>A maps to NM_025112.4 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126178508 C>A maps to NM_025112.4 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143079775 C>A maps to NM_001010972.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143079775 C>A maps to NM_001010972.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3984705 C>A maps to NM_015113.3 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3984705 C>A maps to NM_015113.3 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4005644 G>T maps to NM_015113.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4005644 G>T maps to NM_015113.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:78098304 C>A maps to NM_015534.4 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:78098304 C>A maps to NM_015534.4 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2333252 G>A maps to NM_001089.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2333252 G>A maps to NM_001089.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:66928444 G>T maps to NM_007168.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:66928444 G>T maps to NM_007168.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:16130397 G>A maps to ENST00000399408 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:16130397 G>A maps to ENST00000399408 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:33576959 G>T maps to NM_030955.2 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:33576959 G>T maps to NM_030955.2 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:7727278 C>A maps to NM_020546.2 Y592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:7727278 C>A maps to NM_020546.2 Y592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64794784 G>A maps to ENST00000422803 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64794784 G>A maps to ENST00000422803 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:165667627 G>A maps to NM_000696.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:165667627 G>A maps to NM_000696.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:73679044 G>T maps to NM_015120.4 G1796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:73679044 G>T maps to NM_015120.4 G1796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52283237 G>C maps to NM_182608.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52283237 G>C maps to NM_182608.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:26463462 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:26463462 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:101480520 G>A maps to ENST00000392977 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:101480520 G>A maps to ENST00000392977 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:45744488 G>T maps to NM_001142679.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:45744488 G>T maps to NM_001142679.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:77385315 T>A maps to NM_003664.3 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:77385315 T>A maps to NM_003664.3 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:129950632 C>A maps to NM_033515.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:129950632 C>A maps to NM_033515.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119133385 C>T maps to NM_020754.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119133385 C>T maps to NM_020754.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:46211515 T>A maps to NM_152641.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:46211515 T>A maps to NM_152641.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:31325272 A>T maps to NM_030632.1 R1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:31325272 A>T maps to NM_030632.1 R1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:124381403 G>A maps to NM_014109.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:124381403 G>A maps to NM_014109.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:70040436 T>C maps to NM_001704.2 F1025F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:70040436 T>C maps to NM_001704.2 F1025F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:1394603 A>G maps to NM_003933.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:1394603 A>G maps to NM_003933.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31592973 C>A maps to NM_080686.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31592973 C>A maps to NM_080686.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31631769 G>A maps to NM_033177.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31631769 G>A maps to NM_033177.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:76739973 A>T maps to NM_024685.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:76739973 A>T maps to NM_024685.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118772870 G>C maps to NM_182557.2 Y527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118772870 G>C maps to NM_182557.2 Y527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:133191317 C>T maps to NM_003571.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:133191317 C>T maps to NM_003571.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:61869765 G>T maps to NM_139317.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:61869765 G>T maps to NM_139317.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:121442168 C>T maps to NM_022895.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:121442168 C>T maps to NM_022895.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:10339081 C>T maps to NM_153022.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:10339081 C>T maps to NM_153022.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:97087504 G>T maps to ENST00000342887 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:97087504 G>T maps to ENST00000342887 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75038354 A>T maps to NM_001002912.4 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75038354 A>T maps to NM_001002912.4 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75038801 T>C maps to NM_001002912.4 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75038801 T>C maps to NM_001002912.4 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:746286 G>A maps to NM_033409.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:746286 G>A maps to NM_033409.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119466714 C>T maps to NM_033364.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119466714 C>T maps to NM_033364.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:118865122 C>A maps to NM_152539.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:118865122 C>A maps to NM_152539.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:39082789 G>A maps to NM_018322.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:39082789 G>A maps to NM_018322.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:100033310 G>T maps to NM_145030.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:100033310 G>T maps to NM_145030.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:39288978 G>A maps to NM_001737.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:39288978 G>A maps to NM_001737.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:66880939 G>T maps to NM_005182.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:66880939 G>T maps to NM_005182.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149631369 C>A maps to NM_015981.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149631369 C>A maps to NM_015981.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:44282849 A>T maps to NM_001220.4 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:44282849 A>T maps to NM_001220.4 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:107398941 A>G maps to NM_024814.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:107398941 A>G maps to NM_024814.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119144583 A>T maps to NM_005188.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119144583 A>T maps to NM_005188.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:180397252 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:180397252 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:7636211 C>A maps to NM_004244.4 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:7636211 C>A maps to NM_004244.4 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:35211478 G>A maps to NM_000610.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:35211478 G>A maps to NM_000610.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157804199 C>A maps to NM_005894.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157804199 C>A maps to NM_005894.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:115002122 C>T maps to NM_003903.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:115002122 C>T maps to NM_003903.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:24511576 G>T maps to NM_006727.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:24511576 G>T maps to NM_006727.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:65032651 G>T maps to NM_001797.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:65032651 G>T maps to NM_001797.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:123201726 G>A maps to NM_018249.4 F1224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:123201726 G>A maps to NM_018249.4 F1224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214818771 C>T maps to NM_016343.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214818771 C>T maps to NM_016343.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214819043 C>G maps to NM_016343.3 S2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214819043 C>G maps to NM_016343.3 S2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:117267986 A>G maps to NM_014956.4 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:117267986 A>G maps to NM_014956.4 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:196714945 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:196714945 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:34356222 C>G maps to NM_012125.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:34356222 C>G maps to NM_012125.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:19171031 G>A maps to NM_007098.3 F1566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:19171031 G>A maps to NM_007098.3 F1566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:76555171 T>A maps to NM_033401.3 L833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:76555171 T>A maps to NM_033401.3 L833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:125660660 G>C maps to NM_130773.2 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:125660660 G>C maps to NM_130773.2 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:32167740 G>A maps to NM_001856.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:32167740 G>A maps to NM_001856.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:48391490 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:48391490 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111009826 G>A maps to NM_001846.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111009826 G>A maps to NM_001846.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:228173982 T>C maps to NM_000091.4 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:228173982 T>C maps to NM_000091.4 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:67089173 A>T maps to NM_000756.2 L180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:67089173 A>T maps to NM_000756.2 L180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:17266429 C>A maps to NM_014675.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:17266429 C>A maps to NM_014675.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:97596394 G>A maps to ENST00000182096 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:97596394 G>A maps to ENST00000182096 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:43650779 A>T maps to NM_018590.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:43650779 A>T maps to NM_018590.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34049278 G>A maps to ENST00000373381 L2361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34049278 G>A maps to ENST00000373381 L2361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:23584170 G>A maps to NM_001008693.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:23584170 G>A maps to NM_001008693.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:48996750 C>A maps to NM_025087.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:48996750 C>A maps to NM_025087.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:44874112 G>A maps to NM_001178134.1 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:44874112 G>A maps to NM_001178134.1 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59112837 G>A maps to NM_016651.5 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59112837 G>A maps to NM_016651.5 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:88885767 C>G maps to NM_152418.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:88885767 C>G maps to NM_152418.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69529103 G>A maps to NM_003861.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69529103 G>A maps to NM_003861.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:32270282 A>G maps to NM_001136029.1 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:32270282 A>G maps to NM_001136029.1 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:35060906 G>T maps to ENST00000339266 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:35060906 G>T maps to ENST00000339266 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:990206 C>T maps to NM_021240.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:990206 C>T maps to NM_021240.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:124360010 T>C maps to NM_207437.3 Y2606Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:124360010 T>C maps to NM_207437.3 Y2606Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:13823413 G>A maps to NM_001369.2 D2215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:13823413 G>A maps to NM_001369.2 D2215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72285813 C>A maps to NM_023036.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72285813 C>A maps to NM_023036.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40142373 T>C maps to NM_003315.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40142373 T>C maps to NM_003315.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:51875245 G>T maps to NM_001981.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:51875245 G>T maps to NM_001981.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:212288913 G>T maps to NM_005235.2 I944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:212288913 G>T maps to NM_005235.2 I944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:1137188 G>T maps to NM_178040.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:1137188 G>T maps to NM_178040.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:103492109 C>T maps to NM_017693.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:103492109 C>T maps to NM_017693.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:122722598 C>G maps to NM_001034194.1 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:122722598 C>G maps to NM_001034194.1 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:176831230 C>T maps to NM_000505.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:176831230 C>T maps to NM_000505.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:159076789 C>T maps to NM_001128424.1 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:159076789 C>T maps to NM_001128424.1 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:46248087 G>C maps to ENST00000399588 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:46248087 G>C maps to ENST00000399588 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:34148384 G>A maps to NM_203408.3 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:34148384 G>A maps to NM_203408.3 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:13035002 C>T maps to NM_004461.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:13035002 C>T maps to NM_004461.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:45944566 C>T maps to ENST00000348697 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:45944566 C>T maps to ENST00000348697 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:8148209 C>T maps to NM_032447.3 E2378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:8148209 C>T maps to NM_032447.3 E2378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:159277562 A>G maps to ENST00000368115 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:159277562 A>G maps to ENST00000368115 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:17127347 C>T maps to NM_144997.5 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:17127347 C>T maps to NM_144997.5 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:152326310 C>T maps to NM_001014342.2 Q1317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:152326310 C>T maps to NM_001014342.2 Q1317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:79635142 T>C maps to NM_001013735.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:79635142 T>C maps to NM_001013735.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42635928 G>T maps to NM_001466.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42635928 G>T maps to NM_001466.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:27193364 C>A maps to NM_000810.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:27193364 C>A maps to NM_000810.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:171716262 C>A maps to NM_000817.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:171716262 C>A maps to NM_000817.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:120596318 C>A maps to NM_006836.1 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:120596318 C>A maps to NM_006836.1 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:72623760 C>A maps to ENST00000504199 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:72623760 C>A maps to ENST00000504199 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61958248 C>T maps to NM_002059.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61958248 C>T maps to NM_002059.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:79818430 G>T maps to NM_002069.5 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:79818430 G>T maps to NM_002069.5 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:135433700 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:135433700 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:134884454 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:134884454 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:112724476 C>A maps to NM_018970.6 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:112724476 C>A maps to NM_018970.6 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:236723046 C>A maps to NM_018072.5 A1579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:236723046 C>A maps to NM_018072.5 A1579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:69793919 G>A maps to NM_022079.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:69793919 G>A maps to NM_022079.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:149857920 G>T maps to NM_003528.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:149857920 G>T maps to NM_003528.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:152187576 C>G maps to NM_001009931.1 G2176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:152187576 C>G maps to NM_001009931.1 G2176G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4397-01A-01D-1265-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4397-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52871149 C>T maps to NM_016513.4 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52871149 C>T maps to NM_016513.4 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:65677327 C>A maps to NM_020962.1 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:65677327 C>A maps to NM_020962.1 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:113675248 C>T maps to NM_014439.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:113675248 C>T maps to NM_014439.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28515336 A>G maps to NM_145659.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28515336 A>G maps to NM_145659.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:31522646 C>G maps to ENST00000331075 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:31522646 C>G maps to ENST00000331075 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:15134044 G>T maps to NM_001031853.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:15134044 G>T maps to NM_001031853.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:15197586 C>T maps to NM_001031853.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:15197586 C>T maps to NM_001031853.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:74467990 C>A maps to NM_201526.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:74467990 C>A maps to NM_201526.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:128786319 C>A maps to NM_000890.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:128786319 C>A maps to NM_000890.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:2717918 C>T maps to NM_133497.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:2717918 C>T maps to NM_133497.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:48647873 C>G maps to NM_001080394.1 Y870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:48647873 C>G maps to NM_001080394.1 Y870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:123175387 A>G maps to NM_015312.3 L1987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:123175387 A>G maps to NM_015312.3 L1987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:95539313 T>A maps to NM_015496.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:95539313 T>A maps to NM_015496.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:33235818 C>T maps to NM_020888.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:33235818 C>T maps to NM_020888.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:73959986 G>T maps to NM_001008537.2 R1469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:73959986 G>T maps to NM_001008537.2 R1469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:137519014 G>C maps to NM_005733.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:137519014 G>C maps to NM_005733.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:31654686 G>T maps to NM_001085455.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:31654686 G>T maps to NM_001085455.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:63990183 A>T maps to NM_016571.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:63990183 A>T maps to NM_016571.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75626523 G>T maps to NM_001001933.1 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75626523 G>T maps to NM_001001933.1 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:108862283 C>A maps to NM_001098268.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:108862283 C>A maps to NM_001098268.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:176765533 C>A maps to NM_006816.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:176765533 C>A maps to NM_006816.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156100422 G>A maps to NM_170707.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156100422 G>A maps to NM_170707.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:123302794 T>A maps to NM_207163.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:123302794 T>A maps to NM_207163.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:161027593 C>T maps to NM_005577.2 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:161027593 C>T maps to NM_005577.2 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:188327237 C>G maps to NM_005578.3 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:188327237 C>G maps to NM_005578.3 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:197518271 C>G maps to ENST00000425562 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:197518271 C>G maps to ENST00000425562 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:170002407 G>A maps to NM_004525.2 I4279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:170002407 G>A maps to NM_004525.2 I4279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:7760051 G>C maps to NM_032356.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:7760051 G>C maps to NM_032356.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:11734864 A>G maps to ENST00000376669 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:11734864 A>G maps to ENST00000376669 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:35802718 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:35802718 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7589949 C>G maps to NM_020533.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7589949 C>G maps to NM_020533.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69218141 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69218141 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:70345899 C>T maps to ENST00000333646 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:70345899 C>T maps to ENST00000333646 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21969066 G>C maps to NM_019852.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21969066 G>C maps to NM_019852.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:90874328 C>A maps to NM_007351.2 Y1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:90874328 C>A maps to NM_007351.2 Y1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:10177493 C>T maps to NM_012331.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:10177493 C>T maps to NM_012331.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:17228695 G>A maps to NM_004686.4 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:17228695 G>A maps to NM_004686.4 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:125603416 C>A maps to NM_014751.4 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:125603416 C>A maps to NM_014751.4 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:29855913 C>T maps to NM_001033602.2 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:29855913 C>T maps to NM_001033602.2 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9047973 G>T maps to NM_024690.2 T11219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9047973 G>T maps to NM_024690.2 T11219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10243656 C>A maps to NM_003802.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10243656 C>A maps to NM_003802.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:128381780 C>T maps to ENST00000389524 F1285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:128381780 C>T maps to ENST00000389524 F1285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:15555686 G>A maps to NM_015909.2 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:15555686 G>A maps to NM_015909.2 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:148012568 G>A maps to ENST00000310701 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:148012568 G>A maps to ENST00000310701 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:46276055 A>T maps to NM_181659.2 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:46276055 A>T maps to NM_181659.2 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:115773902 T>A maps to NM_022569.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:115773902 T>A maps to NM_022569.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152423687 C>T maps to NM_001164507.1 Q6050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152423687 C>T maps to NM_001164507.1 Q6050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:29879484 G>C maps to NM_021076.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:29879484 G>C maps to NM_021076.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:70417718 G>C maps to NM_153181.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:70417718 G>C maps to NM_153181.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:31432982 G>A maps to NM_003787.4 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:31432982 G>A maps to NM_003787.4 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:117657885 C>A maps to ENST00000338101 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:117657885 C>A maps to ENST00000338101 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:142780340 C>A maps to NM_001024094.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:142780340 C>A maps to NM_001024094.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:7949816 G>A maps to NM_001004461.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:7949816 G>A maps to NM_001004461.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248512219 C>T maps to NM_001001918.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248512219 C>T maps to NM_001001918.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:143792895 C>A maps to NM_001004135.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:143792895 C>A maps to NM_001004135.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:143657782 G>T maps to NM_012369.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:143657782 G>T maps to NM_012369.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248790327 C>A maps to NM_001001964.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248790327 C>A maps to NM_001001964.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248813330 G>C maps to NM_001001824.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248813330 G>C maps to NM_001001824.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:59283041 G>T maps to NM_001004711.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:59283041 G>T maps to NM_001004711.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:20612580 C>A maps to NM_001004724.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:20612580 C>A maps to NM_001004724.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:5799838 C>T maps to NM_001001922.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:5799838 C>T maps to NM_001001922.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:97983472 A>T maps to NM_001005479.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:97983472 A>T maps to NM_001005479.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:55715171 A>G maps to NM_001005182.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:55715171 A>G maps to NM_001005182.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:57114658 G>T maps to NM_002559.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:57114658 G>T maps to NM_002559.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:31811520 A>G maps to NM_001604.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:31811520 A>G maps to NM_001604.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:91873566 T>A maps to NM_032968.3 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:91873566 T>A maps to NM_032968.3 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140605335 G>T maps to NM_018934.2 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140605335 G>T maps to NM_018934.2 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140531910 G>C maps to NM_018939.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140531910 G>C maps to NM_018939.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140794976 G>T maps to NM_018913.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140794976 G>T maps to NM_018913.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140719050 A>T maps to NM_018915.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140719050 A>T maps to NM_018915.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:31864496 C>A maps to NM_001191057.1 G464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:31864496 C>A maps to NM_001191057.1 G464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149515438 C>A maps to NM_002609.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149515438 C>A maps to NM_002609.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:34396294 A>G maps to NM_152595.4 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:34396294 A>G maps to NM_152595.4 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:133559233 A>G maps to ENST00000394292 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:133559233 A>G maps to ENST00000394292 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118509944 G>A maps to NM_015157.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118509944 G>A maps to NM_015157.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:229890755 G>A maps to NM_017933.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:229890755 G>A maps to NM_017933.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:59739949 G>A maps to NM_176787.4 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:59739949 G>A maps to NM_176787.4 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:81232342 G>C maps to NM_052892.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:81232342 G>C maps to NM_052892.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:118313237 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:118313237 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:23522994 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:23522994 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:11370154 C>A maps to ENST00000435245 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:11370154 C>A maps to ENST00000435245 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:4705649 G>A maps to NM_012409.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:4705649 G>A maps to NM_012409.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:57247239 A>T maps to NM_018304.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:57247239 A>T maps to NM_018304.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:138724870 C>T maps to NM_001134659.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:138724870 C>T maps to NM_001134659.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:52735297 C>T maps to NM_000953.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:52735297 C>T maps to NM_000953.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:103276758 G>T maps to ENST00000428762 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:103276758 G>T maps to ENST00000428762 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101283639 C>G maps to NM_017819.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101283639 C>G maps to NM_017819.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:95067574 C>T maps to NM_014899.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:95067574 C>T maps to NM_014899.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:130912819 G>A maps to NM_015347.4 D755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:130912819 G>A maps to NM_015347.4 D755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89324033 C>T maps to NM_003800.3 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89324033 C>T maps to NM_003800.3 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:35521454 T>G maps to NM_015474.3 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:35521454 T>G maps to NM_015474.3 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:83602053 G>A maps to NM_001037582.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:83602053 G>A maps to NM_001037582.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:166183486 C>A maps to NM_001040142.1 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:166183486 C>A maps to NM_001040142.1 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:169572375 A>G maps to NM_003005.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:169572375 A>G maps to NM_003005.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:74703901 G>A maps to NM_003612.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:74703901 G>A maps to NM_003612.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:61390291 A>T maps to NM_080475.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:61390291 A>T maps to NM_080475.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64863199 G>C maps to NM_014755.2 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64863199 G>C maps to NM_014755.2 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28883955 C>T maps to NM_001145795.1 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28883955 C>T maps to NM_001145795.1 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3675340 G>A maps to NM_023068.3 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3675340 G>A maps to NM_023068.3 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:20004894 G>T maps to NM_001135691.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:20004894 G>T maps to NM_001135691.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:160679774 C>A maps to NM_003058.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:160679774 C>A maps to NM_003058.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:110083919 A>C maps to NM_138773.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:110083919 A>C maps to NM_138773.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44200165 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44200165 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:118598701 G>A maps to NM_001029858.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:118598701 G>A maps to NM_001029858.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21469626 C>T maps to NM_014579.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21469626 C>T maps to NM_014579.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49793478 G>T maps to NM_014037.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49793478 G>T maps to NM_014037.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:87229890 T>A maps to NM_138817.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:87229890 T>A maps to NM_138817.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:40656955 T>C maps to NM_021097.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:40656955 T>C maps to NM_021097.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:20874894 C>A maps to NM_017435.4 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:20874894 C>A maps to NM_017435.4 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:168187940 C>T maps to NM_003062.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:168187940 C>T maps to NM_003062.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:168310298 C>T maps to NM_003062.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:168310298 C>T maps to NM_003062.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:128649711 C>T maps to NM_003069.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:128649711 C>T maps to NM_003069.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:67992311 G>T maps to NM_004232.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:67992311 G>T maps to NM_004232.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:172835416 C>G maps to NM_031955.5 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:172835416 C>G maps to NM_031955.5 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62275216 A>C maps to NM_015894.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62275216 A>C maps to NM_015894.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:124103596 G>T maps to NM_004099.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:124103596 G>T maps to NM_004099.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:134925342 C>T maps to NM_182489.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:134925342 C>T maps to NM_182489.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:93637066 G>T maps to NM_003177.5 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:93637066 G>T maps to NM_003177.5 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:33532834 G>T maps to NM_198992.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:33532834 G>T maps to NM_198992.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120803608 C>A maps to NM_003184.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120803608 C>A maps to NM_003184.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:156841117 C>A maps to NM_005651.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:156841117 C>A maps to NM_005651.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:154517339 C>G maps to NM_001098475.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:154517339 C>G maps to NM_001098475.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:30703089 T>A maps to NM_031271.3 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:30703089 T>A maps to NM_031271.3 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32029429 C>A maps to ENST00000375244 P2412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32029429 C>A maps to ENST00000375244 P2412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:17764828 A>G maps to NM_001082968.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:17764828 A>G maps to NM_001082968.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18057530 T>G maps to ENST00000341556 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18057530 T>G maps to ENST00000341556 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:186306191 C>A maps to NM_003292.2 E1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:186306191 C>A maps to NM_003292.2 E1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:166747499 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:166747499 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179427122 G>T maps to NM_133378.4 T25344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179427122 G>T maps to NM_133378.4 T25344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179431316 A>G maps to NM_133378.4 D23946D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179431316 A>G maps to NM_133378.4 D23946D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179441839 G>A maps to NM_133378.4 S20506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179441839 G>A maps to NM_133378.4 S20506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:8122428 G>A maps to NM_003320.4 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:8122428 G>A maps to NM_003320.4 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:72267536 C>A maps to NM_001145440.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:72267536 C>A maps to NM_001145440.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:10197140 A>G maps to NM_001105562.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:10197140 A>G maps to NM_001105562.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:28905205 C>G maps to NM_016628.3 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:28905205 C>G maps to NM_016628.3 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:190315684 C>T maps to NM_032168.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:190315684 C>T maps to NM_032168.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:33282995 C>A maps to NM_001145338.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:33282995 C>A maps to NM_001145338.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:31809519 G>T maps to NM_001174096.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:31809519 G>T maps to NM_001174096.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:30935921 A>T maps to NM_014717.1 K485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:30935921 A>T maps to NM_014717.1 K485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:30936281 C>A maps to NM_014717.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:30936281 C>A maps to NM_014717.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:247163259 C>G maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:247163259 C>G maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:57768836 C>T maps to NM_178457.1 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:57768836 C>T maps to NM_178457.1 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:58189693 C>T maps to NM_152677.2 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:58189693 C>T maps to NM_152677.2 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:125618603 C>T maps to NM_023928.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:125618603 C>T maps to NM_023928.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:66873754 G>A maps to NM_007168.2 N1328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:66873754 G>A maps to NM_007168.2 N1328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:169791860 A>C maps to NM_003742.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:169791860 A>C maps to NM_003742.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:34218873 T>C maps to NM_145804.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:34218873 T>C maps to NM_145804.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:41923335 C>A maps to ENST00000396512 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:41923335 C>A maps to ENST00000396512 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:2938327 T>A maps to NM_080431.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:2938327 T>A maps to NM_080431.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154571061 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154571061 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:178326700 C>T maps to NM_003659.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:178326700 C>T maps to NM_003659.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:77752624 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:77752624 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:49957632 A>G maps to NM_003886.2 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:49957632 A>G maps to NM_003886.2 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137776545 C>A maps to NM_005989.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137776545 C>A maps to NM_005989.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:111680425 A>G maps to ENST00000428306 Y783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:111680425 A>G maps to ENST00000428306 Y783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:33520878 C>A maps to NM_152462.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:33520878 C>A maps to NM_152462.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:55455693 G>T maps to NM_024669.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:55455693 G>T maps to NM_024669.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:90349373 G>T maps to NM_001150.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:90349373 G>T maps to NM_001150.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:131894468 C>G maps to ENST00000356962 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:131894468 C>G maps to ENST00000356962 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:135825840 G>T maps to NM_004840.2 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:135825840 G>T maps to NM_004840.2 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:123267197 G>T maps to NM_080928.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:123267197 G>T maps to NM_080928.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:161751776 C>T maps to NM_007348.2 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:161751776 C>T maps to NM_007348.2 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:10417182 C>A maps to NM_001001331.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:10417182 C>A maps to NM_001001331.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:142253920 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:142253920 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:28842089 G>T maps to NM_148414.1 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:28842089 G>T maps to NM_148414.1 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:71571615 G>A maps to NM_080742.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:71571615 G>A maps to NM_080742.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:33545227 C>T maps to NM_198428.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:33545227 C>T maps to NM_198428.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49694956 C>T maps to NM_003458.3 A2656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49694956 C>T maps to NM_003458.3 A2656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:105581377 T>A maps to NM_007073.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:105581377 T>A maps to NM_007073.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:4645225 T>C maps to NM_020374.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:4645225 T>C maps to NM_020374.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:74206174 C>A maps to NM_001043318.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:74206174 C>A maps to NM_001043318.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:7330140 C>A maps to NM_175734.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:7330140 C>A maps to NM_175734.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:54025354 C>G maps to ENST00000502396 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:54025354 C>G maps to ENST00000502396 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:57349152 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:57349152 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:89771609 T>C maps to NM_001001709.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:89771609 T>C maps to NM_001001709.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48649378 C>T maps to NM_018896.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48649378 C>T maps to NM_018896.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:67191765 G>T maps to NM_001166222.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:67191765 G>T maps to NM_001166222.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:44581415 G>A maps to NM_138423.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:44581415 G>A maps to NM_138423.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:14024010 G>T maps to NM_017721.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:14024010 G>T maps to NM_017721.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:123633787 A>G maps to NM_022757.4 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:123633787 A>G maps to NM_022757.4 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:17073110 C>T maps to NM_014406.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:17073110 C>T maps to NM_014406.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:51729249 C>T maps to NM_001772.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:51729249 C>T maps to NM_001772.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:44640630 C>A maps to NM_002231.3 C253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:44640630 C>A maps to NM_002231.3 C253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:24488131 G>T maps to NM_006727.3 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:24488131 G>T maps to NM_006727.3 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:64178898 C>A maps to NM_021153.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:64178898 C>A maps to NM_021153.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44815275 C>T maps to NM_021248.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44815275 C>T maps to NM_021248.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:135940544 C>T maps to NM_001807.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:135940544 C>T maps to NM_001807.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:5903185 G>A maps to NM_001819.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:5903185 G>A maps to NM_001819.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71043306 G>A maps to NM_173535.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71043306 G>A maps to NM_173535.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:28498849 G>A maps to NM_000086.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:28498849 G>A maps to NM_000086.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:40959839 T>A maps to NM_173478.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:40959839 T>A maps to NM_173478.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:99715984 C>T maps to NM_014361.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:99715984 C>T maps to NM_014361.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:1445041 C>A maps to NM_014461.2 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:1445041 C>A maps to NM_014461.2 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:71683577 C>A maps to ENST00000356340 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:71683577 C>A maps to ENST00000356340 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121216050 G>T maps to NM_021110.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121216050 G>T maps to NM_021110.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:110831279 C>A maps to NM_001845.4 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:110831279 C>A maps to NM_001845.4 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:111082233 G>T maps to NM_001846.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:111082233 G>T maps to NM_001846.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:131418773 T>G maps to ENST00000502818 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:131418773 T>G maps to ENST00000502818 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211518746 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211518746 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:75944443 A>T maps to NM_031461.5 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:75944443 A>T maps to NM_031461.5 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113332154 C>T maps to NM_198123.1 L2407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113332154 C>T maps to NM_198123.1 L2407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:75968001 G>T maps to NM_001897.4 L2286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:75968001 G>T maps to NM_001897.4 L2286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:75968733 A>T maps to NM_001897.4 T2042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:75968733 A>T maps to NM_001897.4 T2042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:18123563 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:18123563 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:143994819 G>T maps to NM_000498.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:143994819 G>T maps to NM_000498.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:104593790 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:104593790 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:204116832 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:204116832 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:108866741 G>T maps to NM_183075.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:108866741 G>T maps to NM_183075.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:99332707 G>A maps to ENST00000292414 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:99332707 G>A maps to ENST00000292414 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:47582405 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:47582405 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:42818802 C>A maps to NM_145663.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:42818802 C>A maps to NM_145663.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:117864320 G>T maps to ENST00000338728 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:117864320 G>T maps to ENST00000338728 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:118577318 T>C maps to NM_006773.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:118577318 T>C maps to NM_006773.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137080402 G>T maps to NM_004717.2 R1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137080402 G>T maps to NM_004717.2 R1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:30630699 C>T maps to NM_003587.4 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:30630699 C>T maps to NM_003587.4 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:21750233 G>A maps to NM_003777.3 K2256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:21750233 G>A maps to NM_003777.3 K2256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:196821990 G>A maps to NM_018897.2 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:196821990 G>A maps to NM_018897.2 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:86124413 C>T maps to ENST00000256117 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:86124413 C>T maps to ENST00000256117 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:158523983 T>A maps to NM_024007.3 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:158523983 T>A maps to NM_024007.3 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:132958798 A>G maps to NM_015137.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:132958798 A>G maps to NM_015137.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:31472332 G>T maps to NM_014600.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:31472332 G>T maps to NM_014600.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2402300 G>A maps to ENST00000314800 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2402300 G>A maps to ENST00000314800 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:99980852 C>A maps to NM_015904.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:99980852 C>A maps to NM_015904.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1826130 G>T maps to NM_001010865.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1826130 G>T maps to NM_001010865.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:101091000 C>G maps to ENST00000397927 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:101091000 C>G maps to ENST00000397927 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:75178860 T>A maps to ENST00000413830 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:75178860 T>A maps to ENST00000413830 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:89498499 A>T maps to NM_005233.5 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:89498499 A>T maps to NM_005233.5 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:138612908 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:138612908 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:47629392 C>A maps to NM_138371.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:47629392 C>A maps to NM_138371.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:37027550 G>A maps to NM_001013736.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:37027550 G>A maps to NM_001013736.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:43625487 C>A maps to NM_001145196.1 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:43625487 C>A maps to NM_001145196.1 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:13061928 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:13061928 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:8194189 G>T maps to NM_032447.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:8194189 G>T maps to NM_032447.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:137801796 T>A maps to NM_002003.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:137801796 T>A maps to NM_002003.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152282981 G>T maps to NM_002016.1 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152282981 G>T maps to NM_002016.1 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152283358 C>A maps to NM_002016.1 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152283358 C>A maps to NM_002016.1 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52272375 C>A maps to NM_001005738.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52272375 C>A maps to NM_001005738.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52327945 C>A maps to NM_002030.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52327945 C>A maps to NM_002030.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:14797584 T>A maps to ENST00000380880 T1253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:14797584 T>A maps to ENST00000380880 T1253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:32836596 T>A maps to NM_023037.2 I2588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:32836596 T>A maps to NM_023037.2 I2588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:86663275 G>T maps to NM_012193.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:86663275 G>T maps to NM_012193.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:30891520 A>C maps to NM_207359.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:30891520 A>C maps to NM_207359.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79118034 G>A maps to NM_001097636.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79118034 G>A maps to NM_001097636.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:92941702 G>A maps to NM_005263.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:92941702 G>A maps to NM_005263.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:42718754 C>A maps to NM_000163.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:42718754 C>A maps to NM_000163.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150417235 G>A maps to NM_130759.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150417235 G>A maps to NM_130759.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52324423 G>T maps to NM_145262.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52324423 G>T maps to NM_145262.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131020132 C>G maps to NM_004486.4 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131020132 C>G maps to NM_004486.4 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:171822342 C>T maps to NM_015530.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:171822342 C>T maps to NM_015530.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:46826210 C>A maps to NM_015234.4 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:46826210 C>A maps to NM_015234.4 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:134940763 C>T maps to ENST00000368577 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:134940763 C>T maps to ENST00000368577 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:128408647 C>T maps to NM_005291.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:128408647 C>T maps to NM_005291.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:105859085 G>T maps to NM_007227.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:105859085 G>T maps to NM_007227.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:158257769 G>A maps to NM_000826.3 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:158257769 G>A maps to NM_000826.3 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:37271747 C>A maps to NM_000831.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:37271747 C>A maps to NM_000831.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:37324780 G>T maps to NM_000831.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:37324780 G>T maps to NM_000831.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:86416433 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:86416433 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:126173710 G>T maps to NM_001127323.1 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:126173710 G>T maps to NM_001127323.1 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:119720925 G>A maps to NM_002093.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:119720925 G>A maps to NM_002093.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:65409586 G>T maps to NM_138737.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:65409586 G>T maps to NM_138737.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:91728124 C>A maps to NM_001017975.3 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:91728124 C>A maps to NM_001017975.3 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:120389379 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:120389379 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152193134 G>A maps to NM_001009931.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152193134 G>A maps to NM_001009931.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:22157583 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:22157583 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:88039931 G>A maps to NM_000866.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:88039931 G>A maps to NM_000866.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:111088014 C>T maps to NM_001040107.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:111088014 C>T maps to NM_001040107.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:65681619 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:65681619 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:46543513 C>T maps to NM_001002923.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:46543513 C>T maps to NM_001002923.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:18691925 G>T maps to NM_032880.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:18691925 G>T maps to NM_032880.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:143129580 T>A maps to NM_003866.2 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:143129580 T>A maps to NM_003866.2 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:75885524 C>G maps to NM_006633.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:75885524 C>G maps to NM_006633.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31374571 G>T maps to NM_000887.3 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31374571 G>T maps to NM_000887.3 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:24533499 T>A maps to NM_006277.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:24533499 T>A maps to NM_006277.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24040241 G>T maps to NM_032452.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24040241 G>T maps to NM_032452.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110984553 C>A maps to NM_014379.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110984553 C>A maps to NM_014379.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:15703454 G>A maps to NM_014647.3 G1293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:15703454 G>A maps to NM_014647.3 G1293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:27786398 G>T maps to NM_015202.2 P1481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:27786398 G>T maps to NM_015202.2 P1481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:8930076 G>A maps to NM_020738.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:8930076 G>A maps to NM_020738.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:72348398 G>T maps to NM_153209.3 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:72348398 G>T maps to NM_153209.3 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:91522498 A>T maps to ENST00000416354 P1662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:91522498 A>T maps to ENST00000416354 P1662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:45232524 G>T maps to NM_006845.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:45232524 G>T maps to NM_006845.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55341633 C>A maps to NM_013289.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55341633 C>A maps to NM_013289.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:170592411 A>T maps to NM_144711.5 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:170592411 A>T maps to NM_144711.5 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152733251 G>A maps to NM_001025231.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152733251 G>A maps to NM_001025231.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:39118698 G>T maps to NM_213656.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:39118698 G>T maps to NM_213656.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:52985301 G>A maps to NM_080747.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:52985301 G>A maps to NM_080747.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:71124813 C>T maps to NM_018357.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:71124813 C>T maps to NM_018357.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:54347884 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:54347884 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:82409231 C>A maps to ENST00000370717 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:82409231 C>A maps to ENST00000370717 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141680575 G>T maps to NM_018557.2 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141680575 G>T maps to NM_018557.2 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141777507 C>A maps to NM_018557.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141777507 C>A maps to NM_018557.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:40136678 A>G maps to NM_020929.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:40136678 A>G maps to NM_020929.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:54958982 C>A maps to NM_020678.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:54958982 C>A maps to NM_020678.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:160728992 C>A maps to NM_001198759.1 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:160728992 C>A maps to NM_001198759.1 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:161530899 G>T maps to NM_005922.2 A1450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:161530899 G>T maps to NM_005922.2 A1450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:82045297 T>A maps to NM_000429.2 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:82045297 T>A maps to NM_000429.2 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:13885376 C>T maps to NM_000529.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:13885376 C>T maps to NM_000529.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:8813494 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:8813494 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:12061526 C>T maps to NM_014874.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:12061526 C>T maps to NM_014874.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:42042587 A>G maps to ENST00000219905 A2310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:42042587 A>G maps to ENST00000219905 A2310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168352254 G>T maps to ENST00000400822 P1399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168352254 G>T maps to ENST00000400822 P1399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:13883023 G>T maps to NM_001031727.2 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:13883023 G>T maps to NM_001031727.2 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:44815241 C>T maps to NM_016640.3 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:44815241 C>T maps to NM_016640.3 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60152571 C>A maps to NM_206939.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60152571 C>A maps to NM_206939.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:76313919 C>T maps to NM_002440.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:76313919 C>T maps to NM_002440.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100681104 T>A maps to NM_001040105.1 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100681104 T>A maps to NM_001040105.1 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155161952 T>C maps to ENST00000425082 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155161952 T>C maps to ENST00000425082 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:3248371 C>A maps to NM_015419.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:3248371 C>A maps to NM_015419.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10440586 T>A maps to NM_017534.5 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10440586 T>A maps to NM_017534.5 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10360869 G>T maps to NM_017533.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10360869 G>T maps to NM_017533.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10309715 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10309715 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:36691696 G>T maps to NM_002473.4 I1113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:36691696 G>T maps to NM_002473.4 I1113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:52646196 C>T maps to ENST00000358212 K1146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:52646196 C>T maps to ENST00000358212 K1146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:62836920 C>A maps to NM_004535.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:62836920 C>A maps to NM_004535.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:60768353 G>T maps to NM_024611.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:60768353 G>T maps to NM_024611.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152410461 G>T maps to NM_001164507.1 A6502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152410461 G>T maps to NM_001164507.1 A6502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:21592477 C>A maps to NM_006157.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:21592477 C>A maps to NM_006157.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:77221366 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:77221366 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:25481598 C>G maps to NM_025176.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:25481598 C>G maps to NM_025176.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:5821356 C>G maps to ENST00000381093 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:5821356 C>G maps to ENST00000381093 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:54327410 G>C maps to ENST00000391773 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:54327410 G>C maps to ENST00000391773 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:7063622 T>C maps to NM_176822.3 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:7063622 T>C maps to NM_176822.3 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:106890089 G>T maps to ENST00000503451 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:106890089 G>T maps to ENST00000503451 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:5603587 C>A maps to NM_001102654.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:5603587 C>A maps to NM_001102654.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:69124945 T>C maps to NM_020401.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:69124945 T>C maps to NM_020401.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:161953962 G>T maps to ENST00000451379 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:161953962 G>T maps to ENST00000451379 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3195612 G>T maps to ENST00000397187 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3195612 G>T maps to ENST00000397187 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:59271425 C>T maps to NM_001004706.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:59271425 C>T maps to NM_001004706.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:20389718 G>T maps to NM_001005483.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:20389718 G>T maps to NM_001005483.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:5345398 G>T maps to NM_033180.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:5345398 G>T maps to NM_033180.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:4825232 G>T maps to ENST00000380382 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:4825232 G>T maps to ENST00000380382 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:98217147 C>A maps to NM_001004737.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:98217147 C>A maps to NM_001004737.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:56310499 G>T maps to NM_001005245.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:56310499 G>T maps to NM_001005245.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:123813849 A>T maps to NM_001005187.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:123813849 A>T maps to NM_001005187.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:57958654 T>C maps to NM_001005283.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:57958654 T>C maps to NM_001005283.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29648296 A>T maps to NM_183378.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29648296 A>T maps to NM_183378.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:17668496 C>T maps to NM_012387.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:17668496 C>T maps to NM_012387.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:145057391 G>A maps to NM_032789.3 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:145057391 G>A maps to NM_032789.3 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:65559013 G>A maps to NM_017851.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:65559013 G>A maps to NM_017851.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:226576434 C>T maps to NM_001618.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:226576434 C>T maps to NM_001618.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:55839090 C>A maps to NM_001142763.1 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:55839090 C>A maps to NM_001142763.1 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:58207105 G>T maps to NM_001040429.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:58207105 G>T maps to NM_001040429.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140168128 C>T maps to NM_018900.2 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140168128 C>T maps to NM_018900.2 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140605056 G>T maps to NM_018934.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140605056 G>T maps to NM_018934.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140625592 G>C maps to NM_018935.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140625592 G>C maps to NM_018935.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31867987 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31867987 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:72295736 G>A maps to NM_002599.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:72295736 G>A maps to NM_002599.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156874557 G>A maps to NM_001080471.1 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156874557 G>A maps to NM_001080471.1 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:98388153 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:98388153 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:98469378 G>A maps to NM_152309.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:98469378 G>A maps to NM_152309.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151205137 G>T maps to NM_001135638.1 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151205137 G>T maps to NM_001135638.1 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:47867067 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:47867067 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:8630053 A>T maps to NM_015192.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:8630053 A>T maps to NM_015192.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:95791987 G>T maps to ENST00000371380 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:95791987 G>T maps to ENST00000371380 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:208795743 G>A maps to NM_001080475.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:208795743 G>A maps to NM_001080475.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:84563164 G>T maps to ENST00000373145 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:84563164 G>T maps to ENST00000373145 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:16287897 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:16287897 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52729032 C>T maps to NM_014225.5 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52729032 C>T maps to NM_014225.5 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:6349666 C>T maps to NM_181876.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:6349666 C>T maps to NM_181876.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:49035626 C>T maps to NM_006150.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:49035626 C>T maps to NM_006150.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:590069 G>C maps to NM_002735.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:590069 G>C maps to NM_002735.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:125141115 G>T maps to NM_000962.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:125141115 G>T maps to NM_000962.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157414102 G>A maps to NM_002847.3 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157414102 G>A maps to NM_002847.3 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157691363 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157691363 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157985048 G>C maps to NM_002847.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157985048 G>C maps to NM_002847.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:40747084 G>T maps to ENST00000373198 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:40747084 G>T maps to ENST00000373198 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:128849007 C>T maps to ENST00000418265 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:128849007 C>T maps to ENST00000418265 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:46727023 G>A maps to NM_003579.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:46727023 G>A maps to NM_003579.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:4917650 G>A maps to NM_018059.4 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:4917650 G>A maps to NM_018059.4 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:36177703 C>G maps to NM_001082578.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:36177703 C>G maps to NM_001082578.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:100052326 T>A maps to NM_016316.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:100052326 T>A maps to NM_016316.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:77257433 G>T maps to ENST00000396204 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:77257433 G>T maps to ENST00000396204 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:67718784 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:67718784 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237791357 A>T maps to NM_001035.2 K2140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237791357 A>T maps to NM_001035.2 K2140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:51174164 G>T maps to ENST00000251020 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:51174164 G>T maps to ENST00000251020 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:51174491 G>T maps to ENST00000251020 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:51174491 G>T maps to ENST00000251020 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166903467 T>A maps to NM_001165963.1 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166903467 T>A maps to NM_001165963.1 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:65304156 G>C maps to NM_020680.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:65304156 G>C maps to NM_020680.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:29476679 G>T maps to NM_005626.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:29476679 G>T maps to NM_005626.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:112764371 A>G maps to NM_007373.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:112764371 A>G maps to NM_007373.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:1616966 G>T maps to NM_018556.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:1616966 G>T maps to NM_018556.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:56906303 C>A maps to NM_000339.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:56906303 C>A maps to NM_000339.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44664167 G>T maps to NM_001134771.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44664167 G>T maps to NM_001134771.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107408246 C>T maps to NM_000111.2 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107408246 C>T maps to NM_000111.2 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:86912204 C>T maps to NM_022127.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:86912204 C>T maps to NM_022127.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18331686 G>T maps to NM_001145195.1 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18331686 G>T maps to NM_001145195.1 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:33706787 G>A maps to NM_012319.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:33706787 G>A maps to NM_012319.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:135084372 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:135084372 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:142718398 G>A maps to NM_001184749.1 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:142718398 G>A maps to NM_001184749.1 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168910592 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168910592 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:22429317 C>T maps to NM_005775.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:22429317 C>T maps to NM_005775.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:108431125 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:108431125 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106970933 C>T maps to NM_014978.1 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106970933 C>T maps to NM_014978.1 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:101178125 G>A maps to NM_003114.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:101178125 G>A maps to NM_003114.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:64940261 C>A maps to NM_001008778.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:64940261 C>A maps to NM_001008778.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:74382928 G>A maps to NM_182965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:74382928 G>A maps to NM_182965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:54852018 G>T maps to NM_003128.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:54852018 G>T maps to NM_003128.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:17373457 T>C maps to NM_001004470.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:17373457 T>C maps to NM_001004470.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:104125388 C>T maps to NM_017564.9 Y1753Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:104125388 C>T maps to NM_017564.9 Y1753Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:152599232 G>A maps to NM_182961.2 L6188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:152599232 G>A maps to NM_182961.2 L6188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:162272896 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:162272896 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:41658481 G>A maps to ENST00000343317 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:41658481 G>A maps to ENST00000343317 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:44943062 G>T maps to NM_003241.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:44943062 G>T maps to NM_003241.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:39993216 C>A maps to NM_025264.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:39993216 C>A maps to NM_025264.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:154624695 C>T maps to NM_003264.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:154624695 C>T maps to NM_003264.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:120476797 G>T maps to NM_138554.3 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:120476797 G>T maps to NM_138554.3 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:12904106 C>T maps to NM_016562.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:12904106 C>T maps to NM_016562.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:19070735 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:19070735 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:44605101 C>A maps to NM_032256.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:44605101 C>A maps to NM_032256.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:130185163 G>A maps to NM_133448.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:130185163 G>A maps to NM_133448.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:32964722 C>A maps to NM_207313.1 C809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:32964722 C>A maps to NM_207313.1 C809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:120201130 A>C maps to NM_001198670.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:120201130 A>C maps to NM_001198670.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:226054363 C>A maps to NM_014698.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:226054363 C>A maps to NM_014698.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:46159474 G>A maps to NM_016486.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:46159474 G>A maps to NM_016486.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:32052439 C>A maps to ENST00000375244 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:32052439 C>A maps to ENST00000375244 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1308350 C>T maps to NM_012217.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1308350 C>T maps to NM_012217.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:119998087 G>T maps to NM_012101.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:119998087 G>T maps to NM_012101.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100732026 G>C maps to NM_030961.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100732026 G>C maps to NM_030961.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:31324993 C>A maps to NM_002420.4 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:31324993 C>A maps to NM_002420.4 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:77376930 C>T maps to NM_017662.4 K1552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:77376930 C>T maps to NM_017662.4 K1552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:99634667 T>C maps to NM_025244.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:99634667 T>C maps to NM_025244.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130364187 A>G maps to NM_052933.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130364187 A>G maps to NM_052933.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:31768571 G>T maps to NM_020856.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:31768571 G>T maps to NM_020856.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179438510 A>G maps to NM_133378.4 N21548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179438510 A>G maps to NM_133378.4 N21548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:135106115 T>G maps to NM_006659.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:135106115 T>G maps to NM_006659.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:49387022 G>C maps to NM_003323.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:49387022 G>C maps to NM_003323.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:118716548 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:118716548 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:5530284 C>A maps to NM_017481.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:5530284 C>A maps to NM_017481.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:234627525 C>T maps to NM_007120.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:234627525 C>T maps to NM_007120.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:73050705 G>T maps to NM_170744.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:73050705 G>T maps to NM_170744.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:216373151 G>A maps to ENST00000366943 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:216373151 G>A maps to ENST00000366943 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:85678285 C>A maps to NM_014991.4 G1739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:85678285 C>A maps to NM_014991.4 G1739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124132399 C>T maps to NM_145647.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124132399 C>T maps to NM_145647.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141424062 G>A maps to NM_001105558.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141424062 G>A maps to NM_001105558.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:21909901 T>C maps to NM_173531.3 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:21909901 T>C maps to NM_173531.3 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:72353079 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:72353079 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:30935935 G>T maps to NM_014717.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:30935935 G>T maps to NM_014717.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:57769382 G>T maps to NM_178457.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:57769382 G>T maps to NM_178457.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:187698690 G>A maps to NM_182521.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:187698690 G>A maps to NM_182521.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:96810321 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:96810321 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:155029446 C>T maps to NM_207197.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:155029446 C>T maps to NM_207197.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:25284698 G>C maps to NM_001185085.1 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:25284698 G>C maps to NM_001185085.1 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:153664137 C>T maps to NM_001183.4 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:153664137 C>T maps to NM_001183.4 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:171511179 A>G maps to ENST00000392078 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:171511179 A>G maps to ENST00000392078 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:53785858 C>G maps to NM_001128840.1 Y1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:53785858 C>G maps to NM_001128840.1 Y1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:93065407 G>T maps to NM_001164737.1 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:93065407 G>T maps to NM_001164737.1 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:110494844 C>T maps to NM_014289.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:110494844 C>T maps to NM_014289.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:61843459 C>A maps to NM_020198.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:61843459 C>A maps to NM_020198.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:66480331 C>G maps to NM_005582.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:66480331 C>G maps to NM_005582.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:105796298 C>T maps to NM_000494.3 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:105796298 C>T maps to NM_000494.3 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:53676596 C>T maps to NM_000098.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:53676596 C>T maps to NM_000098.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:115273173 C>T maps to NM_001130523.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:115273173 C>T maps to NM_001130523.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:38151718 C>G maps to NM_007335.2 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:38151718 C>G maps to NM_007335.2 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220147599 C>T maps to NM_006736.5 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220147599 C>T maps to NM_006736.5 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr18:28712646 G>A maps to NM_024421.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr18:28712646 G>A maps to NM_024421.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:27016132 C>T maps to NM_203371.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:27016132 C>T maps to NM_203371.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:38048523 G>C maps to NM_013285.2 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:38048523 G>C maps to NM_013285.2 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:18354718 G>A maps to NM_005316.3 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:18354718 G>A maps to NM_005316.3 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:43548607 C>T maps to NM_015052.3 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:43548607 C>T maps to NM_015052.3 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:197106926 A>G maps to NM_020760.1 G1177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:197106926 A>G maps to NM_020760.1 G1177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:3600723 G>A maps to NM_024337.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:3600723 G>A maps to NM_024337.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:200972737 C>T maps to NM_017596.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:200972737 C>T maps to NM_017596.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:43215956 G>A maps to NM_022356.3 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:43215956 G>A maps to NM_022356.3 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57594925 G>A maps to NM_002332.2 E3445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57594925 G>A maps to NM_002332.2 E3445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:66460706 G>A maps to NM_001164664.1 R1900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:66460706 G>A maps to NM_001164664.1 R1900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:35802586 C>T maps to NM_006739.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:35802586 C>T maps to NM_006739.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:43870649 A>T maps to NM_001044370.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:43870649 A>T maps to NM_001044370.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:9057666 G>A maps to NM_024690.2 Q9927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:9057666 G>A maps to NM_024690.2 Q9927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:16701569 C>T maps to NM_012334.2 E978E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:16701569 C>T maps to NM_012334.2 E978E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:52645804 G>C maps to ENST00000358212 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:52645804 G>C maps to ENST00000358212 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:51585289 T>C maps to NM_001145260.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:51585289 T>C maps to NM_001145260.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:106391024 G>T maps to ENST00000372465 C219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:106391024 G>T maps to ENST00000372465 C219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:4661547 C>G maps to NM_001004751.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:4661547 C>G maps to NM_001004751.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:239170884 G>A maps to NM_022817.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:239170884 G>A maps to NM_022817.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:47979819 C>T maps to NM_138295.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:47979819 C>T maps to NM_138295.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:57156548 G>A maps to NM_002728.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:57156548 G>A maps to NM_002728.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:27287916 G>A maps to NM_004103.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:27287916 G>A maps to NM_004103.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:214568285 G>A maps to NM_005401.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:214568285 G>A maps to NM_005401.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:144689206 G>C maps to NM_023078.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:144689206 G>C maps to NM_023078.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:36190906 C>T maps to NM_194301.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:36190906 C>T maps to NM_194301.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:92660373 C>A maps to ENST00000458617 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:92660373 C>A maps to ENST00000458617 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:175268853 C>T maps to NM_024583.4 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:175268853 C>T maps to NM_024583.4 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:95058515 C>A maps to NM_000624.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:95058515 C>A maps to NM_000624.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:112724820 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:112724820 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:62760895 C>T maps to ENST00000430500 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:62760895 C>T maps to ENST00000430500 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96956195 G>A maps to NM_014014.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96956195 G>A maps to NM_014014.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96956426 G>A maps to NM_014014.3 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96956426 G>A maps to NM_014014.3 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:44914529 C>A maps to NM_025137.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:44914529 C>A maps to NM_025137.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:100258035 C>T maps to NM_014290.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:100258035 C>T maps to NM_014290.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:126138199 C>T maps to NM_052907.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:126138199 C>T maps to NM_052907.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:120439040 C>T maps to NM_030577.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:120439040 C>T maps to NM_030577.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:77685838 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:77685838 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:24200844 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:24200844 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:75082845 C>A maps to NM_145170.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:75082845 C>A maps to NM_145170.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:241958534 C>T maps to NM_144625.4 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:241958534 C>T maps to NM_144625.4 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:30936292 G>A maps to NM_014717.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:30936292 G>A maps to NM_014717.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:22941399 G>A maps to ENST00000397104 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:22941399 G>A maps to ENST00000397104 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:45614390 G>C maps to NM_021116.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:45614390 G>C maps to NM_021116.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:27148880 C>A maps to NM_003986.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:27148880 C>A maps to NM_003986.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55814151 G>A maps to NM_032430.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55814151 G>A maps to NM_032430.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:42745036 T>C maps to NM_001145080.2 N586N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:42745036 T>C maps to NM_001145080.2 N586N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:15444287 C>A maps to NM_001135170.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:15444287 C>A maps to NM_001135170.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:56420010 A>T maps to NM_001080433.1 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:56420010 A>T maps to NM_001080433.1 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:28459851 G>T maps to NM_018318.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:28459851 G>T maps to NM_018318.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:2481128 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:2481128 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:35974186 A>G maps to NM_152632.3 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:35974186 A>G maps to NM_152632.3 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:155241864 G>T maps to NM_017639.3 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:155241864 G>T maps to NM_017639.3 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:73662016 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:73662016 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:216737684 C>T maps to NM_001438.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:216737684 C>T maps to NM_001438.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:46867857 C>T maps to NM_001441.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:46867857 C>T maps to NM_001441.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:54735196 A>T maps to NM_001010872.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:54735196 A>T maps to NM_001010872.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:15938262 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:15938262 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:152281323 G>C maps to NM_002016.1 S2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:152281323 G>C maps to NM_002016.1 S2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:74516928 C>A maps to NM_012201.5 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:74516928 C>A maps to NM_012201.5 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:57430245 G>A maps to NM_080425.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:57430245 G>A maps to NM_080425.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:49473085 C>T maps to NM_002103.4 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:49473085 C>T maps to NM_002103.4 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:42265859 G>T maps to NM_016004.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:42265859 G>T maps to NM_016004.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:1471346 C>T maps to NM_002183.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:1471346 C>T maps to NM_002183.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:18096156 G>A maps to ENST00000222249 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:18096156 G>A maps to ENST00000222249 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10573031 G>A maps to NM_007333.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10573031 G>A maps to NM_007333.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10573044 T>C maps to NM_007333.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10573044 T>C maps to NM_007333.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10588480 T>C maps to NM_002260.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10588480 T>C maps to NM_002260.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:132120540 G>T maps to NM_001077637.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:132120540 G>T maps to NM_001077637.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:54958982 C>A maps to NM_020678.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:54958982 C>A maps to NM_020678.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:49634456 G>T maps to NM_139049.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:49634456 G>T maps to NM_139049.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:103932327 T>G maps to ENST00000335102 L289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:103932327 T>G maps to ENST00000335102 L289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:138687137 A>C maps to ENST00000370578 Y666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:138687137 A>C maps to ENST00000370578 Y666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:24122620 C>T maps to NM_005940.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:24122620 C>T maps to NM_005940.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:49927403 C>T maps to NM_002447.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:49927403 C>T maps to NM_002447.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237052595 G>C maps to NM_000254.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237052595 G>C maps to NM_000254.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:119059261 C>T maps to NM_004784.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:119059261 C>T maps to NM_004784.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:248343316 C>A maps to NM_001004688.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:248343316 C>A maps to NM_001004688.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:57268909 G>T maps to NM_021728.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:57268909 G>T maps to NM_021728.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:58207612 T>C maps to NM_001040429.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:58207612 T>C maps to NM_001040429.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:66919296 C>G maps to NM_020786.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:66919296 C>G maps to NM_020786.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:22292796 G>T maps to ENST00000397199 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:22292796 G>T maps to ENST00000397199 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:87076325 G>A maps to ENST00000276616 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:87076325 G>A maps to ENST00000276616 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:47451186 C>T maps to NM_015466.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:47451186 C>T maps to NM_015466.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:119547915 T>C maps to NM_002855.4 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:119547915 T>C maps to NM_002855.4 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:23495306 C>T maps to NM_004914.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:23495306 C>T maps to NM_004914.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:47032556 C>T maps to NM_005676.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:47032556 C>T maps to NM_005676.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr9:3257076 C>A maps to NM_134428.1 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr9:3257076 C>A maps to NM_134428.1 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:31501066 C>G maps to NM_080430.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:31501066 C>G maps to NM_080430.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:74733002 C>G maps to NM_003016.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:74733002 C>G maps to NM_003016.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:13948038 G>A maps to NM_139167.2 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:13948038 G>A maps to NM_139167.2 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:17885293 T>A maps to ENST00000417048 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:17885293 T>A maps to ENST00000417048 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:167833782 G>T maps to NM_016950.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:167833782 G>T maps to NM_016950.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:18637495 G>A maps to NM_194285.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:18637495 G>A maps to NM_194285.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:112424367 A>G maps to NM_022484.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:112424367 A>G maps to NM_022484.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:43250826 G>T maps to NM_032538.1 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:43250826 G>T maps to NM_032538.1 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:10209283 A>T maps to NM_001105562.2 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:10209283 A>T maps to NM_001105562.2 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:101196961 C>A maps to NM_001078.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:101196961 C>A maps to NM_001078.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:87446013 A>G maps to NM_015144.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:87446013 A>G maps to NM_015144.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:4648195 G>A maps to NM_001136046.1 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:4648195 G>A maps to NM_001136046.1 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:1237393 C>A maps to NM_030649.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:1237393 C>A maps to NM_030649.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:33658392 G>T maps to NM_030955.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:33658392 G>T maps to NM_030955.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:4057536 C>A maps to NM_001116.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:4057536 C>A maps to NM_001116.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:52236728 G>T maps to ENST00000441729 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:52236728 G>T maps to ENST00000441729 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:104189908 G>C maps to NM_000035.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:104189908 G>C maps to NM_000035.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:45941035 C>A maps to NM_000698.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:45941035 C>A maps to NM_000698.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:233323381 G>T maps to NM_001631.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:233323381 G>T maps to NM_001631.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:90348374 C>G maps to NM_001150.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:90348374 C>G maps to NM_001150.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:116691783 G>A maps to NM_000482.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:116691783 G>A maps to NM_000482.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:33386152 G>A maps to NM_001170.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:33386152 G>A maps to NM_001170.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:97481663 G>A maps to NM_183356.3 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:97481663 G>A maps to NM_183356.3 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:70231184 C>G maps to NM_015570.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:70231184 C>G maps to NM_015570.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:26798826 C>A maps to NM_001105519.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:26798826 C>A maps to NM_001105519.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:120704290 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:120704290 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:27922221 G>A maps to ENST00000341513 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:27922221 G>A maps to ENST00000341513 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:181701954 G>C maps to ENST00000357570 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:181701954 G>C maps to ENST00000357570 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:181745259 C>A maps to ENST00000357570 V1721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:181745259 C>A maps to ENST00000357570 V1721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:159163315 G>T maps to NM_021189.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:159163315 G>T maps to NM_021189.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:78081896 C>T maps to NM_004354.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:78081896 C>T maps to NM_004354.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:60499427 C>T maps to NM_001794.2 H555H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:60499427 C>T maps to NM_001794.2 H555H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:180047643 A>G maps to NM_014810.4 L1938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:180047643 A>G maps to NM_014810.4 L1938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:55862794 C>A maps to NM_001025195.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:55862794 C>A maps to NM_001025195.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:101964957 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:101964957 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:106171886 C>A maps to NM_001171095.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:106171886 C>A maps to NM_001171095.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:41323637 A>G maps to NM_001843.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:41323637 A>G maps to NM_001843.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:94054500 G>T maps to NM_000089.3 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:94054500 G>T maps to NM_000089.3 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:94057054 C>A maps to NM_000089.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:94057054 C>A maps to NM_000089.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:8607722 C>A maps to NM_001014447.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:8607722 C>A maps to NM_001014447.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:113668559 C>A maps to NM_198123.1 E943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:113668559 C>A maps to NM_198123.1 E943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:49391857 C>T maps to NM_015086.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:49391857 C>T maps to NM_015086.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:14188794 G>T maps to NM_004080.2 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:14188794 G>T maps to NM_004080.2 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:172952819 C>T maps to NM_178120.4 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:172952819 C>T maps to NM_178120.4 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:13820509 C>G maps to NM_001369.2 G2262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:13820509 C>G maps to NM_001369.2 G2262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:117677515 A>T maps to ENST00000276204 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:117677515 A>T maps to ENST00000276204 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:128821560 G>T maps to ENST00000398025 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:128821560 G>T maps to ENST00000398025 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:169509852 G>A maps to NM_004946.2 T1828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:169509852 G>A maps to NM_004946.2 T1828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:33451144 C>G maps to NM_024025.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:33451144 C>G maps to NM_024025.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:102452389 C>T maps to NM_001376.4 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:102452389 C>T maps to NM_001376.4 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:139167714 A>G maps to NM_001195037.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:139167714 A>G maps to NM_001195037.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:3763465 C>A maps to NM_001144958.1 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:3763465 C>A maps to NM_001144958.1 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:10822110 G>A maps to ENST00000429377 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:10822110 G>A maps to ENST00000429377 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:129771316 G>T maps to NM_182314.1 Y428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:129771316 G>T maps to NM_182314.1 Y428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:37028466 C>A maps to NM_001013736.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:37028466 C>A maps to NM_001013736.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:130891659 C>A maps to NM_016623.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:130891659 C>A maps to NM_016623.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:43627705 G>A maps to NM_001145196.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:43627705 G>A maps to NM_001145196.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:73910943 C>A maps to ENST00000389570 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:73910943 C>A maps to ENST00000389570 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55401198 C>T maps to NM_002000.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55401198 C>T maps to NM_002000.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:33014276 G>A maps to NM_007270.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:33014276 G>A maps to NM_007270.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:84609107 C>A maps to NM_001001670.2 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:84609107 C>A maps to NM_001001670.2 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:29237714 C>T maps to NM_005249.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:29237714 C>T maps to NM_005249.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:71015117 T>C maps to NM_032682.4 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:71015117 T>C maps to NM_032682.4 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:101017689 C>A maps to NM_174942.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:101017689 C>A maps to NM_174942.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:34136680 A>C maps to NM_016631.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:34136680 A>C maps to NM_016631.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:150163824 C>A maps to NM_175571.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:150163824 C>A maps to NM_175571.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:132548852 G>A maps to NM_001448.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:132548852 G>A maps to NM_001448.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:22390173 C>G maps to NM_145290.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:22390173 C>G maps to NM_145290.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:78426623 C>A maps to NM_032553.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:78426623 C>A maps to NM_032553.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:105859316 C>A maps to NM_007227.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:105859316 C>A maps to NM_007227.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:94343974 C>A maps to NM_001510.2 Y467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:94343974 C>A maps to NM_001510.2 Y467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:48682426 T>A maps to ENST00000444343 C1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:48682426 T>A maps to ENST00000444343 C1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:43594284 G>A maps to NM_015052.3 T1535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:43594284 G>A maps to NM_015052.3 T1535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:75117983 C>T maps to NM_000189.4 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:75117983 C>T maps to NM_000189.4 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:32411566 A>T maps to NM_019111.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:32411566 A>T maps to NM_019111.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:25699465 C>A maps to NM_001145728.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:25699465 C>A maps to NM_001145728.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:160494946 C>T maps to NM_000876.2 H1702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:160494946 C>T maps to NM_000876.2 H1702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:91449622 G>A maps to NM_007035.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:91449622 G>A maps to NM_007035.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:15696061 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:15696061 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:100056342 C>T maps to ENST00000375206 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:100056342 C>T maps to ENST00000375206 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70681537 T>A maps to NM_020866.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70681537 T>A maps to NM_020866.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153130447 C>A maps to NM_000425.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153130447 C>A maps to NM_000425.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153132928 G>T maps to NM_000425.3 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153132928 G>T maps to NM_000425.3 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153136380 C>A maps to NM_000425.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153136380 C>A maps to NM_000425.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:107752391 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:107752391 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55179178 C>T maps to ENST00000391733 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55179178 C>T maps to ENST00000391733 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:11905847 C>A maps to ENST00000396099 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:11905847 C>A maps to ENST00000396099 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:114422811 C>T maps to NM_020871.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:114422811 C>T maps to NM_020871.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:66502040 C>A maps to NM_015541.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:66502040 C>A maps to NM_015541.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:133650266 G>A maps to ENST00000250173 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:133650266 G>A maps to ENST00000250173 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:33525617 G>A maps to ENST00000354476 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:33525617 G>A maps to ENST00000354476 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:46794187 G>A maps to NM_005588.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:46794187 G>A maps to NM_005588.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:1556668 C>A maps to NM_001174118.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:1556668 C>A maps to NM_001174118.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:9091785 G>T maps to NM_024690.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:9091785 G>T maps to NM_024690.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:158468338 C>A maps to NM_017760.5 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:158468338 C>A maps to NM_017760.5 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:24933897 G>A maps to NM_003743.4 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:24933897 G>A maps to NM_003743.4 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:56538819 C>A maps to NM_153447.4 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:56538819 C>A maps to NM_153447.4 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:101604707 G>T maps to NM_002518.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:101604707 G>T maps to NM_002518.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:124097539 T>C maps to NM_001163278.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:124097539 T>C maps to NM_001163278.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:98188737 T>A maps to NM_001004736.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:98188737 T>A maps to NM_001004736.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:98072804 G>T maps to NM_001005517.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:98072804 G>T maps to NM_001005517.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:158735769 T>G maps to NM_001005185.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:158735769 T>G maps to NM_001005185.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:142749460 C>A maps to NM_001001667.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:142749460 C>A maps to NM_001001667.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:9546641 G>T maps to NM_177990.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:9546641 G>T maps to NM_177990.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:140531775 C>A maps to NM_018939.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:140531775 C>A maps to NM_018939.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:619513 C>A maps to NM_000283.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:619513 C>A maps to NM_000283.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:99956682 C>T maps to ENST00000413850 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:99956682 C>T maps to ENST00000413850 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:242511433 T>A maps to NM_152666.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:242511433 T>A maps to NM_152666.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:48459665 C>A maps to NM_001130082.1 V1052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:48459665 C>A maps to NM_001130082.1 V1052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:75052310 G>A maps to ENST00000257665 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:75052310 G>A maps to ENST00000257665 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:46658030 C>T maps to ENST00000371986 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:46658030 C>T maps to ENST00000371986 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:64728939 A>G maps to NM_002737.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:64728939 A>G maps to NM_002737.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:6498719 C>A maps to NM_006257.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:6498719 C>A maps to NM_006257.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:154493531 G>T maps to NM_171998.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:154493531 G>T maps to NM_171998.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:56774180 C>T maps to NM_058216.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:56774180 C>T maps to NM_058216.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:20563736 A>C maps to NM_020343.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:20563736 A>C maps to NM_020343.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:77147282 C>T maps to ENST00000332191 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:77147282 C>T maps to ENST00000332191 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:51174773 G>A maps to ENST00000251020 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:51174773 G>A maps to ENST00000251020 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:155226463 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:155226463 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:111959711 A>T maps to NM_003002.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:111959711 A>T maps to NM_003002.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:75208255 G>T maps to NM_001039573.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:75208255 G>T maps to NM_001039573.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:33964061 C>A maps to NM_016180.3 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:33964061 C>A maps to NM_016180.3 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:75902272 G>A maps to ENST00000371091 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:75902272 G>A maps to ENST00000371091 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:186231801 G>T maps to NM_031953.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:186231801 G>T maps to NM_031953.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:108380224 G>A maps to NM_001013031.1 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:108380224 G>A maps to NM_001013031.1 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:16265828 C>T maps to NM_015001.2 F3634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:16265828 C>T maps to NM_015001.2 F3634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:147493974 C>A maps to NM_001127698.1 C646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:147493974 C>A maps to NM_001127698.1 C646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:115487070 G>T maps to NM_003176.2 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:115487070 G>T maps to NM_003176.2 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:6631142 A>T maps to NM_138697.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:6631142 A>T maps to NM_138697.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:17299996 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:17299996 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:45145175 G>T maps to ENST00000404564 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:45145175 G>T maps to ENST00000404564 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:35271186 C>T maps to NM_001077653.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:35271186 C>T maps to NM_001077653.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:56688568 G>T maps to ENST00000240361 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:56688568 G>T maps to ENST00000240361 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:30706086 A>T maps to NM_031271.3 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:30706086 A>T maps to NM_031271.3 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:55208436 G>T maps to NM_003222.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:55208436 G>T maps to NM_003222.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:101907146 A>G maps to NM_004612.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:101907146 A>G maps to NM_004612.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:30024943 G>A maps to NM_003257.3 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:30024943 G>A maps to NM_003257.3 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:33134916 C>T maps to NM_001039770.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:33134916 C>T maps to NM_001039770.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:138199922 G>T maps to NM_006290.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:138199922 G>T maps to NM_006290.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:1148429 G>A maps to NM_003327.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:1148429 G>A maps to NM_003327.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:1499812 G>T maps to NM_000547.5 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:1499812 G>T maps to NM_000547.5 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:2225514 G>C maps to NM_032271.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:2225514 G>C maps to NM_032271.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:14482704 C>T maps to NM_007118.2 A2160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:14482704 C>T maps to NM_007118.2 A2160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:77377952 G>A maps to NM_017662.4 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:77377952 G>A maps to NM_017662.4 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:166773862 G>A maps to NM_024753.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:166773862 G>A maps to NM_024753.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:179441914 G>A maps to NM_133378.4 I20481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:179441914 G>A maps to NM_133378.4 I20481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:132235909 C>A maps to NM_080386.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:132235909 C>A maps to NM_080386.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:28856775 C>T maps to NM_003321.4 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:28856775 C>T maps to NM_003321.4 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:90039586 C>A maps to NM_016021.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:90039586 C>A maps to NM_016021.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:156020952 C>A maps to NM_020131.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:156020952 C>A maps to NM_020131.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:141489822 C>A maps to NM_021833.4 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:141489822 C>A maps to NM_021833.4 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:234526901 C>T maps to NM_019076.4 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:234526901 C>T maps to NM_019076.4 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:129054694 G>A maps to NM_006649.3 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:129054694 G>A maps to NM_006649.3 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:9538751 C>T maps to NM_145054.4 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:9538751 C>T maps to NM_145054.4 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:168107426 C>A maps to NM_152381.5 P3175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:168107426 C>A maps to NM_152381.5 P3175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:128901652 G>A maps to NM_003399.5 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:128901652 G>A maps to NM_003399.5 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:100364780 C>T maps to ENST00000349350 N1587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:100364780 C>T maps to ENST00000349350 N1587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:77912692 C>A maps to NM_152694.2 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:77912692 C>A maps to NM_152694.2 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:57931585 A>T maps to NM_006959.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:57931585 A>T maps to NM_006959.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:28240023 C>T maps to NM_001023560.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:28240023 C>T maps to NM_001023560.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:18566443 T>G maps to NM_001145045.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:18566443 T>G maps to NM_001145045.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:27600624 G>A maps to NM_144631.4 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:27600624 G>A maps to NM_144631.4 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:53668344 G>C maps to NM_024733.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:53668344 G>C maps to NM_024733.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:2934602 G>C maps to NM_021217.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:2934602 G>C maps to NM_021217.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:44506099 C>T maps to NM_080752.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:44506099 C>T maps to NM_080752.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:116988238 C>G maps to NM_145062.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:116988238 C>G maps to NM_145062.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:143080396 G>C maps to NM_001010972.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:143080396 G>C maps to NM_001010972.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:137850008 G>T maps to NM_016161.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:137850008 G>T maps to NM_016161.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:67103889 G>C maps to NM_080284.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:67103889 G>C maps to NM_080284.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20691246 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20691246 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20721144 T>C maps to NM_001163941.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20721144 T>C maps to NM_001163941.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:48117855 G>T maps to NM_033226.2 L1319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:48117855 G>T maps to NM_033226.2 L1319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21971083 C>A maps to NM_005691.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21971083 C>A maps to NM_005691.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:22012542 G>A maps to NM_005691.2 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:22012542 G>A maps to NM_005691.2 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39214591 C>T maps to NM_004924.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39214591 C>T maps to NM_004924.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:39646226 G>T maps to NM_001464.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:39646226 G>T maps to NM_001464.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:1229174 C>T maps to NM_018702.2 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:1229174 C>T maps to NM_018702.2 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:7520897 C>T maps to NM_020546.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:7520897 C>T maps to NM_020546.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:100134760 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:100134760 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:3504653 G>A maps to NM_018269.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:3504653 G>A maps to NM_018269.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:87089342 C>A maps to NM_152336.2 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:87089342 C>A maps to NM_152336.2 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:41468293 G>T maps to NM_178819.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:41468293 G>T maps to NM_178819.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:148459391 C>T maps to NM_032049.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:148459391 C>T maps to NM_032049.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:33293231 A>G maps to NM_004274.4 L2071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:33293231 A>G maps to NM_004274.4 L2071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:29519835 T>G maps to NM_004304.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:29519835 T>G maps to NM_004304.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:202494489 G>A maps to ENST00000409099 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:202494489 G>A maps to ENST00000409099 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:114257902 T>C maps to NM_001148.4 D1254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:114257902 T>C maps to NM_001148.4 D1254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:16344419 C>A maps to NM_001130524.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:16344419 C>A maps to NM_001130524.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6896571 C>T maps to ENST00000400091 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6896571 C>T maps to ENST00000400091 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:9839446 G>A maps to NM_001198793.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:9839446 G>A maps to NM_001198793.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:35778811 C>A maps to ENST00000458225 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:35778811 C>A maps to ENST00000458225 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:177142721 A>T maps to NM_080874.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:177142721 A>T maps to NM_080874.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:31324050 C>A maps to NM_030632.1 V1413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:31324050 C>A maps to NM_030632.1 V1413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:1387813 G>T maps to NM_001039211.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:1387813 G>T maps to NM_001039211.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:96807882 C>T maps to NM_018036.5 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:96807882 C>T maps to NM_018036.5 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:130686175 G>T maps to NM_001001486.1 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:130686175 G>T maps to NM_001001486.1 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:80878645 G>T maps to NM_183050.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:80878645 G>T maps to NM_183050.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219527604 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219527604 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:32491767 G>T maps to NM_001714.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:32491767 G>T maps to NM_001714.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:51717913 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:51717913 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:43287085 G>T maps to NM_014753.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:43287085 G>T maps to NM_014753.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:13610218 G>A maps to NM_148894.2 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:13610218 G>A maps to NM_148894.2 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:65888104 G>C maps to ENST00000420799 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:65888104 G>C maps to ENST00000420799 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:81097425 G>A maps to NM_152337.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:81097425 G>A maps to NM_152337.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2511048 C>A maps to NM_025108.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2511048 C>A maps to NM_025108.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:43333281 C>T maps to NM_152343.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:43333281 C>T maps to NM_152343.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119466072 G>T maps to NM_033364.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119466072 G>T maps to NM_033364.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43970829 G>T maps to NM_153246.4 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43970829 G>T maps to NM_153246.4 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100085976 G>A maps to ENST00000423930 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100085976 G>A maps to ENST00000423930 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:21735703 T>A maps to NM_138644.1 L80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:21735703 T>A maps to NM_138644.1 L80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:81593675 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:81593675 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:18439904 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:18439904 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:105209506 G>A maps to NM_015916.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:105209506 G>A maps to NM_015916.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:31592718 C>G maps to NM_194300.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:31592718 C>G maps to NM_194300.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:24838914 C>A maps to NM_001130726.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:24838914 C>A maps to NM_001130726.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:30303883 G>A maps to NM_001238.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:30303883 G>A maps to NM_001238.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:17072297 G>T maps to NM_014406.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:17072297 G>T maps to NM_014406.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:112648057 C>A maps to NM_138806.3 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:112648057 C>A maps to NM_138806.3 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66084210 C>A maps to NM_020404.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66084210 C>A maps to NM_020404.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111342669 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111342669 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:21975200 C>A maps to NM_004061.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:21975200 C>A maps to NM_004061.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:60508074 C>A maps to NM_001794.2 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:60508074 C>A maps to NM_001794.2 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26881388 C>T maps to NM_016279.3 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26881388 C>T maps to NM_016279.3 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:90377055 G>T maps to NM_012395.2 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:90377055 G>T maps to NM_012395.2 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:125864221 T>A maps to ENST00000392693 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:125864221 T>A maps to ENST00000392693 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:95375391 A>G maps to NM_001012267.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:95375391 A>G maps to NM_001012267.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:101443555 C>T maps to ENST00000327230 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:101443555 C>T maps to ENST00000327230 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:14720333 G>T maps to NM_005454.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:14720333 G>T maps to NM_005454.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:66975440 G>T maps to NM_003869.5 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:66975440 G>T maps to NM_003869.5 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:369945 G>T maps to NM_006614.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:369945 G>T maps to NM_006614.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:24976617 A>G maps to NM_001836.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:24976617 A>G maps to NM_001836.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:135106984 T>A maps to NM_001190850.1 K98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:135106984 T>A maps to NM_001190850.1 K98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:76482811 A>G maps to NM_033401.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:76482811 A>G maps to NM_033401.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:103377723 A>T maps to NM_080629.2 P1371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:103377723 A>T maps to NM_080629.2 P1371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:103444660 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:103444660 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:107814668 C>G maps to ENST00000328300 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:107814668 C>G maps to ENST00000328300 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:70944627 C>A maps to NM_001851.4 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:70944627 C>A maps to NM_001851.4 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:40776819 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:40776819 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:88008655 C>T maps to NM_033048.5 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:88008655 C>T maps to NM_033048.5 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:197446846 C>T maps to NM_201253.2 V1353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:197446846 C>T maps to NM_201253.2 V1353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:75932314 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:75932314 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:208988976 G>T maps to NM_006891.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:208988976 G>T maps to NM_006891.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113668413 A>T maps to NM_198123.1 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113668413 A>T maps to NM_198123.1 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:80874768 C>A maps to ENST00000402739 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:80874768 C>A maps to ENST00000402739 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219000009 C>T maps to NM_001168298.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219000009 C>T maps to NM_001168298.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:143994038 G>T maps to NM_000498.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:143994038 G>T maps to NM_000498.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99447309 C>T maps to NM_022820.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99447309 C>T maps to NM_022820.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99463536 G>T maps to NM_022820.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99463536 G>T maps to NM_022820.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:47400231 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:47400231 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:15784337 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:15784337 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:155699057 G>A maps to NM_004632.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:155699057 G>A maps to NM_004632.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33287596 T>C maps to NM_001350.4 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33287596 T>C maps to NM_001350.4 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117841006 C>T maps to ENST00000338728 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117841006 C>T maps to ENST00000338728 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:91063967 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:91063967 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:19352177 G>T maps to NM_017925.4 E1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:19352177 G>T maps to NM_017925.4 E1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:137075974 A>G maps to NM_004717.2 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:137075974 A>G maps to NM_004717.2 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:84245775 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:84245775 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:170592563 G>A maps to NM_005618.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:170592563 G>A maps to NM_005618.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:11556076 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:11556076 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:51370645 C>G maps to NM_004947.4 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:51370645 C>G maps to NM_004947.4 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:28914144 G>T maps to NM_001942.2 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:28914144 G>T maps to NM_001942.2 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184045207 G>T maps to NM_001194947.1 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184045207 G>T maps to NM_001194947.1 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184046478 C>T maps to NM_001194947.1 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184046478 C>T maps to NM_001194947.1 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:14875406 G>A maps to NM_013447.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:14875406 G>A maps to NM_013447.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4856126 G>T maps to NM_053013.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4856126 G>T maps to NM_053013.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:34797801 G>T maps to NM_012156.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:34797801 G>T maps to NM_012156.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:37960402 G>A maps to NM_017549.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:37960402 G>A maps to NM_017549.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:89390123 G>T maps to NM_005233.5 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:89390123 G>T maps to NM_005233.5 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134911467 G>T maps to NM_004441.4 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134911467 G>T maps to NM_004441.4 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:56468699 T>A maps to ENST00000460849 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:56468699 T>A maps to ENST00000460849 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:158178130 G>A maps to NM_001009959.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:158178130 G>A maps to NM_001009959.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:56726658 A>G maps to NM_018261.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:56726658 A>G maps to NM_018261.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:572553 C>T maps to NM_018303.4 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:572553 C>T maps to NM_018303.4 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:113770068 G>T maps to NM_000131.3 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:113770068 G>T maps to NM_000131.3 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:14816389 C>A maps to NM_031453.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:14816389 C>A maps to NM_031453.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:170627005 G>T maps to NM_032448.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:170627005 G>T maps to NM_032448.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:131521381 C>A maps to NM_001105195.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:131521381 C>A maps to NM_001105195.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139158254 C>A maps to NM_015912.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139158254 C>A maps to NM_015912.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:62066779 C>A maps to ENST00000404929 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:62066779 C>A maps to ENST00000404929 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:187527367 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:187527367 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:92534272 C>A maps to ENST00000298047 V2698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:92534272 C>A maps to ENST00000298047 V2698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126336492 G>T maps to NM_024582.4 V2125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126336492 G>T maps to NM_024582.4 V2125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:45996262 G>T maps to ENST00000348697 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:45996262 G>T maps to ENST00000348697 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:97325680 G>T maps to NM_003837.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:97325680 G>T maps to NM_003837.2 T256T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:102375180 C>A maps to NM_175929.2 *253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:102375180 C>A maps to NM_175929.2 *253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:170883613 G>A maps to NM_003862.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:170883613 G>A maps to NM_003862.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:81188289 C>A maps to NM_004464.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:81188289 C>A maps to NM_004464.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50514654 T>A maps to NM_022116.3 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50514654 T>A maps to NM_022116.3 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:33014285 G>C maps to NM_007270.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:33014285 G>C maps to NM_007270.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152277575 G>A maps to NM_002016.1 A3262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152277575 G>A maps to NM_002016.1 A3262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128493675 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128493675 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128496862 C>T maps to NM_001458.4 N2483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128496862 C>T maps to NM_001458.4 N2483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:14306823 C>G maps to NM_198391.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:14306823 C>G maps to NM_198391.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:49777384 C>T maps to NM_001079673.1 Q1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:49777384 C>T maps to NM_001079673.1 Q1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:49186289 C>G maps to NM_004476.1 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:49186289 C>G maps to NM_004476.1 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4796695 G>T maps to ENST00000450194 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4796695 G>T maps to ENST00000450194 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127238613 C>T maps to NM_020369.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127238613 C>T maps to NM_020369.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26518624 C>A maps to NM_001134366.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26518624 C>A maps to NM_001134366.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:230415089 G>T maps to NM_004481.3 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:230415089 G>T maps to NM_004481.3 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:158115853 G>T maps to NM_014568.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:158115853 G>T maps to NM_014568.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:8100775 G>A maps to NM_001002295.1 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:8100775 G>A maps to NM_001002295.1 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:25023490 C>A maps to NM_005265.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:25023490 C>A maps to NM_005265.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27857778 C>A maps to NM_007266.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27857778 C>A maps to NM_007266.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:6732043 G>C maps to NM_001080452.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:6732043 G>C maps to NM_001080452.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:47682492 C>T maps to NM_153838.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:47682492 C>T maps to NM_153838.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:131605421 C>T maps to NM_198827.3 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:131605421 C>T maps to NM_198827.3 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20043587 G>T maps to NM_001002911.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20043587 G>T maps to NM_001002911.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:154147119 G>A maps to NM_001038705.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:154147119 G>A maps to NM_001038705.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:110300857 C>A maps to ENST00000414000 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:110300857 C>A maps to ENST00000414000 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:57712137 C>A maps to NM_170776.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:57712137 C>A maps to NM_170776.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31023524 G>A maps to ENST00000327783 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31023524 G>A maps to ENST00000327783 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:9934561 C>A maps to NM_000833.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:9934561 C>A maps to NM_000833.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:1008896 G>A maps to NM_138690.1 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:1008896 G>A maps to NM_138690.1 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:121086100 T>A maps to NM_005308.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:121086100 T>A maps to NM_005308.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:65429375 G>A maps to NM_000181.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:65429375 G>A maps to NM_000181.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:19078171 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:19078171 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:239990287 C>G maps to NM_006037.3 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:239990287 C>G maps to NM_006037.3 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:18832987 G>A maps to NM_178425.2 W745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:18832987 G>A maps to NM_178425.2 W745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43484129 C>G maps to NM_015052.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43484129 C>G maps to NM_015052.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43548637 G>T maps to NM_015052.3 G1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43548637 G>T maps to NM_015052.3 G1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79662892 C>T maps to NM_004712.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79662892 C>T maps to NM_004712.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108095391 C>G maps to NM_007072.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108095391 C>G maps to NM_007072.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:100515505 C>A maps to NM_033055.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:100515505 C>A maps to NM_033055.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:26217274 C>T maps to NM_021052.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:26217274 C>T maps to NM_021052.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33052925 G>T maps to NM_002121.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33052925 G>T maps to NM_002121.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:43058193 A>T maps to ENST00000338692 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:43058193 A>T maps to ENST00000338692 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:83347645 C>A maps to NM_031372.2 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:83347645 C>A maps to NM_031372.2 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:60287597 A>T maps to NM_015888.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:60287597 A>T maps to NM_015888.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:27213049 C>A maps to NM_018951.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:27213049 C>A maps to NM_018951.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:176958399 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:176958399 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:148847542 G>T maps to NM_032383.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:148847542 G>T maps to NM_032383.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:14205167 G>T maps to NM_006041.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:14205167 G>T maps to NM_006041.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:97484869 A>G maps to NM_153456.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:97484869 A>G maps to NM_153456.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:99006652 C>T maps to NM_000197.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:99006652 C>T maps to NM_000197.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:22222418 C>T maps to NM_005529.5 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:22222418 C>T maps to NM_005529.5 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:88039964 C>G maps to NM_000866.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:88039964 C>G maps to NM_000866.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:47409238 G>A maps to NM_000621.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:47409238 G>A maps to NM_000621.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113803680 C>T maps to NM_006028.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113803680 C>T maps to NM_006028.3 L188L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:154862941 G>C maps to NM_024012.2 R111R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:154862941 G>C maps to NM_024012.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:3201609 G>A maps to NM_002111.6 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:3201609 G>A maps to NM_002111.6 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:18170763 G>A maps to NM_005535.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:18170763 G>A maps to NM_005535.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:15230305 G>T maps to NM_006844.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:15230305 G>T maps to NM_006844.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76715025 C>A maps to NM_001563.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76715025 C>A maps to NM_001563.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:134595382 C>T maps to NM_005539.3 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:134595382 C>T maps to NM_005539.3 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:158983077 T>A maps to NM_001042705.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:158983077 T>A maps to NM_001042705.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:51013673 C>A maps to NM_138334.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:51013673 C>A maps to NM_138334.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:41705438 T>C maps to NM_152903.4 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:41705438 T>C maps to NM_152903.4 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110768630 G>A maps to NM_004978.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110768630 G>A maps to NM_004978.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110768729 C>T maps to NM_004978.4 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110768729 C>T maps to NM_004978.4 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:119915075 C>T maps to NM_012281.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:119915075 C>T maps to NM_012281.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:211192226 G>A maps to NM_172362.2 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:211192226 G>A maps to NM_172362.2 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118969188 C>T maps to NM_181840.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118969188 C>T maps to NM_181840.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36671867 C>T maps to NM_001031836.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36671867 C>T maps to NM_001031836.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:94731486 G>T maps to NM_018039.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:94731486 G>T maps to NM_018039.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:57193888 C>T maps to NM_020722.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:57193888 C>T maps to NM_020722.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:5754899 G>A maps to ENST00000414202 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:5754899 G>A maps to ENST00000414202 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:20986464 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:20986464 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:57970089 C>A maps to NM_004984.2 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:57970089 C>A maps to NM_004984.2 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:21674112 G>A maps to NM_153270.1 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:21674112 G>A maps to NM_153270.1 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:136964067 C>A maps to NM_017415.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:136964067 C>A maps to NM_017415.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52799788 G>A maps to NM_033033.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52799788 G>A maps to NM_033033.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31933542 G>A maps to ENST00000437381 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31933542 G>A maps to ENST00000437381 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:129468101 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:129468101 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:133962939 G>C maps to ENST00000355048 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:133962939 G>C maps to ENST00000355048 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:71124585 G>T maps to NM_018357.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:71124585 G>T maps to NM_018357.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152636661 G>A maps to NM_178430.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152636661 G>A maps to NM_178430.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:165173230 G>A maps to NM_177398.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:165173230 G>A maps to NM_177398.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:39984670 G>A maps to NM_022896.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:39984670 G>A maps to NM_022896.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141747098 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141747098 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194081493 C>A maps to NM_001135057.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194081493 C>A maps to NM_001135057.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:80530200 C>G maps to NM_178839.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:80530200 C>G maps to NM_178839.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:115560788 G>T maps to NM_002338.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:115560788 G>T maps to NM_002338.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:33567971 C>A maps to ENST00000354476 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:33567971 C>A maps to ENST00000354476 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:21343119 T>C maps to NM_006767.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:21343119 T>C maps to NM_006767.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:151935452 G>T maps to NM_005362.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:151935452 G>T maps to NM_005362.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39103296 C>A maps to NM_001042600.1 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39103296 C>A maps to NM_001042600.1 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:3785123 G>T maps to NM_139355.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:3785123 G>T maps to NM_139355.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:89756989 C>A maps to NM_203406.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:89756989 C>A maps to NM_203406.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:112437458 C>A maps to NM_001085377.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:112437458 C>A maps to NM_001085377.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:151083775 A>G maps to NM_053002.4 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:151083775 A>G maps to NM_053002.4 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:8702180 G>T maps to NM_152599.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:8702180 G>T maps to NM_152599.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:88423496 A>T maps to NM_152706.2 *254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:88423496 A>T maps to NM_152706.2 *254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:151945259 T>C maps to ENST00000355193 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:151945259 T>C maps to ENST00000355193 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:90856531 G>A maps to NM_007351.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:90856531 G>A maps to NM_007351.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:31342402 C>A maps to ENST00000397641 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:31342402 C>A maps to ENST00000397641 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:30516970 G>A maps to NM_001584.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:30516970 G>A maps to NM_001584.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60164177 A>T maps to NM_032597.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60164177 A>T maps to NM_032597.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9019326 G>T maps to NM_024690.2 S12520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9019326 G>T maps to NM_024690.2 S12520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9082766 G>T maps to NM_024690.2 L3016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9082766 G>T maps to NM_024690.2 L3016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:42811688 C>A maps to NM_001144925.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:42811688 C>A maps to NM_001144925.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47360128 C>A maps to ENST00000399249 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47360128 C>A maps to ENST00000399249 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48600955 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48600955 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108189604 G>T maps to NM_014981.1 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108189604 G>T maps to NM_014981.1 A461A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:15615812 C>A maps to NM_015909.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:15615812 C>A maps to NM_015909.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:22881253 C>T maps to NM_004540.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:22881253 C>T maps to NM_004540.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:134073738 C>T maps to NM_015261.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:134073738 C>T maps to NM_015261.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:152507312 G>T maps to NM_001164507.1 S2334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:152507312 G>T maps to NM_001164507.1 S2334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:52693476 T>A maps to NM_199289.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:52693476 T>A maps to NM_199289.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:125139560 T>C maps to NM_001040214.1 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:125139560 T>C maps to NM_001040214.1 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:65084125 C>G maps to NM_020726.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:65084125 C>G maps to NM_020726.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151784224 G>A maps to NM_020167.4 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151784224 G>A maps to NM_020167.4 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:30490919 G>T maps to NM_006092.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:30490919 G>T maps to NM_006092.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:10729816 G>A maps to NM_024894.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:10729816 G>A maps to NM_024894.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6669387 T>A maps to ENST00000382421 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6669387 T>A maps to ENST00000382421 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:162337163 C>A maps to NM_014697.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:162337163 C>A maps to NM_014697.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:26116677 G>A maps to NM_000625.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:26116677 G>A maps to NM_000625.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:120461116 G>A maps to NM_024408.2 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:120461116 G>A maps to NM_024408.2 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:32712560 G>T maps to ENST00000265074 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:32712560 G>T maps to ENST00000265074 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:30327198 C>G maps to NM_000475.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:30327198 C>G maps to NM_000475.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:107979326 T>A maps to NM_001113226.1 C432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:107979326 T>A maps to NM_001113226.1 C432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:156846196 G>A maps to NM_002529.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:156846196 G>A maps to NM_002529.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17571645 G>T maps to NM_138454.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17571645 G>T maps to NM_138454.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:71066319 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:71066319 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:107331852 C>T maps to NM_001004483.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:107331852 C>T maps to NM_001004483.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:248487666 G>C maps to NM_001004691.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:248487666 G>C maps to NM_001004691.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20216395 G>A maps to NM_172194.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20216395 G>A maps to NM_172194.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:5842332 T>A maps to NM_001005174.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:5842332 T>A maps to NM_001005174.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:55761252 G>C maps to NM_003697.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:55761252 G>C maps to NM_003697.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:98073304 C>A maps to NM_001005517.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:98073304 C>A maps to NM_001005517.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:56380834 C>A maps to NM_001004740.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:56380834 C>A maps to NM_001004740.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:56043986 C>A maps to NM_001004745.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:56043986 C>A maps to NM_001004745.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158746534 G>A maps to NM_001005278.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158746534 G>A maps to NM_001005278.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20917121 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20917121 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:29604464 G>A maps to NM_183378.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:29604464 G>A maps to NM_183378.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:152553900 C>G maps to NM_002563.2 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:152553900 C>G maps to NM_002563.2 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17674518 G>A maps to NM_012387.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17674518 G>A maps to NM_012387.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:103249049 C>G maps to NM_000277.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:103249049 C>G maps to NM_000277.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:61010338 A>G maps to NM_022894.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:61010338 A>G maps to NM_022894.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:36882088 C>A maps to NM_016734.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:36882088 C>A maps to NM_016734.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:100925600 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:100925600 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:134073016 C>A maps to NM_032961.1 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:134073016 C>A maps to NM_032961.1 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:138449938 C>A maps to NM_019035.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:138449938 C>A maps to NM_019035.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140552727 G>C maps to NM_018940.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140552727 G>C maps to NM_018940.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140745189 C>A maps to NM_018918.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140745189 C>A maps to NM_018918.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76721721 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76721721 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:15111245 G>T maps to NM_015027.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:15111245 G>T maps to NM_015027.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:30974930 G>A maps to NM_014303.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:30974930 G>A maps to NM_014303.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:46105752 T>A maps to ENST00000257821 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:46105752 T>A maps to ENST00000257821 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2160772 G>A maps to NM_001009944.2 P1465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2160772 G>A maps to NM_001009944.2 P1465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:110464484 C>A maps to ENST00000426474 I2161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:110464484 C>A maps to ENST00000426474 I2161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:20440629 G>T maps to ENST00000442610 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:20440629 G>T maps to ENST00000442610 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:8639328 C>A maps to NM_015192.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:8639328 C>A maps to NM_015192.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:153688867 C>T maps to NM_017514.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:153688867 C>T maps to NM_017514.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:131865425 C>A maps to NM_020911.1 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:131865425 C>A maps to NM_020911.1 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:50719225 G>A maps to NM_012401.2 Q1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:50719225 G>A maps to NM_012401.2 Q1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:7416790 C>A maps to NM_000937.4 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:7416790 C>A maps to NM_000937.4 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:130832239 G>T maps to NM_001099771.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:130832239 G>T maps to NM_001099771.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:39500315 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:39500315 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:288085 G>A maps to NM_177543.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:288085 G>A maps to NM_177543.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:49632190 G>T maps to NM_003660.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:49632190 G>T maps to NM_003660.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:203008325 G>T maps to ENST00000367238 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:203008325 G>T maps to ENST00000367238 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:113519997 G>C maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:113519997 G>C maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:43223077 C>A maps to NM_022115.3 E1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:43223077 C>A maps to NM_022115.3 E1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:1578502 C>A maps to NM_006445.3 V1001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:1578502 C>A maps to NM_006445.3 V1001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:79325635 T>G maps to NM_015225.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:79325635 T>G maps to NM_015225.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43268341 A>C maps to NM_182707.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43268341 A>C maps to NM_182707.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:87643511 G>T maps to NM_080685.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:87643511 G>T maps to NM_080685.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:8518098 G>T maps to NM_002839.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:8518098 G>T maps to NM_002839.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:46725741 G>T maps to NM_003579.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:46725741 G>T maps to NM_003579.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:36596038 C>A maps to NM_000448.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:36596038 C>A maps to NM_000448.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:79929483 G>A maps to ENST00000438737 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:79929483 G>A maps to ENST00000438737 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:36117029 A>T maps to NM_021111.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:36117029 A>T maps to NM_021111.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:186515343 T>A maps to NM_181573.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:186515343 T>A maps to NM_181573.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176105680 T>C maps to NM_022457.5 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176105680 T>C maps to NM_022457.5 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:78319271 G>T maps to NM_020914.4 L2428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:78319271 G>T maps to NM_020914.4 L2428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:62380968 G>A maps to NM_000327.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:62380968 G>A maps to NM_000327.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:94486633 G>T maps to NM_004560.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:94486633 G>T maps to NM_004560.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117706998 G>C maps to NM_002944.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117706998 G>C maps to NM_002944.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237947326 C>A maps to NM_001035.2 L4105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237947326 C>A maps to NM_001035.2 L4105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64812108 G>T maps to ENST00000301885 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64812108 G>T maps to ENST00000301885 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:166172033 G>T maps to NM_001040142.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:166172033 G>T maps to NM_001040142.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:62025345 G>T maps to NM_000334.4 Y1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:62025345 G>T maps to NM_000334.4 Y1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:121671605 G>T maps to NM_007190.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:121671605 G>T maps to NM_007190.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48062871 C>A maps to NM_153618.1 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48062871 C>A maps to NM_153618.1 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:30392510 G>T maps to NM_052838.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:30392510 G>T maps to NM_052838.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:135204106 T>A maps to ENST00000372169 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:135204106 T>A maps to ENST00000372169 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26688934 G>T maps to NM_021115.4 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26688934 G>T maps to NM_021115.4 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:70595651 C>A maps to NM_012426.4 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:70595651 C>A maps to NM_012426.4 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:77471193 T>C maps to NM_024776.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:77471193 T>C maps to NM_024776.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:164710185 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:164710185 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:103703647 C>A maps to NM_000452.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:103703647 C>A maps to NM_000452.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:127487035 A>T maps to NM_001046.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:127487035 A>T maps to NM_001046.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:99364134 T>A maps to NM_005073.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:99364134 T>A maps to NM_005073.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:73641465 C>A maps to NM_006517.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:73641465 C>A maps to NM_006517.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:60168525 C>T maps to NM_004731.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:60168525 C>T maps to NM_004731.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:160858106 C>T maps to ENST00000392145 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:160858106 C>T maps to ENST00000392145 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:129492639 G>A maps to ENST00000339231 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:129492639 G>A maps to ENST00000339231 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:10027568 G>T maps to NM_001001290.1 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:10027568 G>T maps to NM_001001290.1 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:57177517 G>A maps to ENST00000428603 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:57177517 G>A maps to ENST00000428603 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:162821589 G>A maps to NM_001178015.1 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:162821589 G>A maps to NM_001178015.1 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20636270 G>T maps to NM_004211.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20636270 G>T maps to NM_004211.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:103300761 C>T maps to NM_003048.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:103300761 C>T maps to NM_003048.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:168151446 C>G maps to NM_003062.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:168151446 C>G maps to NM_003062.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:164906356 G>T maps to NM_014926.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:164906356 G>T maps to NM_014926.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:88390655 T>C maps to NM_198274.3 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:88390655 T>C maps to NM_198274.3 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:115600940 G>C maps to NM_001012994.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:115600940 G>C maps to NM_001012994.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:138589371 C>A maps to NM_001101677.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:138589371 C>A maps to NM_001101677.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:108447970 C>T maps to NM_001013031.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:108447970 C>T maps to NM_001013031.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:106960942 C>T maps to NM_014978.1 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:106960942 C>T maps to NM_014978.1 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:121495846 G>T maps to NM_003105.5 G2075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:121495846 G>T maps to NM_003105.5 G2075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:45993739 G>C maps to NM_003110.5 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:45993739 G>C maps to NM_003110.5 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:22680765 C>A maps to ENST00000376603 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:22680765 C>A maps to ENST00000376603 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:142803912 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:142803912 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151054175 A>T maps to NM_003118.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151054175 A>T maps to NM_003118.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:32259394 T>C maps to NM_144569.4 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:32259394 T>C maps to NM_144569.4 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158596724 G>A maps to NM_003126.2 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158596724 G>A maps to NM_003126.2 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158647624 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158647624 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:52677374 G>A maps to ENST00000435678 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:52677374 G>A maps to ENST00000435678 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:172753011 C>T maps to NM_003714.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:172753011 C>T maps to NM_003714.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219538430 G>T maps to NM_015690.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219538430 G>T maps to NM_015690.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:184930347 G>C maps to NM_020225.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:184930347 G>C maps to NM_020225.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31046342 A>C maps to NM_004604.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31046342 A>C maps to NM_004604.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44237717 G>T maps to NM_014351.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44237717 G>T maps to NM_014351.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:48046854 C>A maps to NM_152782.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:48046854 C>A maps to NM_152782.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:113169031 C>A maps to ENST00000374463 G2953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:113169031 C>A maps to ENST00000374463 G2953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:29779863 C>A maps to NM_021738.2 L1368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:29779863 C>A maps to NM_021738.2 L1368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:29784045 G>A maps to NM_021738.2 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:29784045 G>A maps to NM_021738.2 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:64653252 C>T maps to NM_182914.2 Q5890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:64653252 C>T maps to NM_182914.2 Q5890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:40853934 C>T maps to NM_020783.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:40853934 C>T maps to NM_020783.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:7441796 C>A maps to NM_175733.3 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:7441796 C>A maps to NM_175733.3 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:764306 A>G maps to NM_006755.1 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:764306 A>G maps to NM_006755.1 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:118671560 T>C maps to NM_016281.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:118671560 T>C maps to NM_016281.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15641673 C>A maps to NM_178571.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15641673 C>A maps to NM_178571.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:114823366 C>A maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:114823366 C>A maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:44560666 C>T maps to NM_016427.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:44560666 C>T maps to NM_016427.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20845890 G>A maps to NM_007110.4 L1915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20845890 G>A maps to NM_007110.4 L1915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:70332961 C>A maps to NM_030625.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:70332961 C>A maps to NM_030625.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:30705978 G>T maps to NM_031271.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:30705978 G>T maps to NM_031271.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26902739 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26902739 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:95235490 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:95235490 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:85554095 A>C maps to ENST00000409015 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:85554095 A>C maps to ENST00000409015 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:84202720 C>A maps to NM_005077.3 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:84202720 C>A maps to NM_005077.3 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:50152022 C>T maps to NM_001098576.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:50152022 C>T maps to NM_001098576.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:177019266 C>T maps to NM_017510.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:177019266 C>T maps to NM_017510.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150490382 G>A maps to NM_014020.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150490382 G>A maps to NM_014020.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:1589782 G>T maps to NM_001097620.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:1589782 G>T maps to NM_001097620.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:117838395 C>T maps to NM_002160.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:117838395 C>T maps to NM_002160.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:5410698 C>A maps to NM_001080495.2 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:5410698 C>A maps to NM_001080495.2 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175372525 C>A maps to NM_003285.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175372525 C>A maps to NM_003285.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:1459996 G>T maps to NM_000547.5 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:1459996 G>T maps to NM_000547.5 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10941906 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10941906 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:129695926 C>A maps to NM_007117.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:129695926 C>A maps to NM_007117.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15516138 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15516138 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:140397212 C>A maps to NM_152616.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:140397212 C>A maps to NM_152616.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189068294 G>T maps to NM_178556.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189068294 G>T maps to NM_178556.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189012859 C>G maps to ENST00000326754 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189012859 C>G maps to ENST00000326754 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:111155893 G>T maps to NM_012471.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:111155893 G>T maps to NM_012471.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:2432702 G>A maps to ENST00000452833 Y889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:2432702 G>A maps to ENST00000452833 Y889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:77411734 A>T maps to NM_017662.4 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:77411734 A>T maps to NM_017662.4 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:77442832 G>T maps to NM_017662.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:77442832 G>T maps to NM_017662.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142572887 G>A maps to NM_018646.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142572887 G>A maps to NM_018646.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:3341794 G>A maps to ENST00000398659 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:3341794 G>A maps to ENST00000398659 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179431856 C>T maps to NM_133378.4 W23766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179431856 C>T maps to NM_133378.4 W23766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179473145 T>A maps to NM_133378.4 L14920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179473145 T>A maps to NM_133378.4 L14920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:19752451 G>T maps to NM_006001.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:19752451 G>T maps to NM_006001.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:132238108 C>A maps to NM_080386.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:132238108 C>A maps to NM_080386.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:139564123 C>A maps to ENST00000358430 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:139564123 C>A maps to ENST00000358430 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:19864758 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:19864758 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34249795 C>G maps to NM_001171201.1 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34249795 C>G maps to NM_001171201.1 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:19478260 C>A maps to ENST00000375267 R2363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:19478260 C>A maps to ENST00000375267 R2363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346426 C>A maps to NM_021139.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346426 C>A maps to NM_021139.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346555 G>T maps to NM_021139.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346555 G>T maps to NM_021139.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:35541183 C>A maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:35541183 C>A maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216040370 G>A maps to ENST00000366943 I2941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216040370 G>A maps to ENST00000366943 I2941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:145069548 C>T maps to NM_007124.2 L2703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:145069548 C>T maps to NM_007124.2 L2703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:12414216 G>T maps to NM_015378.2 T3206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:12414216 G>T maps to NM_015378.2 T3206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:22152984 G>C maps to NM_173615.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:22152984 G>C maps to NM_173615.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:85592308 G>A maps to NM_145172.3 W743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:85592308 G>A maps to NM_145172.3 W743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228109635 C>A maps to NM_003395.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228109635 C>A maps to NM_003395.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:98349796 G>T maps to NM_001079.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:98349796 G>T maps to NM_001079.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:56191345 A>T maps to NM_030776.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:56191345 A>T maps to NM_030776.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:31749999 A>G maps to NM_001174096.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:31749999 A>G maps to NM_001174096.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:145156854 G>T maps to NM_014795.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:145156854 G>T maps to NM_014795.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:135524845 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:135524845 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:22155564 G>T maps to NM_007153.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:22155564 G>T maps to NM_007153.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:133768557 G>T maps to NM_001165881.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:133768557 G>T maps to NM_001165881.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:44351433 A>G maps to NM_181845.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:44351433 A>G maps to NM_181845.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:21606119 G>A maps to NM_024697.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:21606119 G>A maps to NM_024697.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:149467541 C>A maps to NM_207336.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:149467541 C>A maps to NM_207336.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52942159 C>T maps to NM_001143939.1 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52942159 C>T maps to NM_001143939.1 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:58370796 C>T maps to NM_032828.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:58370796 C>T maps to NM_032828.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42956150 G>T maps to NM_001134656.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42956150 G>T maps to NM_001134656.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:88966075 C>T maps to NM_181646.2 P1260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:88966075 C>T maps to NM_181646.2 P1260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:58384402 G>A maps to NM_001144989.1 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:58384402 G>A maps to NM_001144989.1 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113608400 C>A maps to NM_004724.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113608400 C>A maps to NM_004724.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4008082 C>A maps to NM_015113.3 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4008082 C>A maps to NM_015113.3 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:48411994 G>T maps to NM_152701.3 A3678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:48411994 G>T maps to NM_152701.3 A3678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:74128467 G>T maps to NM_001615.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:74128467 G>T maps to NM_001615.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:70990219 C>A maps to NM_003814.4 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:70990219 C>A maps to NM_003814.4 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:100537778 C>A maps to NM_139057.2 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:100537778 C>A maps to NM_139057.2 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:233244563 C>A maps to NM_001632.3 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:233244563 C>A maps to NM_001632.3 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:24942255 C>T maps to NM_001006634.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:24942255 C>T maps to NM_001006634.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:117185777 C>T maps to NM_207303.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:117185777 C>T maps to NM_207303.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:62384572 G>T maps to NM_012200.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:62384572 G>T maps to NM_012200.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:88138501 G>A maps to NM_001031743.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:88138501 G>A maps to NM_001031743.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:2721097 C>A maps to NM_199460.2 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:2721097 C>A maps to NM_199460.2 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:27458429 G>T maps to NM_004341.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:27458429 G>T maps to NM_004341.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:110496279 G>T maps to NM_014289.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:110496279 G>T maps to NM_014289.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:65491381 G>T maps to NM_003613.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:65491381 G>T maps to NM_003613.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:38724678 G>A maps to NM_175060.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:38724678 G>A maps to NM_175060.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61468486 C>T maps to NM_001853.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61468486 C>T maps to NM_001853.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:99799532 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:99799532 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:72141382 C>T maps to NM_014003.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:72141382 C>T maps to NM_014003.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:230411703 C>A maps to NM_139072.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:230411703 C>A maps to NM_139072.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:103091377 A>T maps to NM_001080463.1 A2991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:103091377 A>T maps to NM_001080463.1 A2991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:43930153 G>T maps to NM_001127615.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:43930153 G>T maps to NM_001127615.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:56277674 C>A maps to NM_000502.4 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:56277674 C>A maps to NM_000502.4 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:27282987 G>T maps to NM_001989.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:27282987 G>T maps to NM_001989.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:135418890 G>T maps to NM_205855.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:135418890 G>T maps to NM_205855.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:13678059 C>A maps to NM_001165035.1 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:13678059 C>A maps to NM_001165035.1 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:86545095 C>T maps to NM_001451.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:86545095 C>T maps to NM_001451.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:45262154 C>A maps to NM_021072.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:45262154 C>A maps to NM_021072.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:23387343 G>T maps to NM_006547.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:23387343 G>T maps to NM_006547.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:111663783 T>A maps to NM_003640.3 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:111663783 T>A maps to NM_003640.3 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:31388319 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:31388319 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:78771773 A>G maps to NM_001161352.1 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:78771773 A>G maps to NM_001161352.1 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:52756685 G>A maps to NM_002283.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:52756685 G>A maps to NM_002283.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:54850355 G>T maps to NM_012276.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:54850355 G>T maps to NM_012276.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:84199427 T>A maps to NM_178452.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:84199427 T>A maps to NM_178452.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:141074130 G>A maps to ENST00000509479 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:141074130 G>A maps to ENST00000509479 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:39717247 T>C maps to NM_054024.3 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:39717247 T>C maps to NM_054024.3 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:102931226 G>T maps to NM_001142432.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:102931226 G>T maps to NM_001142432.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:11177237 C>T maps to NM_015458.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:11177237 C>T maps to NM_015458.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50735302 G>T maps to NM_001145809.1 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50735302 G>T maps to NM_001145809.1 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:128347776 C>A maps to ENST00000389524 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:128347776 C>A maps to ENST00000389524 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:124914621 G>T maps to NM_014222.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:124914621 G>T maps to NM_014222.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:5925160 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:5925160 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:131745598 G>A maps to NM_015354.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:131745598 G>A maps to NM_015354.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:183713605 C>T maps to NM_001080477.1 D1927D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:183713605 C>T maps to NM_001080477.1 D1927D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:159283996 C>A maps to NM_001004467.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:159283996 C>A maps to NM_001004467.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:5968809 C>A maps to NM_001003443.2 C78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:5968809 C>A maps to NM_001003443.2 C78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:55755477 C>A maps to NM_001142763.1 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:55755477 C>A maps to NM_001142763.1 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:82387974 G>T maps to NM_033026.5 A5115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:82387974 G>T maps to NM_033026.5 A5115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:17462465 C>A maps to NM_002594.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:17462465 C>A maps to NM_002594.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:79697924 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:79697924 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81228607 C>A maps to NM_052892.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81228607 C>A maps to NM_052892.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81253858 G>A maps to NM_052892.3 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81253858 G>A maps to NM_052892.3 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:110516569 G>T maps to ENST00000426474 G3616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:110516569 G>T maps to ENST00000426474 G3616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:99342457 G>T maps to NM_001100426.1 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:99342457 G>T maps to NM_001100426.1 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:51174868 A>G maps to ENST00000251020 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:51174868 A>G maps to ENST00000251020 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:27514323 C>A maps to NM_016240.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:27514323 C>A maps to NM_016240.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:172666786 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:172666786 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:7984357 G>T maps to NM_153449.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:7984357 G>T maps to NM_153449.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:150657177 G>A maps to NM_001145017.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:150657177 G>A maps to NM_001145017.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:172755181 C>A maps to NM_003714.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:172755181 C>A maps to NM_003714.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:29998952 G>A maps to NM_016151.2 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:29998952 G>A maps to NM_016151.2 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:59560747 G>A maps to ENST00000393853 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:59560747 G>A maps to ENST00000393853 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:46658780 A>T maps to NM_001010870.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:46658780 A>T maps to NM_001010870.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:171867900 G>T maps to ENST00000360843 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:171867900 G>T maps to ENST00000360843 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:193051690 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:193051690 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:141952342 C>T maps to NM_001001317.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:141952342 C>T maps to NM_001001317.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:179477550 C>A maps to NM_133378.4 E14065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:179477550 C>A maps to NM_133378.4 E14065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085305 G>A maps to NM_000552.3 Q2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085305 G>A maps to NM_000552.3 Q2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085324 G>A maps to NM_000552.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085324 G>A maps to NM_000552.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:85642648 T>C maps to NM_014991.4 Q2506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:85642648 T>C maps to NM_014991.4 Q2506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:128477084 C>A maps to NM_018383.4 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:128477084 C>A maps to NM_018383.4 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:5256249 G>A maps to NM_015610.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:5256249 G>A maps to NM_015610.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:53645327 C>T maps to NM_001172674.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:53645327 C>T maps to NM_001172674.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:12542604 C>T maps to NM_005815.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:12542604 C>T maps to NM_005815.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:149152474 C>A maps to ENST00000440594 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:149152474 C>A maps to ENST00000440594 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:66982324 G>A maps to NM_080283.3 D1396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:66982324 G>A maps to NM_080283.3 D1396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:44051103 G>T maps to NM_022436.2 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:44051103 G>T maps to NM_022436.2 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23072868 C>A maps to NM_022060.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23072868 C>A maps to NM_022060.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:17405098 C>A maps to NM_024527.4 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:17405098 C>A maps to NM_024527.4 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:20486734 C>A maps to NM_001010845.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:20486734 C>A maps to NM_001010845.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:78399673 G>T maps to NM_020421.3 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:78399673 G>T maps to NM_020421.3 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:131955632 G>T maps to NM_001115.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:131955632 G>T maps to NM_001115.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:88292349 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:88292349 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:31539816 G>C maps to NM_016633.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:31539816 G>C maps to NM_016633.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:243800929 C>A maps to NM_005465.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:243800929 C>A maps to NM_005465.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:165649771 G>T maps to NM_000696.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:165649771 G>T maps to NM_000696.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:73677379 A>T maps to NM_015120.4 T1241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:73677379 A>T maps to NM_015120.4 T1241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:41530017 C>A maps to ENST00000415018 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:41530017 C>A maps to ENST00000415018 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:61946573 G>T maps to NM_020987.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:61946573 G>T maps to NM_020987.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:77818207 A>G maps to NM_001029870.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:77818207 A>G maps to NM_001029870.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:66539449 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:66539449 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:23762406 C>A maps to NM_017707.3 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:23762406 C>A maps to NM_017707.3 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:25967291 G>T maps to NM_018263.4 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:25967291 G>T maps to NM_018263.4 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:160141496 C>A maps to NM_144699.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:160141496 C>A maps to NM_144699.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:169346052 C>T maps to NM_003666.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:169346052 C>T maps to NM_003666.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:112969438 C>T maps to ENST00000273395 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:112969438 C>T maps to ENST00000273395 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:140534555 G>T maps to NM_004333.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:140534555 G>T maps to NM_004333.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:102748794 G>T maps to NM_021830.4 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:102748794 G>T maps to NM_021830.4 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:60600866 G>T maps to ENST00000404681 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:60600866 G>T maps to ENST00000404681 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:77844531 C>A maps to NM_001010860.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:77844531 C>A maps to NM_001010860.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:77493594 C>A maps to NM_024496.2 G181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:77493594 C>A maps to NM_024496.2 G181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55672122 T>C maps to ENST00000301249 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55672122 T>C maps to ENST00000301249 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:11769500 C>G maps to NM_198545.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:11769500 C>G maps to NM_198545.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:40066958 G>C maps to NM_021096.3 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:40066958 G>C maps to NM_021096.3 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:54110042 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:54110042 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:2959088 C>T maps to NM_032415.4 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:2959088 C>T maps to NM_032415.4 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:49200413 G>T maps to NM_022903.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:49200413 G>T maps to NM_022903.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158324239 C>A maps to NM_030893.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158324239 C>A maps to NM_030893.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:2638463 C>A maps to NM_002414.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:2638463 C>A maps to NM_002414.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44815503 G>A maps to NM_021248.1 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44815503 G>A maps to NM_021248.1 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:150754238 C>A maps to NM_004935.3 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:150754238 C>A maps to NM_004935.3 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:125555739 C>A maps to NM_130773.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:125555739 C>A maps to NM_130773.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:228118302 G>T maps to NM_000091.4 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:228118302 G>T maps to NM_000091.4 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:137657570 C>A maps to NM_000093.3 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:137657570 C>A maps to NM_000093.3 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:48603990 C>A maps to NM_000094.3 R2770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:48603990 C>A maps to NM_000094.3 R2770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:211473213 C>A maps to NM_001122633.1 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:211473213 C>A maps to NM_001122633.1 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:211515107 A>T maps to NM_001122633.1 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:211515107 A>T maps to NM_001122633.1 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:207737305 C>A maps to NM_000651.4 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:207737305 C>A maps to NM_000651.4 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:34082548 G>A maps to ENST00000373381 P1951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:34082548 G>A maps to ENST00000373381 P1951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:64506176 G>T maps to NM_022048.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:64506176 G>T maps to NM_022048.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:126214566 A>C maps to NM_020946.1 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:126214566 A>C maps to NM_020946.1 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:35125307 C>A maps to ENST00000339266 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:35125307 C>A maps to ENST00000339266 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:6712897 T>G maps to NM_018198.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:6712897 T>G maps to NM_018198.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:66258797 C>A maps to NM_005700.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:66258797 C>A maps to NM_005700.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:7584148 C>A maps to NM_004415.2 T2218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:7584148 C>A maps to NM_004415.2 T2218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:7585432 G>T maps to NM_004415.2 T2646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:7585432 G>T maps to NM_004415.2 T2646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:95499230 C>T maps to NM_004411.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:95499230 C>T maps to NM_004411.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:207516600 G>A maps to NM_001093730.1 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:207516600 G>A maps to NM_001093730.1 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:31489305 C>T maps to NM_014600.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:31489305 C>T maps to NM_014600.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:80626441 T>C maps to NM_022726.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:80626441 T>C maps to NM_022726.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:129762017 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:129762017 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:131190924 G>T maps to NM_001431.3 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:131190924 G>T maps to NM_001431.3 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:148511212 C>A maps to NM_004456.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:148511212 C>A maps to NM_004456.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:139255225 A>G maps to NM_015912.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:139255225 A>G maps to NM_015912.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:137808248 C>A maps to NM_002003.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:137808248 C>A maps to NM_002003.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:81188268 C>A maps to NM_004464.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:81188268 C>A maps to NM_004464.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:180052945 G>C maps to NM_182925.4 Y448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:180052945 G>C maps to NM_182925.4 Y448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:147026477 G>T maps to NM_002024.5 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:147026477 G>T maps to NM_002024.5 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:37711391 G>C maps to NM_014907.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:37711391 G>C maps to NM_014907.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:49447646 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:49447646 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:81388197 G>T maps to NM_022041.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:81388197 G>T maps to NM_022041.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:75263507 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:75263507 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:172165765 G>A maps to NM_198407.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:172165765 G>A maps to NM_198407.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:117149992 C>A maps to NM_148963.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:117149992 C>A maps to NM_148963.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:9934525 G>A maps to NM_000833.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:9934525 G>A maps to NM_000833.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:121184540 C>T maps to NM_005308.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:121184540 C>T maps to NM_005308.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:5248281 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:5248281 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:69692461 C>A maps to NM_022079.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:69692461 C>A maps to NM_022079.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:30005856 G>T maps to NM_003609.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:30005856 G>T maps to NM_003609.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:21655613 G>T maps to NM_005849.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:21655613 G>T maps to NM_005849.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:37947690 C>A maps to NM_012481.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:37947690 C>A maps to NM_012481.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:61913163 G>T maps to NM_001040694.1 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:61913163 G>T maps to NM_001040694.1 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:26639153 C>A maps to NM_002223.2 A1898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:26639153 C>A maps to NM_002223.2 A1898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:36634757 C>A maps to NM_014657.1 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:36634757 C>A maps to NM_014657.1 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:6526309 C>A maps to NM_014804.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:6526309 C>A maps to NM_014804.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:154394250 G>T maps to NM_001099293.1 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:154394250 G>T maps to NM_001099293.1 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:51410284 C>A maps to NM_004917.3 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:51410284 C>A maps to NM_004917.3 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:53165919 G>T maps to NM_015848.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:53165919 G>T maps to NM_015848.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:71974056 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:71974056 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:202287185 C>A maps to NM_001017403.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:202287185 C>A maps to NM_001017403.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:54782198 C>A maps to ENST00000391747 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:54782198 C>A maps to ENST00000391747 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:15561681 A>G maps to NM_198996.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:15561681 A>G maps to NM_198996.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:40137251 G>C maps to NM_020929.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:40137251 G>C maps to NM_020929.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:14220342 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:14220342 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:149013594 C>A maps to NM_005364.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:149013594 C>A maps to NM_005364.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:90398393 G>T maps to NM_014611.1 P3719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:90398393 G>T maps to NM_014611.1 P3719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:171753005 C>A maps to NM_015935.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:171753005 C>A maps to NM_015935.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:21971721 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:21971721 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:154014609 C>A maps to NM_002436.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:154014609 C>A maps to NM_002436.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:47690291 T>C maps to NM_000251.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:47690291 T>C maps to NM_000251.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:8996402 C>A maps to NM_024690.2 L13723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:8996402 C>A maps to NM_024690.2 L13723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:9089510 G>T maps to NM_024690.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:9089510 G>T maps to NM_024690.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:108107872 C>A maps to NM_014981.1 E1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:108107872 C>A maps to NM_014981.1 E1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:34864955 T>C maps to NM_001163735.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:34864955 T>C maps to NM_001163735.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:124826521 G>A maps to NM_006312.4 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:124826521 G>A maps to NM_006312.4 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:20948921 T>C maps to NM_006157.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:20948921 T>C maps to NM_006157.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:29663768 G>C maps to NM_001042492.2 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:29663768 G>C maps to NM_001042492.2 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:103964602 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:103964602 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55502016 C>A maps to NM_017852.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55502016 C>A maps to NM_017852.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:164271730 C>A maps to NM_006174.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:164271730 C>A maps to NM_006174.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:15918682 G>T maps to NM_013940.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:15918682 G>T maps to NM_013940.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:248308679 C>A maps to NM_001004690.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:248308679 C>A maps to NM_001004690.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55904483 G>T maps to NM_001004064.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55904483 G>T maps to NM_001004064.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55904891 C>A maps to NM_001004064.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55904891 C>A maps to NM_001004064.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:63280184 C>A maps to NM_014562.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:63280184 C>A maps to NM_014562.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:90691247 A>T maps to NM_080832.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:90691247 A>T maps to NM_080832.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140203111 G>A maps to NM_018908.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140203111 G>A maps to NM_018908.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140228508 G>A maps to NM_031857.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140228508 G>A maps to NM_031857.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140573564 G>T maps to NM_018930.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140573564 G>T maps to NM_018930.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140594393 C>A maps to NM_018933.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140594393 C>A maps to NM_018933.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140532099 G>T maps to NM_018939.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140532099 G>T maps to NM_018939.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140755905 C>A maps to NM_018919.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140755905 C>A maps to NM_018919.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:195997348 C>G maps to NM_005017.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:195997348 C>G maps to NM_005017.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:144882847 C>A maps to NM_014644.4 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:144882847 C>A maps to NM_014644.4 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:197729737 C>A maps to NM_024989.3 G612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:197729737 C>A maps to NM_024989.3 G612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:15509287 G>T maps to NM_003662.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:15509287 G>T maps to NM_003662.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:110477208 G>T maps to ENST00000426474 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:110477208 G>T maps to ENST00000426474 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:159530448 C>A maps to NM_003628.3 R1022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:159530448 C>A maps to NM_003628.3 R1022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:42977128 C>A maps to NM_006245.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:42977128 C>A maps to NM_006245.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:32130369 G>T maps to NM_138717.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:32130369 G>T maps to NM_138717.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:169953138 G>T maps to NM_002740.5 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:169953138 G>T maps to NM_002740.5 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:73579615 C>A maps to ENST00000373120 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:73579615 C>A maps to ENST00000373120 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:43382203 T>A maps to NM_006905.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:43382203 T>A maps to NM_006905.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:8504366 C>G maps to NM_002839.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:8504366 C>G maps to NM_002839.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:40770553 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:40770553 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:52232510 T>A maps to NM_144651.4 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:52232510 T>A maps to NM_144651.4 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:122250566 A>G maps to NM_198179.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:122250566 A>G maps to NM_198179.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:114374916 C>A maps to NM_016196.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:114374916 C>A maps to NM_016196.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:109696442 A>T maps to NM_020769.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:109696442 A>T maps to NM_020769.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:192153500 T>A maps to NM_130782.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:192153500 T>A maps to NM_130782.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:24619312 C>T maps to NM_017999.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:24619312 C>T maps to NM_017999.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:78766485 G>T maps to NM_002941.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:78766485 G>T maps to NM_002941.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:36164674 C>A maps to NM_001754.4 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:36164674 C>A maps to NM_001754.4 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:237774249 T>A maps to NM_001035.2 P1624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:237774249 T>A maps to NM_001035.2 P1624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:71427749 C>A maps to NM_001144952.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:71427749 C>A maps to NM_001144952.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:84697505 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:84697505 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:198274608 C>A maps to NM_012433.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:198274608 C>A maps to NM_012433.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:52103483 C>A maps to ENST00000361543 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:52103483 C>A maps to ENST00000361543 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:99337124 A>G maps to NM_005073.3 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:99337124 A>G maps to NM_005073.3 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:92374579 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:92374579 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:173486699 G>T maps to NM_178527.3 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:173486699 G>T maps to NM_178527.3 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:4167987 G>C maps to ENST00000443211 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:4167987 G>C maps to ENST00000443211 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:49067153 C>A maps to ENST00000376407 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:49067153 C>A maps to ENST00000376407 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:155003661 C>G maps to NM_005840.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:155003661 C>G maps to NM_005840.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:37370511 G>T maps to NM_198993.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:37370511 G>T maps to NM_198993.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:4452617 C>A maps to NM_182760.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:4452617 C>A maps to NM_182760.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:152647560 G>A maps to NM_182961.2 L5055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:152647560 G>A maps to NM_182961.2 L5055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:132874343 C>T maps to NM_053278.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:132874343 C>T maps to NM_053278.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:104379501 G>A maps to NM_003211.4 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:104379501 G>A maps to NM_003211.4 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:156831355 T>A maps to NM_005651.2 L204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:156831355 T>A maps to NM_005651.2 L204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:49846498 C>A maps to NM_003598.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:49846498 C>A maps to NM_003598.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:1278899 C>A maps to NM_198253.2 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:1278899 C>A maps to NM_198253.2 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:35219803 C>A maps to NM_021809.6 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:35219803 C>A maps to NM_021809.6 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:2413144 C>G maps to NM_198994.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:2413144 C>G maps to NM_198994.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:119290904 G>T maps to NM_006288.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:119290904 G>T maps to NM_006288.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:27401082 C>T maps to NM_004740.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:27401082 C>T maps to NM_004740.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:25654004 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:25654004 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:73012669 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:73012669 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:140396906 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:140396906 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:43436153 G>A maps to NM_018259.5 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:43436153 G>A maps to NM_018259.5 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:179482721 C>A maps to NM_133378.4 G13218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:179482721 C>A maps to NM_133378.4 G13218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:141483348 C>T maps to NM_021833.4 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:141483348 C>T maps to NM_021833.4 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:33969744 C>A maps to NM_018244.4 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:33969744 C>A maps to NM_018244.4 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:216373188 G>T maps to ENST00000366943 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:216373188 G>T maps to ENST00000366943 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:124619715 C>A maps to NM_014312.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:124619715 C>A maps to NM_014312.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:128471191 G>T maps to NM_018383.4 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:128471191 G>T maps to NM_018383.4 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:72984793 C>G maps to NM_006885.3 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:72984793 C>G maps to NM_006885.3 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:58574841 C>A maps to NM_007134.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:58574841 C>A maps to NM_007134.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:38403680 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:38403680 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:30934717 C>A maps to NM_014717.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:30934717 C>A maps to NM_014717.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:58042442 C>A maps to ENST00000376233 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:58042442 C>A maps to ENST00000376233 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:42583283 C>A maps to ENST00000222339 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:42583283 C>A maps to ENST00000222339 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:123980213 G>A maps to NM_020747.2 P1282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:123980213 G>A maps to NM_020747.2 P1282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:100865999 G>T maps to NM_006349.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:100865999 G>T maps to NM_006349.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:28296422 A>T maps to NM_007038.3 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:28296422 A>T maps to NM_007038.3 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:148037651 G>T maps to NM_002025.3 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:148037651 G>T maps to NM_002025.3 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:69420406 C>T maps to NM_001098805.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:69420406 C>T maps to NM_001098805.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6500371 T>A maps to NM_012402.2 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6500371 T>A maps to NM_012402.2 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:152826287 C>T maps to NM_001001344.2 D998D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:152826287 C>T maps to NM_001001344.2 D998D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:1161881 G>A maps to NM_018354.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:1161881 G>A maps to NM_018354.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201044701 C>A maps to NM_000069.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201044701 C>A maps to NM_000069.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:4267770 G>T maps to NM_018074.4 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:4267770 G>T maps to NM_018074.4 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:31323228 C>A maps to NM_004932.2 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:31323228 C>A maps to NM_004932.2 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:214818475 G>T maps to NM_016343.3 E1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:214818475 G>T maps to NM_016343.3 E1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:424292 G>T maps to NM_006614.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:424292 G>T maps to NM_006614.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:137704348 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:137704348 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:43907549 C>A maps to NM_001145146.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:43907549 C>A maps to NM_001145146.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:75975008 C>G maps to NM_001897.4 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:75975008 C>G maps to NM_001897.4 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:33112196 G>T maps to NM_001326.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:33112196 G>T maps to NM_001326.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:70666760 G>T maps to NM_024045.1 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:70666760 G>T maps to NM_024045.1 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:61542642 C>A maps to NM_033081.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:61542642 C>A maps to NM_033081.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:162376241 C>A maps to NM_020116.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:162376241 C>A maps to NM_020116.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:161324187 T>C maps to NM_001127648.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:161324187 T>C maps to NM_001127648.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:27185180 C>A maps to NM_000810.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:27185180 C>A maps to NM_000810.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:85924771 G>A maps to NM_006433.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:85924771 G>A maps to NM_006433.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:144297308 C>T maps to NM_178172.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:144297308 C>T maps to NM_178172.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:131590397 C>G maps to NM_198827.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:131590397 C>G maps to NM_198827.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:25886828 T>C maps to NM_020752.2 I758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:25886828 T>C maps to NM_020752.2 I758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:80394588 G>T maps to NM_173620.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:80394588 G>T maps to NM_173620.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:176308304 C>G maps to NM_002115.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:176308304 C>G maps to NM_002115.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:137089548 G>A maps to NM_006805.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:137089548 G>A maps to NM_006805.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:152191539 G>T maps to NM_001009931.1 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:152191539 G>T maps to NM_001009931.1 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:135592242 G>A maps to NM_014500.4 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:135592242 G>A maps to NM_014500.4 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:85945191 A>T maps to NM_002163.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:85945191 A>T maps to NM_002163.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:173340412 G>A maps to ENST00000264106 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:173340412 G>A maps to ENST00000264106 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:21318851 C>A maps to NM_021012.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:21318851 C>A maps to NM_021012.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:88652441 G>T maps to NM_138318.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:88652441 G>T maps to NM_138318.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:71978096 C>T maps to NM_003667.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:71978096 C>T maps to NM_003667.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:204587526 G>T maps to NM_201630.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:204587526 G>T maps to NM_201630.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:75652054 C>T maps to NM_006715.2 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:75652054 C>T maps to NM_006715.2 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:53876413 G>T maps to NM_001193511.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:53876413 G>T maps to NM_001193511.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:154884700 C>A maps to NM_007289.2 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:154884700 C>A maps to NM_007289.2 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:10210315 C>A maps to NM_003802.2 V1745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:10210315 C>A maps to NM_003802.2 V1745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:128389268 G>T maps to ENST00000389524 P1705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:128389268 G>T maps to ENST00000389524 P1705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:26114744 T>C maps to NM_000625.4 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:26114744 T>C maps to NM_000625.4 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:64402832 C>A maps to NM_015080.3 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:64402832 C>A maps to NM_015080.3 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:28096576 C>A maps to NM_000275.2 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:28096576 C>A maps to NM_000275.2 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:161970074 G>T maps to ENST00000451379 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:161970074 G>T maps to ENST00000451379 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:19378075 A>C maps to NM_001013354.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:19378075 A>C maps to NM_001013354.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248263534 C>A maps to NM_175911.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248263534 C>A maps to NM_175911.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248308919 C>T maps to NM_001004690.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248308919 C>T maps to NM_001004690.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:20612553 C>T maps to NM_001004724.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:20612553 C>T maps to NM_001004724.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:141335022 C>T maps to NM_016580.2 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:141335022 C>T maps to NM_016580.2 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140517151 G>A maps to NM_015669.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140517151 G>A maps to NM_015669.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140553012 G>T maps to NM_018940.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140553012 G>T maps to NM_018940.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140736242 C>A maps to NM_018917.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140736242 C>A maps to NM_018917.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:3845192 C>T maps to NM_014489.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:3845192 C>T maps to NM_014489.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:81181801 C>A maps to NM_052892.3 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:81181801 C>A maps to NM_052892.3 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118355763 T>A maps to NM_006229.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118355763 T>A maps to NM_006229.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:7405882 G>A maps to NM_000937.4 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:7405882 G>A maps to NM_000937.4 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:96860222 C>T maps to ENST00000434261 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:96860222 C>T maps to ENST00000434261 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:1667443 G>A maps to NM_012293.1 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:1667443 G>A maps to NM_012293.1 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:47041246 G>T maps to NM_005676.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:47041246 G>T maps to NM_005676.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:8161741 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:8161741 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:5800721 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:5800721 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:24620761 A>T maps to NM_017999.4 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:24620761 A>T maps to NM_017999.4 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:119745842 A>G maps to ENST00000379735 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:119745842 A>G maps to ENST00000379735 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:19650022 A>G maps to NM_031892.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:19650022 A>G maps to NM_031892.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:50256082 G>T maps to NM_006841.4 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:50256082 G>T maps to NM_006841.4 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:44474185 G>C maps to NM_201649.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:44474185 G>C maps to NM_201649.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:53722172 C>T maps to NM_001173467.1 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:53722172 C>T maps to NM_001173467.1 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:32289088 G>T maps to NM_014946.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:32289088 G>T maps to NM_014946.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:41081360 G>A maps to NM_020971.2 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:41081360 G>A maps to NM_020971.2 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:75505589 C>A maps to NM_014979.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:75505589 C>A maps to NM_014979.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:31484819 C>A maps to NM_001042454.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:31484819 C>A maps to NM_001042454.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:125834058 C>T maps to NM_052907.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:125834058 C>T maps to NM_052907.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:129559340 G>T maps to NM_133448.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:129559340 G>T maps to NM_133448.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38636950 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38636950 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:152710690 C>A maps to ENST00000402951 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:152710690 C>A maps to ENST00000402951 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:32860297 G>T maps to NM_001039111.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:32860297 G>T maps to NM_001039111.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:179421983 A>T maps to NM_133378.4 A26767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:179421983 A>T maps to NM_133378.4 A26767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:48106929 T>C maps to NM_003328.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:48106929 T>C maps to NM_003328.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53762539 C>A maps to NM_173856.2 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53762539 C>A maps to NM_173856.2 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:100454672 G>T maps to NM_017890.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:100454672 G>T maps to NM_017890.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:58579318 A>G maps to NM_007134.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:58579318 A>G maps to NM_007134.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:57188665 G>T maps to NM_033273.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:57188665 G>T maps to NM_033273.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:30934585 C>A maps to NM_014717.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:30934585 C>A maps to NM_014717.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:22363269 C>A maps to NM_001001411.2 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:22363269 C>A maps to NM_001001411.2 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:57529432 C>A maps to NM_001159279.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:57529432 C>A maps to NM_001159279.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53952871 T>C maps to NM_001008401.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53952871 T>C maps to NM_001008401.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53989992 T>C maps to NM_001004301.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53989992 T>C maps to NM_001004301.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:238048737 G>T maps to NM_021186.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:238048737 G>T maps to NM_021186.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:183669352 C>T maps to NM_005688.2 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:183669352 C>T maps to NM_005688.2 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:5235285 C>A maps to NM_139056.2 Y670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:5235285 C>A maps to NM_139056.2 Y670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:101447432 T>C maps to NM_000693.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:101447432 T>C maps to NM_000693.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:18087754 C>T maps to ENST00000261650 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:18087754 C>T maps to ENST00000261650 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:233244347 G>A maps to NM_001632.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:233244347 G>A maps to NM_001632.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:82938903 T>C maps to ENST00000260047 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:82938903 T>C maps to ENST00000260047 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:83350260 G>T maps to NM_004644.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:83350260 G>T maps to NM_004644.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:153750860 G>T maps to NM_001025595.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:153750860 G>T maps to NM_001025595.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:8959543 C>A maps to NM_020646.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:8959543 C>A maps to NM_020646.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:137500093 A>G maps to NM_139199.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:137500093 A>G maps to NM_139199.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:43796092 C>A maps to NM_145055.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:43796092 C>A maps to NM_145055.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:30617663 C>G maps to NM_001161376.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:30617663 C>G maps to NM_001161376.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135140379 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135140379 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:17072654 A>G maps to NM_014406.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:17072654 A>G maps to NM_014406.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:63492009 C>A maps to NM_004361.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:63492009 C>A maps to NM_004361.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:46052625 A>T maps to NM_176096.1 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:46052625 A>T maps to NM_176096.1 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:240072433 C>A maps to NM_000740.2 C561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:240072433 C>A maps to NM_000740.2 C561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:140285093 A>G maps to NM_022131.2 *956W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:140285093 A>G maps to NM_022131.2 *956W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:79029480 G>T maps to NM_153610.3 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:79029480 G>T maps to NM_153610.3 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:26510755 C>A maps to ENST00000374253 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:26510755 C>A maps to ENST00000374253 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:125367480 G>T maps to NM_130773.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:125367480 G>T maps to NM_130773.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:33985219 C>A maps to ENST00000373381 R3558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:33985219 C>A maps to ENST00000373381 R3558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:70804919 G>A maps to NM_001890.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:70804919 G>A maps to NM_001890.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:15726465 G>T maps to NM_007253.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:15726465 G>T maps to NM_007253.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:155161690 G>A maps to NM_017639.3 Q1998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:155161690 G>A maps to NM_017639.3 Q1998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:39050218 G>T maps to NM_198963.1 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:39050218 G>T maps to NM_198963.1 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:196834819 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:196834819 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:116447481 C>G maps to NM_020868.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:116447481 C>G maps to NM_020868.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:30436638 C>T maps to ENST00000278979 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:30436638 C>T maps to ENST00000278979 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:52344531 G>T maps to NM_018100.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:52344531 G>T maps to NM_018100.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:16464842 C>T maps to NM_004431.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:16464842 C>T maps to NM_004431.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:143053909 G>A maps to NM_001031690.2 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:143053909 G>A maps to NM_001031690.2 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:139263163 G>T maps to NM_015912.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:139263163 G>T maps to NM_015912.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:40417815 C>A maps to NM_138435.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:40417815 C>A maps to NM_138435.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:29423408 C>A maps to NM_018099.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:29423408 C>A maps to NM_018099.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:71319390 C>A maps to NM_018348.5 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:71319390 C>A maps to NM_018348.5 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:151424260 G>T maps to NM_000808.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:151424260 G>T maps to NM_000808.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:97172981 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:97172981 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:167761281 G>A maps to NM_014498.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:167761281 G>A maps to NM_014498.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:165364994 C>T maps to NM_004490.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:165364994 C>T maps to NM_004490.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:42619101 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:42619101 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:48188623 C>G maps to NM_015401.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:48188623 C>G maps to NM_015401.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:935137 G>C maps to NM_001142467.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:935137 G>C maps to NM_001142467.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:21071462 T>A maps to NM_016287.3 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:21071462 T>A maps to NM_016287.3 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:50444255 G>A maps to NM_006060.3 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:50444255 G>A maps to NM_006060.3 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:27356217 G>T maps to NM_000418.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:27356217 G>T maps to NM_000418.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:156810763 G>T maps to NM_014215.2 C1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:156810763 G>T maps to NM_014215.2 C1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:111060704 C>T maps to NM_005549.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:111060704 C>T maps to NM_005549.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:19575002 C>T maps to NM_144633.2 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:19575002 C>T maps to NM_144633.2 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:48309165 A>T maps to NM_001080394.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:48309165 A>T maps to NM_001080394.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:47305840 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:47305840 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:55377867 G>T maps to ENST00000355608 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:55377867 G>T maps to ENST00000355608 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:71960643 C>A maps to NM_003667.2 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:71960643 C>A maps to NM_003667.2 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:2438178 C>T maps to NM_032737.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:2438178 C>T maps to NM_032737.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:197598237 G>T maps to ENST00000425562 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:197598237 G>T maps to ENST00000425562 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:194951 G>A maps to NM_001080478.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:194951 G>A maps to NM_001080478.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:1797082 C>T maps to NM_015133.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:1797082 C>T maps to NM_015133.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:47426713 A>T maps to NM_001113498.2 L651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:47426713 A>T maps to NM_001113498.2 L651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:81295658 G>T maps to NM_022566.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:81295658 G>T maps to NM_022566.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:149783136 G>T maps to NM_000252.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:149783136 G>T maps to NM_000252.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:49425721 G>A maps to NM_000255.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:49425721 G>A maps to NM_000255.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:133721312 C>A maps to NM_207363.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:133721312 C>A maps to NM_207363.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrY:16941628 C>T maps to ENST00000382868 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrY:16941628 C>T maps to ENST00000382868 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:108043481 G>A maps to NM_002519.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:108043481 G>A maps to NM_002519.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:107878194 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:107878194 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:50724852 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:50724852 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:9083205 G>T maps to NM_004822.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:9083205 G>T maps to NM_004822.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:167545348 C>T maps to NM_001122679.1 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:167545348 C>T maps to NM_001122679.1 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:8841573 C>T maps to NM_001004699.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:8841573 C>T maps to NM_001004699.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:4703242 C>A maps to NM_030774.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:4703242 C>A maps to NM_030774.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:14952562 G>A maps to NM_001005190.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:14952562 G>A maps to NM_001005190.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:44553944 G>A maps to NM_001003828.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:44553944 G>A maps to NM_001003828.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:140779850 C>T maps to NM_018925.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:140779850 C>T maps to NM_018925.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20410502 C>A maps to NM_174924.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20410502 C>A maps to NM_174924.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:32048789 G>A maps to NM_178140.2 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:32048789 G>A maps to NM_178140.2 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:153069677 G>A maps to ENST00000393758 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:153069677 G>A maps to ENST00000393758 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:10690004 G>A maps to NM_004565.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:10690004 G>A maps to NM_004565.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:71002377 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:71002377 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:46757059 G>A maps to NM_013270.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:46757059 G>A maps to NM_013270.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:1652347 C>A maps to NM_012293.1 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:1652347 C>A maps to NM_012293.1 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:48389940 G>A maps to NM_002900.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:48389940 G>A maps to NM_002900.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:40627277 A>T maps to NM_012421.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:40627277 A>T maps to NM_012421.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:59483459 G>A maps to NM_173557.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:59483459 G>A maps to NM_173557.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:500625 G>T maps to NM_203389.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:500625 G>T maps to NM_203389.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27830438 G>T maps to NM_000982.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27830438 G>T maps to NM_000982.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:35210035 A>G maps to ENST00000394681 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:35210035 A>G maps to ENST00000394681 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:4281521 C>T maps to NM_152744.3 T2076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:4281521 C>T maps to NM_152744.3 T2076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:48063501 G>A maps to NM_153618.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:48063501 G>A maps to NM_153618.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:42618462 C>A maps to NM_015559.2 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:42618462 C>A maps to NM_015559.2 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:43319550 C>T maps to NM_001146037.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:43319550 C>T maps to NM_001146037.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:25776839 C>T maps to NM_005495.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:25776839 C>T maps to NM_005495.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:58712723 G>A maps to NM_018231.1 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:58712723 G>A maps to NM_018231.1 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:18254566 T>C maps to NM_001145195.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:18254566 T>C maps to NM_001145195.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:33703292 C>A maps to NM_019849.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:33703292 C>A maps to NM_019849.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:21384143 G>C maps to NM_004173.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:21384143 G>C maps to NM_004173.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:40656142 G>T maps to NM_021097.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:40656142 G>T maps to NM_021097.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:158596752 T>A maps to NM_003126.2 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:158596752 T>A maps to NM_003126.2 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:70951418 A>T maps to NM_003171.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:70951418 A>T maps to NM_003171.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:2796158 G>T maps to NM_003249.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:2796158 G>T maps to NM_003249.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:71869203 G>T maps to NM_004817.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:71869203 G>T maps to NM_004817.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:130184929 G>T maps to NM_133448.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:130184929 G>T maps to NM_133448.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:9658629 C>T maps to NM_001130924.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:9658629 C>T maps to NM_001130924.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:32557578 C>A maps to NM_018056.2 Y298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:32557578 C>A maps to NM_018056.2 Y298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:55666159 C>A maps to ENST00000344887 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:55666159 C>A maps to ENST00000344887 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:16323551 G>A maps to NM_016113.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:16323551 G>A maps to NM_016113.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:142627207 C>A maps to NM_019841.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:142627207 C>A maps to NM_019841.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:9854721 A>T maps to NM_001025930.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:9854721 A>T maps to NM_001025930.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:60124574 T>C maps to NM_003338.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:60124574 T>C maps to NM_003338.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:49151717 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:49151717 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:55493427 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:55493427 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:54015096 C>T maps to NM_182758.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:54015096 C>T maps to NM_182758.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:31588954 C>T maps to NM_000379.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:31588954 C>T maps to NM_000379.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:168107679 G>T maps to NM_152381.5 E3260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:168107679 G>T maps to NM_152381.5 E3260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:69256984 C>T maps to NM_004926.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:69256984 C>T maps to NM_004926.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:19823804 T>C maps to NM_021030.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:19823804 T>C maps to NM_021030.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:74583759 C>T maps to NM_007345.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:74583759 C>T maps to NM_007345.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:64966540 C>T maps to NM_015042.1 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:64966540 C>T maps to NM_015042.1 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:30794656 G>T maps to NM_001080417.1 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:30794656 G>T maps to NM_001080417.1 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:219132259 G>A maps to ENST00000444053 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:219132259 G>A maps to ENST00000444053 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:121717988 C>T maps to NM_005763.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:121717988 C>T maps to NM_005763.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:15120590 C>A maps to NM_001039844.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:15120590 C>A maps to NM_001039844.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:63973943 C>A maps to NM_001177387.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:63973943 C>A maps to NM_001177387.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:11696839 G>T maps to NM_001372.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:11696839 G>T maps to NM_001372.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr9:74481837 G>C maps to NM_016014.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr9:74481837 G>C maps to NM_016014.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:142487878 C>T maps to NM_207414.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:142487878 C>T maps to NM_207414.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:183773962 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:183773962 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:1089974 T>A maps to NM_004508.2 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:1089974 T>A maps to NM_004508.2 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:154396898 C>G maps to NM_001099293.1 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:154396898 C>G maps to NM_001099293.1 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:210570425 C>A maps to NM_002374.3 I1569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:210570425 C>A maps to NM_002374.3 I1569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr22:26351203 G>A maps to ENST00000407587 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr22:26351203 G>A maps to ENST00000407587 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051248 C>T maps to ENST00000262283 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051248 C>T maps to ENST00000262283 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:99190256 C>A maps to NM_002629.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:99190256 C>A maps to NM_002629.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:51882391 C>A maps to NM_138694.3 E1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:51882391 C>A maps to NM_138694.3 E1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:237791245 G>T maps to NM_001035.2 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:237791245 G>T maps to NM_001035.2 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:18108505 G>A maps to NM_138421.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:18108505 G>A maps to NM_138421.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:50211517 G>T maps to NM_004186.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:50211517 G>T maps to NM_004186.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:62997040 G>A maps to NM_199352.3 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:62997040 G>A maps to NM_199352.3 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:92459365 G>A maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:92459365 G>A maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:144904728 C>A maps to NM_001144010.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:144904728 C>A maps to NM_001144010.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:70450633 C>G maps to NM_030625.2 S1825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:70450633 C>G maps to NM_030625.2 S1825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:362331 G>A maps to NM_016585.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:362331 G>A maps to NM_016585.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:187003652 A>G maps to NM_003265.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:187003652 A>G maps to NM_003265.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:125463773 G>T maps to NM_017956.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:125463773 G>T maps to NM_017956.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:125464155 G>T maps to NM_017956.3 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:125464155 G>T maps to NM_017956.3 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:30936283 G>C maps to NM_014717.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:30936283 G>C maps to NM_014717.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58864327 G>T maps to NM_130786.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58864327 G>T maps to NM_130786.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:67189377 T>C maps to NM_080282.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:67189377 T>C maps to NM_080282.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:1231131 C>A maps to NM_030649.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:1231131 C>A maps to NM_030649.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:44105127 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:44105127 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:148709277 G>T maps to NM_152406.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:148709277 G>T maps to NM_152406.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:64778626 C>T maps to ENST00000422803 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:64778626 C>T maps to ENST00000422803 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62288696 T>A maps to NM_001620.1 K4398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62288696 T>A maps to NM_001620.1 K4398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:40997146 G>A maps to NM_009590.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:40997146 G>A maps to NM_009590.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:35785455 A>T maps to ENST00000458225 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:35785455 A>T maps to ENST00000458225 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:15266878 G>A maps to NM_001031739.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:15266878 G>A maps to NM_001031739.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:123596232 C>T maps to NM_001001976.1 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:123596232 C>T maps to NM_001001976.1 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:42489544 C>A maps to ENST00000441343 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:42489544 C>A maps to ENST00000441343 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:66114002 G>A maps to NM_006876.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:66114002 G>A maps to NM_006876.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:79973079 C>A maps to NM_153252.4 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:79973079 C>A maps to NM_153252.4 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:113086809 C>A maps to NM_145248.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:113086809 C>A maps to NM_145248.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:90764711 C>A maps to NM_017970.2 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:90764711 C>A maps to NM_017970.2 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:109191436 G>T maps to ENST00000370031 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:109191436 G>T maps to ENST00000370031 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:31671170 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:31671170 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:56735844 A>T maps to NM_178456.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:56735844 A>T maps to NM_178456.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:27805000 C>G maps to NM_032266.3 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:27805000 C>G maps to NM_032266.3 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:109484116 C>T maps to NM_173830.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:109484116 C>T maps to NM_173830.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:170160822 A>G maps to NM_018341.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:170160822 A>G maps to NM_018341.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:148311162 G>T maps to NM_145304.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:148311162 G>T maps to NM_145304.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:9009427 C>A maps to ENST00000413627 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:9009427 C>A maps to ENST00000413627 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:188225373 G>T maps to NM_005795.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:188225373 G>T maps to NM_005795.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200817727 G>T maps to ENST00000236925 G622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200817727 G>T maps to ENST00000236925 G622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:97776051 T>A maps to NM_001159747.1 L168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:97776051 T>A maps to NM_001159747.1 L168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:96292379 C>A maps to NM_182496.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:96292379 C>A maps to NM_182496.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:3781941 C>T maps to NM_021873.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:3781941 C>T maps to NM_021873.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:54606876 G>T maps to NM_201546.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:54606876 G>T maps to NM_201546.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31317987 G>T maps to NM_004932.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31317987 G>T maps to NM_004932.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:26885732 G>T maps to NM_016279.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:26885732 G>T maps to NM_016279.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:117243606 G>T maps to NM_000492.3 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:117243606 G>T maps to NM_000492.3 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:440828 C>G maps to NM_006614.2 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:440828 C>G maps to NM_006614.2 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:154544066 C>T maps to NM_000748.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:154544066 C>T maps to NM_000748.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:10288613 C>T maps to NM_138809.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:10288613 C>T maps to NM_138809.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:87656857 A>G maps to NM_019098.4 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:87656857 A>G maps to NM_019098.4 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:101807015 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:101807015 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70647964 T>A maps to NM_001858.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70647964 T>A maps to NM_001858.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:3087560 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:3087560 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:139060296 T>C maps to NM_016463.7 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:139060296 T>C maps to NM_016463.7 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:30577697 C>A maps to NM_025159.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:30577697 C>A maps to NM_025159.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:50813642 C>G maps to ENST00000311559 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:50813642 C>G maps to ENST00000311559 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:15734866 G>T maps to NM_007253.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:15734866 G>T maps to NM_007253.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:109294181 C>A maps to NM_001917.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:109294181 C>A maps to NM_001917.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159175729 G>T maps to NM_001122951.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159175729 G>T maps to NM_001122951.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:35980933 T>A maps to NM_007010.3 K521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:35980933 T>A maps to NM_007010.3 K521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:61513082 C>A maps to NM_033081.2 E1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:61513082 C>A maps to NM_033081.2 E1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189599404 C>T maps to NM_052952.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189599404 C>T maps to NM_052952.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124399743 C>A maps to ENST00000368915 V2377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124399743 C>A maps to ENST00000368915 V2377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:13841842 T>G maps to NM_001369.2 T1814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:13841842 T>G maps to NM_001369.2 T1814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:10923016 G>T maps to NM_001005361.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:10923016 G>T maps to NM_001005361.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:174870078 G>T maps to NM_000794.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:174870078 G>T maps to NM_000794.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:28737516 G>C maps to NM_024421.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:28737516 G>C maps to NM_024421.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:41719759 G>T maps to NM_001389.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:41719759 G>T maps to NM_001389.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56391359 C>T maps to ENST00000361203 L5765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56391359 C>T maps to ENST00000361203 L5765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:44703539 C>A maps to NM_022076.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:44703539 C>A maps to NM_022076.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71829925 C>T maps to NM_001130987.1 I1316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71829925 C>T maps to NM_001130987.1 I1316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:83402631 C>A maps to NM_005711.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:83402631 C>A maps to NM_005711.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:245180619 G>T maps to ENST00000421886 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:245180619 G>T maps to ENST00000421886 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:37770692 C>A maps to NM_052906.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:37770692 C>A maps to NM_052906.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:6921872 C>T maps to ENST00000381407 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:6921872 C>T maps to ENST00000381407 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:89390221 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:89390221 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97311550 G>T maps to NM_001080448.2 G828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97311550 G>T maps to NM_001080448.2 G828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:23191472 C>G maps to ENST00000400191 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:23191472 C>G maps to ENST00000400191 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:108380886 G>A maps to NM_015065.2 L1783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:108380886 G>A maps to NM_015065.2 L1783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:54159203 T>C maps to NM_017848.4 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:54159203 T>C maps to NM_017848.4 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:61014170 C>A maps to ENST00000442566 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:61014170 C>A maps to ENST00000442566 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:42718991 G>T maps to ENST00000398652 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:42718991 G>T maps to ENST00000398652 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200182768 G>T maps to NM_001105517.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200182768 G>T maps to NM_001105517.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200183299 C>A maps to NM_001105517.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200183299 C>A maps to NM_001105517.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:177249958 C>A maps to NM_021165.2 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:177249958 C>A maps to NM_021165.2 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:190067231 C>A maps to NM_199051.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:190067231 C>A maps to NM_199051.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:37580397 G>C maps to NM_030919.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:37580397 G>C maps to NM_030919.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:137772708 C>A maps to NM_004108.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:137772708 C>A maps to NM_004108.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:216272027 A>G maps to NM_212482.1 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:216272027 A>G maps to NM_212482.1 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52327483 C>T maps to NM_002030.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52327483 C>T maps to NM_002030.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:14823205 C>A maps to ENST00000380880 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:14823205 C>A maps to ENST00000380880 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:37746357 A>C maps to NM_014907.2 G1443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:37746357 A>C maps to NM_014907.2 G1443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:48592823 G>T maps to NM_015030.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:48592823 G>T maps to NM_015030.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:75533498 C>G maps to NM_173540.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:75533498 C>G maps to NM_173540.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161530944 G>T maps to NM_198903.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161530944 G>T maps to NM_198903.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:27777960 G>T maps to NM_033223.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:27777960 G>T maps to NM_033223.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:104123115 A>G maps to NM_004193.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:104123115 A>G maps to NM_004193.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:89849313 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:89849313 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:52993252 T>C maps to NM_003643.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:52993252 T>C maps to NM_003643.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73238542 C>T maps to NM_138619.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73238542 C>T maps to NM_138619.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:155628514 A>C maps to NM_003875.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:155628514 A>C maps to NM_003875.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:231406678 G>T maps to NM_014236.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:231406678 G>T maps to NM_014236.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20329601 C>A maps to NM_001007240.1 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20329601 C>A maps to NM_001007240.1 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:37307393 G>T maps to NM_000831.3 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:37307393 G>T maps to NM_000831.3 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:42510925 C>T maps to NM_002088.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:42510925 C>T maps to NM_002088.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:119925579 G>T maps to ENST00000361035 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:119925579 G>T maps to ENST00000361035 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:65197254 G>C maps to NM_014877.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:65197254 G>C maps to NM_014877.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:46703205 C>A maps to NM_024017.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:46703205 C>A maps to NM_024017.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:177036320 G>T maps to NM_006898.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:177036320 G>T maps to NM_006898.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:91144224 C>A maps to NM_001010987.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:91144224 C>A maps to NM_001010987.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:100976421 C>G maps to NM_016247.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:100976421 C>G maps to NM_016247.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:42744379 C>G maps to NM_020433.4 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:42744379 C>G maps to NM_020433.4 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:19554548 G>T maps to NM_144633.2 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:19554548 G>T maps to NM_144633.2 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160011197 G>T maps to NM_002241.4 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160011197 G>T maps to NM_002241.4 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:90651010 G>C maps to NM_022054.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:90651010 G>C maps to NM_022054.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:196227520 G>T maps to NM_198503.2 S1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:196227520 G>T maps to NM_198503.2 S1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19571463 C>T maps to NM_015047.1 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19571463 C>T maps to NM_015047.1 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:138584557 C>T maps to NM_020340.4 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:138584557 C>T maps to NM_020340.4 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:16316588 C>T maps to NM_024704.4 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:16316588 C>T maps to NM_024704.4 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:43013480 C>A maps to ENST00000438933 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:43013480 C>A maps to ENST00000438933 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:245848963 G>A maps to NM_018012.3 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:245848963 G>A maps to NM_018012.3 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:51901062 C>G maps to NM_032559.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:51901062 C>G maps to NM_032559.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57958725 C>T maps to NM_004984.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57958725 C>T maps to NM_004984.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152733725 G>C maps to NM_001025231.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152733725 G>C maps to NM_001025231.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:39503333 C>A maps to NM_004138.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:39503333 C>A maps to NM_004138.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:143718264 C>T maps to NM_003937.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:143718264 C>T maps to NM_003937.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:107592606 G>T maps to NM_002291.2 C1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:107592606 G>T maps to NM_002291.2 C1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55087568 G>T maps to NM_001130917.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55087568 G>T maps to NM_001130917.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54803139 C>A maps to ENST00000251375 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54803139 C>A maps to ENST00000251375 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:123302674 G>A maps to NM_207163.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:123302674 G>A maps to NM_207163.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:118145780 T>C maps to NM_001031855.1 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:118145780 T>C maps to NM_001031855.1 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:2922154 G>T maps to NM_014646.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:2922154 G>T maps to NM_014646.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:39804662 C>A maps to NM_020862.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:39804662 C>A maps to NM_020862.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:141609220 C>A maps to NM_018557.2 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:141609220 C>A maps to NM_018557.2 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:76372212 C>A maps to NM_001128922.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:76372212 C>A maps to NM_001128922.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:52861975 C>G maps to NM_001024611.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:52861975 C>G maps to NM_001024611.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:102108634 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:102108634 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:235969180 G>T maps to NM_000081.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:235969180 G>T maps to NM_000081.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:103557060 A>G maps to NM_005908.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:103557060 A>G maps to NM_005908.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:151105803 G>T maps to NM_053002.4 L1730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:151105803 G>T maps to NM_053002.4 L1730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:3100497 C>T maps to NM_022468.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:3100497 C>T maps to NM_022468.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9049863 A>G maps to NM_024690.2 S10589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9049863 A>G maps to NM_024690.2 S10589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9059266 T>A maps to NM_024690.2 P9393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9059266 T>A maps to NM_024690.2 P9393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:23902893 C>A maps to NM_000257.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:23902893 C>A maps to NM_000257.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:26400767 T>C maps to ENST00000407587 T2141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:26400767 T>C maps to ENST00000407587 T2141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8601437 T>G maps to NM_012335.3 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8601437 T>G maps to NM_012335.3 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:72191291 C>A maps to ENST00000424560 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:72191291 C>A maps to ENST00000424560 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:1926361 C>T maps to ENST00000399161 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:1926361 C>T maps to ENST00000399161 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:102030992 G>T maps to NM_052867.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:102030992 G>T maps to NM_052867.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:78513134 C>T maps to NM_014903.4 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:78513134 C>T maps to NM_014903.4 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:36202312 G>T maps to ENST00000400445 L2515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:36202312 G>T maps to ENST00000400445 L2515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:16004784 G>A maps to ENST00000395857 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:16004784 G>A maps to ENST00000395857 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:29670032 G>T maps to NM_001042492.2 E2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:29670032 G>T maps to NM_001042492.2 E2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56320397 C>T maps to NM_145007.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56320397 C>T maps to NM_145007.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:145273424 C>T maps to ENST00000454606 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:145273424 C>T maps to ENST00000454606 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:93802948 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:93802948 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2522400 C>A maps to NM_006181.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2522400 C>A maps to NM_006181.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:16910854 G>A maps to ENST00000438489 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:16910854 G>A maps to ENST00000438489 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:78412998 G>T maps to NM_001098816.2 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:78412998 G>T maps to NM_001098816.2 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:62729792 C>T maps to NM_000913.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:62729792 C>T maps to NM_000913.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6891128 C>T maps to NM_001004460.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6891128 C>T maps to NM_001004460.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:29408119 G>T maps to NM_013941.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:29408119 G>T maps to NM_013941.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158368993 G>T maps to NM_001004475.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158368993 G>T maps to NM_001004475.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:107457136 C>A maps to NM_001004484.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:107457136 C>A maps to NM_001004484.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6913518 G>A maps to NM_003700.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6913518 G>A maps to NM_003700.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:248436682 G>T maps to NM_001004695.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:248436682 G>T maps to NM_001004695.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:20444600 T>C maps to NM_001005486.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:20444600 T>C maps to NM_001005486.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5220985 G>C maps to NM_001004760.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5220985 G>C maps to NM_001004760.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5905567 C>T maps to NM_001005165.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5905567 C>T maps to NM_001005165.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5862467 G>T maps to ENST00000379946 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5862467 G>T maps to ENST00000379946 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5776425 G>C maps to NM_001005175.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5776425 G>C maps to NM_001005175.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:4825052 A>T maps to ENST00000380382 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:4825052 A>T maps to ENST00000380382 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6024333 G>A maps to NM_001005179.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6024333 G>A maps to NM_001005179.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97887749 G>A maps to NM_001005515.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97887749 G>A maps to NM_001005515.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:240969525 C>G maps to NM_001005853.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:240969525 C>G maps to NM_001005853.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:133196906 C>A maps to NM_170683.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:133196906 C>A maps to NM_170683.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:73620585 G>T maps to NM_025155.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:73620585 G>T maps to NM_025155.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71429601 C>A maps to NM_020459.1 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71429601 C>A maps to NM_020459.1 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:35454104 G>T maps to NM_015430.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:35454104 G>T maps to NM_015430.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:176679221 C>A maps to NM_020318.2 Y1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:176679221 C>A maps to NM_020318.2 Y1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:162475169 G>T maps to NM_004562.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:162475169 G>T maps to NM_004562.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:14540931 T>A maps to NM_002582.2 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:14540931 T>A maps to NM_002582.2 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:140750197 C>A maps to NM_018924.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:140750197 C>A maps to NM_018924.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:82595230 T>A maps to NM_033026.5 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:82595230 T>A maps to NM_033026.5 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:52732946 A>G maps to NM_052937.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:52732946 A>G maps to NM_052937.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:47773117 G>A maps to NM_006031.5 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:47773117 G>A maps to NM_006031.5 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:19375767 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:19375767 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57327946 A>G maps to NM_006210.2 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57327946 A>G maps to NM_006210.2 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:66235597 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:66235597 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7361762 C>T maps to NM_001131023.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7361762 C>T maps to NM_001131023.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:37848687 A>T maps to NM_018290.3 K382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:37848687 A>T maps to NM_018290.3 K382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:22065242 G>A maps to NM_000444.4 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:22065242 G>A maps to NM_000444.4 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111686523 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111686523 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:60506064 G>T maps to NM_194449.2 G608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:60506064 G>T maps to NM_194449.2 G608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:209188939 A>T maps to NM_015040.3 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:209188939 A>T maps to NM_015040.3 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:9352969 A>T maps to NM_001172646.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:9352969 A>T maps to NM_001172646.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:9368108 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:9368108 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:68028669 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:68028669 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:52159197 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:52159197 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:38151899 C>A maps to NM_006475.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:38151899 C>A maps to NM_006475.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:4934044 C>T maps to NM_002705.4 V1537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:4934044 C>T maps to NM_002705.4 V1537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:104220582 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:104220582 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49378082 G>T maps to NM_014330.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49378082 G>T maps to NM_014330.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2766519 C>T maps to NM_031948.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2766519 C>T maps to NM_031948.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:65419248 G>A maps to NM_198686.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:65419248 G>A maps to NM_198686.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:47034443 G>T maps to NM_005676.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:47034443 G>T maps to NM_005676.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:73554748 C>T maps to NM_021239.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:73554748 C>T maps to NM_021239.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:109694213 T>A maps to NM_020769.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:109694213 T>A maps to NM_020769.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:20979140 C>A maps to ENST00000430083 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:20979140 C>A maps to ENST00000430083 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:10540597 C>T maps to NM_016422.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:10540597 C>T maps to NM_016422.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2312758 G>A maps to NM_080594.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2312758 G>A maps to NM_080594.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:77275584 C>T maps to ENST00000396204 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:77275584 C>T maps to ENST00000396204 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:10480730 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:10480730 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:55541511 A>T maps to NM_006269.1 S1690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:55541511 A>T maps to NM_006269.1 S1690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:17097026 G>A maps to NM_001017.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:17097026 G>A maps to NM_001017.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92998349 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92998349 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237880515 G>T maps to NM_001035.2 E3448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237880515 G>T maps to NM_001035.2 E3448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:34146974 C>A maps to NM_001036.3 L4623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:34146974 C>A maps to NM_001036.3 L4623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:83795889 G>T maps to ENST00000505472 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:83795889 G>T maps to ENST00000505472 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:7269846 C>A maps to NM_001018039.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:7269846 C>A maps to NM_001018039.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52147103 C>A maps to NM_001098612.1 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52147103 C>A maps to NM_001098612.1 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:72176330 G>T maps to NM_015556.1 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:72176330 G>T maps to NM_015556.1 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:103698484 A>C maps to NM_000452.2 *349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:103698484 A>C maps to NM_000452.2 *349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:68396735 C>T maps to NM_022902.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:68396735 C>T maps to NM_022902.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:37357065 G>T maps to NM_080552.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:37357065 G>T maps to NM_080552.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:18292250 T>A maps to NM_001145195.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:18292250 T>A maps to NM_001145195.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:33947282 G>A maps to NM_016180.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:33947282 G>A maps to NM_016180.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:26702708 G>T maps to NM_178498.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:26702708 G>T maps to NM_178498.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:1212463 G>A maps to NM_001003841.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:1212463 G>A maps to NM_001003841.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:107956573 G>C maps to NM_018013.3 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:107956573 G>C maps to NM_018013.3 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158612254 C>A maps to NM_003126.2 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158612254 C>A maps to NM_003126.2 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:134472024 C>A maps to NM_173344.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:134472024 C>A maps to NM_173344.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:40452732 G>A maps to NM_003152.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:40452732 G>A maps to NM_003152.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:171488230 C>G maps to NM_005990.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:171488230 C>G maps to NM_005990.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:220473844 C>T maps to NM_052902.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:220473844 C>T maps to NM_052902.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:85666081 G>A maps to NM_032184.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:85666081 G>A maps to NM_032184.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:45307614 C>A maps to NM_020826.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:45307614 C>A maps to NM_020826.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:74180808 G>T maps to NM_153356.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:74180808 G>T maps to NM_153356.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:89958628 A>T maps to NM_014972.2 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:89958628 A>T maps to NM_014972.2 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:4310162 G>A maps to NM_003223.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:4310162 G>A maps to NM_003223.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:216960770 C>T maps to NM_138390.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:216960770 C>T maps to NM_138390.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:104233399 G>T maps to NM_024789.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:104233399 G>T maps to NM_024789.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:123755311 C>A maps to NM_001013743.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:123755311 C>A maps to NM_001013743.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:16799109 G>A maps to NM_024074.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:16799109 G>A maps to NM_024074.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:16855817 G>A maps to NM_012452.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:16855817 G>A maps to NM_012452.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:161198066 G>T maps to NM_032174.4 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:161198066 G>T maps to NM_032174.4 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:165961466 C>A maps to NM_152620.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:165961466 C>A maps to NM_152620.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:12560661 G>T maps to NM_025265.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:12560661 G>T maps to NM_025265.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:81609826 C>A maps to NM_000369.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:81609826 C>A maps to NM_000369.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179411925 G>T maps to NM_133378.4 G28874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179411925 G>T maps to NM_133378.4 G28874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:132235959 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:132235959 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:90001146 G>C maps to ENST00000304984 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:90001146 G>C maps to ENST00000304984 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62346148 G>A maps to NM_022830.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62346148 G>A maps to NM_022830.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62348607 G>A maps to NM_022830.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62348607 G>A maps to NM_022830.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:41870230 T>C maps to NM_006293.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:41870230 T>C maps to NM_006293.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:234581232 T>G maps to NM_021027.2 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:234581232 T>G maps to NM_021027.2 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216371751 A>T maps to ENST00000366943 L1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216371751 A>T maps to ENST00000366943 L1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:31233060 C>T maps to NM_005800.4 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:31233060 C>T maps to NM_005800.4 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:70796855 C>A maps to NM_018052.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:70796855 C>A maps to NM_018052.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73851354 C>T maps to NM_012478.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73851354 C>T maps to NM_012478.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:85771118 G>A maps to NM_014991.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:85771118 G>A maps to NM_014991.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:177058692 G>T maps to NM_170710.4 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:177058692 G>T maps to NM_170710.4 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:49049968 A>C maps to NM_018031.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:49049968 A>C maps to NM_018031.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62606599 G>A maps to NM_018093.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62606599 G>A maps to NM_018093.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:67303404 T>A maps to NM_024763.4 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:67303404 T>A maps to NM_024763.4 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:180832880 G>T maps to NM_004736.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:180832880 G>T maps to NM_004736.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:33272109 C>T maps to NM_003680.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:33272109 C>T maps to NM_003680.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:187366000 T>G maps to NM_018471.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:187366000 T>G maps to NM_018471.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:111698883 C>T maps to NM_001004308.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:111698883 C>T maps to NM_001004308.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:52193385 G>C maps to NM_006526.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:52193385 G>C maps to NM_006526.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:37006025 T>A maps to NM_001166038.1 K39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:37006025 T>A maps to NM_001166038.1 K39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44590803 G>T maps to NM_001037813.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44590803 G>T maps to NM_001037813.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:178293995 A>T maps to NM_058230.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:178293995 A>T maps to NM_058230.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:30934627 G>T maps to NM_014717.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:30934627 G>T maps to NM_014717.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:38190115 C>A maps to NM_032689.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:38190115 C>A maps to NM_032689.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:57522833 C>A maps to NM_001159279.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:57522833 C>A maps to NM_001159279.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:149174082 G>A maps to NM_001163474.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:149174082 G>A maps to NM_001163474.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:47888036 C>T maps to NM_021035.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:47888036 C>T maps to NM_021035.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56701606 C>A maps to NM_001080456.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56701606 C>A maps to NM_001080456.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:123021952 G>A maps to NM_183357.2 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:123021952 G>A maps to NM_183357.2 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:27056306 C>T maps to NM_006015.4 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:27056306 C>T maps to NM_006015.4 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:112998135 C>T maps to ENST00000273395 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:112998135 C>T maps to ENST00000273395 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr18:30928851 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr18:30928851 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132084685 T>C maps to NM_001012715.3 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132084685 T>C maps to NM_001012715.3 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:61765655 C>T maps to NM_017780.2 F2124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:61765655 C>T maps to NM_017780.2 F2124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:10080322 C>T maps to NM_015719.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:10080322 C>T maps to NM_015719.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:12798544 G>A maps to NM_018340.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:12798544 G>A maps to NM_018340.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:40257095 G>A maps to NM_024119.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:40257095 G>A maps to NM_024119.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:20996704 G>A maps to NM_017539.1 Y2453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:20996704 G>A maps to NM_017539.1 Y2453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:23716364 G>T maps to NM_033266.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:23716364 G>T maps to NM_033266.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:38314895 C>T maps to NM_001174067.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:38314895 C>T maps to NM_001174067.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:45105122 C>A maps to NM_001145107.1 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:45105122 C>A maps to NM_001145107.1 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:43381979 C>T maps to NM_017719.4 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:43381979 C>T maps to NM_017719.4 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:43922332 G>A maps to NM_031451.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:43922332 G>A maps to NM_031451.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:179437058 G>A maps to NM_133378.4 G22032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:179437058 G>A maps to NM_133378.4 G22032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132637633 C>T maps to NM_001008563.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132637633 C>T maps to NM_001008563.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:10914973 T>A maps to NM_001039362.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:10914973 T>A maps to NM_001039362.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:241534076 C>A maps to NM_023083.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:241534076 C>A maps to NM_023083.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr17:8644877 G>T maps to NM_144681.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr17:8644877 G>T maps to NM_144681.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:122741886 T>A maps to NM_001237.3 K202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:122741886 T>A maps to NM_001237.3 K202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:69462816 C>A maps to NM_053056.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:69462816 C>A maps to NM_053056.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:6194247 C>A maps to NM_015557.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:6194247 C>A maps to NM_015557.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:3779781 G>A maps to NM_004380.2 Q1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:3779781 G>A maps to NM_004380.2 Q1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:21272332 C>A maps to NM_005207.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:21272332 C>A maps to NM_005207.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:40657414 C>A maps to NM_033510.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:40657414 C>A maps to NM_033510.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr13:51825613 C>A maps to NM_145019.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr13:51825613 C>A maps to NM_145019.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:22389441 G>A maps to NM_145290.2 N1284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:22389441 G>A maps to NM_145290.2 N1284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:26225699 G>A maps to NM_003532.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:26225699 G>A maps to NM_003532.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:9950948 C>T maps to NM_153483.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:9950948 C>T maps to NM_153483.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:13183548 A>C maps to NM_001136561.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:13183548 A>C maps to NM_001136561.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:169540677 T>A maps to NM_001080460.1 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:169540677 T>A maps to NM_001080460.1 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:49173880 C>A maps to NM_145807.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:49173880 C>A maps to NM_145807.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:55110930 T>C maps to NM_001005274.1 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:55110930 T>C maps to NM_001005274.1 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:65403698 A>G maps to NM_032223.2 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:65403698 A>G maps to NM_032223.2 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:42988084 A>C maps to ENST00000415122 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:42988084 A>C maps to ENST00000415122 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:128853029 C>A maps to ENST00000418265 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:128853029 C>A maps to ENST00000418265 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr20:20582430 G>T maps to NM_020343.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr20:20582430 G>T maps to NM_020343.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:135140264 G>T maps to ENST00000372169 L2494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:135140264 G>T maps to ENST00000372169 L2494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:158627412 G>A maps to NM_003126.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:158627412 G>A maps to NM_003126.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:170736692 A>T maps to NM_021025.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:170736692 A>T maps to NM_021025.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:180687609 C>A maps to NM_032765.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:180687609 C>A maps to NM_032765.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:54825192 A>T maps to ENST00000260323 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:54825192 A>T maps to ENST00000260323 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:234460050 G>T maps to NM_018218.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:234460050 G>T maps to NM_018218.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:107568677 C>T maps to NM_005502.3 W1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:107568677 C>T maps to NM_005502.3 W1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:67082842 C>A maps to NM_080284.2 E1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:67082842 C>A maps to NM_080284.2 E1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:1057025 G>A maps to NM_019112.3 Q1569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:1057025 G>A maps to NM_019112.3 Q1569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:87190634 G>T maps to NM_000927.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:87190634 G>T maps to NM_000927.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:48755286 C>A maps to NM_003786.3 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:48755286 C>A maps to NM_003786.3 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:21960372 T>C maps to NM_005691.2 G1452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:21960372 T>C maps to NM_005691.2 G1452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20702561 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20702561 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20548588 A>T maps to NM_182617.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20548588 A>T maps to NM_182617.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:64580002 G>T maps to NM_182920.1 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:64580002 G>T maps to NM_182920.1 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:84651758 G>T maps to NM_207517.2 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:84651758 G>T maps to NM_207517.2 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:100349700 C>T maps to NM_000673.4 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:100349700 C>T maps to NM_000673.4 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:58128444 G>A maps to NM_001122772.1 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:58128444 G>A maps to NM_001122772.1 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:109681046 C>A maps to NM_031279.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:109681046 C>A maps to NM_031279.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:27877828 T>C maps to NM_001029882.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:27877828 T>C maps to NM_001029882.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:105410705 G>A maps to NM_138420.2 D3694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:105410705 G>A maps to NM_138420.2 D3694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65691778 G>C maps to NM_013410.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65691778 G>C maps to NM_013410.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:119053905 C>T maps to NM_178813.5 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:119053905 C>T maps to NM_178813.5 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:125648219 G>T maps to NM_001195223.1 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:125648219 G>T maps to NM_001195223.1 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:30143132 G>A maps to NM_004304.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:30143132 G>A maps to NM_004304.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:233321858 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:233321858 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:14780019 G>T maps to NM_001145029.1 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:14780019 G>T maps to NM_001145029.1 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83332642 G>T maps to NM_004644.3 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83332642 G>T maps to NM_004644.3 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57004349 G>A maps to NM_005161.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57004349 G>A maps to NM_005161.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:157511282 C>A maps to ENST00000367148 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:157511282 C>A maps to ENST00000367148 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:80750290 T>C maps to NM_014862.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:80750290 T>C maps to NM_014862.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:31324686 G>T maps to NM_030632.1 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:31324686 G>T maps to NM_030632.1 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:20068140 C>T maps to NM_001693.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:20068140 C>T maps to NM_001693.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:40751680 C>T maps to NM_014952.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:40751680 C>T maps to NM_014952.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:127821173 C>T maps to NM_139343.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:127821173 C>T maps to NM_139343.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91358331 G>T maps to NM_000057.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91358331 G>T maps to NM_000057.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:13606444 C>T maps to NM_148894.2 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:13606444 C>T maps to NM_148894.2 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:32914848 C>T maps to NM_000059.3 N2119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:32914848 C>T maps to NM_000059.3 N2119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:128147645 G>T maps to NM_001004298.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:128147645 G>T maps to NM_001004298.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:31495870 A>T maps to NM_032849.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:31495870 A>T maps to NM_032849.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27360749 C>A maps to NM_178553.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27360749 C>A maps to NM_178553.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:118865704 T>C maps to NM_152539.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:118865704 T>C maps to NM_152539.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:118865773 G>A maps to NM_152539.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:118865773 G>A maps to NM_152539.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:41201791 G>T maps to NM_001115131.1 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:41201791 G>T maps to NM_001115131.1 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:120767241 C>T maps to NM_024913.4 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:120767241 C>T maps to NM_024913.4 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:144652141 C>T maps to NM_001100878.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:144652141 C>T maps to NM_001100878.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:81637024 G>T maps to NM_000722.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:81637024 G>T maps to NM_000722.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:1949932 G>T maps to NM_172364.4 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:1949932 G>T maps to NM_172364.4 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:110497564 G>A maps to NM_014289.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:110497564 G>A maps to NM_014289.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:31682504 G>T maps to NM_194300.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:31682504 G>T maps to NM_194300.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:93672777 G>A maps to NM_206886.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:93672777 G>A maps to NM_206886.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:3669110 G>T maps to NM_152492.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:3669110 G>T maps to NM_152492.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:3679922 C>A maps to NM_152492.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:3679922 C>A maps to NM_152492.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43021929 C>T maps to NM_001080850.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43021929 C>T maps to NM_001080850.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:123286246 G>T maps to NM_201435.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:123286246 G>T maps to NM_201435.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71058201 G>C maps to NM_015717.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71058201 G>C maps to NM_015717.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:73995329 G>A maps to NM_001024736.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:73995329 G>A maps to NM_001024736.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43828708 G>A maps to NM_001255.2 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43828708 G>A maps to NM_001255.2 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:24537755 C>A maps to NM_006727.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:24537755 C>A maps to NM_006727.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:44828104 C>T maps to NM_021248.1 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:44828104 C>T maps to NM_021248.1 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73558955 C>A maps to ENST00000398860 P2386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73558955 C>A maps to ENST00000398860 P2386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:31294152 G>T maps to NM_004932.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:31294152 G>T maps to NM_004932.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26988224 T>C maps to NM_016279.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26988224 T>C maps to NM_016279.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109801501 G>T maps to NM_001408.2 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109801501 G>T maps to NM_001408.2 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:56858233 A>G maps to NM_025009.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:56858233 A>G maps to NM_025009.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:55903521 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:55903521 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:111778702 C>A maps to NM_004000.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:111778702 C>A maps to NM_004000.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:136700961 C>A maps to NM_001006628.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:136700961 C>A maps to NM_001006628.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:11889328 C>T maps to ENST00000376496 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:11889328 C>T maps to ENST00000376496 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31538560 G>A maps to NM_012131.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31538560 G>A maps to NM_012131.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:184240783 C>A maps to NM_001111319.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:184240783 C>A maps to NM_001111319.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:123319272 G>A maps to NM_001010852.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:123319272 G>A maps to NM_001010852.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:125671720 C>A maps to NM_130773.2 T1259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:125671720 C>A maps to NM_130773.2 T1259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:103379961 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:103379961 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:86250027 G>A maps to NM_152890.5 Q1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:86250027 G>A maps to NM_152890.5 Q1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:110822945 G>C maps to NM_001845.4 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:110822945 G>C maps to NM_001845.4 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107911594 C>A maps to ENST00000328300 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107911594 C>A maps to ENST00000328300 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129929430 C>T maps to NM_001869.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129929430 C>T maps to NM_001869.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:36737267 T>A maps to NM_016441.2 C548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:36737267 T>A maps to NM_016441.2 C548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:11117570 G>T maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:11117570 G>T maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:119678059 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:119678059 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30577700 T>A maps to NM_025159.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30577700 T>A maps to NM_025159.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:37664300 G>T maps to NM_000397.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:37664300 G>T maps to NM_000397.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:39377208 G>A maps to NM_001343.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:39377208 G>A maps to NM_001343.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:49568630 G>A maps to NM_004393.4 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:49568630 G>A maps to NM_004393.4 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:109292562 C>A maps to NM_001917.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:109292562 C>A maps to NM_001917.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:90263693 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:90263693 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159176164 C>T maps to NM_001122951.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159176164 C>T maps to NM_001122951.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:125299289 G>C maps to NM_001013628.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:125299289 G>C maps to NM_001013628.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:27997758 T>A maps to NM_001017930.1 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:27997758 T>A maps to NM_001017930.1 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:150138537 C>T maps to NM_001135643.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:150138537 C>T maps to NM_001135643.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:169337906 C>T maps to NM_001012967.1 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:169337906 C>T maps to NM_001012967.1 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:54939214 G>T maps to NM_003647.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:54939214 G>T maps to NM_003647.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:3729255 C>A maps to NM_004746.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:3729255 C>A maps to NM_004746.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:11513787 G>A maps to NM_001372.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:11513787 G>A maps to NM_001372.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:6530209 G>T maps to NM_144666.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:6530209 G>T maps to NM_144666.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:99537281 C>A maps to ENST00000428223 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:99537281 C>A maps to ENST00000428223 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:116101468 A>G maps to NM_020868.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:116101468 A>G maps to NM_020868.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105405086 C>G maps to NM_001385.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105405086 C>G maps to NM_001385.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:9783982 A>T maps to NM_000798.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:9783982 A>T maps to NM_000798.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:9784741 C>A maps to NM_000798.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:9784741 C>A maps to NM_000798.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:56328461 C>T maps to ENST00000361203 R7382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:56328461 C>T maps to ENST00000361203 R7382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167095142 C>A maps to NM_001080426.1 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167095142 C>A maps to NM_001080426.1 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71788953 C>A maps to NM_001130987.1 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71788953 C>A maps to NM_001130987.1 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:11565621 G>A maps to NM_001420.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:11565621 G>A maps to NM_001420.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:50610799 G>T maps to NM_021952.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:50610799 G>T maps to NM_021952.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:101331437 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:101331437 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:110294766 C>T maps to NM_139053.1 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:110294766 C>T maps to NM_139053.1 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:110300459 G>A maps to NM_139053.1 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:110300459 G>A maps to NM_139053.1 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:62142647 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:62142647 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:5721079 A>T maps to NM_153717.2 K94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:5721079 A>T maps to NM_153717.2 K94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:75914018 G>A maps to NM_004101.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:75914018 G>A maps to NM_004101.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111801144 C>T maps to NM_001177996.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111801144 C>T maps to NM_001177996.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:130279138 G>T maps to NM_022833.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:130279138 G>T maps to NM_022833.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:177247897 T>A maps to NM_021165.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:177247897 T>A maps to NM_021165.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100042479 A>G maps to NM_153364.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100042479 A>G maps to NM_153364.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:242407607 G>A maps to NM_014808.2 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:242407607 G>A maps to NM_014808.2 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:92533466 G>T maps to ENST00000298047 E2430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:92533466 G>T maps to ENST00000298047 E2430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:126320036 G>A maps to NM_024582.4 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:126320036 G>A maps to NM_024582.4 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:126402751 G>T maps to NM_024582.4 R4225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:126402751 G>T maps to NM_024582.4 R4225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:37457328 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:37457328 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157497605 A>G maps to NM_031281.2 C587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157497605 A>G maps to NM_031281.2 C587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:80478021 G>T maps to NM_004514.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:80478021 G>T maps to NM_004514.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:2974535 G>T maps to NM_202002.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:2974535 G>T maps to NM_202002.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:70321309 G>T maps to NM_005938.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:70321309 G>T maps to NM_005938.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:114302189 G>A maps to NM_148898.3 W598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:114302189 G>A maps to NM_148898.3 W598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:183707256 T>A maps to NM_001463.3 K181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:183707256 T>A maps to NM_001463.3 K181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91423350 G>T maps to NM_002569.2 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91423350 G>T maps to NM_002569.2 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74810460 G>T maps to ENST00000238018 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74810460 G>T maps to ENST00000238018 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:151271896 A>G maps to NM_001146040.1 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:151271896 A>G maps to NM_001146040.1 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:135432389 G>C maps to NM_153834.3 L2175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:135432389 G>C maps to NM_153834.3 L2175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:120702642 G>T maps to NM_014619.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:120702642 G>T maps to NM_014619.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:77796650 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:77796650 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:144966222 G>T maps to NM_001164629.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:144966222 G>T maps to NM_001164629.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:27506660 C>A maps to NM_001520.3 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:27506660 C>A maps to NM_001520.3 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:156482497 A>T maps to NM_001173393.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:156482497 A>T maps to NM_001173393.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:239974809 C>A maps to NM_006037.3 E1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:239974809 C>A maps to NM_006037.3 E1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:242169567 G>T maps to NM_005336.3 Y1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:242169567 G>T maps to NM_005336.3 Y1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:64045284 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:64045284 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:111784228 C>G maps to NM_001541.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:111784228 C>G maps to NM_001541.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:23520675 G>A maps to NM_000864.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:23520675 G>A maps to NM_000864.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113816738 G>A maps to NM_006028.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113816738 G>A maps to NM_006028.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21166572 C>A maps to NM_002175.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21166572 C>A maps to NM_002175.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:1573702 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:1573702 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:1608042 C>A maps to NM_014714.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:1608042 C>A maps to NM_014714.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:99442823 C>T maps to NM_000875.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:99442823 C>T maps to NM_000875.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:160482938 G>T maps to NM_000876.2 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:160482938 G>T maps to NM_000876.2 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:102968096 G>T maps to NM_016232.4 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:102968096 G>T maps to NM_016232.4 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:110526648 C>A maps to NM_032549.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:110526648 C>A maps to NM_032549.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:209965772 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:209965772 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:187533637 G>A maps to NM_002210.3 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:187533637 G>A maps to NM_002210.3 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31371151 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31371151 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:54783878 G>A maps to NM_198510.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:54783878 G>A maps to NM_198510.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:106075104 C>A maps to NM_033397.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:106075104 C>A maps to NM_033397.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:139791671 G>T maps to NM_030647.1 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:139791671 G>T maps to NM_030647.1 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:24040526 C>T maps to NM_032452.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:24040526 C>T maps to NM_032452.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:62739518 G>T maps to NM_181712.4 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:62739518 G>T maps to NM_181712.4 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:223917757 G>T maps to NM_080671.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:223917757 G>T maps to NM_080671.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:49950227 G>A maps to NM_012284.1 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:49950227 G>A maps to NM_012284.1 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:88729805 G>A maps to NM_138318.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:88729805 G>A maps to NM_138318.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:233802491 C>T maps to NM_002245.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:233802491 C>T maps to NM_002245.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:140630623 G>T maps to NM_016601.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:140630623 G>T maps to NM_016601.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:24833391 A>C maps to NM_019590.3 I1731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:24833391 A>C maps to NM_019590.3 I1731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:36851984 A>T maps to NM_001029864.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:36851984 A>T maps to NM_001029864.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:73961079 T>A maps to NM_001008537.2 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:73961079 T>A maps to NM_001008537.2 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:53227807 G>T maps to NM_175834.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:53227807 G>T maps to NM_175834.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31964925 G>T maps to ENST00000399871 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31964925 G>T maps to ENST00000399871 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:16899976 C>T maps to NM_001290.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:16899976 C>T maps to NM_001290.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65897499 C>T maps to NM_017526.4 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65897499 C>T maps to NM_017526.4 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:63990807 G>T maps to NM_016571.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:63990807 G>T maps to NM_016571.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:35298036 G>T maps to NM_005568.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:35298036 G>T maps to NM_005568.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:75596246 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:75596246 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:97833439 C>A maps to NM_014916.3 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:97833439 C>A maps to NM_014916.3 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:118147001 G>T maps to NM_001031855.1 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:118147001 G>T maps to NM_001031855.1 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:161022111 G>A maps to NM_005577.2 Y988Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:161022111 G>A maps to NM_005577.2 Y988Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:114398285 A>G maps to NM_020871.3 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:114398285 A>G maps to NM_020871.3 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:57588381 T>C maps to NM_002332.2 P2697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:57588381 T>C maps to NM_002332.2 P2697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:170090059 G>A maps to NM_004525.2 D1653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:170090059 G>A maps to NM_004525.2 D1653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:6654823 C>A maps to NM_004271.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:6654823 C>A maps to NM_004271.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:235840793 T>A maps to NM_000081.2 I3642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:235840793 T>A maps to NM_000081.2 I3642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:42448756 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:42448756 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:117948253 C>T maps to NM_006699.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:117948253 C>T maps to NM_006699.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:71206861 C>A maps to NM_033141.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:71206861 C>A maps to NM_033141.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:66462833 G>T maps to NM_001164664.1 R2609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:66462833 G>T maps to NM_001164664.1 R2609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3783218 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3783218 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:3304164 C>A maps to NM_000243.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:3304164 C>A maps to NM_000243.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:123367491 C>T maps to ENST00000426959 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:123367491 C>T maps to ENST00000426959 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:2523403 G>T maps to NM_033467.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:2523403 G>T maps to NM_033467.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:90872783 G>T maps to NM_007351.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:90872783 G>T maps to NM_007351.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:14932623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:14932623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:3249690 G>T maps to ENST00000328215 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:3249690 G>T maps to ENST00000328215 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9089858 A>G maps to NM_024690.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9089858 A>G maps to NM_024690.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:100675477 G>T maps to NM_001040105.1 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:100675477 G>T maps to NM_001040105.1 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:135507149 C>A maps to NM_001130173.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:135507149 C>A maps to NM_001130173.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10535201 C>A maps to NM_002470.2 T1696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10535201 C>A maps to NM_002470.2 T1696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:16685845 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:16685845 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:26164761 G>T maps to ENST00000407587 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:26164761 G>T maps to ENST00000407587 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34883450 G>A maps to NM_001163735.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34883450 G>A maps to NM_001163735.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:40104130 C>T maps to NM_018177.3 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:40104130 C>T maps to NM_018177.3 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:15557782 A>C maps to NM_015909.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:15557782 A>C maps to NM_015909.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:145296387 C>T maps to NM_001039703.4 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:145296387 C>T maps to NM_001039703.4 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:240954194 G>A maps to ENST00000404554 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:240954194 G>A maps to ENST00000404554 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:240961673 C>A maps to ENST00000404554 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:240961673 C>A maps to ENST00000404554 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:21592380 A>G maps to NM_006157.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:21592380 A>G maps to NM_006157.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:68156553 C>T maps to NM_173165.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:68156553 C>T maps to NM_173165.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103531828 G>A maps to NM_003998.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103531828 G>A maps to NM_003998.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:156890270 C>G maps to NM_001099287.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:156890270 C>G maps to NM_001099287.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:56424252 A>G maps to NM_176810.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:56424252 A>G maps to NM_176810.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:5463314 C>T maps to NM_033004.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:5463314 C>T maps to NM_033004.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:31537450 A>G maps to NM_003787.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:31537450 A>G maps to NM_003787.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:139411823 C>T maps to NM_017617.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:139411823 C>T maps to NM_017617.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:36339974 G>T maps to NM_004646.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:36339974 G>T maps to NM_004646.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30322835 T>A maps to NM_000475.4 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30322835 T>A maps to NM_000475.4 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:135073436 G>T maps to NM_032536.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:135073436 G>T maps to NM_032536.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62569424 C>A maps to NM_006362.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62569424 C>A maps to NM_006362.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:101092564 T>A maps to ENST00000263032 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:101092564 T>A maps to ENST00000263032 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:28000605 T>A maps to NM_000275.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:28000605 T>A maps to NM_000275.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:128722860 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:128722860 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:124097464 C>A maps to NM_001163278.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:124097464 C>A maps to NM_001163278.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:183652153 C>A maps to NM_001080477.1 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:183652153 C>A maps to NM_001080477.1 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:193377301 A>T maps to NM_130837.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:193377301 A>T maps to NM_130837.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159505254 G>T maps to NM_001004469.1 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159505254 G>T maps to NM_001004469.1 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:29364670 C>A maps to NM_013936.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:29364670 C>A maps to NM_013936.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57971443 G>A maps to NM_001004459.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57971443 G>A maps to NM_001004459.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248685896 A>G maps to NM_001013355.1 *317W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248685896 A>G maps to NM_001013355.1 *317W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248367103 C>A maps to NM_001004689.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248367103 C>A maps to NM_001004689.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:3195447 G>T maps to ENST00000397187 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:3195447 G>T maps to ENST00000397187 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4843568 C>T maps to NM_001004753.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4843568 C>T maps to NM_001004753.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4471180 G>T maps to NM_001005172.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4471180 G>T maps to NM_001005172.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:97806151 G>T maps to NM_054106.1 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:97806151 G>T maps to NM_054106.1 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55587575 C>T maps to ENST00000395203 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55587575 C>T maps to ENST00000395203 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55595191 C>A maps to NM_001004739.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55595191 C>A maps to NM_001004739.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142749622 C>A maps to NM_001001667.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142749622 C>A maps to NM_001001667.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:56113543 G>C maps to NM_001002907.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:56113543 G>C maps to NM_001002907.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:118989775 T>A maps to NM_002581.3 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:118989775 T>A maps to NM_002581.3 A726A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140166919 G>T maps to NM_018900.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140166919 G>T maps to NM_018900.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140181570 C>A maps to NM_018906.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140181570 C>A maps to NM_018906.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140188757 G>T maps to NM_018907.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140188757 G>T maps to NM_018907.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140729928 G>A maps to NM_018922.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140729928 G>A maps to NM_018922.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:17827248 G>A maps to NM_006197.3 E1192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:17827248 G>A maps to NM_006197.3 E1192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:150114743 A>C maps to NM_005389.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:150114743 A>C maps to NM_005389.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:14880789 A>T maps to NM_000922.3 K908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:14880789 A>T maps to NM_000922.3 K908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:144868161 A>T maps to NM_014644.4 T1759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:144868161 A>T maps to NM_014644.4 T1759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:144879315 C>A maps to NM_014644.4 R1378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:144879315 C>A maps to NM_014644.4 R1378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:44108029 C>T maps to NM_002606.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:44108029 C>T maps to NM_002606.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:56763320 G>T maps to NM_021255.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:56763320 G>T maps to NM_021255.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:15579521 G>T maps to NM_052890.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:15579521 G>T maps to NM_052890.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:207107959 G>A maps to NM_002644.3 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:207107959 G>A maps to NM_002644.3 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:81208464 C>A maps to NM_052892.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:81208464 C>A maps to NM_052892.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:102053072 T>A maps to NM_016112.2 K575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:102053072 T>A maps to NM_016112.2 K575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:79513981 G>T maps to NM_181839.1 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:79513981 G>T maps to NM_181839.1 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:186862164 G>T maps to NM_024420.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:186862164 G>T maps to NM_024420.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:9404402 G>T maps to NM_001172646.1 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:9404402 G>T maps to NM_001172646.1 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:143240 G>T maps to NM_052909.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:143240 G>T maps to NM_052909.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:162014 G>T maps to NM_052909.3 G513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:162014 G>T maps to NM_052909.3 G513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:74315474 G>T maps to NM_033238.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:74315474 G>T maps to NM_033238.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:152159023 A>C maps to NM_001184924.1 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:152159023 A>C maps to NM_001184924.1 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:89790744 G>A maps to NM_006813.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:89790744 G>A maps to NM_006813.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:42923008 G>A maps to NM_024664.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:42923008 G>A maps to NM_024664.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:93390349 A>T maps to NM_005398.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:93390349 A>T maps to NM_005398.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:6325265 G>A maps to NM_181876.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:6325265 G>A maps to NM_181876.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:103899473 C>A maps to NM_015062.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:103899473 C>A maps to NM_015062.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:46228588 C>A maps to NM_005400.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:46228588 C>A maps to NM_005400.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:15469011 A>C maps to NM_001128217.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:15469011 A>C maps to NM_001128217.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:38144946 C>T maps to NM_002809.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:38144946 C>T maps to NM_002809.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:54125135 C>A maps to NM_014614.2 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:54125135 C>A maps to NM_014614.2 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:186648544 A>G maps to NM_000963.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:186648544 A>G maps to NM_000963.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:112151515 C>A maps to NM_002829.3 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:112151515 C>A maps to NM_002829.3 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8499799 G>T maps to NM_002839.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8499799 G>T maps to NM_002839.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:52233379 G>C maps to NM_144651.4 R1408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:52233379 G>C maps to NM_144651.4 R1408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:58380796 G>T maps to NM_017771.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:58380796 G>T maps to NM_017771.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:9355208 G>A maps to NM_002864.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:9355208 G>A maps to NM_002864.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:128875700 T>G maps to ENST00000418265 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:128875700 T>G maps to ENST00000418265 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79313966 C>A maps to NM_006507.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79313966 C>A maps to NM_006507.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103185751 G>A maps to ENST00000428762 A2114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103185751 G>A maps to ENST00000428762 A2114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:59483516 C>A maps to NM_173557.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:59483516 C>A maps to NM_173557.2 L60L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:78666911 G>A maps to NM_002941.3 S1385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:78666911 G>A maps to NM_002941.3 S1385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:55540659 A>G maps to NM_006269.1 K1406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:55540659 A>G maps to NM_006269.1 K1406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153628873 A>G maps to NM_006013.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153628873 A>G maps to NM_006013.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:33606994 C>G maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:33606994 C>G maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:20173623 A>T maps to NM_004586.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:20173623 A>T maps to NM_004586.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:25256083 G>T maps to NM_001031680.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:25256083 G>T maps to NM_001031680.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:38934436 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:38934436 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:23915307 G>A maps to NM_014363.4 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:23915307 G>A maps to NM_014363.4 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:21992358 C>T maps to NM_005407.1 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:21992358 C>T maps to NM_005407.1 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:55065090 C>A maps to NM_021626.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:55065090 C>A maps to NM_021626.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:76385183 G>T maps to NM_015571.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:76385183 G>T maps to NM_015571.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:95053824 C>A maps to NM_000624.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:95053824 C>A maps to NM_000624.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:171765891 C>A maps to NM_001017995.2 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:171765891 C>A maps to NM_001017995.2 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:72890351 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:72890351 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:35650509 C>A maps to NM_014450.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:35650509 C>A maps to NM_014450.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121658293 T>C maps to NM_021082.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121658293 T>C maps to NM_021082.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:110778045 G>T maps to NM_033125.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:110778045 G>T maps to NM_033125.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62933576 G>A maps to NM_199352.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62933576 G>A maps to NM_199352.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:128302150 G>T maps to NM_001017372.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:128302150 G>T maps to NM_001017372.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:33984625 G>T maps to NM_016180.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:33984625 G>T maps to NM_016180.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:42335507 G>T maps to NM_000342.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:42335507 G>T maps to NM_000342.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14489309 C>T maps to NM_001134367.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14489309 C>T maps to NM_001134367.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23596442 G>A maps to NM_012244.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23596442 G>A maps to NM_012244.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:70515544 G>T maps to NM_183002.1 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:70515544 G>T maps to NM_183002.1 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:101755678 A>T maps to NM_173488.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:101755678 A>T maps to NM_173488.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:33679959 G>T maps to NM_152270.3 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:33679959 G>T maps to NM_152270.3 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:18853096 C>T maps to ENST00000389467 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:18853096 C>T maps to ENST00000389467 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:71232509 T>C maps to NM_012390.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:71232509 T>C maps to NM_012390.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:93968705 T>G maps to NM_003877.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:93968705 T>G maps to NM_003877.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:34923099 G>T maps to NM_138927.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:34923099 G>T maps to NM_138927.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:108536423 A>G maps to NM_001013031.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:108536423 A>G maps to NM_001013031.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:106974203 C>A maps to NM_014978.1 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:106974203 C>A maps to NM_014978.1 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:39216411 T>A maps to NM_005633.3 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:39216411 T>A maps to NM_005633.3 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:35800161 C>A maps to NM_024867.3 T1641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:35800161 C>A maps to NM_024867.3 T1641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:44876443 C>A maps to NM_025137.3 G1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:44876443 C>A maps to NM_025137.3 G1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:124323228 G>T maps to NM_199327.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:124323228 G>T maps to NM_199327.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53045815 G>A maps to NM_014682.2 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53045815 G>A maps to NM_014682.2 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:77510142 C>A maps to NM_030965.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:77510142 C>A maps to NM_030965.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:40459419 G>T maps to NM_003152.3 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:40459419 G>T maps to NM_003152.3 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4103449 G>T maps to NM_003156.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4103449 G>T maps to NM_003156.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:171488209 G>T maps to NM_005990.3 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:171488209 G>T maps to NM_005990.3 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:37105066 C>A maps to NM_003162.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:37105066 C>A maps to NM_003162.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:46365537 G>T maps to NM_001161841.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:46365537 G>T maps to NM_001161841.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48046872 G>A maps to NM_152782.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48046872 G>A maps to NM_152782.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:115487076 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:115487076 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:93657851 G>A maps to NM_003177.5 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:93657851 G>A maps to NM_003177.5 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:39817888 G>T maps to NM_006116.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:39817888 G>T maps to NM_006116.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47685463 G>T maps to ENST00000371883 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47685463 G>T maps to ENST00000371883 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:162280681 G>T maps to NM_006593.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:162280681 G>T maps to NM_006593.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:45145228 C>T maps to ENST00000404564 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:45145228 C>T maps to ENST00000404564 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:45821846 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:45821846 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49858628 G>A maps to NM_003598.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49858628 G>A maps to NM_003598.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:11521553 G>T maps to ENST00000423059 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:11521553 G>T maps to ENST00000423059 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:165697283 T>G maps to NM_019026.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:165697283 T>G maps to NM_019026.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:122199629 C>T maps to NM_001080825.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:122199629 C>T maps to NM_001080825.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:122199640 C>G maps to NM_001080825.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:122199640 C>G maps to NM_001080825.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:126137135 C>G maps to NM_052907.2 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:126137135 C>G maps to NM_052907.2 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:126138764 T>C maps to NM_052907.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:126138764 T>C maps to NM_052907.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:82373272 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:82373272 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:148690312 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:148690312 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:675548 G>A maps to NM_152834.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:675548 G>A maps to NM_152834.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:2757800 C>G maps to NM_024309.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:2757800 C>G maps to NM_024309.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:175304847 C>A maps to NM_003285.2 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:175304847 C>A maps to NM_003285.2 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:52991147 G>T maps to NM_005486.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:52991147 G>T maps to NM_005486.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:22318676 C>A maps to NM_003935.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:22318676 C>A maps to NM_003935.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:42695415 C>A maps to ENST00000348077 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:42695415 C>A maps to ENST00000348077 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:10959796 C>G maps to NM_199261.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:10959796 C>G maps to NM_199261.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:154216896 G>T maps to NM_015271.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:154216896 G>T maps to NM_015271.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:126319436 A>G maps to NM_001031712.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:126319436 A>G maps to NM_001031712.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:45837908 C>A maps to ENST00000397932 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:45837908 C>A maps to ENST00000397932 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:77436693 G>A maps to NM_017662.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:77436693 G>A maps to NM_017662.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:81554320 T>A maps to NM_000369.2 L114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:81554320 T>A maps to NM_000369.2 L114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:31767545 G>A maps to NM_020856.2 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:31767545 G>A maps to NM_020856.2 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:166771853 T>C maps to NM_024753.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:166771853 T>C maps to NM_024753.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179457382 G>T maps to NM_133378.4 P17215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179457382 G>T maps to NM_133378.4 P17215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179554015 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179554015 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:190903785 G>T maps to ENST00000248151 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:190903785 G>T maps to ENST00000248151 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135103474 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135103474 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:72916384 C>A maps to NM_173477.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:72916384 C>A maps to NM_173477.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216219776 G>T maps to ENST00000366943 V2107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216219776 G>T maps to ENST00000366943 V2107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216372966 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216372966 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:31231662 G>A maps to NM_005800.4 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:31231662 G>A maps to NM_005800.4 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:9936981 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:9936981 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:62276212 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:62276212 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:2847153 G>T maps to NM_022575.2 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:2847153 G>T maps to NM_022575.2 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:22144267 C>A maps to NM_173615.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:22144267 C>A maps to NM_173615.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:71135037 C>T maps to NM_022479.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:71135037 C>T maps to NM_022479.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:117577636 G>A maps to NM_019045.4 W833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:117577636 G>A maps to NM_019045.4 W833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:134879796 T>A maps to NM_014149.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:134879796 T>A maps to NM_014149.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:9598728 G>T maps to NM_003390.3 G354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:9598728 G>T maps to NM_003390.3 G354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141423009 C>A maps to NM_001105558.1 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141423009 C>A maps to NM_001105558.1 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:30954340 G>T maps to NM_000553.4 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:30954340 G>T maps to NM_000553.4 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:123040875 G>T maps to NM_001167.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:123040875 G>T maps to NM_001167.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:39225674 C>A maps to NM_194293.2 T1754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:39225674 C>A maps to NM_194293.2 T1754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168067242 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168067242 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:17264940 G>C maps to NM_175878.3 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:17264940 G>C maps to NM_175878.3 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:125682048 G>A maps to NM_020924.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:125682048 G>A maps to NM_020924.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:195936324 G>T maps to NM_001039617.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:195936324 G>T maps to NM_001039617.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:31810710 C>T maps to NM_001174096.1 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:31810710 C>T maps to NM_001174096.1 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:106813842 T>C maps to NM_012082.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:106813842 T>C maps to NM_012082.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:81065335 G>T maps to NM_020338.3 G801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:81065335 G>T maps to NM_020338.3 G801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:5012904 C>A maps to NM_014519.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:5012904 C>A maps to NM_014519.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:244217637 G>T maps to NM_205768.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:244217637 G>T maps to NM_205768.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:57803157 G>T maps to NM_006635.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:57803157 G>T maps to NM_006635.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:57188766 C>A maps to NM_033273.1 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:57188766 C>A maps to NM_033273.1 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58868092 G>A maps to NM_198458.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58868092 G>A maps to NM_198458.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:31039466 C>A maps to NM_014717.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:31039466 C>A maps to NM_014717.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:58119777 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:58119777 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:67309239 T>C maps to ENST00000392677 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:67309239 T>C maps to ENST00000392677 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:150732735 G>C maps to ENST00000297504 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:150732735 G>C maps to ENST00000297504 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:77317954 G>T maps to NM_199355.2 C1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:77317954 G>T maps to NM_199355.2 C1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:41476484 G>A maps to NM_178819.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:41476484 G>A maps to NM_178819.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:114279343 A>T maps to NM_001148.4 V3190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:114279343 A>T maps to NM_001148.4 V3190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:193132539 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:193132539 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:42480645 C>T maps to ENST00000441343 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:42480645 C>T maps to ENST00000441343 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:34640215 C>T maps to ENST00000438749 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:34640215 C>T maps to ENST00000438749 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:62478118 G>T maps to ENST00000383709 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:62478118 G>T maps to ENST00000383709 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:40912854 T>C maps to NM_170589.3 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:40912854 T>C maps to NM_170589.3 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:158261155 G>A maps to NM_001765.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:158261155 G>A maps to NM_001765.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:31973518 C>A maps to ENST00000357886 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:31973518 C>A maps to ENST00000357886 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:18020341 C>T maps to ENST00000400579 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:18020341 C>T maps to ENST00000400579 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:90038267 C>G maps to NM_145039.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:90038267 C>G maps to NM_145039.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:196928065 G>A maps to ENST00000367421 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:196928065 G>A maps to ENST00000367421 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:233404769 C>A maps to NM_005199.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:233404769 C>A maps to NM_005199.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40958758 C>T maps to NM_173478.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40958758 C>T maps to NM_173478.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:189868183 T>C maps to NM_000090.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:189868183 T>C maps to NM_000090.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:107424190 G>T maps to NM_033641.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:107424190 G>T maps to NM_033641.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:28754529 C>T maps to NM_001304.4 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:28754529 C>T maps to NM_001304.4 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:75119190 G>A maps to NM_001030005.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:75119190 G>A maps to NM_001030005.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:100086549 T>A maps to ENST00000415585 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:100086549 T>A maps to ENST00000415585 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:37658246 G>T maps to NM_000397.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:37658246 G>T maps to NM_000397.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:219674424 G>T maps to NM_000784.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:219674424 G>T maps to NM_000784.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:96534880 G>T maps to NM_000769.1 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:96534880 G>T maps to NM_000769.1 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:99262906 A>G maps to NM_000777.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:99262906 A>G maps to NM_000777.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:50119911 A>G maps to NM_001013742.1 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:50119911 A>G maps to NM_001013742.1 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:234652412 G>A maps to NM_001001394.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:234652412 G>A maps to NM_001001394.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:117395625 T>C maps to NM_020693.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:117395625 T>C maps to NM_020693.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:45387724 C>A maps to NM_014080.4 V1383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:45387724 C>A maps to NM_014080.4 V1383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:61112107 G>C maps to ENST00000442566 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:61112107 G>C maps to ENST00000442566 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:7866921 G>T maps to NM_024091.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:7866921 G>T maps to NM_024091.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:92535010 C>A maps to ENST00000298047 A2944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:92535010 C>A maps to ENST00000298047 A2944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:126411518 C>A maps to NM_024582.4 T4514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:126411518 C>A maps to NM_024582.4 T4514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:173269701 C>T maps to NM_001034845.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:173269701 C>T maps to NM_001034845.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:55214929 A>C maps to NM_207410.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:55214929 A>C maps to NM_207410.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:167025040 G>T maps to NM_005814.1 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:167025040 G>T maps to NM_005814.1 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:87373322 G>T maps to NM_017551.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:87373322 G>T maps to NM_017551.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:22569971 G>C maps to NM_138574.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:22569971 G>C maps to NM_138574.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:222717099 C>G maps to NM_024746.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:222717099 C>G maps to NM_024746.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:23648099 T>A maps to ENST00000414299 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:23648099 T>A maps to ENST00000414299 A244A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4430-01A-02D-1265-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-4430-01A-02D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:23842380 A>T maps to NM_022789.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:23842380 A>T maps to NM_022789.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:3136994 A>G maps to NM_000564.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:3136994 A>G maps to NM_000564.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:53170634 G>T maps to NM_015848.4 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:53170634 G>T maps to NM_015848.4 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:54801975 G>A maps to ENST00000251375 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:54801975 G>A maps to ENST00000251375 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:44204191 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:44204191 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:54961994 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:54961994 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:149638600 G>A maps to NM_005491.3 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:149638600 G>A maps to NM_005491.3 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:149638621 G>A maps to NM_005491.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:149638621 G>A maps to NM_005491.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:149638633 G>A maps to NM_005491.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:149638633 G>A maps to NM_005491.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:150881711 G>T maps to NM_053002.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:150881711 G>T maps to NM_053002.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:313533 C>G maps to NM_017550.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:313533 C>G maps to NM_017550.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:14934406 G>A maps to NM_152581.3 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:14934406 G>A maps to NM_152581.3 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:15839063 G>T maps to NM_001040114.1 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:15839063 G>T maps to NM_001040114.1 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:101265450 C>A maps to NM_138403.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:101265450 C>A maps to NM_138403.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:31075975 G>A maps to NM_015194.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:31075975 G>A maps to NM_015194.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:158450420 G>T maps to NM_001004472.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:158450420 G>T maps to NM_001004472.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:247921321 G>A maps to NM_012353.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:247921321 G>A maps to NM_012353.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:5020469 G>T maps to NM_001004755.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:5020469 G>T maps to NM_001004755.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:5221507 A>G maps to NM_001004760.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:5221507 A>G maps to NM_001004760.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:59132050 G>T maps to NM_001004729.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:59132050 G>T maps to NM_001004729.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:55860900 T>C maps to NM_001003750.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:55860900 T>C maps to NM_001003750.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:241078630 G>A maps to NM_148961.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:241078630 G>A maps to NM_148961.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:79813035 C>A maps to NM_000918.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:79813035 C>A maps to NM_000918.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:150841004 C>A maps to NM_173493.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:150841004 C>A maps to NM_173493.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:95761537 G>A maps to NM_000439.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:95761537 G>A maps to NM_000439.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:183051237 C>A maps to NM_005019.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:183051237 C>A maps to NM_005019.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:129801995 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:129801995 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:228033665 G>C maps to NM_183062.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:228033665 G>C maps to NM_183062.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:121651439 C>A maps to NM_002851.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:121651439 C>A maps to NM_002851.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:55784733 G>C maps to NM_016656.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:55784733 G>C maps to NM_016656.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:110763779 C>A maps to NM_006583.2 C292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:110763779 C>A maps to NM_006583.2 C292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:180017710 C>A maps to NM_052863.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:180017710 C>A maps to NM_052863.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:139304593 C>A maps to NM_001039707.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:139304593 C>A maps to NM_001039707.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:249110822 C>A maps to NM_030645.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:249110822 C>A maps to NM_030645.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:51220029 A>G maps to ENST00000391814 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:51220029 A>G maps to ENST00000391814 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:25799036 T>C maps to NM_005074.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:25799036 T>C maps to NM_005074.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:17599847 C>T maps to NM_198580.1 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:17599847 C>T maps to NM_198580.1 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56629469 C>T maps to NM_001135195.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56629469 C>T maps to NM_001135195.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:142717964 G>T maps to NM_001184749.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:142717964 G>T maps to NM_001184749.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:51362271 C>G maps to NM_018967.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:51362271 C>G maps to NM_018967.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:89598376 C>A maps to NM_003119.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:89598376 C>A maps to NM_003119.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:153048469 C>A maps to NM_014370.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:153048469 C>A maps to NM_014370.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:23016905 G>T maps to NM_001052.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:23016905 G>T maps to NM_001052.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:61498458 C>T maps to ENST00000389520 R1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:61498458 C>T maps to ENST00000389520 R1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:110348912 G>T maps to NM_032300.4 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:110348912 G>T maps to NM_032300.4 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:133953767 C>A maps to NM_003235.4 V1738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:133953767 C>A maps to NM_003235.4 V1738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:169626328 A>T maps to NM_003247.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:169626328 A>T maps to NM_003247.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:122765623 G>T maps to NM_001081550.1 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:122765623 G>T maps to NM_001081550.1 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:13223572 C>A maps to NM_001136035.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:13223572 C>A maps to NM_001136035.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:72998564 C>G maps to NM_005786.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:72998564 C>G maps to NM_005786.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110407674 C>A maps to NM_033035.4 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110407674 C>A maps to NM_033035.4 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:71265914 C>A maps to NM_012339.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:71265914 C>A maps to NM_012339.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:179459083 G>T maps to NM_133378.4 C16811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:179459083 G>T maps to NM_133378.4 C16811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:118975154 C>A maps to NM_080632.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:118975154 C>A maps to NM_080632.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:216019166 C>A maps to ENST00000366943 G3018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:216019166 C>A maps to ENST00000366943 G3018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:41012323 A>G maps to NM_001039590.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:41012323 A>G maps to NM_001039590.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:108507485 C>T maps to NM_006113.4 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:108507485 C>T maps to NM_006113.4 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:215279061 C>A maps to NM_001080500.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:215279061 C>A maps to NM_001080500.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:7684527 G>T maps to NM_020196.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:7684527 G>T maps to NM_020196.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:168102743 C>A maps to NM_152381.5 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:168102743 C>A maps to NM_152381.5 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:29640786 C>T maps to NM_001109809.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:29640786 C>T maps to NM_001109809.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:95637295 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:95637295 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:121738538 C>T maps to NM_005763.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:121738538 C>T maps to NM_005763.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:87179871 G>T maps to NM_000927.3 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:87179871 G>T maps to NM_000927.3 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:183682980 G>A maps to NM_005688.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:183682980 G>A maps to NM_005688.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:109637269 G>T maps to NM_001093.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:109637269 G>T maps to NM_001093.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:40063718 G>A maps to ENST00000401700 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:40063718 G>A maps to ENST00000401700 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236912563 G>A maps to NM_001103.2 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236912563 G>A maps to NM_001103.2 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4202310 C>G maps to NM_000678.3 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4202310 C>G maps to NM_000678.3 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:53819600 A>G maps to NM_020547.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:53819600 A>G maps to NM_020547.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:73987473 C>A maps to NM_032217.3 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:73987473 C>A maps to NM_032217.3 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:74008401 C>G maps to NM_032217.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:74008401 C>G maps to NM_032217.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:26538396 C>T maps to NM_031418.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:26538396 C>T maps to NM_031418.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:139942053 C>A maps to ENST00000354402 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:139942053 C>A maps to ENST00000354402 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:21227176 G>A maps to NM_000384.2 D4017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:21227176 G>A maps to NM_000384.2 D4017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:142586819 G>A maps to NM_015071.4 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:142586819 G>A maps to NM_015071.4 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:97217401 G>T maps to NM_212481.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:97217401 G>T maps to NM_212481.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:197072641 G>A maps to NM_018136.4 A1913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:197072641 G>A maps to NM_018136.4 A1913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:47570993 T>A maps to NM_020453.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:47570993 T>A maps to NM_020453.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:63554270 G>T maps to NM_004655.3 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:63554270 G>T maps to NM_004655.3 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:60687790 C>T maps to NM_022893.3 K752K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:60687790 C>T maps to NM_022893.3 K752K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:16552764 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:16552764 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:870663 G>A maps to NM_001009877.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:870663 G>A maps to NM_001009877.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:66109712 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:66109712 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:108051443 C>G maps to NM_001018072.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:108051443 C>G maps to NM_001018072.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:63586319 C>A maps to NM_138471.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:63586319 C>A maps to NM_138471.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58604954 T>G maps to ENST00000438670 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58604954 T>G maps to ENST00000438670 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:54892330 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:54892330 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:67591502 A>T maps to NM_001013674.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:67591502 A>T maps to NM_001013674.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:1019649 C>A maps to ENST00000448924 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:1019649 C>A maps to ENST00000448924 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:88202560 G>A maps to NM_173824.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:88202560 G>A maps to NM_173824.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:20716571 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:20716571 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54444823 C>T maps to NM_031896.4 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54444823 C>T maps to NM_031896.4 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:200817336 A>G maps to ENST00000236925 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:200817336 A>G maps to ENST00000236925 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:105464840 C>A maps to NM_170662.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:105464840 C>A maps to NM_170662.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:6291133 G>T maps to NM_176875.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:6291133 G>T maps to NM_176875.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160523868 T>A maps to NM_001184879.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160523868 T>A maps to NM_001184879.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51983902 C>A maps to NM_001080405.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51983902 C>A maps to NM_001080405.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:34060657 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:34060657 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:53338271 T>G maps to ENST00000219084 S2118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:53338271 T>G maps to ENST00000219084 S2118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:109931882 G>A maps to NM_001143981.1 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:109931882 G>A maps to NM_001143981.1 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51226832 C>T maps to NM_002975.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51226832 C>T maps to NM_002975.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:28488911 G>T maps to NM_000086.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:28488911 G>T maps to NM_000086.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189862451 A>G maps to NM_000090.3 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189862451 A>G maps to NM_000090.3 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:227983372 T>A maps to ENST00000396625 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:227983372 T>A maps to ENST00000396625 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:173376572 G>T maps to NM_030627.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:173376572 G>T maps to NM_030627.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211421525 G>T maps to NM_001122633.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211421525 G>T maps to NM_001122633.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:2857501 A>G maps to NM_033225.5 S2727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:2857501 A>G maps to NM_033225.5 S2727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113323243 C>A maps to NM_198123.1 G2616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113323243 C>A maps to NM_198123.1 G2616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113516124 T>C maps to NM_198123.1 Q1659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113516124 T>C maps to NM_198123.1 Q1659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:96748683 C>T maps to NM_000771.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:96748683 C>T maps to NM_000771.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:124544668 G>A maps to ENST00000408936 Q1154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:124544668 G>A maps to ENST00000408936 Q1154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155701745 C>G maps to NM_004632.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155701745 C>G maps to NM_004632.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:79571773 C>T maps to NM_004747.3 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:79571773 C>T maps to NM_004747.3 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:32305788 T>A maps to ENST00000357033 S2049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:32305788 T>A maps to ENST00000357033 S2049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:15888819 G>A maps to NM_015291.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:15888819 G>A maps to NM_015291.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:105456611 C>G maps to NM_001385.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:105456611 C>G maps to NM_001385.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:38853122 G>T maps to NM_001396.3 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:38853122 G>T maps to NM_001396.3 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:96293707 C>T maps to NM_198968.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:96293707 C>T maps to NM_198968.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236631556 C>T maps to NM_145861.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236631556 C>T maps to NM_145861.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:68060319 C>T maps to NM_004429.4 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:68060319 C>T maps to NM_004429.4 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:38445799 C>G maps to ENST00000354891 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:38445799 C>G maps to ENST00000354891 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:75469818 G>C maps to NM_014239.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:75469818 G>C maps to NM_014239.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143096453 C>T maps to NM_005232.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143096453 C>T maps to NM_005232.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:96963114 G>T maps to NM_001080448.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:96963114 G>T maps to NM_001080448.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:22915541 G>T maps to NM_020526.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:22915541 G>T maps to NM_020526.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:16535929 C>A maps to ENST00000455140 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:16535929 C>A maps to ENST00000455140 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:13971168 G>A maps to NM_004956.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:13971168 G>A maps to NM_004956.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:61011384 C>T maps to ENST00000442566 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:61011384 C>T maps to ENST00000442566 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15296878 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15296878 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15821092 G>A maps to NM_024948.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15821092 G>A maps to NM_024948.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155223709 C>T maps to ENST00000368370 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155223709 C>T maps to ENST00000368370 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:15406279 G>A maps to NM_145301.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:15406279 G>A maps to NM_145301.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:34961455 G>T maps to NM_152631.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:34961455 G>T maps to NM_152631.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:30041746 G>A maps to NM_031478.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:30041746 G>A maps to NM_031478.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:150947283 A>G maps to NM_001447.2 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:150947283 A>G maps to NM_001447.2 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:15928062 C>A maps to NM_012304.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:15928062 C>A maps to NM_012304.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:97058634 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:97058634 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:46067559 G>A maps to NM_173536.3 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:46067559 G>A maps to NM_173536.3 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:74071266 G>T maps to NM_003857.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:74071266 G>T maps to NM_003857.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:35227241 G>A maps to NM_153212.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:35227241 G>A maps to NM_153212.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:63049633 G>A maps to NM_006572.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:63049633 G>A maps to NM_006572.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:145138041 G>T maps to NM_003801.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:145138041 G>T maps to NM_003801.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:135427277 T>A maps to NM_153834.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:135427277 T>A maps to NM_153834.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:110085967 C>A maps to NM_031936.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:110085967 C>A maps to NM_031936.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:94343932 T>C maps to NM_001510.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:94343932 T>C maps to NM_001510.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:48832428 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:48832428 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46708078 C>T maps to NM_016426.6 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46708078 C>T maps to NM_016426.6 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:35775839 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:35775839 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:3451121 C>T maps to ENST00000511533 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:3451121 C>T maps to ENST00000511533 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:35779115 C>A maps to NM_002133.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:35779115 C>A maps to NM_002133.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:27196008 C>G maps to NM_006896.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:27196008 C>G maps to NM_006896.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:6458850 C>A maps to NM_000613.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:6458850 C>A maps to NM_000613.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:209878313 C>A maps to NM_005525.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:209878313 C>A maps to NM_005525.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:34640769 G>T maps to ENST00000433395 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:34640769 G>T maps to ENST00000433395 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156501026 C>A maps to NM_178229.4 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156501026 C>A maps to NM_178229.4 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:96993503 C>T maps to ENST00000420728 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:96993503 C>T maps to ENST00000420728 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:227922418 C>A maps to NM_023007.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:227922418 C>A maps to NM_023007.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:42747214 C>T maps to NM_020433.4 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:42747214 C>T maps to NM_020433.4 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:18112295 C>T maps to NM_002252.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:18112295 C>T maps to NM_002252.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:196309512 C>A maps to NM_198503.2 G581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:196309512 C>A maps to NM_198503.2 G581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:109740146 G>T maps to NM_020775.3 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:109740146 G>T maps to NM_020775.3 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:1919948 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:1919948 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:21009181 C>A maps to NM_020816.2 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:21009181 C>A maps to NM_020816.2 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:241727623 C>A maps to ENST00000373308 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:241727623 C>A maps to ENST00000373308 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:20819221 C>A maps to NM_032775.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:20819221 C>A maps to NM_032775.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:71293439 G>A maps to ENST00000376535 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:71293439 G>A maps to ENST00000376535 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129833583 G>A maps to NM_000426.3 L2978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129833583 G>A maps to NM_000426.3 L2978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:100942988 C>A maps to ENST00000394113 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:100942988 C>A maps to ENST00000394113 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:75608901 C>A maps to NM_001001933.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:75608901 C>A maps to NM_001001933.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:48304126 G>T maps to NM_031490.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:48304126 G>T maps to NM_031490.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:62775372 G>T maps to ENST00000506720 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:62775372 G>T maps to ENST00000506720 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:141528457 G>T maps to NM_018557.2 S1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:141528457 G>T maps to NM_018557.2 S1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:170009460 G>A maps to NM_004525.2 Y4103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:170009460 G>A maps to NM_004525.2 Y4103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68171003 G>A maps to NM_002335.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68171003 G>A maps to NM_002335.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:131669875 A>T maps to NM_001127244.1 K145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:131669875 A>T maps to NM_001127244.1 K145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:238672083 C>T maps to NM_001137552.1 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:238672083 C>T maps to NM_001137552.1 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:77745882 G>T maps to NM_001134745.1 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:77745882 G>T maps to NM_001134745.1 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:150061877 C>A maps to NM_177964.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:150061877 C>A maps to NM_177964.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47307000 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47307000 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:186961389 T>A maps to NM_139125.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:186961389 T>A maps to NM_139125.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:43933036 C>A maps to ENST00000372754 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:43933036 C>A maps to ENST00000372754 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:108778675 T>C maps to NM_014429.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:108778675 T>C maps to NM_014429.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:174537437 T>A maps to NM_006792.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:174537437 T>A maps to NM_006792.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:28378645 C>A maps to NM_173496.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:28378645 C>A maps to NM_173496.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:1101127 G>T maps to ENST00000441003 T2509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:1101127 G>T maps to ENST00000441003 T2509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:49403210 C>T maps to NM_000255.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:49403210 C>T maps to NM_000255.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10432237 C>T maps to NM_017534.5 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10432237 C>T maps to NM_017534.5 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10558330 G>A maps to NM_002470.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10558330 G>A maps to NM_002470.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:26164506 C>A maps to ENST00000407587 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:26164506 C>A maps to ENST00000407587 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:54925123 C>T maps to NM_005337.4 Q863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:54925123 C>T maps to NM_005337.4 Q863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124862882 C>A maps to NM_006312.4 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124862882 C>A maps to NM_006312.4 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:115760593 T>C maps to NM_022569.1 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:115760593 T>C maps to NM_022569.1 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160340529 C>T maps to NM_005598.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160340529 C>T maps to NM_005598.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:52505827 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:52505827 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:100058048 G>T maps to NM_020202.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:100058048 G>T maps to NM_020202.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:56303673 C>A maps to NM_145007.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:56303673 C>A maps to NM_145007.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:100928737 C>A maps to ENST00000392986 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:100928737 C>A maps to ENST00000392986 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:149357468 T>A maps to ENST00000511528 K182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:149357468 T>A maps to ENST00000511528 K182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:105659883 C>T maps to NM_024928.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:105659883 C>T maps to NM_024928.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161967726 G>A maps to ENST00000451379 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161967726 G>A maps to ENST00000451379 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:132306554 G>T maps to NM_002545.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:132306554 G>T maps to NM_002545.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:57996203 G>T maps to NM_001004471.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:57996203 G>T maps to NM_001004471.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247921240 G>T maps to NM_012353.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247921240 G>T maps to NM_012353.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143747931 C>T maps to NM_012365.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143747931 C>T maps to NM_012365.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248129412 G>A maps to NM_001004491.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248129412 G>A maps to NM_001004491.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248129469 C>T maps to NM_001004491.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248129469 C>T maps to NM_001004491.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247752014 G>T maps to NM_001001915.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247752014 G>T maps to NM_001001915.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248224138 C>T maps to NM_001004687.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248224138 C>T maps to NM_001004687.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:20403986 T>C maps to NM_001004063.2 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:20403986 T>C maps to NM_001004063.2 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:20216281 G>A maps to NM_172194.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:20216281 G>A maps to NM_172194.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5968749 T>A maps to NM_001003443.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5968749 T>A maps to NM_001003443.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55587851 C>T maps to ENST00000395203 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55587851 C>T maps to ENST00000395203 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:97887755 T>C maps to NM_001005515.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:97887755 T>C maps to NM_001005515.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:55715312 A>C maps to NM_001005182.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:55715312 A>C maps to NM_001005182.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14952212 T>C maps to NM_001005190.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14952212 T>C maps to NM_001005190.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:124189357 A>G maps to NM_001002918.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:124189357 A>G maps to NM_001002918.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:55524458 C>T maps to NM_001005243.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:55524458 C>T maps to NM_001005243.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:79817263 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:79817263 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:90691097 G>A maps to NM_080832.2 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:90691097 G>A maps to NM_080832.2 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:105818725 A>G maps to ENST00000458164 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:105818725 A>G maps to ENST00000458164 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:9546830 C>A maps to NM_177990.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:9546830 C>A maps to NM_177990.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:176661379 T>C maps to NM_020318.2 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:176661379 T>C maps to NM_020318.2 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134072017 G>T maps to NM_032961.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134072017 G>T maps to NM_032961.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134072782 C>A maps to NM_032961.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134072782 C>A maps to NM_032961.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134073067 C>A maps to NM_032961.1 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134073067 C>A maps to NM_032961.1 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:56077051 G>A maps to NM_001142763.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:56077051 G>A maps to NM_001142763.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140207846 G>T maps to NM_018909.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140207846 G>T maps to NM_018909.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140559000 C>A maps to NM_019120.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140559000 C>A maps to NM_019120.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140567413 C>A maps to NM_019119.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140567413 C>A maps to NM_019119.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140740421 A>C maps to NM_018923.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140740421 A>C maps to NM_018923.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:96762020 C>G maps to NM_005390.4 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:96762020 C>G maps to NM_005390.4 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:153069794 G>A maps to ENST00000393758 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:153069794 G>A maps to ENST00000393758 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:71006564 G>C maps to NM_021965.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:71006564 G>C maps to NM_021965.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:229890499 C>A maps to NM_017933.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:229890499 C>A maps to NM_017933.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46656285 C>T maps to NM_006071.1 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46656285 C>T maps to NM_006071.1 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:20474887 T>A maps to NM_022819.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:20474887 T>A maps to NM_022819.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:48558261 G>C maps to NM_003706.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:48558261 G>C maps to NM_003706.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:160862201 C>A maps to NM_007366.4 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:160862201 C>A maps to NM_007366.4 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42044932 C>T maps to NM_000930.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42044932 C>T maps to NM_000930.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:68042640 G>A maps to NM_020715.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:68042640 G>A maps to NM_020715.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:132174173 G>T maps to NM_020911.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:132174173 G>T maps to NM_020911.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118350658 A>T maps to NM_006229.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118350658 A>T maps to NM_006229.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:64684431 T>C maps to NM_002737.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:64684431 T>C maps to NM_002737.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:1557162 G>A maps to NM_006445.3 R2045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:1557162 G>A maps to NM_006445.3 R2045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:227073238 C>T maps to ENST00000391872 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:227073238 C>T maps to ENST00000391872 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43258603 G>C maps to NM_182707.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43258603 G>C maps to NM_182707.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43763021 G>T maps to NM_002784.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43763021 G>T maps to NM_002784.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:46945139 C>A maps to NM_000316.2 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:46945139 C>A maps to NM_000316.2 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:8485783 G>A maps to NM_002839.3 F1011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:8485783 G>A maps to NM_002839.3 F1011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:178426889 G>T maps to ENST00000263528 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:178426889 G>T maps to ENST00000263528 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4770301 G>T maps to NM_014737.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4770301 G>T maps to NM_014737.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:110106874 T>A maps to ENST00000405097 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:110106874 T>A maps to ENST00000405097 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:79254298 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:79254298 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:73103418 G>T maps to NM_152222.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:73103418 G>T maps to NM_152222.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:62634765 G>A maps to NM_014836.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:62634765 G>A maps to NM_014836.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42725240 G>A maps to NM_030954.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42725240 G>A maps to NM_030954.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:51175400 C>G maps to ENST00000251020 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:51175400 C>G maps to ENST00000251020 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:92733058 C>A maps to NM_017654.3 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:92733058 C>A maps to NM_017654.3 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:123513340 G>A maps to NM_018400.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:123513340 G>A maps to NM_018400.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:9122841 G>A maps to NM_003966.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:9122841 G>A maps to NM_003966.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:110310789 T>C maps to ENST00000356688 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:110310789 T>C maps to ENST00000356688 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61587110 C>T maps to NM_005024.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61587110 C>T maps to NM_005024.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51217449 G>T maps to ENST00000391814 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51217449 G>T maps to ENST00000391814 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:16973309 G>T maps to NM_015260.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:16973309 G>T maps to NM_015260.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48537079 C>A maps to NM_000338.2 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48537079 C>A maps to NM_000338.2 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:50519375 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:50519375 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:45353678 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:45353678 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:118475608 G>T maps to NM_001029858.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:118475608 G>T maps to NM_001029858.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:21446890 C>A maps to NM_134431.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:21446890 C>A maps to NM_134431.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:105763285 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:105763285 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31484882 C>T maps to ENST00000454496 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31484882 C>T maps to ENST00000454496 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:73449043 G>T maps to NM_006062.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:73449043 G>T maps to NM_006062.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51621444 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51621444 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:22414372 G>A maps to NM_005775.4 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:22414372 G>A maps to NM_005775.4 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:121429396 A>T maps to NM_003105.5 K921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:121429396 A>T maps to NM_003105.5 K921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:88773938 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:88773938 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:123594226 A>G maps to NM_001174046.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:123594226 A>G maps to NM_001174046.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:52951089 G>T maps to NM_145263.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:52951089 G>T maps to NM_145263.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:89764599 C>A maps to NM_152339.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:89764599 C>A maps to NM_152339.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55653023 C>G maps to NM_032681.3 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55653023 C>G maps to NM_032681.3 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55657474 G>T maps to NM_032681.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55657474 G>T maps to NM_032681.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:36708819 C>A maps to NM_025248.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:36708819 C>A maps to NM_025248.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:206566978 C>T maps to ENST00000414359 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:206566978 C>T maps to ENST00000414359 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:629552 T>A maps to NM_080725.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:629552 T>A maps to NM_080725.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:46305850 G>T maps to NM_001161841.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:46305850 G>T maps to NM_001161841.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:149881029 A>G maps to NM_014849.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:149881029 A>G maps to NM_014849.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:113151816 C>T maps to ENST00000374463 V3294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:113151816 C>T maps to ENST00000374463 V3294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:33260910 A>G maps to NM_003490.3 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:33260910 A>G maps to NM_003490.3 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:149700626 G>T maps to NM_015093.4 G526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:149700626 G>T maps to NM_015093.4 G526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:74178874 G>T maps to NM_153356.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:74178874 G>T maps to NM_153356.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120924345 A>T maps to NM_152715.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120924345 A>T maps to NM_152715.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:44255480 C>A maps to NM_182539.3 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:44255480 C>A maps to NM_182539.3 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:30695246 T>C maps to NM_031271.3 T2468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:30695246 T>C maps to NM_031271.3 T2468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:41847786 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:41847786 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:2375140 C>G maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:2375140 C>G maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:54185440 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:54185440 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8079331 G>A maps to NM_032354.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8079331 G>A maps to NM_032354.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:129559151 C>G maps to NM_133448.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:129559151 C>G maps to NM_133448.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:75969071 G>A maps to NM_018247.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:75969071 G>A maps to NM_018247.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:8000138 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:8000138 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10920155 C>A maps to NM_199261.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10920155 C>A maps to NM_199261.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:98574386 G>T maps to ENST00000359863 P2740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:98574386 G>T maps to ENST00000359863 P2740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:167754800 G>A maps to NM_031949.4 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:167754800 G>A maps to NM_031949.4 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179432975 G>A maps to NM_133378.4 Y23393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179432975 G>A maps to NM_133378.4 Y23393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179450006 G>T maps to NM_133378.4 A18920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179450006 G>T maps to NM_133378.4 A18920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179616644 A>C maps to ENST00000375038 S3496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179616644 A>C maps to ENST00000375038 S3496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179659834 G>A maps to NM_133378.4 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179659834 G>A maps to NM_133378.4 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70460880 A>G maps to ENST00000514019 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70460880 A>G maps to ENST00000514019 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:69879758 A>T maps to ENST00000381096 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:69879758 A>T maps to ENST00000381096 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70160484 C>T maps to NM_053039.1 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70160484 C>T maps to NM_053039.1 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:35583677 C>T maps to ENST00000416672 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:35583677 C>T maps to ENST00000416672 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216166437 G>A maps to ENST00000366943 G2243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216166437 G>A maps to ENST00000366943 G2243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:108303495 A>T maps to NM_006113.4 C309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:108303495 A>T maps to NM_006113.4 C309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61077679 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61077679 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:5239289 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:5239289 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:17353088 G>T maps to NM_022166.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:17353088 G>T maps to NM_022166.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:100349668 C>A maps to ENST00000349350 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:100349668 C>A maps to ENST00000349350 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62421330 A>T maps to NM_025224.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62421330 A>T maps to NM_025224.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:110023680 A>T maps to NM_033390.1 K271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:110023680 A>T maps to NM_033390.1 K271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:77765001 G>T maps to NM_024721.4 G1949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:77765001 G>T maps to NM_024721.4 G1949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36884791 A>G maps to NM_133466.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36884791 A>G maps to NM_133466.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:22155158 C>A maps to NM_007153.3 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:22155158 C>A maps to NM_007153.3 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:20003498 A>C maps to NM_021047.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:20003498 A>C maps to NM_021047.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:90484243 G>T maps to NM_182976.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:90484243 G>T maps to NM_182976.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44776033 C>T maps to NM_145044.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44776033 C>T maps to NM_145044.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:52376332 C>A maps to NM_032679.2 G304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:52376332 C>A maps to NM_032679.2 G304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:40773111 T>C maps to NM_033160.5 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:40773111 T>C maps to NM_033160.5 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:63726940 C>T maps to NM_153363.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:63726940 C>T maps to NM_153363.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53086275 G>T maps to NM_001172655.1 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53086275 G>T maps to NM_001172655.1 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:265784 A>T maps to ENST00000419098 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:265784 A>T maps to ENST00000419098 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:20736524 C>A maps to NM_001159293.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:20736524 C>A maps to NM_001159293.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:21116874 G>T maps to NM_003429.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:21116874 G>T maps to NM_003429.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:238053191 C>A maps to NM_021186.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:238053191 C>A maps to NM_021186.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:127426973 C>T maps to ENST00000356792 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:127426973 C>T maps to ENST00000356792 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:62371044 C>T maps to NM_173519.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:62371044 C>T maps to NM_173519.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:95363437 C>A maps to NM_001839.3 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:95363437 C>A maps to NM_001839.3 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:74702789 G>A maps to NM_002993.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:74702789 G>A maps to NM_002993.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:107846994 G>A maps to NM_014421.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:107846994 G>A maps to NM_014421.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:40284373 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:40284373 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:124907980 C>T maps to NM_005519.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:124907980 C>T maps to NM_005519.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:3304665 C>T maps to NM_000243.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:3304665 C>T maps to NM_000243.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:33570261 C>T maps to NM_020884.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:33570261 C>T maps to NM_020884.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:80246365 T>C maps to NM_032693.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:80246365 T>C maps to NM_032693.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:6006964 G>A maps to NM_016588.2 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:6006964 G>A maps to NM_016588.2 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr11:56058355 A>G maps to NM_001005199.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr11:56058355 A>G maps to NM_001005199.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:47269939 C>A maps to NM_020820.3 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:47269939 C>A maps to NM_020820.3 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:45814447 C>A maps to NM_013309.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:45814447 C>A maps to NM_013309.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr19:17992968 G>T maps to NM_000453.2 G395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr19:17992968 G>T maps to NM_000453.2 G395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr13:84453706 G>T maps to NM_052910.1 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr13:84453706 G>T maps to NM_052910.1 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:47685805 G>A maps to ENST00000371883 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:47685805 G>A maps to ENST00000371883 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:190903838 C>A maps to ENST00000248151 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:190903838 C>A maps to ENST00000248151 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:4920916 A>G maps to NM_016936.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:4920916 A>G maps to NM_016936.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:215823978 A>G maps to ENST00000366943 S4766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:215823978 A>G maps to ENST00000366943 S4766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:124266479 G>T maps to NM_007222.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:124266479 G>T maps to NM_007222.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:1063562 G>A maps to NM_019112.3 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:1063562 G>A maps to NM_019112.3 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr16:48244897 C>T maps to NM_032583.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr16:48244897 C>T maps to NM_032583.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:30197041 A>G maps to NM_032204.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:30197041 A>G maps to NM_032204.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:107390627 C>T maps to NM_001080450.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:107390627 C>T maps to NM_001080450.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:127429727 C>T maps to ENST00000356792 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:127429727 C>T maps to ENST00000356792 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:21988399 C>T maps to NM_152612.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:21988399 C>T maps to NM_152612.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr9:35616192 G>C maps to NM_001782.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr9:35616192 G>C maps to NM_001782.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:175742789 G>A maps to NM_001822.4 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:175742789 G>A maps to NM_001822.4 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:76711919 T>C maps to NM_003868.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:76711919 T>C maps to NM_003868.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:76728563 T>A maps to NM_001563.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:76728563 T>A maps to NM_001563.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:37034382 A>G maps to NM_006148.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:37034382 A>G maps to NM_006148.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:10412920 G>A maps to NM_005963.3 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:10412920 G>A maps to NM_005963.3 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:30035168 C>T maps to NM_181832.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:30035168 C>T maps to NM_181832.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:56572883 G>A maps to NM_153447.4 W1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:56572883 G>A maps to NM_153447.4 W1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:8809555 G>A maps to NM_000916.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:8809555 G>A maps to NM_000916.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:140554533 C>T maps to NM_018940.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:140554533 C>T maps to NM_018940.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr7:84644481 G>A maps to NM_152754.2 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr7:84644481 G>A maps to NM_152754.2 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:160679699 C>T maps to NM_003058.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:160679699 C>T maps to NM_003058.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:9460846 T>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:9460846 T>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:152751685 T>C maps to NM_182961.2 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:152751685 T>C maps to NM_182961.2 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:62230408 C>T maps to NM_018469.3 K1019K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:62230408 C>T maps to NM_018469.3 K1019K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr15:35274486 T>C maps to NM_014106.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr15:35274486 T>C maps to NM_014106.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:41245543 G>A maps to ENST00000471181 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:41245543 G>A maps to ENST00000471181 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:32682935 C>A maps to NM_019118.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:32682935 C>A maps to NM_019118.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:158153921 C>T maps to NM_001766.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:158153921 C>T maps to NM_001766.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:45134847 G>T maps to NM_022842.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:45134847 G>T maps to NM_022842.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:165561010 C>A maps to ENST00000392717 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:165561010 C>A maps to ENST00000392717 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:110822017 A>G maps to NM_001845.4 G1278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:110822017 A>G maps to NM_001845.4 G1278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17058019 C>T maps to ENST00000443236 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17058019 C>T maps to ENST00000443236 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:206325296 G>A maps to ENST00000361052 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:206325296 G>A maps to ENST00000361052 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:63999375 G>A maps to NM_005528.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:63999375 G>A maps to NM_005528.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chrX:154128188 G>A maps to NM_000132.3 S2075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chrX:154128188 G>A maps to NM_000132.3 S2075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:19042356 C>T maps to NM_004838.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:19042356 C>T maps to NM_004838.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:7618422 C>T maps to ENST00000256861 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:7618422 C>T maps to ENST00000256861 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:6505921 G>A maps to NM_006854.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:6505921 G>A maps to NM_006854.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:88106792 G>A maps to NM_020803.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:88106792 G>A maps to NM_020803.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587660 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587660 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:68687142 C>A maps to NM_178011.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:68687142 C>A maps to NM_178011.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:62938754 A>T maps to ENST00000393630 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:62938754 A>T maps to ENST00000393630 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:100928725 T>C maps to ENST00000392986 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:100928725 T>C maps to ENST00000392986 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:125289308 G>A maps to ENST00000359439 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:125289308 G>A maps to ENST00000359439 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:52867115 G>A maps to NM_004153.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:52867115 G>A maps to NM_004153.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:110455938 G>T maps to ENST00000426474 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:110455938 G>T maps to ENST00000426474 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:2906185 C>A maps to NM_022119.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:2906185 C>A maps to NM_022119.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:94487167 G>A maps to NM_004560.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:94487167 G>A maps to NM_004560.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:10334756 G>A maps to NM_004230.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:10334756 G>A maps to NM_004230.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr18:33694105 C>A maps to NM_012319.3 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr18:33694105 C>A maps to NM_012319.3 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:11100014 C>T maps to NM_001128849.1 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:11100014 C>T maps to NM_001128849.1 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:220476446 C>T maps to NM_052902.2 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:220476446 C>T maps to NM_052902.2 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:23793961 A>T maps to NM_031414.3 K388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:23793961 A>T maps to NM_031414.3 K388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:143141100 C>A maps to NM_177437.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:143141100 C>A maps to NM_177437.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:145883475 C>A maps to NM_006706.3 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:145883475 C>A maps to NM_006706.3 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:72091177 C>A maps to NM_018279.3 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:72091177 C>A maps to NM_018279.3 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:30128629 G>T maps to NM_006778.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:30128629 G>T maps to NM_006778.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:135053497 G>A maps to NM_014468.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:135053497 G>A maps to NM_014468.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:49510017 G>A maps to NM_181442.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:49510017 G>A maps to NM_181442.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:139907855 T>A maps to ENST00000253810 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:139907855 T>A maps to ENST00000253810 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:46244482 C>A maps to NM_152641.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:46244482 C>A maps to NM_152641.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:127426554 A>T maps to ENST00000356792 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:127426554 A>T maps to ENST00000356792 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:27805333 C>A maps to NM_032266.3 L1965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:27805333 C>A maps to NM_032266.3 L1965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:2229899 G>T maps to NM_020764.3 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:2229899 G>T maps to NM_020764.3 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:28702078 A>T maps to NM_018318.3 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:28702078 A>T maps to NM_018318.3 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:17280754 C>G maps to NM_014675.3 S1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:17280754 C>G maps to NM_014675.3 S1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:44789290 G>T maps to NM_016396.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:44789290 G>T maps to NM_016396.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:7708676 C>T maps to NM_020877.2 N3136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:7708676 C>T maps to NM_020877.2 N3136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:97839178 C>A maps to NM_000110.3 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:97839178 C>A maps to NM_000110.3 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:77438542 T>A maps to NM_203394.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:77438542 T>A maps to NM_203394.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:22237268 G>T maps to NM_013302.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:22237268 G>T maps to NM_013302.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:51829697 G>C maps to NM_001981.2 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:51829697 G>C maps to NM_001981.2 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:157514256 G>T maps to NM_031281.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:157514256 G>T maps to NM_031281.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr13:28602426 T>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr13:28602426 T>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:220307775 G>T maps to NM_018060.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:220307775 G>T maps to NM_018060.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:1718519 G>T maps to NM_001012416.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:1718519 G>T maps to NM_001012416.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:88476272 C>A maps to NM_001171610.1 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:88476272 C>A maps to NM_001171610.1 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr13:76397901 C>T maps to ENST00000357063 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr13:76397901 C>T maps to ENST00000357063 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:238462216 G>T maps to NM_024101.5 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:238462216 G>T maps to NM_024101.5 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:46781865 C>A maps to NM_182493.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:46781865 C>A maps to NM_182493.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:164271826 A>T maps to NM_006174.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:164271826 A>T maps to NM_006174.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:45799762 C>A maps to NM_001004297.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:45799762 C>A maps to NM_001004297.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248684958 C>A maps to NM_001013355.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248684958 C>A maps to NM_001013355.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248458841 T>C maps to NM_001004692.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248458841 T>C maps to NM_001004692.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:55418436 G>T maps to NM_001004059.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:55418436 G>T maps to NM_001004059.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:24537107 G>T maps to NM_001142386.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:24537107 G>T maps to NM_001142386.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:40581050 C>T maps to NM_004573.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:40581050 C>T maps to NM_004573.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:146311745 C>T maps to NM_001085420.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:146311745 C>T maps to NM_001085420.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:17487842 G>A maps to NM_031310.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:17487842 G>A maps to NM_031310.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:41936718 G>A maps to NM_138338.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:41936718 G>A maps to NM_138338.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:120106159 G>A maps to NM_006253.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:120106159 G>A maps to NM_006253.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:48711843 C>G maps to NM_006904.6 G3407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:48711843 C>G maps to NM_006904.6 G3407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:29855756 C>A maps to NM_032932.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:29855756 C>A maps to NM_032932.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:67686372 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:67686372 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:1159281 C>A maps to NM_016176.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:1159281 C>A maps to NM_016176.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:20618728 C>T maps to ENST00000273739 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:20618728 C>T maps to ENST00000273739 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:95162157 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:95162157 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:40453373 C>T maps to NM_003152.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:40453373 C>T maps to NM_003152.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:152059799 G>A maps to NM_001008536.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:152059799 G>A maps to NM_001008536.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:84228379 G>A maps to NM_005077.3 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:84228379 G>A maps to NM_005077.3 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:98129869 G>A maps to NM_012465.3 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:98129869 G>A maps to NM_012465.3 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:35712915 C>G maps to NM_006289.3 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:35712915 C>G maps to NM_006289.3 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:100353717 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:100353717 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:223990465 C>T maps to NM_001031685.2 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:223990465 C>T maps to NM_001031685.2 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:68490852 T>A maps to NM_018227.5 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:68490852 T>A maps to NM_018227.5 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:156268935 C>A maps to NM_001004319.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:156268935 C>A maps to NM_001004319.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:58083956 C>A maps to NM_017879.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:58083956 C>A maps to NM_017879.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:100226947 G>A maps to NM_014361.2 W1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:100226947 G>A maps to NM_014361.2 W1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:35556238 G>T maps to NM_182983.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:35556238 G>T maps to NM_182983.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:233497908 G>T maps to NM_032435.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:233497908 G>T maps to NM_032435.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:183217605 C>A maps to NM_130446.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:183217605 C>A maps to NM_130446.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:71494206 C>A maps to NM_005909.3 G1675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:71494206 C>A maps to NM_005909.3 G1675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:55904779 G>T maps to NM_001004064.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:55904779 G>T maps to NM_001004064.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:140784117 G>A maps to NM_018921.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:140784117 G>A maps to NM_018921.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:2411673 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:2411673 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:125618591 C>T maps to NM_023928.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:125618591 C>T maps to NM_023928.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:121756791 C>T maps to NM_005763.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:121756791 C>T maps to NM_005763.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:66928613 A>T maps to NM_007168.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:66928613 A>T maps to NM_007168.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20432711 G>T maps to NM_017888.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20432711 G>T maps to NM_017888.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:156915449 G>T maps to ENST00000430702 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:156915449 G>T maps to ENST00000430702 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:97506547 T>G maps to NM_144994.7 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:97506547 T>G maps to NM_144994.7 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:36561668 G>T maps to NM_001177506.1 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:36561668 G>T maps to NM_001177506.1 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:61907552 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:61907552 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:235377132 C>A maps to NM_016374.5 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:235377132 C>A maps to NM_016374.5 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:31324968 T>A maps to NM_030632.1 A1719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:31324968 T>A maps to NM_030632.1 A1719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:160106719 C>T maps to NM_000702.3 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:160106719 C>T maps to NM_000702.3 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:77301003 G>A maps to ENST00000355691 W1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:77301003 G>A maps to ENST00000355691 W1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:117040881 C>A maps to NM_207303.2 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:117040881 C>A maps to NM_207303.2 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:31898025 C>T maps to NM_194318.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:31898025 C>T maps to NM_194318.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156622223 T>A maps to NM_021948.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156622223 T>A maps to NM_021948.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:60985524 G>A maps to NM_000633.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:60985524 G>A maps to NM_000633.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:6231696 C>T maps to NM_173525.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:6231696 C>T maps to NM_173525.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:30806758 G>A maps to NM_001105528.1 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:30806758 G>A maps to NM_001105528.1 Q552*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-5428-01A-01D-1625-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-05-5428-01A-01D-1625-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:172425553 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:172425553 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:57351622 C>T maps to NM_000562.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:57351622 C>T maps to NM_000562.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:159170654 C>T maps to NM_021189.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:159170654 C>T maps to NM_021189.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:70209224 G>A maps to NM_182511.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:70209224 G>A maps to NM_182511.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:219870196 C>T maps to NM_194302.2 Q1670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:219870196 C>T maps to NM_194302.2 Q1670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:106152063 C>A maps to NM_001008723.1 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:106152063 C>A maps to NM_001008723.1 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:14135349 G>T maps to NM_004233.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:14135349 G>T maps to NM_004233.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:48207329 A>T maps to NM_001789.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:48207329 A>T maps to NM_001789.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:64604409 C>T maps to NM_017525.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:64604409 C>T maps to NM_017525.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:24491685 C>A maps to NM_006727.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:24491685 C>A maps to NM_006727.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:53999057 G>A maps to NM_001008708.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:53999057 G>A maps to NM_001008708.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:66049782 G>C maps to NM_182553.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:66049782 G>C maps to NM_182553.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:75799843 C>A maps to ENST00000322507 G2975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:75799843 C>A maps to ENST00000322507 G2975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:211512693 C>A maps to NM_001122633.1 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:211512693 C>A maps to NM_001122633.1 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:151908929 C>T maps to ENST00000370291 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:151908929 C>T maps to ENST00000370291 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:16942701 G>A maps to NM_001081.3 Q2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:16942701 G>A maps to NM_001081.3 Q2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:13866015 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:13866015 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:65855118 G>A maps to ENST00000371069 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:65855118 G>A maps to ENST00000371069 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:446548 C>A maps to NM_203447.3 T1920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:446548 C>A maps to NM_203447.3 T1920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:60484418 C>A maps to NM_001144933.1 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:60484418 C>A maps to NM_001144933.1 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:12022454 G>C maps to NM_001987.4 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:12022454 G>C maps to NM_001987.4 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:176832079 G>A maps to NM_000505.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:176832079 G>A maps to NM_000505.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:92353591 G>A maps to ENST00000267620 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:92353591 G>A maps to ENST00000267620 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:73492452 G>T maps to ENST00000295133 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:73492452 G>T maps to ENST00000295133 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:52188725 G>T maps to ENST00000344768 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:52188725 G>T maps to ENST00000344768 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:2279092 C>T maps to NM_013393.1 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:2279092 C>T maps to NM_013393.1 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:161302568 G>A maps to NM_001127648.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:161302568 G>A maps to NM_001127648.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27159958 C>T maps to NM_000810.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27159958 C>T maps to NM_000810.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:46849192 G>A maps to NM_015234.4 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:46849192 G>A maps to NM_015234.4 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:37356599 C>T maps to NM_000831.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:37356599 C>T maps to NM_000831.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:7920966 C>A maps to NM_017545.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:7920966 C>A maps to NM_017545.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:43484720 G>T maps to NM_015052.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:43484720 G>T maps to NM_015052.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:113848527 C>T maps to NM_213621.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:113848527 C>T maps to NM_213621.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:10402219 G>A maps to NM_003259.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:10402219 G>A maps to NM_003259.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:226923449 G>T maps to NM_002221.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:226923449 G>T maps to NM_002221.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:124196145 C>T maps to NM_001024660.3 Q1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:124196145 C>T maps to NM_001024660.3 Q1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:110766517 G>T maps to NM_004978.4 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:110766517 G>T maps to NM_004978.4 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:62046379 G>T maps to NM_172107.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:62046379 G>T maps to NM_172107.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:36788632 C>A maps to NM_001031836.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:36788632 C>A maps to NM_001031836.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:62757845 T>A maps to NM_152688.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:62757845 T>A maps to NM_152688.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:105350345 C>T maps to ENST00000453495 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:105350345 C>T maps to ENST00000453495 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:72292513 C>A maps to NM_014431.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:72292513 C>A maps to NM_014431.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:72300941 C>T maps to NM_014431.2 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:72300941 C>T maps to NM_014431.2 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:94156555 C>T maps to ENST00000393153 A2454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:94156555 C>T maps to ENST00000393153 A2454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:36350468 C>T maps to NM_199180.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:36350468 C>T maps to NM_199180.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:30260370 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:30260370 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:39538047 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:39538047 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:25932627 G>T maps to ENST00000268763 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:25932627 G>T maps to ENST00000268763 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:17597047 C>T maps to NM_015907.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:17597047 C>T maps to NM_015907.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:44626162 C>T maps to NM_001006607.2 Q1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:44626162 C>T maps to NM_001006607.2 Q1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:61744397 C>T maps to NM_203351.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:61744397 C>T maps to NM_203351.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:196733535 G>A maps to NM_005929.5 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:196733535 G>A maps to NM_005929.5 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:41991272 A>T maps to ENST00000219905 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:41991272 A>T maps to ENST00000219905 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:102573541 C>A maps to NM_022122.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:102573541 C>A maps to NM_022122.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:60268516 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:60268516 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:109610050 C>A maps to NM_015011.1 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:109610050 C>A maps to NM_015011.1 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:232389975 G>T maps to NM_006056.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:232389975 G>T maps to NM_006056.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:95076671 C>A maps to NM_017948.5 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:95076671 C>A maps to NM_017948.5 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:164247105 G>A maps to NM_000909.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:164247105 G>A maps to NM_000909.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:167654945 G>A maps to NM_001122679.1 R1768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:167654945 G>A maps to NM_001122679.1 R1768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:53616043 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:53616043 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:98105778 C>A maps to NM_033207.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:98105778 C>A maps to NM_033207.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:22038044 G>A maps to NM_001005465.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:22038044 G>A maps to NM_001005465.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158450320 G>C maps to NM_001004472.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158450320 G>C maps to NM_001004472.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:45798998 A>T maps to NM_001004297.2 L291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:45798998 A>T maps to NM_001004297.2 L291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:107361214 T>G maps to NM_001004482.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:107361214 T>G maps to NM_001004482.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:9204054 C>T maps to ENST00000305465 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:9204054 C>T maps to ENST00000305465 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:248637271 C>A maps to NM_001005495.1 C207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:248637271 C>A maps to NM_001005495.1 C207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:55433433 C>T maps to NM_001004704.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:55433433 C>T maps to NM_001004704.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:4967799 G>A maps to NM_001005329.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:4967799 G>A maps to NM_001005329.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:4608962 A>T maps to NM_001005170.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:4608962 A>T maps to NM_001005170.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:57268854 G>A maps to NM_021728.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:57268854 G>A maps to NM_021728.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:176762726 C>G maps to NM_020318.2 P1684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:176762726 C>G maps to NM_020318.2 P1684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156214603 G>C maps to NM_024897.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156214603 G>C maps to NM_024897.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:31815102 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:31815102 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:134084250 C>T maps to NM_032961.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:134084250 C>T maps to NM_032961.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:71518645 T>C maps to NM_014982.2 S1498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:71518645 T>C maps to NM_014982.2 S1498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:9780179 C>T maps to ENST00000361110 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:9780179 C>T maps to ENST00000361110 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:110477364 G>A maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:110477364 G>A maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:2419130 C>T maps to NM_014638.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:2419130 C>T maps to NM_014638.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:140400119 C>A maps to NM_001098537.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:140400119 C>A maps to NM_001098537.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:121207930 C>A maps to ENST00000393672 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:121207930 C>A maps to ENST00000393672 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:19553697 C>T maps to NM_001005356.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:19553697 C>T maps to NM_001005356.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:30095756 G>A maps to NM_002742.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:30095756 G>A maps to NM_002742.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:27216633 G>A maps to NM_005865.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:27216633 G>A maps to NM_005865.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:43680271 G>T maps to ENST00000270059 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:43680271 G>T maps to ENST00000270059 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:97312031 C>T maps to NM_014754.1 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:97312031 C>T maps to NM_014754.1 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:150240365 G>A maps to NM_001001788.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:150240365 G>A maps to NM_001001788.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:48390445 C>A maps to NM_002900.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:48390445 C>A maps to NM_002900.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:21511198 G>T maps to NM_032572.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:21511198 G>T maps to NM_032572.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:219529493 C>A maps to NM_022453.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:219529493 C>A maps to NM_022453.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:224462308 C>T maps to NM_003469.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:224462308 C>T maps to NM_003469.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:139301806 G>A maps to NM_001039707.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:139301806 G>A maps to NM_001039707.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:71427795 A>T maps to NM_001144952.1 L442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:71427795 A>T maps to NM_001144952.1 L442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:9044622 G>C maps to NM_003966.2 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:9044622 G>C maps to NM_003966.2 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:115782851 C>A maps to ENST00000257414 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:115782851 C>A maps to ENST00000257414 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:99531422 G>A maps to NM_003015.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:99531422 G>A maps to NM_003015.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:44676137 C>T maps to NM_001134771.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:44676137 C>T maps to NM_001134771.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:100459432 G>T maps to NM_020246.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:100459432 G>T maps to NM_020246.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:61424036 C>A maps to NM_194298.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:61424036 C>A maps to NM_194298.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:72332250 G>T maps to NM_001098484.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:72332250 G>T maps to NM_001098484.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:143297459 T>A maps to NM_173653.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:143297459 T>A maps to NM_173653.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:121706014 G>A maps to NM_021021.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:121706014 G>A maps to NM_021021.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:10906287 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:10906287 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:2042715 G>A maps to NM_004209.5 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:2042715 G>A maps to NM_004209.5 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:33455796 G>T maps to ENST00000455217 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:33455796 G>T maps to ENST00000455217 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:44561101 G>T maps to NM_016427.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:44561101 G>T maps to NM_016427.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:11415465 T>A maps to ENST00000423059 R1643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:11415465 T>A maps to ENST00000423059 R1643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:164393185 G>T maps to NM_032136.4 Y567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:164393185 G>T maps to NM_032136.4 Y567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:94975549 C>A maps to NM_020698.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:94975549 C>A maps to NM_020698.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:41121751 G>A maps to NM_178174.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:41121751 G>A maps to NM_178174.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:51872732 G>T maps to NM_173485.5 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:51872732 G>T maps to NM_173485.5 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:31769591 C>T maps to NM_020856.2 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:31769591 C>T maps to NM_020856.2 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20352543 C>T maps to ENST00000424589 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20352543 C>T maps to ENST00000424589 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:62783401 A>T maps to ENST00000280377 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:62783401 A>T maps to ENST00000280377 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:161130615 G>T maps to NM_012475.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:161130615 G>T maps to NM_012475.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:7912985 G>A maps to NM_006786.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:7912985 G>A maps to NM_006786.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:96061493 G>T maps to ENST00000297954 S2059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:96061493 G>T maps to ENST00000297954 S2059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:30584764 C>T maps to NM_001011718.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:30584764 C>T maps to NM_001011718.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:111698291 C>A maps to NM_001004308.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:111698291 C>A maps to NM_001004308.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:85010787 G>A maps to NM_001145548.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:85010787 G>A maps to NM_001145548.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:2307055 G>T maps to NM_020972.2 Y337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:2307055 G>T maps to NM_020972.2 Y337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:11833306 G>A maps to NM_001080493.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:11833306 G>A maps to NM_001080493.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr11:44297152 C>A maps to NM_021926.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr11:44297152 C>A maps to NM_021926.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:37430989 G>T maps to ENST00000374660 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:37430989 G>T maps to ENST00000374660 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chrX:50659037 C>T maps to NM_005448.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chrX:50659037 C>T maps to NM_005448.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr14:95932464 G>A maps to NM_152592.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr14:95932464 G>A maps to NM_152592.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:196706689 G>C maps to NM_000186.3 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:196706689 G>C maps to NM_000186.3 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:1270961 T>G maps to ENST00000413636 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:1270961 T>G maps to ENST00000413636 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr21:41384969 G>T maps to NM_001389.3 T2010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr21:41384969 G>T maps to NM_001389.3 T2010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:87487668 G>A maps to NM_017551.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:87487668 G>A maps to NM_017551.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:60889673 G>A maps to NM_005560.3 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:60889673 G>A maps to NM_005560.3 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr11:34153689 T>C maps to NM_024662.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr11:34153689 T>C maps to NM_024662.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:124840076 G>A maps to NM_006312.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:124840076 G>A maps to NM_006312.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:5283318 G>A maps to NM_144773.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:5283318 G>A maps to NM_144773.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr21:33073367 T>C maps to NM_020706.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr21:33073367 T>C maps to NM_020706.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr5:139751847 C>T maps to ENST00000507527 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr5:139751847 C>T maps to ENST00000507527 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr2:191873762 G>A maps to NM_007315.3 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr2:191873762 G>A maps to NM_007315.3 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:248039631 C>G maps to NM_015431.3 Y434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:248039631 C>G maps to NM_015431.3 Y434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:27088650 C>T maps to NM_006015.4 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:27088650 C>T maps to NM_006015.4 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:123670658 G>A maps to NM_001001976.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:123670658 G>A maps to NM_001001976.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:25958905 G>A maps to NM_024490.3 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:25958905 G>A maps to NM_024490.3 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88677024 C>T maps to NM_004329.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88677024 C>T maps to NM_004329.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:58599889 C>A maps to ENST00000438670 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:58599889 C>A maps to ENST00000438670 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:149944649 G>A maps to ENST00000438086 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:149944649 G>A maps to ENST00000438086 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:214788287 C>G maps to NM_016343.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:214788287 C>G maps to NM_016343.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:154543727 C>T maps to NM_000748.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:154543727 C>T maps to NM_000748.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:165584559 G>A maps to ENST00000392717 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:165584559 G>A maps to ENST00000392717 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:39307727 C>T maps to NM_001171174.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:39307727 C>T maps to NM_001171174.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:143958263 C>G maps to ENST00000377675 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:143958263 C>G maps to ENST00000377675 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:28602409 C>T maps to NM_001941.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:28602409 C>T maps to NM_001941.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:7581354 G>A maps to NM_004415.2 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:7581354 G>A maps to NM_004415.2 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:121591539 C>A maps to NM_018456.4 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:121591539 C>A maps to NM_018456.4 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:29668238 G>A maps to NM_013986.3 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:29668238 G>A maps to NM_013986.3 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:197036344 C>T maps to NM_001994.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:197036344 C>T maps to NM_001994.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:59064388 C>T maps to NM_001040450.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:59064388 C>T maps to NM_001040450.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49469608 G>T maps to NM_000146.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49469608 G>T maps to NM_000146.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr20:42984467 C>T maps to NM_175914.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr20:42984467 C>T maps to NM_175914.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:3156081 G>A maps to NM_002111.6 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:3156081 G>A maps to NM_002111.6 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:7759699 C>A maps to NM_002216.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:7759699 C>A maps to NM_002216.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:6966262 G>A maps to NM_005559.2 D2311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:6966262 G>A maps to NM_005559.2 D2311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:6580190 G>C maps to NM_015274.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:6580190 G>C maps to NM_015274.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:42040833 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:42040833 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:29664476 T>G maps to NM_001042492.2 A2173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:29664476 T>G maps to NM_001042492.2 A2173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:3381996 C>G maps to ENST00000269778 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:3381996 C>G maps to ENST00000269778 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:105167114 A>T maps to NM_198465.2 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:105167114 A>T maps to NM_198465.2 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:241767855 G>A maps to NM_014322.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:241767855 G>A maps to NM_014322.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:143633080 C>T maps to NM_001004685.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:143633080 C>T maps to NM_001004685.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:59224645 C>T maps to NM_001004708.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:59224645 C>T maps to NM_001004708.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:63280139 C>T maps to NM_014562.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:63280139 C>T maps to NM_014562.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:44124205 C>T maps to NM_031292.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:44124205 C>T maps to NM_031292.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:182571202 C>T maps to NM_002928.3 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:182571202 C>T maps to NM_002928.3 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:92763766 G>A maps to NM_152703.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:92763766 G>A maps to NM_152703.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:72139159 G>A maps to NM_015556.1 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:72139159 G>A maps to NM_015556.1 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:47431695 C>G maps to NM_001128225.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:47431695 C>G maps to NM_001128225.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:48584551 C>G maps to NM_005359.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:48584551 C>G maps to NM_005359.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:231135346 G>A maps to NM_007237.4 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:231135346 G>A maps to NM_007237.4 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:50926965 G>A maps to NM_003121.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:50926965 G>A maps to NM_003121.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:217012853 C>T maps to NM_021141.3 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:217012853 C>T maps to NM_021141.3 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:145161554 G>C maps to NM_014795.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:145161554 G>C maps to NM_014795.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:182026920 G>T maps to NM_001009992.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:182026920 G>T maps to NM_001009992.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:87179791 C>A maps to NM_000927.3 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:87179791 C>A maps to NM_000927.3 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:22281165 G>A maps to NM_213599.2 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:22281165 G>A maps to NM_213599.2 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:182635878 C>G maps to NM_014616.1 S1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:182635878 C>G maps to NM_014616.1 S1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:172447276 C>G maps to NM_003945.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:172447276 C>G maps to NM_003945.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:111923111 C>T maps to NM_002973.3 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:111923111 C>T maps to NM_002973.3 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:657407 C>T maps to NM_173593.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:657407 C>T maps to NM_173593.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:180378510 G>T maps to NM_181426.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:180378510 G>T maps to NM_181426.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:97810017 G>A maps to NM_001134375.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:97810017 G>A maps to NM_001134375.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:6196605 G>T maps to NM_015557.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:6196605 G>T maps to NM_015557.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:78652604 C>A maps to ENST00000512485 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:78652604 C>A maps to ENST00000512485 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:722495 C>A maps to NM_022772.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:722495 C>A maps to NM_022772.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:113772898 G>C maps to NM_000131.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:113772898 G>C maps to NM_000131.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:102706854 G>A maps to NM_001136123.1 W998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:102706854 G>A maps to NM_001136123.1 W998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:87487183 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:87487183 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:42927366 C>T maps to NM_002027.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:42927366 C>T maps to NM_002027.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:42930897 C>T maps to NM_018960.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:42930897 C>T maps to NM_018960.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:42491396 C>A maps to NM_173601.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:42491396 C>A maps to NM_173601.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9162083 C>G maps to NM_005810.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9162083 C>G maps to NM_005810.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:131943068 A>T maps to ENST00000403834 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:131943068 A>T maps to ENST00000403834 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9072491 G>T maps to NM_024690.2 S4985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9072491 G>T maps to NM_024690.2 S4985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:16769270 C>A maps to NM_012334.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:16769270 C>A maps to NM_012334.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:101890209 C>A maps to NM_052867.2 G444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:101890209 C>A maps to NM_052867.2 G444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:35630160 C>T maps to ENST00000400445 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:35630160 C>T maps to ENST00000400445 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:56552449 G>A maps to NM_153447.4 Q983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:56552449 G>A maps to NM_153447.4 Q983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:248201628 A>T maps to NM_001004686.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:248201628 A>T maps to NM_001004686.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9361928 C>T maps to NM_001079935.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9361928 C>T maps to NM_001079935.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:58299397 G>C maps to NM_001040429.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:58299397 G>C maps to NM_001040429.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:70963485 C>T maps to NM_001109754.1 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:70963485 C>T maps to NM_001109754.1 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:52321348 C>T maps to NM_144651.4 A945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:52321348 C>T maps to NM_144651.4 A945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:48916811 G>T maps to NM_000321.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:48916811 G>T maps to NM_000321.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:66099815 A>T maps to NM_004292.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:66099815 A>T maps to NM_004292.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:93118140 C>T maps to NM_024832.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:93118140 C>T maps to NM_024832.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25442835 C>T maps to ENST00000381927 H1469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25442835 C>T maps to ENST00000381927 H1469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:33243777 C>T maps to NM_022551.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:33243777 C>T maps to NM_022551.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:213414787 C>T maps to NM_012424.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:213414787 C>T maps to NM_012424.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:26620731 C>T maps to NM_001007538.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:26620731 C>T maps to NM_001007538.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chrX:591646 G>C maps to NM_000451.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chrX:591646 G>C maps to NM_000451.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44224129 G>A maps to NM_178148.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44224129 G>A maps to NM_178148.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:52257314 A>C maps to ENST00000494383 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:52257314 A>C maps to ENST00000494383 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:123709669 C>A maps to NM_006073.2 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:123709669 C>A maps to NM_006073.2 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:28997431 G>A maps to NM_014817.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:28997431 G>A maps to NM_014817.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:42627404 C>G maps to NM_015255.2 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:42627404 C>G maps to NM_015255.2 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:62908991 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:62908991 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:102187939 C>A maps to NM_175056.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:102187939 C>A maps to NM_175056.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:48204060 C>T maps to NM_032583.3 E1282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:48204060 C>T maps to NM_032583.3 E1282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:48174703 C>T maps to NM_033226.2 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:48174703 C>T maps to NM_033226.2 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:44071701 C>G maps to NM_022437.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:44071701 C>G maps to NM_022437.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:32436253 T>C maps to NM_002197.2 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:32436253 T>C maps to NM_002197.2 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:147743991 G>A maps to NM_002025.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:147743991 G>A maps to NM_002025.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:77272896 C>A maps to NM_015305.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:77272896 C>A maps to NM_015305.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:61832646 C>T maps to NM_020987.2 E2664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:61832646 C>T maps to NM_020987.2 E2664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:21255314 G>C maps to NM_000384.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:21255314 G>C maps to NM_000384.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:97217014 G>A maps to NM_212481.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:97217014 G>A maps to NM_212481.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:76397585 G>A maps to NM_080868.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:76397585 G>A maps to NM_080868.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:92447220 G>A maps to ENST00000347608 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:92447220 G>A maps to ENST00000347608 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:37591709 C>T maps to NM_018302.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:37591709 C>T maps to NM_018302.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:98762071 C>A maps to NM_174952.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:98762071 C>A maps to NM_174952.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:90502662 A>G maps to NM_178828.4 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:90502662 A>G maps to NM_178828.4 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:2775888 C>A maps to NM_199460.2 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:2775888 C>A maps to NM_199460.2 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:128449626 G>T maps to NM_022742.3 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:128449626 G>T maps to NM_022742.3 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:46245042 G>T maps to NM_001295.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:46245042 G>T maps to NM_001295.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:227381577 C>A maps to ENST00000366766 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:227381577 C>A maps to ENST00000366766 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:26881505 A>T maps to NM_016279.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:26881505 A>T maps to NM_016279.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:202000804 A>G maps to NM_001127183.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:202000804 A>G maps to NM_001127183.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:45671312 G>A maps to NM_003654.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:45671312 G>A maps to NM_003654.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:123319299 G>A maps to NM_001010852.2 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:123319299 G>A maps to NM_001010852.2 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:101748342 C>T maps to NM_001855.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:101748342 C>T maps to NM_001855.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:113364658 C>A maps to NM_198123.1 G2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:113364658 C>A maps to NM_198123.1 G2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:155011885 G>T maps to NM_152494.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:155011885 G>T maps to NM_152494.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:52740524 A>G maps to ENST00000451288 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:52740524 A>G maps to ENST00000451288 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:53927146 G>T maps to NM_033067.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:53927146 G>T maps to NM_033067.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:84880403 G>A maps to NM_021233.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:84880403 G>A maps to NM_021233.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:103090681 G>A maps to NM_001080463.1 K2957K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:103090681 G>A maps to NM_001080463.1 K2957K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:187088123 C>G maps to ENST00000356371 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:187088123 C>G maps to ENST00000356371 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:72755321 A>G maps to NM_003602.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:72755321 A>G maps to NM_003602.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:4800710 C>T maps to ENST00000450194 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:4800710 C>T maps to ENST00000450194 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:69798188 C>A maps to NM_020692.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:69798188 C>A maps to NM_020692.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:20329667 G>A maps to NM_001007240.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:20329667 G>A maps to NM_001007240.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:50684044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:50684044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:102503455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:102503455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:152191896 T>A maps to NM_001009931.1 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:152191896 T>A maps to NM_001009931.1 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:111146102 G>A maps to NM_004974.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:111146102 G>A maps to NM_004974.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:121878957 G>A maps to ENST00000377071 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:121878957 G>A maps to ENST00000377071 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:30315635 G>T maps to NM_020848.2 G1147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:30315635 G>T maps to NM_020848.2 G1147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:31768823 G>T maps to NM_181599.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:31768823 G>T maps to NM_181599.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:141625750 G>T maps to NM_018557.2 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:141625750 G>T maps to NM_018557.2 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:57602923 C>T maps to NM_002332.2 V4068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:57602923 C>T maps to NM_002332.2 V4068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:40136612 C>A maps to NM_020929.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:40136612 C>A maps to NM_020929.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:30260300 C>A maps to NM_002367.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:30260300 C>A maps to NM_002367.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:7593513 G>T maps to NM_020533.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:7593513 G>T maps to NM_020533.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:41738662 G>T maps to NM_004527.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:41738662 G>T maps to NM_004527.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:48586034 C>T maps to NM_032133.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:48586034 C>T maps to NM_032133.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:10430314 G>T maps to NM_017534.5 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:10430314 G>T maps to NM_017534.5 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:21306049 C>T maps to NM_174928.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:21306049 C>T maps to NM_174928.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:120466411 C>A maps to NM_024408.2 L1569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:120466411 C>A maps to NM_024408.2 L1569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:14991762 G>T maps to NM_030901.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:14991762 G>T maps to NM_030901.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:18915322 G>T maps to NM_000292.2 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:18915322 G>T maps to NM_000292.2 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:42048919 G>T maps to NM_000930.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:42048919 G>T maps to NM_000930.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:145796986 G>C maps to NM_182943.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:145796986 G>C maps to NM_182943.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:22890728 G>T maps to NM_206954.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:22890728 G>T maps to NM_206954.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:64142981 G>T maps to NM_198859.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:64142981 G>T maps to NM_198859.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:106884175 T>A maps to NM_002764.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:106884175 T>A maps to NM_002764.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:142460822 C>T maps to ENST00000486171 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:142460822 C>T maps to ENST00000486171 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:109380883 A>T maps to NM_006267.4 K1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:109380883 A>T maps to NM_006267.4 K1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:46713149 C>A maps to NM_006915.2 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:46713149 C>A maps to NM_006915.2 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:151107785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:151107785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:33073387 G>A maps to NM_020706.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:33073387 G>A maps to NM_020706.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:52031474 C>A maps to NM_001245.5 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:52031474 C>A maps to NM_001245.5 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:38355271 C>T maps to NM_004803.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:38355271 C>T maps to NM_004803.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:48426632 T>C maps to NM_205850.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:48426632 T>C maps to NM_205850.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:43774756 G>A maps to NM_005424.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:43774756 G>A maps to NM_005424.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:60699469 G>A maps to NM_017870.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:60699469 G>A maps to NM_017870.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:35853737 G>T maps to NM_001042590.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:35853737 G>T maps to NM_001042590.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:101375221 G>T maps to NM_004621.5 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:101375221 G>T maps to NM_004621.5 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:37041395 C>T maps to NM_053276.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:37041395 C>T maps to NM_053276.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:113033703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:113033703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:21860755 C>T maps to ENST00000434536 I999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:21860755 C>T maps to ENST00000434536 I999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:843742 C>A maps to NM_024786.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:843742 C>A maps to NM_024786.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:149191293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:149191293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:39678646 G>A maps to NM_001464.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:39678646 G>A maps to NM_001464.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:7870432 C>T maps to NM_001134647.1 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:7870432 C>T maps to NM_001134647.1 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:9256879 C>T maps to NM_015208.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:9256879 C>T maps to NM_015208.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:95157270 C>T maps to NM_016116.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:95157270 C>T maps to NM_016116.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:156622658 T>C maps to NM_021948.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:156622658 T>C maps to NM_021948.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75038450 G>T maps to NM_001002912.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75038450 G>T maps to NM_001002912.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75055723 A>T maps to NM_001002912.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75055723 A>T maps to NM_001002912.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75065523 C>G maps to NM_001002912.4 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75065523 C>G maps to NM_001002912.4 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:47823816 G>A maps to ENST00000355085 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:47823816 G>A maps to ENST00000355085 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57351649 G>A maps to NM_000562.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57351649 G>A maps to NM_000562.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:181701819 C>T maps to ENST00000357570 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:181701819 C>T maps to ENST00000357570 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:81643765 T>C maps to NM_000722.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:81643765 T>C maps to NM_000722.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:83378606 C>A maps to ENST00000268613 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:83378606 C>A maps to ENST00000268613 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:86913415 G>T maps to NM_006536.5 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:86913415 G>T maps to NM_006536.5 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:157232888 A>T maps to NM_001195555.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:157232888 A>T maps to NM_001195555.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:41333203 G>C maps to NM_001843.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:41333203 G>C maps to NM_001843.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121259924 C>T maps to NM_021110.1 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121259924 C>T maps to NM_021110.1 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:94041393 C>A maps to NM_000089.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:94041393 C>A maps to NM_000089.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:48375179 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:48375179 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:106462127 C>T maps to NM_173494.1 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:106462127 C>T maps to NM_173494.1 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:85404022 G>A maps to NM_053281.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:85404022 G>A maps to NM_053281.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:674760 C>A maps to NM_021008.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:674760 C>A maps to NM_021008.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:7667440 C>T maps to NM_020877.2 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:7667440 C>T maps to NM_020877.2 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:52303262 A>T maps to NM_018100.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:52303262 A>T maps to NM_018100.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:36934499 G>T maps to NM_014800.9 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:36934499 G>T maps to NM_014800.9 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:159052015 A>T maps to NM_001128424.1 L425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:159052015 A>T maps to NM_001128424.1 L425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:152276507 T>G maps to NM_002016.1 A3618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:152276507 T>G maps to NM_002016.1 A3618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:46973175 C>A maps to NM_000809.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:46973175 C>A maps to NM_000809.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:22749299 C>G maps to NM_020973.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:22749299 C>G maps to NM_020973.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:20335216 C>A maps to NM_001007240.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:20335216 C>A maps to NM_001007240.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:105623719 T>A maps to NM_000829.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:105623719 T>A maps to NM_000829.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:94411877 G>T maps to NM_001510.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:94411877 G>T maps to NM_001510.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:146720538 G>A maps to NM_000838.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:146720538 G>A maps to NM_000838.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:156476070 T>A maps to NM_001173393.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:156476070 T>A maps to NM_001173393.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:60324149 A>G maps to NM_015888.4 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:60324149 A>G maps to NM_015888.4 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:23842336 C>T maps to NM_022789.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:23842336 C>T maps to NM_022789.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:63316463 T>C maps to NM_139318.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:63316463 T>C maps to NM_139318.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:28998002 G>A maps to NM_015254.3 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:28998002 G>A maps to NM_015254.3 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:39750631 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:39750631 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:38926576 A>T maps to NM_181539.4 C203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:38926576 A>T maps to NM_181539.4 C203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:129802475 A>G maps to NM_000426.3 G2547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:129802475 A>G maps to NM_000426.3 G2547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:112463319 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:112463319 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:165218774 G>T maps to NM_177398.3 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:165218774 G>T maps to NM_177398.3 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:170042167 C>A maps to NM_004525.2 V3230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:170042167 C>A maps to NM_004525.2 V3230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:143867035 G>T maps to NM_003695.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:143867035 G>T maps to NM_003695.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:43821528 C>A maps to ENST00000382031 R2858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:43821528 C>A maps to ENST00000382031 R2858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:10402374 T>A maps to NM_005963.3 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:10402374 T>A maps to NM_005963.3 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:25596689 T>C maps to NM_152667.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:25596689 T>C maps to NM_152667.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:33345446 C>A maps to NM_014071.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:33345446 C>A maps to NM_014071.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:43613235 C>G maps to NM_182977.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:43613235 C>G maps to NM_182977.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:228444508 C>T maps to NM_001098623.1 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:228444508 C>T maps to NM_001098623.1 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:45799859 C>T maps to NM_001004297.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:45799859 C>T maps to NM_001004297.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:248262961 A>T maps to NM_175911.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:248262961 A>T maps to NM_175911.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:20296218 C>T maps to NM_001004723.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:20296218 C>T maps to NM_001004723.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:97852217 T>A maps to NM_001005338.1 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:97852217 T>A maps to NM_001005338.1 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:25671838 C>T maps to NM_030979.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:25671838 C>T maps to NM_030979.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:64323336 T>C maps to NM_020651.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:64323336 T>C maps to NM_020651.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:110394799 C>T maps to ENST00000426474 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:110394799 C>T maps to ENST00000426474 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:64029060 A>T maps to NM_000932.2 K613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:64029060 A>T maps to NM_000932.2 K613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:2230952 T>C maps to NM_181808.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:2230952 T>C maps to NM_181808.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:53103753 A>T maps to NM_182595.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:53103753 A>T maps to NM_182595.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:163956144 A>G maps to ENST00000361752 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:163956144 A>G maps to ENST00000361752 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:36614773 C>T maps to NM_000536.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:36614773 C>T maps to NM_000536.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:9517287 C>T maps to NM_006788.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:9517287 C>T maps to NM_006788.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:35693825 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:35693825 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:103180649 G>T maps to ENST00000428762 I2308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:103180649 G>T maps to ENST00000428762 I2308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:183885735 G>T maps to NM_015149.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:183885735 G>T maps to NM_015149.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:107040986 G>A maps to ENST00000304514 R1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:107040986 G>A maps to ENST00000304514 R1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124765506 T>C maps to NM_019055.5 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124765506 T>C maps to NM_019055.5 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:200137208 C>A maps to NM_001172509.1 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:200137208 C>A maps to NM_001172509.1 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:17771463 A>G maps to NM_001037540.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:17771463 A>G maps to NM_001037540.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:139353684 T>C maps to NM_014866.1 P1770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:139353684 T>C maps to NM_014866.1 P1770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:21350114 T>C maps to NM_006446.4 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:21350114 T>C maps to NM_006446.4 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:107954956 G>A maps to NM_018013.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:107954956 G>A maps to NM_018013.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44862812 C>T maps to NM_025137.3 T2129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44862812 C>T maps to NM_025137.3 T2129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104031839 T>A maps to NM_017564.9 C252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104031839 T>A maps to NM_017564.9 C252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:106155396 G>T maps to ENST00000513237 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:106155396 G>T maps to ENST00000513237 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:50683241 C>A maps to NM_172238.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:50683241 C>A maps to NM_172238.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:40713902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:40713902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:60036548 G>T maps to NM_003839.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:60036548 G>T maps to NM_003839.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:16335350 C>T maps to NM_016113.4 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:16335350 C>T maps to NM_016113.4 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:67860155 C>T maps to ENST00000339830 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:67860155 C>T maps to ENST00000339830 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179465806 G>A maps to NM_133378.4 G16040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179465806 G>A maps to NM_133378.4 G16040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:216373436 G>A maps to ENST00000366943 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:216373436 G>A maps to ENST00000366943 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:135631058 A>T maps to NM_016267.3 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:135631058 A>T maps to NM_016267.3 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:53889378 G>T maps to NM_182758.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:53889378 G>T maps to NM_182758.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44158514 C>T maps to NM_024908.3 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44158514 C>T maps to NM_024908.3 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:75276210 A>T maps to NM_019589.2 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:75276210 A>T maps to NM_019589.2 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:64098704 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:64098704 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:77690535 G>C maps to NM_024721.4 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:77690535 G>C maps to NM_024721.4 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:77767646 C>A maps to NM_024721.4 S2830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:77767646 C>A maps to NM_024721.4 S2830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:136652165 A>C maps to NM_003413.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:136652165 A>C maps to NM_003413.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:27419945 G>A maps to NM_007149.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:27419945 G>A maps to NM_007149.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:247200849 C>T maps to NM_033213.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:247200849 C>T maps to NM_033213.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr17:995057 G>C maps to NM_021962.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr17:995057 G>C maps to NM_021962.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:99109203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:99109203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr16:58301477 A>G maps to NM_014157.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr16:58301477 A>G maps to NM_014157.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:22606880 G>C maps to ENST00000446597 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:22606880 G>C maps to ENST00000446597 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:1606209 G>A maps to NM_001005922.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:1606209 G>A maps to NM_001005922.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:51679625 A>G maps to NM_015106.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:51679625 A>G maps to NM_015106.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:101599389 T>C maps to NM_180991.4 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:101599389 T>C maps to NM_180991.4 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:20618584 C>T maps to ENST00000273739 N1313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:20618584 C>T maps to ENST00000273739 N1313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:104100637 C>G maps to NM_017564.9 V1355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:104100637 C>G maps to NM_017564.9 V1355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:94834210 T>C maps to NM_014639.3 K1142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:94834210 T>C maps to NM_014639.3 K1142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chrX:47271876 A>G maps to NM_003446.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chrX:47271876 A>G maps to NM_003446.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr18:72344028 A>T maps to NM_017757.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr18:72344028 A>T maps to NM_017757.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:87081013 G>T maps to NM_018849.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:87081013 G>T maps to NM_018849.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:72434396 G>T maps to NM_139155.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:72434396 G>T maps to NM_139155.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:8011888 C>A maps to ENST00000380149 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:8011888 C>A maps to ENST00000380149 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:23257338 C>A maps to NM_173081.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:23257338 C>A maps to NM_173081.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:19263677 G>T maps to NM_015681.3 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:19263677 G>T maps to NM_015681.3 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:169338765 T>C maps to NM_003666.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:169338765 T>C maps to NM_003666.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:49689124 G>T maps to NM_003458.3 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:49689124 G>T maps to NM_003458.3 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:40631026 C>T maps to NM_207380.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:40631026 C>T maps to NM_207380.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:156769986 C>T maps to NM_001001343.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:156769986 C>T maps to NM_001001343.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:74554834 G>C maps to ENST00000321288 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:74554834 G>C maps to ENST00000321288 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:176017473 G>A maps to NM_001171976.1 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:176017473 G>A maps to NM_001171976.1 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:42190823 C>A maps to NM_006890.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:42190823 C>A maps to NM_006890.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:136700550 C>A maps to NM_001006628.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:136700550 C>A maps to NM_001006628.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:35763531 G>A maps to NM_001832.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:35763531 G>A maps to NM_001832.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139715563 G>C maps to NM_152888.1 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139715563 G>C maps to NM_152888.1 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:23584334 G>A maps to NM_001008693.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:23584334 G>A maps to NM_001008693.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:135346287 T>C maps to NM_000773.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:135346287 T>C maps to NM_000773.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:103908002 C>A maps to NM_001001711.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:103908002 C>A maps to NM_001001711.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:468955 C>A maps to NM_014974.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:468955 C>A maps to NM_014974.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:76112336 C>T maps to NM_020892.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:76112336 C>T maps to NM_020892.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr18:48513136 G>C maps to NM_018696.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr18:48513136 G>C maps to NM_018696.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:152283734 C>A maps to NM_002016.1 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:152283734 C>A maps to NM_002016.1 G1209G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z005-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:27185072 C>G maps to NM_000810.3 G242G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z005-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:27185072 C>G maps to NM_000810.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:117884488 A>G maps to NM_020399.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:117884488 A>G maps to NM_020399.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:52386428 A>C maps to NM_002203.3 *1182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:52386428 A>C maps to NM_002203.3 *1182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:112525024 G>A maps to ENST00000315987 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:112525024 G>A maps to ENST00000315987 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:21319506 C>A maps to NM_021012.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:21319506 C>A maps to NM_021012.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:225594528 C>A maps to NM_194442.1 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:225594528 C>A maps to NM_194442.1 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:10648124 G>T maps to NM_001098579.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:10648124 G>T maps to NM_001098579.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:3228089 G>T maps to NM_015419.3 G2718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:3228089 G>T maps to NM_015419.3 G2718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:46056783 C>T maps to NM_025136.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:46056783 C>T maps to NM_025136.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:22880658 C>A maps to NM_005028.4 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:22880658 C>A maps to NM_005028.4 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr22:35947785 G>T maps to NM_014310.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr22:35947785 G>T maps to NM_014310.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:72932466 C>A maps to NM_004296.4 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:72932466 C>A maps to NM_004296.4 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:77626671 A>C maps to ENST00000332191 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:77626671 A>C maps to ENST00000332191 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:153410769 G>A maps to NM_001045479.1 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:153410769 G>A maps to NM_001045479.1 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:107955721 C>T maps to NM_018013.3 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:107955721 C>T maps to NM_018013.3 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:45265821 G>T maps to NM_020826.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:45265821 G>T maps to NM_020826.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:6328729 C>G maps to NM_033516.5 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:6328729 C>G maps to NM_033516.5 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:85752721 C>A maps to NM_014991.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:85752721 C>A maps to NM_014991.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:77767550 C>A maps to NM_024721.4 T2798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:77767550 C>A maps to NM_024721.4 T2798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:49672249 G>T maps to NM_015069.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:49672249 G>T maps to NM_015069.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:57175468 G>A maps to NM_001005850.1 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:57175468 G>A maps to NM_001005850.1 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:22012521 A>G maps to NM_005691.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:22012521 A>G maps to NM_005691.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:115304267 G>T maps to NM_000686.4 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:115304267 G>T maps to NM_000686.4 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:26411404 C>G maps to NM_016529.4 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:26411404 C>G maps to NM_016529.4 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:134351250 C>T maps to NM_013318.3 C1245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:134351250 C>T maps to NM_013318.3 C1245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr21:45941909 G>A maps to ENST00000443468 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr21:45941909 G>A maps to ENST00000443468 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:46408020 C>T maps to NM_000741.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:46408020 C>T maps to NM_000741.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:40761279 G>A maps to NM_178126.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:40761279 G>A maps to NM_178126.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:76022196 G>A maps to NM_015687.2 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:76022196 G>A maps to NM_015687.2 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:153476137 T>A maps to NM_052905.3 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:153476137 T>A maps to NM_052905.3 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:77937571 G>A maps to NM_080491.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:77937571 G>A maps to NM_080491.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:147380378 C>T maps to NM_005267.4 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:147380378 C>T maps to NM_005267.4 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:9739736 T>G maps to NM_004246.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:9739736 T>G maps to NM_004246.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:92844777 G>C maps to ENST00000453812 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:92844777 G>C maps to ENST00000453812 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:71142473 G>T maps to ENST00000439900 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:71142473 G>T maps to ENST00000439900 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:38817874 C>T maps to NM_004823.1 H258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:38817874 C>T maps to NM_004823.1 H258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:62936947 G>A maps to ENST00000393630 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:62936947 G>A maps to ENST00000393630 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:44747320 C>T maps to ENST00000444676 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:44747320 C>T maps to ENST00000444676 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:140182818 G>A maps to NM_018906.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:140182818 G>A maps to NM_018906.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:20769251 T>A maps to NM_000921.3 L453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:20769251 T>A maps to NM_000921.3 L453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:249211871 G>A maps to NM_170725.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:249211871 G>A maps to NM_170725.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:76793209 G>A maps to NM_006239.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:76793209 G>A maps to NM_006239.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:231926009 G>T maps to NM_002807.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:231926009 G>T maps to NM_002807.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:78795961 G>T maps to NM_002941.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:78795961 G>T maps to NM_002941.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:27436120 G>A maps to NM_003047.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:27436120 G>A maps to NM_003047.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:140407230 C>T maps to NM_152616.4 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:140407230 C>T maps to NM_152616.4 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:179593262 C>A maps to NM_133378.4 G5220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:179593262 C>A maps to NM_133378.4 G5220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:82849189 G>A maps to NM_004385.4 E3167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:82849189 G>A maps to NM_004385.4 E3167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:53856409 G>T maps to NM_138374.1 E828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:53856409 G>T maps to NM_138374.1 E828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:120437438 G>A maps to NM_021794.2 C507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:120437438 G>A maps to NM_021794.2 C507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:8758006 G>T maps to NM_020661.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:8758006 G>T maps to NM_020661.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:109175688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:109175688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:100808036 G>T maps to NM_016608.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:100808036 G>T maps to NM_016608.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:26133193 C>T maps to NM_016529.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:26133193 C>T maps to NM_016529.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:76764010 G>A maps to NM_000489.3 L2433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:76764010 G>A maps to NM_000489.3 L2433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:90660045 G>T maps to NM_001170794.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:90660045 G>T maps to NM_001170794.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:65056005 C>T maps to NM_172365.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:65056005 C>T maps to NM_172365.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:57832820 G>A maps to NM_032313.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:57832820 G>A maps to NM_032313.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:92158153 G>A maps to NM_032120.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:92158153 G>A maps to NM_032120.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:209785513 C>T maps to NM_020439.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:209785513 C>T maps to NM_020439.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:17072666 C>A maps to NM_014406.4 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:17072666 C>A maps to NM_014406.4 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:22360697 C>G maps to NM_001802.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:22360697 C>G maps to NM_001802.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:13059280 C>T maps to NM_032142.3 L1486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:13059280 C>T maps to NM_032142.3 L1486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:207639898 C>A maps to NM_001006658.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:207639898 C>A maps to NM_001006658.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:97617767 A>G maps to ENST00000182096 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:97617767 A>G maps to ENST00000182096 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:2820852 C>T maps to NM_033225.5 W3115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:2820852 C>T maps to NM_033225.5 W3115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:33985174 T>A maps to ENST00000373381 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:33985174 T>A maps to ENST00000373381 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:84245669 G>A maps to NM_001142699.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:84245669 G>A maps to NM_001142699.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:3879411 C>A maps to NM_004746.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:3879411 C>A maps to NM_004746.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:65871551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:65871551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:169186707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:169186707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:149542537 T>G maps to NM_015630.3 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:149542537 T>G maps to NM_015630.3 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:1137368 C>T maps to NM_178040.2 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:1137368 C>T maps to NM_178040.2 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:92430608 G>T maps to ENST00000298047 E1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:92430608 G>T maps to ENST00000298047 E1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:14964665 C>A maps to NM_152536.3 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:14964665 C>A maps to NM_152536.3 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:67265198 C>T maps to NM_013241.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:67265198 C>T maps to NM_013241.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:28635044 G>A maps to NM_005253.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:28635044 G>A maps to NM_005253.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:58722337 C>A maps to NM_080661.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:58722337 C>A maps to NM_080661.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:30662512 G>T maps to NM_002110.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:30662512 G>T maps to NM_002110.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:176964978 G>C maps to NM_021193.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:176964978 G>C maps to NM_021193.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:103827021 A>C maps to NM_024747.4 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:103827021 A>C maps to NM_024747.4 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:53629543 G>T maps to ENST00000276009 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:53629543 G>T maps to ENST00000276009 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:38341322 C>T maps to ENST00000373026 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:38341322 C>T maps to ENST00000373026 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:15222401 C>A maps to NM_001031853.3 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:15222401 C>A maps to NM_001031853.3 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:48153084 G>T maps to NM_002204.2 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:48153084 G>T maps to NM_002204.2 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:211256133 G>A maps to NM_172362.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:211256133 G>A maps to NM_172362.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:40321496 C>A maps to NM_012285.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:40321496 C>A maps to NM_012285.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:118250613 G>T maps to NM_020721.1 C165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:118250613 G>T maps to NM_020721.1 C165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:86554856 G>T maps to NM_001142749.2 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:86554856 G>T maps to NM_001142749.2 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:35107404 C>A maps to NM_025182.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:35107404 C>A maps to NM_025182.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:111583509 C>T maps to NM_153369.2 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:111583509 C>T maps to NM_153369.2 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:73965458 A>T maps to NM_001008537.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:73965458 A>T maps to NM_001008537.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:28319192 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:28319192 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:66436684 G>T maps to NM_015541.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:66436684 G>T maps to NM_015541.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:138209613 T>C maps to NM_015564.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:138209613 T>C maps to NM_015564.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:32682115 C>T maps to NM_014268.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:32682115 C>T maps to NM_014268.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:160604493 A>G maps to NM_022826.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:160604493 A>G maps to NM_022826.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:149247916 C>T maps to ENST00000404807 D1572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:149247916 C>T maps to ENST00000404807 D1572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:127339644 C>T maps to NM_004526.2 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:127339644 C>T maps to NM_004526.2 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:49576527 G>A maps to NM_014484.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:49576527 G>A maps to NM_014484.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:49576692 A>T maps to NM_014484.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:49576692 A>T maps to NM_014484.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:138119380 G>A maps to NM_001085049.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:138119380 G>A maps to NM_001085049.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:10366660 C>A maps to NM_017533.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:10366660 C>A maps to NM_017533.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:26239764 G>A maps to ENST00000407587 W1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:26239764 G>A maps to ENST00000407587 W1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:17745612 G>C maps to NM_198270.2 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:17745612 G>C maps to NM_198270.2 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:21141408 G>A maps to NM_000271.4 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:21141408 G>A maps to NM_000271.4 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:74947403 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:74947403 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:156834170 C>T maps to NM_002529.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:156834170 C>T maps to NM_002529.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:247920988 G>T maps to NM_012353.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:247920988 G>T maps to NM_012353.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:4928961 C>T maps to NM_001004749.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:4928961 C>T maps to NM_001004749.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:4674586 C>A maps to NM_152430.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:4674586 C>A maps to NM_152430.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:241078679 G>T maps to NM_148961.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:241078679 G>T maps to NM_148961.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:56106160 C>T maps to NM_001142763.1 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:56106160 C>T maps to NM_001142763.1 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:140605041 C>T maps to NM_018934.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:140605041 C>T maps to NM_018934.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:6268300 G>T maps to NM_004566.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:6268300 G>T maps to NM_004566.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:102054706 G>A maps to NM_016112.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:102054706 G>A maps to NM_016112.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:46002479 C>G maps to NM_001080401.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:46002479 C>G maps to NM_001080401.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:322286 C>A maps to NM_013239.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:322286 C>A maps to NM_013239.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:94731782 G>T maps to NM_058237.1 G753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:94731782 G>T maps to NM_058237.1 G753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:54385786 G>T maps to NM_002739.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:54385786 G>T maps to NM_002739.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:7888170 A>G maps to NM_001105244.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:7888170 A>G maps to NM_001105244.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:57648585 C>A maps to ENST00000438036 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:57648585 C>A maps to ENST00000438036 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:102192869 G>T maps to NM_001031834.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:102192869 G>T maps to NM_001031834.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:7231499 C>T maps to NM_001003699.3 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:7231499 C>T maps to NM_001003699.3 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:237753237 C>A maps to NM_001035.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:237753237 C>A maps to NM_001035.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:237961377 C>T maps to NM_001035.2 I4666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:237961377 C>T maps to NM_001035.2 I4666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:91965657 G>A maps to NM_024077.3 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:91965657 G>A maps to NM_024077.3 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:75398285 G>T maps to NM_001113491.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:75398285 G>T maps to NM_001113491.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:51617215 G>A maps to NM_018967.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:51617215 G>A maps to NM_018967.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:44914425 T>G maps to NM_025137.3 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:44914425 T>G maps to NM_025137.3 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:2815037 A>T maps to NM_016333.3 P1503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:2815037 A>T maps to NM_016333.3 P1503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:33194833 G>T maps to NM_015551.1 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:33194833 G>T maps to NM_015551.1 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:152949424 G>A maps to NM_182961.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:152949424 G>A maps to NM_182961.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:52928765 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:52928765 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:90450943 C>A maps to NM_018319.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:90450943 C>A maps to NM_018319.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:104465042 C>A maps to NM_031274.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:104465042 C>A maps to NM_031274.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:36752694 G>C maps to NM_005119.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:36752694 G>C maps to NM_005119.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:19452067 C>T maps to NM_001105248.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:19452067 C>T maps to NM_001105248.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:6479486 T>C maps to NM_033278.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:6479486 T>C maps to NM_033278.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:111195609 C>T maps to NM_012471.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:111195609 C>T maps to NM_012471.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:15930733 A>G maps to NM_017775.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:15930733 A>G maps to NM_017775.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:80751918 A>G maps to NM_003318.4 *858W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:80751918 A>G maps to NM_003318.4 *858W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:145440738 C>T maps to NM_006472.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:145440738 C>T maps to NM_006472.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:128870688 A>T maps to NM_020120.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:128870688 A>T maps to NM_020120.3 R185*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z008-01A-01W-0746-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-17-Z008-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:96171635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:96171635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:177608491 G>T maps to NM_005429.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:177608491 G>T maps to NM_005429.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:133032954 T>C maps to NM_004666.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:133032954 T>C maps to NM_004666.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:46554008 T>A maps to ENST00000242848 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:46554008 T>A maps to ENST00000242848 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:30677324 G>A maps to ENST00000394679 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:30677324 G>A maps to ENST00000394679 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:12243845 A>G maps to NM_021143.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:12243845 A>G maps to NM_021143.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:57188281 G>T maps to NM_033273.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:57188281 G>T maps to NM_033273.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:30934690 C>A maps to NM_014717.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:30934690 C>A maps to NM_014717.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:37643329 C>A maps to ENST00000356958 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:37643329 C>A maps to ENST00000356958 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:63726274 T>A maps to NM_153363.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:63726274 T>A maps to NM_153363.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:57769436 C>T maps to NM_178457.1 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:57769436 C>T maps to NM_178457.1 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:56544821 G>A maps to NM_031885.3 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:56544821 G>A maps to NM_031885.3 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:24923773 A>C maps to NM_018958.2 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:24923773 A>C maps to NM_018958.2 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:125555844 C>A maps to NM_130773.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:125555844 C>A maps to NM_130773.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:21723541 G>T maps to NM_003777.3 V1874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:21723541 G>T maps to NM_003777.3 V1874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:34149594 C>T maps to NM_203408.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:34149594 C>T maps to NM_203408.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:46011807 G>T maps to NM_198688.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:46011807 G>T maps to NM_198688.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:52700337 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:52700337 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:56230508 G>T maps to NM_001004743.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:56230508 G>T maps to NM_001004743.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:56000091 A>T maps to NM_001004746.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:56000091 A>T maps to NM_001004746.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:91134022 C>T maps to NM_032968.3 F928F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:91134022 C>T maps to NM_032968.3 F928F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:141325367 G>A maps to NM_016580.2 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:141325367 G>A maps to NM_016580.2 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:14489270 C>A maps to NM_001134367.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:14489270 C>A maps to NM_001134367.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr17:40475148 G>T maps to NM_139276.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr17:40475148 G>T maps to NM_139276.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:100511564 G>T maps to ENST00000471714 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:100511564 G>T maps to ENST00000471714 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:6307195 C>T maps to NM_133492.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:6307195 C>T maps to NM_133492.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:80655812 C>A maps to NM_130767.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:80655812 C>A maps to NM_130767.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:20435267 C>T maps to NM_017888.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:20435267 C>T maps to NM_017888.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:28302380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:28302380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:105416780 C>T maps to NM_138420.2 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:105416780 C>T maps to NM_138420.2 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:33242913 C>T maps to NM_004274.4 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:33242913 C>T maps to NM_004274.4 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:10692545 G>A maps to ENST00000453102 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:10692545 G>A maps to ENST00000453102 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:128842724 G>A maps to NM_001142685.1 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:128842724 G>A maps to NM_001142685.1 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:73066630 C>T maps to NM_014786.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:73066630 C>T maps to NM_014786.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:155935420 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:155935420 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:2951227 T>A maps to NM_001011719.1 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:2951227 T>A maps to NM_001011719.1 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247737488 C>G maps to NM_145278.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247737488 C>G maps to NM_145278.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:37463237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:37463237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:2797764 C>A maps to NM_199460.2 S2062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:2797764 C>A maps to NM_199460.2 S2062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:181752855 G>T maps to ENST00000357570 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:181752855 G>T maps to ENST00000357570 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:196646636 G>A maps to NM_000186.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:196646636 G>A maps to NM_000186.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:49853405 C>T maps to NM_001127898.1 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:49853405 C>T maps to NM_001127898.1 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:10492114 G>T maps to NM_052964.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:10492114 G>T maps to NM_052964.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:107419022 C>T maps to NM_033641.2 E897E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:107419022 C>T maps to NM_033641.2 E897E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:10077013 G>A maps to NM_015719.3 L1586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:10077013 G>A maps to NM_015719.3 L1586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:211527851 C>A maps to NM_001122633.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:211527851 C>A maps to NM_001122633.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:27003933 C>T maps to NM_001887.3 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:27003933 C>T maps to NM_001887.3 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:104447973 C>T maps to NM_015420.6 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:104447973 C>T maps to NM_015420.6 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:18250028 T>C maps to NM_003472.3 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:18250028 T>C maps to NM_003472.3 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:137341259 T>G maps to NM_004717.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:137341259 T>G maps to NM_004717.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:53119001 C>T maps to NM_014584.1 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:53119001 C>T maps to NM_014584.1 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:63410855 G>A maps to NM_152424.3 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:63410855 G>A maps to NM_152424.3 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:61022235 C>A maps to ENST00000442566 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:61022235 C>A maps to ENST00000442566 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:79698583 C>A maps to NM_001170574.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:79698583 C>A maps to NM_001170574.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:92086010 G>T maps to ENST00000298047 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:92086010 G>T maps to ENST00000298047 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:83440921 G>T maps to NM_001007122.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:83440921 G>T maps to NM_001007122.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:71318328 C>A maps to NM_018348.5 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:71318328 C>A maps to NM_018348.5 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:46930517 A>G maps to NM_000809.2 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:46930517 A>G maps to NM_000809.2 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:42005030 G>A maps to NM_000168.5 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:42005030 G>A maps to NM_000168.5 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:155649576 C>A maps to NM_003875.2 Y528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:155649576 C>A maps to NM_003875.2 Y528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:14552739 G>T maps to ENST00000507975 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:14552739 G>T maps to ENST00000507975 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:27840243 T>A maps to NM_001109763.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:27840243 T>A maps to NM_001109763.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:65427132 C>A maps to NM_138737.3 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:65427132 C>A maps to NM_138737.3 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:65427990 G>T maps to NM_138737.3 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:65427990 G>T maps to NM_138737.3 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:27147962 G>T maps to NM_153631.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:27147962 G>T maps to NM_153631.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:176982040 C>A maps to NM_002148.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:176982040 C>A maps to NM_002148.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156496382 C>A maps to NM_178229.4 L1597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156496382 C>A maps to NM_178229.4 L1597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:35107375 A>C maps to NM_003024.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:35107375 A>C maps to NM_003024.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:17793918 C>T maps to NM_001112741.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:17793918 C>T maps to NM_001112741.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:197428578 C>A maps to NM_014687.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:197428578 C>A maps to NM_014687.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:36870090 C>A maps to NM_001029864.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:36870090 C>A maps to NM_001029864.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:39394359 G>A maps to NM_031963.2 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:39394359 G>A maps to NM_031963.2 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:40359792 C>T maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:40359792 C>T maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:52861507 G>T maps to NM_001024611.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:52861507 G>T maps to NM_001024611.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:140985461 A>G maps to NM_138702.1 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:140985461 A>G maps to NM_138702.1 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:23889628 A>G maps to NM_019066.4 Y1087Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:23889628 A>G maps to NM_019066.4 Y1087Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:62861047 T>C maps to ENST00000393630 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:62861047 T>C maps to ENST00000393630 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:18159366 C>A maps to NM_054031.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:18159366 C>A maps to NM_054031.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:86433235 A>T maps to NM_016622.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:86433235 A>T maps to NM_016622.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:135871275 T>A maps to NM_018133.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:135871275 T>A maps to NM_018133.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237057838 G>A maps to NM_000254.2 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237057838 G>A maps to NM_000254.2 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:9010702 G>T maps to NM_024690.2 T12986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:9010702 G>T maps to NM_024690.2 T12986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:1893090 G>T maps to ENST00000399161 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:1893090 G>T maps to ENST00000399161 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:73928255 G>T maps to NM_016347.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:73928255 G>T maps to NM_016347.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:144828750 G>T maps to NM_001037675.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:144828750 G>T maps to NM_001037675.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:52639626 C>A maps to NM_199289.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:52639626 C>A maps to NM_199289.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247592922 G>T maps to NM_004895.4 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247592922 G>T maps to NM_004895.4 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:128415640 G>T maps to NM_001708.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:128415640 G>T maps to NM_001708.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247978920 C>T maps to NM_001001966.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247978920 C>T maps to NM_001001966.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:57982974 T>C maps to NM_001004458.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:57982974 T>C maps to NM_001004458.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248458256 G>T maps to NM_001004692.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248458256 G>T maps to NM_001004692.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:59211009 C>T maps to NM_001004728.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:59211009 C>T maps to NM_001004728.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:56310157 A>T maps to NM_001005245.1 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:56310157 A>T maps to NM_001005245.1 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:40566419 G>A maps to NM_020168.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:40566419 G>A maps to NM_020168.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:140255725 A>G maps to NM_018903.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:140255725 A>G maps to NM_018903.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:103814369 G>A maps to NM_025208.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:103814369 G>A maps to NM_025208.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:204426903 G>A maps to NM_002646.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:204426903 G>A maps to NM_002646.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:4512252 C>A maps to NM_001080400.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:4512252 C>A maps to NM_001080400.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:152937076 G>T maps to NM_001039582.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:152937076 G>T maps to NM_001039582.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:43441240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:43441240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:117250117 T>A maps to NM_173560.3 C865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:117250117 T>A maps to NM_173560.3 C865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:67809533 C>A maps to NM_173630.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:67809533 C>A maps to NM_173630.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237948032 G>T maps to NM_001035.2 E4341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237948032 G>T maps to NM_001035.2 E4341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:51171411 G>T maps to ENST00000251020 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:51171411 G>T maps to ENST00000251020 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:8224564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:8224564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:72117071 A>T maps to NM_015556.1 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:72117071 A>T maps to NM_015556.1 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:25850351 C>A maps to NM_001098486.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:25850351 C>A maps to NM_001098486.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:19445803 C>A maps to ENST00000395585 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:19445803 C>A maps to ENST00000395585 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:51415441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:51415441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:119563200 C>A maps to NM_194286.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:119563200 C>A maps to NM_194286.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:17363107 G>T maps to NM_001004470.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:17363107 G>T maps to NM_001004470.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:168931720 T>A maps to NM_013233.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:168931720 T>A maps to NM_013233.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:30380610 C>A maps to NM_015527.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:30380610 C>A maps to NM_015527.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:17446184 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:17446184 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:35242074 G>A maps to NM_001077653.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:35242074 G>A maps to NM_001077653.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:151747948 C>A maps to NM_001083965.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:151747948 C>A maps to NM_001083965.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:132352131 G>A maps to NM_016521.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:132352131 G>A maps to NM_016521.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:133984966 C>T maps to NM_003235.4 F2060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:133984966 C>T maps to NM_003235.4 F2060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:43735789 T>A maps to ENST00000330266 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:43735789 T>A maps to ENST00000330266 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:10934114 T>A maps to NM_199261.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:10934114 T>A maps to NM_199261.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:42235933 C>A maps to NM_033502.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:42235933 C>A maps to NM_033502.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:42236656 C>A maps to NM_033502.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:42236656 C>A maps to NM_033502.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:31768400 C>T maps to NM_020856.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:31768400 C>T maps to NM_020856.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179486301 C>T maps to NM_133378.4 R12515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179486301 C>T maps to NM_133378.4 R12515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:51457539 C>A maps to ENST00000273612 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:51457539 C>A maps to ENST00000273612 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:109691364 G>T maps to NM_021224.4 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:109691364 G>T maps to NM_021224.4 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:22063912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:22063912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:147120176 G>A maps to NM_016361.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:147120176 G>A maps to NM_016361.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:131310520 C>T maps to NM_015256.2 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:131310520 C>T maps to NM_015256.2 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:100253209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:100253209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:88247824 T>C maps to ENST00000395847 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:88247824 T>C maps to ENST00000395847 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:40832536 A>G maps to NM_004307.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:40832536 A>G maps to NM_004307.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:112175323 G>T maps to NM_001127510.2 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:112175323 G>T maps to NM_001127510.2 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chrX:100609682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chrX:100609682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:158324233 T>G maps to NM_030893.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:158324233 T>G maps to NM_030893.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:76525508 C>T maps to ENST00000307465 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:76525508 C>T maps to ENST00000307465 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:126661424 G>T maps to ENST00000368325 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:126661424 G>T maps to ENST00000368325 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:39382953 C>A maps to NM_001343.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:39382953 C>A maps to NM_001343.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:182822531 G>A maps to NM_001357.4 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:182822531 G>A maps to NM_001357.4 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:88584102 A>T maps to NM_004407.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:88584102 A>T maps to NM_004407.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:79609709 G>A maps to NM_016010.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:79609709 G>A maps to NM_016010.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:40366229 G>A maps to NM_003890.2 C4668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:40366229 G>A maps to NM_003890.2 C4668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:45262663 G>A maps to NM_021072.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:45262663 G>A maps to NM_021072.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:60314855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:60314855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:1879615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:1879615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:909731 G>A maps to NM_015155.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:909731 G>A maps to NM_015155.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:42856542 C>T maps to ENST00000251268 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:42856542 C>T maps to ENST00000251268 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:40819641 G>A maps to NM_020831.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:40819641 G>A maps to NM_020831.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44695707 G>A maps to NM_020967.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44695707 G>A maps to NM_020967.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44695758 G>A maps to NM_020967.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44695758 G>A maps to NM_020967.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:55582502 T>G maps to NM_001142763.1 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:55582502 T>G maps to NM_001142763.1 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:56423944 G>T maps to NM_001142763.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:56423944 G>T maps to NM_001142763.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:42988051 T>A maps to ENST00000415122 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:42988051 T>A maps to ENST00000415122 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:25384267 G>A maps to NM_001035256.1 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:25384267 G>A maps to NM_001035256.1 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:30094791 C>T maps to NM_002720.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:30094791 C>T maps to NM_002720.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:6013938 C>A maps to NM_012416.2 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:6013938 C>A maps to NM_012416.2 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:196229918 C>A maps to NM_152617.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:196229918 C>A maps to NM_152617.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:1543282 G>C maps to NM_003693.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:1543282 G>C maps to NM_003693.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:42532247 A>T maps to NM_015559.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:42532247 A>T maps to NM_015559.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:72205151 C>T maps to NM_001098484.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:72205151 C>T maps to NM_001098484.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:33690514 G>T maps to NM_152270.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:33690514 G>T maps to NM_152270.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:18637459 G>A maps to NM_194285.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:18637459 G>A maps to NM_194285.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:62505073 C>T maps to NM_199360.1 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:62505073 C>T maps to NM_199360.1 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chrX:2712624 C>A maps to NM_001141919.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chrX:2712624 C>A maps to NM_001141919.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:279018 G>T maps to NM_033089.6 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:279018 G>T maps to NM_033089.6 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:22586296 C>T maps to NM_001098626.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:22586296 C>T maps to NM_001098626.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:970439 G>A maps to NM_021962.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:970439 G>A maps to NM_021962.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:141011428 C>T maps to NM_001037172.1 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:141011428 C>T maps to NM_001037172.1 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:7709394 G>C maps to NM_020546.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:7709394 G>C maps to NM_020546.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:86278795 G>T maps to NM_006738.4 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:86278795 G>T maps to NM_006738.4 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:73677115 C>T maps to NM_015120.4 F1153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:73677115 C>T maps to NM_015120.4 F1153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:104116919 C>T maps to NM_020978.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:104116919 C>T maps to NM_020978.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:129980465 G>T maps to NM_001642.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:129980465 G>T maps to NM_001642.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:100880884 C>T maps to NM_016607.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:100880884 C>T maps to NM_016607.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:50273601 T>A maps to NM_006045.1 K461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:50273601 T>A maps to NM_006045.1 K461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:28382009 T>C maps to NM_022461.3 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:28382009 T>C maps to NM_022461.3 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:156622616 G>T maps to NM_021948.3 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:156622616 G>T maps to NM_021948.3 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:24995031 C>T maps to NM_001178093.1 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:24995031 C>T maps to NM_001178093.1 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:70048923 C>T maps to NM_032735.2 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:70048923 C>T maps to NM_032735.2 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:38988924 G>T maps to NM_207444.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:38988924 G>T maps to NM_207444.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:185125792 C>A maps to NM_030934.4 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:185125792 C>A maps to NM_030934.4 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:23731171 C>T maps to NM_199136.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:23731171 C>T maps to NM_199136.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:54444850 C>T maps to NM_031896.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:54444850 C>T maps to NM_031896.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:96101821 C>T maps to ENST00000508830 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:96101821 C>T maps to ENST00000508830 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:167549960 A>C maps to NM_004367.5 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:167549960 A>C maps to NM_004367.5 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:72700794 G>A maps to ENST00000412086 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:72700794 G>A maps to ENST00000412086 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:23065995 C>G maps to NM_012072.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:23065995 C>G maps to NM_012072.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:137524732 T>C maps to NM_004661.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:137524732 T>C maps to NM_004661.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:227333372 C>T maps to ENST00000366766 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:227333372 C>T maps to ENST00000366766 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:90585060 G>T maps to NM_012395.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:90585060 G>T maps to NM_012395.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:49034265 C>T maps to NM_001194998.1 K1289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:49034265 C>T maps to NM_001194998.1 K1289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:34091162 A>T maps to NM_007186.3 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:34091162 A>T maps to NM_007186.3 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:7797874 T>G maps to NM_001005271.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:7797874 T>G maps to NM_001005271.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:107400277 C>T maps to NM_033641.2 Q1675Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:107400277 C>T maps to NM_033641.2 Q1675Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:4157104 C>G maps to NM_032607.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:4157104 C>G maps to NM_032607.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:17113511 G>T maps to NM_001081.3 I846I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:17113511 G>T maps to NM_001081.3 I846I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:42916000 G>T maps to NM_004391.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:42916000 G>T maps to NM_004391.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:168014231 A>G maps to ENST00000367840 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:168014231 A>G maps to ENST00000367840 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:11831565 T>C maps to NM_001033018.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:11831565 T>C maps to NM_001033018.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:38158307 C>T maps to NM_007335.2 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:38158307 C>T maps to NM_007335.2 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:101200980 C>T maps to NM_003836.5 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:101200980 C>T maps to NM_003836.5 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:76424764 C>T maps to ENST00000389840 E4137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:76424764 C>T maps to ENST00000389840 E4137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:9784054 C>T maps to NM_000798.4 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:9784054 C>T maps to NM_000798.4 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:29056117 G>A maps to NM_001944.2 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:29056117 G>A maps to NM_001944.2 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:65819702 C>A maps to ENST00000450752 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:65819702 C>A maps to ENST00000450752 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:31484431 C>T maps to NM_014600.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:31484431 C>T maps to NM_014600.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:67629996 G>T maps to NM_019002.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:67629996 G>T maps to NM_019002.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:30811120 C>G maps to NM_032222.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:30811120 C>G maps to NM_032222.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:49212035 C>T maps to NM_080829.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:49212035 C>T maps to NM_080829.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:127697461 C>T maps to NM_001999.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:127697461 C>T maps to NM_001999.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:147774425 T>C maps to NM_205836.1 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:147774425 T>C maps to NM_205836.1 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:159652942 G>T maps to NM_032532.2 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:159652942 G>T maps to NM_032532.2 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:71319486 G>A maps to NM_018348.5 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:71319486 G>A maps to NM_018348.5 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:101216454 G>A maps to NM_005458.7 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:101216454 G>A maps to NM_005458.7 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:46390696 G>A maps to ENST00000507069 N9N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:46390696 G>A maps to ENST00000507069 N9N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:161580355 C>G maps to NM_198903.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:161580355 C>G maps to NM_198903.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:153788944 G>A maps to NM_020699.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:153788944 G>A maps to NM_020699.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:155209713 C>G maps to NM_001005742.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:155209713 C>G maps to NM_001005742.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:110376291 G>A maps to NM_057169.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:110376291 G>A maps to NM_057169.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:1960100 C>A maps to NM_001500.2 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:1960100 C>A maps to NM_001500.2 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:236341782 G>T maps to NM_003272.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:236341782 G>T maps to NM_003272.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:89949518 C>T maps to NM_032119.3 D1376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:89949518 C>T maps to NM_032119.3 D1376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:123480926 G>A maps to ENST00000456860 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:123480926 G>A maps to ENST00000456860 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:11770204 G>A maps to NM_014668.3 E1527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:11770204 G>A maps to NM_014668.3 E1527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:88780383 T>G maps to NM_001143831.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:88780383 T>G maps to NM_001143831.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:178408746 G>A maps to NM_000843.3 Q849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:178408746 G>A maps to NM_000843.3 Q849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:49486080 G>A maps to NM_002103.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:49486080 G>A maps to NM_002103.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:36110348 C>T maps to NM_015302.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:36110348 C>T maps to NM_015302.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:156456832 G>A maps to NM_001173393.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:156456832 G>A maps to NM_001173393.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:43540856 C>A maps to NM_015052.3 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:43540856 C>A maps to NM_015052.3 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:93822101 C>T maps to NM_001098672.1 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:93822101 C>T maps to NM_001098672.1 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:222717462 C>G maps to NM_024746.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:222717462 C>G maps to NM_024746.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:27134292 G>T maps to NM_005522.4 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:27134292 G>T maps to NM_005522.4 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:99003132 C>G maps to NM_000197.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:99003132 C>G maps to NM_000197.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:84164007 G>A maps to NM_031463.4 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:84164007 G>A maps to NM_031463.4 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:166896325 T>A maps to NM_199351.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:166896325 T>A maps to NM_199351.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:52812963 A>G maps to NM_002215.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:52812963 A>G maps to NM_002215.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:5021038 C>T maps to NM_000217.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:5021038 C>T maps to NM_000217.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:5153882 C>T maps to NM_002234.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:5153882 C>T maps to NM_002234.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:39272298 C>T maps to NM_031460.3 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:39272298 C>T maps to NM_031460.3 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:138648750 G>C maps to ENST00000298480 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:138648750 G>C maps to ENST00000298480 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:84862622 G>A maps to NM_014895.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:84862622 G>A maps to NM_014895.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:154394492 A>G maps to NM_001099293.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:154394492 A>G maps to NM_001099293.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:51330970 G>T maps to NM_017509.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:51330970 G>T maps to NM_017509.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:152732786 G>A maps to NM_001025231.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:152732786 G>A maps to NM_001025231.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:38978822 G>T maps to NM_000421.3 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:38978822 G>T maps to NM_000421.3 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:36997784 G>A maps to NM_004139.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:36997784 G>A maps to NM_004139.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:140270978 G>A maps to NM_012317.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:140270978 G>A maps to NM_012317.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:113704058 C>T maps to NM_057159.2 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:113704058 C>T maps to NM_057159.2 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:134165170 G>A maps to NM_030626.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:134165170 G>A maps to NM_030626.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:70505058 C>T maps to NM_020794.2 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:70505058 C>T maps to NM_020794.2 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:86050663 G>T maps to NM_033402.4 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:86050663 G>T maps to NM_033402.4 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:85517880 C>T maps to NM_001079910.1 L1197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:85517880 C>T maps to NM_001079910.1 L1197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:140992862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:140992862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:10417435 C>T maps to NM_005885.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:10417435 C>T maps to NM_005885.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:86373795 G>T maps to ENST00000393205 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:86373795 G>T maps to ENST00000393205 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:12379965 C>T maps to NM_032867.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:12379965 C>T maps to NM_032867.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:56573254 C>A maps to NM_004687.4 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:56573254 C>A maps to NM_004687.4 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:9061228 C>T maps to NM_024690.2 K8739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:9061228 C>T maps to NM_024690.2 K8739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:9067105 G>T maps to NM_024690.2 V6780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:9067105 G>T maps to NM_024690.2 V6780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:108158715 G>A maps to NM_014981.1 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:108158715 G>A maps to NM_014981.1 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr22:26422650 G>A maps to ENST00000407587 P2239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr22:26422650 G>A maps to ENST00000407587 P2239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:171248950 A>G maps to NM_138995.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:171248950 A>G maps to NM_138995.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:76602281 G>A maps to ENST00000428345 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:76602281 G>A maps to ENST00000428345 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:30491862 C>A maps to NM_006092.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:30491862 C>A maps to NM_006092.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:108047777 A>G maps to NM_002519.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:108047777 A>G maps to NM_002519.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:44432048 G>A maps to NM_015332.3 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:44432048 G>A maps to NM_015332.3 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:123657345 C>T maps to NM_001163278.1 Q967Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:123657345 C>T maps to NM_001163278.1 Q967Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:167630823 C>T maps to NM_001122679.1 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:167630823 C>T maps to NM_001122679.1 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:107457526 G>A maps to NM_001004484.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:107457526 G>A maps to NM_001004484.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:107267283 G>A maps to NM_001004485.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:107267283 G>A maps to NM_001004485.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:3254809 C>T maps to NM_012360.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:3254809 C>T maps to NM_012360.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:4968171 T>C maps to NM_001005329.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:4968171 T>C maps to NM_001005329.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:56185650 G>T maps to NM_001004744.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:56185650 G>T maps to NM_001004744.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:158669911 G>A maps to NM_001005279.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:158669911 G>A maps to NM_001005279.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:55927703 G>A maps to NM_001004058.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:55927703 G>A maps to NM_001004058.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:20916075 C>A maps to NM_017807.3 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:20916075 C>A maps to NM_017807.3 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:122255086 G>A maps to NM_031458.2 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:122255086 G>A maps to NM_031458.2 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:52682407 G>A maps to ENST00000296302 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:52682407 G>A maps to ENST00000296302 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:164815882 T>C maps to NM_002585.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:164815882 T>C maps to NM_002585.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:140768875 T>A maps to NM_003736.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:140768875 T>A maps to NM_003736.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:82545268 C>T maps to NM_033026.5 L4011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:82545268 C>T maps to NM_033026.5 L4011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr21:47831326 C>T maps to NM_006031.5 A1780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr21:47831326 C>T maps to NM_006031.5 A1780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:71575489 G>A maps to NM_014982.2 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:71575489 G>A maps to NM_014982.2 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:119059199 G>A maps to ENST00000392817 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:119059199 G>A maps to ENST00000392817 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:142836662 C>A maps to NM_002652.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:142836662 C>A maps to NM_002652.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:111427037 G>T maps to ENST00000312791 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:111427037 G>T maps to ENST00000312791 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:144993229 G>A maps to NM_201380.2 L3724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:144993229 G>A maps to NM_201380.2 L3724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:160222218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:160222218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:55873403 T>C maps to NM_033109.3 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:55873403 T>C maps to NM_033109.3 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:94540564 A>G maps to NM_001166160.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:94540564 A>G maps to NM_001166160.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:68873420 G>T maps to NM_138964.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:68873420 G>T maps to NM_138964.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:12828223 G>A maps to NM_001039091.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:12828223 G>A maps to NM_001039091.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr22:51208445 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr22:51208445 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:86672798 C>T maps to NM_002890.1 H762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:86672798 C>T maps to NM_002890.1 H762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:30648079 G>T maps to NM_138328.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:30648079 G>T maps to NM_138328.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:59377887 A>G maps to ENST00000434298 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:59377887 A>G maps to ENST00000434298 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:78319310 G>A maps to NM_020914.4 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:78319310 G>A maps to NM_020914.4 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:201958633 C>T maps to NM_020216.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:201958633 C>T maps to NM_020216.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:155291647 C>T maps to NM_001105203.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:155291647 C>T maps to NM_001105203.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:153520844 C>T maps to NM_002960.1 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:153520844 C>T maps to NM_002960.1 Q39Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z012-01A-01W-0746-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z012-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:144890952 A>G maps to NM_182706.3 N647N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:144890952 A>G maps to NM_182706.3 N647N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:2246846 A>G maps to NM_014853.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:2246846 A>G maps to NM_014853.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:157815866 G>A maps to NM_003030.4 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:157815866 G>A maps to NM_003030.4 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:220026771 G>C maps to NM_001144890.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:220026771 G>C maps to NM_001144890.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:118895961 G>A maps to NM_001164278.1 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:118895961 G>A maps to NM_001164278.1 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:57175354 G>A maps to ENST00000428603 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:57175354 G>A maps to ENST00000428603 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:162751232 G>A maps to NM_001178015.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:162751232 G>A maps to NM_001178015.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:74907573 G>A maps to NM_007256.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:74907573 G>A maps to NM_007256.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:33690265 C>T maps to NM_152270.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:33690265 C>T maps to NM_152270.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:16261545 C>T maps to NM_015001.2 N2937N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:16261545 C>T maps to NM_015001.2 N2937N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:158627404 A>T maps to NM_003126.2 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:158627404 A>T maps to NM_003126.2 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:89856778 G>A maps to NM_152999.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:89856778 G>A maps to NM_152999.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:150028397 C>T maps to NM_001166209.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:150028397 C>T maps to NM_001166209.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:118627673 G>A maps to NM_016281.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:118627673 G>A maps to NM_016281.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:45148652 G>T maps to ENST00000404564 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:45148652 G>T maps to ENST00000404564 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:67815002 G>A maps to NM_006019.3 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:67815002 G>A maps to NM_006019.3 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:2320588 G>T maps to NM_003245.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:2320588 G>T maps to NM_003245.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:85554056 G>T maps to ENST00000409015 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:85554056 G>T maps to ENST00000409015 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:63170220 C>G maps to NM_178505.6 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:63170220 C>G maps to NM_178505.6 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:68691515 A>T maps to NM_004262.2 Y343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:68691515 A>T maps to NM_004262.2 Y343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr21:19687505 G>A maps to NM_002772.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr21:19687505 G>A maps to NM_002772.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:83075446 C>T maps to NM_006670.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:83075446 C>T maps to NM_006670.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:49881338 C>T maps to NM_005879.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:49881338 C>T maps to NM_005879.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:81610006 C>A maps to NM_000369.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:81610006 C>A maps to NM_000369.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:54483228 C>T maps to NM_001003937.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:54483228 C>T maps to NM_001003937.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:154213987 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:154213987 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:43988238 C>T maps to NM_015983.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:43988238 C>T maps to NM_015983.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:116206406 C>T maps to NM_001172412.1 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:116206406 C>T maps to NM_001172412.1 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:150082662 C>T maps to NM_007259.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:150082662 C>T maps to NM_007259.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:64954702 C>T maps to NM_006977.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:64954702 C>T maps to NM_006977.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:72830424 C>T maps to NM_006885.3 P2052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:72830424 C>T maps to NM_006885.3 P2052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:70468872 G>A maps to ENST00000373988 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:70468872 G>A maps to ENST00000373988 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:18296556 C>T maps to ENST00000401790 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:18296556 C>T maps to ENST00000401790 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:44053338 A>G maps to NM_001099284.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr10:44053338 A>G maps to NM_001099284.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:37677489 G>A maps to NM_152279.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:37677489 G>A maps to NM_152279.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:123985340 G>A maps to NM_020747.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:123985340 G>A maps to NM_020747.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:91405077 T>G maps to NM_201269.1 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:91405077 T>G maps to NM_201269.1 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:12575952 G>A maps to ENST00000428311 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:12575952 G>A maps to ENST00000428311 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:130191112 C>T maps to NM_007135.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr9:130191112 C>T maps to NM_007135.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:23545306 T>C maps to NM_003430.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:23545306 T>C maps to NM_003430.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:112174159 A>T maps to NM_001127510.2 K957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:112174159 A>T maps to NM_001127510.2 K957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:77542780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:77542780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:170618823 G>A maps to NM_173872.2 W501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:170618823 G>A maps to NM_173872.2 W501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:3245076 G>A maps to NM_033225.5 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:3245076 G>A maps to NM_033225.5 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:27998440 C>A maps to NM_001017930.1 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:27998440 C>A maps to NM_001017930.1 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:21183972 C>A maps to NM_001198801.1 E1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:21183972 C>A maps to NM_001198801.1 E1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:154159069 C>A maps to NM_000132.3 G999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:154159069 C>A maps to NM_000132.3 G999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:52351367 A>G maps to NM_002203.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:52351367 A>G maps to NM_002203.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:169805872 G>A maps to NM_004137.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:169805872 G>A maps to NM_004137.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:123192675 C>G maps to NM_015312.3 S2666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:123192675 C>G maps to NM_015312.3 S2666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:151900188 G>A maps to NM_005367.5 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:151900188 G>A maps to NM_005367.5 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:152482653 G>T maps to NM_004988.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:152482653 G>T maps to NM_004988.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:113728837 C>T maps to NM_001112732.1 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:113728837 C>T maps to NM_001112732.1 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:116397813 A>T maps to NM_001127500.1 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:116397813 A>T maps to NM_001127500.1 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:88420186 G>T maps to NM_001012338.1 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:88420186 G>T maps to NM_001012338.1 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:57992981 G>A maps to NM_024779.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:57992981 G>A maps to NM_024779.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:2073948 C>A maps to NM_181808.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:2073948 C>A maps to NM_181808.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:53104227 C>T maps to NM_182595.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:53104227 C>T maps to NM_182595.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:140692806 C>T maps to NM_001104647.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:140692806 C>T maps to NM_001104647.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:74035837 G>A maps to NM_014230.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:74035837 G>A maps to NM_014230.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:84670518 G>A maps to NM_003849.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:84670518 G>A maps to NM_003849.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:64168662 G>T maps to NM_016220.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:64168662 G>T maps to NM_016220.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:107560863 C>A maps to NM_005502.3 V1653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:107560863 C>A maps to NM_005502.3 V1653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:123166723 C>T maps to NM_183357.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:123166723 C>T maps to NM_183357.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:64800102 A>G maps to ENST00000422803 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:64800102 A>G maps to ENST00000422803 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:105410042 T>C maps to NM_138420.2 L3915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:105410042 T>C maps to NM_138420.2 L3915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:19612450 T>G maps to NM_012067.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:19612450 T>G maps to NM_012067.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:129811950 A>G maps to NM_001136152.1 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:129811950 A>G maps to NM_001136152.1 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:46568662 G>A maps to ENST00000458649 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:46568662 G>A maps to ENST00000458649 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:10692526 C>A maps to ENST00000453102 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:10692526 C>A maps to ENST00000453102 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:53994751 G>A maps to NM_001130059.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:53994751 G>A maps to NM_001130059.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:113473715 C>T maps to NM_032189.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:113473715 C>T maps to NM_032189.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:113473722 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:113473722 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:194175079 T>A maps to NM_024524.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:194175079 T>A maps to NM_024524.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:77844782 C>G maps to NM_001010860.1 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:77844782 C>G maps to NM_001010860.1 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:56620019 G>A maps to NM_001038704.1 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:56620019 G>A maps to NM_001038704.1 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:210010462 C>A maps to NM_014388.6 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:210010462 C>A maps to NM_014388.6 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181546993 C>A maps to ENST00000357570 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181546993 C>A maps to ENST00000357570 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:55012272 G>T maps to NM_020356.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:55012272 G>T maps to NM_020356.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:49093591 C>T maps to NM_014008.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:49093591 C>T maps to NM_014008.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:43381990 C>A maps to NM_148672.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:43381990 C>A maps to NM_148672.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:59206372 G>T maps to NM_031891.2 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:59206372 G>T maps to NM_031891.2 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:68712777 C>T maps to NM_001793.4 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:68712777 C>T maps to NM_001793.4 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:96694098 A>G maps to NM_002595.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:96694098 A>G maps to NM_002595.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:42231193 C>T maps to NM_004363.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:42231193 C>T maps to NM_004363.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:214819596 A>G maps to NM_016343.3 E2228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:214819596 A>G maps to NM_016343.3 E2228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:26852374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:26852374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:143047737 C>T maps to NM_000083.2 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:143047737 C>T maps to NM_000083.2 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:87656850 T>A maps to NM_019098.4 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:87656850 T>A maps to NM_019098.4 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:46737032 A>C maps to NM_130902.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:46737032 A>C maps to NM_130902.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:88008696 C>A maps to NM_033048.5 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:88008696 C>A maps to NM_033048.5 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:117365196 G>A maps to NM_033427.2 H1390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:117365196 G>A maps to NM_033427.2 H1390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:15807816 C>G maps to NM_023944.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:15807816 C>G maps to NM_023944.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:373023 C>G maps to NM_014974.2 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:373023 C>G maps to NM_014974.2 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:107956732 G>T maps to NM_014421.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:107956732 G>T maps to NM_014421.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:1624760 G>T maps to ENST00000357934 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:1624760 G>T maps to ENST00000357934 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:52433736 C>T maps to ENST00000273600 R4270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:52433736 C>T maps to ENST00000273600 R4270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11622752 C>G maps to NM_001372.3 R1885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11622752 C>G maps to NM_001372.3 R1885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:117749589 C>T maps to ENST00000276204 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:117749589 C>T maps to ENST00000276204 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:137799407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:137799407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:131761675 C>A maps to ENST00000355311 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:131761675 C>A maps to ENST00000355311 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:28380843 A>T maps to NM_198529.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:28380843 A>T maps to NM_198529.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr22:43950874 C>T maps to NM_022785.3 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr22:43950874 C>T maps to NM_022785.3 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:177156556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:177156556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:30915111 A>G maps to ENST00000509504 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:30915111 A>G maps to ENST00000509504 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:127670447 C>A maps to NM_001999.3 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:127670447 C>A maps to NM_001999.3 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:127697427 C>A maps to NM_001999.3 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:127697427 C>A maps to NM_001999.3 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:76828786 G>A maps to NM_006682.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:76828786 G>A maps to NM_006682.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:152279609 A>G maps to NM_002016.1 S2584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:152279609 A>G maps to NM_002016.1 S2584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:37745335 G>T maps to NM_014907.2 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:37745335 G>T maps to NM_014907.2 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:71318472 C>A maps to NM_018348.5 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:71318472 C>A maps to NM_018348.5 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:31178600 C>T maps to NM_024572.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:31178600 C>T maps to NM_024572.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:7842803 G>T maps to NM_020634.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:7842803 G>T maps to NM_020634.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:85901330 C>T maps to ENST00000436406 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:85901330 C>T maps to ENST00000436406 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:46178074 G>C maps to NM_000164.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:46178074 G>C maps to NM_000164.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:20331681 G>A maps to NM_001007240.1 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:20331681 G>A maps to NM_001007240.1 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:9709395 C>T maps to ENST00000380929 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:9709395 C>T maps to ENST00000380929 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:128408863 C>A maps to NM_005291.2 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:128408863 C>A maps to NM_005291.2 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:165404187 G>A maps to NM_004490.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:165404187 G>A maps to NM_004490.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:105192074 G>A maps to NM_020771.3 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:105192074 G>A maps to NM_020771.3 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:19015565 G>T maps to NM_178425.2 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:19015565 G>T maps to NM_178425.2 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:186077689 A>T maps to NM_031935.2 P3650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:186077689 A>T maps to NM_031935.2 P3650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:52840933 C>T maps to NM_002217.3 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:52840933 C>T maps to NM_002217.3 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:155711581 T>C maps to NM_002239.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:155711581 T>C maps to NM_002239.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:57181644 C>G maps to NM_020722.1 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:57181644 C>G maps to NM_020722.1 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:5765718 C>T maps to ENST00000414202 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:5765718 C>T maps to ENST00000414202 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:1345537 A>T maps to NM_020894.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:1345537 A>T maps to NM_020894.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:118719675 G>A maps to NM_001127211.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:118719675 G>A maps to NM_001127211.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:4927271 A>G maps to NM_006612.5 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:4927271 A>G maps to NM_006612.5 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:86877377 G>T maps to NM_057162.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:86877377 G>T maps to NM_057162.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:52824462 G>T maps to ENST00000252245 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:52824462 G>T maps to ENST00000252245 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:29963353 C>T maps to NM_015344.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:29963353 C>T maps to NM_015344.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:1474214 C>A maps to NM_024830.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:1474214 C>A maps to NM_024830.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:100176035 C>T maps to NM_002319.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:100176035 C>T maps to NM_002319.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:25450200 C>T maps to NM_017640.5 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:25450200 C>T maps to NM_017640.5 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:62856867 T>A maps to NM_199340.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:62856867 T>A maps to NM_199340.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:40137749 C>T maps to NM_020929.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:40137749 C>T maps to NM_020929.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70477609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70477609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:39514069 G>A maps to NM_003618.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:39514069 G>A maps to NM_003618.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:27475432 C>T maps to NM_001172303.1 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:27475432 C>T maps to NM_001172303.1 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:60161283 C>T maps to NM_206939.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:60161283 C>T maps to NM_206939.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:9089918 T>G maps to NM_024690.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:9089918 T>G maps to NM_024690.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:49426987 C>A maps to NM_000255.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:49426987 C>A maps to NM_000255.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:102029287 G>A maps to NM_052867.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:102029287 G>A maps to NM_052867.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:21120400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:21120400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27387647 G>A maps to ENST00000396636 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27387647 G>A maps to ENST00000396636 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:69681330 A>G maps to NM_138713.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:69681330 A>G maps to NM_138713.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7981510 C>A maps to NM_176821.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7981510 C>A maps to NM_176821.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:33467823 C>T maps to NM_022917.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:33467823 C>T maps to NM_022917.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:80130239 C>A maps to NM_004796.4 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:80130239 C>A maps to NM_004796.4 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:107979285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:107979285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:125512599 G>A maps to ENST00000373684 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:125512599 G>A maps to ENST00000373684 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:57971020 C>G maps to NM_001004459.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:57971020 C>G maps to NM_001004459.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:143973505 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:143973505 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:4843074 C>T maps to NM_001004753.1 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:4843074 C>T maps to NM_001004753.1 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:4824734 G>A maps to ENST00000380382 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:4824734 G>A maps to ENST00000380382 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:42804210 C>A maps to NM_001145940.1 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:42804210 C>A maps to NM_001145940.1 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:140590653 C>T maps to NM_018932.3 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:140590653 C>T maps to NM_018932.3 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:82532039 C>G maps to NM_033026.5 G4485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:82532039 C>G maps to NM_033026.5 G4485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:94935645 G>T maps to NM_001161778.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:94935645 G>T maps to NM_001161778.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:3147689 G>T maps to NM_002627.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:3147689 G>T maps to NM_002627.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:82560237 A>C maps to NM_199418.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:82560237 A>C maps to NM_199418.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:23397856 T>C maps to NM_173495.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:23397856 T>C maps to NM_173495.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:198675923 A>T maps to ENST00000271610 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:198675923 A>T maps to ENST00000271610 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:155129872 A>G maps to NM_014892.3 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:155129872 A>G maps to NM_014892.3 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:113307818 T>A maps to NM_001143854.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:113307818 T>A maps to NM_001143854.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:35547522 T>A maps to NM_001135999.1 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:35547522 T>A maps to NM_001135999.1 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:50407374 C>T maps to NM_020436.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:50407374 C>T maps to NM_020436.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:9119213 G>A maps to NM_003966.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:9119213 G>A maps to NM_003966.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:94756234 A>T maps to NM_001100607.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:94756234 A>T maps to NM_001100607.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:61569690 A>T maps to NM_001143818.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:61569690 A>T maps to NM_001143818.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:61154282 G>T maps to NM_002639.4 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:61154282 G>T maps to NM_002639.4 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:47098502 C>T maps to NM_014159.6 L2257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:47098502 C>T maps to NM_014159.6 L2257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:85892884 C>A maps to NM_198843.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:85892884 C>A maps to NM_198843.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:28883245 G>A maps to NM_001145795.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:28883245 G>A maps to NM_001145795.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:164758883 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:164758883 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:49934328 C>A maps to NM_020309.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:49934328 C>A maps to NM_020309.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:64359069 C>A maps to NM_144585.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:64359069 C>A maps to NM_144585.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:128320946 T>A maps to NM_001017372.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:128320946 T>A maps to NM_001017372.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:301673 G>T maps to NM_003044.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:301673 G>T maps to NM_003044.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:5833047 G>A maps to NM_003108.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:5833047 G>A maps to NM_003108.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:53775907 C>T maps to NM_138473.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:53775907 C>T maps to NM_138473.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:228881212 G>A maps to NM_001142644.1 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:228881212 G>A maps to NM_001142644.1 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:119951384 A>G maps to NM_133477.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:119951384 A>G maps to NM_133477.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:100014010 A>T maps to ENST00000394144 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:100014010 A>T maps to ENST00000394144 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47444635 C>A maps to NM_003254.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47444635 C>A maps to NM_003254.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153524337 G>T maps to NM_012253.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153524337 G>T maps to NM_012253.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153551619 G>A maps to NM_012253.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153551619 G>A maps to NM_012253.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:38799908 C>A maps to NM_003263.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:38799908 C>A maps to NM_003263.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:12940113 G>A maps to ENST00000311912 Q1003Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:12940113 G>A maps to ENST00000311912 Q1003Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:88589116 T>C maps to NM_181783.3 N812N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:88589116 T>C maps to NM_181783.3 N812N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:103317144 G>T maps to ENST00000376052 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:103317144 G>T maps to ENST00000376052 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:123539832 T>C maps to NM_006073.2 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:123539832 T>C maps to NM_006073.2 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:165961706 G>A maps to NM_152620.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:165961706 G>A maps to NM_152620.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:51872216 G>C maps to NM_173485.5 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:51872216 G>C maps to NM_173485.5 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:179604300 A>T maps to NM_133437.3 T4382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:179604300 A>T maps to NM_133437.3 T4382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:57958409 C>A maps to NM_016261.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:57958409 C>A maps to NM_016261.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:5042784 T>A maps to NM_004505.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:5042784 T>A maps to NM_004505.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47516657 C>A maps to NM_153477.1 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47516657 C>A maps to NM_153477.1 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:154448518 G>A maps to NM_003372.5 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:154448518 G>A maps to NM_003372.5 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:51477788 G>T maps to ENST00000273612 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:51477788 G>T maps to ENST00000273612 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:100832295 G>A maps to NM_017890.3 E3005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:100832295 G>A maps to NM_017890.3 E3005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:177041038 G>A maps to NM_170710.4 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:177041038 G>A maps to NM_170710.4 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:100934398 C>T maps to NM_001161476.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:100934398 C>T maps to NM_001161476.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:54337550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:54337550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:100344278 G>C maps to ENST00000349350 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:100344278 G>C maps to ENST00000349350 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:106456505 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:106456505 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:32332940 A>T maps to ENST00000375200 K59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:32332940 A>T maps to ENST00000375200 K59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:52856957 G>T maps to NM_001161425.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:52856957 G>T maps to NM_001161425.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:46360579 T>A maps to NM_001039891.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:46360579 T>A maps to NM_001039891.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:121733184 A>C maps to NM_005763.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:121733184 A>C maps to NM_005763.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:215843638 T>C maps to NM_173076.2 P1622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:215843638 T>C maps to NM_173076.2 P1622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:44079548 C>A maps to NM_022437.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:44079548 C>A maps to NM_022437.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:74083896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:74083896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:70901939 C>A maps to NM_001185054.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:70901939 C>A maps to NM_001185054.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148038094 T>A maps to NM_002025.3 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148038094 T>A maps to NM_002025.3 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:38396744 G>T maps to NM_000692.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:38396744 G>T maps to NM_000692.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:14799106 T>A maps to NM_001145029.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:14799106 T>A maps to NM_001145029.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:14852040 C>A maps to NM_001145029.1 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:14852040 C>A maps to NM_001145029.1 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:3030287 C>T maps to NM_004042.3 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:3030287 C>T maps to NM_004042.3 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:123264717 G>T maps to NM_080928.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:123264717 G>T maps to NM_080928.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:96794826 G>A maps to NM_018036.5 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:96794826 G>A maps to NM_018036.5 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:119509422 G>T maps to NM_001142447.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:119509422 G>T maps to NM_001142447.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:36045889 G>T maps to NM_000704.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:36045889 G>T maps to NM_000704.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70070770 G>A maps to NM_032735.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70070770 G>A maps to NM_032735.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:7862663 G>T maps to NM_001718.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:7862663 G>T maps to NM_001718.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:33628274 T>A maps to ENST00000389726 S1365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:33628274 T>A maps to ENST00000389726 S1365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:82644075 G>T maps to NM_145018.3 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:82644075 G>T maps to NM_145018.3 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:11444628 A>G maps to NM_152308.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:11444628 A>G maps to NM_152308.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:67558975 T>A maps to NM_001013674.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:67558975 T>A maps to NM_001013674.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:17950903 C>A maps to NM_052865.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:17950903 C>A maps to NM_052865.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:113541201 G>A maps to NM_018392.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:113541201 G>A maps to NM_018392.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:2794919 C>T maps to NM_199460.2 D1947D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:2794919 C>T maps to NM_199460.2 D1947D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:105215147 C>A maps to NM_001001412.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:105215147 C>A maps to NM_001001412.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:149636357 G>T maps to NM_015981.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:149636357 G>T maps to NM_015981.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:104871219 A>G maps to NM_001136112.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:104871219 A>G maps to NM_001136112.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:8787363 C>A maps to NM_001234.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:8787363 C>A maps to NM_001234.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:31682378 C>A maps to NM_194300.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:31682378 C>A maps to NM_194300.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:42784549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:42784549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:41822538 G>T maps to NM_052848.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:41822538 G>T maps to NM_052848.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:43388578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:43388578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:50053673 G>A maps to NM_033031.2 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:50053673 G>A maps to NM_033031.2 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:73467574 A>C maps to NM_006429.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:73467574 A>C maps to NM_006429.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44757606 T>G maps to NM_001250.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44757606 T>G maps to NM_001250.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:31323216 G>C maps to NM_004932.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:31323216 G>C maps to NM_004932.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:51733775 C>G maps to NM_001971.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:51733775 C>G maps to NM_001971.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:33540176 T>G maps to ENST00000359576 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:33540176 T>G maps to ENST00000359576 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:123369764 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:123369764 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:87755831 G>T maps to NM_019098.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:87755831 G>T maps to NM_019098.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:103405969 C>A maps to NM_080629.2 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:103405969 C>A maps to NM_080629.2 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:32164182 C>T maps to NM_001856.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:32164182 C>T maps to NM_001856.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:48609588 G>T maps to NM_000094.3 R2332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:48609588 G>T maps to NM_000094.3 R2332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:3691617 C>T maps to ENST00000418971 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:3691617 C>T maps to ENST00000418971 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:36932410 G>T maps to NM_156039.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:36932410 G>T maps to NM_156039.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:69281659 G>A maps to NM_013266.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:69281659 G>A maps to NM_013266.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:74533540 C>T maps to NM_134268.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:74533540 C>T maps to NM_134268.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:136501611 C>A maps to NM_000787.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:136501611 C>A maps to NM_000787.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:162745597 C>A maps to NM_006182.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:162745597 C>A maps to NM_006182.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:140223131 G>A maps to NM_015689.3 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:140223131 G>A maps to NM_015689.3 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:14722410 G>A maps to NM_004080.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:14722410 G>A maps to NM_004080.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:11593662 C>G maps to NM_001372.3 V1508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:11593662 C>G maps to NM_001372.3 V1508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:225658115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:225658115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:46129365 T>C maps to NM_021572.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:46129365 T>C maps to NM_021572.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:34778239 C>T maps to NM_012156.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:34778239 C>T maps to NM_012156.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:23718102 G>A maps to NM_033266.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:23718102 G>A maps to NM_033266.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153406764 C>A maps to ENST00000442256 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153406764 C>A maps to ENST00000442256 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:89950665 G>T maps to NM_014883.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:89950665 G>T maps to NM_014883.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:187075717 T>G maps to ENST00000356371 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:187075717 T>G maps to ENST00000356371 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:71504424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:71504424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152327810 G>A maps to NM_001014342.2 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152327810 G>A maps to NM_001014342.2 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152283464 C>T maps to NM_002016.1 R1299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152283464 C>T maps to NM_002016.1 R1299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:128564098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:128564098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:118849734 G>T maps to NM_181721.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:118849734 G>T maps to NM_181721.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:52250184 G>T maps to NM_002029.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:52250184 G>T maps to NM_002029.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:79417956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:79417956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:39454432 C>A maps to NM_207361.4 R3007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:39454432 C>A maps to NM_207361.4 R3007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:131271367 G>T maps to NM_001003722.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:131271367 G>T maps to NM_001003722.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:93555526 A>G maps to NM_004126.3 *74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:93555526 A>G maps to NM_004126.3 *74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:119905558 C>A maps to NM_153002.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:119905558 C>A maps to NM_153002.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:37903137 G>A maps to ENST00000445327 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:37903137 G>A maps to ENST00000445327 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:158283986 G>T maps to NM_000826.3 G815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:158283986 G>T maps to NM_000826.3 G815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:146351043 C>T maps to NM_000838.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:146351043 C>T maps to NM_000838.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:46704788 G>T maps to NM_016426.6 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:46704788 G>T maps to NM_016426.6 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:93797495 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:93797495 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:114383949 G>A maps to NM_153612.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:114383949 G>A maps to NM_153612.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:47469741 G>A maps to NM_000621.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:47469741 G>A maps to NM_000621.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:118921761 C>A maps to NM_001130991.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:118921761 C>A maps to NM_001130991.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:130416703 G>A maps to NM_001170961.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:130416703 G>A maps to NM_001170961.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:75954464 G>A maps to NM_006633.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:75954464 G>A maps to NM_006633.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:120373104 C>A maps to NM_012281.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:120373104 C>A maps to NM_012281.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:99441528 C>A maps to NM_020697.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:99441528 C>A maps to NM_020697.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:6984339 A>G maps to NM_015061.3 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:6984339 A>G maps to NM_015061.3 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:55972874 A>G maps to NM_002253.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:55972874 A>G maps to NM_002253.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:8819247 C>T maps to ENST00000456698 R1368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:8819247 C>T maps to ENST00000456698 R1368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:81171176 C>A maps to NM_018689.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:81171176 C>A maps to NM_018689.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:39563848 G>C maps to NM_145027.4 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:39563848 G>C maps to NM_145027.4 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75602867 C>T maps to NM_001001933.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75602867 C>T maps to NM_001001933.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75606692 C>A maps to NM_001001933.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75606692 C>A maps to NM_001001933.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:118123450 T>A maps to NM_001031855.1 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:118123450 T>A maps to NM_001031855.1 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:55565830 A>T maps to NM_017839.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:55565830 A>T maps to NM_017839.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:151303999 G>T maps to NM_021048.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:151303999 G>T maps to NM_021048.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:220805568 C>T maps to NM_018650.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:220805568 C>T maps to NM_018650.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:126732431 G>A maps to NM_032446.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:126732431 G>A maps to NM_032446.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:132397703 C>T maps to NM_014064.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:132397703 C>T maps to NM_014064.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:89179913 T>C maps to NM_005941.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:89179913 T>C maps to NM_005941.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:102394102 C>A maps to NM_002423.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:102394102 C>A maps to NM_002423.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:46766386 C>A maps to NM_182493.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:46766386 C>A maps to NM_182493.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:26436438 C>T maps to NM_017433.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:26436438 C>T maps to NM_017433.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:36046594 G>T maps to ENST00000400445 G2169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:36046594 G>T maps to ENST00000400445 G2169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:51875430 G>A maps to NM_005601.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:51875430 G>A maps to NM_005601.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:160965078 G>A maps to ENST00000472947 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:160965078 G>A maps to ENST00000472947 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:70510514 G>T maps to NM_007363.4 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:70510514 G>T maps to NM_007363.4 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:79580489 C>A maps to NM_017921.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:79580489 C>A maps to NM_017921.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:50280582 G>T maps to ENST00000404971 I1358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:50280582 G>T maps to ENST00000404971 I1358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:47829997 G>A maps to NM_015231.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:47829997 G>A maps to NM_015231.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:102337995 G>T maps to NM_022052.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:102337995 G>T maps to NM_022052.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123870868 C>T maps to NM_001163278.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123870868 C>T maps to NM_001163278.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:70777048 C>G maps to NM_181672.2 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:70777048 C>G maps to NM_181672.2 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:159410294 C>T maps to NM_012351.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:159410294 C>T maps to NM_012351.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57995885 G>T maps to NM_001004471.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57995885 G>T maps to NM_001004471.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:143807166 G>A maps to NM_001005480.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:143807166 G>A maps to NM_001005480.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248487860 C>A maps to NM_001004691.1 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248487860 C>A maps to NM_001004691.1 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248756857 A>T maps to NM_001004693.1 L71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248756857 A>T maps to NM_001004693.1 L71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248059190 C>T maps to NM_001001957.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248059190 C>T maps to NM_001001957.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55419008 T>A maps to NM_001004059.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55419008 T>A maps to NM_001004059.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158735629 G>T maps to NM_001005185.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158735629 G>T maps to NM_001005185.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:54604074 C>A maps to NM_130771.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:54604074 C>A maps to NM_130771.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:72945674 G>T maps to NM_176071.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:72945674 G>T maps to NM_176071.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:2583588 G>T maps to NM_000430.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:2583588 G>T maps to NM_000430.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:145058996 A>T maps to NM_032789.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:145058996 A>T maps to NM_032789.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140203276 C>A maps to NM_018908.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140203276 C>A maps to NM_018908.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140773661 G>T maps to NM_032088.1 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140773661 G>T maps to NM_032088.1 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140769091 C>T maps to NM_003736.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140769091 C>T maps to NM_003736.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:52758275 C>A maps to NM_052937.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:52758275 C>A maps to NM_052937.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:179615933 G>T maps to NM_016559.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:179615933 G>T maps to NM_016559.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:47533763 A>G maps to NM_000293.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:47533763 A>G maps to NM_000293.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:99950618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:99950618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:51923294 C>A maps to NM_138694.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:51923294 C>A maps to NM_138694.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:8637932 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:8637932 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:21142699 C>T maps to NM_018474.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:21142699 C>T maps to NM_018474.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:82764009 G>T maps to NM_000307.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:82764009 G>T maps to NM_000307.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:121684622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:121684622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:178753641 A>G maps to NM_152663.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:178753641 A>G maps to NM_152663.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:130941232 C>A maps to NM_015347.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:130941232 C>A maps to NM_015347.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47120506 C>A maps to NM_080746.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47120506 C>A maps to NM_080746.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:4556050 C>A maps to NM_032108.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:4556050 C>A maps to NM_032108.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:120901791 G>A maps to NM_003769.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:120901791 G>A maps to NM_003769.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16977261 G>A maps to NM_015260.1 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16977261 G>A maps to NM_015260.1 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:8417115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:8417115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:10583457 G>A maps to ENST00000354846 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:10583457 G>A maps to ENST00000354846 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:49098726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:49098726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104046428 A>T maps to NM_017564.9 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104046428 A>T maps to NM_017564.9 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:31641904 A>T maps to NM_178862.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:31641904 A>T maps to NM_178862.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:79279573 C>T maps to NM_016954.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:79279573 C>T maps to NM_016954.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:89177680 C>A maps to NM_138960.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:89177680 C>A maps to NM_138960.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:43526972 C>T maps to NM_201631.3 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:43526972 C>T maps to NM_201631.3 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153540999 T>A maps to NM_012253.3 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153540999 T>A maps to NM_012253.3 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:105360971 C>T maps to NM_030788.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:105360971 C>T maps to NM_030788.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57457953 G>A maps to NM_001130963.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57457953 G>A maps to NM_001130963.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:175049309 C>T maps to NM_022093.1 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:175049309 C>T maps to NM_022093.1 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:41204318 G>C maps to NM_198153.2 *201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:41204318 G>C maps to NM_198153.2 *201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234873363 C>T maps to NM_024080.4 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234873363 C>T maps to NM_024080.4 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:18505560 C>T maps to NM_006292.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:18505560 C>T maps to NM_006292.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:216246297 T>A maps to ENST00000366943 R1930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:216246297 T>A maps to ENST00000366943 R1930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:62519824 G>T maps to NM_024784.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:62519824 G>T maps to NM_024784.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:49671946 G>T maps to NM_015069.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:49671946 G>T maps to NM_015069.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:21720465 C>A maps to NM_001001415.2 Y537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:21720465 C>A maps to NM_001001415.2 Y537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:8654778 G>T maps to NM_030957.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:8654778 G>T maps to NM_030957.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:45743308 G>T maps to NM_021116.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:45743308 G>T maps to NM_021116.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:88029316 A>T maps to NM_001166693.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:88029316 A>T maps to NM_001166693.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:5721838 G>A maps to ENST00000356134 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:5721838 G>A maps to ENST00000356134 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:21225225 A>C maps to NM_000384.2 L4356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:21225225 A>C maps to NM_000384.2 L4356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:116701353 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:116701353 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:57294180 G>T maps to NM_012096.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:57294180 G>T maps to NM_012096.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121305146 G>T maps to NM_001012659.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121305146 G>T maps to NM_001012659.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:129148379 C>G maps to ENST00000303743 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:129148379 C>G maps to ENST00000303743 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:51693011 C>A maps to NM_016293.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:51693011 C>A maps to NM_016293.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:34648890 C>A maps to ENST00000438749 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:34648890 C>A maps to ENST00000438749 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:72588121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:72588121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:67422389 C>T maps to NM_152765.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:67422389 C>T maps to NM_152765.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:24509554 C>T maps to NM_012295.3 A1380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:24509554 C>T maps to NM_012295.3 A1380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:92978025 A>G maps to NM_017667.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:92978025 A>G maps to NM_017667.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:71058893 T>A maps to NM_015717.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:71058893 T>A maps to NM_015717.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:65026937 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:65026937 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:42611339 C>T maps to NM_004198.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:42611339 C>T maps to NM_004198.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76259265 C>T maps to NM_001882.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76259265 C>T maps to NM_001882.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:140287450 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:140287450 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:497486 C>T maps to NM_018303.4 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:497486 C>T maps to NM_018303.4 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:94688134 A>T maps to NM_019053.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:94688134 A>T maps to NM_019053.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29222071 C>T maps to NM_199280.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29222071 C>T maps to NM_199280.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190250804 G>T maps to NM_199051.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190250804 G>T maps to NM_199051.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:164466340 T>C maps to NM_018086.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:164466340 T>C maps to NM_018086.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:86088718 A>G maps to NM_013231.4 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:86088718 A>G maps to NM_013231.4 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20043968 G>T maps to NM_001002911.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20043968 G>T maps to NM_001002911.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:89953779 G>T maps to NM_032119.3 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:89953779 G>T maps to NM_032119.3 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:27565995 G>T maps to NM_001521.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:27565995 G>T maps to NM_001521.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:186086594 A>T maps to NM_031935.2 P3896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:186086594 A>T maps to NM_031935.2 P3896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:6452952 G>T maps to NM_000613.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:6452952 G>T maps to NM_000613.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:47121402 G>A maps to NM_006546.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:47121402 G>A maps to NM_006546.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:160485538 C>T maps to NM_000876.2 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:160485538 C>T maps to NM_000876.2 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:136728999 G>T maps to NM_144717.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:136728999 G>T maps to NM_144717.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:99180084 G>T maps to NM_001134224.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:99180084 G>T maps to NM_001134224.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:124351420 G>T maps to NM_001024660.3 R1777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:124351420 G>T maps to NM_001024660.3 R1777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:36763323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:36763323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:45400638 C>A maps to ENST00000355081 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:45400638 C>A maps to ENST00000355081 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51480935 C>A maps to NM_005046.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51480935 C>A maps to NM_005046.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129785485 T>A maps to NM_000426.3 Y2348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129785485 T>A maps to NM_000426.3 Y2348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:49162899 C>A maps to NM_002292.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:49162899 C>A maps to NM_002292.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:183086516 G>T maps to NM_002293.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:183086516 G>T maps to NM_002293.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115805311 G>T maps to NM_002338.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115805311 G>T maps to NM_002338.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:51319243 G>A maps to NM_014033.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:51319243 G>A maps to NM_014033.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220935099 G>T maps to NM_017898.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220935099 G>T maps to NM_017898.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:151732527 A>T maps to NM_031420.2 *268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:151732527 A>T maps to NM_031420.2 *268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:9083753 G>T maps to NM_024690.2 T2687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:9083753 G>T maps to NM_024690.2 T2687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20070730 C>T maps to ENST00000396087 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20070730 C>T maps to ENST00000396087 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:78513152 G>A maps to NM_014903.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:78513152 G>A maps to NM_014903.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:21134260 C>A maps to ENST00000430741 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:21134260 C>A maps to ENST00000430741 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:70417313 G>A maps to NM_153181.2 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:70417313 G>A maps to NM_153181.2 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:118723941 C>A maps to NM_001173487.1 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:118723941 C>A maps to NM_001173487.1 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:142409564 G>T maps to NM_002511.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:142409564 G>T maps to NM_002511.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:156135258 C>A maps to NM_000910.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:156135258 C>A maps to NM_000910.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:18745157 G>C maps to ENST00000455492 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:18745157 G>C maps to ENST00000455492 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:135262699 C>T maps to NM_015135.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:135262699 C>T maps to NM_015135.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:41667973 G>A maps to NM_016359.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:41667973 G>A maps to NM_016359.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:103572953 G>T maps to NM_024410.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:103572953 G>T maps to NM_024410.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:107332203 T>C maps to NM_001004483.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:107332203 T>C maps to NM_001004483.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248512711 C>A maps to NM_001001918.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248512711 C>A maps to NM_001001918.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:51515364 G>T maps to NM_001004703.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:51515364 G>T maps to NM_001004703.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158517139 G>T maps to NM_001005189.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158517139 G>T maps to NM_001005189.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:56128531 T>A maps to NM_001005205.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:56128531 T>A maps to NM_001005205.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:20922833 C>T maps to NM_017807.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:20922833 C>T maps to NM_017807.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140515334 C>T maps to NM_015669.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140515334 C>T maps to NM_015669.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140568928 C>A maps to NM_019119.3 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140568928 C>A maps to NM_019119.3 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140710331 G>T maps to NM_018912.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140710331 G>T maps to NM_018912.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140764328 G>T maps to NM_018920.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140764328 G>T maps to NM_018920.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:207109004 C>A maps to NM_002644.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:207109004 C>A maps to NM_002644.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:53104134 C>A maps to NM_182595.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:53104134 C>A maps to NM_182595.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:149210433 G>T maps to NM_133263.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:149210433 G>T maps to NM_133263.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:148601523 C>A maps to NM_138364.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:148601523 C>A maps to NM_138364.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:177421210 G>A maps to NM_006261.4 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:177421210 G>A maps to NM_006261.4 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31105977 C>T maps to NM_014069.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31105977 C>T maps to NM_014069.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:87687591 C>T maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:87687591 C>T maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79253248 G>A maps to NM_001008387.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79253248 G>A maps to NM_001008387.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155771557 G>A maps to NM_000337.5 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155771557 G>A maps to NM_000337.5 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:171766496 C>A maps to NM_001017995.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:171766496 C>A maps to NM_001017995.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:52033170 G>T maps to NM_001245.5 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:52033170 G>T maps to NM_001245.5 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:164700807 T>A maps to NM_001041.3 V1743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:164700807 T>A maps to NM_001041.3 V1743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220089057 C>G maps to NM_018713.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220089057 C>G maps to NM_018713.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:67513051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:67513051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:88719863 C>T maps to NM_003087.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:88719863 C>T maps to NM_003087.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:137483967 C>T maps to NM_004189.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:137483967 C>T maps to NM_004189.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:214878755 C>A maps to NM_024532.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:214878755 C>A maps to NM_024532.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:44329628 C>T maps to NM_145026.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:44329628 C>T maps to NM_145026.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:16255644 A>T maps to NM_015001.2 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:16255644 A>T maps to NM_015001.2 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:30722384 G>T maps to NM_006662.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:30722384 G>T maps to NM_006662.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:144507901 A>T maps to NM_003764.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:144507901 A>T maps to NM_003764.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72680484 G>T maps to NM_013381.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72680484 G>T maps to NM_013381.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:72973925 G>T maps to NM_007332.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:72973925 G>T maps to NM_007332.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:73000430 G>T maps to NM_005786.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:73000430 G>T maps to NM_005786.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:126226901 C>A maps to NM_001165974.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:126226901 C>A maps to NM_001165974.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57641419 C>T maps to NM_020903.2 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57641419 C>T maps to NM_020903.2 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:77907353 G>T maps to NM_020798.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:77907353 G>T maps to NM_020798.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:31039048 C>A maps to NM_014717.1 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:31039048 C>A maps to NM_014717.1 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:58290167 G>A maps to NM_017652.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:58290167 G>A maps to NM_017652.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:88965764 A>T maps to NM_181646.2 K1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:88965764 A>T maps to NM_181646.2 K1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:33290933 G>T maps to NM_004274.4 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:33290933 G>T maps to NM_004274.4 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:96761864 T>A maps to NM_018036.5 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:96761864 T>A maps to NM_018036.5 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:36050048 G>A maps to NM_000704.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:36050048 G>A maps to NM_000704.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:32906433 A>T maps to NM_000059.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:32906433 A>T maps to NM_000059.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:207286343 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:207286343 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:27925798 G>A maps to ENST00000341513 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:27925798 G>A maps to ENST00000341513 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:8288250 A>G maps to NM_016184.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:8288250 A>G maps to NM_016184.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:95682071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:95682071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:86304321 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:86304321 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:130020971 G>A maps to NM_001868.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:130020971 G>A maps to NM_001868.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:34383798 G>T maps to ENST00000373381 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:34383798 G>T maps to ENST00000373381 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:6647185 T>A maps to NM_003737.2 T2232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:6647185 T>A maps to NM_003737.2 T2232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr20:61513365 C>A maps to NM_033081.2 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr20:61513365 C>A maps to NM_033081.2 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:29036400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:29036400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:102505473 C>T maps to NM_001376.4 T3781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:102505473 C>T maps to NM_001376.4 T3781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:108344738 C>A maps to NM_014648.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:108344738 C>A maps to NM_014648.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:48830830 G>T maps to NM_001425.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:48830830 G>T maps to NM_001425.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:36334710 C>G maps to NM_016135.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:36334710 C>G maps to NM_016135.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:68749570 G>A maps to NM_015686.2 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:68749570 G>A maps to NM_015686.2 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:216295506 G>A maps to NM_212482.1 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:216295506 G>A maps to NM_212482.1 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:39202803 C>A maps to ENST00000263405 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:39202803 C>A maps to ENST00000263405 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:43593174 G>A maps to NM_019096.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:43593174 G>A maps to NM_019096.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:176310846 G>A maps to NM_002115.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:176310846 G>A maps to NM_002115.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:156608053 T>C maps to NM_005546.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:156608053 T>C maps to NM_005546.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:211263911 G>T maps to NM_172362.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:211263911 G>T maps to NM_172362.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:53205731 G>T maps to NM_002272.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:53205731 G>T maps to NM_002272.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:10049234 G>T maps to NM_001008737.1 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:10049234 G>T maps to NM_001008737.1 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:114226574 G>A maps to NM_001142782.1 W1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:114226574 G>A maps to NM_001142782.1 W1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:45924190 C>T maps to NM_005456.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:45924190 C>T maps to NM_005456.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:24839230 T>C maps to NM_001136022.1 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:24839230 T>C maps to NM_001136022.1 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:116380681 C>A maps to NM_005599.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:116380681 C>A maps to NM_005599.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:142749649 A>T maps to NM_001001667.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:142749649 A>T maps to NM_001001667.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:176526297 T>A maps to NM_020318.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:176526297 T>A maps to NM_020318.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:91133014 C>A maps to NM_032968.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:91133014 C>A maps to NM_032968.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:102783310 C>A maps to NM_001195263.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:102783310 C>A maps to NM_001195263.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:8528596 G>T maps to NM_002839.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:8528596 G>T maps to NM_002839.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:47039330 G>T maps to NM_005676.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:47039330 G>T maps to NM_005676.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:106145411 G>T maps to ENST00000399421 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:106145411 G>T maps to ENST00000399421 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:157920996 A>T maps to NM_016625.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:157920996 A>T maps to NM_016625.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:51174344 C>G maps to ENST00000251020 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:51174344 C>G maps to ENST00000251020 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:84363383 G>A maps to NM_001012980.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:84363383 G>A maps to NM_001012980.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:51918645 G>T maps to NM_033130.4 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:51918645 G>T maps to NM_033130.4 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:19203776 C>T maps to NM_006938.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:19203776 C>T maps to NM_006938.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:28004719 G>A maps to NM_033389.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:28004719 G>A maps to NM_033389.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:30873049 A>G maps to NM_152787.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:30873049 A>G maps to NM_152787.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:59620775 G>T maps to NM_001062.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:59620775 G>T maps to NM_001062.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:179631372 C>T maps to ENST00000444136 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:179631372 C>T maps to ENST00000444136 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:133906049 G>A maps to NM_003235.4 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:133906049 G>A maps to NM_003235.4 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:108572675 C>T maps to NM_016388.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:108572675 C>T maps to NM_016388.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:142499777 G>T maps to ENST00000476941 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:142499777 G>T maps to ENST00000476941 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:45784062 C>G maps to ENST00000397932 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:45784062 C>G maps to ENST00000397932 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:186339796 G>T maps to NM_018359.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:186339796 G>T maps to NM_018359.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:117570672 T>C maps to NM_019045.4 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:117570672 T>C maps to NM_019045.4 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:77913899 T>A maps to NM_152694.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:77913899 T>A maps to NM_152694.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:27176876 C>G maps to NM_032283.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:27176876 C>G maps to NM_032283.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:106431375 G>T maps to NM_012082.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:106431375 G>T maps to NM_012082.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:58551816 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:58551816 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:56701624 C>G maps to NM_001080456.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:56701624 C>G maps to NM_001080456.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:215848371 T>G maps to NM_173076.2 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:215848371 T>G maps to NM_173076.2 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:111789244 G>T maps to NM_001142807.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:111789244 G>T maps to NM_001142807.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:39624683 G>T maps to NM_001464.3 C433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:39624683 G>T maps to NM_001464.3 C433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:43777381 C>A maps to ENST00000389420 V1592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:43777381 C>A maps to ENST00000389420 V1592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:77895266 C>T maps to NM_014913.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:77895266 C>T maps to NM_014913.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:105409859 C>T maps to NM_138420.2 P3976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:105409859 C>T maps to NM_138420.2 P3976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:21233631 G>T maps to NM_000384.2 I2036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:21233631 G>T maps to NM_000384.2 I2036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:43292651 G>T maps to NM_014753.3 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:43292651 G>T maps to NM_014753.3 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:172571919 C>T maps to ENST00000367723 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:172571919 C>T maps to ENST00000367723 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:45941861 C>A maps to ENST00000443468 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:45941861 C>A maps to ENST00000443468 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:184605295 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:184605295 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43859867 G>T maps to NM_020406.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43859867 G>T maps to NM_020406.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:122685674 G>T maps to NM_153223.3 R897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:122685674 G>T maps to NM_153223.3 R897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:203192351 G>A maps to NM_003465.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:203192351 G>A maps to NM_003465.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:106633562 G>A maps to NM_006825.3 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:106633562 G>A maps to NM_006825.3 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:41419070 C>A maps to NM_001843.2 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:41419070 C>A maps to NM_001843.2 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:103471677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:103471677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:238280774 C>A maps to NM_004369.3 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:238280774 C>A maps to NM_004369.3 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:27998106 G>T maps to NM_001017930.1 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:27998106 G>T maps to NM_001017930.1 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:6647527 C>A maps to NM_003737.2 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:6647527 C>A maps to NM_003737.2 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:50213371 G>T maps to NM_001013742.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:50213371 G>T maps to NM_001013742.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:169938309 C>A maps to NM_001142271.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:169938309 C>A maps to NM_001142271.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:83585467 C>A maps to NM_001142699.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:83585467 C>A maps to NM_001142699.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:21655912 G>A maps to NM_003777.3 A1366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:21655912 G>A maps to NM_003777.3 A1366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:142568572 C>A maps to NM_004445.3 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:142568572 C>A maps to NM_004445.3 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:13714430 C>A maps to NM_016649.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:13714430 C>A maps to NM_016649.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:118831992 C>A maps to NM_000127.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:118831992 C>A maps to NM_000127.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:114550399 T>C maps to NM_182495.5 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:114550399 T>C maps to NM_182495.5 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:152277155 C>T maps to NM_002016.1 R3402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:152277155 C>T maps to NM_002016.1 R3402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:86089393 C>A maps to NM_013231.4 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:86089393 C>A maps to NM_013231.4 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:154282907 G>T maps to NM_023934.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:154282907 G>T maps to NM_023934.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:151358393 G>C maps to NM_000808.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:151358393 G>C maps to NM_000808.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:122616717 G>T maps to NM_000828.4 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:122616717 G>T maps to NM_000828.4 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:236749752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:236749752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:91144372 C>A maps to NM_001010987.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:91144372 C>A maps to NM_001010987.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:156510565 C>A maps to NM_178229.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:156510565 C>A maps to NM_178229.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:52814364 C>A maps to NM_002215.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:52814364 C>A maps to NM_002215.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:155711557 C>T maps to NM_002239.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:155711557 C>T maps to NM_002239.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:99441274 G>A maps to NM_020697.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:99441274 G>A maps to NM_020697.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:137045460 G>A maps to NM_017415.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:137045460 G>A maps to NM_017415.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:39394380 C>A maps to NM_031963.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:39394380 C>A maps to NM_031963.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:84203520 G>T maps to NM_178452.4 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:84203520 G>T maps to NM_178452.4 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:102573849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:102573849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:9000567 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:9000567 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:152427079 C>T maps to NM_001164507.1 A5683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:152427079 C>T maps to NM_001164507.1 A5683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:73575341 G>T maps to NM_002499.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:73575341 G>T maps to NM_002499.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:115664628 A>G maps to NM_198514.3 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:115664628 A>G maps to NM_198514.3 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:247608105 C>A maps to NM_004895.4 C998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:247608105 C>A maps to NM_004895.4 C998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:47843374 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:47843374 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:3707285 T>C maps to NM_016320.4 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:3707285 T>C maps to NM_016320.4 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:128692648 T>A maps to NM_000276.3 L160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:128692648 T>A maps to NM_000276.3 L160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:50952127 G>T maps to NM_018245.2 C591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:50952127 G>T maps to NM_018245.2 C591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:57996245 G>C maps to NM_001004471.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:57996245 G>C maps to NM_001004471.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:29604478 C>A maps to NM_183378.2 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:29604478 C>A maps to NM_183378.2 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:58299214 C>A maps to NM_001040429.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:58299214 C>A maps to NM_001040429.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:140588871 C>A maps to NM_018932.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:140588871 C>A maps to NM_018932.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:89868838 C>A maps to NM_002693.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:89868838 C>A maps to NM_002693.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:22330234 G>T maps to NM_018119.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:22330234 G>T maps to NM_018119.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:48930131 G>A maps to ENST00000376358 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:48930131 G>A maps to ENST00000376358 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:47181712 G>A maps to ENST00000449438 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:47181712 G>A maps to ENST00000449438 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:150997257 A>T maps to NM_021222.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:150997257 A>T maps to NM_021222.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:32954591 A>G maps to NM_001076786.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:32954591 A>G maps to NM_001076786.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:204124179 C>A maps to NM_000537.3 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:204124179 C>A maps to NM_000537.3 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:109694087 A>T maps to NM_020769.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:109694087 A>T maps to NM_020769.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:182554507 G>A maps to NM_021133.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:182554507 G>A maps to NM_021133.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:166018881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:166018881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:71334923 C>A maps to NM_001144952.1 S2107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:71334923 C>A maps to NM_001144952.1 S2107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:13971162 C>G maps to NM_025229.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:13971162 C>G maps to NM_025229.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:42388739 C>T maps to NM_145733.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:42388739 C>T maps to NM_145733.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:8185690 C>A maps to NM_001080826.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:8185690 C>A maps to NM_001080826.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:119014860 G>T maps to NM_003054.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:119014860 G>T maps to NM_003054.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:2943330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:2943330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:67992071 C>A maps to NM_004232.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:67992071 C>A maps to NM_004232.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:34924839 G>C maps to NM_138927.1 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:34924839 G>C maps to NM_138927.1 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:20927363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:20927363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:14482689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:14482689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:122853869 G>T maps to NM_001130698.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:122853869 G>T maps to NM_001130698.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:234851352 C>A maps to NM_024080.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:234851352 C>A maps to NM_024080.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:62784974 C>T maps to ENST00000280377 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:62784974 C>T maps to ENST00000280377 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:42454304 C>T maps to ENST00000348544 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:42454304 C>T maps to ENST00000348544 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:26697215 G>T maps to NM_000638.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:26697215 G>T maps to NM_000638.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:180775251 G>T maps to NM_004736.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:180775251 G>T maps to NM_004736.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:44652982 G>T maps to NM_006630.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:44652982 G>T maps to NM_006630.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:85326374 G>T maps to NM_014630.2 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:85326374 G>T maps to NM_014630.2 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:185803624 C>T maps to NM_194250.1 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:185803624 C>T maps to NM_194250.1 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:238048569 G>T maps to NM_021186.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:238048569 G>T maps to NM_021186.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:89400399 C>T maps to NM_013227.3 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:89400399 C>T maps to NM_013227.3 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:100491142 G>T maps to NM_000665.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:100491142 G>T maps to NM_000665.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:110883274 C>A maps to NM_005719.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:110883274 C>A maps to NM_005719.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:172410886 G>C maps to NM_003945.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:172410886 G>C maps to NM_003945.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:32598880 G>A maps to NM_015060.1 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:32598880 G>A maps to NM_015060.1 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:42906617 C>T maps to NM_001296.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:42906617 C>T maps to NM_001296.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:73471670 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:73471670 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:196796070 C>T maps to NM_002113.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:196796070 C>T maps to NM_002113.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:10079105 C>T maps to NM_015719.3 Q1423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:10079105 C>T maps to NM_015719.3 Q1423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:31376691 G>T maps to NM_006892.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:31376691 G>T maps to NM_006892.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:6175038 G>A maps to NM_000129.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:6175038 G>A maps to NM_000129.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:116621055 A>T maps to NM_020940.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:116621055 A>T maps to NM_020940.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:110594384 G>A maps to NM_033088.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:110594384 G>A maps to NM_033088.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:34148897 G>T maps to NM_203408.3 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:34148897 G>T maps to NM_203408.3 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:34149051 C>T maps to NM_203408.3 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:34149051 C>T maps to NM_203408.3 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:61039975 G>T maps to NM_080473.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:61039975 G>T maps to NM_080473.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:47681877 G>T maps to NM_153838.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:47681877 G>T maps to NM_153838.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:32411097 A>T maps to NM_019111.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:32411097 A>T maps to NM_019111.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:102957268 C>A maps to NM_016232.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:102957268 C>A maps to NM_016232.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:95888300 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:95888300 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:49620824 G>T maps to NM_002237.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:49620824 G>T maps to NM_002237.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:200971447 C>A maps to NM_017596.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:200971447 C>A maps to NM_017596.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:49437155 G>C maps to NM_003482.3 A1841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:49437155 G>C maps to NM_003482.3 A1841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:104742406 T>C maps to NM_182931.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:104742406 T>C maps to NM_182931.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:10356998 C>A maps to NM_017533.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:10356998 C>A maps to NM_017533.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:57983115 C>G maps to NM_001004458.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:57983115 C>G maps to NM_001004458.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:248084348 C>T maps to NM_001005522.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:248084348 C>T maps to NM_001005522.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:140572892 C>A maps to NM_018930.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:140572892 C>A maps to NM_018930.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:140553606 C>A maps to NM_018940.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:140553606 C>A maps to NM_018940.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:82583173 C>T maps to NM_033026.5 E2365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:82583173 C>T maps to NM_033026.5 E2365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:207235397 C>T maps to NM_006212.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:207235397 C>T maps to NM_006212.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:33382863 C>T maps to NM_024165.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:33382863 C>T maps to NM_024165.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:99169979 C>T maps to NM_015029.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:99169979 C>T maps to NM_015029.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:175956198 A>T maps to NM_022457.5 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:175956198 A>T maps to NM_022457.5 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:156347137 C>T maps to NM_020407.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:156347137 C>T maps to NM_020407.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:18690843 G>A maps to NM_005406.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:18690843 G>A maps to NM_005406.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:237608810 T>C maps to NM_001035.2 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:237608810 T>C maps to NM_001035.2 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:52163070 C>T maps to NM_014191.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:52163070 C>T maps to NM_014191.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109017869 G>A maps to ENST00000228463 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109017869 G>A maps to ENST00000228463 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:18883651 G>A maps to ENST00000389467 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:18883651 G>A maps to ENST00000389467 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:114925375 C>G maps to NM_030756.4 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:114925375 C>G maps to NM_030756.4 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:44782163 G>A maps to NM_032256.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:44782163 G>A maps to NM_032256.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:6472122 T>A maps to NM_033278.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:6472122 T>A maps to NM_033278.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:42600600 G>T maps to NM_015255.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:42600600 G>T maps to NM_015255.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:43323077 G>C maps to NM_014345.2 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:43323077 G>C maps to NM_014345.2 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:247464456 C>T maps to NM_032752.1 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:247464456 C>T maps to NM_032752.1 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:169850326 G>T maps to NM_003742.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:169850326 G>T maps to NM_003742.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:195063240 T>A maps to NM_012287.5 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:195063240 T>A maps to NM_012287.5 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:20482504 C>A maps to NM_001010845.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:20482504 C>A maps to NM_001010845.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:43945020 G>T maps to ENST00000389420 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:43945020 G>T maps to ENST00000389420 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:114294268 C>A maps to NM_001148.4 P3878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:114294268 C>A maps to NM_001148.4 P3878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:40997143 G>T maps to NM_009590.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:40997143 G>T maps to NM_009590.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:26370769 A>T maps to NM_001197246.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:26370769 A>T maps to NM_001197246.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:81259232 C>T maps to NM_152446.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:81259232 C>T maps to NM_152446.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:67168096 T>C maps to NM_025187.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:67168096 T>C maps to NM_025187.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:13996796 A>T maps to ENST00000454313 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:13996796 A>T maps to ENST00000454313 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:228476172 T>G maps to NM_020161.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:228476172 T>G maps to NM_020161.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:192517356 C>A maps to NM_178496.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:192517356 C>A maps to NM_178496.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:72226649 G>T maps to NM_032649.5 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:72226649 G>T maps to NM_032649.5 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:99827595 G>T maps to NM_014361.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:99827595 G>T maps to NM_014361.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:146818110 G>C maps to NM_014141.5 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:146818110 G>C maps to NM_014141.5 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:147336342 C>A maps to NM_014141.5 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:147336342 C>A maps to NM_014141.5 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:197404112 C>A maps to NM_201253.2 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:197404112 C>A maps to NM_201253.2 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:5862926 C>A maps to NM_001014809.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:5862926 C>A maps to NM_001014809.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:186256670 G>A maps to NM_017541.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:186256670 G>A maps to NM_017541.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:139038397 G>T maps to NM_001013403.2 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:139038397 G>T maps to NM_001013403.2 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:57476946 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:57476946 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:71863874 T>A maps to ENST00000504952 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:71863874 T>A maps to ENST00000504952 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:83846907 C>A maps to NM_015018.2 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:83846907 C>A maps to NM_015018.2 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:162894881 T>A maps to NM_001935.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:162894881 T>A maps to NM_001935.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:100380642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:100380642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:134967156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:134967156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:96239249 G>T maps to NM_001130140.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:96239249 G>T maps to NM_001130140.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:157738453 G>C maps to NM_030764.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:157738453 G>C maps to NM_030764.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:152281969 G>T maps to NM_002016.1 R1798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:152281969 G>T maps to NM_002016.1 R1798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:114294036 C>A maps to NM_148898.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:114294036 C>A maps to NM_148898.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:46060351 C>A maps to NM_173536.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:46060351 C>A maps to NM_173536.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:69204658 A>T maps to NM_019617.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:69204658 A>T maps to NM_019617.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:158041791 C>T maps to NM_001166060.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:158041791 C>T maps to NM_001166060.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:94690495 A>T maps to NM_001510.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:94690495 A>T maps to NM_001510.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:65427987 C>A maps to NM_138737.3 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:65427987 C>A maps to NM_138737.3 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:166904655 G>T maps to NM_199351.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:166904655 G>T maps to NM_199351.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:79749994 C>T maps to NM_015206.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:79749994 C>T maps to NM_015206.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:200967545 T>A maps to NM_017596.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:200967545 T>A maps to NM_017596.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:165182943 G>T maps to NM_177398.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:165182943 G>T maps to NM_177398.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:170063224 G>T maps to NM_004525.2 P2335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:170063224 G>T maps to NM_004525.2 P2335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:24538409 C>T maps to NM_138360.3 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:24538409 C>T maps to NM_138360.3 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:156566061 T>A maps to NM_004270.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:156566061 T>A maps to NM_004270.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:39884032 G>A maps to NM_001098270.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:39884032 G>A maps to NM_001098270.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:19338660 C>A maps to NM_004386.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:19338660 C>A maps to NM_004386.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:124979486 C>A maps to NM_001040214.1 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:124979486 C>A maps to NM_001040214.1 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:247588856 G>T maps to NM_004895.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:247588856 G>T maps to NM_004895.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:80164063 C>G maps to NM_004796.4 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:80164063 C>G maps to NM_004796.4 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248128875 C>A maps to NM_001004491.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248128875 C>A maps to NM_001004491.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248436330 G>T maps to NM_001004695.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248436330 G>T maps to NM_001004695.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:97983439 G>A maps to NM_001005479.1 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:97983439 G>A maps to NM_001005479.1 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:14910177 C>A maps to NM_198944.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:14910177 C>A maps to NM_198944.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:36882058 G>A maps to NM_016734.1 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:36882058 G>A maps to NM_016734.1 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:56140517 C>A maps to NM_002591.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:56140517 C>A maps to NM_002591.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:77378446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:77378446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:204415205 C>G maps to NM_002646.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:204415205 C>G maps to NM_002646.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:208866198 T>A maps to NM_001080475.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:208866198 T>A maps to NM_001080475.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:23803431 C>T maps to NM_013261.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:23803431 C>T maps to NM_013261.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:99031020 C>A maps to NM_001198879.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:99031020 C>A maps to NM_001198879.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:43617229 G>T maps to NM_173050.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:43617229 G>T maps to NM_173050.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:28599219 A>T maps to NM_031459.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:28599219 A>T maps to NM_031459.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:164748532 T>C maps to NM_001041.3 Q953Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:164748532 T>C maps to NM_001041.3 Q953Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:99336993 G>C maps to NM_005073.3 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:99336993 G>C maps to NM_005073.3 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:18292098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:18292098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:173502879 A>G maps to NM_178527.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:173502879 A>G maps to NM_178527.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:70585415 G>C maps to NM_030958.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:70585415 G>C maps to NM_030958.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:70585514 G>C maps to NM_030958.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:70585514 G>C maps to NM_030958.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:160020026 C>T maps to NM_033394.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:160020026 C>T maps to NM_033394.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:61391822 G>T maps to ENST00000389520 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:61391822 G>T maps to ENST00000389520 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:65275157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:65275157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:120466836 C>A maps to NM_138554.3 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:120466836 C>A maps to NM_138554.3 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:103414409 C>T maps to NM_144632.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:103414409 C>T maps to NM_144632.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:30131593 C>T maps to NM_033229.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:30131593 C>T maps to NM_033229.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179442617 A>T maps to NM_133378.4 P20277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179442617 A>T maps to NM_133378.4 P20277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:70346366 C>T maps to NM_021139.2 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:70346366 C>T maps to NM_021139.2 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:70361151 G>T maps to NM_021139.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:70361151 G>T maps to NM_021139.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:48238660 G>A maps to NM_001017535.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:48238660 G>A maps to NM_001017535.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:61026769 G>A maps to NM_152718.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:61026769 G>A maps to NM_152718.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:77616703 A>T maps to NM_024721.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:77616703 A>T maps to NM_024721.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:64167567 G>T maps to NM_016220.3 G296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:64167567 G>T maps to NM_016220.3 G296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:31039642 C>A maps to NM_014717.1 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:31039642 C>A maps to NM_014717.1 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:238053263 G>T maps to NM_021186.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:238053263 G>T maps to NM_021186.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:12785335 C>A maps to NM_001103170.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:12785335 C>A maps to NM_001103170.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87173486 G>T maps to NM_000927.3 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87173486 G>T maps to NM_000927.3 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20739715 G>T maps to NM_001163941.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20739715 G>T maps to NM_001163941.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17483339 C>T maps to ENST00000302539 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17483339 C>T maps to ENST00000302539 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89052257 G>A maps to NM_004827.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89052257 G>A maps to NM_004827.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109637269 G>A maps to NM_001093.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109637269 G>A maps to NM_001093.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121177208 G>T maps to NM_000017.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121177208 G>T maps to NM_000017.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:44092855 G>C maps to NM_032592.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:44092855 G>C maps to NM_032592.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:236906332 T>A maps to NM_001103.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:236906332 T>A maps to NM_001103.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:127185300 A>T maps to NM_138289.3 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:127185300 A>T maps to NM_138289.3 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:64592755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:64592755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:154574328 G>A maps to ENST00000292205 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:154574328 G>A maps to ENST00000292205 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78392144 C>T maps to NM_020421.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78392144 C>T maps to NM_020421.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147967463 T>A maps to NM_002025.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147967463 T>A maps to NM_002025.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87089365 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87089365 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:91632044 A>C maps to NM_005751.4 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:91632044 A>C maps to NM_005751.4 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134212695 C>A maps to NM_020299.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134212695 C>A maps to NM_020299.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:73799764 C>T maps to NM_015120.4 T3586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:73799764 C>T maps to NM_015120.4 T3586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109441768 C>G maps to NM_015365.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109441768 C>G maps to NM_015365.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:112035188 G>A maps to NM_001113490.1 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:112035188 G>A maps to NM_001113490.1 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99106158 C>T maps to NM_181861.1 C968C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99106158 C>T maps to NM_181861.1 C968C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:1462090 C>T maps to NM_005883.2 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:1462090 C>T maps to NM_005883.2 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:143974008 A>G maps to NM_018460.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:143974008 A>G maps to NM_018460.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43473952 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43473952 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:35750562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:35750562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:66765998 G>A maps to NM_000044.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:66765998 G>A maps to NM_000044.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:131130907 C>A maps to NM_018482.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:131130907 C>A maps to NM_018482.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10659646 C>T maps to NM_032885.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10659646 C>T maps to NM_032885.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42479786 C>A maps to ENST00000441343 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42479786 C>A maps to ENST00000441343 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42489243 G>T maps to ENST00000441343 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42489243 G>T maps to ENST00000441343 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152825353 C>G maps to NM_001001344.2 G931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152825353 C>G maps to NM_001001344.2 G931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176043978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176043978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:143558744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:143558744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:76740735 C>A maps to NM_024685.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:76740735 C>A maps to NM_024685.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:107491620 G>A maps to NM_001142568.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:107491620 G>A maps to NM_001142568.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152770097 C>A maps to NM_001711.4 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152770097 C>A maps to NM_001711.4 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102004414 G>C maps to NM_001142530.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102004414 G>C maps to NM_001142530.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:55758868 G>T maps to NM_001719.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:55758868 G>T maps to NM_001719.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112987218 C>A maps to ENST00000273395 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112987218 C>A maps to ENST00000273395 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112998276 C>G maps to ENST00000273395 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112998276 C>G maps to ENST00000273395 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:32914806 A>C maps to NM_000059.3 I2105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:32914806 A>C maps to NM_000059.3 I2105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:108051372 C>T maps to NM_001018072.1 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:108051372 C>T maps to NM_001018072.1 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:93723642 C>A maps to NM_001002860.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:93723642 C>A maps to NM_001002860.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26468737 C>T maps to NM_007049.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26468737 C>T maps to NM_007049.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50902608 G>A maps to NM_001042427.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50902608 G>A maps to NM_001042427.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:27078780 G>A maps to NM_018164.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:27078780 G>A maps to NM_018164.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:31526831 C>A maps to NM_152325.1 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:31526831 C>A maps to NM_152325.1 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:19725532 C>T maps to NM_001012991.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:19725532 C>T maps to NM_001012991.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34191866 G>A maps to NM_152781.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34191866 G>A maps to NM_152781.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210014249 G>T maps to NM_014388.6 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210014249 G>T maps to NM_014388.6 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26162281 G>A maps to NM_024037.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26162281 G>A maps to NM_024037.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:226784575 C>G maps to ENST00000366788 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:226784575 C>G maps to ENST00000366788 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10603339 G>C maps to NM_001009608.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10603339 G>C maps to NM_001009608.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:37169219 C>A maps to NM_023073.3 T2302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:37169219 C>A maps to NM_023073.3 T2302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:97676906 C>A maps to NM_198468.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:97676906 C>A maps to NM_198468.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:114518679 C>A maps to NM_173521.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:114518679 C>A maps to NM_173521.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50008361 C>A maps to NM_001082534.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50008361 C>A maps to NM_001082534.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150235521 C>A maps to NM_012113.1 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150235521 C>A maps to NM_012113.1 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:201030580 G>T maps to NM_000069.2 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:201030580 G>T maps to NM_000069.2 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24373039 C>A maps to NM_006539.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24373039 C>A maps to NM_006539.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:219886502 G>T maps to NM_194302.2 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:219886502 G>T maps to NM_194302.2 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31112686 G>A maps to NM_001105564.1 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31112686 G>A maps to NM_001105564.1 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32688817 G>A maps to NM_002981.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32688817 G>A maps to NM_002981.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:50052404 G>T maps to NM_033031.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:50052404 G>T maps to NM_033031.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6923305 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6923305 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:87013079 G>T maps to ENST00000456996 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:87013079 G>T maps to ENST00000456996 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:62055058 G>T maps to NM_001796.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:62055058 G>T maps to NM_001796.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26890028 G>A maps to NM_016279.3 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26890028 G>A maps to NM_016279.3 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:123215790 C>A maps to NM_018249.4 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:123215790 C>A maps to NM_018249.4 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:92247457 A>G maps to NM_001145306.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:92247457 A>G maps to NM_001145306.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:123924433 C>A maps to NM_007018.4 R1770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:123924433 C>A maps to NM_007018.4 R1770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:54976776 G>T maps to NM_006568.2 G34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:54976776 G>T maps to NM_006568.2 G34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6202512 C>A maps to NM_015557.2 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6202512 C>A maps to NM_015557.2 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:61655553 G>A maps to NM_017780.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:61655553 G>A maps to NM_017780.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:404926 G>T maps to NM_006614.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:404926 G>T maps to NM_006614.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:85211369 G>T maps to NM_000390.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:85211369 G>T maps to NM_000390.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240071405 G>T maps to NM_000740.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240071405 G>T maps to NM_000740.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10174803 C>T maps to NM_001830.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10174803 C>T maps to NM_001830.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10176536 G>C maps to NM_001830.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10176536 G>C maps to NM_001830.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:73753333 G>T maps to NM_003388.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:73753333 G>T maps to NM_003388.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:77333671 T>C maps to NM_001293.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:77333671 T>C maps to NM_001293.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:150912747 C>A maps to NM_005140.1 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:150912747 C>A maps to NM_005140.1 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:99012829 G>T maps to NM_001298.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:99012829 G>T maps to NM_001298.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:2944633 T>A maps to NM_175607.1 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:2944633 T>A maps to NM_175607.1 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:124979372 C>A maps to NM_130773.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:124979372 C>A maps to NM_130773.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33139546 C>T maps to NM_080680.2 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33139546 C>T maps to NM_080680.2 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109767293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109767293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:238274403 G>A maps to NM_004369.3 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:238274403 G>A maps to NM_004369.3 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120960071 G>C maps to NM_032314.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120960071 G>C maps to NM_032314.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5844825 A>T maps to NM_001014809.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5844825 A>T maps to NM_001014809.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:2966134 G>A maps to NM_033225.5 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:2966134 G>A maps to NM_033225.5 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113249506 G>T maps to NM_198123.1 P3513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113249506 G>T maps to NM_198123.1 P3513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:17142109 G>A maps to NM_001081.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:17142109 G>A maps to NM_001081.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:180830694 C>A maps to NM_020943.2 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:180830694 C>A maps to NM_020943.2 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:76957125 G>A maps to NM_005409.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:76957125 G>A maps to NM_005409.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:139038137 C>A maps to NM_001013403.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:139038137 C>A maps to NM_001013403.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:37663179 G>T maps to NM_000397.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:37663179 G>T maps to NM_000397.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:42815765 G>T maps to NM_145663.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:42815765 G>T maps to NM_145663.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:31327811 G>T maps to NM_181807.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:31327811 G>T maps to NM_181807.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134680394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134680394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113599743 T>A maps to NM_001111322.1 K752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113599743 T>A maps to NM_001111322.1 K752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:142161884 C>T maps to NM_014957.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:142161884 C>T maps to NM_014957.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:47882656 C>T maps to NM_138615.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:47882656 C>T maps to NM_138615.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31496455 G>T maps to ENST00000357033 R2902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31496455 G>T maps to ENST00000357033 R2902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:32486716 T>A maps to ENST00000357033 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:32486716 T>A maps to ENST00000357033 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21133418 G>T maps to NM_017539.1 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21133418 G>T maps to NM_017539.1 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13735345 T>A maps to NM_001369.2 R3885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13735345 T>A maps to NM_001369.2 R3885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11550478 A>G maps to NM_001372.3 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11550478 A>G maps to NM_001372.3 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154237653 G>A maps to NM_130797.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154237653 G>A maps to NM_130797.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100496797 T>A maps to NM_001939.2 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100496797 T>A maps to NM_001939.2 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:3979398 C>A maps to NM_001961.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:3979398 C>A maps to NM_001961.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:38427130 C>T maps to ENST00000354891 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:38427130 C>T maps to ENST00000354891 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8008913 G>C maps to ENST00000449102 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8008913 G>C maps to ENST00000449102 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176072391 C>T maps to NM_001099408.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176072391 C>T maps to NM_001099408.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:11568958 C>T maps to NM_001420.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:11568958 C>T maps to NM_001420.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:77708903 G>T maps to NM_178543.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:77708903 G>T maps to NM_178543.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5395637 G>C maps to NM_012307.2 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5395637 G>C maps to NM_012307.2 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5416023 G>A maps to NM_012307.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5416023 G>A maps to NM_012307.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66467530 G>T maps to NM_004439.5 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66467530 G>T maps to NM_004439.5 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142565366 G>A maps to NM_004445.3 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142565366 G>A maps to NM_004445.3 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71426903 G>T maps to NM_017669.2 Y571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71426903 G>T maps to NM_017669.2 Y571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169492509 T>C maps to ENST00000367796 T1996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169492509 T>C maps to ENST00000367796 T1996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:58639443 G>A maps to NM_138805.2 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:58639443 G>A maps to NM_138805.2 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177242682 C>A maps to NM_021165.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177242682 C>A maps to NM_021165.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190234117 G>T maps to NM_199051.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190234117 G>T maps to NM_199051.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:134136571 G>A maps to NM_033387.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:134136571 G>A maps to NM_033387.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:22647319 C>A maps to NM_022725.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:22647319 C>A maps to NM_022725.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92532334 G>T maps to ENST00000298047 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92532334 G>T maps to ENST00000298047 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4554565 C>A maps to NM_020996.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4554565 C>A maps to NM_020996.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:154962043 T>C maps to NM_025207.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:154962043 T>C maps to NM_025207.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:84609842 T>G maps to NM_001001670.2 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:84609842 T>G maps to NM_001001670.2 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:96651792 G>T maps to NM_006581.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:96651792 G>T maps to NM_006581.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151453202 T>A maps to NM_000808.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151453202 T>A maps to NM_000808.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:161116292 G>T maps to NM_000811.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:161116292 G>T maps to NM_000811.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153668785 C>A maps to NM_001493.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153668785 C>A maps to NM_001493.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:37379194 G>T maps to NM_001172713.1 S2137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:37379194 G>T maps to NM_001172713.1 S2137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:56558437 G>A maps to NM_001127236.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:56558437 G>A maps to NM_001127236.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:144297146 G>T maps to NM_178172.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:144297146 G>T maps to NM_178172.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:26534165 G>T maps to NM_001145168.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:26534165 G>T maps to NM_001145168.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:158233870 A>G maps to NM_000826.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:158233870 A>G maps to NM_000826.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:158284151 A>T maps to NM_000826.3 K870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:158284151 A>T maps to NM_000826.3 K870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:102372529 G>A maps to NM_021956.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:102372529 G>A maps to NM_021956.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:121212277 C>G maps to NM_005308.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:121212277 C>G maps to NM_005308.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13238119 C>G maps to NM_001080555.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13238119 C>G maps to NM_001080555.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135933285 G>A maps to NM_001122823.1 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135933285 G>A maps to NM_001122823.1 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:40999794 T>A maps to ENST00000296803 A1524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:40999794 T>A maps to ENST00000296803 A1524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93806600 A>T maps to NM_001098672.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93806600 A>T maps to NM_001098672.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:65393449 C>T maps to NM_138737.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:65393449 C>T maps to NM_138737.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:65420571 C>A maps to NM_138737.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:65420571 C>A maps to NM_138737.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89576323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89576323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81332037 A>G maps to NM_000601.4 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81332037 A>G maps to NM_000601.4 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81388035 G>A maps to NM_000601.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81388035 G>A maps to NM_000601.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26056239 C>T maps to NM_005319.3 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26056239 C>T maps to NM_005319.3 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26045848 C>T maps to NM_003531.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26045848 C>T maps to NM_003531.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26104360 C>T maps to NM_003542.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26104360 C>T maps to NM_003542.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176972319 C>A maps to NM_021192.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176972319 C>A maps to NM_021192.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176965451 C>G maps to NM_021193.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176965451 C>G maps to NM_021193.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:33354566 C>G maps to NM_002143.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:33354566 C>G maps to NM_002143.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:128751909 C>T maps to ENST00000438626 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:128751909 C>T maps to ENST00000438626 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:94973091 G>A maps to ENST00000375660 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:94973091 G>A maps to ENST00000375660 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10444649 G>C maps to NM_002162.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10444649 G>C maps to NM_002162.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:79107492 G>T maps to NM_006820.2 *453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:79107492 G>T maps to NM_006820.2 *453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:217526666 C>A maps to NM_000597.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:217526666 C>A maps to NM_000597.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:103040328 C>A maps to NM_003853.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:103040328 C>A maps to NM_003853.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128049522 G>A maps to NM_000883.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128049522 G>A maps to NM_000883.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145534112 C>T maps to NM_003637.3 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145534112 C>T maps to NM_003637.3 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145534243 G>T maps to NM_003637.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145534243 G>T maps to NM_003637.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:52201707 C>A maps to NM_181501.1 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:52201707 C>A maps to NM_181501.1 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:31419750 C>T maps to ENST00000444228 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:31419750 C>T maps to ENST00000444228 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54781459 C>T maps to NM_198510.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54781459 C>T maps to NM_198510.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152883772 A>T maps to NM_005547.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152883772 A>T maps to NM_005547.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5154950 G>T maps to NM_002234.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5154950 G>T maps to NM_002234.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4920248 C>A maps to NM_002235.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4920248 C>A maps to NM_002235.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47990217 G>T maps to NM_004975.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47990217 G>T maps to NM_004975.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:48098459 C>A maps to NM_004975.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:48098459 C>A maps to NM_004975.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128551 C>T maps to NM_018658.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128551 C>T maps to NM_018658.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128671 C>G maps to NM_018658.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128671 C>G maps to NM_018658.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128680 C>T maps to NM_018658.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128680 C>T maps to NM_018658.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128950 C>G maps to NM_018658.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128950 C>G maps to NM_018658.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68171770 C>T maps to NM_000891.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68171770 C>T maps to NM_000891.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:73964217 C>A maps to NM_001008537.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:73964217 C>A maps to NM_001008537.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5922998 G>A maps to NM_001017969.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5922998 G>A maps to NM_001017969.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200522785 A>G maps to NM_014875.2 Y1559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200522785 A>G maps to NM_014875.2 Y1559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:16253909 G>A maps to NM_024704.4 H1314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:16253909 G>A maps to NM_024704.4 H1314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33372727 C>A maps to NM_002263.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33372727 C>A maps to NM_002263.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39551496 C>T maps to ENST00000393998 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39551496 C>T maps to ENST00000393998 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52946606 G>T maps to NM_033448.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52946606 G>T maps to NM_033448.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:112463443 C>A maps to NM_001105206.1 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:112463443 C>A maps to NM_001105206.1 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152681592 C>A maps to NM_178356.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152681592 C>A maps to NM_178356.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:136569959 G>T maps to NM_002299.2 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:136569959 G>T maps to NM_002299.2 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66058459 C>G maps to NM_002303.5 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66058459 C>G maps to NM_002303.5 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55142737 C>A maps to ENST00000427581 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55142737 C>A maps to ENST00000427581 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:27949429 C>A maps to NM_152570.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:27949429 C>A maps to NM_152570.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:207509172 C>A maps to NM_001102659.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:207509172 C>A maps to NM_001102659.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:40399610 G>A maps to NM_020737.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:40399610 G>A maps to NM_020737.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:68181229 C>G maps to NM_002335.2 Y859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:68181229 C>G maps to NM_002335.2 Y859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:70004027 C>A maps to NM_201550.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:70004027 C>A maps to NM_201550.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70587566 C>A maps to NM_020794.2 V1537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70587566 C>A maps to NM_020794.2 V1537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169540005 G>A maps to NM_001080460.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169540005 G>A maps to NM_001080460.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110763979 C>A maps to NM_018334.4 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110763979 C>A maps to NM_018334.4 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54952836 G>T maps to NM_020678.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54952836 G>T maps to NM_020678.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:102110021 G>A maps to NM_152892.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:102110021 G>A maps to NM_152892.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:30254064 G>C maps to NM_002365.4 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:30254064 G>C maps to NM_002365.4 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:77789354 A>T maps to NM_012301.3 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:77789354 A>T maps to NM_012301.3 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:86988934 T>A maps to NM_138982.2 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:86988934 T>A maps to NM_138982.2 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30129041 G>T maps to NM_002746.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30129041 G>T maps to NM_002746.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:94927251 G>T maps to NM_018349.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:94927251 G>T maps to NM_018349.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141722154 G>T maps to ENST00000475668 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141722154 G>T maps to ENST00000475668 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:109771183 C>G maps to NM_022765.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:109771183 C>G maps to NM_022765.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107169510 G>T maps to NM_012216.3 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107169510 G>T maps to NM_012216.3 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:37067447 G>A maps to NM_000249.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:37067447 G>A maps to NM_000249.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36211922 G>A maps to NM_014727.1 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36211922 G>A maps to NM_014727.1 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:62918363 C>A maps to ENST00000393630 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:62918363 C>A maps to ENST00000393630 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30435855 T>A maps to NM_001584.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30435855 T>A maps to NM_001584.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:84772654 G>A maps to NM_138409.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:84772654 G>A maps to NM_138409.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:19077786 G>A maps to NM_054030.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:19077786 G>A maps to NM_054030.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149807450 C>T maps to NM_000252.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149807450 C>T maps to NM_000252.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:25840040 T>C maps to NM_004685.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:25840040 T>C maps to NM_004685.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:11313973 G>T maps to NM_004958.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:11313973 G>T maps to NM_004958.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9045756 A>G maps to NM_024690.2 H11958H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9045756 A>G maps to NM_024690.2 H11958H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100676088 G>A maps to NM_001040105.1 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100676088 G>A maps to NM_001040105.1 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42315706 A>G maps to NM_002466.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42315706 A>G maps to NM_002466.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16082253 C>A maps to NM_005378.4 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16082253 C>A maps to NM_005378.4 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:10432342 G>T maps to NM_017534.5 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:10432342 G>T maps to NM_017534.5 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76916515 G>A maps to NM_000260.3 E1830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76916515 G>A maps to NM_000260.3 E1830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:59080679 G>A maps to NM_198055.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:59080679 G>A maps to NM_198055.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:780983 C>A maps to NM_022493.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:780983 C>A maps to NM_022493.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:3532548 G>T maps to NM_024845.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:3532548 G>T maps to NM_024845.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:148015797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:148015797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152507101 C>A maps to NM_001164507.1 E2405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152507101 C>A maps to NM_001164507.1 E2405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:41062140 C>T maps to NM_002505.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:41062140 C>T maps to NM_002505.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71359503 G>A maps to NM_001013627.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71359503 G>A maps to NM_001013627.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:107533127 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:107533127 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54313960 G>T maps to ENST00000391773 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54313960 G>T maps to ENST00000391773 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56243815 G>T maps to NM_176820.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56243815 G>T maps to NM_176820.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:106858223 C>T maps to ENST00000503451 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:106858223 C>T maps to ENST00000503451 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35802273 C>G maps to NM_003995.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35802273 C>G maps to NM_003995.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79175700 G>T maps to NM_004796.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79175700 G>T maps to NM_004796.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88483883 C>A maps to NM_001012338.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88483883 C>A maps to NM_001012338.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102337944 G>T maps to NM_022052.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102337944 G>T maps to NM_022052.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:13775791 G>T maps to NM_003611.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:13775791 G>T maps to NM_003611.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50952076 G>T maps to NM_018245.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50952076 G>T maps to NM_018245.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:44736067 C>T maps to ENST00000444676 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:44736067 C>T maps to ENST00000444676 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55103906 C>A maps to NM_004852.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55103906 C>A maps to NM_004852.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:132306118 A>T maps to NM_002545.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:132306118 A>T maps to NM_002545.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20665697 C>G maps to NM_001005503.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20665697 C>G maps to NM_001005503.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248128866 C>A maps to NM_001004491.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248128866 C>A maps to NM_001004491.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248129451 C>A maps to NM_001004491.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248129451 C>A maps to NM_001004491.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248685078 C>A maps to NM_001013355.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248685078 C>A maps to NM_001013355.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29555741 A>G maps to NM_007160.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29555741 A>G maps to NM_007160.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29012466 G>A maps to NM_030903.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29012466 G>A maps to NM_030903.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248059202 G>T maps to NM_001001957.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248059202 G>T maps to NM_001001957.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248059496 G>T maps to NM_001001957.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248059496 G>T maps to NM_001001957.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55322042 C>A maps to NM_001001920.1 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55322042 C>A maps to NM_001001920.1 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:51515605 G>T maps to NM_001004703.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:51515605 G>T maps to NM_001004703.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5344660 G>T maps to NM_033180.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5344660 G>T maps to NM_033180.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55587545 G>T maps to ENST00000395203 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55587545 G>T maps to ENST00000395203 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55595458 C>A maps to NM_001004739.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55595458 C>A maps to NM_001004739.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:56237709 T>C maps to NM_001004742.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:56237709 T>C maps to NM_001004742.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:55726035 A>G maps to NM_054104.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:55726035 A>G maps to NM_054104.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142750144 C>T maps to NM_001001667.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142750144 C>T maps to NM_001001667.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55861151 C>A maps to NM_001003750.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55861151 C>A maps to NM_001003750.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:56113903 A>T maps to NM_001002907.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:56113903 A>T maps to NM_001002907.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121670267 C>T maps to NM_002560.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121670267 C>T maps to NM_002560.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69478985 T>A maps to NM_002565.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69478985 T>A maps to NM_002565.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:39665644 C>G maps to NM_005884.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:39665644 C>G maps to NM_005884.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:78915545 G>C maps to NM_173797.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:78915545 G>C maps to NM_173797.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176734816 C>A maps to NM_020318.2 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176734816 C>A maps to NM_020318.2 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:25000736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:25000736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:19062124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:19062124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67800922 A>C maps to NM_203487.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67800922 A>C maps to NM_203487.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140167893 C>T maps to NM_018900.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140167893 C>T maps to NM_018900.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140182307 C>A maps to NM_018906.2 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140182307 C>A maps to NM_018906.2 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:66617696 G>C maps to NM_022172.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:66617696 G>C maps to NM_022172.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:101179518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:101179518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144882508 C>G maps to NM_014644.4 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144882508 C>G maps to NM_014644.4 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:55144559 C>T maps to ENST00000507166 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:55144559 C>T maps to ENST00000507166 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1961358 G>A maps to NM_024411.4 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1961358 G>A maps to NM_024411.4 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145752462 C>T maps to NM_002614.3 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145752462 C>T maps to NM_002614.3 Q166*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z022-01A-01W-0746-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-17-Z022-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71080083 A>T maps to NM_021965.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71080083 A>T maps to NM_021965.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54029092 C>A maps to NM_001184896.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54029092 C>A maps to NM_001184896.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:106545618 C>A maps to NM_002649.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:106545618 C>A maps to NM_002649.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:123485672 T>A maps to NM_020845.2 K361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:123485672 T>A maps to NM_020845.2 K361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113822706 G>T maps to NM_173542.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113822706 G>T maps to NM_173542.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100855547 G>A maps to NM_001084.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100855547 G>A maps to NM_001084.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:145918865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:145918865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:84586016 C>A maps to ENST00000373145 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:84586016 C>A maps to ENST00000373145 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:53103576 G>T maps to NM_182595.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:53103576 G>T maps to NM_182595.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:147561326 G>A maps to NM_004575.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:147561326 G>A maps to NM_004575.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:39503861 G>A maps to NM_007252.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:39503861 G>A maps to NM_007252.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:113518145 C>A maps to NM_002711.3 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:113518145 C>A maps to NM_002711.3 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6377596 C>T maps to NM_181876.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6377596 C>T maps to NM_181876.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:45117409 C>A maps to NM_020229.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:45117409 C>A maps to NM_020229.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128186269 C>T maps to ENST00000409048 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128186269 C>T maps to ENST00000409048 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:132484546 C>T maps to NM_016307.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:132484546 C>T maps to NM_016307.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:30807571 G>T maps to NM_002815.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:30807571 G>T maps to NM_002815.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:87703390 C>T maps to NM_080685.2 L2005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:87703390 C>T maps to NM_080685.2 L2005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220162804 G>A maps to NM_002846.3 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220162804 G>A maps to NM_002846.3 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:52258449 G>T maps to NM_144651.4 S1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:52258449 G>T maps to NM_144651.4 S1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158906732 G>T maps to NM_152501.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158906732 G>T maps to NM_152501.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:136393710 A>G maps to ENST00000409606 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:136393710 A>G maps to ENST00000409606 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:53524046 G>C maps to NM_005611.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:53524046 G>C maps to NM_005611.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:36105138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:36105138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:139233925 G>A maps to ENST00000367663 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:139233925 G>A maps to ENST00000367663 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:2328560 C>T maps to NM_007033.4 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:2328560 C>T maps to NM_007033.4 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:192153461 A>T maps to NM_130782.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:192153461 A>T maps to NM_130782.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:51501613 G>T maps to NM_024570.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:51501613 G>T maps to NM_024570.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:2515394 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:2515394 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-17-Z022-01A-01W-0746-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-17-Z022-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77623726 G>A maps to ENST00000332191 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77623726 G>A maps to ENST00000332191 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77666735 G>T maps to ENST00000332191 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77666735 G>T maps to ENST00000332191 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:39013885 G>T maps to NM_000540.2 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:39013885 G>T maps to NM_000540.2 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237947500 C>A maps to NM_001035.2 P4163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237947500 C>A maps to NM_001035.2 P4163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:33945071 C>A maps to NM_001036.3 G1432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:33945071 C>A maps to NM_001036.3 G1432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:51175295 G>T maps to ENST00000251020 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:51175295 G>T maps to ENST00000251020 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166850734 T>C maps to NM_001165963.1 K1591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166850734 T>C maps to NM_001165963.1 K1591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166166887 C>T maps to NM_001040142.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166166887 C>T maps to NM_001040142.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166245668 G>T maps to NM_001040142.1 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166245668 G>T maps to NM_001040142.1 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38592977 G>T maps to NM_001099404.1 R1629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38592977 G>T maps to NM_001099404.1 R1629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:167330311 A>T maps to NM_002976.2 L147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:167330311 A>T maps to NM_002976.2 L147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42643105 C>A maps to NM_015559.2 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42643105 C>A maps to NM_015559.2 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150923356 A>T maps to NM_001145415.1 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150923356 A>T maps to NM_001145415.1 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135139985 T>A maps to ENST00000372169 P2587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135139985 T>A maps to ENST00000372169 P2587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:164709181 G>A maps to NM_001041.3 H1689H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:164709181 G>A maps to NM_001041.3 H1689H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:35261996 G>C maps to NM_032214.2 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:35261996 G>C maps to NM_032214.2 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:48541793 C>T maps to NM_000338.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:48541793 C>T maps to NM_000338.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:119027182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:119027182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50819862 C>A maps to NM_003055.2 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50819862 C>A maps to NM_003055.2 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:110752466 C>A maps to NM_033125.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:110752466 C>A maps to NM_033125.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92401581 C>A maps to NM_134266.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92401581 C>A maps to NM_134266.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67470087 C>A maps to NM_015139.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67470087 C>A maps to NM_015139.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:150682853 G>T maps to NM_001145017.1 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:150682853 G>T maps to NM_001145017.1 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48319073 C>G maps to NM_033518.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48319073 C>G maps to NM_033518.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162711523 G>A maps to NM_001178015.1 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162711523 G>A maps to NM_001178015.1 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20652350 G>C maps to NM_004211.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20652350 G>C maps to NM_004211.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:17419519 C>A maps to NM_001164771.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:17419519 C>A maps to NM_001164771.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:20874970 G>T maps to NM_017435.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:20874970 G>T maps to NM_017435.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74880371 G>A maps to NM_007256.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74880371 G>A maps to NM_007256.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123126142 A>T maps to NM_006714.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123126142 A>T maps to NM_006714.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:75942360 G>T maps to NM_153271.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:75942360 G>T maps to NM_153271.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53514576 C>T maps to NM_003578.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53514576 C>T maps to NM_003578.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:21596141 G>T maps to NM_003107.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:21596141 G>T maps to NM_003107.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220336961 C>A maps to NM_005876.4 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220336961 C>A maps to NM_005876.4 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:89611125 G>A maps to NM_003119.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:89611125 G>A maps to NM_003119.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:57686701 C>G maps to ENST00000506738 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:57686701 C>G maps to ENST00000506738 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:155004222 C>T maps to NM_005840.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:155004222 C>T maps to NM_005840.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55653041 G>A maps to NM_032681.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55653041 G>A maps to NM_032681.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179250037 C>T maps to NM_003900.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179250037 C>T maps to NM_003900.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153047619 C>A maps to NM_014370.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153047619 C>A maps to NM_014370.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99920562 T>A maps to NM_014467.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99920562 T>A maps to NM_014467.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:119568488 C>A maps to NM_194286.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:119568488 C>A maps to NM_194286.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:53062519 C>A maps to NM_014682.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:53062519 C>A maps to NM_014682.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:9395239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:9395239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:25288400 C>A maps to ENST00000445298 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:25288400 C>A maps to ENST00000445298 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64428340 C>T maps to NM_182914.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64428340 C>T maps to NM_182914.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:45265683 C>A maps to NM_020826.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:45265683 C>A maps to NM_020826.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:222753118 G>A maps to NM_005681.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:222753118 G>A maps to NM_005681.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179320366 G>A maps to NM_198868.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179320366 G>A maps to NM_198868.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:72988715 C>G maps to NM_012453.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:72988715 C>G maps to NM_012453.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:67400439 C>T maps to NM_005995.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:67400439 C>T maps to NM_005995.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:50810879 C>T maps to ENST00000263046 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:50810879 C>T maps to ENST00000263046 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:3350040 G>A maps to NM_033208.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:3350040 G>A maps to NM_033208.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105360983 G>C maps to NM_030788.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105360983 G>C maps to NM_030788.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:19477480 C>T maps to NM_001105248.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:19477480 C>T maps to NM_001105248.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94975858 G>T maps to NM_020698.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94975858 G>T maps to NM_020698.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:93625729 G>A maps to NM_016040.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:93625729 G>A maps to NM_016040.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:44781885 A>T maps to NM_032256.1 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:44781885 A>T maps to NM_032256.1 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129569091 G>T maps to NM_133448.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129569091 G>T maps to NM_133448.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32963123 C>A maps to NM_207313.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32963123 C>A maps to NM_207313.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102968619 G>C maps to NM_182541.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102968619 G>C maps to NM_182541.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:19642342 G>T maps to NM_002772.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:19642342 G>T maps to NM_002772.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:117838356 C>T maps to NM_002160.2 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:117838356 C>T maps to NM_002160.2 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:60036185 G>T maps to NM_003839.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:60036185 G>T maps to NM_003839.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9413470 C>T maps to NM_003747.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9413470 C>T maps to NM_003747.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325527 G>T maps to NM_003285.2 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325527 G>T maps to NM_003285.2 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325589 C>A maps to NM_003285.2 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325589 C>A maps to NM_003285.2 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:32023847 A>T maps to ENST00000375244 P2749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:32023847 A>T maps to ENST00000375244 P2749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:44958878 C>A maps to NM_006034.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:44958878 C>A maps to NM_006034.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:38130881 G>T maps to NM_001039141.2 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:38130881 G>T maps to NM_001039141.2 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81609868 G>A maps to NM_000369.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81609868 G>A maps to NM_000369.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:43038397 G>A maps to ENST00000263802 R1515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:43038397 G>A maps to ENST00000263802 R1515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:75059367 G>A maps to NM_145170.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:75059367 G>A maps to NM_145170.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179579977 G>A maps to NM_133378.4 F7401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179579977 G>A maps to NM_133378.4 F7401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179632584 A>T maps to NM_133378.4 A3124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179632584 A>T maps to NM_133378.4 A3124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:90001392 G>T maps to ENST00000304984 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:90001392 G>T maps to ENST00000304984 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88924416 C>A maps to NM_000372.4 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88924416 C>A maps to NM_000372.4 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42600414 C>T maps to NM_015255.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42600414 C>T maps to NM_015255.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:19437262 C>T maps to ENST00000375267 L3955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:19437262 C>T maps to ENST00000375267 L3955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:91496491 C>T maps to NM_018671.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:91496491 C>T maps to NM_018671.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:73048445 G>T maps to NM_170744.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:73048445 G>T maps to NM_170744.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:158974391 C>A maps to NM_001135098.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:158974391 C>A maps to NM_001135098.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:6189872 A>G maps to ENST00000404835 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:6189872 A>G maps to ENST00000404835 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:145021221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:145021221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:58276043 C>A maps to NM_001130480.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:58276043 C>A maps to NM_001130480.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:118504444 C>A maps to NM_019086.5 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:118504444 C>A maps to NM_019086.5 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:100820130 C>G maps to NM_173701.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:100820130 C>G maps to NM_173701.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:39230225 C>G maps to NM_194293.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:39230225 C>G maps to NM_194293.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28133054 G>A maps to NM_015171.2 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28133054 G>A maps to NM_015171.2 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100361491 G>T maps to ENST00000349350 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100361491 G>T maps to ENST00000349350 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36205629 C>A maps to NM_014383.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36205629 C>A maps to NM_014383.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77913598 C>A maps to NM_152694.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77913598 C>A maps to NM_152694.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74670724 A>T maps to NM_144969.2 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74670724 A>T maps to NM_144969.2 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:135614377 C>T maps to NM_020863.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:135614377 C>T maps to NM_020863.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77761890 G>T maps to NM_024721.4 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77761890 G>T maps to NM_024721.4 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77768369 A>G maps to NM_024721.4 S3071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77768369 A>G maps to NM_024721.4 S3071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:136649479 C>T maps to NM_003413.3 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:136649479 C>T maps to NM_003413.3 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:35870650 G>T maps to NM_005095.2 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:35870650 G>T maps to NM_005095.2 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:74622667 A>G maps to NM_007345.3 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:74622667 A>G maps to NM_007345.3 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:2464418 G>A maps to NM_024325.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:2464418 G>A maps to NM_024325.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:22000711 A>G maps to NM_003423.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:22000711 A>G maps to NM_003423.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99226889 G>A maps to NM_145115.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99226889 G>A maps to NM_145115.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:63726979 C>G maps to NM_153363.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:63726979 C>G maps to NM_153363.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:247163259 C>T maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:247163259 C>T maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:12059661 G>T maps to NM_144566.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:12059661 G>T maps to NM_144566.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:20759682 G>T maps to NM_003426.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:20759682 G>T maps to NM_003426.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52570210 C>T maps to NM_001136499.1 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52570210 C>T maps to NM_001136499.1 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52887267 A>G maps to NM_001145434.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52887267 A>G maps to NM_001145434.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:50121487 C>A maps to NM_007009.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:50121487 C>A maps to NM_007009.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:57220928 A>T maps to NM_181806.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:57220928 A>T maps to NM_181806.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:23532767 G>A maps to NM_014977.3 Q930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:23532767 G>A maps to NM_014977.3 Q930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:127186047 C>A maps to NM_138289.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:127186047 C>A maps to NM_138289.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:39626919 C>A maps to NM_001464.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:39626919 C>A maps to NM_001464.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:24795298 C>T maps to NM_139247.3 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:24795298 C>T maps to NM_139247.3 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:150814461 G>C maps to NM_031946.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:150814461 G>C maps to NM_031946.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:77763343 C>T maps to NM_174858.1 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:77763343 C>T maps to NM_174858.1 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:114179249 C>T maps to NM_001148.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:114179249 C>T maps to NM_001148.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:101858563 G>T maps to NM_022838.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:101858563 G>T maps to NM_022838.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:94890988 C>T maps to NM_198150.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:94890988 C>T maps to NM_198150.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:175979487 G>A maps to NM_001880.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:175979487 G>A maps to NM_001880.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:96784089 G>C maps to NM_018036.5 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:96784089 G>C maps to NM_018036.5 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:124236930 A>G maps to NM_012463.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:124236930 A>G maps to NM_012463.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:99569381 G>C maps to NM_001185.3 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:99569381 G>C maps to NM_001185.3 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:197241141 C>T maps to NM_203315.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:197241141 C>T maps to NM_203315.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:102564633 C>A maps to NM_001168399.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:102564633 C>A maps to NM_001168399.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:41161793 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:41161793 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:61144929 C>T maps to NM_004056.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:61144929 C>T maps to NM_004056.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:140852089 G>A maps to ENST00000277549 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:140852089 G>A maps to ENST00000277549 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:2786942 G>A maps to NM_199460.2 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:2786942 G>A maps to NM_199460.2 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:15098939 C>A maps to NM_000728.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:15098939 C>A maps to NM_000728.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:49089836 G>A maps to NM_001240.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:49089836 G>A maps to NM_001240.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:45912707 T>G maps to ENST00000423698 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:45912707 T>G maps to ENST00000423698 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:105660901 G>C maps to NM_152750.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:105660901 G>C maps to NM_152750.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:90588910 G>T maps to NM_001039803.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:90588910 G>T maps to NM_001039803.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:61750661 G>T maps to NM_017780.2 E1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:61750661 G>T maps to NM_017780.2 E1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:109937400 C>T maps to NM_001143981.1 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:109937400 C>T maps to NM_001143981.1 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:100169964 T>A maps to NM_014361.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:100169964 T>A maps to NM_014361.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:130284241 C>T maps to NM_001102608.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:130284241 C>T maps to NM_001102608.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:17157574 C>A maps to NM_001081.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:17157574 C>A maps to NM_001081.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:39851748 T>A maps to ENST00000398904 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:39851748 T>A maps to ENST00000398904 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:100681575 C>T maps to NM_001918.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:100681575 C>T maps to NM_001918.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:137330262 C>T maps to NM_004717.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:137330262 C>T maps to NM_004717.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:13729634 T>C maps to NM_001369.2 P3932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:13729634 T>C maps to NM_001369.2 P3932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:230253032 A>G maps to NM_139072.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:230253032 A>G maps to NM_139072.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:129224176 A>T maps to ENST00000398025 K1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:129224176 A>T maps to ENST00000398025 K1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71788995 G>A maps to NM_001130987.1 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71788995 G>A maps to NM_001130987.1 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:94679737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:94679737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:72127697 T>G maps to NM_000503.4 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:72127697 T>G maps to NM_000503.4 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:82195598 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:82195598 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:68587941 G>T maps to NM_213609.2 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:68587941 G>T maps to NM_213609.2 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13716361 C>T maps to NM_000834.3 V1270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13716361 C>T maps to NM_000834.3 V1270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:43227345 G>A maps to NM_006460.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:43227345 G>A maps to NM_006460.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:161495566 T>C maps to NM_002155.3 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:161495566 T>C maps to NM_002155.3 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:42452119 C>A maps to NM_000419.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:42452119 C>A maps to NM_000419.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:90650563 C>T maps to NM_022054.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:90650563 C>T maps to NM_022054.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:142651422 C>A maps to NM_000420.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:142651422 C>A maps to NM_000420.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:39197229 G>T maps to NM_030967.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:39197229 G>T maps to NM_030967.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:112460429 G>T maps to NM_001105206.1 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:112460429 G>T maps to NM_001105206.1 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54778670 C>A maps to ENST00000391747 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54778670 C>A maps to ENST00000391747 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:90537932 C>T maps to NM_001102469.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:90537932 C>T maps to NM_001102469.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:39805952 C>A maps to NM_020862.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:39805952 C>A maps to NM_020862.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:196387776 C>G maps to NM_198565.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:196387776 C>G maps to NM_198565.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:96053764 C>A maps to NM_024641.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:96053764 C>A maps to NM_024641.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:39487786 C>A maps to NM_003618.2 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:39487786 C>A maps to NM_003618.2 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:5009449 C>G maps to NM_021801.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:5009449 C>G maps to NM_021801.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:90857476 A>G maps to NM_007351.2 K882K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:90857476 A>G maps to NM_007351.2 K882K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:60231793 G>T maps to NM_152866.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:60231793 G>T maps to NM_152866.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:9067654 C>T maps to NM_024690.2 V6597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:9067654 C>T maps to NM_024690.2 V6597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:15818777 C>T maps to NM_001040114.1 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:15818777 C>T maps to NM_001040114.1 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:175184863 T>G maps to NM_207015.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:175184863 T>G maps to NM_207015.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:178098809 C>A maps to NM_006164.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:178098809 C>A maps to NM_006164.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:56490757 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:56490757 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16860106 T>G maps to ENST00000438489 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16860106 T>G maps to ENST00000438489 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:125289494 G>A maps to ENST00000359439 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:125289494 G>A maps to ENST00000359439 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55370921 C>A maps to NM_001004700.1 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55370921 C>A maps to NM_001004700.1 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55371654 G>A maps to NM_001004700.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55371654 G>A maps to NM_001004700.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:56233443 G>A maps to NM_012374.1 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:56233443 G>A maps to NM_012374.1 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:48328562 G>T maps to NM_001004725.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:48328562 G>T maps to NM_001004725.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:124179837 A>G maps to NM_001002917.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:124179837 A>G maps to NM_001002917.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:56510822 G>C maps to NM_001005284.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:56510822 G>C maps to NM_001005284.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:57886055 A>T maps to NM_001005211.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:57886055 A>T maps to NM_001005211.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:76750466 C>A maps to NM_020841.4 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:76750466 C>A maps to NM_020841.4 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:140208839 G>T maps to NM_018909.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:140208839 G>T maps to NM_018909.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:144879554 C>A maps to NM_014644.4 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:144879554 C>A maps to NM_014644.4 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:76708953 C>A maps to NM_003719.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:76708953 C>A maps to NM_003719.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:44108032 G>C maps to NM_002606.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:44108032 G>C maps to NM_002606.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:42934364 C>T maps to NM_000287.3 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:42934364 C>T maps to NM_000287.3 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:57994799 G>T maps to NM_024779.4 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:57994799 G>T maps to NM_024779.4 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:110476710 C>T maps to ENST00000426474 T2550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:110476710 C>T maps to ENST00000426474 T2550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:45567058 C>A maps to ENST00000256692 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:45567058 C>A maps to ENST00000256692 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:81851618 T>C maps to NM_003625.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:81851618 T>C maps to NM_003625.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:58318598 G>T maps to NM_001080492.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:58318598 G>T maps to NM_001080492.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:79323714 C>A maps to NM_015225.2 E1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:79323714 C>A maps to NM_015225.2 E1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:43519393 G>A maps to ENST00000306308 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:43519393 G>A maps to ENST00000306308 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:79002131 G>T maps to NM_000959.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:79002131 G>T maps to NM_000959.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:77256163 A>T maps to NM_002835.3 K390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:77256163 A>T maps to NM_002835.3 K390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:8500763 G>T maps to NM_002839.3 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:8500763 G>T maps to NM_002839.3 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:32590413 T>C maps to NM_001098527.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:32590413 T>C maps to NM_001098527.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:237819146 G>A maps to NM_001035.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:237819146 G>A maps to NM_001035.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:77089566 T>C maps to NM_005506.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:77089566 T>C maps to NM_005506.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:95750583 C>A maps to NM_001160210.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:95750583 C>A maps to NM_001160210.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:21051393 A>T maps to NM_019844.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:21051393 A>T maps to NM_019844.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:108357109 C>A maps to NM_001013031.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:108357109 C>A maps to NM_001013031.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:23827749 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:23827749 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:113231318 C>A maps to ENST00000374463 G1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:113231318 C>A maps to ENST00000374463 G1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:33535419 G>T maps to NM_198992.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:33535419 G>T maps to NM_198992.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:37913576 G>T maps to NM_001163334.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:37913576 G>T maps to NM_001163334.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:132967037 C>A maps to NM_138327.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:132967037 C>A maps to NM_138327.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:132891804 T>C maps to NM_175067.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:132891804 T>C maps to NM_175067.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54675652 G>A maps to NM_001145303.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54675652 G>A maps to NM_001145303.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:175066707 C>T maps to NM_022093.1 Q582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:175066707 C>T maps to NM_022093.1 Q582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:51446143 G>A maps to ENST00000338969 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:51446143 G>A maps to ENST00000338969 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:98547351 C>T maps to ENST00000359863 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:98547351 C>T maps to ENST00000359863 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:6433942 C>T maps to NM_152896.1 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:6433942 C>T maps to NM_152896.1 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:57640186 A>T maps to NM_020903.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:57640186 A>T maps to NM_020903.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:49337974 C>T maps to NM_003363.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:49337974 C>T maps to NM_003363.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:108152587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:108152587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:117540865 A>C maps to NM_019045.4 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:117540865 A>C maps to NM_019045.4 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:85550362 G>A maps to NM_145172.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:85550362 G>A maps to NM_145172.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:122399997 G>T maps to NM_144668.4 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:122399997 G>T maps to NM_144668.4 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:67288076 C>G maps to NM_024763.4 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:67288076 C>G maps to NM_024763.4 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:168100622 G>T maps to NM_152381.5 G907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:168100622 G>T maps to NM_152381.5 G907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:135744395 G>A maps to NM_025052.3 N682N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:135744395 G>A maps to NM_025052.3 N682N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36884637 C>A maps to NM_133466.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36884637 C>A maps to NM_133466.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:44778387 C>T maps to NM_181756.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:44778387 C>T maps to NM_181756.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:178310766 T>A maps to NM_058230.2 Y438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:178310766 T>A maps to NM_058230.2 Y438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:109690044 C>T maps to NM_021224.4 I1284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:109690044 C>T maps to NM_021224.4 I1284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:12691672 G>A maps to NM_020714.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:12691672 G>A maps to NM_020714.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:38055972 C>A maps to NM_016536.3 G453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:38055972 C>A maps to NM_016536.3 G453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:53050823 G>C maps to NM_001039886.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:53050823 G>C maps to NM_001039886.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:106967308 G>C maps to NM_001624.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:106967308 G>C maps to NM_001624.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:159035704 G>A maps to NM_004833.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:159035704 G>A maps to NM_004833.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:86129054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:86129054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:29917778 C>A maps to NM_004304.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:29917778 C>A maps to NM_004304.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:41547753 G>T maps to ENST00000415018 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:41547753 G>T maps to ENST00000415018 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:61836087 G>A maps to NM_020987.2 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:61836087 G>A maps to NM_020987.2 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:92677533 C>A maps to NM_014391.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:92677533 C>A maps to NM_014391.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:21236287 G>T maps to NM_000384.2 A1320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:21236287 G>T maps to NM_000384.2 A1320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:100880147 G>A maps to NM_016607.3 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:100880147 G>A maps to NM_016607.3 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:3028171 C>A maps to NM_004042.3 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:3028171 C>A maps to NM_004042.3 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:76854956 G>C maps to NM_000489.3 S1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:76854956 G>C maps to NM_000489.3 S1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:91347826 G>A maps to NM_152638.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:91347826 G>A maps to NM_152638.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:58472919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:58472919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75038497 T>A maps to NM_001002912.4 R966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75038497 T>A maps to NM_001002912.4 R966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:31890880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:31890880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:58817567 C>T maps to ENST00000482387 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:58817567 C>T maps to ENST00000482387 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:132375844 G>T maps to NM_199350.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:132375844 G>T maps to NM_199350.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:13395963 C>A maps to NM_023035.2 E1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:13395963 C>A maps to NM_023035.2 E1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:67699343 G>A maps to NM_018448.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:67699343 G>A maps to NM_018448.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:112643969 G>T maps to NM_138806.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:112643969 G>T maps to NM_138806.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:180013209 T>G maps to NM_014810.4 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:180013209 T>G maps to NM_014810.4 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:30693186 G>A maps to ENST00000348438 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:30693186 G>A maps to ENST00000348438 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:122722483 G>T maps to NM_019604.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:122722483 G>T maps to NM_019604.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:34088982 C>T maps to ENST00000373381 L1863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:34088982 C>T maps to ENST00000373381 L1863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:96802715 G>A maps to NM_000770.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:96802715 G>A maps to NM_000770.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:12943414 T>A maps to NM_182643.2 K1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:12943414 T>A maps to NM_182643.2 K1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7667524 T>C maps to NM_020877.2 T1090T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7667524 T>C maps to NM_020877.2 T1090T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:84864321 G>T maps to NM_021233.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:84864321 G>T maps to NM_021233.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:167097619 C>T maps to NM_001080426.1 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:167097619 C>T maps to NM_001080426.1 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:48830830 G>T maps to NM_001425.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:48830830 G>T maps to NM_001425.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:154156921 G>A maps to NM_000132.3 R1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:154156921 G>A maps to NM_000132.3 R1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:225244580 G>T maps to NM_001122779.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:225244580 G>T maps to NM_001122779.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:33874928 G>T maps to NM_178468.4 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:33874928 G>T maps to NM_178468.4 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:128680586 A>T maps to NM_002017.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:128680586 A>T maps to NM_002017.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:41557831 G>T maps to NM_001012426.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:41557831 G>T maps to NM_001012426.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:58722739 G>A maps to NM_080661.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:58722739 G>A maps to NM_080661.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:113857445 C>A maps to NM_213621.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:113857445 C>A maps to NM_213621.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143130047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143130047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:26636690 C>G maps to NM_002223.2 L1984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:26636690 C>G maps to NM_002223.2 L1984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:40321503 G>A maps to NM_012285.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:40321503 G>A maps to NM_012285.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:36870262 G>T maps to NM_001029864.1 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:36870262 G>T maps to NM_001029864.1 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:115337205 G>A maps to NM_133465.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:115337205 G>A maps to NM_133465.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:5921210 T>C maps to NM_001017969.2 S1595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:5921210 T>C maps to NM_001017969.2 S1595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:141027815 C>T maps to NM_018557.2 V4414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:141027815 C>T maps to NM_018557.2 V4414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21207543 T>G maps to ENST00000381541 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21207543 T>G maps to ENST00000381541 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:38188961 C>A maps to NM_014815.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:38188961 C>A maps to NM_014815.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:23853923 G>T maps to NM_002471.3 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:23853923 G>T maps to NM_002471.3 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161172231 G>T maps to NM_004550.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161172231 G>T maps to NM_004550.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:233785157 C>A maps to NM_019850.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:233785157 C>A maps to NM_019850.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:119045889 G>T maps to NM_024618.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:119045889 G>T maps to NM_024618.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:50744598 C>A maps to NM_022162.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:50744598 C>A maps to NM_022162.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:24145855 C>T maps to NM_080723.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:24145855 C>T maps to NM_080723.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:183522270 C>T maps to NM_001080477.1 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:183522270 C>T maps to NM_001080477.1 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:78381152 G>A maps to NM_001098816.2 A2079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:78381152 G>A maps to NM_001098816.2 A2079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:3101420 C>T maps to NM_012352.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:3101420 C>T maps to NM_012352.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:56380753 G>A maps to NM_001004740.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:56380753 G>A maps to NM_001004740.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:141248393 C>A maps to NM_032420.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:141248393 C>A maps to NM_032420.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:105173784 T>C maps to NM_014976.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:105173784 T>C maps to NM_014976.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:54978396 C>A maps to NM_002625.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:54978396 C>A maps to NM_002625.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:118498237 G>T maps to NM_015157.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:118498237 G>T maps to NM_015157.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:23524601 C>A maps to NM_020227.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:23524601 C>A maps to NM_020227.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:25276278 C>T maps to NM_002862.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:25276278 C>T maps to NM_002862.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:49578831 G>T maps to NM_000324.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:49578831 G>T maps to NM_000324.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237765335 T>C maps to NM_001035.2 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237765335 T>C maps to NM_001035.2 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237872293 G>T maps to NM_001035.2 G3346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237872293 G>T maps to NM_001035.2 G3346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:84751072 G>T maps to NM_152754.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:84751072 G>T maps to NM_152754.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:156144917 G>T maps to NM_022367.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:156144917 G>T maps to NM_022367.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:3682055 C>T maps to NM_023068.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:3682055 C>T maps to NM_023068.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:164735437 T>G maps to NM_001041.3 P1219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:164735437 T>G maps to NM_001041.3 P1219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:18887483 G>A maps to ENST00000389467 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:18887483 G>A maps to ENST00000389467 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:104149121 C>A maps to NM_017564.9 R2253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:104149121 C>A maps to NM_017564.9 R2253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:152083861 C>A maps to NM_007113.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:152083861 C>A maps to NM_007113.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:56638912 C>A maps to ENST00000240361 V1421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:56638912 C>A maps to ENST00000240361 V1421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:52971718 C>A maps to NM_018676.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:52971718 C>A maps to NM_018676.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:186326649 G>A maps to NM_003292.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:186326649 G>A maps to NM_003292.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:84373138 C>A maps to NM_024686.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:84373138 C>A maps to NM_024686.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:179590741 T>A maps to NM_133378.4 I5525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:179590741 T>A maps to NM_133378.4 I5525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:100451510 C>A maps to NM_015054.1 E1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:100451510 C>A maps to NM_015054.1 E1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:41504622 G>A maps to NM_017886.2 H1116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:41504622 G>A maps to NM_017886.2 H1116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:167711433 G>A maps to NM_018974.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:167711433 G>A maps to NM_018974.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:39233831 C>T maps to NM_025132.3 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:39233831 C>T maps to NM_025132.3 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:28056533 G>C maps to NM_003447.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:28056533 G>C maps to NM_003447.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:23542620 C>A maps to NM_003430.2 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:23542620 C>A maps to NM_003430.2 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:22939801 T>A maps to ENST00000397104 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:22939801 T>A maps to ENST00000397104 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:9010578 C>T maps to NM_144670.3 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:9010578 C>T maps to NM_144670.3 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:17432167 C>G maps to ENST00000302539 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:17432167 C>G maps to ENST00000302539 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:23072499 G>C maps to NM_022060.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:23072499 G>C maps to NM_022060.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:148630008 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:148630008 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109654628 C>T maps to NM_001093.3 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109654628 C>T maps to NM_001093.3 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:32483251 G>T maps to NM_001094.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:32483251 G>T maps to NM_001094.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87780626 G>A maps to NM_021723.3 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87780626 G>A maps to NM_021723.3 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:33637776 G>C maps to NM_030955.2 S598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:33637776 G>C maps to NM_030955.2 S598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:64524896 G>A maps to NM_182920.1 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:64524896 G>A maps to NM_182920.1 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:154575012 G>A maps to ENST00000292205 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:154575012 G>A maps to ENST00000292205 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:25061435 C>A maps to NM_004036.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:25061435 C>A maps to NM_004036.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123051503 G>A maps to NM_183357.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123051503 G>A maps to NM_183357.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31126080 C>G maps to ENST00000409489 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31126080 C>G maps to ENST00000409489 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:228384752 A>G maps to NM_001135187.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:228384752 A>G maps to NM_001135187.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:29448339 G>T maps to NM_004304.3 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:29448339 G>T maps to NM_004304.3 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73717354 G>T maps to NM_015120.4 E2756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73717354 G>T maps to NM_015120.4 E2756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:61833744 C>A maps to NM_020987.2 S2298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:61833744 C>A maps to NM_020987.2 S2298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190541597 C>T maps to NM_144708.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190541597 C>T maps to NM_144708.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:54559907 G>A maps to NM_153228.2 *764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:54559907 G>A maps to NM_153228.2 *764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4085564 C>A maps to NM_016376.3 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4085564 C>A maps to NM_016376.3 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:27317874 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:27317874 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:10471850 C>G maps to ENST00000423585 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:10471850 C>G maps to ENST00000423585 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:7805421 G>T maps to NM_001644.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:7805421 G>T maps to NM_001644.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:39425496 C>T maps to NM_152426.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:39425496 C>T maps to NM_152426.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:21255356 C>T maps to NM_000384.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:21255356 C>T maps to NM_000384.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:64216780 G>C maps to NM_000042.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:64216780 G>C maps to NM_000042.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:35192824 G>A maps to NM_014691.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:35192824 G>A maps to NM_014691.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:72406622 C>T maps to NM_001040118.2 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:72406622 C>T maps to NM_001040118.2 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57872990 G>A maps to ENST00000393797 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57872990 G>A maps to ENST00000393797 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111896543 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111896543 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235383691 C>T maps to NM_016374.5 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235383691 C>T maps to NM_016374.5 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:63852623 G>A maps to NM_032199.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:63852623 G>A maps to NM_032199.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:2990081 C>T maps to NM_004042.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:2990081 C>T maps to NM_004042.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131073090 G>A maps to NM_018482.2 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131073090 G>A maps to NM_018482.2 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155324276 C>G maps to ENST00000368346 G2405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155324276 C>G maps to ENST00000368346 G2405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:96775858 G>A maps to NM_018036.5 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:96775858 G>A maps to NM_018036.5 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:138857045 G>A maps to NM_173694.4 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:138857045 G>A maps to NM_173694.4 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:119513325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:119513325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:89996905 T>A maps to ENST00000428670 K992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:89996905 T>A maps to ENST00000428670 K992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:55338752 C>A maps to NM_005603.4 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:55338752 C>A maps to NM_005603.4 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:17931575 C>T maps to NM_145691.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:17931575 C>T maps to NM_145691.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:42613777 C>G maps to NM_012105.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:42613777 C>G maps to NM_012105.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57007917 C>G maps to NM_013449.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57007917 C>G maps to NM_013449.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:129149327 C>T maps to ENST00000303743 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:129149327 C>T maps to ENST00000303743 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:32458938 G>C maps to NM_001714.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:32458938 G>C maps to NM_001714.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79832344 C>T maps to NM_198892.1 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79832344 C>T maps to NM_198892.1 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31604873 G>A maps to NM_025227.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31604873 G>A maps to NM_025227.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:9785986 G>A maps to NM_001003694.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:9785986 G>A maps to NM_001003694.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:111395585 A>G maps to NM_004336.3 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:111395585 A>G maps to NM_004336.3 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:13526176 C>G maps to ENST00000318426 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:13526176 C>G maps to ENST00000318426 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:97147596 G>T maps to ENST00000342887 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:97147596 G>T maps to ENST00000342887 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:45373678 G>A maps to NM_001017923.1 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:45373678 G>A maps to NM_001017923.1 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8146358 C>T maps to NM_025099.5 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8146358 C>T maps to NM_025099.5 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:77798590 C>T maps to NM_024805.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:77798590 C>T maps to NM_024805.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:36496282 C>T maps to ENST00000455847 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:36496282 C>T maps to ENST00000455847 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:7242748 C>A maps to ENST00000290575 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:7242748 C>A maps to ENST00000290575 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:169390791 G>A maps to ENST00000367806 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:169390791 G>A maps to ENST00000367806 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170964570 C>A maps to NM_001163629.1 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170964570 C>A maps to NM_001163629.1 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247737458 C>A maps to NM_145278.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247737458 C>A maps to NM_145278.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:23696035 G>A maps to ENST00000507744 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:23696035 G>A maps to ENST00000507744 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31044010 C>T maps to NM_080616.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31044010 C>T maps to NM_080616.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30617579 C>A maps to ENST00000300415 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30617579 C>A maps to ENST00000300415 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:88825150 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:88825150 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74043092 C>A maps to NM_001080474.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74043092 C>A maps to NM_001080474.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:47846856 G>A maps to NM_001013732.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:47846856 G>A maps to NM_001013732.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:133118162 G>A maps to NM_052831.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:133118162 G>A maps to NM_052831.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:27898705 C>A maps to ENST00000341513 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:27898705 C>A maps to ENST00000341513 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:24458475 A>T maps to NM_012295.3 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:24458475 A>T maps to NM_012295.3 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48533814 C>T maps to NM_019855.3 *174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48533814 C>T maps to NM_019855.3 *174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181727928 G>C maps to ENST00000357570 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181727928 G>C maps to ENST00000357570 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48646275 G>A maps to NM_018896.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48646275 G>A maps to NM_018896.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37343839 T>C maps to NM_000723.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37343839 T>C maps to NM_000723.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:86010711 G>A maps to NM_153184.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:86010711 G>A maps to NM_153184.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:7356308 G>C maps to NM_001170692.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:7356308 G>C maps to NM_001170692.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:78156488 C>T maps to NM_024110.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:78156488 C>T maps to NM_024110.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:121994735 G>A maps to NM_001178065.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:121994735 G>A maps to NM_001178065.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:38849156 G>A maps to NM_021185.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:38849156 G>A maps to NM_021185.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:96284692 G>C maps to NM_182496.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:96284692 G>C maps to NM_182496.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41828557 G>T maps to NM_052848.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41828557 G>T maps to NM_052848.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:6292376 C>T maps to NM_176875.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:6292376 C>T maps to NM_176875.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:119263472 G>T maps to NM_005191.3 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:119263472 G>T maps to NM_005191.3 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64846929 G>A maps to ENST00000404147 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64846929 G>A maps to ENST00000404147 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:45153866 G>A maps to NM_022842.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:45153866 G>A maps to NM_022842.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:31323243 C>G maps to NM_004932.2 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:31323243 C>G maps to NM_004932.2 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:26906095 G>A maps to NM_016279.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:26906095 G>A maps to NM_016279.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:110988771 A>G maps to NM_015076.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:110988771 A>G maps to NM_015076.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50802719 A>G maps to ENST00000356146 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50802719 A>G maps to ENST00000356146 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151499484 G>T maps to NM_020770.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151499484 G>T maps to NM_020770.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:203151967 C>A maps to NM_001276.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:203151967 C>A maps to NM_001276.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240071236 C>A maps to NM_000740.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240071236 C>A maps to NM_000740.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:157241261 C>A maps to NM_001195555.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:157241261 C>A maps to NM_001195555.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:100543591 G>T maps to NM_206808.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:100543591 G>T maps to NM_206808.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:72180809 G>A maps to NM_018235.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:72180809 G>A maps to NM_018235.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57949203 G>C maps to NM_001297.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57949203 G>C maps to NM_001297.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:147600732 C>A maps to NM_014141.5 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:147600732 C>A maps to NM_014141.5 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40716075 C>T maps to NM_001042532.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40716075 C>T maps to NM_001042532.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46083855 C>T maps to NM_031431.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46083855 C>T maps to NM_031431.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103471864 G>A maps to NM_080629.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103471864 G>A maps to NM_080629.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:33153522 G>C maps to NM_080680.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:33153522 G>C maps to NM_080680.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:75860866 G>C maps to ENST00000322507 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:75860866 G>C maps to ENST00000322507 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:70866083 T>A maps to NM_001858.4 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:70866083 T>A maps to NM_001858.4 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:94041432 C>A maps to NM_000089.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:94041432 C>A maps to NM_000089.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56661649 G>C maps to NM_144576.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56661649 G>C maps to NM_144576.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207851642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207851642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:208986483 C>A maps to NM_006891.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:208986483 C>A maps to NM_006891.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:149433715 C>T maps to NM_005211.3 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:149433715 C>T maps to NM_005211.3 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:23473695 C>A maps to NM_005492.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:23473695 C>A maps to NM_005492.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:19996718 A>T maps to NM_172241.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:19996718 A>T maps to NM_172241.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:111706258 G>A maps to NM_003798.2 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:111706258 G>A maps to NM_003798.2 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:11082865 G>T maps to NM_001332.2 C910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:11082865 G>T maps to NM_001332.2 C910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:48994051 C>T maps to NM_025087.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:48994051 C>T maps to NM_025087.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:99311121 G>A maps to ENST00000292414 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:99311121 G>A maps to ENST00000292414 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:16034627 C>T maps to NM_021187.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:16034627 C>T maps to NM_021187.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:27766454 G>A maps to NM_001136533.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:27766454 G>A maps to NM_001136533.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169158900 T>A maps to NM_017631.5 R1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169158900 T>A maps to NM_017631.5 R1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:145541078 G>A maps to NM_012079.4 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:145541078 G>A maps to NM_012079.4 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127540982 G>C maps to NM_018180.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127540982 G>C maps to NM_018180.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:96213114 G>T maps to NM_006729.4 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:96213114 G>T maps to NM_006729.4 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:233001237 C>G maps to NM_152383.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:233001237 C>G maps to NM_152383.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21042460 G>T maps to NM_017539.1 S1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21042460 G>T maps to NM_017539.1 S1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21063027 G>T maps to NM_017539.1 R1401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21063027 G>T maps to NM_017539.1 R1401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74752170 G>C maps to NM_133637.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74752170 G>C maps to NM_133637.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:118176763 G>A maps to NM_173666.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:118176763 G>A maps to NM_173666.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:102498628 C>T maps to NM_001376.4 Q3302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:102498628 C>T maps to NM_001376.4 Q3302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:38464006 C>T maps to ENST00000354891 F991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:38464006 C>T maps to ENST00000354891 F991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:110920852 C>T maps to NM_001963.4 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:110920852 C>T maps to NM_001963.4 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41573856 C>T maps to NM_001429.3 Q2048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41573856 C>T maps to NM_001429.3 Q2048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:34807690 G>A maps to NM_012156.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:34807690 G>A maps to NM_012156.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184295456 C>T maps to NM_004443.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184295456 C>T maps to NM_004443.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30915195 C>T maps to ENST00000509504 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30915195 C>T maps to ENST00000509504 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:129096470 T>A maps to ENST00000450266 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:129096470 T>A maps to ENST00000450266 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:43626912 G>T maps to NM_001145196.1 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:43626912 G>T maps to NM_001145196.1 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:89824527 G>T maps to NM_001113378.1 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:89824527 G>T maps to NM_001113378.1 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:13035801 C>T maps to NM_004461.2 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:13035801 C>T maps to NM_004461.2 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:92085739 G>A maps to ENST00000298047 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:92085739 G>A maps to ENST00000298047 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:112942901 G>A maps to NM_153214.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:112942901 G>A maps to NM_153214.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127609547 G>T maps to NM_001999.3 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127609547 G>T maps to NM_001999.3 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:114860289 G>A maps to NM_020177.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:114860289 G>A maps to NM_020177.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:14862089 G>A maps to NM_152536.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:14862089 G>A maps to NM_152536.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:167446088 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:167446088 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:80680681 A>T maps to NM_024619.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:80680681 A>T maps to NM_024619.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:135438866 G>C maps to ENST00000443774 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:135438866 G>C maps to ENST00000443774 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:48340054 G>T maps to NM_012280.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:48340054 G>T maps to NM_012280.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:47408702 C>A maps to NM_000812.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:47408702 C>A maps to NM_000812.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:45593434 C>T maps to NM_024707.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:45593434 C>T maps to NM_024707.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61958481 C>T maps to NM_002059.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61958481 C>T maps to NM_002059.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:78511975 C>G maps to NM_017655.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:78511975 C>G maps to NM_017655.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:35260488 G>C maps to NM_002060.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:35260488 G>C maps to NM_002060.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42882275 G>A maps to NM_001080383.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42882275 G>A maps to NM_001080383.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:74537460 G>A maps to NM_012201.5 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:74537460 G>A maps to NM_012201.5 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:96690295 C>T maps to NM_207328.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:96690295 C>T maps to NM_207328.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:176561959 C>A maps to NM_005277.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:176561959 C>A maps to NM_005277.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:25464426 C>T maps to NM_020752.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:25464426 C>T maps to NM_020752.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:167570896 C>G maps to NM_005299.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:167570896 C>G maps to NM_005299.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:11716527 C>T maps to NM_014668.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:11716527 C>T maps to NM_014668.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:102570808 C>T maps to NM_024915.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:102570808 C>T maps to NM_024915.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47422324 C>T maps to NM_004491.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47422324 C>T maps to NM_004491.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:13543373 C>T maps to NM_024827.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:13543373 C>T maps to NM_024827.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:31613463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:31613463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124731845 G>A maps to NM_020733.1 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124731845 G>A maps to NM_020733.1 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:66698700 C>T maps to NM_033647.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:66698700 C>T maps to NM_033647.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124805827 C>T maps to NM_152722.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124805827 C>T maps to NM_152722.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:28361809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:28361809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:26216649 G>A maps to NM_003518.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:26216649 G>A maps to NM_003518.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30460193 G>C maps to NM_005516.5 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30460193 G>C maps to NM_005516.5 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30142618 T>C maps to NM_178581.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30142618 T>C maps to NM_178581.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:177036401 C>T maps to NM_006898.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:177036401 C>T maps to NM_006898.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:115216389 C>T maps to NM_032303.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:115216389 C>T maps to NM_032303.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:87725672 C>T maps to NM_000865.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:87725672 C>T maps to NM_000865.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:34632983 G>T maps to NM_207585.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:34632983 G>T maps to NM_207585.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:103040547 A>C maps to NM_003853.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:103040547 A>C maps to NM_003853.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:27460063 G>T maps to NM_181079.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:27460063 G>T maps to NM_181079.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:68619521 G>A maps to NM_018402.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:68619521 G>A maps to NM_018402.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:77635797 C>T maps to NM_033547.3 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:77635797 C>T maps to NM_033547.3 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:30787165 G>C maps to NM_006390.3 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:30787165 G>C maps to NM_006390.3 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:32673605 C>T maps to NM_001160042.1 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:32673605 C>T maps to NM_001160042.1 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:33033184 C>G maps to ENST00000262650 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:33033184 C>G maps to ENST00000262650 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:52240773 C>G maps to NM_181501.1 S1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:52240773 C>G maps to NM_181501.1 S1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45384960 C>T maps to NM_000212.2 F753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45384960 C>T maps to NM_000212.2 F753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:7773946 C>T maps to NM_002216.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:7773946 C>T maps to NM_002216.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:35147372 G>A maps to NM_003024.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:35147372 G>A maps to NM_003024.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:63447715 C>T maps to NM_139318.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:63447715 C>T maps to NM_139318.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:163256900 G>C maps to NM_033272.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:163256900 G>C maps to NM_033272.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62046307 C>T maps to NM_172107.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62046307 C>T maps to NM_172107.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62046309 G>T maps to NM_172107.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62046309 G>T maps to NM_172107.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:406209 G>A maps to NM_001042603.1 Q1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:406209 G>A maps to NM_001042603.1 Q1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:79749184 C>T maps to NM_015206.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:79749184 C>T maps to NM_015206.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:123192443 C>T maps to NM_015312.3 Q2589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:123192443 C>T maps to NM_015312.3 Q2589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:70776072 C>T maps to NM_015634.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:70776072 C>T maps to NM_015634.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94088192 C>A maps to ENST00000393153 I1560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94088192 C>A maps to ENST00000393153 I1560I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z026-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:138522651 C>T maps to ENST00000413208 Q65*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z026-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:138522651 C>T maps to ENST00000413208 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:5922046 G>A maps to NM_001017969.2 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:5922046 G>A maps to NM_001017969.2 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55377284 G>C maps to ENST00000355608 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55377284 G>C maps to ENST00000355608 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50246942 C>T maps to NM_014315.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50246942 C>T maps to NM_014315.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:152733200 C>G maps to NM_001025231.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:152733200 C>G maps to NM_001025231.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39521736 C>T maps to ENST00000394004 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39521736 C>T maps to ENST00000394004 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37074946 G>A maps to NM_006148.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37074946 G>A maps to NM_006148.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136575240 C>A maps to NM_002299.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136575240 C>A maps to NM_002299.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71977970 C>T maps to NM_003667.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71977970 C>T maps to NM_003667.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151774292 G>T maps to NM_001004432.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151774292 G>T maps to NM_001004432.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:165173116 T>C maps to NM_177398.3 *383W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:165173116 T>C maps to NM_177398.3 *383W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:161011991 C>A maps to NM_005577.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:161011991 C>A maps to NM_005577.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151829937 C>T maps to NM_006726.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151829937 C>T maps to NM_006726.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:99828100 G>T maps to NM_144598.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:99828100 G>T maps to NM_144598.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:47647499 C>G maps to NM_002340.5 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:47647499 C>G maps to NM_002340.5 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:99907837 G>A maps to NM_174898.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:99907837 G>A maps to NM_174898.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:149013507 C>T maps to NM_005364.4 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:149013507 C>T maps to NM_005364.4 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:53876153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:53876153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:54824868 T>C maps to ENST00000371389 *361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:54824868 T>C maps to ENST00000371389 *361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:100395738 T>A maps to NM_032503.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:100395738 T>A maps to NM_032503.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:47660845 C>A maps to NM_003906.3 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:47660845 C>A maps to NM_003906.3 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:118533129 G>T maps to NM_080651.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:118533129 G>T maps to NM_080651.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:73010569 C>T maps to NM_032951.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:73010569 C>T maps to NM_032951.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45904480 C>G maps to NM_145255.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45904480 C>G maps to NM_145255.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:47690167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:47690167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:48027171 C>T maps to NM_000179.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:48027171 C>T maps to NM_000179.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:23409754 C>T maps to ENST00000277598 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:23409754 C>T maps to ENST00000277598 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:107371700 C>T maps to NM_025198.3 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:107371700 C>T maps to NM_025198.3 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9017373 G>T maps to NM_024690.2 T12650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9017373 G>T maps to NM_024690.2 T12650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9072067 G>T maps to NM_024690.2 T5126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9072067 G>T maps to NM_024690.2 T5126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9088055 G>T maps to NM_024690.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9088055 G>T maps to NM_024690.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:57749650 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:57749650 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10360770 A>T maps to NM_017533.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10360770 A>T maps to NM_017533.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:16711276 G>C maps to NM_012334.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:16711276 G>C maps to NM_012334.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:59480398 C>A maps to NM_004998.2 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:59480398 C>A maps to NM_004998.2 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:101721104 A>T maps to NM_052867.2 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:101721104 A>T maps to NM_052867.2 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:78444769 C>A maps to NM_014903.4 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:78444769 C>A maps to NM_014903.4 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152531008 C>G maps to NM_001164507.1 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152531008 C>G maps to NM_001164507.1 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:104157428 C>T maps to NM_001077494.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:104157428 C>T maps to NM_001077494.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:129739493 T>C maps to NM_006165.3 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:129739493 T>C maps to NM_006165.3 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51875445 C>A maps to NM_005601.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51875445 C>A maps to NM_005601.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:16952928 G>T maps to ENST00000382868 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:16952928 G>T maps to ENST00000382868 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:32476635 G>A maps to NM_021209.4 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:32476635 G>A maps to NM_021209.4 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:139395165 T>G maps to NM_017617.3 T1924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:139395165 T>G maps to NM_017617.3 T1924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:51254934 G>T maps to ENST00000404971 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:51254934 G>T maps to ENST00000404971 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:163325228 G>A maps to NM_145697.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:163325228 G>A maps to NM_145697.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134014771 A>T maps to ENST00000451030 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134014771 A>T maps to ENST00000451030 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134014780 G>T maps to ENST00000451030 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134014780 G>T maps to ENST00000451030 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:228550382 C>T maps to NM_001098623.1 P6256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:228550382 C>T maps to NM_001098623.1 P6256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:123870931 C>T maps to NM_001163278.1 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:123870931 C>T maps to NM_001163278.1 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158549248 T>C maps to NM_001004477.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158549248 T>C maps to NM_001004477.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:29343003 G>A maps to ENST00000396806 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:29343003 G>A maps to ENST00000396806 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125316158 C>A maps to NM_001004457.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125316158 C>A maps to NM_001004457.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247695435 G>T maps to NM_198074.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247695435 G>T maps to NM_198074.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247752137 C>A maps to NM_001001915.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247752137 C>A maps to NM_001001915.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248343685 C>A maps to NM_001004688.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248343685 C>A maps to NM_001004688.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:22133667 G>T maps to NM_001001912.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:22133667 G>T maps to NM_001001912.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:5344954 A>T maps to NM_033180.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:5344954 A>T maps to NM_033180.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:4673878 T>A maps to NM_152430.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:4673878 T>A maps to NM_152430.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:4944804 G>T maps to NM_001005237.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:4944804 G>T maps to NM_001005237.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58190686 G>T maps to NM_001005566.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58190686 G>T maps to NM_001005566.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247875435 G>A maps to NM_001005286.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247875435 G>A maps to NM_001005286.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:21109584 G>C maps to NM_001001968.1 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:21109584 G>C maps to NM_001001968.1 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124252846 C>G maps to NM_001005468.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124252846 C>G maps to NM_001005468.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:123777581 C>A maps to NM_001005197.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:123777581 C>A maps to NM_001005197.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:57958804 G>A maps to NM_001005283.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:57958804 G>A maps to NM_001005283.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:24901332 G>T maps to NM_015550.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:24901332 G>T maps to NM_015550.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20824168 C>T maps to NM_005484.3 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20824168 C>T maps to NM_005484.3 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:61985376 C>G maps to NM_022843.3 *952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:61985376 C>G maps to NM_022843.3 *952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140530411 G>T maps to NM_018939.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140530411 G>T maps to NM_018939.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140735630 A>T maps to NM_018917.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140735630 A>T maps to NM_018917.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140789007 G>A maps to NM_018926.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140789007 G>A maps to NM_018926.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:120388168 G>A maps to NM_001029996.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:120388168 G>A maps to NM_001029996.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:17849060 G>A maps to NM_006197.3 V1514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:17849060 G>A maps to NM_006197.3 V1514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62904847 G>T maps to NM_018257.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62904847 G>T maps to NM_018257.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66620060 C>T maps to NM_022172.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66620060 C>T maps to NM_022172.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:33863495 A>G maps to NM_001162429.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:33863495 A>G maps to NM_001162429.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:144946726 C>T maps to NM_014644.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:144946726 C>T maps to NM_014644.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:98155360 G>A maps to ENST00000325141 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:98155360 G>A maps to ENST00000325141 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:49754363 C>T maps to NM_138733.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:49754363 C>T maps to NM_138733.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:18943784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:18943784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:209218815 C>T maps to NM_015040.3 L2013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:209218815 C>T maps to NM_015040.3 L2013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51484223 G>T maps to NM_138694.3 V3960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51484223 G>T maps to NM_138694.3 V3960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96005701 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96005701 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:16838532 C>A maps to ENST00000448080 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:16838532 C>A maps to ENST00000448080 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12008051 G>C maps to ENST00000376369 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12008051 G>C maps to ENST00000376369 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:118236244 C>T maps to NM_001011709.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:118236244 C>T maps to NM_001011709.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:62481961 C>A maps to NM_007215.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:62481961 C>A maps to NM_007215.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:23527707 T>A maps to NM_020227.2 C837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:23527707 T>A maps to NM_020227.2 C837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:37487371 G>A maps to NM_005813.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:37487371 G>A maps to NM_005813.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:48866264 T>C maps to NM_006904.6 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:48866264 T>C maps to NM_006904.6 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71275485 C>G maps to NM_021225.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71275485 C>G maps to NM_021225.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:52874342 G>A maps to NM_032864.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:52874342 G>A maps to NM_032864.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:126883538 G>T maps to ENST00000330542 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:126883538 G>T maps to ENST00000330542 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:143763501 G>T maps to ENST00000301258 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:143763501 G>T maps to ENST00000301258 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:87656019 C>T maps to NM_080685.2 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:87656019 C>T maps to NM_080685.2 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:8636818 G>C maps to NM_002839.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:8636818 G>C maps to NM_002839.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:157959950 G>T maps to NM_002847.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:157959950 G>T maps to NM_002847.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:15704554 G>T maps to NM_030667.1 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:15704554 G>T maps to NM_030667.1 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71286584 G>T maps to NM_002849.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71286584 G>T maps to NM_002849.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40864876 G>A maps to ENST00000373198 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40864876 G>A maps to ENST00000373198 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40877403 C>T maps to ENST00000373198 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40877403 C>T maps to ENST00000373198 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:121674343 G>A maps to NM_002851.2 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:121674343 G>A maps to NM_002851.2 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:144902886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:144902886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:38345516 C>A maps to ENST00000456989 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:38345516 C>A maps to ENST00000456989 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:38487574 C>G maps to NM_001145301.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:38487574 C>G maps to NM_001145301.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:114364966 C>T maps to NM_016196.3 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:114364966 C>T maps to NM_016196.3 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:139237322 C>T maps to NM_002899.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:139237322 C>T maps to NM_002899.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:46214581 C>A maps to ENST00000405162 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:46214581 C>A maps to ENST00000405162 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:25701838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:25701838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:38953091 G>A maps to ENST00000296782 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:38953091 G>A maps to ENST00000296782 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:72960916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:72960916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:73110205 C>T maps to NM_014989.4 V1623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:73110205 C>T maps to NM_014989.4 V1623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105105840 C>G maps to ENST00000436393 S955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105105840 C>G maps to ENST00000436393 S955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:21053584 C>T maps to NM_003831.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:21053584 C>T maps to NM_003831.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:90775203 A>T maps to NM_003821.5 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:90775203 A>T maps to NM_003821.5 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20978752 C>T maps to ENST00000430083 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20978752 C>T maps to ENST00000430083 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90077867 C>G maps to NM_021244.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90077867 C>G maps to NM_021244.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155292330 G>A maps to NM_001105203.1 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155292330 G>A maps to NM_001105203.1 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:133942681 A>C maps to NM_016103.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:133942681 A>C maps to NM_016103.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38622505 G>A maps to NM_001099404.1 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38622505 G>A maps to NM_001099404.1 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:17354336 C>T maps to NM_003000.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:17354336 C>T maps to NM_003000.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:83739784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:83739784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:30393196 C>T maps to NM_052838.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:30393196 C>T maps to NM_052838.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:61310739 C>T maps to NM_002974.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:61310739 C>T maps to NM_002974.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26689002 G>A maps to NM_021115.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26689002 G>A maps to NM_021115.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:27189777 C>T maps to NM_006142.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:27189777 C>T maps to NM_006142.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:52147181 G>T maps to NM_001098612.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:52147181 G>T maps to NM_001098612.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:111575716 C>T maps to NM_015191.1 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:111575716 C>T maps to NM_015191.1 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:164766994 G>T maps to NM_001041.3 C545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:164766994 G>T maps to NM_001041.3 C545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107352991 C>T maps to NM_000441.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107352991 C>T maps to NM_000441.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:103014986 T>C maps to ENST00000354356 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:103014986 T>C maps to ENST00000354356 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168093539 G>T maps to NM_003062.2 Y1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168093539 G>T maps to NM_003062.2 Y1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168250305 G>T maps to NM_003062.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168250305 G>T maps to NM_003062.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:86368536 C>A maps to NM_032229.2 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:86368536 C>A maps to NM_032229.2 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:2182166 G>C maps to NM_003070.3 R1462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:2182166 G>C maps to NM_003070.3 R1462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:62551056 T>C maps to NM_022739.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:62551056 T>C maps to NM_022739.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73450602 C>T maps to NM_006062.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73450602 C>T maps to NM_006062.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:52944958 C>A maps to NM_145263.2 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:52944958 C>A maps to NM_145263.2 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:95011343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:95011343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54853247 C>T maps to NM_003128.2 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54853247 C>T maps to NM_003128.2 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54856192 G>A maps to NM_003128.2 W641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54856192 G>A maps to NM_003128.2 W641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:36709060 C>T maps to NM_025248.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:36709060 C>T maps to NM_025248.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:33684071 C>T maps to NM_178007.2 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:33684071 C>T maps to NM_178007.2 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:23811830 G>A maps to NM_031414.3 K633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:23811830 G>A maps to NM_031414.3 K633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7705870 C>T maps to ENST00000441779 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7705870 C>T maps to ENST00000441779 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:29762820 C>T maps to NM_021738.2 E1825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:29762820 C>T maps to NM_021738.2 E1825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:64449498 C>G maps to NM_182914.2 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:64449498 C>G maps to NM_182914.2 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:33410884 T>A maps to NM_006772.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:33410884 T>A maps to NM_006772.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:76167872 C>T maps to NM_004710.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:76167872 C>T maps to NM_004710.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:35945441 C>T maps to NM_007247.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:35945441 C>T maps to NM_007247.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:110022118 G>A maps to NM_001040709.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:110022118 G>A maps to NM_001040709.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:149700304 C>T maps to NM_015093.4 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:149700304 C>T maps to NM_015093.4 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29994516 C>G maps to NM_016151.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29994516 C>G maps to NM_016151.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100463678 C>T maps to NM_001007565.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100463678 C>T maps to NM_001007565.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:3447317 C>T maps to NM_139214.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:3447317 C>T maps to NM_139214.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:65123347 C>G maps to NM_145719.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:65123347 C>G maps to NM_145719.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105360887 C>A maps to NM_030788.2 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105360887 C>A maps to NM_030788.2 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30729321 G>A maps to NM_014742.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30729321 G>A maps to NM_014742.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:53798104 C>T maps to NM_001099640.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:53798104 C>T maps to NM_001099640.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:32046819 C>T maps to ENST00000375244 V1455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:32046819 C>T maps to ENST00000375244 V1455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:133342988 G>A maps to NM_007027.3 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:133342988 G>A maps to NM_007027.3 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:21963404 G>A maps to NM_014828.2 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:21963404 G>A maps to NM_014828.2 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:20010404 G>A maps to NM_199254.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:20010404 G>A maps to NM_199254.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:17201211 G>T maps to NM_004412.5 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:17201211 G>T maps to NM_004412.5 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30131760 C>T maps to NM_033229.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30131760 C>T maps to NM_033229.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:104414407 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:104414407 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49704026 C>T maps to NM_017636.3 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49704026 C>T maps to NM_017636.3 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:45149029 G>C maps to NM_183422.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:45149029 G>C maps to NM_183422.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:75107923 G>C maps to NM_145170.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:75107923 G>C maps to NM_145170.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:166781138 G>C maps to NM_024753.3 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:166781138 G>C maps to NM_024753.3 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30521612 C>T maps to NM_001008409.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30521612 C>T maps to NM_001008409.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179400234 G>T maps to NM_133378.4 R31135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179400234 G>T maps to NM_133378.4 R31135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179437529 G>A maps to NM_133378.4 C21875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179437529 G>A maps to NM_133378.4 C21875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179438785 C>A maps to NM_133378.4 E21457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179438785 C>A maps to NM_133378.4 E21457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:48115326 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:48115326 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70460322 G>T maps to ENST00000514019 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70460322 G>T maps to ENST00000514019 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:34802577 C>A maps to NM_017754.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:34802577 C>A maps to NM_017754.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:73048712 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:73048712 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:229783447 C>T maps to NM_014777.2 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:229783447 C>T maps to NM_014777.2 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:17214815 C>G maps to ENST00000285681 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:17214815 C>G maps to ENST00000285681 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113679904 G>A maps to NM_020886.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113679904 G>A maps to NM_020886.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:58332589 C>T maps to NM_032582.3 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:58332589 C>T maps to NM_032582.3 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:118939978 G>T maps to NM_021729.4 *87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:118939978 G>T maps to NM_021729.4 *87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:62221814 C>T maps to NM_020821.2 L2057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:62221814 C>T maps to NM_020821.2 L2057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12475196 C>T maps to NM_015378.2 L4030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12475196 C>T maps to NM_015378.2 L4030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:60901508 C>A maps to NM_017966.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:60901508 C>A maps to NM_017966.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:49842350 G>C maps to NM_198570.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:49842350 G>C maps to NM_198570.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:85623504 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:85623504 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:54398737 G>A maps to NM_015285.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:54398737 G>A maps to NM_015285.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:17280688 G>A maps to NM_175878.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:17280688 G>A maps to NM_175878.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:56015035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:56015035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41318432 C>T maps to NM_022098.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41318432 C>T maps to NM_022098.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64828638 C>T maps to NM_007235.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64828638 C>T maps to NM_007235.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:75266343 C>G maps to NM_019589.2 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:75266343 C>G maps to NM_019589.2 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:6641241 G>A maps to NM_005341.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:6641241 G>A maps to NM_005341.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47570647 G>A maps to NM_015168.1 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47570647 G>A maps to NM_015168.1 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:145156751 C>A maps to NM_014795.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:145156751 C>A maps to NM_014795.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:38084405 G>A maps to NM_021943.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:38084405 G>A maps to NM_021943.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:27425158 C>A maps to NM_007149.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:27425158 C>A maps to NM_007149.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44570266 G>T maps to NM_013361.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44570266 G>T maps to NM_013361.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:71482162 T>A maps to NM_145911.1 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:71482162 T>A maps to NM_145911.1 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:14815882 G>T maps to NM_032433.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:14815882 G>T maps to NM_032433.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:25656822 C>T maps to NM_015655.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:25656822 C>T maps to NM_015655.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:52468934 T>A maps to NM_021632.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:52468934 T>A maps to NM_021632.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:21719512 A>T maps to NM_001001415.2 K220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:21719512 A>T maps to NM_001001415.2 K220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:12460636 G>T maps to NM_030824.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:12460636 G>T maps to NM_030824.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:109690338 G>A maps to NM_021224.4 W1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:109690338 G>A maps to NM_021224.4 W1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:37904466 G>A maps to NM_152484.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:37904466 G>A maps to NM_152484.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58490389 G>C maps to NM_025027.3 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58490389 G>C maps to NM_025027.3 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:249149985 G>A maps to NM_001136036.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:249149985 G>A maps to NM_001136036.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:24087218 G>A maps to NM_021916.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:24087218 G>A maps to NM_021916.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33288890 G>A maps to NM_052857.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33288890 G>A maps to NM_052857.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:50532447 G>T maps to NM_001135196.1 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:50532447 G>T maps to NM_001135196.1 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:94055081 C>T maps to NM_000089.3 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:94055081 C>T maps to NM_000089.3 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:139040233 G>T maps to NM_001013403.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:139040233 G>T maps to NM_001013403.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:231954126 A>T maps to NM_001164537.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:231954126 A>T maps to NM_001164537.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:13259056 A>T maps to NM_182643.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:13259056 A>T maps to NM_182643.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr11:83544764 G>A maps to NM_001142699.1 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr11:83544764 G>A maps to NM_001142699.1 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:31224707 T>A maps to ENST00000357033 K3214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:31224707 T>A maps to ENST00000357033 K3214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:212273759 C>G maps to NM_016448.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:212273759 C>G maps to NM_016448.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:1289830 C>T maps to NM_178040.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:1289830 C>T maps to NM_178040.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:187608302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:187608302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:15364371 G>A maps to NM_004469.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:15364371 G>A maps to NM_004469.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:100653423 A>C maps to NM_000169.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:100653423 A>C maps to NM_000169.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:81334810 A>G maps to NM_000601.4 Y635Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:81334810 A>G maps to NM_000601.4 Y635Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:136594171 G>T maps to NM_006558.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:136594171 G>T maps to NM_006558.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:113909203 C>A maps to NM_022363.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:113909203 C>A maps to NM_022363.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr21:47611872 C>T maps to NM_002340.5 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr21:47611872 C>T maps to NM_002340.5 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:195477784 C>A maps to NM_018406.5 G5282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:195477784 C>A maps to NM_018406.5 G5282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr19:8595412 A>G maps to NM_012335.3 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr19:8595412 A>G maps to NM_012335.3 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:174814952 G>A maps to NM_207015.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:174814952 G>A maps to NM_207015.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:104156243 C>T maps to NM_001077494.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:104156243 C>T maps to NM_001077494.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr11:55135667 T>C maps to NM_001005275.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr11:55135667 T>C maps to NM_001005275.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:141618908 C>T maps to NM_001001656.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:141618908 C>T maps to NM_001001656.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:50723380 A>G maps to ENST00000515869 *1062Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:50723380 A>G maps to ENST00000515869 *1062Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:22245655 G>A maps to NM_000444.4 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:22245655 G>A maps to NM_000444.4 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:45270160 C>A maps to NM_004073.2 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:45270160 C>A maps to NM_004073.2 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:144904452 G>T maps to NM_001144010.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chrX:144904452 G>T maps to NM_001144010.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr9:139270915 A>T maps to NM_003086.2 G1434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr9:139270915 A>T maps to NM_003086.2 G1434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:33579378 A>T maps to NM_198992.3 L68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:33579378 A>T maps to NM_198992.3 L68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:35648014 C>T maps to ENST00000416672 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:35648014 C>T maps to ENST00000416672 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:148801966 A>G maps to NM_001001661.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:148801966 A>G maps to NM_001001661.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:47295249 C>T maps to NM_016428.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:47295249 C>T maps to NM_016428.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:89392930 A>G maps to NM_013227.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:89392930 A>G maps to NM_013227.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:51182597 C>T maps to NM_001097.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:51182597 C>T maps to NM_001097.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:79478069 G>T maps to NM_001614.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:79478069 G>T maps to NM_001614.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:111617730 C>T maps to NM_006686.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:111617730 C>T maps to NM_006686.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:42854946 C>T maps to NM_002390.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:42854946 C>T maps to NM_002390.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:123003541 G>C maps to NM_183357.2 Y1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:123003541 G>C maps to NM_183357.2 Y1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:15484838 G>C maps to NM_005858.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:15484838 G>C maps to NM_005858.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:114276238 G>A maps to NM_001148.4 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:114276238 G>A maps to NM_001148.4 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:99837587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:99837587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:36616224 T>A maps to NM_001177506.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:36616224 T>A maps to NM_001177506.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:69153633 G>A maps to NM_006407.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:69153633 G>A maps to NM_006407.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:80750268 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:80750268 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:177030245 C>A maps to ENST00000281881 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:177030245 C>A maps to ENST00000281881 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:94750175 G>A maps to NM_005172.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:94750175 G>A maps to NM_005172.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:152806887 C>T maps to NM_001001344.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:152806887 C>T maps to NM_001001344.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:50303040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:50303040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:50224124 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:50224124 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:34085916 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:34085916 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:32134159 G>T maps to NM_018169.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:32134159 G>T maps to NM_018169.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:74729618 G>T maps to ENST00000317409 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:74729618 G>T maps to ENST00000317409 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:55167806 G>A maps to ENST00000454855 K1139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:55167806 G>A maps to ENST00000454855 K1139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:14756869 G>A maps to NM_032137.4 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:14756869 G>A maps to NM_032137.4 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:43121363 C>G maps to NM_032806.4 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:43121363 C>G maps to NM_032806.4 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:121615755 A>G maps to ENST00000275159 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:121615755 A>G maps to ENST00000275159 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:81634804 G>A maps to NM_000722.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:81634804 G>A maps to NM_000722.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:31683377 C>A maps to NM_194300.2 C798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:31683377 C>A maps to NM_194300.2 C798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:125851150 T>A maps to ENST00000392693 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:125851150 T>A maps to ENST00000392693 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:143039109 G>A maps to NM_000083.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:143039109 G>A maps to NM_000083.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:10205372 T>C maps to NM_207345.2 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:10205372 T>C maps to NM_207345.2 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:79028949 A>T maps to NM_153610.3 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:79028949 A>T maps to NM_153610.3 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:111158939 C>T maps to NM_001846.2 H1527H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:111158939 C>T maps to NM_001846.2 H1527H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:99825362 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:99825362 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47808935 G>T maps to NM_006587.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47808935 G>T maps to NM_006587.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:130008320 C>A maps to NM_080385.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:130008320 C>A maps to NM_080385.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:49825115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:49825115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:17249186 G>A maps to NM_014675.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:17249186 G>A maps to NM_014675.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:115262198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:115262198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:113392685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:113392685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43152182 G>A maps to ENST00000354495 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43152182 G>A maps to ENST00000354495 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:115593078 A>G maps to NM_001017978.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:115593078 A>G maps to NM_001017978.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:143999130 G>T maps to NM_000498.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:143999130 G>T maps to NM_000498.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:96802751 A>T maps to NM_000770.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:96802751 A>T maps to NM_000770.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:32488877 T>A maps to NM_014314.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:32488877 T>A maps to NM_014314.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:7636532 T>C maps to NM_020877.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:7636532 T>C maps to NM_020877.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:102957422 C>T maps to NM_014377.1 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:102957422 C>T maps to NM_014377.1 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:73140966 G>A maps to NM_012074.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:73140966 G>A maps to NM_012074.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:107518318 C>A maps to NM_018712.3 Y182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:107518318 C>A maps to NM_018712.3 Y182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:43798205 G>A maps to NM_001127615.1 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:43798205 G>A maps to NM_001127615.1 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56272419 C>T maps to NM_000502.4 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56272419 C>T maps to NM_000502.4 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56280503 C>A maps to NM_000502.4 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56280503 C>A maps to NM_000502.4 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:45717914 G>A maps to ENST00000360649 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:45717914 G>A maps to ENST00000360649 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:138351857 G>C maps to NM_001033030.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:138351857 G>C maps to NM_001033030.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:45481231 T>G maps to ENST00000361462 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:45481231 T>G maps to ENST00000361462 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:24276805 G>C maps to NM_004116.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:24276805 G>C maps to NM_004116.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:171310611 C>T maps to NM_002022.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:171310611 C>T maps to NM_002022.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:79447787 C>A maps to NM_025074.6 A3634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:79447787 C>A maps to NM_025074.6 A3634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:101216262 C>T maps to NM_005458.7 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:101216262 C>T maps to NM_005458.7 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:42689016 C>A maps to NM_000163.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:42689016 C>A maps to NM_000163.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:183942809 C>A maps to NM_015101.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:183942809 C>A maps to NM_015101.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:79846621 C>A maps to NM_002069.5 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:79846621 C>A maps to NM_002069.5 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:93299471 C>T maps to NM_005113.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:93299471 C>T maps to NM_005113.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:7216392 G>A maps to NM_004489.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:7216392 G>A maps to NM_004489.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123471180 C>T maps to ENST00000456860 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123471180 C>T maps to ENST00000456860 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:30949367 G>T maps to ENST00000327783 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:30949367 G>T maps to ENST00000327783 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:222717027 C>T maps to NM_024746.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:222717027 C>T maps to NM_024746.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26104273 G>T maps to NM_003542.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26104273 G>T maps to NM_003542.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35873613 C>A maps to NM_002185.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35873613 C>A maps to NM_002185.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:7774361 C>A maps to NM_002216.2 S570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:7774361 C>A maps to NM_002216.2 S570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:5154194 C>T maps to NM_002234.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:5154194 C>T maps to NM_002234.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36671879 C>T maps to NM_001031836.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36671879 C>T maps to NM_001031836.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95503859 C>A maps to NM_015496.3 G1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95503859 C>A maps to NM_015496.3 G1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:100077003 C>A maps to ENST00000375206 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:100077003 C>A maps to ENST00000375206 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:138555916 T>A maps to NM_001164665.1 K1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:138555916 T>A maps to NM_001164665.1 K1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:124663934 C>T maps to NM_001081675.2 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:124663934 C>T maps to NM_001081675.2 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:32253684 C>T maps to NM_175858.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:32253684 C>T maps to NM_175858.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:7016520 G>A maps to NM_005559.2 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:7016520 G>A maps to NM_005559.2 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:107692542 C>A maps to NM_007356.2 A1305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:107692542 C>A maps to NM_007356.2 A1305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:25974144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:25974144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:151749750 G>A maps to NM_006726.3 S1584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:151749750 G>A maps to NM_006726.3 S1584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:42356550 C>A maps to NM_152447.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:42356550 C>A maps to NM_152447.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141607710 A>T maps to NM_018557.2 A1633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141607710 A>T maps to NM_018557.2 A1633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160786462 C>T maps to ENST00000263285 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160786462 C>T maps to ENST00000263285 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10415777 C>T maps to NM_005885.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10415777 C>T maps to NM_005885.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:112740431 A>T maps to NM_006343.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:112740431 A>T maps to NM_006343.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:19584404 G>T maps to NM_016183.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:19584404 G>T maps to NM_016183.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:29599884 G>C maps to NM_001033602.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:29599884 G>C maps to NM_001033602.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:241069408 G>A maps to NM_138336.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:241069408 G>A maps to NM_138336.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:41790451 G>A maps to NM_006766.3 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:41790451 G>A maps to NM_006766.3 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:172351585 A>T maps to NM_001146276.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:172351585 A>T maps to NM_001146276.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:24846004 G>A maps to NM_001136022.1 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:24846004 G>A maps to NM_001136022.1 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:37027498 G>A maps to NM_133433.3 E1949E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:37027498 G>A maps to NM_133433.3 E1949E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:56543980 C>A maps to NM_153447.4 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:56543980 C>A maps to NM_153447.4 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:167642068 C>A maps to NM_001122679.1 Y1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:167642068 C>A maps to NM_001122679.1 Y1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123847657 G>C maps to NM_001004474.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123847657 G>C maps to NM_001004474.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:4929495 G>A maps to NM_001004749.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:4929495 G>A maps to NM_001004749.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:88375548 C>T maps to NM_181837.2 I677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:88375548 C>T maps to NM_181837.2 I677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:23792259 C>T maps to NM_004643.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:23792259 C>T maps to NM_004643.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:118982342 G>T maps to NM_002581.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:118982342 G>T maps to NM_002581.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:79986433 G>A maps to NM_002583.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:79986433 G>A maps to NM_002583.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140559783 G>T maps to NM_019120.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140559783 G>T maps to NM_019120.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140720007 T>A maps to NM_018915.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140720007 T>A maps to NM_018915.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140725093 G>T maps to NM_018916.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140725093 G>T maps to NM_018916.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156880521 C>T maps to NM_001080471.1 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156880521 C>T maps to NM_001080471.1 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:88940613 C>T maps to NM_000297.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:88940613 C>T maps to NM_000297.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:28828815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:28828815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:155241684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:155241684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:27786364 G>T maps to NM_003622.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:27786364 G>T maps to NM_003622.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:23521199 G>A maps to NM_020227.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:23521199 G>A maps to NM_020227.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:48772320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:48772320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:120021731 T>C maps to NM_016644.1 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:120021731 T>C maps to NM_016644.1 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:228003842 C>G maps to NM_183062.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:228003842 C>G maps to NM_183062.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:137028345 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:137028345 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:70963526 C>A maps to NM_001109754.1 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:70963526 C>A maps to NM_001109754.1 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:121659301 G>T maps to NM_002851.2 V1656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:121659301 G>T maps to NM_002851.2 V1656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:52320773 G>T maps to NM_144651.4 S1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:52320773 G>T maps to NM_144651.4 S1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:102193079 T>C maps to NM_001031834.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:102193079 T>C maps to NM_001031834.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:10068243 G>A maps to ENST00000377192 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:10068243 G>A maps to ENST00000377192 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:22873256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:22873256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:33493810 G>A maps to NM_033103.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:33493810 G>A maps to NM_033103.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:79174642 G>T maps to NM_002941.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:79174642 G>T maps to NM_002941.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:10466150 C>A maps to NM_178857.5 A1819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:10466150 C>A maps to NM_178857.5 A1819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:23909956 C>A maps to NM_014363.4 L2686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:23909956 C>A maps to NM_014363.4 L2686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:236604 C>A maps to NM_004168.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:236604 C>A maps to NM_004168.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61256060 G>T maps to NM_012397.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61256060 G>T maps to NM_012397.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:164704959 C>T maps to NM_001041.3 Q1721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:164704959 C>T maps to NM_001041.3 Q1721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:92307882 A>G maps to NM_134266.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:92307882 A>G maps to NM_134266.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:18331728 C>G maps to NM_001145195.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:18331728 C>G maps to NM_001145195.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33947414 C>G maps to NM_016180.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33947414 C>G maps to NM_016180.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:40656448 T>A maps to NM_021097.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:40656448 T>A maps to NM_021097.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:21392038 C>A maps to NM_006446.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:21392038 C>A maps to NM_006446.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:4163479 C>T maps to ENST00000443211 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:4163479 C>T maps to ENST00000443211 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:121360804 C>G maps to NM_003105.5 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:121360804 C>G maps to NM_003105.5 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:228886676 A>G maps to NM_001142644.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:228886676 A>G maps to NM_001142644.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:68447162 T>A maps to NM_012108.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:68447162 T>A maps to NM_012108.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:80553736 C>A maps to NM_007029.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:80553736 C>A maps to NM_007029.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:64469442 C>T maps to NM_182914.2 I1264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:64469442 C>T maps to NM_182914.2 I1264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:39813816 G>A maps to NM_006116.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:39813816 G>A maps to NM_006116.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:115120978 G>A maps to NM_016569.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:115120978 G>A maps to NM_016569.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:124184346 C>T maps to NM_024809.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:124184346 C>T maps to NM_024809.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:105885839 G>A maps to NM_004257.4 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:105885839 G>A maps to NM_004257.4 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:43772921 C>T maps to NM_005424.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:43772921 C>T maps to NM_005424.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:98170136 G>T maps to NM_012465.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:98170136 G>T maps to NM_012465.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:117984016 G>T maps to NM_019894.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:117984016 G>T maps to NM_019894.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:57080340 G>C maps to NM_033396.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:57080340 G>C maps to NM_033396.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:72372741 C>T maps to ENST00000389376 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:72372741 C>T maps to ENST00000389376 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:154164570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:154164570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:101359686 C>T maps to NM_004621.5 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:101359686 C>T maps to NM_004621.5 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:12571269 C>T maps to NM_025265.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:12571269 C>T maps to NM_025265.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:166799851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:166799851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156555589 G>T maps to NM_001105669.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156555589 G>T maps to NM_001105669.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:117626661 T>C maps to NM_003594.3 H642H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:117626661 T>C maps to NM_003594.3 H642H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179470390 G>A maps to NM_133378.4 S15309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179470390 G>A maps to NM_133378.4 S15309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:9887621 C>A maps to NM_001098529.1 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:9887621 C>A maps to NM_001098529.1 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:30882660 G>A maps to NM_001167734.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:30882660 G>A maps to NM_001167734.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:54561569 C>G maps to NM_198481.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:54561569 C>G maps to NM_198481.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:149374754 G>A maps to NM_001168278.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:149374754 G>A maps to NM_001168278.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:142123762 T>C maps to NM_019001.3 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:142123762 T>C maps to NM_019001.3 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:77776275 C>A maps to NM_024721.4 V3442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:77776275 C>A maps to NM_024721.4 V3442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:42742933 G>C maps to NM_022473.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:42742933 G>C maps to NM_022473.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:106813564 G>T maps to NM_012082.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:106813564 G>T maps to NM_012082.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:81065349 C>T maps to NM_020338.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:81065349 C>T maps to NM_020338.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:33760818 C>T maps to NM_152493.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:33760818 C>T maps to NM_152493.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71756117 G>A maps to NM_152625.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71756117 G>A maps to NM_152625.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71756207 G>A maps to NM_152625.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71756207 G>A maps to NM_152625.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:37149258 C>A maps to NM_153257.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:37149258 C>A maps to NM_153257.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:52381732 G>A maps to NM_032679.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:52381732 G>A maps to NM_032679.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:3140534 C>A maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:3140534 C>A maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48431670 G>A maps to NM_152701.3 L3936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48431670 G>A maps to NM_152701.3 L3936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48520640 A>T maps to NM_152701.3 P4328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48520640 A>T maps to NM_152701.3 P4328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:72520524 G>T maps to NM_139155.2 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:72520524 G>T maps to NM_139155.2 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:128984535 C>A maps to NM_133638.3 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:128984535 C>A maps to NM_133638.3 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:7789843 C>A maps to NM_020546.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:7789843 C>A maps to NM_020546.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:236708123 G>A maps to NM_001037131.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:236708123 G>A maps to NM_001037131.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:86077001 A>T maps to NM_006738.4 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:86077001 A>T maps to NM_006738.4 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:29754878 G>A maps to NM_004304.3 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:29754878 G>A maps to NM_004304.3 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:233322031 C>T maps to NM_001631.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:233322031 C>T maps to NM_001631.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:114294556 C>A maps to NM_001148.4 S3937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:114294556 C>A maps to NM_001148.4 S3937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:90582698 T>G maps to NM_144590.2 *192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:90582698 T>G maps to NM_144590.2 *192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:28507876 G>T maps to NM_018690.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:28507876 G>T maps to NM_018690.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21229929 G>A maps to NM_000384.2 F3270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21229929 G>A maps to NM_000384.2 F3270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21232296 C>A maps to NM_000384.2 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21232296 C>A maps to NM_000384.2 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:118454054 G>T maps to ENST00000359415 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:118454054 G>T maps to ENST00000359415 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:110451558 G>T maps to NM_020809.2 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:110451558 G>T maps to NM_020809.2 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:137953877 G>T maps to ENST00000469044 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:137953877 G>T maps to ENST00000469044 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155452240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155452240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:62123878 A>G maps to NM_025080.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:62123878 A>G maps to NM_025080.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:119976721 G>T maps to ENST00000313400 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:119976721 G>T maps to ENST00000313400 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:31024004 G>T maps to ENST00000375687 G1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:31024004 G>T maps to ENST00000375687 G1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:26127929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:26127929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:3542926 G>A maps to NM_139321.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:3542926 G>A maps to NM_139321.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:118937519 G>A maps to NM_212543.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:118937519 G>A maps to NM_212543.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:60985503 C>A maps to NM_000633.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:60985503 C>A maps to NM_000633.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:127826586 C>A maps to NM_139343.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:127826586 C>A maps to NM_139343.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:34085925 G>A maps to NM_133468.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:34085925 G>A maps to NM_133468.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:104557799 A>T maps to NM_001083913.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:104557799 A>T maps to NM_001083913.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:93100911 C>T maps to NM_001037671.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:93100911 C>T maps to NM_001037671.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:60903700 T>A maps to NM_174978.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:60903700 T>A maps to NM_174978.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:95921872 C>A maps to NM_152592.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:95921872 C>A maps to NM_152592.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:24921529 G>A maps to NM_018958.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:24921529 G>A maps to NM_018958.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:34647927 T>C maps to ENST00000438749 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:34647927 T>C maps to ENST00000438749 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:170967492 C>A maps to NM_025063.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:170967492 C>A maps to NM_025063.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:116666736 C>A maps to NM_152367.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:116666736 C>A maps to NM_152367.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:75102077 T>C maps to NM_001002912.4 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:75102077 T>C maps to NM_001002912.4 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:101879005 C>T maps to NM_017546.4 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:101879005 C>T maps to NM_017546.4 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:26671556 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:26671556 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:29295618 A>T maps to NM_001029883.1 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:29295618 A>T maps to NM_001029883.1 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:86357416 C>T maps to NM_005181.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:86357416 C>T maps to NM_005181.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:7797433 G>T maps to NM_015215.2 R1154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:7797433 G>T maps to NM_015215.2 R1154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:104869610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:104869610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:78063607 G>A maps to NM_017950.2 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:78063607 G>A maps to NM_017950.2 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:117311374 A>G maps to NM_001767.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:117311374 A>G maps to NM_001767.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:21817108 A>T maps to NM_004061.3 L316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:21817108 A>T maps to NM_004061.3 L316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:19839134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:19839134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:136700124 G>T maps to NM_001006628.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:136700124 G>T maps to NM_001006628.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:87029452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:87029452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98999889 C>T maps to NM_001298.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98999889 C>T maps to NM_001298.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:41316171 T>C maps to NM_001843.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:41316171 T>C maps to NM_001843.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:51097084 C>A maps to ENST00000395542 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:51097084 C>A maps to ENST00000395542 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:103345237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:103345237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:103467507 T>C maps to NM_080629.2 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:103467507 T>C maps to NM_080629.2 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:101788229 C>A maps to NM_001855.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:101788229 C>A maps to NM_001855.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70916935 C>A maps to NM_001858.4 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70916935 C>A maps to NM_001858.4 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:238005468 A>T maps to NM_006710.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:238005468 A>T maps to NM_006710.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:15789215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:15789215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:52392593 G>T maps to ENST00000273600 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:52392593 G>T maps to ENST00000273600 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:196729162 C>A maps to NM_018897.2 E2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:196729162 C>A maps to NM_018897.2 E2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:196788435 C>A maps to NM_018897.2 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:196788435 C>A maps to NM_018897.2 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:225637951 C>T maps to NM_014689.2 E2042E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:225637951 C>T maps to NM_014689.2 E2042E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:11326603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:11326603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:30436607 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:30436607 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104698155 T>G maps to NM_001008394.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104698155 T>G maps to NM_001008394.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:79387375 G>C maps to NM_022159.3 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:79387375 G>C maps to NM_022159.3 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:143098638 T>A maps to NM_005232.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:143098638 T>A maps to NM_005232.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:95680240 G>T maps to NM_017697.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:95680240 G>T maps to NM_017697.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:92531047 C>A maps to ENST00000298047 I1623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:92531047 C>A maps to ENST00000298047 I1623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:127641272 G>T maps to NM_001999.3 I1868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:127641272 G>T maps to NM_001999.3 I1868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:125015437 C>A maps to NM_001039112.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:125015437 C>A maps to NM_001039112.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:159642651 C>A maps to NM_032532.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:159642651 C>A maps to NM_032532.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:109719545 C>A maps to NM_213596.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:109719545 C>A maps to NM_213596.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:44975464 A>T maps to NM_032135.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:44975464 A>T maps to NM_032135.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:27572005 T>A maps to NM_033223.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:27572005 T>A maps to NM_033223.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:110745572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:110745572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:237074745 G>T maps to NM_001485.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:237074745 G>T maps to NM_001485.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9729481 C>A maps to NM_004246.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9729481 C>A maps to NM_004246.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:42566720 C>A maps to NM_002088.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:42566720 C>A maps to NM_002088.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:106579320 C>A maps to ENST00000282249 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:106579320 C>A maps to ENST00000282249 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52220290 C>T maps to NM_001523.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52220290 C>T maps to NM_001523.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:45262889 C>A maps to NM_021072.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:45262889 C>A maps to NM_021072.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:55145159 T>A maps to NM_001526.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:55145159 T>A maps to NM_001526.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:126080722 C>A maps to NM_012259.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:126080722 C>A maps to NM_012259.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:43298641 C>T maps to NM_002130.6 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:43298641 C>T maps to NM_002130.6 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:176981710 C>A maps to NM_002148.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:176981710 C>A maps to NM_002148.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:63256397 G>C maps to NM_000524.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:63256397 G>C maps to NM_000524.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:23391090 C>A maps to NM_006547.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:23391090 C>A maps to NM_006547.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:142650998 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:142650998 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:145539418 G>T maps to NM_003637.3 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:145539418 G>T maps to NM_003637.3 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68607987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68607987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:31425862 T>A maps to ENST00000444228 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:31425862 T>A maps to ENST00000444228 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:78618572 C>A maps to NM_004867.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:78618572 C>A maps to NM_004867.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124438260 C>A maps to NM_001024660.3 R2969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124438260 C>A maps to NM_001024660.3 R2969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:81229224 A>T maps to NM_018689.1 K1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:81229224 A>T maps to NM_018689.1 K1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:51901062 C>T maps to NM_032559.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:51901062 C>T maps to NM_032559.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:36357306 G>T maps to NM_199180.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:36357306 G>T maps to NM_199180.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:39436087 G>T maps to NM_175737.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:39436087 G>T maps to NM_175737.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183396890 T>A maps to NM_017644.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183396890 T>A maps to NM_017644.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:201352444 C>A maps to NM_005558.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:201352444 C>A maps to NM_005558.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:203740012 C>A maps to NM_017773.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:203740012 C>A maps to NM_017773.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40197259 C>A maps to NM_203471.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40197259 C>A maps to NM_203471.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:71918218 C>A maps to NM_003667.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:71918218 C>A maps to NM_003667.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55106733 G>T maps to NM_006863.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55106733 G>T maps to NM_006863.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:97823188 G>T maps to NM_014916.3 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:97823188 G>T maps to NM_014916.3 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:57552239 G>T maps to NM_002332.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:57552239 G>T maps to NM_002332.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:194080143 G>T maps to NM_001135057.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:194080143 G>T maps to NM_001135057.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:1940100 G>A maps to NM_001163926.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:1940100 G>A maps to NM_001163926.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:35804347 G>T maps to NM_002361.3 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:35804347 G>T maps to NM_002361.3 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:43814039 G>A maps to ENST00000382031 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:43814039 G>A maps to ENST00000382031 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:45783903 A>T maps to NM_031417.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:45783903 A>T maps to NM_031417.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:54824387 C>T maps to ENST00000371389 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:54824387 C>T maps to ENST00000371389 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:112767570 A>T maps to NM_006343.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:112767570 A>T maps to NM_006343.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:170913131 G>A maps to NM_021647.6 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:170913131 G>A maps to NM_021647.6 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:33568394 C>T maps to NM_020884.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:33568394 C>T maps to NM_020884.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:92927565 A>T maps to NM_004538.5 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:92927565 A>T maps to NM_004538.5 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:177580532 C>A maps to NM_017838.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:177580532 C>A maps to NM_017838.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:236148781 G>A maps to NM_002508.2 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:236148781 G>A maps to NM_002508.2 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:63831056 G>T maps to NM_173688.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:63831056 G>T maps to NM_173688.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:56549543 C>A maps to NM_153447.4 C923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:56549543 C>A maps to NM_153447.4 C923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55451463 G>A maps to ENST00000446217 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55451463 G>A maps to ENST00000446217 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:96122586 C>A maps to NM_022451.9 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:96122586 C>A maps to NM_022451.9 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:57995948 C>A maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:57995948 C>A maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:3336373 G>C maps to NM_003554.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:3336373 G>C maps to NM_003554.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:51515307 G>A maps to NM_001004703.1 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:51515307 G>A maps to NM_001004703.1 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:20483241 G>A maps to NM_001004712.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:20483241 G>A maps to NM_001004712.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:97852074 C>A maps to NM_001005338.1 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:97852074 C>A maps to NM_001005338.1 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158736112 G>C maps to NM_001005185.1 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158736112 G>C maps to NM_001005185.1 Y120*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z030-01A-01W-0746-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z030-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:55872680 C>T maps to NM_001005200.1 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:55872680 C>T maps to NM_001005200.1 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:242065749 T>C maps to ENST00000358649 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:242065749 T>C maps to ENST00000358649 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:58208383 G>C maps to NM_001040429.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:58208383 G>C maps to NM_001040429.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140249659 G>A maps to NM_018902.3 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140249659 G>A maps to NM_018902.3 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140215965 G>A maps to NM_018910.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140215965 G>A maps to NM_018910.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140605188 G>T maps to NM_018934.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140605188 G>T maps to NM_018934.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:120527899 C>A maps to NM_001083.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:120527899 C>A maps to NM_001083.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:230472852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:230472852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:81208494 C>A maps to NM_052892.3 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:81208494 C>A maps to NM_052892.3 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:110457306 G>T maps to ENST00000426474 G1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:110457306 G>T maps to ENST00000426474 G1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:40590489 C>A maps to NM_004573.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:40590489 C>A maps to NM_004573.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:129285419 G>A maps to NM_015103.2 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:129285419 G>A maps to NM_015103.2 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:154901622 C>A maps to NM_006556.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:154901622 C>A maps to NM_006556.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:244855204 G>T maps to NM_016076.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:244855204 G>T maps to NM_016076.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:30100228 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:30100228 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153512878 C>A maps to ENST00000410080 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153512878 C>A maps to ENST00000410080 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40900085 C>A maps to NM_181882.2 R1391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40900085 C>A maps to NM_181882.2 R1391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:87060978 G>A maps to ENST00000276616 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:87060978 G>A maps to ENST00000276616 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:40980817 C>G maps to ENST00000373198 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:40980817 C>G maps to ENST00000373198 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:6154178 G>T maps to NM_001145547.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:6154178 G>T maps to NM_001145547.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:40503706 C>A maps to NM_002930.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:40503706 C>A maps to NM_002930.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113307696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113307696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:33936548 C>T maps to NM_001036.3 I1198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:33936548 C>T maps to NM_001036.3 I1198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:54179818 T>A maps to NM_152540.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:54179818 T>A maps to NM_152540.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:169823653 T>G maps to NM_181093.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:169823653 T>G maps to NM_181093.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:71354343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:71354343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:122646649 G>T maps to NM_001031702.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:122646649 G>T maps to NM_001031702.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:48056264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:48056264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:42533271 G>T maps to NM_015559.2 E1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:42533271 G>T maps to NM_015559.2 E1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:160604646 G>T maps to NM_003037.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:160604646 G>T maps to NM_003037.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:119026323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:119026323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:36679860 C>A maps to NM_004172.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:36679860 C>A maps to NM_004172.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:15072905 G>T maps to NM_005071.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:15072905 G>T maps to NM_005071.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:92330586 C>A maps to NM_134266.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:92330586 C>A maps to NM_134266.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:101795358 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:101795358 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:48584797 G>T maps to NM_005359.5 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:48584797 G>T maps to NM_005359.5 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:88410029 G>A maps to NM_198274.3 *491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:88410029 G>A maps to NM_198274.3 *491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:25222148 C>A maps to NM_022805.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:25222148 C>A maps to NM_022805.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:51705340 T>A maps to NM_018967.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:51705340 T>A maps to NM_018967.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:118558769 T>A maps to NM_206996.2 K1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:118558769 T>A maps to NM_206996.2 K1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:44903123 G>A maps to NM_025137.3 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:44903123 G>A maps to NM_025137.3 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158622333 C>A maps to NM_003126.2 E1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158622333 C>A maps to NM_003126.2 E1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158622400 A>T maps to NM_003126.2 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158622400 A>T maps to NM_003126.2 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:53084628 T>C maps to NM_014682.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:53084628 T>C maps to NM_014682.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:191855976 C>G maps to NM_007315.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:191855976 C>G maps to NM_007315.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:30097620 G>C maps to NM_004608.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:30097620 G>C maps to NM_004608.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:30703671 C>T maps to NM_031271.3 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:30703671 C>T maps to NM_031271.3 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrY:3447686 C>T maps to NM_139214.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrY:3447686 C>T maps to NM_139214.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:32639192 G>A maps to NM_003253.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:32639192 G>A maps to NM_003253.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:30020221 C>T maps to NM_003257.3 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:30020221 C>T maps to NM_003257.3 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:117826312 G>T maps to NM_002160.2 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:117826312 G>T maps to NM_002160.2 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:179815259 C>A maps to NM_145034.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:179815259 C>A maps to NM_145034.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:42229534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:42229534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:38320457 G>T maps to NM_003306.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:38320457 G>T maps to NM_003306.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:142569473 C>A maps to NM_018646.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:142569473 C>A maps to NM_018646.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:72998441 G>T maps to NM_005786.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:72998441 G>T maps to NM_005786.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:115596059 G>T maps to NM_005725.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:115596059 G>T maps to NM_005725.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:33003037 A>G maps to NM_017735.4 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:33003037 A>G maps to NM_017735.4 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:80744815 A>T maps to NM_003318.4 K577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:80744815 A>T maps to NM_003318.4 K577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:179443596 G>A maps to NM_133378.4 A20152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:179443596 G>A maps to NM_133378.4 A20152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:50656173 C>T maps to NM_020461.3 Q1817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:50656173 C>T maps to NM_020461.3 Q1817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:70980139 A>G maps to NM_018003.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:70980139 A>G maps to NM_018003.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:69535946 A>G maps to NM_001076.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:69535946 A>G maps to NM_001076.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:179483593 G>T maps to NM_003940.2 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:179483593 G>T maps to NM_003940.2 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:160385650 G>T maps to NM_020335.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:160385650 G>T maps to NM_020335.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:133073611 G>A maps to NM_004665.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:133073611 G>A maps to NM_004665.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67299718 C>A maps to NM_024763.4 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67299718 C>A maps to NM_024763.4 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:32413610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:32413610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183432967 A>T maps to NM_018023.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183432967 A>T maps to NM_018023.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:77912648 C>T maps to NM_152694.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:77912648 C>T maps to NM_152694.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:31813003 G>A maps to NM_001174096.1 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:31813003 G>A maps to NM_001174096.1 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:72057189 G>A maps to NM_144982.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:72057189 G>A maps to NM_144982.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:18296739 T>C maps to ENST00000401790 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:18296739 T>C maps to ENST00000401790 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:44681151 G>T maps to NM_001032372.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:44681151 G>T maps to NM_001032372.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37005528 C>T maps to NM_001166038.1 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37005528 C>T maps to NM_001166038.1 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:9271827 G>T maps to NM_020933.4 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:9271827 G>T maps to NM_020933.4 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:54080156 G>T maps to NM_001079907.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:54080156 G>T maps to NM_001079907.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37618138 A>G maps to NM_144689.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37618138 A>G maps to NM_144689.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:44762980 A>T maps to NM_033210.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:44762980 A>T maps to NM_033210.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52937329 C>T maps to NM_001143939.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52937329 C>T maps to NM_001143939.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:38102960 A>T maps to NM_152606.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:38102960 A>T maps to NM_152606.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37428073 G>T maps to NM_198539.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37428073 G>T maps to NM_198539.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57133590 G>T maps to NM_021216.4 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57133590 G>T maps to NM_021216.4 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57985205 G>A maps to NM_001024596.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57985205 G>A maps to NM_001024596.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8990975 C>A maps to NM_144670.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8990975 C>A maps to NM_144670.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215819925 C>A maps to NM_173076.2 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215819925 C>A maps to NM_173076.2 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48311972 G>T maps to NM_152701.3 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48311972 G>T maps to NM_152701.3 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67081857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67081857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87148757 G>A maps to NM_000927.3 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87148757 G>A maps to NM_000927.3 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87076409 G>T maps to NM_018849.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87076409 G>T maps to NM_018849.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:20691041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:20691041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30553990 C>T maps to NM_001025091.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30553990 C>T maps to NM_001025091.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:183911182 A>T maps to NM_018358.2 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:183911182 A>T maps to NM_018358.2 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133738223 G>T maps to NM_007313.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133738223 G>T maps to NM_007313.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15060055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15060055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:44074272 A>G maps to NM_001031854.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:44074272 A>G maps to NM_001031854.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19424710 C>A maps to NM_001010887.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19424710 C>A maps to NM_001010887.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7476107 C>A maps to NM_001080454.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7476107 C>A maps to NM_001080454.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:127186092 G>T maps to NM_138289.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:127186092 G>T maps to NM_138289.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158406902 A>G maps to NM_145259.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158406902 A>G maps to NM_145259.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156917448 C>A maps to ENST00000430702 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156917448 C>A maps to ENST00000430702 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:130319698 C>A maps to NM_139055.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:130319698 C>A maps to NM_139055.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49166295 C>A maps to NM_015270.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49166295 C>A maps to NM_015270.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100063886 G>T maps to ENST00000505590 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100063886 G>T maps to ENST00000505590 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36558941 A>G maps to NM_017825.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36558941 A>G maps to NM_017825.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47698821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47698821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:84457903 G>C maps to NM_032717.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:84457903 G>C maps to NM_032717.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148459427 G>T maps to NM_032049.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148459427 G>T maps to NM_032049.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109684039 G>C maps to NM_031279.3 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109684039 G>C maps to NM_031279.3 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:105412493 C>A maps to NM_138420.2 T3098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:105412493 C>A maps to NM_138420.2 T3098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109819102 G>A maps to NM_001145128.2 D1704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109819102 G>A maps to NM_001145128.2 D1704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:117129924 G>A maps to NM_030767.4 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:117129924 G>A maps to NM_030767.4 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29455248 G>T maps to NM_004304.3 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29455248 G>T maps to NM_004304.3 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73678172 G>T maps to NM_015120.4 G1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73678172 G>T maps to NM_015120.4 G1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:113333029 G>T maps to NM_025144.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:113333029 G>T maps to NM_025144.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:91972512 C>A maps to NM_019004.1 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:91972512 C>A maps to NM_019004.1 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:2115418 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:2115418 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115205761 G>T maps to NM_001284.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115205761 G>T maps to NM_001284.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115238580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115238580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:129996649 A>T maps to NM_001642.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:129996649 A>T maps to NM_001642.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28508885 G>T maps to NM_018690.2 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28508885 G>T maps to NM_018690.2 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:36163085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:36163085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68138278 T>C maps to NM_006421.3 K1352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68138278 T>C maps to NM_006421.3 K1352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:58817916 G>T maps to NM_002892.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:58817916 G>T maps to NM_002892.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:48965033 G>T maps to NM_006321.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:48965033 G>T maps to NM_006321.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231115006 G>T maps to NM_022786.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231115006 G>T maps to NM_022786.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:9437489 A>G maps to NM_003887.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:9437489 A>G maps to NM_003887.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:101090598 C>A maps to NM_006828.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:101090598 C>A maps to NM_006828.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:1743180 G>A maps to NM_001171038.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:1743180 G>A maps to NM_001171038.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176857283 G>T maps to ENST00000281881 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176857283 G>T maps to ENST00000281881 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7050064 C>G maps to NM_001940.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7050064 C>G maps to NM_001940.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182602613 C>G maps to NM_014616.1 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182602613 C>G maps to NM_014616.1 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19770476 G>A maps to NM_020410.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19770476 G>A maps to NM_020410.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:116919960 T>C maps to NM_207303.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:116919960 T>C maps to NM_207303.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:117309037 C>A maps to NM_207303.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:117309037 C>A maps to NM_207303.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47247030 C>A maps to NM_153446.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47247030 C>A maps to NM_153446.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90661199 C>A maps to NM_001170794.1 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90661199 C>A maps to NM_001170794.1 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143561118 G>T maps to NM_001702.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143561118 G>T maps to NM_001702.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69349324 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69349324 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:70797397 G>T maps to NM_018429.2 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:70797397 G>T maps to NM_018429.2 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55659146 C>A maps to NM_021073.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55659146 C>A maps to NM_021073.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55739648 T>C maps to NM_021073.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55739648 T>C maps to NM_021073.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96025610 C>A maps to ENST00000440890 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96025610 C>A maps to ENST00000440890 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:203329571 G>T maps to NM_001204.6 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:203329571 G>T maps to NM_001204.6 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:83931884 C>G maps to NM_001717.3 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:83931884 C>G maps to NM_001717.3 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16436589 A>T maps to NM_017637.5 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16436589 A>T maps to NM_017637.5 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49689787 C>A maps to NM_003458.3 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49689787 C>A maps to NM_003458.3 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:93711233 G>T maps to NM_003972.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:93711233 G>T maps to NM_003972.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107713181 C>A maps to NM_001018072.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107713181 C>A maps to NM_001018072.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124036379 G>T maps to ENST00000368994 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124036379 G>T maps to ENST00000368994 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:16721014 C>A maps to NM_014038.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:16721014 C>A maps to NM_014038.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5788149 G>T maps to NM_017782.4 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5788149 G>T maps to NM_017782.4 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:50531555 C>A maps to NM_001135196.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:50531555 C>A maps to NM_001135196.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33596336 C>A maps to ENST00000389726 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33596336 C>A maps to ENST00000389726 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:101953854 T>G maps to NM_032930.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:101953854 T>G maps to NM_032930.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:103699928 C>A maps to NM_001099336.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:103699928 C>A maps to NM_001099336.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65899625 T>A maps to ENST00000420799 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65899625 T>A maps to ENST00000420799 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22986050 C>A maps to NM_000491.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22986050 C>A maps to NM_000491.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111494008 T>C maps to NM_018372.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111494008 T>C maps to NM_018372.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55161093 C>T maps to ENST00000454855 Y994Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55161093 C>T maps to ENST00000454855 Y994Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35238009 C>T maps to NM_018840.4 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35238009 C>T maps to NM_018840.4 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219222788 G>T maps to NM_198559.1 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219222788 G>T maps to NM_198559.1 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:175717055 C>T maps to ENST00000443967 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:175717055 C>T maps to ENST00000443967 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:47976477 G>A maps to NM_001013732.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:47976477 G>A maps to NM_001013732.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:127898551 T>G maps to NM_001010905.1 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:127898551 T>G maps to NM_001010905.1 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10557833 C>A maps to NM_001040032.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10557833 C>A maps to NM_001040032.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13419010 G>T maps to NM_023035.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13419010 G>T maps to NM_023035.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2675716 C>T maps to NM_199460.2 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2675716 C>T maps to NM_199460.2 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105209245 G>T maps to NM_015916.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105209245 G>T maps to NM_015916.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230916349 C>T maps to NM_006615.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230916349 C>T maps to NM_006615.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55601072 G>A maps to NM_032330.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55601072 G>A maps to NM_032330.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:18891235 G>T maps to NM_033328.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:18891235 G>T maps to NM_033328.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:41604854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:41604854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:131596096 C>A maps to NM_004059.4 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:131596096 C>A maps to NM_004059.4 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15131384 C>A maps to NM_173482.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15131384 C>A maps to NM_173482.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:77290614 G>T maps to NM_001042784.1 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:77290614 G>T maps to NM_001042784.1 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:32806871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:32806871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66359145 C>A maps to NM_018219.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66359145 C>A maps to NM_018219.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:55563917 G>A maps to ENST00000436346 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:55563917 G>A maps to ENST00000436346 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32683574 G>T maps to NM_005408.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32683574 G>T maps to NM_005408.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158300658 C>T maps to NM_001764.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158300658 C>T maps to NM_001764.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51728726 T>C maps to NM_001772.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51728726 T>C maps to NM_001772.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54415662 G>T maps to NM_001170402.1 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54415662 G>T maps to NM_001170402.1 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:21975281 G>T maps to NM_004061.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:21975281 G>T maps to NM_004061.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44815305 G>T maps to NM_021248.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44815305 G>T maps to NM_021248.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73544805 C>T maps to ENST00000398860 T1892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73544805 C>T maps to ENST00000398860 T1892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:25532210 G>T maps to NM_001792.3 S876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:25532210 G>T maps to NM_001792.3 S876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68713831 G>T maps to NM_001793.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68713831 G>T maps to NM_001793.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66424345 C>A maps to NM_001795.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66424345 C>A maps to NM_001795.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:61687697 G>T maps to NM_001796.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:61687697 G>T maps to NM_001796.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176016153 C>A maps to NM_001171976.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176016153 C>A maps to NM_001171976.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:1636272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:1636272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149563051 C>T maps to NM_001804.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149563051 C>T maps to NM_001804.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117265079 G>T maps to NM_014956.4 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117265079 G>T maps to NM_014956.4 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180006107 G>T maps to NM_014810.4 E1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180006107 G>T maps to NM_014810.4 E1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55862836 C>G maps to NM_001025195.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55862836 C>G maps to NM_001025195.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196797376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196797376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40033946 C>T maps to NM_032221.3 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40033946 C>T maps to NM_032221.3 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40049654 C>A maps to NM_032221.3 E1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40049654 C>A maps to NM_032221.3 E1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40102042 C>A maps to NM_032221.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40102042 C>A maps to NM_032221.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241798501 G>A maps to NM_001821.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241798501 G>A maps to NM_001821.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240070780 G>T maps to NM_000740.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240070780 G>T maps to NM_000740.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:105151494 G>T maps to NM_018413.5 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:105151494 G>T maps to NM_018413.5 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113514404 T>C maps to NM_152515.3 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113514404 T>C maps to NM_152515.3 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86960012 G>T maps to NM_001285.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86960012 G>T maps to NM_001285.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31538608 G>A maps to NM_012131.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31538608 G>A maps to NM_012131.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79028115 A>T maps to NM_153610.3 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79028115 A>T maps to NM_153610.3 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47942861 A>T maps to NM_001142564.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47942861 A>T maps to NM_001142564.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:99012598 T>C maps to NM_001298.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:99012598 T>C maps to NM_001298.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:99013353 C>A maps to NM_001298.2 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:99013353 C>A maps to NM_001298.2 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104679103 C>T maps to NM_017649.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104679103 C>T maps to NM_017649.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41422923 C>A maps to NM_001843.2 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41422923 C>A maps to NM_001843.2 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:39176062 G>T maps to NM_033655.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:39176062 G>T maps to NM_033655.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125660603 C>A maps to NM_130773.2 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125660603 C>A maps to NM_130773.2 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75798879 T>A maps to ENST00000322507 G2984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75798879 T>A maps to ENST00000322507 G2984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70745794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70745794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139629198 G>A maps to NM_152888.1 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139629198 G>A maps to NM_152888.1 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189856421 G>T maps to NM_000090.3 G309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189856421 G>T maps to NM_000090.3 G309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189866154 A>C maps to NM_000090.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189866154 A>C maps to NM_000090.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110822020 G>T maps to NM_001845.4 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110822020 G>T maps to NM_001845.4 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47667171 C>T maps to NM_006587.2 W489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47667171 C>T maps to NM_006587.2 W489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93813685 C>G maps to NM_182971.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93813685 C>G maps to NM_182971.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148586790 C>A maps to NM_001870.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148586790 C>A maps to NM_001870.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130007796 C>A maps to NM_080385.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130007796 C>A maps to NM_080385.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:194062981 G>T maps to NM_001080513.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:194062981 G>T maps to NM_001080513.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211527881 T>A maps to NM_001122633.1 A1327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211527881 T>A maps to NM_001122633.1 A1327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29111967 C>T maps to NM_031311.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29111967 C>T maps to NM_031311.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207680056 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207680056 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17266477 A>T maps to NM_014675.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17266477 A>T maps to NM_014675.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3046425 C>A maps to NM_033225.5 E1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3046425 C>A maps to NM_033225.5 E1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3046429 A>T maps to NM_033225.5 V1834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3046429 A>T maps to NM_033225.5 V1834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75983078 G>A maps to NM_001897.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75983078 G>A maps to NM_001897.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:18168093 C>A maps to NM_020536.4 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:18168093 C>A maps to NM_020536.4 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70904436 G>T maps to NM_001902.5 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70904436 G>T maps to NM_001902.5 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80085186 C>A maps to ENST00000402739 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80085186 C>A maps to ENST00000402739 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11236871 G>A maps to NM_001332.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11236871 G>A maps to NM_001332.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16960651 T>A maps to NM_001081.3 T2323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16960651 T>A maps to NM_001081.3 T2323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143996513 C>A maps to NM_000498.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143996513 C>A maps to NM_000498.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284380 T>C maps to NM_001099772.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284380 T>C maps to NM_001099772.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16025116 G>A maps to NM_021187.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16025116 G>A maps to NM_021187.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61106795 C>A maps to NM_015533.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61106795 C>A maps to NM_015533.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:88885653 G>A maps to NM_152418.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:88885653 G>A maps to NM_152418.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:27766652 C>A maps to NM_001136533.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:27766652 C>A maps to NM_001136533.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31327936 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31327936 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6653760 A>T maps to NM_003737.2 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6653760 A>T maps to NM_003737.2 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182665024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182665024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49231389 C>A maps to NM_004818.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49231389 C>A maps to NM_004818.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40980947 G>A maps to NM_022774.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40980947 G>A maps to NM_022774.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197479706 T>C maps to NM_001195215.1 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197479706 T>C maps to NM_001195215.1 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:50167245 C>A maps to NM_001013742.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:50167245 C>A maps to NM_001013742.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21075494 C>G maps to NM_015510.3 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21075494 C>G maps to NM_015510.3 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51830520 G>A maps to NM_001174116.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51830520 G>A maps to NM_001174116.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760404 A>G maps to NM_003777.3 K2406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760404 A>G maps to NM_003777.3 K2406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52392659 C>T maps to ENST00000273600 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52392659 C>T maps to ENST00000273600 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196729268 C>A maps to NM_018897.2 G2370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196729268 C>A maps to NM_018897.2 G2370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128181683 C>A maps to NM_153330.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128181683 C>A maps to NM_153330.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6592888 G>T maps to NM_144666.2 T4645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6592888 G>T maps to NM_144666.2 T4645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:117810667 G>T maps to ENST00000276204 E1810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:117810667 G>T maps to ENST00000276204 E1810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:420996 A>C maps to NM_203447.3 R1358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:420996 A>C maps to NM_203447.3 R1358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:103348125 G>T maps to NM_015448.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:103348125 G>T maps to NM_015448.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66262852 G>T maps to NM_005700.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66262852 G>T maps to NM_005700.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:109050770 G>T maps to NM_018189.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:109050770 G>T maps to NM_018189.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27165428 G>T maps to NM_020134.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27165428 G>T maps to NM_020134.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117310620 G>T maps to NM_020693.2 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117310620 G>T maps to NM_020693.2 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28934678 T>G maps to NM_001942.2 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28934678 T>G maps to NM_001942.2 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28980939 T>A maps to NM_001134453.1 Y458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28980939 T>A maps to NM_001134453.1 Y458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74001051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74001051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44028816 C>A maps to NM_001193464.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44028816 C>A maps to NM_001193464.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150483445 G>A maps to ENST00000369049 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150483445 G>A maps to ENST00000369049 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:110884341 C>T maps to NM_001963.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:110884341 C>T maps to NM_001963.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36380998 G>T maps to NM_012199.2 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36380998 G>T maps to NM_012199.2 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:109240539 G>A maps to NM_001568.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:109240539 G>A maps to NM_001568.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:23762136 C>A maps to ENST00000359598 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:23762136 C>A maps to ENST00000359598 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50610780 C>A maps to NM_021952.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50610780 C>A maps to NM_021952.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:45003280 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:45003280 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39991416 G>C maps to NM_052846.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39991416 G>C maps to NM_052846.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62375671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62375671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:111441429 T>A maps to NM_001977.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:111441429 T>A maps to NM_001977.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:46609130 C>T maps to NM_001430.4 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:46609130 C>T maps to NM_001430.4 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111570403 G>T maps to NM_022140.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111570403 G>T maps to NM_022140.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:236406743 C>A maps to NM_019891.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:236406743 C>A maps to NM_019891.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56531638 C>G maps to NM_001184796.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56531638 C>G maps to NM_001184796.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157069147 G>T maps to NM_001004341.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157069147 G>T maps to NM_001004341.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5812715 G>T maps to NM_153717.2 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5812715 G>T maps to NM_153717.2 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108381672 C>A maps to NM_015065.2 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108381672 C>A maps to NM_015065.2 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169489848 T>A maps to ENST00000367796 P2039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169489848 T>A maps to ENST00000367796 P2039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:51049382 T>A maps to NM_007051.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:51049382 T>A maps to NM_007051.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:50284483 C>A maps to NM_012306.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:50284483 C>A maps to NM_012306.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153414480 C>G maps to ENST00000442256 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153414480 C>G maps to ENST00000442256 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131520622 C>T maps to NM_001105195.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131520622 C>T maps to NM_001105195.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45475265 G>A maps to ENST00000361462 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45475265 G>A maps to ENST00000361462 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:97088022 G>C maps to NM_017561.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:97088022 G>C maps to NM_017561.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:29972986 C>A maps to ENST00000269209 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:29972986 C>A maps to ENST00000269209 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:43625221 T>C maps to NM_001145196.1 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:43625221 T>C maps to NM_001145196.1 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:90535242 A>C maps to NM_001145124.1 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:90535242 A>C maps to NM_001145124.1 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:187522508 C>A maps to ENST00000260147 E3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:187522508 C>A maps to ENST00000260147 E3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150934204 T>C maps to NM_001447.2 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150934204 T>C maps to NM_001447.2 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:92616191 G>T maps to ENST00000298047 T4190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:92616191 G>T maps to ENST00000298047 T4190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127610316 C>A maps to NM_001999.3 L2551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127610316 C>A maps to NM_001999.3 L2551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:123550108 G>C maps to NM_012164.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:123550108 G>C maps to NM_012164.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157771894 C>G maps to NM_052938.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157771894 C>G maps to NM_052938.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157508978 G>T maps to NM_031281.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157508978 G>T maps to NM_031281.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:108290504 G>T maps to NM_005246.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:108290504 G>T maps to NM_005246.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95795118 T>C maps to NM_033086.2 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95795118 T>C maps to NM_033086.2 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241672064 G>A maps to NM_000143.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241672064 G>A maps to NM_000143.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:76124486 T>A maps to NM_015687.2 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:76124486 T>A maps to NM_015687.2 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152324582 T>G maps to NM_001014342.2 S1893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152324582 T>G maps to NM_001014342.2 S1893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:84603913 C>T maps to NM_001001670.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:84603913 C>T maps to NM_001001670.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240256719 T>A maps to ENST00000406993 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240256719 T>A maps to ENST00000406993 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47774471 T>A maps to NM_015308.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47774471 T>A maps to NM_015308.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172052792 G>A maps to NM_022763.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172052792 G>A maps to NM_022763.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89403575 C>A maps to NM_153696.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89403575 C>A maps to NM_153696.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116940 C>T maps to NM_207305.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116940 C>T maps to NM_207305.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30432901 G>T maps to NM_004118.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30432901 G>T maps to NM_004118.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52327465 C>A maps to NM_002030.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52327465 C>A maps to NM_002030.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:69225772 G>A maps to NM_015123.1 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:69225772 G>A maps to NM_015123.1 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48569379 A>G maps to NM_015030.1 Y1018Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48569379 A>G maps to NM_015030.1 Y1018Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61897778 C>A maps to NM_017647.3 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61897778 C>A maps to NM_017647.3 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:91419748 G>T maps to NM_002569.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:91419748 G>T maps to NM_002569.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5831810 G>A maps to NM_001040701.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5831810 G>A maps to NM_001040701.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5832191 C>T maps to NM_001040701.1 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5832191 C>T maps to NM_001040701.1 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:96651471 C>A maps to NM_006581.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:96651471 C>A maps to NM_006581.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29599209 G>A maps to NM_001470.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29599209 G>A maps to NM_001470.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99758405 C>A maps to NM_024637.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99758405 C>A maps to NM_024637.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230339027 G>T maps to NM_004481.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230339027 G>T maps to NM_004481.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11362512 G>A maps to NM_198516.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11362512 G>A maps to NM_198516.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:8100535 A>T maps to NM_001002295.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:8100535 A>T maps to NM_001002295.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89729610 C>T maps to NM_052942.3 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89729610 C>T maps to NM_052942.3 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:74325436 A>G maps to NM_016591.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:74325436 A>G maps to NM_016591.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55264236 T>C maps to NM_207410.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55264236 T>C maps to NM_207410.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61958486 C>A maps to NM_002059.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61958486 C>A maps to NM_002059.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150389578 G>T maps to NM_015660.2 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150389578 G>T maps to NM_015660.2 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42883059 G>A maps to NM_001080383.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42883059 G>A maps to NM_001080383.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:3937123 T>A maps to NM_001042413.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:3937123 T>A maps to NM_001042413.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93263811 G>A maps to NM_005113.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93263811 G>A maps to NM_005113.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155726843 G>A maps to ENST00000368331 L1808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155726843 G>A maps to ENST00000368331 L1808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55526376 G>T maps to NM_001083899.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55526376 G>T maps to NM_001083899.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:93518664 G>A maps to NM_004466.4 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:93518664 G>A maps to NM_004466.4 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:135428675 T>C maps to NM_153834.3 Y937Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:135428675 T>C maps to NM_153834.3 Y937Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:71804186 G>T maps to NM_018971.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:71804186 G>T maps to NM_018971.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51274756 T>A maps to NM_001506.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51274756 T>A maps to NM_001506.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:174417407 G>C maps to NM_005684.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:174417407 G>C maps to NM_005684.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:110300596 G>T maps to ENST00000414000 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:110300596 G>T maps to ENST00000414000 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123477486 T>G maps to ENST00000456860 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123477486 T>G maps to ENST00000456860 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:125824488 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:125824488 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102134197 C>A maps to NM_021956.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102134197 C>A maps to NM_021956.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120831680 G>T maps to NM_014619.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120831680 G>T maps to NM_014619.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3029697 C>T maps to NM_182982.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3029697 C>T maps to NM_182982.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:6903104 C>A maps to NM_181874.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:6903104 C>A maps to NM_181874.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38126821 G>T maps to NM_178171.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38126821 G>T maps to NM_178171.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3627903 A>T maps to NM_031965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3627903 A>T maps to NM_031965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:42620421 C>T maps to NM_007102.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:42620421 C>T maps to NM_007102.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19371793 G>T maps to NM_023002.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19371793 G>T maps to NM_023002.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52222629 C>T maps to NM_001523.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52222629 C>T maps to NM_001523.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19080547 C>A maps to NM_017645.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19080547 C>A maps to NM_017645.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55113464 C>T maps to NM_001526.3 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55113464 C>T maps to NM_001526.3 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93803633 T>A maps to NM_001098672.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93803633 T>A maps to NM_001098672.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93806537 G>A maps to NM_001098672.1 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93806537 G>A maps to NM_001098672.1 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:27100572 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:27100572 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12120864 A>T maps to NM_002114.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12120864 A>T maps to NM_002114.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143091671 C>A maps to NM_006734.3 E1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143091671 C>A maps to NM_006734.3 E1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185931767 T>C maps to NM_031935.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185931767 T>C maps to NM_031935.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186050511 G>T maps to NM_031935.2 G2925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186050511 G>T maps to NM_031935.2 G2925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:175111180 T>G maps to NM_001131055.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:175111180 T>G maps to NM_001131055.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152192918 G>A maps to NM_001009931.1 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152192918 G>A maps to NM_001009931.1 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:21977318 C>T maps to NM_005144.4 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:21977318 C>T maps to NM_005144.4 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:209879154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:209879154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:45033780 G>T maps to NM_007031.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:45033780 G>T maps to NM_007031.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:183822694 C>T maps to NM_182589.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:183822694 C>T maps to NM_182589.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204801540 A>T maps to NM_012092.3 K2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204801540 A>T maps to NM_012092.3 K2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:129233291 G>T maps to NM_052985.2 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:129233291 G>T maps to NM_052985.2 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:26990193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:26990193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:99459971 G>T maps to NM_000875.3 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:99459971 G>T maps to NM_000875.3 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151163145 G>A maps to NM_178822.4 F1541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151163145 G>A maps to NM_178822.4 F1541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18688690 C>A maps to NM_032880.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18688690 C>A maps to NM_032880.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:76713659 A>T maps to NM_001563.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:76713659 A>T maps to NM_001563.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:62321802 C>T maps to NM_176877.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:62321802 C>T maps to NM_176877.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220439497 A>G maps to NM_002191.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220439497 A>G maps to NM_002191.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:59956112 A>G maps to NM_152230.4 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:59956112 A>G maps to NM_152230.4 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:46310028 T>A maps to NM_000211.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:46310028 T>A maps to NM_000211.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:54817492 G>T maps to NM_198510.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:54817492 G>T maps to NM_198510.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7618493 C>A maps to ENST00000256861 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7618493 C>A maps to ENST00000256861 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:62728896 G>T maps to NM_181712.4 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:62728896 G>T maps to NM_181712.4 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:163241387 C>T maps to NM_033272.2 K924K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:163241387 C>T maps to NM_033272.2 K924K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:68171861 C>A maps to NM_000891.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:68171861 C>A maps to NM_000891.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78708917 G>T maps to NM_001161352.1 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78708917 G>T maps to NM_001161352.1 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:18112325 C>A maps to NM_002252.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:18112325 C>A maps to NM_002252.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:138669215 G>A maps to ENST00000298480 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:138669215 G>A maps to ENST00000298480 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196577361 T>G maps to NM_198503.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196577361 T>G maps to NM_198503.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215760008 G>T maps to NM_016121.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215760008 G>T maps to NM_016121.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:404813 G>A maps to NM_001042603.1 D1460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:404813 G>A maps to NM_001042603.1 D1460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:53222184 C>G maps to NM_004187.3 L1549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:53222184 C>G maps to NM_004187.3 L1549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55964400 G>T maps to NM_002253.2 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55964400 G>T maps to NM_002253.2 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73952132 G>A maps to ENST00000370385 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73952132 G>A maps to ENST00000370385 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:34832327 G>T maps to NM_014686.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:34832327 G>T maps to NM_014686.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34971408 T>A maps to NM_015297.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34971408 T>A maps to NM_015297.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141366213 T>A maps to NM_001080392.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141366213 T>A maps to NM_001080392.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94088849 C>A maps to ENST00000393153 P1779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94088849 C>A maps to ENST00000393153 P1779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30336462 C>A maps to NM_020848.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30336462 C>A maps to NM_020848.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118689513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118689513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:20912887 G>A maps to NM_017794.3 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:20912887 G>A maps to NM_017794.3 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233511713 A>G maps to NM_032435.2 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233511713 A>G maps to NM_032435.2 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113376754 C>T maps to NM_001009899.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113376754 C>T maps to NM_001009899.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:44869001 G>T maps to NM_020242.2 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:44869001 G>T maps to NM_020242.2 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30898857 G>T maps to NM_004798.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30898857 G>T maps to NM_004798.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:117079538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:117079538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51412524 G>T maps to NM_004917.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51412524 G>T maps to NM_004917.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53070111 G>T maps to NM_006121.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53070111 G>T maps to NM_006121.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52913792 G>T maps to NM_000424.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52913792 G>T maps to NM_000424.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52886966 G>T maps to NM_005554.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52886966 G>T maps to NM_005554.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53086371 G>T maps to NM_175078.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53086371 G>T maps to NM_175078.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39183047 G>T maps to NM_031957.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39183047 G>T maps to NM_031957.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:143742744 C>T maps to NM_003937.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:143742744 C>T maps to NM_003937.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50735894 C>A maps to NM_024884.2 G298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50735894 C>A maps to NM_024884.2 G298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6958476 C>A maps to NM_005559.2 E2655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6958476 C>A maps to NM_005559.2 E2655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129618939 T>C maps to NM_000426.3 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129618939 T>C maps to NM_000426.3 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129802527 T>C maps to NM_000426.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129802527 T>C maps to NM_000426.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152784984 T>A maps to NM_178349.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152784984 T>A maps to NM_178349.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22138962 C>T maps to NM_001013693.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22138962 C>T maps to NM_001013693.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25014121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25014121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124971943 G>T maps to NM_014368.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124971943 G>T maps to NM_014368.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54802621 G>T maps to ENST00000251375 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54802621 G>T maps to ENST00000251375 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145487436 G>T maps to NM_153713.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145487436 G>T maps to NM_153713.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75116744 G>T maps to NM_021819.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75116744 G>T maps to NM_021819.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:123303144 C>G maps to NM_207163.1 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:123303144 C>G maps to NM_207163.1 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:62453098 T>A maps to ENST00000506720 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:62453098 T>A maps to ENST00000506720 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39805628 C>A maps to NM_020862.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39805628 C>A maps to NM_020862.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141081473 T>A maps to NM_018557.2 K4168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141081473 T>A maps to NM_018557.2 K4168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24528927 A>C maps to NM_138360.3 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24528927 A>C maps to NM_138360.3 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51022251 G>T maps to NM_001080457.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51022251 G>T maps to NM_001080457.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52861920 C>A maps to NM_001024611.1 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52861920 C>A maps to NM_001024611.1 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70446072 G>C maps to NM_020794.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70446072 G>C maps to NM_020794.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:77745713 G>T maps to NM_001134745.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:77745713 G>T maps to NM_001134745.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143846157 C>A maps to NM_023946.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143846157 C>A maps to NM_023946.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235918831 A>T maps to NM_000081.2 L2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235918831 A>T maps to NM_000081.2 L2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:27840244 A>C maps to NM_182506.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:27840244 A>C maps to NM_182506.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:30261046 C>A maps to NM_002367.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:30261046 C>A maps to NM_002367.3 P265P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z031-01A-01W-0746-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z031-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77649213 G>A maps to NM_012301.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77649213 G>A maps to NM_012301.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95825223 T>C maps to NM_032427.1 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95825223 T>C maps to NM_032427.1 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63670187 A>T maps to NM_001039469.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63670187 A>T maps to NM_001039469.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:6302907 G>T maps to NM_024596.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:6302907 G>T maps to NM_024596.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41614041 G>A maps to NM_005586.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41614041 G>A maps to NM_005586.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60059766 T>C maps to NM_005121.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60059766 T>C maps to NM_005121.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100230590 A>T maps to ENST00000338042 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100230590 A>T maps to ENST00000338042 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:48703428 C>A maps to NM_016626.4 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:48703428 C>A maps to NM_016626.4 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141730528 C>G maps to ENST00000475668 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141730528 C>G maps to ENST00000475668 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109771520 C>A maps to NM_022765.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109771520 C>A maps to NM_022765.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:70014047 G>T maps to ENST00000448226 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:70014047 G>T maps to ENST00000448226 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:89179958 A>G maps to NM_005941.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:89179958 A>G maps to NM_005941.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:49576692 A>G maps to NM_014484.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:49576692 A>G maps to NM_014484.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:102931490 T>A maps to NM_001142432.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:102931490 T>A maps to NM_001142432.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:174537449 A>C maps to NM_006792.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:174537449 A>C maps to NM_006792.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:123694649 C>A maps to NM_022782.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:123694649 C>A maps to NM_022782.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:202547585 C>A maps to NM_033066.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:202547585 C>A maps to NM_033066.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17076054 G>C maps to NM_015134.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17076054 G>C maps to NM_015134.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19582446 G>T maps to NM_016183.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19582446 G>T maps to NM_016183.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60156903 T>C maps to NM_206939.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60156903 T>C maps to NM_206939.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30654299 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30654299 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26584731 A>G maps to NM_001135091.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26584731 A>G maps to NM_001135091.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9002504 G>T maps to NM_024690.2 V13437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9002504 G>T maps to NM_024690.2 V13437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9064621 A>T maps to NM_024690.2 S7608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9064621 A>T maps to NM_024690.2 S7608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9070918 A>C maps to NM_024690.2 S5509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9070918 A>C maps to NM_024690.2 S5509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:102078203 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:102078203 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:135520131 T>A maps to NM_001130173.1 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:135520131 T>A maps to NM_001130173.1 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108135676 C>T maps to NM_014981.1 Q1330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108135676 C>T maps to NM_014981.1 Q1330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23851756 G>A maps to NM_002471.3 N1892N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23851756 G>A maps to NM_002471.3 N1892N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192273772 C>T maps to NM_001130158.1 Q879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192273772 C>T maps to NM_001130158.1 Q879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31087343 T>C maps to NM_015194.1 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31087343 T>C maps to NM_015194.1 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:59494581 C>G maps to NM_004998.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:59494581 C>G maps to NM_004998.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:12666918 C>A maps to NM_001146312.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:12666918 C>A maps to NM_001146312.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:76788499 G>A maps to NM_012330.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:76788499 G>A maps to NM_012330.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1946753 C>A maps to ENST00000399161 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1946753 C>A maps to ENST00000399161 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:40146364 G>C maps to NM_018177.3 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:40146364 G>C maps to NM_018177.3 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101710323 G>A maps to NM_052867.2 Q1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101710323 G>A maps to NM_052867.2 Q1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:34149017 T>C maps to NM_024662.2 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:34149017 T>C maps to NM_024662.2 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133540443 G>T maps to NM_207363.2 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133540443 G>T maps to NM_207363.2 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133542196 A>G maps to NM_207363.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133542196 A>G maps to NM_207363.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:115767153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:115767153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152522014 C>A maps to NM_001164507.1 G1690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152522014 C>A maps to NM_001164507.1 G1690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:72241942 G>T maps to NM_173808.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:72241942 G>T maps to NM_173808.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:675314 G>T maps to NM_016533.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:675314 G>T maps to NM_016533.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:5821359 G>T maps to ENST00000381093 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:5821359 G>T maps to ENST00000381093 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:6069309 G>T maps to ENST00000381093 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:6069309 G>T maps to ENST00000381093 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:5462875 G>C maps to NM_033004.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:5462875 G>C maps to NM_033004.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:183230189 C>A maps to NM_015039.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:183230189 C>A maps to NM_015039.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26094791 C>A maps to NM_000625.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26094791 C>A maps to NM_000625.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45668160 G>T maps to NM_006310.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45668160 G>T maps to NM_006310.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:51255087 C>G maps to ENST00000404971 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:51255087 C>G maps to ENST00000404971 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:106500285 A>T maps to NM_014840.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:106500285 A>T maps to NM_014840.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27613886 C>A maps to NM_020772.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27613886 C>A maps to NM_020772.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73230880 C>T maps to NM_024844.3 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73230880 C>T maps to NM_024844.3 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56871537 G>T maps to NM_014669.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56871537 G>T maps to NM_014669.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24878082 G>T maps to NM_025081.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24878082 G>T maps to NM_025081.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228565291 C>A maps to NM_001098623.1 S7794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228565291 C>A maps to NM_001098623.1 S7794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167671429 T>C maps to NM_001122679.1 H1833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167671429 T>C maps to NM_001122679.1 H1833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:183650130 C>T maps to NM_001080477.1 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:183650130 C>T maps to NM_001080477.1 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72011637 C>A maps to NM_024576.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72011637 C>A maps to NM_024576.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:88416012 C>T maps to NM_001030015.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:88416012 C>T maps to NM_001030015.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123909483 C>A maps to NM_001004463.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123909483 C>A maps to NM_001004463.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16059889 C>T maps to NM_001004465.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16059889 C>T maps to NM_001004465.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20691978 T>C maps to NM_001004480.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20691978 T>C maps to NM_001004480.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3336583 G>T maps to NM_003554.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3336583 G>T maps to NM_003554.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:143633044 G>T maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:143633044 G>T maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248685462 C>T maps to NM_001013355.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248685462 C>T maps to NM_001013355.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29080005 A>T maps to NM_001005216.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29080005 A>T maps to NM_001005216.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248224540 G>C maps to NM_001004687.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248224540 G>C maps to NM_001004687.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248112716 G>C maps to NM_001001963.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248112716 G>C maps to NM_001001963.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247654701 C>G maps to NM_001004698.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247654701 C>G maps to NM_001004698.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55136264 T>A maps to NM_001005275.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55136264 T>A maps to NM_001005275.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55136270 T>G maps to NM_001005275.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55136270 T>G maps to NM_001005275.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:50003743 T>C maps to NM_001005270.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:50003743 T>C maps to NM_001005270.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:48347427 T>A maps to NM_001004702.1 Y312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:48347427 T>A maps to NM_001004702.1 Y312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56247354 C>T maps to NM_001004707.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56247354 C>T maps to NM_001004707.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123810905 T>C maps to NM_001001965.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123810905 T>C maps to NM_001001965.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20585585 C>T maps to NM_001004715.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20585585 C>T maps to NM_001004715.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20295924 C>T maps to NM_001004723.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20295924 C>T maps to NM_001004723.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22383137 C>A maps to NM_001005241.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22383137 C>A maps to NM_001005241.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20216350 C>T maps to NM_172194.1 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20216350 C>T maps to NM_172194.1 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5474876 C>A maps to NM_001004754.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5474876 C>A maps to NM_001004754.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:97806571 C>T maps to NM_054106.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:97806571 C>T maps to NM_054106.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55798328 T>C maps to NM_001001921.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55798328 T>C maps to NM_001001921.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:58275239 C>A maps to NM_001005218.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:58275239 C>A maps to NM_001005218.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56230559 G>A maps to NM_001004743.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56230559 G>A maps to NM_001004743.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55725637 C>T maps to NM_054104.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55725637 C>T maps to NM_054104.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55820396 T>C maps to NM_001005183.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55820396 T>C maps to NM_001005183.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158517481 T>C maps to NM_001005189.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158517481 T>C maps to NM_001005189.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14938363 T>C maps to NM_017506.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14938363 T>C maps to NM_017506.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56086191 C>A maps to NM_001005202.1 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56086191 C>A maps to NM_001005202.1 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56511218 G>T maps to NM_001005284.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56511218 G>T maps to NM_001005284.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56468741 T>C maps to NM_001013358.1 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56468741 T>C maps to NM_001013358.1 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55524037 C>A maps to NM_001005243.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55524037 C>A maps to NM_001005243.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57946993 T>C maps to NM_001005212.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57946993 T>C maps to NM_001005212.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:190619988 A>T maps to NM_022353.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:190619988 A>T maps to NM_022353.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:4190627 C>A maps to NM_177998.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:4190627 C>A maps to NM_177998.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17682563 G>A maps to NM_012387.2 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17682563 G>A maps to NM_012387.2 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:55248300 T>A maps to NM_130467.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:55248300 T>A maps to NM_130467.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:77070047 C>A maps to NM_001128620.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:77070047 C>A maps to NM_001128620.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93912878 G>C maps to NM_015368.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93912878 G>C maps to NM_015368.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176526165 G>A maps to NM_020318.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176526165 G>A maps to NM_020318.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:79856273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:79856273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:206166422 G>A maps to ENST00000406610 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:206166422 G>A maps to ENST00000406610 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14576589 C>T maps to NM_002582.2 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14576589 C>T maps to NM_002582.2 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:223084954 G>T maps to NM_181459.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:223084954 G>T maps to NM_181459.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154919081 C>T maps to NM_020524.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154919081 C>T maps to NM_020524.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140263697 G>T maps to NM_018904.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140263697 G>T maps to NM_018904.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140605065 G>T maps to NM_018934.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140605065 G>T maps to NM_018934.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140626792 G>C maps to NM_018935.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140626792 G>C maps to NM_018935.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140515357 G>C maps to NM_015669.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140515357 G>C maps to NM_015669.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140552679 G>A maps to NM_018940.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140552679 G>A maps to NM_018940.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140559228 C>A maps to NM_019120.2 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140559228 C>A maps to NM_019120.2 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140811612 C>T maps to NM_003735.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140811612 C>T maps to NM_003735.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82584628 T>A maps to NM_033026.5 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82584628 T>A maps to NM_033026.5 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82584924 C>A maps to NM_033026.5 E1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82584924 C>A maps to NM_033026.5 E1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31793147 A>T maps to NM_001191057.1 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31793147 A>T maps to NM_001191057.1 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149324062 G>A maps to NM_000440.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149324062 G>A maps to NM_000440.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149515316 C>A maps to NM_002609.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149515316 C>A maps to NM_002609.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:131606651 T>C maps to NM_003687.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:131606651 T>C maps to NM_003687.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31799690 T>A maps to NM_178140.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31799690 T>A maps to NM_178140.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:73440204 C>T maps to NM_015009.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:73440204 C>T maps to NM_015009.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10473252 A>T maps to NM_002631.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10473252 A>T maps to NM_002631.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33794654 A>G maps to ENST00000419414 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33794654 A>G maps to ENST00000419414 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:106509635 C>A maps to NM_002649.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:106509635 C>A maps to NM_002649.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6367110 G>A maps to NM_031220.3 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6367110 G>A maps to NM_031220.3 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160813100 C>T maps to NM_007366.4 W981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160813100 C>T maps to NM_007366.4 W981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:57078966 C>T maps to NM_002655.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:57078966 C>T maps to NM_002655.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198949518 T>G maps to NM_006226.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198949518 T>G maps to NM_006226.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198950364 C>T maps to NM_006226.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198950364 C>T maps to NM_006226.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:126708357 G>T maps to NM_032242.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:126708357 G>T maps to NM_032242.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151400442 C>A maps to NM_015100.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151400442 C>A maps to NM_015100.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131984434 A>T maps to NM_001083538.1 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131984434 A>T maps to NM_001083538.1 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:23815428 A>G maps to NM_013261.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:23815428 A>G maps to NM_013261.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202391819 A>G maps to ENST00000367270 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202391819 A>G maps to ENST00000367270 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49378903 C>T maps to NM_014330.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49378903 C>T maps to NM_014330.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54976576 G>A maps to NM_006741.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54976576 G>A maps to NM_006741.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:22287777 C>G maps to ENST00000397199 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:22287777 C>G maps to ENST00000397199 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142460762 A>C maps to ENST00000486171 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142460762 A>C maps to ENST00000486171 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10396301 G>C maps to NM_198464.3 *353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10396301 G>C maps to NM_198464.3 *353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:79328502 T>C maps to NM_015225.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:79328502 T>C maps to NM_015225.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43575864 T>C maps to NM_031246.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43575864 T>C maps to NM_031246.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43268389 G>C maps to NM_182707.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43268389 G>C maps to NM_182707.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43762591 G>T maps to NM_002784.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43762591 G>T maps to NM_002784.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72347216 C>G maps to NM_001099666.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72347216 C>G maps to NM_001099666.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42883812 C>A maps to NM_138296.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42883812 C>A maps to NM_138296.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:89685268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:89685268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16528616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16528616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57066594 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57066594 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47127353 C>T maps to NM_000960.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47127353 C>T maps to NM_000960.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125154486 A>G maps to NM_000962.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125154486 A>G maps to NM_000962.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8485849 T>C maps to NM_002839.3 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8485849 T>C maps to NM_002839.3 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:52323921 C>A maps to NM_144651.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:52323921 C>A maps to NM_144651.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9344804 A>T maps to NM_002864.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9344804 A>T maps to NM_002864.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:238494767 G>A maps to NM_022449.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:238494767 G>A maps to NM_022449.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:82693359 G>T maps to NM_014488.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:82693359 G>T maps to NM_014488.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:102192660 G>T maps to NM_001031834.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:102192660 G>T maps to NM_001031834.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130738128 G>A maps to NM_032144.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130738128 G>A maps to NM_032144.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:114786935 C>A maps to ENST00000389544 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:114786935 C>A maps to ENST00000389544 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:65278515 C>T maps to ENST00000294428 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:65278515 C>T maps to ENST00000294428 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:53573762 C>A maps to NM_014781.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:53573762 C>A maps to NM_014781.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50085712 G>T maps to NM_005777.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50085712 G>T maps to NM_005777.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79349995 C>T maps to NM_002909.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79349995 C>T maps to NM_002909.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103141203 G>T maps to ENST00000428762 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103141203 G>T maps to ENST00000428762 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:61149450 C>A maps to NM_002908.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:61149450 C>A maps to NM_002908.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204130498 G>T maps to NM_000537.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204130498 G>T maps to NM_000537.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:34404009 T>C maps to NM_002915.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:34404009 T>C maps to NM_002915.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:186507929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:186507929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6026249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6026249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:107041677 G>A maps to ENST00000304514 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:107041677 G>A maps to ENST00000304514 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:19955659 C>T maps to ENST00000255006 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:19955659 C>T maps to ENST00000255006 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:96513553 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:96513553 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40697320 A>T maps to NM_012421.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40697320 A>T maps to NM_012421.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154669892 G>T maps to ENST00000274068 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154669892 G>T maps to ENST00000274068 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:64624701 C>T maps to NM_005012.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:64624701 C>T maps to NM_005012.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:84955399 A>C maps to NM_025065.6 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:84955399 A>C maps to NM_025065.6 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:53670418 C>A maps to NM_015272.2 E1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:53670418 C>A maps to NM_015272.2 E1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24021208 G>T maps to NM_000975.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24021208 G>T maps to NM_000975.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:146017269 C>A maps to NM_000973.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:146017269 C>A maps to NM_000973.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7231128 G>T maps to NM_001003699.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7231128 G>T maps to NM_001003699.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122992896 G>A maps to NM_023012.5 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122992896 G>A maps to NM_023012.5 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237756931 G>T maps to NM_001035.2 E1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237756931 G>T maps to NM_001035.2 E1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237791134 C>T maps to NM_001035.2 T2065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237791134 C>T maps to NM_001035.2 T2065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153362655 G>A maps to NM_002964.4 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153362655 G>A maps to NM_002964.4 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:134994547 G>T maps to NM_018666.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:134994547 G>T maps to NM_018666.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130505332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130505332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165994466 G>A maps to NM_006922.3 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165994466 G>A maps to NM_006922.3 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62034575 G>A maps to NM_000334.4 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62034575 G>A maps to NM_000334.4 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71410866 C>T maps to NM_001144952.1 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71410866 C>T maps to NM_001144952.1 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84636207 A>G maps to NM_152754.2 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84636207 A>G maps to NM_152754.2 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50223737 G>T maps to NM_004186.3 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50223737 G>T maps to NM_004186.3 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9052121 G>T maps to NM_003966.2 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9052121 G>T maps to NM_003966.2 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122632802 C>A maps to NM_001031702.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122632802 C>A maps to NM_001031702.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48058161 C>T maps to NM_153618.1 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48058161 C>T maps to NM_153618.1 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87369132 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87369132 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25160708 G>A maps to NM_016955.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25160708 G>A maps to NM_016955.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61379923 T>C maps to NM_080475.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61379923 T>C maps to NM_080475.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61231352 G>T maps to ENST00000382768 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61231352 G>T maps to ENST00000382768 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65819873 G>T maps to NM_006842.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65819873 G>T maps to NM_006842.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84257443 A>T maps to ENST00000434347 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84257443 A>T maps to ENST00000434347 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87181525 A>G maps to ENST00000482504 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87181525 A>G maps to ENST00000482504 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:77660381 G>C maps to NM_020859.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:77660381 G>C maps to NM_020859.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52002707 G>T maps to NM_053003.2 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52002707 G>T maps to NM_053003.2 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43405707 C>T maps to NM_213602.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43405707 C>T maps to NM_213602.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72165839 G>T maps to NM_015556.1 E1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72165839 G>T maps to NM_015556.1 E1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:69666587 A>G maps to NM_012238.4 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:69666587 A>G maps to NM_012238.4 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:120741789 C>T maps to NM_012240.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:120741789 C>T maps to NM_012240.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164760930 T>C maps to NM_001041.3 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164760930 T>C maps to NM_001041.3 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:50819661 C>A maps to NM_003055.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:50819661 C>A maps to NM_003055.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37641525 C>T maps to NM_030631.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37641525 C>T maps to NM_030631.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58018914 A>T maps to NM_133489.2 K452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58018914 A>T maps to NM_133489.2 K452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107315472 C>A maps to NM_000441.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107315472 C>A maps to NM_000441.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:9097800 G>T maps to NM_003039.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:9097800 G>T maps to NM_003039.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27480054 C>A maps to NM_003459.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27480054 C>A maps to NM_003459.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:8435680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:8435680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62656035 C>T maps to NM_001012661.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62656035 C>T maps to NM_001012661.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:190439989 G>A maps to NM_014585.5 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:190439989 G>A maps to NM_014585.5 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162735741 C>T maps to NM_001178015.1 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162735741 C>T maps to NM_001178015.1 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17988771 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17988771 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28548790 A>G maps to ENST00000394821 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28548790 A>G maps to ENST00000394821 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14526391 G>T maps to NM_001134367.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14526391 G>T maps to NM_001134367.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44476398 T>A maps to NM_201649.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44476398 T>A maps to NM_201649.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101606328 T>A maps to NM_180991.4 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101606328 T>A maps to NM_180991.4 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20543081 C>T maps to ENST00000273739 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20543081 C>T maps to ENST00000273739 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:91948453 C>A maps to ENST00000417249 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:91948453 C>A maps to ENST00000417249 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:107022241 G>T maps to NM_014978.1 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:107022241 G>T maps to NM_014978.1 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:137483919 C>A maps to NM_004189.2 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:137483919 C>A maps to NM_004189.2 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231120198 G>T maps to NM_007237.4 G398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231120198 G>T maps to NM_007237.4 G398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21469848 G>T maps to NM_003112.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21469848 G>T maps to NM_003112.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:22653939 G>T maps to ENST00000376603 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:22653939 G>T maps to ENST00000376603 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151046004 G>T maps to NM_003118.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151046004 G>T maps to NM_003118.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151049240 G>A maps to NM_003118.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151049240 G>A maps to NM_003118.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3343455 C>T maps to NM_001170695.1 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3343455 C>T maps to NM_001170695.1 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64938908 G>T maps to NM_001008778.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64938908 G>T maps to NM_001008778.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220309868 G>T maps to NM_005876.4 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220309868 G>T maps to NM_005876.4 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74383159 A>T maps to NM_182965.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74383159 A>T maps to NM_182965.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228882761 C>A maps to NM_001142644.1 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228882761 C>A maps to NM_001142644.1 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:4352682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:4352682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:167675842 T>A maps to NM_016950.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:167675842 T>A maps to NM_016950.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158612233 A>G maps to NM_003126.2 C1568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158612233 A>G maps to NM_003126.2 C1568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158632542 C>A maps to NM_003126.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158632542 C>A maps to NM_003126.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41071433 T>A maps to NM_020971.2 S2007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41071433 T>A maps to NM_020971.2 S2007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79616339 T>A maps to NM_032567.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79616339 T>A maps to NM_032567.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64536283 C>T maps to NM_020762.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64536283 C>T maps to NM_020762.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9106198 C>A maps to NM_014850.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9106198 C>A maps to NM_014850.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27958697 C>A maps to NM_033389.2 E1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27958697 C>A maps to NM_033389.2 E1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48047125 C>A maps to NM_021015.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48047125 C>A maps to NM_021015.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:107460147 G>A maps to NM_001142351.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:107460147 G>A maps to NM_001142351.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52558143 C>A maps to NM_015136.2 S2524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52558143 C>A maps to NM_015136.2 S2524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70865519 A>G maps to NM_003154.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70865519 A>G maps to NM_003154.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220473359 G>C maps to NM_052902.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220473359 G>C maps to NM_052902.2 R564R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z031-01A-01W-0746-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z031-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:113168920 T>G maps to ENST00000374463 R2990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:113168920 T>G maps to ENST00000374463 R2990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:113312281 G>T maps to ENST00000374463 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:113312281 G>T maps to ENST00000374463 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58443525 T>A maps to NM_014258.2 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58443525 T>A maps to NM_014258.2 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152782764 C>G maps to NM_182961.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152782764 C>G maps to NM_182961.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:34003352 C>G maps to NM_003895.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:34003352 C>G maps to NM_003895.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:63466558 C>A maps to NM_001130003.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:63466558 C>A maps to NM_001130003.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:62463150 T>G maps to NM_031914.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:62463150 T>G maps to NM_031914.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71164608 G>T maps to NM_001057.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71164608 G>T maps to NM_001057.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:100530247 C>A maps to NM_024885.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:100530247 C>A maps to NM_024885.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159457473 G>T maps to NM_054114.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159457473 G>T maps to NM_054114.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19166620 G>C maps to NM_152232.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19166620 G>C maps to NM_152232.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:114793507 G>T maps to NM_000192.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:114793507 G>T maps to NM_000192.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59620691 G>A maps to NM_001062.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59620691 G>A maps to NM_001062.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141682712 T>A maps to NM_001178139.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141682712 T>A maps to NM_001178139.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:43771094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:43771094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137990655 G>T maps to ENST00000272643 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137990655 G>T maps to ENST00000272643 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:138413069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:138413069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171871452 C>T maps to ENST00000360843 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171871452 C>T maps to ENST00000360843 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60683535 G>A maps to ENST00000326270 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60683535 G>A maps to ENST00000326270 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38848891 G>A maps to NM_031940.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38848891 G>A maps to NM_031940.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:126135489 C>A maps to NM_052907.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:126135489 C>A maps to NM_052907.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129558884 G>T maps to NM_133448.2 Y945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129558884 G>T maps to NM_133448.2 Y945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129566495 C>G maps to NM_133448.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129566495 C>G maps to NM_133448.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86868445 G>T maps to NM_022918.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86868445 G>T maps to NM_022918.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120198203 G>T maps to NM_001198670.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120198203 G>T maps to NM_001198670.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15433804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15433804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74365094 T>C maps to NM_013390.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74365094 T>C maps to NM_013390.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20926798 G>A maps to NM_001100814.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20926798 G>A maps to NM_001100814.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:69094993 C>T maps to NM_182502.3 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:69094993 C>T maps to NM_182502.3 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37494470 G>T maps to ENST00000381792 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37494470 G>T maps to ENST00000381792 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101287160 G>A maps to NM_032813.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101287160 G>A maps to NM_032813.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101321049 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101321049 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:1953716 C>A maps to ENST00000397301 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:1953716 C>A maps to ENST00000397301 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175048829 G>T maps to NM_022093.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175048829 G>T maps to NM_022093.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:10952929 T>C maps to NM_199261.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:10952929 T>C maps to NM_199261.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123714766 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123714766 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30128458 G>T maps to NM_006778.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30128458 G>T maps to NM_006778.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55036729 G>T maps to ENST00000357530 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55036729 G>T maps to ENST00000357530 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230693987 C>T maps to ENST00000389044 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230693987 C>T maps to ENST00000389044 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230723818 A>T maps to ENST00000389044 C232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230723818 A>T maps to ENST00000389044 C232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:101374792 C>A maps to NM_004621.5 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:101374792 C>A maps to NM_004621.5 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:31342758 C>T maps to NM_002420.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:31342758 C>T maps to NM_002420.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:45774529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:45774529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77386752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77386752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:16338249 C>T maps to NM_016113.4 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:16338249 C>T maps to NM_016113.4 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43220496 G>T maps to NM_032538.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43220496 G>T maps to NM_032538.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231097013 C>A maps to NM_024525.4 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231097013 C>A maps to NM_024525.4 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:138849885 C>T maps to NM_024926.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:138849885 C>T maps to NM_024926.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74718474 A>T maps to NM_022492.4 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74718474 A>T maps to NM_022492.4 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46847393 C>T maps to NM_001130918.1 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46847393 C>T maps to NM_001130918.1 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179443954 G>C maps to NM_133378.4 S20033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179443954 G>C maps to NM_133378.4 S20033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179472329 C>T maps to NM_133378.4 V15127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179472329 C>T maps to NM_133378.4 V15127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179473549 A>G maps to NM_133378.4 D14828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179473549 A>G maps to NM_133378.4 D14828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179537182 T>A maps to NM_133378.4 P10326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179537182 T>A maps to NM_133378.4 P10326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179583274 G>A maps to NM_133378.4 S6942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179583274 G>A maps to NM_133378.4 S6942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179611073 T>A maps to ENST00000375038 P5353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179611073 T>A maps to ENST00000375038 P5353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:72248389 T>A maps to NM_032646.5 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:72248389 T>A maps to NM_032646.5 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49666755 G>T maps to NM_032704.3 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49666755 G>T maps to NM_032704.3 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:94594 C>A maps to NM_177987.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:94594 C>A maps to NM_177987.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44196109 T>A maps to NM_002822.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44196109 T>A maps to NM_002822.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:125398152 G>A maps to NM_021009.5 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:125398152 G>A maps to NM_021009.5 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202304772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202304772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865546 G>T maps to NM_012474.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865546 G>T maps to NM_012474.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:43529798 G>C maps to NM_173568.3 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:43529798 G>C maps to NM_173568.3 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20357558 G>T maps to ENST00000424589 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20357558 G>T maps to ENST00000424589 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216052419 G>T maps to ENST00000366943 L2748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216052419 G>T maps to ENST00000366943 L2748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:76703977 A>G maps to NM_003715.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:76703977 A>G maps to NM_003715.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23099056 C>A maps to NM_020718.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23099056 C>A maps to NM_020718.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144806606 C>T maps to NM_007124.2 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144806606 C>T maps to NM_007124.2 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:7907834 G>T maps to NM_006786.3 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:7907834 G>T maps to NM_006786.3 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:171675513 C>A maps to NM_003762.4 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:171675513 C>A maps to NM_003762.4 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108313275 A>G maps to NM_006113.4 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108313275 A>G maps to NM_006113.4 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247420194 G>T maps to NM_173858.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247420194 G>T maps to NM_173858.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159825854 G>T maps to NM_001013661.1 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159825854 G>T maps to NM_001013661.1 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:27256783 G>T maps to NM_006646.5 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:27256783 G>T maps to NM_006646.5 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36590380 G>T maps to NM_001083961.1 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36590380 G>T maps to NM_001083961.1 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48918081 C>A maps to NM_175575.5 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48918081 C>A maps to NM_175575.5 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40939378 G>A maps to NM_032387.4 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40939378 G>A maps to NM_032387.4 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102242449 C>A maps to NM_003393.3 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102242449 C>A maps to NM_003393.3 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:10085241 C>T maps to NM_015691.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:10085241 C>T maps to NM_015691.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39227078 G>T maps to NM_194293.2 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39227078 G>T maps to NM_194293.2 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39228032 C>T maps to NM_194293.2 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39228032 C>T maps to NM_194293.2 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100389699 A>G maps to ENST00000349350 V2547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100389699 A>G maps to ENST00000349350 V2547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:111312892 G>T maps to NM_024508.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:111312892 G>T maps to NM_024508.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:114069646 T>C maps to NM_001164342.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:114069646 T>C maps to NM_001164342.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:73524208 T>C maps to NM_203303.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:73524208 T>C maps to NM_203303.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:207174981 A>C maps to NM_020923.1 S1910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:207174981 A>C maps to NM_020923.1 S1910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38126700 A>G maps to NM_014898.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38126700 A>G maps to NM_014898.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29643737 C>T maps to NM_001109809.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29643737 C>T maps to NM_001109809.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73448513 G>A maps to NM_021260.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73448513 G>A maps to NM_021260.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:15116212 G>A maps to NM_022340.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:15116212 G>A maps to NM_022340.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62366087 C>A maps to NM_032527.4 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62366087 C>A maps to NM_032527.4 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19790268 A>C maps to NM_033204.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19790268 A>C maps to NM_033204.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:64168334 C>A maps to NM_016220.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:64168334 C>A maps to NM_016220.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22156941 C>G maps to NM_007153.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22156941 C>G maps to NM_007153.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:22842727 C>T maps to NM_080764.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:22842727 C>T maps to NM_080764.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43308231 C>A maps to NM_014345.2 V1168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43308231 C>A maps to NM_014345.2 V1168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64158503 A>T maps to NM_014951.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64158503 A>T maps to NM_014951.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21478513 C>A maps to NM_024697.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21478513 C>A maps to NM_024697.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72345692 G>T maps to NM_017757.2 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72345692 G>T maps to NM_017757.2 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50549718 C>T maps to NM_015428.1 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50549718 C>T maps to NM_015428.1 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22847836 A>T maps to NM_020855.2 K456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22847836 A>T maps to NM_020855.2 K456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22805577 C>T maps to NM_015461.2 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22805577 C>T maps to NM_015461.2 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:37482136 C>T maps to ENST00000444991 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:37482136 C>T maps to ENST00000444991 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:23836620 C>A maps to NM_138330.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:23836620 C>A maps to NM_138330.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22939746 C>A maps to ENST00000397104 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22939746 C>A maps to ENST00000397104 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22940568 A>G maps to ENST00000397104 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22940568 A>G maps to ENST00000397104 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60635066 C>G maps to NM_207341.2 Y11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60635066 C>G maps to NM_207341.2 Y11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238048068 G>T maps to NM_021186.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238048068 G>T maps to NM_021186.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:102196309 C>T maps to NM_175056.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:102196309 C>T maps to NM_175056.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:124793960 A>T maps to NM_001609.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:124793960 A>T maps to NM_001609.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:52377795 G>A maps to NM_020328.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:52377795 G>A maps to NM_020328.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:67517005 G>C maps to NM_001138.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:67517005 G>C maps to NM_001138.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:44296989 G>A maps to NM_021926.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:44296989 G>A maps to NM_021926.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:876251 G>A maps to NM_001009877.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:876251 G>A maps to NM_001009877.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:61539136 G>A maps to NM_001127392.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:61539136 G>A maps to NM_001127392.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:50101404 G>T maps to NM_018139.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:50101404 G>T maps to NM_018139.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:77598774 C>A maps to NM_152420.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:77598774 C>A maps to NM_152420.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13325396 G>A maps to NM_023035.2 D1923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13325396 G>A maps to NM_023035.2 D1923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:3677864 G>T maps to NM_152492.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:3677864 G>T maps to NM_152492.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:214826277 C>T maps to NM_016343.3 L2756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:214826277 C>T maps to NM_016343.3 L2756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:74334528 C>G maps to NM_020872.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:74334528 C>G maps to NM_020872.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:227924918 C>T maps to ENST00000396625 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:227924918 C>T maps to ENST00000396625 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113358404 C>A maps to NM_198123.1 V2121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113358404 C>A maps to NM_198123.1 V2121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:91572167 G>A maps to NM_133503.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:91572167 G>A maps to NM_133503.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:114128537 G>A maps to NM_001014283.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:114128537 G>A maps to NM_001014283.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:31236919 G>A maps to NM_030653.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:31236919 G>A maps to NM_030653.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:12136102 C>T maps to NM_018706.5 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:12136102 C>T maps to NM_018706.5 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:34961803 G>T maps to NM_152631.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:34961803 G>T maps to NM_152631.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:29237816 G>A maps to NM_005249.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:29237816 G>A maps to NM_005249.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:14859370 G>A maps to ENST00000380880 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:14859370 G>A maps to ENST00000380880 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:150439288 T>A maps to ENST00000447239 L57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:150439288 T>A maps to ENST00000447239 L57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:37365368 C>T maps to NM_001172713.1 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:37365368 C>T maps to NM_001172713.1 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:134896056 C>T maps to ENST00000368577 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:134896056 C>T maps to ENST00000368577 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:178418426 G>A maps to NM_000843.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:178418426 G>A maps to NM_000843.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:106826353 T>C maps to NM_012257.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:106826353 T>C maps to NM_012257.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:149783680 G>A maps to ENST00000427880 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:149783680 G>A maps to ENST00000427880 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:32632626 C>T maps to ENST00000374943 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:32632626 C>T maps to ENST00000374943 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:42174362 G>T maps to NM_001556.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:42174362 G>T maps to NM_001556.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120373016 G>C maps to NM_012281.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120373016 G>C maps to NM_012281.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19574961 C>T maps to NM_144633.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19574961 C>T maps to NM_144633.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:90188651 C>A maps to NM_198525.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:90188651 C>A maps to NM_198525.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:47910196 C>T maps to NM_020160.1 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:47910196 C>T maps to NM_020160.1 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42052640 G>T maps to ENST00000219905 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42052640 G>T maps to ENST00000219905 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:10417173 G>A maps to NM_005963.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:10417173 G>A maps to NM_005963.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:10542451 T>A maps to NM_002470.2 K1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:10542451 T>A maps to NM_002470.2 K1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:5811256 C>A maps to ENST00000381093 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:5811256 C>A maps to ENST00000381093 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:5020849 C>G maps to NM_001004755.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:5020849 C>G maps to NM_001004755.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:140249779 C>T maps to NM_018902.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:140249779 C>T maps to NM_018902.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:130832620 G>T maps to NM_001099771.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:130832620 G>T maps to NM_001099771.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:174200394 A>G maps to NM_014857.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:174200394 A>G maps to NM_014857.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:15572098 T>C maps to NM_022904.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:15572098 T>C maps to NM_022904.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:11375868 G>A maps to NM_004850.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:11375868 G>A maps to NM_004850.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:33878259 G>A maps to NM_001036.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:33878259 G>A maps to NM_001036.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:61600404 C>T maps to NM_005024.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:61600404 C>T maps to NM_005024.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:85133173 C>G maps to NM_021103.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:85133173 C>G maps to NM_021103.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:18042605 C>A maps to ENST00000341556 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:18042605 C>A maps to ENST00000341556 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:239234518 C>T maps to NM_015650.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:239234518 C>T maps to NM_015650.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:123020084 C>A maps to NM_001167.2 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:123020084 C>A maps to NM_001167.2 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:2407350 G>A maps to NM_004729.3 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:2407350 G>A maps to NM_004729.3 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:37129905 C>T maps to NM_153257.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:37129905 C>T maps to NM_153257.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:58601463 G>A maps to NM_001145542.1 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:58601463 G>A maps to NM_001145542.1 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:169787279 C>A maps to NM_003742.2 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:169787279 C>A maps to NM_003742.2 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:109665276 G>T maps to NM_001093.3 P1328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:109665276 G>T maps to NM_001093.3 P1328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:182920509 A>G maps to ENST00000287709 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:182920509 A>G maps to ENST00000287709 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:219231791 C>T maps to NM_198559.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:219231791 C>T maps to NM_198559.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:3254981 C>G maps to NM_001042690.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:3254981 C>G maps to NM_001042690.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:42187791 G>A maps to NM_006890.3 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:42187791 G>A maps to NM_006890.3 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:21864051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:21864051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:48369121 G>A maps to NM_001844.4 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:48369121 G>A maps to NM_001844.4 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:155006926 G>T maps to NM_152494.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:155006926 G>T maps to NM_152494.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:185018488 G>A maps to NM_153343.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:185018488 G>A maps to NM_153343.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:41572504 G>A maps to NM_001429.3 E1678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:41572504 G>A maps to NM_001429.3 E1678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:19186824 G>T maps to NM_014964.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:19186824 G>T maps to NM_014964.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:184764488 G>A maps to NM_052966.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:184764488 G>A maps to NM_052966.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:130270747 C>A maps to NM_022833.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:130270747 C>A maps to NM_022833.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:34961739 C>A maps to NM_152631.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:34961739 C>A maps to NM_152631.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:157665170 T>A maps to NM_052939.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:157665170 T>A maps to NM_052939.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:67266052 G>C maps to NM_013241.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:67266052 G>C maps to NM_013241.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:153230085 C>A maps to ENST00000369984 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:153230085 C>A maps to ENST00000369984 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:75094767 G>T maps to NM_000189.4 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:75094767 G>T maps to NM_000189.4 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:71000487 C>A maps to NM_025130.3 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:71000487 C>A maps to NM_025130.3 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:151164576 C>A maps to NM_178822.4 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:151164576 C>A maps to NM_178822.4 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:35874617 C>A maps to NM_002185.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:35874617 C>A maps to NM_002185.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:78669849 G>A maps to NM_001161352.1 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:78669849 G>A maps to NM_001161352.1 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:69595966 G>T maps to NM_012310.4 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:69595966 G>T maps to NM_012310.4 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:85331431 G>A maps to NM_012152.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:85331431 G>A maps to NM_012152.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:151092879 C>A maps to ENST00000427663 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:151092879 C>A maps to ENST00000427663 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:20113208 G>A maps to NM_001080480.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:20113208 G>A maps to NM_001080480.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:36873841 T>G maps to NM_005937.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:36873841 T>G maps to NM_005937.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:120800881 C>A maps to NM_002442.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:120800881 C>A maps to NM_002442.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:10222424 G>T maps to NM_003802.2 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:10222424 G>T maps to NM_003802.2 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:59553678 G>A maps to NM_004998.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:59553678 G>A maps to NM_004998.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:102335099 G>A maps to NM_022052.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:102335099 G>A maps to NM_022052.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:28000611 G>C maps to NM_000275.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:28000611 G>C maps to NM_000275.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:123519886 G>T maps to NM_001163278.1 R1906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:123519886 G>T maps to NM_001163278.1 R1906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:180582494 T>C maps to NM_206880.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:180582494 T>C maps to NM_206880.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:5878152 T>A maps to NM_001005168.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:5878152 T>A maps to NM_001005168.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:5989571 G>T maps to NM_001146033.1 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:5989571 G>T maps to NM_001146033.1 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:36846920 C>A maps to NM_016734.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:36846920 C>A maps to NM_016734.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:140725411 G>T maps to NM_018916.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:140725411 G>T maps to NM_018916.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:1961229 G>T maps to NM_024411.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:1961229 G>T maps to NM_024411.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:152937445 G>T maps to NM_001039582.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:152937445 G>T maps to NM_001039582.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:63920451 G>A maps to ENST00000422769 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:63920451 G>A maps to ENST00000422769 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:72358888 G>A maps to NM_005041.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:72358888 G>A maps to NM_005041.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:24615757 C>A maps to ENST00000429021 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:24615757 C>A maps to ENST00000429021 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:94747018 G>A maps to NM_203390.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:94747018 G>A maps to NM_203390.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:33955862 C>A maps to NM_001036.3 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:33955862 C>A maps to NM_001036.3 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:134990726 T>A maps to NM_018666.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:134990726 T>A maps to NM_018666.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:62049173 G>C maps to NM_000334.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:62049173 G>C maps to NM_000334.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:38639327 A>G maps to NM_001099404.1 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:38639327 A>G maps to NM_001099404.1 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:100774658 C>A maps to NM_139319.2 C94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:100774658 C>A maps to NM_139319.2 C94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:150867730 G>T maps to NM_078483.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:150867730 G>T maps to NM_078483.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:52938290 C>T maps to NM_145263.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:52938290 C>T maps to NM_145263.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:47466578 C>T maps to NM_006950.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:47466578 C>T maps to NM_006950.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:43995535 C>T maps to NM_033542.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:43995535 C>T maps to NM_033542.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:43086858 C>T maps to ENST00000263802 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:43086858 C>T maps to ENST00000263802 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:91155921 G>T maps to NM_001010854.1 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:91155921 G>T maps to NM_001010854.1 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:57398383 A>G maps to NM_014830.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:57398383 A>G maps to NM_014830.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:3142080 G>T maps to NM_032805.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:3142080 G>T maps to NM_032805.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr3:105243203 T>C maps to NM_001627.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr3:105243203 T>C maps to NM_001627.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:114179204 G>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:114179204 G>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:11206877 G>T maps to NM_013427.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:11206877 G>T maps to NM_013427.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:197070922 G>A maps to NM_018136.4 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:197070922 G>A maps to NM_018136.4 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:160047783 C>T maps to NM_025153.2 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:160047783 C>T maps to NM_025153.2 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:111795047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:111795047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:47846566 C>T maps to NM_001013732.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:47846566 C>T maps to NM_001013732.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:55924942 C>T maps to NM_030820.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:55924942 C>T maps to NM_030820.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:31579339 G>A maps to NM_144973.3 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:31579339 G>A maps to NM_144973.3 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr21:38877680 G>A maps to NM_001396.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr21:38877680 G>A maps to NM_001396.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr10:11791540 G>T maps to NM_024693.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr10:11791540 G>T maps to NM_024693.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:176072395 G>T maps to NM_001099408.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:176072395 G>T maps to NM_001099408.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:34150188 G>A maps to NM_203408.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:34150188 G>A maps to NM_203408.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:153190617 G>T maps to NM_001114183.1 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:153190617 G>T maps to NM_001114183.1 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr14:25100276 T>C maps to ENST00000382542 *282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr14:25100276 T>C maps to ENST00000382542 *282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:132091281 G>A maps to NM_001077188.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:132091281 G>A maps to NM_001077188.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:226378338 C>T maps to NM_020864.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:226378338 C>T maps to NM_020864.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr9:5920904 A>G maps to NM_001017969.2 N1697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr9:5920904 A>G maps to NM_001017969.2 N1697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:97533207 G>A maps to NM_052904.3 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:97533207 G>A maps to NM_052904.3 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr13:52676356 C>G maps to NM_199289.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr13:52676356 C>G maps to NM_199289.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr10:91352983 G>A maps to NM_148977.1 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr10:91352983 G>A maps to NM_148977.1 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:23521180 C>A maps to NM_020227.2 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:23521180 C>A maps to NM_020227.2 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:237947545 C>T maps to NM_001035.2 N4178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:237947545 C>T maps to NM_001035.2 N4178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr9:109688043 C>T maps to NM_021224.4 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr9:109688043 C>T maps to NM_021224.4 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:5961119 C>G maps to ENST00000324058 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:5961119 C>G maps to ENST00000324058 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:167973204 A>T maps to ENST00000367840 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:167973204 A>T maps to ENST00000367840 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:147380357 C>G maps to NM_005267.4 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:147380357 C>G maps to NM_005267.4 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:24632299 C>T maps to NM_006084.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:24632299 C>T maps to NM_006084.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:62739506 C>T maps to NM_181712.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:62739506 C>T maps to NM_181712.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:4920769 A>T maps to NM_002235.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:4920769 A>T maps to NM_002235.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:36136535 C>A maps to NM_001007527.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:36136535 C>A maps to NM_001007527.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:80529444 G>T maps to NM_178839.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:80529444 G>T maps to NM_178839.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:23239012 C>G maps to NM_005015.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:23239012 C>G maps to NM_005015.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:57358430 G>A maps to NM_001135690.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:57358430 G>A maps to NM_001135690.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:145008877 C>T maps to NM_201380.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:145008877 C>T maps to NM_201380.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:43984325 G>A maps to NM_172069.3 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:43984325 G>A maps to NM_172069.3 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:62493020 C>T maps to NM_007215.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:62493020 C>T maps to NM_007215.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:45899437 C>T maps to NM_001142502.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:45899437 C>T maps to NM_001142502.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:186917761 A>T maps to NM_153708.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:186917761 A>T maps to NM_153708.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:55058572 C>A maps to NM_021626.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:55058572 C>A maps to NM_021626.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:129299351 G>A maps to ENST00000376744 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:129299351 G>A maps to ENST00000376744 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:39214706 A>G maps to NM_005633.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:39214706 A>G maps to NM_005633.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:43577064 C>A maps to NM_052955.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:43577064 C>A maps to NM_052955.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:7606725 A>T maps to NM_018081.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:7606725 A>T maps to NM_018081.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:17464265 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:17464265 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:43708162 C>T maps to NM_004915.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:43708162 C>T maps to NM_004915.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:77327080 G>A maps to NM_199355.2 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:77327080 G>A maps to NM_199355.2 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:159035744 A>G maps to NM_004833.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:159035744 A>G maps to NM_004833.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:116151290 G>C maps to ENST00000277315 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:116151290 G>C maps to ENST00000277315 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr18:43666457 G>T maps to NM_001001937.1 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr18:43666457 G>T maps to NM_001001937.1 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:128292392 G>A maps to NM_007354.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:128292392 G>A maps to NM_007354.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:109807586 C>T maps to NM_001408.2 T1854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:109807586 C>T maps to NM_001408.2 T1854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:68374580 C>A maps to NM_001812.2 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:68374580 C>A maps to NM_001812.2 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:136700367 C>T maps to NM_001006628.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:136700367 C>T maps to NM_001006628.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:90321153 G>A maps to NM_004938.2 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:90321153 G>A maps to NM_004938.2 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:41711172 C>T maps to NM_001389.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:41711172 C>T maps to NM_001389.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:71425004 T>C maps to NM_017669.2 V1204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:71425004 T>C maps to NM_017669.2 V1204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:6305707 G>A maps to NM_000129.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:6305707 G>A maps to NM_000129.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:35076824 T>A maps to NM_004629.1 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:35076824 T>A maps to NM_004629.1 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:157650552 A>G maps to NM_052939.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:157650552 A>G maps to NM_052939.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:14848753 G>A maps to ENST00000380880 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:14848753 G>A maps to ENST00000380880 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:37746018 G>A maps to NM_014907.2 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:37746018 G>A maps to NM_014907.2 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:158282245 A>G maps to NM_001083619.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:158282245 A>G maps to NM_001083619.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679297 G>A maps to NM_001040708.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679297 G>A maps to NM_001040708.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:123192464 A>T maps to NM_015312.3 R2596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:123192464 A>T maps to NM_015312.3 R2596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:94044288 G>A maps to ENST00000393153 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:94044288 G>A maps to ENST00000393153 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:39594555 G>A maps to NM_006771.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:39594555 G>A maps to NM_006771.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:52865968 C>T maps to NM_173086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:52865968 C>T maps to NM_173086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:149638792 G>A maps to NM_005491.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:149638792 G>A maps to NM_005491.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:151970910 G>T maps to ENST00000355193 C297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:151970910 G>T maps to ENST00000355193 C297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:151209071 C>T maps to NM_015440.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:151209071 C>T maps to NM_015440.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:16699586 C>T maps to NM_012334.2 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:16699586 C>T maps to NM_012334.2 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:8587291 G>A maps to NM_012335.3 N1063N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:8587291 G>A maps to NM_012335.3 N1063N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:95162102 G>A maps to NM_013451.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:95162102 G>A maps to NM_013451.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:56538690 C>T maps to NM_153447.4 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:56538690 C>T maps to NM_153447.4 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:120539848 G>A maps to NM_024408.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:120539848 G>A maps to NM_024408.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:248813366 A>G maps to NM_001001824.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:248813366 A>G maps to NM_001001824.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:6191529 G>A maps to NM_001004052.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:6191529 G>A maps to NM_001004052.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:107763108 T>C maps to NM_001198533.1 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:107763108 T>C maps to NM_001198533.1 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:140581714 C>T maps to NM_018931.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:140581714 C>T maps to NM_018931.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:170892656 G>T maps to NM_002598.3 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:170892656 G>T maps to NM_002598.3 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:69129862 C>T maps to NM_024870.2 S1539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:69129862 C>T maps to NM_024870.2 S1539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:104173680 C>T maps to NM_002779.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:104173680 C>T maps to NM_002779.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:198668830 C>A maps to ENST00000271610 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:198668830 C>A maps to ENST00000271610 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:33937261 G>A maps to NM_016568.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:33937261 G>A maps to NM_016568.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:236580 C>T maps to NM_004168.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:236580 C>T maps to NM_004168.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:156779566 G>A maps to NM_001161441.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:156779566 G>A maps to NM_001161441.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:100841681 C>T maps to ENST00000262901 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:100841681 C>T maps to ENST00000262901 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:55690764 G>A maps to NM_001043.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:55690764 G>A maps to NM_001043.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:33687334 A>G maps to NM_152270.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:33687334 A>G maps to NM_152270.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:18896865 A>G maps to ENST00000389467 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:18896865 A>G maps to ENST00000389467 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:24801234 C>A maps to NM_003102.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:24801234 C>A maps to NM_003102.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:137988704 C>T maps to ENST00000272643 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:137988704 C>T maps to ENST00000272643 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:186307307 T>A maps to NM_003292.2 R1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:186307307 T>A maps to NM_003292.2 R1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:228758627 T>G maps to NM_178821.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:228758627 T>G maps to NM_178821.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:54335696 G>T maps to NM_020922.4 C254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:54335696 G>T maps to NM_020922.4 C254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:36884571 T>A maps to NM_133466.2 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:36884571 T>A maps to NM_133466.2 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:38190761 C>T maps to NM_032689.4 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:38190761 C>T maps to NM_032689.4 G90G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z038-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:173232765 G>A maps to ENST00000308120 G1G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z038-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:173232765 G>A maps to ENST00000308120 G1G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:37475309 G>C maps to NM_144736.4 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:37475309 G>C maps to NM_144736.4 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:48800926 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:48800926 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:139606335 C>A maps to NM_152888.1 R1513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:139606335 C>A maps to NM_152888.1 R1513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:28776720 A>T maps to NM_001304.4 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:28776720 A>T maps to NM_001304.4 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:113243834 A>C maps to NM_198123.1 T3589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:113243834 A>C maps to NM_198123.1 T3589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:143998596 C>A maps to NM_000498.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:143998596 C>A maps to NM_000498.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:59112171 T>A maps to NM_016651.5 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:59112171 T>A maps to NM_016651.5 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:30053332 C>T maps to NM_001037500.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:30053332 C>T maps to NM_001037500.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:22924647 C>T maps to NM_020526.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:22924647 C>T maps to NM_020526.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:26596287 G>T maps to NM_033505.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:26596287 G>T maps to NM_033505.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:91813031 A>C maps to NM_001017975.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:91813031 A>C maps to NM_001017975.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:48165214 C>T maps to NM_002204.2 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:48165214 C>T maps to NM_002204.2 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:86716547 G>T maps to NM_001146688.1 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:86716547 G>T maps to NM_001146688.1 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:97587156 G>C maps to NM_052904.3 *621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:97587156 G>C maps to NM_052904.3 *621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr18:7026048 G>A maps to NM_005559.2 Y777Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr18:7026048 G>A maps to NM_005559.2 Y777Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:7090770 G>A maps to NM_005768.5 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:7090770 G>A maps to NM_005768.5 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:15852738 C>T maps to NM_013938.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:15852738 C>T maps to NM_013938.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:248202306 A>G maps to NM_001004686.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:248202306 A>G maps to NM_001004686.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:55587674 C>T maps to ENST00000395203 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:55587674 C>T maps to ENST00000395203 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:6816141 C>A maps to NM_003696.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:6816141 C>A maps to NM_003696.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:146073744 G>A maps to ENST00000447906 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:146073744 G>A maps to ENST00000447906 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:15587252 G>C maps to NM_052890.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:15587252 G>C maps to NM_052890.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:48130813 G>T maps to NM_000961.3 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:48130813 G>T maps to NM_000961.3 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:214638115 G>T maps to NM_005401.4 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:214638115 G>T maps to NM_005401.4 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:18763945 C>T maps to NM_032781.3 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:18763945 C>T maps to NM_032781.3 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:46355634 G>A maps to NM_004819.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:46355634 G>A maps to NM_004819.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:33579266 A>C maps to NM_198992.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:33579266 A>C maps to NM_198992.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:115985846 C>G maps to NM_198795.1 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:115985846 C>G maps to NM_198795.1 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:72832069 C>T maps to NM_017728.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:72832069 C>T maps to NM_017728.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:18722634 G>A maps to NM_153347.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:18722634 G>A maps to NM_153347.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:30128212 G>A maps to NM_006778.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:30128212 G>A maps to NM_006778.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:184586747 C>G maps to ENST00000437079 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:184586747 C>G maps to ENST00000437079 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:77775483 A>G maps to NM_024721.4 S3178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:77775483 A>G maps to NM_024721.4 S3178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:43414129 G>C maps to NM_020727.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:43414129 G>C maps to NM_020727.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:73152066 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:73152066 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87792440 C>T maps to NM_021723.3 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87792440 C>T maps to NM_021723.3 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:32459004 C>T maps to NM_001714.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:32459004 C>T maps to NM_001714.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:105942138 G>A maps to ENST00000389588 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:105942138 G>A maps to ENST00000389588 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:128910976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:128910976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:26886164 T>A maps to NM_024828.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:26886164 T>A maps to NM_024828.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:32162566 G>A maps to NM_001856.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:32162566 G>A maps to NM_001856.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:128850971 C>T maps to ENST00000398025 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:128850971 C>T maps to ENST00000398025 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:15338903 G>T maps to NM_001142886.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:15338903 G>T maps to NM_001142886.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:57430211 C>A maps to NM_080425.2 S631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:57430211 C>A maps to NM_080425.2 S631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:149783692 G>T maps to ENST00000427880 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:149783692 G>T maps to ENST00000427880 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:124271530 G>C maps to NM_002775.4 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:124271530 G>C maps to NM_002775.4 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:43881757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:43881757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:113578471 G>T maps to ENST00000509061 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:113578471 G>T maps to ENST00000509061 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:26695490 G>A maps to NM_194248.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:26695490 G>A maps to NM_194248.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:11022137 T>G maps to ENST00000303905 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:11022137 T>G maps to ENST00000303905 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:144991967 G>A maps to NM_201380.2 A4144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:144991967 G>A maps to NM_201380.2 A4144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:48389203 C>G maps to NM_002900.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:48389203 C>G maps to NM_002900.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:83905765 C>T maps to NM_033411.3 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:83905765 C>T maps to NM_033411.3 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:220336997 G>T maps to NM_005876.4 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:220336997 G>T maps to NM_005876.4 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:35470214 G>T maps to NM_003136.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:35470214 G>T maps to NM_003136.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:106196706 G>A maps to ENST00000513237 Q1701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:106196706 G>A maps to ENST00000513237 Q1701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:45575761 G>A maps to NM_145288.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:45575761 G>A maps to NM_145288.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:21240397 C>G maps to NM_025189.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:21240397 C>G maps to NM_025189.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:21217054 A>G maps to NM_003460.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:21217054 A>G maps to NM_003460.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:137850092 C>T maps to NM_016161.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:137850092 C>T maps to NM_016161.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:31438992 C>A maps to NM_183377.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:31438992 C>A maps to NM_183377.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:53911339 T>A maps to NM_022899.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:53911339 T>A maps to NM_022899.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:113351752 G>A maps to NM_025144.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:113351752 G>A maps to NM_025144.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:36230754 C>T maps to NM_015230.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:36230754 C>T maps to NM_015230.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155327183 C>T maps to ENST00000368346 E2331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155327183 C>T maps to ENST00000368346 E2331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:32848269 C>A maps to NM_001672.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:32848269 C>A maps to NM_001672.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:171509979 C>T maps to ENST00000392078 N1125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:171509979 C>T maps to ENST00000392078 N1125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:13603789 T>C maps to NM_148894.2 A1578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:13603789 T>C maps to NM_148894.2 A1578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:32841967 C>A maps to NM_174932.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:32841967 C>A maps to NM_174932.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:41244213 C>A maps to ENST00000471181 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:41244213 C>A maps to ENST00000471181 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:74824463 G>T maps to NM_018228.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:74824463 G>T maps to NM_018228.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:43045077 C>A maps to NM_006688.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:43045077 C>A maps to NM_006688.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:27804469 C>T maps to NM_032266.3 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:27804469 C>T maps to NM_032266.3 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:5975501 C>A maps to ENST00000324058 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:5975501 C>A maps to ENST00000324058 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:31080012 C>A maps to NM_014070.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:31080012 C>A maps to NM_014070.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:31735161 G>A maps to NM_006658.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:31735161 G>A maps to NM_006658.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:89887464 T>C maps to NM_001039706.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:89887464 T>C maps to NM_001039706.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:39316032 A>C maps to NM_001737.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:39316032 A>C maps to NM_001737.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:2024089 C>T maps to NM_172364.4 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:2024089 C>T maps to NM_172364.4 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:44620905 G>T maps to NM_138423.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:44620905 G>T maps to NM_138423.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:122002777 C>T maps to NM_001178065.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:122002777 C>T maps to NM_001178065.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:112358550 C>A maps to ENST00000447230 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:112358550 C>A maps to ENST00000447230 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:121838341 G>C maps to NM_175862.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:121838341 G>C maps to NM_175862.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:24491816 G>A maps to NM_006727.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:24491816 G>A maps to NM_006727.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:26906107 C>A maps to NM_016279.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:26906107 C>A maps to NM_016279.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:64824355 C>A maps to NM_022145.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:64824355 C>A maps to NM_022145.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:101804357 T>A maps to NM_001855.3 L848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:101804357 T>A maps to NM_001855.3 L848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:110839511 C>A maps to NM_001845.4 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:110839511 C>A maps to NM_001845.4 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:107802317 G>T maps to ENST00000328300 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:107802317 G>T maps to ENST00000328300 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:27943985 G>T maps to ENST00000345068 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:27943985 G>T maps to ENST00000345068 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:24542766 C>A maps to NM_006032.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:24542766 C>A maps to NM_006032.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:43907805 C>A maps to NM_001145146.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:43907805 C>A maps to NM_001145146.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:101514310 A>T maps to NM_015960.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:101514310 A>T maps to NM_015960.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:36103456 C>G maps to NM_173695.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:36103456 C>G maps to NM_173695.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:6646565 G>A maps to NM_003737.2 L2337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:6646565 G>A maps to NM_003737.2 L2337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:61528109 T>A maps to NM_033081.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:61528109 T>A maps to NM_033081.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:21813388 G>T maps to NM_003777.3 V3043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:21813388 G>T maps to NM_003777.3 V3043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:71747321 C>A maps to NM_001130987.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:71747321 C>A maps to NM_001130987.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:83362383 G>C maps to NM_005711.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:83362383 G>C maps to NM_005711.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:64573953 G>A maps to NM_001136178.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:64573953 G>A maps to NM_001136178.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184295234 G>T maps to NM_004443.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184295234 G>T maps to NM_004443.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:58552960 G>A maps to ENST00000474531 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:58552960 G>A maps to ENST00000474531 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38879975 G>T maps to NM_138389.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38879975 G>T maps to NM_138389.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:139164944 C>A maps to NM_015912.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:139164944 C>A maps to NM_015912.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:49994657 C>T maps to NM_032130.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:49994657 C>T maps to NM_032130.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:62148787 C>A maps to NM_178539.3 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:62148787 C>A maps to NM_178539.3 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:108380494 A>T maps to NM_005246.2 K610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:108380494 A>T maps to NM_005246.2 K610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:14905646 G>A maps to NM_152536.3 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:14905646 G>A maps to NM_152536.3 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:155528067 G>A maps to ENST00000407946 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:155528067 G>A maps to ENST00000407946 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:128490514 G>T maps to NM_001458.4 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:128490514 G>T maps to NM_001458.4 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:94278600 G>A maps to NM_002033.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:94278600 G>A maps to NM_002033.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:137589487 G>A maps to NM_001496.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:137589487 G>A maps to NM_001496.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:1721832 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:1721832 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:135427079 A>C maps to NM_153834.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:135427079 A>C maps to NM_153834.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:113658765 G>A maps to NM_017577.4 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:113658765 G>A maps to NM_017577.4 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:153144083 G>T maps to NM_001114183.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:153144083 G>T maps to NM_001114183.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:126544738 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:126544738 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155253817 C>T maps to NM_020897.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155253817 C>T maps to NM_020897.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:65427075 G>T maps to NM_138737.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:65427075 G>T maps to NM_138737.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91851360 C>A maps to NM_001017975.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91851360 C>A maps to NM_001017975.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:222717204 C>G maps to NM_024746.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:222717204 C>G maps to NM_024746.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:71103346 G>A maps to NM_032821.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:71103346 G>A maps to NM_032821.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:8268291 T>A maps to ENST00000422063 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:8268291 T>A maps to ENST00000422063 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:91035817 C>T maps to NM_003870.3 A1501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:91035817 C>T maps to NM_003870.3 A1501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:15714632 G>A maps to NM_003638.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:15714632 G>A maps to NM_003638.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:6147571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:6147571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:47991189 G>A maps to NM_004975.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:47991189 G>A maps to NM_004975.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:73480015 C>A maps to NM_004770.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:73480015 C>A maps to NM_004770.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:215259900 G>C maps to NM_001017425.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:215259900 G>C maps to NM_001017425.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:36691146 A>C maps to NM_001031836.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:36691146 A>C maps to NM_001031836.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:94007177 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:94007177 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:135027498 C>A maps to ENST00000368572 S1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:135027498 C>A maps to ENST00000368572 S1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:53071141 G>T maps to NM_006121.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:53071141 G>T maps to NM_006121.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:39521462 A>G maps to ENST00000394004 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:39521462 A>G maps to ENST00000394004 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:46101810 G>T maps to NM_181686.1 C76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:46101810 G>T maps to NM_181686.1 C76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:143798073 G>A maps to NM_003937.2 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:143798073 G>A maps to NM_003937.2 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:42158946 G>T maps to NM_032107.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:42158946 G>T maps to NM_032107.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:152671550 C>A maps to NM_178428.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:152671550 C>A maps to NM_178428.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141819715 G>T maps to NM_018557.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141819715 G>T maps to NM_018557.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:110763520 C>A maps to NM_018334.4 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:110763520 C>A maps to NM_018334.4 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:47037777 C>G maps to NM_003684.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:47037777 C>G maps to NM_003684.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:23811384 G>T maps to NM_005664.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:23811384 G>T maps to NM_005664.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:56291139 G>A maps to NM_017777.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:56291139 G>A maps to NM_017777.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:151970871 A>T maps to ENST00000355193 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:151970871 A>T maps to ENST00000355193 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:21959418 G>A maps to NM_004641.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:21959418 G>A maps to NM_004641.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:102819850 C>A maps to NM_002427.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:102819850 C>A maps to NM_002427.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:60233576 G>T maps to NM_152866.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:60233576 G>T maps to NM_152866.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:55481788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:55481788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:17542024 G>A maps to NM_001001924.2 R884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:17542024 G>A maps to NM_001001924.2 R884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:108112925 C>A maps to NM_014981.1 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:108112925 C>A maps to NM_014981.1 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:78362296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:78362296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:15432848 C>A maps to NM_015909.2 V1613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:15432848 C>A maps to NM_015909.2 V1613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:75567204 C>T maps to NM_003635.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:75567204 C>T maps to NM_003635.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236192967 G>T maps to NM_002508.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236192967 G>T maps to NM_002508.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:23538979 T>C maps to NM_006167.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:23538979 T>C maps to NM_006167.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56369277 G>T maps to NM_134444.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56369277 G>T maps to NM_134444.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:30326994 C>T maps to NM_000475.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:30326994 C>T maps to NM_000475.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:229636556 G>A maps to NM_018230.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:229636556 G>A maps to NM_018230.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:159284104 C>A maps to NM_001004467.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:159284104 C>A maps to NM_001004467.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158450125 C>G maps to NM_001004472.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158450125 C>G maps to NM_001004472.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:35957690 C>A maps to NM_019897.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:35957690 C>A maps to NM_019897.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:5173455 C>T maps to NM_012375.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:5173455 C>T maps to NM_012375.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:55563783 C>A maps to NM_001004735.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:55563783 C>A maps to NM_001004735.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:55579085 G>C maps to NM_001004738.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:55579085 G>C maps to NM_001004738.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:56127955 C>A maps to NM_001005205.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:56127955 C>A maps to NM_001005205.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:90691131 C>A maps to NM_080832.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:90691131 C>A maps to NM_080832.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:206265803 C>T maps to ENST00000406610 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:206265803 C>T maps to ENST00000406610 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:140215842 G>T maps to NM_018910.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:140215842 G>T maps to NM_018910.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:140810505 G>T maps to NM_003735.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:140810505 G>T maps to NM_003735.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98469657 C>A maps to NM_152309.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98469657 C>A maps to NM_152309.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:209204747 G>T maps to NM_015040.3 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:209204747 G>T maps to NM_015040.3 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:125255524 C>T maps to NM_022062.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:125255524 C>T maps to NM_022062.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:8769322 G>T maps to NM_015192.2 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:8769322 G>T maps to NM_015192.2 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:133250241 C>T maps to ENST00000455752 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:133250241 C>T maps to ENST00000455752 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:38143959 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:38143959 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55614841 C>A maps to NM_017607.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55614841 C>A maps to NM_017607.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:48755809 G>T maps to NM_005710.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:48755809 G>T maps to NM_005710.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:71029627 G>A maps to NM_001109754.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:71029627 G>A maps to NM_001109754.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:49039353 C>G maps to NM_000321.2 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:49039353 C>G maps to NM_000321.2 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:79349190 G>A maps to NM_002909.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:79349190 G>A maps to NM_002909.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:3270425 C>A maps to NM_134428.1 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:3270425 C>A maps to NM_134428.1 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108487651 G>T maps to NM_182588.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108487651 G>T maps to NM_182588.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:163044229 C>G maps to NM_001102445.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:163044229 C>G maps to NM_001102445.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:123699417 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:123699417 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:10467119 G>T maps to NM_178857.5 T1496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:10467119 G>T maps to NM_178857.5 T1496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:46713305 C>A maps to NM_006915.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:46713305 C>A maps to NM_006915.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:237777470 T>C maps to NM_001035.2 D1681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:237777470 T>C maps to NM_001035.2 D1681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:92735074 T>C maps to NM_017654.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:92735074 T>C maps to NM_017654.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:167262665 G>T maps to NM_002976.2 Y1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:167262665 G>T maps to NM_002976.2 Y1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:167168244 C>A maps to ENST00000303354 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:167168244 C>A maps to ENST00000303354 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:4014039 G>T maps to NM_152744.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:4014039 G>T maps to NM_152744.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:83590814 G>T maps to NM_006080.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:83590814 G>T maps to NM_006080.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:118774739 C>A maps to ENST00000394612 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:118774739 C>A maps to ENST00000394612 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:64020381 G>A maps to ENST00000513458 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:64020381 G>A maps to ENST00000513458 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:51961203 C>G maps to NM_014442.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:51961203 C>G maps to NM_014442.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:36184064 T>C maps to ENST00000308927 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:36184064 T>C maps to ENST00000308927 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108614426 C>A maps to NM_021815.2 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108614426 C>A maps to NM_021815.2 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:101577934 G>A maps to NM_145913.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:101577934 G>A maps to NM_145913.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:20619253 G>T maps to ENST00000273739 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:20619253 G>T maps to ENST00000273739 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:88328536 G>A maps to NM_015567.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:88328536 G>A maps to NM_015567.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:59179172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:59179172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:31762254 G>C maps to ENST00000446633 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:31762254 G>C maps to ENST00000446633 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:142596805 G>A maps to NM_001009609.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:142596805 G>A maps to NM_001009609.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:228881495 A>G maps to NM_001142644.1 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:228881495 A>G maps to NM_001142644.1 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:153012668 G>A maps to NM_006945.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:153012668 G>A maps to NM_006945.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:70415729 G>T maps to NM_006927.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:70415729 G>T maps to NM_006927.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:28619880 A>G maps to NM_177529.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:28619880 A>G maps to NM_177529.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:12209920 G>T maps to NM_133625.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:12209920 G>T maps to NM_133625.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:162087710 A>G maps to NM_004180.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:162087710 A>G maps to NM_004180.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:17413736 C>A maps to NM_001134381.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:17413736 C>A maps to NM_001134381.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:6722662 C>A maps to NM_053285.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:6722662 C>A maps to NM_053285.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:79366217 C>A maps to NM_003248.4 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:79366217 C>A maps to NM_003248.4 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:138378216 C>A maps to ENST00000272643 C1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:138378216 C>A maps to ENST00000272643 C1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:43770804 G>T maps to NM_005424.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:43770804 G>T maps to NM_005424.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:98449143 G>T maps to NM_001134450.1 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:98449143 G>T maps to NM_001134450.1 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:248039403 G>A maps to NM_015431.3 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:248039403 G>A maps to NM_015431.3 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:77353446 C>A maps to NM_017662.4 R1884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:77353446 C>A maps to NM_017662.4 R1884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:179581897 G>A maps to NM_133378.4 G7277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:179581897 G>A maps to NM_133378.4 G7277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:35477039 A>T maps to NM_003322.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:35477039 A>T maps to NM_003322.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:669135 C>T maps to NM_001071.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:669135 C>T maps to NM_001071.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:215987216 G>T maps to ENST00000366943 P3200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:215987216 G>T maps to ENST00000366943 P3200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:149208152 A>T maps to NM_005715.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:149208152 A>T maps to NM_005715.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:77850896 G>T maps to NM_020927.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:77850896 G>T maps to NM_020927.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:97304097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:97304097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:39279779 G>T maps to NM_025132.3 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:39279779 G>T maps to NM_025132.3 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:142090171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:142090171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:22837824 G>T maps to NM_014870.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:22837824 G>T maps to NM_014870.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:135533235 T>A maps to NM_020863.3 K1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:135533235 T>A maps to NM_020863.3 K1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:28053588 G>T maps to NM_003447.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:28053588 G>T maps to NM_003447.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:46722523 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:46722523 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:31134131 C>A maps to NM_182755.2 G749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:31134131 C>A maps to NM_182755.2 G749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:22574464 G>T maps to NM_001098626.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:22574464 G>T maps to NM_001098626.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:14851707 A>T maps to NM_001145029.1 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:14851707 A>T maps to NM_001145029.1 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:135464767 C>A maps to NM_020064.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:135464767 C>A maps to NM_020064.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:19591213 T>A maps to NM_004934.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:19591213 T>A maps to NM_004934.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7801418 C>T maps to NM_001005271.2 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7801418 C>T maps to NM_001005271.2 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:101806866 G>A maps to NM_001855.3 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:101806866 G>A maps to NM_001855.3 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:116931658 C>A maps to NM_032888.2 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:116931658 C>A maps to NM_032888.2 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:14496147 C>A maps to NM_001144061.1 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:14496147 C>A maps to NM_001144061.1 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:101829548 G>T maps to NM_001308.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:101829548 G>T maps to NM_001308.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7701481 G>T maps to NM_020877.2 R2746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7701481 G>T maps to NM_020877.2 R2746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:225709557 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:225709557 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:29122616 C>T maps to NM_001943.3 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:29122616 C>T maps to NM_001943.3 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:25899679 G>T maps to NM_022659.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:25899679 G>T maps to NM_022659.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:90537779 C>T maps to NM_001145124.1 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:90537779 C>T maps to NM_001145124.1 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:413122 T>C maps to NM_183421.1 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:413122 T>C maps to NM_183421.1 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:152283677 G>A maps to NM_002016.1 D1228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:152283677 G>A maps to NM_002016.1 D1228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:151820166 C>A maps to NM_018558.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:151820166 C>A maps to NM_018558.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:7843253 C>T maps to NM_020634.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:7843253 C>T maps to NM_020634.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:35896884 C>A maps to NM_153368.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:35896884 C>A maps to NM_153368.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:135432047 T>C maps to NM_153834.3 S2061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:135432047 T>C maps to NM_153834.3 S2061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:13717203 G>T maps to NM_000834.3 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:13717203 G>T maps to NM_000834.3 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:156727535 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:156727535 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:22569902 C>T maps to NM_138574.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:22569902 C>T maps to NM_138574.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:26818886 G>A maps to NM_002223.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:26818886 G>A maps to NM_002223.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:48915564 G>T maps to NM_000233.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:48915564 G>T maps to NM_000233.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:72061135 C>A maps to NM_207119.1 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:72061135 C>A maps to NM_207119.1 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:70478655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:70478655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:151935512 C>T maps to NM_005362.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:151935512 C>T maps to NM_005362.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:154007589 G>T maps to NM_002436.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:154007589 G>T maps to NM_002436.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10209811 C>T maps to NM_003802.2 K1810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10209811 C>T maps to NM_003802.2 K1810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:23858084 C>T maps to NM_002471.3 E1386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:23858084 C>T maps to NM_002471.3 E1386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:109507807 T>C maps to NM_015011.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:109507807 T>C maps to NM_015011.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:30932129 C>A maps to NM_015194.1 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:30932129 C>A maps to NM_015194.1 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:72433352 C>A maps to NM_021963.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:72433352 C>A maps to NM_021963.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:42076368 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:42076368 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:25485522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:25485522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:282700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:282700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:114182961 A>T maps to NM_006169.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:114182961 A>T maps to NM_006169.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:200017309 C>T maps to NM_205860.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:200017309 C>T maps to NM_205860.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:33057179 T>C maps to NM_001002010.1 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:33057179 T>C maps to NM_001002010.1 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:184022189 T>G maps to NM_138285.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:184022189 T>G maps to NM_138285.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153421992 C>A maps to NM_020061.4 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153421992 C>A maps to NM_020061.4 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:20586107 C>A maps to NM_001004715.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:20586107 C>A maps to NM_001004715.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:55563947 T>G maps to NM_001004735.1 L306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:55563947 T>G maps to NM_001004735.1 L306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:55587308 C>G maps to ENST00000395203 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:55587308 C>G maps to ENST00000395203 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:56310715 G>T maps to NM_001005245.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:56310715 G>T maps to NM_001005245.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:124189501 G>A maps to NM_001002918.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:124189501 G>A maps to NM_001002918.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:149943153 G>A maps to NM_020205.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:149943153 G>A maps to NM_020205.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:55581629 A>C maps to NM_001142763.1 S1959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:55581629 A>C maps to NM_001142763.1 S1959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:105607675 A>G maps to NM_022361.4 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:105607675 A>G maps to NM_022361.4 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:57301532 G>C maps to NM_002703.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:57301532 G>C maps to NM_002703.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:22892422 G>T maps to NM_206954.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:22892422 G>T maps to NM_206954.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:107600086 G>T maps to NM_018137.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:107600086 G>T maps to NM_018137.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43680280 G>A maps to ENST00000270059 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43680280 G>A maps to ENST00000270059 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:119805398 C>A maps to ENST00000369199 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:119805398 C>A maps to ENST00000369199 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:101078437 T>C maps to NM_015668.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:101078437 T>C maps to NM_015668.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:130941202 C>A maps to NM_015347.4 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:130941202 C>A maps to NM_015347.4 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:169677567 G>C maps to NM_000655.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:169677567 G>C maps to NM_000655.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:43836132 T>C maps to NM_003007.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:43836132 T>C maps to NM_003007.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:25264767 G>T maps to NM_001039948.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:25264767 G>T maps to NM_001039948.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:64976347 C>T maps to NM_019072.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:64976347 C>T maps to NM_019072.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:164907124 T>C maps to NM_014926.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:164907124 T>C maps to NM_014926.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:220354244 C>G maps to NM_005876.4 L2835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:220354244 C>G maps to NM_005876.4 L2835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:79368107 A>G maps to NM_003248.4 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:79368107 A>G maps to NM_003248.4 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:949543 C>A maps to NM_032326.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:949543 C>A maps to NM_032326.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7834427 T>C maps to NM_001166621.1 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7834427 T>C maps to NM_001166621.1 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:96261978 C>A maps to NM_138800.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:96261978 C>A maps to NM_138800.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:179414450 G>T maps to NM_133378.4 A28098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:179414450 G>T maps to NM_133378.4 A28098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:17785515 C>G maps to ENST00000428389 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:17785515 C>G maps to ENST00000428389 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:12043819 T>A maps to NM_015542.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:12043819 T>A maps to NM_015542.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:12566972 G>A maps to NM_015378.2 L4287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:12566972 G>A maps to NM_015378.2 L4287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:57396733 C>A maps to NM_014830.2 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:57396733 C>A maps to NM_014830.2 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:30935618 G>T maps to NM_014717.1 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:30935618 G>T maps to NM_014717.1 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:57769598 C>A maps to NM_178457.1 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:57769598 C>A maps to NM_178457.1 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:102792954 C>T maps to NM_018335.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:102792954 C>T maps to NM_018335.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:5455750 C>G maps to NM_181710.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:5455750 C>G maps to NM_181710.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:44506135 C>T maps to NM_080752.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:44506135 C>T maps to NM_080752.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:21225813 G>A maps to NM_000384.2 G4160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:21225813 G>A maps to NM_000384.2 G4160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:21229633 G>T maps to NM_000384.2 S3369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:21229633 G>T maps to NM_000384.2 S3369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:1844524 A>G maps to ENST00000398564 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:1844524 A>G maps to ENST00000398564 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:190531043 C>G maps to NM_019048.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:190531043 C>G maps to NM_019048.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:43927613 C>T maps to NM_172095.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:43927613 C>T maps to NM_172095.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:83251005 G>A maps to ENST00000268613 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:83251005 G>A maps to ENST00000268613 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:5903865 G>A maps to NM_001819.2 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:5903865 G>A maps to NM_001819.2 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:137886024 T>A maps to NM_016216.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:137886024 T>A maps to NM_016216.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:21062988 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:21062988 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:52250112 C>G maps to NM_002029.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:52250112 C>G maps to NM_002029.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:44975065 A>T maps to NM_032135.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:44975065 A>T maps to NM_032135.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:39153584 T>C maps to ENST00000263405 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:39153584 T>C maps to ENST00000263405 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:58010268 G>A maps to NM_001111270.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:58010268 G>A maps to NM_001111270.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:35223434 A>G maps to NM_005268.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:35223434 A>G maps to NM_005268.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:35223473 A>G maps to NM_005268.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:35223473 A>G maps to NM_005268.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:42004992 T>A maps to NM_000168.5 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:42004992 T>A maps to NM_000168.5 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:37672452 C>A maps to NM_032777.9 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:37672452 C>A maps to NM_032777.9 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:55789090 C>A maps to NM_012267.4 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:55789090 C>A maps to NM_012267.4 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140037230 T>G maps to NM_006083.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140037230 T>G maps to NM_006083.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:107977312 A>G maps to NM_003604.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:107977312 A>G maps to NM_003604.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:2812305 T>C maps to NM_014878.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:2812305 T>C maps to NM_014878.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:34791650 C>T maps to NM_014686.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:34791650 C>T maps to NM_014686.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:31744327 C>G maps to NM_181621.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:31744327 C>G maps to NM_181621.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:152681700 C>A maps to NM_178356.2 C50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:152681700 C>A maps to NM_178356.2 C50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:66850174 G>A maps to NM_207338.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:66850174 G>A maps to NM_207338.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:62903540 T>A maps to ENST00000506720 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:62903540 T>A maps to ENST00000506720 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:151945106 A>T maps to ENST00000355193 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:151945106 A>T maps to ENST00000355193 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:10541665 G>T maps to NM_002470.2 A1141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:10541665 G>T maps to NM_002470.2 A1141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:29548865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:29548865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:102512214 C>A maps to NM_024057.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:102512214 C>A maps to NM_024057.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:154412189 C>T maps to NM_001145279.1 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:154412189 C>T maps to NM_001145279.1 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:123886969 C>G maps to NM_001004462.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:123886969 C>G maps to NM_001004462.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:27879545 C>T maps to NM_033057.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:27879545 C>T maps to NM_033057.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:55587140 G>T maps to ENST00000395203 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:55587140 G>T maps to ENST00000395203 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:55587800 C>T maps to ENST00000395203 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:55587800 C>T maps to ENST00000395203 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140580678 C>A maps to NM_018931.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140580678 C>A maps to NM_018931.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:92131251 G>A maps to NM_000466.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:92131251 G>A maps to NM_000466.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:32974304 C>A maps to NM_004572.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:32974304 C>A maps to NM_004572.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:8626753 G>A maps to NM_015192.2 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:8626753 G>A maps to NM_015192.2 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:157691364 C>A maps to NM_002847.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:157691364 C>A maps to NM_002847.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:134501636 G>A maps to NM_198679.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:134501636 G>A maps to NM_198679.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:107052702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:107052702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:92982957 C>A maps to NM_175634.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:92982957 C>A maps to NM_175634.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:158549152 A>G maps to NM_032861.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:158549152 A>G maps to NM_032861.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:108439435 C>A maps to NM_001013031.1 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:108439435 C>A maps to NM_001013031.1 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:125482927 C>G maps to NM_152713.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:125482927 C>G maps to NM_152713.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:89177554 G>T maps to NM_138960.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:89177554 G>T maps to NM_138960.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:45807213 C>T maps to NM_025077.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:45807213 C>T maps to NM_025077.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:167719509 C>A maps to NM_018974.3 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:167719509 C>A maps to NM_018974.3 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:78187555 T>C maps to NM_015017.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:78187555 T>C maps to NM_015017.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:123598270 G>A maps to NM_003455.2 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:123598270 G>A maps to NM_003455.2 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:22154762 C>A maps to NM_007153.3 G1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:22154762 C>A maps to NM_007153.3 G1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:81582793 C>G maps to NM_001033723.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:81582793 C>G maps to NM_001033723.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:436824 T>C maps to NM_133474.2 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:436824 T>C maps to NM_133474.2 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48313591 T>C maps to NM_152701.3 N1443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48313591 T>C maps to NM_152701.3 N1443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:48201238 C>T maps to NM_032583.3 K1365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:48201238 C>T maps to NM_032583.3 K1365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:65473743 G>A maps to NM_001005386.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:65473743 G>A maps to NM_001005386.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:28296686 C>A maps to NM_007038.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:28296686 C>A maps to NM_007038.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7626394 C>A maps to NM_020546.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7626394 C>A maps to NM_020546.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7626401 C>A maps to NM_020546.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7626401 C>A maps to NM_020546.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:131796003 T>A maps to NM_001115.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:131796003 T>A maps to NM_001115.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:131848680 C>A maps to NM_001115.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:131848680 C>A maps to NM_001115.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:186331121 T>C maps to ENST00000273784 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:186331121 T>C maps to ENST00000273784 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:106975227 A>G maps to NM_001624.2 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:106975227 A>G maps to NM_001624.2 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:130630758 G>A maps to ENST00000223836 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:130630758 G>A maps to ENST00000223836 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:202211398 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:202211398 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:71471903 C>A maps to NM_016519.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:71471903 C>A maps to NM_016519.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:110815422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:110815422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220100210 G>T maps to NM_001042410.1 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220100210 G>T maps to NM_001042410.1 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:24975515 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:24975515 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:119128424 G>C maps to NM_020754.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:119128424 G>C maps to NM_020754.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:23321834 A>T maps to NM_173081.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:23321834 A>T maps to NM_173081.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138845532 C>A maps to NM_173694.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138845532 C>A maps to NM_173694.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:45007671 C>G maps to NM_004048.2 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:45007671 C>G maps to NM_004048.2 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:33945218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:33945218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:9781177 G>T maps to NM_001003694.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:9781177 G>T maps to NM_001003694.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:32134158 A>G maps to NM_018169.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:32134158 A>G maps to NM_018169.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:2795874 G>T maps to NM_080739.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:2795874 G>T maps to NM_080739.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74803612 G>T maps to NM_138804.3 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74803612 G>T maps to NM_138804.3 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:165703509 A>T maps to NM_144980.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:165703509 A>T maps to NM_144980.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:181702005 A>T maps to ENST00000357570 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:181702005 A>T maps to ENST00000357570 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2022227 G>A maps to NM_172364.4 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2022227 G>A maps to NM_172364.4 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:86028353 C>A maps to NM_153184.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:86028353 C>A maps to NM_153184.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:219869056 G>A maps to NM_194302.2 S1724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:219869056 G>A maps to NM_194302.2 S1724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74574129 G>C maps to ENST00000321288 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74574129 G>C maps to ENST00000321288 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:7531613 A>T maps to ENST00000416109 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:7531613 A>T maps to ENST00000416109 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:35832041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:35832041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:121828230 C>A maps to NM_175862.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:121828230 C>A maps to NM_175862.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:59221421 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:59221421 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:25568620 T>C maps to NM_001792.3 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:25568620 T>C maps to NM_001792.3 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:61687544 G>C maps to NM_001796.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:61687544 G>C maps to NM_001796.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:243336058 A>G maps to NM_014812.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:243336058 A>G maps to NM_014812.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:13087591 A>G maps to NM_032142.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:13087591 A>G maps to NM_032142.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:111861778 G>A maps to NM_201653.2 W318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:111861778 G>A maps to NM_201653.2 W318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:240070930 G>A maps to NM_000740.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:240070930 G>A maps to NM_000740.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:101959778 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:101959778 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:78416081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:78416081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143017865 C>A maps to NM_000083.2 Y137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143017865 C>A maps to NM_000083.2 Y137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155233107 C>A maps to ENST00000368361 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155233107 C>A maps to ENST00000368361 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:100126552 G>C maps to NM_014361.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:100126552 G>C maps to NM_014361.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:111130464 T>A maps to NM_001846.2 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:111130464 T>A maps to NM_001846.2 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:238245033 T>C maps to NM_004369.3 P2903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:238245033 T>C maps to NM_004369.3 P2903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:61468463 A>C maps to NM_001853.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:61468463 A>C maps to NM_001853.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:207827199 A>G maps to NM_173077.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:207827199 A>G maps to NM_173077.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:197404271 G>T maps to NM_201253.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:197404271 G>T maps to NM_201253.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34174808 G>T maps to ENST00000373381 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34174808 G>T maps to ENST00000373381 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34190164 C>A maps to ENST00000373381 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34190164 C>A maps to ENST00000373381 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:101882786 A>T maps to ENST00000360264 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:101882786 A>T maps to ENST00000360264 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:39841120 G>C maps to ENST00000398904 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:39841120 G>C maps to ENST00000398904 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:125686416 C>A maps to NM_178470.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:125686416 C>A maps to NM_178470.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:27998032 G>T maps to NM_001017930.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:27998032 G>T maps to NM_001017930.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:169204671 G>C maps to NM_017631.5 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:169204671 G>C maps to NM_017631.5 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:115144126 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:115144126 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:436003 C>A maps to NM_014974.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:436003 C>A maps to NM_014974.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:196892697 C>A maps to NM_018897.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:196892697 C>A maps to NM_018897.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11660890 G>T maps to NM_001372.3 G2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11660890 G>T maps to NM_001372.3 G2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:101648709 C>A maps to ENST00000342239 E1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:101648709 C>A maps to ENST00000342239 E1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:29037051 G>T maps to NM_001944.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:29037051 G>T maps to NM_001944.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:67914656 G>A maps to NM_014329.3 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:67914656 G>A maps to NM_014329.3 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:83362355 C>A maps to NM_005711.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:83362355 C>A maps to NM_005711.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:137803055 C>G maps to NM_001964.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:137803055 C>G maps to NM_001964.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:77077086 G>A maps to NM_001042573.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:77077086 G>A maps to NM_001042573.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:132171232 G>T maps to NM_006208.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:132171232 G>T maps to NM_006208.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:5419721 C>G maps to NM_012307.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:5419721 C>G maps to NM_012307.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:72229802 G>A maps to NM_000503.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:72229802 G>A maps to NM_000503.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:118166263 A>T maps to NM_017709.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:118166263 A>T maps to NM_017709.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:79698088 G>A maps to NM_001170574.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:79698088 G>A maps to NM_001170574.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:29867047 C>T maps to ENST00000269209 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:29867047 C>T maps to ENST00000269209 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:58468385 C>A maps to NM_001114636.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:58468385 C>A maps to NM_001114636.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:187532545 T>A maps to ENST00000260147 K3286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:187532545 T>A maps to ENST00000260147 K3286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:207135630 G>T maps to NM_001170631.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:207135630 G>T maps to NM_001170631.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:157494129 G>C maps to NM_031281.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:157494129 G>C maps to NM_031281.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141993533 G>A maps to NM_001144935.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141993533 G>A maps to NM_001144935.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:176516638 G>T maps to NM_213647.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:176516638 G>T maps to NM_213647.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:34081943 C>T maps to NM_025135.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:34081943 C>T maps to NM_025135.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:39266238 C>A maps to NM_207361.4 T1586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:39266238 C>A maps to NM_207361.4 T1586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:5642886 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:5642886 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:96651789 C>A maps to NM_006581.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:96651789 C>A maps to NM_006581.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:39202015 G>T maps to ENST00000263405 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:39202015 G>T maps to ENST00000263405 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:33267089 G>A maps to NM_020474.3 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:33267089 G>A maps to NM_020474.3 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:96010438 A>T maps to NM_016417.2 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:96010438 A>T maps to NM_016417.2 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135428012 C>T maps to NM_153834.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135428012 C>T maps to NM_153834.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135431945 T>A maps to NM_153834.3 P2027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135431945 T>A maps to NM_153834.3 P2027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:8588828 C>A maps to NM_080819.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:8588828 C>A maps to NM_080819.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:94436365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:94436365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:94690558 G>C maps to NM_001510.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:94690558 G>C maps to NM_001510.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:102074321 A>T maps to NM_021956.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:102074321 A>T maps to NM_021956.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:23345106 C>T maps to NM_022482.3 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:23345106 C>T maps to NM_022482.3 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:18687613 T>A maps to NM_178425.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:18687613 T>A maps to NM_178425.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:19015513 C>A maps to NM_178425.2 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:19015513 C>A maps to NM_178425.2 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:26225651 G>A maps to NM_003532.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:26225651 G>A maps to NM_003532.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:143081223 T>C maps to NM_006734.3 K2067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:143081223 T>C maps to NM_006734.3 K2067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:186036966 A>G maps to NM_031935.2 V2569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:186036966 A>G maps to NM_031935.2 V2569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:54448763 C>A maps to NM_153633.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:54448763 C>A maps to NM_153633.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135594123 T>C maps to NM_014500.4 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135594123 T>C maps to NM_014500.4 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:63256622 G>T maps to NM_000524.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:63256622 G>T maps to NM_000524.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:154862698 C>A maps to NM_024012.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:154862698 C>A maps to NM_024012.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:130412614 C>A maps to NM_001170961.1 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:130412614 C>A maps to NM_001170961.1 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:133790154 C>A maps to NM_014987.1 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:133790154 C>A maps to NM_014987.1 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42186653 G>T maps to NM_001556.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42186653 G>T maps to NM_001556.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:70328488 A>G maps to NM_000206.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:70328488 A>G maps to NM_000206.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:170366650 C>A maps to NM_006063.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:170366650 C>A maps to NM_006063.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:19436594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:19436594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:18112662 G>T maps to NM_002252.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:18112662 G>T maps to NM_002252.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:143586459 G>T maps to NM_020768.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:143586459 G>T maps to NM_020768.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:62757887 C>A maps to NM_152688.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:62757887 C>A maps to NM_152688.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:61304154 G>T maps to NM_001129993.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:61304154 G>T maps to NM_001129993.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:107688430 C>A maps to NM_007356.2 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:107688430 C>A maps to NM_007356.2 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:126161781 A>T maps to NM_005573.3 K532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:126161781 A>T maps to NM_005573.3 K532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:2432449 C>A maps to NM_032737.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:2432449 C>A maps to NM_032737.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:141259432 G>T maps to NM_018557.2 C2891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:141259432 G>T maps to NM_018557.2 C2891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:165532868 C>A maps to NM_001005214.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:165532868 C>A maps to NM_001005214.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:91502283 A>T maps to NM_002345.3 L158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:91502283 A>T maps to NM_002345.3 L158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:30269347 C>A maps to NM_177404.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:30269347 C>A maps to NM_177404.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:141291191 G>T maps to NM_016249.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:141291191 G>T maps to NM_016249.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:16067612 C>A maps to NM_001102562.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:16067612 C>A maps to NM_001102562.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:58039570 G>A maps to NM_005912.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:58039570 G>A maps to NM_005912.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:8701313 A>G maps to NM_152599.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:8701313 A>G maps to NM_152599.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:89180005 C>A maps to NM_005941.4 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:89180005 C>A maps to NM_005941.4 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:50957558 G>T maps to NM_004533.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:50957558 G>T maps to NM_004533.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:59668400 G>T maps to NM_199290.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:59668400 G>T maps to NM_199290.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:23361955 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:23361955 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:115997622 T>C maps to NM_022569.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:115997622 T>C maps to NM_022569.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:152467371 G>T maps to NM_001164507.1 Y3938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:152467371 G>T maps to NM_001164507.1 Y3938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:73562349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:73562349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:104179253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:104179253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:16874685 G>T maps to ENST00000438489 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:16874685 G>T maps to ENST00000438489 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:102337744 C>A maps to NM_022052.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:102337744 C>A maps to NM_022052.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:86826107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:86826107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:67283821 G>A maps to NM_002547.2 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:67283821 G>A maps to NM_002547.2 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6866922 G>T maps to ENST00000379831 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6866922 G>T maps to ENST00000379831 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:125512434 C>A maps to ENST00000373684 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:125512434 C>A maps to ENST00000373684 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143792733 T>C maps to NM_001004135.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143792733 T>C maps to NM_001004135.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248637469 T>A maps to NM_001005495.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248637469 T>A maps to NM_001005495.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56247585 T>A maps to NM_001004707.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56247585 T>A maps to NM_001004707.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5462057 G>T maps to NM_001005288.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5462057 G>T maps to NM_001005288.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5142799 C>A maps to NM_001005222.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5142799 C>A maps to NM_001005222.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:55794779 C>A maps to NM_001005518.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:55794779 C>A maps to NM_001005518.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:118974077 G>A maps to NM_002581.3 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:118974077 G>A maps to NM_002581.3 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:58209102 C>A maps to NM_001040429.2 S808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:58209102 C>A maps to NM_001040429.2 S808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:67800784 C>A maps to NM_203487.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:67800784 C>A maps to NM_203487.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140306845 C>T maps to NM_018898.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140306845 C>T maps to NM_018898.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140563360 C>A maps to NM_020957.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140563360 C>A maps to NM_020957.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140736947 T>A maps to NM_018917.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140736947 T>A maps to NM_018917.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140782983 A>G maps to NM_018921.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140782983 A>G maps to NM_018921.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:82595464 T>G maps to NM_033026.5 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:82595464 T>G maps to NM_033026.5 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:92136427 G>A maps to NM_000466.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:92136427 G>A maps to NM_000466.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:209142259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:209142259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110535120 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110535120 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:51512865 T>A maps to NM_138694.3 S3787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:51512865 T>A maps to NM_138694.3 S3787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:28739720 G>A maps to NM_153021.4 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:28739720 G>A maps to NM_153021.4 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:118354339 G>T maps to NM_006229.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:118354339 G>T maps to NM_006229.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:7894004 C>A maps to NM_001142389.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:7894004 C>A maps to NM_001142389.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:43197381 C>A maps to NM_001005365.2 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:43197381 C>A maps to NM_001005365.2 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:130832524 C>T maps to NM_001099771.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:130832524 C>T maps to NM_001099771.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:43259795 C>A maps to NM_022115.3 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:43259795 C>A maps to NM_022115.3 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:68882116 C>T maps to NM_138964.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:68882116 C>T maps to NM_138964.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:120022253 C>A maps to NM_016644.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:120022253 C>A maps to NM_016644.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:98242851 C>A maps to NM_000264.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:98242851 C>A maps to NM_000264.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:8340468 T>C maps to NM_002839.3 R1709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:8340468 T>C maps to NM_002839.3 R1709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:157926394 C>G maps to NM_002847.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:157926394 C>G maps to NM_002847.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:58120940 G>T maps to NM_138453.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:58120940 G>T maps to NM_138453.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:160277143 G>T maps to NM_014247.2 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:160277143 G>T maps to NM_014247.2 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:24642161 G>T maps to NM_005132.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:24642161 G>T maps to NM_005132.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:117248702 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:117248702 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:89760498 C>A maps to NM_000326.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:89760498 C>A maps to NM_000326.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:68895599 C>T maps to NM_000329.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:68895599 C>T maps to NM_000329.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:49506545 C>G maps to NM_006666.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:49506545 C>G maps to NM_006666.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237617850 C>A maps to NM_001035.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237617850 C>A maps to NM_001035.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237620012 G>T maps to NM_001035.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237620012 G>T maps to NM_001035.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237995919 G>T maps to NM_001035.2 R4959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237995919 G>T maps to NM_001035.2 R4959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:33855183 T>G maps to NM_001036.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:33855183 T>G maps to NM_001036.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:26711500 C>A maps to ENST00000379061 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:26711500 C>A maps to ENST00000379061 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9238003 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9238003 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:58552872 C>A maps to NM_001160305.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:58552872 C>A maps to NM_001160305.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:123504057 G>A maps to NM_002351.4 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:123504057 G>A maps to NM_002351.4 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:99364188 G>T maps to NM_005073.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:99364188 G>T maps to NM_005073.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42302218 C>G maps to NM_006749.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42302218 C>G maps to NM_006749.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:19261612 C>A maps to NM_020689.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:19261612 C>A maps to NM_020689.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:118604334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:118604334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:85488008 G>T maps to NM_004213.3 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:85488008 G>T maps to NM_004213.3 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:205764003 C>T maps to NM_173854.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:205764003 C>T maps to NM_173854.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:95311003 G>T maps to NM_001114106.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:95311003 G>T maps to NM_001114106.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:8398029 C>T maps to ENST00000377479 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:8398029 C>T maps to ENST00000377479 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:20874845 T>A maps to NM_017435.4 L295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:20874845 T>A maps to NM_017435.4 L295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:151638446 G>C maps to ENST00000458013 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:151638446 G>C maps to ENST00000458013 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:118550774 T>C maps to NM_206996.2 V1493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:118550774 T>C maps to NM_206996.2 V1493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:44328185 C>A maps to NM_145026.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:44328185 C>A maps to NM_145026.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:42169373 C>A maps to ENST00000320955 V1217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:42169373 C>A maps to ENST00000320955 V1217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:90733066 C>A maps to ENST00000371927 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:90733066 C>A maps to ENST00000371927 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:197004483 T>C maps to NM_004226.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:197004483 T>C maps to NM_004226.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:48807909 C>A maps to NM_172311.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:48807909 C>A maps to NM_172311.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48046871 C>A maps to NM_152782.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48046871 C>A maps to NM_152782.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:104577476 C>A maps to NM_001059.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:104577476 C>A maps to NM_001059.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:102242440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:102242440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:120998995 G>T maps to NM_005422.2 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:120998995 G>T maps to NM_005422.2 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:20837664 T>C maps to NM_007110.4 E2498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:20837664 T>C maps to NM_007110.4 E2498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:106180774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:106180774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43525418 G>T maps to NM_201631.3 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43525418 G>T maps to NM_201631.3 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:44782157 A>G maps to NM_032256.1 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:44782157 A>G maps to NM_032256.1 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:108985619 G>A maps to NM_181724.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:108985619 G>A maps to NM_181724.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:60695129 C>T maps to NM_017870.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:60695129 C>T maps to NM_017870.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:94797463 C>T maps to NM_153704.5 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:94797463 C>T maps to NM_153704.5 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:24565622 C>A maps to NM_024893.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:24565622 C>A maps to NM_024893.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:52990024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:52990024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:235277205 T>C maps to NM_014765.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:235277205 T>C maps to NM_014765.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:10970031 G>C maps to NM_199261.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:10970031 G>C maps to NM_199261.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5655031 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5655031 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:14508071 G>T maps to NM_007118.2 T2945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:14508071 G>T maps to NM_007118.2 T2945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:135587493 T>C maps to NM_020389.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:135587493 T>C maps to NM_020389.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:45811201 G>A maps to ENST00000397932 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:45811201 G>A maps to ENST00000397932 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:12560565 A>G maps to NM_025265.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:12560565 A>G maps to NM_025265.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179434376 G>A maps to NM_133378.4 D22926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179434376 G>A maps to NM_133378.4 D22926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215901464 G>T maps to ENST00000366943 P3991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215901464 G>T maps to ENST00000366943 P3991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:30400248 G>A maps to NM_006447.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:30400248 G>A maps to NM_006447.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:132161730 G>C maps to NM_031907.1 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:132161730 G>C maps to NM_031907.1 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:43649514 C>A maps to NM_001195831.1 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:43649514 C>A maps to NM_001195831.1 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:100334678 C>A maps to ENST00000349350 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:100334678 C>A maps to ENST00000349350 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:141163053 A>T maps to NM_001080412.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:141163053 A>T maps to NM_001080412.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:147113996 G>C maps to NM_001168379.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:147113996 G>C maps to NM_001168379.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:74620297 C>T maps to NM_007345.3 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:74620297 C>T maps to NM_007345.3 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30935353 C>T maps to NM_014717.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30935353 C>T maps to NM_014717.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30935950 C>T maps to NM_014717.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30935950 C>T maps to NM_014717.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30936550 C>G maps to NM_014717.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30936550 C>G maps to NM_014717.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:31038848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:31038848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:125989913 C>A maps to NM_152412.2 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:125989913 C>A maps to NM_152412.2 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9027055 C>T maps to NM_144670.3 I1419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9027055 C>T maps to NM_144670.3 I1419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:20739700 A>G maps to NM_001163941.1 A760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:20739700 A>G maps to NM_001163941.1 A760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:33643509 T>C maps to NM_030955.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:33643509 T>C maps to NM_030955.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:49170885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:49170885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:10517224 C>T maps to NM_000480.2 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:10517224 C>T maps to NM_000480.2 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:108334145 G>A maps to NM_001146.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:108334145 G>A maps to NM_001146.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:114277465 G>A maps to NM_001148.4 V2564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:114277465 G>A maps to NM_001148.4 V2564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:37451776 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:37451776 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:99056232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:99056232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:21232754 C>A maps to NM_000384.2 E2329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:21232754 C>A maps to NM_000384.2 E2329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:24436372 G>A maps to NM_001650.4 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:24436372 G>A maps to NM_001650.4 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:69150987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:69150987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:31473872 G>T maps to ENST00000408912 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:31473872 G>T maps to ENST00000408912 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:55746029 G>T maps to NM_001719.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:55746029 G>T maps to NM_001719.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:49054301 G>A maps to NM_017822.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:49054301 G>A maps to NM_017822.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:64746740 A>G maps to NM_001170633.1 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:64746740 A>G maps to NM_001170633.1 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:24466138 T>A maps to NM_001007537.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:24466138 T>A maps to NM_001007537.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:35796646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:35796646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:131822123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:131822123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:61192386 A>T maps to NM_004056.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:61192386 A>T maps to NM_004056.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:64880681 T>C maps to NM_014404.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:64880681 T>C maps to NM_014404.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:57105360 A>T maps to NM_133459.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:57105360 A>T maps to NM_133459.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:32636279 A>T maps to NM_001008391.2 C528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:32636279 A>T maps to NM_001008391.2 C528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:37014313 G>C maps to NM_003914.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:37014313 G>C maps to NM_003914.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:14118280 G>T maps to NM_004233.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:14118280 G>T maps to NM_004233.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:19591192 G>T maps to NM_004934.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:19591192 G>T maps to NM_004934.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:19747346 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:19747346 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:80718705 C>T maps to NM_152342.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:80718705 C>T maps to NM_152342.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:369897 G>T maps to NM_006614.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:369897 G>T maps to NM_006614.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:19655528 C>A maps to NM_153221.2 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:19655528 C>A maps to NM_153221.2 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:86921162 A>C maps to NM_006536.5 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:86921162 A>C maps to NM_006536.5 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:3095549 G>T maps to NM_175607.1 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:3095549 G>T maps to NM_175607.1 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:238275929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:238275929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:130284366 T>C maps to NM_001102608.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:130284366 T>C maps to NM_001102608.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:129999467 C>A maps to NM_080385.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:129999467 C>A maps to NM_080385.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:93999765 G>T maps to NM_014912.4 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:93999765 G>T maps to NM_014912.4 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:2886895 C>A maps to NM_033225.5 L2600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:2886895 C>A maps to NM_033225.5 L2600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:68024265 G>T maps to ENST00000389042 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:68024265 G>T maps to ENST00000389042 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:117432022 G>T maps to NM_033427.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:117432022 G>T maps to NM_033427.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:145151543 C>T maps to NM_001916.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:145151543 C>T maps to NM_001916.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:57480688 G>A maps to ENST00000371231 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:57480688 G>A maps to ENST00000371231 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:27997671 G>T maps to NM_001017930.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:27997671 G>T maps to NM_001017930.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:56335291 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:56335291 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:169952147 T>A maps to NM_001142271.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:169952147 T>A maps to NM_001142271.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:32613933 C>T maps to ENST00000357033 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:32613933 C>T maps to ENST00000357033 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:70210004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:70210004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:11845781 G>T maps to NM_001372.3 E4275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:11845781 G>T maps to NM_001372.3 E4275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:225658115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:225658115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:113286151 A>G maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:113286151 A>G maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:71508495 A>G maps to NM_031889.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:71508495 A>G maps to NM_031889.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:77708994 G>T maps to NM_178543.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:77708994 G>T maps to NM_178543.3 E185*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z046-01A-01W-0746-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z046-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:212251659 G>T maps to NM_005235.2 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:212251659 G>T maps to NM_005235.2 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:166039813 C>G maps to NM_001017961.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:166039813 C>G maps to NM_001017961.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:15936727 C>T maps to NM_012304.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:15936727 C>T maps to NM_012304.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:27016639 G>T maps to NM_203371.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:27016639 G>T maps to NM_203371.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:159653964 G>C maps to NM_032532.2 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:159653964 G>C maps to NM_032532.2 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:52250064 G>T maps to NM_002029.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:52250064 G>T maps to NM_002029.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:48566014 C>A maps to NM_015030.1 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:48566014 C>A maps to NM_015030.1 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153792212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153792212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:54060341 G>A maps to NM_147193.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:54060341 G>A maps to NM_147193.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:194117583 C>T maps to NM_004488.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:194117583 C>T maps to NM_004488.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:34003900 C>G maps to NM_000841.1 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:34003900 C>G maps to NM_000841.1 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:613920 C>A maps to NM_001194.3 S632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:613920 C>A maps to NM_001194.3 S632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:31856407 T>A maps to ENST00000389961 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:31856407 T>A maps to ENST00000389961 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:28412877 C>A maps to NM_004667.4 L3503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:28412877 C>A maps to NM_004667.4 L3503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:139285161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:139285161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:245019446 G>A maps to NM_031844.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:245019446 G>A maps to NM_031844.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:152188370 G>A maps to NM_001009931.1 Q1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:152188370 G>A maps to NM_001009931.1 Q1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:102813361 G>T maps to NM_001111285.1 C109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:102813361 G>T maps to NM_001111285.1 C109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:50455157 A>T maps to NM_006060.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:50455157 A>T maps to NM_006060.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:55204168 C>A maps to NM_139017.4 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:55204168 C>A maps to NM_139017.4 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:1416815 G>A maps to NM_016532.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:1416815 G>A maps to NM_016532.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:271197 C>A maps to NM_001170738.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:271197 C>A maps to NM_001170738.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:54784970 G>T maps to NM_198510.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:54784970 G>T maps to NM_198510.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:8565261 G>A maps to NM_000216.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:8565261 G>A maps to NM_000216.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:155555928 G>T maps to NM_002239.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:155555928 G>T maps to NM_002239.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:133141907 C>A maps to NM_004519.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:133141907 C>A maps to NM_004519.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:57181701 C>T maps to NM_020722.1 N678N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:57181701 C>T maps to NM_020722.1 N678N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:72339178 C>A maps to NM_153209.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:72339178 C>A maps to NM_153209.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:39513460 C>A maps to NM_145027.4 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:39513460 C>A maps to NM_145027.4 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:55564615 G>T maps to NM_000222.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:55564615 G>T maps to NM_000222.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:38926661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:38926661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:9547771 G>T maps to NM_198560.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:9547771 G>T maps to NM_198560.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:90528675 C>T maps to NM_001102469.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:90528675 C>T maps to NM_001102469.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:7231198 G>A maps to NM_001105581.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:7231198 G>A maps to NM_001105581.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:21205486 C>T maps to NM_145109.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:21205486 C>T maps to NM_145109.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:220752760 C>T maps to NM_018650.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:220752760 C>T maps to NM_018650.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:13825937 A>T maps to NM_005913.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:13825937 A>T maps to NM_005913.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:88766208 T>C maps to ENST00000395102 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:88766208 T>C maps to ENST00000395102 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:74928823 C>A maps to NM_198955.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:74928823 C>A maps to NM_198955.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:42042456 G>T maps to ENST00000219905 E2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:42042456 G>T maps to ENST00000219905 E2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:154858047 C>A maps to NM_007289.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:154858047 C>A maps to NM_007289.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:181024399 G>A maps to NM_001531.2 *342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:181024399 G>A maps to NM_001531.2 *342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100684926 G>T maps to NM_001040105.1 P3410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100684926 G>T maps to NM_001040105.1 P3410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:195516951 C>T maps to NM_018406.5 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:195516951 C>T maps to NM_018406.5 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:1251243 C>A maps to ENST00000447027 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:1251243 C>A maps to ENST00000447027 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:10415821 C>A maps to NM_005963.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:10415821 C>A maps to NM_005963.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:786371 C>T maps to NM_022493.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:786371 C>T maps to NM_022493.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:97007829 G>T maps to NM_015341.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:97007829 G>T maps to NM_015341.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:29562684 A>G maps to NM_001042492.2 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:29562684 A>G maps to NM_001042492.2 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:54327143 C>T maps to ENST00000391773 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:54327143 C>T maps to ENST00000391773 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:55501455 G>A maps to NM_017852.3 Q811Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:55501455 G>A maps to NM_017852.3 Q811Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:74064820 A>G maps to NM_014886.3 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:74064820 A>G maps to NM_014886.3 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:229611465 G>A maps to NM_018230.2 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:229611465 G>A maps to NM_018230.2 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:228529172 G>C maps to NM_001098623.1 G5964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:228529172 G>C maps to NM_001098623.1 G5964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:50946007 C>T maps to NM_018245.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:50946007 C>T maps to NM_018245.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:29342470 G>A maps to NM_030959.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:29342470 G>A maps to NM_030959.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:6807164 G>T maps to NM_001004489.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:6807164 G>T maps to NM_001004489.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248085209 A>C maps to NM_001005522.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248085209 A>C maps to NM_001005522.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:22382624 A>T maps to NM_001005241.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:22382624 A>T maps to NM_001005241.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:4929315 C>T maps to NM_001004749.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:4929315 C>T maps to NM_001004749.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:55944950 C>T maps to NM_001005492.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:55944950 C>T maps to NM_001005492.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:141619403 C>T maps to NM_001001656.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:141619403 C>T maps to NM_001001656.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:150828257 C>A maps to NM_173493.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:150828257 C>A maps to NM_173493.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:19029762 C>T maps to NM_002584.2 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:19029762 C>T maps to NM_002584.2 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:31918700 C>A maps to NM_001191057.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:31918700 C>A maps to NM_001191057.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:68040018 G>A maps to NM_020715.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:68040018 G>A maps to NM_020715.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:79781774 C>A maps to NM_007055.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:79781774 C>A maps to NM_007055.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:12422845 T>A maps to NM_015869.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:12422845 T>A maps to NM_015869.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:160783242 C>T maps to NM_139245.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:160783242 C>T maps to NM_139245.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:186273330 C>A maps to NM_005807.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:186273330 C>A maps to NM_005807.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:23482714 C>G maps to NM_178161.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:23482714 C>G maps to NM_178161.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:23482795 C>T maps to NM_178161.2 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:23482795 C>T maps to NM_178161.2 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:41101011 G>C maps to ENST00000373198 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:41101011 G>C maps to ENST00000373198 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:180144453 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:180144453 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:17699558 G>C maps to ENST00000395776 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:17699558 G>C maps to ENST00000395776 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:114781671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:114781671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:129251464 G>T maps to NM_000539.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:129251464 G>T maps to NM_000539.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:12859270 C>A maps to NM_014859.4 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:12859270 C>A maps to NM_014859.4 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:55541304 A>G maps to NM_006269.1 K1621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:55541304 A>G maps to NM_006269.1 K1621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:187416469 C>T maps to NM_001004312.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:187416469 C>T maps to NM_001004312.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:179025800 A>G maps to NM_025158.3 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:179025800 A>G maps to NM_025158.3 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:38768369 G>A maps to NM_006514.2 F938F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:38768369 G>A maps to NM_006514.2 F938F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:37410516 C>T maps to NM_017438.3 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:37410516 C>T maps to NM_017438.3 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:14022191 A>G maps to NM_139167.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:14022191 A>G maps to NM_139167.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:156785869 G>T maps to NM_001161441.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:156785869 G>T maps to NM_001161441.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:75681540 A>T maps to NM_152697.4 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:75681540 A>T maps to NM_152697.4 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:40342701 C>G maps to NM_021097.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:40342701 C>G maps to NM_021097.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:40657407 G>T maps to NM_021097.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:40657407 G>T maps to NM_021097.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:144904539 T>C maps to NM_001144010.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:144904539 T>C maps to NM_001144010.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:95204270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:95204270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:55652954 C>T maps to NM_032681.3 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:55652954 C>T maps to NM_032681.3 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:105897157 C>A maps to NM_004257.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:105897157 C>A maps to NM_004257.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:82267548 C>T maps to ENST00000376537 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:82267548 C>T maps to ENST00000376537 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:7577141 C>A maps to NM_001126112.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:7577141 C>A maps to NM_001126112.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:26386765 T>A maps to NM_032588.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:26386765 T>A maps to NM_032588.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:894986 G>T maps to NM_004237.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:894986 G>T maps to NM_004237.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:112769635 C>A maps to NM_032028.3 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:112769635 C>A maps to NM_032028.3 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:30584428 G>C maps to NM_001011718.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:30584428 G>C maps to NM_001011718.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:217006039 C>T maps to NM_021141.3 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:217006039 C>T maps to NM_021141.3 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:751703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:751703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:145157427 C>T maps to NM_014795.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:145157427 C>T maps to NM_014795.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:22271934 T>C maps to NM_033468.2 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:22271934 T>C maps to NM_033468.2 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:45130998 C>A maps to NM_018102.3 G327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:45130998 C>A maps to NM_018102.3 G327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:57081647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:57081647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:52825490 C>T maps to NM_144684.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:52825490 C>T maps to NM_144684.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:22847467 G>T maps to NM_020855.2 G333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:22847467 G>T maps to NM_020855.2 G333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:31039160 G>T maps to NM_014717.1 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:31039160 G>T maps to NM_014717.1 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:113955336 C>T maps to NM_007136.3 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:113955336 C>T maps to NM_007136.3 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:28284105 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:28284105 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:20232313 C>T maps to ENST00000389655 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:20232313 C>T maps to ENST00000389655 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:13080791 C>T maps to NM_152654.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:13080791 C>T maps to NM_152654.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr14:95592940 T>C maps to NM_177438.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr14:95592940 T>C maps to NM_177438.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chrX:34149570 G>A maps to NM_203408.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chrX:34149570 G>A maps to NM_203408.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr9:84606359 G>A maps to NM_001001670.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr9:84606359 G>A maps to NM_001001670.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr4:158281078 G>A maps to NM_000826.3 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr4:158281078 G>A maps to NM_000826.3 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:42734572 G>C maps to NM_020707.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:42734572 G>C maps to NM_020707.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:26107823 G>A maps to NM_005323.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:26107823 G>A maps to NM_005323.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:51961676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:51961676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr9:2056742 C>T maps to NM_003070.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr9:2056742 C>T maps to NM_003070.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:113667648 C>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:113667648 C>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:39832385 G>A maps to NM_015035.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:39832385 G>A maps to NM_015035.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:39832733 G>A maps to NM_015035.3 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:39832733 G>A maps to NM_015035.3 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:97916894 C>G maps to NM_014803.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:97916894 C>G maps to NM_014803.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:25038480 G>C maps to NM_032501.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:25038480 G>C maps to NM_032501.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:1323906 A>G maps to NM_030782.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:1323906 A>G maps to NM_030782.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:57493629 C>T maps to NM_020312.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:57493629 C>T maps to NM_020312.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:46871355 C>T maps to NM_001441.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:46871355 C>T maps to NM_001441.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:152860003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:152860003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:39202819 C>T maps to ENST00000263405 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:39202819 C>T maps to ENST00000263405 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr10:26581847 C>A maps to NM_001134366.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr10:26581847 C>A maps to NM_001134366.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:35789560 G>A maps to NM_002133.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:35789560 G>A maps to NM_002133.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:30898036 C>T maps to NM_004798.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:30898036 C>T maps to NM_004798.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:76363722 T>G maps to NM_002440.2 Y829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:76363722 T>G maps to NM_002440.2 Y829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:10432553 G>A maps to NM_017534.5 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:10432553 G>A maps to NM_017534.5 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:57424943 T>C maps to NM_005379.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:57424943 T>C maps to NM_005379.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:66847734 A>T maps to ENST00000359087 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:66847734 A>T maps to ENST00000359087 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:58314361 C>T maps to NM_001080492.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:58314361 C>T maps to NM_001080492.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr21:37418121 G>A maps to NM_017438.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr21:37418121 G>A maps to NM_017438.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:154148673 T>C maps to NM_001043351.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:154148673 T>C maps to NM_001043351.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:22868966 G>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:22868966 G>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:17743622 G>A maps to ENST00000428389 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:17743622 G>A maps to ENST00000428389 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:52603770 C>A maps to NM_138932.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:52603770 C>A maps to NM_138932.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:89385033 G>A maps to NM_013227.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:89385033 G>A maps to NM_013227.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20648731 C>A maps to NM_052956.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20648731 C>A maps to NM_052956.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:4218087 C>T maps to ENST00000262970 N1067N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:4218087 C>T maps to ENST00000262970 N1067N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:241631350 C>T maps to ENST00000429564 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:241631350 C>T maps to ENST00000429564 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:115298844 C>T maps to NM_173800.4 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:115298844 C>T maps to NM_173800.4 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:5683787 C>T maps to NM_024701.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:5683787 C>T maps to NM_024701.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:63544124 C>T maps to NM_000706.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:63544124 C>T maps to NM_000706.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:1394318 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:1394318 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:31480657 G>T maps to NM_032849.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:31480657 G>T maps to NM_032849.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:54502969 C>A maps to NM_145814.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:54502969 C>A maps to NM_145814.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:112324419 C>A maps to ENST00000447230 R910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:112324419 C>A maps to ENST00000447230 R910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:44856176 C>A maps to NM_021248.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:44856176 C>A maps to NM_021248.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:175995736 G>C maps to NM_001171976.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:175995736 G>C maps to NM_001171976.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:86891152 T>A maps to NM_006536.5 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:86891152 T>A maps to NM_006536.5 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:70850844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:70850844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139614396 G>A maps to NM_152888.1 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139614396 G>A maps to NM_152888.1 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:227973938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:227973938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:228009237 T>C maps to ENST00000396625 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:228009237 T>C maps to ENST00000396625 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:62228014 G>T maps to NM_152516.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:62228014 G>T maps to NM_152516.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:49426537 T>C maps to NM_001143887.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:49426537 T>C maps to NM_001143887.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:12798850 C>A maps to NM_018340.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:12798850 C>A maps to NM_018340.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:8621241 C>T maps to NM_001014447.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:8621241 C>T maps to NM_001014447.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:197404098 G>T maps to NM_201253.2 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:197404098 G>T maps to NM_201253.2 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:3205672 T>A maps to NM_033225.5 G1105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:3205672 T>A maps to NM_033225.5 G1105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:113421256 C>A maps to NM_198123.1 V1800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:113421256 C>A maps to NM_198123.1 V1800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:138260224 A>T maps to ENST00000355078 K525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:138260224 A>T maps to ENST00000355078 K525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:156787322 C>T maps to ENST00000442283 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:156787322 C>T maps to ENST00000442283 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:113603730 G>A maps to NM_001111322.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:113603730 G>A maps to NM_001111322.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:19132105 C>A maps to NM_022719.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:19132105 C>A maps to NM_022719.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:46972732 C>T maps to NM_147192.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:46972732 C>T maps to NM_147192.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167096833 C>T maps to NM_001080426.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167096833 C>T maps to NM_001080426.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:95662046 T>C maps to NM_004411.4 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:95662046 T>C maps to NM_004411.4 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:44109565 T>C maps to ENST00000420999 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:44109565 T>C maps to ENST00000420999 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:39992302 G>T maps to NM_052846.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:39992302 G>T maps to NM_052846.1 Y163*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z049-01A-01W-0746-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z049-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:89499353 C>A maps to NM_005233.5 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:89499353 C>A maps to NM_005233.5 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:62135164 G>A maps to NM_001433.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:62135164 G>A maps to NM_001433.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:38937412 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:38937412 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76828894 G>A maps to NM_006682.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76828894 G>A maps to NM_006682.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97053947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97053947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:133780762 G>T maps to NM_001145106.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:133780762 G>T maps to NM_001145106.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:109268417 C>T maps to NM_001144937.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:109268417 C>T maps to NM_001144937.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42635671 A>T maps to NM_001466.3 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42635671 A>T maps to NM_001466.3 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42636024 G>A maps to NM_001466.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42636024 G>A maps to NM_001466.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:6604785 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:6604785 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167038195 C>T maps to NM_005814.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167038195 C>T maps to NM_005814.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131487497 G>T maps to NM_207364.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131487497 G>T maps to NM_207364.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:90021006 T>G maps to NM_032119.3 L3337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:90021006 T>G maps to NM_032119.3 L3337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:90085635 A>T maps to NM_032119.3 R4671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:90085635 A>T maps to NM_032119.3 R4671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:126173023 T>A maps to NM_001127323.1 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:126173023 T>A maps to NM_001127323.1 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:45946097 C>G maps to NM_152312.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:45946097 C>G maps to NM_152312.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:228646195 C>T maps to NM_175055.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:228646195 C>T maps to NM_175055.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:143092971 G>A maps to NM_006734.3 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:143092971 G>A maps to NM_006734.3 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:161495986 C>T maps to NM_002155.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:161495986 C>T maps to NM_002155.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:47115535 C>T maps to NM_006546.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:47115535 C>T maps to NM_006546.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:57828905 C>T maps to NM_005538.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:57828905 C>T maps to NM_005538.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:75979001 G>T maps to NM_006633.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:75979001 G>T maps to NM_006633.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17945770 G>T maps to NM_000215.3 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17945770 G>T maps to NM_000215.3 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:154510156 C>T maps to NM_001131007.1 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:154510156 C>T maps to NM_001131007.1 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:138576797 G>T maps to NM_020340.4 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:138576797 G>T maps to NM_020340.4 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:10338103 C>T maps to ENST00000377086 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:10338103 C>T maps to ENST00000377086 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:66031146 A>T maps to NM_022822.2 K257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:66031146 A>T maps to NM_022822.2 K257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:70293520 C>A maps to NM_020866.2 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:70293520 C>A maps to NM_020866.2 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:32127564 G>T maps to NM_181619.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:32127564 G>T maps to NM_181619.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11213427 G>A maps to NM_000527.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11213427 G>A maps to NM_000527.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:226076565 G>A maps to NM_020997.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:226076565 G>A maps to NM_020997.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:206767040 G>T maps to NM_006893.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:206767040 G>T maps to NM_006893.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96315553 C>T maps to NM_005575.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96315553 C>T maps to NM_005575.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:82456357 A>T maps to ENST00000370717 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:82456357 A>T maps to ENST00000370717 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:47317081 A>T maps to NM_003682.3 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:47317081 A>T maps to NM_003682.3 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:27839659 C>T maps to NM_182506.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:27839659 C>T maps to NM_182506.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:23889964 G>T maps to NM_019066.4 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:23889964 G>T maps to NM_019066.4 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:136926373 C>A maps to NM_005923.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:136926373 C>A maps to NM_005923.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:30747104 G>A maps to NM_005204.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:30747104 G>A maps to NM_005204.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:58162891 C>A maps to ENST00000408972 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:58162891 C>A maps to ENST00000408972 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:39883914 C>A maps to ENST00000425303 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:39883914 C>A maps to ENST00000425303 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:131208915 T>A maps to ENST00000425847 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:131208915 T>A maps to ENST00000425847 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:237058850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:237058850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100676861 C>A maps to NM_001040105.1 S722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100676861 C>A maps to NM_001040105.1 S722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30408010 G>C maps to NM_033118.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30408010 G>C maps to NM_033118.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:18058424 C>A maps to ENST00000205890 A2742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:18058424 C>A maps to ENST00000205890 A2742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:109817396 C>A maps to NM_015011.1 S1749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:109817396 C>A maps to NM_015011.1 S1749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:8601851 G>T maps to NM_012335.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:8601851 G>T maps to NM_012335.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:54925988 C>A maps to NM_005337.4 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:54925988 C>A maps to NM_005337.4 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56569689 C>T maps to NM_153447.4 N1128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56569689 C>T maps to NM_153447.4 N1128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:120429207 G>T maps to NM_002514.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:120429207 G>T maps to NM_002514.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:139232108 G>T maps to NM_013982.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:139232108 G>T maps to NM_013982.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:88576115 C>T maps to NM_001012338.1 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:88576115 C>T maps to NM_001012338.1 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16870092 G>T maps to ENST00000438489 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16870092 G>T maps to ENST00000438489 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:123785935 G>T maps to NM_001163278.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:123785935 G>T maps to NM_001163278.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248309177 T>C maps to NM_001004690.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248309177 T>C maps to NM_001004690.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:3195486 G>T maps to ENST00000397187 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:3195486 G>T maps to ENST00000397187 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:140590239 C>A maps to NM_018932.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:140590239 C>A maps to NM_018932.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:41966200 C>T maps to NM_001164595.1 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:41966200 C>T maps to NM_001164595.1 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76984658 G>C maps to NM_017439.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76984658 G>C maps to NM_017439.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:144995162 C>A maps to NM_201380.2 L3079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:144995162 C>A maps to NM_201380.2 L3079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:41974849 C>T maps to NM_002676.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:41974849 C>T maps to NM_002676.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:89870506 C>A maps to NM_002693.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:89870506 C>A maps to NM_002693.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:40902380 G>T maps to NM_181882.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:40902380 G>T maps to NM_181882.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43519364 A>T maps to ENST00000306308 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43519364 A>T maps to ENST00000306308 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:173855581 T>C maps to NM_007023.3 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:173855581 T>C maps to NM_007023.3 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:173891807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:173891807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:130897669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:130897669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:48916850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:48916850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:103294652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:103294652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:14080873 G>A maps to NM_002918.4 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:14080873 G>A maps to NM_002918.4 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:40554089 G>C maps to NM_002930.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:40554089 G>C maps to NM_002930.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:78320201 C>T maps to NM_020914.4 I2738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:78320201 C>T maps to NM_020914.4 I2738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:7035937 G>T maps to NM_080657.4 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:7035937 G>T maps to NM_080657.4 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:46318260 T>A maps to NM_030785.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:46318260 T>A maps to NM_030785.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39037099 G>T maps to NM_000540.2 E4010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39037099 G>T maps to NM_000540.2 E4010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:65745040 G>T maps to NM_005146.4 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:65745040 G>T maps to NM_005146.4 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:108954774 C>A maps to NM_014706.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:108954774 C>A maps to NM_014706.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:38622697 G>T maps to NM_001099404.1 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:38622697 G>T maps to NM_001099404.1 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:101990178 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:101990178 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:42529997 C>A maps to NM_015559.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:42529997 C>A maps to NM_015559.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:164780196 C>A maps to NM_001041.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:164780196 C>A maps to NM_001041.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:48500072 G>T maps to NM_000338.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:48500072 G>T maps to NM_000338.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:101370758 C>A maps to NM_031212.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:101370758 C>A maps to NM_031212.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:142228514 C>A maps to NM_001080431.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:142228514 C>A maps to NM_001080431.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:47940788 C>G maps to NM_015063.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:47940788 C>G maps to NM_015063.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:45361250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:45361250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220342496 G>T maps to NM_005876.4 E1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220342496 G>T maps to NM_005876.4 E1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:40996037 G>T maps to NM_020971.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:40996037 G>T maps to NM_020971.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:126276452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:126276452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:184938370 G>T maps to NM_020225.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:184938370 G>T maps to NM_020225.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:48046776 G>A maps to NM_152782.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:48046776 G>A maps to NM_152782.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:46345508 C>A maps to NM_004819.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:46345508 C>A maps to NM_004819.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:123846989 G>T maps to NM_206862.2 E1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:123846989 G>T maps to NM_206862.2 E1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:46663670 G>T maps to NM_001010870.2 E2054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:46663670 G>T maps to NM_001010870.2 E2054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:27197412 T>C maps to NM_000459.3 Y575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:27197412 T>C maps to NM_000459.3 Y575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:70342447 C>T maps to NM_005078.2 E769E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:70342447 C>T maps to NM_005078.2 E769E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:166986902 C>T maps to ENST00000507499 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:166986902 C>T maps to ENST00000507499 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:38829071 C>A maps to NM_006068.3 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:38829071 C>A maps to NM_006068.3 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:129389290 C>A maps to NM_001017395.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:129389290 C>A maps to NM_001017395.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:129559373 C>A maps to NM_133448.2 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:129559373 C>A maps to NM_133448.2 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:201334413 C>A maps to ENST00000421663 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:201334413 C>A maps to ENST00000421663 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:62521252 A>T maps to NM_199360.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:62521252 A>T maps to NM_199360.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:21498832 C>A maps to NM_173846.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:21498832 C>A maps to NM_173846.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:45504113 G>T maps to NM_003274.4 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:45504113 G>T maps to NM_003274.4 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:41197839 C>A maps to NM_198153.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:41197839 C>A maps to NM_198153.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:72945893 G>T maps to NM_007332.2 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:72945893 G>T maps to NM_007332.2 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:38320544 G>A maps to NM_003306.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:38320544 G>A maps to NM_003306.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:98557025 G>T maps to ENST00000359863 V2127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:98557025 G>T maps to ENST00000359863 V2127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:39162657 G>A maps to ENST00000301819 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:39162657 G>A maps to ENST00000301819 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:96222766 C>T maps to NM_003728.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:96222766 C>T maps to NM_003728.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:6965283 G>T maps to NM_001098536.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:6965283 G>T maps to NM_001098536.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:12304474 C>T maps to NM_015378.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:12304474 C>T maps to NM_015378.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:140048959 C>G maps to NM_017706.4 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:140048959 C>G maps to NM_017706.4 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:37381787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:37381787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:50278347 G>T maps to NM_014838.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:50278347 G>T maps to NM_014838.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:52926895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:52926895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:18297070 G>T maps to ENST00000401790 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:18297070 G>T maps to ENST00000401790 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:337569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:337569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:133764455 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:133764455 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178505711 A>G maps to NM_014594.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178505711 A>G maps to NM_014594.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:148801675 C>T maps to NM_001001661.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:148801675 C>T maps to NM_001001661.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:89034565 G>T maps to NM_004827.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:89034565 G>T maps to NM_004827.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:98129747 T>G maps to NM_025190.3 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:98129747 T>G maps to NM_025190.3 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:201464398 G>A maps to NM_001159.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:201464398 G>A maps to NM_001159.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:141039357 G>A maps to NM_022481.5 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:141039357 G>A maps to NM_022481.5 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:197074075 C>T maps to NM_018136.4 K1435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:197074075 C>T maps to NM_018136.4 K1435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:119737556 C>A maps to ENST00000313400 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:119737556 C>A maps to ENST00000313400 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:60688843 G>A maps to NM_022893.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:60688843 G>A maps to NM_022893.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:113533733 T>G maps to NM_018392.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:113533733 T>G maps to NM_018392.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:54466476 C>G maps to NM_031895.5 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:54466476 C>G maps to NM_031895.5 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:78073487 C>A maps to NM_017950.2 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:78073487 C>A maps to NM_017950.2 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:25593715 C>T maps to NM_001792.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:25593715 C>T maps to NM_001792.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:130290028 C>A maps to NM_001102608.1 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:130290028 C>A maps to NM_001102608.1 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:207648400 C>T maps to NM_001006658.2 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:207648400 C>T maps to NM_001006658.2 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:28843964 G>A maps to NM_182898.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:28843964 G>A maps to NM_182898.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:94704545 T>G maps to NM_016403.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:94704545 T>G maps to NM_016403.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:13868089 G>A maps to NM_001369.2 A1282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:13868089 G>A maps to NM_001369.2 A1282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:109027098 A>G maps to NM_138815.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:109027098 A>G maps to NM_138815.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:22927467 C>T maps to NM_020526.3 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:22927467 C>T maps to NM_020526.3 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:1390694 C>T maps to NM_001452.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:1390694 C>T maps to NM_001452.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:183772674 G>A maps to NM_130770.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:183772674 G>A maps to NM_130770.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:15688875 G>A maps to NM_003638.1 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:15688875 G>A maps to NM_003638.1 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:137759815 C>A maps to NM_016604.3 S1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:137759815 C>A maps to NM_016604.3 S1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:57182421 G>A maps to NM_020722.1 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:57182421 G>A maps to NM_020722.1 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:160243896 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:160243896 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr21:46032169 C>T maps to NM_198695.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr21:46032169 C>T maps to NM_198695.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:152777924 G>A maps to NM_178351.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:152777924 G>A maps to NM_178351.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:25972922 G>T maps to NM_009587.2 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:25972922 G>T maps to NM_009587.2 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:77764362 G>A maps to NM_012301.3 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:77764362 G>A maps to NM_012301.3 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:16877804 G>A maps to NM_012334.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:16877804 G>A maps to NM_012334.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:57430773 C>T maps to NM_005379.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:57430773 C>T maps to NM_005379.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:171258114 C>T maps to NM_138995.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:171258114 C>T maps to NM_138995.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:133489352 C>T maps to NM_207363.2 G1800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:133489352 C>T maps to NM_207363.2 G1800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:247586535 A>C maps to NM_004895.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:247586535 A>C maps to NM_004895.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:7950013 A>G maps to NM_001004461.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:7950013 A>G maps to NM_001004461.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:247920883 G>T maps to NM_012353.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:247920883 G>T maps to NM_012353.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:49974693 C>A maps to NM_001001955.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:49974693 C>A maps to NM_001001955.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:55432992 C>T maps to NM_001004704.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:55432992 C>T maps to NM_001004704.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chrX:38211914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chrX:38211914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:152553813 G>A maps to NM_002563.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:152553813 G>A maps to NM_002563.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:48535580 C>T maps to NM_001166686.1 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:48535580 C>T maps to NM_001166686.1 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:13228215 C>T maps to NM_030948.1 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:13228215 C>T maps to NM_030948.1 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:72158692 T>C maps to NM_031293.2 K854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:72158692 T>C maps to NM_031293.2 K854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:23526759 T>A maps to NM_020227.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:23526759 T>A maps to NM_020227.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:45258348 G>A maps to ENST00000352766 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:45258348 G>A maps to ENST00000352766 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:2968982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:2968982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:43696228 C>T maps to ENST00000374459 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:43696228 C>T maps to ENST00000374459 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:7164553 C>T maps to NM_014746.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:7164553 C>T maps to NM_014746.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:40009751 T>A maps to NM_182704.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:40009751 T>A maps to NM_182704.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:61324184 G>T maps to NM_006919.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:61324184 G>T maps to NM_006919.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:164758795 G>A maps to NM_001041.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:164758795 G>A maps to NM_001041.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:92307873 T>C maps to NM_134266.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:92307873 T>C maps to NM_134266.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75716950 G>A maps to NM_152697.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75716950 G>A maps to NM_152697.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:55730215 C>T maps to NM_001043.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:55730215 C>T maps to NM_001043.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:168233476 G>T maps to NM_003062.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:168233476 G>T maps to NM_003062.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:70420143 C>T maps to NM_001034852.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:70420143 C>T maps to NM_001034852.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:31008313 G>T maps to NM_052874.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:31008313 G>T maps to NM_052874.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:25313015 C>T maps to NM_024838.4 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:25313015 C>T maps to NM_024838.4 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:248028108 G>T maps to NM_015431.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:248028108 G>T maps to NM_015431.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:116616125 C>G maps to NM_014112.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:116616125 C>G maps to NM_014112.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:179616665 T>C maps to ENST00000375038 R3489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:179616665 T>C maps to ENST00000375038 R3489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:54793049 G>A maps to ENST00000260323 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:54793049 G>A maps to ENST00000260323 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:61577740 G>A maps to NM_014709.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:61577740 G>A maps to NM_014709.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:69203447 G>A maps to NM_001031732.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:69203447 G>A maps to NM_001031732.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:62407079 G>A maps to NM_025224.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:62407079 G>A maps to NM_025224.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:41106914 C>A maps to NM_001136042.2 G485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:41106914 C>A maps to NM_001136042.2 G485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:150554718 C>G maps to ENST00000416793 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:150554718 C>G maps to ENST00000416793 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:29398931 G>T maps to NM_005503.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:29398931 G>T maps to NM_005503.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:201683536 C>T maps to ENST00000452790 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:201683536 C>T maps to ENST00000452790 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:93065483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:93065483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:37964469 C>T maps to NM_152243.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:37964469 C>T maps to NM_152243.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:50833699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:50833699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:136700193 C>A maps to NM_001006628.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:136700193 C>A maps to NM_001006628.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:151135180 G>A maps to NM_144727.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:151135180 G>A maps to NM_144727.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:131409602 C>A maps to NM_000758.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:131409602 C>A maps to NM_000758.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:16990534 G>T maps to NM_001081.3 V1717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:16990534 G>T maps to NM_001081.3 V1717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:117303887 C>G maps to NM_020693.2 L1724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:117303887 C>G maps to NM_020693.2 L1724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:63999764 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:63999764 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:171687700 A>T maps to NM_000817.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:171687700 A>T maps to NM_000817.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:155208061 C>T maps to NM_001005742.2 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:155208061 C>T maps to NM_001005742.2 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:46184988 G>T maps to NM_000164.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:46184988 G>T maps to NM_000164.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:39341673 G>A maps to NM_030772.4 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:39341673 G>A maps to NM_030772.4 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:48665047 C>T maps to ENST00000444343 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:48665047 C>T maps to ENST00000444343 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:20349774 G>T maps to NM_002196.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:20349774 G>T maps to NM_002196.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:2749502 C>T maps to NM_033267.4 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:2749502 C>T maps to NM_033267.4 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:51901863 T>A maps to NM_032559.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:51901863 T>A maps to NM_032559.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:51022504 C>T maps to NM_001080457.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:51022504 C>T maps to NM_001080457.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:23306130 C>T maps to NM_004995.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:23306130 C>T maps to NM_004995.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:50580511 T>C maps to NM_018995.2 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:50580511 T>C maps to NM_018995.2 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:100681800 T>A maps to NM_001040105.1 P2368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:100681800 T>A maps to NM_001040105.1 P2368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:3229154 C>T maps to NM_015419.3 V2363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:3229154 C>T maps to NM_015419.3 V2363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:103517298 C>G maps to NM_003998.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:103517298 C>G maps to NM_003998.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:74879876 C>G maps to NM_015901.4 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:74879876 C>G maps to NM_015901.4 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:150840816 G>T maps to NM_173493.2 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:150840816 G>T maps to NM_173493.2 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:37627428 C>T maps to NM_002872.3 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:37627428 C>T maps to NM_002872.3 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:48383952 G>T maps to NM_002900.2 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:48383952 G>T maps to NM_002900.2 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:50408808 C>A maps to NM_020436.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:50408808 C>A maps to NM_020436.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:219255991 C>G maps to NM_000578.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:219255991 C>G maps to NM_000578.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:32445601 A>C maps to NM_001193513.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:32445601 A>C maps to NM_001193513.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:142716994 G>T maps to NM_001184749.1 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:142716994 G>T maps to NM_001184749.1 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:41019461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:41019461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:30700550 G>A maps to NM_031271.3 Q1995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:30700550 G>A maps to NM_031271.3 Q1995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:151820328 G>T maps to NM_182578.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:151820328 G>T maps to NM_182578.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:48754089 G>T maps to NM_001167947.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:48754089 G>T maps to NM_001167947.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:130356549 G>A maps to NM_052933.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:130356549 G>A maps to NM_052933.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:79929508 A>G maps to ENST00000376646 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:79929508 A>G maps to ENST00000376646 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:219736486 A>T maps to NM_006522.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:219736486 A>T maps to NM_006522.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:53344721 C>T maps to NM_001008801.1 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:53344721 C>T maps to NM_001008801.1 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:71591197 A>T maps to NM_014497.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:71591197 A>T maps to NM_014497.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:115335600 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:115335600 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:76740087 G>A maps to NM_024685.3 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:76740087 G>A maps to NM_024685.3 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:100615128 G>A maps to NM_000061.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:100615128 G>A maps to NM_000061.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:14015674 C>A maps to ENST00000454313 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:14015674 C>A maps to ENST00000454313 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:60503479 C>T maps to NM_001794.2 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:60503479 C>T maps to NM_001794.2 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:121237373 T>A maps to NM_021110.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:121237373 T>A maps to NM_021110.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:101797642 C>A maps to NM_001855.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:101797642 C>A maps to NM_001855.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:140953388 G>T maps to ENST00000398557 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:140953388 G>T maps to ENST00000398557 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:154132271 A>G maps to NM_000132.3 N1969N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:154132271 A>G maps to NM_000132.3 N1969N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:157666024 G>A maps to NM_052939.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:157666024 G>A maps to NM_052939.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr18:11752921 C>T maps to NM_182978.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr18:11752921 C>T maps to NM_182978.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:22394314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:22394314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:156721097 G>T maps to ENST00000502959 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:156721097 G>T maps to ENST00000502959 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:29938086 G>T maps to NM_014271.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:29938086 G>T maps to NM_014271.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:155566146 C>A maps to NM_002239.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:155566146 C>A maps to NM_002239.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:200960256 C>A maps to NM_017596.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:200960256 C>A maps to NM_017596.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:52017210 T>C maps to NM_153374.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:52017210 T>C maps to NM_153374.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:9003350 A>G maps to NM_024690.2 L13362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:9003350 A>G maps to NM_024690.2 L13362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:54377403 G>T maps to NM_001020818.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:54377403 G>T maps to NM_001020818.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:10399400 C>A maps to NM_005963.3 E1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:10399400 C>A maps to NM_005963.3 E1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:204939792 C>T maps to ENST00000367172 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:204939792 C>T maps to ENST00000367172 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:153659681 C>T maps to NM_000906.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:153659681 C>T maps to NM_000906.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:156135900 G>C maps to NM_000910.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:156135900 G>C maps to NM_000910.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:64434818 C>A maps to NM_015080.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:64434818 C>A maps to NM_015080.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:123525994 C>T maps to NM_001163278.1 T1865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:123525994 C>T maps to NM_001163278.1 T1865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:247752434 C>A maps to NM_001001915.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:247752434 C>A maps to NM_001001915.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:55433271 T>C maps to NM_001004704.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:55433271 T>C maps to NM_001004704.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:48328541 C>A maps to NM_001004725.1 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:48328541 C>A maps to NM_001004725.1 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:35454044 C>A maps to NM_015430.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:35454044 C>A maps to NM_015430.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:75070314 C>A maps to ENST00000257665 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:75070314 C>A maps to ENST00000257665 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:84233709 C>T maps to NM_153362.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:84233709 C>T maps to NM_153362.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:17698661 G>T maps to ENST00000395776 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:17698661 G>T maps to ENST00000395776 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:130926459 C>A maps to NM_015347.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:130926459 C>A maps to NM_015347.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:104314691 C>T maps to NM_019592.5 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:104314691 C>T maps to NM_019592.5 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:10465304 T>C maps to NM_178857.5 V2101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:10465304 T>C maps to NM_178857.5 V2101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:92909096 C>A maps to NM_153646.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:92909096 C>A maps to NM_153646.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:220101686 G>T maps to NM_018713.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:220101686 G>T maps to NM_018713.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:135510102 G>T maps to NM_001001419.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:135510102 G>T maps to NM_001001419.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:88405917 G>T maps to NM_198274.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:88405917 G>T maps to NM_198274.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr18:67992311 G>T maps to NM_004232.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr18:67992311 G>T maps to NM_004232.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:26383939 C>A maps to NM_005086.4 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:26383939 C>A maps to NM_005086.4 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:1479314 C>A maps to NM_014188.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:1479314 C>A maps to NM_014188.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:57409554 G>A maps to NM_013251.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:57409554 G>A maps to NM_013251.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:153556304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:153556304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:209955489 C>A maps to NM_025228.2 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:209955489 C>A maps to NM_025228.2 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:113222826 G>T maps to NM_017868.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:113222826 G>T maps to NM_017868.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:122667741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:122667741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:128476970 G>A maps to NM_018383.4 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:128476970 G>A maps to NM_018383.4 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:122361784 G>A maps to NM_144668.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:122361784 G>A maps to NM_144668.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:72056937 G>A maps to NM_144982.4 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:72056937 G>A maps to NM_144982.4 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:5455969 C>A maps to NM_181710.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:5455969 C>A maps to NM_181710.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:8870280 G>T maps to NM_001127448.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:8870280 G>T maps to NM_001127448.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:73150995 G>T maps to NM_148912.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:73150995 G>T maps to NM_148912.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:43213882 C>T maps to NM_001135706.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:43213882 C>T maps to NM_001135706.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:277249 G>T maps to NM_004300.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:277249 G>T maps to NM_004300.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:46602545 A>G maps to NM_015833.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:46602545 A>G maps to NM_015833.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:143754989 A>G maps to NM_182503.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:143754989 A>G maps to NM_182503.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:78001584 C>A maps to NM_174858.1 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:78001584 C>A maps to NM_174858.1 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:115220123 C>T maps to NM_000036.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:115220123 C>T maps to NM_000036.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:241463552 C>A maps to ENST00000401804 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:241463552 C>A maps to ENST00000401804 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:98175298 T>A maps to NM_025190.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:98175298 T>A maps to NM_025190.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:112174893 A>G maps to NM_001127510.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:112174893 A>G maps to NM_001127510.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:28508140 G>A maps to NM_018690.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:28508140 G>A maps to NM_018690.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:143973997 G>T maps to NM_018460.3 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:143973997 G>T maps to NM_018460.3 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:63852788 G>C maps to NM_032199.2 *1189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:63852788 G>C maps to NM_032199.2 *1189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:98985773 G>A maps to NM_005720.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:98985773 G>A maps to NM_005720.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:175983097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:175983097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:36168791 C>T maps to NM_015695.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:36168791 C>T maps to NM_015695.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:124049434 A>T maps to ENST00000368994 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:124049434 A>T maps to ENST00000368994 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:122830080 G>T maps to NM_024806.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:122830080 G>T maps to NM_024806.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:90135398 G>A maps to NM_152259.3 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:90135398 G>A maps to NM_152259.3 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:162829264 G>A maps to NM_178550.4 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:162829264 G>A maps to NM_178550.4 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:75107013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:75107013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:100458827 C>A maps to NM_032149.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:100458827 C>A maps to NM_032149.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:121563385 A>G maps to ENST00000275159 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:121563385 A>G maps to ENST00000275159 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:46915350 C>G maps to NM_032040.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:46915350 C>G maps to NM_032040.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:44387331 C>T maps to NM_001253.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:44387331 C>T maps to NM_001253.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:95164220 C>T maps to NM_001144663.1 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:95164220 C>T maps to NM_001144663.1 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:61774814 C>T maps to NM_017780.2 R2631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:61774814 C>T maps to NM_017780.2 R2631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:7828196 G>A maps to NM_014257.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:7828196 G>A maps to NM_014257.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:122862098 G>C maps to ENST00000302528 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:122862098 G>C maps to ENST00000302528 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:228137669 G>C maps to NM_000091.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:228137669 G>C maps to NM_000091.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:3778777 G>C maps to NM_004380.2 L2090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:3778777 G>C maps to NM_004380.2 L2090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:114186082 T>A maps to NM_198123.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:114186082 T>A maps to NM_198123.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:80101224 G>T maps to ENST00000402739 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:80101224 G>T maps to ENST00000402739 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:32007877 G>T maps to NM_000500.5 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:32007877 G>T maps to NM_000500.5 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:59404998 G>A maps to NM_000780.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:59404998 G>A maps to NM_000780.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:88885128 G>C maps to NM_152418.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:88885128 G>C maps to NM_152418.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:155287360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:155287360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:220290415 C>A maps to NM_001927.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:220290415 C>A maps to NM_001927.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:154011602 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:154011602 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:38905909 C>G maps to ENST00000327475 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:38905909 C>G maps to ENST00000327475 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:113890710 G>A maps to NM_000796.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:113890710 G>A maps to NM_000796.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:117375699 A>G maps to NM_020693.2 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:117375699 A>G maps to NM_020693.2 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:28991302 C>T maps to NM_001134453.1 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:28991302 C>T maps to NM_001134453.1 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:67632269 C>A maps to NM_019002.3 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:67632269 C>A maps to NM_019002.3 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:6175085 T>G maps to NM_000129.3 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:6175085 T>G maps to NM_000129.3 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:92087587 G>T maps to ENST00000298047 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:92087587 G>T maps to ENST00000298047 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:126384716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:126384716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:125131083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:125131083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:65655165 C>A maps to NM_198897.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:65655165 C>A maps to NM_198897.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:110146372 C>T maps to NM_014845.5 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:110146372 C>T maps to NM_014845.5 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:159653379 G>T maps to NM_032532.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:159653379 G>T maps to NM_032532.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:49221941 A>T maps to NM_004476.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:49221941 A>T maps to NM_004476.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150439758 C>A maps to ENST00000447239 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150439758 C>A maps to ENST00000447239 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:57415310 C>T maps to NM_016592.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:57415310 C>T maps to NM_016592.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:102153822 G>C maps to NM_024312.4 Y1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:102153822 G>C maps to NM_024312.4 Y1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:131488756 A>T maps to NM_198827.3 K391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:131488756 A>T maps to NM_198827.3 K391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:31062243 G>C maps to ENST00000327783 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:31062243 G>C maps to ENST00000327783 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:110201680 C>T maps to NM_000850.4 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:110201680 C>T maps to NM_000850.4 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:197184182 A>G maps to NM_020760.1 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:197184182 A>G maps to NM_020760.1 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:174254254 C>G maps to NM_002129.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:174254254 C>G maps to NM_002129.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:3231756 C>T maps to NM_002111.6 A2751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:3231756 C>T maps to NM_002111.6 A2751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:65682626 C>T maps to NM_020962.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:65682626 C>T maps to NM_020962.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:54318156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:54318156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:50760886 C>A maps to NM_024884.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:50760886 C>A maps to NM_024884.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:19389462 G>T maps to NM_001001671.3 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:19389462 G>T maps to NM_001001671.3 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:47637442 C>T maps to NM_000251.1 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:47637442 C>T maps to NM_000251.1 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:11319409 C>A maps to NM_004958.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:11319409 C>A maps to NM_004958.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:69063508 C>T maps to NM_138768.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:69063508 C>T maps to NM_138768.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:31094725 G>A maps to NM_015194.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:31094725 G>A maps to NM_015194.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:35793019 A>G maps to NM_003995.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:35793019 A>G maps to NM_003995.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17571669 G>A maps to NM_138454.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17571669 G>A maps to NM_138454.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123894264 C>A maps to NM_001001953.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123894264 C>A maps to NM_001001953.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:248551472 C>A maps to NM_001005471.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:248551472 C>A maps to NM_001005471.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:4661247 G>C maps to NM_001004751.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:4661247 G>C maps to NM_001004751.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:55945510 T>C maps to NM_001005494.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:55945510 T>C maps to NM_001005494.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:124294722 C>A maps to NM_001005196.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:124294722 C>A maps to NM_001005196.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:11022705 A>T maps to ENST00000303905 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:11022705 A>T maps to ENST00000303905 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:71838618 C>T maps to ENST00000373539 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:71838618 C>T maps to ENST00000373539 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:130437286 G>C maps to NM_014602.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:130437286 G>C maps to NM_014602.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:128815035 T>A maps to NM_014264.4 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:128815035 T>A maps to NM_014264.4 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:130832308 G>T maps to NM_001099771.2 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:130832308 G>T maps to NM_001099771.2 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:82763624 C>A maps to NM_000307.3 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:82763624 C>A maps to NM_000307.3 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:12835252 G>T maps to NM_001080830.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:12835252 G>T maps to NM_001080830.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:142459837 G>A maps to ENST00000486171 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:142459837 G>A maps to ENST00000486171 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:88945911 G>A maps to NM_007039.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:88945911 G>A maps to NM_007039.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:34807957 T>C maps to NM_001145521.1 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:34807957 T>C maps to NM_001145521.1 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:38903628 G>T maps to ENST00000405332 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:38903628 G>T maps to ENST00000405332 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:101076250 C>A maps to NM_015668.3 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:101076250 C>A maps to NM_015668.3 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:134990673 G>T maps to NM_018666.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:134990673 G>T maps to NM_018666.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:84651815 T>A maps to NM_152754.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:84651815 T>A maps to NM_152754.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:102738134 C>T maps to NM_017893.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:102738134 C>T maps to NM_017893.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:156186283 G>C maps to NM_000337.5 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:156186283 G>C maps to NM_000337.5 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41096893 C>A maps to NM_138392.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41096893 C>A maps to NM_138392.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:3669804 C>A maps to NM_023068.3 T1689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:3669804 C>A maps to NM_023068.3 T1689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:25914896 A>G maps to NM_005835.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:25914896 A>G maps to NM_005835.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:21242931 T>C maps to ENST00000381541 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:21242931 T>C maps to ENST00000381541 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:89611152 C>T maps to NM_003119.2 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:89611152 C>T maps to NM_003119.2 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:36545949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:36545949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:123229239 C>T maps to NM_001042750.1 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:123229239 C>T maps to NM_001042750.1 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:32633771 G>T maps to NM_153809.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:32633771 G>T maps to NM_153809.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41847855 C>T maps to NM_000660.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41847855 C>T maps to NM_000660.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:7833932 C>A maps to NM_001166621.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:7833932 C>A maps to NM_001166621.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:179605005 A>G maps to NM_133437.3 S4147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:179605005 A>G maps to NM_133437.3 S4147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:179613695 A>T maps to ENST00000375038 P4479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:179613695 A>T maps to ENST00000375038 P4479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:44047544 C>T maps to NM_006297.2 *634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:44047544 C>T maps to NM_006297.2 *634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:146156798 T>C maps to NM_006958.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:146156798 T>C maps to NM_006958.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:178139060 C>T maps to NM_005649.2 *606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:178139060 C>T maps to NM_005649.2 *606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr19:45655240 G>T maps to NM_198478.3 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr19:45655240 G>T maps to NM_198478.3 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr4:186539746 C>T maps to ENST00000355634 Q977Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr4:186539746 C>T maps to ENST00000355634 Q977Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:215846999 G>C maps to NM_173076.2 S1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:215846999 G>C maps to NM_173076.2 S1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:48311677 G>A maps to NM_152701.3 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:48311677 G>A maps to NM_152701.3 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:179076924 C>A maps to NM_007314.3 V1159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:179076924 C>A maps to NM_007314.3 V1159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:20439153 C>T maps to NM_017888.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:20439153 C>T maps to NM_017888.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156957828 A>G maps to ENST00000430702 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156957828 A>G maps to ENST00000430702 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:130275919 G>A maps to NM_007037.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:130275919 G>A maps to NM_007037.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:62287344 C>T maps to NM_001620.1 K4848K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:62287344 C>T maps to NM_001620.1 K4848K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:186338571 C>T maps to ENST00000273784 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:186338571 C>T maps to ENST00000273784 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:5128823 G>T maps to NM_019109.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:5128823 G>T maps to NM_019109.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:41585512 C>A maps to ENST00000415018 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:41585512 C>A maps to ENST00000415018 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114280093 C>T maps to NM_001148.4 S3440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114280093 C>T maps to NM_001148.4 S3440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:69933991 G>A maps to NM_018043.5 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:69933991 G>A maps to NM_018043.5 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:201488582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:201488582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:161192311 C>T maps to NM_001643.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:161192311 C>T maps to NM_001643.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6500083 C>A maps to NM_012402.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6500083 C>A maps to NM_012402.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:130215893 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:130215893 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:11196309 G>C maps to NM_013427.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:11196309 G>C maps to NM_013427.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:148999940 G>T maps to NM_001001669.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:148999940 G>T maps to NM_001001669.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:27097664 C>G maps to NM_006015.4 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:27097664 C>G maps to NM_006015.4 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:100911626 C>A maps to NM_177949.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:100911626 C>A maps to NM_177949.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:177136780 C>A maps to NM_080874.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:177136780 C>A maps to NM_080874.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:182584168 A>T maps to NM_014616.1 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:182584168 A>T maps to NM_014616.1 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:36050742 C>A maps to NM_000704.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:36050742 C>A maps to NM_000704.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:96706898 C>A maps to NM_000623.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:96706898 C>A maps to NM_000623.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:11405587 C>A maps to ENST00000427279 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:11405587 C>A maps to ENST00000427279 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:220236272 C>A maps to NM_006085.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:220236272 C>A maps to NM_006085.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:50192204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:50192204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:38548124 T>C maps to NM_052893.1 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:38548124 T>C maps to NM_052893.1 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75072441 C>T maps to NM_001002912.4 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75072441 C>T maps to NM_001002912.4 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:9498867 C>T maps to NM_012261.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:9498867 C>T maps to NM_012261.3 F219F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z055-01A-01W-0747-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-17-Z055-01A-01W-0747-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:86705174 C>A maps to NM_001239.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:86705174 C>A maps to NM_001239.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:25583116 G>T maps to NM_001792.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:25583116 G>T maps to NM_001792.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:18622561 C>A maps to NM_001037343.1 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:18622561 C>A maps to NM_001037343.1 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:184098564 G>T maps to NM_003741.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:184098564 G>T maps to NM_003741.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:19654862 C>T maps to NM_153221.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:19654862 C>T maps to NM_153221.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:87041100 T>A maps to ENST00000263723 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:87041100 T>A maps to ENST00000263723 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:205034236 C>A maps to NM_005076.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:205034236 C>A maps to NM_005076.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139668137 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139668137 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:189871661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:189871661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:175306001 G>A maps to NM_001008220.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:175306001 G>A maps to NM_001008220.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:20018209 C>T maps to NM_016652.4 W712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:20018209 C>T maps to NM_016652.4 W712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75175923 A>T maps to NM_001889.3 L163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75175923 A>T maps to NM_001889.3 L163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:149449435 C>A maps to NM_005211.3 G504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:149449435 C>A maps to NM_005211.3 G504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:3263597 T>A maps to NM_033225.5 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:3263597 T>A maps to NM_033225.5 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:138160262 A>G maps to ENST00000355078 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:138160262 A>G maps to ENST00000355078 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:74702982 C>A maps to NM_002993.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:74702982 C>A maps to NM_002993.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:96535208 C>A maps to NM_000769.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:96535208 C>A maps to NM_000769.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:59410853 G>T maps to NM_000780.3 Y85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:59410853 G>T maps to NM_000780.3 Y85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:39383130 C>A maps to NM_001343.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:39383130 C>A maps to NM_001343.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:30435739 G>A maps to NM_024096.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:30435739 G>A maps to NM_024096.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:50011297 G>T maps to NM_001037498.1 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:50011297 G>T maps to NM_001037498.1 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6468427 A>G maps to NM_024898.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6468427 A>G maps to NM_024898.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:59943223 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:59943223 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:387245 G>C maps to NM_014974.2 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:387245 G>C maps to NM_014974.2 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:48051291 G>T maps to NM_138281.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:48051291 G>T maps to NM_138281.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:21640542 G>T maps to NM_003777.3 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:21640542 G>T maps to NM_003777.3 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:76565322 G>C maps to ENST00000389840 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:76565322 G>C maps to ENST00000389840 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169101389 C>A maps to NM_004946.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169101389 C>A maps to NM_004946.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:65178452 C>A maps to NM_032160.2 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:65178452 C>A maps to NM_032160.2 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:29126201 G>T maps to NM_001943.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:29126201 G>T maps to NM_001943.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32428316 G>T maps to NM_001390.4 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32428316 G>T maps to NM_001390.4 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:167096068 C>T maps to NM_001080426.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:167096068 C>T maps to NM_001080426.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:4708298 G>T maps to NM_003845.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:4708298 G>T maps to NM_003845.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108409750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108409750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:8080124 A>G maps to NM_004280.4 *175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:8080124 A>G maps to NM_004280.4 *175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:34400393 C>A maps to NM_022073.3 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:34400393 C>A maps to NM_022073.3 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:31484530 G>T maps to NM_014600.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:31484530 G>T maps to NM_014600.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:37382321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:37382321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100367276 A>T maps to NM_001008707.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100367276 A>T maps to NM_001008707.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:34761683 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:34761683 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:38227521 G>A maps to NM_001099439.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:38227521 G>A maps to NM_001099439.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:94066636 C>T maps to NM_004440.3 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:94066636 C>T maps to NM_004440.3 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:22895779 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:22895779 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142562016 C>A maps to NM_004445.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142562016 C>A maps to NM_004445.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:102814755 C>A maps to NM_015051.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:102814755 C>A maps to NM_015051.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216850619 G>T maps to NM_001438.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216850619 G>T maps to NM_001438.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:128333508 G>T maps to NM_001143820.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:128333508 G>T maps to NM_001143820.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:128359245 G>A maps to NM_001143820.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:128359245 G>A maps to NM_001143820.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:40194595 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:40194595 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:34148839 G>T maps to NM_203408.3 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:34148839 G>T maps to NM_203408.3 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:34150080 G>A maps to NM_203408.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:34150080 G>A maps to NM_203408.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114401093 G>C maps to ENST00000424269 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114401093 G>C maps to ENST00000424269 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114569356 G>C maps to NM_182495.5 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114569356 G>C maps to NM_182495.5 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:54805190 C>A maps to NM_001010872.1 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:54805190 C>A maps to NM_001010872.1 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:92086801 C>G maps to ENST00000298047 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:92086801 C>G maps to ENST00000298047 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:92087705 C>T maps to ENST00000298047 Q810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:92087705 C>T maps to ENST00000298047 Q810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:15937085 C>T maps to NM_012304.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:15937085 C>T maps to NM_012304.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:157660279 G>A maps to NM_052939.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:157660279 G>A maps to NM_052939.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:159785242 G>T maps to NM_001004310.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:159785242 G>T maps to NM_001004310.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:14862491 C>A maps to NM_152536.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:14862491 C>A maps to NM_152536.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:135290119 G>A maps to NM_001159699.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:135290119 G>A maps to NM_001159699.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:27016682 C>T maps to NM_203371.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:27016682 C>T maps to NM_203371.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:152325344 T>G maps to NM_001014342.2 T1639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:152325344 T>G maps to NM_001014342.2 T1639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:52272423 T>C maps to NM_001005738.1 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:52272423 T>C maps to NM_001005738.1 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:52328053 A>G maps to NM_002030.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:52328053 A>G maps to NM_002030.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:79158661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:79158661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:69965980 A>T maps to NM_006654.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:69965980 A>T maps to NM_006654.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:44975659 T>C maps to NM_032135.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:44975659 T>C maps to NM_032135.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:169764516 C>A maps to NM_021176.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:169764516 C>A maps to NM_021176.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150864101 C>A maps to NM_001098834.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150864101 C>A maps to NM_001098834.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:120572171 C>A maps to NM_006836.1 G2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:120572171 C>A maps to NM_006836.1 G2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150269487 C>T maps to ENST00000430830 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150269487 C>T maps to ENST00000430830 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:35045188 C>T maps to NM_020660.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:35045188 C>T maps to NM_020660.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:235747042 G>C maps to NM_004485.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:235747042 G>C maps to NM_004485.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:22415262 G>A maps to NM_145290.2 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:22415262 G>A maps to NM_145290.2 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:112724233 A>T maps to NM_018970.6 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:112724233 A>T maps to NM_018970.6 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100118679 G>T maps to NM_001127258.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100118679 G>T maps to NM_001127258.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186113344 C>A maps to NM_031935.2 C4655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186113344 C>A maps to NM_031935.2 C4655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:42828542 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:42828542 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:25704415 G>A maps to NM_006040.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:25704415 G>A maps to NM_006040.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:183776233 C>A maps to NM_130770.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:183776233 C>A maps to NM_130770.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47109329 C>G maps to NM_006546.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47109329 C>G maps to NM_006546.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28513377 G>A maps to NM_145659.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28513377 G>A maps to NM_145659.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:2748642 T>A maps to NM_033267.4 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:2748642 T>A maps to NM_033267.4 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:2930909 A>T maps to NM_018463.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:2930909 A>T maps to NM_018463.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:15614332 G>A maps to NM_003638.1 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:15614332 G>A maps to NM_003638.1 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:39085299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:39085299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5021275 C>A maps to NM_000217.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5021275 C>A maps to NM_000217.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:119915393 C>A maps to NM_012281.2 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:119915393 C>A maps to NM_012281.2 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:21926523 C>T maps to NM_004982.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:21926523 C>T maps to NM_004982.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:233802734 G>A maps to NM_002245.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:233802734 G>A maps to NM_002245.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:42161646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:42161646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:86312942 C>T maps to NM_022480.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:86312942 C>T maps to NM_022480.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:166160027 C>T maps to NM_001161521.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:166160027 C>T maps to NM_001161521.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:7050761 G>T maps to NM_005559.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:7050761 G>T maps to NM_005559.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183177097 C>G maps to NM_005562.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183177097 C>G maps to NM_005562.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36248824 G>T maps to NM_174902.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36248824 G>T maps to NM_174902.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:111914405 G>T maps to NM_178175.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:111914405 G>T maps to NM_178175.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:35773617 G>A maps to NM_182548.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:35773617 G>A maps to NM_182548.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:54804155 C>A maps to ENST00000251375 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:54804155 C>A maps to ENST00000251375 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:126140539 G>T maps to NM_005573.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:126140539 G>T maps to NM_005573.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:82409388 C>A maps to ENST00000370717 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:82409388 C>A maps to ENST00000370717 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:85984515 G>T maps to NM_001017924.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:85984515 G>T maps to NM_001017924.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:127669172 G>T maps to NM_022143.4 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:127669172 G>T maps to NM_022143.4 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:25357144 C>T maps to NM_001001660.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:25357144 C>T maps to NM_001001660.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:179663482 C>A maps to NM_002752.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:179663482 C>A maps to NM_002752.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:47806387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:47806387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:54824717 C>A maps to ENST00000371389 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:54824717 C>A maps to ENST00000371389 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:151078260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:151078260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:128138161 C>A maps to NM_018396.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:128138161 C>A maps to NM_018396.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:118376836 A>G maps to NM_001197104.1 P3410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:118376836 A>G maps to NM_001197104.1 P3410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:60164086 C>T maps to NM_032597.3 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:60164086 C>T maps to NM_032597.3 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:42762540 T>A maps to NM_002463.1 L261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:42762540 T>A maps to NM_002463.1 L261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:50944202 G>A maps to NM_004533.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:50944202 G>A maps to NM_004533.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:16680172 G>A maps to NM_012334.2 Y1475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:16680172 G>A maps to NM_012334.2 Y1475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:26239789 G>T maps to ENST00000407587 T1101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:26239789 G>T maps to ENST00000407587 T1101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:24433564 G>T maps to ENST00000330966 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:24433564 G>T maps to ENST00000330966 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:145311785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:145311785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:71075712 G>A maps to NM_006540.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:71075712 G>A maps to NM_006540.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:21124439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:21124439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:152553886 T>A maps to NM_001164507.1 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:152553886 T>A maps to NM_001164507.1 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:29527460 C>T maps to NM_001042492.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:29527460 C>T maps to NM_001042492.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:24795650 C>G maps to NM_020448.4 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:24795650 C>G maps to NM_020448.4 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56544054 G>A maps to NM_153447.4 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56544054 G>A maps to NM_153447.4 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56561897 C>T maps to NM_153447.4 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56561897 C>T maps to NM_153447.4 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55451424 G>T maps to ENST00000446217 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55451424 G>T maps to ENST00000446217 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:31709891 C>G maps to NM_003787.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:31709891 C>G maps to NM_003787.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:66191383 C>T maps to NM_178864.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:66191383 C>T maps to NM_178864.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:50847159 C>T maps to ENST00000404971 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:50847159 C>T maps to ENST00000404971 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5603742 G>A maps to NM_001102654.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5603742 G>A maps to NM_001102654.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:132177642 C>A maps to NM_001144058.1 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:132177642 C>A maps to NM_001144058.1 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:131760827 A>T maps to NM_015354.1 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:131760827 A>T maps to NM_015354.1 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:23240331 A>T maps to NM_007342.2 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:23240331 A>T maps to NM_007342.2 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:24878208 G>A maps to NM_025081.2 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:24878208 G>A maps to NM_025081.2 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:113403718 C>G maps to NM_006187.2 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:113403718 C>G maps to NM_006187.2 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:28090144 C>A maps to NM_000275.2 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:28090144 C>A maps to NM_000275.2 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:28096534 G>A maps to NM_000275.2 C777C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:28096534 G>A maps to NM_000275.2 C777C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:7949837 A>T maps to NM_001004461.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:7949837 A>T maps to NM_001004461.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248202222 C>A maps to NM_001004686.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248202222 C>A maps to NM_001004686.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:48238837 C>T maps to NM_001005470.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:48238837 C>T maps to NM_001005470.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:50003261 G>T maps to NM_001005270.2 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:50003261 G>T maps to NM_001005270.2 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:49974684 C>G maps to NM_001001955.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:49974684 C>G maps to NM_001001955.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20611947 C>A maps to NM_001004724.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20611947 C>A maps to NM_001004724.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4944708 G>T maps to NM_001005237.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4944708 G>T maps to NM_001005237.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4936137 A>G maps to NM_001005238.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4936137 A>G maps to NM_001005238.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:5906065 G>T maps to NM_001005165.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:5906065 G>T maps to NM_001005165.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6007542 G>T maps to NM_001005173.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6007542 G>T maps to NM_001005173.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:5969235 C>G maps to NM_001003443.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:5969235 C>G maps to NM_001003443.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:58126400 G>A maps to NM_001005489.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:58126400 G>A maps to NM_001005489.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:56310559 G>T maps to NM_001005245.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:56310559 G>T maps to NM_001005245.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142723538 G>A maps to NM_001001658.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142723538 G>A maps to NM_001001658.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:77732460 A>T maps to NM_012383.4 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:77732460 A>T maps to NM_012383.4 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:3802968 C>G maps to NM_002558.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:3802968 C>G maps to NM_002558.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:89475486 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:89475486 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:242065755 C>A maps to ENST00000358649 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:242065755 C>A maps to ENST00000358649 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:31812339 C>A maps to NM_001604.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:31812339 C>A maps to NM_001604.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140263034 C>T maps to NM_018904.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140263034 C>T maps to NM_018904.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140347940 C>T maps to NM_018899.5 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140347940 C>T maps to NM_018899.5 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140736530 G>T maps to NM_018917.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140736530 G>T maps to NM_018917.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:57334136 G>T maps to NM_006210.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:57334136 G>T maps to NM_006210.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:120266065 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:120266065 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:209191038 C>T maps to NM_015040.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:209191038 C>T maps to NM_015040.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:46657467 A>G maps to NM_006071.1 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:46657467 A>G maps to NM_006071.1 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:110509296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:110509296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:51656118 C>G maps to NM_138694.3 V2785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:51656118 C>G maps to NM_138694.3 V2785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:89279416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:89279416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:28828766 A>G maps to NM_153021.4 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:28828766 A>G maps to NM_153021.4 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:49357341 C>A maps to NM_020904.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:49357341 C>A maps to NM_020904.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:131848972 G>T maps to NM_020911.1 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:131848972 G>T maps to NM_020911.1 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:203029442 G>T maps to ENST00000367238 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:203029442 G>T maps to ENST00000367238 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:37536784 C>A maps to NM_015568.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:37536784 C>A maps to NM_015568.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150315815 A>G maps to NM_004698.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150315815 A>G maps to NM_004698.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36424880 G>C maps to NM_001160167.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36424880 G>C maps to NM_001160167.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:87687591 C>G maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:87687591 C>G maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:121651280 T>A maps to NM_002851.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:121651280 T>A maps to NM_002851.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:100157239 C>A maps to NM_032709.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:100157239 C>A maps to NM_032709.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36597067 G>C maps to NM_000448.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36597067 G>C maps to NM_000448.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:38506136 C>T maps to NM_001145301.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:38506136 C>T maps to NM_001145301.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:79384812 G>T maps to NM_138937.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:79384812 G>T maps to NM_138937.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:3248067 C>T maps to NM_134428.1 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:3248067 C>T maps to NM_134428.1 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:109694147 C>A maps to NM_020769.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:109694147 C>A maps to NM_020769.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:46940530 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:46940530 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:49604437 G>A maps to NM_000324.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:49604437 G>A maps to NM_000324.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20978830 G>T maps to ENST00000430083 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20978830 G>T maps to ENST00000430083 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:10469635 G>T maps to NM_178857.5 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:10469635 G>T maps to NM_178857.5 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:55533649 A>T maps to NM_006269.1 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:55533649 A>T maps to NM_006269.1 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:218938550 C>A maps to NM_198483.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:218938550 C>A maps to NM_198483.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:158980357 G>A maps to NM_001197113.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:158980357 G>A maps to NM_001197113.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:9227080 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:9227080 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:42089579 G>C maps to NM_006275.5 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:42089579 G>C maps to NM_006275.5 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:51650071 C>A maps to NM_014385.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:51650071 C>A maps to NM_014385.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:133979773 G>C maps to NM_032826.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:133979773 G>C maps to NM_032826.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:205779242 T>G maps to NM_173854.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:205779242 T>G maps to NM_173854.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:27462237 G>A maps to ENST00000454389 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:27462237 G>A maps to ENST00000454389 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:108609530 T>A maps to NM_021815.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:108609530 T>A maps to NM_021815.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:20648267 G>A maps to NM_004211.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:20648267 G>A maps to NM_004211.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:14489270 C>A maps to NM_001134367.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:14489270 C>A maps to NM_001134367.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:1093879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:1093879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:106916949 A>T maps to NM_014978.1 K513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:106916949 A>T maps to NM_014978.1 K513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:136448122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:136448122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:55655698 G>T maps to NM_032681.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:55655698 G>T maps to NM_032681.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:123217306 G>A maps to NM_001042750.1 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:123217306 G>A maps to NM_001042750.1 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:39564833 C>A maps to NM_145286.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:39564833 C>A maps to NM_145286.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:81743374 C>A maps to NM_033104.2 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:81743374 C>A maps to NM_033104.2 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:152642999 A>C maps to NM_182961.2 T5313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:152642999 A>C maps to NM_182961.2 T5313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:40850356 A>T maps to NM_020783.3 C409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:40850356 A>T maps to NM_020783.3 C409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:120774806 C>A maps to NM_003184.3 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:120774806 C>A maps to NM_003184.3 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:33455691 G>T maps to ENST00000455217 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:33455691 G>T maps to ENST00000455217 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:179620107 T>A maps to ENST00000444136 L636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:179620107 T>A maps to ENST00000444136 L636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:70451364 G>T maps to NM_030625.2 E2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:70451364 G>T maps to NM_030625.2 E2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:89177554 G>T maps to NM_138960.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:89177554 G>T maps to NM_138960.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133980046 C>T maps to NM_003235.4 Q1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133980046 C>T maps to NM_003235.4 Q1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:54208148 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:54208148 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:133099997 C>T maps to NM_001136469.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:133099997 C>T maps to NM_001136469.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:159028349 C>T maps to NM_020823.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:159028349 C>T maps to NM_020823.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:57915654 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:57915654 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:117800546 G>T maps to NM_002160.2 G1835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:117800546 G>T maps to NM_002160.2 G1835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:135602027 G>T maps to NM_020389.2 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:135602027 G>T maps to NM_020389.2 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:98289595 C>T maps to NM_033512.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:98289595 C>T maps to NM_033512.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179414360 T>A maps to NM_133378.4 A28128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179414360 T>A maps to NM_133378.4 A28128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:35965802 C>A maps to NM_152404.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:35965802 C>A maps to NM_152404.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216270502 T>G maps to ENST00000366943 A1560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216270502 T>G maps to ENST00000366943 A1560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:17370516 G>A maps to NM_031941.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:17370516 G>A maps to NM_031941.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:49153912 C>T maps to ENST00000434032 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:49153912 C>T maps to ENST00000434032 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:132637848 C>T maps to NM_001008563.3 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:132637848 C>T maps to NM_001008563.3 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:58313587 G>A maps to NM_032582.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:58313587 G>A maps to NM_032582.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:136653574 G>A maps to NM_001134398.1 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:136653574 G>A maps to NM_001134398.1 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:150573463 G>T maps to ENST00000370361 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:150573463 G>T maps to ENST00000370361 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:62208221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:62208221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:41188134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:41188134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:58315575 C>A maps to NM_001130480.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:58315575 C>A maps to NM_001130480.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:123334767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:123334767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:70853322 C>A maps to NM_022479.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:70853322 C>A maps to NM_022479.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:65462664 T>A maps to NM_007191.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:65462664 T>A maps to NM_007191.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:175440099 C>A maps to NM_003387.4 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:175440099 C>A maps to NM_003387.4 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:32414251 A>G maps to NM_024426.4 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:32414251 A>G maps to NM_024426.4 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168102687 C>T maps to NM_152381.5 Q1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168102687 C>T maps to NM_152381.5 Q1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168107270 T>C maps to NM_152381.5 F3123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168107270 T>C maps to NM_152381.5 F3123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:37587591 C>T maps to NM_021083.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:37587591 C>T maps to NM_021083.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:61833965 C>A maps to NM_017798.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:61833965 C>A maps to NM_017798.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:155629621 T>G maps to ENST00000368339 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:155629621 T>G maps to ENST00000368339 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:113088699 A>G maps to NM_198581.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:113088699 A>G maps to NM_198581.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:219508190 C>T maps to NM_001105537.1 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:219508190 C>T maps to NM_001105537.1 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:14830004 G>A maps to NM_032433.2 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:14830004 G>A maps to NM_032433.2 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:21466981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:21466981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:109692894 G>T maps to NM_021224.4 T1979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:109692894 G>T maps to NM_021224.4 T1979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:31039942 C>A maps to NM_014717.1 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:31039942 C>A maps to NM_014717.1 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:37643140 C>A maps to ENST00000356958 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:37643140 C>A maps to ENST00000356958 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:22941729 G>T maps to ENST00000397104 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:22941729 G>T maps to ENST00000397104 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:102175128 A>G maps to NM_175056.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:102175128 A>G maps to NM_175056.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:20767982 C>T maps to NM_001163941.1 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:20767982 C>T maps to NM_001163941.1 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:48226494 G>T maps to NM_032583.3 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:48226494 G>T maps to NM_032583.3 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:30545195 G>A maps to NM_001025091.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:30545195 G>A maps to NM_001025091.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20696551 A>G maps to NM_052956.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20696551 A>G maps to NM_052956.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:29451870 C>T maps to NM_004304.3 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:29451870 C>T maps to NM_004304.3 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:115220953 A>G maps to NM_000036.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:115220953 A>G maps to NM_000036.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:22272494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:22272494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:36537716 G>C maps to NM_145640.2 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:36537716 G>C maps to NM_145640.2 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:32089084 G>T maps to NM_004381.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:32089084 G>T maps to NM_004381.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:193032854 C>A maps to NM_198505.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:193032854 C>A maps to NM_198505.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:110777087 C>T maps to NM_170665.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:110777087 C>T maps to NM_170665.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:122850097 G>T maps to NM_001098169.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:122850097 G>T maps to NM_001098169.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:89735692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:89735692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:109191325 C>A maps to ENST00000370031 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:109191325 C>A maps to ENST00000370031 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:73850837 G>A maps to ENST00000334126 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:73850837 G>A maps to ENST00000334126 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57843022 C>T maps to NM_032313.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57843022 C>T maps to NM_032313.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:2714277 C>T maps to NM_199460.2 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:2714277 C>T maps to NM_199460.2 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:110494201 C>A maps to NM_014289.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:110494201 C>A maps to NM_014289.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158324256 G>A maps to NM_030893.3 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158324256 G>A maps to NM_030893.3 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:31317543 T>C maps to NM_004932.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:31317543 T>C maps to NM_004932.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:96704919 G>T maps to NM_002595.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:96704919 G>T maps to NM_002595.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:34061701 G>T maps to NM_007186.3 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:34061701 G>T maps to NM_007186.3 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:203149612 G>C maps to NM_001276.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:203149612 G>C maps to NM_001276.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:21545046 C>A maps to NM_014927.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:21545046 C>A maps to NM_014927.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:41421698 T>A maps to NM_001843.2 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:41421698 T>A maps to NM_001843.2 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:139737680 G>A maps to NM_152888.1 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:139737680 G>A maps to NM_152888.1 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:189922114 G>T maps to NM_000393.3 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:189922114 G>T maps to NM_000393.3 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:130285828 A>C maps to NM_001102608.1 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:130285828 A>C maps to NM_001102608.1 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:128987440 G>A maps to NM_016128.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:128987440 G>A maps to NM_016128.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:111786099 C>A maps to NM_015267.3 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:111786099 C>A maps to NM_015267.3 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:91763537 G>A maps to NM_000786.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:91763537 G>A maps to NM_000786.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:61502410 G>A maps to NM_006133.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:61502410 G>A maps to NM_006133.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:118579436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:118579436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:231829653 A>G maps to NM_001164537.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:231829653 A>G maps to NM_001164537.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:46280927 G>A maps to NM_004409.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:46280927 G>A maps to NM_004409.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:3706126 C>A maps to NM_005223.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:3706126 C>A maps to NM_005223.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:154561256 C>A maps to NM_130797.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:154561256 C>A maps to NM_130797.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:44032290 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:44032290 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:103495004 C>T maps to NM_153448.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:103495004 C>T maps to NM_153448.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:37780831 G>C maps to NM_016042.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:37780831 G>C maps to NM_016042.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:103434286 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:103434286 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:34149639 G>T maps to NM_203408.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:34149639 G>T maps to NM_203408.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:89818611 G>A maps to NM_000135.2 H1000H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:89818611 G>A maps to NM_000135.2 H1000H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:196311059 A>G maps to NM_001105573.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:196311059 A>G maps to NM_001105573.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:27939492 G>A maps to NM_005248.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:27939492 G>A maps to NM_005248.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:29001429 G>T maps to NM_002019.4 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:29001429 G>T maps to NM_002019.4 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:78430611 C>A maps to ENST00000436586 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:78430611 C>A maps to ENST00000436586 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:30538474 G>A maps to NM_024051.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:30538474 G>A maps to NM_024051.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:150270129 T>G maps to ENST00000430830 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:150270129 T>G maps to ENST00000430830 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:6553454 C>A maps to NM_000170.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:6553454 C>A maps to NM_000170.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:22389681 G>A maps to NM_145290.2 N1204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:22389681 G>A maps to NM_145290.2 N1204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:174417608 C>T maps to NM_005684.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:174417608 C>T maps to NM_005684.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:88301012 G>C maps to NM_001143831.2 S613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:88301012 G>C maps to NM_001143831.2 S613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:148730754 A>T maps to NM_152407.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:148730754 A>T maps to NM_152407.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:33539580 C>T maps to NM_000178.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:33539580 C>T maps to NM_000178.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:60773886 G>A maps to NM_015666.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:60773886 G>A maps to NM_015666.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26043588 C>T maps to NM_021062.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26043588 C>T maps to NM_021062.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:101038617 G>A maps to NM_016247.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:101038617 G>A maps to NM_016247.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:30500666 G>T maps to NM_002209.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:30500666 G>T maps to NM_002209.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:170367346 A>T maps to NM_006063.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:170367346 A>T maps to NM_006063.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:211192454 C>T maps to NM_172362.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:211192454 C>T maps to NM_172362.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:163374375 C>A maps to NM_033272.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:163374375 C>A maps to NM_033272.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21926238 G>A maps to NM_004982.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21926238 G>A maps to NM_004982.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:108278851 C>A maps to NM_020890.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:108278851 C>A maps to NM_020890.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840213 C>T maps to NM_004522.1 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840213 C>T maps to NM_004522.1 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:70681449 C>A maps to NM_020866.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:70681449 C>A maps to NM_020866.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9751093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9751093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:165218683 C>A maps to NM_177398.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:165218683 C>A maps to NM_177398.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:99772454 C>A maps to NM_014839.4 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:99772454 C>A maps to NM_014839.4 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:7231727 C>T maps to NM_001105581.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:7231727 C>T maps to NM_001105581.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:52863951 C>T maps to NM_001024611.1 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:52863951 C>T maps to NM_001024611.1 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:54962004 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:54962004 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21201839 G>T maps to ENST00000381541 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21201839 G>T maps to ENST00000381541 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74999204 A>T maps to NM_000428.2 C637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74999204 A>T maps to NM_000428.2 C637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:20030536 G>A maps to NM_001168465.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:20030536 G>A maps to NM_001168465.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:29340104 G>A maps to NM_001034172.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:29340104 G>A maps to NM_001034172.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:141740553 C>A maps to ENST00000475668 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:141740553 C>A maps to ENST00000475668 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:151850039 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:151850039 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:43804243 C>T maps to NM_005373.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:43804243 C>T maps to NM_005373.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:9011387 G>A maps to NM_024690.2 Q12949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:9011387 G>A maps to NM_024690.2 Q12949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:26432510 C>T maps to NM_017433.4 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:26432510 C>T maps to NM_017433.4 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:134072753 C>A maps to NM_015261.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:134072753 C>A maps to NM_015261.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:152553213 G>A maps to NM_001164507.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:152553213 G>A maps to NM_001164507.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:100058771 C>A maps to NM_020202.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:100058771 C>A maps to NM_020202.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:56321473 A>G maps to NM_145007.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:56321473 A>G maps to NM_145007.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55452863 C>T maps to ENST00000446217 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55452863 C>T maps to ENST00000446217 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:119531735 C>T maps to NM_022002.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:119531735 C>T maps to NM_022002.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108501528 G>A maps to ENST00000368983 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108501528 G>A maps to ENST00000368983 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:92923848 C>A maps to NM_005654.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:92923848 C>A maps to NM_005654.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:61391393 C>A maps to NM_002531.2 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:61391393 C>A maps to NM_002531.2 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:228437915 G>C maps to NM_001098623.1 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:228437915 G>C maps to NM_001098623.1 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:123900934 T>G maps to ENST00000375021 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:123900934 T>G maps to ENST00000375021 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158576518 T>C maps to NM_001004478.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158576518 T>C maps to NM_001004478.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:107331795 C>A maps to NM_001004483.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:107331795 C>A maps to NM_001004483.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:3301515 G>T maps to NM_003553.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:3301515 G>T maps to NM_003553.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:248569765 T>A maps to NM_030904.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:248569765 T>A maps to NM_030904.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:69515 G>A maps to NM_001005484.1 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:69515 G>A maps to NM_001005484.1 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:55861055 C>A maps to NM_001003750.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:55861055 C>A maps to NM_001003750.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:56500855 C>T maps to NM_006191.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:56500855 C>T maps to NM_006191.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:125616205 A>T maps to NM_138294.2 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:125616205 A>T maps to NM_138294.2 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:55582805 A>G maps to NM_001142763.1 S1567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:55582805 A>G maps to NM_001142763.1 S1567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:96761627 G>C maps to NM_005390.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:96761627 G>C maps to NM_005390.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:209190982 A>T maps to NM_015040.3 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:209190982 A>T maps to NM_015040.3 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:53104215 C>A maps to NM_182595.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:53104215 C>A maps to NM_182595.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:131976448 C>A maps to NM_001083538.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:131976448 C>A maps to NM_001083538.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:145719676 C>T maps to NM_002700.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:145719676 C>T maps to NM_002700.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:23527713 G>T maps to NM_020227.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:23527713 G>T maps to NM_020227.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:68882356 C>G maps to NM_138964.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:68882356 C>G maps to NM_138964.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:96827071 G>A maps to NM_177995.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:96827071 G>A maps to NM_177995.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57351180 C>T maps to NM_003708.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57351180 C>T maps to NM_003708.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:192548397 A>G maps to NM_002922.3 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:192548397 A>G maps to NM_002922.3 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:63204047 T>A maps to NM_003835.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:63204047 T>A maps to NM_003835.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:30319882 T>A maps to NM_015565.2 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:30319882 T>A maps to NM_015565.2 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:159533308 C>T maps to ENST00000440678 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:159533308 C>T maps to ENST00000440678 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:237886546 T>C maps to NM_001035.2 L3558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:237886546 T>C maps to NM_001035.2 L3558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:33954734 C>A maps to NM_001036.3 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:33954734 C>A maps to NM_001036.3 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:50408103 C>A maps to NM_020436.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:50408103 C>A maps to NM_020436.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:13846070 A>T maps to NM_025229.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:13846070 A>T maps to NM_025229.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:83606483 C>A maps to NM_006080.2 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:83606483 C>A maps to NM_006080.2 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:150913869 C>T maps to NM_001145415.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:150913869 C>T maps to NM_001145415.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:20216188 T>C maps to NM_001012410.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:20216188 T>C maps to NM_001012410.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:7536068 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:7536068 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:591811 G>C maps to NM_000451.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:591811 G>C maps to NM_000451.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:122768941 G>T maps to NM_022444.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:122768941 G>T maps to NM_022444.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:91195874 C>T maps to NM_213606.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:91195874 C>T maps to NM_213606.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:63057975 A>T maps to NM_001039752.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:63057975 A>T maps to NM_001039752.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:73273564 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:73273564 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78225180 C>T maps to NM_173626.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78225180 C>T maps to NM_173626.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:196573496 C>T maps to NM_001127257.1 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:196573496 C>T maps to NM_001127257.1 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27426161 C>T maps to NM_021095.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27426161 C>T maps to NM_021095.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:142985597 C>A maps to NM_173653.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:142985597 C>A maps to NM_173653.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:164907997 C>T maps to NM_014926.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:164907997 C>T maps to NM_014926.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:57908710 T>A maps to ENST00000428312 C785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:57908710 T>A maps to ENST00000428312 C785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:130785060 G>A maps to NM_014758.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:130785060 G>A maps to NM_014758.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:23016842 G>T maps to NM_001052.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:23016842 G>T maps to NM_001052.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:47716839 T>A maps to NM_001048166.1 K1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:47716839 T>A maps to NM_001048166.1 K1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:80567104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:80567104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:152552537 T>A maps to NM_182961.2 L7009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:152552537 T>A maps to NM_182961.2 L7009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:75886872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:75886872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:35280502 G>T maps to NM_001077653.2 Y267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:35280502 G>T maps to NM_001077653.2 Y267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:152080151 C>G maps to NM_007113.2 A1847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:152080151 C>G maps to NM_007113.2 A1847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:97440279 C>A maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:97440279 C>A maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:138208559 A>C maps to ENST00000272643 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:138208559 A>C maps to ENST00000272643 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:126128650 G>T maps to NM_052907.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:126128650 G>T maps to NM_052907.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:72419373 G>T maps to NM_173490.6 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:72419373 G>T maps to NM_173490.6 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:129813779 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:129813779 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:136573445 T>C maps to NM_025246.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:136573445 T>C maps to NM_025246.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:12164496 C>T maps to NM_001243.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:12164496 C>T maps to NM_001243.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:175092569 G>A maps to NM_022093.1 W895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:175092569 G>A maps to NM_022093.1 W895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:122853998 C>A maps to NM_001130698.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:122853998 C>A maps to NM_001130698.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:142627276 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:142627276 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:43251484 C>A maps to NM_032538.1 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:43251484 C>A maps to NM_032538.1 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:96505870 C>A maps to NM_020121.3 G1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:96505870 C>A maps to NM_020121.3 G1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:51457357 T>C maps to ENST00000273612 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:51457357 T>C maps to ENST00000273612 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:991214 A>T maps to NM_001184985.1 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:991214 A>T maps to NM_001184985.1 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:69970319 C>T maps to NM_007014.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:69970319 C>T maps to NM_007014.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:41742175 G>T maps to ENST00000351589 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:41742175 G>T maps to ENST00000351589 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:77618300 G>T maps to NM_024721.4 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:77618300 G>T maps to NM_024721.4 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:68598295 C>A maps to NM_133458.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:68598295 C>A maps to NM_133458.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:147130437 G>T maps to NM_003412.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:147130437 G>T maps to NM_003412.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:53644587 G>C maps to NM_001172674.1 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:53644587 G>C maps to NM_001172674.1 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:57509949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:57509949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:52566489 C>T maps to NM_138932.2 *595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:52566489 C>T maps to NM_138932.2 *595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20721219 G>A maps to NM_001163941.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20721219 G>A maps to NM_001163941.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:43822329 G>C maps to ENST00000389420 S1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:43822329 G>C maps to ENST00000389420 S1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:17382561 A>G maps to NM_001621.4 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:17382561 A>G maps to NM_001621.4 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:186330902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:186330902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62105604 C>A maps to NM_025080.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62105604 C>A maps to NM_025080.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:182616475 C>A maps to NM_014616.1 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:182616475 C>A maps to NM_014616.1 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193220353 G>T maps to NM_032279.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193220353 G>T maps to NM_032279.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:13604518 T>A maps to NM_148894.2 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:13604518 T>A maps to NM_148894.2 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:65928064 G>C maps to ENST00000321892 V2189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:65928064 G>C maps to ENST00000321892 V2189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:137480930 G>A maps to NM_139199.1 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:137480930 G>A maps to NM_139199.1 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:37707162 C>A maps to NM_018310.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:37707162 C>A maps to NM_018310.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:33557476 C>G maps to NM_031446.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:33557476 C>G maps to NM_031446.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:104238915 A>G maps to NM_032342.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:104238915 A>G maps to NM_032342.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:181701771 C>T maps to ENST00000357570 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:181701771 C>T maps to ENST00000357570 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:15096642 C>A maps to NM_000728.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:15096642 C>A maps to NM_000728.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:76823720 C>T maps to ENST00000360841 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:76823720 C>T maps to ENST00000360841 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:219885895 G>T maps to NM_194302.2 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:219885895 G>T maps to NM_194302.2 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:17978516 G>T maps to ENST00000400579 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:17978516 G>T maps to ENST00000400579 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:104061194 C>G maps to NM_001813.2 V1985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:104061194 C>G maps to NM_001813.2 V1985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:88854042 G>T maps to NM_016083.4 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:88854042 G>T maps to NM_016083.4 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:106459968 C>G maps to NM_173494.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:106459968 C>G maps to NM_173494.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:39388915 A>T maps to NM_001343.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:39388915 A>T maps to NM_001343.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:159175966 G>T maps to NM_001122951.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:159175966 G>T maps to NM_001122951.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:57910624 C>G maps to NM_001195056.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:57910624 C>G maps to NM_001195056.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118572406 C>G maps to NM_006773.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118572406 C>G maps to NM_006773.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:12957379 G>T maps to NM_182643.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:12957379 G>T maps to NM_182643.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:130699748 G>A maps to ENST00000373110 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:130699748 G>A maps to ENST00000373110 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:9783934 C>G maps to NM_000798.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:9783934 C>G maps to NM_000798.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:45426447 C>G maps to NM_175940.1 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:45426447 C>G maps to NM_175940.1 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:129801716 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:129801716 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:89448577 C>A maps to NM_005233.5 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:89448577 C>A maps to NM_005233.5 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:203630378 C>T maps to NM_173511.3 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:203630378 C>T maps to NM_173511.3 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:170657263 A>G maps to NM_032448.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:170657263 A>G maps to NM_032448.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:91230571 A>G maps to NM_001145065.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:91230571 A>G maps to NM_001145065.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:59064337 C>T maps to NM_001040450.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:59064337 C>T maps to NM_001040450.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:187539601 G>C maps to ENST00000260147 S2716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:187539601 G>C maps to ENST00000260147 S2716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:126373591 G>T maps to NM_024582.4 V3807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:126373591 G>T maps to NM_024582.4 V3807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:107216862 G>A maps to NM_001163315.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:107216862 G>A maps to NM_001163315.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7755300 C>T maps to NM_002002.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7755300 C>T maps to NM_002002.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:40406006 C>A maps to NM_003890.2 A1613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:40406006 C>A maps to NM_003890.2 A1613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:47767697 C>T maps to NM_015308.2 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:47767697 C>T maps to NM_015308.2 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:49190744 G>A maps to NM_000145.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:49190744 G>A maps to NM_000145.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:20043221 C>A maps to NM_001002911.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:20043221 C>A maps to NM_001002911.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:91700938 G>T maps to ENST00000238699 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:91700938 G>T maps to ENST00000238699 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:87482851 G>A maps to NM_017551.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:87482851 G>A maps to NM_017551.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:33533874 G>C maps to NM_000178.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:33533874 G>C maps to NM_000178.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:240066312 G>T maps to NM_006037.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:240066312 G>T maps to NM_006037.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:28375357 G>A maps to NM_004667.4 V4251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:28375357 G>A maps to NM_004667.4 V4251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:54423643 C>T maps to NM_004503.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:54423643 C>T maps to NM_004503.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:114378978 G>A maps to NM_153612.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:114378978 G>A maps to NM_153612.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:183824453 C>A maps to NM_182589.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:183824453 C>A maps to NM_182589.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:53578369 G>A maps to ENST00000276009 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:53578369 G>A maps to ENST00000276009 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:27994969 T>G maps to NM_022873.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:27994969 T>G maps to NM_022873.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:133795690 C>T maps to NM_014987.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:133795690 C>T maps to NM_014987.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:99156081 C>G maps to NM_001134224.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:99156081 C>G maps to NM_001134224.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:155838621 C>A maps to NM_172160.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:155838621 C>A maps to NM_172160.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:50589842 T>C maps to NM_173605.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:50589842 T>C maps to NM_173605.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:91498222 C>T maps to ENST00000416354 Q1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:91498222 C>T maps to ENST00000416354 Q1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:51901578 T>C maps to NM_032559.4 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:51901578 T>C maps to NM_032559.4 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:183072670 C>T maps to NM_002293.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:183072670 C>T maps to NM_002293.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:45565505 C>T maps to NM_015340.3 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:45565505 C>T maps to NM_015340.3 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:59271634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:59271634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:165532799 G>A maps to NM_001005214.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:165532799 G>A maps to NM_001005214.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20198441 G>A maps to NM_182762.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20198441 G>A maps to NM_182762.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63767230 G>T maps to NM_014067.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63767230 G>T maps to NM_014067.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:51043817 C>T maps to ENST00000329492 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:51043817 C>T maps to ENST00000329492 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:182812356 T>A maps to NM_020166.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:182812356 T>A maps to NM_020166.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:116339632 G>A maps to NM_001127500.1 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:116339632 G>A maps to NM_001127500.1 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:49438021 G>A maps to NM_003482.3 Q1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:49438021 G>A maps to NM_003482.3 Q1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:36863737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:36863737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:174537308 G>C maps to NM_006792.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:174537308 G>C maps to NM_006792.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:10362639 C>T maps to NM_017533.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:10362639 C>T maps to NM_017533.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:52611477 C>T maps to ENST00000358212 L1671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:52611477 C>T maps to ENST00000358212 L1671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:23931652 C>A maps to NM_002487.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:23931652 C>A maps to NM_002487.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:3606913 C>T maps to ENST00000448023 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:3606913 C>T maps to ENST00000448023 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:108059913 G>A maps to NM_002519.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:108059913 G>A maps to NM_002519.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:200080374 T>C maps to NM_205860.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:200080374 T>C maps to NM_205860.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:132177676 G>T maps to NM_001144058.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:132177676 G>T maps to NM_001144058.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:73229200 C>T maps to NM_024844.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:73229200 C>T maps to NM_024844.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:161968139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:161968139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:54147394 G>A maps to NM_000912.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:54147394 G>A maps to NM_000912.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:248512966 G>T maps to NM_001001918.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:248512966 G>T maps to NM_001001918.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:248637568 G>A maps to NM_001005495.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:248637568 G>A maps to NM_001005495.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:123814446 C>A maps to NM_001005187.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:123814446 C>A maps to NM_001005187.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:56128651 C>A maps to NM_001005205.1 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:56128651 C>A maps to NM_001005205.1 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:79804358 C>T maps to NM_000918.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:79804358 C>T maps to NM_000918.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:140773999 G>A maps to NM_032088.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:140773999 G>A maps to NM_032088.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:36896595 G>C maps to NM_007144.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:36896595 G>C maps to NM_007144.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:24665110 G>A maps to NM_004845.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:24665110 G>A maps to NM_004845.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:125301228 G>T maps to NM_022062.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:125301228 G>T maps to NM_022062.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:94620959 A>T maps to NM_005761.1 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:94620959 A>T maps to NM_005761.1 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:55970088 G>T maps to NM_173814.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:55970088 G>T maps to NM_173814.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:66270235 G>A maps to ENST00000451741 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:66270235 G>A maps to ENST00000451741 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:103207174 C>T maps to ENST00000428762 G1540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:103207174 C>T maps to ENST00000428762 G1540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:150444485 C>G maps to NM_015203.3 S1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:150444485 C>G maps to NM_015203.3 S1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:39449254 C>T maps to ENST00000443003 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:39449254 C>T maps to ENST00000443003 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:11931799 C>A maps to NM_015659.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:11931799 C>A maps to NM_015659.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:134022558 C>A maps to NM_021982.1 S524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:134022558 C>A maps to NM_021982.1 S524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:23808790 C>T maps to NM_000231.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:23808790 C>T maps to NM_000231.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:25280125 G>A maps to NM_001039948.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:25280125 G>A maps to NM_001039948.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:40804796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:40804796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:52132707 G>A maps to ENST00000222107 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:52132707 G>A maps to ENST00000222107 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:44664477 C>T maps to NM_001134771.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:44664477 C>T maps to NM_001134771.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:86894926 C>G maps to NM_022127.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:86894926 C>G maps to NM_022127.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:115652022 G>A maps to NM_033051.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:115652022 G>A maps to NM_033051.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:23598915 C>A maps to NM_012244.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:23598915 C>A maps to NM_012244.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:1168844 T>C maps to NM_018968.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:1168844 T>C maps to NM_018968.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:37809960 C>T maps to NM_006804.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:37809960 C>T maps to NM_006804.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:67941311 T>A maps to NM_017635.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:67941311 T>A maps to NM_017635.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:152673178 G>A maps to NM_182961.2 Q3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:152673178 G>A maps to NM_182961.2 Q3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:27802713 C>A maps to NM_020791.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:27802713 C>A maps to NM_020791.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:101646185 T>A maps to NM_001102426.1 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:101646185 T>A maps to NM_001102426.1 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:2375101 C>A maps to NM_198994.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:2375101 C>A maps to NM_198994.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:83839863 C>G maps to NM_024672.4 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:83839863 C>G maps to NM_024672.4 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:63055812 C>T maps to NM_015059.2 N1671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:63055812 C>T maps to NM_015059.2 N1671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98307730 G>A maps to NM_020123.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98307730 G>A maps to NM_020123.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:48360467 G>A maps to NM_001143842.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:48360467 G>A maps to NM_001143842.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:44121557 C>T maps to NM_018426.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:44121557 C>T maps to NM_018426.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:31267869 G>T maps to NM_015544.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:31267869 G>T maps to NM_015544.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:32018015 C>T maps to ENST00000375244 L3066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:32018015 C>T maps to ENST00000375244 L3066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:110100052 C>A maps to NM_003301.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:110100052 C>A maps to NM_003301.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:20767520 G>A maps to NM_138376.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:20767520 G>A maps to NM_138376.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:162535799 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:162535799 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:43313526 G>C maps to NM_174916.2 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:43313526 G>C maps to NM_174916.2 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216373194 A>T maps to ENST00000366943 C1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216373194 A>T maps to ENST00000366943 C1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:36564348 C>T maps to NM_001083961.1 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:36564348 C>T maps to NM_001083961.1 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:980451 C>T maps to NM_001184985.1 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:980451 C>T maps to NM_001184985.1 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7685329 C>T maps to NM_020196.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7685329 C>T maps to NM_020196.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:114121117 G>T maps to NM_001018011.1 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:114121117 G>T maps to NM_001018011.1 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:157963721 C>T maps to NM_024630.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:157963721 C>T maps to NM_024630.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:26637641 G>A maps to NM_024639.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:26637641 G>A maps to NM_024639.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:90903721 C>G maps to NM_001004309.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:90903721 C>G maps to NM_001004309.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:100801841 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:100801841 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:41004562 G>T maps to NM_003734.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:41004562 G>T maps to NM_003734.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:68165701 T>C maps to NM_006421.3 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:68165701 T>C maps to NM_006421.3 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:53779848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:53779848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:87073891 T>A maps to NM_172213.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:87073891 T>A maps to NM_172213.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:16358321 C>T maps to NM_004070.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:16358321 C>T maps to NM_004070.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:189851865 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:189851865 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:70728877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:70728877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:47838009 C>T maps to NM_017895.7 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:47838009 C>T maps to NM_017895.7 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:98995156 G>A maps to NM_182562.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:98995156 G>A maps to NM_182562.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:129034607 G>T maps to NM_006026.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:129034607 G>T maps to NM_006026.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:239975262 G>A maps to NM_006037.3 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:239975262 G>A maps to NM_006037.3 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:1903427 G>T maps to ENST00000434971 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:1903427 G>T maps to ENST00000434971 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:42909603 G>T maps to NM_005357.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:42909603 G>T maps to NM_005357.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:32229892 C>T maps to NM_001040446.1 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:32229892 C>T maps to NM_001040446.1 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:80246395 A>G maps to NM_032693.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:80246395 A>G maps to NM_032693.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:69744935 C>T maps to NM_000903.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:69744935 C>T maps to NM_000903.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:228527675 G>T maps to NM_001098623.1 T5763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:228527675 G>T maps to NM_001098623.1 T5763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:76253195 G>A maps to NM_004582.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:76253195 G>A maps to NM_004582.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:12684299 C>T maps to NM_001112706.2 Y617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:12684299 C>T maps to NM_001112706.2 Y617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:42340031 G>T maps to NM_000342.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:42340031 G>T maps to NM_000342.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:1545619 C>T maps to NM_016111.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:1545619 C>T maps to NM_016111.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:3599744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:3599744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50245222 C>T maps to NM_021733.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50245222 C>T maps to NM_021733.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:73830749 C>A maps to ENST00000412096 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:73830749 C>A maps to ENST00000412096 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:49823451 C>A maps to NM_015069.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:49823451 C>A maps to NM_015069.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:30793473 G>A maps to NM_001080417.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:30793473 G>A maps to NM_001080417.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:52314646 C>T maps to NM_001077401.1 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:52314646 C>T maps to NM_001077401.1 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:101434169 C>A maps to NM_000693.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:101434169 C>A maps to NM_000693.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:19555059 C>T maps to NM_001031806.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:19555059 C>T maps to NM_001031806.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:46722808 G>A maps to NM_147129.3 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:46722808 G>A maps to NM_147129.3 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:23897064 T>C maps to NM_024122.4 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:23897064 T>C maps to NM_024122.4 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:27102065 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:27102065 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:124368697 G>C maps to NM_014109.3 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:124368697 G>C maps to NM_014109.3 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:160105633 C>T maps to NM_000702.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:160105633 C>T maps to NM_000702.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:152826266 C>T maps to NM_001001344.2 H991H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:152826266 C>T maps to NM_001001344.2 H991H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:57039069 C>A maps to NM_001686.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:57039069 C>A maps to NM_001686.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:6560158 C>T maps to NM_001242.4 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:6560158 C>T maps to NM_001242.4 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:23522739 G>C maps to NM_022478.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:23522739 G>C maps to NM_022478.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:26906095 G>A maps to NM_016279.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:26906095 G>A maps to NM_016279.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:7832416 C>T maps to NM_014257.4 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:7832416 C>T maps to NM_014257.4 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:48604137 C>A maps to NM_000094.3 V2753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:48604137 C>A maps to NM_000094.3 V2753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:334870 C>A maps to NM_130386.2 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:334870 C>A maps to NM_130386.2 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:149460351 G>T maps to NM_005211.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:149460351 G>T maps to NM_005211.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:42916063 C>G maps to NM_004391.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:42916063 C>G maps to NM_004391.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:98518497 G>A maps to ENST00000326857 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:98518497 G>A maps to ENST00000326857 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:28574376 G>T maps to NM_001440.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:28574376 G>T maps to NM_001440.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:197009737 T>A maps to NM_001994.2 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:197009737 T>A maps to NM_001994.2 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:95766311 G>C maps to NM_033086.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:95766311 G>C maps to NM_033086.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:236762788 T>A maps to NM_018072.5 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:236762788 T>A maps to NM_018072.5 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:151163927 C>A maps to NM_178822.4 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:151163927 C>A maps to NM_178822.4 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:121509046 C>T maps to NM_001023570.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:121509046 C>T maps to NM_001023570.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:33626577 C>T maps to ENST00000374316 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:33626577 C>T maps to ENST00000374316 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:17954674 C>A maps to NM_000215.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:17954674 C>A maps to NM_000215.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:42788289 G>A maps to NM_020433.4 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:42788289 G>A maps to NM_020433.4 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:138643961 G>A maps to ENST00000394800 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:138643961 G>A maps to ENST00000394800 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:43805735 C>A maps to NM_005373.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:43805735 C>A maps to NM_005373.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:248059046 C>A maps to NM_001001957.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:248059046 C>A maps to NM_001001957.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:158517160 G>T maps to NM_001005189.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:158517160 G>T maps to NM_001005189.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:74813241 G>A maps to NM_000917.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:74813241 G>A maps to NM_000917.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:140476014 G>T maps to NM_018936.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:140476014 G>T maps to NM_018936.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:43269800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:43269800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:4917271 C>A maps to NM_018059.4 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:4917271 C>A maps to NM_018059.4 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:103275909 G>T maps to ENST00000428762 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:103275909 G>T maps to ENST00000428762 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:183869310 C>T maps to NM_015149.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:183869310 C>T maps to NM_015149.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:72055392 G>A maps to NM_015556.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:72055392 G>A maps to NM_015556.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:42335047 C>T maps to NM_000342.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:42335047 C>T maps to NM_000342.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:53084451 G>T maps to NM_014682.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:53084451 G>T maps to NM_014682.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:52529464 C>T maps to NM_015136.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:52529464 C>T maps to NM_015136.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:40476747 T>A maps to NM_139276.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:40476747 T>A maps to NM_139276.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:132351569 C>A maps to NM_016521.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:132351569 C>A maps to NM_016521.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:54173272 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:54173272 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:92008880 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:92008880 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:179575542 C>T maps to NM_133378.4 K8183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:179575542 C>T maps to NM_133378.4 K8183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:12439541 A>G maps to NM_015378.2 R3694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:12439541 A>G maps to NM_015378.2 R3694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:49359952 A>G maps to NM_003394.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:49359952 A>G maps to NM_003394.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:28121476 G>C maps to NM_006298.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:28121476 G>C maps to NM_006298.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:58452653 G>A maps to NM_005773.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:58452653 G>A maps to NM_005773.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:35687288 A>G maps to NM_198834.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:35687288 A>G maps to NM_198834.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:236898980 C>A maps to NM_001103.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:236898980 C>A maps to NM_001103.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:7626380 T>C maps to NM_020546.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:7626380 T>C maps to NM_020546.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:105406156 C>A maps to NM_138420.2 G5211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:105406156 C>A maps to NM_138420.2 G5211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:114274541 G>T maps to NM_001148.4 E1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:114274541 G>T maps to NM_001148.4 E1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:29390775 G>A maps to NM_005503.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:29390775 G>A maps to NM_005503.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:116691951 C>A maps to NM_000482.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:116691951 C>A maps to NM_000482.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:21263871 A>C maps to NM_000384.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:21263871 A>C maps to NM_000384.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33386083 G>A maps to NM_001170.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33386083 G>A maps to NM_001170.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:31250635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:31250635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:150245264 G>T maps to NM_024579.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:150245264 G>T maps to NM_024579.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:26676331 G>T maps to NM_145038.2 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:26676331 G>T maps to NM_145038.2 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:18825106 A>G maps to NM_201596.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:18825106 A>G maps to NM_201596.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:106121899 G>C maps to NM_001008723.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:106121899 G>C maps to NM_001008723.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:18022492 G>C maps to ENST00000400579 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:18022492 G>C maps to ENST00000400579 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:100672087 C>T maps to NM_001918.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:100672087 C>T maps to NM_001918.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:124341757 C>A maps to NM_207437.3 V2080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:124341757 C>A maps to NM_207437.3 V2080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:432258 T>C maps to NM_203447.3 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:432258 T>C maps to NM_203447.3 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:236645849 C>A maps to NM_145861.2 C183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:236645849 C>A maps to NM_145861.2 C183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:22269909 C>T maps to NM_013302.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:22269909 C>T maps to NM_013302.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:49637301 C>T maps to NM_024593.3 *212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:49637301 C>T maps to NM_024593.3 *212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:233421189 G>T maps to NM_004846.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:233421189 G>T maps to NM_004846.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:56274427 C>T maps to NM_000502.4 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:56274427 C>T maps to NM_000502.4 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:18284915 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:18284915 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:88939886 T>C maps to ENST00000298786 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:88939886 T>C maps to ENST00000298786 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:54805295 G>T maps to NM_001010872.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:54805295 G>T maps to NM_001010872.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:187531124 C>A maps to ENST00000260147 E3303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:187531124 C>A maps to ENST00000260147 E3303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:19185000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:19185000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:155507347 G>C maps to NM_000508.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:155507347 G>C maps to NM_000508.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:38061775 C>A maps to NM_004496.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:38061775 C>A maps to NM_004496.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:17445724 T>C maps to NM_001037814.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:17445724 T>C maps to NM_001037814.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:651063 G>T maps to NM_015721.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:651063 G>T maps to NM_015721.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:51274219 G>T maps to NM_001506.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:51274219 G>T maps to NM_001506.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:34008346 G>T maps to NM_000841.1 Y449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:34008346 G>T maps to NM_000841.1 Y449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:27476786 C>A maps to NM_001520.3 E1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:27476786 C>A maps to NM_001520.3 E1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:13546158 G>T maps to NM_024827.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:13546158 G>T maps to NM_024827.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:66698689 C>T maps to NM_033647.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:66698689 C>T maps to NM_033647.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:145416842 C>G maps to NM_213653.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:145416842 C>G maps to NM_213653.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:2156600 G>T maps to NM_001127598.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:2156600 G>T maps to NM_001127598.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:242651390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:242651390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:7611658 G>T maps to ENST00000256861 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:7611658 G>T maps to ENST00000256861 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:150648008 C>A maps to NM_000238.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:150648008 C>A maps to NM_000238.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:139164444 C>G maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:139164444 C>G maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:59277357 G>A maps to NM_153377.3 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:59277357 G>A maps to NM_153377.3 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:160789136 C>T maps to ENST00000263285 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:160789136 C>T maps to ENST00000263285 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:26212995 C>A maps to NM_173523.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:26212995 C>A maps to NM_173523.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:43933170 C>A maps to ENST00000372754 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:43933170 C>A maps to ENST00000372754 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:58979597 G>C maps to NM_001039396.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:58979597 G>C maps to NM_001039396.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:68777384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:68777384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:1267037 C>A maps to ENST00000447027 A2979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:1267037 C>A maps to ENST00000447027 A2979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:128331591 G>A maps to ENST00000389524 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:128331591 G>A maps to ENST00000389524 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:50953849 C>A maps to NM_018245.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:50953849 C>A maps to NM_018245.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:161970074 G>A maps to ENST00000451379 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:161970074 G>A maps to ENST00000451379 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:140216004 G>A maps to NM_018910.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:140216004 G>A maps to NM_018910.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:106509745 C>A maps to NM_002649.2 Y580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:106509745 C>A maps to NM_002649.2 Y580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:52387682 G>A maps to NM_144651.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:52387682 G>A maps to NM_144651.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:4917467 G>A maps to NM_018059.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:4917467 G>A maps to NM_018059.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:43896061 G>T maps to NM_080860.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:43896061 G>T maps to NM_080860.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:66456123 G>A maps to NM_016038.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:66456123 G>A maps to NM_016038.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:156237396 C>G maps to NM_015327.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:156237396 C>G maps to NM_015327.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:12662398 G>C maps to NM_001080530.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:12662398 G>C maps to NM_001080530.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:113275212 G>T maps to ENST00000374463 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:113275212 G>T maps to ENST00000374463 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:64428309 C>T maps to NM_182914.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:64428309 C>T maps to NM_182914.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:66807602 G>T maps to NM_001177880.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:66807602 G>T maps to NM_001177880.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:12904931 T>A maps to NM_016562.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:12904931 T>A maps to NM_016562.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:19381870 G>A maps to NM_001001524.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:19381870 G>A maps to NM_001001524.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:72256329 G>A maps to NM_032646.5 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:72256329 G>A maps to NM_032646.5 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:69127008 T>A maps to NM_003968.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:69127008 T>A maps to NM_003968.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:48546712 C>A maps to NM_000377.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:48546712 C>A maps to NM_000377.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:67370901 G>A maps to NM_024763.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:67370901 G>A maps to NM_024763.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:64722401 C>T maps to NM_001010888.3 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:64722401 C>T maps to NM_001010888.3 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:21910504 T>C maps to NM_173531.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:21910504 T>C maps to NM_173531.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:116750741 G>A maps to ENST00000374126 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:116750741 G>A maps to ENST00000374126 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:56736247 C>A maps to NM_024303.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:56736247 C>A maps to NM_024303.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:101605388 G>C maps to NM_000392.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:101605388 G>C maps to NM_000392.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:47322160 C>A maps to NM_006111.2 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:47322160 C>A maps to NM_006111.2 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:80655734 A>G maps to NM_130767.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:80655734 A>G maps to NM_130767.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:56203479 G>A maps to NM_052947.3 S1313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:56203479 G>A maps to NM_052947.3 S1313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:47846938 T>A maps to NM_001013732.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:47846938 T>A maps to NM_001013732.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:116187351 A>G maps to ENST00000451722 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:116187351 A>G maps to ENST00000451722 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:49315226 G>A maps to NM_004352.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:49315226 G>A maps to NM_004352.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:119909873 G>A maps to NM_178499.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:119909873 G>A maps to NM_178499.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:137708876 C>T maps to NM_000093.3 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:137708876 C>T maps to NM_000093.3 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:17091487 T>C maps to ENST00000443236 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:17091487 T>C maps to ENST00000443236 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:113421175 C>A maps to NM_198123.1 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:113421175 C>A maps to NM_198123.1 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:50734080 G>T maps to NM_005215.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:50734080 G>T maps to NM_005215.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:162741928 G>T maps to NM_006182.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:162741928 G>T maps to NM_006182.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:107847034 C>A maps to NM_014421.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:107847034 C>A maps to NM_014421.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:83691637 C>A maps to NM_001142699.1 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:83691637 C>A maps to NM_001142699.1 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:88583610 G>A maps to NM_004407.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:88583610 G>A maps to NM_004407.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:117722181 T>A maps to ENST00000276204 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:117722181 T>A maps to ENST00000276204 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:71740731 G>A maps to NM_001142958.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:71740731 G>A maps to NM_001142958.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:161476250 T>C maps to NM_001136219.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:161476250 T>C maps to NM_001136219.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:135440216 G>C maps to ENST00000443774 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:135440216 G>C maps to ENST00000443774 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:155206035 C>T maps to NM_001005742.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:155206035 C>T maps to NM_001005742.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:147928400 A>T maps to NM_001040173.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:147928400 A>T maps to NM_001040173.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:10435100 G>A maps to ENST00000377086 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:10435100 G>A maps to ENST00000377086 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:27521052 T>C maps to NM_018362.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:27521052 T>C maps to NM_018362.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:141113971 T>A maps to NM_018557.2 T3823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:141113971 T>A maps to NM_018557.2 T3823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:39750084 A>G maps to ENST00000361689 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:39750084 A>G maps to ENST00000361689 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:151869822 C>T maps to NM_005363.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:151869822 C>T maps to NM_005363.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:128865084 T>C maps to NM_152778.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:128865084 T>C maps to NM_152778.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:56350205 C>T maps to ENST00000340482 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:56350205 C>T maps to ENST00000340482 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:121437551 T>A maps to NM_014078.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:121437551 T>A maps to NM_014078.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:247587296 G>A maps to NM_004895.4 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:247587296 G>A maps to NM_004895.4 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:6942267 G>A maps to NM_001004684.1 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:6942267 G>A maps to NM_001004684.1 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:99962907 C>T maps to ENST00000457907 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:99962907 C>T maps to ENST00000457907 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:53418774 G>A maps to NM_002590.2 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:53418774 G>A maps to NM_002590.2 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:53420597 C>A maps to NM_002590.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:53420597 C>A maps to NM_002590.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:7361711 G>A maps to NM_001131023.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:7361711 G>A maps to NM_001131023.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:20416368 G>A maps to NM_000929.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:20416368 G>A maps to NM_000929.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:113309470 T>C maps to NM_019014.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:113309470 T>C maps to NM_019014.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:49690769 C>T maps to ENST00000451891 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:49690769 C>T maps to ENST00000451891 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:70974894 G>T maps to NM_001109754.1 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:70974894 G>T maps to NM_001109754.1 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:40733346 C>A maps to ENST00000373198 V1156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:40733346 C>A maps to ENST00000373198 V1156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:152300041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:152300041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:78649340 A>G maps to NM_002941.3 N1621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:78649340 A>G maps to NM_002941.3 N1621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:30977307 C>T maps to NM_014712.1 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:30977307 C>T maps to NM_014712.1 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:91656986 C>T maps to NM_016848.5 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:91656986 C>T maps to NM_016848.5 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:42302221 G>A maps to NM_006749.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:42302221 G>A maps to NM_006749.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:56212691 C>T maps to NM_024592.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:56212691 C>T maps to NM_024592.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:149502580 C>G maps to NM_198455.2 R2799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:149502580 C>G maps to NM_198455.2 R2799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:113170490 G>C maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:113170490 G>C maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:113259168 T>A maps to ENST00000374463 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:113259168 T>A maps to ENST00000374463 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:152652223 C>T maps to NM_182961.2 V4532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:152652223 C>T maps to NM_182961.2 V4532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:33461818 C>T maps to ENST00000455217 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:33461818 C>T maps to ENST00000455217 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:30699764 G>A maps to NM_031271.3 Q2257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:30699764 G>A maps to NM_031271.3 Q2257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:246707917 A>G maps to NM_022366.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:246707917 A>G maps to NM_022366.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:137814683 C>G maps to ENST00000272643 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:137814683 C>G maps to ENST00000272643 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:63031647 G>T maps to NM_015059.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:63031647 G>T maps to NM_015059.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:7579493 T>A maps to NM_001126112.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:7579493 T>A maps to NM_001126112.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:90799469 C>A maps to ENST00000438251 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:90799469 C>A maps to ENST00000438251 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179417149 G>T maps to NM_133378.4 P27591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179417149 G>T maps to NM_133378.4 P27591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179616021 A>T maps to ENST00000375038 L3704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179616021 A>T maps to ENST00000375038 L3704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:15605884 A>T maps to NM_006765.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:15605884 A>T maps to NM_006765.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:57839444 G>C maps to NM_213598.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:57839444 G>C maps to NM_213598.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:102798179 G>A maps to NM_018335.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:102798179 G>A maps to NM_018335.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:7759056 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:7759056 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:98274559 C>A maps to NM_005735.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:98274559 C>A maps to NM_005735.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:109962786 T>C maps to NM_001145128.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:109962786 T>C maps to NM_001145128.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:58258025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:58258025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:114276797 G>T maps to NM_001148.4 G2342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:114276797 G>T maps to NM_001148.4 G2342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:241448842 T>C maps to ENST00000401804 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:241448842 T>C maps to ENST00000401804 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:26463525 C>A maps to NM_031418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:26463525 C>A maps to NM_031418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:169049309 G>T maps to NM_007193.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:169049309 G>T maps to NM_007193.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:36634037 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:36634037 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:119976739 C>A maps to ENST00000313400 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:119976739 C>A maps to ENST00000313400 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:119977021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:119977021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:33644805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:33644805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:96075790 C>A maps to ENST00000440890 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:96075790 C>A maps to ENST00000440890 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:56385037 C>A maps to NM_004758.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:56385037 C>A maps to NM_004758.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:24922504 C>T maps to NM_018958.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:24922504 C>T maps to NM_018958.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:58506877 C>A maps to NM_181707.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:58506877 C>A maps to NM_181707.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:31532419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:31532419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:32260790 T>A maps to ENST00000447241 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:32260790 T>A maps to ENST00000447241 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:165715669 C>A maps to NM_144980.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:165715669 C>A maps to NM_144980.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:64875162 G>A maps to NM_014404.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:64875162 G>A maps to NM_014404.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:54109681 C>A maps to NM_020898.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:54109681 C>A maps to NM_020898.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:93065452 G>A maps to NM_001164737.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:93065452 G>A maps to NM_001164737.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:32724417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:32724417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:7522157 G>T maps to ENST00000416109 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:7522157 G>T maps to ENST00000416109 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:21854831 G>T maps to NM_004061.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:21854831 G>T maps to NM_004061.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:202677285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:202677285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:3767007 C>A maps to NM_001810.5 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:3767007 C>A maps to NM_001810.5 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:21859723 C>A maps to NM_001170629.1 V2321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:21859723 C>A maps to NM_001170629.1 V2321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:45672158 G>T maps to NM_003654.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:45672158 G>T maps to NM_003654.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70847590 A>T maps to NM_001858.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70847590 A>T maps to NM_001858.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:139707073 C>A maps to NM_152888.1 E881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:139707073 C>A maps to NM_152888.1 E881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:107930916 A>G maps to ENST00000328300 Q1507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:107930916 A>G maps to ENST00000328300 Q1507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:130293295 G>T maps to NM_001102608.1 V1158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:130293295 G>T maps to NM_001102608.1 V1158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:48620454 C>A maps to NM_000094.3 A1503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:48620454 C>A maps to NM_000094.3 A1503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:117431239 G>A maps to NM_033427.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:117431239 G>A maps to NM_033427.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:37668872 G>T maps to NM_000397.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:37668872 G>T maps to NM_000397.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:122075648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:122075648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:36779985 C>T maps to NM_033403.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:36779985 C>T maps to NM_033403.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:112309028 A>T maps to NM_007204.4 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:112309028 A>T maps to NM_007204.4 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:1497608 G>T maps to ENST00000357934 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:1497608 G>T maps to ENST00000357934 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:169122863 C>A maps to NM_004946.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:169122863 C>A maps to NM_004946.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:154645511 G>T maps to NM_130797.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:154645511 G>T maps to NM_130797.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:48624495 C>T maps to NM_001025248.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:48624495 C>T maps to NM_001025248.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:89390950 C>T maps to NM_005233.5 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:89390950 C>T maps to NM_005233.5 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169511450 G>T maps to ENST00000367796 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169511450 G>T maps to ENST00000367796 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:34961676 C>G maps to NM_152631.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:34961676 C>G maps to NM_152631.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:152281931 C>T maps to NM_002016.1 Q1810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:152281931 C>T maps to NM_002016.1 Q1810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:44166262 G>T maps to NM_032892.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:44166262 G>T maps to NM_032892.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:40034008 T>A maps to NM_152597.4 K218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:40034008 T>A maps to NM_152597.4 K218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:89907908 A>G maps to NM_002042.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:89907908 A>G maps to NM_002042.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:150174228 G>T maps to NM_175571.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:150174228 G>T maps to NM_175571.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:121748104 C>T maps to NM_005270.4 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:121748104 C>T maps to NM_005270.4 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:29037044 C>T maps to NM_006582.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:29037044 C>T maps to NM_006582.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40365464 C>A maps to NM_004810.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40365464 C>A maps to NM_004810.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:86416286 G>T maps to NM_000840.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:86416286 G>T maps to NM_000840.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:28375307 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:28375307 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:91816379 A>G maps to NM_001017975.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:91816379 A>G maps to NM_001017975.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:3444490 A>T maps to ENST00000511533 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:3444490 A>T maps to ENST00000511533 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:46804190 C>T maps to NM_006361.5 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:46804190 C>T maps to NM_006361.5 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:117131682 C>A maps to NM_001542.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:117131682 C>A maps to NM_001542.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:100949990 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:100949990 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:2748675 G>A maps to NM_033267.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:2748675 G>A maps to NM_033267.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:68596156 G>A maps to ENST00000423218 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:68596156 G>A maps to ENST00000423218 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:156655368 T>A maps to NM_005546.3 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:156655368 T>A maps to NM_005546.3 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:19384092 A>T maps to NM_144633.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:19384092 A>T maps to NM_144633.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrY:21894529 C>T maps to NM_001146705.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrY:21894529 C>T maps to NM_001146705.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:3662520 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:3662520 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:30317993 C>T maps to NM_020848.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:30317993 C>T maps to NM_020848.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:51902346 T>A maps to NM_032559.4 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:51902346 T>A maps to NM_032559.4 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:7037597 G>C maps to NM_005559.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:7037597 G>C maps to NM_005559.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:50867904 A>G maps to ENST00000429001 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:50867904 A>G maps to ENST00000429001 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:152552268 G>T maps to NM_032563.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:152552268 G>T maps to NM_032563.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:189681779 C>A maps to NM_018192.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:189681779 C>A maps to NM_018192.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:113909174 G>A maps to NM_022363.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:113909174 G>A maps to NM_022363.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:30639729 C>A maps to NM_002309.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:30639729 C>A maps to NM_002309.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:62778448 G>T maps to ENST00000506720 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:62778448 G>T maps to ENST00000506720 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:141083399 C>A maps to NM_018557.2 E4091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:141083399 C>A maps to NM_018557.2 E4091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:40137278 G>T maps to NM_020929.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:40137278 G>T maps to NM_020929.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:60821889 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:60821889 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:42839470 G>T maps to ENST00000251268 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:42839470 G>T maps to ENST00000251268 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:43245924 T>C maps to NM_153361.2 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:43245924 T>C maps to NM_153361.2 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:14345717 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:14345717 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:27964307 C>T maps to NM_173576.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:27964307 C>T maps to NM_173576.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:60744808 C>T maps to NM_006039.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:60744808 C>T maps to NM_006039.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:80040323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:80040323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:9063442 C>A maps to NM_024690.2 V8001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:9063442 C>A maps to NM_024690.2 V8001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:3240107 C>G maps to NM_015419.3 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:3240107 C>G maps to NM_015419.3 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:10206755 C>T maps to NM_003802.2 K1842K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:10206755 C>T maps to NM_003802.2 K1842K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:41941682 A>C maps to NM_024561.4 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:41941682 A>C maps to NM_024561.4 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:179336200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:179336200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120468433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120468433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:71716299 G>T maps to ENST00000393695 T1942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:71716299 G>T maps to ENST00000393695 T1942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121461897 T>A maps to NM_003733.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121461897 T>A maps to NM_003733.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:55406717 C>A maps to NM_001004124.1 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:55406717 C>A maps to NM_001004124.1 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:56380108 A>G maps to NM_001004740.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:56380108 A>G maps to NM_001004740.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:123676202 A>G maps to NM_001005325.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:123676202 A>G maps to NM_001005325.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:123624623 G>T maps to NM_001005188.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:123624623 G>T maps to NM_001005188.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:56113825 C>A maps to NM_001002907.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:56113825 C>A maps to NM_001002907.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:57958873 C>A maps to NM_001005283.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:57958873 C>A maps to NM_001005283.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:58114581 G>T maps to NM_006812.3 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:58114581 G>T maps to NM_006812.3 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:17555219 G>T maps to NM_013358.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:17555219 G>T maps to NM_013358.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:55913024 G>T maps to NM_001142763.1 S545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:55913024 G>T maps to NM_001142763.1 S545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:31144175 G>A maps to NM_001173523.1 W1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:31144175 G>A maps to NM_001173523.1 W1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140249938 G>A maps to NM_018902.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140249938 G>A maps to NM_018902.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140215323 C>A maps to NM_018910.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140215323 C>A maps to NM_018910.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140740472 G>T maps to NM_018923.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140740472 G>T maps to NM_018923.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:77685113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:77685113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:94301942 C>T maps to NM_152431.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:94301942 C>T maps to NM_152431.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:51889987 T>A maps to NM_138694.3 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:51889987 T>A maps to NM_138694.3 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:118314955 G>T maps to NM_000936.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:118314955 G>T maps to NM_000936.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:23886434 G>A maps to NM_013261.3 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:23886434 G>A maps to NM_013261.3 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:12854068 G>A maps to NM_023013.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:12854068 G>A maps to NM_023013.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:22892502 T>A maps to NM_206954.1 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:22892502 T>A maps to NM_206954.1 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:119259401 A>T maps to NM_003619.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:119259401 A>T maps to NM_003619.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:136939604 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:136939604 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70970273 C>T maps to NM_001109754.1 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70970273 C>T maps to NM_001109754.1 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:121637944 C>A maps to NM_002851.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:121637944 C>A maps to NM_002851.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:30332326 G>T maps to NM_001008712.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:30332326 G>T maps to NM_001008712.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:104898360 T>C maps to NM_001100117.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:104898360 T>C maps to NM_001100117.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:3111187 T>C maps to NM_003804.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:3111187 T>C maps to NM_003804.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:94486258 C>T maps to NM_004560.2 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:94486258 C>T maps to NM_004560.2 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:92007406 C>A maps to NM_006378.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:92007406 C>A maps to NM_006378.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:26688943 G>T maps to NM_021115.4 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:26688943 G>T maps to NM_021115.4 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:48559801 G>A maps to NM_000338.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:48559801 G>A maps to NM_000338.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:43262342 G>C maps to NM_007163.3 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:43262342 G>C maps to NM_007163.3 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:22384369 C>T maps to NM_020346.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:22384369 C>T maps to NM_020346.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:116577933 G>A maps to NM_018420.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:116577933 G>A maps to NM_018420.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:62782096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:62782096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:61296405 C>T maps to NM_016354.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:61296405 C>T maps to NM_016354.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:24864908 G>T maps to ENST00000424834 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:24864908 G>T maps to ENST00000424834 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:147693700 C>A maps to NM_032566.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:147693700 C>A maps to NM_032566.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:121355924 C>T maps to NM_152546.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:121355924 C>T maps to NM_152546.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:99786547 T>C maps to NM_012447.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:99786547 T>C maps to NM_012447.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:113139549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:113139549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:123969978 C>T maps to NM_206862.2 F2013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:123969978 C>T maps to NM_206862.2 F2013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:222734834 C>A maps to NM_005681.2 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:222734834 C>A maps to NM_005681.2 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60698116 A>T maps to NM_017870.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60698116 A>T maps to NM_017870.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:150498727 C>A maps to NM_018487.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:150498727 C>A maps to NM_018487.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:175046688 C>T maps to NM_022093.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:175046688 C>T maps to NM_022093.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40661742 A>G maps to ENST00000454349 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40661742 A>G maps to ENST00000454349 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:42694686 G>T maps to ENST00000348077 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:42694686 G>T maps to ENST00000348077 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186315293 T>C maps to NM_003292.2 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186315293 T>C maps to NM_003292.2 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:41746638 C>A maps to NM_017886.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:41746638 C>A maps to NM_017886.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:216260105 G>A maps to ENST00000366943 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:216260105 G>A maps to ENST00000366943 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108247586 G>A maps to NM_006113.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108247586 G>A maps to NM_006113.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:113120583 T>A maps to NM_001164496.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:113120583 T>A maps to NM_001164496.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:85561703 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:85561703 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:31595227 C>A maps to NM_000379.3 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:31595227 C>A maps to NM_000379.3 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:28112853 T>C maps to NM_015171.2 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:28112853 T>C maps to NM_015171.2 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:756704 T>C maps to NM_005433.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:756704 T>C maps to NM_005433.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100344251 G>A maps to ENST00000349350 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100344251 G>A maps to ENST00000349350 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:28053455 A>T maps to NM_003447.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:28053455 A>T maps to NM_003447.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:37917229 C>T maps to NM_152484.2 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:37917229 C>T maps to NM_152484.2 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:60023 T>C maps to NM_182524.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:60023 T>C maps to NM_182524.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:182026293 G>T maps to NM_001009992.1 C284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:182026293 G>T maps to NM_001009992.1 C284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:22363350 C>A maps to NM_001001411.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:22363350 C>A maps to NM_001001411.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:22586188 C>A maps to NM_001098626.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:22586188 C>A maps to NM_001098626.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:119024779 C>A maps to NM_001142505.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:119024779 C>A maps to NM_001142505.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:161166643 C>T maps to NM_005099.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:161166643 C>T maps to NM_005099.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:78140366 C>A maps to NM_006020.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:78140366 C>A maps to NM_006020.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:37430688 G>T maps to ENST00000374660 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:37430688 G>T maps to ENST00000374660 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:14803803 C>A maps to NM_001145029.1 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:14803803 C>A maps to NM_001145029.1 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:46244360 C>T maps to NM_152641.2 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:46244360 C>T maps to NM_152641.2 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:32850662 C>T maps to NM_001672.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:32850662 C>T maps to NM_001672.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr13:26129180 C>A maps to NM_016529.4 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr13:26129180 C>A maps to NM_016529.4 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:83932640 G>A maps to NM_001717.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:83932640 G>A maps to NM_001717.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:79517502 C>T maps to NM_025161.5 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:79517502 C>T maps to NM_025161.5 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:207200841 T>A maps to NM_023938.5 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:207200841 T>A maps to NM_023938.5 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:57349287 G>T maps to NM_000562.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:57349287 G>T maps to NM_000562.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:54109765 C>T maps to NM_020898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:54109765 C>T maps to NM_020898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:3041473 C>A maps to NM_001014437.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:3041473 C>A maps to NM_001014437.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:26491829 G>A maps to NM_000730.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:26491829 G>A maps to NM_000730.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:51018160 G>A maps to NM_005198.4 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:51018160 G>A maps to NM_005198.4 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:85838570 G>A maps to NM_001861.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:85838570 G>A maps to NM_001861.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr13:95114415 G>T maps to NM_001129889.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr13:95114415 G>T maps to NM_001129889.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:56492021 G>A maps to ENST00000361203 Q1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:56492021 G>A maps to ENST00000361203 Q1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:15902235 G>A maps to NM_024948.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:15902235 G>A maps to NM_024948.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:10600509 C>A maps to NM_203500.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:10600509 C>A maps to NM_203500.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:134322837 C>T maps to NM_178554.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:134322837 C>T maps to NM_178554.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:141946048 G>T maps to NM_018557.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:141946048 G>T maps to NM_018557.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr8:20110502 G>A maps to NM_021020.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr8:20110502 G>A maps to NM_021020.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:132326280 G>A maps to NM_016155.4 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:132326280 G>A maps to NM_016155.4 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:233897386 G>A maps to NM_005383.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:233897386 G>A maps to NM_005383.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chrX:152027453 G>T maps to NM_015922.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chrX:152027453 G>T maps to NM_015922.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:58170745 A>T maps to NM_001005469.1 L46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:58170745 A>T maps to NM_001005469.1 L46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:55996690 C>A maps to NM_001142763.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:55996690 C>A maps to NM_001142763.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:140741991 G>T maps to NM_018923.2 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:140741991 G>T maps to NM_018923.2 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:186643667 G>A maps to NM_000963.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:186643667 G>A maps to NM_000963.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:5105124 G>T maps to NM_021163.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:5105124 G>T maps to NM_021163.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:169580745 G>T maps to NM_003005.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:169580745 G>T maps to NM_003005.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:51032015 C>T maps to NM_032802.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:51032015 C>T maps to NM_032802.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:1220716 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:1220716 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:29997962 C>T maps to NM_016151.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:29997962 C>T maps to NM_016151.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:10398886 C>T maps to ENST00000379613 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:10398886 C>T maps to ENST00000379613 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:38991094 C>T maps to NM_001195386.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:38991094 C>T maps to NM_001195386.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:69101201 G>A maps to NM_007114.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:69101201 G>A maps to NM_007114.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:110007728 C>T maps to NM_033390.1 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:110007728 C>T maps to NM_033390.1 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:57868089 G>T maps to ENST00000391705 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:57868089 G>T maps to ENST00000391705 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175897287 C>G maps to NM_014269.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175897287 C>G maps to NM_014269.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:112043034 G>C maps to NM_000677.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:112043034 G>C maps to NM_000677.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:12340268 G>A maps to NM_006796.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:12340268 G>A maps to NM_006796.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:4832528 C>A maps to NM_018836.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:4832528 C>A maps to NM_018836.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:2249447 C>T maps to NM_000479.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:2249447 C>T maps to NM_000479.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:90669503 T>C maps to NM_020801.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:90669503 T>C maps to NM_020801.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:54714429 G>A maps to NM_015941.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:54714429 G>A maps to NM_015941.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:50235516 C>G maps to NM_006045.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:50235516 C>G maps to NM_006045.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:63981399 G>A maps to NM_001177387.1 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:63981399 G>A maps to NM_001177387.1 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:134252845 G>T maps to NM_054025.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:134252845 G>T maps to NM_054025.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:29295087 C>T maps to NM_001029883.1 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:29295087 C>T maps to NM_001029883.1 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:15578884 C>A maps to NM_173550.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:15578884 C>A maps to NM_173550.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:105400604 C>T maps to NM_170662.3 K753K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:105400604 C>T maps to NM_170662.3 K753K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:146747842 G>A maps to NM_004284.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:146747842 G>A maps to NM_004284.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:170613431 C>G maps to NM_173872.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:170613431 C>G maps to NM_173872.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160268766 C>T maps to NM_001098398.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160268766 C>T maps to NM_001098398.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:113253964 G>A maps to NM_198123.1 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:113253964 G>A maps to NM_198123.1 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:96443608 C>A maps to NM_000772.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:96443608 C>A maps to NM_000772.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:162745570 C>A maps to NM_006182.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:162745570 C>A maps to NM_006182.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:42784848 G>T maps to NM_178009.2 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:42784848 G>T maps to NM_178009.2 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:137308270 A>G maps to NM_004717.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:137308270 A>G maps to NM_004717.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:13894779 C>A maps to NM_001369.2 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:13894779 C>A maps to NM_001369.2 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:111368371 G>T maps to ENST00000428084 G1962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:111368371 G>T maps to ENST00000428084 G1962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:21560097 T>C maps to NM_001397.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:21560097 T>C maps to NM_001397.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:22902780 C>T maps to NM_020526.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:22902780 C>T maps to NM_020526.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:57318977 C>T maps to NM_174912.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:57318977 C>T maps to NM_174912.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:67575921 C>A maps to NM_001193523.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:67575921 C>A maps to NM_001193523.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:45970489 C>A maps to NM_006486.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:45970489 C>A maps to NM_006486.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:6683888 C>T maps to NM_153230.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:6683888 C>T maps to NM_153230.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:172096131 C>A maps to NM_022763.3 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:172096131 C>A maps to NM_022763.3 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:108985208 G>A maps to NM_001455.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:108985208 G>A maps to NM_001455.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:79360061 A>T maps to NM_025074.6 S1791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:79360061 A>T maps to NM_025074.6 S1791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:155735335 G>A maps to ENST00000368331 Q1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:155735335 G>A maps to ENST00000368331 Q1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:45645553 A>G maps to NM_021072.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:45645553 A>G maps to NM_021072.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:43048961 C>A maps to ENST00000458501 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:43048961 C>A maps to ENST00000458501 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:12122959 A>T maps to NM_002114.2 K978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:12122959 A>T maps to NM_002114.2 K978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:185834870 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:185834870 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:18330608 C>A maps to NM_181507.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:18330608 C>A maps to NM_181507.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:152191000 G>T maps to NM_001009931.1 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:152191000 G>T maps to NM_001009931.1 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:152191908 C>T maps to NM_001009931.1 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:152191908 C>T maps to NM_001009931.1 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:94568259 A>G maps to NM_206949.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:94568259 A>G maps to NM_206949.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:41166313 T>A maps to NM_005533.4 *289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:41166313 T>A maps to NM_005533.4 *289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:23509711 G>T maps to NM_006547.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:23509711 G>T maps to NM_006547.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:52816081 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:52816081 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:93412787 C>A maps to NM_014216.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:93412787 C>A maps to NM_014216.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:170359634 C>T maps to ENST00000419050 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:170359634 C>T maps to ENST00000419050 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:111216207 C>T maps to NM_002232.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:111216207 C>T maps to NM_002232.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:155555400 G>T maps to NM_002239.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:155555400 G>T maps to NM_002239.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:36641963 A>G maps to NM_001031836.2 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:36641963 A>G maps to NM_001031836.2 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:36640041 G>C maps to NM_014657.1 S726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:36640041 G>C maps to NM_014657.1 S726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:58941425 G>T maps to ENST00000354386 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:58941425 G>T maps to ENST00000354386 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:128696921 T>C maps to NM_020741.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:128696921 T>C maps to NM_020741.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:8888085 G>T maps to NM_020738.2 G1153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:8888085 G>T maps to NM_020738.2 G1153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:135020831 G>A maps to ENST00000368572 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:135020831 G>A maps to ENST00000368572 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:38859774 G>A maps to NM_019016.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:38859774 G>A maps to NM_019016.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:53090180 G>A maps to NM_175078.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:53090180 G>A maps to NM_175078.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:149982924 C>A maps to NM_004690.2 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:149982924 C>A maps to NM_004690.2 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:48915894 T>C maps to NM_000233.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:48915894 T>C maps to NM_000233.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:54754667 G>A maps to NM_001081442.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:54754667 G>A maps to NM_001081442.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:160968970 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:160968970 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:99771305 C>A maps to NM_014839.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:99771305 C>A maps to NM_014839.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:15652161 C>A maps to NM_005924.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:15652161 C>A maps to NM_005924.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:50925882 C>A maps to NM_017584.5 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:50925882 C>A maps to NM_017584.5 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:24449046 G>T maps to NM_005932.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:24449046 G>T maps to NM_005932.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:49437166 C>A maps to NM_003482.3 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:49437166 C>A maps to NM_003482.3 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:49576221 G>A maps to NM_014484.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:49576221 G>A maps to NM_014484.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:57025677 G>C maps to NM_005372.1 Y288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:57025677 G>C maps to NM_005372.1 Y288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60070117 T>C maps to NM_148975.1 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60070117 T>C maps to NM_148975.1 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:9046506 A>G maps to NM_024690.2 F11708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:9046506 A>G maps to NM_024690.2 F11708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:1247869 G>A maps to ENST00000447027 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:1247869 G>A maps to ENST00000447027 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:10356615 A>T maps to NM_017533.2 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:10356615 A>T maps to NM_017533.2 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:12656521 G>T maps to NM_001146312.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:12656521 G>T maps to NM_001146312.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:201950244 T>C maps to NM_002491.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:201950244 T>C maps to NM_002491.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:55452323 T>C maps to ENST00000446217 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:55452323 T>C maps to ENST00000446217 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:108057297 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:108057297 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:129350834 A>T maps to NM_001030013.1 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:129350834 A>T maps to NM_001030013.1 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:78399144 T>G maps to NM_001098816.2 I1738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:78399144 T>G maps to NM_001098816.2 I1738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:27925332 G>T maps to NM_012367.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:27925332 G>T maps to NM_012367.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:247694973 G>A maps to NM_198074.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:247694973 G>A maps to NM_198074.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:248789556 G>A maps to NM_001001964.1 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:248789556 G>A maps to NM_001001964.1 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:247875403 A>G maps to NM_001005286.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:247875403 A>G maps to NM_001005286.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:123813615 G>T maps to NM_001005187.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:123813615 G>T maps to NM_001005187.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:128697855 G>C maps to ENST00000373487 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:128697855 G>C maps to ENST00000373487 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrY:4925347 G>T maps to NM_032973.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrY:4925347 G>T maps to NM_032973.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:233190058 C>A maps to NM_014801.3 G1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:233190058 C>A maps to NM_014801.3 G1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:65385567 C>T maps to NM_032223.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:65385567 C>T maps to NM_032223.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:65385574 G>T maps to NM_032223.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:65385574 G>T maps to NM_032223.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:66713196 C>A maps to NM_001037341.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:66713196 C>A maps to NM_001037341.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160001424 A>G maps to NM_145167.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160001424 A>G maps to NM_145167.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:72499544 C>A maps to ENST00000419739 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:72499544 C>A maps to ENST00000419739 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:20335797 G>T maps to NM_032812.7 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:20335797 G>T maps to NM_032812.7 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:113558625 G>T maps to NM_002711.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:113558625 G>T maps to NM_002711.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:9550048 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:9550048 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:40900894 G>A maps to NM_181882.2 Q1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:40900894 G>A maps to NM_181882.2 Q1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:209309586 G>A maps to NM_005048.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:209309586 G>A maps to NM_005048.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:125004273 C>G maps to NM_033117.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:125004273 C>G maps to NM_033117.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:35752768 A>G maps to ENST00000456972 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:35752768 A>G maps to ENST00000456972 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:152273318 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:152273318 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:75115887 C>T maps to NM_001005.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:75115887 C>T maps to NM_001005.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:93026809 T>A maps to NM_175634.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:93026809 T>A maps to NM_175634.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:165378823 G>A maps to NM_006917.4 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:165378823 G>A maps to NM_006917.4 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:38954166 G>C maps to NM_000540.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:38954166 G>C maps to NM_000540.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:56042602 C>T maps to NM_001101401.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:56042602 C>T maps to NM_001101401.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:144890967 G>C maps to NM_182706.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:144890967 G>C maps to NM_182706.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:44674596 C>A maps to NM_001134771.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:44674596 C>A maps to NM_001134771.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:118596767 G>T maps to NM_001029858.3 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:118596767 G>T maps to NM_001029858.3 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:48604460 C>T maps to NM_005985.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:48604460 C>T maps to NM_005985.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:22415692 C>A maps to NM_005775.4 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:22415692 C>A maps to NM_005775.4 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:124116914 A>G maps to NM_004099.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:124116914 A>G maps to NM_004099.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:10410283 C>G maps to ENST00000379613 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:10410283 C>G maps to ENST00000379613 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:38776143 G>T maps to NM_030956.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:38776143 G>T maps to NM_030956.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:179453979 A>T maps to NM_133378.4 A18256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:179453979 A>T maps to NM_133378.4 A18256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:33475290 G>A maps to NM_173167.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:33475290 G>A maps to NM_173167.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:74951892 A>G maps to NM_030581.3 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:74951892 A>G maps to NM_030581.3 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:75230866 G>A maps to NM_019589.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:75230866 G>A maps to NM_019589.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:52192872 A>G maps to NM_006526.2 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:52192872 A>G maps to NM_006526.2 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:111846827 G>C maps to NM_021994.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:111846827 G>C maps to NM_021994.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:23688995 G>A maps to NM_001077195.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:23688995 G>A maps to NM_001077195.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:151262665 T>C maps to NM_020832.1 H1011H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:151262665 T>C maps to NM_020832.1 H1011H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:123434443 C>T maps to NM_203444.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:123434443 C>T maps to NM_203444.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:44079960 C>A maps to NM_022437.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:44079960 C>A maps to NM_022437.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:50472280 C>T maps to NM_020039.2 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:50472280 C>T maps to NM_020039.2 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:7709406 C>A maps to NM_020546.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:7709406 C>A maps to NM_020546.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:117139108 C>G maps to NM_030767.4 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:117139108 C>G maps to NM_030767.4 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:21902328 C>A maps to NM_000478.4 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:21902328 C>A maps to NM_000478.4 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:129851285 G>A maps to NM_012098.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:129851285 G>A maps to NM_012098.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:38229003 A>G maps to NM_138797.2 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:38229003 A>G maps to NM_138797.2 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:60641387 C>T maps to NM_001002858.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:60641387 C>T maps to NM_001002858.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:17983153 G>A maps to NM_018125.3 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:17983153 G>A maps to NM_018125.3 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:3002329 C>A maps to NM_004042.3 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:3002329 C>A maps to NM_004042.3 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:77254173 G>T maps to ENST00000355691 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:77254173 G>T maps to ENST00000355691 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31608183 G>T maps to NM_025227.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31608183 G>T maps to NM_025227.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:107914367 G>T maps to NM_001018072.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:107914367 G>T maps to NM_001018072.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:165715669 C>A maps to NM_144980.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:165715669 C>A maps to NM_144980.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:201043677 G>T maps to NM_000069.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:201043677 G>T maps to NM_000069.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:138714661 C>G maps to ENST00000409386 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:138714661 C>G maps to ENST00000409386 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:37518590 G>C maps to NM_001236.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:37518590 G>C maps to NM_001236.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:78021137 C>A maps to NM_017950.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:78021137 C>A maps to NM_017950.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:117561103 A>C maps to NM_004258.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:117561103 A>C maps to NM_004258.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:43027804 C>G maps to NM_138477.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:43027804 C>G maps to NM_138477.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:45206811 T>A maps to ENST00000396750 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:45206811 T>A maps to ENST00000396750 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:383703 T>A maps to NM_006614.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:383703 T>A maps to NM_006614.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:101982737 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:101982737 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:76573653 G>T maps to NM_033401.3 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:76573653 G>T maps to NM_033401.3 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:34071499 G>T maps to NM_052896.3 A2104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:34071499 G>T maps to NM_052896.3 A2104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:122060407 C>T maps to NM_005213.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:122060407 C>T maps to NM_005213.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:35333796 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:35333796 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:100182492 C>T maps to NM_006668.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:100182492 C>T maps to NM_006668.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:15769364 G>A maps to NM_000896.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:15769364 G>A maps to NM_000896.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:162748380 T>A maps to NM_006182.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:162748380 T>A maps to NM_006182.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:47954023 G>T maps to ENST00000318711 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:47954023 G>T maps to ENST00000318711 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:37617640 C>T maps to NM_005128.2 D1121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:37617640 C>T maps to NM_005128.2 D1121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:236645936 C>T maps to NM_145861.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:236645936 C>T maps to NM_145861.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142563341 C>G maps to NM_004445.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142563341 C>G maps to NM_004445.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:75246764 G>A maps to NM_001432.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:75246764 G>A maps to NM_001432.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:187626437 C>A maps to NM_177454.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:187626437 C>A maps to NM_177454.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:150946773 G>A maps to NM_001447.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:150946773 G>A maps to NM_001447.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92086705 G>T maps to ENST00000298047 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92086705 G>T maps to ENST00000298047 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92616482 C>G maps to ENST00000298047 P4287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92616482 C>G maps to ENST00000298047 P4287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:5540693 G>A maps to ENST00000312577 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:5540693 G>A maps to ENST00000312577 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:230861623 A>T maps to NM_174899.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:230861623 A>T maps to NM_174899.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:39974500 C>A maps to NM_021939.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:39974500 C>A maps to NM_021939.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:152284187 G>T maps to NM_002016.1 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:152284187 G>T maps to NM_002016.1 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:29005448 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:29005448 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:79343065 G>A maps to NM_025074.6 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:79343065 G>A maps to NM_025074.6 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:90895970 G>T maps to NM_003505.1 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:90895970 G>T maps to NM_003505.1 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:99773221 C>G maps to NM_152742.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:99773221 C>G maps to NM_152742.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:113803682 G>T maps to NM_006028.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:113803682 G>T maps to NM_006028.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:656683 C>G maps to NM_148959.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:656683 C>G maps to NM_148959.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:71007833 G>T maps to NM_032821.2 A1708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:71007833 G>T maps to NM_032821.2 A1708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:53494881 C>A maps to NM_002178.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:53494881 C>A maps to NM_002178.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:133790343 C>A maps to NM_014987.1 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:133790343 C>A maps to NM_014987.1 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:117864125 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:117864125 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:6086640 C>A maps to NM_001099433.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:6086640 C>A maps to NM_001099433.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:63246541 G>T maps to NM_139318.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:63246541 G>T maps to NM_139318.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:13232873 C>G maps to NM_020853.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:13232873 C>G maps to NM_020853.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:17817464 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:17817464 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:21441623 G>A maps to ENST00000416669 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:21441623 G>A maps to ENST00000416669 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:97821046 C>T maps to NM_014916.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:97821046 C>T maps to NM_014916.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:121413407 G>A maps to NM_002317.5 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:121413407 G>A maps to NM_002317.5 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:70004183 G>T maps to NM_201550.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:70004183 G>T maps to NM_201550.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:242161852 G>A maps to NM_001004343.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:242161852 G>A maps to NM_001004343.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:29340602 C>A maps to NM_001034172.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:29340602 C>A maps to NM_001034172.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:89053847 C>A maps to NM_005941.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:89053847 C>A maps to NM_005941.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:88703607 C>A maps to NM_024756.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:88703607 C>A maps to NM_024756.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:10253942 C>T maps to NM_003802.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:10253942 C>T maps to NM_003802.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:34859854 C>A maps to NM_001163735.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:34859854 C>A maps to NM_001163735.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:1926244 G>T maps to ENST00000399161 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:1926244 G>T maps to ENST00000399161 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:19334855 C>A maps to NM_004386.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:19334855 C>A maps to NM_004386.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:233834988 G>T maps to NM_019850.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:233834988 G>T maps to NM_019850.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:247588095 C>T maps to NM_004895.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:247588095 C>T maps to NM_004895.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:3019783 C>A maps to NM_000904.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:3019783 C>A maps to NM_000904.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:64390551 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:64390551 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:102512146 C>A maps to NM_024057.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:102512146 C>A maps to NM_024057.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:228482093 C>T maps to NM_001098623.1 T3791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:228482093 C>T maps to NM_001098623.1 T3791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:55615131 C>A maps to NM_001005280.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:55615131 C>A maps to NM_001005280.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:6806978 C>A maps to NM_001004489.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:6806978 C>A maps to NM_001004489.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:59224870 G>A maps to NM_001004708.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:59224870 G>A maps to NM_001004708.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:5776386 C>A maps to NM_001005175.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:5776386 C>A maps to NM_001005175.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:5969346 C>A maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:5969346 C>A maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:98002177 G>T maps to NM_001005482.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:98002177 G>T maps to NM_001005482.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:158517139 G>C maps to NM_001005189.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:158517139 G>C maps to NM_001005189.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:9225998 G>T maps to ENST00000293614 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:9225998 G>T maps to ENST00000293614 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:48920046 C>T maps to NM_001005203.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:48920046 C>T maps to NM_001005203.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:56468504 G>T maps to NM_001013358.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:56468504 G>T maps to NM_001013358.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:140581683 T>C maps to NM_018931.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:140581683 T>C maps to NM_018931.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:95394517 G>T maps to NM_006204.3 G375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:95394517 G>T maps to NM_006204.3 G375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:6255622 C>A maps to NM_004566.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:6255622 C>A maps to NM_004566.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:86271324 C>T maps to NM_015425.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:86271324 C>T maps to NM_015425.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:70118298 G>T maps to NM_003626.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:70118298 G>T maps to NM_003626.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:12919587 G>T maps to NM_023014.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:12919587 G>T maps to NM_023014.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:53822337 C>A maps to NM_001098512.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:53822337 C>A maps to NM_001098512.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:3677878 C>A maps to NM_019854.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:3677878 C>A maps to NM_019854.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:198665955 C>A maps to ENST00000271610 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:198665955 C>A maps to ENST00000271610 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:103193922 G>A maps to ENST00000428762 T2019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:103193922 G>A maps to ENST00000428762 T2019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:176799027 C>T maps to ENST00000398128 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:176799027 C>T maps to ENST00000398128 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:21790023 G>A maps to NM_020366.3 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:21790023 G>A maps to NM_020366.3 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:60213092 A>G maps to NM_021136.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:60213092 A>G maps to NM_021136.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:237895399 C>T maps to NM_001035.2 L3664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:237895399 C>T maps to NM_001035.2 L3664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:165986746 A>T maps to NM_006922.3 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:165986746 A>T maps to NM_006922.3 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:29909284 C>A maps to NM_201575.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:29909284 C>A maps to NM_201575.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:155935667 G>T maps to NM_000337.5 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:155935667 G>T maps to NM_000337.5 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:72890282 G>C maps to NM_018130.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:72890282 G>C maps to NM_018130.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:95360465 C>T maps to NM_001114106.1 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:95360465 C>T maps to NM_001114106.1 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:84454310 C>A maps to NM_052910.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:84454310 C>A maps to NM_052910.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:220354240 C>A maps to NM_005876.4 S2834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:220354240 C>A maps to NM_005876.4 S2834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:23016164 G>T maps to NM_001052.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:23016164 G>T maps to NM_001052.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:131285835 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:131285835 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129566309 G>T maps to NM_133448.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129566309 G>T maps to NM_133448.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77709293 A>T maps to NM_020431.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77709293 A>T maps to NM_020431.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:5360179 G>A maps to NM_001080495.2 Q2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:5360179 G>A maps to NM_001080495.2 Q2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:165961742 A>G maps to NM_152620.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:165961742 A>G maps to NM_152620.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:101353722 G>T maps to NM_004621.5 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:101353722 G>T maps to NM_004621.5 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:45825877 C>A maps to ENST00000397932 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:45825877 C>A maps to ENST00000397932 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:41716672 G>A maps to ENST00000351589 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:41716672 G>A maps to ENST00000351589 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:77766326 C>A maps to NM_024721.4 P2390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:77766326 C>A maps to NM_024721.4 P2390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:9534019 G>T maps to NM_003442.5 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:9534019 G>T maps to NM_003442.5 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:22157391 G>T maps to NM_007153.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:22157391 G>T maps to NM_007153.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:21552500 G>T maps to NM_024697.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:21552500 G>T maps to NM_024697.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:72346332 A>T maps to NM_017757.2 K1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:72346332 A>T maps to NM_017757.2 K1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:31040158 C>T maps to NM_014717.1 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:31040158 C>T maps to NM_014717.1 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:53855115 A>T maps to NM_138374.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:53855115 A>T maps to NM_138374.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44053559 C>A maps to NM_022436.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44053559 C>A maps to NM_022436.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33588880 C>T maps to NM_030955.2 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33588880 C>T maps to NM_030955.2 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:5306810 G>A maps to NM_139056.2 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:5306810 G>A maps to NM_139056.2 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:167825401 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:167825401 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:86807970 T>C maps to NM_152336.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:86807970 T>C maps to NM_152336.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:27874643 G>C maps to NM_001029882.2 S1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:27874643 G>C maps to NM_001029882.2 S1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:105418112 G>T maps to NM_138420.2 G1225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:105418112 G>T maps to NM_138420.2 G1225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:151674268 C>T maps to NM_005100.3 H1581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:151674268 C>T maps to NM_005100.3 H1581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:202582932 C>A maps to NM_020919.3 G1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:202582932 C>A maps to NM_020919.3 G1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:22281219 G>A maps to NM_213599.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:22281219 G>A maps to NM_213599.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:41004382 C>T maps to NM_003734.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:41004382 C>T maps to NM_003734.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:201683038 C>T maps to ENST00000452790 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:201683038 C>T maps to ENST00000452790 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:103566612 T>A maps to NM_001077594.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:103566612 T>A maps to NM_001077594.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:13885475 C>T maps to NM_014047.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:13885475 C>T maps to NM_014047.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:86163065 C>T maps to NM_198584.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:86163065 C>T maps to NM_198584.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:67698482 A>T maps to NM_018448.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:67698482 A>T maps to NM_018448.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:119961557 C>T maps to NM_178499.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:119961557 C>T maps to NM_178499.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:44371572 A>G maps to NM_001253.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:44371572 A>G maps to NM_001253.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:22358636 C>T maps to NM_001802.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:22358636 C>T maps to NM_001802.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:51984863 A>T maps to NM_001080405.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:51984863 A>T maps to NM_001080405.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:6215696 G>A maps to NM_015557.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:6215696 G>A maps to NM_015557.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:175622694 C>T maps to NM_001039523.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:175622694 C>T maps to NM_001039523.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:58621299 G>T maps to NM_016284.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:58621299 G>T maps to NM_016284.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:230795244 T>C maps to NM_007357.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:230795244 T>C maps to NM_007357.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:103449746 C>A maps to NM_080629.2 G847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:103449746 C>A maps to NM_080629.2 G847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:99625319 G>A maps to NM_018058.4 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:99625319 G>A maps to NM_018058.4 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:51025875 G>A maps to NM_005215.3 Q1369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:51025875 G>A maps to NM_005215.3 Q1369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:162729652 G>T maps to NM_006182.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:162729652 G>T maps to NM_006182.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:134713797 A>T maps to NM_182540.4 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:134713797 A>T maps to NM_182540.4 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:111743051 G>A maps to NM_024901.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:111743051 G>A maps to NM_024901.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:13830205 T>A maps to NM_001369.2 K2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:13830205 T>A maps to NM_001369.2 K2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:38758182 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:38758182 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:225635347 T>A maps to NM_014689.2 P2073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:225635347 T>A maps to NM_014689.2 P2073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102510612 C>T maps to NM_001376.4 G4229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102510612 C>T maps to NM_001376.4 G4229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:71741005 G>T maps to NM_001130987.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:71741005 G>T maps to NM_001130987.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184042134 G>A maps to NM_001194947.1 T880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184042134 G>A maps to NM_001194947.1 T880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:77705080 C>T maps to NM_178543.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:77705080 C>T maps to NM_178543.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:23191569 G>T maps to ENST00000400191 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:23191569 G>T maps to ENST00000400191 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:56196892 C>T maps to NM_001130071.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:56196892 C>T maps to NM_001130071.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:61112134 G>A maps to ENST00000442566 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:61112134 G>A maps to ENST00000442566 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:144812632 C>A maps to NM_198488.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:144812632 C>A maps to NM_198488.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:1313598 G>T maps to NM_033260.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:1313598 G>T maps to NM_033260.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:52327525 C>T maps to NM_002030.3 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:52327525 C>T maps to NM_002030.3 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:153927567 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:153927567 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:161116289 G>A maps to NM_000811.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:161116289 G>A maps to NM_000811.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:150325195 G>T maps to ENST00000438845 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:150325195 G>T maps to ENST00000438845 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:102160037 A>C maps to NM_024312.4 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:102160037 A>C maps to NM_024312.4 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:117128029 G>A maps to NM_148963.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:117128029 G>A maps to NM_148963.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:9857329 G>T maps to NM_000833.3 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:9857329 G>T maps to NM_000833.3 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:222696209 T>C maps to NM_024746.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:222696209 T>C maps to NM_024746.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:228612716 G>A maps to NM_003493.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:228612716 G>A maps to NM_003493.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:32976018 G>T maps to NM_002119.3 Y34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:32976018 G>T maps to NM_002119.3 Y34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:46607741 G>C maps to NM_002144.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:46607741 G>C maps to NM_002144.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:20818971 C>A maps to NM_022460.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:20818971 C>A maps to NM_022460.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:206945735 C>A maps to NM_000572.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:206945735 C>A maps to NM_000572.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:50397695 C>A maps to NM_172374.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:50397695 C>A maps to NM_172374.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:201844050 T>G maps to NM_018085.4 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:201844050 T>G maps to NM_018085.4 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17949155 G>A maps to NM_000215.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17949155 G>A maps to NM_000215.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:163361084 A>T maps to NM_033272.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:163361084 A>T maps to NM_033272.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752587 G>C maps to NM_001080424.1 V994V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752587 G>C maps to NM_001080424.1 V994V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752683 G>A maps to NM_001080424.1 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752683 G>A maps to NM_001080424.1 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752914 G>C maps to NM_001080424.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752914 G>C maps to NM_001080424.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7753195 G>A maps to NM_001080424.1 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7753195 G>A maps to NM_001080424.1 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:46677780 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:46677780 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:24762578 A>G maps to NM_019590.3 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:24762578 A>G maps to NM_019590.3 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:71553274 T>G maps to NM_016027.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:71553274 T>G maps to NM_016027.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:7080457 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:7080457 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:96315307 A>T maps to NM_005575.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:96315307 A>T maps to NM_005575.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:40399543 G>A maps to NM_020737.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:40399543 G>A maps to NM_020737.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:141707802 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:141707802 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:70478697 C>A maps to NM_020794.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:70478697 C>A maps to NM_020794.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:21900703 C>T maps to NM_015884.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:21900703 C>T maps to NM_015884.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:182789018 G>A maps to NM_020166.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:182789018 G>A maps to NM_020166.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:90402560 G>A maps to NM_014611.1 A3396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:90402560 G>A maps to NM_014611.1 A3396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:141750532 A>T maps to ENST00000475668 K892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:141750532 A>T maps to ENST00000475668 K892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:37838829 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:37838829 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:135521438 C>T maps to NM_001130173.1 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:135521438 C>T maps to NM_001130173.1 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:10366497 T>C maps to NM_017533.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:10366497 T>C maps to NM_017533.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:2017596 G>T maps to NM_003970.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:2017596 G>T maps to NM_003970.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:114167427 C>T maps to NM_006169.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:114167427 C>T maps to NM_006169.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:139395152 C>A maps to NM_017617.3 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:139395152 C>A maps to NM_017617.3 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158450116 G>T maps to NM_001004472.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158450116 G>T maps to NM_001004472.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:248844993 C>T maps to NM_001004734.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:248844993 C>T maps to NM_001004734.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:57970939 G>A maps to NM_001004459.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:57970939 G>A maps to NM_001004459.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:247695585 C>G maps to NM_198074.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:247695585 C>G maps to NM_198074.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:248309309 C>A maps to NM_001004690.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:248309309 C>A maps to NM_001004690.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:20502512 G>T maps to NM_001004714.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:20502512 G>T maps to NM_001004714.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176564365 G>T maps to NM_020318.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176564365 G>T maps to NM_020318.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:56287632 G>A maps to NM_001142763.1 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:56287632 G>A maps to NM_001142763.1 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:107533453 C>G maps to NM_020381.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:107533453 C>G maps to NM_020381.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:28269748 A>T maps to NM_032507.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:28269748 A>T maps to NM_032507.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:65108868 G>A maps to ENST00000333425 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:65108868 G>A maps to ENST00000333425 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:18435366 C>T maps to NM_004570.4 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:18435366 C>T maps to NM_004570.4 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:17051998 A>G maps to NM_001144382.1 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:17051998 A>G maps to NM_001144382.1 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:12012719 C>T maps to ENST00000376369 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:12012719 C>T maps to ENST00000376369 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:51820114 G>T maps to NM_007195.2 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:51820114 G>T maps to NM_007195.2 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7402374 T>C maps to NM_000937.4 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7402374 T>C maps to NM_000937.4 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:1095299 C>T maps to NM_002695.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:1095299 C>T maps to NM_002695.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44428592 T>C maps to NM_002706.4 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44428592 T>C maps to NM_002706.4 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:47273726 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:47273726 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:42689589 G>T maps to NM_000322.4 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:42689589 G>T maps to NM_000322.4 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:50099341 G>T maps to NM_020719.1 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:50099341 G>T maps to NM_020719.1 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:52321963 G>A maps to NM_144651.4 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:52321963 G>A maps to NM_144651.4 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:10433904 G>A maps to NM_133452.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:10433904 G>A maps to NM_133452.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:48954376 A>T maps to NM_000321.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:48954376 A>T maps to NM_000321.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:145742149 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:145742149 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:79313627 G>T maps to NM_006507.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:79313627 G>T maps to NM_006507.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:237789018 G>T maps to NM_001035.2 G2027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:237789018 G>T maps to NM_001035.2 G2027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:38908895 T>A maps to ENST00000302328 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:38908895 T>A maps to ENST00000302328 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:167145087 A>G maps to ENST00000303354 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:167145087 A>G maps to ENST00000303354 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:71412115 C>T maps to NM_001144952.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:71412115 C>T maps to NM_001144952.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:150933450 T>G maps to NM_001145415.1 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:150933450 T>G maps to NM_001145415.1 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:100838548 C>T maps to ENST00000262901 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:100838548 C>T maps to ENST00000262901 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:46239859 G>T maps to NM_003726.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:46239859 G>T maps to NM_003726.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:173486707 C>A maps to NM_178527.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:173486707 C>A maps to NM_178527.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:164906952 G>A maps to NM_014926.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:164906952 G>A maps to NM_014926.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:11170530 G>T maps to NM_001128849.1 E1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:11170530 G>T maps to NM_001128849.1 E1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:96943346 C>T maps to NM_014014.3 W1954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:96943346 C>T maps to NM_014014.3 W1954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:23716277 C>A maps to NM_006940.4 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:23716277 C>A maps to NM_006940.4 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158624418 C>G maps to NM_003126.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158624418 C>G maps to NM_003126.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158636288 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158636288 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:103984724 A>C maps to NM_017564.9 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:103984724 A>C maps to NM_017564.9 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:132785214 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:132785214 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:132909898 G>T maps to NM_003967.2 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:132909898 G>T maps to NM_003967.2 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33457372 G>C maps to ENST00000455217 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33457372 G>C maps to ENST00000455217 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:69097042 T>G maps to NM_182502.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:69097042 T>G maps to NM_182502.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:72338117 G>T maps to ENST00000389376 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:72338117 G>T maps to ENST00000389376 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:80749411 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:80749411 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:17522676 G>T maps to NM_153676.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:17522676 G>T maps to NM_153676.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:17202920 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:17202920 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:10099382 G>A maps to NM_017491.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:10099382 G>A maps to NM_017491.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:122396982 C>T maps to NM_144668.4 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:122396982 C>T maps to NM_144668.4 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:184233491 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:184233491 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:88694394 C>G maps to ENST00000452588 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:88694394 C>G maps to ENST00000452588 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:22154535 A>T maps to NM_007153.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:22154535 A>T maps to NM_007153.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:44792867 A>G maps to NM_004234.4 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:44792867 A>G maps to NM_004234.4 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:71590291 T>C maps to NM_014497.3 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:71590291 T>C maps to NM_014497.3 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:238048521 G>A maps to NM_021186.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:238048521 G>A maps to NM_021186.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2328070 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2328070 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:18681847 G>C maps to NM_001040272.4 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:18681847 G>C maps to NM_001040272.4 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:58126628 C>T maps to NM_001122772.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:58126628 C>T maps to NM_001122772.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:100340790 C>G maps to ENST00000311030 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:100340790 C>G maps to ENST00000311030 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:42869851 G>T maps to NM_016248.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:42869851 G>T maps to NM_016248.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:110607490 G>A maps to NM_006492.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:110607490 G>A maps to NM_006492.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26568987 C>T maps to NM_031418.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26568987 C>T maps to NM_031418.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154293723 G>A maps to NM_080429.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154293723 G>A maps to NM_080429.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:153803942 C>A maps to NM_001025595.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:153803942 C>A maps to NM_001025595.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7516152 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7516152 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:119976663 C>A maps to ENST00000313400 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:119976663 C>A maps to ENST00000313400 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:28912102 C>A maps to NM_173201.3 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:28912102 C>A maps to NM_173201.3 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:33217114 G>T maps to NM_198428.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:33217114 G>T maps to NM_198428.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:118769540 G>A maps to NM_182557.2 N1361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:118769540 G>A maps to NM_182557.2 N1361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:120069236 G>A maps to NM_001017927.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:120069236 G>A maps to NM_001017927.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:62636554 G>T maps to ENST00000383709 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:62636554 G>T maps to ENST00000383709 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:202074064 C>T maps to NM_032977.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:202074064 C>T maps to NM_032977.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:71282453 G>A maps to NM_012121.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:71282453 G>A maps to NM_012121.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:176002978 C>A maps to NM_001171976.1 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:176002978 C>A maps to NM_001171976.1 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:125891245 C>A maps to ENST00000392693 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:125891245 C>A maps to ENST00000392693 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:37775117 C>T maps to NM_005441.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:37775117 C>T maps to NM_005441.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:6206462 C>A maps to NM_015557.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:6206462 C>A maps to NM_015557.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:103986585 G>A maps to NM_001823.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:103986585 G>A maps to NM_001823.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:140285094 G>T maps to NM_022131.2 *956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:140285094 G>T maps to NM_022131.2 *956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:33144975 G>A maps to NM_080680.2 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:33144975 G>A maps to NM_080680.2 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:70647992 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:70647992 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:7571509 G>C maps to NM_001037763.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:7571509 G>C maps to NM_001037763.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:48630048 G>A maps to NM_000094.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:48630048 G>A maps to NM_000094.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:17292344 C>T maps to NM_014675.3 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:17292344 C>T maps to NM_014675.3 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:104388027 C>T maps to NM_138455.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:104388027 C>T maps to NM_138455.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:80816439 G>T maps to ENST00000402739 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:80816439 G>T maps to ENST00000402739 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:143960554 G>A maps to ENST00000377675 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:143960554 G>A maps to ENST00000377675 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:86068171 G>T maps to NM_053281.3 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:86068171 G>T maps to NM_053281.3 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6651356 C>T maps to NM_003737.2 E1556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6651356 C>T maps to NM_003737.2 E1556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:36779849 C>A maps to NM_033403.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:36779849 C>A maps to NM_033403.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:108709289 G>T maps to NM_004398.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:108709289 G>T maps to NM_004398.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:50134574 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:50134574 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:21603894 C>A maps to NM_003777.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:21603894 C>A maps to NM_003777.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:76433797 G>A maps to ENST00000389840 N3980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:76433797 G>A maps to ENST00000389840 N3980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:130985089 G>T maps to ENST00000372923 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:130985089 G>T maps to ENST00000372923 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:225695308 T>A maps to NM_014689.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:225695308 T>A maps to NM_014689.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:340165 A>G maps to NM_203447.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:340165 A>G maps to NM_203447.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:41667980 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:41667980 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:7585771 C>A maps to NM_004415.2 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:7585771 C>A maps to NM_004415.2 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:95285067 C>T maps to NM_001393.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:95285067 C>T maps to NM_001393.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:3979398 C>A maps to NM_001961.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:3979398 C>A maps to NM_001961.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:38893430 C>A maps to NM_138389.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:38893430 C>A maps to NM_138389.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:139160790 G>A maps to NM_015912.3 H1140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:139160790 G>A maps to NM_015912.3 H1140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:88911170 C>T maps to ENST00000298786 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:88911170 C>T maps to ENST00000298786 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:114569275 C>A maps to NM_182495.5 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:114569275 C>A maps to NM_182495.5 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:43627279 G>T maps to NM_001145196.1 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:43627279 G>T maps to NM_001145196.1 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30937209 C>T maps to NM_001099784.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30937209 C>T maps to NM_001099784.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:5956139 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:5956139 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:87367538 C>A maps to NM_024735.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:87367538 C>A maps to NM_024735.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:152324369 G>T maps to NM_001014342.2 P1964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:152324369 G>T maps to NM_001014342.2 P1964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:58154383 A>T maps to NM_001164317.1 T2503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:58154383 A>T maps to NM_001164317.1 T2503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:240371459 G>A maps to ENST00000406993 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:240371459 G>A maps to ENST00000406993 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:32783855 T>A maps to NM_023037.2 V1470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:32783855 T>A maps to NM_023037.2 V1470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:71318667 C>A maps to NM_018348.5 G386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:71318667 C>A maps to NM_018348.5 G386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:39341358 G>A maps to NM_030772.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:39341358 G>A maps to NM_030772.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:6554778 C>A maps to NM_000170.2 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:6554778 C>A maps to NM_000170.2 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:133357452 C>T maps to NM_005895.3 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:133357452 C>T maps to NM_005895.3 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:23313758 C>T maps to ENST00000435486 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:23313758 C>T maps to ENST00000435486 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:154146867 G>A maps to NM_001038705.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:154146867 G>A maps to NM_001038705.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:133174632 C>T maps to NM_001508.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:133174632 C>T maps to NM_001508.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:122641152 G>T maps to NM_005328.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:122641152 G>T maps to NM_005328.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:155254544 G>A maps to NM_020897.1 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:155254544 G>A maps to NM_020897.1 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:78697766 C>T maps to NM_004272.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:78697766 C>T maps to NM_004272.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:11400897 C>T maps to NM_005114.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:11400897 C>T maps to NM_005114.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:118824885 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:118824885 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:13264218 G>T maps to NM_004907.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:13264218 G>T maps to NM_004907.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160062750 G>A maps to NM_052868.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160062750 G>A maps to NM_052868.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:113832766 G>A maps to NM_032556.4 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:113832766 G>A maps to NM_032556.4 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7267398 C>A maps to NM_000208.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7267398 C>A maps to NM_000208.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15646308 G>A maps to NM_003638.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15646308 G>A maps to NM_003638.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:31332581 C>T maps to NM_001145808.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:31332581 C>T maps to NM_001145808.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:187506202 A>G maps to NM_002210.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:187506202 A>G maps to NM_002210.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:123813743 G>A maps to NM_001024660.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:123813743 G>A maps to NM_001024660.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:63246454 C>G maps to NM_139318.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:63246454 C>G maps to NM_139318.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:43497740 G>A maps to NM_020964.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:43497740 G>A maps to NM_020964.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:135012103 G>T maps to ENST00000368572 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:135012103 G>T maps to ENST00000368572 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:53009974 C>A maps to NM_175068.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:53009974 C>A maps to NM_175068.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32127564 G>T maps to NM_181619.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32127564 G>T maps to NM_181619.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:53307451 G>A maps to NM_007015.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:53307451 G>A maps to NM_007015.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:77907656 G>A maps to NM_032808.5 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:77907656 G>A maps to NM_032808.5 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:155665771 C>A maps to NM_004744.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:155665771 C>A maps to NM_004744.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141665494 G>T maps to NM_018557.2 C1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141665494 G>T maps to NM_018557.2 C1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:76376989 G>T maps to NM_001128922.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:76376989 G>T maps to NM_001128922.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51051825 G>C maps to NM_001080457.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51051825 G>C maps to NM_001080457.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:133650260 C>A maps to ENST00000250173 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:133650260 C>A maps to ENST00000250173 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:143856770 G>A maps to NM_177457.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:143856770 G>A maps to NM_177457.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:17838466 G>T maps to NM_018174.4 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:17838466 G>T maps to NM_018174.4 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:144803919 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:144803919 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30129406 C>A maps to NM_002746.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30129406 C>A maps to NM_002746.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:135076303 C>T maps to NM_002410.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:135076303 C>T maps to NM_002410.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107084576 C>T maps to NM_012216.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107084576 C>T maps to NM_012216.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:89209475 G>A maps to NM_005941.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:89209475 G>A maps to NM_005941.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:60744813 G>A maps to NM_006039.3 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:60744813 G>A maps to NM_006039.3 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:17998015 G>T maps to NM_001105569.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:17998015 G>T maps to NM_001105569.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:816887 G>T maps to NM_013404.4 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:816887 G>T maps to NM_013404.4 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9077692 G>T maps to NM_024690.2 A3251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9077692 G>T maps to NM_024690.2 A3251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1262981 C>A maps to ENST00000447027 T1627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1262981 C>A maps to ENST00000447027 T1627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1279597 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1279597 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1026436 G>T maps to NM_005961.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1026436 G>T maps to NM_005961.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:3240857 T>A maps to NM_015419.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:3240857 T>A maps to NM_015419.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:52664515 C>A maps to ENST00000358212 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:52664515 C>A maps to ENST00000358212 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:40192631 C>A maps to NM_015460.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:40192631 C>A maps to NM_015460.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:23932115 C>A maps to NM_002487.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:23932115 C>A maps to NM_002487.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:45001030 G>T maps to NM_001145107.1 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:45001030 G>T maps to NM_001145107.1 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:56413552 C>A maps to NM_176810.2 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:56413552 C>A maps to NM_176810.2 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:150696412 G>A maps to NM_000603.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:150696412 G>A maps to NM_000603.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:57269553 C>A maps to NM_024663.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:57269553 C>A maps to NM_024663.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:25266429 C>T maps to NM_022150.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:25266429 C>T maps to NM_022150.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:200143262 C>T maps to NM_205860.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:200143262 C>T maps to NM_205860.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:88476241 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:88476241 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:61340876 C>A maps to NM_002531.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:61340876 C>A maps to NM_002531.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6806723 A>G maps to NM_001004489.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6806723 A>G maps to NM_001004489.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:20389217 G>C maps to NM_001005483.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:20389217 G>C maps to NM_001005483.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:20248810 G>C maps to NM_001005500.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:20248810 G>C maps to NM_001005500.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56431718 C>A maps to NM_001004730.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56431718 C>A maps to NM_001004730.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:97887953 C>A maps to NM_001005515.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:97887953 C>A maps to NM_001005515.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56237376 T>A maps to NM_001004742.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56237376 T>A maps to NM_001004742.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56258336 G>T maps to NM_001005282.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56258336 G>T maps to NM_001005282.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:55820132 G>T maps to NM_001005183.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:55820132 G>T maps to NM_001005183.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158517679 G>T maps to NM_001005189.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158517679 G>T maps to NM_001005189.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56085805 G>T maps to NM_001005202.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56085805 G>T maps to NM_001005202.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56468594 G>T maps to NM_001013358.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56468594 G>T maps to NM_001013358.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:29592259 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:29592259 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:131544998 C>G maps to NM_001142599.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:131544998 C>G maps to NM_001142599.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:51978184 C>A maps to NM_001003931.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:51978184 C>A maps to NM_001003931.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140230311 G>C maps to NM_031857.1 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140230311 G>C maps to NM_031857.1 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140580417 A>T maps to NM_018931.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140580417 A>T maps to NM_018931.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140720931 C>A maps to NM_018915.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140720931 C>A maps to NM_018915.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:60994098 G>T maps to NM_032439.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:60994098 G>T maps to NM_032439.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:51612662 C>A maps to NM_138694.3 E3251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:51612662 C>A maps to NM_138694.3 E3251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:118368609 C>T maps to NM_006229.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:118368609 C>T maps to NM_006229.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:65048470 C>T maps to NM_002689.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:65048470 C>T maps to NM_002689.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:76247598 G>A maps to NM_012230.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:76247598 G>A maps to NM_012230.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:146070759 C>T maps to ENST00000394414 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:146070759 C>T maps to ENST00000394414 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141537762 G>T maps to NM_001008270.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141537762 G>T maps to NM_001008270.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:70989841 G>A maps to NM_001109754.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:70989841 G>A maps to NM_001109754.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:198691571 G>T maps to ENST00000271610 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:198691571 G>T maps to ENST00000271610 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:8465464 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:8465464 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:41101119 G>T maps to ENST00000373198 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:41101119 G>T maps to ENST00000373198 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:1691402 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:1691402 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:58368427 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:58368427 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:36615025 G>T maps to NM_000536.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:36615025 G>T maps to NM_000536.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:36154335 C>A maps to NM_194301.2 G859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:36154335 C>A maps to NM_194301.2 G859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:178425833 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:178425833 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:151316172 C>T maps to NM_000449.3 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:151316172 C>T maps to NM_000449.3 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:134993769 G>T maps to NM_018666.2 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:134993769 G>T maps to NM_018666.2 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:18276281 C>A maps to NM_006089.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:18276281 C>A maps to NM_006089.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38951597 G>T maps to ENST00000302328 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38951597 G>T maps to ENST00000302328 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:165952084 G>T maps to NM_006922.3 S1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:165952084 G>T maps to NM_006922.3 S1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:102732997 C>G maps to NM_017893.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:102732997 C>G maps to NM_017893.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:57382044 C>T maps to ENST00000403558 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:57382044 C>T maps to ENST00000403558 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:99857221 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:99857221 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154940997 G>A maps to NM_001130040.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154940997 G>A maps to NM_001130040.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:50350457 C>T maps to NM_020717.3 E1228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:50350457 C>T maps to NM_020717.3 E1228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:164748523 T>A maps to NM_001041.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:164748523 T>A maps to NM_001041.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:147438204 T>A maps to ENST00000507030 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:147438204 T>A maps to ENST00000507030 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110763978 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110763978 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:35469351 T>C maps to NM_006933.4 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:35469351 T>C maps to NM_006933.4 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:115590105 C>T maps to NM_007231.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:115590105 C>T maps to NM_007231.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:111950282 A>G maps to NM_183061.1 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:111950282 A>G maps to NM_183061.1 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:33738842 G>A maps to NM_018042.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:33738842 G>A maps to NM_018042.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:168135052 C>T maps to NM_003062.2 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:168135052 C>T maps to NM_003062.2 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:48591908 G>T maps to NM_005359.5 G358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:48591908 G>T maps to NM_005359.5 G358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:50490682 C>T maps to NM_003076.4 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:50490682 C>T maps to NM_003076.4 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:53126805 C>T maps to NM_014682.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:53126805 C>T maps to NM_014682.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:152651068 C>A maps to NM_182961.2 L4917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:152651068 C>A maps to NM_182961.2 L4917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:152722271 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:152722271 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:132910325 G>T maps to NM_003967.2 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:132910325 G>T maps to NM_003967.2 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:123845206 G>A maps to NM_206862.2 A1064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:123845206 G>A maps to NM_206862.2 A1064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:11286553 C>T maps to NM_001097643.1 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:11286553 C>T maps to NM_001097643.1 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:156841130 G>T maps to NM_005651.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:156841130 G>T maps to NM_005651.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:26892177 G>A maps to NM_012143.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:26892177 G>A maps to NM_012143.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:169626292 C>A maps to NM_003247.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:169626292 C>A maps to NM_003247.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:155532365 A>T maps to ENST00000456144 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:155532365 A>T maps to ENST00000456144 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:156381591 T>A maps to NM_138379.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:156381591 T>A maps to NM_138379.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:103338819 G>T maps to NM_001198812.1 G435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:103338819 G>T maps to NM_001198812.1 G435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:77685275 C>A maps to NM_020431.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:77685275 C>A maps to NM_020431.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:42861482 C>G maps to NM_001135099.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:42861482 C>G maps to NM_001135099.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:45315856 T>A maps to NM_033550.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:45315856 T>A maps to NM_033550.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:141294040 T>A maps to NM_031466.5 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:141294040 T>A maps to NM_031466.5 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:72727231 G>A maps to NM_178125.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:72727231 G>A maps to NM_178125.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:46684476 C>T maps to NM_017931.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:46684476 C>T maps to NM_017931.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:117626716 G>T maps to NM_003594.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:117626716 G>T maps to NM_003594.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:80741182 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:80741182 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:57599324 C>A maps to NM_030773.3 Y281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:57599324 C>A maps to NM_030773.3 Y281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:128870687 C>T maps to NM_020120.3 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:128870687 C>T maps to NM_020120.3 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216256821 G>A maps to ENST00000366943 N1758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216256821 G>A maps to ENST00000366943 N1758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:85875929 G>C maps to NM_006590.2 *566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:85875929 G>C maps to NM_006590.2 *566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:116206454 C>T maps to NM_001172412.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:116206454 C>T maps to NM_001172412.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:108138840 G>T maps to NM_006113.4 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:108138840 G>T maps to NM_006113.4 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:35061053 G>A maps to NM_007126.3 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:35061053 G>A maps to NM_007126.3 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:31105879 G>T maps to ENST00000319788 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:31105879 G>T maps to ENST00000319788 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:117532433 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:117532433 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:106815564 T>A maps to NM_012082.3 A1085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:106815564 T>A maps to NM_012082.3 A1085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:68222715 T>C maps to NM_015346.3 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:68222715 T>C maps to NM_015346.3 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:28244326 C>T maps to NM_001023560.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:28244326 C>T maps to NM_001023560.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:38120852 G>C maps to NM_021045.1 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:38120852 G>C maps to NM_021045.1 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:21478545 C>A maps to NM_024697.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:21478545 C>A maps to NM_024697.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:30934597 C>T maps to NM_014717.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:30934597 C>T maps to NM_014717.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:23927876 C>A maps to NM_138286.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:23927876 C>A maps to NM_138286.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:146806893 C>A maps to ENST00000508784 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:146806893 C>A maps to ENST00000508784 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:33289355 T>C maps to NM_052857.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:33289355 T>C maps to NM_052857.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:89039395 G>T maps to NM_004827.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:89039395 G>T maps to NM_004827.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:119027326 G>T maps to NM_001142505.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:119027326 G>T maps to NM_001142505.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:27048009 T>A maps to NM_005470.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:27048009 T>A maps to NM_005470.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74140675 G>T maps to NM_001615.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74140675 G>T maps to NM_001615.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:110925491 C>T maps to NM_001099922.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:110925491 C>T maps to NM_001099922.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:47342739 G>A maps to NM_004069.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:47342739 G>A maps to NM_004069.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:21233784 G>A maps to NM_000384.2 T1985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:21233784 G>A maps to NM_000384.2 T1985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:42490069 C>T maps to ENST00000441343 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:42490069 C>T maps to ENST00000441343 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:32446999 C>A maps to NM_001714.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:32446999 C>A maps to NM_001714.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:37704487 C>A maps to NM_018310.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:37704487 C>A maps to NM_018310.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:5782211 G>A maps to NM_017782.4 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:5782211 G>A maps to NM_017782.4 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:97114181 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:97114181 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:34663387 C>A maps to NM_001134734.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:34663387 C>A maps to NM_001134734.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:159166147 C>A maps to NM_138803.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:159166147 C>A maps to NM_138803.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:158299699 G>T maps to NM_001764.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:158299699 G>T maps to NM_001764.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:93496622 A>T maps to NM_001271.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:93496622 A>T maps to NM_001271.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:101717775 T>G maps to NM_014918.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:101717775 T>G maps to NM_014918.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:2942375 T>A maps to NM_175607.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:2942375 T>A maps to NM_175607.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:101797629 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:101797629 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:189904124 T>A maps to NM_000393.3 P1266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:189904124 T>A maps to NM_000393.3 P1266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:43906654 C>G maps to NM_001145146.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:43906654 C>G maps to NM_001145146.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:2855611 C>A maps to NM_033225.5 T2766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:2855611 C>A maps to NM_033225.5 T2766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:34083157 C>A maps to ENST00000373381 E1923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:34083157 C>A maps to ENST00000373381 E1923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:125298617 C>A maps to NM_001013628.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:125298617 C>A maps to NM_001013628.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74593019 C>T maps to NM_004082.4 K962K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74593019 C>T maps to NM_004082.4 K962K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:69565368 T>C maps to NM_021800.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:69565368 T>C maps to NM_021800.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:117302316 C>A maps to NM_020693.2 V1829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:117302316 C>A maps to NM_020693.2 V1829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:56418453 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:56418453 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:71795381 G>C maps to NM_001130987.1 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:71795381 G>C maps to NM_001130987.1 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:207564940 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:207564940 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:94120813 G>T maps to NM_004440.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:94120813 G>T maps to NM_004440.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:28573839 G>T maps to NM_001440.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:28573839 G>T maps to NM_001440.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:116608451 G>T maps to NM_020940.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:116608451 G>T maps to NM_020940.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:19184744 C>A maps to NM_152898.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:19184744 C>A maps to NM_152898.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:155487718 G>T maps to NM_005141.4 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:155487718 G>T maps to NM_005141.4 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:152279645 G>A maps to NM_002016.1 D2572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:152279645 G>A maps to NM_002016.1 D2572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:128493587 G>T maps to NM_001458.4 E2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:128493587 G>T maps to NM_001458.4 E2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:39134974 T>G maps to ENST00000263405 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:39134974 T>G maps to ENST00000263405 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:48414371 G>A maps to NM_016204.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:48414371 G>A maps to NM_016204.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:121743870 C>T maps to NM_005270.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:121743870 C>T maps to NM_005270.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:135482264 A>T maps to NM_153834.3 L2855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:135482264 A>T maps to NM_153834.3 L2855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:207041254 C>A maps to NM_005279.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:207041254 C>A maps to NM_005279.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:101911403 G>T maps to NM_001184727.1 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:101911403 G>T maps to NM_001184727.1 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:9943737 C>A maps to NM_000833.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:9943737 C>A maps to NM_000833.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:27492446 C>T maps to NM_001520.3 R1383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:27492446 C>T maps to NM_001520.3 R1383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:43531768 A>G maps to NM_015052.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:43531768 A>G maps to NM_015052.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:100995382 G>A maps to NM_021828.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:100995382 G>A maps to NM_021828.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:114141542 G>A maps to NM_000868.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:114141542 G>A maps to NM_000868.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:118623643 G>A maps to NM_152538.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:118623643 G>A maps to NM_152538.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:130408103 C>A maps to NM_001170961.1 G1281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:130408103 C>A maps to NM_001170961.1 G1281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:31384711 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:31384711 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:41705564 T>A maps to NM_152903.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:41705564 T>A maps to NM_152903.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:16355029 C>A maps to NM_024704.4 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:16355029 C>A maps to NM_024704.4 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:47289506 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:47289506 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:53519983 T>C maps to NM_001003760.4 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:53519983 T>C maps to NM_001003760.4 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:31864088 C>A maps to ENST00000433652 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:31864088 C>A maps to ENST00000433652 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153141231 G>A maps to NM_000425.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153141231 G>A maps to NM_000425.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:127892139 C>T maps to NM_000230.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:127892139 C>T maps to NM_000230.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:15537619 A>T maps to NM_198996.2 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:15537619 A>T maps to NM_198996.2 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:78010953 C>G maps to NM_005296.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:78010953 C>G maps to NM_005296.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:141135855 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:141135855 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:99015916 G>A maps to ENST00000254898 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:99015916 G>A maps to ENST00000254898 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:126754828 C>G maps to NM_032446.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:126754828 C>G maps to NM_032446.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:126792949 C>T maps to NM_032446.2 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:126792949 C>T maps to NM_032446.2 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:170912687 T>A maps to NM_021647.6 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:170912687 T>A maps to NM_021647.6 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:12089846 G>T maps to NM_021933.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:12089846 G>T maps to NM_021933.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:23811792 C>T maps to NM_005664.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:23811792 C>T maps to NM_005664.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:78830508 C>T maps to NM_020236.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:78830508 C>T maps to NM_020236.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:100677756 C>A maps to NM_001040105.1 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:100677756 C>A maps to NM_001040105.1 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:67492484 C>T maps to NM_001080416.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:67492484 C>T maps to NM_001080416.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:56485016 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:56485016 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:96099535 G>T maps to NM_022451.9 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:96099535 G>T maps to NM_022451.9 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:154112394 G>A maps to NM_207308.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:154112394 G>A maps to NM_207308.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:102338132 C>A maps to NM_022052.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:102338132 C>A maps to NM_022052.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:101096044 C>A maps to ENST00000263032 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:101096044 C>A maps to ENST00000263032 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:95163437 C>T maps to NM_033014.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:95163437 C>T maps to NM_033014.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:7530737 C>A maps to NM_198474.3 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:7530737 C>A maps to NM_198474.3 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153496192 G>T maps to NM_000513.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153496192 G>T maps to NM_000513.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:247921474 G>T maps to NM_012353.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:247921474 G>T maps to NM_012353.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:248263129 G>T maps to NM_175911.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:248263129 G>T maps to NM_175911.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:180166173 G>A maps to NM_001001657.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:180166173 G>A maps to NM_001001657.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:20215963 C>A maps to NM_172194.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:20215963 C>A maps to NM_172194.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55587431 G>A maps to ENST00000395203 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55587431 G>A maps to ENST00000395203 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:98188902 G>T maps to NM_001004736.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:98188902 G>T maps to NM_001004736.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55579853 G>C maps to NM_001004738.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55579853 G>C maps to NM_001004738.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:55945334 G>T maps to NM_001005494.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:55945334 G>T maps to NM_001005494.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:9213199 G>T maps to NM_001005193.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:9213199 G>T maps to NM_001005193.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55890174 T>C maps to NM_001005201.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55890174 T>C maps to NM_001005201.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:127255559 C>T maps to NM_006193.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:127255559 C>T maps to NM_006193.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:82583785 C>A maps to NM_033026.5 S2161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:82583785 C>A maps to NM_033026.5 S2161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:72297214 C>A maps to NM_002599.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:72297214 C>A maps to NM_002599.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:119043972 C>A maps to NM_173791.3 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:119043972 C>A maps to NM_173791.3 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:18972503 G>T maps to NM_000292.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:18972503 G>T maps to NM_000292.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:59777143 C>G maps to NM_176787.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:59777143 C>G maps to NM_176787.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:625203 G>A maps to NM_005035.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:625203 G>A maps to NM_005035.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:76797516 C>A maps to NM_006239.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:76797516 C>A maps to NM_006239.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:13448265 C>A maps to NM_001024661.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:13448265 C>A maps to NM_001024661.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:23522765 C>G maps to NM_020227.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:23522765 C>G maps to NM_020227.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:219695054 G>A maps to NM_017431.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:219695054 G>A maps to NM_017431.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:128178937 C>A maps to ENST00000409048 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:128178937 C>A maps to ENST00000409048 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:36484284 G>T maps to NM_001160167.1 *369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:36484284 G>T maps to NM_001160167.1 *369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:40748572 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:40748572 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:103214660 G>T maps to ENST00000428762 Y1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:103214660 G>T maps to ENST00000428762 Y1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:129251249 C>A maps to NM_000539.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:129251249 C>A maps to NM_000539.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:38132699 G>C maps to ENST00000339363 S932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:38132699 G>C maps to ENST00000339363 S932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:38169931 C>A maps to NM_001034853.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:38169931 C>A maps to NM_001034853.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:83372408 G>T maps to NM_014496.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:83372408 G>T maps to NM_014496.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237947041 G>C maps to NM_001035.2 V4010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237947041 G>C maps to NM_001035.2 V4010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:33926870 C>A maps to NM_001036.3 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:33926870 C>A maps to NM_001036.3 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:92731290 C>A maps to NM_017654.3 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:92731290 C>A maps to NM_017654.3 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:102249903 C>G maps to NM_015490.3 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:102249903 C>G maps to NM_015490.3 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:38435024 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:38435024 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:101952176 C>T maps to ENST00000306803 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:101952176 C>T maps to ENST00000306803 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:232577114 G>A maps to NM_020808.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:232577114 G>A maps to NM_020808.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:164709250 G>T maps to NM_001041.3 G1666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:164709250 G>T maps to NM_001041.3 G1666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:54839362 C>T maps to NM_003128.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:54839362 C>T maps to NM_003128.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:57245565 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:57245565 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:149885085 G>T maps to NM_014849.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:149885085 G>T maps to NM_014849.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:152725440 A>C maps to NM_182961.2 V2244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:152725440 A>C maps to NM_182961.2 V2244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:234565956 G>A maps to NM_005646.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:234565956 G>A maps to NM_005646.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:75936626 C>A maps to ENST00000431480 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:75936626 C>A maps to ENST00000431480 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:119469161 G>A maps to ENST00000369429 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:119469161 G>A maps to ENST00000369429 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:89967041 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:89967041 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:45522848 C>T maps to NM_003274.4 D1179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:45522848 C>T maps to NM_003274.4 D1179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:31294303 G>T maps to NM_002420.4 V1511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:31294303 G>T maps to NM_002420.4 V1511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:130479637 G>T maps to NM_144965.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:130479637 G>T maps to NM_144965.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:103723774 G>A maps to NM_181890.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:103723774 G>A maps to NM_181890.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:215820888 C>T maps to ENST00000366943 W4922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:215820888 C>T maps to ENST00000366943 W4922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:168102023 C>A maps to NM_152381.5 V1374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:168102023 C>A maps to NM_152381.5 V1374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:77764797 G>T maps to NM_024721.4 E1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:77764797 G>T maps to NM_024721.4 E1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:71756813 C>A maps to NM_152625.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:71756813 C>A maps to NM_152625.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:40514426 G>T maps to NM_178544.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:40514426 G>T maps to NM_178544.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:59024578 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:59024578 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr5:137527958 G>A maps to NM_004661.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr5:137527958 G>A maps to NM_004661.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:34071023 G>A maps to ENST00000373381 G2090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:34071023 G>A maps to ENST00000373381 G2090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chrX:31496380 T>A maps to ENST00000357033 R2927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chrX:31496380 T>A maps to ENST00000357033 R2927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr18:13826013 C>T maps to NM_005913.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr18:13826013 C>T maps to NM_005913.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr16:14340355 G>A maps to NM_014048.3 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr16:14340355 G>A maps to NM_014048.3 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chrX:3235706 G>A maps to NM_015419.3 H2005H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chrX:3235706 G>A maps to NM_015419.3 H2005H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:36597478 C>T maps to NM_000448.2 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:36597478 C>T maps to NM_000448.2 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr14:94780976 G>A maps to NM_001756.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr14:94780976 G>A maps to NM_001756.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:143550931 C>A maps to NM_173653.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:143550931 C>A maps to NM_173653.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:27829671 C>A maps to NM_020791.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:27829671 C>A maps to NM_020791.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr2:179440814 G>A maps to NM_133378.4 A20780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr2:179440814 G>A maps to NM_133378.4 A20780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:84611521 C>T maps to NM_207517.2 H764H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:84611521 C>T maps to NM_207517.2 H764H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:57282530 C>A maps to NM_012106.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:57282530 C>A maps to NM_012106.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:36054336 C>A maps to NM_000704.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:36054336 C>A maps to NM_000704.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:26343229 C>A maps to NM_016529.4 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:26343229 C>A maps to NM_016529.4 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:19702684 C>T maps to NM_020314.5 N935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:19702684 C>T maps to NM_020314.5 N935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:151498137 C>T maps to NM_020770.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:151498137 C>T maps to NM_020770.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:32440004 A>G maps to NM_176812.4 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:32440004 A>G maps to NM_176812.4 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:86071035 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:86071035 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:118971517 G>A maps to NM_001382.3 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:118971517 G>A maps to NM_001382.3 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:147782065 A>G maps to NM_205836.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:147782065 A>G maps to NM_205836.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:157666997 C>T maps to NM_052939.3 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:157666997 C>T maps to NM_052939.3 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:1961435 C>T maps to NM_000815.4 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:1961435 C>T maps to NM_000815.4 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:151821212 C>T maps to NM_018558.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:151821212 C>T maps to NM_018558.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:42006186 C>T maps to NM_000168.5 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:42006186 C>T maps to NM_000168.5 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:3446353 T>A maps to ENST00000511533 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:3446353 T>A maps to ENST00000511533 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:151155694 G>A maps to NM_178822.4 P2218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:151155694 G>A maps to NM_178822.4 P2218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:63246580 C>A maps to NM_139318.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:63246580 C>A maps to NM_139318.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:38824023 C>T maps to NM_152868.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:38824023 C>T maps to NM_152868.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:215259841 A>T maps to NM_001017425.2 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:215259841 A>T maps to NM_001017425.2 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:85695048 G>T maps to NM_014615.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:85695048 G>T maps to NM_014615.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:69563563 G>A maps to NM_012310.4 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:69563563 G>A maps to NM_012310.4 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:50088219 G>T maps to NM_002408.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:50088219 G>T maps to NM_002408.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:41988516 G>T maps to ENST00000219905 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:41988516 G>T maps to ENST00000219905 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:160218466 C>T maps to NM_014161.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:160218466 C>T maps to NM_014161.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:77755943 A>G maps to NM_015057.4 D1611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:77755943 A>G maps to NM_015057.4 D1611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:32030657 C>T maps to NM_025152.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:32030657 C>T maps to NM_025152.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:122446792 C>T maps to NM_017554.2 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:122446792 C>T maps to NM_017554.2 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:57889907 T>C maps to NM_000938.1 Y949Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:57889907 T>C maps to NM_000938.1 Y949Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:45885836 C>T maps to NM_001142502.1 W799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:45885836 C>T maps to NM_001142502.1 W799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:29825754 C>A maps to NM_145239.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:29825754 C>A maps to NM_145239.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:29325908 G>A maps to NM_032322.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:29325908 G>A maps to NM_032322.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:38082222 G>A maps to NM_001038633.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:38082222 G>A maps to NM_001038633.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:39025445 C>T maps to NM_000540.2 I3782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:39025445 C>T maps to NM_000540.2 I3782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:36018820 G>A maps to NM_001166034.1 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:36018820 G>A maps to NM_001166034.1 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:99848690 G>A maps to NM_032870.2 R715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:99848690 G>A maps to NM_032870.2 R715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:48510921 G>A maps to NM_016479.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:48510921 G>A maps to NM_016479.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:76026892 G>A maps to NM_080744.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:76026892 G>A maps to NM_080744.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:149485538 C>A maps to NM_198455.2 P1316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:149485538 C>A maps to NM_198455.2 P1316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:901101 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:901101 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:36520068 A>G maps to NM_145803.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:36520068 A>G maps to NM_145803.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:45821602 C>T maps to ENST00000397932 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:45821602 C>T maps to ENST00000397932 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr18:670728 C>G maps to NM_001071.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr18:670728 C>G maps to NM_001071.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:48918349 C>T maps to NM_175575.5 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:48918349 C>T maps to NM_175575.5 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:21861373 T>A maps to NM_015884.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:21861373 T>A maps to NM_015884.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:57768041 G>T maps to NM_178457.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:57768041 G>T maps to NM_178457.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:20782585 C>A maps to NM_001163941.1 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:20782585 C>A maps to NM_001163941.1 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:69347640 C>T maps to NM_001130004.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:69347640 C>T maps to NM_001130004.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:88769445 G>A maps to NM_133447.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:88769445 G>A maps to NM_133447.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:27291498 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:27291498 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:38514959 T>C maps to NM_001635.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:38514959 T>C maps to NM_001635.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:28506502 G>T maps to NM_018690.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:28506502 G>T maps to NM_018690.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:25265297 G>T maps to NM_001185085.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:25265297 G>T maps to NM_001185085.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:49692178 C>G maps to NM_003458.3 T1730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:49692178 C>G maps to NM_003458.3 T1730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:3544800 G>A maps to NM_001080524.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:3544800 G>A maps to NM_001080524.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:2788839 C>A maps to NM_199460.2 A1822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:2788839 C>A maps to NM_199460.2 A1822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76834861 G>A maps to ENST00000360841 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76834861 G>A maps to ENST00000360841 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:111274656 T>A maps to NM_018210.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:111274656 T>A maps to NM_018210.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:10713961 C>A maps to NM_001079843.1 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:10713961 C>A maps to NM_001079843.1 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:46506740 G>T maps to NM_001080402.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:46506740 G>T maps to NM_001080402.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:66432426 G>A maps to NM_001795.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:66432426 G>A maps to NM_001795.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:50863272 T>A maps to NM_020549.4 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:50863272 T>A maps to NM_020549.4 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:76528858 C>A maps to NM_033401.3 Y710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:76528858 C>A maps to NM_033401.3 Y710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:2820156 C>A maps to NM_033225.5 V3153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:2820156 C>A maps to NM_033225.5 V3153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:32827694 G>A maps to ENST00000357033 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:32827694 G>A maps to ENST00000357033 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:21775401 G>T maps to NM_003777.3 E2536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:21775401 G>T maps to NM_003777.3 E2536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:108353816 C>T maps to NM_014648.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:108353816 C>T maps to NM_014648.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:131520565 C>T maps to NM_001105195.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:131520565 C>T maps to NM_001105195.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:135418862 G>A maps to NM_205855.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:135418862 G>A maps to NM_205855.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:54294192 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:54294192 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:134217326 G>A maps to NM_138342.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:134217326 G>A maps to NM_138342.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:6602205 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:6602205 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:27333928 C>A maps to NM_005288.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:27333928 C>A maps to NM_005288.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:5290731 C>T maps to NM_005330.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:5290731 C>T maps to NM_005330.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:27147987 G>T maps to NM_153631.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:27147987 G>T maps to NM_153631.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:103826163 G>C maps to NM_024747.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:103826163 G>C maps to NM_024747.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:103826181 A>G maps to NM_024747.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:103826181 A>G maps to NM_024747.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:99459899 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:99459899 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:61922991 G>A maps to NM_001134779.1 K965K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:61922991 G>A maps to NM_001134779.1 K965K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:107977955 G>T maps to NM_003604.2 S540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:107977955 G>T maps to NM_003604.2 S540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:145533104 G>A maps to NM_003637.3 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:145533104 G>A maps to NM_003637.3 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:40312059 A>T maps to NM_012285.2 *1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:40312059 A>T maps to NM_012285.2 *1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:196309546 C>T maps to NM_198503.2 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:196309546 C>T maps to NM_198503.2 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:2719073 C>A maps to NM_133497.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:2719073 C>A maps to NM_133497.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrY:21869167 C>T maps to NM_001146705.1 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrY:21869167 C>T maps to NM_001146705.1 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:3821781 C>T maps to NM_001300.5 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:3821781 C>T maps to NM_001300.5 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:62758578 C>T maps to ENST00000506720 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:62758578 C>T maps to ENST00000506720 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:51021451 C>T maps to NM_001080457.1 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:51021451 C>T maps to NM_001080457.1 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:71357870 G>T maps to NM_005791.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:71357870 G>T maps to NM_005791.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:18022482 C>T maps to ENST00000205890 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:18022482 C>T maps to ENST00000205890 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76900499 C>T maps to NM_000260.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76900499 C>T maps to NM_000260.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936319 G>C maps to NM_052867.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936319 G>C maps to NM_052867.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:48719040 T>C maps to NM_016453.2 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:48719040 T>C maps to NM_016453.2 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:115998177 C>T maps to NM_022569.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:115998177 C>T maps to NM_022569.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:7220797 G>A maps to NM_032442.2 R1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:7220797 G>A maps to NM_032442.2 R1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:151784305 C>G maps to NM_020167.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:151784305 C>G maps to NM_020167.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:164271982 A>T maps to NM_006174.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:164271982 A>T maps to NM_006174.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:50964931 G>T maps to NM_018245.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:50964931 G>T maps to NM_018245.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:7960722 C>T maps to NM_001003745.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:7960722 C>T maps to NM_001003745.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:29408139 C>T maps to NM_013941.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:29408139 C>T maps to NM_013941.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:144015468 C>A maps to NM_001005287.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:144015468 C>A maps to NM_001005287.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:248436672 G>A maps to NM_001004695.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:248436672 G>A maps to NM_001004695.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:55579094 C>A maps to NM_001004738.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:55579094 C>A maps to NM_001004738.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:140167782 C>G maps to NM_018900.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:140167782 C>G maps to NM_018900.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:105173721 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:105173721 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:103814198 G>A maps to NM_025208.4 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:103814198 G>A maps to NM_025208.4 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:42036483 G>T maps to NM_000930.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:42036483 G>T maps to NM_000930.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:8769148 G>A maps to NM_015192.2 K1055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:8769148 G>A maps to NM_015192.2 K1055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:62202176 G>T maps to NM_001037335.2 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:62202176 G>T maps to NM_001037335.2 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:96860848 A>T maps to ENST00000434261 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:96860848 A>T maps to ENST00000434261 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:17701268 G>A maps to ENST00000395776 T1669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:17701268 G>A maps to ENST00000395776 T1669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:36217804 C>A maps to NM_194301.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:36217804 C>A maps to NM_194301.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:48381909 G>A maps to NM_002900.2 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:48381909 G>A maps to NM_002900.2 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:108487259 G>T maps to NM_182588.2 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:108487259 G>T maps to NM_182588.2 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:116269564 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:116269564 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:20647420 C>T maps to NM_004040.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:20647420 C>T maps to NM_004040.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:33517468 C>T maps to NM_033103.4 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:33517468 C>T maps to NM_033103.4 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:56439903 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:56439903 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:49304864 G>A maps to NM_001193489.1 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:49304864 G>A maps to NM_001193489.1 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:101080668 C>A maps to NM_020654.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:101080668 C>A maps to NM_020654.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:3672023 C>A maps to NM_023068.3 G1518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:3672023 C>A maps to NM_023068.3 G1518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:11169546 C>T maps to NM_001128849.1 F1571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:11169546 C>T maps to NM_001128849.1 F1571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:66475713 C>T maps to NM_006946.2 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:66475713 C>T maps to NM_006946.2 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:104099501 C>T maps to NM_017564.9 V1331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:104099501 C>T maps to NM_017564.9 V1331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:20859919 C>T maps to NM_007110.4 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:20859919 C>T maps to NM_007110.4 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:169648694 G>T maps to NM_003247.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:169648694 G>T maps to NM_003247.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:83791515 T>A maps to NM_023003.3 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:83791515 T>A maps to NM_023003.3 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:30113787 G>A maps to ENST00000376724 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:30113787 G>A maps to ENST00000376724 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:38320577 G>T maps to NM_003306.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:38320577 G>T maps to NM_003306.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57640927 C>A maps to NM_020903.2 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57640927 C>A maps to NM_020903.2 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:157131777 T>A maps to NM_001167912.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:157131777 T>A maps to NM_001167912.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:134095108 C>T maps to NM_052875.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:134095108 C>T maps to NM_052875.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:119575581 T>C maps to NM_015836.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:119575581 T>C maps to NM_015836.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:38162186 G>A maps to NM_023034.1 Y843Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:38162186 G>A maps to NM_023034.1 Y843Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:3339735 C>T maps to NM_005741.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:3339735 C>T maps to NM_005741.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:57187792 G>T maps to NM_033273.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:57187792 G>T maps to NM_033273.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:5085736 G>A maps to NM_032530.1 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:5085736 G>A maps to NM_032530.1 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:12502032 G>A maps to NM_001080821.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:12502032 G>A maps to NM_001080821.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:223786027 C>G maps to NM_203372.1 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:223786027 C>G maps to NM_203372.1 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:105418952 C>G maps to NM_138420.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:105418952 C>G maps to NM_138420.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:43481668 C>T maps to ENST00000428638 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:43481668 C>T maps to ENST00000428638 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:1800442 G>A maps to NM_138813.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:1800442 G>A maps to NM_138813.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:128114598 G>A maps to NM_001004298.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:128114598 G>A maps to NM_001004298.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:27070631 G>T maps to NM_018164.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:27070631 G>T maps to NM_018164.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:220870012 C>T maps to NM_024709.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:220870012 C>T maps to NM_024709.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:24451494 C>A maps to NM_012295.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:24451494 C>A maps to NM_012295.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:64961110 C>T maps to NM_014405.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:64961110 C>T maps to NM_014405.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:34113551 C>T maps to NM_005898.4 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:34113551 C>T maps to NM_005898.4 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:5170849 G>C maps to NM_003818.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:5170849 G>C maps to NM_003818.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:194063200 C>T maps to NM_001080513.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:194063200 C>T maps to NM_001080513.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:35009107 G>A maps to NM_015283.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:35009107 G>A maps to NM_015283.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:102516517 G>T maps to NM_001376.4 E4599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:102516517 G>T maps to NM_001376.4 E4599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:5251930 C>G maps to NM_014674.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:5251930 C>G maps to NM_014674.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:99092213 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:99092213 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:15928575 C>A maps to NM_012304.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:15928575 C>A maps to NM_012304.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:49440182 G>C maps to NM_001018071.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:49440182 G>C maps to NM_001018071.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:46009261 G>A maps to NM_024513.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:46009261 G>A maps to NM_024513.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:19612197 C>T maps to ENST00000404158 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:19612197 C>T maps to ENST00000404158 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:95050857 C>T maps to NM_005708.3 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:95050857 C>T maps to NM_005708.3 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:26775202 C>T maps to NM_002223.2 Q1086Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:26775202 C>T maps to NM_002223.2 Q1086Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:58317463 G>A maps to NM_004811.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:58317463 G>A maps to NM_004811.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:131678376 C>T maps to NM_001127244.1 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:131678376 C>T maps to NM_001127244.1 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:42099415 C>T maps to NM_152513.3 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:42099415 C>T maps to NM_152513.3 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:121531008 C>T maps to NM_022045.3 F854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:121531008 C>T maps to NM_022045.3 F854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:100685799 C>G maps to NM_001040105.1 V3701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:100685799 C>G maps to NM_001040105.1 V3701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:55420632 G>A maps to NM_021191.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:55420632 G>A maps to NM_021191.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:46443288 G>A maps to NM_002516.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:46443288 G>A maps to NM_002516.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:29142164 C>G maps to NM_030905.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:29142164 C>G maps to NM_030905.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:55524127 T>G maps to NM_001005243.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:55524127 T>G maps to NM_001005243.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:122353865 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:122353865 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:145010068 G>A maps to NM_201380.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:145010068 G>A maps to NM_201380.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:69104733 C>T maps to NM_024870.2 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:69104733 C>T maps to NM_024870.2 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:131784696 C>A maps to ENST00000372554 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:131784696 C>A maps to ENST00000372554 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:6454686 G>A maps to NM_024103.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:6454686 G>A maps to NM_024103.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:20255608 C>A maps to ENST00000273739 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:20255608 C>A maps to ENST00000273739 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:146467853 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:146467853 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:169051406 C>T maps to NM_022138.2 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:169051406 C>T maps to NM_022138.2 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:16258746 G>A maps to NM_015001.2 P2004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:16258746 G>A maps to NM_015001.2 P2004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:55655666 A>C maps to NM_032681.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:55655666 A>C maps to NM_032681.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:63967503 G>A maps to ENST00000358794 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:63967503 G>A maps to ENST00000358794 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:70533430 C>G maps to NM_001128206.1 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:70533430 C>G maps to NM_001128206.1 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730434 G>T maps to NM_006342.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730434 G>T maps to NM_006342.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:5921731 G>A maps to NM_015939.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:5921731 G>A maps to NM_015939.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:140137953 C>A maps to NM_006088.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:140137953 C>A maps to NM_006088.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:90052102 G>A maps to NM_016021.2 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:90052102 G>A maps to NM_016021.2 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:44684350 C>T maps to NM_006991.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:44684350 C>T maps to NM_006991.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:2877778 C>T maps to NM_024967.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:2877778 C>T maps to NM_024967.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:55050419 G>T maps to NM_015547.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:55050419 G>T maps to NM_015547.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70811980 T>A maps to NM_052957.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70811980 T>A maps to NM_052957.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20576095 G>A maps to NM_182617.3 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20576095 G>A maps to NM_182617.3 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:175898482 G>T maps to NM_014269.4 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:175898482 G>T maps to NM_014269.4 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:28296445 G>T maps to NM_007038.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:28296445 G>T maps to NM_007038.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41206253 C>A maps to NM_024876.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41206253 C>A maps to NM_024876.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:123166345 G>T maps to NM_183357.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:123166345 G>T maps to NM_183357.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:4202211 G>C maps to NM_000678.3 Y559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:4202211 G>C maps to NM_000678.3 Y559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:143605318 G>T maps to NM_016108.2 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:143605318 G>T maps to NM_016108.2 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:45713742 C>G maps to NM_000383.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:45713742 C>G maps to NM_000383.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:113332984 G>C maps to NM_025144.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:113332984 G>C maps to NM_025144.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:79503386 G>T maps to NM_005139.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:79503386 G>T maps to NM_005139.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:42012411 G>T maps to NM_006803.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:42012411 G>T maps to NM_006803.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:241622086 C>G maps to NM_001102467.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:241622086 C>G maps to NM_001102467.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:110450209 G>A maps to NM_020809.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:110450209 G>A maps to NM_020809.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:46233110 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:46233110 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100912508 G>T maps to NM_177949.2 Y22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100912508 G>T maps to NM_177949.2 Y22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:13378643 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:13378643 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:152818573 C>A maps to NM_001001344.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:152818573 C>A maps to NM_001001344.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:50346456 C>A maps to NM_006045.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:50346456 C>A maps to NM_006045.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:76889200 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:76889200 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:129147050 C>T maps to ENST00000303743 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:129147050 C>T maps to ENST00000303743 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50197938 G>A maps to ENST00000342989 Y479Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50197938 G>A maps to ENST00000342989 Y479Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:135570362 T>C maps to NM_001727.1 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:135570362 T>C maps to NM_001727.1 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180338528 C>A maps to NM_001040462.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180338528 C>A maps to NM_001040462.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:118116962 G>T maps to NM_198515.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:118116962 G>T maps to NM_198515.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:8135133 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:8135133 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:33651132 C>A maps to NM_018944.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:33651132 C>A maps to NM_018944.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:24939993 C>A maps to ENST00000266155 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:24939993 C>A maps to ENST00000266155 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:85049049 G>T maps to ENST00000409520 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:85049049 G>T maps to ENST00000409520 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:93065290 G>T maps to NM_001164737.1 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:93065290 G>T maps to NM_001164737.1 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:71275384 G>T maps to NM_031468.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:71275384 G>T maps to NM_031468.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:41495913 C>A maps to ENST00000378163 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:41495913 C>A maps to ENST00000378163 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:55012263 T>A maps to NM_020356.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:55012263 T>A maps to NM_020356.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:74628614 G>C maps to NM_138357.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:74628614 G>C maps to NM_138357.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109408184 A>G maps to NM_144978.1 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109408184 A>G maps to NM_144978.1 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109415039 G>T maps to NM_144978.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109415039 G>T maps to NM_144978.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:35829248 C>G maps to NM_001771.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:35829248 C>G maps to NM_001771.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:95158252 A>G maps to NM_001144663.1 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:95158252 A>G maps to NM_001144663.1 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:61823357 C>A maps to NM_001796.2 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:61823357 C>A maps to NM_001796.2 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:19629015 C>A maps to NM_024944.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:19629015 C>A maps to NM_024944.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:45671408 G>T maps to NM_003654.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:45671408 G>T maps to NM_003654.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:96936995 G>T maps to NM_004804.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:96936995 G>T maps to NM_004804.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:154507269 A>G maps to NM_001289.4 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:154507269 A>G maps to NM_001289.4 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:140265369 C>A maps to NM_022131.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:140265369 C>A maps to NM_022131.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:74334492 A>G maps to NM_020872.1 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:74334492 A>G maps to NM_020872.1 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:74411126 C>G maps to NM_020872.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:74411126 C>G maps to NM_020872.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:125281973 G>A maps to NM_130773.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:125281973 G>A maps to NM_130773.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:101788184 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:101788184 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94024364 C>A maps to NM_000089.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94024364 C>A maps to NM_000089.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:139833474 C>A maps to NM_152888.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:139833474 C>A maps to NM_152888.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:107417734 G>T maps to NM_033641.2 R1025R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:107417734 G>T maps to NM_033641.2 R1025R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:10091369 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:10091369 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130290118 C>G maps to NM_001102608.1 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130290118 C>G maps to NM_001102608.1 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:120118126 G>A maps to NM_006438.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:120118126 G>A maps to NM_006438.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:346493 G>T maps to NM_130386.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:346493 G>T maps to NM_130386.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137612986 G>A maps to NM_194071.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137612986 G>A maps to NM_194071.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:43906639 C>T maps to NM_001145146.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:43906639 C>T maps to NM_001145146.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3443691 G>C maps to NM_033225.5 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3443691 G>C maps to NM_033225.5 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3565936 G>T maps to NM_033225.5 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3565936 G>T maps to NM_033225.5 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:68024300 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:68024300 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:56087659 A>T maps to ENST00000423479 Y493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:56087659 A>T maps to ENST00000423479 Y493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:11384963 G>T maps to NM_001332.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:11384963 G>T maps to NM_001332.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17152916 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17152916 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:95095717 A>G maps to NM_001129889.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:95095717 A>G maps to NM_001129889.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:79994491 C>A maps to NM_016286.3 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:79994491 C>A maps to NM_016286.3 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137363341 G>T maps to NM_004717.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137363341 G>T maps to NM_004717.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:54567930 T>A maps to NM_019030.2 R950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:54567930 T>A maps to NM_019030.2 R950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7095231 G>A maps to NM_001365.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7095231 G>A maps to NM_001365.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7095234 G>C maps to NM_001365.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7095234 G>C maps to NM_001365.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:79603413 C>A maps to NM_004747.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:79603413 C>A maps to NM_004747.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:35128632 C>T maps to ENST00000339266 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:35128632 C>T maps to ENST00000339266 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:172952918 C>A maps to NM_178120.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:172952918 C>A maps to NM_178120.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:32591655 T>C maps to ENST00000357033 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:32591655 T>C maps to ENST00000357033 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:32591897 G>A maps to ENST00000357033 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:32591897 G>A maps to ENST00000357033 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:124268651 C>A maps to NM_207437.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:124268651 C>A maps to NM_207437.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:25190084 G>T maps to NM_016544.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:25190084 G>T maps to NM_016544.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:66963822 C>A maps to NM_033105.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:66963822 C>A maps to NM_033105.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:154143393 G>T maps to NM_130797.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:154143393 G>T maps to NM_130797.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:154684100 C>A maps to NM_130797.2 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:154684100 C>A maps to NM_130797.2 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:42080434 G>T maps to NM_001389.3 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:42080434 G>T maps to NM_001389.3 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:35390862 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:35390862 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:88533715 G>T maps to NM_014208.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:88533715 G>T maps to NM_014208.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:31484545 A>T maps to NM_014600.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:31484545 A>T maps to NM_014600.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:184049276 G>C maps to NM_001194947.1 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:184049276 G>C maps to NM_001194947.1 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:10820817 T>C maps to ENST00000429377 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:10820817 T>C maps to ENST00000429377 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:131247752 C>A maps to NM_001431.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:131247752 C>A maps to NM_001431.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:212248510 G>A maps to NM_005235.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:212248510 G>A maps to NM_005235.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:457102 G>T maps to ENST00000315013 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:457102 G>T maps to ENST00000315013 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:98995129 C>G maps to NM_182562.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:98995129 C>G maps to NM_182562.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:124672364 C>A maps to NM_001029888.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:124672364 C>A maps to NM_001029888.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:34150341 C>T maps to NM_203408.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:34150341 C>T maps to NM_203408.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:37028756 C>G maps to NM_001013736.2 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:37028756 C>G maps to NM_001013736.2 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:29867398 C>A maps to ENST00000269209 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:29867398 C>A maps to ENST00000269209 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:190067567 G>T maps to NM_199051.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:190067567 G>T maps to NM_199051.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:3129680 T>C maps to NM_021826.4 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:3129680 T>C maps to NM_021826.4 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:92616380 G>T maps to ENST00000298047 V4253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:92616380 G>T maps to ENST00000298047 V4253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:126369619 C>T maps to NM_024582.4 S2483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:126369619 C>T maps to NM_024582.4 S2483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:28877396 G>T maps to NM_002019.4 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:28877396 G>T maps to NM_002019.4 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:171306561 A>G maps to NM_002022.1 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:171306561 A>G maps to NM_002022.1 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:147011476 G>T maps to NM_002024.5 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:147011476 G>T maps to NM_002024.5 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:52781806 G>T maps to NM_013409.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:52781806 G>T maps to NM_013409.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:46252333 G>T maps to ENST00000507069 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:46252333 G>T maps to ENST00000507069 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:170235646 T>C maps to NM_014211.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:170235646 T>C maps to NM_014211.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109067568 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109067568 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:135864467 G>T maps to NM_004188.4 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:135864467 G>T maps to NM_004188.4 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:110134686 A>T maps to NM_006496.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:110134686 A>T maps to NM_006496.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:57485074 T>C maps to NM_080425.2 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:57485074 T>C maps to NM_080425.2 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72368432 C>G maps to ENST00000440684 G1324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72368432 C>G maps to ENST00000440684 G1324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119900181 G>T maps to NM_153002.2 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119900181 G>T maps to NM_153002.2 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:19031888 T>A maps to NM_001079858.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:19031888 T>A maps to NM_001079858.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:42895637 C>T maps to NM_001080476.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:42895637 C>T maps to NM_001080476.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:27544623 C>T maps to NM_001520.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:27544623 C>T maps to NM_001520.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:65413470 G>T maps to NM_138737.3 G508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:65413470 G>T maps to NM_138737.3 G508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:65428008 T>C maps to NM_138737.3 N882N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:65428008 T>C maps to NM_138737.3 N882N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:122284812 A>T maps to NM_002150.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:122284812 A>T maps to NM_002150.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:99465613 G>C maps to NM_000875.3 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:99465613 G>C maps to NM_000875.3 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151156245 G>A maps to NM_178822.4 L2035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151156245 G>A maps to NM_178822.4 L2035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151162965 G>T maps to NM_178822.4 S1601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151162965 G>T maps to NM_178822.4 S1601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130409601 G>A maps to NM_001170961.1 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130409601 G>A maps to NM_001170961.1 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:117122425 A>G maps to NM_001542.2 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:117122425 A>G maps to NM_001542.2 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:206653243 A>G maps to NM_014002.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:206653243 A>G maps to NM_014002.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:30795406 C>A maps to NM_006774.4 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:30795406 C>A maps to NM_006774.4 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:24655131 C>T maps to ENST00000458132 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:24655131 C>T maps to ENST00000458132 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:209974727 T>A maps to NM_006147.2 K11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:209974727 T>A maps to NM_006147.2 K11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:68628072 G>T maps to ENST00000423218 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:68628072 G>T maps to ENST00000423218 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:182344886 A>T maps to NM_000885.4 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:182344886 A>T maps to NM_000885.4 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:46330267 C>T maps to NM_000211.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:46330267 C>T maps to NM_000211.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26955576 C>A maps to NM_014680.2 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26955576 C>A maps to NM_014680.2 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:42832694 G>T maps to NM_015349.1 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:42832694 G>T maps to NM_015349.1 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:5461255 T>C maps to NM_015325.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:5461255 T>C maps to NM_015325.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:226446930 C>T maps to NM_020864.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:226446930 C>T maps to NM_020864.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:180905360 C>T maps to NM_020950.1 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:180905360 C>T maps to NM_020950.1 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51411734 C>A maps to NM_004917.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51411734 C>A maps to NM_004917.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:31655172 G>T maps to NM_001085455.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:31655172 G>T maps to NM_001085455.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153137772 G>T maps to NM_000425.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153137772 G>T maps to NM_000425.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:104377164 G>A maps to NM_199000.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:104377164 G>A maps to NM_199000.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:54758730 A>T maps to NM_001081442.1 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:54758730 A>T maps to NM_001081442.1 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31661988 G>C maps to NM_001031801.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31661988 G>C maps to NM_001031801.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:12907902 T>C maps to NM_001013631.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:12907902 T>C maps to NM_001013631.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:99418781 A>T maps to NM_001037317.1 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:99418781 A>T maps to NM_001037317.1 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170042415 G>T maps to NM_004525.2 R3148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170042415 G>T maps to NM_004525.2 R3148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:7231798 C>A maps to NM_001105581.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:7231798 C>A maps to NM_001105581.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:70505178 G>A maps to NM_020794.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:70505178 G>A maps to NM_020794.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:33484661 T>A maps to ENST00000354476 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:33484661 T>A maps to ENST00000354476 T801T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-38-4631-01A-01D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-38-4631-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:148798267 G>T maps to NM_005366.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:148798267 G>T maps to NM_005366.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:140996471 C>A maps to NM_005462.4 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:140996471 C>A maps to NM_005462.4 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:140985491 C>G maps to NM_138702.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:140985491 C>G maps to NM_138702.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:210574773 C>T maps to NM_002374.3 P1623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:210574773 C>T maps to NM_002374.3 P1623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:40704285 G>T maps to NM_002446.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:40704285 G>T maps to NM_002446.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:48255620 G>C maps to NM_002747.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:48255620 G>C maps to NM_002747.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:63666129 G>T maps to NM_001039469.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:63666129 G>T maps to NM_001039469.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:31194359 G>T maps to NM_002379.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:31194359 G>T maps to NM_002379.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:100395639 G>A maps to NM_032503.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:100395639 G>A maps to NM_032503.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:90382347 G>C maps to NM_014611.1 L4516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:90382347 G>C maps to NM_014611.1 L4516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:126734442 G>T maps to NM_032446.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:126734442 G>T maps to NM_032446.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128116824 C>T maps to NM_018396.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128116824 C>T maps to NM_018396.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:73263868 G>T maps to NM_020679.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:73263868 G>T maps to NM_020679.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:49444340 C>T maps to NM_003482.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:49444340 C>T maps to NM_003482.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:4947149 C>A maps to NM_001100600.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:4947149 C>A maps to NM_001100600.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:102745612 G>A maps to ENST00000326227 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:102745612 G>A maps to ENST00000326227 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:823009 C>A maps to NM_001025190.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:823009 C>A maps to NM_001025190.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:17157478 G>C maps to NM_004686.4 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:17157478 G>C maps to NM_004686.4 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:1246914 C>T maps to ENST00000447027 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:1246914 C>T maps to ENST00000447027 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:3240047 G>T maps to NM_015419.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:3240047 G>T maps to NM_015419.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:3240385 C>A maps to NM_015419.3 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:3240385 C>A maps to NM_015419.3 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:16085777 G>T maps to NM_005378.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:16085777 G>T maps to NM_005378.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23893160 C>G maps to NM_000257.2 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23893160 C>G maps to NM_000257.2 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128367542 G>T maps to ENST00000389524 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128367542 G>T maps to ENST00000389524 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:39942312 G>C maps to NM_015460.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:39942312 G>C maps to NM_015460.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:101890222 A>T maps to NM_052867.2 C439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:101890222 A>T maps to NM_052867.2 C439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:19339041 G>T maps to NM_004386.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:19339041 G>T maps to NM_004386.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50957719 G>T maps to NM_001185011.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50957719 G>T maps to NM_001185011.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:152432207 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:152432207 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:880904 C>A maps to NM_015658.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:880904 C>A maps to NM_015658.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:110886807 G>T maps to NM_000272.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:110886807 G>T maps to NM_000272.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:132407564 A>T maps to ENST00000393156 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:132407564 A>T maps to ENST00000393156 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119533824 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119533824 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:28000590 G>T maps to NM_000275.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:28000590 G>T maps to NM_000275.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:145113226 C>G maps to ENST00000360660 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:145113226 C>G maps to ENST00000360660 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247978137 C>T maps to NM_001001966.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247978137 C>T maps to NM_001001966.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248845176 T>A maps to NM_001004734.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248845176 T>A maps to NM_001004734.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248366413 G>T maps to NM_001004689.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248366413 G>T maps to NM_001004689.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:20502862 T>A maps to NM_001004714.1 K19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:20502862 T>A maps to NM_001004714.1 K19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:158517436 G>T maps to NM_001005189.1 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:158517436 G>T maps to NM_001005189.1 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:24892121 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:24892121 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72921750 G>T maps to NM_178160.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72921750 G>T maps to NM_178160.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:50111264 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:50111264 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:55570365 C>A maps to NM_001142769.1 E1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:55570365 C>A maps to NM_001142769.1 E1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:140181957 C>T maps to NM_018906.2 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:140181957 C>T maps to NM_018906.2 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:140746230 G>T maps to NM_018918.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:140746230 G>T maps to NM_018918.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:233394782 C>A maps to NM_014801.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:233394782 C>A maps to NM_014801.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:41239371 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:41239371 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:105197798 C>T maps to NM_014976.1 N1291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:105197798 C>T maps to NM_014976.1 N1291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:58273026 G>T maps to NM_001104631.1 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:58273026 G>T maps to NM_001104631.1 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:38468616 G>A maps to NM_012407.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:38468616 G>A maps to NM_012407.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130435260 A>C maps to NM_014602.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130435260 A>C maps to NM_014602.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:8809051 G>T maps to NM_001142633.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:8809051 G>T maps to NM_001142633.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:47852795 C>T maps to NM_138295.3 E2423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:47852795 C>T maps to NM_138295.3 E2423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110408304 G>T maps to ENST00000426474 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110408304 G>T maps to ENST00000426474 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110432915 G>T maps to ENST00000426474 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110432915 G>T maps to ENST00000426474 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110453507 C>A maps to ENST00000426474 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110453507 C>A maps to ENST00000426474 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:198950286 G>T maps to NM_006226.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:198950286 G>T maps to NM_006226.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:205809436 G>A maps to NM_152491.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:205809436 G>A maps to NM_152491.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:81751859 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:81751859 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:228003479 G>T maps to NM_183062.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:228003479 G>T maps to NM_183062.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11591677 G>T maps to NM_020780.1 E1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11591677 G>T maps to NM_020780.1 E1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11596646 T>G maps to NM_020780.1 G1361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11596646 T>G maps to NM_020780.1 G1361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:52370124 G>T maps to NM_144651.4 C305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:52370124 G>T maps to NM_144651.4 C305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109380141 A>G maps to NM_006267.4 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109380141 A>G maps to NM_006267.4 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:175956123 T>A maps to NM_022457.5 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:175956123 T>A maps to NM_022457.5 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:90021157 G>T maps to NM_016321.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:90021157 G>T maps to NM_016321.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:121001250 G>A maps to ENST00000458409 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:121001250 G>A maps to ENST00000458409 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77282815 A>G maps to ENST00000396204 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77282815 A>G maps to ENST00000396204 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:26887236 G>T maps to NM_001006665.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:26887236 G>T maps to NM_001006665.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46299363 T>C maps to NM_030785.3 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46299363 T>C maps to NM_030785.3 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46307976 C>A maps to NM_030785.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46307976 C>A maps to NM_030785.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:12145986 C>T maps to NM_032167.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:12145986 C>T maps to NM_032167.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:237881822 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:237881822 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:153512580 C>G maps to ENST00000359215 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:153512580 C>G maps to ENST00000359215 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55748125 C>A maps to ENST00000443936 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55748125 C>A maps to ENST00000443936 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:166901689 G>A maps to NM_001165963.1 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:166901689 G>A maps to NM_001165963.1 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:13858198 G>T maps to NM_025229.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:13858198 G>T maps to NM_025229.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:122629685 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:122629685 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:115838023 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:115838023 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:47158146 C>A maps to NM_014159.6 E1518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:47158146 C>A maps to NM_014159.6 E1518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:85894863 G>A maps to NM_198843.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:85894863 G>A maps to NM_198843.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44680366 G>T maps to NM_001134771.1 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44680366 G>T maps to NM_001134771.1 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43204723 C>A maps to NM_007163.3 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43204723 C>A maps to NM_007163.3 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:108681710 C>T maps to NM_013386.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:108681710 C>T maps to NM_013386.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140126578 C>A maps to NM_080877.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140126578 C>A maps to NM_080877.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:28539836 C>T maps to ENST00000394821 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:28539836 C>T maps to ENST00000394821 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:103090301 T>A maps to NM_001011552.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:103090301 T>A maps to NM_001011552.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:33802073 T>C maps to ENST00000361112 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:33802073 T>C maps to ENST00000361112 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:67457256 G>T maps to NM_005902.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:67457256 G>T maps to NM_005902.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:128650468 G>T maps to NM_003069.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:128650468 G>T maps to NM_003069.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:11138490 G>T maps to NM_001128849.1 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:11138490 G>T maps to NM_001128849.1 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:33071821 G>A maps to NM_018225.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:33071821 G>A maps to NM_018225.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:84350817 T>G maps to NM_014841.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:84350817 T>G maps to NM_014841.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:54872431 C>T maps to NM_003128.2 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:54872431 C>T maps to NM_003128.2 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:65338162 G>A maps to NM_006396.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:65338162 G>A maps to NM_006396.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17363208 C>A maps to NM_001004470.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17363208 C>A maps to NM_001004470.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17365137 G>T maps to NM_001004470.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17365137 G>T maps to NM_001004470.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:123220442 A>T maps to NM_001042750.1 R1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:123220442 A>T maps to NM_001042750.1 R1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:40468915 C>G maps to NM_139276.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:40468915 C>G maps to NM_139276.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:883153 A>T maps to ENST00000456758 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:883153 A>T maps to ENST00000456758 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:179290819 C>G maps to NM_198868.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:179290819 C>G maps to NM_198868.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:44554665 G>T maps to NM_145653.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:44554665 G>T maps to NM_145653.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:20876105 C>A maps to NM_007110.4 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:20876105 C>A maps to NM_007110.4 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:122004482 G>A maps to NM_014553.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:122004482 G>A maps to NM_014553.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:89177644 C>A maps to NM_138960.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:89177644 C>A maps to NM_138960.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:43797576 C>A maps to ENST00000330266 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:43797576 C>A maps to ENST00000330266 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:130184919 G>T maps to NM_133448.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:130184919 G>T maps to NM_133448.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:72691080 C>T maps to NM_001080462.1 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:72691080 C>T maps to NM_001080462.1 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:4292731 G>T maps to NM_144615.2 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:4292731 G>T maps to NM_144615.2 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:68964602 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:68964602 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:122063060 G>T maps to ENST00000509841 C342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:122063060 G>T maps to ENST00000509841 C342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:10916475 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:10916475 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:189068507 A>C maps to NM_178556.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:189068507 A>C maps to NM_178556.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:101375479 C>A maps to NM_004621.5 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:101375479 C>A maps to NM_004621.5 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:98508004 A>C maps to ENST00000359863 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:98508004 A>C maps to ENST00000359863 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:91007747 G>T maps to NM_001010854.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:91007747 G>T maps to NM_001010854.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:43576789 C>T maps to NM_015140.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:43576789 C>T maps to NM_015140.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179594233 C>A maps to NM_133378.4 E4973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179594233 C>A maps to NM_133378.4 E4973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:139569030 C>A maps to ENST00000358430 G365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:139569030 C>A maps to ENST00000358430 G365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:103359294 C>A maps to NM_015902.4 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:103359294 C>A maps to NM_015902.4 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:17758110 G>A maps to ENST00000428389 D757D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:17758110 G>A maps to ENST00000428389 D757D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:73836586 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:73836586 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:57640594 G>T maps to NM_020903.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:57640594 G>T maps to NM_020903.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:30207727 C>A maps to NM_018428.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:30207727 C>A maps to NM_018428.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:108303502 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:108303502 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:71148363 G>T maps to NM_012476.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:71148363 G>T maps to NM_012476.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:17830708 C>A maps to NM_003385.4 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:17830708 C>A maps to NM_003385.4 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:131398629 C>T maps to NM_052844.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:131398629 C>T maps to NM_052844.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:187371498 A>G maps to NM_018471.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:187371498 A>G maps to NM_018471.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:77768312 G>T maps to NM_024721.4 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:77768312 G>T maps to NM_024721.4 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58572989 G>T maps to NM_007134.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58572989 G>T maps to NM_007134.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:52193349 C>A maps to NM_006526.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:52193349 C>A maps to NM_006526.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58724290 C>T maps to NM_133502.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58724290 C>T maps to NM_133502.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:31138373 T>A maps to NM_182755.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:31138373 T>A maps to NM_182755.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:37129922 C>A maps to NM_153257.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:37129922 C>A maps to NM_153257.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56934257 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56934257 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:37677514 A>T maps to NM_152279.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:37677514 A>T maps to NM_152279.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:59438 G>T maps to NM_182524.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:59438 G>T maps to NM_182524.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:249144509 C>A maps to NM_001136036.2 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:249144509 C>A maps to NM_001136036.2 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247150364 T>A maps to NM_020394.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247150364 T>A maps to NM_020394.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53855100 C>G maps to NM_138374.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53855100 C>G maps to NM_138374.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:183645219 T>A maps to NM_005688.2 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:183645219 T>A maps to NM_005688.2 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:119029412 C>A maps to NM_001142505.1 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:119029412 C>A maps to NM_001142505.1 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:131312362 G>C maps to NM_001009185.1 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:131312362 G>C maps to NM_001009185.1 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:136321308 C>T maps to NM_139025.3 V1229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:136321308 C>T maps to NM_139025.3 V1229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:96781456 C>A maps to NM_000682.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:96781456 C>A maps to NM_000682.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44152341 C>A maps to NM_001129.3 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44152341 C>A maps to NM_001129.3 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:125876314 G>T maps to ENST00000273450 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:125876314 G>T maps to ENST00000273450 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:112054521 C>A maps to NM_001113490.1 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:112054521 C>A maps to NM_001113490.1 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:197873683 T>A maps to NM_001195144.1 K666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:197873683 T>A maps to NM_001195144.1 K666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:150199077 C>G maps to NM_030920.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:150199077 C>G maps to NM_030920.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:118463521 G>T maps to ENST00000359415 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:118463521 G>T maps to ENST00000359415 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:2998959 C>A maps to NM_004042.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:2998959 C>A maps to NM_004042.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:177136755 G>A maps to NM_080874.3 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:177136755 G>A maps to NM_080874.3 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:101103673 A>G maps to NM_006828.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:101103673 A>G maps to NM_006828.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176915132 C>A maps to ENST00000281881 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176915132 C>A maps to ENST00000281881 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:70034898 T>C maps to NM_001704.2 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:70034898 T>C maps to NM_001704.2 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:34118559 G>A maps to NM_133468.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:34118559 G>A maps to NM_133468.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:21146658 G>A maps to NM_152914.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:21146658 G>A maps to NM_152914.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:74729666 G>T maps to ENST00000317409 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:74729666 G>T maps to ENST00000317409 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:31903836 A>G maps to NM_000063.4 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:31903836 A>G maps to NM_000063.4 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:71020080 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:71020080 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:2778096 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:2778096 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:181763997 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:181763997 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:85932593 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:85932593 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44259816 G>T maps to NM_001220.4 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44259816 G>T maps to NM_001220.4 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:128758689 G>A maps to NM_024768.2 *599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:128758689 G>A maps to NM_024768.2 *599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:60785468 C>A maps to NM_006725.3 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:60785468 C>A maps to NM_006725.3 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:137542337 G>A maps to NM_004661.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:137542337 G>A maps to NM_004661.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:233396060 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:233396060 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:77569227 T>G maps to NM_006493.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:77569227 T>G maps to NM_006493.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:77569332 A>G maps to NM_006493.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:77569332 A>G maps to NM_006493.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:88249303 A>G maps to NM_173538.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:88249303 A>G maps to NM_173538.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:146805425 C>A maps to NM_014141.5 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:146805425 C>A maps to NM_014141.5 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:110819541 C>T maps to NM_001845.4 K1304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:110819541 C>T maps to NM_001845.4 K1304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:107930772 T>A maps to ENST00000328300 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:107930772 T>A maps to ENST00000328300 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:238274646 A>G maps to NM_004369.3 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:238274646 A>G maps to NM_004369.3 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:207867944 T>C maps to NM_175710.1 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:207867944 T>C maps to NM_175710.1 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:2949080 A>T maps to NM_033225.5 T2414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:2949080 A>T maps to NM_033225.5 T2414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:23425463 C>A maps to NM_138283.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:23425463 C>A maps to NM_138283.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:41594959 G>T maps to NM_000766.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:41594959 G>T maps to NM_000766.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:59410880 G>A maps to NM_000780.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:59410880 G>A maps to NM_000780.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:88885434 A>T maps to NM_152418.3 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:88885434 A>T maps to NM_152418.3 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:95092210 C>A maps to NM_001129889.1 G534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:95092210 C>A maps to NM_001129889.1 G534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:61890702 G>T maps to NM_203499.1 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:61890702 G>T maps to NM_203499.1 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:107557756 G>A maps to NM_000108.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:107557756 G>A maps to NM_000108.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11584037 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11584037 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:129172390 G>A maps to ENST00000398025 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:129172390 G>A maps to ENST00000398025 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:74063857 G>T maps to NM_001025290.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:74063857 G>T maps to NM_001025290.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:37771373 G>C maps to NM_052906.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:37771373 G>C maps to NM_052906.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:77079623 C>T maps to NM_001042573.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:77079623 C>T maps to NM_001042573.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:14028124 A>T maps to NM_005236.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:14028124 A>T maps to NM_005236.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:50282943 G>A maps to NM_012306.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:50282943 G>A maps to NM_012306.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:29474838 G>A maps to NM_018099.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:29474838 G>A maps to NM_018099.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:150905490 C>T maps to NM_001447.2 L3448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:150905490 C>T maps to NM_001447.2 L3448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:126240577 C>T maps to NM_024582.4 T1004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:126240577 C>T maps to NM_024582.4 T1004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:125072896 C>T maps to NM_001039112.2 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:125072896 C>T maps to NM_001039112.2 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:15964477 C>T maps to NM_031950.3 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:15964477 C>T maps to NM_031950.3 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:34298530 G>A maps to NM_025135.2 W915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:34298530 G>A maps to NM_025135.2 W915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:183699581 G>T maps to NM_001463.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:183699581 G>T maps to NM_001463.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:162307216 C>A maps to NM_020116.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:162307216 C>A maps to NM_020116.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:47034432 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:47034432 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:88902641 C>A maps to NM_000512.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:88902641 C>A maps to NM_000512.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:173804034 G>T maps to NM_001034845.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:173804034 G>T maps to NM_001034845.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:19749276 T>C maps to NM_016573.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:19749276 T>C maps to NM_016573.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:75557765 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:75557765 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:176622814 A>C maps to NM_005277.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:176622814 A>C maps to NM_005277.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:135429848 G>A maps to NM_153834.3 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:135429848 G>A maps to NM_153834.3 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:153065835 C>A maps to NM_001114183.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:153065835 C>A maps to NM_001114183.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:18705918 G>T maps to NM_178425.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:18705918 G>T maps to NM_178425.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:37289110 C>T maps to NM_019024.1 W556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:37289110 C>T maps to NM_019024.1 W556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:126080785 G>T maps to NM_012259.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:126080785 G>T maps to NM_012259.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:100503813 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:100503813 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:88040363 T>A maps to NM_000866.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:88040363 T>A maps to NM_000866.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:47409208 C>A maps to NM_000621.3 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:47409208 C>A maps to NM_000621.3 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:6104075 G>A maps to NM_000417.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:6104075 G>A maps to NM_000417.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:6814717 A>T maps to NM_015061.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:6814717 A>T maps to NM_015061.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45748180 C>T maps to NM_002265.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45748180 C>T maps to NM_002265.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:169714975 C>G maps to NM_005565.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:169714975 C>G maps to NM_005565.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:929611 C>A maps to ENST00000262301 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:929611 C>A maps to ENST00000262301 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1474682 C>A maps to NM_024830.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1474682 C>A maps to NM_024830.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:141607773 G>A maps to NM_018557.2 D1612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:141607773 G>A maps to NM_018557.2 D1612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:90399290 G>T maps to NM_001134479.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:90399290 G>T maps to NM_001134479.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:33505173 C>T maps to ENST00000354476 Q1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:33505173 C>T maps to ENST00000354476 Q1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:151302987 C>A maps to NM_021048.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:151302987 C>A maps to NM_021048.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:78150962 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:78150962 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:112326314 G>A maps to NM_139078.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:112326314 G>A maps to NM_139078.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:22532983 G>A maps to ENST00000441815 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:22532983 G>A maps to ENST00000441815 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56848061 G>T maps to NM_012064.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56848061 G>T maps to NM_012064.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:102562550 G>A maps to NM_022122.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:102562550 G>A maps to NM_022122.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:56355386 G>A maps to ENST00000340482 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:56355386 G>A maps to ENST00000340482 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:68777420 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:68777420 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:50804967 G>A maps to NM_001145809.1 K1840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:50804967 G>A maps to NM_001145809.1 K1840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:26343715 G>T maps to ENST00000407587 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:26343715 G>T maps to ENST00000407587 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:24929491 C>A maps to NM_003743.4 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:24929491 C>A maps to NM_003743.4 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:145660444 C>A maps to NM_013432.4 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:145660444 C>A maps to NM_013432.4 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:99264811 G>A maps to NM_024759.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:99264811 G>A maps to NM_024759.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:247587737 C>T maps to NM_004895.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:247587737 C>T maps to NM_004895.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:55447800 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:55447800 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:50850507 C>A maps to ENST00000404971 G393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:50850507 C>A maps to ENST00000404971 G393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24884815 C>T maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24884815 C>T maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:123893725 A>T maps to NM_001001953.1 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:123893725 A>T maps to NM_001001953.1 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:248512747 C>A maps to NM_001001918.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:248512747 C>A maps to NM_001001918.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:143826999 T>C maps to NM_001001659.1 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:143826999 T>C maps to NM_001001659.1 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:247614654 G>A maps to NM_001004492.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:247614654 G>A maps to NM_001004492.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:248058992 C>A maps to NM_001001957.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:248058992 C>A maps to NM_001001957.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:5079999 T>A maps to NM_001005164.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:5079999 T>A maps to NM_001005164.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9324916 C>T maps to NM_001005191.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9324916 C>T maps to NM_001005191.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:55117811 G>T maps to NM_207339.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:55117811 G>T maps to NM_207339.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:39591612 C>A maps to NM_001004318.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:39591612 C>A maps to NM_001004318.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176525706 C>A maps to NM_020318.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176525706 C>A maps to NM_020318.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140475996 G>A maps to NM_018936.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140475996 G>A maps to NM_018936.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:82582363 T>C maps to NM_033026.5 S2635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:82582363 T>C maps to NM_033026.5 S2635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:95748051 G>T maps to NM_000439.4 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:95748051 G>T maps to NM_000439.4 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:173451115 G>A maps to ENST00000392571 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:173451115 G>A maps to ENST00000392571 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32037440 C>G maps to NM_178140.2 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32037440 C>G maps to NM_178140.2 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:22210611 G>T maps to NM_001135721.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:22210611 G>T maps to NM_001135721.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:47937646 T>A maps to NM_138295.3 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:47937646 T>A maps to NM_138295.3 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:111426935 G>T maps to ENST00000312791 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:111426935 G>T maps to ENST00000312791 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:160241521 G>A maps to NM_173516.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:160241521 G>A maps to NM_173516.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:53103525 C>A maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:53103525 C>A maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:14542896 A>G maps to ENST00000444806 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:14542896 A>G maps to ENST00000444806 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:113518830 C>A maps to NM_002711.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:113518830 C>A maps to NM_002711.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:146070804 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:146070804 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:68956758 C>A maps to NM_024870.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:68956758 C>A maps to NM_024870.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10387191 A>G maps to NM_198464.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10387191 A>G maps to NM_198464.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:40979266 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:40979266 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:68695996 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:68695996 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:25622074 C>G maps to NM_000965.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:25622074 C>G maps to NM_000965.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:114773055 C>A maps to ENST00000389544 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:114773055 C>A maps to ENST00000389544 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:80369241 C>T maps to NM_006909.1 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:80369241 C>T maps to NM_006909.1 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:33774800 G>T maps to NM_170672.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:33774800 G>T maps to NM_170672.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:48390037 C>A maps to NM_002900.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:48390037 C>A maps to NM_002900.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:103207068 G>A maps to ENST00000428762 R1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:103207068 G>A maps to ENST00000428762 R1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:100038093 A>G maps to NM_016316.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:100038093 A>G maps to NM_016316.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:105261775 C>G maps to NM_001100117.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:105261775 C>G maps to NM_001100117.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:78656192 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:78656192 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:124742359 G>T maps to NM_022370.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:124742359 G>T maps to NM_022370.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10466377 C>A maps to NM_178857.5 E1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10466377 C>A maps to NM_178857.5 E1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237711772 G>A maps to NM_001035.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237711772 G>A maps to NM_001035.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:35652806 C>A maps to NM_005066.2 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:35652806 C>A maps to NM_005066.2 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:201860533 G>T maps to NM_198149.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:201860533 G>T maps to NM_198149.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:20003353 G>T maps to NM_001135691.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:20003353 G>T maps to NM_001135691.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:72332162 C>A maps to NM_001098484.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:72332162 C>A maps to NM_001098484.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:108626707 T>A maps to NM_021815.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:108626707 T>A maps to NM_021815.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:70148046 T>G maps to NM_032803.5 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:70148046 T>G maps to NM_032803.5 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:99157098 A>G maps to NM_015976.4 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:99157098 A>G maps to NM_015976.4 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108489871 C>T maps to NM_001013031.1 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108489871 C>T maps to NM_001013031.1 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10584168 C>T maps to ENST00000354846 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10584168 C>T maps to ENST00000354846 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158617447 G>A maps to NM_003126.2 D1259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158617447 G>A maps to NM_003126.2 D1259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:149492317 G>T maps to NM_198455.2 L2070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:149492317 G>T maps to NM_198455.2 L2070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:113261338 G>A maps to ENST00000374463 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:113261338 G>A maps to ENST00000374463 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:64899784 G>A maps to NM_172230.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:64899784 G>A maps to NM_172230.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:132351099 G>A maps to NM_016521.2 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:132351099 G>A maps to NM_016521.2 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:11441425 A>G maps to ENST00000423059 C1469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:11441425 A>G maps to ENST00000423059 C1469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:137872774 G>A maps to ENST00000272643 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:137872774 G>A maps to ENST00000272643 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:103261149 A>G maps to NM_001198812.1 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:103261149 A>G maps to NM_001198812.1 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:16875340 G>A maps to NM_012452.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:16875340 G>A maps to NM_012452.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:57070016 G>A maps to NM_033396.2 S1533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:57070016 G>A maps to NM_033396.2 S1533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:175372465 C>T maps to NM_003285.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:175372465 C>T maps to NM_003285.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:84417624 T>A maps to NM_024686.4 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:84417624 T>A maps to NM_024686.4 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179530102 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179530102 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:78189128 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:78189128 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:111633123 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:111633123 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:57396913 C>T maps to NM_014830.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:57396913 C>T maps to NM_014830.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:73440836 G>A maps to NM_021260.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:73440836 G>A maps to NM_021260.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:147120536 G>T maps to NM_001168379.1 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:147120536 G>T maps to NM_001168379.1 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:101139126 T>G maps to NM_001011657.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:101139126 T>G maps to NM_001011657.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:40532225 T>A maps to NM_024645.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:40532225 T>A maps to NM_024645.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9677031 C>A maps to NM_001008727.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9677031 C>A maps to NM_001008727.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:44933334 C>A maps to NM_014518.2 G541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:44933334 C>A maps to NM_014518.2 G541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:38305839 G>T maps to NM_006954.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:38305839 G>T maps to NM_006954.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:21706376 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:21706376 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:12691646 G>C maps to NM_020714.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:12691646 G>C maps to NM_020714.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:88966204 C>A maps to NM_181646.2 A1303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:88966204 C>A maps to NM_181646.2 A1303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:108010911 G>T maps to NM_000019.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:108010911 G>T maps to NM_000019.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:141049580 T>C maps to NM_022481.5 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:141049580 T>C maps to NM_022481.5 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:47559750 G>A maps to NM_020453.3 W632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:47559750 G>A maps to NM_020453.3 W632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:21971024 G>A maps to NM_001195132.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:21971024 G>A maps to NM_001195132.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:214815961 G>A maps to NM_016343.3 Q1427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:214815961 G>A maps to NM_016343.3 Q1427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495853 C>T maps to ENST00000429130 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495853 C>T maps to ENST00000429130 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:87011404 C>T maps to NM_001143935.1 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:87011404 C>T maps to NM_001143935.1 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:118971726 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:118971726 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:65113155 G>A maps to NM_006268.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:65113155 G>A maps to NM_006268.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:37271783 G>A maps to NM_000831.3 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:37271783 G>A maps to NM_000831.3 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:43360300 G>A maps to NM_015052.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:43360300 G>A maps to NM_015052.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr12:44180499 A>G maps to NM_016123.3 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr12:44180499 A>G maps to NM_016123.3 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:10248921 C>T maps to NM_003802.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:10248921 C>T maps to NM_003802.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:26423043 G>T maps to ENST00000407587 P2370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:26423043 G>T maps to ENST00000407587 P2370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:33345398 T>C maps to NM_014071.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:33345398 T>C maps to NM_014071.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:125391043 G>T maps to NM_001004450.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:125391043 G>T maps to NM_001004450.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:248551127 C>A maps to NM_001005471.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:248551127 C>A maps to NM_001005471.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:17405775 G>A maps to NM_007365.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:17405775 G>A maps to NM_007365.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:48689544 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:48689544 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:87696608 G>T maps to NM_080685.2 G1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:87696608 G>T maps to NM_080685.2 G1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:46202150 G>A maps to NM_017659.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:46202150 G>A maps to NM_017659.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:184570664 C>T maps to ENST00000326397 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:184570664 C>T maps to ENST00000326397 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:165370601 G>T maps to NM_006917.4 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:165370601 G>T maps to NM_006917.4 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:37953842 T>A maps to ENST00000223214 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:37953842 T>A maps to ENST00000223214 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:108831633 T>G maps to NM_152621.5 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:108831633 T>G maps to NM_152621.5 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:36671140 G>A maps to NM_004172.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:36671140 G>A maps to NM_004172.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:172691270 T>C maps to NM_003705.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:172691270 T>C maps to NM_003705.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:62701743 C>T maps to NM_003195.4 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:62701743 C>T maps to NM_003195.4 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:152084546 C>T maps to NM_007113.2 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:152084546 C>T maps to NM_007113.2 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:44250095 G>A maps to NM_182539.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:44250095 G>A maps to NM_182539.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:109635560 C>G maps to NM_020141.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:109635560 C>G maps to NM_020141.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:1499823 C>A maps to NM_000547.5 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:1499823 C>A maps to NM_000547.5 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:186322930 T>G maps to NM_003292.2 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:186322930 T>G maps to NM_003292.2 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:52370413 G>A maps to NM_012288.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:52370413 G>A maps to NM_012288.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:179577962 G>T maps to NM_133378.4 I7722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:179577962 G>T maps to NM_133378.4 I7722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:13275788 C>A maps to NM_145314.1 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:13275788 C>A maps to NM_145314.1 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:55604670 A>T maps to NM_015306.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:55604670 A>T maps to NM_015306.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:145124170 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:145124170 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:108185291 G>C maps to NM_006113.4 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:108185291 G>C maps to NM_006113.4 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:98354269 C>A maps to NM_001079.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:98354269 C>A maps to NM_001079.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:200377573 G>A maps to NM_012482.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:200377573 G>A maps to NM_012482.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:84611368 G>T maps to NM_207517.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:84611368 G>T maps to NM_207517.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:62287632 G>A maps to NM_001620.1 G4752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:62287632 G>A maps to NM_001620.1 G4752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:178834572 C>G maps to NM_004673.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:178834572 C>G maps to NM_004673.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:135770093 G>T maps to NM_004840.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:135770093 G>T maps to NM_004840.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:39932096 G>A maps to NM_001123385.1 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:39932096 G>A maps to NM_001123385.1 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:42127650 C>T maps to NM_207406.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:42127650 C>T maps to NM_207406.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:112993282 C>A maps to ENST00000273395 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:112993282 C>A maps to ENST00000273395 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:131822191 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:131822191 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:122002990 C>A maps to NM_001178065.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:122002990 C>A maps to NM_001178065.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:40948053 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:40948053 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:55563912 A>G maps to ENST00000436346 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:55563912 A>G maps to ENST00000436346 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:123920081 G>T maps to NM_007018.4 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:123920081 G>T maps to NM_007018.4 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:117232482 G>A maps to NM_000492.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:117232482 G>A maps to NM_000492.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:139737683 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:139737683 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:130285780 C>A maps to NM_001102608.1 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:130285780 C>A maps to NM_001102608.1 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:30693084 G>A maps to ENST00000348438 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:30693084 G>A maps to ENST00000348438 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:67662412 G>T maps to NM_006565.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:67662412 G>T maps to NM_006565.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:67663407 C>T maps to NM_006565.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:67663407 C>T maps to NM_006565.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:43152464 G>A maps to ENST00000354495 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:43152464 G>A maps to ENST00000354495 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:44028080 C>T maps to NM_022785.3 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:44028080 C>T maps to NM_022785.3 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:27209237 C>T maps to ENST00000394906 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:27209237 C>T maps to ENST00000394906 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:78430041 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:78430041 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:28385431 T>A maps to NM_017412.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:28385431 T>A maps to NM_017412.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:141900396 T>C maps to NM_001039547.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:141900396 T>C maps to NM_001039547.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:134916302 C>T maps to ENST00000368577 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:134916302 C>T maps to ENST00000368577 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:50742266 C>A maps to NM_005311.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:50742266 C>A maps to NM_005311.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:33053643 C>T maps to NM_002121.4 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:33053643 C>T maps to NM_002121.4 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:114141815 T>A maps to NM_000868.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:114141815 T>A maps to NM_000868.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:219922284 G>A maps to NM_002181.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:219922284 G>A maps to NM_002181.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:42178305 T>C maps to NM_001556.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:42178305 T>C maps to NM_001556.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:75989203 G>T maps to NM_006633.2 V1310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:75989203 G>T maps to NM_006633.2 V1310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:44180314 T>C maps to NM_016123.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:44180314 T>C maps to NM_016123.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:29035077 C>A maps to NM_015254.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:29035077 C>A maps to NM_015254.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:47288895 C>T maps to NM_182902.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:47288895 C>T maps to NM_182902.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:55014925 G>T maps to NM_002288.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:55014925 G>T maps to NM_002288.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:36250715 G>T maps to NM_174902.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:36250715 G>T maps to NM_174902.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:99418684 G>T maps to NM_001037317.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:99418684 G>T maps to NM_001037317.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:40136264 G>T maps to NM_020929.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:40136264 G>T maps to NM_020929.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:75650120 G>T maps to NM_020932.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:75650120 G>T maps to NM_020932.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:9089294 G>T maps to NM_024690.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:9089294 G>T maps to NM_024690.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:130881249 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:130881249 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:13427850 C>A maps to NM_024923.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:13427850 C>A maps to NM_024923.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:143748276 C>A maps to NM_012365.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:143748276 C>A maps to NM_012365.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:48510589 C>A maps to NM_001005512.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:48510589 C>A maps to NM_001005512.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:55761411 C>G maps to NM_003697.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:55761411 C>G maps to NM_003697.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:161221084 G>T maps to NM_001080440.1 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:161221084 G>T maps to NM_001080440.1 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:56720126 C>T maps to NM_001127460.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:56720126 C>T maps to NM_001127460.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:21695368 C>A maps to NM_006192.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:21695368 C>A maps to NM_006192.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:145001142 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:145001142 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:106821052 A>T maps to NM_018082.5 K394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:106821052 A>T maps to NM_018082.5 K394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:144689139 G>A maps to NM_023078.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:144689139 G>A maps to NM_023078.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:88228553 T>A maps to NM_020320.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:88228553 T>A maps to NM_020320.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:86672762 A>T maps to NM_002890.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:86672762 A>T maps to NM_002890.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:79265680 C>T maps to NM_002891.4 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:79265680 C>T maps to NM_002891.4 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:47044718 C>T maps to NM_005676.3 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:47044718 C>T maps to NM_005676.3 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:33945029 C>A maps to NM_001036.3 A1418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:33945029 C>A maps to NM_001036.3 A1418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:91617196 C>A maps to NM_005226.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:91617196 C>A maps to NM_005226.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:84362714 G>T maps to NM_001012980.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:84362714 G>T maps to NM_001012980.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:165969466 G>T maps to NM_006922.3 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:165969466 G>T maps to NM_006922.3 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:123508904 G>T maps to NM_018400.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:123508904 G>T maps to NM_018400.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:94964179 G>T maps to NM_173850.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:94964179 G>T maps to NM_173850.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:26769421 C>T maps to NM_021115.4 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:26769421 C>T maps to NM_021115.4 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:100787145 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:100787145 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:42287589 C>A maps to NM_006749.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:42287589 C>A maps to NM_006749.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:150656992 G>T maps to NM_001145017.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:150656992 G>T maps to NM_001145017.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:96954406 G>A maps to NM_014014.3 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:96954406 G>A maps to NM_014014.3 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:53814754 G>T maps to NM_052870.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:53814754 G>T maps to NM_052870.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:48818790 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:48818790 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:35913988 C>T maps to NM_007247.4 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:35913988 C>T maps to NM_007247.4 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:60575247 G>A maps to NM_003185.3 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:60575247 G>A maps to NM_003185.3 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:179562934 C>A maps to ENST00000444136 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:179562934 C>A maps to ENST00000444136 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:126137132 C>A maps to NM_052907.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:126137132 C>A maps to NM_052907.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:1590516 G>A maps to NM_001097620.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:1590516 G>A maps to NM_001097620.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:32052274 C>A maps to ENST00000375244 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:32052274 C>A maps to ENST00000375244 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:20352501 C>G maps to ENST00000424589 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:20352501 C>G maps to ENST00000424589 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:49357466 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:49357466 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:75265918 G>T maps to NM_019589.2 E1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:75265918 G>T maps to NM_019589.2 E1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:46619112 T>C maps to ENST00000242848 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:46619112 T>C maps to ENST00000242848 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:77618185 G>T maps to NM_024721.4 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:77618185 G>T maps to NM_024721.4 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:28056963 C>T maps to NM_003447.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:28056963 C>T maps to NM_003447.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:52794387 T>C maps to NM_001010851.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:52794387 T>C maps to NM_001010851.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:149153029 G>A maps to ENST00000440594 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:149153029 G>A maps to ENST00000440594 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:57176422 C>A maps to NM_001005850.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:57176422 C>A maps to NM_001005850.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:151474961 G>A maps to NM_207365.3 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:151474961 G>A maps to NM_207365.3 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:67151276 C>A maps to NM_080282.3 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:67151276 C>A maps to NM_080282.3 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:6756062 G>T maps to NM_032489.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:6756062 G>T maps to NM_032489.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:5319166 C>A maps to NM_139056.2 C1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:5319166 C>A maps to NM_139056.2 C1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:131797655 G>T maps to NM_001115.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:131797655 G>T maps to NM_001115.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:114107680 C>T maps to NM_138430.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:114107680 C>T maps to NM_138430.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:88035721 G>T maps to NM_001166693.1 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:88035721 G>T maps to NM_001166693.1 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:147743878 G>T maps to NM_002025.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:147743878 G>T maps to NM_002025.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:132270356 G>A maps to NM_014423.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:132270356 G>A maps to NM_014423.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:86838536 C>A maps to NM_152336.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:86838536 C>A maps to NM_152336.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125872400 C>G maps to ENST00000273450 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125872400 C>G maps to ENST00000273450 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110168959 G>T maps to ENST00000393689 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110168959 G>T maps to ENST00000393689 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:45810525 C>T maps to NM_001142679.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:45810525 C>T maps to NM_001142679.1 L686L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:21239498 G>T maps to NM_000384.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:21239498 G>T maps to NM_000384.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:11187672 G>T maps to NM_013427.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:11187672 G>T maps to NM_013427.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:1893702 C>T maps to ENST00000398564 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:1893702 C>T maps to ENST00000398564 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150878457 C>A maps to ENST00000422024 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150878457 C>A maps to ENST00000422024 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:152814179 G>A maps to NM_001001344.2 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:152814179 G>A maps to NM_001001344.2 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:232262810 G>C maps to NM_145236.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:232262810 G>C maps to NM_145236.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:171482233 C>G maps to ENST00000392078 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:171482233 C>G maps to ENST00000392078 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:31614236 G>C maps to ENST00000404765 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:31614236 G>C maps to ENST00000404765 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:33545220 G>A maps to NM_198428.2 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:33545220 G>A maps to NM_198428.2 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:99641150 C>G maps to NM_138576.2 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:99641150 C>G maps to NM_138576.2 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:101005478 G>A maps to NM_020836.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:101005478 G>A maps to NM_020836.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:18209220 G>T maps to NM_153346.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:18209220 G>T maps to NM_153346.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:11406562 C>A maps to ENST00000427279 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:11406562 C>A maps to ENST00000427279 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:59961503 T>A maps to NM_004330.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:59961503 T>A maps to NM_004330.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:13605955 A>G maps to NM_148894.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:13605955 A>G maps to NM_148894.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28464260 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28464260 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:79936969 T>C maps to NM_153252.4 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:79936969 T>C maps to NM_153252.4 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90095675 C>T maps to NM_001214.3 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90095675 C>T maps to NM_001214.3 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22986095 C>A maps to NM_000491.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22986095 C>A maps to NM_000491.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75042609 T>A maps to NM_001002912.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75042609 T>A maps to NM_001002912.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75097612 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75097612 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:31873971 C>T maps to NM_033197.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:31873971 C>T maps to NM_033197.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:45598868 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:45598868 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:98865109 A>G maps to NM_174952.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:98865109 A>G maps to NM_174952.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:35045841 C>A maps to NM_203299.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:35045841 C>A maps to NM_203299.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:139959972 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:139959972 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:86570402 C>A maps to NM_032307.3 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:86570402 C>A maps to NM_032307.3 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:27556698 C>T maps to NM_018325.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:27556698 C>T maps to NM_018325.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:105209689 G>T maps to NM_015916.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:105209689 G>T maps to NM_015916.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:149644578 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:149644578 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:74440083 A>T maps to NM_133493.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:74440083 A>T maps to NM_133493.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:35836515 C>A maps to NM_001771.3 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:35836515 C>A maps to NM_001771.3 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160811266 C>A maps to NM_001166663.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160811266 C>A maps to NM_001166663.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:157803125 T>A maps to NM_005894.2 K299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:157803125 T>A maps to NM_005894.2 K299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:80869846 T>C maps to NM_001098802.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:80869846 T>C maps to NM_001098802.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196871740 C>A maps to NM_006684.2 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196871740 C>A maps to NM_006684.2 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:6173019 G>A maps to NM_015557.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:6173019 G>A maps to NM_015557.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:43890470 C>T maps to ENST00000413657 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:43890470 C>T maps to ENST00000413657 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87645121 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87645121 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:205030381 C>A maps to NM_005076.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:205030381 C>A maps to NM_005076.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:1415641 A>C maps to NM_014461.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:1415641 A>C maps to NM_014461.2 A660A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:51111276 C>A maps to ENST00000395542 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:51111276 C>A maps to ENST00000395542 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:103347307 G>T maps to NM_080629.2 S1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:103347307 G>T maps to NM_080629.2 S1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101817382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101817382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:189849688 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:189849688 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:189872627 G>A maps to NM_000090.3 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:189872627 G>A maps to NM_000090.3 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:111132682 G>T maps to NM_001846.2 G902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:111132682 G>T maps to NM_001846.2 G902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:61460981 C>A maps to NM_001853.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:61460981 C>A maps to NM_001853.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:83215960 G>A maps to ENST00000261723 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:83215960 G>A maps to ENST00000261723 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:1706002 G>T maps to NM_020825.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:1706002 G>T maps to NM_020825.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:2967786 C>A maps to NM_033225.5 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:2967786 C>A maps to NM_033225.5 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:113668509 T>A maps to NM_198123.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:113668509 T>A maps to NM_198123.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:61121426 C>G maps to NM_001161454.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:61121426 C>G maps to NM_001161454.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:85404013 C>A maps to NM_053281.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:85404013 C>A maps to NM_053281.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:155298497 G>T maps to NM_017639.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:155298497 G>T maps to NM_017639.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:33054338 G>A maps to NM_001077242.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:33054338 G>A maps to NM_001077242.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:14216489 C>A maps to NM_004080.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:14216489 C>A maps to NM_004080.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:60545245 C>A maps to NM_001042517.1 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:60545245 C>A maps to NM_001042517.1 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117387250 C>A maps to NM_020693.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117387250 C>A maps to NM_020693.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:28934273 C>A maps to NM_001942.2 Y705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:28934273 C>A maps to NM_001942.2 Y705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:30454915 T>A maps to NM_080611.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:30454915 T>A maps to NM_080611.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:102476787 G>T maps to NM_001376.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:102476787 G>T maps to NM_001376.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:65824891 G>A maps to ENST00000450752 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:65824891 G>A maps to ENST00000450752 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:103988648 A>T maps to NM_152310.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:103988648 A>T maps to NM_152310.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:2891214 G>T maps to NM_032048.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:2891214 G>T maps to NM_032048.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:225699551 C>A maps to ENST00000284563 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:225699551 C>A maps to ENST00000284563 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:38201006 G>A maps to NM_001099439.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:38201006 G>A maps to NM_001099439.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:56270729 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:56270729 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:44820665 C>T maps to NM_024066.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:44820665 C>T maps to NM_024066.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23713520 T>C maps to NM_033266.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23713520 T>C maps to NM_033266.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:152265374 C>A maps to NM_001122741.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:152265374 C>A maps to NM_001122741.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:154157068 G>A maps to NM_000132.3 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:154157068 G>A maps to NM_000132.3 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139209900 G>A maps to NM_015912.3 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139209900 G>A maps to NM_015912.3 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:190250720 C>A maps to NM_199051.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:190250720 C>A maps to NM_199051.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:67675061 C>T maps to NM_173526.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:67675061 C>T maps to NM_173526.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:33876671 G>T maps to NM_178468.4 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:33876671 G>T maps to NM_178468.4 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:85139043 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:85139043 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:92531038 A>T maps to ENST00000298047 L1620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:92531038 A>T maps to ENST00000298047 L1620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:16096938 C>T maps to NM_017556.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:16096938 C>T maps to NM_017556.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:161680652 G>A maps to NM_001184866.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:161680652 G>A maps to NM_001184866.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:114257954 A>T maps to NM_012184.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:114257954 A>T maps to NM_012184.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:89878658 G>T maps to NM_001085471.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:89878658 G>T maps to NM_001085471.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:49444597 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:49444597 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:49450215 A>T maps to NM_001018071.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:49450215 A>T maps to NM_001018071.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:47427875 G>T maps to NM_000812.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:47427875 G>T maps to NM_000812.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:151131076 G>A maps to NM_004961.3 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:151131076 G>A maps to NM_004961.3 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:89895077 G>A maps to NM_002042.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:89895077 G>A maps to NM_002042.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:130101922 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:130101922 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:131958333 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:131958333 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:135429795 C>T maps to NM_153834.3 Q1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:135429795 C>T maps to NM_153834.3 Q1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:105518392 G>T maps to NM_013345.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:105518392 G>T maps to NM_013345.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:105804493 C>A maps to NM_000829.3 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:105804493 C>A maps to NM_000829.3 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:86415734 C>T maps to NM_000840.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:86415734 C>T maps to NM_000840.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:126173068 G>A maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:126173068 G>A maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:108628500 A>C maps to ENST00000218006 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:108628500 A>C maps to ENST00000218006 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:25075913 G>T maps to NM_033423.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:25075913 G>T maps to NM_033423.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:6995464 C>A maps to NM_001135565.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:6995464 C>A maps to NM_001135565.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:42738368 C>A maps to NM_020707.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:42738368 C>A maps to NM_020707.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:76472699 C>A maps to NM_004133.4 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:76472699 C>A maps to NM_004133.4 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:27147953 G>T maps to NM_153631.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:27147953 G>T maps to NM_153631.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:159998597 T>A maps to ENST00000483754 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:159998597 T>A maps to ENST00000483754 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:151164626 C>A maps to NM_178822.4 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:151164626 C>A maps to NM_178822.4 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:14153293 G>T maps to NM_004843.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:14153293 G>T maps to NM_004843.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:15243084 G>T maps to NM_001031853.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:15243084 G>T maps to NM_001031853.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:59962346 G>A maps to NM_020748.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:59962346 G>A maps to NM_020748.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:128632152 G>T maps to NM_015693.3 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:128632152 G>T maps to NM_015693.3 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:30837233 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:30837233 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:50163051 G>C maps to NM_001571.5 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:50163051 G>C maps to NM_001571.5 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3939949 G>T maps to NM_170678.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3939949 G>T maps to NM_170678.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52818396 C>T maps to NM_002215.2 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52818396 C>T maps to NM_002215.2 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:7773793 C>A maps to NM_002216.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:7773793 C>A maps to NM_002216.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118960760 C>T maps to NM_181840.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118960760 C>T maps to NM_181840.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:215759873 G>C maps to NM_016121.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:215759873 G>C maps to NM_016121.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2732500 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2732500 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:86718114 C>T maps to NM_001146688.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:86718114 C>T maps to NM_001146688.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:2820098 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:2820098 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43909129 T>C maps to NM_015284.2 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43909129 T>C maps to NM_015284.2 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:55356792 G>A maps to NM_001098815.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:55356792 G>A maps to NM_001098815.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:72293677 G>T maps to NM_014431.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:72293677 G>T maps to NM_014431.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:59942666 T>A maps to NM_020854.3 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:59942666 T>A maps to NM_020854.3 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:126306856 G>A maps to NM_032531.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:126306856 G>A maps to NM_032531.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:52910578 A>G maps to NM_000424.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:52910578 A>G maps to NM_000424.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:130378623 G>T maps to NM_032438.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:130378623 G>T maps to NM_032438.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:129511366 A>T maps to NM_000426.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:129511366 A>T maps to NM_000426.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:36993348 G>T maps to NM_004139.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:36993348 G>T maps to NM_004139.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152552358 T>G maps to NM_032563.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152552358 T>G maps to NM_032563.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152552406 G>T maps to NM_032563.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152552406 G>T maps to NM_032563.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152681628 C>T maps to NM_178356.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152681628 C>T maps to NM_178356.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:25014017 G>A maps to NM_018176.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:25014017 G>A maps to NM_018176.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:22005800 C>A maps to NM_139278.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:22005800 C>A maps to NM_139278.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197890481 C>A maps to NM_020204.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197890481 C>A maps to NM_020204.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:108861584 G>A maps to NM_001098268.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:108861584 G>A maps to NM_001098268.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55146211 C>A maps to ENST00000427581 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55146211 C>A maps to ENST00000427581 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:52860544 T>G maps to NM_001024611.1 *881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:52860544 T>G maps to NM_001024611.1 *881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:80530119 C>A maps to NM_178839.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:80530119 C>A maps to NM_178839.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:77745830 G>A maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:77745830 G>A maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:115805318 C>A maps to NM_002338.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:115805318 C>A maps to NM_002338.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24785582 G>A maps to NM_181657.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24785582 G>A maps to NM_181657.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:109117173 G>C maps to NM_002372.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:109117173 G>C maps to NM_002372.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:220752847 G>A maps to NM_018650.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:220752847 G>A maps to NM_018650.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:47601037 C>T maps to NM_001113498.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:47601037 C>T maps to NM_001113498.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141734529 G>T maps to ENST00000475668 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141734529 G>T maps to ENST00000475668 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141765176 C>A maps to ENST00000475668 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141765176 C>A maps to ENST00000475668 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:38664294 G>A maps to NM_021242.4 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:38664294 G>A maps to NM_021242.4 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:2537710 C>T maps to NM_033467.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:2537710 C>T maps to NM_033467.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18159296 G>A maps to NM_054031.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18159296 G>A maps to NM_054031.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:72754931 A>T maps to NM_005098.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:72754931 A>T maps to NM_005098.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:815524 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:815524 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:9047920 G>T maps to NM_024690.2 S11237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:9047920 G>T maps to NM_024690.2 S11237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:100680894 A>C maps to NM_001040105.1 T2066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:100680894 A>C maps to NM_001040105.1 T2066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:42771257 C>T maps to NM_002463.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:42771257 C>T maps to NM_002463.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:10448801 G>A maps to NM_017534.5 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:10448801 G>A maps to NM_017534.5 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:31105501 C>A maps to NM_015194.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:31105501 C>A maps to NM_015194.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:24388532 G>A maps to ENST00000330966 H1282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:24388532 G>A maps to ENST00000330966 H1282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:76736088 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:76736088 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:15417225 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:15417225 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21486633 G>T maps to NM_201537.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21486633 G>T maps to NM_201537.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119158233 C>A maps to NM_004784.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119158233 C>A maps to NM_004784.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:152512819 G>A maps to NM_001164507.1 H2114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:152512819 G>A maps to NM_001164507.1 H2114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:72400909 C>A maps to NM_173808.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:72400909 C>A maps to NM_173808.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:70423368 G>T maps to NM_153181.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:70423368 G>T maps to NM_153181.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:69660387 C>T maps to NM_138713.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:69660387 C>T maps to NM_138713.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:40175883 C>T maps to ENST00000316082 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:40175883 C>T maps to ENST00000316082 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:32477680 G>T maps to NM_021209.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:32477680 G>T maps to NM_021209.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:144097390 G>A maps to ENST00000467773 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:144097390 G>A maps to ENST00000467773 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:21140247 G>A maps to NM_000271.4 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:21140247 G>A maps to NM_000271.4 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132440851 C>T maps to ENST00000393156 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132440851 C>T maps to ENST00000393156 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:163298634 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:163298634 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:62569273 G>A maps to NM_006362.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:62569273 G>A maps to NM_006362.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228464949 G>C maps to NM_001098623.1 A2230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228464949 G>C maps to NM_001098623.1 A2230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228523917 C>A maps to NM_001098623.1 S5495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228523917 C>A maps to NM_001098623.1 S5495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:123848122 G>T maps to NM_001004474.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:123848122 G>T maps to NM_001004474.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:247695357 C>T maps to NM_198074.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:247695357 C>T maps to NM_198074.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248685279 G>A maps to NM_001013355.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248685279 G>A maps to NM_001013355.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:29141789 T>C maps to NM_030905.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:29141789 T>C maps to NM_030905.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248487613 A>T maps to NM_001004691.1 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248487613 A>T maps to NM_001004691.1 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248569630 C>G maps to NM_030904.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248569630 C>G maps to NM_030904.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248551409 G>T maps to NM_001005471.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248551409 G>T maps to NM_001005471.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:20528424 C>T maps to NM_001004717.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:20528424 C>T maps to NM_001004717.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:4661634 C>G maps to NM_001004751.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:4661634 C>G maps to NM_001004751.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55563648 C>T maps to NM_001004735.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55563648 C>T maps to NM_001004735.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:98188533 C>G maps to NM_001004736.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:98188533 C>G maps to NM_001004736.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:55688350 G>T maps to NM_001005493.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:55688350 G>T maps to NM_001005493.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158687392 G>T maps to ENST00000368146 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158687392 G>T maps to ENST00000368146 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:124413478 G>T maps to NM_001005195.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:124413478 G>T maps to NM_001005195.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:56510306 T>C maps to NM_001005284.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:56510306 T>C maps to NM_001005284.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21737979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21737979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:26696879 C>A maps to NM_194248.2 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:26696879 C>A maps to NM_194248.2 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:66001696 G>A maps to NM_018026.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:66001696 G>A maps to NM_018026.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:154775015 C>A maps to NM_007349.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:154775015 C>A maps to NM_007349.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140255191 G>T maps to NM_018903.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140255191 G>T maps to NM_018903.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140264057 C>A maps to NM_018904.2 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140264057 C>A maps to NM_018904.2 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140181996 C>T maps to NM_018906.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140181996 C>T maps to NM_018906.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140559207 G>A maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140559207 G>A maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140712338 G>T maps to NM_018912.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140712338 G>T maps to NM_018912.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140774233 G>C maps to NM_032088.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140774233 G>C maps to NM_032088.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140783352 A>T maps to NM_018921.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140783352 A>T maps to NM_018921.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:95425129 A>T maps to NM_006204.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:95425129 A>T maps to NM_006204.3 S844S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:33320129 A>T maps to ENST00000400481 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:33320129 A>T maps to ENST00000400481 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:73673724 G>T maps to NM_015009.1 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:73673724 G>T maps to NM_015009.1 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:11022087 G>T maps to ENST00000303905 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:11022087 G>T maps to ENST00000303905 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:11068426 A>T maps to ENST00000303905 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:11068426 A>T maps to ENST00000303905 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45975092 C>A maps to ENST00000257821 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45975092 C>A maps to ENST00000257821 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:41750471 C>A maps to NM_003924.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:41750471 C>A maps to NM_003924.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:36935737 C>T maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:36935737 C>T maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:65688808 C>A maps to NM_012417.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:65688808 C>A maps to NM_012417.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28855887 C>T maps to NM_153021.4 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28855887 C>T maps to NM_153021.4 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:219492944 A>T maps to ENST00000432688 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:219492944 A>T maps to ENST00000432688 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:131866250 G>A maps to NM_020911.1 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:131866250 G>A maps to NM_020911.1 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:129279566 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:129279566 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:121209248 C>A maps to ENST00000393672 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:121209248 C>A maps to ENST00000393672 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:27787876 T>C maps to NM_003622.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:27787876 T>C maps to NM_003622.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94731787 C>T maps to NM_058237.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94731787 C>T maps to NM_058237.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:47087208 C>T maps to NM_005972.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:47087208 C>T maps to NM_005972.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:24046866 C>A maps to NM_002738.6 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:24046866 C>A maps to NM_002738.6 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:128183673 T>A maps to ENST00000409048 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:128183673 T>A maps to ENST00000409048 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:109241224 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:109241224 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:50099832 C>T maps to NM_020719.1 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:50099832 C>T maps to NM_020719.1 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:120022157 G>T maps to NM_016644.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:120022157 G>T maps to NM_016644.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:11594436 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:11594436 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18754823 C>A maps to NM_032781.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18754823 C>A maps to NM_032781.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:65417767 C>T maps to NM_198686.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:65417767 C>T maps to NM_198686.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:154490315 G>T maps to NM_171998.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:154490315 G>T maps to NM_171998.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50368056 G>A maps to NM_170714.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50368056 G>A maps to NM_170714.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:57351413 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:57351413 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:34404942 A>T maps to NM_002915.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:34404942 A>T maps to NM_002915.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:73165951 A>T maps to NM_001080479.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:73165951 A>T maps to NM_001080479.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:73189084 C>T maps to NM_001080479.2 A1210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:73189084 C>T maps to NM_001080479.2 A1210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:22868121 C>T maps to NM_001160036.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:22868121 C>T maps to NM_001160036.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21424253 C>A maps to NM_002934.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21424253 C>A maps to NM_002934.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:25356049 G>A maps to ENST00000381927 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:25356049 G>A maps to ENST00000381927 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:10469885 G>T maps to NM_178857.5 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:10469885 G>T maps to NM_178857.5 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62312041 C>T maps to ENST00000482936 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62312041 C>T maps to ENST00000482936 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:67795688 C>A maps to NM_173630.3 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:67795688 C>A maps to NM_173630.3 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237729942 G>A maps to NM_001035.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237729942 G>A maps to NM_001035.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237955445 G>T maps to NM_001035.2 T4535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237955445 G>T maps to NM_001035.2 T4535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237798279 G>A maps to NM_001035.2 P2260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237798279 G>A maps to NM_001035.2 P2260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:224463261 C>A maps to NM_003469.4 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:224463261 C>A maps to NM_003469.4 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:62018709 C>G maps to NM_000334.4 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:62018709 C>G maps to NM_000334.4 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:139301895 G>A maps to NM_001039707.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:139301895 G>A maps to NM_001039707.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94914952 G>T maps to NM_001080451.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94914952 G>T maps to NM_001080451.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:61231211 T>A maps to ENST00000382768 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:61231211 T>A maps to ENST00000382768 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:29897070 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:29897070 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:26761402 C>A maps to NM_021115.4 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:26761402 C>A maps to NM_021115.4 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:28878263 G>T maps to NM_001145795.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:28878263 G>T maps to NM_001145795.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:51143399 G>T maps to NM_001080420.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:51143399 G>T maps to NM_001080420.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51914384 G>A maps to NM_033130.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51914384 G>A maps to NM_033130.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26779577 G>A maps to NM_003930.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26779577 G>A maps to NM_003930.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:25769243 C>A maps to NM_005495.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:25769243 C>A maps to NM_005495.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:36686205 C>A maps to NM_004172.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:36686205 C>A maps to NM_004172.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:38316549 G>T maps to NM_004256.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:38316549 G>T maps to NM_004256.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:95750586 T>A maps to NM_001160210.1 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:95750586 T>A maps to NM_001160210.1 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:27481081 C>T maps to NM_003459.4 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:27481081 C>T maps to NM_003459.4 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:58036698 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:58036698 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:1213591 C>A maps to NM_001003841.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:1213591 C>A maps to NM_001003841.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:11145652 G>T maps to NM_001128849.1 E1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:11145652 G>T maps to NM_001128849.1 E1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:45802672 T>A maps to NM_148674.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:45802672 T>A maps to NM_148674.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:53515142 C>T maps to NM_003578.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:53515142 C>T maps to NM_003578.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:137483857 C>A maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:137483857 C>A maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:35793322 G>T maps to NM_024867.3 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:35793322 G>T maps to NM_024867.3 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:35779449 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:35779449 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:153005015 C>A maps to NM_003125.2 C65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:153005015 C>A maps to NM_003125.2 C65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:68436839 T>A maps to NM_012108.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:68436839 T>A maps to NM_012108.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:134040417 G>T maps to NM_173575.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:134040417 G>T maps to NM_173575.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:152763329 G>T maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:152763329 G>T maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:85459315 T>A maps to NM_001162953.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:85459315 T>A maps to NM_001162953.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:102197167 C>T maps to NM_152334.2 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:102197167 C>T maps to NM_152334.2 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:6639556 C>A maps to NM_138697.3 Y813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:6639556 C>A maps to NM_138697.3 Y813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62697831 G>T maps to NM_003195.4 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62697831 G>T maps to NM_003195.4 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:46657598 G>T maps to NM_001010870.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:46657598 G>T maps to NM_001010870.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:107224573 G>A maps to NM_031273.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:107224573 G>A maps to NM_031273.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:62272301 C>A maps to NM_018469.3 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:62272301 C>A maps to NM_018469.3 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:92174228 C>A maps to NM_003243.4 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:92174228 C>A maps to NM_003243.4 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:134125712 C>A maps to NM_003235.4 Y2540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:134125712 C>A maps to NM_003235.4 Y2540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:2185531 C>A maps to NM_199292.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:2185531 C>A maps to NM_199292.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:56811917 C>A maps to NM_003920.3 E1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:56811917 C>A maps to NM_003920.3 E1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43472821 G>A maps to NM_001146016.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43472821 G>A maps to NM_001146016.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:166981295 A>T maps to ENST00000507499 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:166981295 A>T maps to ENST00000507499 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:76113394 C>A maps to NM_007267.6 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:76113394 C>A maps to NM_007267.6 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:87494879 C>A maps to NM_153354.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:87494879 C>A maps to NM_153354.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150500823 C>T maps to NM_018487.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150500823 C>T maps to NM_018487.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:117826977 A>C maps to NM_002160.2 Y1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:117826977 A>C maps to NM_002160.2 Y1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:12157230 G>T maps to NM_001243.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:12157230 G>T maps to NM_001243.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:189068504 C>A maps to NM_178556.3 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:189068504 C>A maps to NM_178556.3 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:43225569 G>A maps to NM_032538.1 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:43225569 G>A maps to NM_032538.1 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:124751500 C>G maps to NM_001139442.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:124751500 C>G maps to NM_001139442.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:179592522 C>T maps to NM_133378.4 K5350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:179592522 C>T maps to NM_133378.4 K5350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:52486660 G>A maps to NM_015913.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:52486660 G>A maps to NM_015913.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:76134926 C>T maps to NM_006002.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:76134926 C>T maps to NM_006002.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:39515800 C>A maps to NM_003359.3 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:39515800 C>A maps to NM_003359.3 G56*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216051128 C>T maps to ENST00000366943 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216051128 C>T maps to ENST00000366943 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:75290090 C>T maps to NM_152586.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:75290090 C>T maps to NM_152586.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:41043660 C>T maps to NM_001039590.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:41043660 C>T maps to NM_001039590.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:65252541 C>T maps to NM_007268.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:65252541 C>T maps to NM_007268.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:124007381 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:124007381 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110446485 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110446485 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:110440496 A>T maps to NM_139281.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:110440496 A>T maps to NM_139281.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:29070323 C>G maps to NM_016258.2 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:29070323 C>G maps to NM_016258.2 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22817989 A>G maps to NM_014870.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22817989 A>G maps to NM_014870.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:64139002 A>T maps to NM_018684.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:64139002 A>T maps to NM_018684.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:77690475 C>A maps to NM_024721.4 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:77690475 C>A maps to NM_024721.4 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:35847280 G>T maps to NM_005095.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:35847280 G>T maps to NM_005095.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:74672731 C>G maps to NM_007345.3 Y1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:74672731 C>G maps to NM_007345.3 Y1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:44891466 T>A maps to NM_152354.3 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:44891466 T>A maps to NM_152354.3 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:178506335 A>T maps to NM_014594.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:178506335 A>T maps to NM_014594.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:54767847 G>C maps to NM_001130967.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:54767847 G>C maps to NM_001130967.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:149174739 G>C maps to NM_001163474.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:149174739 G>C maps to NM_001163474.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:238051763 C>A maps to NM_021186.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:238051763 C>A maps to NM_021186.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:44505619 C>T maps to NM_080752.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:44505619 C>T maps to NM_080752.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87179274 G>T maps to NM_000927.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87179274 G>T maps to NM_000927.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:61568577 G>T maps to NM_000789.3 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:61568577 G>T maps to NM_000789.3 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:79063992 G>A maps to ENST00000258883 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:79063992 G>A maps to ENST00000258883 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:100129926 G>C maps to NM_001102470.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:100129926 G>C maps to NM_001102470.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:148037248 G>C maps to NM_002025.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:148037248 G>C maps to NM_002025.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:62284434 C>G maps to NM_001620.1 G5818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:62284434 C>G maps to NM_001620.1 G5818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:151669912 G>A maps to NM_005100.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:151669912 G>A maps to NM_005100.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:177001816 G>T maps to ENST00000281881 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:177001816 G>T maps to ENST00000281881 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:31612762 C>T maps to ENST00000404765 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:31612762 C>T maps to ENST00000404765 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:69093485 C>A maps to NM_014482.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:69093485 C>A maps to NM_014482.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55816253 G>A maps to NM_032430.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55816253 G>A maps to NM_032430.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:11903468 C>T maps to NM_014962.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:11903468 C>T maps to NM_014962.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:50583009 G>A maps to NM_024558.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:50583009 G>A maps to NM_024558.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:57209874 A>G maps to NM_001004303.4 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:57209874 A>G maps to NM_001004303.4 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:206239420 A>T maps to NM_001007544.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:206239420 A>T maps to NM_001007544.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:35737067 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:35737067 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:87808957 C>G maps to NM_144645.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:87808957 C>G maps to NM_144645.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:49063288 C>G maps to NM_005183.2 G1764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:49063288 C>G maps to NM_005183.2 G1764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:40055838 G>T maps to NM_021096.3 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:40055838 G>T maps to NM_021096.3 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:119169117 G>T maps to NM_005188.2 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:119169117 G>T maps to NM_005188.2 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219896344 C>T maps to NM_194302.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219896344 C>T maps to NM_194302.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73574860 C>T maps to ENST00000398860 L3302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73574860 C>T maps to ENST00000398860 L3302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:28488845 C>T maps to NM_000086.2 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:28488845 C>T maps to NM_000086.2 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:9801203 C>A maps to NM_001009566.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:9801203 C>A maps to NM_001009566.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:62212571 C>G maps to NM_173519.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:62212571 C>G maps to NM_173519.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:41337887 C>A maps to NM_001843.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:41337887 C>A maps to NM_001843.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:134947927 C>A maps to NM_001172288.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:134947927 C>A maps to NM_001172288.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:57756645 G>T maps to ENST00000371231 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:57756645 G>T maps to ENST00000371231 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:35060938 C>A maps to ENST00000339266 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:35060938 C>A maps to ENST00000339266 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:11554418 G>T maps to NM_001372.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:11554418 G>T maps to NM_001372.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:225688307 G>T maps to NM_014689.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:225688307 G>T maps to NM_014689.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:169509813 G>A maps to NM_004946.2 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:169509813 G>A maps to NM_004946.2 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:207527705 T>C maps to NM_001093730.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:207527705 T>C maps to NM_001093730.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:67630779 G>A maps to NM_019002.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:67630779 G>A maps to NM_019002.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:25744118 G>T maps to NM_152704.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:25744118 G>T maps to NM_152704.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:139268930 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:139268930 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137346773 G>A maps to NM_016603.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137346773 G>A maps to NM_016603.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190067912 G>T maps to NM_199051.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190067912 G>T maps to NM_199051.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:150923859 G>T maps to NM_001447.2 V2276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:150923859 G>T maps to NM_001447.2 V2276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:126372424 A>T maps to NM_024582.4 P3418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:126372424 A>T maps to NM_024582.4 P3418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:125359481 A>G maps to NM_005103.4 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:125359481 A>G maps to NM_005103.4 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:72756805 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:72756805 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:152323526 G>C maps to NM_001014342.2 S2245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:152323526 G>C maps to NM_001014342.2 S2245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:43323890 C>T maps to NM_005892.3 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:43323890 C>T maps to NM_005892.3 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:46023126 C>A maps to NM_024513.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:46023126 C>A maps to NM_024513.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:74962575 G>A maps to NM_001480.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:74962575 G>A maps to NM_001480.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:34143676 C>A maps to NM_016631.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:34143676 C>A maps to NM_016631.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:52993666 A>T maps to NM_003643.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:52993666 A>T maps to NM_003643.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:20331622 G>T maps to NM_001007240.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:20331622 G>T maps to NM_001007240.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:140058265 C>A maps to ENST00000371546 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:140058265 C>A maps to ENST00000371546 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:52222511 C>A maps to NM_001523.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:52222511 C>A maps to NM_001523.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:81335059 G>T maps to NM_000601.4 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:81335059 G>T maps to NM_000601.4 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:176308745 C>T maps to NM_002115.2 Q780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:176308745 C>T maps to NM_002115.2 Q780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:27149788 G>T maps to NM_153631.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:27149788 G>T maps to NM_153631.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:209878280 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:209878280 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:114141545 T>A maps to NM_000868.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:114141545 T>A maps to NM_000868.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:45957003 G>T maps to NM_001013398.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:45957003 G>T maps to NM_001013398.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:130407899 G>T maps to NM_001170961.1 S1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:130407899 G>T maps to NM_001170961.1 S1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:18740275 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:18740275 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:67685288 G>T maps to NM_144701.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:67685288 G>T maps to NM_144701.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:31384695 C>T maps to NM_000887.3 Y831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:31384695 C>T maps to NM_000887.3 Y831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:49626461 C>A maps to NM_002237.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:49626461 C>A maps to NM_002237.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:49626476 C>A maps to NM_002237.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:49626476 C>A maps to NM_002237.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:215792538 C>T maps to NM_016121.3 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:215792538 C>T maps to NM_016121.3 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:22676357 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:22676357 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:5768968 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:5768968 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:166231703 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:166231703 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:52841599 G>A maps to NM_005555.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:52841599 G>A maps to NM_005555.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:5705940 G>A maps to NM_004793.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:5705940 G>A maps to NM_004793.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:42356875 A>T maps to NM_152447.3 K350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:42356875 A>T maps to NM_152447.3 K350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:40692295 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:40692295 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1908757 G>T maps to ENST00000381758 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1908757 G>T maps to ENST00000381758 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:143867038 C>T maps to NM_003695.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:143867038 C>T maps to NM_003695.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:18300617 G>A maps to NM_015241.2 S1603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:18300617 G>A maps to NM_015241.2 S1603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:60765738 C>T maps to NM_006039.3 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:60765738 C>T maps to NM_006039.3 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:39691003 G>C maps to NM_001001414.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:39691003 G>C maps to NM_001001414.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:115997478 T>C maps to NM_022569.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:115997478 T>C maps to NM_022569.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:5821791 C>T maps to ENST00000381093 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:5821791 C>T maps to ENST00000381093 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:7981814 A>G maps to NM_176821.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:7981814 A>G maps to NM_176821.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:163309230 A>G maps to NM_145697.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:163309230 A>G maps to NM_145697.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:55103682 T>C maps to NM_004852.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:55103682 T>C maps to NM_004852.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:16060155 C>A maps to NM_001004465.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:16060155 C>A maps to NM_001004465.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158390596 C>A maps to NM_001004476.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158390596 C>A maps to NM_001004476.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248616383 C>T maps to NM_001004136.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248616383 C>T maps to NM_001004136.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:4674575 C>T maps to NM_152430.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:4674575 C>T maps to NM_152430.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:5411261 C>T maps to NM_001004756.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:5411261 C>T maps to NM_001004756.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:55587647 G>A maps to ENST00000395203 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:55587647 G>A maps to ENST00000395203 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:56380708 C>T maps to NM_001004740.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:56380708 C>T maps to NM_001004740.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:90690947 C>A maps to NM_080832.2 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:90690947 C>A maps to NM_080832.2 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:25029153 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:25029153 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140553150 G>A maps to NM_018940.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140553150 G>A maps to NM_018940.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:32089085 C>T maps to NM_178140.2 G1844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:32089085 C>T maps to NM_178140.2 G1844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:156877440 C>T maps to NM_001080471.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:156877440 C>T maps to NM_001080471.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:45730917 G>A maps to NM_002626.4 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:45730917 G>A maps to NM_002626.4 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:106509706 C>T maps to NM_002649.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:106509706 C>T maps to NM_002649.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:9416205 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:9416205 G>T did not map to a codon.
Alternatively spliced codon TCGA-44-2657-01A-01D-1105-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2657-01A-01D-1105-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219495488 G>A maps to ENST00000432688 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219495488 G>A maps to ENST00000432688 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:131872243 G>T maps to NM_020911.1 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:131872243 G>T maps to NM_020911.1 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:23509207 C>A maps to NM_020227.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:23509207 C>A maps to NM_020227.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186276758 C>A maps to NM_005807.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186276758 C>A maps to NM_005807.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:6527123 C>T maps to NM_006257.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:6527123 C>T maps to NM_006257.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:138738864 G>T maps to NM_001013650.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:138738864 G>T maps to NM_001013650.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100958529 G>C maps to NM_022777.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100958529 G>C maps to NM_022777.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:79298769 G>A maps to NM_002891.4 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:79298769 G>A maps to NM_002891.4 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:53160011 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:53160011 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:71350871 G>A maps to NM_001024455.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:71350871 G>A maps to NM_001024455.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:119243226 G>T maps to NM_139282.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:119243226 G>T maps to NM_139282.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:1551211 G>A maps to NM_031430.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:1551211 G>A maps to NM_031430.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:39075605 G>T maps to NM_000540.2 V4890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:39075605 G>T maps to NM_000540.2 V4890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:54232057 C>A maps to NM_152540.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:54232057 C>A maps to NM_152540.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:62049512 G>C maps to NM_000334.4 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:62049512 G>C maps to NM_000334.4 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:118771018 C>T maps to ENST00000394612 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:118771018 C>T maps to ENST00000394612 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:118783986 G>A maps to ENST00000394612 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:118783986 G>A maps to ENST00000394612 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:61262396 C>T maps to NM_012397.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:61262396 C>T maps to NM_012397.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:37429496 C>A maps to NM_017438.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:37429496 C>A maps to NM_017438.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:65829420 A>T maps to NM_006842.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:65829420 A>T maps to NM_006842.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:171766608 T>A maps to NM_001017995.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:171766608 T>A maps to NM_001017995.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:77680772 G>A maps to NM_020859.3 E1758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:77680772 G>A maps to NM_020859.3 E1758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:45169953 C>T maps to NM_005413.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:45169953 C>T maps to NM_005413.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100454718 C>T maps to NM_020246.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100454718 C>T maps to NM_020246.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:119015005 G>T maps to NM_003054.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:119015005 G>T maps to NM_003054.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:228552160 C>A maps to NM_025243.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:228552160 C>A maps to NM_025243.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:138714948 G>A maps to NM_152685.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:138714948 G>A maps to NM_152685.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:128321029 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:128321029 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:110738260 G>T maps to NM_001010898.2 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:110738260 G>T maps to NM_001010898.2 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:170219102 G>A maps to NM_020949.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:170219102 G>A maps to NM_020949.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:144904138 C>T maps to NM_001144010.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:144904138 C>T maps to NM_001144010.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:112722332 C>A maps to NM_005986.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:112722332 C>A maps to NM_005986.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:187387014 C>T maps to NM_001048.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:187387014 C>T maps to NM_001048.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:67937355 C>A maps to NM_001142503.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:67937355 C>A maps to NM_001142503.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219553475 G>T maps to NM_015690.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219553475 G>T maps to NM_015690.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:70968562 C>T maps to NM_003171.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:70968562 C>T maps to NM_003171.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:64557633 G>T maps to NM_182914.2 V3948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:64557633 G>T maps to NM_182914.2 V3948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:32633636 G>C maps to NM_153809.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:32633636 G>C maps to NM_153809.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:1264700 C>A maps to NM_198253.2 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:1264700 C>A maps to NM_198253.2 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:141671483 G>A maps to NM_001178139.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:141671483 G>A maps to NM_001178139.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44943080 A>C maps to NM_003241.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44943080 A>C maps to NM_003241.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:159028286 G>C maps to NM_020823.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:159028286 G>C maps to NM_020823.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:175362955 G>T maps to NM_003285.2 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:175362955 G>T maps to NM_003285.2 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:15499941 C>T maps to ENST00000455584 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:15499941 C>T maps to ENST00000455584 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:51489621 G>T maps to ENST00000338969 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:51489621 G>T maps to ENST00000338969 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:51872756 C>T maps to NM_173485.5 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:51872756 C>T maps to NM_173485.5 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:73686561 C>T maps to NM_003355.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:73686561 C>T maps to NM_003355.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:11531200 C>A maps to NM_001080491.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:11531200 C>A maps to NM_001080491.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:135618241 G>A maps to NM_016267.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:135618241 G>A maps to NM_016267.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:17125802 G>C maps to NM_152415.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:17125802 G>C maps to NM_152415.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:77618315 G>T maps to NM_024721.4 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:77618315 G>T maps to NM_024721.4 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:116811996 C>T maps to ENST00000374126 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:116811996 C>T maps to ENST00000374126 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:40580835 C>A maps to NM_001142577.1 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:40580835 C>A maps to NM_001142577.1 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:90699438 G>T maps to NM_001141945.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:90699438 G>T maps to NM_001141945.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:28296389 G>T maps to NM_007038.3 C925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:28296389 G>T maps to NM_007038.3 C925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31104472 C>A maps to ENST00000409489 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31104472 C>A maps to ENST00000409489 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:4875555 C>A maps to NM_001040177.1 C74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:4875555 C>A maps to NM_001040177.1 C74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:233321920 C>A maps to NM_001631.3 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:233321920 C>A maps to NM_001631.3 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:61894040 T>A maps to NM_020987.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:61894040 T>A maps to NM_020987.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:37482151 C>A maps to ENST00000374660 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:37482151 C>A maps to ENST00000374660 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:127231265 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:127231265 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:11196360 C>T maps to NM_013427.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:11196360 C>T maps to NM_013427.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:1561077 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:1561077 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:10420008 G>A maps to NM_001001331.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:10420008 G>A maps to NM_001001331.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:28381958 T>C maps to NM_022461.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:28381958 T>C maps to NM_022461.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:143623593 G>T maps to NM_001702.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:143623593 G>T maps to NM_001702.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:165548020 A>T maps to NM_000055.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:165548020 A>T maps to NM_000055.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:28521251 C>T maps to NM_004899.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:28521251 C>T maps to NM_004899.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:6804696 G>A maps to NM_153685.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:6804696 G>A maps to NM_153685.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:97052114 T>C maps to ENST00000342887 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:97052114 T>C maps to ENST00000342887 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:77044100 C>A maps to ENST00000392445 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:77044100 C>A maps to ENST00000392445 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:73768560 C>T maps to ENST00000334126 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:73768560 C>T maps to ENST00000334126 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:29287785 G>T maps to NM_001029883.1 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:29287785 G>T maps to NM_001029883.1 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:17072819 C>G maps to NM_014406.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:17072819 C>G maps to NM_014406.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:158323686 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:158323686 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:59217421 C>A maps to NM_031891.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:59217421 C>A maps to NM_031891.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:17630515 C>G maps to NM_033070.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:17630515 C>G maps to NM_033070.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:10226001 G>T maps to NM_016511.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:10226001 G>T maps to NM_016511.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:130293211 C>T maps to NM_001102608.1 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:130293211 C>T maps to NM_001102608.1 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:67726504 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:67726504 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:112999275 G>T maps to NM_018704.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:112999275 G>T maps to NM_018704.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:6661904 G>A maps to NM_003737.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:6661904 G>A maps to NM_003737.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:61886918 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:61886918 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:54572987 T>C maps to NM_019030.2 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:54572987 T>C maps to NM_019030.2 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:60490350 C>A maps to NM_001042517.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:60490350 C>A maps to NM_001042517.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:27150119 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:27150119 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:143096425 C>A maps to NM_005232.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:143096425 C>A maps to NM_005232.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:144942383 G>A maps to NM_031308.1 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:144942383 G>A maps to NM_031308.1 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:51855349 G>A maps to NM_145019.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:51855349 G>A maps to NM_145019.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:33810354 C>A maps to ENST00000395190 G350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:33810354 C>A maps to ENST00000395190 G350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:150948411 G>T maps to NM_001447.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:150948411 G>T maps to NM_001447.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:150923124 G>A maps to NM_001447.2 I2521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:150923124 G>A maps to NM_001447.2 I2521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:92531656 G>T maps to ENST00000298047 V1826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:92531656 G>T maps to ENST00000298047 V1826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:117604776 T>A maps to NM_033624.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:117604776 T>A maps to NM_033624.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:125083826 G>A maps to NM_001039112.2 P1349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:125083826 G>A maps to NM_001039112.2 P1349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:128486497 C>A maps to NM_001458.4 R1370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:128486497 C>A maps to NM_001458.4 R1370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:128487757 G>A maps to NM_001458.4 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:128487757 G>A maps to NM_001458.4 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:13782540 G>A maps to NM_018027.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:13782540 G>A maps to NM_018027.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:11607723 C>G maps to NM_002052.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:11607723 C>G maps to NM_002052.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:120614021 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:120614021 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42988647 G>T maps to NM_002055.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42988647 G>T maps to NM_002055.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42989120 G>C maps to NM_002055.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42989120 G>C maps to NM_002055.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:9757859 G>T maps to NM_004246.1 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:9757859 G>T maps to NM_004246.1 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:27333070 A>G maps to NM_005288.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:27333070 A>G maps to NM_005288.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:19883303 G>T maps to NM_016235.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:19883303 G>T maps to NM_016235.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:104432902 G>T maps to NM_133445.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:104432902 G>T maps to NM_133445.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:108638598 G>T maps to ENST00000218006 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:108638598 G>T maps to ENST00000218006 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:41049235 A>G maps to ENST00000296803 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:41049235 A>G maps to ENST00000296803 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:46690584 C>A maps to NM_024016.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:46690584 C>A maps to NM_024016.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:50326123 C>A maps to ENST00000336089 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:50326123 C>A maps to ENST00000336089 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:118624530 G>T maps to NM_152538.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:118624530 G>T maps to NM_152538.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:67833707 G>T maps to NM_001559.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:67833707 G>T maps to NM_001559.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:123105064 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:123105064 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:30492757 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:30492757 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:111146879 G>T maps to NM_004974.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:111146879 G>T maps to NM_004974.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:26950706 C>T maps to NM_002246.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:26950706 C>T maps to NM_002246.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:55979648 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:55979648 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:57180981 C>A maps to NM_020722.1 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:57180981 C>A maps to NM_020722.1 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:113388976 G>A maps to NM_001009899.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:113388976 G>A maps to NM_001009899.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:38950231 G>A maps to NM_181535.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:38950231 G>A maps to NM_181535.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:31914107 A>T maps to ENST00000437381 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:31914107 A>T maps to ENST00000437381 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:129674482 C>T maps to NM_000426.3 R1566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:129674482 C>T maps to NM_000426.3 R1566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:133932443 G>T maps to ENST00000355048 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:133932443 G>T maps to ENST00000355048 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:169697831 G>T maps to NM_005565.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:169697831 G>T maps to NM_005565.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:133673736 G>T maps to ENST00000250173 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:133673736 G>T maps to ENST00000250173 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:131912667 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:131912667 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:4794818 G>A maps to NM_153827.4 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:4794818 G>A maps to NM_153827.4 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:47656892 G>T maps to NM_000251.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:47656892 G>T maps to NM_000251.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:89891341 G>T maps to NM_005467.3 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:89891341 G>T maps to NM_005467.3 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:34139978 G>T maps to NM_024662.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:34139978 G>T maps to NM_024662.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31378426 G>A maps to NM_022728.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31378426 G>A maps to NM_022728.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:29657517 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:29657517 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:3452609 G>T maps to ENST00000269778 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:3452609 G>T maps to ENST00000269778 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:9967990 C>T maps to NM_058164.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:9967990 C>T maps to NM_058164.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:154411266 C>A maps to NM_001145279.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:154411266 C>A maps to NM_001145279.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:247835560 G>C maps to NM_001005487.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:247835560 G>C maps to NM_001005487.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:248343332 G>T maps to NM_001004688.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:248343332 G>T maps to NM_001004688.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:5364169 C>G maps to NM_001005567.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:5364169 C>G maps to NM_001005567.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:5799228 A>T maps to NM_001001922.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:5799228 A>T maps to NM_001001922.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:21109283 G>T maps to NM_001001968.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:21109283 G>T maps to NM_001001968.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:19681553 G>A maps to NM_025245.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:19681553 G>A maps to NM_025245.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:140789265 G>T maps to NM_018926.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:140789265 G>T maps to NM_018926.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:50719027 C>A maps to NM_012401.2 T1355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:50719027 C>A maps to NM_012401.2 T1355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:70981462 G>T maps to NM_024504.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:70981462 G>T maps to NM_024504.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:198703338 C>G maps to ENST00000271610 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:198703338 C>G maps to ENST00000271610 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:52320976 G>T maps to NM_144651.4 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:52320976 G>T maps to NM_144651.4 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:49224135 G>T maps to NM_017805.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:49224135 G>T maps to NM_017805.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:50900254 C>A maps to ENST00000337034 R881R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:50900254 C>A maps to ENST00000337034 R881R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:102249074 G>C maps to NM_015490.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:102249074 G>C maps to NM_015490.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:151338092 C>A maps to ENST00000435071 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:151338092 C>A maps to ENST00000435071 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:84669986 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:84669986 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:95088803 G>T maps to ENST00000393080 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:95088803 G>T maps to ENST00000393080 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:42531705 G>T maps to NM_015559.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:42531705 G>T maps to NM_015559.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:28880416 G>T maps to NM_001145795.1 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:28880416 G>T maps to NM_001145795.1 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:3677978 C>A maps to NM_023068.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:3677978 C>A maps to NM_023068.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:36152974 G>T maps to NM_005983.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:36152974 G>T maps to NM_005983.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:18069983 C>A maps to NM_031481.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:18069983 C>A maps to NM_031481.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:48694625 C>T maps to NM_001135181.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:48694625 C>T maps to NM_001135181.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:168093467 C>A maps to NM_003062.2 A1521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:168093467 C>A maps to NM_003062.2 A1521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:168201304 C>A maps to NM_003062.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:168201304 C>A maps to NM_003062.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:18844353 C>A maps to ENST00000389467 L2900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:18844353 C>A maps to ENST00000389467 L2900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:214162029 G>T maps to NM_024532.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:214162029 G>T maps to NM_024532.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:912907 G>A maps to ENST00000456758 W955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:912907 G>A maps to ENST00000456758 W955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:33400563 C>T maps to NM_006772.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:33400563 C>T maps to NM_006772.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:51135682 C>T maps to NM_001160329.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:51135682 C>T maps to NM_001160329.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:32633200 G>T maps to NM_153809.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:32633200 G>T maps to NM_153809.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:152058155 G>A maps to NM_001008536.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:152058155 G>A maps to NM_001008536.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:43552760 G>A maps to NM_201631.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:43552760 G>A maps to NM_201631.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:134042064 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:134042064 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:120476353 C>T maps to NM_138554.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:120476353 C>T maps to NM_138554.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:12270058 T>C maps to NM_018374.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:12270058 T>C maps to NM_018374.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:48845849 G>A maps to NM_018273.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:48845849 G>A maps to NM_018273.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:12777052 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:12777052 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:205053310 G>A maps to NM_203376.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:205053310 G>A maps to NM_203376.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:7578555 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:7578555 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:45052014 C>A maps to NM_182985.3 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:45052014 C>A maps to NM_182985.3 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:65715520 C>T maps to NM_152762.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:65715520 C>T maps to NM_152762.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:179542346 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:179542346 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:179396278 G>A maps to NM_133378.4 G32453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:179396278 G>A maps to NM_133378.4 G32453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:12708115 G>T maps to NM_000550.2 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:12708115 G>T maps to NM_000550.2 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:17554814 G>T maps to NM_153676.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:17554814 G>T maps to NM_153676.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:30415862 T>C maps to NM_006447.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:30415862 T>C maps to NM_006447.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:161130697 C>T maps to NM_012475.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:161130697 C>T maps to NM_012475.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:87018100 C>A maps to NM_016206.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:87018100 C>A maps to NM_016206.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:38040836 G>T maps to NM_015873.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:38040836 G>T maps to NM_015873.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:10755797 C>A maps to NM_173683.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:10755797 C>A maps to NM_173683.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:37126596 G>T maps to NM_032226.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:37126596 G>T maps to NM_032226.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:56954087 G>T maps to ENST00000342634 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:56954087 G>T maps to ENST00000342634 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:64004154 C>G maps to NM_178558.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:64004154 C>G maps to NM_178558.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:183909003 C>T maps to NM_018358.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:183909003 C>T maps to NM_018358.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr11:62289393 G>A maps to NM_001620.1 I4165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr11:62289393 G>A maps to NM_001620.1 I4165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:65546941 C>T maps to NM_000048.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:65546941 C>T maps to NM_000048.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:42472956 C>T maps to ENST00000441343 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:42472956 C>T maps to ENST00000441343 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr22:23653922 C>T maps to NM_004327.3 C1074C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr22:23653922 C>T maps to NM_004327.3 C1074C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:27289706 G>A maps to NM_020641.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:27289706 G>A maps to NM_020641.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:10677772 G>A maps to NM_079421.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:10677772 G>A maps to NM_079421.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:88486597 G>T maps to NM_025114.3 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:88486597 G>T maps to NM_025114.3 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:116930258 C>A maps to NM_032888.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:116930258 C>A maps to NM_032888.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:14866618 C>A maps to NM_013447.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:14866618 C>A maps to NM_013447.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:24382712 T>C maps to NM_001136234.1 N612N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:24382712 T>C maps to NM_001136234.1 N612N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:200182894 G>T maps to NM_001105517.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:200182894 G>T maps to NM_001105517.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:190067975 G>A maps to NM_199051.1 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:190067975 G>A maps to NM_199051.1 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:44938571 C>T maps to NM_021140.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:44938571 C>T maps to NM_021140.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:141598529 C>A maps to NM_018557.2 G1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:141598529 C>A maps to NM_018557.2 G1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:148797857 C>A maps to NM_005366.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:148797857 C>A maps to NM_005366.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:173997032 T>C maps to NM_014932.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:173997032 T>C maps to NM_014932.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr5:140174708 C>T maps to NM_018905.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr5:140174708 C>T maps to NM_018905.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr20:58381220 C>A maps to NM_080672.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr20:58381220 C>A maps to NM_080672.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:95931188 C>A maps to ENST00000371380 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:95931188 C>A maps to ENST00000371380 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:30164790 C>T maps to ENST00000436066 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:30164790 C>T maps to ENST00000436066 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr15:64455119 G>C maps to NM_000942.4 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr15:64455119 G>C maps to NM_000942.4 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:31499013 T>C maps to ENST00000431354 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:31499013 T>C maps to ENST00000431354 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:44474143 G>A maps to NM_201649.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:44474143 G>A maps to NM_201649.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:136342080 A>G maps to NM_005862.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:136342080 A>G maps to NM_005862.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:179413469 T>C maps to NM_133378.4 K28393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:179413469 T>C maps to NM_133378.4 K28393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:79946994 G>T maps to ENST00000376646 E2021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:79946994 G>T maps to ENST00000376646 E2021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr11:46726803 C>T maps to NM_024741.2 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr11:46726803 C>T maps to NM_024741.2 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:53344103 C>A maps to NM_001008801.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:53344103 C>A maps to NM_001008801.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:73150990 G>A maps to NM_148912.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:73150990 G>A maps to NM_148912.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:111878415 C>T maps to NM_016824.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:111878415 C>T maps to NM_016824.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:40745963 G>A maps to NM_001626.3 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:40745963 G>A maps to NM_001626.3 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:103390270 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:103390270 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:114438395 G>T maps to NM_006594.2 S592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:114438395 G>T maps to NM_006594.2 S592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:19154840 C>T maps to ENST00000392336 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:19154840 C>T maps to ENST00000392336 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:97486050 G>A maps to NM_183356.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:97486050 G>A maps to NM_183356.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:7045359 C>G maps to NM_001940.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:7045359 C>G maps to NM_001940.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:1807187 G>A maps to NM_138813.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:1807187 G>A maps to NM_138813.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:75263783 G>A maps to NM_001170714.1 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:75263783 G>A maps to NM_001170714.1 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:140870386 C>G maps to ENST00000277549 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:140870386 C>G maps to ENST00000277549 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:49086775 T>A maps to NM_005183.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:49086775 T>A maps to NM_005183.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:65027116 G>T maps to NM_014405.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:65027116 G>T maps to NM_014405.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:66358452 C>T maps to NM_018219.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:66358452 C>T maps to NM_018219.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:33743967 G>C maps to NM_203331.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:33743967 G>C maps to NM_203331.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:89695225 C>A maps to NM_004365.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:89695225 C>A maps to NM_004365.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:58580599 C>T maps to NM_016284.3 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:58580599 C>T maps to NM_016284.3 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:17298311 G>T maps to NM_017738.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:17298311 G>T maps to NM_017738.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:148596501 T>C maps to NM_001870.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:148596501 T>C maps to NM_001870.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:211542707 A>G maps to NM_001122633.1 *1507W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:211542707 A>G maps to NM_001122633.1 *1507W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:2876053 A>G maps to NM_033225.5 H2658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:2876053 A>G maps to NM_033225.5 H2658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:24756941 C>A maps to NM_001127453.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:24756941 C>A maps to NM_001127453.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:38790665 G>T maps to ENST00000327475 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:38790665 G>T maps to ENST00000327475 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:51297693 C>T maps to NM_004947.4 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:51297693 C>T maps to NM_004947.4 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:17581486 C>T maps to NM_006870.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:17581486 C>T maps to NM_006870.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:53156717 G>A maps to ENST00000370918 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:53156717 G>A maps to ENST00000370918 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:45916955 G>A maps to NM_202001.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:45916955 G>A maps to NM_202001.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:22778144 C>G maps to NM_018638.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:22778144 C>G maps to NM_018638.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:93159384 G>A maps to NM_005665.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:93159384 G>A maps to NM_005665.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:25743888 G>T maps to NM_152704.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:25743888 G>T maps to NM_152704.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:73486383 C>T maps to ENST00000295133 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:73486383 C>T maps to ENST00000295133 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:17122442 C>A maps to NM_144997.5 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:17122442 C>A maps to NM_144997.5 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:180671581 C>T maps to NM_005087.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:180671581 C>T maps to NM_005087.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:30661019 G>A maps to NM_002047.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:30661019 G>A maps to NM_002047.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:72634140 G>T maps to ENST00000504199 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:72634140 G>T maps to ENST00000504199 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:33581686 A>G maps to NM_018025.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:33581686 A>G maps to NM_018025.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:99947430 C>G maps to NM_004951.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:99947430 C>G maps to NM_004951.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:71804102 C>T maps to NM_018971.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:71804102 C>T maps to NM_018971.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:176859747 G>C maps to NM_002082.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:176859747 G>C maps to NM_002082.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:176867753 C>T maps to NM_002082.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:176867753 C>T maps to NM_002082.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:65476146 T>A maps to NM_138737.3 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:65476146 T>A maps to NM_138737.3 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:43917150 G>A maps to NM_001190880.1 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:43917150 G>A maps to NM_001190880.1 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:18735941 C>T maps to NM_173588.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:18735941 C>T maps to NM_173588.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:128263324 C>A maps to NM_017969.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:128263324 C>A maps to NM_017969.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:43893318 C>T maps to NM_015284.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:43893318 C>T maps to NM_015284.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:136963998 G>T maps to NM_017415.2 C526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:136963998 G>T maps to NM_017415.2 C526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:187149393 T>A maps to NM_000892.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:187149393 T>A maps to NM_000892.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:96350699 G>A maps to NM_005575.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:96350699 G>A maps to NM_005575.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:800570 G>A maps to NM_145886.3 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:800570 G>A maps to NM_145886.3 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:57567683 C>T maps to NM_002332.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:57567683 C>T maps to NM_002332.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:185169073 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:185169073 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:18255867 G>T maps to NM_015016.1 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:18255867 G>T maps to NM_015016.1 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:70351936 C>G maps to ENST00000333646 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:70351936 C>G maps to ENST00000333646 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:70352265 C>A maps to ENST00000333646 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:70352265 C>A maps to ENST00000333646 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:37059087 C>T maps to NM_000249.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:37059087 C>T maps to NM_000249.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:49575978 C>T maps to NM_014484.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:49575978 C>T maps to NM_014484.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:77760048 C>G maps to NM_015057.4 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:77760048 C>G maps to NM_015057.4 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:169498414 A>G maps to NM_018657.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:169498414 A>G maps to NM_018657.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:175812221 C>T maps to ENST00000451293 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:175812221 C>T maps to ENST00000451293 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:30326415 G>A maps to NM_000475.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:30326415 G>A maps to NM_000475.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:123870874 G>T maps to NM_001163278.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:123870874 G>T maps to NM_001163278.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:247920841 G>T maps to NM_012353.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:247920841 G>T maps to NM_012353.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:123814523 G>A maps to NM_001005187.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:123814523 G>A maps to NM_001005187.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:82763877 C>T maps to NM_033026.5 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:82763877 C>T maps to NM_033026.5 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:62896763 C>T maps to NM_018257.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:62896763 C>T maps to NM_018257.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:70190451 C>T maps to NM_017990.3 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:70190451 C>T maps to NM_017990.3 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:51889441 G>A maps to NM_138694.3 I1722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:51889441 G>A maps to NM_138694.3 I1722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:103044263 C>T maps to NM_000533.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:103044263 C>T maps to NM_000533.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:140441329 G>A maps to NM_001098537.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:140441329 G>A maps to NM_001098537.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:74880721 C>T maps to NM_016218.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:74880721 C>T maps to NM_016218.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:124503574 G>A maps to NM_015450.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:124503574 G>A maps to NM_015450.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:14218165 G>A maps to NM_002730.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:14218165 G>A maps to NM_002730.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:115024747 G>C maps to NM_001163790.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:115024747 G>C maps to NM_001163790.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:34145244 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:34145244 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:127420137 C>T maps to NM_001046.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:127420137 C>T maps to NM_001046.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:1089244 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:1089244 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:44222520 G>C maps to NM_178148.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:44222520 G>C maps to NM_178148.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:165755216 G>T maps to ENST00000409662 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:165755216 G>T maps to ENST00000409662 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:48575670 C>G maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:48575670 C>G maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:1133329 C>T maps to NM_018968.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:1133329 C>T maps to NM_018968.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:77094489 G>C maps to NM_152996.2 *306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:77094489 G>C maps to NM_152996.2 *306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:70596266 G>A maps to NM_014465.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:70596266 G>A maps to NM_014465.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:158489688 C>T maps to NM_003898.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:158489688 C>T maps to NM_003898.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:51718529 C>T maps to NM_015926.4 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:51718529 C>T maps to NM_015926.4 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:98497312 G>A maps to ENST00000359863 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:98497312 G>A maps to ENST00000359863 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:99696502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:99696502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:150385793 G>C maps to NM_024518.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:150385793 G>C maps to NM_024518.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:145103244 C>G maps to NM_007124.2 L2940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:145103244 C>G maps to NM_007124.2 L2940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:72821293 C>T maps to NM_006885.3 A3627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:72821293 C>T maps to NM_006885.3 A3627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:106813278 G>A maps to NM_012082.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:106813278 G>A maps to NM_012082.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:52619759 G>T maps to NM_178523.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:52619759 G>T maps to NM_178523.3 G219G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-2662-01A-01D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:31073108 C>T maps to ENST00000417110 F99F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-2662-01A-01D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:31073108 C>T maps to ENST00000417110 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:10500112 C>T maps to NM_000480.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:10500112 C>T maps to NM_000480.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:34666633 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:34666633 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:202131374 G>T maps to NM_001080125.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:202131374 G>T maps to NM_001080125.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:112068652 G>C maps to NM_001004196.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:112068652 G>C maps to NM_001004196.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:125671705 C>T maps to NM_130773.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:125671705 C>T maps to NM_130773.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:162740300 A>G maps to NM_006182.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:162740300 A>G maps to NM_006182.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr18:28671106 G>A maps to ENST00000438199 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr18:28671106 G>A maps to ENST00000438199 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:79698598 C>A maps to NM_001170574.1 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:79698598 C>A maps to NM_001170574.1 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:128409115 C>T maps to NM_005291.2 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:128409115 C>T maps to NM_005291.2 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:89923107 C>A maps to NM_032119.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:89923107 C>A maps to NM_032119.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:65482335 C>G maps to NM_182710.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:65482335 C>G maps to NM_182710.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr13:45582974 A>G maps to NM_018559.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr13:45582974 A>G maps to NM_018559.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:77746184 C>T maps to NM_001134745.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:77746184 C>T maps to NM_001134745.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chrX:64959736 C>T maps to NM_002444.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chrX:64959736 C>T maps to NM_002444.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:49928031 G>A maps to NM_002447.2 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:49928031 G>A maps to NM_002447.2 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chrX:3241385 C>T maps to NM_015419.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chrX:3241385 C>T maps to NM_015419.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr4:140265338 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr4:140265338 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr8:32621514 G>A maps to NM_013956.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr8:32621514 G>A maps to NM_013956.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr15:44038799 C>T maps to NM_005313.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr15:44038799 C>T maps to NM_005313.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:2340211 G>A maps to NM_153818.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:2340211 G>A maps to NM_153818.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr21:45738375 G>A maps to NM_002626.4 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr21:45738375 G>A maps to NM_002626.4 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:126747836 G>A maps to NM_032242.3 E1557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:126747836 G>A maps to NM_032242.3 E1557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:86993021 A>G maps to NM_022780.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:86993021 A>G maps to NM_022780.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr14:21167802 A>G maps to NM_194431.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr14:21167802 A>G maps to NM_194431.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:167301340 T>C maps to NM_002976.2 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:167301340 T>C maps to NM_002976.2 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr10:29819538 G>A maps to NM_021738.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr10:29819538 G>A maps to NM_021738.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:68941375 G>A maps to NM_024562.1 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:68941375 G>A maps to NM_024562.1 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr8:22926499 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr8:22926499 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:76083028 G>A maps to NM_001142640.1 P1216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:76083028 G>A maps to NM_001142640.1 P1216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:229779278 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:229779278 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr18:72344696 A>G maps to NM_017757.2 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr18:72344696 A>G maps to NM_017757.2 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chrX:2933386 G>A maps to NM_001011719.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chrX:2933386 G>A maps to NM_001011719.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:32583776 C>T maps to NM_002982.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:32583776 C>T maps to NM_002982.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr6:27114409 G>C maps to NM_080593.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr6:27114409 G>C maps to NM_080593.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr21:46020607 C>G maps to ENST00000380102 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr21:46020607 C>G maps to ENST00000380102 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:11087523 G>A maps to NM_006610.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:11087523 G>A maps to NM_006610.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr19:50864306 A>G maps to NM_004851.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr19:50864306 A>G maps to NM_004851.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr5:176562832 A>G maps to NM_022455.4 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr5:176562832 A>G maps to NM_022455.4 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:92734749 G>A maps to NM_017654.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:92734749 G>A maps to NM_017654.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:47162161 G>A maps to NM_014159.6 R1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:47162161 G>A maps to NM_014159.6 R1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:152856990 C>A maps to NM_030663.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:152856990 C>A maps to NM_030663.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:20009541 C>A maps to NM_181719.4 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:20009541 C>A maps to NM_181719.4 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr16:4920908 G>T maps to NM_016936.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr16:4920908 G>T maps to NM_016936.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr18:54339838 G>C maps to NM_015285.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr18:54339838 G>C maps to NM_015285.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:43706024 G>T maps to NM_004915.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:43706024 G>T maps to NM_004915.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:161165311 C>A maps to NM_005099.4 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:161165311 C>A maps to NM_005099.4 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:7698358 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:7698358 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:75435610 C>T maps to NM_001144000.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:75435610 C>T maps to NM_001144000.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:27355418 A>G maps to NM_014915.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:27355418 A>G maps to NM_014915.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:14851710 A>T maps to NM_001145029.1 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:14851710 A>T maps to NM_001145029.1 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:45782067 G>A maps to NM_001142679.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:45782067 G>A maps to NM_001142679.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:69034444 A>G maps to NM_001007231.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:69034444 A>G maps to NM_001007231.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:31319720 G>T maps to NM_030632.1 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:31319720 G>T maps to NM_030632.1 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:138825774 T>C maps to NM_173694.4 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:138825774 T>C maps to NM_173694.4 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:154319214 C>T maps to NM_020452.3 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:154319214 C>T maps to NM_020452.3 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:45253100 G>A maps to NM_153274.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:45253100 G>A maps to NM_153274.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:56109843 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:56109843 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:31619550 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:31619550 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:128772477 G>A maps to NM_145013.1 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:128772477 G>A maps to NM_145013.1 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:93015489 G>T maps to NM_153040.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:93015489 G>T maps to NM_153040.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:90128937 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:90128937 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:172437622 C>A maps to NM_139240.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:172437622 C>A maps to NM_139240.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:162353097 G>A maps to NM_001135240.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:162353097 G>A maps to NM_001135240.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:24964570 C>A maps to NM_020531.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:24964570 C>A maps to NM_020531.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:31740878 G>A maps to NM_025258.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:31740878 G>A maps to NM_025258.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:86559771 G>A maps to NM_032307.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:86559771 G>A maps to NM_032307.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:104825537 A>G maps to NM_001225.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:104825537 A>G maps to NM_001225.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158325683 T>C maps to NM_030893.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158325683 T>C maps to NM_030893.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:112648180 C>A maps to NM_138806.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:112648180 C>A maps to NM_138806.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:59166450 C>A maps to NM_031891.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:59166450 C>A maps to NM_031891.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:109812141 G>A maps to NM_001408.2 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:109812141 G>A maps to NM_001408.2 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:110670478 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:110670478 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:57731243 A>G maps to NM_032866.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:57731243 A>G maps to NM_032866.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:53330937 A>T maps to ENST00000219084 R1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:53330937 A>T maps to ENST00000219084 R1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:10194218 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:10194218 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:6262723 T>A maps to NM_001037329.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:6262723 T>A maps to NM_001037329.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:146741087 G>T maps to NM_014141.5 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:146741087 G>T maps to NM_014141.5 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:32163593 G>T maps to NM_001856.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:32163593 G>T maps to NM_001856.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:88027473 C>T maps to NM_001814.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:88027473 C>T maps to NM_001814.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:27945229 T>A maps to ENST00000435845 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:27945229 T>A maps to ENST00000435845 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:2209644 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:2209644 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:50885023 C>T maps to NM_032110.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:50885023 C>T maps to NM_032110.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:72297288 G>A maps to NM_023036.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:72297288 G>A maps to NM_023036.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:169506136 C>A maps to NM_004946.2 S1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:169506136 C>A maps to NM_004946.2 S1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:68021438 G>T maps to NM_022355.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:68021438 G>T maps to NM_022355.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:28604458 A>G maps to NM_001941.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:28604458 A>G maps to NM_001941.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:82122229 G>T maps to ENST00000372198 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:82122229 G>T maps to ENST00000372198 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:77710991 G>A maps to NM_178543.3 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:77710991 G>A maps to NM_178543.3 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:37864638 G>A maps to NM_004448.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:37864638 G>A maps to NM_004448.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:236384243 G>A maps to NM_019891.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:236384243 G>A maps to NM_019891.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:58555485 C>A maps to ENST00000474531 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:58555485 C>A maps to ENST00000474531 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:225266017 G>T maps to NM_001122779.1 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:225266017 G>T maps to NM_001122779.1 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:17664236 T>C maps to ENST00000335393 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:17664236 T>C maps to ENST00000335393 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:179782939 C>A maps to NM_173509.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:179782939 C>A maps to NM_173509.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:177250579 G>T maps to NM_021165.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:177250579 G>T maps to NM_021165.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:54805780 C>A maps to NM_001010872.1 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:54805780 C>A maps to NM_001010872.1 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:172628514 G>T maps to NM_000639.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:172628514 G>T maps to NM_000639.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:150889896 A>T maps to NM_033085.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:150889896 A>T maps to NM_033085.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:34324148 C>A maps to NM_025135.2 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:34324148 C>A maps to NM_025135.2 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:152286757 C>A maps to NM_002016.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:152286757 C>A maps to NM_002016.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:240370499 C>A maps to ENST00000406993 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:240370499 C>A maps to ENST00000406993 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:114284742 G>T maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:114284742 G>T maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:183723562 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:183723562 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:174219403 C>T maps to NM_017423.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:174219403 C>T maps to NM_017423.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:137593428 C>A maps to NM_001496.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:137593428 C>A maps to NM_001496.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:55223727 G>A maps to NM_207410.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:55223727 G>A maps to NM_207410.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:40344424 C>T maps to NM_032484.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:40344424 C>T maps to NM_032484.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:121726404 C>G maps to NM_005270.4 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:121726404 C>G maps to NM_005270.4 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:94482464 G>T maps to NM_005708.3 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:94482464 G>T maps to NM_005708.3 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:135438315 C>A maps to NM_153834.3 R2307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:135438315 C>A maps to NM_153834.3 R2307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:27333528 G>A maps to NM_005288.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:27333528 G>A maps to NM_005288.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:110086510 C>A maps to NM_031936.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:110086510 C>A maps to NM_031936.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:101972151 G>A maps to NM_138437.5 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:101972151 G>A maps to NM_138437.5 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:94436451 G>T maps to NM_001510.2 G695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:94436451 G>T maps to NM_001510.2 G695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:121212200 A>T maps to NM_005308.2 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:121212200 A>T maps to NM_005308.2 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:103267764 G>A maps to NM_001002916.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:103267764 G>A maps to NM_001002916.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:27182746 C>T maps to NM_019102.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:27182746 C>T maps to NM_019102.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:176965301 C>A maps to NM_021193.3 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:176965301 C>A maps to NM_021193.3 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:26860725 T>A maps to NM_022081.4 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:26860725 T>A maps to NM_022081.4 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:119617366 G>T maps to NM_014365.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:119617366 G>T maps to NM_014365.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:70841869 G>T maps to NM_032821.2 P4992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:70841869 G>T maps to NM_032821.2 P4992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:113832363 C>T maps to NM_032556.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:113832363 C>T maps to NM_032556.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:35876455 C>G maps to NM_002185.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:35876455 C>G maps to NM_002185.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31424229 C>A maps to ENST00000444228 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31424229 C>A maps to ENST00000444228 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31429490 C>A maps to ENST00000444228 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31429490 C>A maps to ENST00000444228 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31384648 G>T maps to NM_000887.3 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31384648 G>T maps to NM_000887.3 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:4920244 G>T maps to NM_002235.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:4920244 G>T maps to NM_002235.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:4919482 C>T maps to NM_002235.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:4919482 C>T maps to NM_002235.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:226447290 C>T maps to NM_020864.1 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:226447290 C>T maps to NM_020864.1 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:43497730 G>C maps to NM_020964.2 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:43497730 G>C maps to NM_020964.2 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:149419946 G>T maps to NM_032534.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:149419946 G>T maps to NM_032534.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:19818480 C>G maps to NM_000237.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:19818480 C>G maps to NM_000237.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:90179863 C>T maps to NM_032270.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:90179863 C>T maps to NM_032270.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:40689415 A>C maps to NM_198578.3 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:40689415 A>C maps to NM_198578.3 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:75052555 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:75052555 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:219383917 A>T maps to NM_138794.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:219383917 A>T maps to NM_138794.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:14066277 C>T maps to ENST00000310348 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:14066277 C>T maps to ENST00000310348 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:126253785 C>G maps to NM_178450.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:126253785 C>G maps to NM_178450.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:31194491 G>T maps to NM_002379.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:31194491 G>T maps to NM_002379.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:183013261 T>A maps to NM_015078.2 K501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:183013261 T>A maps to NM_015078.2 K501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:12244188 C>T maps to NM_014632.2 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:12244188 C>T maps to NM_014632.2 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:89131070 T>A maps to NM_005941.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:89131070 T>A maps to NM_005941.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:60102397 C>G maps to NM_139249.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:60102397 C>G maps to NM_139249.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:9024496 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:9024496 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:9075970 T>G maps to NM_024690.2 P3825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:9075970 T>G maps to NM_024690.2 P3825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:10204268 C>T maps to NM_003802.2 *1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:10204268 C>T maps to NM_003802.2 *1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:10428360 C>A maps to NM_017534.5 G1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:10428360 C>A maps to NM_017534.5 G1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23853902 C>T maps to NM_002471.3 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23853902 C>T maps to NM_002471.3 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:24433661 C>T maps to ENST00000330966 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:24433661 C>T maps to ENST00000330966 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:62839146 G>T maps to NM_004535.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:62839146 G>T maps to NM_004535.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:101795439 G>A maps to NM_052867.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:101795439 G>A maps to NM_052867.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:52507528 C>G maps to NM_007361.3 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:52507528 C>G maps to NM_007361.3 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:55508759 C>T maps to NM_017852.3 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:55508759 C>T maps to NM_017852.3 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:32184740 G>T maps to NM_004557.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:32184740 G>T maps to NM_004557.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:50765774 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:50765774 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:24878985 A>T maps to NM_025081.2 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:24878985 A>T maps to NM_025081.2 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:228511035 G>T maps to NM_001098623.1 V5127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:228511035 G>T maps to NM_001098623.1 V5127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158548786 G>A maps to NM_001004477.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158548786 G>A maps to NM_001004477.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:22368979 C>A maps to NM_001004719.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:22368979 C>A maps to NM_001004719.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:142749604 C>G maps to NM_001001667.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:142749604 C>G maps to NM_001001667.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:31871585 T>A maps to NM_017784.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:31871585 T>A maps to NM_017784.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:205978256 A>T maps to ENST00000406610 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:205978256 A>T maps to ENST00000406610 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:55721652 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:55721652 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:140346518 G>A maps to NM_018899.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:140346518 G>A maps to NM_018899.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:15134400 G>A maps to NM_006205.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:15134400 G>A maps to NM_006205.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:110396315 C>T maps to ENST00000426474 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:110396315 C>T maps to ENST00000426474 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:110439381 A>G maps to ENST00000426474 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:110439381 A>G maps to ENST00000426474 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:110477364 G>T maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:110477364 G>T maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:44441504 G>T maps to NM_004571.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:44441504 G>T maps to NM_004571.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:38508176 G>A maps to NM_003560.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:38508176 G>A maps to NM_003560.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:14533094 C>A maps to ENST00000444806 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:14533094 C>A maps to ENST00000444806 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:11558264 C>T maps to ENST00000436195 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:11558264 C>T maps to ENST00000436195 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:82096114 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:82096114 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:50188236 G>A maps to NM_001536.3 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:50188236 G>A maps to NM_001536.3 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:138762886 G>T maps to NM_001134657.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:138762886 G>T maps to NM_001134657.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:141712745 G>A maps to NM_005607.4 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:141712745 G>A maps to NM_005607.4 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:198668801 C>T maps to ENST00000271610 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:198668801 C>T maps to ENST00000271610 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:121608167 T>C maps to NM_002851.2 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:121608167 T>C maps to NM_002851.2 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:37735070 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:37735070 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:114310968 G>A maps to NM_018364.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:114310968 G>A maps to NM_018364.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:21992889 G>A maps to NM_005407.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:21992889 G>A maps to NM_005407.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:83626447 G>A maps to NM_001037582.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:83626447 G>A maps to NM_001037582.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:64863747 G>A maps to NM_014755.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:64863747 G>A maps to NM_014755.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:48381848 C>G maps to NM_020846.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:48381848 C>G maps to NM_020846.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:108123470 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:108123470 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:32482261 T>A maps to NM_000343.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:32482261 T>A maps to NM_000343.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:32631036 G>T maps to NM_014227.2 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:32631036 G>T maps to NM_014227.2 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:85279238 A>T maps to NM_182767.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:85279238 A>T maps to NM_182767.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:20623177 G>T maps to NM_004211.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:20623177 G>T maps to NM_004211.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:95197501 G>T maps to NM_001128429.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:95197501 G>T maps to NM_001128429.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:7594074 G>T maps to NM_152551.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:7594074 G>T maps to NM_152551.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158583602 G>T maps to NM_003126.2 C2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158583602 G>T maps to NM_003126.2 C2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:85648857 A>G maps to NM_032184.1 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:85648857 A>G maps to NM_032184.1 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:110019409 C>A maps to NM_001040709.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:110019409 C>A maps to NM_001040709.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:122634998 G>A maps to NM_016945.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:122634998 G>A maps to NM_016945.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:132351138 T>C maps to NM_016521.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:132351138 T>C maps to NM_016521.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:43801862 C>T maps to ENST00000330266 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:43801862 C>T maps to ENST00000330266 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:126139091 A>T maps to NM_052907.2 K1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:126139091 A>T maps to NM_052907.2 K1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrY:9305907 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrY:9305907 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:179584083 T>C maps to NM_133378.4 S6767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:179584083 T>C maps to NM_133378.4 S6767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:39511521 T>C maps to NM_003359.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:39511521 T>C maps to NM_003359.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:96140294 G>T maps to NM_003728.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:96140294 G>T maps to NM_003728.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:70765432 C>T maps to NM_018052.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:70765432 C>T maps to NM_018052.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:100205157 C>G maps to NM_017890.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:100205157 C>G maps to NM_017890.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:64065847 T>C maps to NM_080666.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:64065847 T>C maps to NM_080666.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:168106862 G>A maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:168106862 G>A maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:30936619 C>A maps to NM_014717.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:30936619 C>A maps to NM_014717.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:135621050 G>A maps to NM_138326.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:135621050 G>A maps to NM_138326.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:91700232 A>G maps to NM_005751.4 K2174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:91700232 A>G maps to NM_005751.4 K2174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:134755106 C>T maps to ENST00000368586 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:134755106 C>T maps to ENST00000368586 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:10614343 A>T maps to NM_020233.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:10614343 A>T maps to NM_020233.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr21:45987863 C>T maps to ENST00000443468 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr21:45987863 C>T maps to ENST00000443468 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:106694259 C>A maps to NM_032411.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:106694259 C>A maps to NM_032411.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:42777197 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:42777197 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:139865752 C>T maps to NM_004065.2 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:139865752 C>T maps to NM_004065.2 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:48342692 G>A maps to NM_000554.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:48342692 G>A maps to NM_000554.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:106466058 C>T maps to NM_173494.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:106466058 C>T maps to NM_173494.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:26774058 G>T maps to NM_024887.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:26774058 G>T maps to NM_024887.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:80629226 C>T maps to NM_022726.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:80629226 C>T maps to NM_022726.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:13035486 G>A maps to NM_004461.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:13035486 G>A maps to NM_004461.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:58080587 G>T maps to NM_001164317.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:58080587 G>T maps to NM_001164317.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:89846102 C>T maps to NM_198460.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:89846102 C>T maps to NM_198460.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:7915176 G>T maps to NM_017545.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:7915176 G>T maps to NM_017545.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:6055779 G>C maps to NM_001099433.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:6055779 G>C maps to NM_001099433.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:95508681 G>A maps to NM_015496.3 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:95508681 G>A maps to NM_015496.3 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:113375009 G>C maps to NM_001009899.2 S1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:113375009 G>C maps to NM_001009899.2 S1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:11740466 G>T maps to ENST00000376669 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:11740466 G>T maps to ENST00000376669 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:37566051 G>A maps to NM_004774.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:37566051 G>A maps to NM_004774.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:74690084 T>G maps to NM_006302.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:74690084 T>G maps to NM_006302.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:49724891 G>A maps to NM_020998.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:49724891 G>A maps to NM_020998.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:36985802 C>T maps to NM_133433.3 R841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:36985802 C>T maps to NM_133433.3 R841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:33460194 G>C maps to NM_018096.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:33460194 G>C maps to NM_018096.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:57063702 C>T maps to NM_032206.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:57063702 C>T maps to NM_032206.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:51239056 C>A maps to NM_018159.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:51239056 C>A maps to NM_018159.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:56258675 G>T maps to NM_001005282.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:56258675 G>T maps to NM_001005282.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:49042347 G>T maps to NM_177938.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:49042347 G>T maps to NM_177938.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:55912863 G>T maps to NM_001142763.1 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:55912863 G>T maps to NM_001142763.1 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:140580729 C>T maps to NM_018931.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:140580729 C>T maps to NM_018931.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:77373667 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:77373667 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:30768315 C>A maps to NM_000294.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:30768315 C>A maps to NM_000294.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:62492600 C>T maps to NM_007215.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:62492600 C>T maps to NM_007215.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr9:8518127 C>G maps to NM_002839.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr9:8518127 C>G maps to NM_002839.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:120651680 G>A maps to NM_001080855.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:120651680 G>A maps to NM_001080855.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:17755623 T>A maps to NM_018715.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:17755623 T>A maps to NM_018715.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:85576585 C>T maps to NM_017750.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:85576585 C>T maps to NM_017750.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:73048995 G>A maps to NM_001080479.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:73048995 G>A maps to NM_001080479.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47456481 C>A maps to NM_012235.2 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47456481 C>A maps to NM_012235.2 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:1222559 C>A maps to NM_001130413.2 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:1222559 C>A maps to NM_001130413.2 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:83640501 G>A maps to NM_006080.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:83640501 G>A maps to NM_006080.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:30972796 C>T maps to NM_014712.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:30972796 C>T maps to NM_014712.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:31924784 C>T maps to NM_001007467.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:31924784 C>T maps to NM_001007467.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:154940730 G>A maps to NM_001130040.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:154940730 G>A maps to NM_001130040.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:70732858 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:70732858 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:45981367 C>G maps to NM_021199.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:45981367 C>G maps to NM_021199.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:138373848 G>A maps to ENST00000272643 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:138373848 G>A maps to ENST00000272643 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:57089341 G>A maps to NM_033396.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:57089341 G>A maps to NM_033396.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:40093097 C>G maps to ENST00000377543 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:40093097 C>G maps to ENST00000377543 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:179479391 G>T maps to NM_133378.4 T13715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:179479391 G>T maps to NM_133378.4 T13715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:9396446 G>A maps to NM_020648.5 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:9396446 G>A maps to NM_020648.5 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:69682205 G>T maps to NM_001075.4 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:69682205 G>T maps to NM_001075.4 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:74920198 G>A maps to NM_030581.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:74920198 G>A maps to NM_030581.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:47569696 C>A maps to NM_015168.1 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:47569696 C>A maps to NM_015168.1 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:77913581 T>C maps to NM_152694.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:77913581 T>C maps to NM_152694.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:47835778 G>T maps to NM_006962.1 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:47835778 G>T maps to NM_006962.1 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:52618738 G>A maps to NM_178523.3 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:52618738 G>A maps to NM_178523.3 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:12087894 G>T maps to NM_001012753.1 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:12087894 G>T maps to NM_001012753.1 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:16215881 C>T maps to ENST00000399408 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:16215881 C>T maps to ENST00000399408 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:148617108 T>A maps to NM_014945.2 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:148617108 T>A maps to NM_014945.2 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:38524627 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:38524627 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:222843270 A>T maps to NM_022831.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:222843270 A>T maps to NM_022831.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:49958058 T>A maps to NM_003886.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:49958058 T>A maps to NM_003886.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:108348463 C>T maps to NM_001146.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:108348463 C>T maps to NM_001146.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17942587 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17942587 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:4621907 G>A maps to ENST00000412477 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:4621907 G>A maps to ENST00000412477 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:31607498 G>T maps to NM_025227.1 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:31607498 G>T maps to NM_025227.1 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:40037180 C>A maps to NM_021096.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:40037180 C>A maps to NM_021096.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:104872880 G>A maps to NM_001136112.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:104872880 G>A maps to NM_001136112.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:46915989 G>C maps to NM_032040.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:46915989 G>C maps to NM_032040.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:24487846 G>C maps to NM_006727.3 Y764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:24487846 G>C maps to NM_006727.3 Y764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:40053840 G>A maps to NM_032221.3 L1441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:40053840 G>A maps to NM_032221.3 L1441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:70747664 C>T maps to NM_014515.5 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:70747664 C>T maps to NM_014515.5 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:27024277 C>A maps to NM_001886.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:27024277 C>A maps to NM_001886.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:173822599 C>G maps to NM_018122.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:173822599 C>G maps to NM_018122.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:169111324 C>G maps to NM_004946.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:169111324 C>G maps to NM_004946.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:6928182 C>T maps to ENST00000381407 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:6928182 C>T maps to ENST00000381407 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:121942173 G>A maps to NM_001024613.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:121942173 G>A maps to NM_001024613.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:37730992 G>T maps to NM_014907.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:37730992 G>T maps to NM_014907.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:50314902 C>T maps to NM_025129.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:50314902 C>T maps to NM_025129.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:34937809 G>T maps to NM_024835.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:34937809 G>T maps to NM_024835.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:24462986 T>C maps to NM_001503.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:24462986 T>C maps to NM_001503.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:122318380 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:122318380 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:23424311 G>A maps to NM_017815.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:23424311 G>A maps to NM_017815.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:14153284 C>A maps to NM_004843.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:14153284 C>A maps to NM_004843.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:234072374 G>A maps to ENST00000359570 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:234072374 G>A maps to ENST00000359570 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:155566152 C>T maps to NM_002239.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:155566152 C>T maps to NM_002239.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:42796704 C>T maps to NM_015349.1 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:42796704 C>T maps to NM_015349.1 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:35739604 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:35739604 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:112471752 T>C maps to NM_001105206.1 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:112471752 T>C maps to NM_001105206.1 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:136552260 G>C maps to NM_002299.2 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:136552260 G>C maps to NM_002299.2 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:43817873 G>A maps to ENST00000382031 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:43817873 G>A maps to ENST00000382031 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:161508850 C>T maps to NM_005922.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:161508850 C>T maps to NM_005922.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:21887671 A>G maps to NM_015884.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:21887671 A>G maps to NM_015884.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:70340929 C>A maps to ENST00000333646 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:70340929 C>A maps to ENST00000333646 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:21837987 G>A maps to NM_002451.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:21837987 G>A maps to NM_002451.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:9076465 T>C maps to NM_024690.2 E3660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:9076465 T>C maps to NM_024690.2 E3660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:42461774 C>T maps to NM_000262.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:42461774 C>T maps to NM_000262.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:55481502 G>A maps to NM_017852.3 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:55481502 G>A maps to NM_017852.3 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:56382294 G>T maps to NM_134444.4 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:56382294 G>T maps to NM_134444.4 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:62737698 C>A maps to NM_005286.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:62737698 C>A maps to NM_005286.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:101092627 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:101092627 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:161969906 C>T maps to ENST00000451379 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:161969906 C>T maps to ENST00000451379 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:15904893 C>T maps to NM_001004466.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:15904893 C>T maps to NM_001004466.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:55607015 A>G maps to NM_001005496.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:55607015 A>G maps to NM_001005496.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:56310154 G>C maps to NM_001005245.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:56310154 G>C maps to NM_001005245.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:91134238 C>A maps to NM_032968.3 T1000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:91134238 C>A maps to NM_032968.3 T1000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:140255899 C>T maps to NM_018903.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:140255899 C>T maps to NM_018903.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:140741282 C>T maps to NM_018923.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:140741282 C>T maps to NM_018923.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:60646291 C>T maps to NM_194449.2 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:60646291 C>T maps to NM_194449.2 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:205065902 C>A maps to NM_005057.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:205065902 C>A maps to NM_005057.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:66834239 G>T maps to NM_014578.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:66834239 G>T maps to NM_014578.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:39019688 G>C maps to NM_000540.2 T3711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:39019688 G>C maps to NM_000540.2 T3711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:4558144 G>A maps to NM_032108.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:4558144 G>A maps to NM_032108.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:7474714 C>T maps to ENST00000321337 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:7474714 C>T maps to ENST00000321337 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:135205013 C>T maps to ENST00000372169 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:135205013 C>T maps to ENST00000372169 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:153909104 A>G maps to NM_015595.3 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:153909104 A>G maps to NM_015595.3 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:7335003 G>T maps to NM_175733.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:7335003 G>T maps to NM_175733.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:24682633 G>C maps to NM_014169.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:24682633 G>C maps to NM_014169.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:129559172 G>C maps to NM_133448.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:129559172 G>C maps to NM_133448.2 L849L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-3398-01A-01D-1105-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-3398-01A-01D-1105-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:175372525 C>A maps to NM_003285.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:175372525 C>A maps to NM_003285.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:114969874 A>G maps to NM_015906.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:114969874 A>G maps to NM_015906.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:67860419 C>G maps to ENST00000339830 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:67860419 C>G maps to ENST00000339830 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:116574052 G>A maps to ENST00000368611 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:116574052 G>A maps to ENST00000368611 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:180322026 A>G maps to NM_133462.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:180322026 A>G maps to NM_133462.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:46671250 C>T maps to NM_017931.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:46671250 C>T maps to NM_017931.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:167753645 G>T maps to NM_031949.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:167753645 G>T maps to NM_031949.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:3102774 C>A maps to NM_014948.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:3102774 C>A maps to NM_014948.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:46559777 C>G maps to ENST00000242848 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:46559777 C>G maps to ENST00000242848 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:127014854 T>A maps to NM_176814.3 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:127014854 T>A maps to NM_176814.3 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:185802746 T>G maps to NM_194250.1 L875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:185802746 T>G maps to NM_194250.1 L875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:67181701 C>A maps to NM_080282.3 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:67181701 C>A maps to NM_080282.3 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:101606845 G>T maps to NM_000392.3 G1425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:101606845 G>T maps to NM_000392.3 G1425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:22078927 C>A maps to NM_005691.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:22078927 C>A maps to NM_005691.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:27893423 G>T maps to NM_198147.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:27893423 G>T maps to NM_198147.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:148683667 C>T maps to NM_001616.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:148683667 C>T maps to NM_001616.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:39535049 A>G maps to NM_014237.2 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:39535049 A>G maps to NM_014237.2 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:5146294 C>A maps to NM_139056.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:5146294 C>A maps to NM_139056.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161161116 C>T maps to NM_005099.4 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161161116 C>T maps to NM_005099.4 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161165958 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161165958 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:1313243 G>C maps to NM_018702.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:1313243 G>C maps to NM_018702.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45662260 G>T maps to NM_021116.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45662260 G>T maps to NM_021116.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45726178 G>T maps to NM_021116.2 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45726178 G>T maps to NM_021116.2 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7626389 C>T maps to NM_020546.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7626389 C>T maps to NM_020546.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:26074882 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:26074882 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:7795472 C>A maps to NM_001134647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:7795472 C>A maps to NM_001134647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:58121758 G>A maps to NM_001122772.1 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:58121758 G>A maps to NM_001122772.1 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159035798 C>A maps to NM_004833.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159035798 C>A maps to NM_004833.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:45709651 G>T maps to NM_000383.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:45709651 G>T maps to NM_000383.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:4879694 G>T maps to NM_001040177.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:4879694 G>T maps to NM_001040177.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33093032 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33093032 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:37438727 T>A maps to ENST00000374660 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:37438727 T>A maps to ENST00000374660 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:17444343 C>A maps to NM_020959.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:17444343 C>A maps to NM_020959.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:120176787 G>T maps to ENST00000313400 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:120176787 G>T maps to ENST00000313400 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:160029652 C>A maps to NM_025153.2 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:160029652 C>A maps to NM_025153.2 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:160059374 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:160059374 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:43664301 T>C maps to NM_001001937.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:43664301 T>C maps to NM_001001937.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:104065050 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:104065050 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:1796076 C>T maps to NM_138813.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:1796076 C>T maps to NM_138813.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47236503 C>A maps to NM_153446.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47236503 C>A maps to NM_153446.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143570777 C>T maps to NM_001702.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143570777 C>T maps to NM_001702.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:127414292 A>T maps to ENST00000356792 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:127414292 A>T maps to ENST00000356792 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:88379803 T>A maps to NM_152589.1 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:88379803 T>A maps to NM_152589.1 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:77880277 C>A maps to NM_001113475.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:77880277 C>A maps to NM_001113475.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:67154013 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:67154013 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:40832376 C>A maps to ENST00000357884 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:40832376 C>A maps to ENST00000357884 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:75086427 T>C maps to NM_001002912.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:75086427 T>C maps to NM_001002912.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31541485 A>G maps to NM_018356.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31541485 A>G maps to NM_018356.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:43446491 C>A maps to NM_022483.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:43446491 C>A maps to NM_022483.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:57431534 G>T maps to NM_000066.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:57431534 G>T maps to NM_000066.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:2786311 C>A maps to NM_199460.2 Y1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:2786311 C>A maps to NM_199460.2 Y1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:48655738 C>A maps to NM_018896.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:48655738 C>A maps to NM_018896.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:65040955 C>A maps to NM_000727.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:65040955 C>A maps to NM_000727.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:64873632 C>A maps to NM_014404.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:64873632 C>A maps to NM_014404.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27457405 T>A maps to NM_004341.3 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27457405 T>A maps to NM_004341.3 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:43939635 C>A maps to NM_172095.1 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:43939635 C>A maps to NM_172095.1 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33392155 G>A maps to NM_032816.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33392155 G>A maps to NM_032816.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66368019 G>T maps to NM_005125.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66368019 G>T maps to NM_005125.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66082935 A>T maps to NM_020404.2 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66082935 A>T maps to NM_020404.2 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:121825184 G>T maps to NM_175862.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:121825184 G>T maps to NM_175862.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:66436897 G>T maps to NM_001795.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:66436897 G>T maps to NM_001795.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:26881640 G>T maps to NM_016279.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:26881640 G>T maps to NM_016279.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:15788108 C>A maps to ENST00000375924 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:15788108 C>A maps to ENST00000375924 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:196871707 C>A maps to NM_006684.2 C73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:196871707 C>A maps to NM_006684.2 C73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6185834 C>A maps to NM_015557.2 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6185834 C>A maps to NM_015557.2 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240070813 A>T maps to NM_000740.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240070813 A>T maps to NM_000740.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:6978390 G>T maps to NM_182906.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:6978390 G>T maps to NM_182906.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:45077112 G>A maps to NM_003278.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:45077112 G>A maps to NM_003278.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:86246908 A>C maps to NM_152890.5 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:86246908 A>C maps to NM_152890.5 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:110829280 C>T maps to NM_001845.4 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:110829280 C>T maps to NM_001845.4 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111092174 C>T maps to NM_001846.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111092174 C>T maps to NM_001846.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:107403708 G>T maps to NM_033641.2 A1503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:107403708 G>T maps to NM_033641.2 A1503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10108082 G>T maps to NM_015719.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10108082 G>T maps to NM_015719.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:68334753 T>C maps to NM_020361.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:68334753 T>C maps to NM_020361.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:3000071 G>A maps to NM_033225.5 A2052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:3000071 G>A maps to NM_033225.5 A2052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:225346794 C>A maps to NM_003590.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:225346794 C>A maps to NM_003590.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:144909467 C>A maps to NM_004709.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:144909467 C>A maps to NM_004709.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:134303588 G>A maps to NM_001031705.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:134303588 G>A maps to NM_001031705.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:100165800 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:100165800 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15769109 C>A maps to NM_000896.2 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15769109 C>A maps to NM_000896.2 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:69520615 T>A maps to NM_003861.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:69520615 T>A maps to NM_003861.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:61091480 G>C maps to NM_001923.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:61091480 G>C maps to NM_001923.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94545841 C>A maps to NM_020414.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94545841 C>A maps to NM_020414.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132624411 T>C maps to NM_175066.3 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132624411 T>C maps to NM_175066.3 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:101200977 C>A maps to NM_003836.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:101200977 C>A maps to NM_003836.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:46275985 T>A maps to NM_004409.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:46275985 T>A maps to NM_004409.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:21747330 G>A maps to NM_003777.3 L2194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:21747330 G>A maps to NM_003777.3 L2194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11786979 C>A maps to NM_001372.3 S3628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11786979 C>A maps to NM_001372.3 S3628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:128769017 A>T maps to ENST00000398025 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:128769017 A>T maps to ENST00000398025 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:169141186 G>T maps to NM_004946.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:169141186 G>T maps to NM_004946.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:25226114 C>T maps to NM_024940.6 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:25226114 C>T maps to NM_024940.6 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:46783426 C>T maps to NM_017653.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:46783426 C>T maps to NM_017653.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21216182 G>C maps to NM_006683.4 *148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21216182 G>C maps to NM_006683.4 *148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:73520448 G>A maps to NM_001965.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:73520448 G>A maps to NM_001965.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:141567244 G>A maps to NM_012154.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:141567244 G>A maps to NM_012154.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:77081424 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:77081424 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:43935508 G>T maps to NM_001127615.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:43935508 G>T maps to NM_001127615.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142568608 C>A maps to NM_004445.3 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142568608 C>A maps to NM_004445.3 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:97749975 C>A maps to NM_199336.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:97749975 C>A maps to NM_199336.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137354123 G>A maps to NM_016603.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137354123 G>A maps to NM_016603.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:43629301 G>T maps to NM_001145196.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:43629301 G>T maps to NM_001145196.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127730961 T>A maps to NM_001999.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127730961 T>A maps to NM_001999.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8176861 G>A maps to NM_032447.3 H1320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8176861 G>A maps to NM_032447.3 H1320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161187845 C>A maps to NM_004106.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161187845 C>A maps to NM_004106.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157659675 A>T maps to NM_052939.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157659675 A>T maps to NM_052939.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124989712 C>A maps to NM_001039112.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124989712 C>A maps to NM_001039112.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:152328818 T>C maps to NM_001014342.2 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:152328818 T>C maps to NM_001014342.2 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:83440920 G>T maps to NM_001007122.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:83440920 G>T maps to NM_001007122.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:17468884 C>T maps to NM_001037814.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:17468884 C>T maps to NM_001037814.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:69800211 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:69800211 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:129373262 C>A maps to ENST00000442111 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:129373262 C>A maps to ENST00000442111 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:88651389 C>A maps to ENST00000376023 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:88651389 C>A maps to ENST00000376023 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99773278 G>T maps to NM_152742.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99773278 G>T maps to NM_152742.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:23299710 G>T maps to ENST00000435486 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:23299710 G>T maps to ENST00000435486 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:37692864 C>T maps to NM_032777.9 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:37692864 C>T maps to NM_032777.9 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:154055652 G>C maps to NM_001038705.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:154055652 G>C maps to NM_001038705.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:25510016 G>T maps to NM_020752.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:25510016 G>T maps to NM_020752.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:241570037 C>G maps to NM_001195381.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:241570037 C>G maps to NM_001195381.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:158257623 C>T maps to NM_000826.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:158257623 C>T maps to NM_000826.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:94344040 C>A maps to NM_001510.2 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:94344040 C>A maps to NM_001510.2 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:104449332 G>C maps to NM_133445.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:104449332 G>C maps to NM_133445.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:126173449 G>A maps to NM_001127323.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:126173449 G>A maps to NM_001127323.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:135933327 T>C maps to NM_001122823.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:135933327 T>C maps to NM_001122823.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:156479504 C>A maps to NM_001173393.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:156479504 C>A maps to NM_001173393.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:153224148 C>T maps to ENST00000369984 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:153224148 C>T maps to ENST00000369984 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:65146101 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:65146101 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:26156938 C>G maps to NM_005321.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:26156938 C>G maps to NM_005321.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:149858691 C>G maps to NM_003517.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:149858691 C>G maps to NM_003517.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33037433 G>A maps to NM_033554.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33037433 G>A maps to NM_033554.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:76472577 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:76472577 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:118814642 G>A maps to NM_000414.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:118814642 G>A maps to NM_000414.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:70934908 C>A maps to NM_032821.2 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:70934908 C>A maps to NM_032821.2 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:70935047 C>G maps to NM_032821.2 R2968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:70935047 C>G maps to NM_032821.2 R2968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10449400 G>A maps to NM_002162.3 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10449400 G>A maps to NM_002162.3 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:65678330 C>T maps to NM_020962.1 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:65678330 C>T maps to NM_020962.1 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45931535 C>A maps to NM_000596.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45931535 C>A maps to NM_000596.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23915734 C>A maps to NM_020070.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23915734 C>A maps to NM_020070.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:219922302 G>T maps to NM_002181.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:219922302 G>T maps to NM_002181.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:103010926 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:103010926 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3119199 G>T maps to ENST00000416912 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3119199 G>T maps to ENST00000416912 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3119311 G>T maps to ENST00000416912 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3119311 G>T maps to ENST00000416912 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201832720 G>C maps to NM_018085.4 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201832720 G>C maps to NM_018085.4 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:118969761 T>A maps to NM_181840.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:118969761 T>A maps to NM_181840.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:6893232 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:6893232 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:55357526 G>T maps to NM_001098815.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:55357526 G>T maps to NM_001098815.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123192196 A>T maps to NM_015312.3 P2506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123192196 A>T maps to NM_015312.3 P2506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94088825 C>A maps to ENST00000393153 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94088825 C>A maps to ENST00000393153 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113377383 G>A maps to NM_001009899.2 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113377383 G>A maps to NM_001009899.2 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:17764657 C>A maps to NM_022113.4 E1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:17764657 C>A maps to NM_022113.4 E1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:70514350 C>A maps to NM_020866.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:70514350 C>A maps to NM_020866.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51411999 G>T maps to NM_004917.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51411999 G>T maps to NM_004917.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:187178396 C>T maps to ENST00000511608 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:187178396 C>T maps to ENST00000511608 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:39383031 C>A maps to NM_031961.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:39383031 C>A maps to NM_031961.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:39406097 C>A maps to ENST00000431129 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:39406097 C>A maps to ENST00000431129 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107720069 G>T maps to NM_007356.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107720069 G>T maps to NM_007356.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:133951286 C>T maps to ENST00000355048 Y1188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:133951286 C>T maps to ENST00000355048 Y1188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:71946858 G>T maps to NM_003667.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:71946858 G>T maps to NM_003667.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:35300289 G>T maps to NM_005568.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:35300289 G>T maps to NM_005568.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:38496682 A>G maps to NM_002310.5 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:38496682 A>G maps to NM_002310.5 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:61776058 G>T maps to NM_030576.3 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:61776058 G>T maps to NM_030576.3 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:42356853 T>A maps to NM_152447.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:42356853 T>A maps to NM_152447.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76370953 G>T maps to NM_001128922.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76370953 G>T maps to NM_001128922.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:40137637 C>A maps to NM_020929.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:40137637 C>A maps to NM_020929.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:70541827 G>A maps to NM_020794.2 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:70541827 G>A maps to NM_020794.2 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53876885 G>A maps to NM_001193511.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53876885 G>A maps to NM_001193511.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:217124301 G>A maps to NM_020814.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:217124301 G>A maps to NM_020814.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:119699918 G>T maps to NM_006770.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:119699918 G>T maps to NM_006770.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:149227674 G>T maps to ENST00000404807 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:149227674 G>T maps to ENST00000404807 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:116434321 C>A maps to NM_015335.4 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:116434321 C>A maps to NM_015335.4 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:71058047 G>A maps to ENST00000430055 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:71058047 G>A maps to ENST00000430055 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74738049 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74738049 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:1560536 C>T maps to NM_080875.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:1560536 C>T maps to NM_080875.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:5011950 C>T maps to NM_021801.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:5011950 C>T maps to NM_021801.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:11852385 T>C maps to ENST00000376585 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:11852385 T>C maps to ENST00000376585 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9064315 G>T maps to NM_024690.2 I7710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9064315 G>T maps to NM_024690.2 I7710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9084425 C>A maps to NM_024690.2 S2463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9084425 C>A maps to NM_024690.2 S2463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:15831438 C>A maps to NM_001040114.1 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:15831438 C>A maps to NM_001040114.1 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:10219041 C>A maps to NM_003802.2 E1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:10219041 C>A maps to NM_003802.2 E1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23859649 G>C maps to NM_002471.3 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23859649 G>C maps to NM_002471.3 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76872032 G>T maps to NM_000260.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76872032 G>T maps to NM_000260.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76910852 C>T maps to NM_000260.3 N1614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76910852 C>T maps to NM_000260.3 N1614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:12656506 C>A maps to NM_001146312.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:12656506 C>A maps to NM_001146312.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:17743007 C>T maps to NM_002478.4 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:17743007 C>T maps to NM_002478.4 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:2054353 G>T maps to NM_003970.2 G989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:2054353 G>T maps to NM_003970.2 G989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:101714424 C>A maps to NM_052867.2 L1550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:101714424 C>A maps to NM_052867.2 L1550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:183832072 G>C maps to NM_205842.1 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:183832072 G>C maps to NM_205842.1 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:41309565 C>T maps to NM_004828.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:41309565 C>T maps to NM_004828.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:170498204 G>A maps to ENST00000507142 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:170498204 G>A maps to ENST00000507142 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:24845993 G>T maps to NM_001136022.1 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:24845993 G>T maps to NM_001136022.1 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7982252 G>A maps to NM_176821.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7982252 G>A maps to NM_176821.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247607997 C>A maps to NM_004895.4 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247607997 C>A maps to NM_004895.4 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6027357 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6027357 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107878201 C>A maps to ENST00000379032 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107878201 C>A maps to ENST00000379032 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:206610594 G>T maps to NM_201266.1 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:206610594 G>T maps to NM_201266.1 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:104171765 G>A maps to NM_001031701.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:104171765 G>A maps to NM_001031701.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16910887 C>G maps to ENST00000438489 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16910887 C>G maps to ENST00000438489 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220421266 G>T maps to NM_015311.2 I1415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220421266 G>T maps to NM_015311.2 I1415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220424001 G>T maps to NM_015311.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220424001 G>T maps to NM_015311.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:97619368 G>T maps to NM_006188.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:97619368 G>T maps to NM_006188.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13175537 G>T maps to NM_021980.4 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13175537 G>T maps to NM_021980.4 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158435416 G>A maps to NM_001004473.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158435416 G>A maps to NM_001004473.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:29054812 G>T maps to NM_001005226.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:29054812 G>T maps to NM_001005226.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143632386 G>A maps to NM_001004685.1 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143632386 G>A maps to NM_001004685.1 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247769735 C>A maps to NM_001001914.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247769735 C>A maps to NM_001001914.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:4869646 G>T maps to NM_001004758.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:4869646 G>T maps to NM_001004758.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:55798169 C>A maps to NM_001001921.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:55798169 C>A maps to NM_001001921.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158670321 C>A maps to NM_001005279.1 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158670321 C>A maps to NM_001005279.1 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158724611 C>T maps to NM_001005184.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158724611 C>T maps to NM_001005184.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:56468588 C>A maps to NM_001013358.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:56468588 C>A maps to NM_001013358.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:76752582 G>A maps to NM_020841.4 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:76752582 G>A maps to NM_020841.4 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:36966698 C>T maps to NM_016734.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:36966698 C>T maps to NM_016734.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19018402 G>T maps to NM_002584.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19018402 G>T maps to NM_002584.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:138453098 T>A maps to NM_019035.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:138453098 T>A maps to NM_019035.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140590443 C>T maps to NM_018932.3 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140590443 C>T maps to NM_018932.3 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140595758 C>A maps to NM_018933.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140595758 C>A maps to NM_018933.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140481801 C>A maps to NM_018937.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140481801 C>A maps to NM_018937.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140812311 G>T maps to NM_003735.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140812311 G>T maps to NM_003735.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140745822 C>G maps to NM_018918.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140745822 C>G maps to NM_018918.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:165863739 G>T maps to NM_001130690.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:165863739 G>T maps to NM_001130690.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:103814330 C>A maps to NM_025208.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:103814330 C>A maps to NM_025208.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:45309811 G>A maps to NM_138415.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:45309811 G>A maps to NM_138415.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:229890731 C>T maps to NM_017933.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:229890731 C>T maps to NM_017933.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:397118 C>G maps to NM_007183.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:397118 C>G maps to NM_007183.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:186934604 G>T maps to NM_024420.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:186934604 G>T maps to NM_024420.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:199011650 G>T maps to NM_006226.3 E1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:199011650 G>T maps to NM_006226.3 E1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:67859504 C>T maps to NM_016445.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:67859504 C>T maps to NM_016445.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:57755823 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:57755823 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:17476328 C>A maps to NM_031310.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:17476328 C>A maps to NM_031310.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:131825443 C>A maps to NM_020911.1 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:131825443 C>A maps to NM_020911.1 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:55894184 C>A maps to NM_033109.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:55894184 C>A maps to NM_033109.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:121230732 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:121230732 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:130832809 C>A maps to NM_001099771.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:130832809 C>A maps to NM_001099771.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:19566062 T>C maps to NM_001005356.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:19566062 T>C maps to NM_001005356.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287852 G>T maps to NM_001136213.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287852 G>T maps to NM_001136213.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:102503827 C>A maps to ENST00000451606 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:102503827 C>A maps to ENST00000451606 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:202391828 C>T maps to ENST00000367270 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:202391828 C>T maps to ENST00000367270 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:148575241 C>A maps to NM_138364.2 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:148575241 C>A maps to NM_138364.2 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:58314358 G>T maps to NM_001080492.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:58314358 G>T maps to NM_001080492.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:79002162 C>A maps to NM_000959.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:79002162 C>A maps to NM_000959.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:100146993 T>C maps to NM_032709.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:100146993 T>C maps to NM_032709.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:56385938 G>T maps to NM_002868.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:56385938 G>T maps to NM_002868.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:25542752 C>T maps to NM_000965.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:25542752 C>T maps to NM_000965.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:155749035 C>A maps to NM_144979.3 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:155749035 C>A maps to NM_144979.3 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55568078 C>A maps to NM_001145971.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55568078 C>A maps to NM_001145971.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57351014 C>A maps to NM_003708.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57351014 C>A maps to NM_003708.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:73657141 C>T maps to NM_004259.5 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:73657141 C>T maps to NM_004259.5 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79314056 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79314056 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:116276912 G>T maps to NM_144488.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:116276912 G>T maps to NM_144488.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240969526 G>T maps to ENST00000407727 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240969526 G>T maps to ENST00000407727 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:5339539 C>A maps to NM_006911.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:5339539 C>A maps to NM_006911.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:237993831 C>T maps to NM_001035.2 T4886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:237993831 C>T maps to NM_001035.2 T4886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:200246528 C>A maps to NM_001172509.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:200246528 C>A maps to NM_001172509.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:78173883 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:78173883 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156146367 C>T maps to NM_022367.3 Y622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156146367 C>T maps to NM_022367.3 Y622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94914724 G>T maps to NM_001080451.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94914724 G>T maps to NM_001080451.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:42531801 A>T maps to NM_015559.2 R833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:42531801 A>T maps to NM_015559.2 R833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:92364057 C>A maps to NM_134266.1 C387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:92364057 C>A maps to NM_134266.1 C387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:1479965 G>A maps to ENST00000382147 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:1479965 G>A maps to ENST00000382147 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:108136901 C>A maps to NM_080546.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:108136901 C>A maps to NM_080546.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:70617324 T>C maps to NM_030958.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:70617324 T>C maps to NM_030958.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:168187880 G>T maps to NM_003062.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:168187880 G>T maps to NM_003062.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:64404770 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:64404770 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:231065681 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:231065681 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:123594256 G>A maps to NM_001174046.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:123594256 G>A maps to NM_001174046.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:74464372 G>A maps to NM_001164380.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:74464372 G>A maps to NM_001164380.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:23802538 G>A maps to NM_031414.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:23802538 G>A maps to NM_031414.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120957868 T>A maps to NM_014980.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120957868 T>A maps to NM_014980.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:11183829 C>A maps to NM_176885.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:11183829 C>A maps to NM_176885.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:38037261 G>C maps to NM_015173.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:38037261 G>C maps to NM_015173.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:141590958 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:141590958 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:44554580 G>A maps to NM_145653.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:44554580 G>A maps to NM_145653.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:31129473 C>T maps to NM_007109.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:31129473 C>T maps to NM_007109.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:52942960 A>T maps to ENST00000398339 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:52942960 A>T maps to ENST00000398339 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:31018993 C>G maps to NM_000355.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:31018993 C>G maps to NM_000355.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:61057958 G>T maps to NM_001146070.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:61057958 G>T maps to NM_001146070.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:30703266 C>A maps to NM_031271.3 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:30703266 C>A maps to NM_031271.3 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:71220882 T>G maps to NM_144582.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:71220882 T>G maps to NM_144582.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:117969813 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:117969813 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:1953726 G>T maps to ENST00000397301 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:1953726 G>T maps to ENST00000397301 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175053003 A>T maps to NM_022093.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175053003 A>T maps to NM_022093.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175299341 G>A maps to NM_003285.2 Q1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175299341 G>A maps to NM_003285.2 Q1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:6328618 C>G maps to NM_033516.5 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:6328618 C>G maps to NM_033516.5 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:18051102 A>G maps to ENST00000341556 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:18051102 A>G maps to ENST00000341556 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:103301781 A>T maps to ENST00000376052 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:103301781 A>T maps to ENST00000376052 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10933879 G>T maps to NM_199261.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10933879 G>T maps to NM_199261.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10951374 G>A maps to NM_199261.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10951374 G>A maps to NM_199261.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110099839 C>T maps to NM_003301.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110099839 C>T maps to NM_003301.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57128684 G>A maps to NM_015294.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57128684 G>A maps to NM_015294.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:16321155 C>G maps to NM_016113.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:16321155 C>G maps to NM_016113.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:150128498 G>T maps to NM_014779.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:150128498 G>T maps to NM_014779.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76507337 G>A maps to NM_015516.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76507337 G>A maps to NM_015516.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:67860158 C>A maps to ENST00000339830 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:67860158 C>A maps to ENST00000339830 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179440901 G>A maps to NM_133378.4 I20751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179440901 G>A maps to NM_133378.4 I20751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179440973 G>A maps to NM_133378.4 A20727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179440973 G>A maps to NM_133378.4 A20727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:88924512 C>A maps to NM_000372.4 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:88924512 C>A maps to NM_000372.4 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154223999 C>G maps to NM_014847.3 S512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154223999 C>G maps to NM_014847.3 S512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:42600432 G>A maps to NM_015255.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:42600432 G>A maps to NM_015255.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:124453974 A>T maps to NM_000373.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:124453974 A>T maps to NM_000373.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:215901707 T>C maps to ENST00000366943 E3910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:215901707 T>C maps to ENST00000366943 E3910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:215972390 C>A maps to ENST00000366943 P3272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:215972390 C>A maps to ENST00000366943 P3272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:216498838 C>A maps to ENST00000366943 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:216498838 C>A maps to ENST00000366943 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57642508 C>A maps to NM_020903.2 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57642508 C>A maps to NM_020903.2 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:82837227 C>A maps to NM_004385.4 S2802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:82837227 C>A maps to NM_004385.4 S2802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35062998 C>A maps to NM_007126.3 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35062998 C>A maps to NM_007126.3 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:108641766 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:108641766 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:39227261 G>T maps to NM_194293.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:39227261 G>T maps to NM_194293.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:114069769 G>A maps to NM_001164342.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:114069769 G>A maps to NM_001164342.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:144621344 G>A maps to NM_015117.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:144621344 G>A maps to NM_015117.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:77765474 T>G maps to NM_024721.4 S2106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:77765474 T>G maps to NM_024721.4 S2106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57646287 A>G maps to NM_052882.1 *473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57646287 A>G maps to NM_052882.1 *473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:44933602 G>A maps to NM_014518.2 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:44933602 G>A maps to NM_014518.2 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:133768116 G>T maps to NM_001165881.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:133768116 G>T maps to NM_001165881.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:22805772 G>A maps to NM_015461.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:22805772 G>A maps to NM_015461.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56586481 C>T maps to NM_018181.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56586481 C>T maps to NM_018181.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:30934951 G>T maps to NM_014717.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:30934951 G>T maps to NM_014717.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:53747150 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:53747150 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:35344012 A>G maps to NM_012138.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:35344012 A>G maps to NM_012138.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr13:32972776 C>G maps to NM_000059.3 S3376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr13:32972776 C>G maps to NM_000059.3 S3376*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-3919-01A-02D-1458-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-44-3919-01A-02D-1458-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:19839363 C>A maps to NM_024627.5 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:19839363 C>A maps to NM_024627.5 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:165878523 C>G maps to NM_153027.1 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:165878523 C>G maps to NM_153027.1 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:109027920 G>A maps to NM_138815.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:109027920 G>A maps to NM_138815.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:58001193 C>A maps to NM_178502.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:58001193 C>A maps to NM_178502.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr15:49776610 T>G maps to NM_002009.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr15:49776610 T>G maps to NM_002009.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:76063271 C>T maps to NM_015687.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:76063271 C>T maps to NM_015687.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:48636352 A>C maps to NM_015030.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:48636352 A>C maps to NM_015030.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:227921231 G>C maps to NM_023007.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:227921231 G>C maps to NM_023007.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:29816618 T>C maps to NM_007317.1 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:29816618 T>C maps to NM_007317.1 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr21:46057393 C>T maps to NM_181688.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr21:46057393 C>T maps to NM_181688.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:140641169 C>G maps to ENST00000509479 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:140641169 C>G maps to ENST00000509479 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr18:70416304 A>G maps to NM_153181.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr18:70416304 A>G maps to NM_153181.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:140581560 C>T maps to NM_018931.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:140581560 C>T maps to NM_018931.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:16267026 G>C maps to NM_001136213.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:16267026 G>C maps to NM_001136213.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:171765852 C>T maps to NM_001017995.2 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:171765852 C>T maps to NM_001017995.2 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:37462202 G>A maps to ENST00000381792 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:37462202 G>A maps to ENST00000381792 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:113120481 G>A maps to NM_001164496.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:113120481 G>A maps to NM_001164496.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:48550738 A>T maps to NM_152701.3 T4528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:48550738 A>T maps to NM_152701.3 T4528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:183667662 C>A maps to NM_005688.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:183667662 C>A maps to NM_005688.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:8418164 C>T maps to NM_003501.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:8418164 C>T maps to NM_003501.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:39581360 C>A maps to NM_014237.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:39581360 C>A maps to NM_014237.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3654110 G>T maps to NM_025220.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3654110 G>T maps to NM_025220.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:178770884 C>T maps to NM_014244.4 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:178770884 C>T maps to NM_014244.4 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:203134619 C>T maps to NM_001048230.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:203134619 C>T maps to NM_001048230.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:434429 G>A maps to NM_020731.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:434429 G>A maps to NM_020731.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:186335057 G>C maps to ENST00000273784 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:186335057 G>C maps to ENST00000273784 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:11188890 C>T maps to NM_054028.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:11188890 C>T maps to NM_054028.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:41581078 C>A maps to ENST00000415018 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:41581078 C>A maps to ENST00000415018 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:58465265 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:58465265 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:1403795 G>C maps to NM_001039211.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:1403795 G>C maps to NM_001039211.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:1396021 G>T maps to NM_003933.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:1396021 G>T maps to NM_003933.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:76740021 C>G maps to NM_024685.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:76740021 C>G maps to NM_024685.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:22487493 C>A maps to NM_018688.4 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:22487493 C>A maps to NM_018688.4 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:69098253 C>A maps to NM_014482.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:69098253 C>A maps to NM_014482.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:11908753 G>A maps to NM_153256.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:11908753 G>A maps to NM_153256.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:23468205 G>A maps to NM_021944.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:23468205 G>A maps to NM_021944.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:61576188 C>T maps to NM_017896.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:61576188 C>T maps to NM_017896.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3234370 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3234370 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:135602878 C>T maps to NM_152572.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:135602878 C>T maps to NM_152572.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:49142168 G>T maps to NM_001217.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:49142168 G>T maps to NM_001217.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:54913115 G>T maps to NM_018398.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:54913115 G>T maps to NM_018398.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54445372 C>T maps to NM_031896.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54445372 C>T maps to NM_031896.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:138713800 C>A maps to ENST00000409386 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:138713800 C>A maps to ENST00000409386 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:50801306 A>G maps to NM_004196.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:50801306 A>G maps to NM_004196.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:6709106 C>A maps to ENST00000309577 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:6709106 C>A maps to ENST00000309577 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:40042044 C>T maps to NM_032221.3 E2350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:40042044 C>T maps to NM_032221.3 E2350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:71571551 C>A maps to NM_001166395.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:71571551 C>A maps to NM_001166395.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:87012867 C>A maps to ENST00000263723 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:87012867 C>A maps to ENST00000263723 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:22208544 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:22208544 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:147914551 C>G maps to NM_014141.5 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:147914551 C>G maps to NM_014141.5 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:111130347 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:111130347 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113421166 G>T maps to NM_198123.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113421166 G>T maps to NM_198123.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113657363 C>T maps to NM_198123.1 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113657363 C>T maps to NM_198123.1 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:16025584 G>T maps to NM_021187.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:16025584 G>T maps to NM_021187.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:50923678 C>A maps to NM_005215.3 S897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:50923678 C>A maps to NM_005215.3 S897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:32487950 G>A maps to NM_014314.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:32487950 G>A maps to NM_014314.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:50016256 G>T maps to NM_001037498.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:50016256 G>T maps to NM_001037498.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:88583969 C>G maps to NM_004407.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:88583969 C>G maps to NM_004407.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:13820608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:13820608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:196718075 G>T maps to NM_018897.2 T2924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:196718075 G>T maps to NM_018897.2 T2924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:7585489 G>T maps to NM_004415.2 T2665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:7585489 G>T maps to NM_004415.2 T2665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:58949494 A>T maps to NM_015177.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:58949494 A>T maps to NM_015177.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:101183241 T>G maps to ENST00000397927 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:101183241 T>G maps to ENST00000397927 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:89391034 G>T maps to NM_005233.5 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:89391034 G>T maps to NM_005233.5 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:29867329 C>A maps to ENST00000269209 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:29867329 C>A maps to ENST00000269209 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3128051 T>A maps to NM_021826.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3128051 T>A maps to NM_021826.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:97052765 C>T maps to NM_020482.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:97052765 C>T maps to NM_020482.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:153588256 G>C maps to NM_001110556.1 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:153588256 G>C maps to NM_001110556.1 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:43320573 C>A maps to NM_005892.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:43320573 C>A maps to NM_005892.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:169533119 C>G maps to NM_012188.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:169533119 C>G maps to NM_012188.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:44974150 A>T maps to NM_032135.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:44974150 A>T maps to NM_032135.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:44976030 C>A maps to NM_032135.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:44976030 C>A maps to NM_032135.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:71318652 C>A maps to NM_018348.5 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:71318652 C>A maps to NM_018348.5 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:27910596 C>A maps to NM_001085454.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:27910596 C>A maps to NM_001085454.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:64067495 T>A maps to ENST00000261887 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:64067495 T>A maps to ENST00000261887 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:143081589 G>A maps to NM_006734.3 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:143081589 G>A maps to NM_006734.3 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:162909665 C>T maps to NM_001142556.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:162909665 C>T maps to NM_001142556.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:173491285 A>T maps to NM_015980.3 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:173491285 A>T maps to NM_015980.3 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:18301446 G>C maps to NM_181507.1 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:18301446 G>C maps to NM_181507.1 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:21976734 C>G maps to NM_005144.4 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:21976734 C>G maps to NM_005144.4 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:102964543 T>A maps to NM_016232.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:102964543 T>A maps to NM_016232.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:33067497 A>T maps to ENST00000262650 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:33067497 A>T maps to ENST00000262650 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:52211397 G>T maps to NM_181501.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:52211397 G>T maps to NM_181501.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:48835305 C>T maps to NM_021999.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:48835305 C>T maps to NM_021999.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:36694373 G>T maps to NM_001031836.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:36694373 G>T maps to NM_001031836.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:55961742 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:55961742 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:30317503 G>A maps to NM_020848.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:30317503 G>A maps to NM_020848.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:39761734 C>A maps to ENST00000395670 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:39761734 C>A maps to ENST00000395670 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:129649484 C>G maps to NM_000426.3 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:129649484 C>G maps to NM_000426.3 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:28996610 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:28996610 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55107392 G>C maps to NM_006863.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55107392 G>C maps to NM_006863.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:68857482 G>T maps to NM_178011.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:68857482 G>T maps to NM_178011.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:34264777 G>A maps to NM_020426.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:34264777 G>A maps to NM_020426.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:151101921 G>A maps to NM_053002.4 T1579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:151101921 G>A maps to NM_053002.4 T1579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:131937142 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:131937142 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:5011854 G>A maps to NM_021801.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:5011854 G>A maps to NM_021801.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:62929425 C>T maps to ENST00000393630 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:62929425 C>T maps to ENST00000393630 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:108819262 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:108819262 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:30066846 G>C maps to NM_001033602.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:30066846 G>C maps to NM_001033602.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:9071875 A>G maps to NM_024690.2 P5190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:9071875 A>G maps to NM_024690.2 P5190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9012893 A>T maps to NM_024690.2 A12850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9012893 A>T maps to NM_024690.2 A12850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:207003265 C>A maps to ENST00000455934 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:207003265 C>A maps to ENST00000455934 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr22:29886352 G>A maps to NM_021076.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr22:29886352 G>A maps to NM_021076.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:101093866 T>A maps to NM_001011717.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:101093866 T>A maps to NM_001011717.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:28230274 C>A maps to NM_000275.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:28230274 C>A maps to NM_000275.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:107288800 C>T maps to NM_001001919.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:107288800 C>T maps to NM_001001919.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:29012091 C>A maps to NM_030903.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:29012091 C>A maps to NM_030903.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:56344906 G>T maps to NM_001004741.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:56344906 G>T maps to NM_001004741.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:124294272 C>A maps to NM_001005196.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:124294272 C>A maps to NM_001005196.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:56128507 C>A maps to NM_001005205.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:56128507 C>A maps to NM_001005205.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3869921 C>T maps to NM_153638.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3869921 C>T maps to NM_153638.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140502029 A>G maps to NM_018938.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140502029 A>G maps to NM_018938.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140812209 G>T maps to NM_003735.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140812209 G>T maps to NM_003735.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140731095 G>A maps to NM_018922.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140731095 G>A maps to NM_018922.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140799010 G>T maps to NM_018927.2 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140799010 G>T maps to NM_018927.2 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:71413832 G>T maps to NM_014982.2 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:71413832 G>T maps to NM_014982.2 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:153303329 C>A maps to NM_020393.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:153303329 C>A maps to NM_020393.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:20416374 C>A maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:20416374 C>A maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:8862494 G>C maps to NM_015192.2 *1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:8862494 G>C maps to NM_015192.2 *1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:202406947 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:202406947 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:48775079 C>A maps to NM_006904.6 E1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:48775079 C>A maps to NM_006904.6 E1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:125145834 G>T maps to NM_000962.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:125145834 G>T maps to NM_000962.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:157997860 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:157997860 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:9333632 A>T maps to NM_002864.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:9333632 A>T maps to NM_002864.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:47028849 G>T maps to NM_005676.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:47028849 G>T maps to NM_005676.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:10468145 C>A maps to NM_178857.5 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:10468145 C>A maps to NM_178857.5 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:60072160 C>A maps to NM_021136.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:60072160 C>A maps to NM_021136.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:25291041 G>A maps to NM_001031680.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:25291041 G>A maps to NM_001031680.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:33937085 C>A maps to NM_016568.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:33937085 C>A maps to NM_016568.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:166258948 A>T maps to NM_006745.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:166258948 A>T maps to NM_006745.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:35212535 A>G maps to ENST00000394681 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:35212535 A>G maps to ENST00000394681 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:71397870 G>A maps to NM_001144952.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:71397870 G>A maps to NM_001144952.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:74707190 C>T maps to NM_003612.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:74707190 C>T maps to NM_003612.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:185341816 A>T maps to ENST00000427465 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:185341816 A>T maps to ENST00000427465 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:146247375 T>A maps to ENST00000367503 I1095I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:146247375 T>A maps to ENST00000367503 I1095I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:117058368 T>A maps to NM_001040455.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:117058368 T>A maps to NM_001040455.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:46247979 G>A maps to NM_003726.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:46247979 G>A maps to NM_003726.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:160604514 G>T maps to NM_003037.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:160604514 G>T maps to NM_003037.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:43217059 C>T maps to NM_007163.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:43217059 C>T maps to NM_007163.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:19674053 C>A maps to NM_020689.3 Y492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:19674053 C>A maps to NM_020689.3 Y492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:170216487 C>A maps to NM_020949.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:170216487 C>A maps to NM_020949.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:33687260 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:33687260 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:2698037 A>T maps to NM_015295.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:2698037 A>T maps to NM_015295.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:130910223 C>T maps to NM_017951.4 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:130910223 C>T maps to NM_017951.4 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:118539079 G>A maps to NM_206996.2 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:118539079 G>A maps to NM_206996.2 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:2818262 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:2818262 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:132938807 G>T maps to NM_001033080.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:132938807 G>T maps to NM_001033080.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:27372189 A>T maps to NM_175769.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:27372189 A>T maps to NM_175769.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:71216144 G>A maps to NM_144582.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:71216144 G>A maps to NM_144582.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:89177107 G>T maps to NM_138960.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:89177107 G>T maps to NM_138960.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:20748249 T>A maps to ENST00000431224 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:20748249 T>A maps to ENST00000431224 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:2597906 G>A maps to NM_080751.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:2597906 G>A maps to NM_080751.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:130762208 G>T maps to NM_052913.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:130762208 G>T maps to NM_052913.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:29924384 A>G maps to NM_016127.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:29924384 A>G maps to NM_016127.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:88589424 A>T maps to NM_181783.3 *915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:88589424 A>T maps to NM_181783.3 *915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:175067546 C>G maps to NM_022093.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:175067546 C>G maps to NM_022093.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:42695473 G>T maps to ENST00000348077 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:42695473 G>T maps to ENST00000348077 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:116430677 C>T maps to NM_014112.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:116430677 C>T maps to NM_014112.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:116631412 C>A maps to NM_014112.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:116631412 C>A maps to NM_014112.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:2337895 C>A maps to NM_139022.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:2337895 C>A maps to NM_139022.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:10238754 A>T maps to NM_001105562.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:10238754 A>T maps to NM_001105562.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:176306802 C>T maps to NM_133369.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:176306802 C>T maps to NM_133369.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:18968169 G>C maps to ENST00000418384 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:18968169 G>C maps to ENST00000418384 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:113699990 A>T maps to NM_020886.2 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:113699990 A>T maps to NM_020886.2 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:82785998 T>A maps to NM_004385.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:82785998 T>A maps to NM_004385.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:48238558 C>A maps to NM_001017535.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:48238558 C>A maps to NM_001017535.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:37000952 C>T maps to NM_053276.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:37000952 C>T maps to NM_053276.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:1640948 A>T maps to NM_001163809.1 S1932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:1640948 A>T maps to NM_001163809.1 S1932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:17228385 G>A maps to NM_022166.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:17228385 G>A maps to NM_022166.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:82615027 T>A maps to NM_024699.2 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:82615027 T>A maps to NM_024699.2 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:58579297 C>A maps to NM_007134.1 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:58579297 C>A maps to NM_007134.1 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:71482342 C>A maps to NM_145911.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:71482342 C>A maps to NM_145911.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53311269 C>A maps to NM_006969.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53311269 C>A maps to NM_006969.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:57529051 C>A maps to NM_001159279.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:57529051 C>A maps to NM_001159279.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:5237116 G>T maps to NM_139056.2 G687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:5237116 G>T maps to NM_139056.2 G687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:113348781 C>T maps to NM_025144.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:113348781 C>T maps to NM_025144.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:122953874 G>A maps to NM_024769.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:122953874 G>A maps to NM_024769.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:24922492 C>G maps to NM_018958.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:24922492 C>G maps to NM_018958.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:80159586 G>A maps to ENST00000445854 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:80159586 G>A maps to ENST00000445854 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:73569656 C>T maps to ENST00000398860 R2940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:73569656 C>T maps to ENST00000398860 R2940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:34355793 C>A maps to NM_012125.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:34355793 C>A maps to NM_012125.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:147336252 C>T maps to NM_014141.5 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:147336252 C>T maps to NM_014141.5 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:103540212 C>T maps to NM_080629.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:103540212 C>T maps to NM_080629.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:28791657 C>T maps to NM_001304.4 C1323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:28791657 C>T maps to NM_001304.4 C1323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:113657408 G>T maps to NM_198123.1 S1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:113657408 G>T maps to NM_198123.1 S1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:115200394 C>T maps to NM_020868.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:115200394 C>T maps to NM_020868.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:48687961 C>A maps to NM_181532.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:48687961 C>A maps to NM_181532.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:34174787 C>A maps to NM_025135.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:34174787 C>A maps to NM_025135.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:56688494 C>T maps to NM_033106.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:56688494 C>T maps to NM_033106.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:11750921 G>A maps to NM_014668.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:11750921 G>A maps to NM_014668.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:58127024 C>T maps to NM_022070.4 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:58127024 C>T maps to NM_022070.4 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118451918 C>T maps to NM_025015.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118451918 C>T maps to NM_025015.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:24447963 G>A maps to NM_021258.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:24447963 G>A maps to NM_021258.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:15689004 T>C maps to NM_003638.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:15689004 T>C maps to NM_003638.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:24533249 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:24533249 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:30033076 G>T maps to NM_002233.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:30033076 G>T maps to NM_002233.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:55331432 A>T maps to ENST00000355608 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:55331432 A>T maps to ENST00000355608 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:70371026 G>T maps to NM_020866.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:70371026 G>T maps to NM_020866.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:123067517 A>G maps to NM_014708.4 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:123067517 A>G maps to NM_014708.4 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:88441311 C>T maps to NM_001171610.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:88441311 C>T maps to NM_001171610.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:7964660 G>A maps to NM_025061.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:7964660 G>A maps to NM_025061.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:101567856 C>T maps to NM_024652.3 Y847Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:101567856 C>T maps to NM_024652.3 Y847Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:160636570 C>T maps to NM_001198759.1 W1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:160636570 C>T maps to NM_001198759.1 W1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:100395746 G>A maps to NM_032503.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:100395746 G>A maps to NM_032503.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:3294566 A>G maps to NM_000243.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:3294566 A>G maps to NM_000243.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:41894956 C>A maps to NM_024561.4 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:41894956 C>A maps to NM_024561.4 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:89891356 C>T maps to NM_005467.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:89891356 C>T maps to NM_005467.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66189681 A>C maps to NM_178864.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66189681 A>C maps to NM_178864.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:158576833 C>T maps to NM_001004478.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:158576833 C>T maps to NM_001004478.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:22369132 G>T maps to NM_001004719.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:22369132 G>T maps to NM_001004719.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:18329146 G>A maps to NM_000923.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:18329146 G>A maps to NM_000923.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:123626343 C>T maps to NM_015651.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:123626343 C>T maps to NM_015651.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:17124379 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:17124379 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:134364900 G>T maps to NM_002653.4 Y171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:134364900 G>T maps to NM_002653.4 Y171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118231352 C>A maps to NM_001011709.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118231352 C>A maps to NM_001011709.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:1994858 C>T maps to NM_005061.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:1994858 C>T maps to NM_005061.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:78811790 G>A maps to NM_020761.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:78811790 G>A maps to NM_020761.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:2234505 C>T maps to NM_003036.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:2234505 C>T maps to NM_003036.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:22364897 C>T maps to NM_020346.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:22364897 C>T maps to NM_020346.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:108700188 T>C maps to NM_013386.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:108700188 T>C maps to NM_013386.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:98799805 G>A maps to NM_003061.2 R746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:98799805 G>A maps to NM_003061.2 R746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:30053373 G>A maps to NM_003257.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:30053373 G>A maps to NM_003257.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:12186059 C>T maps to NM_001243.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:12186059 C>T maps to NM_001243.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:47062564 G>T maps to NM_153280.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:47062564 G>T maps to NM_153280.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:177077245 C>A maps to NM_170710.4 S850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:177077245 C>A maps to NM_170710.4 S850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:20411848 T>A maps to NM_001142684.1 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:20411848 T>A maps to NM_001142684.1 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:62298186 G>C maps to NM_001620.1 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:62298186 G>C maps to NM_001620.1 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr15:50211113 G>A maps to NM_024837.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr15:50211113 G>A maps to NM_024837.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr4:56830456 A>C maps to NM_025009.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr4:56830456 A>C maps to NM_025009.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:49178266 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:49178266 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:62455858 T>A maps to NM_176877.2 Y1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:62455858 T>A maps to NM_176877.2 Y1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:50167984 A>G maps to NM_001571.5 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:50167984 A>G maps to NM_001571.5 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:38260315 C>G maps to NM_001113482.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:38260315 C>G maps to NM_001113482.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:58165039 G>A maps to ENST00000408972 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:58165039 G>A maps to ENST00000408972 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:21083677 C>G maps to NM_058004.2 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:21083677 C>G maps to NM_058004.2 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:38592972 T>A maps to NM_001099404.1 I1630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:38592972 T>A maps to NM_001099404.1 I1630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:54701405 G>T maps to NM_015360.4 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:54701405 G>T maps to NM_015360.4 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:19786258 G>A maps to NM_020344.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:19786258 G>A maps to NM_020344.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chrX:153553708 C>T maps to NM_012253.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chrX:153553708 C>T maps to NM_012253.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr17:7573966 G>A maps to NM_001126112.1 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr17:7573966 G>A maps to NM_001126112.1 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr7:44806174 G>A maps to NM_031449.3 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr7:44806174 G>A maps to NM_031449.3 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:2338147 G>A maps to NM_001089.2 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:2338147 G>A maps to NM_001089.2 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97506535 A>G maps to NM_144994.7 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97506535 A>G maps to NM_144994.7 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:25264845 A>C maps to NM_001185085.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:25264845 A>C maps to NM_001185085.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:90642500 G>A maps to NM_001170794.1 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:90642500 G>A maps to NM_001170794.1 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:96730466 C>A maps to NM_000710.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:96730466 C>A maps to NM_000710.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54417827 G>T maps to NM_031896.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54417827 G>T maps to NM_031896.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:30888022 C>A maps to NM_001002259.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:30888022 C>A maps to NM_001002259.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:160163609 T>C maps to NM_001231.4 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:160163609 T>C maps to NM_001231.4 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:135947048 C>A maps to NM_001807.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:135947048 C>A maps to NM_001807.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:121215954 A>G maps to NM_021110.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:121215954 A>G maps to NM_021110.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:211507347 G>T maps to NM_001122633.1 E1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:211507347 G>T maps to NM_001122633.1 E1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:2944742 C>T maps to NM_033225.5 A2450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:2944742 C>T maps to NM_033225.5 A2450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:113599347 C>A maps to NM_198123.1 G1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:113599347 C>A maps to NM_198123.1 G1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:74117808 G>A maps to NM_018665.2 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:74117808 G>A maps to NM_018665.2 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:9228270 T>A maps to NM_015213.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:9228270 T>A maps to NM_015213.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:83183790 C>A maps to NM_001142699.1 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:83183790 C>A maps to NM_001142699.1 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:63128797 C>A maps to ENST00000371140 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:63128797 C>A maps to ENST00000371140 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:231509812 C>A maps to NM_022051.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:231509812 C>A maps to NM_022051.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:156590417 C>T maps to NM_130899.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:156590417 C>T maps to NM_130899.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:43628677 C>A maps to NM_001145196.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:43628677 C>A maps to NM_001145196.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:48800777 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:48800777 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:71797820 C>T maps to NM_001142958.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:71797820 C>T maps to NM_001142958.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:157737279 G>A maps to NM_030764.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:157737279 G>A maps to NM_030764.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:52272882 C>A maps to NM_001005738.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:52272882 C>A maps to NM_001005738.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:74525009 C>A maps to NM_012201.5 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:74525009 C>A maps to NM_012201.5 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:100693000 C>A maps to NM_018437.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:100693000 C>A maps to NM_018437.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:27799269 G>T maps to NM_003541.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:27799269 G>T maps to NM_003541.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:82950158 C>A maps to NM_015525.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:82950158 C>A maps to NM_015525.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:68595651 A>T maps to NM_018402.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:68595651 A>T maps to NM_018402.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201839916 G>A maps to NM_018085.4 E780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201839916 G>A maps to NM_018085.4 E780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:41231330 T>G maps to NM_025194.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:41231330 T>G maps to NM_025194.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:78844414 C>T maps to NM_001161352.1 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:78844414 C>T maps to NM_001161352.1 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:67013472 A>T maps to NM_012308.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:67013472 A>T maps to NM_012308.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:137759900 G>T maps to NM_016604.3 V1370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:137759900 G>T maps to NM_016604.3 V1370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:75552465 A>T maps to NM_015037.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:75552465 A>T maps to NM_015037.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:70681366 A>G maps to NM_020866.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:70681366 A>G maps to NM_020866.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:133942410 C>A maps to ENST00000355048 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:133942410 C>A maps to ENST00000355048 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:74976010 C>A maps to NM_000428.2 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:74976010 C>A maps to NM_000428.2 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:112786011 C>G maps to NM_006343.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:112786011 C>G maps to NM_006343.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:135076255 C>T maps to NM_002410.3 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:135076255 C>T maps to NM_002410.3 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:102482489 A>G maps to NM_004771.3 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:102482489 A>G maps to NM_004771.3 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:105449934 A>G maps to NM_001171020.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:105449934 A>G maps to NM_001171020.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:69948774 G>T maps to NM_032578.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:69948774 G>T maps to NM_032578.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:164087831 G>A maps to NM_138386.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:164087831 G>A maps to NM_138386.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:61554014 A>T maps to NM_001145512.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:61554014 A>T maps to NM_001145512.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:117715774 G>A maps to ENST00000338101 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:117715774 G>A maps to ENST00000338101 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:102334542 A>G maps to NM_022052.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:102334542 A>G maps to NM_022052.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:228402004 G>T maps to NM_001098623.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:228402004 G>T maps to NM_001098623.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:3101508 C>T maps to NM_012352.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:3101508 C>T maps to NM_012352.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:55579751 T>A maps to NM_001004738.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:55579751 T>A maps to NM_001004738.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:3114833 C>T maps to NM_020896.3 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:3114833 C>T maps to NM_020896.3 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:47204065 G>A maps to NM_016223.4 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:47204065 G>A maps to NM_016223.4 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:31890286 G>A maps to NM_001191057.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:31890286 G>A maps to NM_001191057.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:144994079 C>A maps to NM_201380.2 L3440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:144994079 C>A maps to NM_201380.2 L3440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:102494992 T>A maps to ENST00000451606 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:102494992 T>A maps to ENST00000451606 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:24046815 C>T maps to NM_002738.6 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:24046815 C>T maps to NM_002738.6 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:130799843 G>A maps to ENST00000514667 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:130799843 G>A maps to ENST00000514667 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:108475846 G>T maps to NM_182588.2 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:108475846 G>T maps to NM_182588.2 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:152128886 G>T maps to NM_001122965.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:152128886 G>T maps to NM_001122965.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:237777894 A>T maps to NM_001035.2 K1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:237777894 A>T maps to NM_001035.2 K1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:166897827 G>T maps to NM_001165963.1 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:166897827 G>T maps to NM_001165963.1 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:232650755 G>A maps to NM_020808.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:232650755 G>A maps to NM_020808.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:48512829 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:48512829 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:20629073 C>A maps to NM_004211.3 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:20629073 C>A maps to NM_004211.3 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:86369929 T>C maps to NM_032229.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:86369929 T>C maps to NM_032229.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:38019713 T>C maps to NM_024700.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:38019713 T>C maps to NM_024700.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:97327388 G>A maps to NM_173499.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:97327388 G>A maps to NM_173499.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:179247950 C>A maps to NM_003900.4 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:179247950 C>A maps to NM_003900.4 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:1218446 A>T maps to NM_000455.4 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:1218446 A>T maps to NM_000455.4 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:152792794 C>A maps to NM_182961.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:152792794 C>A maps to NM_182961.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48876781 C>T maps to NM_012451.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48876781 C>T maps to NM_012451.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:114682355 G>T maps to ENST00000369545 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:114682355 G>T maps to ENST00000369545 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:77918563 G>C maps to NM_020927.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:77918563 G>C maps to NM_020927.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:39229100 T>A maps to NM_194293.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:39229100 T>A maps to NM_194293.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:64168598 A>T maps to NM_016220.3 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:64168598 A>T maps to NM_016220.3 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:151474790 T>C maps to NM_207365.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:151474790 T>C maps to NM_207365.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:9257678 G>T maps to NM_015208.3 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:9257678 G>T maps to NM_015208.3 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:77133994 G>T maps to NM_198531.3 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:77133994 G>T maps to NM_198531.3 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:379987 G>T maps to NM_178537.4 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:379987 G>T maps to NM_178537.4 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:136597525 T>C maps to NM_014739.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:136597525 T>C maps to NM_014739.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55805584 C>A maps to NM_032430.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55805584 C>A maps to NM_032430.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:43796478 G>T maps to NM_145055.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:43796478 G>T maps to NM_145055.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:150027588 A>G maps to NM_138434.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:150027588 A>G maps to NM_138434.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:135447818 G>A maps to NM_207417.1 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:135447818 G>A maps to NM_207417.1 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:58234888 A>T maps to NM_000717.3 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:58234888 A>T maps to NM_000717.3 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:31294066 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:31294066 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:30198004 C>T maps to NM_007074.3 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:30198004 C>T maps to NM_007074.3 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:111782352 C>A maps to NM_001885.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:111782352 C>A maps to NM_001885.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:49281192 G>T maps to NM_020377.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:49281192 G>T maps to NM_020377.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:122075576 T>A maps to NM_014618.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:122075576 T>A maps to NM_014618.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:176887644 C>T maps to ENST00000393565 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:176887644 C>T maps to ENST00000393565 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:155226378 G>T maps to NM_017639.3 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:155226378 G>T maps to NM_017639.3 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:46398735 C>T maps to NM_001105540.1 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:46398735 C>T maps to NM_001105540.1 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:225710296 G>A maps to NM_014689.2 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:225710296 G>A maps to NM_014689.2 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:348144 C>T maps to ENST00000457386 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:348144 C>T maps to ENST00000457386 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:71753444 G>C maps to NM_001130987.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:71753444 G>C maps to NM_001130987.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:101090976 G>A maps to ENST00000397927 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:101090976 G>A maps to ENST00000397927 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:37746165 C>A maps to NM_014907.2 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:37746165 C>A maps to NM_014907.2 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:26806080 G>T maps to NM_021912.4 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:26806080 G>T maps to NM_021912.4 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:46086070 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:46086070 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:34072003 C>A maps to NM_139285.2 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:34072003 C>A maps to NM_139285.2 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:61958499 G>T maps to NM_002059.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:61958499 G>T maps to NM_002059.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:21661495 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:21661495 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:40366980 G>T maps to NM_004810.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:40366980 G>T maps to NM_004810.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:27135408 C>A maps to NM_005522.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:27135408 C>A maps to NM_005522.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:113820089 C>A maps to NM_173170.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:113820089 C>A maps to NM_173170.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:104440259 C>A maps to NM_017416.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:104440259 C>A maps to NM_017416.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:39788641 C>A maps to NM_172140.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:39788641 C>A maps to NM_172140.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:57850273 G>T maps to NM_031479.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:57850273 G>T maps to NM_031479.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:58941419 A>G maps to ENST00000354386 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:58941419 A>G maps to ENST00000354386 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:200960045 G>T maps to NM_017596.2 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:200960045 G>T maps to NM_017596.2 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:39034617 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:39034617 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:53096690 G>A maps to NM_175078.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:53096690 G>A maps to NM_175078.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55086240 G>C maps to NM_001130917.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55086240 G>C maps to NM_001130917.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54849249 G>T maps to NM_012276.3 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54849249 G>T maps to NM_012276.3 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:34652347 G>T maps to NM_153613.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:34652347 G>T maps to NM_153613.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:26751339 T>G maps to NM_052953.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:26751339 T>G maps to NM_052953.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:85518289 G>T maps to NM_001079910.1 E1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:85518289 G>T maps to NM_001079910.1 E1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:235918892 T>A maps to NM_000081.2 K2372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:235918892 T>A maps to NM_000081.2 K2372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:47530707 C>T maps to NM_001113498.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:47530707 C>T maps to NM_001113498.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:60754844 A>T maps to NM_006039.3 K684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:60754844 A>T maps to NM_006039.3 K684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:10543657 C>G maps to NM_002470.2 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:10543657 C>G maps to NM_002470.2 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:2057200 C>A maps to NM_003970.2 S1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:2057200 C>A maps to NM_003970.2 S1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:71303831 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:71303831 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:15358905 G>A maps to NM_015909.2 P2141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:15358905 G>A maps to NM_015909.2 P2141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:152551034 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:152551034 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:70451041 T>A maps to NM_153181.2 K246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:70451041 T>A maps to NM_153181.2 K246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:3452573 C>T maps to ENST00000269778 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:3452573 C>T maps to ENST00000269778 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:107871485 C>T maps to ENST00000379032 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:107871485 C>T maps to ENST00000379032 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:88679798 G>T maps to NM_001012338.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:88679798 G>T maps to NM_001012338.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:143657536 G>C maps to NM_012369.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:143657536 G>C maps to NM_012369.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:20443946 G>C maps to NM_001005486.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:20443946 G>C maps to NM_001005486.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:22383395 T>A maps to NM_001005241.1 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:22383395 T>A maps to NM_001005241.1 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:5410855 C>A maps to NM_001004756.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:5410855 C>A maps to NM_001004756.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:5776692 T>C maps to NM_001005175.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:5776692 T>C maps to NM_001005175.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:26689580 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:26689580 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:39660360 C>T maps to NM_005884.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:39660360 C>T maps to NM_005884.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:5534763 C>A maps to NM_025239.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:5534763 C>A maps to NM_025239.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:20522823 A>T maps to NM_000921.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:20522823 A>T maps to NM_000921.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:113812723 C>T maps to NM_173542.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:113812723 C>T maps to NM_173542.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:38143959 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:38143959 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:153535965 G>T maps to ENST00000410080 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:153535965 G>T maps to ENST00000410080 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:3018721 C>T maps to NM_002836.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:3018721 C>T maps to NM_002836.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:31426787 A>G maps to ENST00000373741 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:31426787 A>G maps to ENST00000373741 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:108086636 G>T maps to NM_007062.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:108086636 G>T maps to NM_007062.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:74288677 C>T maps to NM_032134.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:74288677 C>T maps to NM_032134.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:113557021 C>A maps to NM_001193520.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:113557021 C>A maps to NM_001193520.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:49243434 C>T maps to NM_017805.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:49243434 C>T maps to NM_017805.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:10468154 G>C maps to NM_178857.5 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:10468154 G>C maps to NM_178857.5 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:99144969 C>A maps to NM_015179.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:99144969 C>A maps to NM_015179.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:38621382 C>A maps to NM_015073.1 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:38621382 C>A maps to NM_015073.1 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:1617080 G>T maps to NM_018556.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:1617080 G>T maps to NM_018556.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:138713676 G>T maps to NM_152685.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:138713676 G>T maps to NM_152685.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:41486065 C>G maps to NM_144990.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:41486065 C>G maps to NM_144990.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:98799742 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:98799742 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:123950104 C>G maps to NM_180699.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:123950104 C>G maps to NM_180699.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:35753775 G>T maps to NM_024867.3 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:35753775 G>T maps to NM_024867.3 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:74383633 C>G maps to NM_182965.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:74383633 C>G maps to NM_182965.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:158592829 C>A maps to NM_003126.2 L2021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:158592829 C>A maps to NM_003126.2 L2021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:162274295 G>T maps to NM_006593.2 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:162274295 G>T maps to NM_006593.2 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:97852405 C>A maps to ENST00000379795 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:97852405 C>A maps to ENST00000379795 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:89177128 G>T maps to NM_138960.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:89177128 G>T maps to NM_138960.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:29670371 G>T maps to NM_001193451.1 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:29670371 G>T maps to NM_001193451.1 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:116698035 G>T maps to NM_139169.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:116698035 G>T maps to NM_139169.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:93407 G>T maps to NM_177987.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:93407 G>T maps to NM_177987.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:69962327 A>T maps to NM_001074.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:69962327 A>T maps to NM_001074.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:95927531 T>C maps to NM_032147.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:95927531 T>C maps to NM_032147.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:219294031 C>T maps to NM_007127.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:219294031 C>T maps to NM_007127.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:37032693 G>T maps to NM_053276.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:37032693 G>T maps to NM_053276.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:123349178 T>C maps to NM_003941.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:123349178 T>C maps to NM_003941.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:52941034 C>T maps to NM_001143939.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:52941034 C>T maps to NM_001143939.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:58196641 G>T maps to ENST00000356715 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:58196641 G>T maps to ENST00000356715 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:89293776 G>T maps to NM_182531.2 G333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:89293776 G>T maps to NM_182531.2 G333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:57765063 G>T maps to NM_001023563.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:57765063 G>T maps to NM_001023563.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr4:114253214 C>A maps to NM_001148.4 T1071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr4:114253214 C>A maps to NM_001148.4 T1071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:26903856 G>A maps to NM_016279.3 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:26903856 G>A maps to NM_016279.3 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:53564228 G>A maps to NM_015989.4 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:53564228 G>A maps to NM_015989.4 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:95131259 C>A maps to NM_001129889.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:95131259 C>A maps to NM_001129889.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr9:90535184 T>C maps to NM_001145124.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr9:90535184 T>C maps to NM_001145124.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:27772630 C>T maps to NM_033223.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:27772630 C>T maps to NM_033223.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr17:72846416 G>A maps to NM_000835.3 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr17:72846416 G>A maps to NM_000835.3 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:43025813 C>T maps to ENST00000458501 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:43025813 C>T maps to ENST00000458501 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:8926113 G>A maps to NM_020738.2 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:8926113 G>A maps to NM_020738.2 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:201355987 T>C maps to NM_005558.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:201355987 T>C maps to NM_005558.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr18:6958504 G>A maps to NM_005559.2 G2645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr18:6958504 G>A maps to NM_005559.2 G2645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:105510146 A>G maps to NM_013437.4 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:105510146 A>G maps to NM_013437.4 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:232390131 G>A maps to NM_006056.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:232390131 G>A maps to NM_006056.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:100079004 G>T maps to NM_016316.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:100079004 G>T maps to NM_016316.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:46357676 C>T maps to NM_198849.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:46357676 C>T maps to NM_198849.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:56822746 G>A maps to NM_003920.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:56822746 G>A maps to NM_003920.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:73047491 C>T maps to NM_170744.3 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:73047491 C>T maps to NM_170744.3 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:11504481 C>T maps to NM_001080491.2 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:11504481 C>T maps to NM_001080491.2 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:28900788 C>T maps to NM_016628.3 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:28900788 C>T maps to NM_016628.3 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:7703883 C>T maps to NM_145891.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:7703883 C>T maps to NM_145891.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:67119513 G>A maps to NM_080284.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:67119513 G>A maps to NM_080284.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:43743968 G>A maps to NM_016006.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:43743968 G>A maps to NM_016006.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:34179552 A>T maps to NM_032834.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:34179552 A>T maps to NM_032834.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:114278605 C>A maps to NM_001148.4 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:114278605 C>A maps to NM_001148.4 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:150509006 G>A maps to NM_001155.4 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:150509006 G>A maps to NM_001155.4 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:75312419 G>T maps to NM_001657.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:75312419 G>T maps to NM_001657.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:27105722 A>G maps to NM_006015.4 E1778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:27105722 A>G maps to NM_006015.4 E1778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:27106494 G>T maps to NM_006015.4 E2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:27106494 G>T maps to NM_006015.4 E2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203652428 C>A maps to NM_001001396.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203652428 C>A maps to NM_001001396.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:116889226 C>T maps to NM_207303.2 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:116889226 C>T maps to NM_207303.2 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:201044650 G>A maps to NM_000069.2 Y640Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:201044650 G>A maps to NM_000069.2 Y640Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:33370118 G>A maps to NM_032816.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:33370118 G>A maps to NM_032816.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:29874030 C>T maps to NM_006319.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:29874030 C>T maps to NM_006319.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:74441857 G>T maps to NM_015424.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:74441857 G>T maps to NM_015424.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:41323803 C>A maps to NM_001843.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:41323803 C>A maps to NM_001843.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:100170105 G>A maps to NM_014361.2 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:100170105 G>A maps to NM_014361.2 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:32145268 G>T maps to NM_001856.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:32145268 G>T maps to NM_001856.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:70916659 T>C maps to NM_001858.4 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:70916659 T>C maps to NM_001858.4 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139611018 C>T maps to NM_152888.1 E1436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139611018 C>T maps to NM_152888.1 E1436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:86581034 T>C maps to NM_152890.5 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:86581034 T>C maps to NM_152890.5 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:34209108 G>A maps to ENST00000373381 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:34209108 G>A maps to ENST00000373381 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:25044574 G>T maps to NM_001911.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:25044574 G>T maps to NM_001911.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:40660664 C>A maps to NM_033510.1 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:40660664 C>A maps to NM_033510.1 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:183948267 C>T maps to NM_080876.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:183948267 C>T maps to NM_080876.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:1299835 C>T maps to NM_001405.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:1299835 C>T maps to NM_001405.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:53663491 T>C maps to NM_012291.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:53663491 T>C maps to NM_012291.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:63411897 C>A maps to NM_152424.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:63411897 C>A maps to NM_152424.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:177199215 T>C maps to NM_021165.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:177199215 T>C maps to NM_021165.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152279938 C>A maps to NM_002016.1 G2475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152279938 C>A maps to NM_002016.1 G2475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:76045407 C>A maps to NM_017791.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:76045407 C>A maps to NM_017791.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:48583535 C>T maps to NM_015030.1 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:48583535 C>T maps to NM_015030.1 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:151821551 C>A maps to NM_018558.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:151821551 C>A maps to NM_018558.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:89735196 G>A maps to NM_052942.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:89735196 G>A maps to NM_052942.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:6903371 G>C maps to NM_181874.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:6903371 G>C maps to NM_181874.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:23520466 G>T maps to NM_000864.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:23520466 G>T maps to NM_000864.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:107978287 C>A maps to NM_003604.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:107978287 C>A maps to NM_003604.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:50683564 C>A maps to NM_002202.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:50683564 C>A maps to NM_002202.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:156234122 G>A maps to NM_172159.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:156234122 G>A maps to NM_172159.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:163693087 G>T maps to NM_033272.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:163693087 G>T maps to NM_033272.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:68128481 G>A maps to NM_018658.1 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:68128481 G>A maps to NM_018658.1 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:66103259 G>A maps to ENST00000451741 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:66103259 G>A maps to ENST00000451741 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:183273318 G>T maps to NM_130446.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:183273318 G>T maps to NM_130446.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152732099 G>T maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152732099 G>T maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:52797657 C>T maps to NM_033033.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:52797657 C>T maps to NM_033033.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:54744953 G>T maps to ENST00000245620 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:54744953 G>T maps to ENST00000245620 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:141214101 G>T maps to NM_018557.2 T3295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:141214101 G>T maps to NM_018557.2 T3295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:1905190 C>A maps to ENST00000381758 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:1905190 C>A maps to ENST00000381758 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:25098930 A>C maps to NM_001009909.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:25098930 A>C maps to NM_001009909.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:210557722 G>T maps to NM_002374.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:210557722 G>T maps to NM_002374.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:2537762 G>C maps to NM_033467.3 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:2537762 G>C maps to NM_033467.3 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:102709382 G>A maps to NM_002422.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:102709382 G>A maps to NM_002422.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:55478804 A>C maps to NM_138962.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:55478804 A>C maps to NM_138962.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:10535948 G>A maps to NM_002470.2 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:10535948 G>A maps to NM_002470.2 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:55421050 C>G maps to NM_021191.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:55421050 C>G maps to NM_021191.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:102632568 C>A maps to NM_206915.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:102632568 C>A maps to NM_206915.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:15026683 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:15026683 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:62729692 C>A maps to NM_000913.3 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:62729692 C>A maps to NM_000913.3 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:125273565 C>A maps to ENST00000444856 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:125273565 C>A maps to ENST00000444856 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248366863 C>T maps to NM_001004689.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248366863 C>T maps to NM_001004689.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:20248933 G>T maps to NM_001005500.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:20248933 G>T maps to NM_001005500.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:9226301 G>C maps to ENST00000293614 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:9226301 G>C maps to ENST00000293614 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:140220965 C>A maps to NM_018911.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:140220965 C>A maps to NM_018911.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:140581503 G>T maps to NM_018931.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:140581503 G>T maps to NM_018931.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:92147357 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:92147357 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:160832629 G>A maps to NM_007366.4 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:160832629 G>A maps to NM_007366.4 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:108119757 T>C maps to NM_015723.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:108119757 T>C maps to NM_015723.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:55603622 C>A maps to NM_017607.2 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:55603622 C>A maps to NM_017607.2 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:12854180 A>G maps to NM_023013.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:12854180 A>G maps to NM_023013.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:43439664 C>A maps to NM_002783.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:43439664 C>A maps to NM_002783.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:46196732 A>T maps to NM_017659.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:46196732 A>T maps to NM_017659.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:49582477 C>A maps to NM_000324.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:49582477 C>A maps to NM_000324.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:130926813 G>A maps to NM_015347.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:130926813 G>A maps to NM_015347.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr21:15872984 C>A maps to ENST00000285670 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr21:15872984 C>A maps to ENST00000285670 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:156784940 C>A maps to NM_001161441.1 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:156784940 C>A maps to NM_001161441.1 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:22397549 G>T maps to NM_020346.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:22397549 G>T maps to NM_020346.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:44268815 C>A maps to NM_013305.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:44268815 C>A maps to NM_013305.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:77395087 C>A maps to NM_015975.4 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:77395087 C>A maps to NM_015975.4 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:104373741 C>T maps to NM_003211.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:104373741 C>T maps to NM_003211.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:175362996 C>T maps to NM_003285.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:175362996 C>T maps to NM_003285.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:99636893 G>A maps to NM_025244.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:99636893 G>A maps to NM_025244.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:6021386 T>A maps to NM_015253.1 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:6021386 T>A maps to NM_015253.1 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:227843216 C>T maps to NM_178549.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:227843216 C>T maps to NM_178549.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:130198190 T>G maps to NM_007135.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:130198190 T>G maps to NM_007135.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:237172865 C>T maps to NM_212556.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:237172865 C>T maps to NM_212556.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:131521594 C>T maps to NM_001105195.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:131521594 C>T maps to NM_001105195.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr17:39594399 G>T maps to NM_006771.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr17:39594399 G>T maps to NM_006771.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:156146628 A>T maps to NM_022367.3 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:156146628 A>T maps to NM_022367.3 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:207460797 C>A maps to NM_003812.2 C757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:207460797 C>A maps to NM_003812.2 C757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:39634566 G>T maps to NM_001464.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:39634566 G>T maps to NM_001464.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:38948861 A>G maps to NM_003816.2 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:38948861 A>G maps to NM_003816.2 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:236706517 G>T maps to NM_001037131.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:236706517 G>T maps to NM_001037131.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:151673209 G>C maps to NM_005100.3 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:151673209 G>C maps to NM_005100.3 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:26664730 T>C maps to NM_031418.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:26664730 T>C maps to NM_031418.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:29737725 C>A maps to NM_001127.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:29737725 C>A maps to NM_001127.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:45448462 G>A maps to NM_001646.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:45448462 G>A maps to NM_001646.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:23287229 C>A maps to NM_173081.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:23287229 C>A maps to NM_173081.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:31476035 A>T maps to ENST00000408912 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:31476035 A>T maps to ENST00000408912 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:234200894 C>T maps to ENST00000392018 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:234200894 C>T maps to ENST00000392018 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:13337045 G>T maps to NM_001135995.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:13337045 G>T maps to NM_001135995.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:11414293 C>T maps to ENST00000427279 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:11414293 C>T maps to ENST00000427279 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:36196765 G>T maps to NM_015695.2 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:36196765 G>T maps to NM_015695.2 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:49694473 G>A maps to NM_003458.3 L2495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:49694473 G>A maps to NM_003458.3 L2495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:92554450 C>T maps to NM_183242.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:92554450 C>T maps to NM_183242.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:60505797 G>A maps to NM_152377.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:60505797 G>A maps to NM_152377.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:85051249 C>T maps to ENST00000409520 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:85051249 C>T maps to ENST00000409520 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:175716949 A>G maps to ENST00000443967 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:175716949 A>G maps to ENST00000443967 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:74573105 C>T maps to ENST00000321288 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:74573105 C>T maps to ENST00000321288 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:19520858 T>A maps to NM_004934.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:19520858 T>A maps to NM_004934.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:34850767 C>A maps to NM_020180.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:34850767 C>A maps to NM_020180.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:71570874 C>A maps to NM_001166395.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:71570874 C>A maps to NM_001166395.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:6260973 G>T maps to NM_001037329.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:6260973 G>T maps to NM_001037329.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:125232345 A>T maps to NM_130773.2 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:125232345 A>T maps to NM_130773.2 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739212 T>C maps to NM_000651.4 Y1299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739212 T>C maps to NM_000651.4 Y1299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:3265538 C>A maps to NM_033225.5 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:3265538 C>A maps to NM_033225.5 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:50544320 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:50544320 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:31633190 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:31633190 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:24435559 G>C maps to NM_021004.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:24435559 G>C maps to NM_021004.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:125453083 G>T maps to NM_032656.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:125453083 G>T maps to NM_032656.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:124362332 G>T maps to NM_207437.3 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:124362332 G>T maps to NM_207437.3 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:76112317 G>T maps to NM_020892.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:76112317 G>T maps to NM_020892.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:183885371 A>T maps to NM_004423.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:183885371 A>T maps to NM_004423.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:13624573 C>A maps to NM_001167890.1 Y199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:13624573 C>A maps to NM_001167890.1 Y199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:22920042 C>A maps to NM_020526.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:22920042 C>A maps to NM_020526.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:148525873 C>A maps to NM_004456.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:148525873 C>A maps to NM_004456.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:6152179 G>T maps to NM_000129.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:6152179 G>T maps to NM_000129.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:2661631 A>T maps to ENST00000324666 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:2661631 A>T maps to ENST00000324666 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:34148513 G>A maps to NM_203408.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:34148513 G>A maps to NM_203408.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:127664435 C>A maps to NM_001999.3 E1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:127664435 C>A maps to NM_001999.3 E1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:48416854 G>T maps to NM_207102.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:48416854 G>T maps to NM_207102.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:155490894 C>A maps to NM_005141.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:155490894 C>A maps to NM_005141.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54497807 C>A maps to NM_004463.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54497807 C>A maps to NM_004463.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:162380416 G>A maps to NM_020116.3 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:162380416 G>A maps to NM_020116.3 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:39047363 C>A maps to NM_002062.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:39047363 C>A maps to NM_002062.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:72368402 G>T maps to ENST00000440684 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:72368402 G>T maps to ENST00000440684 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:150349617 C>A maps to NM_004224.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:150349617 C>A maps to NM_004224.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:19027776 A>T maps to NM_001079858.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:19027776 A>T maps to NM_001079858.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:10031859 G>A maps to NM_000833.3 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:10031859 G>A maps to NM_000833.3 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:55113435 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:55113435 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:16342122 C>A maps to ENST00000375714 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:16342122 C>A maps to ENST00000375714 P243P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-6774-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-6774-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:70977729 C>T maps to NM_032821.2 L2217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:70977729 C>T maps to NM_032821.2 L2217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:154422456 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:154422456 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:62626588 G>T maps to NM_176877.2 L1796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:62626588 G>T maps to NM_176877.2 L1796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:33690859 A>G maps to NM_054111.4 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:33690859 A>G maps to NM_054111.4 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:63447816 T>A maps to NM_139318.3 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:63447816 T>A maps to NM_139318.3 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:175237374 A>C maps to NM_001145314.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:175237374 A>C maps to NM_001145314.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:20946797 G>T maps to NM_017794.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:20946797 G>T maps to NM_017794.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:51901011 G>T maps to NM_032559.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:51901011 G>T maps to NM_032559.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:21675720 G>T maps to NM_153270.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:21675720 G>T maps to NM_153270.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:17597143 C>A maps to NM_015907.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:17597143 C>A maps to NM_015907.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:152648742 C>A maps to NM_178429.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:152648742 C>A maps to NM_178429.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:53286962 A>T maps to NM_007015.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:53286962 A>T maps to NM_007015.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:15561487 A>T maps to NM_198996.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:15561487 A>T maps to NM_198996.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:82432280 G>T maps to ENST00000370717 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:82432280 G>T maps to ENST00000370717 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:194080593 G>T maps to NM_001135057.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:194080593 G>T maps to NM_001135057.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:52860730 C>A maps to NM_001024611.1 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:52860730 C>A maps to NM_001024611.1 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:26157297 G>T maps to NM_173699.3 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:26157297 G>T maps to NM_173699.3 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:5958577 C>T maps to NM_032485.4 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:5958577 C>T maps to NM_032485.4 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:90428641 A>T maps to NM_014611.1 C2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:90428641 A>T maps to NM_014611.1 C2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:41738725 G>T maps to NM_004527.3 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:41738725 G>T maps to NM_004527.3 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:228205012 A>T maps to NM_020194.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:228205012 A>T maps to NM_020194.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:2524403 G>T maps to NM_033467.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:2524403 G>T maps to NM_033467.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:15851755 G>T maps to NM_001040114.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:15851755 G>T maps to NM_001040114.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:19735465 G>T maps to ENST00000396087 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:19735465 G>T maps to ENST00000396087 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:24811217 G>A maps to ENST00000221169 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:24811217 G>A maps to ENST00000221169 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:7981772 G>T maps to NM_176821.3 Y462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:7981772 G>T maps to NM_176821.3 Y462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:78387378 G>A maps to NM_001098816.2 L1772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:78387378 G>A maps to NM_001098816.2 L1772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:29622581 G>T maps to NM_002544.4 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:29622581 G>T maps to NM_002544.4 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:3255073 G>T maps to NM_012360.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:3255073 G>T maps to NM_012360.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:248486946 G>T maps to NM_001004691.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:248486946 G>T maps to NM_001004691.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:102079389 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:102079389 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:118997533 G>T maps to NM_002581.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:118997533 G>T maps to NM_002581.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:138453001 C>A maps to NM_019035.3 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:138453001 C>A maps to NM_019035.3 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:140744068 G>T maps to NM_018918.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:140744068 G>T maps to NM_018918.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:47783459 G>A maps to NM_006031.5 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:47783459 G>A maps to NM_006031.5 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:233394269 G>T maps to NM_014801.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:233394269 G>T maps to NM_014801.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:66631268 C>A maps to NM_022172.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:66631268 C>A maps to NM_022172.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:95216780 T>C maps to NM_002612.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:95216780 T>C maps to NM_002612.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:9438111 G>C maps to NM_001172646.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:9438111 G>C maps to NM_001172646.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:153694525 C>A maps to NM_017514.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:153694525 C>A maps to NM_017514.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:124475444 T>A maps to NM_015450.2 K465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:124475444 T>A maps to NM_015450.2 K465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:65847231 A>T maps to NM_016395.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:65847231 A>T maps to NM_016395.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:157959944 C>A maps to NM_002847.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:157959944 C>A maps to NM_002847.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:41306575 G>C maps to ENST00000373198 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:41306575 G>C maps to ENST00000373198 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:220406194 T>C maps to ENST00000358951 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:220406194 T>C maps to ENST00000358951 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:10444192 C>T maps to NM_133452.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:10444192 C>T maps to NM_133452.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:47120852 G>T maps to NM_080746.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:47120852 G>T maps to NM_080746.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:62292694 G>C maps to ENST00000482936 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:62292694 G>C maps to ENST00000482936 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:134983833 G>A maps to NM_018666.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:134983833 G>A maps to NM_018666.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:224462974 A>T maps to NM_003469.4 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:224462974 A>T maps to NM_003469.4 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:70599101 C>T maps to NM_012426.4 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:70599101 C>T maps to NM_012426.4 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:77471207 C>A maps to NM_024776.2 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:77471207 C>A maps to NM_024776.2 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:51215271 C>A maps to ENST00000391814 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:51215271 C>A maps to ENST00000391814 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:25773865 G>C maps to NM_005495.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:25773865 G>C maps to NM_005495.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:48762072 C>A maps to ENST00000452555 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:48762072 C>A maps to ENST00000452555 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:49812161 C>A maps to NM_014037.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:49812161 C>A maps to NM_014037.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:68405826 G>T maps to NM_018667.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:68405826 G>T maps to NM_018667.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:48600677 C>T maps to NM_005985.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:48600677 C>T maps to NM_005985.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67992885 G>T maps to NM_004232.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67992885 G>T maps to NM_004232.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:131293250 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:131293250 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:33260991 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:33260991 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:222736578 C>A maps to NM_005681.2 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:222736578 C>A maps to NM_005681.2 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:6703488 G>A maps to NM_053285.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:6703488 G>A maps to NM_053285.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:156346502 C>A maps to NM_138379.2 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:156346502 C>A maps to NM_138379.2 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:19765250 G>T maps to NM_152774.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:19765250 G>T maps to NM_152774.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:29669311 G>T maps to NM_001193451.1 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:29669311 G>T maps to NM_001193451.1 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:170858244 C>A maps to NM_015028.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:170858244 C>A maps to NM_015028.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:111195528 C>A maps to NM_012471.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:111195528 C>A maps to NM_012471.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54466892 G>T maps to NM_058163.1 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54466892 G>T maps to NM_058163.1 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:179588667 C>A maps to NM_133378.4 L5862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:179588667 C>A maps to NM_133378.4 L5862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:4910737 C>T maps to NM_016936.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:4910737 C>T maps to NM_016936.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:33513322 C>A maps to NM_173167.2 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:33513322 C>A maps to NM_173167.2 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:132160952 G>T maps to NM_031907.1 C432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:132160952 G>T maps to NM_031907.1 C432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:55513305 G>A maps to NM_201286.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:55513305 G>A maps to NM_201286.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:8995983 C>A maps to NM_003470.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:8995983 C>A maps to NM_003470.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:25631887 G>T maps to NM_015626.8 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:25631887 G>T maps to NM_015626.8 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:100178003 C>A maps to ENST00000328526 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:100178003 C>A maps to ENST00000328526 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:69195781 C>A maps to NM_001031732.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:69195781 C>A maps to NM_001031732.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:119387449 C>A maps to NM_001184742.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:119387449 C>A maps to NM_001184742.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:72056982 C>A maps to NM_144982.4 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:72056982 C>A maps to NM_144982.4 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:39898873 G>A maps to NM_003407.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:39898873 G>A maps to NM_003407.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:37005407 C>A maps to NM_001166038.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:37005407 C>A maps to NM_001166038.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:2464341 G>T maps to NM_024325.4 S422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:2464341 G>T maps to NM_024325.4 S422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:52376254 C>A maps to NM_032679.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:52376254 C>A maps to NM_032679.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:127014764 C>A maps to NM_176814.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:127014764 C>A maps to NM_176814.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:33546239 C>T maps to NM_030955.2 W1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:33546239 C>T maps to NM_030955.2 W1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:17966798 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:17966798 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:74755111 G>A maps to ENST00000258081 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:74755111 G>A maps to ENST00000258081 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:66294223 C>A maps to NM_024649.4 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:66294223 C>A maps to NM_024649.4 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:129171499 C>T maps to ENST00000303743 D1562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:129171499 C>T maps to ENST00000303743 D1562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:18209127 G>T maps to NM_153346.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:18209127 G>T maps to NM_153346.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:45687539 T>C maps to NM_018353.4 K929K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:45687539 T>C maps to NM_018353.4 K929K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:113323387 G>T maps to NM_198123.1 Y2568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:113323387 G>T maps to NM_198123.1 Y2568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:116534782 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:116534782 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:6080555 G>T maps to NM_014413.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:6080555 G>T maps to NM_014413.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:231472492 G>T maps to NM_175876.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:231472492 G>T maps to NM_175876.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:108380299 G>C maps to NM_015065.2 Y1978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:108380299 G>C maps to NM_015065.2 Y1978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:41934093 C>T maps to NM_012176.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:41934093 C>T maps to NM_012176.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:1131385 C>A maps to NM_001505.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:1131385 C>A maps to NM_001505.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:124080759 C>A maps to NM_000177.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:124080759 C>A maps to NM_000177.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:10395636 C>G maps to NM_000201.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:10395636 C>G maps to NM_000201.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:30032875 T>C maps to NM_002233.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:30032875 T>C maps to NM_002233.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:73848237 G>A maps to NM_004770.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:73848237 G>A maps to NM_004770.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:245849587 C>A maps to NM_018012.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:245849587 C>A maps to NM_018012.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:39155964 G>A maps to NM_031959.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:39155964 G>A maps to NM_031959.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr10:68686704 G>T maps to NM_178011.3 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr10:68686704 G>T maps to NM_178011.3 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:123370268 A>G maps to ENST00000426959 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:123370268 A>G maps to ENST00000426959 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:106185199 G>T maps to NM_024657.4 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:106185199 G>T maps to NM_024657.4 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:13162688 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:13162688 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:17213240 G>A maps to NM_004145.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:17213240 G>A maps to NM_004145.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr20:62854713 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr20:62854713 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:29490290 G>T maps to NM_001042492.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:29490290 G>T maps to NM_001042492.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr16:69748916 C>A maps to NM_000903.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr16:69748916 C>A maps to NM_000903.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:31725314 C>A maps to NM_017784.4 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:31725314 C>A maps to NM_017784.4 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:105860985 G>T maps to ENST00000458164 G898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:105860985 G>T maps to ENST00000458164 G898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:140719806 C>A maps to NM_018915.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:140719806 C>A maps to NM_018915.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:140782869 C>T maps to NM_018921.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:140782869 C>T maps to NM_018921.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:57325603 G>A maps to NM_006210.2 A1402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:57325603 G>A maps to NM_006210.2 A1402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:18942541 C>A maps to NM_000292.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:18942541 C>A maps to NM_000292.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:152226179 C>T maps to NM_013364.4 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:152226179 C>T maps to NM_013364.4 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:8998684 G>T maps to NM_024607.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:8998684 G>T maps to NM_024607.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:94540004 C>A maps to NM_001166160.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:94540004 C>A maps to NM_001166160.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:123593719 T>C maps to NM_005047.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:123593719 T>C maps to NM_005047.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:160274996 C>A maps to NM_014247.2 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:160274996 C>A maps to NM_014247.2 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:110882746 C>T maps to NM_022768.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:110882746 C>T maps to NM_022768.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:39291650 T>C maps to ENST00000381897 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:39291650 T>C maps to ENST00000381897 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:78766485 G>T maps to NM_002941.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:78766485 G>T maps to NM_002941.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr6:108070972 C>T maps to NM_198081.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr6:108070972 C>T maps to NM_198081.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:77660331 C>A maps to NM_020859.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:77660331 C>A maps to NM_020859.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:62744845 C>A maps to NM_004790.3 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:62744845 C>A maps to NM_004790.3 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:95011207 G>A maps to NM_031952.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:95011207 G>A maps to NM_031952.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:220355211 C>A maps to NM_005876.4 A3001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:220355211 C>A maps to NM_005876.4 A3001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:223465897 G>T maps to NM_017982.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:223465897 G>T maps to NM_017982.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:120816176 C>T maps to NM_003184.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:120816176 C>T maps to NM_003184.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:62549736 C>A maps to NM_006473.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:62549736 C>A maps to NM_006473.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:72985559 G>T maps to NM_012453.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:72985559 G>T maps to NM_012453.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:155172165 C>A maps to NM_007112.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:155172165 C>A maps to NM_007112.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:9867507 C>A maps to NM_001025930.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:9867507 C>A maps to NM_001025930.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:154456754 G>A maps to NM_003372.5 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:154456754 G>A maps to NM_003372.5 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr13:20411810 A>G maps to NM_001142684.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr13:20411810 A>G maps to NM_001142684.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:215821446 A>T maps to NM_173076.2 L2058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:215821446 A>T maps to NM_173076.2 L2058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:104244123 T>A maps to NM_005736.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:104244123 T>A maps to NM_005736.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24800250 G>C maps to NM_139247.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24800250 G>C maps to NM_139247.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:70906009 C>G maps to NM_001185054.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:70906009 C>G maps to NM_001185054.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:144062359 G>T maps to NM_005435.3 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:144062359 G>T maps to NM_005435.3 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:74825220 G>T maps to NM_018228.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:74825220 G>T maps to NM_018228.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:156703952 G>T maps to NM_015997.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:156703952 G>T maps to NM_015997.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:27459688 C>T maps to NM_004341.3 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:27459688 C>T maps to NM_004341.3 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:17688151 G>A maps to NM_017424.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:17688151 G>A maps to NM_017424.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:34263295 C>A maps to NM_022467.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:34263295 C>A maps to NM_022467.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:103364516 G>A maps to NM_080629.2 Q1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:103364516 G>A maps to NM_080629.2 Q1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:56963965 G>T maps to NM_181654.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:56963965 G>T maps to NM_181654.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:1389174 C>T maps to NM_175918.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:1389174 C>T maps to NM_175918.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:150121677 G>T maps to NM_001135643.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:150121677 G>T maps to NM_001135643.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:65989641 T>C maps to ENST00000443035 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:65989641 T>C maps to ENST00000443035 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:15928305 C>A maps to NM_012304.3 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:15928305 C>A maps to NM_012304.3 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:125094555 A>T maps to NM_001039112.2 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:125094555 A>T maps to NM_001039112.2 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:30433324 G>A maps to NM_004118.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:30433324 G>A maps to NM_004118.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:151818268 T>A maps to NM_018558.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:151818268 T>A maps to NM_018558.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:58007843 C>T maps to NM_001111270.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:58007843 C>T maps to NM_001111270.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:108684588 C>A maps to ENST00000218006 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:108684588 C>A maps to ENST00000218006 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:50546388 G>T maps to NM_002112.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:50546388 G>T maps to NM_002112.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:82936911 G>T maps to NM_015525.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:82936911 G>T maps to NM_015525.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:67795396 C>T maps to NM_001559.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:67795396 C>T maps to NM_001559.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:81201517 G>A maps to NM_018689.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:81201517 G>A maps to NM_018689.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:116859703 G>A maps to ENST00000259410 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:116859703 G>A maps to ENST00000259410 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:69550031 T>A maps to NM_012310.4 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:69550031 T>A maps to NM_012310.4 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:187177230 G>T maps to ENST00000511608 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:187177230 G>T maps to ENST00000511608 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:17590483 C>T maps to NM_015907.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:17590483 C>T maps to NM_015907.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:55086240 G>A maps to NM_001130917.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:55086240 G>A maps to NM_001130917.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:71490201 C>T maps to NM_005909.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:71490201 C>T maps to NM_005909.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:50547204 A>T maps to NM_018995.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:50547204 A>T maps to NM_018995.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:47630473 G>A maps to NM_000251.1 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:47630473 G>A maps to NM_000251.1 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:3248299 G>T maps to NM_015419.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:3248299 G>T maps to NM_015419.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:73012883 C>A maps to NM_004885.2 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:73012883 C>A maps to NM_004885.2 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:115356916 A>G maps to ENST00000369358 S1461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:115356916 A>G maps to ENST00000369358 S1461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24885565 G>A maps to NM_025081.2 P1537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24885565 G>A maps to NM_025081.2 P1537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:123810709 C>A maps to NM_001001965.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:123810709 C>A maps to NM_001001965.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:169611776 G>A maps to NM_001166108.1 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:169611776 G>A maps to NM_001166108.1 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:140736275 C>G maps to NM_018917.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:140736275 C>G maps to NM_018917.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:67589620 G>T maps to ENST00000396611 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:67589620 G>T maps to ENST00000396611 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:39379532 G>A maps to NM_007252.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:39379532 G>A maps to NM_007252.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:48767901 T>C maps to NM_006904.6 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:48767901 T>C maps to NM_006904.6 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:103080665 C>A maps to NM_016370.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:103080665 C>A maps to NM_016370.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:74473846 G>A maps to NM_024599.5 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:74473846 G>A maps to NM_024599.5 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:104930686 T>C maps to NM_001100117.2 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:104930686 T>C maps to NM_001100117.2 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:153430322 G>A maps to NM_002963.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:153430322 G>A maps to NM_002963.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:1294130 C>A maps to NM_080489.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:1294130 C>A maps to NM_080489.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:42977284 A>G maps to NM_032237.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:42977284 A>G maps to NM_032237.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:150460020 G>A maps to NM_005067.5 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:150460020 G>A maps to NM_005067.5 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:85438234 C>A maps to NM_004213.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:85438234 C>A maps to NM_004213.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:153048493 G>A maps to NM_014370.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:153048493 G>A maps to NM_014370.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:1220639 C>T maps to NM_000455.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:1220639 C>T maps to NM_000455.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:48873793 C>A maps to NM_172311.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:48873793 C>A maps to NM_172311.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:72419664 C>T maps to NM_173490.6 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:72419664 C>T maps to NM_173490.6 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:35957470 C>A maps to NM_152404.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:35957470 C>A maps to NM_152404.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:144124647 T>C maps to NM_032557.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:144124647 T>C maps to NM_032557.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:37035874 G>T maps to NM_053276.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:37035874 G>T maps to NM_053276.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:33255770 G>T maps to NM_005452.5 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:33255770 G>T maps to NM_005452.5 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:1952803 G>T maps to NM_133335.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:1952803 G>T maps to NM_133335.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:10093090 C>A maps to NM_015691.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:10093090 C>A maps to NM_015691.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:44638038 C>A maps to NM_182592.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:44638038 C>A maps to NM_182592.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:49672666 C>A maps to NM_015069.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:49672666 C>A maps to NM_015069.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:227843490 G>T maps to NM_178549.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:227843490 G>T maps to NM_178549.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:66883271 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:66883271 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:6749348 G>A maps to NM_032489.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:6749348 G>A maps to NM_032489.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8657673 C>T maps to NM_030957.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8657673 C>T maps to NM_030957.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:131826458 G>T maps to NM_001115.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:131826458 G>T maps to NM_001115.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:87066166 C>A maps to NM_152336.2 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:87066166 C>A maps to NM_152336.2 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:135787304 C>A maps to NM_017651.4 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:135787304 C>A maps to NM_017651.4 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67250703 C>T maps to NM_003977.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67250703 C>T maps to NM_003977.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:77763334 G>A maps to NM_174858.1 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:77763334 G>A maps to NM_174858.1 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:55052310 C>A maps to NM_000032.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:55052310 C>A maps to NM_000032.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:42492225 C>T maps to ENST00000441343 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:42492225 C>T maps to ENST00000441343 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:154344445 G>T maps to NM_024332.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:154344445 G>T maps to NM_024332.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62435065 G>C maps to ENST00000431002 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62435065 G>C maps to ENST00000431002 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:73319245 C>A maps to ENST00000377815 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:73319245 C>A maps to ENST00000377815 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:59942717 T>A maps to NM_144581.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:59942717 T>A maps to NM_144581.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:20051545 C>A maps to ENST00000389655 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:20051545 C>A maps to ENST00000389655 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:8212739 G>T maps to NM_004054.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:8212739 G>T maps to NM_004054.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:10555136 C>A maps to NM_001040032.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:10555136 C>A maps to NM_001040032.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:1965187 T>A maps to NM_172364.4 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:1965187 T>A maps to NM_172364.4 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:110560282 C>A maps to NM_001744.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:110560282 C>A maps to NM_001744.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:77300478 A>G maps to NM_001042784.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:77300478 A>G maps to NM_001042784.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:72522082 G>A maps to NM_174892.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:72522082 G>A maps to NM_174892.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:207498072 C>A maps to NM_001114752.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:207498072 C>A maps to NM_001114752.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:54415704 T>G maps to NM_001170402.1 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:54415704 T>G maps to NM_001170402.1 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:26988489 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:26988489 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:55004778 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:55004778 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:130941407 G>A maps to NM_012127.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:130941407 G>A maps to NM_012127.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150911088 G>T maps to NM_005140.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150911088 G>T maps to NM_005140.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:230814765 G>A maps to NM_007357.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:230814765 G>A maps to NM_007357.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:189929291 T>A maps to NM_000393.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:189929291 T>A maps to NM_000393.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:207870914 C>A maps to NM_175710.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:207870914 C>A maps to NM_175710.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51470323 C>A maps to NM_030809.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51470323 C>A maps to NM_030809.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:10781720 G>A maps to NM_014633.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:10781720 G>A maps to NM_014633.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:35969250 G>T maps to NM_152632.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:35969250 G>T maps to NM_152632.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30862314 G>A maps to NM_013994.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30862314 G>A maps to NM_013994.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:134147432 C>T maps to ENST00000452510 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:134147432 C>T maps to ENST00000452510 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:54573087 G>C maps to NM_019030.2 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:54573087 G>C maps to NM_019030.2 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51108374 A>G maps to NM_173602.2 Q949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51108374 A>G maps to NM_173602.2 Q949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:32482741 C>A maps to ENST00000357033 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:32482741 C>A maps to ENST00000357033 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:51743894 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:51743894 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13737490 C>A maps to NM_001369.2 L3775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13737490 C>A maps to NM_001369.2 L3775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:169423143 A>G maps to NM_004946.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:169423143 A>G maps to NM_004946.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:89704488 G>A maps to NM_004413.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:89704488 G>A maps to NM_004413.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:32949373 C>T maps to NM_001172774.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:32949373 C>T maps to NM_001172774.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:131277562 A>G maps to NM_001431.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:131277562 A>G maps to NM_001431.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:110301167 G>T maps to NM_139053.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:110301167 G>T maps to NM_139053.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:197031045 A>G maps to NM_001994.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:197031045 A>G maps to NM_001994.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:131521385 G>T maps to NM_001105195.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:131521385 G>T maps to NM_001105195.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:92965125 G>A maps to NM_173698.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:92965125 G>A maps to NM_173698.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:18950802 C>T maps to NM_153707.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:18950802 C>T maps to NM_153707.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:92613927 G>T maps to ENST00000298047 T4053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:92613927 G>T maps to ENST00000298047 T4053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161647155 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161647155 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39974663 C>T maps to NM_021939.3 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39974663 C>T maps to NM_021939.3 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:79301109 G>T maps to NM_025074.6 E1175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:79301109 G>T maps to NM_025074.6 E1175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:160763717 T>A maps to NM_021911.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:160763717 T>A maps to NM_021911.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:153783749 G>T maps to NM_198321.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:153783749 G>T maps to NM_198321.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:150417565 C>T maps to NM_130759.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:150417565 C>T maps to NM_130759.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:75807463 A>T maps to ENST00000378692 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:75807463 A>T maps to ENST00000378692 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:194118855 G>C maps to NM_004488.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:194118855 G>C maps to NM_004488.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150345267 G>T maps to NM_004224.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150345267 G>T maps to NM_004224.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:94690552 G>A maps to NM_001510.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:94690552 G>A maps to NM_001510.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:120531065 G>T maps to NM_014619.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:120531065 G>T maps to NM_014619.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:9857857 G>A maps to NM_000833.3 N1181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:9857857 G>A maps to NM_000833.3 N1181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:141535732 T>C maps to NM_139209.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:141535732 T>C maps to NM_139209.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:228335393 G>T maps to ENST00000366720 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:228335393 G>T maps to ENST00000366720 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:73617679 C>A maps to NM_005477.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:73617679 C>A maps to NM_005477.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:83724223 T>A maps to NM_144657.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:83724223 T>A maps to NM_144657.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:27107278 G>A maps to NM_003495.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:27107278 G>A maps to NM_003495.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:10395693 G>C maps to NM_000201.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:10395693 G>C maps to NM_000201.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:79128522 T>A maps to NM_006417.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:79128522 T>A maps to NM_006417.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:1621514 G>A maps to NM_014714.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:1621514 G>A maps to NM_014714.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:27441409 C>A maps to NM_181079.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:27441409 C>A maps to NM_181079.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:1460678 G>T maps to NM_002183.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:1460678 G>T maps to NM_002183.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:143045851 C>T maps to NM_003866.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:143045851 C>T maps to NM_003866.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:62703975 C>T maps to NM_181712.4 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:62703975 C>T maps to NM_181712.4 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:73479986 C>A maps to NM_004770.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:73479986 C>A maps to NM_004770.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:18113189 G>A maps to NM_002252.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:18113189 G>A maps to NM_002252.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:42830319 C>A maps to NM_015349.1 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:42830319 C>A maps to NM_015349.1 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:19454665 C>T maps to NM_015329.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:19454665 C>T maps to NM_015329.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:123234841 G>T maps to NM_015312.3 E3438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:123234841 G>T maps to NM_015312.3 E3438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:57182100 G>T maps to NM_020722.1 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:57182100 G>T maps to NM_020722.1 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:44249068 T>A maps to NM_015443.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:44249068 T>A maps to NM_015443.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:95507123 T>A maps to NM_015496.3 P1535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:95507123 T>A maps to NM_015496.3 P1535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:138556068 G>C maps to NM_001164665.1 S1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:138556068 G>C maps to NM_001164665.1 S1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39535670 C>A maps to NM_021013.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39535670 C>A maps to NM_021013.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:53189643 G>C maps to ENST00000309505 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:53189643 G>C maps to ENST00000309505 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:48665537 C>A maps to NM_000234.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:48665537 C>A maps to NM_000234.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:145492315 C>A maps to NM_153713.1 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:145492315 C>A maps to NM_153713.1 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:73569270 C>T maps to NM_001031803.1 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:73569270 C>T maps to NM_001031803.1 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:58318699 T>G maps to NM_004811.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:58318699 T>G maps to NM_004811.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:52861432 T>A maps to NM_001024611.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:52861432 T>A maps to NM_001024611.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:151504237 C>G maps to NM_006439.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:151504237 C>G maps to NM_006439.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:39782999 C>T maps to ENST00000361689 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:39782999 C>T maps to ENST00000361689 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:56160758 C>T maps to NM_005921.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:56160758 C>T maps to NM_005921.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:75298415 G>T maps to NM_033063.1 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:75298415 G>T maps to NM_033063.1 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:36075267 C>G maps to NM_139012.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:36075267 C>G maps to NM_139012.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:7636006 C>T maps to NM_019005.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:7636006 C>T maps to NM_019005.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:151845607 C>A maps to ENST00000355193 T4525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:151845607 C>A maps to ENST00000355193 T4525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:102824900 C>T maps to NM_002427.3 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:102824900 C>T maps to NM_002427.3 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9083144 C>T maps to NM_024690.2 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9083144 C>T maps to NM_024690.2 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:1018048 G>T maps to NM_005961.2 P1584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:1018048 G>T maps to NM_005961.2 P1584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:149932857 C>A maps to NM_001543.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:149932857 C>A maps to NM_001543.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:27061970 C>T maps to NM_178170.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:27061970 C>T maps to NM_178170.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:23060864 C>A maps to NM_144599.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:23060864 C>A maps to NM_144599.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:120510123 G>C maps to NM_024408.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:120510123 G>C maps to NM_024408.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:100106266 C>T maps to NM_007052.4 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:100106266 C>T maps to NM_007052.4 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:15045459 C>A maps to NM_003298.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:15045459 C>A maps to NM_003298.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161953506 G>A maps to ENST00000451379 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161953506 G>A maps to ENST00000451379 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:7949729 T>C maps to NM_001004461.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:7949729 T>C maps to NM_001004461.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:248366685 C>A maps to NM_001004689.1 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:248366685 C>A maps to NM_001004689.1 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55432932 C>A maps to NM_001004704.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55432932 C>A maps to NM_001004704.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55703540 T>A maps to NM_006637.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55703540 T>A maps to NM_006637.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55579769 G>T maps to NM_001004738.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55579769 G>T maps to NM_001004738.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247875385 G>T maps to NM_001005286.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247875385 G>T maps to NM_001005286.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:25833257 C>G maps to NM_017897.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:25833257 C>G maps to NM_017897.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:34690785 C>A maps to NM_019619.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:34690785 C>A maps to NM_019619.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140306689 C>A maps to NM_018898.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140306689 C>A maps to NM_018898.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140801456 C>T maps to NM_018914.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140801456 C>T maps to NM_018914.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140866245 A>G maps to NM_018928.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140866245 A>G maps to NM_018928.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:98411382 C>T maps to NM_152309.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:98411382 C>T maps to NM_152309.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:159488325 G>T maps to NM_003628.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:159488325 G>T maps to NM_003628.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:84559396 C>A maps to ENST00000373145 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:84559396 C>A maps to ENST00000373145 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:133209095 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:133209095 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:25384027 G>T maps to NM_001035256.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:25384027 G>T maps to NM_001035256.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:18802078 A>T maps to NM_006240.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:18802078 A>T maps to NM_006240.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:42957396 A>T maps to NM_006245.2 K26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:42957396 A>T maps to NM_006245.2 K26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:94708735 C>T maps to NM_058237.1 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:94708735 C>T maps to NM_058237.1 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:11545942 G>T maps to NM_006248.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:11545942 G>T maps to NM_006248.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:23482675 A>G maps to NM_178161.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:23482675 A>G maps to NM_178161.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:1653261 C>A maps to NM_012293.1 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:1653261 C>A maps to NM_012293.1 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:154490324 G>A maps to NM_171998.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:154490324 G>A maps to NM_171998.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38959969 G>A maps to ENST00000296782 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38959969 G>A maps to ENST00000296782 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:46712937 G>T maps to NM_006915.2 G44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:46712937 G>T maps to NM_006915.2 G44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:45213248 G>T maps to NM_003683.5 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:45213248 G>T maps to NM_003683.5 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:16794556 G>T maps to NM_012425.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:16794556 G>T maps to NM_012425.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:70154088 G>C maps to NM_017987.4 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:70154088 G>C maps to NM_017987.4 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:153430434 G>A maps to NM_002963.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:153430434 G>A maps to NM_002963.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:113873250 G>C maps to NM_138432.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:113873250 G>C maps to NM_138432.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:52474798 G>T maps to NM_020163.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:52474798 G>T maps to NM_020163.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:46615700 C>A maps to NM_024745.4 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:46615700 C>A maps to NM_024745.4 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62782142 C>G maps to ENST00000430500 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62782142 C>G maps to ENST00000430500 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:19216419 C>T maps to NM_178526.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:19216419 C>T maps to NM_178526.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:32633297 C>A maps to NM_014227.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:32633297 C>A maps to NM_014227.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:47752262 G>A maps to NM_003074.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:47752262 G>A maps to NM_003074.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:106918651 C>A maps to NM_014978.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:106918651 C>A maps to NM_014978.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:48522884 A>G maps to NM_006038.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:48522884 A>G maps to NM_006038.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:42166579 G>A maps to ENST00000320955 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:42166579 G>A maps to ENST00000320955 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:149492428 A>T maps to NM_198455.2 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:149492428 A>T maps to NM_198455.2 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:8019212 G>T maps to NM_031923.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:8019212 G>T maps to NM_031923.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:152058336 C>G maps to NM_001008536.1 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:152058336 C>G maps to NM_001008536.1 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154141851 G>C maps to ENST00000328159 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154141851 G>C maps to ENST00000328159 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:41250403 T>C maps to NM_018643.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:41250403 T>C maps to NM_018643.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:14479402 C>T maps to NM_007118.2 Q2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:14479402 C>T maps to NM_007118.2 Q2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:179560073 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:179560073 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:125397468 G>A maps to NM_021009.5 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:125397468 G>A maps to NM_021009.5 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161123853 C>A maps to NM_016406.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161123853 C>A maps to NM_016406.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:234681012 C>G maps to ENST00000373460 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:234681012 C>G maps to ENST00000373460 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:69962774 T>A maps to NM_001074.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:69962774 T>A maps to NM_001074.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:706347 C>T maps to NM_145294.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:706347 C>T maps to NM_145294.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:145147140 C>A maps to NM_014795.3 T1174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:145147140 C>A maps to NM_014795.3 T1174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9677451 C>A maps to NM_001008727.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9677451 C>A maps to NM_001008727.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:44470667 C>T maps to NM_013359.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:44470667 C>T maps to NM_013359.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:148801710 C>A maps to NM_001001661.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:148801710 C>A maps to NM_001001661.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:52918882 C>T maps to NM_032423.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:52918882 C>T maps to NM_032423.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9452606 A>T maps to NM_032497.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9452606 A>T maps to NM_032497.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:52868948 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:52868948 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:40528913 C>A maps to NM_001145082.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:40528913 C>A maps to NM_001145082.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:22363098 C>A maps to NM_001001411.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:22363098 C>A maps to NM_001001411.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11833103 G>T maps to NM_001080493.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11833103 G>T maps to NM_001080493.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:12785398 G>T maps to NM_001103170.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:12785398 G>T maps to NM_001103170.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:215855533 G>T maps to NM_173076.2 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:215855533 G>T maps to NM_173076.2 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:72490000 C>A maps to NM_139155.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:72490000 C>A maps to NM_139155.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:77317918 C>T maps to NM_199355.2 Q1200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:77317918 C>T maps to NM_199355.2 Q1200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:91980362 A>C maps to NM_019004.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:91980362 A>C maps to NM_019004.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:69420353 T>A maps to NM_001098805.1 L415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:69420353 T>A maps to NM_001098805.1 L415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:10025082 G>T maps to NM_198798.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:10025082 G>T maps to NM_198798.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:69933977 C>A maps to NM_018043.5 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:69933977 C>A maps to NM_018043.5 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:86916249 G>T maps to NM_001025616.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:86916249 G>T maps to NM_001025616.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:3527984 T>C maps to NM_139321.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:3527984 T>C maps to NM_139321.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:61725727 C>A maps to NM_001139443.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:61725727 C>A maps to NM_001139443.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:69092864 G>T maps to NM_014482.1 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:69092864 G>T maps to NM_014482.1 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:13427329 G>C maps to NM_032320.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:13427329 G>C maps to NM_032320.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:16760378 A>T maps to NM_014267.5 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:16760378 A>T maps to NM_014267.5 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:77805851 G>T maps to NM_024805.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:77805851 G>T maps to NM_024805.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:106690423 G>T maps to NM_032411.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:106690423 G>T maps to NM_032411.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:123731376 G>A maps to NM_001735.2 Y1394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:123731376 G>A maps to NM_001735.2 Y1394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:47976770 G>C maps to NM_001013732.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:47976770 G>C maps to NM_001013732.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:49147767 C>T maps to NM_001217.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:49147767 C>T maps to NM_001217.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:181708383 T>A maps to ENST00000357570 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:181708383 T>A maps to ENST00000357570 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:3041535 G>A maps to NM_001014437.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:3041535 G>A maps to NM_001014437.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:66504560 T>C maps to NM_024781.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:66504560 T>C maps to NM_024781.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179701636 C>A maps to NM_173648.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179701636 C>A maps to NM_173648.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:19612582 G>C maps to NM_004934.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:19612582 G>C maps to NM_004934.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:26915771 T>C maps to NM_016279.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:26915771 T>C maps to NM_016279.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:61707559 C>T maps to NM_017780.2 D704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:61707559 C>T maps to NM_017780.2 D704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:101824293 G>T maps to NM_001855.3 A1148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:101824293 G>T maps to NM_001855.3 A1148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:75927085 G>T maps to NM_031461.5 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:75927085 G>T maps to NM_031461.5 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:19995629 A>T maps to NM_172241.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:19995629 A>T maps to NM_172241.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:196681687 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:196681687 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:94337786 T>C maps to NM_014597.4 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:94337786 T>C maps to NM_014597.4 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:49917564 C>T maps to NM_001144955.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:49917564 C>T maps to NM_001144955.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:71838609 C>T maps to NM_001130987.1 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:71838609 C>T maps to NM_001130987.1 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:55724737 T>A maps to NM_130810.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:55724737 T>A maps to NM_130810.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:212522552 C>A maps to NM_005235.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:212522552 C>A maps to NM_005235.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:119123234 G>A maps to NM_000127.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:119123234 G>A maps to NM_000127.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:51826249 C>A maps to NM_145019.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:51826249 C>A maps to NM_145019.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:139165276 C>A maps to NM_015912.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:139165276 C>A maps to NM_015912.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:43627174 T>A maps to NM_001145196.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:43627174 T>A maps to NM_001145196.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:155489561 G>T maps to NM_005141.4 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:155489561 G>T maps to NM_005141.4 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:86088697 G>T maps to NM_013231.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:86088697 G>T maps to NM_013231.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:33330311 C>A maps to ENST00000291421 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:33330311 C>A maps to ENST00000291421 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:79635400 C>A maps to NM_001013735.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:79635400 C>A maps to NM_001013735.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:151079675 A>C maps to NM_144618.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:151079675 A>C maps to NM_144618.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:33602646 C>T maps to NM_018025.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:33602646 C>T maps to NM_018025.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:37691585 G>T maps to NM_032777.9 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:37691585 G>T maps to NM_032777.9 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:19371852 T>A maps to NM_023002.2 K85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:19371852 T>A maps to NM_023002.2 K85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:19063029 T>C maps to NM_017645.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:19063029 T>C maps to NM_017645.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:42984470 G>C maps to NM_175914.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:42984470 G>C maps to NM_175914.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:118835178 C>T maps to NM_000414.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:118835178 C>T maps to NM_000414.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:46733630 C>T maps to NM_198541.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:46733630 C>T maps to NM_198541.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:76660392 G>T maps to NM_001563.2 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:76660392 G>T maps to NM_001563.2 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:48726008 G>A maps to ENST00000395509 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:48726008 G>A maps to ENST00000395509 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:41794613 C>T maps to NM_002220.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:41794613 C>T maps to NM_002220.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:30032965 G>A maps to NM_002233.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:30032965 G>A maps to NM_002233.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:155904188 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:155904188 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:81224241 C>A maps to NM_018689.1 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:81224241 C>A maps to NM_018689.1 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:26203667 C>T maps to NM_002254.6 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:26203667 C>T maps to NM_002254.6 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:66033335 C>T maps to NM_022822.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:66033335 C>T maps to NM_022822.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:129714271 C>A maps to NM_000426.3 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:129714271 C>A maps to NM_000426.3 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:107642143 G>T maps to NM_002291.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:107642143 G>T maps to NM_002291.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:20361675 C>A maps to ENST00000324290 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:20361675 C>A maps to ENST00000324290 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55107720 G>T maps to NM_006863.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55107720 G>T maps to NM_006863.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:54760089 C>T maps to NM_001081442.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:54760089 C>T maps to NM_001081442.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:19805736 C>A maps to NM_000237.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:19805736 C>A maps to NM_000237.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:141299375 G>T maps to NM_018557.2 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:141299375 G>T maps to NM_018557.2 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57603848 C>G maps to NM_002332.2 L4159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57603848 C>G maps to NM_002332.2 L4159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:35790539 G>T maps to NM_002361.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:35790539 G>T maps to NM_002361.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:135301624 G>A maps to NM_024597.3 D865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:135301624 G>A maps to NM_024597.3 D865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:138708795 C>T maps to ENST00000370578 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:138708795 C>T maps to ENST00000370578 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:156565908 T>C maps to NM_004270.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:156565908 T>C maps to NM_004270.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:222800921 G>T maps to NM_198551.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:222800921 G>T maps to NM_198551.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:43870646 C>T maps to NM_001044370.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:43870646 C>T maps to NM_001044370.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:49935560 C>A maps to NM_002447.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:49935560 C>A maps to NM_002447.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10400384 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10400384 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10299914 G>A maps to NM_002472.2 L1495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10299914 G>A maps to NM_002472.2 L1495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:7230116 C>T maps to NM_032442.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:7230116 C>T maps to NM_032442.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:53852565 G>A maps to NM_005285.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:53852565 G>A maps to NM_005285.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:21965371 C>A maps to NM_024815.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:21965371 C>A maps to NM_024815.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:134077032 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:134077032 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:29365228 T>C maps to NM_013936.3 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:29365228 T>C maps to NM_013936.3 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:3119639 C>A maps to NM_014565.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:3119639 C>A maps to NM_014565.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:143792514 G>A maps to NM_001004135.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:143792514 G>A maps to NM_001004135.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:58207549 G>C maps to NM_001004733.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:58207549 G>C maps to NM_001004733.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55606871 C>A maps to NM_001005496.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55606871 C>A maps to NM_001005496.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:158669914 G>T maps to NM_001005279.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:158669914 G>T maps to NM_001005279.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:9361943 C>A maps to NM_001079935.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:9361943 C>A maps to NM_001079935.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:9543539 G>A maps to NM_177990.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:9543539 G>A maps to NM_177990.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrY:4967790 C>A maps to NM_032973.1 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrY:4967790 C>A maps to NM_032973.1 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:156873708 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:156873708 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:47622832 G>T maps to NM_000293.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:47622832 G>T maps to NM_000293.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:71713314 T>G maps to NM_015020.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:71713314 T>G maps to NM_015020.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:46655393 G>T maps to NM_006071.1 R1276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:46655393 G>T maps to NM_006071.1 R1276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:95931001 A>T maps to ENST00000371380 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:95931001 A>T maps to ENST00000371380 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:6435619 G>A maps to NM_001144856.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:6435619 G>A maps to NM_001144856.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:153689938 G>T maps to NM_017514.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:153689938 G>T maps to NM_017514.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:46973122 C>T maps to NM_018215.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:46973122 C>T maps to NM_018215.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:19573143 G>A maps to NM_001005356.2 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:19573143 G>A maps to NM_001005356.2 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:94540576 T>A maps to NM_001166160.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:94540576 T>A maps to NM_001166160.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:23713961 C>A maps to NM_144662.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:23713961 C>A maps to NM_144662.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:53173933 C>T maps to NM_002806.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:53173933 C>T maps to NM_002806.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:28926031 C>A maps to NM_024816.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:28926031 C>A maps to NM_024816.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:7111235 A>T maps to NM_014469.4 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:7111235 A>T maps to NM_014469.4 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:48389677 C>A maps to NM_002900.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:48389677 C>A maps to NM_002900.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:105105697 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:105105697 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:96503331 A>G maps to NM_018343.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:96503331 A>G maps to NM_018343.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237777446 C>A maps to NM_001035.2 A1673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237777446 C>A maps to NM_001035.2 A1673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237780584 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237780584 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:101705385 C>T maps to NM_001400.4 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:101705385 C>T maps to NM_001400.4 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:122645243 G>T maps to NM_001031702.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:122645243 G>T maps to NM_001031702.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:151108131 T>C maps to NM_001178061.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:151108131 T>C maps to NM_001178061.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41122770 C>T maps to NM_003012.4 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41122770 C>T maps to NM_003012.4 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:235949598 G>A maps to NM_014521.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:235949598 G>A maps to NM_014521.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:50350570 G>A maps to NM_020717.3 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:50350570 G>A maps to NM_020717.3 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:3674160 G>T maps to NM_023068.3 Y1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:3674160 G>T maps to NM_023068.3 Y1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:73096183 G>T maps to ENST00000450736 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:73096183 G>T maps to ENST00000450736 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:25861851 C>A maps to NM_001098486.1 G209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:25861851 C>A maps to NM_001098486.1 G209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:22391655 C>A maps to NM_020346.2 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:22391655 C>A maps to NM_020346.2 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:1508533 G>T maps to NM_001636.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:1508533 G>T maps to NM_001636.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:58056109 T>A maps to NM_001080455.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:58056109 T>A maps to NM_001080455.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:149485869 G>T maps to NM_198455.2 G1364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:149485869 G>T maps to NM_198455.2 G1364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:152443810 C>T maps to NM_182961.2 R8718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:152443810 C>T maps to NM_182961.2 R8718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:104577452 G>A maps to NM_001059.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:104577452 G>A maps to NM_001059.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:32956213 C>A maps to NM_207313.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:32956213 C>A maps to NM_207313.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:122682831 C>A maps to NM_152399.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:122682831 C>A maps to NM_152399.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:98938260 T>A maps to NM_001032283.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:98938260 T>A maps to NM_001032283.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:132586259 G>A maps to ENST00000437532 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:132586259 G>A maps to ENST00000437532 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:30164346 C>A maps to NM_003449.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:30164346 C>A maps to NM_003449.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:178417115 C>A maps to NM_152517.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:178417115 C>A maps to NM_152517.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:135106638 G>A maps to NM_006659.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:135106638 G>A maps to NM_006659.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:86284186 G>A maps to NM_013438.4 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:86284186 G>A maps to NM_013438.4 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:79980488 G>A maps to ENST00000376646 K2776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:79980488 G>A maps to ENST00000376646 K2776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:141429402 G>A maps to NM_001105558.1 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:141429402 G>A maps to NM_001105558.1 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:168104771 A>C maps to NM_152381.5 P2290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:168104771 A>C maps to NM_152381.5 P2290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:100377141 C>A maps to ENST00000349350 R2131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:100377141 C>A maps to ENST00000349350 R2131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:106815426 A>T maps to NM_012082.3 R1039R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:106815426 A>T maps to NM_012082.3 R1039R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:238045793 G>T maps to NM_021186.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:238045793 G>T maps to NM_021186.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:152549329 G>A maps to NM_020445.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:152549329 G>A maps to NM_020445.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:66863199 A>T maps to NM_000044.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:66863199 A>T maps to NM_000044.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:168726188 C>A maps to NM_020981.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:168726188 C>A maps to NM_020981.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:13604662 C>T maps to NM_148894.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:13604662 C>T maps to NM_148894.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:73766252 G>A maps to NM_001042367.1 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:73766252 G>A maps to NM_001042367.1 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:32646552 G>T maps to ENST00000394620 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:32646552 G>T maps to ENST00000394620 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:49843569 C>A maps to NM_001774.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:49843569 C>A maps to NM_001774.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:113694835 C>A maps to NM_198123.1 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:113694835 C>A maps to NM_198123.1 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:110714106 A>T maps to NM_003649.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:110714106 A>T maps to NM_003649.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:61541329 G>A maps to NM_033081.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:61541329 G>A maps to NM_033081.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:29314233 C>A maps to NM_001166005.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:29314233 C>A maps to NM_001166005.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:144940512 G>A maps to NM_031308.1 A2303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:144940512 G>A maps to NM_031308.1 A2303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:190068053 G>T maps to NM_199051.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:190068053 G>T maps to NM_199051.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:60297986 G>T maps to NM_012182.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:60297986 G>T maps to NM_012182.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:101969871 G>A maps to NM_138437.5 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:101969871 G>A maps to NM_138437.5 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:26199201 G>A maps to NM_021065.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:26199201 G>A maps to NM_021065.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:71142249 C>A maps to ENST00000439900 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:71142249 C>A maps to ENST00000439900 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:4920463 A>T maps to NM_002235.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:4920463 A>T maps to NM_002235.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:55340831 G>A maps to NM_013289.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:55340831 G>A maps to NM_013289.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr9:130263349 T>C maps to NM_001005374.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr9:130263349 T>C maps to NM_001005374.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:5821242 C>T maps to ENST00000381093 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:5821242 C>T maps to ENST00000381093 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:5821248 A>G maps to ENST00000381093 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:5821248 A>G maps to ENST00000381093 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:5317414 G>A maps to NM_002532.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:5317414 G>A maps to NM_002532.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:56031202 G>T maps to NM_206899.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:56031202 G>T maps to NM_206899.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:49366454 A>G maps to NM_032521.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:49366454 A>G maps to NM_032521.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:24906175 C>A maps to ENST00000379068 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:24906175 C>A maps to ENST00000379068 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr21:15596756 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr21:15596756 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:124756660 G>A maps to NM_019055.5 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:124756660 G>A maps to NM_019055.5 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:166900384 G>A maps to NM_001165963.1 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:166900384 G>A maps to NM_001165963.1 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:144904435 C>T maps to NM_001144010.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:144904435 C>T maps to NM_001144010.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:1220684 A>T maps to NM_000455.4 K235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:1220684 A>T maps to NM_000455.4 K235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:48848036 G>T maps to NM_172311.2 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:48848036 G>T maps to NM_172311.2 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:43892286 G>A maps to NM_153700.2 Q1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:43892286 G>A maps to NM_153700.2 Q1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:88485518 G>T maps to NM_018271.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:88485518 G>T maps to NM_018271.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710466 C>T maps to NM_001143819.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710466 C>T maps to NM_001143819.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715133 C>T maps to NM_001143819.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715133 C>T maps to NM_001143819.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715146 C>T maps to NM_001143819.1 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715146 C>T maps to NM_001143819.1 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113717995 C>T maps to NM_001143819.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113717995 C>T maps to NM_001143819.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:31769001 G>T maps to NM_020856.2 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:31769001 G>T maps to NM_020856.2 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:61574335 G>T maps to NM_000789.3 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:61574335 G>T maps to NM_000789.3 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:185697769 G>C maps to NM_001995.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:185697769 G>C maps to NM_001995.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:20638524 G>A maps to NM_052956.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:20638524 G>A maps to NM_052956.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:100606230 G>A maps to NM_022496.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:100606230 G>A maps to NM_022496.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:32150921 C>T maps to ENST00000375070 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:32150921 C>T maps to ENST00000375070 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:105413012 C>T maps to NM_138420.2 L2925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:105413012 C>T maps to NM_138420.2 L2925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:91712591 G>T maps to NM_005751.4 E2757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:91712591 G>T maps to NM_005751.4 E2757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:54450166 C>T maps to NM_153228.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:54450166 C>T maps to NM_153228.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:6889984 C>T maps to ENST00000400091 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:6889984 C>T maps to ENST00000400091 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:6890047 C>T maps to ENST00000400091 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:6890047 C>T maps to ENST00000400091 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:119134030 C>A maps to NM_020754.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:119134030 C>A maps to NM_020754.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:113514623 G>A maps to NM_032189.3 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:113514623 G>A maps to NM_032189.3 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:16437285 C>T maps to NM_017637.5 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:16437285 C>T maps to NM_017637.5 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:79514604 C>A maps to NM_025161.5 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:79514604 C>A maps to NM_025161.5 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:94146905 C>A maps to NM_022900.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:94146905 C>A maps to NM_022900.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:15819509 C>T maps to NM_001229.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:15819509 C>T maps to NM_001229.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:62533819 C>A maps to NM_138363.1 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:62533819 C>A maps to NM_138363.1 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:69993721 G>C maps to NM_006431.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:69993721 G>C maps to NM_006431.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:46931713 C>A maps to NM_014246.1 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:46931713 C>A maps to NM_014246.1 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:90038108 C>G maps to NM_145039.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:90038108 C>G maps to NM_145039.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:117280523 C>A maps to NM_014956.4 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:117280523 C>A maps to NM_014956.4 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:27462597 G>A maps to NM_001831.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:27462597 G>A maps to NM_001831.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:31349862 G>A maps to NM_004086.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:31349862 G>A maps to NM_004086.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:46908345 G>T maps to ENST00000359759 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:46908345 G>T maps to ENST00000359759 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:4171671 C>T maps to NM_032607.1 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:4171671 C>T maps to NM_032607.1 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:209007436 C>T maps to NM_005210.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:209007436 C>T maps to NM_005210.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:125685235 T>G maps to NM_178470.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:125685235 T>G maps to NM_178470.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:153911513 G>C maps to NM_014856.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:153911513 G>C maps to NM_014856.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:74177855 C>A maps to NM_080916.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:74177855 C>A maps to NM_080916.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:3729133 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:3729133 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:21923946 C>T maps to NM_003777.3 I4149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:21923946 C>T maps to NM_003777.3 I4149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:99977859 G>T maps to NM_015904.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:99977859 G>T maps to NM_015904.3 E166*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4486-01A-01D-1265-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-49-4486-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:46124836 G>A maps to NM_001193268.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:46124836 G>A maps to NM_001193268.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:637752 C>T maps to NM_018303.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:637752 C>T maps to NM_018303.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:72945354 C>T maps to NM_015189.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:72945354 C>T maps to NM_015189.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:88427553 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:88427553 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:145581358 G>A maps to NM_012162.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:145581358 G>A maps to NM_012162.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:157557311 G>A maps to NM_031282.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:157557311 G>A maps to NM_031282.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:186370113 G>T maps to NM_014375.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:186370113 G>T maps to NM_014375.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:30708996 C>T maps to NM_005803.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:30708996 C>T maps to NM_005803.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:26851621 C>G maps to NM_003593.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:26851621 C>G maps to NM_003593.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:46307712 G>T maps to ENST00000507069 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:46307712 G>T maps to ENST00000507069 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:48908349 G>A maps to NM_000836.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:48908349 G>A maps to NM_000836.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:156634680 C>G maps to NM_001130684.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:156634680 C>G maps to NM_001130684.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:153223607 G>A maps to ENST00000369984 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:153223607 G>A maps to ENST00000369984 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:89607913 C>A maps to NM_014606.1 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:89607913 C>A maps to NM_014606.1 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:67833506 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:67833506 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:81592195 C>T maps to NM_172217.3 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:81592195 C>T maps to NM_172217.3 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:41350979 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:41350979 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:7125476 G>T maps to NM_000208.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:7125476 G>T maps to NM_000208.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:12961966 C>G maps to ENST00000429247 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:12961966 C>G maps to ENST00000429247 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:128781479 C>T maps to NM_000890.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:128781479 C>T maps to NM_000890.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:39082721 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:39082721 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:134999868 G>T maps to ENST00000368572 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:134999868 G>T maps to ENST00000368572 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:52826901 C>T maps to ENST00000252245 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:52826901 C>T maps to ENST00000252245 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:140270932 G>A maps to NM_012317.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:140270932 G>A maps to NM_012317.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:128434781 C>A maps to NM_001006617.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:128434781 C>A maps to NM_001006617.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:119245036 G>C maps to ENST00000316316 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:119245036 G>C maps to ENST00000316316 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:71844960 G>T maps to ENST00000396051 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:71844960 G>T maps to ENST00000396051 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:75010726 C>A maps to NM_016065.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:75010726 C>A maps to NM_016065.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:97256211 C>A maps to NM_015942.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:97256211 C>A maps to NM_015942.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:1275484 C>A maps to ENST00000447027 A5130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:1275484 C>A maps to ENST00000447027 A5130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:2685594 G>A maps to NM_001012418.3 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:2685594 G>A maps to NM_001012418.3 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:26317264 A>G maps to ENST00000407587 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:26317264 A>G maps to ENST00000407587 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:236144993 C>T maps to NM_002508.2 A1048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:236144993 C>T maps to NM_002508.2 A1048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:46827466 C>G maps to NM_199044.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:46827466 C>G maps to NM_199044.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:135310103 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:135310103 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:107332059 G>C maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:107332059 G>C maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:107332125 G>A maps to NM_001004483.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:107332125 G>A maps to NM_001004483.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:59282630 G>A maps to NM_001004711.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:59282630 G>A maps to NM_001004711.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:55873051 C>T maps to NM_001005200.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:55873051 C>T maps to NM_001005200.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:206023444 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:206023444 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:140222270 C>T maps to NM_018911.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:140222270 C>T maps to NM_018911.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:79867408 G>A maps to NM_001184917.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:79867408 G>A maps to NM_001184917.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:230486820 C>G maps to ENST00000321327 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:230486820 C>G maps to ENST00000321327 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:18924679 C>G maps to NM_000292.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:18924679 C>G maps to NM_000292.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:21174156 C>G maps to NM_058004.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:21174156 C>G maps to NM_058004.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:131976379 C>T maps to NM_001083538.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:131976379 C>T maps to NM_001083538.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:11560100 A>G maps to ENST00000436195 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:11560100 A>G maps to ENST00000436195 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:43680049 G>C maps to ENST00000270059 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:43680049 G>C maps to ENST00000270059 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:15486912 G>C maps to NM_001128217.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:15486912 G>C maps to NM_001128217.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:808702 C>T maps to NM_002819.4 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:808702 C>T maps to NM_002819.4 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:157387989 C>T maps to NM_002847.3 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:157387989 C>T maps to NM_002847.3 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:10132254 C>T maps to NM_015725.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:10132254 C>T maps to NM_015725.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:111695224 C>A maps to NM_002912.3 G1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:111695224 C>A maps to NM_002912.3 G1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:151316754 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:151316754 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:19312512 C>A maps to NM_003721.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:19312512 C>A maps to NM_003721.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:108488038 G>A maps to NM_182588.2 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:108488038 G>A maps to NM_182588.2 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:130929756 C>A maps to NM_015347.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:130929756 C>A maps to NM_015347.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:95033574 G>A maps to NM_006215.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:95033574 G>A maps to NM_006215.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:51629007 C>T maps to NM_014441.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:51629007 C>T maps to NM_014441.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:9097677 C>G maps to NM_003039.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:9097677 C>G maps to NM_003039.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:62656062 C>T maps to NM_001012661.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:62656062 C>T maps to NM_001012661.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:150773143 C>G maps to NM_003040.3 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:150773143 C>G maps to NM_003040.3 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:40656136 G>T maps to NM_021097.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:40656136 G>T maps to NM_021097.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:70617447 G>A maps to NM_030958.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:70617447 G>A maps to NM_030958.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:168149325 C>T maps to NM_003062.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:168149325 C>T maps to NM_003062.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:135496713 C>T maps to NM_001001419.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:135496713 C>T maps to NM_001001419.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:39910293 C>G maps to NM_019008.4 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:39910293 C>G maps to NM_019008.4 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:53777320 G>A maps to NM_138473.2 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:53777320 G>A maps to NM_138473.2 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:121355963 G>A maps to NM_152546.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:121355963 G>A maps to NM_152546.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:67925796 G>T maps to NM_017635.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:67925796 G>T maps to NM_017635.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:158487539 C>A maps to NM_003898.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:158487539 C>A maps to NM_003898.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:159161475 C>T maps to NM_018342.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:159161475 C>T maps to NM_018342.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:32568033 C>T maps to NM_018056.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:32568033 C>T maps to NM_018056.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:45846541 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:45846541 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:43251403 C>T maps to NM_032538.1 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:43251403 C>T maps to NM_032538.1 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:156555559 C>T maps to NM_001105669.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:156555559 C>T maps to NM_001105669.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrY:15372252 G>A maps to NM_007125.3 Q1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrY:15372252 G>A maps to NM_007125.3 Q1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:117589583 G>A maps to NM_182645.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:117589583 G>A maps to NM_182645.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:153076458 C>T maps to NM_003381.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:153076458 C>T maps to NM_003381.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:118948941 C>T maps to NM_021729.4 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:118948941 C>T maps to NM_021729.4 F606F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4486-01A-01D-1265-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-49-4486-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:154987711 G>T maps to ENST00000417934 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:154987711 G>T maps to ENST00000417934 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:35862213 C>A maps to NM_005095.2 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:35862213 C>A maps to NM_005095.2 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:3380815 G>A maps to NM_001130520.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:3380815 G>A maps to NM_001130520.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:12157505 G>A maps to NM_001080404.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:12157505 G>A maps to NM_001080404.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:48226556 G>T maps to NM_032583.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:48226556 G>T maps to NM_032583.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:43705991 T>C maps to NM_004915.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:43705991 T>C maps to NM_004915.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:44065078 G>T maps to NM_022436.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:44065078 G>T maps to NM_022436.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:179095583 C>A maps to NM_007314.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:179095583 C>A maps to NM_007314.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:207435495 C>G maps to NM_003812.2 Y509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:207435495 C>G maps to NM_003812.2 Y509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:100131597 A>G maps to NM_001102470.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:100131597 A>G maps to NM_001102470.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:19634650 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:19634650 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:69271871 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:69271871 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:201473800 C>A maps to NM_001159.3 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:201473800 C>A maps to NM_001159.3 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:6423817 C>A maps to ENST00000389906 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:6423817 C>A maps to ENST00000389906 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:45452504 A>T maps to NM_000483.3 *102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:45452504 A>T maps to NM_000483.3 *102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:79650869 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:79650869 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:190532187 C>A maps to NM_019048.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:190532187 C>A maps to NM_019048.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:102942738 A>G maps to NM_017935.4 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:102942738 A>G maps to NM_017935.4 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:107937904 C>A maps to NM_001018072.1 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:107937904 C>A maps to NM_001018072.1 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:41897939 G>T maps to NM_004053.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:41897939 G>T maps to NM_004053.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:91626658 G>T maps to NM_001102368.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:91626658 G>T maps to NM_001102368.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:8138500 G>A maps to NM_025099.5 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:8138500 G>A maps to NM_025099.5 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:7283153 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:7283153 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:75086562 A>G maps to NM_001002912.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:75086562 A>G maps to NM_001002912.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:26663340 A>G maps to NM_145038.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:26663340 A>G maps to NM_145038.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:200819109 A>G maps to ENST00000236925 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:200819109 A>G maps to ENST00000236925 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:66721317 G>T maps to NM_024781.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:66721317 G>T maps to NM_024781.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:73548713 G>C maps to ENST00000398860 L1951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:73548713 G>C maps to ENST00000398860 L1951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:73548779 G>A maps to ENST00000398860 V1973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:73548779 G>A maps to ENST00000398860 V1973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:117279604 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:117279604 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:8688714 C>T maps to NM_014358.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:8688714 C>T maps to NM_014358.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:74350796 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:74350796 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:32138037 C>T maps to NM_001856.3 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:32138037 C>T maps to NM_001856.3 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:100893275 G>A maps to NM_052820.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:100893275 G>A maps to NM_052820.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:50204051 C>G maps to NM_152359.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:50204051 C>G maps to NM_152359.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:34554702 C>A maps to ENST00000373381 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:34554702 C>A maps to ENST00000373381 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:77455260 G>T maps to NM_004715.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:77455260 G>T maps to NM_004715.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:57564428 G>T maps to NM_001085458.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:57564428 G>T maps to NM_001085458.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:59409191 C>A maps to NM_000780.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:59409191 C>A maps to NM_000780.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:103908281 C>G maps to NM_001001711.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:103908281 C>G maps to NM_001001711.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:134920437 G>T maps to NM_004441.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:134920437 G>T maps to NM_004441.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:242042434 C>T maps to NM_006027.4 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:242042434 C>T maps to NM_006027.4 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:466931 A>T maps to ENST00000315013 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:466931 A>T maps to ENST00000315013 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:120889069 A>C maps to NM_207009.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:120889069 A>C maps to NM_207009.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:10106095 C>T maps to NM_033084.3 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:10106095 C>T maps to NM_033084.3 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:157771367 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:157771367 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:135440222 G>T maps to ENST00000443774 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:135440222 G>T maps to ENST00000443774 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:163004008 G>C maps to ENST00000233604 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:163004008 G>C maps to ENST00000233604 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:650507 C>A maps to NM_015721.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:650507 C>A maps to NM_015721.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:183909712 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:183909712 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131019540 G>A maps to NM_004486.4 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131019540 G>A maps to NM_004486.4 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:23299725 C>T maps to ENST00000435486 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:23299725 C>T maps to ENST00000435486 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:123186930 G>T maps to NM_177551.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:123186930 G>T maps to NM_177551.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:11136728 C>T maps to NM_005333.4 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:11136728 C>T maps to NM_005333.4 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:176981699 G>T maps to NM_002148.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:176981699 G>T maps to NM_002148.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:152193050 C>A maps to NM_001009931.1 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:152193050 C>A maps to NM_001009931.1 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:94985760 G>A maps to ENST00000375660 N1142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:94985760 G>A maps to ENST00000375660 N1142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:118621428 C>A maps to NM_152538.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:118621428 C>A maps to NM_152538.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:38341285 T>A maps to ENST00000373026 K674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:38341285 T>A maps to ENST00000373026 K674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:52836351 C>T maps to NM_002217.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:52836351 C>T maps to NM_002217.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:5029786 C>T maps to NM_004972.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:5029786 C>T maps to NM_004972.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:75444887 G>A maps to NM_139137.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:75444887 G>A maps to NM_139137.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:72292489 G>C maps to NM_014431.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:72292489 G>C maps to NM_014431.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:8919883 G>A maps to NM_020738.2 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:8919883 G>A maps to NM_020738.2 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:136969801 G>A maps to NM_017415.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:136969801 G>A maps to NM_017415.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51530734 C>A maps to NM_144947.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51530734 C>A maps to NM_144947.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:39644972 G>A maps to NM_003771.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:39644972 G>A maps to NM_003771.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:31933419 A>G maps to NM_181614.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:31933419 A>G maps to NM_181614.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:152595393 G>T maps to NM_178431.1 C62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:152595393 G>T maps to NM_178431.1 C62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:32745302 A>C maps to ENST00000373562 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:32745302 A>C maps to ENST00000373562 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55143932 C>A maps to ENST00000427581 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55143932 C>A maps to ENST00000427581 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55179364 G>A maps to ENST00000391733 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55179364 G>A maps to ENST00000391733 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:50589611 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:50589611 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:28319035 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:28319035 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:39844974 C>A maps to ENST00000361689 L2397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:39844974 C>A maps to ENST00000361689 L2397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:10764812 G>T maps to NM_005906.3 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:10764812 G>T maps to NM_005906.3 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:151945169 G>C maps to ENST00000355193 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:151945169 G>C maps to ENST00000355193 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:9013854 G>T maps to NM_024690.2 P12845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:9013854 G>T maps to NM_024690.2 P12845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:38182677 C>T maps to NM_001172567.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:38182677 C>T maps to NM_001172567.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:16145360 C>G maps to NM_013262.3 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:16145360 C>G maps to NM_013262.3 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:26423256 G>T maps to ENST00000407587 V2441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:26423256 G>T maps to ENST00000407587 V2441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:2088652 A>T maps to NM_003970.2 K1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:2088652 A>T maps to NM_003970.2 K1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160313246 C>T maps to NM_015331.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160313246 C>T maps to NM_015331.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:206994877 G>A maps to ENST00000455934 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:206994877 G>A maps to ENST00000455934 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:90808964 C>T maps to NM_001033088.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:90808964 C>T maps to NM_001033088.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:105168968 A>C maps to NM_198465.2 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:105168968 A>C maps to NM_198465.2 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131735482 T>C maps to NM_015354.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131735482 T>C maps to NM_015354.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:77057380 C>A maps to ENST00000458189 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:77057380 C>A maps to ENST00000458189 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:101096644 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:101096644 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:15905245 C>T maps to NM_001004466.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:15905245 C>T maps to NM_001004466.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158450077 G>A maps to NM_001004472.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158450077 G>A maps to NM_001004472.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:4944909 G>T maps to NM_001005237.1 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:4944909 G>T maps to NM_001005237.1 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158517802 G>T maps to NM_001005189.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158517802 G>T maps to NM_001005189.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:48919524 G>T maps to NM_001005203.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:48919524 G>T maps to NM_001005203.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:60864346 C>T maps to NM_144498.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:60864346 C>T maps to NM_144498.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:24874131 C>A maps to NM_015550.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:24874131 C>A maps to NM_015550.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:17664567 C>T maps to NM_012387.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:17664567 C>T maps to NM_012387.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65553263 T>A maps to NM_017851.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65553263 T>A maps to NM_017851.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:99663319 C>G maps to NM_001184880.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:99663319 C>G maps to NM_001184880.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:140531058 G>T maps to NM_018939.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:140531058 G>T maps to NM_018939.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:66384347 C>T maps to NM_001037341.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:66384347 C>T maps to NM_001037341.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:44151934 G>A maps to NM_002606.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:44151934 G>A maps to NM_002606.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:57327814 G>T maps to NM_006210.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:57327814 G>T maps to NM_006210.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49351252 C>A maps to NM_020904.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49351252 C>A maps to NM_020904.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:160240111 C>A maps to NM_173516.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:160240111 C>A maps to NM_173516.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:118314904 G>T maps to NM_000936.2 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:118314904 G>T maps to NM_000936.2 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:68992816 A>G maps to NM_024870.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:68992816 A>G maps to NM_024870.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:60715997 A>T maps to NM_002792.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:60715997 A>T maps to NM_002792.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:40550483 G>A maps to NM_003720.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:40550483 G>A maps to NM_003720.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:204305194 G>A maps to ENST00000374493 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:204305194 G>A maps to ENST00000374493 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:25611291 G>A maps to NM_000965.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:25611291 G>A maps to NM_000965.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:103205756 C>T maps to ENST00000428762 K1726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:103205756 C>T maps to ENST00000428762 K1726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:117249928 T>C maps to NM_173560.3 Y802Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:117249928 T>C maps to NM_173560.3 Y802Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:3429844 A>T maps to NM_198229.2 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:3429844 A>T maps to NM_198229.2 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:74150403 A>G maps to NM_052916.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:74150403 A>G maps to NM_052916.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:21795867 G>T maps to NM_020366.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:21795867 G>T maps to NM_020366.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:114354884 A>C maps to NM_018364.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:114354884 A>C maps to NM_018364.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:12142250 G>T maps to NM_032167.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:12142250 G>T maps to NM_032167.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55751267 C>A maps to ENST00000443936 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55751267 C>A maps to ENST00000443936 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:47162938 T>A maps to NM_014159.6 R1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:47162938 T>A maps to NM_014159.6 R1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:70602364 G>T maps to NM_012426.4 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:70602364 G>T maps to NM_012426.4 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:164735353 C>A maps to NM_001041.3 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:164735353 C>A maps to NM_001041.3 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:140683345 G>A maps to NM_031947.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:140683345 G>A maps to NM_031947.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:45564934 C>A maps to NM_004212.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:45564934 C>A maps to NM_004212.3 T604T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4487-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-49-4487-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:88328486 G>T maps to NM_015567.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:88328486 G>T maps to NM_015567.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:57313401 C>A maps to ENST00000457912 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:57313401 C>A maps to ENST00000457912 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:13145411 T>G maps to NM_018327.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:13145411 T>G maps to NM_018327.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:87837824 A>G maps to NM_003130.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:87837824 A>G maps to NM_003130.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:1207119 G>T maps to NM_000455.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:1207119 G>T maps to NM_000455.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:109306414 G>A maps to NM_018711.2 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:109306414 G>A maps to NM_018711.2 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:20847168 C>A maps to NM_007110.4 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:20847168 C>A maps to NM_007110.4 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:56650540 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:56650540 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:41854259 C>T maps to NM_000660.4 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:41854259 C>T maps to NM_000660.4 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:177020658 G>A maps to NM_017510.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:177020658 G>A maps to NM_017510.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:103596403 G>T maps to NM_006291.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:103596403 G>T maps to NM_006291.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:49866941 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:49866941 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:6495432 G>A maps to NM_006087.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:6495432 G>A maps to NM_006087.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:229771835 G>T maps to NM_014777.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:229771835 G>T maps to NM_014777.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:77921492 C>T maps to NM_020798.2 Y864Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:77921492 C>T maps to NM_020798.2 Y864Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:177649042 C>T maps to NM_005429.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:177649042 C>T maps to NM_005429.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:156979108 C>T maps to NM_001167912.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:156979108 C>T maps to NM_001167912.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:71036293 G>T maps to NM_022479.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:71036293 G>T maps to NM_022479.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:141408875 C>A maps to NM_001105558.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:141408875 C>A maps to NM_001105558.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:147131310 T>A maps to NM_003412.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:147131310 T>A maps to NM_003412.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:44582428 C>A maps to NM_022095.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:44582428 C>A maps to NM_022095.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:114289740 G>T maps to NM_133464.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:114289740 G>T maps to NM_133464.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:35258314 C>T maps to NM_001007248.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:35258314 C>T maps to NM_001007248.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:40774878 T>A maps to NM_033160.5 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:40774878 T>A maps to NM_033160.5 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:20749692 C>A maps to NM_003426.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:20749692 C>A maps to NM_003426.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:58551839 C>T maps to NM_182572.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:58551839 C>T maps to NM_182572.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:48320967 C>T maps to NM_152701.3 Q2919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:48320967 C>T maps to NM_152701.3 Q2919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:23723692 G>T maps to NM_001037171.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:23723692 G>T maps to NM_001037171.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:104247995 C>A maps to NM_005736.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:104247995 C>A maps to NM_005736.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:128994399 A>T maps to NM_133638.3 K793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:128994399 A>T maps to NM_133638.3 K793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:18574146 T>C maps to NM_001040272.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:18574146 T>C maps to NM_001040272.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:96361532 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:96361532 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:41519407 G>A maps to ENST00000415018 Q1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:41519407 G>A maps to ENST00000415018 Q1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:114275527 C>A maps to NM_001148.4 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:114275527 C>A maps to NM_001148.4 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:37433953 G>A maps to ENST00000374660 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:37433953 G>A maps to ENST00000374660 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:50296348 G>T maps to NM_014203.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:50296348 G>T maps to NM_014203.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:193039468 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:193039468 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:88381708 T>A maps to NM_152589.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:88381708 T>A maps to NM_152589.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:39586309 C>A maps to NM_025138.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:39586309 C>A maps to NM_025138.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:87936057 A>T maps to NM_001739.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:87936057 A>T maps to NM_001739.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6291447 G>T maps to NM_176875.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6291447 G>T maps to NM_176875.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:66492421 G>T maps to NM_005582.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:66492421 G>T maps to NM_005582.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:157805681 C>A maps to NM_005894.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:157805681 C>A maps to NM_005894.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:3766047 G>A maps to NM_001810.5 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:3766047 G>A maps to NM_001810.5 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:124783244 G>T maps to NM_130773.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:124783244 G>T maps to NM_130773.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:148927061 G>T maps to NM_000096.3 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:148927061 G>T maps to NM_000096.3 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:126133023 C>A maps to NM_173689.5 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:126133023 C>A maps to NM_173689.5 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:18710442 G>T maps to NM_004750.4 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:18710442 G>T maps to NM_004750.4 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:11364841 C>T maps to NM_001332.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:11364841 C>T maps to NM_001332.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:118676545 G>T maps to NM_022101.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:118676545 G>T maps to NM_022101.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:30633332 C>A maps to NM_003587.4 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:30633332 C>A maps to NM_003587.4 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:10886571 C>T maps to NM_001005361.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:10886571 C>T maps to NM_001005361.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:37349651 G>C maps to NM_001135651.1 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:37349651 G>C maps to NM_001135651.1 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:133785996 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:133785996 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:172635119 G>A maps to NM_000639.1 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:172635119 G>A maps to NM_000639.1 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:55817594 C>T maps to NM_152231.1 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:55817594 C>T maps to NM_152231.1 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:125324085 G>T maps to NM_005103.4 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:125324085 G>T maps to NM_005103.4 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:32735019 G>A maps to NM_139241.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:32735019 G>A maps to NM_139241.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:183731208 C>A maps to NM_001463.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:183731208 C>A maps to NM_001463.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:117693432 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:117693432 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:97731231 G>A maps to NM_001105580.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:97731231 G>A maps to NM_001105580.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:31189074 G>T maps to NM_024572.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:31189074 G>T maps to NM_024572.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:90605635 G>A maps to NM_032602.1 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:90605635 G>A maps to NM_032602.1 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:122528961 C>A maps to NM_000828.4 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:122528961 C>A maps to NM_000828.4 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:222696184 T>A maps to NM_024746.3 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:222696184 T>A maps to NM_024746.3 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:222712015 C>A maps to NM_024746.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:222712015 C>A maps to NM_024746.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:15243093 T>A maps to NM_001031853.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:15243093 T>A maps to NM_001031853.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:19554469 C>T maps to NM_144633.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:19554469 C>T maps to NM_144633.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:27585277 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:27585277 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:51901792 G>T maps to NM_032559.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:51901792 G>T maps to NM_032559.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:39506805 C>A maps to NM_004138.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:39506805 C>A maps to NM_004138.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:39324028 G>T maps to NM_033187.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:39324028 G>T maps to NM_033187.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr18:7080333 G>T maps to NM_005559.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr18:7080333 G>T maps to NM_005559.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:169574169 C>T maps to NM_024727.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:169574169 C>T maps to NM_024727.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:151504264 C>A maps to NM_006439.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:151504264 C>A maps to NM_006439.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:75004592 G>A maps to NM_138703.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:75004592 G>A maps to NM_138703.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:112720710 C>A maps to NM_001085377.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:112720710 C>A maps to NM_001085377.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:46806779 C>A maps to NM_005588.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:46806779 C>A maps to NM_005588.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:75515140 C>T maps to NM_001040108.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:75515140 C>T maps to NM_001040108.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:10439864 T>G maps to NM_017534.5 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:10439864 T>G maps to NM_017534.5 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:203054888 C>T maps to NM_002479.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:203054888 C>T maps to NM_002479.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:101748032 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:101748032 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:29553701 G>T maps to NM_001042492.2 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:29553701 G>T maps to NM_001042492.2 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:23944435 G>A maps to NM_001042635.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:23944435 G>A maps to NM_001042635.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:123657420 G>A maps to NM_001163278.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:123657420 G>A maps to NM_001163278.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:248112647 C>T maps to NM_001001963.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:248112647 C>T maps to NM_001001963.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:55322372 G>A maps to NM_001001920.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:55322372 G>A maps to NM_001001920.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:22382660 G>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:22382660 G>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:99961383 C>A maps to ENST00000457907 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:99961383 C>A maps to ENST00000457907 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:73008426 G>A maps to NM_004154.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:73008426 G>A maps to NM_004154.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:233122107 C>T maps to NM_014801.3 S1990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:233122107 C>T maps to NM_014801.3 S1990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:49754614 G>A maps to NM_138733.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:49754614 G>A maps to NM_138733.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:103041585 C>A maps to NM_000533.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:103041585 C>A maps to NM_000533.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:118202625 C>A maps to NM_001011709.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:118202625 C>A maps to NM_001011709.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:16279253 T>C maps to NM_001136213.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:16279253 T>C maps to NM_001136213.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:61917612 C>T maps to NM_006255.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:61917612 C>T maps to NM_006255.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:71830725 G>T maps to NM_001126128.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:71830725 G>T maps to NM_001126128.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:95941742 G>T maps to NM_144707.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:95941742 G>T maps to NM_144707.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:40681205 G>T maps to NM_000958.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:40681205 G>T maps to NM_000958.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:1537677 G>T maps to NM_001013658.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:1537677 G>T maps to NM_001013658.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:73627304 G>A maps to NM_004259.5 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:73627304 G>A maps to NM_004259.5 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:46949271 C>T maps to NM_152869.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:46949271 C>T maps to NM_152869.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:241094037 C>A maps to ENST00000407727 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:241094037 C>A maps to ENST00000407727 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:104303257 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:104303257 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:75388073 G>T maps to NM_031464.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:75388073 G>T maps to NM_031464.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:15064948 G>A maps to NM_005071.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:15064948 G>A maps to NM_005071.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:110763798 C>A maps to NM_033125.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:110763798 C>A maps to NM_033125.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:164907670 A>T maps to NM_014926.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:164907670 A>T maps to NM_014926.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:51571150 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:51571150 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158612762 C>T maps to NM_003126.2 W1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158612762 C>T maps to NM_003126.2 W1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158648303 G>T maps to NM_003126.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158648303 G>T maps to NM_003126.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:38031143 G>T maps to NM_006307.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:38031143 G>T maps to NM_006307.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:171533718 G>C maps to NM_005990.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:171533718 G>C maps to NM_005990.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:119427377 G>A maps to ENST00000369429 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:119427377 G>A maps to ENST00000369429 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:65170926 A>G maps to NM_001010874.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:65170926 A>G maps to NM_001010874.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:30701124 G>T maps to NM_031271.3 C1803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:30701124 G>T maps to NM_031271.3 C1803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:72969994 A>T maps to NM_007332.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:72969994 A>T maps to NM_007332.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:110236694 A>G maps to NM_021625.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:110236694 A>G maps to NM_021625.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:93392 C>A maps to NM_177987.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:93392 C>A maps to NM_177987.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:70361498 C>A maps to NM_021139.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:70361498 C>A maps to NM_021139.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:43557547 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:43557547 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:17758167 C>A maps to ENST00000428389 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:17758167 C>A maps to ENST00000428389 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:96091426 G>T maps to NM_003728.3 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:96091426 G>T maps to NM_003728.3 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:31749538 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:31749538 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:168108350 G>T maps to NM_152381.5 T3483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:168108350 G>T maps to NM_152381.5 T3483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:100459594 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:100459594 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:58385170 G>T maps to NM_053023.4 G569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:58385170 G>T maps to NM_053023.4 G569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:35863112 G>T maps to NM_005095.2 E1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:35863112 G>T maps to NM_005095.2 E1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:44891283 C>A maps to NM_152354.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:44891283 C>A maps to NM_152354.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:21706479 A>T maps to NM_024697.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:21706479 A>T maps to NM_024697.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:57936548 G>T maps to NM_007156.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:57936548 G>T maps to NM_007156.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:16215936 C>T maps to ENST00000399408 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:16215936 C>T maps to ENST00000399408 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:12367059 C>T maps to NM_006796.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:12367059 C>T maps to NM_006796.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:4881967 C>T maps to NM_001040177.1 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:4881967 C>T maps to NM_001040177.1 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:135239585 G>A maps to NM_022568.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:135239585 G>A maps to NM_022568.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:79650120 T>C maps to NM_001040025.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:79650120 T>C maps to NM_001040025.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:152772564 C>A maps to NM_001711.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:152772564 C>A maps to NM_001711.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:19839739 G>A maps to NM_024627.5 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:19839739 G>A maps to NM_024627.5 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:2985558 C>T maps to NM_032415.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:2985558 C>T maps to NM_032415.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr19:1031149 C>A maps to NM_004368.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr19:1031149 C>A maps to NM_004368.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:75801214 T>C maps to ENST00000322507 K2892K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:75801214 T>C maps to ENST00000322507 K2892K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr4:126389826 C>T maps to NM_024582.4 G4020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr4:126389826 C>T maps to NM_024582.4 G4020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:161117219 A>T maps to NM_000811.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:161117219 A>T maps to NM_000811.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:178408744 C>T maps to NM_000843.3 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:178408744 C>T maps to NM_000843.3 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:118460543 G>A maps to NM_025015.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:118460543 G>A maps to NM_025015.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:217542954 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:217542954 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr19:14150581 C>A maps to NM_004843.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr19:14150581 C>A maps to NM_004843.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:103969532 G>T maps to NM_199000.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:103969532 G>T maps to NM_199000.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:10352022 G>C maps to NM_017533.2 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:10352022 G>C maps to NM_017533.2 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:55541386 C>T maps to NM_001001967.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:55541386 C>T maps to NM_001001967.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:32089580 C>A maps to NM_178140.2 P2009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:32089580 C>A maps to NM_178140.2 P2009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:20442054 G>A maps to ENST00000442610 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:20442054 G>A maps to ENST00000442610 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:14107310 C>T maps to NM_012231.4 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:14107310 C>T maps to NM_012231.4 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:23522506 T>C maps to NM_020227.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:23522506 T>C maps to NM_020227.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:141716267 C>A maps to NM_005607.4 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:141716267 C>A maps to NM_005607.4 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:24621035 C>T maps to NM_017999.4 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:24621035 C>T maps to NM_017999.4 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:148869468 C>T maps to NM_015278.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:148869468 C>T maps to NM_015278.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:67734615 C>T maps to NM_013257.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:67734615 C>T maps to NM_013257.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:17412164 G>A maps to NM_001164771.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:17412164 G>A maps to NM_001164771.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:63965324 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:63965324 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:100532630 C>A maps to NM_024885.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:100532630 C>A maps to NM_024885.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:50791271 C>A maps to ENST00000263046 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:50791271 C>A maps to ENST00000263046 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:172224320 G>A maps to ENST00000382750 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:172224320 G>A maps to ENST00000382750 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:30309600 G>A maps to NM_021253.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:30309600 G>A maps to NM_021253.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:56591553 T>C maps to NM_013444.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:56591553 T>C maps to NM_013444.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:8976458 C>G maps to NM_144670.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:8976458 C>G maps to NM_144670.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:2939236 C>A maps to NM_080431.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:2939236 C>A maps to NM_080431.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:87780636 T>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:87780636 T>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:24908653 C>A maps to NM_020824.3 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:24908653 C>A maps to NM_020824.3 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:50264908 A>T maps to NM_024837.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:50264908 A>T maps to NM_024837.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:34118586 G>A maps to NM_133468.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:34118586 G>A maps to NM_133468.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:32370727 C>A maps to ENST00000468270 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:32370727 C>A maps to ENST00000468270 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:5777378 G>A maps to NM_017782.4 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:5777378 G>A maps to NM_017782.4 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:3721735 G>C maps to NM_001114118.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:3721735 G>C maps to NM_001114118.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:100086912 G>T maps to ENST00000423930 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:100086912 G>T maps to ENST00000423930 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:181745280 C>A maps to ENST00000357570 Y1728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:181745280 C>A maps to ENST00000357570 Y1728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:122002642 C>T maps to NM_001178065.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:122002642 C>T maps to NM_001178065.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:74559017 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:74559017 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:175624090 G>A maps to NM_001039523.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:175624090 G>A maps to NM_001039523.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:33586291 G>A maps to ENST00000359576 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:33586291 G>A maps to ENST00000359576 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:51012809 C>T maps to NM_152245.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:51012809 C>T maps to NM_152245.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:3265421 G>T maps to NM_033225.5 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:3265421 G>T maps to NM_033225.5 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:52781003 G>T maps to NM_000782.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:52781003 G>T maps to NM_000782.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:94342194 G>A maps to NM_014597.4 N432N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:94342194 G>A maps to NM_014597.4 N432N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:62373359 T>C maps to ENST00000278845 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:62373359 T>C maps to ENST00000278845 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:76028403 A>T maps to NM_001992.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:76028403 A>T maps to NM_001992.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131008459 A>G maps to NM_133372.2 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131008459 A>G maps to NM_133372.2 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:27765181 G>A maps to NM_033223.4 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:27765181 G>A maps to NM_033223.4 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:81410933 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:81410933 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:69148655 A>T maps to NM_005329.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:69148655 A>T maps to NM_005329.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:38822910 C>T maps to NM_152868.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:38822910 C>T maps to NM_152868.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:53215787 C>A maps to NM_175834.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:53215787 C>A maps to NM_175834.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:197707306 C>T maps to NM_001136049.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:197707306 C>T maps to NM_001136049.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:44204415 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:44204415 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:42042147 G>T maps to ENST00000219905 E2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:42042147 G>T maps to ENST00000219905 E2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:34964760 A>G maps to NM_024864.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:34964760 A>G maps to NM_024864.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:41791381 C>A maps to NM_006766.3 A1452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:41791381 C>A maps to NM_006766.3 A1452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:19890505 A>T maps to ENST00000396087 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:19890505 A>T maps to ENST00000396087 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:233785095 G>A maps to NM_019850.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:233785095 G>A maps to NM_019850.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:56363726 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:56363726 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:89088202 G>A maps to NM_016931.3 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:89088202 G>A maps to NM_016931.3 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:86268246 G>T maps to NM_006183.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:86268246 G>T maps to NM_006183.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:20443787 G>T maps to NM_001005486.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:20443787 G>T maps to NM_001005486.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:58170033 C>A maps to NM_001005469.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:58170033 C>A maps to NM_001005469.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:148715892 C>A maps to NM_181742.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:148715892 C>A maps to NM_181742.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:140182644 G>A maps to NM_018906.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:140182644 G>A maps to NM_018906.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:140503214 G>A maps to NM_018938.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:140503214 G>A maps to NM_018938.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:142548566 G>A maps to NM_013363.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:142548566 G>A maps to NM_013363.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:13283718 C>T maps to NM_030948.1 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:13283718 C>T maps to NM_030948.1 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:52735014 G>T maps to NM_000953.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:52735014 G>T maps to NM_000953.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:53607013 C>T maps to NM_000966.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:53607013 C>T maps to NM_000966.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:47034491 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:47034491 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:103159822 G>T maps to ENST00000428762 G2603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:103159822 G>T maps to ENST00000428762 G2603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:30611730 G>A maps to NM_138328.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:30611730 G>A maps to NM_138328.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:40701711 G>A maps to NM_012421.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:40701711 G>A maps to NM_012421.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:45992752 C>T maps to NM_005619.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:45992752 C>T maps to NM_005619.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:62037699 G>T maps to NM_002411.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:62037699 G>T maps to NM_002411.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:101047371 T>A maps to NM_020654.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:101047371 T>A maps to NM_020654.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:25921559 G>T maps to NM_005835.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:25921559 G>T maps to NM_005835.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17994524 C>T maps to NM_000453.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17994524 C>T maps to NM_000453.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:60575635 C>A maps to NM_003185.3 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:60575635 C>A maps to NM_003185.3 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:231349584 G>A maps to NM_001004342.3 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:231349584 G>A maps to NM_001004342.3 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:53114869 A>C maps to NM_022117.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:53114869 A>C maps to NM_022117.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:178416999 G>C maps to NM_152517.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:178416999 G>C maps to NM_152517.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:93686678 C>T maps to NM_175748.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:93686678 C>T maps to NM_175748.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:177608434 G>A maps to NM_005429.2 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:177608434 G>A maps to NM_005429.2 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:1741937 C>A maps to NM_032642.2 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:1741937 C>A maps to NM_032642.2 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:58439200 C>T maps to NM_133460.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:58439200 C>T maps to NM_133460.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:31025802 G>T maps to NM_014717.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:31025802 G>T maps to NM_014717.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:85327612 G>A maps to NM_014630.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:85327612 G>A maps to NM_014630.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52876488 G>T maps to NM_001145434.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52876488 G>T maps to NM_001145434.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:21213574 G>A maps to NM_003460.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:21213574 G>A maps to NM_003460.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:236659076 G>A maps to NM_001037131.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:236659076 G>A maps to NM_001037131.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:76939964 G>A maps to NM_000489.3 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:76939964 G>A maps to NM_000489.3 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:654046 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:654046 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:44144682 C>T maps to NM_007058.3 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:44144682 C>T maps to NM_007058.3 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:72250878 C>T maps to NM_032649.5 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:72250878 C>T maps to NM_032649.5 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:32930059 G>A maps to NM_001172774.1 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:32930059 G>A maps to NM_001172774.1 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:102493717 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:102493717 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:22548528 C>A maps to NM_004430.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:22548528 C>A maps to NM_004430.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr10:102677017 G>A maps to NM_001136123.1 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr10:102677017 G>A maps to NM_001136123.1 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:140055780 C>A maps to ENST00000371546 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:140055780 C>A maps to ENST00000371546 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:111668632 C>T maps to NM_003640.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:111668632 C>T maps to NM_003640.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:146991889 T>C maps to NM_014790.3 Q797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:146991889 T>C maps to NM_014790.3 Q797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:202704716 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:202704716 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:94173126 G>A maps to ENST00000393153 P2617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:94173126 G>A maps to ENST00000393153 P2617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:173703049 G>A maps to NM_014458.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:173703049 G>A maps to NM_014458.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:33629296 C>T maps to NM_004795.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:33629296 C>T maps to NM_004795.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr21:46000422 G>A maps to NM_198694.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr21:46000422 G>A maps to NM_198694.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:70164437 G>A maps to NM_002357.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:70164437 G>A maps to NM_002357.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:10538772 C>T maps to NM_002470.2 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:10538772 C>T maps to NM_002470.2 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr10:69959229 C>T maps to NM_032578.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr10:69959229 C>T maps to NM_032578.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:130884336 C>T maps to NM_024800.4 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:130884336 C>T maps to NM_024800.4 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:123909324 C>T maps to NM_001004463.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:123909324 C>T maps to NM_001004463.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:161781118 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:161781118 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:77256456 C>G maps to NM_002835.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:77256456 C>G maps to NM_002835.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:38903680 G>A maps to ENST00000405332 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:38903680 G>A maps to ENST00000405332 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:127765391 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:127765391 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:78176220 G>A maps to NM_144777.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:78176220 G>A maps to NM_144777.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:122642571 G>A maps to NM_001031702.2 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:122642571 G>A maps to NM_001031702.2 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:27472894 G>A maps to ENST00000454389 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:27472894 G>A maps to ENST00000454389 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:65239967 C>A maps to ENST00000389723 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:65239967 C>A maps to ENST00000389723 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:114201654 G>T maps to NM_017905.4 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:114201654 G>T maps to NM_017905.4 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:62783683 C>A maps to ENST00000280377 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:62783683 C>A maps to ENST00000280377 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:155127855 G>A maps to NM_005638.5 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:155127855 G>A maps to NM_005638.5 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:219301980 C>T maps to NM_007127.2 H702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:219301980 C>T maps to NM_007127.2 H702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:2635510 G>A maps to NM_003383.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:2635510 G>A maps to NM_003383.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:38270002 G>T maps to NM_024640.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:38270002 G>T maps to NM_024640.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:22806285 A>G maps to NM_015461.2 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:22806285 A>G maps to NM_015461.2 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:148048525 G>A maps to NM_002025.3 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:148048525 G>A maps to NM_002025.3 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:153575350 G>T maps to NM_152522.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:153575350 G>T maps to NM_152522.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:50192226 C>G maps to ENST00000342989 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:50192226 C>G maps to ENST00000342989 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:107914363 C>A maps to NM_001018072.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:107914363 C>A maps to NM_001018072.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:26509305 C>A maps to NM_001732.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:26509305 C>A maps to NM_001732.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:746118 C>T maps to NM_033409.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:746118 C>T maps to NM_033409.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:179976928 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:179976928 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:48614315 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:48614315 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:194062054 C>T maps to NM_001080513.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:194062054 C>T maps to NM_001080513.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:72134054 G>A maps to ENST00000359684 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:72134054 G>A maps to ENST00000359684 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:61657204 G>T maps to NM_005828.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:61657204 G>T maps to NM_005828.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:74166085 A>G maps to NM_080916.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:74166085 A>G maps to NM_080916.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:95556996 C>A maps to NM_177438.2 P1869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:95556996 C>A maps to NM_177438.2 P1869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:48244175 G>T maps to NM_014601.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:48244175 G>T maps to NM_014601.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:111480848 G>T maps to NM_001977.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:111480848 G>T maps to NM_001977.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:142562292 G>T maps to NM_004445.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:142562292 G>T maps to NM_004445.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:103460021 C>T maps to NM_017693.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:103460021 C>T maps to NM_017693.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:19110321 A>G maps to NM_052911.2 N835N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:19110321 A>G maps to NM_052911.2 N835N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:49218950 G>A maps to NM_080829.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:49218950 G>A maps to NM_080829.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:126389832 G>C maps to NM_024582.4 R4022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:126389832 G>C maps to NM_024582.4 R4022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:37099078 C>A maps to NM_001008777.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:37099078 C>A maps to NM_001008777.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:142451830 C>A maps to NM_207414.2 G956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:142451830 C>A maps to NM_207414.2 G956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:173734826 C>A maps to NM_001034845.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:173734826 C>A maps to NM_001034845.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:179734238 C>A maps to NM_005110.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:179734238 C>A maps to NM_005110.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:117885021 G>T maps to NM_005264.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:117885021 G>T maps to NM_005264.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:20327354 G>T maps to NM_001007240.1 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:20327354 G>T maps to NM_001007240.1 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:88300588 G>T maps to NM_001143831.2 C754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:88300588 G>T maps to NM_001143831.2 C754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:91816322 G>T maps to NM_001017975.3 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:91816322 G>T maps to NM_001017975.3 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:186121912 G>T maps to NM_031935.2 R4976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:186121912 G>T maps to NM_031935.2 R4976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:21409375 T>C maps to NM_002170.3 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:21409375 T>C maps to NM_002170.3 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:47075133 C>T maps to NM_006546.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:47075133 C>T maps to NM_006546.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:1535816 G>A maps to ENST00000389470 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:1535816 G>A maps to ENST00000389470 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:55360396 C>A maps to NM_024335.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:55360396 C>A maps to NM_024335.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:31283250 G>C maps to NM_001145808.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:31283250 G>C maps to NM_001145808.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:20449247 C>A maps to NM_002214.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:20449247 C>A maps to NM_002214.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:210970994 G>T maps to NM_172362.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:210970994 G>T maps to NM_172362.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:51901329 C>T maps to NM_032559.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:51901329 C>T maps to NM_032559.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:70681813 T>A maps to NM_020866.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:70681813 T>A maps to NM_020866.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:21513859 T>A maps to ENST00000416669 S2943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:21513859 T>A maps to ENST00000416669 S2943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:31765614 G>A maps to NM_021177.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:31765614 G>A maps to NM_021177.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:75078523 T>A maps to NM_000428.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:75078523 T>A maps to NM_000428.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:24759848 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:24759848 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:55532289 C>T maps to NM_004530.4 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:55532289 C>T maps to NM_004530.4 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:206992594 G>A maps to ENST00000455934 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:206992594 G>A maps to ENST00000455934 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:17624951 G>A maps to ENST00000430136 P1369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:17624951 G>A maps to ENST00000430136 P1369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:101095867 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:101095867 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:248637256 G>T maps to NM_001005495.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:248637256 G>T maps to NM_001005495.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:5068621 C>T maps to NM_001001916.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:5068621 C>T maps to NM_001001916.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:55798577 C>A maps to NM_001001921.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:55798577 C>A maps to NM_001001921.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:58125639 C>T maps to NM_001005489.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:58125639 C>T maps to NM_001005489.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:17634767 C>A maps to NM_012387.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:17634767 C>A maps to NM_012387.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:55156544 G>C maps to ENST00000507166 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:55156544 G>C maps to ENST00000507166 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:57995328 T>C maps to NM_024779.4 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:57995328 T>C maps to NM_024779.4 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:144993917 G>A maps to NM_201380.2 L3494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:144993917 G>A maps to NM_201380.2 L3494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:19566041 A>G maps to NM_001005356.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:19566041 A>G maps to NM_001005356.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:79461572 T>C maps to NM_015225.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:79461572 T>C maps to NM_015225.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:79461593 A>G maps to NM_015225.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:79461593 A>G maps to NM_015225.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:240979706 A>G maps to ENST00000407727 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:240979706 A>G maps to ENST00000407727 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:38949876 C>G maps to NM_000540.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:38949876 C>G maps to NM_000540.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:38835489 G>A maps to NM_006514.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:38835489 G>A maps to NM_006514.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:94915054 A>T maps to NM_001080451.1 C19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:94915054 A>T maps to NM_001080451.1 C19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:44222604 G>A maps to NM_178148.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:44222604 G>A maps to NM_178148.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:162830769 T>C maps to NM_001178015.1 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:162830769 T>C maps to NM_001178015.1 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:32439310 C>A maps to NM_000343.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:32439310 C>A maps to NM_000343.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:132938903 G>T maps to NM_001033080.1 Y147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:132938903 G>T maps to NM_001033080.1 Y147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:59626663 T>C maps to NM_001062.3 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:59626663 T>C maps to NM_001062.3 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:79351686 G>T maps to NM_003248.4 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:79351686 G>T maps to NM_003248.4 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:10908866 G>T maps to NM_199261.2 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:10908866 G>T maps to NM_199261.2 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:38225509 G>A maps to NM_003306.1 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:38225509 G>A maps to NM_003306.1 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:73053227 G>A maps to NM_170744.3 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:73053227 G>A maps to NM_170744.3 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:154464553 G>A maps to NM_003372.5 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:154464553 G>A maps to NM_003372.5 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:31926643 C>G maps to NM_003414.4 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:31926643 C>G maps to NM_003414.4 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:64589669 C>G maps to NM_182920.1 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:64589669 C>G maps to NM_182920.1 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:84659932 G>T maps to NM_207517.2 G1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:84659932 G>T maps to NM_207517.2 G1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:112838173 C>T maps to NM_000681.3 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:112838173 C>T maps to NM_000681.3 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:14851639 G>T maps to NM_001145029.1 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:14851639 G>T maps to NM_001145029.1 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:14578063 T>C maps to NM_018179.3 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:14578063 T>C maps to NM_018179.3 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:49054773 G>A maps to NM_001194998.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:49054773 G>A maps to NM_001194998.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:11896113 G>A maps to ENST00000376496 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:11896113 G>A maps to ENST00000376496 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:10102466 G>A maps to NM_015719.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:10102466 G>A maps to NM_015719.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr21:34974652 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr21:34974652 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:124358326 A>C maps to ENST00000368915 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:124358326 A>C maps to ENST00000368915 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:117758500 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:117758500 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:116066912 C>A maps to NM_020868.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:116066912 C>A maps to NM_020868.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:103006490 G>T maps to NM_001080463.1 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:103006490 G>T maps to NM_001080463.1 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:14854510 G>T maps to NM_013447.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:14854510 G>T maps to NM_013447.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:28574047 C>T maps to NM_001440.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:28574047 C>T maps to NM_001440.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:83451731 C>A maps to NM_001007122.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:83451731 C>A maps to NM_001007122.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:57311874 T>C maps to NM_182569.3 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:57311874 T>C maps to NM_182569.3 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:92560220 C>A maps to NM_004466.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:92560220 C>A maps to NM_004466.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:93518616 A>T maps to NM_004466.4 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:93518616 A>T maps to NM_004466.4 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:155257692 G>T maps to NM_020897.1 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:155257692 G>T maps to NM_020897.1 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:81386503 C>T maps to ENST00000453018 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:81386503 C>T maps to ENST00000453018 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:6860174 G>T maps to NM_014743.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:6860174 G>T maps to NM_014743.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:19449664 G>T maps to NM_015329.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:19449664 G>T maps to NM_015329.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:10668511 C>A maps to NM_023008.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:10668511 C>A maps to NM_023008.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:152749164 C>T maps to NM_178354.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:152749164 C>T maps to NM_178354.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:141625675 T>A maps to NM_018557.2 T1442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:141625675 T>A maps to NM_018557.2 T1442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:23889140 T>C maps to NM_019066.4 *1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:23889140 T>C maps to NM_019066.4 *1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:100839573 G>T maps to NM_178176.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:100839573 G>T maps to NM_178176.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:131197484 G>T maps to ENST00000481105 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:131197484 G>T maps to ENST00000481105 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:3238913 T>C maps to NM_015419.3 Q1604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:3238913 T>C maps to NM_015419.3 Q1604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:16680115 G>A maps to NM_012334.2 N1494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:16680115 G>A maps to NM_012334.2 N1494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:113076777 C>A maps to ENST00000316851 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:113076777 C>A maps to ENST00000316851 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:151784152 G>A maps to NM_020167.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:151784152 G>A maps to NM_020167.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:30492654 C>T maps to NM_006092.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:30492654 C>T maps to NM_006092.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:34243682 T>C maps to NM_001164749.1 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:34243682 T>C maps to NM_001164749.1 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:64375347 C>A maps to NM_015080.3 E1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:64375347 C>A maps to NM_015080.3 E1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:78412982 G>A maps to NM_001098816.2 R1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:78412982 G>A maps to NM_001098816.2 R1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:6806453 G>T maps to NM_001004489.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:6806453 G>T maps to NM_001004489.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:29614909 A>T maps to NM_183378.2 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:29614909 A>T maps to NM_183378.2 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:58207732 C>A maps to NM_001040429.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:58207732 C>A maps to NM_001040429.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:242264083 T>A maps to NM_152666.2 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:242264083 T>A maps to NM_152666.2 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:149221869 C>T maps to NM_133263.3 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:149221869 C>T maps to NM_133263.3 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:101705214 C>A maps to NM_001400.4 Y225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:101705214 C>A maps to NM_001400.4 Y225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:122942516 T>G maps to NM_012430.4 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:122942516 T>G maps to NM_012430.4 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:131456047 C>A maps to NM_001122821.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:131456047 C>A maps to NM_001122821.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:33769260 C>A maps to NM_144682.5 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:33769260 C>A maps to NM_144682.5 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:106937931 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:106937931 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:50600929 C>A maps to NM_006939.2 G996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:50600929 C>A maps to NM_006939.2 G996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:10320618 G>A maps to NM_014760.3 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:10320618 G>A maps to NM_014760.3 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:56695310 C>T maps to NM_024831.6 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:56695310 C>T maps to NM_024831.6 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:2127676 C>A maps to NM_000548.3 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:2127676 C>A maps to NM_000548.3 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:130953905 G>T maps to NM_207312.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:130953905 G>T maps to NM_207312.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:31751988 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:31751988 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:177069484 T>C maps to NM_170710.4 Y656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:177069484 T>C maps to NM_170710.4 Y656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:17211811 C>A maps to NM_022166.3 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:17211811 C>A maps to NM_022166.3 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:185731220 T>A maps to NM_194250.1 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:185731220 T>A maps to NM_194250.1 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:74295223 A>G maps to NM_004299.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:74295223 A>G maps to NM_004299.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:81593167 G>C maps to NM_024560.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:81593167 G>C maps to NM_024560.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:130332081 C>T maps to NM_139055.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:130332081 C>T maps to NM_139055.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:77752670 G>T maps to NM_174858.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:77752670 G>T maps to NM_174858.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:112178161 C>T maps to NM_001127510.2 Q2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:112178161 C>T maps to NM_001127510.2 Q2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:1455540 G>T maps to NM_018188.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:1455540 G>T maps to NM_018188.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:47247053 C>T maps to NM_153446.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:47247053 C>T maps to NM_153446.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:56992464 G>A maps to NM_013449.3 I1885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:56992464 G>A maps to NM_013449.3 I1885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:98741602 G>A maps to NM_015652.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:98741602 G>A maps to NM_015652.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:35433299 A>G maps to NM_080627.2 N975N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:35433299 A>G maps to NM_080627.2 N975N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258363 G>C maps to NM_012073.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258363 G>C maps to NM_012073.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258620 G>T maps to NM_012073.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258620 G>T maps to NM_012073.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:46054188 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:46054188 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:173772115 A>C maps to NM_001127181.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:173772115 A>C maps to NM_001127181.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:122363411 T>A maps to NM_015282.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:122363411 T>A maps to NM_015282.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:137717892 C>A maps to NM_001002026.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:137717892 C>A maps to NM_001002026.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:47682794 T>C maps to NM_001316.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:47682794 T>C maps to NM_001316.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:107904542 C>T maps to NM_003478.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:107904542 C>T maps to NM_003478.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:111772464 G>A maps to NM_015267.3 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:111772464 G>A maps to NM_015267.3 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:41596043 G>T maps to NM_000766.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:41596043 G>T maps to NM_000766.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:96637043 G>A maps to NM_005222.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:96637043 G>A maps to NM_005222.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:11757474 C>T maps to NM_001372.3 F3221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:11757474 C>T maps to NM_001372.3 F3221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:56462572 G>A maps to ENST00000361203 Q3843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:56462572 G>A maps to ENST00000361203 Q3843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:49647698 C>T maps to NM_024593.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:49647698 C>T maps to NM_024593.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:169526010 G>T maps to ENST00000367796 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:169526010 G>T maps to ENST00000367796 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr13:49761277 G>T maps to NM_001079673.1 G593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr13:49761277 G>T maps to NM_001079673.1 G593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:44976336 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:44976336 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:31202718 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:31202718 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:17472979 G>T maps to NM_001037814.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:17472979 G>T maps to NM_001037814.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:9850261 C>G maps to NM_201433.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:9850261 C>G maps to NM_201433.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:74764525 C>T maps to ENST00000238018 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:74764525 C>T maps to ENST00000238018 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70443954 G>A maps to NM_000166.5 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70443954 G>A maps to NM_000166.5 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:14748447 G>A maps to NM_002063.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:14748447 G>A maps to NM_002063.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:231403467 C>T maps to NM_014236.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:231403467 C>T maps to NM_014236.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:20331721 C>T maps to NM_001007240.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:20331721 C>T maps to NM_001007240.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:49316527 C>A maps to NM_016246.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:49316527 C>A maps to NM_016246.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:108958089 G>T maps to NM_213595.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:108958089 G>T maps to NM_213595.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:66104161 C>T maps to NM_153033.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:66104161 C>T maps to NM_153033.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:113389015 C>T maps to NM_001009899.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:113389015 C>T maps to NM_001009899.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:34255857 T>C maps to NM_194313.2 E1249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:34255857 T>C maps to NM_194313.2 E1249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:23417972 G>A maps to NM_001142546.1 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:23417972 G>A maps to NM_001142546.1 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:71346521 G>T maps to NM_152291.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:71346521 G>T maps to NM_152291.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48603495 T>C maps to NM_032133.4 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48603495 T>C maps to NM_032133.4 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:36723528 T>A maps to NM_002473.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:36723528 T>A maps to NM_002473.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:20066787 C>A maps to ENST00000396087 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:20066787 C>A maps to ENST00000396087 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:15771719 C>T maps to NM_001143979.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:15771719 C>T maps to NM_001143979.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:25470570 C>T maps to NM_025176.4 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:25470570 C>T maps to NM_025176.4 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:50664758 A>C maps to NM_033119.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:50664758 A>C maps to NM_033119.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:248616355 C>G maps to NM_001004136.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:248616355 C>G maps to NM_001004136.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:97887971 G>T maps to NM_001005515.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:97887971 G>T maps to NM_001005515.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:201785051 A>C maps to NM_006190.4 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:201785051 A>C maps to NM_006190.4 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:140307478 C>T maps to NM_018898.3 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:140307478 C>T maps to NM_018898.3 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:140768713 G>A maps to NM_003736.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:140768713 G>A maps to NM_003736.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:82387922 T>A maps to NM_033026.5 K5133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:82387922 T>A maps to NM_033026.5 K5133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:82784915 C>A maps to NM_033026.5 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:82784915 C>A maps to NM_033026.5 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:135163596 A>C maps to ENST00000368554 R1R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:135163596 A>C maps to ENST00000368554 R1R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:38830505 C>G maps to NM_006514.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:38830505 C>G maps to NM_006514.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:91943572 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:91943572 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:54654398 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:54654398 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:19786747 G>T maps to NM_020344.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:19786747 G>T maps to NM_020344.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:105199028 G>A maps to NM_032148.3 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:105199028 G>A maps to NM_032148.3 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:158654954 G>T maps to NM_003126.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:158654954 G>T maps to NM_003126.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:159890119 C>A maps to ENST00000368096 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:159890119 C>A maps to ENST00000368096 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:235600786 G>T maps to NM_003193.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:235600786 G>T maps to NM_003193.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:2025659 C>T maps to NM_006453.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:2025659 C>T maps to NM_006453.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:44945469 C>A maps to NM_003241.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:44945469 C>A maps to NM_003241.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:179610710 A>G maps to ENST00000375038 D5474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:179610710 A>G maps to ENST00000375038 D5474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:101188708 C>G maps to NM_001078.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:101188708 C>G maps to NM_001078.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:743352 G>A maps to NM_005433.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:743352 G>A maps to NM_005433.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:18296556 C>T maps to ENST00000401790 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:18296556 C>T maps to ENST00000401790 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:23927472 C>T maps to NM_138286.2 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:23927472 C>T maps to NM_138286.2 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:185803191 C>A maps to NM_194250.1 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:185803191 C>A maps to NM_194250.1 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:238048821 C>G maps to NM_021186.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:238048821 C>G maps to NM_021186.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:33616057 C>A maps to NM_030955.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:33616057 C>A maps to NM_030955.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:86800112 C>A maps to NM_152336.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:86800112 C>A maps to NM_152336.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:46034631 C>A maps to NM_153326.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:46034631 C>A maps to NM_153326.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:108236106 G>T maps to NM_000051.3 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:108236106 G>T maps to NM_000051.3 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:55342225 G>T maps to NM_005603.4 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:55342225 G>T maps to NM_005603.4 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:56545112 A>G maps to NM_031885.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:56545112 A>G maps to NM_031885.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:39923700 G>T maps to NM_001123385.1 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:39923700 G>T maps to NM_001123385.1 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:15560312 C>A maps to NM_203281.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:15560312 C>A maps to NM_203281.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:36952396 G>A maps to NM_001725.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:36952396 G>A maps to NM_001725.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:3639147 G>T maps to NM_032444.2 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:3639147 G>T maps to NM_032444.2 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:80356140 C>A maps to NM_175902.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:80356140 C>A maps to NM_175902.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:51892103 C>A maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:51892103 C>A maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:99739595 G>T maps to NM_032511.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:99739595 G>T maps to NM_032511.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:2231837 G>T maps to NM_020764.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:2231837 G>T maps to NM_020764.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:145699073 T>A maps to NM_007053.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:145699073 T>A maps to NM_007053.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:21947981 G>T maps to NM_018719.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:21947981 G>T maps to NM_018719.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:40045329 C>A maps to NM_032221.3 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:40045329 C>A maps to NM_032221.3 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:113504152 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:113504152 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:66613978 C>A maps to NM_144673.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:66613978 C>A maps to NM_144673.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:95363336 G>T maps to NM_001839.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:95363336 G>T maps to NM_001839.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:48608080 C>A maps to NM_000094.3 P2445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:48608080 C>A maps to NM_000094.3 P2445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:113649130 C>T maps to NM_198123.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:113649130 C>T maps to NM_198123.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:61541215 C>A maps to NM_033081.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:61541215 C>A maps to NM_033081.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:124416361 C>A maps to NM_207437.3 R4248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:124416361 C>A maps to NM_207437.3 R4248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:21856245 C>A maps to NM_003777.3 P3505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:21856245 C>A maps to NM_003777.3 P3505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:21906170 C>A maps to NM_003777.3 S3867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:21906170 C>A maps to NM_003777.3 S3867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:38825304 G>T maps to ENST00000327475 L1903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:38825304 G>T maps to ENST00000327475 L1903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:56222358 G>T maps to NM_032364.5 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:56222358 G>T maps to NM_032364.5 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:212273850 C>A maps to NM_016448.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:212273850 C>A maps to NM_016448.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:10827584 C>A maps to ENST00000429377 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:10827584 C>A maps to ENST00000429377 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:59059694 C>T maps to NM_147189.2 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:59059694 C>T maps to NM_147189.2 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:31011593 C>A maps to NM_000823.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:31011593 C>A maps to NM_000823.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:182353653 G>A maps to NM_002065.5 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:182353653 G>A maps to NM_002065.5 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:6954757 C>A maps to NM_002075.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:6954757 C>A maps to NM_002075.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:65113803 G>T maps to ENST00000418919 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:65113803 G>T maps to ENST00000418919 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:74212332 G>T maps to NM_173537.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:74212332 G>T maps to NM_173537.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:104337631 G>T maps to NM_003299.1 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:104337631 G>T maps to NM_003299.1 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:21166212 G>T maps to NM_002175.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:21166212 G>T maps to NM_002175.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:5020768 C>A maps to NM_000217.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:5020768 C>A maps to NM_000217.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:6509270 C>A maps to NM_006854.3 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:6509270 C>A maps to NM_006854.3 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:241755403 C>A maps to NM_003679.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:241755403 C>A maps to NM_003679.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:113568632 C>A maps to ENST00000509061 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:113568632 C>A maps to ENST00000509061 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:23417946 G>T maps to NM_001142546.1 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:23417946 G>T maps to NM_001142546.1 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:119212362 C>A maps to NM_031433.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:119212362 C>A maps to NM_031433.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:99279513 C>A maps to NM_012214.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:99279513 C>A maps to NM_012214.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:38016133 G>T maps to NM_001195296.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:38016133 G>T maps to NM_001195296.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:36868108 C>A maps to NM_005937.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:36868108 C>A maps to NM_005937.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:9695403 C>A maps to NM_001077525.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:9695403 C>A maps to NM_001077525.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:52522456 C>A maps to NM_007184.3 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:52522456 C>A maps to NM_007184.3 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:15300123 C>A maps to NM_000435.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:15300123 C>A maps to NM_000435.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:108032007 G>T maps to NM_002519.2 R1269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:108032007 G>T maps to NM_002519.2 R1269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:5603829 G>T maps to NM_001102654.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:5603829 G>T maps to NM_001102654.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:149936221 T>C maps to NM_020205.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:149936221 T>C maps to NM_020205.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:140753829 G>T maps to NM_018919.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:140753829 G>T maps to NM_018919.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:47831522 G>T maps to NM_006031.5 E1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:47831522 G>T maps to NM_006031.5 E1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:15126762 C>A maps to NM_015027.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:15126762 C>A maps to NM_015027.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:145747064 C>A maps to NM_002614.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:145747064 C>A maps to NM_002614.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:143792567 C>T maps to NM_003630.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:143792567 C>T maps to NM_003630.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:110445368 G>T maps to ENST00000426474 V1088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:110445368 G>T maps to ENST00000426474 V1088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:62492666 G>T maps to NM_007215.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:62492666 G>T maps to NM_007215.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:109381161 A>T maps to NM_006267.4 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:109381161 A>T maps to NM_006267.4 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:158428548 G>T maps to NM_206963.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:158428548 G>T maps to NM_206963.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:73658966 G>T maps to NM_004259.5 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:73658966 G>T maps to NM_004259.5 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:33260885 C>A maps to NM_004761.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:33260885 C>A maps to NM_004761.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:124765701 C>A maps to NM_019055.5 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:124765701 C>A maps to NM_019055.5 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:169644745 C>A maps to NM_182610.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:169644745 C>A maps to NM_182610.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:68312365 G>T maps to NM_001164160.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:68312365 G>T maps to NM_001164160.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:68377482 C>A maps to NM_001164160.1 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:68377482 C>A maps to NM_001164160.1 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:113286455 G>T maps to ENST00000393830 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:113286455 G>T maps to ENST00000393830 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:48696369 C>A maps to NM_001135181.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:48696369 C>A maps to NM_001135181.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:170198378 C>A maps to NM_020949.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:170198378 C>A maps to NM_020949.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:98797489 C>A maps to NM_003061.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:98797489 C>A maps to NM_003061.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:71566659 A>C maps to NM_001044305.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:71566659 A>C maps to NM_001044305.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:1161274 C>A maps to NM_018968.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:1161274 C>A maps to NM_018968.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:167656220 C>A maps to NM_016950.2 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:167656220 C>A maps to NM_016950.2 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:57099699 G>T maps to NM_003146.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:57099699 G>T maps to NM_003146.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:883104 C>A maps to ENST00000456758 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:883104 C>A maps to ENST00000456758 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:132874424 G>T maps to NM_053278.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:132874424 G>T maps to NM_053278.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:125534427 A>G maps to NM_032026.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:125534427 A>G maps to NM_032026.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:37298890 C>A maps to NM_017772.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:37298890 C>A maps to NM_017772.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:92268647 A>T maps to NM_001128596.1 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:92268647 A>T maps to NM_001128596.1 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:53453881 C>A maps to NM_170754.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:53453881 C>A maps to NM_170754.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:229773335 C>A maps to NM_014777.2 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:229773335 C>A maps to NM_014777.2 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:44847408 G>A maps to ENST00000412927 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:44847408 G>A maps to ENST00000412927 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:38241750 T>C maps to NM_145011.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:38241750 T>C maps to NM_145011.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:30934651 C>A maps to NM_014717.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:30934651 C>A maps to NM_014717.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:53678701 G>T maps to NM_024733.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:53678701 G>T maps to NM_024733.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:100491460 G>A maps to NM_000665.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:100491460 G>A maps to NM_000665.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:7706886 C>T maps to NM_020546.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:7706886 C>T maps to NM_020546.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:91645513 G>A maps to NM_005751.4 E1228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:91645513 G>A maps to NM_005751.4 E1228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:100911743 C>A maps to NM_177949.2 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:100911743 C>A maps to NM_177949.2 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:2828020 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:2828020 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:66931529 T>A maps to NM_000044.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:66931529 T>A maps to NM_000044.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:50216779 T>G maps to ENST00000342989 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:50216779 T>G maps to ENST00000342989 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:73467658 C>A maps to NM_006429.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:73467658 C>A maps to NM_006429.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:621376 G>T maps to NM_021924.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:621376 G>T maps to NM_021924.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:36145569 C>A maps to ENST00000392201 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:36145569 C>A maps to ENST00000392201 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:61508791 G>A maps to NM_006133.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:61508791 G>A maps to NM_006133.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:102956535 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:102956535 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:16548579 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:16548579 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:68266595 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:68266595 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:64011313 G>T maps to NM_057092.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:64011313 G>T maps to NM_057092.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:9857311 G>A maps to NM_000833.3 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:9857311 G>A maps to NM_000833.3 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:235950597 G>A maps to NM_000081.2 L1588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:235950597 G>A maps to NM_000081.2 L1588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:40569229 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:40569229 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:51171226 G>A maps to ENST00000251020 N1257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:51171226 G>A maps to ENST00000251020 N1257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:160679384 G>T maps to NM_003058.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:160679384 G>T maps to NM_003058.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:172835182 A>G maps to NM_031955.5 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:172835182 A>G maps to NM_031955.5 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:140083650 A>G maps to NM_003731.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:140083650 A>G maps to NM_003731.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:70429066 G>T maps to NM_006927.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:70429066 G>T maps to NM_006927.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:107460325 A>G maps to NM_001142351.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:107460325 A>G maps to NM_001142351.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:10788535 C>A maps to NM_144674.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:10788535 C>A maps to NM_144674.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:48256676 C>T maps to NM_032583.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:48256676 C>T maps to NM_032583.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:20702412 G>C maps to NM_052956.2 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:20702412 G>C maps to NM_052956.2 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:175898085 T>A maps to NM_014269.4 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:175898085 T>A maps to NM_014269.4 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:39068731 G>T maps to NM_145004.5 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:39068731 G>T maps to NM_145004.5 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:70819935 C>T maps to NM_030816.4 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:70819935 C>T maps to NM_030816.4 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:97509717 G>A maps to NM_144994.7 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:97509717 G>A maps to NM_144994.7 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:58571906 G>C maps to NM_006380.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:58571906 G>C maps to NM_006380.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:65552719 C>G maps to NM_000048.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:65552719 C>G maps to NM_000048.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32086643 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32086643 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:36051325 G>T maps to NM_000704.2 C242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:36051325 G>T maps to NM_000704.2 C242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:1309388 T>C maps to NM_001127230.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:1309388 T>C maps to NM_001127230.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:79058647 G>A maps to NM_017451.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:79058647 G>A maps to NM_017451.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:56857322 C>T maps to NM_152731.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:56857322 C>T maps to NM_152731.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:159169550 G>T maps to NM_021189.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:159169550 G>T maps to NM_021189.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:42781128 G>A maps to NM_144719.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:42781128 G>A maps to NM_144719.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:157804206 G>C maps to NM_005894.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:157804206 G>C maps to NM_005894.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:11363182 G>C maps to NM_006561.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:11363182 G>C maps to NM_006561.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:31918139 C>T maps to ENST00000437789 F1030F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:31918139 C>T maps to ENST00000437789 F1030F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:246829095 C>T maps to NM_152609.2 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:246829095 C>T maps to NM_152609.2 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:48370305 A>T maps to NM_001844.4 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:48370305 A>T maps to NM_001844.4 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:11159691 G>A maps to NM_001332.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:11159691 G>A maps to NM_001332.2 L719L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4514-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-49-4514-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:117241033 C>T maps to NM_015404.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:117241033 C>T maps to NM_015404.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:28584106 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:28584106 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:137783471 G>A maps to NM_173543.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:137783471 G>A maps to NM_173543.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:44073893 C>G maps to NM_022785.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:44073893 C>G maps to NM_022785.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:2409265 G>A maps to ENST00000314800 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:2409265 G>A maps to ENST00000314800 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:54045060 C>A maps to NM_015701.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:54045060 C>A maps to NM_015701.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:5805686 C>T maps to NM_024896.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:5805686 C>T maps to NM_024896.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:38945162 G>A maps to NM_138389.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:38945162 G>A maps to NM_138389.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:8764316 T>C maps to NM_174951.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:8764316 T>C maps to NM_174951.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92616311 C>A maps to ENST00000298047 V4230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92616311 C>A maps to ENST00000298047 V4230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92616506 C>A maps to ENST00000298047 C4295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92616506 C>A maps to ENST00000298047 C4295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:35928959 C>T maps to NM_031866.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:35928959 C>T maps to NM_031866.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:132688112 G>T maps to NM_001122636.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:132688112 G>T maps to NM_001122636.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:173734718 C>A maps to NM_001034845.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:173734718 C>A maps to NM_001034845.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:31008551 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:31008551 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:24707944 C>T maps to ENST00000348719 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:24707944 C>T maps to ENST00000348719 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:23438484 C>T maps to NM_002073.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:23438484 C>T maps to NM_002073.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:132437227 T>A maps to NM_001448.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:132437227 T>A maps to NM_001448.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:47681808 C>A maps to NM_153838.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:47681808 C>A maps to NM_153838.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:139228960 C>T maps to NM_001145638.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:139228960 C>T maps to NM_001145638.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:13906651 G>A maps to NM_000834.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:13906651 G>A maps to NM_000834.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:146480565 C>A maps to NM_000838.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:146480565 C>A maps to NM_000838.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:19369647 G>A maps to NM_023002.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:19369647 G>A maps to NM_023002.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:124731532 T>A maps to NM_020733.1 K964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:124731532 T>A maps to NM_020733.1 K964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:26043663 G>A maps to NM_021062.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:26043663 G>A maps to NM_021062.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:176317680 G>A maps to NM_002115.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:176317680 G>A maps to NM_002115.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:2927443 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:2927443 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:5126725 C>T maps to NM_004972.3 Q1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:5126725 C>T maps to NM_004972.3 Q1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:27066140 G>A maps to NM_021219.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:27066140 G>A maps to NM_021219.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:6422414 C>T maps to NM_003685.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:6422414 C>T maps to NM_003685.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:26962060 C>T maps to NM_014680.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:26962060 C>T maps to NM_014680.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:233518099 C>T maps to NM_032435.2 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:233518099 C>T maps to NM_032435.2 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:200574419 G>T maps to NM_014875.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:200574419 G>T maps to NM_014875.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:69516869 C>A maps to NM_012310.4 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:69516869 C>A maps to NM_012310.4 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:51447018 G>T maps to NM_012427.4 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:51447018 G>T maps to NM_012427.4 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:130378626 G>A maps to NM_032438.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:130378626 G>A maps to NM_032438.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:41687769 A>T maps to NM_014988.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:41687769 A>T maps to NM_014988.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:46917794 A>T maps to ENST00000256991 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:46917794 A>T maps to ENST00000256991 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:151870188 C>T maps to NM_005363.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:151870188 C>T maps to NM_005363.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:242159523 C>A maps to NM_001004343.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:242159523 C>A maps to NM_001004343.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:14340373 G>T maps to NM_014048.3 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:14340373 G>T maps to NM_014048.3 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:18159486 G>A maps to NM_054031.3 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:18159486 G>A maps to NM_054031.3 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:60215230 G>T maps to NM_023945.2 *201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:60215230 G>T maps to NM_023945.2 *201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:195475819 A>G maps to NM_018406.5 C5329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:195475819 A>G maps to NM_018406.5 C5329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:34167642 G>A maps to NM_024662.2 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:34167642 G>A maps to NM_024662.2 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:52639650 G>A maps to NM_199289.1 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:52639650 G>A maps to NM_199289.1 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:14951443 C>G maps to ENST00000456867 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:14951443 C>G maps to ENST00000456867 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:96877534 G>T maps to NM_021005.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:96877534 G>T maps to NM_021005.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:56485054 G>A maps to NM_007006.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:56485054 G>A maps to NM_007006.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:47656115 G>T maps to ENST00000513748 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:47656115 G>T maps to ENST00000513748 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:53624887 C>A maps to NM_006418.3 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:53624887 C>A maps to NM_006418.3 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:143826660 C>T maps to NM_001001659.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:143826660 C>T maps to NM_001001659.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:27925440 C>A maps to NM_012367.1 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:27925440 C>A maps to NM_012367.1 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:72943236 C>T maps to NM_178233.1 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:72943236 C>T maps to NM_178233.1 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:150780225 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:150780225 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:91131799 C>T maps to NM_032968.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:91131799 C>T maps to NM_032968.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:140750983 T>C maps to NM_018924.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:140750983 T>C maps to NM_018924.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:72289311 G>T maps to NM_002599.3 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:72289311 G>T maps to NM_002599.3 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:96427979 C>G maps to NM_005392.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:96427979 C>G maps to NM_005392.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:17056291 G>T maps to NM_001144382.1 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:17056291 G>T maps to NM_001144382.1 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:145049531 C>A maps to NM_000445.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:145049531 C>A maps to NM_000445.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:55874525 C>A maps to NM_033109.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:55874525 C>A maps to NM_033109.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:103898374 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:103898374 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:43576026 C>A maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:43576026 C>A maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:27703038 G>T maps to NM_001034842.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:27703038 G>T maps to NM_001034842.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:35943005 C>A maps to NM_014310.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:35943005 C>A maps to NM_014310.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:155880280 G>A maps to ENST00000368322 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:155880280 G>A maps to ENST00000368322 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:31410942 C>A maps to NM_013235.4 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:31410942 C>A maps to NM_013235.4 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:145663205 C>G maps to NM_014455.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:145663205 C>G maps to NM_014455.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:17602406 C>T maps to ENST00000377813 E1084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:17602406 C>T maps to ENST00000377813 E1084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:23904721 C>T maps to NM_014363.4 R4431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:23904721 C>T maps to NM_014363.4 R4431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:47465463 G>C maps to NM_012235.2 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:47465463 G>C maps to NM_012235.2 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:115783223 G>A maps to ENST00000257414 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:115783223 G>A maps to ENST00000257414 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:164780172 G>A maps to NM_001041.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:164780172 G>A maps to NM_001041.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:140128970 C>T maps to NM_080877.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:140128970 C>T maps to NM_080877.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:74880440 C>T maps to NM_007256.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:74880440 C>T maps to NM_007256.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:20600009 C>T maps to ENST00000273739 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:20600009 C>T maps to ENST00000273739 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:127729611 G>T maps to NM_014390.2 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:127729611 G>T maps to NM_014390.2 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:215274945 C>A maps to NM_024532.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:215274945 C>A maps to NM_024532.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:44336164 A>G maps to NM_145026.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:44336164 A>G maps to NM_145026.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:220353373 C>A maps to NM_005876.4 T2671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:220353373 C>A maps to NM_005876.4 T2671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:28995568 G>T maps to NM_032038.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:28995568 G>T maps to NM_032038.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:28620116 G>A maps to NM_177529.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:28620116 G>A maps to NM_177529.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:16778404 G>T maps to NM_032796.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:16778404 G>T maps to NM_032796.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:33592448 G>A maps to NM_198992.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:33592448 G>A maps to NM_198992.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:69898724 T>A maps to NM_001003811.1 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:69898724 T>A maps to NM_001003811.1 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:55209277 G>A maps to NM_003222.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:55209277 G>A maps to NM_003222.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:44951753 C>A maps to NM_003241.3 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:44951753 C>A maps to NM_003241.3 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:11630168 C>A maps to ENST00000423059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:11630168 C>A maps to ENST00000423059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:156396124 C>T maps to NM_015508.4 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:156396124 C>T maps to NM_015508.4 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:12940137 G>A maps to ENST00000311912 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:12940137 G>A maps to ENST00000311912 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:129825205 C>G maps to NM_032842.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:129825205 C>G maps to NM_032842.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179438297 G>C maps to NM_133378.4 L21619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179438297 G>C maps to NM_133378.4 L21619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179455350 C>A maps to NM_133378.4 R17799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179455350 C>A maps to NM_133378.4 R17799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179466607 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179466607 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:22866790 C>A maps to NM_052903.4 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:22866790 C>A maps to NM_052903.4 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:100453137 T>A maps to NM_015054.1 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:100453137 T>A maps to NM_015054.1 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:160385935 C>A maps to NM_020335.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:160385935 C>A maps to NM_020335.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:85738543 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:85738543 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:1005334 G>A maps to NM_001184985.1 V2154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:1005334 G>A maps to NM_001184985.1 V2154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:21833877 G>A maps to ENST00000434536 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:21833877 G>A maps to ENST00000434536 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:77767111 G>A maps to NM_024721.4 W2652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:77767111 G>A maps to NM_024721.4 W2652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:77158902 G>A maps to NM_032772.4 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:77158902 G>A maps to NM_032772.4 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:94508893 G>C maps to NM_000350.2 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:94508893 G>C maps to NM_000350.2 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:183639186 C>T maps to NM_005688.2 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:183639186 C>T maps to NM_005688.2 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:133750267 C>A maps to NM_007313.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:133750267 C>A maps to NM_007313.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:24324369 G>T maps to ENST00000380789 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:24324369 G>T maps to ENST00000380789 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:64747408 G>A maps to NM_197941.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:64747408 G>A maps to NM_197941.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:70933522 G>T maps to NM_001185054.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:70933522 G>T maps to NM_001185054.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:202920102 G>T maps to NM_015999.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:202920102 G>T maps to NM_015999.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:150817228 C>T maps to NM_031946.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:150817228 C>T maps to NM_031946.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:110172892 C>T maps to ENST00000393689 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:110172892 C>T maps to ENST00000393689 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30963078 G>A maps to ENST00000509504 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30963078 G>A maps to ENST00000509504 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73125036 C>T maps to NM_024585.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73125036 C>T maps to NM_024585.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:66863121 T>G maps to NM_000044.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:66863121 T>G maps to NM_000044.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:176853570 C>A maps to ENST00000281881 E1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:176853570 C>A maps to ENST00000281881 E1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:26043142 G>A maps to NM_016529.4 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:26043142 G>A maps to NM_016529.4 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:33264327 C>T maps to NM_004323.5 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:33264327 C>T maps to NM_004323.5 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:121402009 C>T maps to ENST00000275159 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:121402009 C>T maps to ENST00000275159 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:39996547 C>T maps to NM_021096.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:39996547 C>T maps to NM_021096.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:57765097 G>T maps to NM_032269.5 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:57765097 G>T maps to NM_032269.5 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:27598008 C>A maps to NM_018246.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:27598008 C>A maps to NM_018246.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:119909846 G>C maps to NM_178499.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:119909846 G>C maps to NM_178499.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158225932 G>T maps to NM_001763.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158225932 G>T maps to NM_001763.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:40040831 C>G maps to NM_032221.3 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:40040831 C>G maps to NM_032221.3 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:10996624 G>T maps to NM_000246.3 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:10996624 G>T maps to NM_000246.3 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:103462665 T>C maps to NM_080629.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:103462665 T>C maps to NM_080629.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:107840674 T>G maps to ENST00000328300 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:107840674 T>G maps to ENST00000328300 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:88886264 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:88886264 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:1497623 C>T maps to ENST00000357934 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:1497623 C>T maps to ENST00000357934 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:74154041 G>A maps to NM_031427.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:74154041 G>A maps to NM_031427.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:10287990 G>A maps to NM_001130823.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:10287990 G>A maps to NM_001130823.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:169508966 C>A maps to NM_004946.2 V1803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:169508966 C>A maps to NM_004946.2 V1803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:1936832 C>T maps to NM_001383.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:1936832 C>T maps to NM_001383.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:102302091 C>T maps to NM_018370.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:102302091 C>T maps to NM_018370.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:55790479 C>A maps to NM_130810.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:55790479 C>A maps to NM_130810.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:45347296 C>T maps to NM_020365.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:45347296 C>T maps to NM_020365.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:145134857 C>A maps to NM_019037.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:145134857 C>A maps to NM_019037.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:5540615 G>A maps to ENST00000312577 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:5540615 G>A maps to ENST00000312577 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:159277621 C>G maps to ENST00000368115 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:159277621 C>G maps to ENST00000368115 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:59737984 T>A maps to NM_002012.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:59737984 T>A maps to NM_002012.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:202899456 C>T maps to NM_003507.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:202899456 C>T maps to NM_003507.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:74325766 T>C maps to NM_016591.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:74325766 T>C maps to NM_016591.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:30739035 C>T maps to ENST00000378948 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:30739035 C>T maps to ENST00000378948 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:100551821 G>A maps to ENST00000266746 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:100551821 G>A maps to ENST00000266746 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:133353278 G>A maps to NM_005895.3 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:133353278 G>A maps to NM_005895.3 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:106558340 A>C maps to ENST00000282249 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:106558340 A>C maps to ENST00000282249 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21800809 C>T maps to NM_015094.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21800809 C>T maps to NM_015094.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:110618327 G>A maps to NM_014055.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:110618327 G>A maps to NM_014055.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:44223519 C>T maps to NM_019612.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:44223519 C>T maps to NM_019612.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:53223698 G>C maps to NM_004187.3 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:53223698 G>C maps to NM_004187.3 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:24762917 C>T maps to NM_019590.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:24762917 C>T maps to NM_019590.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:51901605 G>T maps to NM_032559.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:51901605 G>T maps to NM_032559.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:21526202 C>T maps to ENST00000416669 I3104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:21526202 C>T maps to ENST00000416669 I3104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:36103257 T>C maps to NM_174902.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:36103257 T>C maps to NM_174902.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:35773659 C>T maps to NM_182548.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:35773659 C>T maps to NM_182548.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:160661620 G>A maps to NM_002349.3 F1701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:160661620 G>A maps to NM_002349.3 F1701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:47663460 C>T maps to NM_003906.3 E1738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:47663460 C>T maps to NM_003906.3 E1738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158815571 T>C maps to NM_002432.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158815571 T>C maps to NM_002432.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:145302755 C>T maps to NM_001039703.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:145302755 C>T maps to NM_001039703.4 L398L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-49-6742-01A-11D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-49-6742-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:49245625 G>A maps to ENST00000393198 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:49245625 G>A maps to ENST00000393198 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:92929472 C>T maps to NM_005654.4 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:92929472 C>T maps to NM_005654.4 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:71727041 G>A maps to ENST00000393695 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:71727041 G>A maps to ENST00000393695 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:167420062 G>A maps to NM_001122679.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:167420062 G>A maps to NM_001122679.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:137815157 C>T maps to NM_175747.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:137815157 C>T maps to NM_175747.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158450024 C>T maps to NM_001004472.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158450024 C>T maps to NM_001004472.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:247921159 A>G maps to NM_012353.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:247921159 A>G maps to NM_012353.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:3030290 C>G maps to ENST00000381953 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:3030290 C>G maps to ENST00000381953 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248756475 G>A maps to NM_001004693.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248756475 G>A maps to NM_001004693.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248616757 G>A maps to NM_001004136.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248616757 G>A maps to NM_001004136.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:125551303 C>T maps to NM_001001923.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:125551303 C>T maps to NM_001001923.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:56043713 T>A maps to NM_001004745.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:56043713 T>A maps to NM_001004745.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:35453912 A>G maps to NM_015430.2 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:35453912 A>G maps to NM_015430.2 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:118949433 G>A maps to NM_002581.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:118949433 G>A maps to NM_002581.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140719743 C>A maps to NM_018915.2 Y402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140719743 C>A maps to NM_018915.2 Y402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:30975750 C>A maps to NM_014303.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:30975750 C>A maps to NM_014303.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:42437818 C>A maps to ENST00000397272 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:42437818 C>A maps to ENST00000397272 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:46974055 C>G maps to NM_018215.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:46974055 C>G maps to NM_018215.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:43582053 C>A maps to NM_006502.2 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:43582053 C>A maps to NM_006502.2 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:121230865 G>A maps to ENST00000393672 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:121230865 G>A maps to ENST00000393672 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:131976394 G>A maps to NM_001083538.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:131976394 G>A maps to NM_001083538.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:130877668 C>T maps to NM_001099771.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:130877668 C>T maps to NM_001099771.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:23847513 G>T maps to NM_002738.6 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:23847513 G>T maps to NM_002738.6 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:170695455 C>T maps to NM_022716.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:170695455 C>T maps to NM_022716.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:43430043 G>C maps to NM_002783.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:43430043 G>C maps to NM_002783.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99022693 G>A maps to NM_001198879.1 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99022693 G>A maps to NM_001198879.1 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:209355383 C>T maps to NM_005048.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:209355383 C>T maps to NM_005048.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:24582308 G>T maps to NM_006910.4 E1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:24582308 G>T maps to NM_006910.4 E1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:93306113 G>T maps to NM_000969.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:93306113 G>T maps to NM_000969.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:100757054 C>T maps to NM_001130841.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:100757054 C>T maps to NM_001130841.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:92762500 G>A maps to NM_152703.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:92762500 G>A maps to NM_152703.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:113830940 G>T maps to NM_006843.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:113830940 G>T maps to NM_006843.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:45567458 C>T maps to NM_007056.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:45567458 C>T maps to NM_007056.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:77660855 G>A maps to NM_020859.3 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:77660855 G>A maps to NM_020859.3 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:60714086 G>C maps to NM_016582.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:60714086 G>C maps to NM_016582.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:2929521 C>T maps to NM_002555.5 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:2929521 C>T maps to NM_002555.5 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:40655728 A>G maps to NM_021097.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:40655728 A>G maps to NM_021097.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:173472448 G>A maps to NM_178527.3 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:173472448 G>A maps to NM_178527.3 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:11106947 C>A maps to NM_001128849.1 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:11106947 C>A maps to NM_001128849.1 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:11168982 G>T maps to NM_001128849.1 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:11168982 G>T maps to NM_001128849.1 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:68405583 G>T maps to NM_018667.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:68405583 G>T maps to NM_018667.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:35771818 G>T maps to NM_024867.3 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:35771818 G>T maps to NM_024867.3 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:27008930 G>A maps to NM_003170.3 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:27008930 G>A maps to NM_003170.3 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21354219 C>T maps to NM_030573.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21354219 C>T maps to NM_030573.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:19997284 C>A maps to NM_199254.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:19997284 C>A maps to NM_199254.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179579142 A>C maps to NM_133378.4 S7542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179579142 A>C maps to NM_133378.4 S7542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179604933 T>C maps to NM_133437.3 K4171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179604933 T>C maps to NM_133437.3 K4171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:113675627 C>A maps to NM_020886.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:113675627 C>A maps to NM_020886.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50277564 G>A maps to NM_014838.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50277564 G>A maps to NM_014838.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:31868935 G>A maps to NM_181842.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:31868935 G>A maps to NM_181842.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:64718934 C>A maps to NM_001010888.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:64718934 C>A maps to NM_001010888.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:219508460 G>T maps to NM_001105537.1 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:219508460 G>T maps to NM_001105537.1 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:44701144 C>T maps to NM_003420.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:44701144 C>T maps to NM_003420.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:56648816 G>T maps to NM_018181.4 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:56648816 G>T maps to NM_018181.4 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:437397 A>G maps to NM_133474.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:437397 A>G maps to NM_133474.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:17483330 G>T maps to ENST00000302539 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:17483330 G>T maps to ENST00000302539 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35608974 C>T maps to NM_198834.1 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35608974 C>T maps to NM_198834.1 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:24359040 G>A maps to ENST00000380789 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:24359040 G>A maps to ENST00000380789 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:33576821 C>T maps to NM_030955.2 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:33576821 C>T maps to NM_030955.2 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:33881487 G>A maps to NM_030955.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:33881487 G>A maps to NM_030955.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:47712124 C>A maps to ENST00000357610 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:47712124 C>A maps to ENST00000357610 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:970663 C>A maps to NM_198576.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:970663 C>A maps to NM_198576.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:151626886 A>G maps to NM_005100.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:151626886 A>G maps to NM_005100.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:89346598 C>A maps to NM_013275.4 P2117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:89346598 C>A maps to NM_013275.4 P2117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:89351263 G>C maps to NM_013275.4 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:89351263 G>C maps to NM_013275.4 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:101504242 C>A maps to ENST00000392977 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:101504242 C>A maps to ENST00000392977 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:36579923 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:36579923 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:46703731 C>T maps to NM_004308.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:46703731 C>T maps to NM_004308.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:119133226 C>A maps to NM_020754.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:119133226 C>A maps to NM_020754.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:74882170 C>T maps to ENST00000395077 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:74882170 C>T maps to ENST00000395077 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:18120709 G>T maps to NM_015683.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:18120709 G>T maps to NM_015683.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:155448133 A>G maps to ENST00000368346 S1509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:155448133 A>G maps to ENST00000368346 S1509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:176915099 C>T maps to ENST00000281881 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:176915099 C>T maps to ENST00000281881 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:193201779 G>A maps to NM_032279.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:193201779 G>A maps to NM_032279.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:203652494 C>G maps to NM_001001396.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:203652494 C>G maps to NM_001001396.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36046179 C>T maps to NM_000704.2 K738K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36046179 C>T maps to NM_000704.2 K738K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:117026330 C>A maps to NM_207303.2 Y610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:117026330 C>A maps to NM_207303.2 Y610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:160804095 T>C maps to NM_033168.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:160804095 T>C maps to NM_033168.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:70049037 G>T maps to NM_032735.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:70049037 G>T maps to NM_032735.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:6759009 A>G maps to NM_001200.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:6759009 A>G maps to NM_001200.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:116633960 G>C maps to NM_032725.3 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:116633960 G>C maps to NM_032725.3 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:127442260 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:127442260 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105939595 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105939595 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:95932327 C>A maps to NM_152592.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:95932327 C>A maps to NM_152592.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:42745462 T>C maps to NM_001145080.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:42745462 T>C maps to NM_001145080.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:210016916 G>T maps to NM_014388.6 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:210016916 G>T maps to NM_014388.6 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207271572 C>A maps to NM_001017367.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207271572 C>A maps to NM_001017367.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:170179307 G>A maps to NM_018341.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:170179307 G>A maps to NM_018341.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:181727922 G>A maps to ENST00000357570 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:181727922 G>A maps to ENST00000357570 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:81714109 G>C maps to NM_000722.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:81714109 G>C maps to NM_000722.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:62423880 G>T maps to ENST00000383709 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:62423880 G>T maps to ENST00000383709 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:241537348 G>T maps to NM_023083.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:241537348 G>T maps to NM_023083.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:70516154 C>G maps to NM_018237.2 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:70516154 C>G maps to NM_018237.2 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:85630435 G>A maps to NM_173556.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:85630435 G>A maps to NM_173556.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7522231 C>A maps to ENST00000416109 E1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7522231 C>A maps to ENST00000416109 E1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:174231036 G>A maps to NM_031942.4 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:174231036 G>A maps to NM_031942.4 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:65016162 T>A maps to NM_001797.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:65016162 T>A maps to NM_001797.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:26890651 A>T maps to NM_016279.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:26890651 A>T maps to NM_016279.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125848197 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125848197 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:139865923 C>T maps to NM_004065.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:139865923 C>T maps to NM_004065.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:46772988 G>A maps to ENST00000415402 F1743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:46772988 G>A maps to ENST00000415402 F1743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:10217377 C>A maps to NM_207345.2 Y173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:10217377 C>A maps to NM_207345.2 Y173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:74548835 T>G maps to NM_020872.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:74548835 T>G maps to NM_020872.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:100095500 C>A maps to NM_014361.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:100095500 C>A maps to NM_014361.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:86590638 G>A maps to NM_152890.5 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:86590638 G>A maps to NM_152890.5 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:130284020 C>G maps to NM_001102608.1 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:130284020 C>G maps to NM_001102608.1 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:71009822 G>T maps to NM_001851.4 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:71009822 G>T maps to NM_001851.4 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:3685138 A>G maps to ENST00000418971 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:3685138 A>G maps to ENST00000418971 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:148904391 T>C maps to NM_000096.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:148904391 T>C maps to NM_000096.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49660566 C>T maps to ENST00000211238 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49660566 C>T maps to ENST00000211238 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49696538 A>G maps to NM_001190986.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49696538 A>G maps to NM_001190986.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:37334172 C>A maps to ENST00000262825 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:37334172 C>A maps to ENST00000262825 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:113960089 A>G maps to NM_198123.1 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:113960089 A>G maps to NM_198123.1 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:54661162 G>T maps to NM_001031672.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:54661162 G>T maps to NM_001031672.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:61490343 C>T maps to NM_006133.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:61490343 C>T maps to NM_006133.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:125685964 C>A maps to NM_178470.4 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:125685964 C>A maps to NM_178470.4 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:153916598 C>A maps to NM_014856.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:153916598 C>A maps to NM_014856.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:124377605 C>A maps to ENST00000368915 Y1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:124377605 C>A maps to ENST00000368915 Y1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:6588994 C>T maps to NM_144666.2 Q4086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:6588994 C>T maps to NM_144666.2 Q4086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:51400008 C>T maps to NM_004947.4 L1733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:51400008 C>T maps to NM_004947.4 L1733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38709568 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38709568 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:32928176 A>T maps to NM_001172774.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:32928176 A>T maps to NM_001172774.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:28719709 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:28719709 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:102506695 G>C maps to NM_001376.4 L3938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:102506695 G>C maps to NM_001376.4 L3938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:55240711 G>T maps to NM_005228.3 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:55240711 G>T maps to NM_005228.3 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:109260898 C>A maps to NM_001568.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:109260898 C>A maps to NM_001568.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:79401978 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:79401978 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132514350 G>C maps to ENST00000333577 L1865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132514350 G>C maps to ENST00000333577 L1865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:134898723 C>G maps to NM_004441.4 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:134898723 C>G maps to NM_004441.4 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:103498884 C>T maps to NM_153448.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:103498884 C>T maps to NM_153448.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:93170109 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:93170109 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:92086966 T>C maps to ENST00000298047 N563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:92086966 T>C maps to ENST00000298047 N563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:92531737 G>A maps to ENST00000298047 V1853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:92531737 G>A maps to ENST00000298047 V1853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:147807316 G>T maps to NM_205836.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:147807316 G>T maps to NM_205836.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:11718336 C>T maps to ENST00000376768 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:11718336 C>T maps to ENST00000376768 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161475295 C>T maps to NM_001136219.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161475295 C>T maps to NM_001136219.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161693310 C>G maps to NM_001002901.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161693310 C>G maps to NM_001002901.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:95602830 G>A maps to NM_018351.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:95602830 G>A maps to NM_018351.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:110113827 C>G maps to NM_014845.5 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:110113827 C>G maps to NM_014845.5 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:39265302 A>G maps to NM_207361.4 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:39265302 A>G maps to NM_207361.4 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:52179251 G>T maps to ENST00000344768 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:52179251 G>T maps to ENST00000344768 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29576386 G>A maps to NM_001470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29576386 G>A maps to NM_001470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51753050 G>T maps to NM_007210.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51753050 G>T maps to NM_007210.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:38026075 G>T maps to ENST00000381756 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:38026075 G>T maps to ENST00000381756 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:121768043 C>T maps to NM_000165.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:121768043 C>T maps to NM_000165.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:58714571 G>A maps to ENST00000317391 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:58714571 G>A maps to ENST00000317391 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121396160 G>A maps to ENST00000393667 Q3004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121396160 G>A maps to ENST00000393667 Q3004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128780875 C>G maps to NM_000174.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128780875 C>G maps to NM_000174.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:95335954 C>T maps to NM_181745.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:95335954 C>T maps to NM_181745.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:27333673 G>A maps to NM_005288.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:27333673 G>A maps to NM_005288.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:90052968 A>T maps to NM_032119.3 A3977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:90052968 A>T maps to NM_032119.3 A3977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:50660723 C>A maps to NM_005311.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:50660723 C>A maps to NM_005311.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:59944430 G>A maps to NM_004492.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:59944430 G>A maps to NM_004492.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:30876867 C>T maps to NM_001517.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:30876867 C>T maps to NM_001517.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:44683137 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:44683137 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:7886946 G>C maps to NM_017545.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:7886946 G>C maps to NM_017545.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:156533887 G>T maps to NM_032782.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:156533887 G>T maps to NM_032782.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:73617521 A>G maps to NM_005477.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:73617521 A>G maps to NM_005477.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:18705894 G>A maps to NM_178425.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:18705894 G>A maps to NM_178425.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242179036 G>A maps to NM_005336.3 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242179036 G>A maps to NM_005336.3 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:65427034 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:65427034 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:75187481 G>A maps to NM_005338.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:75187481 G>A maps to NM_005338.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:27775546 C>G maps to NM_003519.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:27775546 C>G maps to NM_003519.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29797447 G>T maps to ENST00000376828 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29797447 G>T maps to ENST00000376828 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:27147571 C>A maps to NM_153631.2 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:27147571 C>A maps to NM_153631.2 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46673819 C>A maps to NM_018952.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46673819 C>A maps to NM_018952.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46691844 G>A maps to NM_024016.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46691844 G>A maps to NM_024016.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:175110496 C>G maps to NM_001131055.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:175110496 C>G maps to NM_001131055.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:43775600 A>G maps to NM_016142.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:43775600 A>G maps to NM_016142.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:22174304 G>A maps to NM_005529.5 I2634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:22174304 G>A maps to NM_005529.5 I2634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:21187074 A>T maps to NM_021068.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:21187074 A>T maps to NM_021068.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:35871200 A>G maps to NM_002185.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:35871200 A>G maps to NM_002185.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:156815060 A>T maps to NM_014215.2 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:156815060 A>T maps to NM_014215.2 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:1524940 G>A maps to ENST00000389470 A1214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:1524940 G>A maps to ENST00000389470 A1214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55362639 G>T maps to NM_024335.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55362639 G>T maps to NM_024335.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:30516759 G>A maps to NM_002209.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:30516759 G>A maps to NM_002209.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:31332814 C>A maps to NM_001145808.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:31332814 C>A maps to NM_001145808.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160914947 T>C maps to NM_080878.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160914947 T>C maps to NM_080878.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:119915237 C>A maps to NM_012281.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:119915237 C>A maps to NM_012281.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:61611611 C>G maps to NM_030779.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:61611611 C>G maps to NM_030779.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:90651130 G>A maps to NM_022054.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:90651130 G>A maps to NM_022054.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:73487508 A>T maps to ENST00000375248 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:73487508 A>T maps to ENST00000375248 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:126051106 G>A maps to ENST00000377985 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:126051106 G>A maps to ENST00000377985 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:138545902 C>A maps to NM_001164665.1 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:138545902 C>A maps to NM_001164665.1 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:45223724 G>T maps to NM_006845.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:45223724 G>T maps to NM_006845.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:86312159 G>T maps to NM_022480.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:86312159 G>T maps to NM_022480.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124658089 G>A maps to NM_001081675.2 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124658089 G>A maps to NM_001081675.2 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51451955 C>G maps to NM_012427.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51451955 C>G maps to NM_012427.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:31986076 A>G maps to NM_181602.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:31986076 A>G maps to NM_181602.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:112466085 C>A maps to NM_001105206.1 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:112466085 C>A maps to NM_001105206.1 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:21788508 C>T maps to NM_002300.6 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:21788508 C>T maps to NM_002300.6 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:65639479 C>T maps to NM_014319.4 Q807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:65639479 C>T maps to NM_014319.4 Q807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:39292691 C>A maps to NM_006149.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:39292691 C>A maps to NM_006149.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:55106661 C>G maps to NM_006863.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:55106661 C>G maps to NM_006863.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12907643 G>T maps to NM_001013631.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12907643 G>T maps to NM_001013631.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:141115560 T>C maps to NM_018557.2 Q3794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:141115560 T>C maps to NM_018557.2 Q3794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:79982203 C>T maps to NM_144999.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:79982203 C>T maps to NM_144999.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:80530455 G>A maps to NM_178839.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:80530455 G>A maps to NM_178839.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:115560779 C>T maps to NM_002338.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:115560779 C>T maps to NM_002338.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:151870084 C>A maps to NM_005363.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:151870084 C>A maps to NM_005363.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:68065080 A>G maps to NM_145160.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:68065080 A>G maps to NM_145160.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:128072408 C>A maps to NM_006609.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:128072408 C>A maps to NM_006609.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:220808734 G>C maps to NM_018650.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:220808734 G>C maps to NM_018650.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:123370268 A>G maps to ENST00000426959 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:123370268 A>G maps to ENST00000426959 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:37184517 T>A maps to NM_170675.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:37184517 T>A maps to NM_170675.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:42021491 C>A maps to ENST00000219905 S1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:42021491 C>A maps to ENST00000219905 S1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:43277258 C>A maps to NM_153361.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:43277258 C>A maps to NM_153361.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:10427695 C>T maps to NM_001193277.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:10427695 C>T maps to NM_001193277.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:129903224 T>C maps to NM_002417.4 P2293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:129903224 T>C maps to NM_002417.4 P2293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:50515284 G>T maps to NM_015166.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:50515284 G>T maps to NM_015166.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:89128819 G>T maps to NM_005941.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:89128819 G>T maps to NM_005941.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:41345257 G>C maps to NM_005830.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:41345257 G>C maps to NM_005830.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:9065837 G>C maps to NM_024690.2 S7203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:9065837 G>C maps to NM_024690.2 S7203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:195498652 G>C maps to NM_018406.5 S4371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:195498652 G>C maps to NM_018406.5 S4371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49403170 G>A maps to NM_000255.3 Q708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49403170 G>A maps to NM_000255.3 Q708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:47363609 C>T maps to ENST00000399249 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:47363609 C>T maps to ENST00000399249 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48451077 G>A maps to NM_016132.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48451077 G>A maps to NM_016132.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23872644 C>T maps to NM_002471.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23872644 C>T maps to NM_002471.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:26168353 C>T maps to ENST00000407587 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:26168353 C>T maps to ENST00000407587 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52646176 G>C maps to ENST00000358212 S1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52646176 G>C maps to ENST00000358212 S1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52517701 C>A maps to NM_018728.3 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52517701 C>A maps to NM_018728.3 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101707769 A>T maps to NM_052867.2 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101707769 A>T maps to NM_052867.2 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:92926977 G>A maps to NM_004538.5 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:92926977 G>A maps to NM_004538.5 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:133721291 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:133721291 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:18122333 C>T maps to NM_198586.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:18122333 C>T maps to NM_198586.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89185033 T>A maps to NM_016931.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89185033 T>A maps to NM_016931.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:5993290 G>A maps to NM_015102.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:5993290 G>A maps to NM_015102.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:129349024 C>T maps to ENST00000393231 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:129349024 C>T maps to ENST00000393231 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:88680695 G>A maps to NM_001012338.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:88680695 G>A maps to NM_001012338.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:121465578 G>C maps to NM_003733.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:121465578 G>C maps to NM_003733.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228529167 G>T maps to NM_001098623.1 E5963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228529167 G>T maps to NM_001098623.1 E5963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228559661 C>T maps to NM_001098623.1 F7061F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228559661 C>T maps to NM_001098623.1 F7061F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:28231771 T>A maps to NM_000275.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:28231771 T>A maps to NM_000275.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:143657161 C>A maps to NM_012369.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:143657161 C>A maps to NM_012369.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29555765 C>T maps to NM_007160.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29555765 C>T maps to NM_007160.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248262730 C>A maps to NM_175911.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248262730 C>A maps to NM_175911.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248309309 C>A maps to NM_001004690.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248309309 C>A maps to NM_001004690.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248458348 C>A maps to NM_001004692.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248458348 C>A maps to NM_001004692.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248436750 C>A maps to NM_001004695.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248436750 C>A maps to NM_001004695.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248525428 C>T maps to NM_001004696.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248525428 C>T maps to NM_001004696.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:102358574 C>A maps to NM_001001674.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:102358574 C>A maps to NM_001001674.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20296191 G>A maps to NM_001004723.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20296191 G>A maps to NM_001004723.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:48328182 C>A maps to NM_001004725.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:48328182 C>A maps to NM_001004725.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:4389381 G>T maps to NM_001005161.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:4389381 G>T maps to NM_001005161.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:56258246 A>T maps to NM_001005282.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:56258246 A>T maps to NM_001005282.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:56185519 G>A maps to NM_001004744.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:56185519 G>A maps to NM_001004744.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240969744 G>T maps to NM_001005853.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240969744 G>T maps to NM_001005853.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240984556 G>T maps to NM_173351.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240984556 G>T maps to NM_173351.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:124412647 C>T maps to NM_001005195.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:124412647 C>T maps to NM_001005195.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:141619430 C>A maps to NM_001001656.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:141619430 C>A maps to NM_001001656.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:3114893 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:3114893 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:55617002 C>T maps to NM_001142763.1 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:55617002 C>T maps to NM_001142763.1 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:140432665 G>T maps to NM_013340.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:140432665 G>T maps to NM_013340.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82583766 C>A maps to NM_033026.5 E2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82583766 C>A maps to NM_033026.5 E2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82583851 T>C maps to NM_033026.5 E2139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82583851 T>C maps to NM_033026.5 E2139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:71485879 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:71485879 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:142537260 G>T maps to NM_013363.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:142537260 G>T maps to NM_013363.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165809840 G>A maps to NM_001130690.1 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165809840 G>A maps to NM_001130690.1 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7343063 C>A maps to NM_001131023.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7343063 C>A maps to NM_001131023.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42934569 G>C maps to NM_000287.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42934569 G>C maps to NM_000287.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45736371 C>A maps to NM_002626.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45736371 C>A maps to NM_002626.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45736373 G>C maps to NM_002626.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45736373 G>C maps to NM_002626.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:77381314 C>T maps to NM_000291.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:77381314 C>T maps to NM_000291.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:67588927 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:67588927 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:47866970 C>T maps to NM_138295.3 E2277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:47866970 C>T maps to NM_138295.3 E2277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:95791157 C>T maps to ENST00000371380 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:95791157 C>T maps to ENST00000371380 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:155212151 G>A maps to ENST00000340059 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:155212151 G>A maps to ENST00000340059 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:204218335 C>A maps to ENST00000367191 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:204218335 C>A maps to ENST00000367191 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6528570 G>A maps to NM_198681.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6528570 G>A maps to NM_198681.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:55887293 C>A maps to NM_033109.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:55887293 C>A maps to NM_033109.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:79782082 A>T maps to NM_007055.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:79782082 A>T maps to NM_007055.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:145594088 G>T maps to NM_006468.6 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:145594088 G>T maps to NM_006468.6 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:22106629 A>T maps to NM_001722.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:22106629 A>T maps to NM_001722.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:89781467 T>C maps to NM_006467.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:89781467 T>C maps to NM_006467.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:53103858 C>T maps to NM_182595.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:53103858 C>T maps to NM_182595.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:159631958 G>A maps to NM_005038.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:159631958 G>A maps to NM_005038.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:43131648 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:43131648 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12952860 C>A maps to NM_001039361.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12952860 C>A maps to NM_001039361.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:11552076 G>T maps to ENST00000436195 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:11552076 G>T maps to ENST00000436195 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:128179007 C>T maps to ENST00000409048 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:128179007 C>T maps to ENST00000409048 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:138739044 C>T maps to NM_001013650.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:138739044 C>T maps to NM_001013650.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:53178229 G>T maps to NM_002806.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:53178229 G>T maps to NM_002806.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:78959093 C>A maps to NM_000959.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:78959093 C>A maps to NM_000959.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:49135439 G>A maps to NM_005051.1 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:49135439 G>A maps to NM_005051.1 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:79253843 G>T maps to NM_001008387.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:79253843 G>T maps to NM_001008387.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:107080805 C>T maps to ENST00000357881 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:107080805 C>T maps to ENST00000357881 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:11505190 G>A maps to NM_001161616.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:11505190 G>A maps to NM_001161616.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:86018322 C>A maps to ENST00000358110 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:86018322 C>A maps to ENST00000358110 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:130898774 C>T maps to NM_015347.4 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:130898774 C>T maps to NM_015347.4 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:43161900 C>A maps to ENST00000352483 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:43161900 C>A maps to ENST00000352483 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:167344530 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:167344530 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:60803662 C>A maps to NM_134260.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:60803662 C>A maps to NM_134260.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:10480174 G>T maps to NM_178857.5 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:10480174 G>T maps to NM_178857.5 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128356926 C>T maps to NM_002950.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128356926 C>T maps to NM_002950.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41750014 G>A maps to NM_015138.4 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41750014 G>A maps to NM_015138.4 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237837441 C>A maps to NM_001035.2 A2879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237837441 C>A maps to NM_001035.2 A2879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:166852588 C>T maps to NM_001165963.1 K1505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:166852588 C>T maps to NM_001165963.1 K1505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30887626 G>A maps to NM_174977.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30887626 G>A maps to NM_174977.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121652417 C>T maps to NM_007190.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121652417 C>T maps to NM_007190.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:9044499 C>A maps to NM_003966.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:9044499 C>A maps to NM_003966.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:19707368 C>T maps to NM_002688.5 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:19707368 C>T maps to NM_002688.5 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:1720180 G>T maps to NM_005088.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:1720180 G>T maps to NM_005088.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:201400786 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:201400786 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51217149 G>A maps to ENST00000391814 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51217149 G>A maps to ENST00000391814 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:103718715 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:103718715 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:63067050 G>A maps to NM_001039752.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:63067050 G>A maps to NM_001039752.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:113742145 G>T maps to NM_024959.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:113742145 G>T maps to NM_024959.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:118165312 T>C maps to NM_173851.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:118165312 T>C maps to NM_173851.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:75685014 G>T maps to NM_152697.4 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:75685014 G>T maps to NM_152697.4 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51883653 G>T maps to NM_001039960.1 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51883653 G>T maps to NM_001039960.1 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32477865 C>A maps to NM_000343.3 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32477865 C>A maps to NM_000343.3 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:33355670 G>A maps to NM_014270.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:33355670 G>A maps to NM_014270.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:84290251 G>C maps to NM_014841.2 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:84290251 G>C maps to NM_014841.2 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:220353802 C>G maps to NM_005876.4 S2726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:220353802 C>G maps to NM_005876.4 S2726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:44865870 G>A maps to NM_025137.3 Q2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:44865870 G>A maps to NM_025137.3 Q2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27959178 C>T maps to NM_033389.2 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27959178 C>T maps to NM_033389.2 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:104089374 C>T maps to NM_017564.9 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:104089374 C>T maps to NM_017564.9 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:74515975 T>C maps to NM_001164380.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:74515975 T>C maps to NM_001164380.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:63967651 C>T maps to ENST00000358794 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:63967651 C>T maps to ENST00000358794 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242441096 G>C maps to NM_006374.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242441096 G>C maps to NM_006374.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:43910165 C>G maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:43910165 C>G maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:53150367 G>T maps to NM_178509.5 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:53150367 G>T maps to NM_178509.5 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27011620 C>G maps to NM_003170.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27011620 C>G maps to NM_003170.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113275338 G>T maps to ENST00000374463 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113275338 G>T maps to ENST00000374463 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152832220 A>G maps to NM_182961.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152832220 A>G maps to NM_182961.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:27831773 G>A maps to ENST00000409980 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:27831773 G>A maps to ENST00000409980 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:80887118 C>T maps to NM_005993.4 R942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:80887118 C>T maps to NM_005993.4 R942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:152084936 C>A maps to NM_007113.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:152084936 C>A maps to NM_007113.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:104470656 T>G maps to NM_153046.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:104470656 T>G maps to NM_153046.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169637358 G>A maps to NM_003247.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169637358 G>A maps to NM_003247.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68725317 G>T maps to NM_004262.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68725317 G>T maps to NM_004262.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68956359 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68956359 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51252603 T>C maps to NM_182559.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51252603 T>C maps to NM_182559.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:19744626 C>A maps to NM_002772.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:19744626 C>A maps to NM_002772.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:7995186 T>A maps to NM_001561.5 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:7995186 T>A maps to NM_001561.5 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:31769849 G>C maps to NM_020856.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:31769849 G>C maps to NM_020856.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:43251342 C>T maps to NM_032538.1 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:43251342 C>T maps to NM_032538.1 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:83733733 C>A maps to NM_198920.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:83733733 C>A maps to NM_198920.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:99226377 G>A maps to ENST00000409347 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:99226377 G>A maps to ENST00000409347 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:216172294 T>A maps to ENST00000366943 T2197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:216172294 T>A maps to ENST00000366943 T2197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:132630678 G>T maps to NM_001008563.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:132630678 G>T maps to NM_001008563.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:132162272 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:132162272 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:50789392 G>A maps to NM_005154.3 W1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:50789392 G>A maps to NM_005154.3 W1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12342994 C>T maps to NM_015378.2 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12342994 C>T maps to NM_015378.2 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:85656258 C>T maps to NM_014991.4 W2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:85656258 C>T maps to NM_014991.4 W2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:53997422 T>A maps to NM_182758.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:53997422 T>A maps to NM_182758.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:48917893 C>T maps to NM_175575.5 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:48917893 C>T maps to NM_175575.5 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:168105191 C>A maps to NM_152381.5 P2430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:168105191 C>A maps to NM_152381.5 P2430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:30585070 G>C maps to NM_001011718.1 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:30585070 G>C maps to NM_001011718.1 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:135744470 A>T maps to NM_025052.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:135744470 A>T maps to NM_025052.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:37126664 A>T maps to NM_032226.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:37126664 A>T maps to NM_032226.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:74742845 C>T maps to NM_144969.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:74742845 C>T maps to NM_144969.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:31810746 G>C maps to NM_001174096.1 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:31810746 G>C maps to NM_001174096.1 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:77768282 G>A maps to NM_024721.4 Q3042Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:77768282 G>A maps to NM_024721.4 Q3042Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:50769143 C>T maps to NM_018197.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:50769143 C>T maps to NM_018197.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52090621 G>A maps to NM_007147.2 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52090621 G>A maps to NM_007147.2 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:22156887 T>C maps to NM_007153.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:22156887 T>C maps to NM_007153.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:74587598 C>T maps to NM_007345.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:74587598 C>T maps to NM_007345.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:148903825 C>A maps to NM_003575.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:148903825 C>A maps to NM_003575.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44139647 C>T maps to NM_006973.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44139647 C>T maps to NM_006973.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:57188188 G>T maps to NM_033273.1 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:57188188 G>T maps to NM_033273.1 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:31040290 C>A maps to NM_014717.1 P1255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:31040290 C>A maps to NM_014717.1 P1255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:56973726 G>T maps to ENST00000342634 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:56973726 G>T maps to ENST00000342634 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:20727616 C>A maps to NM_001159293.1 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:20727616 C>A maps to NM_001159293.1 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:149558927 C>T maps to NM_001099220.1 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:149558927 C>T maps to NM_001099220.1 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:72511353 G>T maps to NM_139155.2 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:72511353 G>T maps to NM_139155.2 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:31498490 A>T maps to NM_032849.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:31498490 A>T maps to NM_032849.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:142637619 G>C maps to NM_178829.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:142637619 G>C maps to NM_178829.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:40948086 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:40948086 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:7043209 C>A maps to NM_153376.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:7043209 C>A maps to NM_153376.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:101977790 T>A maps to NM_001278.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:101977790 T>A maps to NM_001278.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:86954791 C>A maps to NM_001285.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:86954791 C>A maps to NM_001285.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:146741007 G>T maps to NM_014141.5 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:146741007 G>T maps to NM_014141.5 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:147914434 A>G maps to NM_014141.5 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:147914434 A>G maps to NM_014141.5 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:189904154 C>A maps to NM_000393.3 A1256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:189904154 C>A maps to NM_000393.3 A1256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:11384918 G>T maps to NM_001332.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:11384918 G>T maps to NM_001332.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:16975089 T>A maps to NM_001081.3 R2040R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:16975089 T>A maps to NM_001081.3 R2040R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:119668354 G>T maps to NM_003588.3 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:119668354 G>T maps to NM_003588.3 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:47858717 C>A maps to NM_017895.7 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:47858717 C>A maps to NM_017895.7 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:196718110 C>A maps to NM_018897.2 G2913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:196718110 C>A maps to NM_018897.2 G2913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:38818064 A>T maps to ENST00000327475 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:38818064 A>T maps to ENST00000327475 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:220246786 G>A maps to NM_012100.2 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:220246786 G>A maps to NM_012100.2 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:25799720 C>A maps to NM_021907.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:25799720 C>A maps to NM_021907.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:167095996 C>A maps to NM_001080426.1 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:167095996 C>A maps to NM_001080426.1 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:43632903 C>A maps to NM_001159936.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:43632903 C>A maps to NM_001159936.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:207026076 G>T maps to NM_021121.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:207026076 G>T maps to NM_021121.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:169511382 C>T maps to ENST00000367796 W987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:169511382 C>T maps to ENST00000367796 W987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:71233696 C>A maps to NM_001162529.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:71233696 C>A maps to NM_001162529.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:102683759 A>G maps to NM_001136123.1 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:102683759 A>G maps to NM_001136123.1 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:152283026 C>T maps to NM_002016.1 V1445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:152283026 C>T maps to NM_002016.1 V1445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:171154953 T>G maps to NM_001460.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:171154953 T>G maps to NM_001460.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:41740638 C>A maps to NM_006653.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:41740638 C>A maps to NM_006653.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:121187964 C>A maps to NM_177478.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:121187964 C>A maps to NM_177478.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:172735813 G>A maps to NM_001034845.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:172735813 G>A maps to NM_001034845.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:101910103 C>A maps to NM_001184727.1 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:101910103 C>A maps to NM_001184727.1 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:83730390 A>T maps to NM_144657.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:83730390 A>T maps to NM_144657.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:236730017 G>A maps to NM_018072.5 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:236730017 G>A maps to NM_018072.5 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:104440286 G>T maps to NM_017416.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:104440286 G>T maps to NM_017416.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:145536119 C>T maps to NM_003637.3 Q738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:145536119 C>T maps to NM_003637.3 Q738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:8825176 G>T maps to ENST00000456698 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:8825176 G>T maps to ENST00000456698 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:5462197 G>A maps to NM_015325.1 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:5462197 G>A maps to NM_015325.1 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:113378248 A>T maps to NM_001009899.2 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:113378248 A>T maps to NM_001009899.2 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:44584644 G>T maps to NM_173484.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:44584644 G>T maps to NM_173484.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:39138575 T>A maps to NM_182497.3 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:39138575 T>A maps to NM_182497.3 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:66857163 G>T maps to NM_207338.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:66857163 G>T maps to NM_207338.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:4276495 C>A maps to NM_017816.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:4276495 C>A maps to NM_017816.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:45953763 C>A maps to NM_145021.4 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:45953763 C>A maps to NM_145021.4 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:108819310 C>A maps to NM_014429.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:108819310 C>A maps to NM_014429.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:36455434 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:36455434 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9066577 G>C maps to NM_024690.2 T6956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9066577 G>C maps to NM_024690.2 T6956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100680747 C>T maps to NM_001040105.1 T2017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100680747 C>T maps to NM_001040105.1 T2017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:3235810 C>A maps to NM_015419.3 E1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:3235810 C>A maps to NM_015419.3 E1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:69954181 A>T maps to NM_032578.2 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:69954181 A>T maps to NM_032578.2 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:130829230 G>A maps to NM_197956.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:130829230 G>A maps to NM_197956.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:70417389 G>T maps to NM_153181.2 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:70417389 G>T maps to NM_153181.2 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248402508 T>C maps to NM_017504.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248402508 T>C maps to NM_017504.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:5862539 G>T maps to ENST00000379946 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:5862539 G>T maps to ENST00000379946 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:58125858 T>A maps to NM_001005489.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:58125858 T>A maps to NM_001005489.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:55594858 C>A maps to NM_001004739.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:55594858 C>A maps to NM_001004739.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:57114032 C>T maps to NM_002559.2 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:57114032 C>T maps to NM_002559.2 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:176525865 G>A maps to NM_020318.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:176525865 G>A maps to NM_020318.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr21:47359948 A>T maps to NM_020528.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr21:47359948 A>T maps to NM_020528.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140215056 C>A maps to NM_018910.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140215056 C>A maps to NM_018910.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:95380393 C>T maps to NM_006204.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:95380393 C>T maps to NM_006204.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:73651528 C>A maps to NM_015009.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:73651528 C>A maps to NM_015009.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:41966756 G>T maps to NM_001164595.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:41966756 G>T maps to NM_001164595.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:156878709 C>G maps to NM_001080471.1 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:156878709 C>G maps to NM_001080471.1 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:18562678 C>A maps to NM_017929.5 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:18562678 C>A maps to NM_017929.5 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:28800396 C>A maps to NM_023923.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:28800396 C>A maps to NM_023923.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:145580300 T>C maps to NM_006099.3 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:145580300 T>C maps to NM_006099.3 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:51920528 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:51920528 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:53104089 C>A maps to NM_182595.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:53104089 C>A maps to NM_182595.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:39500185 G>C maps to NM_007252.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:39500185 G>C maps to NM_007252.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:160786689 C>T maps to NM_139245.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:160786689 C>T maps to NM_139245.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:12828214 C>A maps to NM_001039091.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:12828214 C>A maps to NM_001039091.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:54122796 A>T maps to NM_014614.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:54122796 A>T maps to NM_014614.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:32375637 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:32375637 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:37177414 A>T maps to NM_020336.2 R996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:37177414 A>T maps to NM_020336.2 R996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:80409611 T>C maps to NM_006909.1 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:80409611 T>C maps to NM_006909.1 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:21996975 G>T maps to NM_025232.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:21996975 G>T maps to NM_025232.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:79349964 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:79349964 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:45541023 A>G maps to ENST00000221452 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:45541023 A>G maps to ENST00000221452 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100457847 G>A maps to NM_020246.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100457847 G>A maps to NM_020246.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:119029955 T>A maps to NM_003054.4 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:119029955 T>A maps to NM_003054.4 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:48414086 C>A maps to NM_205850.2 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:48414086 C>A maps to NM_205850.2 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:68308952 G>T maps to NM_003983.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:68308952 G>T maps to NM_003983.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:127361381 G>T maps to NM_014390.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:127361381 G>T maps to NM_014390.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:2446398 C>A maps to ENST00000339610 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:2446398 C>A maps to ENST00000339610 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:7717038 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:7717038 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:123594319 C>T maps to NM_001174046.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:123594319 C>T maps to NM_001174046.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:52948664 A>T maps to NM_145263.2 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:52948664 A>T maps to NM_145263.2 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:2097598 C>A maps to NM_080836.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:2097598 C>A maps to NM_080836.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:7324268 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:7324268 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:35831203 C>A maps to NM_001166105.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:35831203 C>A maps to NM_001166105.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:179562701 G>T maps to ENST00000444136 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:179562701 G>T maps to ENST00000444136 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:179603745 G>T maps to ENST00000444136 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:179603745 G>T maps to ENST00000444136 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:35606260 A>T maps to NM_006285.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:35606260 A>T maps to NM_006285.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:77377967 G>A maps to NM_017662.4 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:77377967 G>A maps to NM_017662.4 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:144698278 G>A maps to NM_003313.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:144698278 G>A maps to NM_003313.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:94830476 C>A maps to NM_014639.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:94830476 C>A maps to NM_014639.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:179395804 G>C maps to NM_133378.4 T32611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:179395804 G>C maps to NM_133378.4 T32611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:62302682 C>A maps to NM_020821.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:62302682 C>A maps to NM_020821.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100388610 G>T maps to ENST00000349350 A2468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100388610 G>T maps to ENST00000349350 A2468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:77616715 C>A maps to NM_024721.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:77616715 C>A maps to NM_024721.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:43161515 G>T maps to ENST00000509156 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:43161515 G>T maps to ENST00000509156 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:37005825 G>A maps to NM_001166038.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:37005825 G>A maps to NM_001166038.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9270788 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9270788 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:22804599 G>T maps to NM_015461.2 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:22804599 G>T maps to NM_015461.2 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57985661 G>T maps to NM_001024596.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57985661 G>T maps to NM_001024596.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:23562714 G>T maps to NM_014977.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:23562714 G>T maps to NM_014977.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:18777139 C>T maps to NM_001040272.4 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:18777139 C>T maps to NM_001040272.4 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:100346960 C>A maps to ENST00000311030 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:100346960 C>A maps to ENST00000311030 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:105418709 G>T maps to NM_138420.2 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:105418709 G>T maps to NM_138420.2 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:3744966 G>A maps to ENST00000403787 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:3744966 G>A maps to ENST00000403787 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:55623913 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:55623913 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:112997024 C>A maps to ENST00000273395 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:112997024 C>A maps to ENST00000273395 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:185153947 A>G maps to NM_001105518.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:185153947 A>G maps to NM_001105518.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:63632549 G>T maps to NM_001218.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:63632549 G>T maps to NM_001218.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:77290604 C>A maps to NM_001042784.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:77290604 C>A maps to NM_001042784.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:60498690 C>T maps to NM_001794.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:60498690 C>T maps to NM_001794.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:105664963 C>T maps to NM_152750.4 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:105664963 C>T maps to NM_152750.4 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:68380365 C>T maps to NM_001812.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:68380365 C>T maps to NM_001812.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:580695 G>A maps to NM_004066.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:580695 G>A maps to NM_004066.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:117235030 G>A maps to NM_000492.3 W846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:117235030 G>A maps to NM_000492.3 W846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:1339045 C>T maps to NM_030782.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:1339045 C>T maps to NM_030782.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:41463833 C>T maps to NM_001843.2 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:41463833 C>T maps to NM_001843.2 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr13:111088677 G>A maps to NM_001846.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr13:111088677 G>A maps to NM_001846.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:155018644 C>A maps to NM_152494.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:155018644 C>A maps to NM_152494.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:38905909 C>G maps to ENST00000327475 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:38905909 C>G maps to ENST00000327475 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:100405019 C>T maps to NM_004444.4 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:100405019 C>T maps to NM_004444.4 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:56274463 G>A maps to NM_000502.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:56274463 G>A maps to NM_000502.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:5800410 G>A maps to NM_153717.2 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:5800410 G>A maps to NM_153717.2 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:59058926 G>A maps to NM_147189.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:59058926 G>A maps to NM_147189.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:37118262 T>G maps to NM_001008777.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:37118262 T>G maps to NM_001008777.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:53331253 A>C maps to NM_001134999.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:53331253 A>C maps to NM_001134999.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:14819376 G>A maps to ENST00000380880 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:14819376 G>A maps to ENST00000380880 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007141 G>A maps to NM_001111270.1 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007141 G>A maps to NM_001111270.1 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007228 G>T maps to NM_001111270.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007228 G>T maps to NM_001111270.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:20335276 G>A maps to NM_001007240.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:20335276 G>A maps to NM_001007240.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:27861500 C>G maps to NM_003527.4 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:27861500 C>G maps to NM_003527.4 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:86406603 C>T maps to NM_006839.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:86406603 C>T maps to NM_006839.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:7658062 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:7658062 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:94089156 C>T maps to ENST00000393153 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:94089156 C>T maps to ENST00000393153 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:86518051 C>A maps to NM_017576.1 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:86518051 C>A maps to NM_017576.1 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:55341714 T>A maps to NM_013289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:55341714 T>A maps to NM_013289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:30740625 C>T maps to NM_005204.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:30740625 C>T maps to NM_005204.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:207621659 C>T maps to NM_001039845.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:207621659 C>T maps to NM_001039845.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:90449993 G>A maps to NM_014611.1 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:90449993 G>A maps to NM_014611.1 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:116412043 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:116412043 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:42003302 C>G maps to ENST00000219905 S947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:42003302 C>G maps to ENST00000219905 S947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr22:50553670 G>T maps to NM_018995.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr22:50553670 G>T maps to NM_018995.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:18025525 C>T maps to ENST00000205890 Q1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:18025525 C>T maps to ENST00000205890 Q1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:1371285 C>A maps to NM_001080779.1 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:1371285 C>A maps to NM_001080779.1 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:41791407 G>A maps to NM_006766.3 Q1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:41791407 G>A maps to NM_006766.3 Q1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:41792077 G>T maps to NM_006766.3 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:41792077 G>T maps to NM_006766.3 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131849959 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131849959 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:119367416 G>A maps to NM_022135.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:119367416 G>A maps to NM_022135.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:47269226 G>T maps to NM_020820.3 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:47269226 G>T maps to NM_020820.3 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:43359740 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:43359740 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:184026273 G>A maps to NM_002808.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:184026273 G>A maps to NM_002808.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:21940150 G>A maps to NM_001145658.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:21940150 G>A maps to NM_001145658.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:43615592 C>A maps to NM_020975.4 S891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:43615592 C>A maps to NM_020975.4 S891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:102269108 C>A maps to NM_015490.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:102269108 C>A maps to NM_015490.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:123950179 C>T maps to NM_180699.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:123950179 C>T maps to NM_180699.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:86248582 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:86248582 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:220355149 C>T maps to NM_005876.4 R2981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:220355149 C>T maps to NM_005876.4 R2981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:126135201 G>A maps to NM_003139.3 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:126135201 G>A maps to NM_003139.3 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:64634012 C>G maps to NM_182914.2 L5556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:64634012 C>G maps to NM_182914.2 L5556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:138000025 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:138000025 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:7963022 G>T maps to NM_021156.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:7963022 G>T maps to NM_021156.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:77377179 C>T maps to NM_017662.4 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:77377179 C>T maps to NM_017662.4 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:2127686 C>A maps to NM_000548.3 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:2127686 C>A maps to NM_000548.3 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:71265911 G>T maps to NM_012339.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:71265911 G>T maps to NM_012339.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:179644902 G>A maps to NM_133378.4 Q1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:179644902 G>A maps to NM_133378.4 Q1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:43480051 C>T maps to ENST00000506469 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:43480051 C>T maps to ENST00000506469 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:52911671 A>G maps to NM_001009881.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:52911671 A>G maps to NM_001009881.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:58578971 C>T maps to NM_007134.1 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:58578971 C>T maps to NM_007134.1 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:195516 G>T maps to NM_001042416.1 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:195516 G>T maps to NM_001042416.1 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:40772607 C>T maps to NM_033160.5 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:40772607 C>T maps to NM_033160.5 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:44506471 C>T maps to NM_080752.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:44506471 C>T maps to NM_080752.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:108881887 G>T maps to NM_032859.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:108881887 G>T maps to NM_032859.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:156787351 T>C maps to NM_017419.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:156787351 T>C maps to NM_017419.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:15603663 C>G maps to NM_021804.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:15603663 C>G maps to NM_021804.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:64587297 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:64587297 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:150531541 G>A maps to ENST00000369039 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:150531541 G>A maps to ENST00000369039 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:112838281 G>T maps to NM_000681.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:112838281 G>T maps to NM_000681.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:147743757 G>T maps to NM_002025.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:147743757 G>T maps to NM_002025.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:105420365 G>T maps to NM_138420.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:105420365 G>T maps to NM_138420.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:62298828 C>A maps to NM_001620.1 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:62298828 C>A maps to NM_001620.1 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:55040069 T>G maps to NM_000032.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:55040069 T>G maps to NM_000032.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:102097954 G>A maps to NM_017621.3 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:102097954 G>A maps to NM_017621.3 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29498007 G>C maps to NM_004304.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29498007 G>C maps to NM_004304.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29498358 G>A maps to NM_004304.3 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29498358 G>A maps to NM_004304.3 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:56438862 G>A maps to NM_001144.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:56438862 G>A maps to NM_001144.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:113266828 C>T maps to NM_178510.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:113266828 C>T maps to NM_178510.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:27935035 G>T maps to NM_152345.4 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:27935035 G>T maps to NM_152345.4 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:34044367 G>T maps to NM_001030006.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:34044367 G>T maps to NM_001030006.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:148744108 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:148744108 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:11204552 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:11204552 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:138455935 C>G maps to NM_130840.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:138455935 C>G maps to NM_130840.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:97941429 G>T maps to NM_018842.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:97941429 G>T maps to NM_018842.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:55758936 G>T maps to NM_001719.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:55758936 G>T maps to NM_001719.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:50217164 C>A maps to ENST00000342989 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:50217164 C>A maps to ENST00000342989 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:92445139 G>A maps to ENST00000347608 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:92445139 G>A maps to ENST00000347608 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:55474246 C>A maps to NM_057176.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:55474246 C>A maps to NM_057176.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:102589844 A>T maps to NM_017915.3 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:102589844 A>T maps to NM_017915.3 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:24921595 C>A maps to NM_018958.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:24921595 C>A maps to NM_018958.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119760064 T>A maps to NM_152692.4 *319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119760064 T>A maps to NM_152692.4 *319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:38155360 C>A maps to NM_017850.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:38155360 C>A maps to NM_017850.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:119236106 C>T maps to NM_016589.3 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:119236106 C>T maps to NM_016589.3 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:47846146 G>A maps to NM_001013732.3 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:47846146 G>A maps to NM_001013732.3 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:40945337 T>C maps to NM_000587.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:40945337 T>C maps to NM_000587.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:76993506 G>A maps to NM_138793.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:76993506 G>A maps to NM_138793.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:18891414 C>A maps to NM_033328.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:18891414 C>A maps to NM_033328.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:149962191 A>G maps to ENST00000438086 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:149962191 A>G maps to ENST00000438086 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:85961603 G>T maps to NM_033100.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:85961603 G>T maps to NM_033100.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:72667526 C>A maps to NM_005193.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:72667526 C>A maps to NM_005193.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61981901 G>C maps to NM_000744.5 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61981901 G>C maps to NM_000744.5 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:10218182 G>T maps to NM_207345.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:10218182 G>T maps to NM_207345.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:201726035 A>G maps to NM_001162407.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:201726035 A>G maps to NM_001162407.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:76486439 T>A maps to NM_033401.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:76486439 T>A maps to NM_033401.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:76513433 C>A maps to NM_033401.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:76513433 C>A maps to NM_033401.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:103474072 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:103474072 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:88009013 C>A maps to NM_033048.5 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:88009013 C>A maps to NM_033048.5 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:113484936 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:113484936 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:101993007 G>T maps to NM_018294.4 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:101993007 G>T maps to NM_018294.4 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:125299760 G>A maps to NM_001013628.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:125299760 G>A maps to NM_001013628.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:134680667 A>T maps to NM_182540.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:134680667 A>T maps to NM_182540.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:234365974 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:234365974 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:35365841 G>T maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:35365841 G>T maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:124393957 G>T maps to NM_207437.3 S3204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:124393957 G>T maps to NM_207437.3 S3204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:124409643 C>T maps to NM_207437.3 Y3820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:124409643 C>T maps to NM_207437.3 Y3820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:21646323 A>C maps to NM_003777.3 A1275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:21646323 A>C maps to NM_003777.3 A1275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:83829488 C>T maps to NM_015018.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:83829488 C>T maps to NM_015018.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:113866280 C>G maps to NM_000796.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:113866280 C>G maps to NM_000796.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:56328452 T>A maps to ENST00000361203 S7385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:56328452 T>A maps to ENST00000361203 S7385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:60484500 G>A maps to NM_001144933.1 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:60484500 G>A maps to NM_001144933.1 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142566875 G>T maps to NM_004445.3 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142566875 G>T maps to NM_004445.3 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:216737621 T>A maps to NM_001438.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:216737621 T>A maps to NM_001438.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:169528534 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:169528534 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:138643881 C>G maps to NM_000133.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:138643881 C>G maps to NM_000133.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:43616453 C>T maps to NM_001101376.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:43616453 C>T maps to NM_001101376.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:37029345 G>T maps to NM_001013736.2 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:37029345 G>T maps to NM_001013736.2 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:8377323 G>T maps to NM_018088.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:8377323 G>T maps to NM_018088.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:45645709 T>C maps to NM_020937.2 D1251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:45645709 T>C maps to NM_020937.2 D1251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:8131063 G>A maps to NM_032447.3 I2723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:8131063 G>A maps to NM_032447.3 I2723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:19184871 G>T maps to NM_152898.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:19184871 G>T maps to NM_152898.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:28599081 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:28599081 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:79387360 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:79387360 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:151123292 G>A maps to NM_004961.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:151123292 G>A maps to NM_004961.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:46099302 G>T maps to NM_173536.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:46099302 G>T maps to NM_173536.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:8100556 G>A maps to NM_001002295.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:8100556 G>A maps to NM_001002295.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:19611939 G>A maps to ENST00000404158 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:19611939 G>A maps to ENST00000404158 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:121554949 G>T maps to NM_005270.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:121554949 G>T maps to NM_005270.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:143928045 G>T maps to NM_002066.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:143928045 G>T maps to NM_002066.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:56377843 G>T maps to NM_138736.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:56377843 G>T maps to NM_138736.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:72368429 G>T maps to ENST00000440684 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:72368429 G>T maps to ENST00000440684 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:6313831 G>A maps to NM_207370.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:6313831 G>A maps to NM_207370.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:158262430 C>A maps to NM_000826.3 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:158262430 C>A maps to NM_000826.3 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:87379646 G>T maps to NM_017551.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:87379646 G>T maps to NM_017551.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:104432626 G>A maps to NM_133445.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:104432626 G>A maps to NM_133445.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:6389579 C>A maps to NM_002096.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:6389579 C>A maps to NM_002096.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:89414160 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:89414160 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:27115266 G>A maps to NM_080596.1 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:27115266 G>A maps to NM_080596.1 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:27148136 G>T maps to NM_153631.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:27148136 G>T maps to NM_153631.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:54379591 C>A maps to NM_017409.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:54379591 C>A maps to NM_017409.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:152187705 G>A maps to NM_001009931.1 Y2133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:152187705 G>A maps to NM_001009931.1 Y2133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:16343585 C>A maps to ENST00000375714 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:16343585 C>A maps to ENST00000375714 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:47409355 G>T maps to NM_000621.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:47409355 G>T maps to NM_000621.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88731894 T>A maps to NM_004967.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88731894 T>A maps to NM_004967.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:51864583 C>A maps to NM_001085479.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:51864583 C>A maps to NM_001085479.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:107978506 G>T maps to NM_003604.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:107978506 G>T maps to NM_003604.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:133930852 G>C maps to NM_001105521.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:133930852 G>C maps to NM_001105521.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:87678335 C>A maps to NM_020655.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:87678335 C>A maps to NM_020655.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4920340 G>T maps to NM_002235.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4920340 G>T maps to NM_002235.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:26965368 G>A maps to NM_014680.2 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:26965368 G>A maps to NM_014680.2 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:86544145 C>A maps to NM_001142749.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:86544145 C>A maps to NM_001142749.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:51900966 C>A maps to NM_032559.4 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:51900966 C>A maps to NM_032559.4 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:86887408 C>A maps to NM_057162.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:86887408 C>A maps to NM_057162.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:10531200 A>T maps to NM_007360.3 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:10531200 A>T maps to NM_007360.3 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:6943236 T>C maps to NM_005559.2 P3003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:6943236 T>C maps to NM_005559.2 P3003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141625342 A>T maps to NM_018557.2 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141625342 A>T maps to NM_018557.2 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:25004826 G>T maps to NM_001009909.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:25004826 G>T maps to NM_001009909.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:90499591 T>A maps to NM_014611.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:90499591 T>A maps to NM_014611.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:109459024 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:109459024 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:128346069 A>G maps to ENST00000389524 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:128346069 A>G maps to ENST00000389524 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:17296810 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:17296810 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:117828411 G>T maps to NM_016200.4 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:117828411 G>T maps to NM_016200.4 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:52802577 C>A maps to NM_003157.4 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:52802577 C>A maps to NM_003157.4 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:182543485 G>A maps to NM_002500.2 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:182543485 G>A maps to NM_002500.2 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:173322579 G>T maps to NM_014932.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:173322579 G>T maps to NM_014932.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:5811274 G>T maps to ENST00000381093 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:5811274 G>T maps to ENST00000381093 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:247607376 G>T maps to NM_004895.4 G925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:247607376 G>T maps to NM_004895.4 G925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:66189699 C>G maps to NM_178864.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:66189699 C>G maps to NM_178864.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:107790397 G>T maps to ENST00000379032 S1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:107790397 G>T maps to ENST00000379032 S1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:123515009 G>C maps to NM_001163278.1 V2525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:123515009 G>C maps to NM_001163278.1 V2525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:50953476 G>C maps to NM_018245.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:50953476 G>C maps to NM_018245.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61444331 G>T maps to NM_007346.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61444331 G>T maps to NM_007346.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:161953797 G>T maps to ENST00000451379 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:161953797 G>T maps to ENST00000451379 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:47754281 C>T maps to ENST00000489301 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:47754281 C>T maps to ENST00000489301 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:107380044 C>G maps to NM_001001956.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:107380044 C>G maps to NM_001001956.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:107266854 C>T maps to NM_001004485.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:107266854 C>T maps to NM_001004485.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:247921237 G>T maps to NM_012353.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:247921237 G>T maps to NM_012353.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248128776 C>A maps to NM_001004491.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248128776 C>A maps to NM_001004491.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:55110711 C>A maps to NM_001005274.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:55110711 C>A maps to NM_001005274.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:56247252 C>A maps to NM_001004707.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:56247252 C>A maps to NM_001004707.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:55406105 C>A maps to NM_001004124.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:55406105 C>A maps to NM_001004124.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4661967 C>A maps to NM_001004751.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4661967 C>A maps to NM_001004751.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4842746 T>A maps to NM_001004753.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4842746 T>A maps to NM_001004753.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4843385 C>A maps to NM_001004753.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4843385 C>A maps to NM_001004753.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4389408 G>A maps to NM_001005161.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4389408 G>A maps to NM_001005161.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:6007893 C>A maps to NM_001005173.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:6007893 C>A maps to NM_001005173.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:56043776 C>G maps to NM_001004745.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:56043776 C>G maps to NM_001004745.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:55715042 C>A maps to NM_001005182.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:55715042 C>A maps to NM_001005182.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:23237369 C>T maps to NM_005015.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:23237369 C>T maps to NM_005015.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:31811562 G>T maps to NM_001604.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:31811562 G>T maps to NM_001604.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:47783763 G>T maps to NM_006031.5 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:47783763 G>T maps to NM_006031.5 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:72292013 G>A maps to NM_002599.3 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:72292013 G>A maps to NM_002599.3 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:49754639 G>A maps to NM_138733.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:49754639 G>A maps to NM_138733.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:8770948 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:8770948 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:81181897 G>A maps to NM_052892.3 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:81181897 G>A maps to NM_052892.3 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:131883345 A>T maps to ENST00000409158 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:131883345 A>T maps to ENST00000409158 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:131913209 C>A maps to NM_020911.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:131913209 C>A maps to NM_020911.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:50724600 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:50724600 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:82763625 G>A maps to NM_000307.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:82763625 G>A maps to NM_000307.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:50189880 G>T maps to NM_001536.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:50189880 G>T maps to NM_001536.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:55964742 A>T maps to NM_173814.4 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:55964742 A>T maps to NM_173814.4 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:43420610 G>A maps to NM_002782.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:43420610 G>A maps to NM_002782.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:54114546 T>A maps to NM_014614.2 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:54114546 T>A maps to NM_014614.2 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:157475566 C>A maps to NM_002847.3 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:157475566 C>A maps to NM_002847.3 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:40748599 T>A maps to ENST00000373198 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:40748599 T>A maps to ENST00000373198 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:32956352 A>T maps to NM_001076786.1 A1054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:32956352 A>T maps to NM_001076786.1 A1054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:4917440 G>T maps to NM_018059.4 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:4917440 G>T maps to NM_018059.4 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:33490546 T>A maps to NM_033103.4 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:33490546 T>A maps to NM_033103.4 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:38082183 G>T maps to NM_001038633.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:38082183 G>T maps to NM_001038633.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237944869 C>A maps to NM_001035.2 S3962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237944869 C>A maps to NM_001035.2 S3962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:148761493 G>T maps to NM_015278.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:148761493 G>T maps to NM_015278.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:192700894 G>A maps to NM_004657.5 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:192700894 G>A maps to NM_004657.5 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:27306715 G>A maps to NM_178860.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:27306715 G>A maps to NM_178860.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:100838542 G>T maps to ENST00000262901 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:100838542 G>T maps to ENST00000262901 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:60714149 C>A maps to NM_016582.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:60714149 C>A maps to NM_016582.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:25777187 G>T maps to ENST00000397076 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:25777187 G>T maps to ENST00000397076 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:53558281 G>T maps to NM_006671.4 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:53558281 G>T maps to NM_006671.4 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:113417306 T>C maps to NM_005415.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:113417306 T>C maps to NM_005415.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:48921536 C>A maps to NM_000387.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:48921536 C>A maps to NM_000387.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:130166263 G>T maps to NM_014580.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:130166263 G>T maps to NM_014580.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:135067717 C>A maps to NM_001042537.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:135067717 C>A maps to NM_001042537.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:20890205 T>C maps to NM_017435.4 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:20890205 T>C maps to NM_017435.4 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:11105641 G>T maps to NM_001128849.1 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:11105641 G>T maps to NM_001128849.1 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:48600832 C>A maps to NM_005985.3 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:48600832 C>A maps to NM_005985.3 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:231311580 G>T maps to NM_001080391.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:231311580 G>T maps to NM_001080391.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131356465 G>T maps to NM_001130438.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131356465 G>T maps to NM_001130438.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109186490 C>A maps to NM_018984.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109186490 C>A maps to NM_018984.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:38679166 C>A maps to NM_001049.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:38679166 C>A maps to NM_001049.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152623135 C>T maps to NM_182961.2 K5803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152623135 C>T maps to NM_182961.2 K5803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152658014 C>T maps to NM_182961.2 L4163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152658014 C>T maps to NM_182961.2 L4163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:46967662 T>C maps to NM_031912.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:46967662 T>C maps to NM_031912.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:138169389 C>A maps to ENST00000272643 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:138169389 C>A maps to ENST00000272643 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:54219384 G>T maps to NM_014464.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:54219384 G>T maps to NM_014464.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:64882401 C>T maps to NM_003273.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:64882401 C>T maps to NM_003273.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:30730904 G>T maps to NM_014742.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:30730904 G>T maps to NM_014742.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:98392317 C>T maps to NM_015348.1 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:98392317 C>T maps to NM_015348.1 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:87502891 T>A maps to NM_153354.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:87502891 T>A maps to NM_153354.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:218713342 G>A maps to NM_022648.4 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:218713342 G>A maps to NM_022648.4 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:10910327 C>G maps to NM_199261.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:10910327 C>G maps to NM_199261.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:110131488 C>T maps to NM_003301.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:110131488 C>T maps to NM_003301.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:139564043 G>T maps to ENST00000358430 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:139564043 G>T maps to ENST00000358430 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:41864677 C>T maps to NM_006293.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:41864677 C>T maps to NM_006293.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:88911909 C>A maps to NM_000372.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:88911909 C>A maps to NM_000372.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:70352325 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:70352325 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:17752260 C>T maps to ENST00000428389 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:17752260 C>T maps to ENST00000428389 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:100182371 C>T maps to NM_017890.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:100182371 C>T maps to NM_017890.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:100183083 G>C maps to ENST00000328526 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:100183083 G>C maps to ENST00000328526 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131502331 G>A maps to NM_006336.2 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131502331 G>A maps to NM_006336.2 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:72026207 C>A maps to NM_144982.4 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:72026207 C>A maps to NM_144982.4 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:147114032 G>T maps to NM_001168379.1 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:147114032 G>T maps to NM_001168379.1 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:99129088 T>A maps to NM_014569.3 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:99129088 T>A maps to NM_014569.3 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:9578910 T>A maps to NM_152476.2 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:9578910 T>A maps to NM_152476.2 R238*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-6767-01A-11D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-49-6767-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:52619983 C>A maps to NM_178523.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:52619983 C>A maps to NM_178523.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:90903396 G>T maps to NM_001004309.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:90903396 G>T maps to NM_001004309.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:47886770 C>T maps to NM_021035.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:47886770 C>T maps to NM_021035.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:238048491 T>A maps to NM_021186.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:238048491 T>A maps to NM_021186.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2331081 G>C maps to NM_001089.2 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2331081 G>C maps to NM_001089.2 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:67691945 C>T maps to NM_001082486.1 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:67691945 C>T maps to NM_001082486.1 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:147743946 C>T maps to NM_002025.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:147743946 C>T maps to NM_002025.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:151670161 T>G maps to NM_005100.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:151670161 T>G maps to NM_005100.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:33242895 G>T maps to NM_004274.4 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:33242895 G>T maps to NM_004274.4 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:66250611 G>A maps to NM_016627.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:66250611 G>A maps to NM_016627.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:99056293 G>A maps to NM_181861.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:99056293 G>A maps to NM_181861.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:108139267 C>A maps to NM_000051.3 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:108139267 C>A maps to NM_000051.3 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:58201497 C>A maps to NM_006576.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:58201497 C>A maps to NM_006576.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:1997365 G>T maps to NM_017797.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:1997365 G>T maps to NM_017797.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:118986935 G>A maps to NM_014807.3 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:118986935 G>A maps to NM_014807.3 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:56667419 G>C maps to ENST00000447900 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:56667419 G>C maps to ENST00000447900 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:31683039 C>T maps to NM_194300.2 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:31683039 C>T maps to NM_194300.2 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:149782840 G>A maps to NM_001025159.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:149782840 G>A maps to NM_001025159.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:64235725 C>A maps to NM_021153.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:64235725 C>A maps to NM_021153.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:63527017 G>T maps to NM_004361.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:63527017 G>T maps to NM_004361.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:45016957 G>T maps to NM_001102597.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:45016957 G>T maps to NM_001102597.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:31701436 C>T maps to NM_001288.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:31701436 C>T maps to NM_001288.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:135352458 C>A maps to NM_000773.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:135352458 C>A maps to NM_000773.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:69520960 C>T maps to NM_003861.2 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:69520960 C>T maps to NM_003861.2 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2296867 G>A maps to NM_001919.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2296867 G>A maps to NM_001919.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:50531021 G>A maps to NM_000790.3 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:50531021 G>A maps to NM_000790.3 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:71827929 G>T maps to NM_001130987.1 S1285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:71827929 G>T maps to NM_001130987.1 S1285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:103988654 C>G maps to NM_152310.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:103988654 C>G maps to NM_152310.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:38227380 C>T maps to NM_001099439.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:38227380 C>T maps to NM_001099439.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:454097 C>A maps to ENST00000315013 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:454097 C>A maps to ENST00000315013 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:159640747 G>A maps to NM_001040442.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:159640747 G>A maps to NM_001040442.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:68749636 G>T maps to NM_015686.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:68749636 G>T maps to NM_015686.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:146126545 C>A maps to NM_032145.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:146126545 C>A maps to NM_032145.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:147819232 G>A maps to NM_205836.1 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:147819232 G>A maps to NM_205836.1 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:132569144 C>A maps to NM_015082.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:132569144 C>A maps to NM_015082.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:92220653 C>T maps to NM_006705.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:92220653 C>T maps to NM_006705.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:24702537 C>A maps to ENST00000348719 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:24702537 C>A maps to ENST00000348719 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:935104 G>C maps to NM_001142467.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:935104 G>C maps to NM_001142467.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:155094106 C>A maps to ENST00000344756 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:155094106 C>A maps to ENST00000344756 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:75970456 C>A maps to NM_006633.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:75970456 C>A maps to NM_006633.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:67021783 C>A maps to NM_012308.2 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:67021783 C>A maps to NM_012308.2 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:43893379 C>T maps to NM_015284.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:43893379 C>T maps to NM_015284.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:39658759 G>A maps to NM_153490.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:39658759 G>A maps to NM_153490.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:38953258 G>C maps to NM_181535.3 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:38953258 G>C maps to NM_181535.3 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:37966317 C>T maps to NM_006498.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:37966317 C>T maps to NM_006498.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:76381853 C>A maps to ENST00000357063 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:76381853 C>A maps to ENST00000357063 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:127339965 C>G maps to NM_004526.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:127339965 C>G maps to NM_004526.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4715112 G>T maps to NM_015246.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4715112 G>T maps to NM_015246.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:55463885 G>A maps to NM_002453.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:55463885 G>A maps to NM_002453.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:30075295 C>G maps to NM_001033602.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:30075295 C>G maps to NM_001033602.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:26584812 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:26584812 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:6626080 C>A maps to NM_014865.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:6626080 C>A maps to NM_014865.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:42679412 T>C maps to NM_005385.3 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:42679412 T>C maps to NM_005385.3 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:119528971 C>A maps to NM_022002.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:119528971 C>A maps to NM_022002.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:24134590 G>A maps to NM_080723.4 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:24134590 G>A maps to NM_080723.4 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:131761474 C>A maps to NM_015354.1 I1180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:131761474 C>A maps to NM_015354.1 I1180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:114090197 G>A maps to ENST00000374428 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:114090197 G>A maps to ENST00000374428 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:48238561 G>T maps to NM_001005470.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:48238561 G>T maps to NM_001005470.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr21:44445024 G>A maps to NM_004571.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr21:44445024 G>A maps to NM_004571.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45271230 C>A maps to NM_004073.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45271230 C>A maps to NM_004073.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:108119700 C>G maps to NM_015723.2 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:108119700 C>G maps to NM_015723.2 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:16019963 G>A maps to NM_006017.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:16019963 G>A maps to NM_006017.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:13644814 G>A maps to NM_005493.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:13644814 G>A maps to NM_005493.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:19970782 G>T maps to ENST00000255006 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:19970782 G>T maps to ENST00000255006 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:77607239 G>T maps to ENST00000332191 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:77607239 G>T maps to ENST00000332191 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:54603852 A>G maps to NM_015360.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:54603852 A>G maps to NM_015360.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:73089907 C>T maps to ENST00000450736 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:73089907 C>T maps to ENST00000450736 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:27004687 T>C maps to ENST00000382009 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:27004687 T>C maps to ENST00000382009 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:27016440 G>A maps to NM_003170.3 K1068K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:27016440 G>A maps to NM_003170.3 K1068K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:7335009 C>A maps to NM_175733.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:7335009 C>A maps to NM_175733.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:10954611 G>A maps to NM_023919.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:10954611 G>A maps to NM_023919.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4312330 G>A maps to NM_003223.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4312330 G>A maps to NM_003223.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4312569 G>T maps to NM_003223.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4312569 G>T maps to NM_003223.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56826269 G>A maps to NM_003920.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56826269 G>A maps to NM_003920.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:100153955 G>A maps to NM_004800.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:100153955 G>A maps to NM_004800.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:36872627 C>A maps to NM_014831.2 E2772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:36872627 C>A maps to NM_014831.2 E2772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:22840266 G>C maps to NM_052903.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:22840266 G>C maps to NM_052903.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:19499492 G>C maps to ENST00000375267 S1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:19499492 G>C maps to ENST00000375267 S1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:20348642 G>C maps to ENST00000424589 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:20348642 G>C maps to ENST00000424589 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:101761654 G>A maps to NM_014503.2 L2095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:101761654 G>A maps to NM_014503.2 L2095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:95840796 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:95840796 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:15591572 C>A maps to NM_021804.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:15591572 C>A maps to NM_021804.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:32407427 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:32407427 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:18777115 C>A maps to NM_001040272.4 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:18777115 C>A maps to NM_001040272.4 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:100341785 G>T maps to NM_000673.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:100341785 G>T maps to NM_000673.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:65242116 C>A maps to NM_182703.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:65242116 C>A maps to NM_182703.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:125591731 C>G maps to NM_020337.2 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:125591731 C>G maps to NM_020337.2 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:36277798 A>G maps to ENST00000007510 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:36277798 A>G maps to ENST00000007510 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:63850815 G>T maps to NM_032199.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:63850815 G>T maps to NM_032199.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:99640498 C>A maps to NM_138576.2 E892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:99640498 C>A maps to NM_138576.2 E892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:82187221 G>A maps to NM_032333.4 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:82187221 G>A maps to NM_032333.4 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:170102857 G>A maps to ENST00000439249 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:170102857 G>A maps to ENST00000439249 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:121980613 C>G maps to NM_001178065.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:121980613 C>G maps to NM_001178065.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:117552673 C>T maps to NM_004258.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:117552673 C>T maps to NM_004258.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:158299788 C>A maps to NM_001764.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:158299788 C>A maps to NM_001764.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:6203991 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:6203991 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:71046532 T>G maps to NM_173535.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:71046532 T>G maps to NM_173535.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:211532907 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:211532907 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:117424407 G>A maps to NM_033427.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:117424407 G>A maps to NM_033427.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:57476937 G>T maps to ENST00000371231 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:57476937 G>T maps to ENST00000371231 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:125298593 C>T maps to NM_001013628.2 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:125298593 C>T maps to NM_001013628.2 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:169158467 G>C maps to NM_017631.5 L1460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:169158467 G>C maps to NM_017631.5 L1460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:220284871 C>A maps to NM_001927.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:220284871 C>A maps to NM_001927.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:88584414 C>G maps to NM_004407.3 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:88584414 C>G maps to NM_004407.3 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:334313 C>T maps to NM_203447.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:334313 C>T maps to NM_203447.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:56417868 C>A maps to ENST00000361203 E5030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:56417868 C>A maps to ENST00000361203 E5030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:44178096 T>A maps to NM_022785.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:44178096 T>A maps to NM_022785.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:5397197 C>A maps to NM_012307.2 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:5397197 C>A maps to NM_012307.2 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:91371880 C>G maps to NM_004950.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:91371880 C>G maps to NM_004950.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:27283044 C>A maps to NM_001989.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:27283044 C>A maps to NM_001989.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:50957419 G>A maps to NM_007051.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:50957419 G>A maps to NM_007051.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:18881049 T>A maps to NM_001039999.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:18881049 T>A maps to NM_001039999.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:13669356 G>T maps to NM_001165035.1 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:13669356 G>T maps to NM_001165035.1 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:241665846 C>A maps to NM_000143.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:241665846 C>A maps to NM_000143.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:110059537 G>T maps to NM_014845.5 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:110059537 G>T maps to NM_014845.5 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:180048746 C>A maps to NM_182925.4 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:180048746 C>A maps to NM_182925.4 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:230379103 G>T maps to NM_004481.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:230379103 G>T maps to NM_004481.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:39341323 G>C maps to NM_030772.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:39341323 G>C maps to NM_030772.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:92560247 C>T maps to NM_004466.4 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:92560247 C>T maps to NM_004466.4 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:110086057 G>T maps to NM_031936.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:110086057 G>T maps to NM_031936.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:94006167 C>G maps to NM_001510.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:94006167 C>G maps to NM_001510.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:78172322 C>A maps to NM_000863.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:78172322 C>A maps to NM_000863.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:113742496 C>A maps to NM_019618.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:113742496 C>A maps to NM_019618.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:76744340 C>T maps to NM_001563.2 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:76744340 C>T maps to NM_001563.2 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:102250507 G>T maps to NM_004791.1 G292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:102250507 G>T maps to NM_004791.1 G292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:19498289 C>A maps to NM_144633.2 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:19498289 C>A maps to NM_144633.2 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:47748863 G>A maps to NM_022055.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:47748863 G>A maps to NM_022055.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:34810999 G>T maps to NM_014686.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:34810999 G>T maps to NM_014686.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:74219593 C>A maps to NM_005576.2 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:74219593 C>A maps to NM_005576.2 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:115805270 G>A maps to NM_002338.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:115805270 G>A maps to NM_002338.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:4285409 C>T maps to NM_017816.2 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:4285409 C>T maps to NM_017816.2 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:39549928 A>T maps to ENST00000361689 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:39549928 A>T maps to ENST00000361689 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:140640517 C>A maps to ENST00000509479 E1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:140640517 C>A maps to ENST00000509479 E1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:91450650 C>T maps to NM_006122.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:91450650 C>T maps to NM_006122.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:186978604 G>T maps to NM_139125.3 C157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:186978604 G>T maps to NM_139125.3 C157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:13825904 T>G maps to NM_005913.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:13825904 T>G maps to NM_005913.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:70014209 G>C maps to ENST00000448226 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:70014209 G>C maps to ENST00000448226 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:113562895 C>T maps to ENST00000189978 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:113562895 C>T maps to ENST00000189978 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:18079763 C>T maps to NM_001160176.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:18079763 C>T maps to NM_001160176.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:29665720 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:29665720 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:26109132 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:26109132 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:164247684 G>A maps to NM_000909.4 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:164247684 G>A maps to NM_000909.4 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:123805543 G>T maps to NM_001163278.1 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:123805543 G>T maps to NM_001163278.1 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:19378024 C>T maps to NM_001013354.1 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:19378024 C>T maps to NM_001013354.1 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:248512311 C>G maps to NM_001001918.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:248512311 C>G maps to NM_001001918.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:143793021 C>A maps to NM_001004135.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:143793021 C>A maps to NM_001004135.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:247751823 G>T maps to NM_001001915.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:247751823 G>T maps to NM_001001915.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:29555747 C>A maps to NM_007160.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:29555747 C>A maps to NM_007160.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:180166827 G>T maps to NM_001001657.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:180166827 G>T maps to NM_001001657.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:5153347 T>A maps to NM_001005160.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:5153347 T>A maps to NM_001005160.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:55587404 A>T maps to ENST00000395203 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:55587404 A>T maps to ENST00000395203 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:99961617 C>T maps to ENST00000457907 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:99961617 C>T maps to ENST00000457907 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:242066663 C>A maps to ENST00000358649 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:242066663 C>A maps to ENST00000358649 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:123489892 C>T maps to NM_020845.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:123489892 C>T maps to NM_020845.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:8717676 T>A maps to NM_015192.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:8717676 T>A maps to NM_015192.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:18848011 C>A maps to ENST00000266505 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:18848011 C>A maps to ENST00000266505 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:53564426 C>A maps to NM_001098512.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:53564426 C>A maps to NM_001098512.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:121652108 T>C maps to NM_002851.2 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:121652108 T>C maps to NM_002851.2 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:121653455 G>A maps to NM_002851.2 Q1452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:121653455 G>A maps to NM_002851.2 Q1452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:40871810 G>T maps to NM_007341.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:40871810 G>T maps to NM_007341.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:103324830 C>A maps to NM_003048.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:103324830 C>A maps to NM_003048.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:108427546 C>A maps to NM_001013031.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:108427546 C>A maps to NM_001013031.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:88773892 C>T maps to NM_030960.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:88773892 C>T maps to NM_030960.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:41149043 C>T maps to NM_181642.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:41149043 C>T maps to NM_181642.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:92988093 C>A maps to NM_006011.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:92988093 C>A maps to NM_006011.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:52553398 T>C maps to NM_015136.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:52553398 T>C maps to NM_015136.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:36527654 G>T maps to NM_003149.1 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:36527654 G>T maps to NM_003149.1 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:2097420 A>T maps to NM_080836.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:2097420 A>T maps to NM_080836.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:158492669 G>A maps to NM_003898.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:158492669 G>A maps to NM_003898.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:84217021 A>T maps to NM_005679.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:84217021 A>T maps to NM_005679.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:7578223 T>A maps to NM_001126112.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:7578223 T>A maps to NM_001126112.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:31230608 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:31230608 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:72233551 G>T maps to NM_032646.5 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:72233551 G>T maps to NM_032646.5 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:72875738 T>A maps to NM_032175.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:72875738 T>A maps to NM_032175.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:119575562 C>A maps to NM_015836.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:119575562 C>A maps to NM_015836.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:195935335 C>A maps to NM_001039617.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:195935335 C>A maps to NM_001039617.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:147108803 G>T maps to NM_001168379.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:147108803 G>T maps to NM_001168379.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:12692408 C>A maps to NM_020714.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:12692408 C>A maps to NM_020714.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:10447451 G>A maps to NM_053042.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:10447451 G>A maps to NM_053042.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:91405404 C>A maps to NM_201269.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:91405404 C>A maps to NM_201269.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:247162721 C>A maps to NM_020394.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:247162721 C>A maps to NM_020394.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:1056363 G>T maps to NM_019112.3 V1484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:1056363 G>T maps to NM_019112.3 V1484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:43645890 A>T maps to NM_004915.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:43645890 A>T maps to NM_004915.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:43744034 A>G maps to NM_016006.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:43744034 A>G maps to NM_016006.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:89400831 C>A maps to NM_013227.3 A1672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:89400831 C>A maps to NM_013227.3 A1672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:236924412 G>T maps to NM_001103.2 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:236924412 G>T maps to NM_001103.2 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:156915443 G>T maps to ENST00000430702 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:156915443 G>T maps to ENST00000430702 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:33527361 G>C maps to NM_030955.2 P1572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:33527361 G>C maps to NM_030955.2 P1572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:130340917 C>T maps to NM_139055.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:130340917 C>T maps to NM_139055.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:84611674 G>C maps to NM_207517.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:84611674 G>C maps to NM_207517.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203134388 G>T maps to NM_001048230.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203134388 G>T maps to NM_001048230.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:32873371 C>T maps to NM_000687.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:32873371 C>T maps to NM_000687.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105416309 G>C maps to NM_138420.2 P1826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105416309 G>C maps to NM_138420.2 P1826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105418991 C>T maps to NM_138420.2 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105418991 C>T maps to NM_138420.2 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:4872892 A>G maps to NM_001040177.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:4872892 A>G maps to NM_001040177.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:113351863 G>T maps to NM_025144.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:113351863 G>T maps to NM_025144.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:37451741 C>G maps to ENST00000374660 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:37451741 C>G maps to ENST00000374660 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50302619 G>T maps to NM_014203.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50302619 G>T maps to NM_014203.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112111324 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112111324 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:69049694 C>A maps to NM_001007231.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:69049694 C>A maps to NM_001007231.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:73071466 G>T maps to NM_014786.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:73071466 G>T maps to NM_014786.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:18810033 A>G maps to NM_015161.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:18810033 A>G maps to NM_015161.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:177030246 T>C maps to ENST00000281881 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:177030246 T>C maps to ENST00000281881 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:108218051 G>A maps to NM_000051.3 L2877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:108218051 G>A maps to NM_000051.3 L2877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:3839651 C>A maps to NM_174953.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:3839651 C>A maps to NM_174953.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:118279713 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:118279713 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:57743930 G>T maps to NM_001015878.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:57743930 G>T maps to NM_001015878.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:160804473 C>A maps to NM_033168.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:160804473 C>A maps to NM_033168.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:56386311 C>A maps to NM_004758.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:56386311 C>A maps to NM_004758.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50657930 C>A maps to NM_152358.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50657930 C>A maps to NM_152358.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57252873 C>A maps to NM_001004303.4 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57252873 C>A maps to NM_001004303.4 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:75037556 G>T maps to NM_001002912.4 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:75037556 G>T maps to NM_001002912.4 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:55134562 C>T maps to ENST00000454855 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:55134562 C>T maps to ENST00000454855 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:47823414 G>T maps to ENST00000355085 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:47823414 G>T maps to ENST00000355085 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:175763869 C>G maps to ENST00000443967 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:175763869 C>G maps to ENST00000443967 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:25194711 C>G maps to NM_138811.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:25194711 C>G maps to NM_138811.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100086048 T>C maps to ENST00000423930 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100086048 T>C maps to ENST00000423930 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:10702958 C>A maps to NM_001079843.1 R1373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:10702958 C>A maps to NM_001079843.1 R1373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:54573762 C>A maps to NM_080617.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:54573762 C>A maps to NM_080617.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:3669131 C>A maps to NM_152492.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:3669131 C>A maps to NM_152492.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:107096574 T>A maps to NM_032600.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:107096574 T>A maps to NM_032600.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:32636434 G>A maps to NM_001008391.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:32636434 G>A maps to NM_001008391.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:55555428 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:55555428 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:46916051 C>A maps to NM_032040.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:46916051 C>A maps to NM_032040.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:74497099 G>T maps to NM_133493.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:74497099 G>T maps to NM_133493.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:1573206 C>A maps to ENST00000401097 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:1573206 C>A maps to ENST00000401097 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150752433 C>A maps to NM_004935.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150752433 C>A maps to NM_004935.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45015706 C>T maps to NM_001102597.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45015706 C>T maps to NM_001102597.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:95099902 G>T maps to NM_001012267.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:95099902 G>T maps to NM_001012267.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:424235 C>T maps to NM_006614.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:424235 C>T maps to NM_006614.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:42611333 T>A maps to NM_004198.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:42611333 T>A maps to NM_004198.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:233398754 G>T maps to NM_000751.1 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:233398754 G>T maps to NM_000751.1 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:142841088 G>T maps to NM_004267.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:142841088 G>T maps to NM_004267.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:139695042 G>A maps to NM_006079.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:139695042 G>A maps to NM_006079.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:143016968 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:143016968 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:57725718 C>A maps to NM_004859.3 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:57725718 C>A maps to NM_004859.3 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:139668138 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:139668138 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:86591501 G>A maps to NM_152890.5 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:86591501 G>A maps to NM_152890.5 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:189870984 G>A maps to NM_000090.3 K1031K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:189870984 G>A maps to NM_000090.3 K1031K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:238253292 C>T maps to NM_004369.3 T2456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:238253292 C>T maps to NM_004369.3 T2456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:130023601 C>G maps to NM_001868.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:130023601 C>G maps to NM_001868.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211438023 A>C maps to NM_001122633.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211438023 A>C maps to NM_001122633.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211525276 C>T maps to NM_001122633.1 F1281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211525276 C>T maps to NM_001122633.1 F1281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211525285 G>T maps to NM_001122633.1 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211525285 G>T maps to NM_001122633.1 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:52782352 A>T maps to NM_000782.4 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:52782352 A>T maps to NM_000782.4 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57476877 G>T maps to ENST00000371231 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57476877 G>T maps to ENST00000371231 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:110714246 C>A maps to NM_003649.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:110714246 C>A maps to NM_003649.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:162745480 C>A maps to NM_006182.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:162745480 C>A maps to NM_006182.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56330337 A>G maps to NM_201554.1 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56330337 A>G maps to NM_201554.1 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:3534573 T>A maps to NM_004746.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:3534573 T>A maps to NM_004746.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:101195326 C>A maps to NM_003836.5 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:101195326 C>A maps to NM_003836.5 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:32862917 C>A maps to ENST00000357033 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:32862917 C>A maps to ENST00000357033 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:13824388 T>C maps to NM_001369.2 G2166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:13824388 T>C maps to NM_001369.2 G2166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:11593506 G>A maps to NM_001372.3 R1456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:11593506 G>A maps to NM_001372.3 R1456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131847035 G>T maps to NM_020438.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131847035 G>T maps to NM_020438.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:168670288 G>T maps to NM_001937.4 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:168670288 G>T maps to NM_001937.4 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:28586987 A>T maps to NM_001941.3 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:28586987 A>T maps to NM_001941.3 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:56399961 C>A maps to ENST00000361203 S5422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:56399961 C>A maps to ENST00000361203 S5422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:122287985 T>A maps to NM_138287.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:122287985 T>A maps to NM_138287.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:31489369 G>T maps to NM_014600.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:31489369 G>T maps to NM_014600.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:74439635 G>A maps to NM_001249.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:74439635 G>A maps to NM_001249.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:212251682 G>A maps to NM_005235.2 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:212251682 G>A maps to NM_005235.2 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:128356000 G>C maps to NM_001143820.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:128356000 G>C maps to NM_001143820.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:22985288 T>A maps to NM_032581.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:22985288 T>A maps to NM_032581.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:37027103 G>T maps to NM_001013736.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:37027103 G>T maps to NM_001013736.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:92616228 A>T maps to ENST00000298047 K4203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:92616228 A>T maps to ENST00000298047 K4203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:126355442 A>T maps to NM_024582.4 V2354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:126355442 A>T maps to NM_024582.4 V2354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:37437683 T>A maps to NM_032875.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:37437683 T>A maps to NM_032875.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:147806774 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:147806774 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:121341475 C>A maps to NM_016298.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:121341475 C>A maps to NM_016298.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161188690 G>A maps to NM_004106.1 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161188690 G>A maps to NM_004106.1 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:157490894 C>A maps to NM_031281.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:157490894 C>A maps to NM_031281.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:24276808 G>A maps to NM_004116.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:24276808 G>A maps to NM_004116.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128492993 G>A maps to NM_001458.4 G2039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128492993 G>A maps to NM_001458.4 G2039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:33333800 G>T maps to ENST00000291421 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:33333800 G>T maps to ENST00000291421 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:202899447 G>C maps to NM_003507.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:202899447 G>C maps to NM_003507.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:46099312 C>T maps to NM_173536.3 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:46099312 C>T maps to NM_173536.3 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:30951022 C>A maps to NM_004861.1 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:30951022 C>A maps to NM_004861.1 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39871798 G>T maps to NM_000805.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39871798 G>T maps to NM_000805.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:42005085 G>A maps to NM_000168.5 N1195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:42005085 G>A maps to NM_000168.5 N1195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:58604650 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:58604650 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:135431490 C>T maps to NM_153834.3 Q1876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:135431490 C>T maps to NM_153834.3 Q1876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:100362477 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:100362477 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:25887284 G>A maps to NM_020752.2 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:25887284 G>A maps to NM_020752.2 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:158224836 A>T maps to NM_000826.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:158224836 A>T maps to NM_000826.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:108631742 G>T maps to ENST00000218006 V977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:108631742 G>T maps to ENST00000218006 V977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:2238062 T>A maps to NM_024511.5 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:2238062 T>A maps to NM_024511.5 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:12123582 C>T maps to NM_002114.2 H1185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:12123582 C>T maps to NM_002114.2 H1185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:221057722 G>T maps to NM_021958.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:221057722 G>T maps to NM_021958.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148857789 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148857789 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6461960 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6461960 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:22826314 G>C maps to NM_006043.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:22826314 G>C maps to NM_006043.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:78172305 G>T maps to NM_000863.1 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:78172305 G>T maps to NM_000863.1 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65622727 A>T maps to NM_004884.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65622727 A>T maps to NM_004884.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65677372 C>A maps to NM_020962.1 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65677372 C>A maps to NM_020962.1 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:15233751 A>T maps to NM_006844.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:15233751 A>T maps to NM_006844.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:51942032 T>C maps to NM_012141.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:51942032 T>C maps to NM_012141.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42457993 G>T maps to NM_000419.3 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42457993 G>T maps to NM_000419.3 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:156608056 C>T maps to NM_005546.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:156608056 C>T maps to NM_005546.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:64975021 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:64975021 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:111145925 G>C maps to NM_004974.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:111145925 G>C maps to NM_004974.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:68128794 T>G maps to NM_018658.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:68128794 T>G maps to NM_018658.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:196395109 A>T maps to NM_198503.2 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:196395109 A>T maps to NM_198503.2 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:42263516 T>A maps to NM_015058.1 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:42263516 T>A maps to NM_015058.1 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:95524281 G>C maps to NM_015496.3 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:95524281 G>C maps to NM_015496.3 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:95539139 C>A maps to NM_015496.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:95539139 C>A maps to NM_015496.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:30336558 C>G maps to NM_020848.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:30336558 C>G maps to NM_020848.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:20820324 G>T maps to NM_017794.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:20820324 G>T maps to NM_017794.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55330025 C>A maps to ENST00000355608 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55330025 C>A maps to ENST00000355608 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36349666 T>A maps to NM_199180.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36349666 T>A maps to NM_199180.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:126319003 G>T maps to NM_032531.3 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:126319003 G>T maps to NM_032531.3 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:205308823 G>T maps to NM_018203.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:205308823 G>T maps to NM_018203.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:241725626 G>T maps to NM_003679.3 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:241725626 G>T maps to NM_003679.3 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31797993 G>T maps to NM_181622.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31797993 G>T maps to NM_181622.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31802607 C>A maps to NM_181600.1 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31802607 C>A maps to NM_181600.1 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:1643104 G>T maps to ENST00000359229 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:1643104 G>T maps to ENST00000359229 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:130372451 G>T maps to NM_032438.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:130372451 G>T maps to NM_032438.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:107580555 G>T maps to NM_002291.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:107580555 G>T maps to NM_002291.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:8321906 G>A maps to NM_024552.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:8321906 G>A maps to NM_024552.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:152648700 C>A maps to NM_178429.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:152648700 C>A maps to NM_178429.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55144092 C>A maps to ENST00000427581 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55144092 C>A maps to ENST00000427581 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:54721090 G>C maps to NM_001081450.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:54721090 G>C maps to NM_001081450.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:99772548 C>A maps to NM_014839.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:99772548 C>A maps to NM_014839.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:105503206 T>C maps to NM_013437.4 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:105503206 T>C maps to NM_013437.4 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:141122262 C>A maps to NM_018557.2 G3700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:141122262 C>A maps to NM_018557.2 G3700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:85449966 A>T maps to NM_001079910.1 K466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:85449966 A>T maps to NM_001079910.1 K466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:80529462 C>A maps to NM_178839.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:80529462 C>A maps to NM_178839.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:54527922 G>A maps to NM_000242.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:54527922 G>A maps to NM_000242.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:5966773 A>T maps to NM_032485.4 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:5966773 A>T maps to NM_032485.4 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36212498 C>T maps to NM_014727.1 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36212498 C>T maps to NM_014727.1 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:202550694 C>A maps to NM_033066.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:202550694 C>A maps to NM_033066.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:72754952 C>A maps to NM_005098.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:72754952 C>A maps to NM_005098.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100684016 T>A maps to NM_001040105.1 L3107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100684016 T>A maps to NM_001040105.1 L3107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:3239783 T>A maps to NM_015419.3 P1314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:3239783 T>A maps to NM_015419.3 P1314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50958470 C>A maps to NM_004533.3 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50958470 C>A maps to NM_004533.3 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:77662999 T>A maps to NM_015057.4 L3564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:77662999 T>A maps to NM_015057.4 L3564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:45299180 G>T maps to NM_002476.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:45299180 G>T maps to NM_002476.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:41836296 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:41836296 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:113102910 C>A maps to ENST00000316851 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:113102910 C>A maps to ENST00000316851 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:91963392 T>C maps to NM_022351.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:91963392 T>C maps to NM_022351.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:15273347 C>A maps to NM_000435.2 A1947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:15273347 C>A maps to NM_000435.2 A1947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36340176 G>T maps to NM_004646.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36340176 G>T maps to NM_004646.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:139231258 G>T maps to NM_013982.2 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:139231258 G>T maps to NM_013982.2 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39985170 G>A maps to NM_052935.4 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39985170 G>A maps to NM_052935.4 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:104200707 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:104200707 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:175006615 G>A maps to ENST00000409546 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:175006615 G>A maps to ENST00000409546 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:29395247 G>T maps to NM_013937.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:29395247 G>T maps to NM_013937.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6942648 T>C maps to NM_001004684.1 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6942648 T>C maps to NM_001004684.1 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248344003 G>T maps to NM_001004688.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248344003 G>T maps to NM_001004688.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248308454 A>G maps to NM_001004690.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248308454 A>G maps to NM_001004690.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:20389361 T>C maps to NM_001005483.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:20389361 T>C maps to NM_001005483.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5221657 C>A maps to NM_001004760.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5221657 C>A maps to NM_001004760.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5173071 G>T maps to NM_012375.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5173071 G>T maps to NM_012375.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:4470649 C>A maps to NM_001005172.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:4470649 C>A maps to NM_001005172.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5799255 G>T maps to NM_001001922.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5799255 G>T maps to NM_001001922.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:4824944 C>A maps to ENST00000380382 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:4824944 C>A maps to ENST00000380382 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5758675 C>A maps to NM_001005180.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5758675 C>A maps to NM_001005180.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:7847204 C>T maps to NM_153445.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:7847204 C>T maps to NM_153445.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:29323885 G>T maps to NM_030876.5 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:29323885 G>T maps to NM_030876.5 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:57799342 C>T maps to NM_001005186.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:57799342 C>T maps to NM_001005186.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:123624809 G>T maps to NM_001005188.1 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:123624809 G>T maps to NM_001005188.1 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:55927528 G>T maps to NM_001004058.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:55927528 G>T maps to NM_001004058.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:169611825 C>T maps to NM_001166108.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:169611825 C>T maps to NM_001166108.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:206480372 A>T maps to ENST00000406610 K1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:206480372 A>T maps to ENST00000406610 K1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:91134010 A>T maps to NM_032968.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:91134010 A>T maps to NM_032968.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140229633 C>A maps to NM_031857.1 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140229633 C>A maps to NM_031857.1 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140559504 G>A maps to NM_019120.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140559504 G>A maps to NM_019120.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140711648 C>T maps to NM_018912.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140711648 C>T maps to NM_018912.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140774113 G>T maps to NM_032088.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140774113 G>T maps to NM_032088.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:31913021 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:31913021 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:20766474 G>T maps to NM_000921.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:20766474 G>T maps to NM_000921.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:55152084 G>T maps to ENST00000507166 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:55152084 G>T maps to ENST00000507166 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:153070178 G>T maps to ENST00000393758 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:153070178 G>T maps to ENST00000393758 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:119043174 C>A maps to NM_173791.3 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:119043174 C>A maps to NM_173791.3 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:8051527 G>T maps to NM_002616.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:8051527 G>T maps to NM_002616.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:153309768 C>A maps to NM_020393.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:153309768 C>A maps to NM_020393.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:133807004 G>C maps to ENST00000395386 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:133807004 G>C maps to ENST00000395386 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:44048031 C>T maps to NM_015937.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:44048031 C>T maps to NM_015937.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:98408475 G>A maps to NM_152309.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:98408475 G>A maps to NM_152309.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:18273926 G>C maps to NM_005027.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:18273926 G>C maps to NM_005027.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:28755040 C>T maps to NM_153021.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:28755040 C>T maps to NM_153021.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105398444 C>A maps to NM_138790.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105398444 C>A maps to NM_138790.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100850972 C>A maps to NM_001084.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100850972 C>A maps to NM_001084.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:153041514 G>T maps to NM_005393.2 G1525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:153041514 G>T maps to NM_005393.2 G1525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:151377694 G>C maps to NM_015100.3 V1272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:151377694 G>C maps to NM_015100.3 V1272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:134165626 C>A maps to NM_032728.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:134165626 C>A maps to NM_032728.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:42866306 C>T maps to NM_153026.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:42866306 C>T maps to NM_153026.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:93624697 A>G maps to NM_000313.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:93624697 A>G maps to NM_000313.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43575947 G>A maps to NM_031246.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43575947 G>A maps to NM_031246.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43579539 G>A maps to NM_031246.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43579539 G>A maps to NM_031246.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:32827218 G>C maps to NM_002800.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:32827218 G>C maps to NM_002800.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55710185 G>T maps to NM_002842.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55710185 G>T maps to NM_002842.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:52320838 G>C maps to NM_144651.4 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:52320838 G>C maps to NM_144651.4 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74288491 G>T maps to NM_032134.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74288491 G>T maps to NM_032134.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:25622194 C>A maps to NM_000965.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:25622194 C>A maps to NM_000965.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:113553488 C>T maps to NM_001193520.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:113553488 C>T maps to NM_001193520.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:95360225 G>C maps to NM_006744.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:95360225 G>C maps to NM_006744.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79348007 C>A maps to NM_002909.4 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79348007 C>A maps to NM_002909.4 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79253236 C>A maps to NM_001008387.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79253236 C>A maps to NM_001008387.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:107041515 A>G maps to ENST00000304514 T969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:107041515 A>G maps to ENST00000304514 T969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:8158922 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:8158922 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74157642 G>T maps to NM_052916.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74157642 G>T maps to NM_052916.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:25362200 C>T maps to ENST00000381927 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:25362200 C>T maps to ENST00000381927 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:30782715 T>A maps to NM_001017981.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:30782715 T>A maps to NM_001017981.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77275591 G>T maps to ENST00000396204 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77275591 G>T maps to ENST00000396204 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38997148 G>T maps to NM_000540.2 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38997148 G>T maps to NM_000540.2 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:33990136 G>T maps to NM_001036.3 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:33990136 G>T maps to NM_001036.3 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:34015045 C>A maps to NM_001036.3 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:34015045 C>A maps to NM_001036.3 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:130465705 C>A maps to ENST00000457563 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:130465705 C>A maps to ENST00000457563 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:200137221 C>A maps to NM_001172509.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:200137221 C>A maps to NM_001172509.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62022923 C>A maps to NM_000334.4 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62022923 C>A maps to NM_000334.4 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:240506 G>T maps to NM_004168.2 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:240506 G>T maps to NM_004168.2 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4550173 G>T maps to NM_032108.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4550173 G>T maps to NM_032108.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:110325409 C>T maps to ENST00000356688 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:110325409 C>T maps to ENST00000356688 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:95030067 G>T maps to NM_006215.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:95030067 G>T maps to NM_006215.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4290476 G>T maps to NM_020209.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4290476 G>T maps to NM_020209.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51919588 G>A maps to NM_033130.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51919588 G>A maps to NM_033130.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:52132674 G>T maps to ENST00000222107 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:52132674 G>T maps to ENST00000222107 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38689107 C>G maps to NM_015073.1 P1640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38689107 C>G maps to NM_015073.1 P1640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:45169935 C>A maps to NM_005413.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:45169935 C>A maps to NM_005413.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:170108877 C>T maps to NM_005414.3 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:170108877 C>T maps to NM_005414.3 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:36608587 A>T maps to NM_004172.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:36608587 A>T maps to NM_004172.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:54960596 C>A maps to NM_173514.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:54960596 C>A maps to NM_173514.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:33984643 G>T maps to NM_016180.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:33984643 G>T maps to NM_016180.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220505176 G>C maps to NM_201574.2 V1128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220505176 G>C maps to NM_201574.2 V1128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:170198681 A>T maps to NM_020949.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:170198681 A>T maps to NM_020949.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:36748987 G>A maps to ENST00000511166 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:36748987 G>A maps to ENST00000511166 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:121429298 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:121429298 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:44046938 G>A maps to NM_175064.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:44046938 G>A maps to NM_175064.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:35644576 G>T maps to NM_024867.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:35644576 G>T maps to NM_024867.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:81744277 C>A maps to NM_033104.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:81744277 C>A maps to NM_033104.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:31416469 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:31416469 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:147646093 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:147646093 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136198958 C>A maps to NM_006753.4 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136198958 C>A maps to NM_006753.4 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:59622150 G>T maps to NM_001062.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:59622150 G>T maps to NM_001062.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:35088394 C>T maps to NM_001093728.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:35088394 C>T maps to NM_001093728.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:89177795 G>T maps to NM_138960.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:89177795 G>T maps to NM_138960.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:171910293 C>A maps to ENST00000360843 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:171910293 C>A maps to ENST00000360843 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:120474984 A>C maps to NM_138554.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:120474984 A>C maps to NM_138554.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:12905855 A>T maps to NM_016562.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:12905855 A>T maps to NM_016562.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:12940185 G>A maps to ENST00000311912 K1027K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:12940185 G>A maps to ENST00000311912 K1027K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:32959727 C>T maps to NM_207313.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:32959727 C>T maps to NM_207313.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:42824589 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:42824589 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:63170400 G>A maps to NM_178505.6 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:63170400 G>A maps to NM_178505.6 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:218700934 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:218700934 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:32064729 G>T maps to ENST00000375244 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:32064729 G>T maps to ENST00000375244 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:36603507 G>A maps to NM_014408.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:36603507 G>A maps to NM_014408.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5729477 G>T maps to NM_006074.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5729477 G>T maps to NM_006074.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:189060756 C>A maps to NM_178556.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:189060756 C>A maps to NM_178556.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:230657799 G>A maps to ENST00000389044 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:230657799 G>A maps to ENST00000389044 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:111155829 G>A maps to NM_012471.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:111155829 G>A maps to NM_012471.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77397634 G>T maps to NM_017662.4 Y1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77397634 G>T maps to NM_017662.4 Y1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:31769269 C>A maps to NM_020856.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:31769269 C>A maps to NM_020856.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:167753612 G>A maps to NM_031949.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:167753612 G>A maps to NM_031949.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:30512839 G>A maps to NM_001008409.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:30512839 G>A maps to NM_001008409.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:179455491 G>T maps to NM_133378.4 V17752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:179455491 G>T maps to NM_133378.4 V17752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:5436253 T>A maps to NM_024803.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:5436253 T>A maps to NM_024803.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:50659382 C>A maps to NM_020461.3 G1135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:50659382 C>A maps to NM_020461.3 G1135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:20357477 G>T maps to ENST00000424589 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:20357477 G>T maps to ENST00000424589 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:48637933 G>A maps to NM_003365.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:48637933 G>A maps to NM_003365.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:215847617 A>T maps to ENST00000366943 P4545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:215847617 A>T maps to ENST00000366943 P4545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:23080338 G>C maps to NM_020718.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:23080338 G>C maps to NM_020718.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:23085136 C>G maps to NM_020718.3 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:23085136 C>G maps to NM_020718.3 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:82815783 A>T maps to NM_004385.4 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:82815783 A>T maps to NM_004385.4 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:100832256 C>A maps to NM_017890.3 I2992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:100832256 C>A maps to NM_017890.3 I2992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:65253607 G>T maps to NM_007268.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:65253607 G>T maps to NM_007268.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36558727 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36558727 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:17202755 C>A maps to NM_022166.3 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:17202755 C>A maps to NM_022166.3 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:102033252 A>T maps to NM_001130145.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:102033252 A>T maps to NM_001130145.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74077484 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74077484 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:207169695 C>A maps to NM_020923.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:207169695 C>A maps to NM_020923.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:97062214 A>T maps to NM_194320.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:97062214 A>T maps to NM_194320.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:104170865 A>G maps to NM_003452.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:104170865 A>G maps to NM_003452.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:45130107 C>A maps to NM_018102.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:45130107 C>A maps to NM_018102.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:2464826 C>A maps to NM_024325.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:2464826 C>A maps to NM_024325.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:57839240 A>T maps to NM_213598.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:57839240 A>T maps to NM_213598.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:37643909 T>A maps to ENST00000356958 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:37643909 T>A maps to ENST00000356958 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:89294045 G>T maps to NM_182531.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:89294045 G>T maps to NM_182531.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:185801376 C>A maps to NM_194250.1 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:185801376 C>A maps to NM_194250.1 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:9868261 T>C maps to NM_001077624.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:9868261 T>C maps to NM_001077624.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:21131980 A>T maps to NM_003429.4 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:21131980 A>T maps to NM_003429.4 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:20027412 G>T maps to NM_031218.3 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:20027412 G>T maps to NM_031218.3 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:70823861 C>A maps to NM_052957.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:70823861 C>A maps to NM_052957.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:28210755 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:28210755 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:148206844 C>A maps to NM_000024.5 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:148206844 C>A maps to NM_000024.5 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:100151828 C>T maps to NM_006076.4 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:100151828 C>T maps to NM_006076.4 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:117139158 G>T maps to NM_030767.4 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:117139158 G>T maps to NM_030767.4 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:68772345 T>C maps to NM_173545.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:68772345 T>C maps to NM_173545.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:21229323 G>T maps to NM_000384.2 T3472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:21229323 G>T maps to NM_000384.2 T3472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:27284176 T>A maps to NM_000484.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:27284176 T>A maps to NM_000484.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:69261741 G>T maps to NM_001002254.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:69261741 G>T maps to NM_001002254.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:71665880 G>A maps to NM_080742.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:71665880 G>A maps to NM_080742.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:66297386 C>A maps to NM_024649.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:66297386 C>A maps to NM_024649.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:99439331 G>T maps to NM_207362.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:99439331 G>T maps to NM_207362.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:14708425 C>A maps to NM_016474.4 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:14708425 C>A maps to NM_016474.4 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:56695041 A>G maps to ENST00000447900 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:56695041 A>G maps to ENST00000447900 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:30617598 G>T maps to NM_001161376.1 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:30617598 G>T maps to NM_001161376.1 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:1250432 C>T maps to NM_021098.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:1250432 C>T maps to NM_021098.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:54930774 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:54930774 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:197565879 G>T maps to NM_001080539.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:197565879 G>T maps to NM_001080539.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:68473355 C>T maps to NM_031966.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:68473355 C>T maps to NM_031966.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:122862286 C>A maps to ENST00000302528 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:122862286 C>A maps to ENST00000302528 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:34557977 C>T maps to NM_147164.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:34557977 C>T maps to NM_147164.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:113237149 A>T maps to NM_198123.1 P3658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:113237149 A>T maps to NM_198123.1 P3658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:15956965 C>T maps to NM_032341.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:15956965 C>T maps to NM_032341.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:197564418 C>A maps to NM_001195215.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:197564418 C>A maps to NM_001195215.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:21742410 C>A maps to NM_003777.3 P2095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:21742410 C>A maps to NM_003777.3 P2095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:8028582 G>A maps to ENST00000351593 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:8028582 G>A maps to ENST00000351593 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:132504686 G>T maps to ENST00000333577 T1493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:132504686 G>T maps to ENST00000333577 T1493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:79698295 T>A maps to NM_001170574.1 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:79698295 T>A maps to NM_001170574.1 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:86089366 G>T maps to NM_013231.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:86089366 G>T maps to NM_013231.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr13:28602365 G>A maps to NM_004119.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr13:28602365 G>A maps to NM_004119.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:161128526 G>T maps to NM_000811.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:161128526 G>T maps to NM_000811.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:117885009 G>A maps to NM_005264.4 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:117885009 G>A maps to NM_005264.4 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:183942763 C>A maps to NM_015101.2 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:183942763 C>A maps to NM_015101.2 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:27223851 G>T maps to NM_022078.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:27223851 G>T maps to NM_022078.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:25887113 G>T maps to NM_020752.2 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:25887113 G>T maps to NM_020752.2 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:7620335 C>A maps to NM_181874.2 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:7620335 C>A maps to NM_181874.2 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:26437999 C>A maps to NM_000182.4 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:26437999 C>A maps to NM_000182.4 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:182395301 G>T maps to NM_000885.4 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:182395301 G>T maps to NM_000885.4 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:123987957 C>T maps to NM_001024660.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:123987957 C>T maps to NM_001024660.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:55367261 C>A maps to NM_001098815.1 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:55367261 C>A maps to NM_001098815.1 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:1347163 C>G maps to NM_020894.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:1347163 C>G maps to NM_020894.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:39092708 C>T maps to NM_015515.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:39092708 C>T maps to NM_015515.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:16590419 G>T maps to NM_001290.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:16590419 G>T maps to NM_001290.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:180243617 C>A maps to NM_033343.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:180243617 C>A maps to NM_033343.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:141707939 C>A maps to NM_018557.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:141707939 C>A maps to NM_018557.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:57604564 G>T maps to NM_002332.2 A4273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:57604564 G>T maps to NM_002332.2 A4273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:54952686 C>A maps to NM_020678.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:54952686 C>A maps to NM_020678.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:149638270 C>A maps to NM_005491.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:149638270 C>A maps to NM_005491.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:48874139 G>T maps to NM_182746.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:48874139 G>T maps to NM_182746.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:90424409 T>A maps to NM_014611.1 G2307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:90424409 T>A maps to NM_014611.1 G2307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:9068782 G>T maps to NM_024690.2 L6221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:9068782 G>T maps to NM_024690.2 L6221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:2678500 C>A maps to NM_001012418.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:2678500 C>A maps to NM_001012418.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:47880673 T>A maps to NM_152995.4 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:47880673 T>A maps to NM_152995.4 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:99661990 G>A maps to NM_001184880.1 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:99661990 G>A maps to NM_001184880.1 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:140480847 G>A maps to NM_018937.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:140480847 G>A maps to NM_018937.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:140740859 G>T maps to NM_018923.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:140740859 G>T maps to NM_018923.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:24566320 C>T maps to NM_004563.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:24566320 C>T maps to NM_004563.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:144874681 T>C maps to NM_014644.4 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:144874681 T>C maps to NM_014644.4 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:61015998 C>A maps to ENST00000422676 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:61015998 C>A maps to ENST00000422676 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:128807323 C>A maps to NM_014264.4 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:128807323 C>A maps to NM_014264.4 R267R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5051-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:46998167 C>A maps to ENST00000377652 G93G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5051-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:46998167 C>A maps to ENST00000377652 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:103345713 C>T maps to NM_013274.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:103345713 C>T maps to NM_013274.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:149215859 C>A maps to NM_133263.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:149215859 C>A maps to NM_133263.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:45901298 G>T maps to NM_001142502.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:45901298 G>T maps to NM_001142502.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:18832240 C>A maps to NM_002767.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:18832240 C>A maps to NM_002767.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:56380776 G>T maps to NM_002868.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:56380776 G>T maps to NM_002868.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:130926968 C>A maps to NM_015347.4 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:130926968 C>A maps to NM_015347.4 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:174948944 C>A maps to NM_022754.5 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:174948944 C>A maps to NM_022754.5 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:119029580 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:119029580 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:45993673 C>A maps to NM_003110.5 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:45993673 C>A maps to NM_003110.5 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:126276876 C>G maps to ENST00000356132 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:126276876 C>G maps to ENST00000356132 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:107459839 G>T maps to NM_001142351.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:107459839 G>T maps to NM_001142351.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:33405956 C>A maps to NM_006772.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:33405956 C>A maps to NM_006772.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:35271146 G>T maps to NM_001077653.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:35271146 G>T maps to NM_001077653.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:43552355 C>T maps to NM_201631.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:43552355 C>T maps to NM_201631.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:9413115 G>T maps to NM_015453.2 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:9413115 G>T maps to NM_015453.2 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:25668107 C>A maps to ENST00000264331 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:25668107 C>A maps to ENST00000264331 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:113711404 C>A maps to NM_001143819.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:113711404 C>A maps to NM_001143819.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:41166017 G>T maps to ENST00000373108 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:41166017 G>T maps to ENST00000373108 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:111195407 C>A maps to NM_012471.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:111195407 C>A maps to NM_012471.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:33986766 G>T maps to NM_018449.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:33986766 G>T maps to NM_018449.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:4648622 C>T maps to NM_001136046.1 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:4648622 C>T maps to NM_001136046.1 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:44489137 G>T maps to NM_181489.5 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:44489137 G>T maps to NM_181489.5 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:11598551 C>A maps to NM_138783.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:11598551 C>A maps to NM_138783.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr8:39525665 C>T maps to NM_014237.2 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr8:39525665 C>T maps to NM_014237.2 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr4:90169158 G>A maps to NM_198281.2 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr4:90169158 G>A maps to NM_198281.2 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr5:153149874 G>T maps to NM_001114183.1 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr5:153149874 G>T maps to NM_001114183.1 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:74759023 C>A maps to NM_005050.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:74759023 C>A maps to NM_005050.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:33649001 G>T maps to NM_030955.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:33649001 G>T maps to NM_030955.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:3502844 C>G maps to NM_018269.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:3502844 C>G maps to NM_018269.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:2740343 C>A maps to NM_133463.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:2740343 C>A maps to NM_133463.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:41582017 G>A maps to ENST00000415018 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:41582017 G>A maps to ENST00000415018 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:7188192 C>A maps to ENST00000290575 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:7188192 C>A maps to ENST00000290575 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:31643258 C>T maps to NM_182658.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:31643258 C>T maps to NM_182658.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:172537594 C>A maps to NM_153607.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:172537594 C>A maps to NM_153607.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:90870297 C>T maps to NM_006888.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:90870297 C>T maps to NM_006888.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:13050437 C>T maps to NM_004343.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:13050437 C>T maps to NM_004343.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:36633999 C>T maps to NM_001749.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:36633999 C>T maps to NM_001749.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:175618339 G>T maps to NM_001039523.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:175618339 G>T maps to NM_001039523.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:11364913 G>C maps to NM_001332.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:11364913 G>C maps to NM_001332.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:47395891 G>C maps to ENST00000371904 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:47395891 G>C maps to ENST00000371904 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:122004411 C>G maps to NM_014618.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:122004411 C>G maps to NM_014618.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:957012 G>C maps to NM_001347.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:957012 G>C maps to NM_001347.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:5364390 G>A maps to ENST00000457531 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:5364390 G>A maps to ENST00000457531 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:39050299 G>A maps to NM_198963.1 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:39050299 G>A maps to NM_198963.1 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:169446069 C>T maps to NM_004946.2 D1113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:169446069 C>T maps to NM_004946.2 D1113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:55220239 G>T maps to NM_005228.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:55220239 G>T maps to NM_005228.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:80634725 C>A maps to NM_022726.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:80634725 C>A maps to NM_022726.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:40468908 G>A maps to NM_001248.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:40468908 G>A maps to NM_001248.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:38227422 C>T maps to NM_001099439.1 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:38227422 C>T maps to NM_001099439.1 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:71235312 T>C maps to NM_001162529.1 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:71235312 T>C maps to NM_001162529.1 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:126242333 T>C maps to NM_024582.4 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:126242333 T>C maps to NM_024582.4 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:170883631 G>A maps to NM_003862.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:170883631 G>A maps to NM_003862.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:34205612 C>A maps to NM_025135.2 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:34205612 C>A maps to NM_025135.2 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:89656942 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:89656942 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:79117887 C>G maps to NM_001097636.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:79117887 C>G maps to NM_001097636.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:133375048 G>T maps to NM_005895.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:133375048 G>T maps to NM_005895.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:156533647 G>T maps to NM_032782.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:156533647 G>T maps to NM_032782.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:5290727 C>A maps to NM_005330.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:5290727 C>A maps to NM_005330.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:21800488 G>T maps to NM_015094.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:21800488 G>T maps to NM_015094.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:137013242 T>G maps to NM_017415.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:137013242 T>G maps to NM_017415.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:1651150 C>T maps to NM_001001480.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:1651150 C>T maps to NM_001001480.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:7040235 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:7040235 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59828638 C>T maps to NM_006138.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59828638 C>T maps to NM_006138.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10541662 C>T maps to NM_002470.2 R1142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10541662 C>T maps to NM_002470.2 R1142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:26423475 C>T maps to ENST00000407587 S2514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:26423475 C>T maps to ENST00000407587 S2514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:16895566 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:16895566 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:133541070 A>G maps to NM_207363.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:133541070 A>G maps to NM_207363.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:52508880 C>A maps to NM_007361.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:52508880 C>A maps to NM_007361.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:51192619 G>A maps to NM_182946.1 N2081N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:51192619 G>A maps to NM_182946.1 N2081N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:1038313 G>A maps to NM_033120.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:1038313 G>A maps to NM_033120.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:56369521 C>A maps to NM_134444.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:56369521 C>A maps to NM_134444.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:67919706 C>T maps to NM_198443.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:67919706 C>T maps to NM_198443.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:79175639 C>A maps to NM_004796.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:79175639 C>A maps to NM_004796.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:77775522 C>T maps to NM_001105663.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:77775522 C>T maps to NM_001105663.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:29394971 G>T maps to NM_013937.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:29394971 G>T maps to NM_013937.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248685219 C>A maps to NM_001013355.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248685219 C>A maps to NM_001013355.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248343379 C>A maps to NM_001004688.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248343379 C>A maps to NM_001004688.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:4870357 G>T maps to NM_001004758.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:4870357 G>T maps to NM_001004758.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:56020313 T>A maps to NM_001004747.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:56020313 T>A maps to NM_001004747.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:29630271 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:29630271 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:176564455 C>A maps to NM_020318.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:176564455 C>A maps to NM_020318.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:33049566 G>T maps to NM_004572.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:33049566 G>T maps to NM_004572.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:23815781 T>A maps to NM_013261.3 K442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:23815781 T>A maps to NM_013261.3 K442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:203024682 C>A maps to ENST00000367238 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:203024682 C>A maps to ENST00000367238 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:179315751 G>T maps to NM_003690.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:179315751 G>T maps to NM_003690.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:138739119 C>A maps to NM_001013650.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:138739119 C>A maps to NM_001013650.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43762450 G>T maps to NM_002784.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43762450 G>T maps to NM_002784.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:150443310 G>A maps to NM_015203.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:150443310 G>A maps to NM_015203.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:18028279 G>A maps to NM_012139.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:18028279 G>A maps to NM_012139.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:180014088 T>C maps to NM_178123.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:180014088 T>C maps to NM_178123.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:72191384 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:72191384 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:118588222 C>A maps to NM_001029858.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:118588222 C>A maps to NM_001029858.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:65540931 C>T maps to NM_181784.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:65540931 C>T maps to NM_181784.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:22354577 C>A maps to NM_003034.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:22354577 C>A maps to NM_003034.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:13011368 G>A maps to NM_001105578.1 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:13011368 G>A maps to NM_001105578.1 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:12183493 C>T maps to NM_133625.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:12183493 C>T maps to NM_133625.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:23861997 C>T maps to ENST00000418698 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:23861997 C>T maps to ENST00000418698 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:100548045 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:100548045 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:90437533 G>T maps to NM_018319.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:90437533 G>T maps to NM_018319.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:65188409 G>T maps to NM_001010874.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:65188409 G>T maps to NM_001010874.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:50683151 G>T maps to NM_172238.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:50683151 G>T maps to NM_172238.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:11485769 G>T maps to ENST00000423059 C994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:11485769 G>T maps to ENST00000423059 C994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:7758929 C>A maps to NM_203411.1 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:7758929 C>A maps to NM_203411.1 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:68699043 G>T maps to NM_004262.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:68699043 G>T maps to NM_004262.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:132238048 G>A maps to NM_080386.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:132238048 G>A maps to NM_080386.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229773857 A>C maps to NM_014777.2 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229773857 A>C maps to NM_014777.2 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:62292764 C>A maps to NM_020821.2 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:62292764 C>A maps to NM_020821.2 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:53010451 G>C maps to NM_016075.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:53010451 G>C maps to NM_016075.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:147108755 C>T maps to NM_001168379.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:147108755 C>T maps to NM_001168379.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:27420577 C>A maps to NM_007149.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:27420577 C>A maps to NM_007149.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:48371204 C>T maps to NM_153034.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:48371204 C>T maps to NM_153034.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:12575151 C>A maps to ENST00000428311 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:12575151 C>A maps to ENST00000428311 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chrX:74288883 C>A maps to NM_004299.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chrX:74288883 C>A maps to NM_004299.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr14:58701085 A>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr14:58701085 A>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr5:7520954 C>T maps to NM_020546.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr5:7520954 C>T maps to NM_020546.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:71464084 T>C maps to NM_016519.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:71464084 T>C maps to NM_016519.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:5843982 C>A maps to NM_152504.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:5843982 C>A maps to NM_152504.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:105218097 T>G maps to NM_001001412.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:105218097 T>G maps to NM_001001412.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:15834373 T>A maps to NM_001229.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:15834373 T>A maps to NM_001229.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:6262814 G>T maps to NM_001037329.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:6262814 G>T maps to NM_001037329.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:2908580 G>T maps to NM_175607.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:2908580 G>T maps to NM_175607.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:70881869 A>C maps to NM_001858.4 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:70881869 A>C maps to NM_001858.4 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr8:114326897 A>G maps to NM_198123.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr8:114326897 A>G maps to NM_198123.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:30037859 T>C maps to NM_153324.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:30037859 T>C maps to NM_153324.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr18:29126288 T>C maps to NM_001943.3 A980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr18:29126288 T>C maps to NM_001943.3 A980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:32694335 C>T maps to NM_003757.2 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:32694335 C>T maps to NM_003757.2 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:35849908 C>T maps to NM_005304.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:35849908 C>T maps to NM_005304.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:71906938 A>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:71906938 A>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:75444671 A>C maps to NM_139137.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:75444671 A>C maps to NM_139137.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:215259894 C>A maps to NM_001017425.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:215259894 C>A maps to NM_001017425.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:33246129 C>A maps to ENST00000354476 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:33246129 C>A maps to ENST00000354476 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:91502246 C>T maps to NM_002345.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:91502246 C>T maps to NM_002345.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:171753361 C>T maps to NM_015935.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:171753361 C>T maps to NM_015935.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:29624865 G>T maps to NM_183378.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:29624865 G>T maps to NM_183378.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:106508506 C>T maps to NM_002649.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:106508506 C>T maps to NM_002649.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:47942011 T>G maps to NM_138295.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:47942011 T>G maps to NM_138295.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:62664297 C>T maps to NM_012469.3 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:62664297 C>T maps to NM_012469.3 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:803636 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:803636 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:50145580 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:50145580 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:173931108 G>A maps to NM_172071.2 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:173931108 G>A maps to NM_172071.2 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:122342158 T>A maps to NM_198085.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:122342158 T>A maps to NM_198085.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:9064912 G>T maps to NM_207420.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:9064912 G>T maps to NM_207420.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:152615181 G>C maps to NM_182961.2 S5921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:152615181 G>C maps to NM_182961.2 S5921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:39741459 G>A maps to NM_003286.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:39741459 G>A maps to NM_003286.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:53994016 C>T maps to NM_001004301.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:53994016 C>T maps to NM_001004301.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:36053477 T>C maps to NM_000704.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:36053477 T>C maps to NM_000704.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:97960806 T>A maps to NM_013314.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:97960806 T>A maps to NM_013314.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:7334276 T>A maps to NM_001170692.1 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:7334276 T>A maps to NM_001170692.1 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:104901056 C>A maps to NM_033292.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:104901056 C>A maps to NM_033292.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55653055 T>A maps to ENST00000442196 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55653055 T>A maps to ENST00000442196 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:157805888 C>A maps to NM_005894.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:157805888 C>A maps to NM_005894.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:12870965 C>T maps to NM_004064.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:12870965 C>T maps to NM_004064.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:21876960 C>T maps to NM_001170629.1 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:21876960 C>T maps to NM_001170629.1 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:76350352 C>T maps to NM_033401.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:76350352 C>T maps to NM_033401.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:120008903 C>A maps to NM_001145718.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:120008903 C>A maps to NM_001145718.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:196681572 A>G maps to NM_018897.2 N3180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:196681572 A>G maps to NM_018897.2 N3180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:2191239 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:2191239 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:79403964 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:79403964 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:46750357 G>T maps to NM_000506.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:46750357 G>T maps to NM_000506.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:67671599 G>T maps to NM_173526.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:67671599 G>T maps to NM_173526.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:157738450 G>T maps to NM_030764.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:157738450 G>T maps to NM_030764.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:135290071 G>T maps to NM_001159699.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:135290071 G>T maps to NM_001159699.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:180039568 C>A maps to NM_182925.4 A1158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:180039568 C>A maps to NM_182925.4 A1158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:86662264 C>T maps to NM_012193.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:86662264 C>T maps to NM_012193.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:31147107 G>T maps to NM_024572.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:31147107 G>T maps to NM_024572.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:22569815 C>T maps to NM_138574.2 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:22569815 C>T maps to NM_138574.2 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:319882 A>T maps to NM_021034.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:319882 A>T maps to NM_021034.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:24596748 G>A maps to NM_014809.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:24596748 G>A maps to NM_014809.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:133948699 C>A maps to ENST00000355048 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:133948699 C>A maps to ENST00000355048 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:46490395 G>T maps to NM_002343.3 C390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:46490395 G>T maps to NM_002343.3 C390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:235933477 C>A maps to NM_000081.2 L1968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:235933477 C>A maps to NM_000081.2 L1968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:151900215 G>T maps to NM_005367.5 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:151900215 G>T maps to NM_005367.5 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr18:13884809 C>T maps to NM_000529.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr18:13884809 C>T maps to NM_000529.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:90472077 G>A maps to NM_014611.1 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:90472077 G>A maps to NM_014611.1 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:141727024 G>T maps to ENST00000475668 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:141727024 G>T maps to ENST00000475668 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18195147 C>G maps to NM_054032.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18195147 C>G maps to NM_054032.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:3238682 G>T maps to NM_015419.3 P1681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:3238682 G>T maps to NM_015419.3 P1681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:102036301 C>G maps to NM_002465.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:102036301 C>G maps to NM_002465.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:21101767 G>A maps to ENST00000430741 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:21101767 G>A maps to ENST00000430741 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:24146170 C>T maps to NM_080723.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:24146170 C>T maps to NM_080723.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:6789735 C>A maps to NM_001004490.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:6789735 C>A maps to NM_001004490.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:31819479 C>A maps to ENST00000382902 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:31819479 C>A maps to ENST00000382902 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:55566680 G>T maps to ENST00000373965 S1571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:55566680 G>T maps to ENST00000373965 S1571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:55943218 C>T maps to NM_001142763.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:55943218 C>T maps to NM_001142763.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:140589507 C>T maps to NM_018932.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:140589507 C>T maps to NM_018932.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:65417041 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:65417041 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:57346752 C>A maps to NM_003708.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:57346752 C>A maps to NM_003708.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:24626763 C>A maps to NM_017999.4 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:24626763 C>A maps to NM_017999.4 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55489022 G>A maps to NM_016304.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55489022 G>A maps to NM_016304.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:50418833 G>T maps to NM_020436.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:50418833 G>T maps to NM_020436.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:15884834 G>T maps to ENST00000285670 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:15884834 G>T maps to ENST00000285670 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr18:61264450 G>T maps to NM_012397.3 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr18:61264450 G>T maps to NM_012397.3 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:16942394 C>T maps to NM_015260.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:16942394 C>T maps to NM_015260.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:71232647 T>A maps to NM_012390.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:71232647 T>A maps to NM_012390.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:125208250 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:125208250 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:53044593 G>A maps to NM_014682.2 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:53044593 G>A maps to NM_014682.2 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:1218414 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:1218414 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:134040456 G>A maps to NM_173575.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:134040456 G>A maps to NM_173575.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:142880729 C>A maps to NM_176881.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:142880729 C>A maps to NM_176881.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:5353294 G>T maps to NM_001080495.2 P2409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:5353294 G>T maps to NM_001080495.2 P2409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:114482981 G>A maps to NM_018700.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:114482981 G>A maps to NM_018700.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:62910725 C>G maps to NM_003368.4 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:62910725 C>G maps to NM_003368.4 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55540619 C>A maps to NM_030796.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55540619 C>A maps to NM_030796.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:47585438 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:47585438 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:37117731 C>T maps to NM_032825.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:37117731 C>T maps to NM_032825.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55980358 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55980358 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:152991455 C>T maps to NM_000033.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:152991455 C>T maps to NM_000033.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:74061970 G>C maps to NM_152331.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:74061970 G>C maps to NM_152331.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20451222 A>G maps to NM_017888.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20451222 A>G maps to NM_017888.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:127755306 C>A maps to NM_003474.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:127755306 C>A maps to NM_003474.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:39587425 C>A maps to NM_014237.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:39587425 C>A maps to NM_014237.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:207482344 C>A maps to NM_003812.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:207482344 C>A maps to NM_003812.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:10655477 G>T maps to NM_032885.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:10655477 G>T maps to NM_032885.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:138880429 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:138880429 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:152825272 C>A maps to NM_001001344.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:152825272 C>A maps to NM_001001344.2 P904P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5931-01A-11D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-50-5931-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:50154563 G>T maps to NM_024837.2 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:50154563 G>T maps to NM_024837.2 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:50158549 T>A maps to NM_024837.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:50158549 T>A maps to NM_024837.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:70092757 A>G maps to NM_001704.2 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:70092757 A>G maps to NM_001704.2 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:134351523 A>G maps to NM_013318.3 A1336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:134351523 A>G maps to NM_013318.3 A1336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:147092255 G>C maps to NM_004326.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:147092255 G>C maps to NM_004326.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:26509111 G>T maps to NM_001732.2 G431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:26509111 G>T maps to NM_001732.2 G431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:76496244 C>T maps to NM_152335.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:76496244 C>T maps to NM_152335.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:47859103 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:47859103 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:26527427 C>T maps to NM_198137.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:26527427 C>T maps to NM_198137.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:33439178 T>C maps to NM_032816.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:33439178 T>C maps to NM_032816.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:74528209 G>T maps to NM_133493.3 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:74528209 G>T maps to NM_133493.3 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:72584764 G>A maps to NM_001115152.1 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:72584764 G>A maps to NM_001115152.1 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:160651120 C>A maps to NM_001778.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:160651120 C>A maps to NM_001778.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:61689396 A>T maps to NM_001796.2 L628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:61689396 A>T maps to NM_001796.2 L628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:26916032 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:26916032 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:67864377 G>A maps to NM_025082.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:67864377 G>A maps to NM_025082.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:100061935 G>A maps to NM_014361.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:100061935 G>A maps to NM_014361.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:55924963 G>T maps to NM_030820.3 C820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:55924963 G>T maps to NM_030820.3 C820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:71004157 G>C maps to NM_001851.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:71004157 G>C maps to NM_001851.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:5837731 C>T maps to NM_001014809.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:5837731 C>T maps to NM_001014809.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:40496312 C>G maps to NM_144970.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:40496312 C>G maps to NM_144970.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:76688498 C>A maps to NM_004762.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:76688498 C>A maps to NM_004762.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:77078117 G>T maps to NM_001042573.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:77078117 G>T maps to NM_001042573.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:5754651 G>T maps to NM_153717.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:5754651 G>T maps to NM_153717.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:122734442 A>T maps to NM_001034194.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:122734442 A>T maps to NM_001034194.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:138642898 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:138642898 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:86131529 C>A maps to ENST00000372088 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:86131529 C>A maps to ENST00000372088 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:92088373 G>T maps to ENST00000298047 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:92088373 G>T maps to ENST00000298047 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:58111326 G>C maps to NM_001164317.1 V1306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:58111326 G>C maps to NM_001164317.1 V1306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:180047709 C>A maps to NM_182925.4 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:180047709 C>A maps to NM_182925.4 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:17488962 T>G maps to NM_001037814.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:17488962 T>G maps to NM_001037814.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:27159948 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:27159948 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:27726406 C>A maps to NM_001486.3 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:27726406 C>A maps to NM_001486.3 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:55216093 T>C maps to NM_207410.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:55216093 T>C maps to NM_207410.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48972657 G>C maps to NM_015698.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48972657 G>C maps to NM_015698.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:28501898 C>T maps to NM_001509.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:28501898 C>T maps to NM_001509.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:31066377 C>A maps to ENST00000327783 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:31066377 C>A maps to ENST00000327783 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:13717084 G>A maps to NM_000834.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:13717084 G>A maps to NM_000834.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:126410119 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:126410119 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:51486782 G>T maps to NM_018094.4 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:51486782 G>T maps to NM_018094.4 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:124746193 C>A maps to NM_020733.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:124746193 C>A maps to NM_020733.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:66638981 C>T maps to NM_007199.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:66638981 C>T maps to NM_007199.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:31372508 G>A maps to NM_000887.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:31372508 G>A maps to NM_000887.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:123271218 A>T maps to NM_015312.3 S4613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:123271218 A>T maps to NM_015312.3 S4613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:112513052 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:112513052 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:85449836 A>T maps to NM_001079910.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:85449836 A>T maps to NM_001079910.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:35821059 C>A maps to ENST00000422348 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:35821059 C>A maps to ENST00000422348 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:45805709 G>T maps to ENST00000262891 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:45805709 G>T maps to ENST00000262891 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:3779790 G>T maps to NM_002378.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:3779790 G>T maps to NM_002378.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:89209481 C>T maps to NM_005941.4 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:89209481 C>T maps to NM_005941.4 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:151247408 G>T maps to NM_015440.3 G412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:151247408 G>T maps to NM_015440.3 G412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:9049764 T>C maps to NM_024690.2 L10622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:9049764 T>C maps to NM_024690.2 L10622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:24775338 G>T maps to NM_005382.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:24775338 G>T maps to NM_005382.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:56320319 A>G maps to NM_145007.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:56320319 A>G maps to NM_145007.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:125316137 G>A maps to NM_001004457.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:125316137 G>A maps to NM_001004457.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:6942636 C>A maps to NM_001004684.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:6942636 C>A maps to NM_001004684.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:248616202 C>A maps to NM_001004136.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:248616202 C>A maps to NM_001004136.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4790454 G>A maps to ENST00000380383 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4790454 G>A maps to ENST00000380383 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4825432 C>A maps to ENST00000380382 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4825432 C>A maps to ENST00000380382 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48780528 C>A maps to NM_017602.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48780528 C>A maps to NM_017602.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:107752608 A>G maps to NM_001198533.1 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:107752608 A>G maps to NM_001198533.1 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:169842779 G>T maps to NM_001166108.1 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:169842779 G>T maps to NM_001166108.1 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:140475630 C>A maps to NM_018936.2 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:140475630 C>A maps to NM_018936.2 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:82579279 G>T maps to NM_033026.5 R3542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:82579279 G>T maps to NM_033026.5 R3542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:57989696 C>T maps to NM_024779.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:57989696 C>T maps to NM_024779.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:47256394 C>A maps to NM_020820.3 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:47256394 C>A maps to NM_020820.3 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:49034396 G>T maps to NM_006150.3 C300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:49034396 G>T maps to NM_006150.3 C300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:121653413 C>A maps to NM_002851.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:121653413 C>A maps to NM_002851.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:129306209 G>T maps to NM_004794.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:129306209 G>T maps to NM_004794.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:127440427 C>A maps to ENST00000368317 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:127440427 C>A maps to ENST00000368317 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:60193879 C>A maps to NM_021136.2 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:60193879 C>A maps to NM_021136.2 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:237538082 G>T maps to NM_001035.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:237538082 G>T maps to NM_001035.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:237580396 T>A maps to NM_001035.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:237580396 T>A maps to NM_001035.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:16664606 G>A maps to NM_024881.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:16664606 G>A maps to NM_024881.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:66455338 C>A maps to NM_006946.2 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:66455338 C>A maps to NM_006946.2 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:65289695 G>T maps to ENST00000389723 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:65289695 G>T maps to ENST00000389723 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:26744201 C>T maps to NM_018317.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:26744201 C>T maps to NM_018317.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:121999985 G>T maps to NM_014553.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:121999985 G>T maps to NM_014553.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:43552772 T>C maps to NM_201631.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:43552772 T>C maps to NM_201631.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:74876054 C>T maps to NM_001105579.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:74876054 C>T maps to NM_001105579.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:138189107 G>A maps to NM_015905.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:138189107 G>A maps to NM_015905.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:230678747 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:230678747 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179553412 G>T maps to NM_133378.4 R9486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179553412 G>T maps to NM_133378.4 R9486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:135631063 C>T maps to NM_016267.3 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:135631063 C>T maps to NM_016267.3 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:17271972 C>T maps to NM_003380.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:17271972 C>T maps to NM_003380.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:119575682 C>A maps to NM_015836.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:119575682 C>A maps to NM_015836.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:77764394 G>T maps to NM_024721.4 T1746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:77764394 G>T maps to NM_024721.4 T1746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:6977309 C>T maps to NM_013250.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:6977309 C>T maps to NM_013250.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:21992460 C>T maps to NM_003423.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:21992460 C>T maps to NM_003423.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:22379528 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:22379528 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:101560181 G>A maps to NM_000392.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:101560181 G>A maps to NM_000392.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:46624491 G>T maps to NM_015833.3 G570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:46624491 G>T maps to NM_015833.3 G570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:4057494 G>A maps to NM_001116.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:4057494 G>A maps to NM_001116.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chrX:153662570 C>T maps to NM_001183.4 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chrX:153662570 C>T maps to NM_001183.4 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr19:48339552 G>T maps to NM_000554.4 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr19:48339552 G>T maps to NM_000554.4 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:79428720 C>T maps to NM_025074.6 Q3155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:79428720 C>T maps to NM_025074.6 Q3155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:20418672 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:20418672 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:42797676 G>T maps to NM_015349.1 G536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:42797676 G>T maps to NM_015349.1 G536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:129905292 G>C maps to NM_002417.4 S1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:129905292 G>C maps to NM_002417.4 S1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr3:9704013 G>T maps to NM_001077525.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr3:9704013 G>T maps to NM_001077525.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:22368727 A>G maps to NM_001004719.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:22368727 A>G maps to NM_001004719.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr3:8809378 C>T maps to NM_000916.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr3:8809378 C>T maps to NM_000916.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:31877566 T>A maps to NM_001191057.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:31877566 T>A maps to NM_001191057.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:56149702 G>T maps to NM_006213.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:56149702 G>T maps to NM_006213.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:76950084 C>T maps to NM_017439.3 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:76950084 C>T maps to NM_017439.3 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:28748150 G>A maps to NM_153021.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:28748150 G>A maps to NM_153021.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr18:77679236 C>A maps to NM_025078.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr18:77679236 C>A maps to NM_025078.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:1652104 C>T maps to NM_012293.1 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:1652104 C>T maps to NM_012293.1 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:237777542 G>T maps to NM_001035.2 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:237777542 G>T maps to NM_001035.2 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:242009518 G>A maps to NM_001080437.1 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:242009518 G>A maps to NM_001080437.1 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:1372745 C>A maps to NM_022834.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:1372745 C>A maps to NM_022834.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:43752487 C>A maps to NM_080869.1 *112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:43752487 C>A maps to NM_080869.1 *112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:132063769 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:132063769 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:111625426 C>A maps to NM_006687.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:111625426 C>A maps to NM_006687.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:236881159 C>A maps to NM_001103.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:236881159 C>A maps to NM_001103.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:49172025 C>A maps to NM_015270.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:49172025 C>A maps to NM_015270.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:109664983 G>T maps to NM_031279.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:109664983 G>T maps to NM_031279.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:91708553 G>A maps to NM_005751.4 K2369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:91708553 G>A maps to NM_005751.4 K2369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:243736347 C>G maps to NM_005465.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:243736347 C>G maps to NM_005465.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:165118544 G>A maps to NM_012403.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:165118544 G>A maps to NM_012403.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:145773605 C>T maps to NM_025251.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:145773605 C>T maps to NM_025251.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:3002689 G>T maps to NM_004042.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:3002689 G>T maps to NM_004042.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:152818718 C>A maps to NM_001001344.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:152818718 C>A maps to NM_001001344.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:58786658 T>C maps to ENST00000407086 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:58786658 T>C maps to ENST00000407086 S98S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5933-01A-11D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-50-5933-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:32135454 G>A maps to NM_018169.3 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:32135454 G>A maps to NM_018169.3 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:49433158 G>T maps to NM_144602.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:49433158 G>T maps to NM_144602.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:6631426 G>T maps to NM_024067.2 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:6631426 G>T maps to NM_024067.2 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:33370059 G>T maps to NM_001102401.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:33370059 G>T maps to NM_001102401.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:32210931 C>T maps to NM_005093.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:32210931 C>T maps to NM_005093.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:111318978 G>A maps to NM_152591.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:111318978 G>A maps to NM_152591.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:33256050 C>A maps to NM_006584.3 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:33256050 C>A maps to NM_006584.3 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55844546 G>T maps to NM_001025195.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55844546 G>T maps to NM_001025195.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:62677633 G>A maps to NM_000738.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:62677633 G>A maps to NM_000738.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:32393543 G>T maps to NM_001190455.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:32393543 G>T maps to NM_001190455.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:73245827 G>T maps to NM_001305.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:73245827 G>T maps to NM_001305.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7164149 G>A maps to NM_001185022.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7164149 G>A maps to NM_001185022.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:57762457 T>C maps to NM_004859.3 N1492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:57762457 T>C maps to NM_004859.3 N1492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103428211 T>A maps to NM_080629.2 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103428211 T>A maps to NM_080629.2 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:75839937 C>A maps to ENST00000322507 G2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:75839937 C>A maps to ENST00000322507 G2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:1389357 G>T maps to NM_175918.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:1389357 G>T maps to NM_175918.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:41622110 A>T maps to NM_000774.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:41622110 A>T maps to NM_000774.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:15648394 C>A maps to NM_173483.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:15648394 C>A maps to NM_173483.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:38110568 A>G maps to NM_001164232.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:38110568 A>G maps to NM_001164232.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:79601668 C>A maps to NM_004747.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:79601668 C>A maps to NM_004747.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:3534267 C>T maps to NM_004746.2 Q801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:3534267 C>T maps to NM_004746.2 Q801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:134013941 C>A maps to NM_006426.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:134013941 C>A maps to NM_006426.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:55242488 G>T maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:55242488 G>T maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:5434023 C>T maps to NM_012307.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:5434023 C>T maps to NM_012307.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143097014 C>A maps to NM_005232.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143097014 C>A maps to NM_005232.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:89391112 G>T maps to NM_005233.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:89391112 G>T maps to NM_005233.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:23718183 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:23718183 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:8074128 G>C maps to NM_018948.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:8074128 G>C maps to NM_018948.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:128974032 G>C maps to NM_001039762.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:128974032 G>C maps to NM_001039762.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:37593534 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:37593534 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:153253846 G>A maps to NM_033632.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:153253846 G>A maps to NM_033632.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:35850520 G>T maps to NM_005304.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:35850520 G>T maps to NM_005304.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:152329305 G>T maps to NM_001014342.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:152329305 G>T maps to NM_001014342.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:79634848 C>T maps to NM_001013735.1 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:79634848 C>T maps to NM_001013735.1 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:29237306 G>T maps to NM_005249.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:29237306 G>T maps to NM_005249.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:52188790 A>T maps to ENST00000344768 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:52188790 A>T maps to ENST00000344768 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:30880602 C>A maps to NM_207359.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:30880602 C>A maps to NM_207359.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:155158100 A>C maps to NM_052917.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:155158100 A>C maps to NM_052917.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:89849284 C>A maps to NM_198460.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:89849284 C>A maps to NM_198460.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:18499156 G>C maps to NM_004864.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:18499156 G>C maps to NM_004864.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:154055988 C>T maps to NM_001038705.1 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:154055988 C>T maps to NM_001038705.1 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:168065746 T>A maps to NM_153832.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:168065746 T>A maps to NM_153832.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:150349227 A>G maps to NM_004224.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:150349227 A>G maps to NM_004224.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:123471195 G>T maps to ENST00000456860 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:123471195 G>T maps to ENST00000456860 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:165365353 C>A maps to NM_004490.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:165365353 C>A maps to NM_004490.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:120776195 C>T maps to NM_014619.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:120776195 C>T maps to NM_014619.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:2240764 C>A maps to NM_024511.5 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:2240764 C>A maps to NM_024511.5 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:80679498 G>A maps to NM_001040708.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:80679498 G>A maps to NM_001040708.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:62199166 G>T maps to ENST00000394997 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:62199166 G>T maps to ENST00000394997 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:126298797 C>T maps to NM_138571.4 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:126298797 C>T maps to NM_138571.4 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:118960401 G>C maps to NM_000190.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:118960401 G>C maps to NM_000190.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:46628224 G>T maps to NM_002146.4 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:46628224 G>T maps to NM_002146.4 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:21239472 C>T maps to NM_002172.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:21239472 C>T maps to NM_002172.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:143081564 C>T maps to NM_003866.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:143081564 C>T maps to NM_003866.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:124065999 G>A maps to NM_001024660.3 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:124065999 G>A maps to NM_001024660.3 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:73849101 C>A maps to NM_004770.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:73849101 C>A maps to NM_004770.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:112524478 C>A maps to ENST00000315987 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:112524478 C>A maps to ENST00000315987 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:18207729 A>G maps to ENST00000388870 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:18207729 A>G maps to ENST00000388870 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:138629991 G>T maps to NM_020340.4 G1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:138629991 G>T maps to NM_020340.4 G1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:59855221 G>T maps to NM_020854.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:59855221 G>T maps to NM_020854.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:245849483 C>A maps to NM_018012.3 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:245849483 C>A maps to NM_018012.3 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:39594373 G>T maps to NM_006771.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:39594373 G>T maps to NM_006771.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:52799697 C>A maps to NM_033033.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:52799697 C>A maps to NM_033033.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:1651135 G>A maps to NM_001001480.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:1651135 G>A maps to NM_001001480.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:82456780 A>T maps to ENST00000370717 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:82456780 A>T maps to ENST00000370717 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62862035 C>T maps to ENST00000506720 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62862035 C>T maps to ENST00000506720 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62894600 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62894600 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:59274657 C>T maps to NM_153377.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:59274657 C>T maps to NM_153377.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:170097558 C>A maps to NM_004525.2 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:170097558 C>A maps to NM_004525.2 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:68183796 G>A maps to NM_002335.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:68183796 G>A maps to NM_002335.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:151102897 C>T maps to NM_053002.4 V1634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:151102897 C>T maps to NM_053002.4 V1634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:126769091 G>A maps to NM_032446.2 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:126769091 G>A maps to NM_032446.2 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:44097384 C>T maps to NM_005926.2 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:44097384 C>T maps to NM_005926.2 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9064858 A>T maps to NM_024690.2 T7529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9064858 A>T maps to NM_024690.2 T7529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9065530 G>C maps to NM_024690.2 T7305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9065530 G>C maps to NM_024690.2 T7305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:1271324 T>A maps to ENST00000447027 T4408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:1271324 T>A maps to ENST00000447027 T4408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:128322929 C>A maps to ENST00000389524 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:128322929 C>A maps to ENST00000389524 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:80436674 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:80436674 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:24929508 C>T maps to NM_003743.4 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:24929508 C>T maps to NM_003743.4 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:211848790 A>G maps to NM_002497.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:211848790 A>G maps to NM_002497.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:52802406 G>A maps to NM_003157.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:52802406 G>A maps to NM_003157.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:156642539 C>T maps to NM_006617.1 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:156642539 C>T maps to NM_006617.1 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:113436286 C>A maps to NM_024019.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:113436286 C>A maps to NM_024019.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:204985516 G>T maps to ENST00000367172 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:204985516 G>T maps to ENST00000367172 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:219942057 G>T maps to NM_024782.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:219942057 G>T maps to NM_024782.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:50149279 G>C maps to ENST00000404971 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:50149279 G>C maps to ENST00000404971 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:40131790 C>A maps to NM_032526.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:40131790 C>A maps to NM_032526.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:50411624 C>A maps to NM_012346.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:50411624 C>A maps to NM_012346.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:158435389 C>A maps to NM_001004473.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:158435389 C>A maps to NM_001004473.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:29142068 T>G maps to NM_030905.2 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:29142068 T>G maps to NM_030905.2 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248263099 G>T maps to NM_175911.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248263099 G>T maps to NM_175911.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248367166 C>A maps to NM_001004689.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248367166 C>A maps to NM_001004689.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:55433223 C>A maps to NM_001004704.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:55433223 C>A maps to NM_001004704.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20482704 C>G maps to NM_001004712.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20482704 C>G maps to NM_001004712.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20295660 C>A maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20295660 C>A maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:5021144 A>G maps to NM_001004755.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:5021144 A>G maps to NM_001004755.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:4470601 A>T maps to NM_001005172.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:4470601 A>T maps to NM_001005172.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:5969355 G>A maps to NM_001003443.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:5969355 G>A maps to NM_001003443.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:151055928 G>A maps to NM_022788.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:151055928 G>A maps to NM_022788.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:122432420 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:122432420 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:31740991 G>A maps to NM_014323.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:31740991 G>A maps to NM_014323.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:55782675 A>T maps to NM_001142763.1 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:55782675 A>T maps to NM_001142763.1 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:140531097 G>A maps to NM_018939.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:140531097 G>A maps to NM_018939.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:82893517 T>C maps to NM_015885.3 I1467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:82893517 T>C maps to NM_015885.3 I1467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:58271611 G>A maps to NM_001104631.1 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:58271611 G>A maps to NM_001104631.1 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:8047129 T>G maps to NM_002616.2 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:8047129 T>G maps to NM_002616.2 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:209169636 C>T maps to NM_015040.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:209169636 C>T maps to NM_015040.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:51907899 C>A maps to NM_138694.3 G952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:51907899 C>A maps to NM_138694.3 G952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:118196235 C>T maps to NM_001011709.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:118196235 C>T maps to NM_001011709.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:53103645 C>T maps to NM_182595.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:53103645 C>T maps to NM_182595.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:19553586 C>A maps to NM_001005356.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:19553586 C>A maps to NM_001005356.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:142459765 C>A maps to ENST00000486171 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:142459765 C>A maps to ENST00000486171 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43679577 G>A maps to ENST00000270059 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43679577 G>A maps to ENST00000270059 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:71029808 A>G maps to NM_001109754.1 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:71029808 A>G maps to NM_001109754.1 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:33133871 C>A maps to NM_005610.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:33133871 C>A maps to NM_005610.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:41347407 G>T maps to NM_014248.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:41347407 G>T maps to NM_014248.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:10465552 C>A maps to NM_178857.5 E2019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:10465552 C>A maps to NM_178857.5 E2019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:40503437 A>G maps to NM_001034996.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:40503437 A>G maps to NM_001034996.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:35826892 G>T maps to NM_002951.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:35826892 G>T maps to NM_002951.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:219458846 A>T maps to NM_005444.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:219458846 A>T maps to NM_005444.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237620006 C>G maps to NM_001035.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237620006 C>G maps to NM_001035.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:92731108 T>C maps to NM_017654.3 L1434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:92731108 T>C maps to NM_017654.3 L1434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:50902832 G>A maps to ENST00000337034 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:50902832 G>A maps to ENST00000337034 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:91940393 C>T maps to NM_024077.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:91940393 C>T maps to NM_024077.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:132097247 G>A maps to NM_001098811.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:132097247 G>A maps to NM_001098811.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:201436412 C>T maps to NM_152524.5 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:201436412 C>T maps to NM_152524.5 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:34542847 C>T maps to NM_133647.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:34542847 C>T maps to NM_133647.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:110746218 G>T maps to NM_033125.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:110746218 G>T maps to NM_033125.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92346638 G>A maps to NM_134266.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92346638 G>A maps to NM_134266.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:162751274 C>T maps to NM_001178015.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:162751274 C>T maps to NM_001178015.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55730143 C>A maps to NM_001043.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55730143 C>A maps to NM_001043.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:103120016 G>C maps to NM_001011552.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:103120016 G>C maps to NM_001011552.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:34923231 G>T maps to NM_138927.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:34923231 G>T maps to NM_138927.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:97144022 G>A maps to NM_001034954.1 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:97144022 G>A maps to NM_001034954.1 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7324722 G>T maps to NM_199339.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7324722 G>T maps to NM_199339.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:4349455 C>T maps to NM_182538.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:4349455 C>T maps to NM_182538.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:149483225 C>A maps to NM_198455.2 Y1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:149483225 C>A maps to NM_198455.2 Y1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:27000439 C>T maps to NM_003170.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:27000439 C>T maps to NM_003170.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:91835637 T>C maps to NM_014848.4 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:91835637 T>C maps to NM_014848.4 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:123844294 T>C maps to NM_206862.2 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:123844294 T>C maps to NM_206862.2 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:6636488 C>A maps to NM_138697.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:6636488 C>A maps to NM_138697.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:19167001 G>T maps to NM_152232.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:19167001 G>T maps to NM_152232.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143175789 C>A maps to NM_176883.2 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143175789 C>A maps to NM_176883.2 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:19475096 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:19475096 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:69377432 G>A maps to NM_144676.3 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:69377432 G>A maps to NM_144676.3 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:36230815 G>A maps to NM_024660.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:36230815 G>A maps to NM_024660.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:122682990 G>T maps to NM_152399.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:122682990 G>T maps to NM_152399.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:675508 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:675508 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:18729266 C>T maps to NM_012109.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:18729266 C>T maps to NM_012109.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:136384028 G>T maps to NM_001080483.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:136384028 G>T maps to NM_001080483.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:117787939 C>A maps to ENST00000413475 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:117787939 C>A maps to ENST00000413475 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:2410316 C>T maps to NM_182973.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:2410316 C>T maps to NM_182973.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:72201203 A>G maps to NM_002270.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:72201203 A>G maps to NM_002270.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7578289 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7578289 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:6328768 G>T maps to NM_033516.5 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:6328768 G>T maps to NM_033516.5 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:10969089 G>T maps to NM_199261.2 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:10969089 G>T maps to NM_199261.2 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:140406834 T>C maps to NM_152616.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:140406834 T>C maps to NM_152616.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:72948635 C>A maps to NM_007332.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:72948635 C>A maps to NM_007332.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:31767929 G>T maps to NM_020856.2 I923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:31767929 G>T maps to NM_020856.2 I923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:31768284 G>T maps to NM_020856.2 S805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:31768284 G>T maps to NM_020856.2 S805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:41865601 G>T maps to NM_006293.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:41865601 G>T maps to NM_006293.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:75204453 G>A maps to NM_138467.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:75204453 G>A maps to NM_138467.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:76168548 C>T maps to NM_173469.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:76168548 C>T maps to NM_173469.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:86293364 T>A maps to NM_013438.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:86293364 T>A maps to NM_013438.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:69817244 A>G maps to NM_024743.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:69817244 A>G maps to NM_024743.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:35769859 G>T maps to NM_003367.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:35769859 G>T maps to NM_003367.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:215802170 G>T maps to ENST00000366943 G5192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:215802170 G>T maps to ENST00000366943 G5192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:134225225 G>T maps to NM_003882.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:134225225 G>T maps to NM_003882.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:228238441 C>A maps to ENST00000366753 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:228238441 C>A maps to ENST00000366753 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:31573032 C>T maps to NM_000379.3 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:31573032 C>T maps to NM_000379.3 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:45498927 C>T maps to NM_006963.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:45498927 C>T maps to NM_006963.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:52538202 G>T maps to NM_014650.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:52538202 G>T maps to NM_014650.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:22363426 G>T maps to NM_001001411.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:22363426 G>T maps to NM_001001411.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:27506907 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:27506907 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:62284241 G>A maps to NM_001620.1 L5883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:62284241 G>A maps to NM_001620.1 L5883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:293449 A>G maps to ENST00000409479 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:293449 A>G maps to ENST00000409479 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:96707414 G>T maps to NM_000623.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:96707414 G>T maps to NM_000623.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:121629165 C>A maps to ENST00000275159 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:121629165 C>A maps to ENST00000275159 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:30364597 C>T maps to NM_006110.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:30364597 C>T maps to NM_006110.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:7295904 C>A maps to NM_014718.3 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:7295904 C>A maps to NM_014718.3 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:105798251 C>T maps to NM_000494.3 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:105798251 C>T maps to NM_000494.3 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:38136441 C>T maps to NM_007335.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:38136441 C>T maps to NM_007335.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:32561035 C>T maps to NM_025209.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:32561035 C>T maps to NM_025209.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:34149207 C>A maps to NM_203408.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:34149207 C>A maps to NM_203408.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:30676241 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:30676241 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:145140568 C>T maps to NM_003801.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:145140568 C>T maps to NM_003801.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:206649521 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:206649521 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:32672630 C>T maps to NM_001160042.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:32672630 C>T maps to NM_001160042.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:38935858 C>T maps to NM_181537.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:38935858 C>T maps to NM_181537.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr21:46117436 C>A maps to NM_198699.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr21:46117436 C>A maps to NM_198699.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:141092094 G>A maps to NM_018557.2 S4050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:141092094 G>A maps to NM_018557.2 S4050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:60024296 G>A maps to NM_005121.2 Q2125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:60024296 G>A maps to NM_005121.2 Q2125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:23861782 C>G maps to NM_002471.3 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:23861782 C>G maps to NM_002471.3 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:17264842 C>G maps to NM_004145.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:17264842 C>G maps to NM_004145.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:15629147 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:15629147 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:117723101 C>T maps to ENST00000338101 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:117723101 C>T maps to ENST00000338101 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:84744852 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:84744852 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:8790639 C>G maps to NM_152745.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:8790639 C>G maps to NM_152745.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:5969262 G>C maps to NM_001003443.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:5969262 G>C maps to NM_001003443.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:72942966 C>T maps to NM_178233.1 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:72942966 C>T maps to NM_178233.1 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:17804747 A>G maps to NM_006197.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:17804747 A>G maps to NM_006197.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:62891578 G>A maps to NM_018257.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:62891578 G>A maps to NM_018257.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:11461678 C>A maps to NM_002723.3 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:11461678 C>A maps to NM_002723.3 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:68995473 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:68995473 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:61957767 G>A maps to NM_006552.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:61957767 G>A maps to NM_006552.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:38760173 G>A maps to NM_006514.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:38760173 G>A maps to NM_006514.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:148427472 C>T maps to NM_024577.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:148427472 C>T maps to NM_024577.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:33770903 G>A maps to NM_144682.5 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:33770903 G>A maps to NM_144682.5 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:36826828 G>A maps to ENST00000373130 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:36826828 G>A maps to ENST00000373130 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:139575436 G>A maps to ENST00000422328 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:139575436 G>A maps to ENST00000422328 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:152082860 C>T maps to NM_007113.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:152082860 C>T maps to NM_007113.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:89986022 C>T maps to ENST00000304984 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:89986022 C>T maps to ENST00000304984 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:22033295 G>A maps to NM_032236.5 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:22033295 G>A maps to NM_032236.5 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:41007725 G>A maps to NM_001039590.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:41007725 G>A maps to NM_001039590.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:57019257 C>A maps to NM_004738.4 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:57019257 C>A maps to NM_004738.4 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:100866416 C>T maps to NM_017890.3 F3625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:100866416 C>T maps to NM_017890.3 F3625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:69259640 G>C maps to NM_004926.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:69259640 G>C maps to NM_004926.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:44051073 G>T maps to NM_022436.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:44051073 G>T maps to NM_022436.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:79058499 G>A maps to ENST00000258883 S1251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:79058499 G>A maps to ENST00000258883 S1251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:137761343 C>G maps to NM_005989.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:137761343 C>G maps to NM_005989.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:80869213 G>A maps to NM_014862.3 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:80869213 G>A maps to NM_014862.3 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:80869216 G>A maps to NM_014862.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:80869216 G>A maps to NM_014862.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:66282098 C>T maps to NM_024649.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:66282098 C>T maps to NM_024649.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:27066580 G>A maps to NM_018164.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:27066580 G>A maps to NM_018164.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:153907269 C>T maps to NM_014856.2 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:153907269 C>T maps to NM_014856.2 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:39089318 T>A maps to NM_198963.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:39089318 T>A maps to NM_198963.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:11631219 T>A maps to NM_001372.3 L1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:11631219 T>A maps to NM_001372.3 L1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:30451753 G>A maps to NM_080611.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:30451753 G>A maps to NM_080611.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:197019965 T>A maps to NM_001994.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:197019965 T>A maps to NM_001994.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:230415080 G>C maps to NM_004481.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:230415080 G>C maps to NM_004481.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:4872540 C>T maps to NM_017417.1 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:4872540 C>T maps to NM_017417.1 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:107115455 G>A maps to NM_005295.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:107115455 G>A maps to NM_005295.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:149858559 C>T maps to NM_003517.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:149858559 C>T maps to NM_003517.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:90634803 C>T maps to NM_002168.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:90634803 C>T maps to NM_002168.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:145535837 C>T maps to NM_003637.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:145535837 C>T maps to NM_003637.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:110984679 G>A maps to NM_014379.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:110984679 G>A maps to NM_014379.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:10610573 G>A maps to NM_203500.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:10610573 G>A maps to NM_203500.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:30316109 G>C maps to NM_020848.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:30316109 G>C maps to NM_020848.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:158322895 C>T maps to NM_001195432.1 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:158322895 C>T maps to NM_001195432.1 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:48719903 G>A maps to NM_016453.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:48719903 G>A maps to NM_016453.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:124906575 C>A maps to NM_014222.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:124906575 C>A maps to NM_014222.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:25781183 T>A maps to NM_018297.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:25781183 T>A maps to NM_018297.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:27613316 G>A maps to NM_020772.2 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:27613316 G>A maps to NM_020772.2 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:123810835 T>C maps to NM_001001965.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:123810835 T>C maps to NM_001001965.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:124310357 A>C maps to NM_012378.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:124310357 A>C maps to NM_012378.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:550630 C>A maps to NM_002607.5 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:550630 C>A maps to NM_002607.5 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:3202410 T>G maps to ENST00000380989 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:3202410 T>G maps to ENST00000380989 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:139241421 C>A maps to ENST00000367663 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:139241421 C>A maps to ENST00000367663 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:50818878 G>A maps to NM_003055.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:50818878 G>A maps to NM_003055.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:11100020 C>T maps to NM_001128849.1 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:11100020 C>T maps to NM_001128849.1 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:39962249 A>G maps to NM_003169.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:39962249 A>G maps to NM_003169.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:9609135 T>G maps to NM_003747.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:9609135 T>G maps to NM_003747.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:50769638 T>G maps to NM_005154.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:50769638 T>G maps to NM_005154.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100847836 C>T maps to NM_001161476.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100847836 C>T maps to NM_001161476.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:168104900 G>A maps to NM_152381.5 K2333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:168104900 G>A maps to NM_152381.5 K2333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:72022763 T>G maps to NM_144982.4 R1294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:72022763 T>G maps to NM_144982.4 R1294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:106814835 G>T maps to NM_012082.3 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:106814835 G>T maps to NM_012082.3 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:50548182 C>T maps to NM_015428.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:50548182 C>T maps to NM_015428.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:238048575 G>T maps to NM_021186.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:238048575 G>T maps to NM_021186.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:12785266 C>A maps to NM_001103170.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:12785266 C>A maps to NM_001103170.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:4877970 C>G maps to NM_001040177.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:4877970 C>G maps to NM_001040177.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:8959614 C>A maps to NM_020646.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:8959614 C>A maps to NM_020646.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:160114889 C>T maps to NM_025153.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:160114889 C>T maps to NM_025153.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:76556002 C>A maps to NM_033401.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:76556002 C>A maps to NM_033401.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:189950489 T>C maps to NM_000393.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:189950489 T>C maps to NM_000393.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chrX:32361372 G>A maps to ENST00000357033 L1873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chrX:32361372 G>A maps to ENST00000357033 L1873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:35384134 G>A maps to NM_001145315.1 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:35384134 G>A maps to NM_001145315.1 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:71508555 T>A maps to NM_031889.2 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:71508555 T>A maps to NM_031889.2 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:2242225 G>A maps to NM_024511.5 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:2242225 G>A maps to NM_024511.5 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:54675628 A>G maps to NM_031157.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:54675628 A>G maps to NM_031157.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:6664535 C>A maps to NM_001193457.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:6664535 C>A maps to NM_001193457.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:2811462 C>A maps to NM_014878.4 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:2811462 C>A maps to NM_014878.4 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:53074042 C>T maps to NM_006121.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:53074042 C>T maps to NM_006121.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:40136624 G>T maps to NM_020929.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:40136624 G>T maps to NM_020929.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:57919410 C>T maps to NM_052897.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:57919410 C>T maps to NM_052897.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr18:33779984 G>A maps to NM_017947.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr18:33779984 G>A maps to NM_017947.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:7315482 C>T maps to NM_020795.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:7315482 C>T maps to NM_020795.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:164272189 C>T maps to NM_006174.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:164272189 C>T maps to NM_006174.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:52283747 G>A maps to NM_002525.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:52283747 G>A maps to NM_002525.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:22382658 C>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:22382658 C>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:73007895 C>T maps to NM_004154.3 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:73007895 C>T maps to NM_004154.3 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:102782063 G>A maps to NM_001195263.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:102782063 G>A maps to NM_001195263.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:1220716 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:1220716 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:3725360 G>A maps to NM_016292.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:3725360 G>A maps to NM_016292.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:126445603 C>T maps to NM_025195.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:126445603 C>T maps to NM_025195.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:231700635 A>G maps to NM_005999.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:231700635 A>G maps to NM_005999.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:7726786 T>C maps to NM_145891.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:7726786 T>C maps to NM_145891.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:89382143 C>T maps to NM_013227.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:89382143 C>T maps to NM_013227.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:18149851 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:18149851 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:24326278 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:24326278 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:75778405 G>A maps to NM_000700.1 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:75778405 G>A maps to NM_000700.1 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:33935315 G>T maps to NM_001030006.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:33935315 G>T maps to NM_001030006.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:1391158 C>T maps to NM_003933.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:1391158 C>T maps to NM_003933.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:140494267 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:140494267 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:15677045 G>T maps to NM_000060.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:15677045 G>T maps to NM_000060.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:81095023 C>A maps to NM_152337.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:81095023 C>A maps to NM_152337.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:19656205 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:19656205 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:9496976 G>C maps to NM_012261.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:9496976 G>C maps to NM_012261.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:62187725 C>A maps to NM_024059.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:62187725 C>A maps to NM_024059.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:7639557 G>T maps to NM_004244.4 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:7639557 G>T maps to NM_004244.4 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:83378558 G>C maps to ENST00000268613 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:83378558 G>C maps to ENST00000268613 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:63529983 G>T maps to NM_004361.2 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:63529983 G>T maps to NM_004361.2 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:46783743 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:46783743 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:143039236 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:143039236 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:78064458 C>A maps to NM_005752.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:78064458 C>A maps to NM_005752.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:101747955 G>A maps to NM_001855.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:101747955 G>A maps to NM_001855.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:107807110 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:107807110 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:70964867 C>A maps to NM_001851.4 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:70964867 C>A maps to NM_001851.4 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113668536 T>C maps to NM_198123.1 E950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113668536 T>C maps to NM_198123.1 E950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:111772476 C>A maps to NM_015267.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:111772476 C>A maps to NM_015267.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:47489620 C>A maps to NM_178033.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:47489620 C>A maps to NM_178033.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:90312087 G>T maps to NM_004938.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:90312087 G>T maps to NM_004938.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:1430350 G>T maps to NM_018959.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:1430350 G>T maps to NM_018959.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:88885722 G>T maps to NM_152418.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:88885722 G>T maps to NM_152418.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:232172459 G>A maps to NM_001164537.1 Q848Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:232172459 G>A maps to NM_001164537.1 Q848Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:32380906 T>A maps to ENST00000357033 K1775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:32380906 T>A maps to ENST00000357033 K1775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:13923424 G>A maps to NM_001369.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:13923424 G>A maps to NM_001369.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:72301558 G>T maps to NM_023036.4 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:72301558 G>T maps to NM_023036.4 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:102496194 G>T maps to NM_001376.4 E3228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:102496194 G>T maps to NM_001376.4 E3228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:65635361 A>T maps to NM_016938.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:65635361 A>T maps to NM_016938.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:40352528 T>A maps to NM_005875.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:40352528 T>A maps to NM_005875.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:36917704 G>T maps to NM_014800.9 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:36917704 G>T maps to NM_014800.9 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:43933985 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:43933985 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:37026686 G>T maps to NM_001013736.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:37026686 G>T maps to NM_001013736.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:156589904 C>A maps to NM_130899.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:156589904 C>A maps to NM_130899.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:10107089 G>T maps to NM_033084.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:10107089 G>T maps to NM_033084.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:92534671 C>G maps to ENST00000298047 T2831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:92534671 C>G maps to ENST00000298047 T2831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:159275976 G>T maps to ENST00000368115 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:159275976 G>T maps to ENST00000368115 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:4488553 G>T maps to NM_020638.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:4488553 G>T maps to NM_020638.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:49195970 A>G maps to NM_000145.3 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:49195970 A>G maps to NM_000145.3 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:161580233 G>T maps to NM_198903.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:161580233 G>T maps to NM_198903.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:242741366 C>A maps to NM_022134.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:242741366 C>A maps to NM_022134.2 L97L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5941-01A-11D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-50-5941-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:46094545 C>A maps to NM_005282.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:46094545 C>A maps to NM_005282.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:156469676 C>A maps to NM_001173393.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:156469676 C>A maps to NM_001173393.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:30662468 G>T maps to NM_002110.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:30662468 G>T maps to NM_002110.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:114378648 C>T maps to NM_153612.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:114378648 C>T maps to NM_153612.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:117127642 C>A maps to NM_001542.2 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:117127642 C>A maps to NM_001542.2 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:18188418 G>T maps to NM_005535.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:18188418 G>T maps to NM_005535.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:160958300 A>G maps to NM_000888.3 N771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:160958300 A>G maps to NM_000888.3 N771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:35229037 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:35229037 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:15468782 G>T maps to NM_004973.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:15468782 G>T maps to NM_004973.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:62739866 G>T maps to NM_181712.4 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:62739866 G>T maps to NM_181712.4 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:30032821 G>T maps to NM_002233.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:30032821 G>T maps to NM_002233.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:29437774 G>C maps to NM_014939.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:29437774 G>C maps to NM_014939.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:118223470 A>C maps to NM_020721.1 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:118223470 A>C maps to NM_020721.1 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:118284524 C>A maps to NM_020721.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:118284524 C>A maps to NM_020721.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:5920562 C>A maps to NM_001017969.2 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:5920562 C>A maps to NM_001017969.2 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:7804420 T>A maps to NM_012311.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:7804420 T>A maps to NM_012311.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:31971136 T>A maps to NM_181604.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:31971136 T>A maps to NM_181604.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:152648532 C>G maps to NM_178429.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:152648532 C>G maps to NM_178429.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:40137191 C>G maps to NM_020929.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:40137191 C>G maps to NM_020929.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:120053874 C>T maps to NM_001099678.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:120053874 C>T maps to NM_001099678.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:204588511 G>T maps to NM_201630.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:204588511 G>T maps to NM_201630.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:235860530 G>A maps to NM_000081.2 Y3472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:235860530 G>A maps to NM_000081.2 Y3472Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5941-01A-11D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-50-5941-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:13119527 G>A maps to ENST00000319217 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:13119527 G>A maps to ENST00000319217 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:13125263 C>T maps to ENST00000319217 Q1586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:13125263 C>T maps to ENST00000319217 Q1586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:11790300 C>T maps to NM_078629.3 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:11790300 C>T maps to NM_078629.3 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:10403985 G>T maps to NM_005963.3 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:10403985 G>T maps to NM_005963.3 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:23898509 C>G maps to NM_000257.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:23898509 C>G maps to NM_000257.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:41792281 C>T maps to NM_006766.3 W1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:41792281 C>T maps to NM_006766.3 W1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:101756711 G>A maps to NM_052867.2 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:101756711 G>A maps to NM_052867.2 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:115997568 G>T maps to NM_022569.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:115997568 G>T maps to NM_022569.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:72400930 C>A maps to NM_173808.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:72400930 C>A maps to NM_173808.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:247588043 C>A maps to NM_004895.4 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:247588043 C>A maps to NM_004895.4 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:26110041 G>A maps to NM_000625.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:26110041 G>A maps to NM_000625.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:48619793 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:48619793 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:67395478 T>A maps to ENST00000376693 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:67395478 T>A maps to ENST00000376693 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:70783032 A>T maps to NM_181672.2 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:70783032 A>T maps to NM_181672.2 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:55735246 G>A maps to NM_001005491.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:55735246 G>A maps to NM_001005491.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123886883 C>T maps to NM_001004462.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123886883 C>T maps to NM_001004462.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:15838972 G>T maps to NM_013939.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:15838972 G>T maps to NM_013939.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:15839524 C>T maps to NM_013939.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:15839524 C>T maps to NM_013939.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:107267231 C>A maps to NM_001004485.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:107267231 C>A maps to NM_001004485.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248402652 T>C maps to NM_017504.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248402652 T>C maps to NM_017504.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:48511135 C>T maps to NM_001005512.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:48511135 C>T maps to NM_001005512.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:4790229 G>A maps to ENST00000380383 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:4790229 G>A maps to ENST00000380383 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29323942 A>G maps to NM_030876.5 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29323942 A>G maps to NM_030876.5 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:240969108 G>T maps to NM_001005853.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:240969108 G>T maps to NM_001005853.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158670175 C>T maps to NM_001005279.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158670175 C>T maps to NM_001005279.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29614828 G>T maps to NM_183378.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29614828 G>T maps to NM_183378.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:41870397 C>T maps to NM_000436.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:41870397 C>T maps to NM_000436.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:133196473 C>A maps to NM_170683.2 C142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:133196473 C>A maps to NM_170683.2 C142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:55116443 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:55116443 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:60998765 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:60998765 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:140186909 C>A maps to NM_018907.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:140186909 C>A maps to NM_018907.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:140774086 A>G maps to NM_032088.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:140774086 A>G maps to NM_032088.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:47801664 G>T maps to NM_006031.5 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:47801664 G>T maps to NM_006031.5 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:233394395 G>A maps to NM_014801.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:233394395 G>A maps to NM_014801.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:51524525 C>T maps to NM_138694.3 R3466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:51524525 C>T maps to NM_138694.3 R3466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:42046461 C>A maps to NM_000930.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:42046461 C>A maps to NM_000930.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:118220523 C>A maps to NM_001011709.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:118220523 C>A maps to NM_001011709.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:44566423 C>A maps to NM_001171603.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:44566423 C>A maps to NM_001171603.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:68942817 C>T maps to NM_024870.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:68942817 C>T maps to NM_024870.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:120021827 C>T maps to NM_016644.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:120021827 C>T maps to NM_016644.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:10383136 G>T maps to NM_198464.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:10383136 G>T maps to NM_198464.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:117504135 A>G maps to NM_020440.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:117504135 A>G maps to NM_020440.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:28116577 G>T maps to ENST00000354417 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:28116577 G>T maps to ENST00000354417 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8340447 A>T maps to NM_002839.3 A1716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8340447 A>T maps to NM_002839.3 A1716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:24580931 T>A maps to NM_006910.4 L974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:24580931 T>A maps to NM_006910.4 L974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:73668692 A>G maps to NM_181471.1 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:73668692 A>G maps to NM_181471.1 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:94486198 G>A maps to NM_004560.2 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:94486198 G>A maps to NM_004560.2 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:45220426 G>T maps to NM_003683.5 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:45220426 G>T maps to NM_003683.5 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:39008032 T>C maps to NM_000540.2 C3240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:39008032 T>C maps to NM_000540.2 C3240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:33895446 G>T maps to NM_001036.3 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:33895446 G>T maps to NM_001036.3 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:33962752 C>T maps to NM_001036.3 C1952C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:33962752 C>T maps to NM_001036.3 C1952C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:50406726 C>A maps to NM_020436.3 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:50406726 C>A maps to NM_020436.3 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:71913617 C>G maps to NM_020150.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:71913617 C>G maps to NM_020150.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:99356686 T>C maps to NM_005073.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:99356686 T>C maps to NM_005073.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:153932915 G>A maps to NM_014437.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:153932915 G>A maps to NM_014437.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:103148978 G>T maps to NM_001011552.3 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:103148978 G>T maps to NM_001011552.3 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:49110447 C>A maps to NM_133498.2 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:49110447 C>A maps to NM_133498.2 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:49156968 T>A maps to ENST00000376407 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:49156968 T>A maps to ENST00000376407 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:9416201 G>T maps to NM_025106.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:9416201 G>T maps to NM_025106.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:99920571 C>A maps to NM_014467.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:99920571 C>A maps to NM_014467.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:10910379 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:10910379 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:210267754 G>T maps to NM_001146261.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:210267754 G>T maps to NM_001146261.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:114682454 A>G maps to ENST00000369545 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:114682454 A>G maps to ENST00000369545 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:84212612 G>T maps to NM_005679.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:84212612 G>T maps to NM_005679.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:45141141 G>A maps to ENST00000404564 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:45141141 G>A maps to ENST00000404564 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:104462106 T>A maps to NM_153046.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:104462106 T>A maps to NM_153046.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:32961967 C>T maps to NM_207313.1 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:32961967 C>T maps to NM_207313.1 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:32961988 G>A maps to NM_207313.1 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:32961988 G>A maps to NM_207313.1 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:20024285 G>C maps to NM_199254.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:20024285 G>C maps to NM_199254.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:10934070 G>T maps to NM_199261.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:10934070 G>T maps to NM_199261.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:89537472 G>A maps to NM_020358.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:89537472 G>A maps to NM_020358.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:230724102 G>A maps to ENST00000389044 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:230724102 G>A maps to ENST00000389044 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:116426403 A>G maps to NM_014112.2 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:116426403 A>G maps to NM_014112.2 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:99678232 G>A maps to NM_022905.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:99678232 G>A maps to NM_022905.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:38537962 A>T maps to NM_003316.3 A1149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:38537962 A>T maps to NM_003316.3 A1149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179614244 A>G maps to ENST00000375038 F4296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179614244 A>G maps to ENST00000375038 F4296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:43281044 G>A maps to NM_174916.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:43281044 G>A maps to NM_174916.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:128941254 A>G maps to NM_020120.3 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:128941254 A>G maps to NM_020120.3 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:96124010 C>A maps to NM_003728.3 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:96124010 C>A maps to NM_003728.3 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:160388875 A>T maps to NM_020335.2 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:160388875 A>T maps to NM_020335.2 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:87017812 G>A maps to NM_016206.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:87017812 G>A maps to NM_016206.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:73249146 G>A maps to NM_152559.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:73249146 G>A maps to NM_152559.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:85750187 C>A maps to NM_014991.4 G309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:85750187 C>A maps to NM_014991.4 G309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:22271584 C>T maps to NM_033468.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:22271584 C>T maps to NM_033468.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:56999641 C>T maps to NM_001031623.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:56999641 C>T maps to NM_001031623.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:30536016 C>A maps to NM_024671.3 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:30536016 C>A maps to NM_024671.3 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:6185605 T>G maps to NM_030924.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:6185605 T>G maps to NM_030924.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:43249763 G>A maps to NM_000022.2 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:43249763 G>A maps to NM_000022.2 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr12:21679860 G>T maps to NM_030572.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr12:21679860 G>T maps to NM_030572.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:40842258 G>A maps to ENST00000357884 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:40842258 G>A maps to ENST00000357884 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:57252851 C>A maps to NM_001004303.4 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:57252851 C>A maps to NM_001004303.4 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:36211992 T>A maps to NM_001085411.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:36211992 T>A maps to NM_001085411.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr7:6840707 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr7:6840707 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr4:77283378 T>C maps to NM_001042784.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr4:77283378 T>C maps to NM_001042784.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:99994323 G>A maps to NM_005190.3 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:99994323 G>A maps to NM_005190.3 Q209*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5942-01A-21D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-50-5942-01A-21D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:90074797 C>A maps to NM_032119.3 L4322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:90074797 C>A maps to NM_032119.3 L4322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:48738496 A>T maps to NM_001135629.2 K735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:48738496 A>T maps to NM_001135629.2 K735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr17:39552824 G>A maps to ENST00000393998 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr17:39552824 G>A maps to ENST00000393998 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr7:107696312 A>G maps to NM_007356.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr7:107696312 A>G maps to NM_007356.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:197890682 C>A maps to NM_020204.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:197890682 C>A maps to NM_020204.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:140985256 G>A maps to NM_138702.1 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:140985256 G>A maps to NM_138702.1 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:248059652 C>A maps to NM_001001957.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:248059652 C>A maps to NM_001001957.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:55322399 C>T maps to NM_001001920.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:55322399 C>T maps to NM_001001920.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:140626216 C>A maps to NM_018935.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:140626216 C>A maps to NM_018935.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:35091858 C>A maps to NM_032634.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:35091858 C>A maps to NM_032634.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:90128520 C>T maps to NM_001098173.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:90128520 C>T maps to NM_001098173.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:6016243 A>C maps to NM_000635.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:6016243 A>C maps to NM_000635.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:77378461 G>A maps to NM_016578.3 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:77378461 G>A maps to NM_016578.3 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:47142963 G>A maps to NM_014159.6 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:47142963 G>A maps to NM_014159.6 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:40342548 C>A maps to NM_021097.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:40342548 C>A maps to NM_021097.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:24565544 G>A maps to NM_024893.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:24565544 G>A maps to NM_024893.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:54707188 A>G maps to ENST00000260323 Q1619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:54707188 A>G maps to ENST00000260323 Q1619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr4:85626627 G>A maps to NM_014991.4 L2752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr4:85626627 G>A maps to NM_014991.4 L2752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chrX:76875915 G>T maps to NM_000489.3 S1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chrX:76875915 G>T maps to NM_000489.3 S1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:32362584 G>A maps to ENST00000468270 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:32362584 G>A maps to ENST00000468270 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:30791979 T>A maps to NM_001105528.1 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:30791979 T>A maps to NM_001105528.1 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:41904477 C>G maps to NM_175921.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:41904477 C>G maps to NM_175921.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:105800829 G>A maps to NM_000494.3 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:105800829 G>A maps to NM_000494.3 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:57850081 G>A maps to NM_031479.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:57850081 G>A maps to NM_031479.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:52360755 G>A maps to NM_002203.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:52360755 G>A maps to NM_002203.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:60040304 G>T maps to NM_005121.2 I1624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:60040304 G>T maps to NM_005121.2 I1624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102743680 G>A maps to ENST00000326227 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102743680 G>A maps to ENST00000326227 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102565709 G>A maps to NM_022122.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102565709 G>A maps to NM_022122.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102565800 G>A maps to NM_022122.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102565800 G>A maps to NM_022122.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167551957 C>A maps to NM_001122679.1 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167551957 C>A maps to NM_001122679.1 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:59283059 G>A maps to NM_001004711.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:59283059 G>A maps to NM_001004711.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:81151064 G>T maps to NM_052892.3 I2227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:81151064 G>T maps to NM_052892.3 I2227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:97321847 T>C maps to NM_014754.1 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:97321847 T>C maps to NM_014754.1 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:5286436 G>A maps to NM_004703.4 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:5286436 G>A maps to NM_004703.4 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:76752164 C>A maps to NM_171999.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:76752164 C>A maps to NM_171999.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:68337295 T>C maps to NM_001164160.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:68337295 T>C maps to NM_001164160.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:51630512 T>A maps to NM_014441.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:51630512 T>A maps to NM_014441.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207179 G>A maps to NM_003116.1 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207179 G>A maps to NM_003116.1 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:152671317 T>C maps to NM_182961.2 Q3962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:152671317 T>C maps to NM_182961.2 Q3962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:65146796 G>T maps to NM_001010874.4 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:65146796 G>T maps to NM_001010874.4 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:60695270 C>T maps to NM_017870.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:60695270 C>T maps to NM_017870.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:22323137 A>G maps to NM_003935.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:22323137 A>G maps to NM_003935.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:180320180 C>T maps to NM_133462.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:180320180 C>T maps to NM_133462.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:31598367 G>A maps to NM_000379.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:31598367 G>A maps to NM_000379.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:3990762 C>T maps to NM_015113.3 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:3990762 C>T maps to NM_015113.3 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:12779533 C>T maps to NM_001103170.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:12779533 C>T maps to NM_001103170.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:169836374 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:169836374 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:27112234 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:27112234 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:148563036 C>A maps to NM_014945.2 Y12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:148563036 C>A maps to NM_014945.2 Y12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:236917278 C>G maps to NM_001103.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:236917278 C>G maps to NM_001103.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:87746059 G>T maps to NM_021723.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:87746059 G>T maps to NM_021723.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:130332434 C>A maps to NM_139055.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:130332434 C>A maps to NM_139055.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:28212699 C>A maps to NM_006988.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:28212699 C>A maps to NM_006988.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:77894244 G>T maps to NM_014913.3 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:77894244 G>T maps to NM_014913.3 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:67046684 C>A maps to NM_001619.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:67046684 C>A maps to NM_001619.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:105415109 C>A maps to NM_138420.2 V2226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:105415109 C>A maps to NM_138420.2 V2226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:870863 C>A maps to NM_015985.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:870863 C>A maps to NM_015985.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:14782612 G>T maps to NM_001145029.1 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:14782612 G>T maps to NM_001145029.1 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:21261822 T>C maps to NM_145865.2 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:21261822 T>C maps to NM_145865.2 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:232104711 G>T maps to ENST00000359743 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:232104711 G>T maps to ENST00000359743 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:117045738 A>G maps to NM_207303.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:117045738 A>G maps to NM_207303.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:69599542 G>T maps to NM_015570.2 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:69599542 G>T maps to NM_015570.2 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104240320 C>A maps to ENST00000297574 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104240320 C>A maps to ENST00000297574 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70049261 C>T maps to NM_001704.2 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70049261 C>T maps to NM_001704.2 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160229597 G>A maps to NM_013450.2 Q1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160229597 G>A maps to NM_013450.2 Q1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:165548501 G>T maps to NM_000055.2 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:165548501 G>T maps to NM_000055.2 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:93761035 T>C maps to NM_001002860.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:93761035 T>C maps to NM_001002860.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26509122 C>G maps to NM_001732.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26509122 C>G maps to NM_001732.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:68029493 C>A maps to NM_022338.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:68029493 C>A maps to NM_022338.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:6804644 G>T maps to NM_153685.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:6804644 G>T maps to NM_153685.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:100795347 G>T maps to NM_207117.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:100795347 G>T maps to NM_207117.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:90167029 C>A maps to NM_152259.3 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:90167029 C>A maps to NM_152259.3 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:29756143 C>A maps to NM_175900.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:29756143 C>A maps to NM_175900.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:49430385 A>G maps to NM_144602.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:49430385 A>G maps to NM_144602.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:2099251 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:2099251 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:179348611 T>C maps to NM_144696.4 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:179348611 T>C maps to NM_144696.4 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:170934322 C>A maps to NM_001163629.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:170934322 C>A maps to NM_001163629.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:75037409 C>T maps to NM_001002912.4 K1328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:75037409 C>T maps to NM_001002912.4 K1328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:3802910 C>T maps to NM_018347.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:3802910 C>T maps to NM_018347.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47976529 G>T maps to NM_001013732.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47976529 G>T maps to NM_001013732.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:54095708 C>A maps to ENST00000502396 C972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:54095708 C>A maps to ENST00000502396 C972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:53694252 C>T maps to NM_001128840.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:53694252 C>T maps to NM_001128840.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:48699018 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:48699018 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:122261606 T>C maps to NM_001167940.1 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:122261606 T>C maps to NM_001167940.1 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:67699248 G>T maps to NM_018448.3 G601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:67699248 G>T maps to NM_018448.3 G601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:44442841 C>G maps to NM_144974.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:44442841 C>G maps to NM_144974.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:106139942 C>A maps to NM_001008723.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:106139942 C>A maps to NM_001008723.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:27371932 T>C maps to NM_030771.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:27371932 T>C maps to NM_030771.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:117303198 C>T maps to NM_001767.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:117303198 C>T maps to NM_001767.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72470715 C>G maps to NM_007261.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72470715 C>G maps to NM_007261.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118209936 G>A maps to NM_000732.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118209936 G>A maps to NM_000732.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:80273285 G>T maps to NM_006137.6 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:80273285 G>T maps to NM_006137.6 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:61859036 C>T maps to NM_001796.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:61859036 C>T maps to NM_001796.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:214787201 G>A maps to NM_016343.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:214787201 G>A maps to NM_016343.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67006789 C>T maps to NM_024922.5 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67006789 C>T maps to NM_024922.5 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:85211304 G>T maps to NM_000390.2 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:85211304 G>T maps to NM_000390.2 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240071723 G>T maps to NM_000740.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240071723 G>T maps to NM_000740.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:46812052 C>T maps to ENST00000415402 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:46812052 C>T maps to ENST00000415402 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:86952402 G>T maps to NM_001285.3 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:86952402 G>T maps to NM_001285.3 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:104678641 G>T maps to NM_017649.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:104678641 G>T maps to NM_017649.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:32745454 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:32745454 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:121224716 G>T maps to NM_021110.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:121224716 G>T maps to NM_021110.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70926770 A>T maps to NM_001851.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70926770 A>T maps to NM_001851.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:36145554 C>A maps to ENST00000392201 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:36145554 C>A maps to ENST00000392201 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:46656574 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:46656574 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:61187393 C>A maps to NM_024811.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:61187393 C>A maps to NM_024811.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:113678504 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:113678504 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:114186068 C>A maps to NM_198123.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:114186068 C>A maps to NM_198123.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:68139030 C>A maps to NM_013266.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:68139030 C>A maps to NM_013266.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:41450571 C>G maps to NM_001905.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:41450571 C>G maps to NM_001905.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:117424333 A>T maps to NM_033427.2 L748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:117424333 A>T maps to NM_033427.2 L748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:144909467 C>A maps to NM_004709.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:144909467 C>A maps to NM_004709.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:125685682 C>A maps to NM_178470.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:125685682 C>A maps to NM_178470.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:88885965 C>A maps to NM_152418.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:88885965 C>A maps to NM_152418.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:50547536 C>A maps to NM_000790.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:50547536 C>A maps to NM_000790.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:70733332 G>T maps to NM_004728.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:70733332 G>T maps to NM_004728.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:50135413 G>T maps to NM_001013742.1 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:50135413 G>T maps to NM_001013742.1 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12790351 T>C maps to NM_001930.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12790351 T>C maps to NM_001930.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:125441675 G>A maps to NM_032656.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:125441675 G>A maps to NM_032656.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:41567781 G>C maps to NM_004941.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:41567781 G>C maps to NM_004941.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:21789411 G>T maps to NM_003777.3 L2937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:21789411 G>T maps to NM_003777.3 L2937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:38747766 C>T maps to ENST00000327475 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:38747766 C>T maps to ENST00000327475 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:28586947 C>A maps to NM_001941.3 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:28586947 C>A maps to NM_001941.3 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:28993188 G>A maps to NM_001134453.1 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:28993188 G>A maps to NM_001134453.1 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:76111984 G>T maps to NM_020892.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:76111984 G>T maps to NM_020892.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:19251861 C>T maps to NM_024680.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:19251861 C>T maps to NM_024680.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33703448 G>C maps to NM_018217.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33703448 G>C maps to NM_018217.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:2406158 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:2406158 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:96706223 C>T maps to NM_001080448.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:96706223 C>T maps to NM_001080448.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100320626 G>T maps to NM_000799.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100320626 G>T maps to NM_000799.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103468880 G>C maps to NM_017693.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103468880 G>C maps to NM_017693.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:53119805 C>A maps to NM_014584.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:53119805 C>A maps to NM_014584.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:53663689 C>T maps to NM_012291.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:53663689 C>T maps to NM_012291.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:158552763 C>G maps to NM_020728.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:158552763 C>G maps to NM_020728.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:6145983 G>T maps to NM_000129.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:6145983 G>T maps to NM_000129.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:222920373 G>T maps to NM_207468.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:222920373 G>T maps to NM_207468.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:128363285 C>T maps to NM_032599.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:128363285 C>T maps to NM_032599.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:10084738 T>C maps to NM_033084.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:10084738 T>C maps to NM_033084.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:101153929 G>T maps to NM_001029860.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:101153929 G>T maps to NM_001029860.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:192053164 G>T maps to NM_021032.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:192053164 G>T maps to NM_021032.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240370907 C>A maps to ENST00000406993 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240370907 C>A maps to ENST00000406993 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:172025272 A>T maps to NM_022763.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:172025272 A>T maps to NM_022763.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:79635337 C>A maps to NM_001013735.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:79635337 C>A maps to NM_001013735.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:70177794 C>A maps to NM_001126334.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:70177794 C>A maps to NM_001126334.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:39448685 G>A maps to NM_207361.4 E2748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:39448685 G>A maps to NM_207361.4 E2748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:12728531 G>T maps to ENST00000429478 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:12728531 G>T maps to ENST00000429478 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:49190147 C>G maps to NM_000145.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:49190147 C>G maps to NM_000145.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:121187927 G>T maps to NM_177478.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:121187927 G>T maps to NM_177478.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:39202771 G>A maps to ENST00000263405 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:39202771 G>A maps to ENST00000263405 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:101151281 G>T maps to NM_005458.7 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:101151281 G>T maps to NM_005458.7 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34072747 G>A maps to NM_139285.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34072747 G>A maps to NM_139285.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:72618363 C>G maps to ENST00000504199 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:72618363 C>G maps to ENST00000504199 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:135862118 C>T maps to NM_004188.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:135862118 C>T maps to NM_004188.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:233671354 C>T maps to ENST00000373566 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:233671354 C>T maps to ENST00000373566 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:80091553 G>T maps to NM_001102386.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:80091553 G>T maps to NM_001102386.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:133357431 C>T maps to NM_005895.3 Q1178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:133357431 C>T maps to NM_005895.3 Q1178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47682165 G>T maps to NM_153838.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47682165 G>T maps to NM_153838.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:131622689 C>G maps to NM_198827.3 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:131622689 C>G maps to NM_198827.3 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145894569 G>T maps to NM_194251.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145894569 G>T maps to NM_194251.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:19042028 C>A maps to NM_001079858.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:19042028 C>A maps to NM_001079858.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:140058238 C>T maps to ENST00000371546 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:140058238 C>T maps to ENST00000371546 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:106680948 T>A maps to ENST00000282249 K488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:106680948 T>A maps to ENST00000282249 K488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:32086598 C>A maps to NM_001525.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:32086598 C>A maps to NM_001525.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:55119931 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:55119931 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:185940983 G>T maps to NM_001029887.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:185940983 G>T maps to NM_001029887.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:28478364 A>G maps to NM_004667.4 F1534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:28478364 A>G maps to NM_004667.4 F1534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32609932 C>T maps to NM_002122.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32609932 C>T maps to NM_002122.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32713751 C>T maps to NM_020056.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32713751 C>T maps to NM_020056.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29692181 C>T maps to NM_001098479.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29692181 C>T maps to NM_001098479.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30136874 G>T maps to NM_178581.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30136874 G>T maps to NM_178581.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:186084073 C>A maps to NM_031935.2 V3800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:186084073 C>A maps to NM_031935.2 V3800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:176957938 C>T maps to NM_000523.3 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:176957938 C>T maps to NM_000523.3 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:26864522 C>T maps to NM_022081.4 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:26864522 C>T maps to NM_022081.4 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:21350556 A>T maps to NM_021002.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:21350556 A>T maps to NM_021002.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:103013337 G>T maps to NM_003855.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:103013337 G>T maps to NM_003855.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:41730009 G>T maps to NM_002192.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:41730009 G>T maps to NM_002192.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:247542 C>A maps to NM_001170738.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:247542 C>A maps to NM_001170738.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:68620470 G>A maps to ENST00000423218 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:68620470 G>A maps to ENST00000423218 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:20431052 G>T maps to NM_002214.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:20431052 G>T maps to NM_002214.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:65323401 C>G maps to NM_002227.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:65323401 C>G maps to NM_002227.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111146417 G>T maps to NM_004974.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111146417 G>T maps to NM_004974.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111216141 G>A maps to NM_002232.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111216141 G>A maps to NM_002232.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:63416959 C>G maps to NM_139318.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:63416959 C>G maps to NM_139318.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:39286894 G>T maps to NM_032115.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:39286894 G>T maps to NM_032115.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55970999 G>T maps to NM_002253.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55970999 G>T maps to NM_002253.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55976849 G>T maps to NM_002253.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55976849 G>T maps to NM_002253.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:75150053 C>T maps to NM_001039479.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:75150053 C>T maps to NM_001039479.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:75561136 C>A maps to NM_015037.2 R1797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:75561136 C>A maps to NM_015037.2 R1797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4905403 A>C maps to NM_006612.5 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4905403 A>C maps to NM_006612.5 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:154394126 G>T maps to NM_001099293.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:154394126 G>T maps to NM_001099293.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:10188396 G>T maps to NM_003597.4 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:10188396 G>T maps to NM_003597.4 V311V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-6590-01A-12D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:30349927 C>A maps to ENST00000426194 T52T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-6590-01A-12D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:30349927 C>A maps to ENST00000426194 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:60886056 G>C maps to NM_005560.3 L3394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:60886056 G>C maps to NM_005560.3 L3394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107756606 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107756606 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:37514996 G>A maps to NM_001170331.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:37514996 G>A maps to NM_001170331.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:93183806 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:93183806 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:75608952 G>T maps to NM_001001933.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:75608952 G>T maps to NM_001001933.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62598883 G>A maps to ENST00000506720 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62598883 G>A maps to ENST00000506720 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:188583986 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:188583986 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:140992363 T>A maps to NM_018557.2 L4550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:140992363 T>A maps to NM_018557.2 L4550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:7021986 C>T maps to NM_201650.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:7021986 C>T maps to NM_201650.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:46746158 C>T maps to ENST00000254454 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:46746158 C>T maps to ENST00000254454 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:70505160 A>G maps to NM_020794.2 Q1180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:70505160 A>G maps to NM_020794.2 Q1180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:23890519 G>A maps to NM_019066.4 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:23890519 G>A maps to NM_019066.4 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:21207865 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:21207865 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:112389553 C>A maps to NM_001085377.1 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:112389553 C>A maps to NM_001085377.1 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:30672203 G>A maps to NM_014641.2 Q1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:30672203 G>A maps to NM_014641.2 Q1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:90466039 C>T maps to NM_014611.1 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:90466039 C>T maps to NM_014611.1 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:41874857 G>A maps to NM_004275.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:41874857 G>A maps to NM_004275.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:145736022 C>T maps to NM_138431.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:145736022 C>T maps to NM_138431.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:43280084 G>T maps to NM_153361.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:43280084 G>T maps to NM_153361.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:76346999 G>T maps to NM_002440.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:76346999 G>T maps to NM_002440.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:135913853 G>C maps to NM_018133.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:135913853 G>C maps to NM_018133.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:42836679 C>G maps to ENST00000405094 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:42836679 C>G maps to ENST00000405094 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:38281086 C>T maps to NM_005955.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:38281086 C>T maps to NM_005955.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:29598828 G>C maps to NM_001033602.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:29598828 G>C maps to NM_001033602.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100681896 A>C maps to NM_001040105.1 T2400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100681896 A>C maps to NM_001040105.1 T2400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:49409662 T>A maps to NM_000255.3 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:49409662 T>A maps to NM_000255.3 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10533024 G>C maps to NM_002470.2 T1895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10533024 G>C maps to NM_002470.2 T1895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:128354110 C>T maps to ENST00000389524 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:128354110 C>T maps to ENST00000389524 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:120377483 T>A maps to NM_001047980.1 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:120377483 T>A maps to NM_001047980.1 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:45169921 A>T maps to NM_001145107.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:45169921 A>T maps to NM_001145107.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:120547952 T>A maps to NM_024408.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:120547952 T>A maps to NM_024408.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:164246586 C>A maps to NM_000909.4 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:164246586 C>A maps to NM_000909.4 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:84118522 C>T maps to ENST00000404547 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:84118522 C>T maps to ENST00000404547 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:50280528 A>T maps to ENST00000404971 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:50280528 A>T maps to ENST00000404971 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:176637040 C>T maps to NM_022455.4 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:176637040 C>T maps to NM_022455.4 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71063864 C>T maps to NM_017855.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71063864 C>T maps to NM_017855.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47776035 C>A maps to ENST00000489301 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47776035 C>A maps to ENST00000489301 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6867089 C>A maps to ENST00000379831 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6867089 C>A maps to ENST00000379831 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123894621 G>T maps to NM_001001953.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123894621 G>T maps to NM_001001953.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247978623 C>T maps to NM_001001966.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247978623 C>T maps to NM_001001966.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6807059 C>A maps to NM_001004489.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6807059 C>A maps to NM_001004489.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6789237 C>G maps to NM_001004490.1 *317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6789237 C>G maps to NM_001004490.1 *317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29054629 A>G maps to NM_001005226.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29054629 A>G maps to NM_001005226.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:27925656 C>A maps to NM_012367.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:27925656 C>A maps to NM_012367.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:143657206 G>T maps to NM_012369.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:143657206 G>T maps to NM_012369.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247769355 C>T maps to NM_001001914.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247769355 C>T maps to NM_001001914.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247769615 C>A maps to NM_001001914.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247769615 C>A maps to NM_001001914.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248402586 T>A maps to NM_017504.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248402586 T>A maps to NM_017504.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248487471 G>T maps to NM_001004691.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248487471 G>T maps to NM_001004691.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248789924 G>T maps to NM_001001964.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248789924 G>T maps to NM_001001964.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:55136240 C>A maps to NM_001005275.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:55136240 C>A maps to NM_001005275.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:51515952 G>A maps to NM_001004703.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:51515952 G>A maps to NM_001004703.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:5373150 G>A maps to NM_001004750.1 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:5373150 G>A maps to NM_001004750.1 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:5444011 C>A maps to NM_001004757.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:5444011 C>A maps to NM_001004757.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:59211573 G>A maps to NM_001004728.1 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:59211573 G>A maps to NM_001004728.1 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179214116 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179214116 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:97639077 A>G maps to NM_080818.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:97639077 A>G maps to NM_080818.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:90690623 C>A maps to NM_080832.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:90690623 C>A maps to NM_080832.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:103240675 G>T maps to NM_000277.1 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:103240675 G>T maps to NM_000277.1 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:176525706 C>T maps to NM_020318.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:176525706 C>T maps to NM_020318.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:24608166 G>T maps to NM_004845.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:24608166 G>T maps to NM_004845.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:178494167 G>T maps to NM_016953.3 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:178494167 G>T maps to NM_016953.3 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:178681582 G>A maps to NM_016953.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:178681582 G>A maps to NM_016953.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:22439035 C>T maps to NM_021630.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:22439035 C>T maps to NM_021630.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:28254866 C>T maps to NM_032507.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:28254866 C>T maps to NM_032507.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:11068307 G>T maps to ENST00000303905 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:11068307 G>T maps to ENST00000303905 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:170557702 C>T maps to NM_001008489.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:170557702 C>T maps to NM_001008489.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:18715655 G>T maps to NM_004570.4 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:18715655 G>T maps to NM_004570.4 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:130831589 T>A maps to NM_004764.4 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:130831589 T>A maps to NM_004764.4 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:51938334 T>C maps to NM_138694.3 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:51938334 T>C maps to NM_138694.3 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160807913 G>C maps to NM_007366.4 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160807913 G>C maps to NM_007366.4 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:59811014 A>T maps to NM_173801.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:59811014 A>T maps to NM_173801.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:113822052 G>A maps to NM_173542.3 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:113822052 G>A maps to NM_173542.3 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:8770174 G>T maps to NM_015192.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:8770174 G>T maps to NM_015192.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:144998618 C>A maps to NM_201380.2 R1963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:144998618 C>A maps to NM_201380.2 R1963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:84562266 T>A maps to ENST00000373145 K356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:84562266 T>A maps to ENST00000373145 K356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:12458630 T>A maps to NM_015869.4 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:12458630 T>A maps to NM_015869.4 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:202464797 C>T maps to ENST00000367270 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:202464797 C>T maps to ENST00000367270 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:111622951 C>A maps to NM_181699.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:111622951 C>A maps to NM_181699.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94731754 G>T maps to NM_058237.1 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94731754 G>T maps to NM_058237.1 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62198634 C>A maps to NM_001037335.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62198634 C>A maps to NM_001037335.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20486091 G>T maps to NM_005788.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20486091 G>T maps to NM_005788.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:23398555 C>A maps to NM_006109.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:23398555 C>A maps to NM_006109.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:37312669 T>C maps to NM_000950.2 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:37312669 T>C maps to NM_000950.2 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43762510 T>A maps to NM_002784.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43762510 T>A maps to NM_002784.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:47124656 C>A maps to NM_000960.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:47124656 C>A maps to NM_000960.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:87680173 A>G maps to NM_080685.2 A1167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:87680173 A>G maps to NM_080685.2 A1167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:45375314 G>A maps to NM_001042724.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:45375314 G>A maps to NM_001042724.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:135848565 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:135848565 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:4839262 C>A maps to NM_018059.4 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:4839262 C>A maps to NM_018059.4 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:152880647 C>T maps to NM_002886.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:152880647 C>T maps to NM_002886.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:50114545 C>A maps to NM_005777.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:50114545 C>A maps to NM_005777.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:107040327 G>T maps to ENST00000304514 Y1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:107040327 G>T maps to ENST00000304514 Y1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:192335235 A>G maps to NM_001039152.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:192335235 A>G maps to NM_001039152.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:125498687 C>T maps to NM_007218.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:125498687 C>T maps to NM_007218.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124763627 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124763627 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:10469018 G>T maps to NM_178857.5 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:10469018 G>T maps to NM_178857.5 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:26887625 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:26887625 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:54711355 G>T maps to NM_001013.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:54711355 G>T maps to NM_001013.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:45217389 C>A maps to NM_003683.5 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:45217389 C>A maps to NM_003683.5 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237666759 C>A maps to NM_001035.2 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237666759 C>A maps to NM_001035.2 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237780725 C>T maps to NM_001035.2 N1952N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237780725 C>T maps to NM_001035.2 N1952N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237886430 G>T maps to NM_001035.2 E3520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237886430 G>T maps to NM_001035.2 E3520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:34130390 T>C maps to NM_001036.3 F4070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:34130390 T>C maps to NM_001036.3 F4070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:10335473 G>T maps to NM_004230.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:10335473 G>T maps to NM_004230.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:92764150 T>C maps to NM_152703.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:92764150 T>C maps to NM_152703.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:166859122 A>T maps to NM_001165963.1 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:166859122 A>T maps to NM_001165963.1 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77917576 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77917576 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94908972 C>A maps to NM_001080451.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94908972 C>A maps to NM_001080451.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:167183058 A>T maps to NM_006217.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:167183058 A>T maps to NM_006217.3 T267T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-6590-01A-12D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52003552 C>G maps to NM_053003.2 A143A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-6590-01A-12D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52003552 C>G maps to NM_053003.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:147215232 G>A maps to ENST00000507030 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:147215232 G>A maps to ENST00000507030 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:63057948 T>A maps to NM_001039752.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:63057948 T>A maps to NM_001039752.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64360945 C>T maps to NM_144585.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64360945 C>T maps to NM_144585.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:22272313 G>T maps to NM_001135153.1 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:22272313 G>T maps to NM_001135153.1 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101603518 C>A maps to NM_145913.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101603518 C>A maps to NM_145913.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1240699 C>A maps to NM_182632.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1240699 C>A maps to NM_182632.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1208873 C>T maps to NM_001003841.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1208873 C>T maps to NM_001003841.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:121823891 G>A maps to NM_021021.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:121823891 G>A maps to NM_021021.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:1263176 C>T maps to NM_018968.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:1263176 C>T maps to NM_018968.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:107012558 C>A maps to NM_014978.1 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:107012558 C>A maps to NM_014978.1 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:67075136 G>A maps to NM_017857.3 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:67075136 G>A maps to NM_017857.3 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149523229 C>A maps to NM_198455.2 A4777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149523229 C>A maps to NM_198455.2 A4777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:17363208 C>A maps to NM_001004470.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:17363208 C>A maps to NM_001004470.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:37406599 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:37406599 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:40850491 A>T maps to NM_020783.3 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:40850491 A>T maps to NM_020783.3 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:159457708 G>T maps to NM_054114.3 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:159457708 G>T maps to NM_054114.3 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160005758 C>A maps to NM_033394.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160005758 C>A maps to NM_033394.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:30688618 C>T maps to ENST00000403477 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:30688618 C>T maps to ENST00000403477 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:11485952 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:11485952 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166795202 T>C maps to ENST00000507499 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166795202 T>C maps to ENST00000507499 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:63102153 G>T maps to NM_015059.2 E2232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:63102153 G>T maps to NM_015059.2 E2232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:120470839 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:120470839 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:102896654 G>T maps to NM_005521.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:102896654 G>T maps to NM_005521.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:105367343 G>A maps to NM_030788.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:105367343 G>A maps to NM_030788.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:2616631 G>T maps to NM_080751.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:2616631 G>T maps to NM_080751.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:120439109 G>A maps to NM_030577.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:120439109 G>A maps to NM_030577.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:130762883 G>T maps to NM_052913.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:130762883 G>T maps to NM_052913.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:25785239 C>T maps to NM_018202.4 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:25785239 C>T maps to NM_018202.4 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175048553 C>T maps to NM_022093.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175048553 C>T maps to NM_022093.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175328853 A>G maps to NM_003285.2 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175328853 A>G maps to NM_003285.2 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32035473 G>T maps to ENST00000375244 R2170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32035473 G>T maps to ENST00000375244 R2170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52400607 G>A maps to NM_012288.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52400607 G>A maps to NM_012288.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:4406814 G>C maps to NM_003141.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:4406814 G>C maps to NM_003141.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:5923322 G>C maps to NM_015939.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:5923322 G>C maps to NM_015939.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:141955392 G>A maps to NM_001001317.2 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:141955392 G>A maps to NM_001001317.2 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130353958 T>G maps to NM_052933.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130353958 T>G maps to NM_052933.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:31770503 G>T maps to NM_020856.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:31770503 G>T maps to NM_020856.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:41011323 C>T maps to NM_001159726.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:41011323 C>T maps to NM_001159726.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:112769534 T>C maps to NM_032028.3 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:112769534 T>C maps to NM_032028.3 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:76259371 C>T maps to NM_015072.4 Q1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:76259371 C>T maps to NM_015072.4 Q1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179399494 G>C maps to NM_133378.4 T31381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179399494 G>C maps to NM_133378.4 T31381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179447085 C>A maps to NM_133378.4 E19465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179447085 C>A maps to NM_133378.4 E19465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:132238276 C>A maps to NM_080386.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:132238276 C>A maps to NM_080386.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:216051136 C>A maps to ENST00000366943 G2882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:216051136 C>A maps to ENST00000366943 G2882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:30216302 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:30216302 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87424097 A>G maps to NM_007013.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87424097 A>G maps to NM_007013.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:168099599 G>A maps to NM_152381.5 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:168099599 G>A maps to NM_152381.5 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100350634 C>A maps to ENST00000349350 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100350634 C>A maps to ENST00000349350 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:28454783 A>G maps to NM_001040432.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:28454783 A>G maps to NM_001040432.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:77767958 G>T maps to NM_024721.4 T2934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:77767958 G>T maps to NM_024721.4 T2934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:106813428 G>A maps to NM_012082.3 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:106813428 G>A maps to NM_012082.3 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:44660543 C>A maps to NM_006630.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:44660543 C>A maps to NM_006630.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:22271619 T>G maps to NM_033468.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:22271619 T>G maps to NM_033468.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:37117542 C>A maps to NM_032825.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:37117542 C>A maps to NM_032825.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:49671242 G>T maps to NM_015069.2 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:49671242 G>T maps to NM_015069.2 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:22804791 G>A maps to NM_015461.2 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:22804791 G>A maps to NM_015461.2 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52994604 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52994604 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:23836221 C>A maps to NM_138330.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:23836221 C>A maps to NM_138330.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:151259783 C>T maps to NM_020832.1 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:151259783 C>T maps to NM_020832.1 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149174025 T>A maps to NM_001163474.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149174025 T>A maps to NM_001163474.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:80789946 C>T maps to NM_024702.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:80789946 C>T maps to NM_024702.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:88962751 C>A maps to NM_181646.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:88962751 C>A maps to NM_181646.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:57767459 C>A maps to NM_178457.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:57767459 C>A maps to NM_178457.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:13939466 G>A maps to NM_023072.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:13939466 G>A maps to NM_023072.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:102317991 C>A maps to NM_018476.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:102317991 C>A maps to NM_018476.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:15686793 G>A maps to NM_000060.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:15686793 G>A maps to NM_000060.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:56389822 C>A maps to NM_004758.2 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:56389822 C>A maps to NM_004758.2 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:34049272 C>T maps to ENST00000373381 E2363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:34049272 C>T maps to ENST00000373381 E2363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr10:104597000 G>A maps to NM_000102.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr10:104597000 G>A maps to NM_000102.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:340237 C>G maps to NM_203447.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:340237 C>G maps to NM_203447.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:102453875 G>T maps to NM_001376.4 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:102453875 G>T maps to NM_001376.4 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:45642256 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:45642256 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:32868708 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:32868708 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:151820133 C>A maps to NM_018558.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:151820133 C>A maps to NM_018558.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:90106985 C>T maps to NM_032119.3 F5303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:90106985 C>T maps to NM_032119.3 F5303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:26271321 G>A maps to NM_003534.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:26271321 G>A maps to NM_003534.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:39183255 G>T maps to NM_031957.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:39183255 G>T maps to NM_031957.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr11:64566285 C>A maps to NM_004579.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr11:64566285 C>A maps to NM_004579.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:36923550 A>T maps to NM_031280.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:36923550 A>T maps to NM_031280.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:248308637 C>A maps to NM_001004690.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:248308637 C>A maps to NM_001004690.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:40558062 G>A maps to NM_020168.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:40558062 G>A maps to NM_020168.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:150842573 T>A maps to NM_173493.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:150842573 T>A maps to NM_173493.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:53422136 G>A maps to NM_002590.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:53422136 G>A maps to NM_002590.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:91527270 C>A maps to NM_003981.2 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:91527270 C>A maps to NM_003981.2 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:42168341 G>T maps to ENST00000320955 A1364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:42168341 G>T maps to ENST00000320955 A1364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr21:42852431 C>A maps to NM_001135099.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr21:42852431 C>A maps to NM_001135099.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:48940622 T>C maps to NM_005749.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:48940622 T>C maps to NM_005749.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:87104727 C>T maps to NM_018849.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:87104727 C>T maps to NM_018849.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:22086857 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:22086857 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:130343038 C>T maps to NM_139055.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:130343038 C>T maps to NM_139055.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:4535474 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:4535474 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:104121932 G>A maps to NM_020978.3 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:104121932 G>A maps to NM_020978.3 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:14769114 C>T maps to NM_054027.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:14769114 C>T maps to NM_054027.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:51065402 G>A maps to ENST00000395624 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:51065402 G>A maps to ENST00000395624 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:19965106 C>A maps to NM_001670.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:19965106 C>A maps to NM_001670.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:155452126 C>T maps to ENST00000368346 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:155452126 C>T maps to ENST00000368346 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:177001757 G>T maps to ENST00000281881 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:177001757 G>T maps to ENST00000281881 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:119382626 G>A maps to ENST00000313400 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:119382626 G>A maps to ENST00000313400 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:153663817 C>A maps to NM_001183.4 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:153663817 C>A maps to NM_001183.4 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:77542696 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:77542696 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:24706265 T>C maps to ENST00000374409 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:24706265 T>C maps to ENST00000374409 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:26678074 C>T maps to NM_145038.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:26678074 C>T maps to NM_145038.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:136251402 G>A maps to NM_153710.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:136251402 G>A maps to NM_153710.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:2621975 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:2621975 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:32751961 C>A maps to NM_001026383.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:32751961 C>A maps to NM_001026383.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:119248737 A>G maps to NM_005191.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:119248737 A>G maps to NM_005191.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:46795763 G>A maps to NM_014246.1 H1754H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:46795763 G>A maps to NM_014246.1 H1754H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:241797472 C>T maps to NM_001821.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:241797472 C>T maps to NM_001821.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:42611771 G>A maps to NM_004198.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:42611771 G>A maps to NM_004198.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:26864167 C>T maps to NM_001029881.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:26864167 C>T maps to NM_001029881.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:83240092 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:83240092 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:3820747 C>A maps to NM_004380.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:3820747 C>A maps to NM_004380.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:3000194 A>T maps to NM_033225.5 G2011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:3000194 A>T maps to NM_033225.5 G2011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:23431199 A>G maps to NM_130794.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:23431199 A>G maps to NM_130794.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:42780200 C>T maps to NM_178009.2 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:42780200 C>T maps to NM_178009.2 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:117308125 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:117308125 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:233431655 G>T maps to NM_004846.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:233431655 G>T maps to NM_004846.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:2891555 C>T maps to NM_032048.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:2891555 C>T maps to NM_032048.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:2892119 T>C maps to NM_032048.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:2892119 T>C maps to NM_032048.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:21926531 G>T maps to ENST00000265800 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:21926531 G>T maps to ENST00000265800 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:164468116 A>C maps to NM_018086.2 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:164468116 A>C maps to NM_018086.2 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:154956262 C>T maps to NM_025207.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:154956262 C>T maps to NM_025207.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:89909083 G>A maps to NM_002042.3 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:89909083 G>A maps to NM_002042.3 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:89630437 C>T maps to NM_207398.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:89630437 C>T maps to NM_207398.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:6605136 C>T maps to NM_000170.2 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:6605136 C>T maps to NM_000170.2 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:117127976 C>T maps to NM_148963.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:117127976 C>T maps to NM_148963.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:42049868 G>T maps to NM_024503.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:42049868 G>T maps to NM_024503.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:47469795 G>T maps to NM_000621.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:47469795 G>T maps to NM_000621.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:997817 G>A maps to NM_000203.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:997817 G>A maps to NM_000203.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:160477508 G>A maps to NM_000876.2 W916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:160477508 G>A maps to NM_000876.2 W916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:31414912 C>A maps to ENST00000444228 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:31414912 C>A maps to ENST00000444228 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:30814602 T>C maps to NM_032116.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:30814602 T>C maps to NM_032116.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:155711421 C>A maps to NM_002239.2 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:155711421 C>A maps to NM_002239.2 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:22623827 G>C maps to ENST00000446597 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:22623827 G>C maps to ENST00000446597 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:11985481 G>A maps to ENST00000376576 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:11985481 G>A maps to ENST00000376576 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:136562354 G>A maps to NM_002299.2 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:136562354 G>A maps to NM_002299.2 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1823940 C>T maps to NM_012318.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1823940 C>T maps to NM_012318.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:40095886 C>T maps to NM_013268.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:40095886 C>T maps to NM_013268.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:26998233 G>T maps to NM_022901.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:26998233 G>T maps to NM_022901.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:196387755 C>A maps to NM_198565.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:196387755 C>A maps to NM_198565.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:12032560 G>T maps to ENST00000415385 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:12032560 G>T maps to ENST00000415385 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:32270927 T>A maps to NM_001040446.1 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:32270927 T>A maps to NM_001040446.1 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:81101698 C>A maps to NM_002469.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:81101698 C>A maps to NM_002469.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10448684 G>A maps to NM_017534.5 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10448684 G>A maps to NM_017534.5 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10360812 A>T maps to NM_017533.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10360812 A>T maps to NM_017533.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:2693021 G>A maps to NM_001012418.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:2693021 G>A maps to NM_001012418.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:84035949 G>A maps to NM_019065.2 *387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:84035949 G>A maps to NM_019065.2 *387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:233899562 G>A maps to NM_005383.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:233899562 G>A maps to NM_005383.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:44228229 G>C maps to NM_004556.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:44228229 G>C maps to NM_004556.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:123540179 A>T maps to NM_001163278.1 Y1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:123540179 A>T maps to NM_001163278.1 Y1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20444177 G>C maps to NM_001005486.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20444177 G>C maps to NM_001005486.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:82584973 A>G maps to NM_033026.5 P1765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:82584973 A>G maps to NM_033026.5 P1765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:335704 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:335704 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:39617690 G>T maps to ENST00000398870 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:39617690 G>T maps to ENST00000398870 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:3321338 C>T maps to NM_022114.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:3321338 C>T maps to NM_022114.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:47296203 C>T maps to NM_020820.3 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:47296203 C>T maps to NM_020820.3 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:68972958 T>G maps to NM_024870.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:68972958 T>G maps to NM_024870.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:804557 G>T maps to NM_002819.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:804557 G>T maps to NM_002819.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:209358128 G>T maps to NM_005048.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:209358128 G>T maps to NM_005048.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:2313104 G>A maps to NM_080594.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:2313104 G>A maps to NM_080594.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:34030760 C>T maps to NM_001036.3 F2542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:34030760 C>T maps to NM_001036.3 F2542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:40009423 C>T maps to NM_182704.1 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:40009423 C>T maps to NM_182704.1 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:90771739 C>T maps to NM_198925.2 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:90771739 C>T maps to NM_198925.2 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:29475665 G>A maps to NM_005626.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:29475665 G>A maps to NM_005626.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:164764689 C>T maps to NM_001041.3 W609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:164764689 C>T maps to NM_001041.3 W609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:73740832 G>T maps to NM_006517.3 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:73740832 G>T maps to NM_006517.3 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:110752418 C>A maps to NM_033125.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:110752418 C>A maps to NM_033125.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:190428700 C>A maps to NM_014585.5 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:190428700 C>A maps to NM_014585.5 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:95206109 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:95206109 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:231174739 T>A maps to NM_007237.4 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:231174739 T>A maps to NM_007237.4 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:133525471 G>T maps to NM_021203.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:133525471 G>T maps to NM_021203.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:48822395 C>T maps to NM_001198595.1 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:48822395 C>T maps to NM_001198595.1 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:154480954 A>T maps to NM_001098475.1 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:154480954 A>T maps to NM_001098475.1 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:48170629 T>A maps to NM_003215.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:48170629 T>A maps to NM_003215.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:38776688 T>G maps to NM_030956.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:38776688 T>G maps to NM_030956.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:32557332 C>G maps to NM_018056.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:32557332 C>G maps to NM_018056.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:189590691 G>A maps to NM_003722.4 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:189590691 G>A maps to NM_003722.4 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:118006122 C>A maps to NM_152402.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:118006122 C>A maps to NM_152402.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:73012715 C>A maps to NM_013381.2 Y744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:73012715 C>A maps to NM_013381.2 Y744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:180651800 C>T maps to NM_033549.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:180651800 C>T maps to NM_033549.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:2104433 A>G maps to NM_000548.3 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:2104433 A>G maps to NM_000548.3 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:50251356 G>T maps to NM_021733.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:50251356 G>T maps to NM_021733.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20757804 G>T maps to NM_138376.2 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20757804 G>T maps to NM_138376.2 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:69692147 G>T maps to NM_001075.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:69692147 G>T maps to NM_001075.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:216017806 G>A maps to ENST00000366943 V3029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:216017806 G>A maps to ENST00000366943 V3029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:184654066 G>T maps to ENST00000437079 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:184654066 G>T maps to ENST00000437079 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:71134994 A>G maps to NM_022479.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:71134994 A>G maps to NM_022479.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:1126035 C>G maps to ENST00000416775 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:1126035 C>G maps to ENST00000416775 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37734244 G>A maps to NM_152604.1 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37734244 G>A maps to NM_152604.1 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37619575 T>C maps to NM_144689.3 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37619575 T>C maps to NM_144689.3 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37314610 T>A maps to NM_206894.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37314610 T>A maps to NM_206894.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:220396523 G>T maps to NM_018674.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:220396523 G>T maps to NM_018674.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20429493 G>C maps to NM_017888.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20429493 G>C maps to NM_017888.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:207452813 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:207452813 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:148038040 A>C maps to NM_002025.3 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:148038040 A>C maps to NM_002025.3 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:27292957 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:27292957 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:61910346 G>T maps to NM_175609.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:61910346 G>T maps to NM_175609.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:9540190 G>T maps to NM_003887.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:9540190 G>T maps to NM_003887.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:197112564 C>A maps to NM_018136.4 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:197112564 C>A maps to NM_018136.4 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:31323960 C>T maps to NM_030632.1 A1383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:31323960 C>T maps to NM_030632.1 A1383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:64678616 C>A maps to ENST00000421419 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:64678616 C>A maps to ENST00000421419 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:160061466 G>T maps to NM_025153.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:160061466 G>T maps to NM_025153.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:10444021 C>G maps to NM_001001331.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:10444021 C>G maps to NM_001001331.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:10917754 G>A maps to NM_001039362.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:10917754 G>A maps to NM_001039362.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:80838876 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:80838876 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:55472786 C>T maps to NM_057176.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:55472786 C>T maps to NM_057176.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:61541489 G>T maps to NM_001127392.1 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:61541489 G>T maps to NM_001127392.1 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:75086593 G>C maps to NM_001002912.4 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:75086593 G>C maps to NM_001002912.4 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:41154095 C>A maps to NM_001115131.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:41154095 C>A maps to NM_001115131.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:97823055 C>A maps to NM_001193329.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:97823055 C>A maps to NM_001193329.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:81667467 C>G maps to NM_000722.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:81667467 C>G maps to NM_000722.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:115080336 G>A maps to NM_014333.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:115080336 G>A maps to NM_014333.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:124857202 C>T maps to NM_025004.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:124857202 C>T maps to NM_025004.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:45104117 G>C maps to NM_001029835.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:45104117 G>C maps to NM_001029835.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160535530 C>A maps to NM_001184879.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160535530 C>A maps to NM_001184879.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:202671455 C>A maps to ENST00000450471 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:202671455 C>A maps to ENST00000450471 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:101090478 C>T maps to NM_020348.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:101090478 C>T maps to NM_020348.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:55932125 C>A maps to NM_030820.3 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:55932125 C>A maps to NM_030820.3 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:47423461 G>T maps to NM_001848.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:47423461 G>T maps to NM_001848.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:8616158 C>T maps to NM_001014447.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:8616158 C>T maps to NM_001014447.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:114326963 A>T maps to NM_198123.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:114326963 A>T maps to NM_198123.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:56099045 C>G maps to ENST00000423479 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:56099045 C>G maps to ENST00000423479 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117432193 G>T maps to NM_033427.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117432193 G>T maps to NM_033427.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:16942696 C>A maps to NM_001081.3 L2779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:16942696 C>A maps to NM_001081.3 L2779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:59112609 A>G maps to NM_016651.5 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:59112609 A>G maps to NM_016651.5 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:66963857 C>T maps to NM_033105.4 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:66963857 C>T maps to NM_033105.4 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:169446012 G>A maps to NM_004946.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:169446012 G>A maps to NM_004946.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:71839887 C>T maps to NM_001130987.1 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:71839887 C>T maps to NM_001130987.1 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:130586660 C>G maps to NM_001114753.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:130586660 C>G maps to NM_001114753.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:132498100 G>T maps to ENST00000333577 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:132498100 G>T maps to ENST00000333577 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:45702912 C>A maps to ENST00000360649 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:45702912 C>A maps to ENST00000360649 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:82437305 G>T maps to NM_001105281.1 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:82437305 G>T maps to NM_001105281.1 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:139209828 A>T maps to NM_015912.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:139209828 A>T maps to NM_015912.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:179013191 G>A maps to NM_014864.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:179013191 G>A maps to NM_014864.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:125052163 C>A maps to NM_001039112.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:125052163 C>A maps to NM_001039112.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:34335225 G>T maps to NM_025135.2 R1284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:34335225 G>T maps to NM_025135.2 R1284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:84606401 T>C maps to NM_001001670.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:84606401 T>C maps to NM_001001670.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:79373506 A>T maps to NM_025074.6 P2254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:79373506 A>T maps to NM_025074.6 P2254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:78425922 G>A maps to ENST00000436586 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:78425922 G>A maps to ENST00000436586 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:85712181 A>G maps to NM_016095.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:85712181 A>G maps to NM_016095.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:47845054 G>T maps to NM_018485.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:47845054 G>T maps to NM_018485.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:146480614 C>A maps to NM_000838.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:146480614 C>A maps to NM_000838.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:51486790 G>T maps to NM_018094.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:51486790 G>T maps to NM_018094.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:37227728 C>A maps to NM_019024.1 E1849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:37227728 C>A maps to NM_019024.1 E1849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:175443104 T>C maps to NM_000860.4 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:175443104 T>C maps to NM_000860.4 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:35874575 C>A maps to NM_002185.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:35874575 C>A maps to NM_002185.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:128584606 G>A maps to NM_015693.3 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:128584606 G>A maps to NM_015693.3 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:196227444 A>C maps to NM_198503.2 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:196227444 A>C maps to NM_198503.2 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:5486894 G>T maps to NM_015325.1 S2194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:5486894 G>T maps to NM_015325.1 S2194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:94060028 G>A maps to ENST00000393153 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:94060028 G>A maps to ENST00000393153 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:39739907 C>T maps to NM_000526.4 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:39739907 C>T maps to NM_000526.4 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:55143392 C>G maps to ENST00000427581 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:55143392 C>G maps to ENST00000427581 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:140995719 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:140995719 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:50121501 T>C maps to NM_001006939.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:50121501 T>C maps to NM_001006939.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:131670204 G>T maps to NM_001127244.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:131670204 G>T maps to NM_001127244.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:7965608 G>A maps to NM_025061.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:7965608 G>A maps to NM_025061.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:131943062 T>A maps to ENST00000403834 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:131943062 T>A maps to ENST00000403834 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:4965099 G>T maps to NM_001100600.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:4965099 G>T maps to NM_001100600.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:89209451 G>T maps to NM_005941.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:89209451 G>T maps to NM_005941.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:42883391 A>T maps to ENST00000405094 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:42883391 A>T maps to ENST00000405094 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:52509063 T>A maps to NM_007361.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:52509063 T>A maps to NM_007361.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:120097541 G>A maps to NM_178507.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:120097541 G>A maps to NM_178507.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:144015558 G>A maps to NM_001005287.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:144015558 G>A maps to NM_001005287.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:248458340 G>A maps to NM_001004692.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:248458340 G>A maps to NM_001004692.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:248458343 G>C maps to NM_001004692.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:248458343 G>C maps to NM_001004692.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:59225047 G>T maps to NM_001004708.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:59225047 G>T maps to NM_001004708.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:20612415 C>A maps to NM_001004724.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:20612415 C>A maps to NM_001004724.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:3121424 C>T maps to NM_020896.3 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:3121424 C>T maps to NM_020896.3 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:26683599 C>A maps to NM_194248.2 E1910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:26683599 C>A maps to NM_194248.2 E1910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:17666216 G>A maps to NM_012387.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:17666216 G>A maps to NM_012387.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:176762717 T>C maps to NM_020318.2 C1681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:176762717 T>C maps to NM_020318.2 C1681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:140256412 G>T maps to NM_018903.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:140256412 G>T maps to NM_018903.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:42284448 G>T maps to NM_138370.2 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:42284448 G>T maps to NM_138370.2 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:208270153 C>A maps to NM_025179.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:208270153 C>A maps to NM_025179.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:89860636 G>C maps to NM_172240.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:89860636 G>C maps to NM_172240.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526568 G>T maps to NM_020227.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526568 G>T maps to NM_020227.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526585 G>A maps to NM_020227.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526585 G>A maps to NM_020227.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:52781373 G>T maps to NM_000956.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:52781373 G>T maps to NM_000956.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:104897786 C>G maps to NM_001100117.2 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:104897786 C>G maps to NM_001100117.2 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:92999138 T>G maps to NM_175634.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:92999138 T>G maps to NM_175634.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:237813178 A>G maps to NM_001035.2 A2505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:237813178 A>G maps to NM_001035.2 A2505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:33936677 C>T maps to NM_001036.3 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:33936677 C>T maps to NM_001036.3 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:1551450 C>A maps to NM_006065.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:1551450 C>A maps to NM_006065.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:48381722 A>G maps to NM_020846.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:48381722 A>G maps to NM_020846.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:56913483 C>T maps to NM_000339.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:56913483 C>T maps to NM_000339.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:138718264 C>T maps to NM_152685.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:138718264 C>T maps to NM_152685.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:55729297 G>A maps to NM_001043.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:55729297 G>A maps to NM_001043.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:21033900 C>T maps to NM_019844.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:21033900 C>T maps to NM_019844.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:130064042 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:130064042 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:39959769 C>T maps to NM_003169.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:39959769 C>T maps to NM_003169.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:223465925 T>C maps to NM_017982.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:223465925 T>C maps to NM_017982.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:46660739 G>C maps to NM_001010870.2 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:46660739 G>C maps to NM_001010870.2 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:32537364 C>A maps to NM_003253.2 E969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:32537364 C>A maps to NM_003253.2 E969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:28656338 G>A maps to NM_206832.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:28656338 G>A maps to NM_206832.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:7577608 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:7577608 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:50485614 T>A maps to NM_001080447.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:50485614 T>A maps to NM_001080447.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:179449531 A>C maps to NM_133378.4 A19044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:179449531 A>C maps to NM_133378.4 A19044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:70160246 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:70160246 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:33510507 G>T maps to NM_173167.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:33510507 G>T maps to NM_173167.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:48646609 A>G maps to NM_003365.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:48646609 A>G maps to NM_003365.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:133073885 G>C maps to NM_004665.2 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:133073885 G>C maps to NM_004665.2 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:79908411 A>G maps to ENST00000376646 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:79908411 A>G maps to ENST00000376646 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:168549358 G>A maps to NM_002995.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:168549358 G>A maps to NM_002995.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:168511286 C>T maps to NM_003175.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:168511286 C>T maps to NM_003175.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:69197846 C>A maps to NM_001031732.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:69197846 C>A maps to NM_001031732.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:2407790 G>A maps to NM_004729.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:2407790 G>A maps to NM_004729.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:128975780 C>A maps to NM_016032.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:128975780 C>A maps to NM_016032.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:11978561 C>T maps to NM_152262.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:11978561 C>T maps to NM_152262.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153008743 G>A maps to NM_000033.3 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153008743 G>A maps to NM_000033.3 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:44064971 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:44064971 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:43743797 G>A maps to NM_016006.4 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:43743797 G>A maps to NM_016006.4 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:20497894 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:20497894 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:25003718 T>A maps to NM_032501.2 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:25003718 T>A maps to NM_032501.2 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:39027464 A>T maps to NM_145004.5 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:39027464 A>T maps to NM_145004.5 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:5306771 C>A maps to NM_139056.2 C1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:5306771 C>A maps to NM_139056.2 C1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:905425 C>A maps to NM_001117.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:905425 C>A maps to NM_001117.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:112838131 G>T maps to NM_000681.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:112838131 G>T maps to NM_000681.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:236706530 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:236706530 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:89351665 G>A maps to NM_013275.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:89351665 G>A maps to NM_013275.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:48866731 A>G maps to NM_012404.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:48866731 A>G maps to NM_012404.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:183894822 G>C maps to ENST00000411763 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:183894822 G>C maps to ENST00000411763 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:9463316 G>T maps to NM_003887.2 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:9463316 G>T maps to NM_003887.2 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:101166052 T>A maps to NM_006828.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:101166052 T>A maps to NM_006828.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:155449758 T>A maps to ENST00000368346 K968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:155449758 T>A maps to ENST00000368346 K968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176934373 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176934373 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47571098 G>C maps to NM_020453.3 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47571098 G>C maps to NM_020453.3 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:76920184 C>A maps to NM_000489.3 E1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:76920184 C>A maps to NM_000489.3 E1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:32193110 G>T maps to NM_001703.2 P1556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:32193110 G>T maps to NM_001703.2 P1556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:97949369 G>A maps to NM_018842.4 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:97949369 G>A maps to NM_018842.4 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:171504658 C>T maps to ENST00000392078 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:171504658 C>T maps to ENST00000392078 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:88683406 C>T maps to NM_004329.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:88683406 C>T maps to NM_004329.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:74196469 C>A maps to NM_001043318.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:74196469 C>A maps to NM_001043318.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:24923235 C>A maps to NM_018958.2 S741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:24923235 C>A maps to NM_018958.2 S741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:55158163 G>T maps to ENST00000454855 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:55158163 G>T maps to ENST00000454855 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:109191531 C>A maps to ENST00000370031 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:109191531 C>A maps to ENST00000370031 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:41195922 G>T maps to NM_001115131.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:41195922 G>T maps to NM_001115131.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:5431904 G>A maps to NM_018465.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:5431904 G>A maps to NM_018465.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:49713293 C>T maps to NM_001082534.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:49713293 C>T maps to NM_001082534.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:2949712 C>T maps to NM_032415.4 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:2949712 C>T maps to NM_032415.4 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:44483092 G>A maps to ENST00000398168 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:44483092 G>A maps to ENST00000398168 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:180381657 T>A maps to NM_181426.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:180381657 T>A maps to NM_181426.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61833628 C>A maps to NM_020198.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61833628 C>A maps to NM_020198.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:119942924 C>A maps to NM_178499.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:119942924 C>A maps to NM_178499.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32657240 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32657240 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:72005146 C>A maps to NM_030813.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:72005146 C>A maps to NM_030813.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:70894798 G>T maps to NM_001858.4 G950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:70894798 G>T maps to NM_001858.4 G950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:189925509 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:189925509 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:3691503 C>T maps to ENST00000418971 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:3691503 C>T maps to ENST00000418971 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:131283073 G>T maps to ENST00000502818 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:131283073 G>T maps to ENST00000502818 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61988147 C>T maps to NM_022579.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61988147 C>T maps to NM_022579.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:113326135 T>A maps to NM_198123.1 I2565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:113326135 T>A maps to NM_198123.1 I2565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:100087794 C>A maps to ENST00000415585 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:100087794 C>A maps to ENST00000415585 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:37658309 C>T maps to NM_000397.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:37658309 C>T maps to NM_000397.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:143957749 G>T maps to ENST00000377675 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:143957749 G>T maps to ENST00000377675 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:172337512 A>G maps to NM_025000.3 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:172337512 A>G maps to NM_025000.3 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:41984937 G>T maps to NM_001029955.3 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:41984937 G>T maps to NM_001029955.3 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:49989687 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:49989687 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:71146759 G>A maps to NM_001360.2 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:71146759 G>A maps to NM_001360.2 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:41597598 G>T maps to NM_004941.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:41597598 G>T maps to NM_004941.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:223178056 C>T maps to NM_032890.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:223178056 C>T maps to NM_032890.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:28906835 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:28906835 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:29054363 T>A maps to NM_001944.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:29054363 T>A maps to NM_001944.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:49644011 C>A maps to NM_024593.3 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:49644011 C>A maps to NM_024593.3 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:101063284 G>T maps to ENST00000397927 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:101063284 G>T maps to ENST00000397927 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:71425015 C>A maps to NM_017669.2 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:71425015 C>A maps to NM_017669.2 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:15883598 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:15883598 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:92088205 C>G maps to ENST00000298047 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:92088205 C>G maps to ENST00000298047 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:161188513 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:161188513 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:125047631 G>T maps to NM_001039112.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:125047631 G>T maps to NM_001039112.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:138665315 G>A maps to NM_023067.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:138665315 G>A maps to NM_023067.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:12736043 T>C maps to ENST00000429478 D1023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:12736043 T>C maps to ENST00000429478 D1023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:40018854 C>A maps to NM_152597.4 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:40018854 C>A maps to NM_152597.4 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:151166232 C>T maps to NM_198395.1 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:151166232 C>T maps to NM_198395.1 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46060348 G>A maps to NM_173536.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46060348 G>A maps to NM_173536.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:89732128 T>C maps to NM_052942.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:89732128 T>C maps to NM_052942.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:158409160 C>T maps to ENST00000264263 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:158409160 C>T maps to ENST00000264263 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:168066240 G>A maps to NM_153832.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:168066240 G>A maps to NM_153832.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:11728878 G>T maps to NM_014668.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:11728878 G>T maps to NM_014668.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:144714906 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:144714906 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:108631888 C>A maps to ENST00000218006 E929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:108631888 C>A maps to ENST00000218006 E929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:45262166 T>C maps to NM_021072.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:45262166 T>C maps to NM_021072.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:124732514 G>A maps to NM_020733.1 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:124732514 G>A maps to NM_020733.1 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:43227462 G>A maps to NM_006460.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:43227462 G>A maps to NM_006460.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43042430 G>C maps to ENST00000338692 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43042430 G>C maps to ENST00000338692 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:60791901 C>A maps to ENST00000317393 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:60791901 C>A maps to ENST00000317393 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:120056731 C>A maps to ENST00000235547 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:120056731 C>A maps to ENST00000235547 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:147889329 G>C maps to NM_001040173.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:147889329 G>C maps to NM_001040173.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:130411006 C>A maps to NM_001170961.1 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:130411006 C>A maps to NM_001170961.1 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:113742502 C>A maps to NM_019618.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:113742502 C>A maps to NM_019618.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:55201964 C>A maps to NM_139017.4 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:55201964 C>A maps to NM_139017.4 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31391127 G>T maps to NM_000887.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31391127 G>T maps to NM_000887.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:54817377 A>G maps to NM_198510.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:54817377 A>G maps to NM_198510.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:44627235 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:44627235 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:163374549 T>C maps to NM_033272.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:163374549 T>C maps to NM_033272.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:55971026 A>T maps to NM_002253.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:55971026 A>T maps to NM_002253.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:70681522 C>A maps to NM_020866.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:70681522 C>A maps to NM_020866.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:143685269 A>G maps to NM_003937.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:143685269 A>G maps to NM_003937.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:95557397 G>A maps to NM_005097.2 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:95557397 G>A maps to NM_005097.2 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:19809434 G>C maps to NM_000237.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:19809434 G>C maps to NM_000237.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:46894954 G>T maps to ENST00000256991 P1518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:46894954 G>T maps to ENST00000256991 P1518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:74507408 C>A maps to NM_001105659.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:74507408 C>A maps to NM_001105659.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:71493792 C>A maps to NM_005909.3 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:71493792 C>A maps to NM_005909.3 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:39086174 G>A maps to NM_001042600.1 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:39086174 G>A maps to NM_001042600.1 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:87019675 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:87019675 C>T did not map to a codon.
Alternatively spliced codon TCGA-50-6594-01A-11D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-50-6594-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:13825811 C>A maps to NM_005913.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:13825811 C>A maps to NM_005913.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:47530667 C>A maps to NM_001113498.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:47530667 C>A maps to NM_001113498.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:70341001 G>A maps to ENST00000333646 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:70341001 G>A maps to ENST00000333646 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88766961 A>T maps to ENST00000395102 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88766961 A>T maps to ENST00000395102 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:112786077 G>A maps to NM_006343.2 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:112786077 G>A maps to NM_006343.2 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:29627267 T>C maps to NM_002433.4 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:29627267 T>C maps to NM_002433.4 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:138395819 G>T maps to NM_016034.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:138395819 G>T maps to NM_016034.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:59947339 C>A maps to NM_152852.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:59947339 C>A maps to NM_152852.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:76867813 C>T maps to NM_000260.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:76867813 C>T maps to NM_000260.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:15372559 G>T maps to NM_015909.2 A2074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:15372559 G>T maps to NM_015909.2 A2074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:6631033 C>G maps to NM_014865.3 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:6631033 C>G maps to NM_014865.3 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:233791841 C>A maps to NM_019850.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:233791841 C>A maps to NM_019850.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:47583904 C>T maps to NM_002507.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:47583904 C>T maps to NM_002507.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:23060867 C>A maps to NM_144599.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:23060867 C>A maps to NM_144599.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:63502280 G>T maps to NM_173688.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:63502280 G>T maps to NM_173688.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:10041187 A>G maps to NM_022787.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:10041187 A>G maps to NM_022787.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:135102362 C>A maps to NM_032536.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:135102362 C>A maps to NM_032536.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24884536 C>A maps to NM_025081.2 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24884536 C>A maps to NM_025081.2 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:158435354 G>T maps to NM_001004473.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:158435354 G>T maps to NM_001004473.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:130678718 C>A maps to NM_001004486.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:130678718 C>A maps to NM_001004486.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:248436888 C>G maps to NM_001004695.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:248436888 C>G maps to NM_001004695.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:6007392 A>G maps to NM_001005173.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:6007392 A>G maps to NM_001005173.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:57799281 G>T maps to NM_001005186.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:57799281 G>T maps to NM_001005186.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:123777146 A>T maps to NM_001005197.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:123777146 A>T maps to NM_001005197.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:201800585 C>A maps to NM_006190.4 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:201800585 C>A maps to NM_006190.4 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:43535035 G>C maps to NM_006451.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:43535035 G>C maps to NM_006451.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:73733265 C>G maps to ENST00000427855 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:73733265 C>G maps to ENST00000427855 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176709300 G>T maps to NM_020318.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176709300 G>T maps to NM_020318.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:55626443 A>T maps to NM_001142763.1 T1230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:55626443 A>T maps to NM_001142763.1 T1230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:30723484 G>T maps to NM_001173523.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:30723484 G>T maps to NM_001173523.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:140182887 C>T maps to NM_018906.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:140182887 C>T maps to NM_018906.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:82585287 C>A maps to NM_033026.5 G1661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:82585287 C>A maps to NM_033026.5 G1661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:57325335 C>A maps to NM_006210.2 E1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:57325335 C>A maps to NM_006210.2 E1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:133806688 G>A maps to ENST00000395386 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:133806688 G>A maps to ENST00000395386 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:128812263 A>T maps to NM_014264.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:128812263 A>T maps to NM_014264.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:44540079 G>A maps to NM_006227.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:44540079 G>A maps to NM_006227.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:129275993 T>A maps to NM_015103.2 K1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:129275993 T>A maps to NM_015103.2 K1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12854357 T>A maps to NM_023013.2 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12854357 T>A maps to NM_023013.2 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:156770210 A>T maps to NM_005973.4 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:156770210 A>T maps to NM_005973.4 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:82125933 C>A maps to NM_006259.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:82125933 C>A maps to NM_006259.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:214170993 G>T maps to NM_002763.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:214170993 G>T maps to NM_002763.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:157387959 C>T maps to NM_002847.3 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:157387959 C>T maps to NM_002847.3 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:52366223 T>A maps to NM_144651.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:52366223 T>A maps to NM_144651.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:107100453 A>G maps to NM_018292.4 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:107100453 A>G maps to NM_018292.4 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:108496517 T>A maps to NM_182588.2 L1673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:108496517 T>A maps to NM_182588.2 L1673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:25404637 G>A maps to ENST00000381927 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:25404637 G>A maps to ENST00000381927 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:68895517 G>T maps to NM_000329.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:68895517 G>T maps to NM_000329.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:68904917 C>A maps to NM_000329.2 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:68904917 C>A maps to NM_000329.2 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237732577 C>A maps to NM_001035.2 S1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237732577 C>A maps to NM_001035.2 S1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:130535489 T>A maps to ENST00000457563 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:130535489 T>A maps to ENST00000457563 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:76882213 T>C maps to NM_018115.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:76882213 T>C maps to NM_018115.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:115814323 G>A maps to ENST00000257414 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:115814323 G>A maps to ENST00000257414 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43851751 T>C maps to NM_003008.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43851751 T>C maps to NM_003008.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:8234235 T>A maps to NM_001080826.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:8234235 T>A maps to NM_001080826.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:3677377 G>T maps to NM_023068.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:3677377 G>T maps to NM_023068.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:232568020 C>A maps to NM_020808.3 E1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:232568020 C>A maps to NM_020808.3 E1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:45362392 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:45362392 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:48762038 C>A maps to ENST00000452555 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:48762038 C>A maps to ENST00000452555 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:11078612 C>A maps to NM_003042.3 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:11078612 C>A maps to NM_003042.3 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:34205715 C>A maps to NM_003116.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:34205715 C>A maps to NM_003116.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:121311045 G>T maps to NM_152546.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:121311045 G>T maps to NM_152546.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:7712287 G>T maps to ENST00000441779 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:7712287 G>T maps to ENST00000441779 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:48558669 G>A maps to NM_003173.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:48558669 G>A maps to NM_003173.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:46330800 G>A maps to NM_004819.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:46330800 G>A maps to NM_004819.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:75276687 G>A maps to NM_001058.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:75276687 G>A maps to NM_001058.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:9629952 G>C maps to NM_019599.2 Y64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:9629952 G>C maps to NM_019599.2 Y64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:120983878 C>A maps to NM_005422.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:120983878 C>A maps to NM_005422.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:50791265 G>T maps to ENST00000263046 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:50791265 G>T maps to ENST00000263046 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:169648613 G>A maps to NM_003247.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:169648613 G>A maps to NM_003247.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:155167904 C>A maps to NM_007112.3 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:155167904 C>A maps to NM_007112.3 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:129563212 C>A maps to NM_133448.2 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:129563212 C>A maps to NM_133448.2 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:175049401 C>A maps to NM_022093.1 Y296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:175049401 C>A maps to NM_022093.1 Y296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:43857595 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:43857595 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:142967582 G>T maps to NM_001012989.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:142967582 G>T maps to NM_001012989.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:96137360 T>A maps to NM_003728.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:96137360 T>A maps to NM_003728.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:216262460 A>G maps to ENST00000366943 T1593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:216262460 A>G maps to ENST00000366943 T1593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:41088906 C>T maps to NM_001039590.2 Q2436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:41088906 C>T maps to NM_001039590.2 Q2436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129063439 G>A maps to NM_006649.3 K724K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129063439 G>A maps to NM_006649.3 K724K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:100168775 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:100168775 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43355731 C>A maps to NM_003881.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43355731 C>A maps to NM_003881.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:119389208 C>T maps to NM_001184742.1 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:119389208 C>T maps to NM_001184742.1 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:111698204 A>T maps to NM_001004308.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:111698204 A>T maps to NM_001004308.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:49557648 G>T maps to NM_015069.2 V1237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:49557648 G>T maps to NM_015069.2 V1237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:178392949 G>A maps to NM_182594.2 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:178392949 G>A maps to NM_182594.2 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:57187551 C>A maps to NM_033273.1 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:57187551 C>A maps to NM_033273.1 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:56114164 G>T maps to NM_153219.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:56114164 G>T maps to NM_153219.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:131309042 G>A maps to NM_001009185.1 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:131309042 G>A maps to NM_001009185.1 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:151670665 C>A maps to NM_005100.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:151670665 C>A maps to NM_005100.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr21:27372471 C>A maps to NM_000484.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr21:27372471 C>A maps to NM_000484.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:111750307 C>T maps to NM_022761.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:111750307 C>T maps to NM_022761.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr14:81251328 C>A maps to NM_152446.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr14:81251328 C>A maps to NM_152446.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:60885645 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:60885645 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:29104408 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:29104408 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:73316466 G>T maps to NM_002086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:73316466 G>T maps to NM_002086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:26156806 G>A maps to NM_005321.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:26156806 G>A maps to NM_005321.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:39789086 G>A maps to NM_172140.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:39789086 G>A maps to NM_172140.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:78674703 G>A maps to NM_001161352.1 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:78674703 G>A maps to NM_001161352.1 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:173735413 C>T maps to NM_014458.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:173735413 C>T maps to NM_014458.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:39092762 A>G maps to NM_015515.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:39092762 A>G maps to NM_015515.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:54967152 C>A maps to ENST00000431846 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:54967152 C>A maps to ENST00000431846 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr3:45637519 C>G maps to NM_014240.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr3:45637519 C>G maps to NM_014240.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:8968944 G>T maps to NM_024690.2 L14357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:8968944 G>T maps to NM_024690.2 L14357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:109707854 C>T maps to NM_015011.1 Q1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:109707854 C>T maps to NM_015011.1 Q1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:56539578 G>C maps to NM_153447.4 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:56539578 G>C maps to NM_153447.4 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:78413334 G>T maps to NM_001098816.2 V1441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:78413334 G>T maps to NM_001098816.2 V1441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:50111357 G>A maps to ENST00000505697 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:50111357 G>A maps to ENST00000505697 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:76624846 C>A maps to NM_003719.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:76624846 C>A maps to NM_003719.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr3:184081292 C>T maps to NM_006232.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr3:184081292 C>T maps to NM_006232.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:50118928 C>A maps to NM_018191.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:50118928 C>A maps to NM_018191.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:19312473 G>A maps to NM_003721.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:19312473 G>A maps to NM_003721.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:46713256 G>A maps to NM_006915.2 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:46713256 G>A maps to NM_006915.2 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:92374657 C>T maps to NM_134266.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:92374657 C>T maps to NM_134266.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:17421113 T>C maps to NM_001164771.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:17421113 T>C maps to NM_001164771.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:64472703 G>A maps to NM_020762.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:64472703 G>A maps to NM_020762.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr9:35717690 C>A maps to NM_006289.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr9:35717690 C>A maps to NM_006289.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:100453665 C>A maps to NM_015054.1 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:100453665 C>A maps to NM_015054.1 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:65445188 C>T maps to NM_007191.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:65445188 C>T maps to NM_007191.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:62364616 C>T maps to NM_032527.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:62364616 C>T maps to NM_032527.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:44681619 C>T maps to NM_001032372.1 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:44681619 C>T maps to NM_001032372.1 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:50548236 A>T maps to NM_015428.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:50548236 A>T maps to NM_015428.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:146791526 G>A maps to ENST00000508784 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:146791526 G>A maps to ENST00000508784 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:47261719 G>A maps to NM_001610.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:47261719 G>A maps to NM_001610.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:77327094 G>A maps to NM_194287.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:77327094 G>A maps to NM_194287.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:62187705 C>T maps to NM_024059.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:62187705 C>T maps to NM_024059.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:96281432 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:96281432 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:143028370 C>A maps to NM_000083.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:143028370 C>A maps to NM_000083.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:38840726 G>A maps to ENST00000327475 W2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:38840726 G>A maps to ENST00000327475 W2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:27332766 G>A maps to NM_052943.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:27332766 G>A maps to NM_052943.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:65156897 C>A maps to NM_031904.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:65156897 C>A maps to NM_031904.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:7866403 G>A maps to NM_017545.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:7866403 G>A maps to NM_017545.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:29911193 C>T maps to ENST00000376806 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:29911193 C>T maps to ENST00000376806 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:186057108 G>T maps to NM_031935.2 G3137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:186057108 G>T maps to NM_031935.2 G3137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:46627240 G>T maps to NM_207393.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:46627240 G>T maps to NM_207393.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:38824041 G>A maps to NM_152868.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:38824041 G>A maps to NM_152868.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:142640390 G>A maps to NM_000420.2 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:142640390 G>A maps to NM_000420.2 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:5811409 C>T maps to ENST00000381093 W653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:5811409 C>T maps to ENST00000381093 W653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:15102637 C>T maps to NM_015027.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:15102637 C>T maps to NM_015027.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:153698804 G>C maps to NM_017514.3 V1669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:153698804 G>C maps to NM_017514.3 V1669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:15142887 G>A maps to NM_000304.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:15142887 G>A maps to NM_000304.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:48368170 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:48368170 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:85597693 T>C maps to NM_152573.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:85597693 T>C maps to NM_152573.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:29834950 C>T maps to NM_021026.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:29834950 C>T maps to NM_021026.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:64533556 G>C maps to NM_201995.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:64533556 G>C maps to NM_201995.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:115651959 G>A maps to NM_033051.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:115651959 G>A maps to NM_033051.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:144905472 C>A maps to NM_001144010.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:144905472 C>A maps to NM_001144010.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr13:37427570 C>T maps to NM_001127217.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr13:37427570 C>T maps to NM_001127217.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:38798355 G>T maps to NM_003263.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:38798355 G>T maps to NM_003263.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:28996324 G>A maps to NM_014817.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:28996324 G>A maps to NM_014817.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:189012796 G>A maps to ENST00000326754 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:189012796 G>A maps to ENST00000326754 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:231064839 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:231064839 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:215963478 C>T maps to ENST00000366943 Q3368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:215963478 C>T maps to ENST00000366943 Q3368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:219301246 G>A maps to NM_007127.2 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:219301246 G>A maps to NM_007127.2 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:120969619 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:120969619 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr3:142133084 G>A maps to NM_019001.3 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr3:142133084 G>A maps to NM_019001.3 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:44495994 G>A maps to NM_003445.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:44495994 G>A maps to NM_003445.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:114293153 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:114293153 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:61555353 G>T maps to NM_000789.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:61555353 G>T maps to NM_000789.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20636756 C>A maps to NM_052956.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20636756 C>A maps to NM_052956.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:43856733 C>T maps to ENST00000389420 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:43856733 C>T maps to ENST00000389420 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:7690925 G>T maps to NM_020546.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:7690925 G>T maps to NM_020546.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:7727284 C>T maps to NM_020546.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:7727284 C>T maps to NM_020546.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:230845984 C>A maps to NM_000029.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:230845984 C>A maps to NM_000029.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:47471975 A>G maps to NM_001143668.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:47471975 A>G maps to NM_001143668.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:61874083 T>C maps to NM_020987.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:61874083 T>C maps to NM_020987.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:165118749 T>A maps to NM_012403.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:165118749 T>A maps to NM_012403.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:69304604 A>G maps to NM_032208.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:69304604 A>G maps to NM_032208.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:28260242 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:28260242 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:11382131 A>G maps to NM_006395.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:11382131 A>G maps to NM_006395.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:11911909 G>T maps to NM_153256.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:11911909 G>T maps to NM_153256.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:81428996 G>A maps to ENST00000458088 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:81428996 G>A maps to ENST00000458088 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:30554588 C>A maps to NM_001105528.1 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:30554588 C>A maps to NM_001105528.1 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:31661395 G>T maps to NM_182658.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:31661395 G>T maps to NM_182658.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:3340198 C>T maps to NM_001009984.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:3340198 C>T maps to NM_001009984.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:73825445 C>T maps to ENST00000334126 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:73825445 C>T maps to ENST00000334126 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:97597754 C>T maps to NM_198468.2 W1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:97597754 C>T maps to NM_198468.2 W1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:122261549 C>A maps to NM_001167940.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:122261549 C>A maps to NM_001167940.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:76993152 C>T maps to NM_138793.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:76993152 C>T maps to NM_138793.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:97779093 T>C maps to NM_001159747.1 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:97779093 T>C maps to NM_001159747.1 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42761275 C>A maps to NM_144609.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42761275 C>A maps to NM_144609.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:72540856 C>T maps to NM_006678.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:72540856 C>T maps to NM_006678.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:103412023 G>C maps to NM_006035.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:103412023 G>C maps to NM_006035.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:31294118 A>G maps to NM_004932.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:31294118 A>G maps to NM_004932.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:123920101 A>C maps to NM_007018.4 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:123920101 A>C maps to NM_007018.4 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:150932244 C>A maps to NM_019015.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:150932244 C>A maps to NM_019015.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:95677188 C>G maps to NM_024734.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:95677188 C>G maps to NM_024734.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:140277664 C>T maps to NM_022131.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:140277664 C>T maps to NM_022131.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:108686655 C>T maps to NM_001142344.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:108686655 C>T maps to NM_001142344.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:58580243 G>C maps to NM_016284.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:58580243 G>C maps to NM_016284.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207867884 G>A maps to NM_175710.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207867884 G>A maps to NM_175710.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:137586169 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:137586169 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:113651000 A>G maps to NM_198123.1 Y1150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:113651000 A>G maps to NM_198123.1 Y1150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:113275988 T>A maps to NM_198123.1 T3247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:113275988 T>A maps to NM_198123.1 T3247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:35327985 C>A maps to NM_001198778.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:35327985 C>A maps to NM_001198778.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:76927398 A>T maps to NM_002416.1 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:76927398 A>T maps to NM_002416.1 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:99358456 A>C maps to NM_017460.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:99358456 A>C maps to NM_017460.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:169348278 A>T maps to NM_001012967.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:169348278 A>T maps to NM_001012967.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:14661112 G>A maps to NM_004080.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:14661112 G>A maps to NM_004080.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:107845747 T>A maps to NM_014421.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:107845747 T>A maps to NM_014421.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118971089 C>A maps to NM_001382.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118971089 C>A maps to NM_001382.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:41948216 C>T maps to NM_001956.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:41948216 C>T maps to NM_001956.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:82533697 C>A maps to NM_024580.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:82533697 C>A maps to NM_024580.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:117658740 C>A maps to ENST00000411422 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:117658740 C>A maps to ENST00000411422 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:42530317 A>G maps to NM_019063.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:42530317 A>G maps to NM_019063.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:53668749 C>G maps to NM_012291.4 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:53668749 C>G maps to NM_012291.4 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:175919293 G>A maps to NM_014613.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:175919293 G>A maps to NM_014613.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:49042449 C>A maps to ENST00000336769 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:49042449 C>A maps to ENST00000336769 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:163055369 A>T maps to NM_004460.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:163055369 A>T maps to NM_004460.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:29486612 C>T maps to NM_018099.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:29486612 C>T maps to NM_018099.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:32735076 T>C maps to NM_139241.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:32735076 T>C maps to NM_139241.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:45603641 T>A maps to NM_002013.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:45603641 T>A maps to NM_002013.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:84607512 C>T maps to NM_001001670.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:84607512 C>T maps to NM_001001670.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:46376129 A>T maps to NM_004497.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:46376129 A>T maps to NM_004497.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118851197 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118851197 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:37724226 T>C maps to NM_014907.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:37724226 T>C maps to NM_014907.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:32776614 A>T maps to NM_023037.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:32776614 A>T maps to NM_023037.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:52779454 G>A maps to NM_013409.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:52779454 G>A maps to NM_013409.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:61995376 G>T maps to NM_000515.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:61995376 G>T maps to NM_000515.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:14627185 C>T maps to NM_002063.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:14627185 C>T maps to NM_002063.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:44713077 T>C maps to NM_138335.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:44713077 T>C maps to NM_138335.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:55543669 C>G maps to NM_001083899.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:55543669 C>G maps to NM_001083899.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973450 C>T maps to NM_015698.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973450 C>T maps to NM_015698.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:26534033 G>C maps to NM_001145168.1 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:26534033 G>C maps to NM_001145168.1 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:47682492 C>T maps to NM_153838.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:47682492 C>T maps to NM_153838.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:41554924 C>G maps to NM_005300.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:41554924 C>G maps to NM_005300.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:122641019 C>T maps to NM_005328.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:122641019 C>T maps to NM_005328.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:37302746 G>A maps to NM_019024.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:37302746 G>A maps to NM_019024.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:58134603 C>T maps to NM_022070.4 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:58134603 C>T maps to NM_022070.4 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:27782452 G>T maps to NM_021066.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:27782452 G>T maps to NM_021066.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:143080971 G>C maps to NM_006734.3 Y2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:143080971 G>C maps to NM_006734.3 Y2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:43297158 T>C maps to NM_002130.6 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:43297158 T>C maps to NM_002130.6 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:245018902 C>T maps to NM_031844.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:245018902 C>T maps to NM_031844.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:122930823 C>T maps to NM_006597.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:122930823 C>T maps to NM_006597.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:27456537 C>G maps to NM_181079.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:27456537 C>G maps to NM_181079.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:121712503 C>A maps to ENST00000344209 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:121712503 C>A maps to ENST00000344209 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:76728443 G>A maps to NM_001563.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:76728443 G>A maps to NM_001563.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:99193583 C>T maps to NM_001134224.1 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:99193583 C>T maps to NM_001134224.1 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:170336018 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:170336018 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:111146591 C>T maps to NM_004974.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:111146591 C>T maps to NM_004974.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:75444632 C>A maps to NM_139137.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:75444632 C>A maps to NM_139137.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:78708950 G>C maps to NM_001161352.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:78708950 G>C maps to NM_001161352.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:57181272 G>T maps to NM_020722.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:57181272 G>T maps to NM_020722.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:152595432 C>G maps to NM_178431.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:152595432 C>G maps to NM_178431.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:48620930 G>A maps to NM_000234.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:48620930 G>A maps to NM_000234.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:48653354 G>A maps to NM_000234.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:48653354 G>A maps to NM_000234.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:78010953 C>A maps to NM_005296.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:78010953 C>A maps to NM_005296.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:166973414 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:166973414 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:47799765 C>A maps to ENST00000424334 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:47799765 C>A maps to ENST00000424334 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:37565296 G>C maps to NM_004774.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:37565296 G>C maps to NM_004774.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:48703797 G>A maps to NM_016626.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:48703797 G>A maps to NM_016626.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:109765933 G>T maps to NM_022765.3 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:109765933 G>T maps to NM_022765.3 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:129907465 C>A maps to NM_002417.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:129907465 C>A maps to NM_002417.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:4864773 C>A maps to NM_002448.3 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:4864773 C>A maps to NM_002448.3 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:10369628 C>T maps to NM_017533.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:10369628 C>T maps to NM_017533.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:36029490 G>A maps to NM_001014839.1 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:36029490 G>A maps to NM_001014839.1 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:79434537 G>T maps to NM_004796.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:79434537 G>T maps to NM_004796.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:73743881 G>A maps to NM_001005743.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:73743881 G>A maps to NM_001005743.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:50969206 C>A maps to NM_001014440.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:50969206 C>A maps to NM_001014440.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:123631059 G>C maps to NM_001163278.1 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:123631059 G>C maps to NM_001163278.1 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:7961051 G>A maps to NM_001003745.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:7961051 G>A maps to NM_001003745.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:2995963 G>A maps to NM_002548.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:2995963 G>A maps to NM_002548.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:55136183 C>A maps to NM_001005275.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:55136183 C>A maps to NM_001005275.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:48346725 C>T maps to NM_001004702.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:48346725 C>T maps to NM_001004702.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:4674112 G>T maps to NM_152430.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:4674112 G>T maps to NM_152430.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158735614 G>A maps to NM_001005185.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158735614 G>A maps to NM_001005185.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:14991870 G>C maps to NM_030901.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:14991870 G>C maps to NM_030901.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:21739596 C>T maps to ENST00000286149 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:21739596 C>T maps to ENST00000286149 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:72926821 G>A maps to NM_178160.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:72926821 G>A maps to NM_178160.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:31862302 A>G maps to ENST00000382902 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:31862302 A>G maps to ENST00000382902 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:89475535 C>G maps to NM_001015880.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:89475535 C>G maps to NM_001015880.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:242063432 C>A maps to ENST00000358649 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:242063432 C>A maps to ENST00000358649 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:142567170 A>T maps to NM_013363.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:142567170 A>T maps to NM_013363.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20410589 C>T maps to NM_174924.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20410589 C>T maps to NM_174924.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:58318160 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:58318160 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207112587 C>A maps to NM_002644.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207112587 C>A maps to NM_002644.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:44047575 A>T maps to NM_015937.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:44047575 A>T maps to NM_015937.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:106524640 C>T maps to NM_002649.2 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:106524640 C>T maps to NM_002649.2 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:8784283 G>A maps to NM_001142633.1 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:8784283 G>A maps to NM_001142633.1 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42434277 G>A maps to ENST00000397272 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42434277 G>A maps to ENST00000397272 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:118203901 A>G maps to NM_001011709.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:118203901 A>G maps to NM_001011709.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:14513720 A>G maps to ENST00000444806 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:14513720 A>G maps to ENST00000444806 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:120175881 G>A maps to NM_014352.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:120175881 G>A maps to NM_014352.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:82763574 G>T maps to NM_000307.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:82763574 G>T maps to NM_000307.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:104251167 G>A maps to NM_015316.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:104251167 G>A maps to NM_015316.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:23522756 C>T maps to NM_020227.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:23522756 C>T maps to NM_020227.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:23527608 T>C maps to NM_020227.2 Y804Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:23527608 T>C maps to NM_020227.2 Y804Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:148559745 T>C maps to NM_138364.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:148559745 T>C maps to NM_138364.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:18905887 C>T maps to NM_016335.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:18905887 C>T maps to NM_016335.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:21011690 G>T maps to NM_001010915.3 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:21011690 G>T maps to NM_001010915.3 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:89016692 C>A maps to NM_007039.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:89016692 C>A maps to NM_007039.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:71139814 C>A maps to NM_002849.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:71139814 C>A maps to NM_002849.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:125782612 A>T maps to NM_012197.3 K557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:125782612 A>T maps to NM_012197.3 K557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:163043249 G>C maps to NM_001102445.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:163043249 G>C maps to NM_001102445.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:213445952 G>C maps to NM_012424.3 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:213445952 G>C maps to NM_012424.3 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:107035615 G>A maps to NM_032730.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:107035615 G>A maps to NM_032730.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:33937436 C>A maps to NM_016568.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:33937436 C>A maps to NM_016568.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:237802405 G>A maps to NM_001035.2 G2340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:237802405 G>A maps to NM_001035.2 G2340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33955874 G>A maps to NM_001036.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33955874 G>A maps to NM_001036.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:76753742 A>G maps to NM_171999.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:76753742 A>G maps to NM_171999.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:71394317 G>T maps to NM_001144952.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:71394317 G>T maps to NM_001144952.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:43837269 C>T maps to NM_003007.3 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:43837269 C>T maps to NM_003007.3 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:7325986 G>A maps to NM_001018039.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:7325986 G>A maps to NM_001018039.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:3672715 C>A maps to NM_023068.3 T1388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:3672715 C>A maps to NM_023068.3 T1388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:87470972 T>C maps to NM_018843.3 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:87470972 T>C maps to NM_018843.3 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:103017306 A>T maps to ENST00000354356 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:103017306 A>T maps to ENST00000354356 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:58031050 G>T maps to NM_001080455.1 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:58031050 G>T maps to NM_001080455.1 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:205631991 C>G maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:205631991 C>G maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:101560477 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:101560477 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:11059649 T>A maps to NM_003042.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:11059649 T>A maps to NM_003042.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:16727320 C>T maps to NM_198546.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:16727320 C>T maps to NM_198546.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:220333306 G>A maps to NM_005876.4 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:220333306 G>A maps to NM_005876.4 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:94794785 C>G maps to NM_006415.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:94794785 C>G maps to NM_006415.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:23016251 G>T maps to NM_001052.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:23016251 G>T maps to NM_001052.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:134478231 C>A maps to NM_173344.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:134478231 C>A maps to NM_173344.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:16773136 C>T maps to NM_032796.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:16773136 C>T maps to NM_032796.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156381702 C>G maps to NM_138379.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156381702 C>G maps to NM_138379.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:105361662 C>T maps to NM_030788.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:105361662 C>T maps to NM_030788.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:48358150 C>T maps to NM_001143842.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:48358150 C>T maps to NM_001143842.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:150488636 G>A maps to NM_014020.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:150488636 G>A maps to NM_014020.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:119155825 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:119155825 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:49719371 G>T maps to NM_005480.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:49719371 G>T maps to NM_005480.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:167754836 A>T maps to NM_031949.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:167754836 A>T maps to NM_031949.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:40818441 C>T maps to NM_016437.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:40818441 C>T maps to NM_016437.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42286811 G>A maps to NM_014233.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42286811 G>A maps to NM_014233.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:54446672 T>C maps to NM_015285.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:54446672 T>C maps to NM_015285.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:22837736 C>A maps to NM_014870.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:22837736 C>A maps to NM_014870.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38031515 C>T maps to NM_199321.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38031515 C>T maps to NM_199321.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38031553 C>T maps to NM_199321.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38031553 C>T maps to NM_199321.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:178402820 A>G maps to NM_003659.3 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:178402820 A>G maps to NM_003659.3 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:201469468 A>G maps to NM_001159.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:201469468 A>G maps to NM_001159.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:113505179 A>C maps to NM_001690.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:113505179 A>C maps to NM_001690.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:56999682 C>T maps to NM_013449.3 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:56999682 C>T maps to NM_013449.3 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:91691110 G>T maps to NM_001102368.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:91691110 G>T maps to NM_001102368.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:49048413 G>A maps to NM_001194998.1 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:49048413 G>A maps to NM_001194998.1 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:201719418 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:201719418 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:139894883 C>T maps to NM_022131.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:139894883 C>T maps to NM_022131.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:126683169 C>A maps to NM_022802.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:126683169 C>A maps to NM_022802.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:41222860 A>T maps to NM_019074.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:41222860 A>T maps to NM_019074.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:57509469 C>T maps to NM_018110.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:57509469 C>T maps to NM_018110.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:131646711 G>A maps to ENST00000355311 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:131646711 G>A maps to ENST00000355311 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:220156530 C>T maps to NM_004446.2 E1100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:220156530 C>T maps to NM_004446.2 E1100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:153593043 G>A maps to NM_001110556.1 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:153593043 G>A maps to NM_001110556.1 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:99757601 G>A maps to NM_024637.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:99757601 G>A maps to NM_024637.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:151818707 C>T maps to NM_022087.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:151818707 C>T maps to NM_022087.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:93518679 C>T maps to NM_004466.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:93518679 C>T maps to NM_004466.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:94452137 C>G maps to NM_002729.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:94452137 C>G maps to NM_002729.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:23885761 C>T maps to NM_002167.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:23885761 C>T maps to NM_002167.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:31408682 C>T maps to ENST00000444228 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:31408682 C>T maps to ENST00000444228 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:19126880 A>T maps to NM_001034841.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:19126880 A>T maps to NM_001034841.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:67338378 T>C maps to NM_001100915.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:67338378 T>C maps to NM_001100915.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:15705447 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:15705447 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:205306640 G>A maps to NM_018203.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:205306640 G>A maps to NM_018203.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:68119494 C>G maps to ENST00000380035 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:68119494 C>G maps to ENST00000380035 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:33329064 G>A maps to NM_013975.3 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:33329064 G>A maps to NM_013975.3 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:100179735 G>T maps to NM_002319.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:100179735 G>T maps to NM_002319.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:170148766 T>A maps to NM_004525.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:170148766 T>A maps to NM_004525.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:40136579 T>A maps to NM_020929.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:40136579 T>A maps to NM_020929.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:20112536 G>A maps to NM_021020.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:20112536 G>A maps to NM_021020.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:117944870 A>C maps to NM_006699.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:117944870 A>C maps to NM_006699.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:108776233 G>A maps to NM_014429.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:108776233 G>A maps to NM_014429.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:47709955 G>C maps to NM_000251.1 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:47709955 G>C maps to NM_000251.1 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:128366434 G>A maps to ENST00000389524 Q932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:128366434 G>A maps to ENST00000389524 Q932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:204948556 C>A maps to ENST00000367172 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:204948556 C>A maps to ENST00000367172 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:47892632 T>G maps to NM_152995.4 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:47892632 T>G maps to NM_152995.4 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:236205494 C>A maps to NM_002508.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:236205494 C>A maps to NM_002508.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:18937478 C>T maps to NM_182543.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:18937478 C>T maps to NM_182543.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:3938097 G>A maps to NM_020367.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:3938097 G>A maps to NM_020367.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:140503319 G>A maps to NM_018938.2 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:140503319 G>A maps to NM_018938.2 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:1483661 G>A maps to NM_017573.3 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:1483661 G>A maps to NM_017573.3 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:27235900 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:27235900 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:64029531 C>T maps to NM_000932.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:64029531 C>T maps to NM_000932.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:129308192 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:129308192 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:56227471 G>A maps to NM_020182.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:56227471 G>A maps to NM_020182.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:93118639 C>T maps to NM_024832.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:93118639 C>T maps to NM_024832.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:35827583 C>G maps to NM_002951.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:35827583 C>G maps to NM_002951.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:4996625 A>T maps to NM_006638.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:4996625 A>T maps to NM_006638.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:46305468 C>A maps to NM_030785.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:46305468 C>A maps to NM_030785.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:12939475 C>T maps to NM_031429.1 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:12939475 C>T maps to NM_031429.1 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:1298988 G>A maps to NM_080489.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:1298988 G>A maps to NM_080489.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:88218186 G>A maps to NM_006416.4 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:88218186 G>A maps to NM_006416.4 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:31833120 C>T maps to NM_025257.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:31833120 C>T maps to NM_025257.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:85266386 T>A maps to NM_182767.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:85266386 T>A maps to NM_182767.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:101631627 G>A maps to NM_180991.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:101631627 G>A maps to NM_180991.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:88328773 G>T maps to NM_015567.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:88328773 G>T maps to NM_015567.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:123599914 G>A maps to NM_001174046.1 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:123599914 G>A maps to NM_001174046.1 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:74622173 G>A maps to NM_018414.3 H473H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:74622173 G>A maps to NM_018414.3 H473H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:20846396 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:20846396 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:58011791 G>A maps to NM_199046.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:58011791 G>A maps to NM_199046.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:99854064 C>G maps to NM_022144.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:99854064 C>G maps to NM_022144.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:100100547 C>A maps to NM_014820.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:100100547 C>A maps to NM_014820.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:32829544 G>C maps to NM_052841.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:32829544 G>C maps to NM_052841.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:43225668 C>T maps to NM_032538.1 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:43225668 C>T maps to NM_032538.1 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:90062267 C>A maps to NM_016021.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:90062267 C>A maps to NM_016021.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:6189290 C>T maps to ENST00000404835 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:6189290 C>T maps to ENST00000404835 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:11941941 C>T maps to ENST00000399455 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:11941941 C>T maps to ENST00000399455 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:122748722 T>A maps to NM_022916.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:122748722 T>A maps to NM_022916.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:54545618 G>A maps to NM_198481.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:54545618 G>A maps to NM_198481.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:37587669 T>C maps to NM_021083.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:37587669 T>C maps to NM_021083.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:77617597 C>A maps to NM_024721.4 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:77617597 C>A maps to NM_024721.4 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:22154331 G>T maps to NM_007153.3 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:22154331 G>T maps to NM_007153.3 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:36967452 G>A maps to NM_001145343.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:36967452 G>A maps to NM_001145343.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:99171065 C>T maps to NM_001083956.1 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:99171065 C>T maps to NM_001083956.1 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:24087098 G>A maps to NM_021916.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:24087098 G>A maps to NM_021916.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:57935582 G>A maps to NM_007156.4 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:57935582 G>A maps to NM_007156.4 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:67013931 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:67013931 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:16284194 C>A maps to NM_001171.5 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:16284194 C>A maps to NM_001171.5 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:42854900 G>T maps to NM_002390.4 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:42854900 G>T maps to NM_002390.4 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:5303443 C>A maps to NM_139056.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:5303443 C>A maps to NM_139056.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:74277727 G>C maps to NM_000477.5 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:74277727 G>C maps to NM_000477.5 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:77817345 C>A maps to NM_001029870.1 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:77817345 C>A maps to NM_001029870.1 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:207297524 A>T maps to NM_000715.3 K174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:207297524 A>T maps to NM_000715.3 K174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:71200917 T>A maps to NM_033122.3 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:71200917 T>A maps to NM_033122.3 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:47846656 G>T maps to NM_001013732.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:47846656 G>T maps to NM_001013732.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:86352058 T>C maps to NM_005181.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:86352058 T>C maps to NM_005181.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:1260866 G>T maps to NM_021098.2 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:1260866 G>T maps to NM_021098.2 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:2962897 C>G maps to NM_032415.4 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:2962897 C>G maps to NM_032415.4 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:133541765 A>G maps to NM_002715.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:133541765 A>G maps to NM_002715.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:80642133 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:80642133 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:55004903 G>T maps to NM_006568.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:55004903 G>T maps to NM_006568.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:21868346 C>A maps to NM_001170629.1 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:21868346 C>A maps to NM_001170629.1 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:37833633 G>T maps to NM_001146077.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:37833633 G>T maps to NM_001146077.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48342704 C>A maps to NM_000554.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48342704 C>A maps to NM_000554.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:113246619 C>A maps to NM_198123.1 E3572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:113246619 C>A maps to NM_198123.1 E3572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:80773161 C>A maps to ENST00000402739 S505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:80773161 C>A maps to ENST00000402739 S505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:137170140 G>C maps to NM_004717.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:137170140 G>C maps to NM_004717.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:32509488 C>A maps to ENST00000357033 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:32509488 C>A maps to ENST00000357033 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:76548887 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:76548887 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:220239585 G>A maps to NM_012100.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:220239585 G>A maps to NM_012100.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41313711 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41313711 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:112025333 T>C maps to NM_019114.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:112025333 T>C maps to NM_019114.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:66356314 T>A maps to NM_004439.5 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:66356314 T>A maps to NM_004439.5 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:97167530 C>A maps to NM_001080448.2 Y617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:97167530 C>A maps to NM_001080448.2 Y617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:14861864 C>T maps to NM_152536.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:14861864 C>T maps to NM_152536.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:132682498 C>A maps to NM_001122636.1 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:132682498 C>A maps to NM_001122636.1 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135426563 T>C maps to NM_153834.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135426563 T>C maps to NM_153834.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135428318 A>C maps to NM_153834.3 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135428318 A>C maps to NM_153834.3 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:72368676 G>T maps to ENST00000440684 E1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:72368676 G>T maps to ENST00000440684 E1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:45262862 A>G maps to NM_021072.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:45262862 A>G maps to NM_021072.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153052270 G>A maps to NM_004135.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153052270 G>A maps to NM_004135.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:31427912 G>T maps to ENST00000444228 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:31427912 G>T maps to ENST00000444228 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:7708825 C>A maps to ENST00000256861 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:7708825 C>A maps to ENST00000256861 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:38690564 G>T maps to NM_016531.5 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:38690564 G>T maps to NM_016531.5 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:198571773 G>T maps to NM_138395.3 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:198571773 G>T maps to NM_138395.3 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:46801129 G>A maps to NM_005588.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:46801129 G>A maps to NM_005588.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:108780902 C>A maps to NM_014429.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:108780902 C>A maps to NM_014429.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:76343981 G>T maps to NM_002440.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:76343981 G>T maps to NM_002440.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:153043127 C>T maps to NM_025107.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:153043127 C>T maps to NM_025107.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:10415290 C>A maps to NM_005963.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:10415290 C>A maps to NM_005963.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:52539166 C>A maps to NM_018728.3 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:52539166 C>A maps to NM_018728.3 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:149919744 C>G maps to NM_001543.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:149919744 C>G maps to NM_001543.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:115998012 A>G maps to NM_022569.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:115998012 A>G maps to NM_022569.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:107867517 G>T maps to NM_001113226.1 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:107867517 G>T maps to NM_001113226.1 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:167625974 C>A maps to NM_001122679.1 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:167625974 C>A maps to NM_001122679.1 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:248262793 G>C maps to NM_175911.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:248262793 G>C maps to NM_175911.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:59211048 C>A maps to NM_001004728.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:59211048 C>A maps to NM_001004728.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:55682035 G>T maps to NM_001001960.1 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:55682035 G>T maps to NM_001001960.1 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:1584614 C>A maps to NM_178129.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:1584614 C>A maps to NM_178129.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:176563987 G>T maps to NM_020318.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:176563987 G>T maps to NM_020318.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:141336579 C>T maps to NM_016580.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:141336579 C>T maps to NM_016580.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:140481423 A>G maps to NM_018937.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:140481423 A>G maps to NM_018937.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:66620018 G>A maps to NM_022172.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:66620018 G>A maps to NM_022172.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:96761789 C>T maps to NM_005390.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:96761789 C>T maps to NM_005390.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:32077587 C>G maps to NM_178140.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:32077587 C>G maps to NM_178140.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:152622521 G>A maps to NM_004564.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:152622521 G>A maps to NM_004564.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:75756214 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:75756214 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:96064272 G>A maps to ENST00000371380 E1831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:96064272 G>A maps to ENST00000371380 E1831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:19119763 C>A maps to NM_001122.2 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:19119763 C>A maps to NM_001122.2 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:72184551 G>A maps to NM_031293.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:72184551 G>A maps to NM_031293.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:130877800 G>A maps to NM_001099771.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:130877800 G>A maps to NM_001099771.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:16526804 C>G maps to NM_030664.3 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:16526804 C>G maps to NM_030664.3 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:8492980 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:8492980 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:17697104 C>A maps to NM_001099218.2 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:17697104 C>A maps to NM_001099218.2 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:79349205 C>A maps to NM_002909.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:79349205 C>A maps to NM_002909.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:86992311 A>G maps to NM_022780.3 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:86992311 A>G maps to NM_022780.3 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:237880547 G>T maps to NM_001035.2 R3458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:237880547 G>T maps to NM_001035.2 R3458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:18535780 A>C maps to NM_001172745.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:18535780 A>C maps to NM_001172745.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:148388513 G>T maps to NM_024577.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:148388513 G>T maps to NM_024577.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153716543 T>A maps to ENST00000440701 K301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153716543 T>A maps to ENST00000440701 K301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:139751894 G>A maps to ENST00000507527 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:139751894 G>A maps to ENST00000507527 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:34207126 C>A maps to NM_003116.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:34207126 C>A maps to NM_003116.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:155003883 T>A maps to NM_005840.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:155003883 T>A maps to NM_005840.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158645962 G>T maps to NM_003126.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158645962 G>T maps to NM_003126.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41078080 G>A maps to NM_020971.2 K2492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41078080 G>A maps to NM_020971.2 K2492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57457865 G>A maps to NM_001130963.1 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57457865 G>A maps to NM_001130963.1 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:154736680 G>T maps to NM_018196.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:154736680 G>T maps to NM_018196.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:135567122 G>A maps to NM_020389.2 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:135567122 G>A maps to NM_020389.2 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:216420068 C>T maps to ENST00000366943 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:216420068 C>T maps to ENST00000366943 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:55515249 C>A maps to NM_201286.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:55515249 C>A maps to NM_201286.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:65242212 T>C maps to NM_007268.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:65242212 T>C maps to NM_007268.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:88644073 G>A maps to ENST00000452588 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:88644073 G>A maps to ENST00000452588 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:44932747 G>A maps to NM_014518.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:44932747 G>A maps to NM_014518.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:151261158 C>T maps to NM_020832.1 H757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:151261158 C>T maps to NM_020832.1 H757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:68139537 T>A maps to NM_006421.3 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:68139537 T>A maps to NM_006421.3 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:155935546 G>A maps to NM_001162383.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:155935546 G>A maps to NM_001162383.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:343555 C>T maps to NM_003502.3 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:343555 C>T maps to NM_003502.3 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:171481268 G>C maps to ENST00000392078 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:171481268 G>C maps to ENST00000392078 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:4563766 C>A maps to ENST00000359075 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:4563766 C>A maps to ENST00000359075 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:73539146 C>T maps to ENST00000398860 R1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:73539146 C>T maps to ENST00000398860 R1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:65499309 G>A maps to NM_003613.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:65499309 G>A maps to NM_003613.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:86898147 C>T maps to NM_006536.5 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:86898147 C>T maps to NM_006536.5 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:54896977 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:54896977 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:103544260 G>T maps to NM_080629.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:103544260 G>T maps to NM_080629.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:113246673 A>G maps to NM_198123.1 L3554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:113246673 A>G maps to NM_198123.1 L3554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:113254005 T>A maps to NM_198123.1 K3471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:113254005 T>A maps to NM_198123.1 K3471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:37708204 G>T maps to NM_013385.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:37708204 G>T maps to NM_013385.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:39869181 G>C maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:39869181 G>C maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:59113520 C>A maps to NM_016651.5 S727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:59113520 C>A maps to NM_016651.5 S727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:82574914 G>T maps to NM_001008226.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:82574914 G>T maps to NM_001008226.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:92526039 G>A maps to ENST00000298047 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:92526039 G>A maps to ENST00000298047 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:115965312 A>G maps to ENST00000446284 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:115965312 A>G maps to ENST00000446284 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr13:49752747 C>A maps to NM_001079673.1 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr13:49752747 C>A maps to NM_001079673.1 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:95265332 T>C maps to NM_181702.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:95265332 T>C maps to NM_181702.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:34943641 C>T maps to NM_024835.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:34943641 C>T maps to NM_024835.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:94973151 G>A maps to ENST00000375660 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:94973151 G>A maps to ENST00000375660 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr12:68549133 T>A maps to NM_000619.2 *167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr12:68549133 T>A maps to NM_000619.2 *167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:15729638 C>T maps to NM_014647.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:15729638 C>T maps to NM_014647.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:30349753 G>T maps to NM_020805.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:30349753 G>T maps to NM_020805.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:18434299 A>G maps to NM_017448.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:18434299 A>G maps to NM_017448.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:62598910 A>G maps to ENST00000506720 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:62598910 A>G maps to ENST00000506720 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:85991732 G>A maps to NM_015613.2 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:85991732 G>A maps to NM_015613.2 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:141122288 C>T maps to NM_018557.2 W3691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:141122288 C>T maps to NM_018557.2 W3691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:70488885 C>A maps to NM_020794.2 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:70488885 C>A maps to NM_020794.2 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:41799787 G>A maps to NM_002344.5 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:41799787 G>A maps to NM_002344.5 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:71267477 C>A maps to NM_033141.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:71267477 C>A maps to NM_033141.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:55530912 C>T maps to NM_004530.4 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:55530912 C>T maps to NM_004530.4 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:75881898 C>T maps to NM_014763.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:75881898 C>T maps to NM_014763.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:10297636 C>A maps to NM_002472.2 E1699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:10297636 C>A maps to NM_002472.2 E1699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:123375979 T>C maps to NM_053025.3 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:123375979 T>C maps to NM_053025.3 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:55721651 C>A maps to NM_001142763.1 G962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:55721651 C>A maps to NM_001142763.1 G962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:71444880 T>C maps to NM_014982.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:71444880 T>C maps to NM_014982.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:96416741 C>G maps to NM_005392.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:96416741 C>G maps to NM_005392.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:23524574 C>A maps to NM_020227.2 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:23524574 C>A maps to NM_020227.2 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:44057084 G>A maps to NM_002840.3 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:44057084 G>A maps to NM_002840.3 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:40980916 G>T maps to ENST00000373198 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:40980916 G>T maps to ENST00000373198 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:110852500 C>A maps to NM_015480.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:110852500 C>A maps to NM_015480.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:6013603 T>G maps to NM_012416.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:6013603 T>G maps to NM_012416.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:178412213 G>T maps to ENST00000263528 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:178412213 G>T maps to ENST00000263528 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:72945022 C>G maps to NM_004296.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:72945022 C>G maps to NM_004296.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:30339447 C>T maps to NM_015565.2 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:30339447 C>T maps to NM_015565.2 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:237880667 G>A maps to NM_001035.2 L3498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:237880667 G>A maps to NM_001035.2 L3498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:166010961 C>T maps to NM_006922.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:166010961 C>T maps to NM_006922.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:18523046 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:18523046 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:57367767 C>T maps to ENST00000403558 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:57367767 C>T maps to ENST00000403558 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:12506571 C>A maps to NM_001128626.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:12506571 C>A maps to NM_001128626.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:141693947 G>A maps to NM_030964.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:141693947 G>A maps to NM_030964.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:70539459 C>A maps to NM_001128206.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:70539459 C>A maps to NM_001128206.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:11633038 G>T maps to ENST00000423059 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:11633038 G>T maps to ENST00000423059 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:76130575 C>T maps to NM_152468.4 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:76130575 C>T maps to NM_152468.4 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:142503716 A>T maps to ENST00000476941 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:142503716 A>T maps to ENST00000476941 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:179600340 T>A maps to NM_133378.4 T3700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:179600340 T>A maps to NM_133378.4 T3700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:90042805 G>T maps to NM_016021.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:90042805 G>T maps to NM_016021.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:46345932 C>A maps to NM_058238.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:46345932 C>A maps to NM_058238.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:151259951 G>A maps to NM_020832.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:151259951 G>A maps to NM_020832.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:57829575 C>T maps to NM_178457.1 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:57829575 C>T maps to NM_178457.1 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:12726346 A>G maps to NM_001013630.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:12726346 A>G maps to NM_001013630.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:48337961 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:48337961 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:48249114 G>A maps to NM_032583.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:48249114 G>A maps to NM_032583.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:33588843 G>A maps to NM_030955.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:33588843 G>A maps to NM_030955.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:2901113 G>A maps to NM_014189.2 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:2901113 G>A maps to NM_014189.2 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:100205961 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:100205961 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:99996200 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:99996200 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:62293041 G>T maps to NM_001620.1 P2949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:62293041 G>T maps to NM_001620.1 P2949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:33015818 C>T maps to NM_004274.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:33015818 C>T maps to NM_004274.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:32563471 A>T maps to NM_001030055.1 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:32563471 A>T maps to NM_001030055.1 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:62459864 C>G maps to NM_001130702.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:62459864 C>G maps to NM_001130702.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:33564734 C>A maps to ENST00000389726 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:33564734 C>A maps to ENST00000389726 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:95932315 G>C maps to NM_152592.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:95932315 G>C maps to NM_152592.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:30602723 C>A maps to ENST00000300415 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:30602723 C>A maps to ENST00000300415 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:73748714 G>A maps to ENST00000334126 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:73748714 G>A maps to ENST00000334126 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:184626182 G>T maps to NM_021942.4 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:184626182 G>T maps to NM_021942.4 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:43477340 G>T maps to NM_001012974.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:43477340 G>T maps to NM_001012974.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:15721813 G>T maps to NM_173550.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:15721813 G>T maps to NM_173550.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:86354305 G>A maps to NM_005181.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:86354305 G>A maps to NM_005181.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:13365935 G>A maps to NM_023035.2 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:13365935 G>A maps to NM_023035.2 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:27462632 A>C maps to NM_004341.3 P1821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:27462632 A>C maps to NM_004341.3 P1821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:2972220 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:2972220 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:10714190 G>A maps to NM_001079843.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:10714190 G>A maps to NM_001079843.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:28603338 A>T maps to NM_018318.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:28603338 A>T maps to NM_018318.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:15780138 C>A maps to NM_001775.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:15780138 C>A maps to NM_001775.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:38168929 C>T maps to NM_018101.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:38168929 C>T maps to NM_018101.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:65026827 T>C maps to NM_001797.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:65026827 T>C maps to NM_001797.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:31299712 C>T maps to NM_004932.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:31299712 C>T maps to NM_004932.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:63548087 C>A maps to NM_004361.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:63548087 C>A maps to NM_004361.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:205495284 G>A maps to NM_212503.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:205495284 G>A maps to NM_212503.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:196794685 T>C maps to NM_002113.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:196794685 T>C maps to NM_002113.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:90042181 C>T maps to NM_001185072.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:90042181 C>T maps to NM_001185072.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:6265579 G>T maps to NM_001037329.2 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:6265579 G>T maps to NM_001037329.2 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:129962386 C>T maps to NM_016352.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:129962386 C>T maps to NM_016352.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:36710125 G>T maps to NM_020939.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:36710125 G>T maps to NM_020939.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:1709951 G>C maps to NM_020825.3 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:1709951 G>C maps to NM_020825.3 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:219856955 G>A maps to NM_057094.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:219856955 G>A maps to NM_057094.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:18919472 C>T maps to NM_001338.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:18919472 C>T maps to NM_001338.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:99261602 G>A maps to NM_000777.3 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:99261602 G>A maps to NM_000777.3 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:49231324 C>T maps to NM_004818.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:49231324 C>T maps to NM_004818.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:140246655 G>A maps to NM_015689.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:140246655 G>A maps to NM_015689.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:24531294 C>T maps to NM_001358.2 W733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:24531294 C>T maps to NM_001358.2 W733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52416446 C>T maps to ENST00000273600 I2639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52416446 C>T maps to ENST00000273600 I2639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:13766117 C>T maps to NM_001369.2 L3356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:13766117 C>T maps to NM_001369.2 L3356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:196749413 T>A maps to NM_018897.2 R1886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:196749413 T>A maps to NM_018897.2 R1886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:230456400 C>T maps to NM_139072.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:230456400 C>T maps to NM_139072.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:28711631 C>T maps to NM_024421.2 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:28711631 C>T maps to NM_024421.2 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:28934525 A>T maps to NM_001942.2 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:28934525 A>T maps to NM_001942.2 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:118183793 G>A maps to NM_173666.2 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:118183793 G>A maps to NM_173666.2 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56164474 C>T maps to NM_080677.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56164474 C>T maps to NM_080677.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:71827869 G>T maps to NM_001130987.1 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:71827869 G>T maps to NM_001130987.1 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:77423928 C>T maps to NM_203394.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:77423928 C>T maps to NM_203394.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:11005667 G>A maps to NM_017770.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:11005667 G>A maps to NM_017770.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:56487889 C>T maps to NM_001982.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:56487889 C>T maps to NM_001982.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:158178193 C>T maps to NM_001009959.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:158178193 C>T maps to NM_001009959.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:242030244 A>T maps to NM_006027.4 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:242030244 A>T maps to NM_006027.4 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:72127687 T>A maps to NM_000503.4 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:72127687 T>A maps to NM_000503.4 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:139263226 G>T maps to NM_015912.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:139263226 G>T maps to NM_015912.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:163051220 G>T maps to NM_004460.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:163051220 G>T maps to NM_004460.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:16091648 G>A maps to NM_017556.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:16091648 G>A maps to NM_017556.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:15937075 C>G maps to NM_012304.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:15937075 C>G maps to NM_012304.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:58135871 C>G maps to NM_001164317.1 V2126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:58135871 C>G maps to NM_001164317.1 V2126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:162841739 G>A maps to NM_020116.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:162841739 G>A maps to NM_020116.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:88406292 C>A maps to NM_000153.2 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:88406292 C>A maps to NM_000153.2 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:31013714 C>G maps to NM_000823.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:31013714 C>G maps to NM_000823.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:42006171 G>C maps to NM_000168.5 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:42006171 G>C maps to NM_000168.5 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:183920144 C>A maps to NM_015101.2 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:183920144 C>A maps to NM_015101.2 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135438315 C>A maps to NM_153834.3 R2307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135438315 C>A maps to NM_153834.3 R2307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:1004960 G>A maps to NM_138690.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:1004960 G>A maps to NM_138690.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:28368063 G>T maps to NM_145657.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:28368063 G>T maps to NM_145657.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:45262466 C>T maps to NM_021072.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:45262466 C>T maps to NM_021072.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:43351606 G>A maps to NM_015052.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:43351606 G>A maps to NM_015052.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:137519416 G>A maps to NM_000416.2 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:137519416 G>A maps to NM_000416.2 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:15199881 T>A maps to NM_001031853.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:15199881 T>A maps to NM_001031853.3 V203V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-5899-01A-11D-1625-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-55-5899-01A-11D-1625-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:110438031 G>C maps to NM_003749.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:110438031 G>C maps to NM_003749.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:26809336 A>T maps to NM_002223.2 C779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:26809336 A>T maps to NM_002223.2 C779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:21319541 G>T maps to NM_021012.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:21319541 G>T maps to NM_021012.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:5032933 C>T maps to NM_015015.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:5032933 C>T maps to NM_015015.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:44928906 C>T maps to NM_021140.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:44928906 C>T maps to NM_021140.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:51900705 G>T maps to NM_032559.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:51900705 G>T maps to NM_032559.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:226075724 G>T maps to ENST00000419724 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:226075724 G>T maps to ENST00000419724 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:128415048 C>A maps to NM_017980.4 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:128415048 C>A maps to NM_017980.4 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:70386116 G>T maps to NM_018368.3 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:70386116 G>T maps to NM_018368.3 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:2434012 C>A maps to NM_032737.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:2434012 C>A maps to NM_032737.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:141093287 C>T maps to NM_018557.2 L4004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:141093287 C>T maps to NM_018557.2 L4004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:101597146 C>A maps to NM_024652.3 A1473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:101597146 C>A maps to NM_024652.3 A1473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:12247750 G>T maps to NM_014632.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:12247750 G>T maps to NM_014632.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:97686194 G>A maps to NM_153182.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:97686194 G>A maps to NM_153182.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:10398274 C>T maps to NM_005963.3 K1813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:10398274 C>T maps to NM_005963.3 K1813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:95116583 G>A maps to NM_013451.3 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:95116583 G>A maps to NM_013451.3 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:14146718 A>T maps to ENST00000397581 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:14146718 A>T maps to ENST00000397581 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:103504054 G>T maps to NM_003998.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:103504054 G>T maps to NM_003998.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:7059876 G>A maps to NM_176822.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:7059876 G>A maps to NM_176822.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:64415749 C>T maps to NM_015080.3 W1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:64415749 C>T maps to NM_015080.3 W1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:33055307 G>A maps to NM_001002010.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:33055307 G>A maps to NM_001002010.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:15905664 G>T maps to NM_001004466.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:15905664 G>T maps to NM_001004466.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:57996272 A>G maps to NM_001004471.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:57996272 A>G maps to NM_001004471.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:107379867 G>A maps to NM_001001956.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:107379867 G>A maps to NM_001001956.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:247921053 C>A maps to NM_012353.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:247921053 C>A maps to NM_012353.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:125288810 G>A maps to ENST00000359439 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:125288810 G>A maps to ENST00000359439 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:48286047 G>A maps to NM_001004726.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:48286047 G>A maps to NM_001004726.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:56128531 T>A maps to NM_001005205.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:56128531 T>A maps to NM_001005205.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:55523902 C>A maps to NM_001005243.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:55523902 C>A maps to NM_001005243.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:29614941 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:29614941 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:183547409 G>A maps to NM_018622.5 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:183547409 G>A maps to NM_018622.5 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:242065725 G>A maps to ENST00000358649 N868N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:242065725 G>A maps to ENST00000358649 N868N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:127255535 G>T maps to NM_006193.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:127255535 G>T maps to NM_006193.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:134072044 C>T maps to NM_032961.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:134072044 C>T maps to NM_032961.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:67802317 A>T maps to NM_203487.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:67802317 A>T maps to NM_203487.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:140573672 C>G maps to NM_018930.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:140573672 C>G maps to NM_018930.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:85722152 G>A maps to ENST00000393343 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:85722152 G>A maps to ENST00000393343 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:28855875 C>T maps to NM_153021.4 A1356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:28855875 C>T maps to NM_153021.4 A1356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:121737721 G>A maps to NM_018699.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:121737721 G>A maps to NM_018699.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:16014961 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:16014961 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:97236292 A>G maps to ENST00000370197 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:97236292 A>G maps to ENST00000370197 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:79255045 G>C maps to NM_001008387.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:79255045 G>C maps to NM_001008387.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:241094037 C>A maps to ENST00000407727 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:241094037 C>A maps to ENST00000407727 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:43399959 G>A maps to NM_182970.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:43399959 G>A maps to NM_182970.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:83390110 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:83390110 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:7230138 G>T maps to NM_001003699.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:7230138 G>T maps to NM_001003699.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:38995478 C>G maps to NM_000540.2 S2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:38995478 C>G maps to NM_000540.2 S2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:38592216 G>T maps to NM_001099404.1 A1882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:38592216 G>T maps to NM_001099404.1 A1882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:192700753 C>T maps to NM_004657.5 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:192700753 C>T maps to NM_004657.5 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:20216035 G>C maps to NM_001012410.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:20216035 G>C maps to NM_001012410.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:152069309 G>A maps to NM_001009555.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:152069309 G>A maps to NM_001009555.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:232600609 G>A maps to NM_020808.3 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:232600609 G>A maps to NM_020808.3 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:61180535 T>A maps to NM_017420.4 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:61180535 T>A maps to NM_017420.4 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:61594721 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:61594721 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:103038451 C>A maps to ENST00000354356 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:103038451 C>A maps to ENST00000354356 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:164906389 G>T maps to NM_014926.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:164906389 G>T maps to NM_014926.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:139586802 C>A maps to NM_005634.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:139586802 C>A maps to NM_005634.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:34508805 G>A maps to NM_012391.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:34508805 G>A maps to NM_012391.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:37961593 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:37961593 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:143175819 C>T maps to NM_176883.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:143175819 C>T maps to NM_176883.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:10721631 G>A maps to NM_144674.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:10721631 G>A maps to NM_144674.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:169637774 G>A maps to NM_003247.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:169637774 G>A maps to NM_003247.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:138169177 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:138169177 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:98408867 C>A maps to NM_015348.1 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:98408867 C>A maps to NM_015348.1 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:130761971 T>A maps to NM_052913.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:130761971 T>A maps to NM_052913.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:68780440 G>A maps to NM_182606.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:68780440 G>A maps to NM_182606.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:73046137 A>T maps to NM_013381.2 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:73046137 A>T maps to NM_013381.2 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:72946497 G>T maps to NM_007332.2 I890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:72946497 G>T maps to NM_007332.2 I890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142573310 G>T maps to NM_018646.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142573310 G>T maps to NM_018646.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:51872435 C>T maps to NM_173485.5 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:51872435 C>T maps to NM_173485.5 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:40818412 C>T maps to NM_016437.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:40818412 C>T maps to NM_016437.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:234436079 T>C maps to NM_018218.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:234436079 T>C maps to NM_018218.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:144769761 G>T maps to NM_007124.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:144769761 G>T maps to NM_007124.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:82837720 G>T maps to NM_004385.4 E2967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:82837720 G>T maps to NM_004385.4 E2967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:100865783 C>T maps to NM_017890.3 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:100865783 C>T maps to NM_017890.3 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:122630691 A>T maps to NM_018117.11 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:122630691 A>T maps to NM_018117.11 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:100996230 G>T maps to NM_001161476.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:100996230 G>T maps to NM_001161476.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:74982428 G>A maps to NM_030581.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:74982428 G>A maps to NM_030581.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:77618690 A>T maps to NM_024721.4 K790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:77618690 A>T maps to NM_024721.4 K790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:45905073 G>A maps to ENST00000471951 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:45905073 G>A maps to ENST00000471951 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:30696360 G>T maps to ENST00000394679 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:30696360 G>T maps to ENST00000394679 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:87123 C>T maps to NM_182524.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:87123 C>T maps to NM_182524.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:238048072 G>A maps to NM_021186.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:238048072 G>A maps to NM_021186.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:12726493 A>G maps to NM_001013630.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:12726493 A>G maps to NM_001013630.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr15:40756668 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr15:40756668 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chrX:119664013 T>A maps to NM_003588.3 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chrX:119664013 T>A maps to NM_003588.3 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr19:49445799 C>T maps to NM_014475.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr19:49445799 C>T maps to NM_014475.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr17:10436695 G>A maps to NM_017534.5 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr17:10436695 G>A maps to NM_017534.5 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:146030241 G>A maps to ENST00000394414 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:146030241 G>A maps to ENST00000394414 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr15:34150087 C>A maps to NM_001036.3 P4705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr15:34150087 C>A maps to NM_001036.3 P4705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:102256137 C>G maps to NM_015490.3 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:102256137 C>G maps to NM_015490.3 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr7:100478962 G>A maps to NM_015908.5 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr7:100478962 G>A maps to NM_015908.5 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:113158398 C>A maps to NM_006322.4 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:113158398 C>A maps to NM_006322.4 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:1042353 C>A maps to NM_019112.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:1042353 C>A maps to NM_019112.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:100343332 C>T maps to ENST00000311030 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:100343332 C>T maps to ENST00000311030 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:83333168 G>T maps to NM_004644.3 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:83333168 G>T maps to NM_004644.3 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:108123622 C>T maps to NM_000051.3 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:108123622 C>T maps to NM_000051.3 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:32135901 A>G maps to NM_018169.3 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:32135901 A>G maps to NM_018169.3 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:24924481 G>T maps to NM_018958.2 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:24924481 G>T maps to NM_018958.2 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:159170597 C>A maps to NM_021189.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:159170597 C>A maps to NM_021189.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:28947910 C>T maps to NM_001178098.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:28947910 C>T maps to NM_001178098.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:145624758 C>A maps to NM_013291.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:145624758 C>A maps to NM_013291.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:41703807 G>T maps to ENST00000301173 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:41703807 G>T maps to ENST00000301173 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:115141903 G>T maps to ENST00000393274 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:115141903 G>T maps to ENST00000393274 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:9694561 G>A maps to ENST00000330255 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:9694561 G>A maps to ENST00000330255 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:216850478 C>A maps to NM_001438.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:216850478 C>A maps to NM_001438.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:33427033 C>A maps to NM_012157.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:33427033 C>A maps to NM_012157.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:76023009 G>T maps to NM_015687.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:76023009 G>T maps to NM_015687.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:84607545 G>T maps to NM_001001670.2 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:84607545 G>T maps to NM_001001670.2 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:171303750 C>T maps to NM_002022.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:171303750 C>T maps to NM_002022.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:109719545 C>T maps to NM_213596.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:109719545 C>T maps to NM_213596.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:54456927 T>A maps to NM_001008397.2 L104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:54456927 T>A maps to NM_001008397.2 L104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:122733873 G>T maps to NM_004506.3 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:122733873 G>T maps to NM_004506.3 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:87725648 G>T maps to NM_000865.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:87725648 G>T maps to NM_000865.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:124273856 C>A maps to NM_002775.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:124273856 C>A maps to NM_002775.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:2932972 C>T maps to NM_018463.3 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:2932972 C>T maps to NM_018463.3 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:138601583 C>A maps to NM_001164665.1 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:138601583 C>A maps to NM_001164665.1 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:1943634 G>A maps to NM_001163926.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:1943634 G>A maps to NM_001163926.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1818200 C>A maps to NM_015133.3 A1187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1818200 C>A maps to NM_015133.3 A1187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:63668537 C>A maps to NM_001039469.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:63668537 C>A maps to NM_001039469.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:42977156 C>A maps to NM_031903.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:42977156 C>A maps to NM_031903.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:7981826 G>T maps to NM_176821.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:7981826 G>T maps to NM_176821.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:6669426 C>A maps to ENST00000382421 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:6669426 C>A maps to ENST00000382421 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:78433920 G>A maps to NM_001098816.2 Q1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:78433920 G>A maps to NM_001098816.2 Q1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:7960401 C>A maps to NM_001003745.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:7960401 C>A maps to NM_001003745.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:4703443 G>C maps to NM_030774.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:4703443 G>C maps to NM_030774.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:77103408 G>T maps to NM_001128620.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:77103408 G>T maps to NM_001128620.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:73720460 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:73720460 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:206480504 C>A maps to ENST00000406610 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:206480504 C>A maps to ENST00000406610 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:140221013 C>A maps to NM_018911.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:140221013 C>A maps to NM_018911.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:140725309 C>T maps to NM_018916.3 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:140725309 C>T maps to NM_018916.3 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:28293846 G>T maps to NM_012399.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:28293846 G>T maps to NM_012399.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:102057199 G>A maps to NM_016112.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:102057199 G>A maps to NM_016112.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:79745854 G>A maps to NM_007055.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:79745854 G>A maps to NM_007055.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:43171052 A>T maps to NM_001005365.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:43171052 A>T maps to NM_001005365.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:128306975 C>A maps to ENST00000368210 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:128306975 C>A maps to ENST00000368210 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:128319959 C>A maps to ENST00000368210 G874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:128319959 C>A maps to ENST00000368210 G874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:26899812 C>A maps to NM_001006665.1 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:26899812 C>A maps to NM_001006665.1 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:71354263 C>A maps to NM_001144952.1 P1849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:71354263 C>A maps to NM_001144952.1 P1849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:13868478 C>A maps to NM_025229.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:13868478 C>A maps to NM_025229.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:9488801 G>A maps to ENST00000407969 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:9488801 G>A maps to ENST00000407969 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:51215302 C>T maps to ENST00000391814 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:51215302 C>T maps to ENST00000391814 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:92915519 C>T maps to NM_153646.3 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:92915519 C>T maps to NM_153646.3 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:37356235 G>T maps to NM_080552.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:37356235 G>T maps to NM_080552.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:231327147 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:231327147 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:131388917 C>A maps to NM_001130438.2 T2176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:131388917 C>A maps to NM_001130438.2 T2176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:80724478 C>A maps to ENST00000380182 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:80724478 C>A maps to ENST00000380182 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:149503132 G>T maps to NM_198455.2 T2880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:149503132 G>T maps to NM_198455.2 T2880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:28144411 C>T maps to ENST00000373939 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:28144411 C>T maps to ENST00000373939 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:119947973 C>A maps to NM_133477.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:119947973 C>A maps to NM_133477.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:62567299 G>T maps to NM_031914.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:62567299 G>T maps to NM_031914.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:114640499 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:114640499 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:19168238 G>A maps to NM_152232.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:19168238 G>A maps to NM_152232.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:20854331 C>A maps to NM_007110.4 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:20854331 C>A maps to NM_007110.4 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:119945314 G>T maps to NM_002546.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:119945314 G>T maps to NM_002546.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:175375610 G>T maps to NM_003285.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:175375610 G>T maps to NM_003285.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:31323248 G>T maps to NM_002420.4 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:31323248 G>T maps to NM_002420.4 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:145438882 G>T maps to NM_006472.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:145438882 G>T maps to NM_006472.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:215956215 C>T maps to ENST00000366943 G3483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:215956215 C>T maps to ENST00000366943 G3483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:128481959 C>A maps to NM_018383.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:128481959 C>A maps to NM_018383.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:57647011 G>T maps to NM_052882.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:57647011 G>T maps to NM_052882.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:109701362 G>T maps to NM_021224.4 P2134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:109701362 G>T maps to NM_021224.4 P2134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:63720640 G>T maps to NM_153363.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:63720640 G>T maps to NM_153363.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:204267335 C>G maps to ENST00000295851 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:204267335 C>G maps to ENST00000295851 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20648731 C>T maps to NM_052956.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20648731 C>T maps to NM_052956.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:25044431 G>C maps to NM_004036.3 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:25044431 G>C maps to NM_004036.3 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:105409805 G>T maps to NM_138420.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:105409805 G>T maps to NM_138420.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:86893266 G>C maps to NM_001025616.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:86893266 G>C maps to NM_001025616.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:33384213 G>T maps to NM_198428.2 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:33384213 G>T maps to NM_198428.2 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:16736595 G>A maps to NM_014038.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:16736595 G>A maps to NM_014038.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:82645328 T>G maps to NM_145018.3 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:82645328 T>G maps to NM_145018.3 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr21:47706940 G>C maps to NM_058181.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr21:47706940 G>C maps to NM_058181.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:99890703 A>G maps to NM_032359.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:99890703 A>G maps to NM_032359.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:41160463 G>T maps to NM_001115131.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:41160463 G>T maps to NM_001115131.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:30619166 C>A maps to NM_001161376.1 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:30619166 C>A maps to NM_001161376.1 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:151789866 G>A maps to NM_024573.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:151789866 G>A maps to NM_024573.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:6639661 C>A maps to NM_024067.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:6639661 C>A maps to NM_024067.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:2566831 C>T maps to NM_199460.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:2566831 C>T maps to NM_199460.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:48670421 G>T maps to NM_022911.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:48670421 G>T maps to NM_022911.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:134280256 C>A maps to NM_025180.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:134280256 C>A maps to NM_025180.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:117282537 C>G maps to NM_000492.3 S1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:117282537 C>G maps to NM_000492.3 S1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:129676622 G>A maps to NM_152311.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:129676622 G>A maps to NM_152311.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:641486 G>A maps to NM_199167.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:641486 G>A maps to NM_199167.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:103548460 C>A maps to NM_080629.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:103548460 C>A maps to NM_080629.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:94038732 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:94038732 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:1389321 C>A maps to NM_175918.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:1389321 C>A maps to NM_175918.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:75924671 G>A maps to NM_031461.5 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:75924671 G>A maps to NM_031461.5 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:10800532 G>T maps to NM_014633.3 E1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:10800532 G>T maps to NM_014633.3 E1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:187122496 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:187122496 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:100774381 G>A maps to NM_014395.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:100774381 G>A maps to NM_014395.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:112337368 G>A maps to NM_152624.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:112337368 G>A maps to NM_152624.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:62498279 C>A maps to NM_004396.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:62498279 C>A maps to NM_004396.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:67365638 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:67365638 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:113850094 G>T maps to NM_000796.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:113850094 G>T maps to NM_000796.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:28588281 G>A maps to NM_001941.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:28588281 G>A maps to NM_001941.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:132958768 C>T maps to NM_015137.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:132958768 C>T maps to NM_015137.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:12897820 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:12897820 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:80636030 A>C maps to NM_022726.3 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:80636030 A>C maps to NM_022726.3 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:4858834 C>A maps to NM_053013.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:4858834 C>A maps to NM_053013.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:131973769 G>A maps to NM_005021.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:131973769 G>A maps to NM_005021.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:55170247 G>C maps to NM_001166699.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:55170247 G>C maps to NM_001166699.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:126372721 C>G maps to NM_024582.4 V3517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:126372721 C>G maps to NM_024582.4 V3517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:97053871 C>T maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:97053871 C>T maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:152285801 C>A maps to NM_002016.1 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:152285801 C>A maps to NM_002016.1 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:127240302 C>A maps to NM_020369.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:127240302 C>A maps to NM_020369.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:17449262 G>T maps to NM_001037814.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:17449262 G>T maps to NM_001037814.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:97172694 G>T maps to NM_001001557.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:97172694 G>T maps to NM_001001557.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:8062111 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:8062111 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100275741 A>T maps to NM_005273.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100275741 A>T maps to NM_005273.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:36484438 G>T maps to ENST00000398597 P1672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:36484438 G>T maps to ENST00000398597 P1672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:105795123 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:105795123 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:122626660 G>T maps to NM_005328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:122626660 G>T maps to NM_005328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:93247528 C>A maps to ENST00000446394 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:93247528 C>A maps to ENST00000446394 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:155093316 G>T maps to ENST00000344756 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:155093316 G>T maps to ENST00000344756 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:55361653 C>T maps to NM_024335.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:55361653 C>T maps to NM_024335.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:45369786 C>A maps to NM_000212.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:45369786 C>A maps to NM_000212.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:42127269 G>A maps to NM_005090.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:42127269 G>A maps to NM_005090.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:47990221 G>T maps to NM_004975.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:47990221 G>T maps to NM_004975.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:34372821 G>T maps to NM_020702.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:34372821 G>T maps to NM_020702.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:81171077 T>G maps to NM_018689.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:81171077 T>G maps to NM_018689.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:5769138 C>A maps to ENST00000414202 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:5769138 C>A maps to ENST00000414202 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:117079538 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:117079538 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:50570900 C>A maps to NM_001113546.1 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:50570900 C>A maps to NM_001113546.1 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:42052654 C>G maps to ENST00000219905 L2491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:42052654 C>G maps to ENST00000219905 L2491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:22015198 C>T maps to NM_004641.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:22015198 C>T maps to NM_004641.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:11227549 C>G maps to NM_004958.3 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:11227549 C>G maps to NM_004958.3 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:9071028 G>A maps to NM_024690.2 Q5473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:9071028 G>A maps to NM_024690.2 Q5473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:10354165 C>T maps to NM_017533.2 Q1304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:10354165 C>T maps to NM_017533.2 Q1304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:76885841 C>A maps to NM_000260.3 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:76885841 C>A maps to NM_000260.3 S659*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-6712-01A-11D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-55-6712-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:134022910 G>T maps to NM_015261.2 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:134022910 G>T maps to NM_015261.2 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:140402693 C>A maps to NM_004546.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:140402693 C>A maps to NM_004546.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:21108394 C>T maps to ENST00000430741 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:21108394 C>T maps to ENST00000430741 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:45173774 C>A maps to NM_001145107.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:45173774 C>A maps to NM_001145107.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:156135228 G>A maps to NM_000910.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:156135228 G>A maps to NM_000910.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:167673883 C>T maps to NM_001122679.1 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:167673883 C>T maps to NM_001122679.1 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:123909540 G>T maps to NM_001004463.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:123909540 G>T maps to NM_001004463.1 P56P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-6712-01A-11D-1855-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-55-6712-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:7722002 C>A maps to NM_198185.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:7722002 C>A maps to NM_198185.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140590314 C>A maps to NM_018932.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140590314 C>A maps to NM_018932.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140740397 C>T maps to NM_018923.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140740397 C>T maps to NM_018923.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:74733991 C>T maps to NM_032673.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:74733991 C>T maps to NM_032673.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:35091479 G>T maps to NM_032634.2 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:35091479 G>T maps to NM_032634.2 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:99956585 C>G maps to ENST00000413850 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:99956585 C>G maps to ENST00000413850 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:47870861 C>T maps to NM_138295.3 G2142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:47870861 C>T maps to NM_138295.3 G2142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:198948756 G>T maps to NM_006226.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:198948756 G>T maps to NM_006226.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:6528640 G>C maps to NM_198681.2 S829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:6528640 G>C maps to NM_198681.2 S829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:46997852 G>T maps to NM_020709.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:46997852 G>T maps to NM_020709.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:30804434 C>T maps to NM_015352.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:30804434 C>T maps to NM_015352.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:145724388 C>T maps to NM_032902.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:145724388 C>T maps to NM_032902.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:11420642 C>A maps to NM_006249.4 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:11420642 C>A maps to NM_006249.4 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:91512757 C>G maps to NM_003981.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:91512757 C>G maps to NM_003981.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:53569133 C>T maps to NM_014781.4 Q1085Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:53569133 C>T maps to NM_014781.4 Q1085Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:107080751 G>A maps to ENST00000357881 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:107080751 G>A maps to ENST00000357881 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:100994287 A>G maps to NM_015668.3 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:100994287 A>G maps to NM_015668.3 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:117647510 G>A maps to NM_002944.2 C1811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:117647510 G>A maps to NM_002944.2 C1811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:237617732 C>A maps to NM_001035.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:237617732 C>A maps to NM_001035.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:76757144 C>A maps to NM_171999.2 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:76757144 C>A maps to NM_171999.2 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:31351583 G>A maps to NM_014654.3 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:31351583 G>A maps to NM_014654.3 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:4273010 G>A maps to NM_152744.3 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:4273010 G>A maps to NM_152744.3 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:61654401 C>A maps to NM_198833.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:61654401 C>A maps to NM_198833.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:42281613 A>T maps to NM_015559.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:42281613 A>T maps to NM_015559.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:77406518 C>G maps to NM_024776.2 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:77406518 C>G maps to NM_024776.2 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:56938351 C>A maps to NM_000339.2 R977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:56938351 C>A maps to NM_000339.2 R977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:50819934 A>T maps to NM_003055.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:50819934 A>T maps to NM_003055.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:44463224 G>T maps to NM_201649.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:44463224 G>T maps to NM_201649.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:68344679 C>A maps to NM_032178.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:68344679 C>A maps to NM_032178.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:41078029 C>G maps to NM_020971.2 L2475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:41078029 C>G maps to NM_020971.2 L2475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:91769555 C>T maps to NM_014848.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:91769555 C>T maps to NM_014848.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:45274043 G>A maps to NM_020826.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:45274043 G>A maps to NM_020826.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:234529175 G>A maps to NM_005646.3 Q1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:234529175 G>A maps to NM_005646.3 Q1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:76446948 G>T maps to NM_003239.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:76446948 G>T maps to NM_003239.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:43779385 G>A maps to ENST00000330266 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:43779385 G>A maps to ENST00000330266 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:76130522 C>A maps to NM_152468.4 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:76130522 C>A maps to NM_152468.4 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:117846713 C>A maps to NM_002160.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:117846713 C>A maps to NM_002160.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:173155819 C>T maps to NM_003326.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:173155819 C>T maps to NM_003326.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:175355362 G>A maps to NM_003285.2 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:175355362 G>A maps to NM_003285.2 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:47409036 C>A maps to NM_022748.11 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:47409036 C>A maps to NM_022748.11 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:1418188 G>A maps to NM_000547.5 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:1418188 G>A maps to NM_000547.5 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:45052005 G>T maps to NM_182985.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:45052005 G>T maps to NM_182985.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:31770029 G>A maps to NM_020856.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:31770029 G>A maps to NM_020856.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:76507337 G>T maps to NM_015516.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:76507337 G>T maps to NM_015516.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:179468735 C>T maps to NM_133378.4 L15658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:179468735 C>T maps to NM_133378.4 L15658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:6495312 C>A maps to NM_006087.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:6495312 C>A maps to NM_006087.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:19865698 C>G maps to NM_006440.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:19865698 C>G maps to NM_006440.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:69536160 G>T maps to NM_001076.2 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:69536160 G>T maps to NM_001076.2 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:216348700 G>T maps to ENST00000366943 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:216348700 G>T maps to ENST00000366943 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:85687161 C>T maps to NM_014991.4 V1663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:85687161 C>T maps to NM_014991.4 V1663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:52940850 C>A maps to NM_001009881.2 G794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:52940850 C>A maps to NM_001009881.2 G794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:69256497 C>A maps to NM_004926.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:69256497 C>A maps to NM_004926.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:50701361 G>A maps to NM_199427.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:50701361 G>A maps to NM_199427.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:3273905 G>T maps to NM_198088.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:3273905 G>T maps to NM_198088.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:15619790 C>G maps to NM_020652.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:15619790 C>G maps to NM_020652.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:57188672 G>C maps to NM_033273.1 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:57188672 G>C maps to NM_033273.1 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:12060173 C>A maps to NM_144566.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:12060173 C>A maps to NM_144566.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48218374 G>T maps to NM_032583.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48218374 G>T maps to NM_032583.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:211085420 C>G maps to NM_001608.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:211085420 C>G maps to NM_001608.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:229568342 G>T maps to NM_001100.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:229568342 G>T maps to NM_001100.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:43925995 C>A maps to ENST00000389420 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:43925995 C>A maps to ENST00000389420 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:28296584 G>A maps to NM_007038.3 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:28296584 G>A maps to NM_007038.3 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:33562426 C>T maps to ENST00000373441 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:33562426 C>T maps to ENST00000373441 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:32878561 G>A maps to NM_000687.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:32878561 G>A maps to NM_000687.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:33205040 G>T maps to NM_004274.4 E1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:33205040 G>T maps to NM_004274.4 E1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:112235925 G>T maps to NM_000690.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:112235925 G>T maps to NM_000690.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:94014518 A>T maps to NM_032290.3 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:94014518 A>T maps to NM_032290.3 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:21261201 T>A maps to NM_145865.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:21261201 T>A maps to NM_145865.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:2127178 G>A maps to ENST00000355272 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:2127178 G>A maps to ENST00000355272 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:28906165 C>A maps to NM_173201.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:28906165 C>A maps to NM_173201.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:44441770 G>A maps to NM_004047.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:44441770 G>A maps to NM_004047.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:26043256 C>A maps to NM_016529.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:26043256 C>A maps to NM_016529.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:160294972 C>A maps to NM_013450.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:160294972 C>A maps to NM_013450.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:156618447 C>G maps to NM_021948.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:156618447 C>G maps to NM_021948.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:108042980 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:108042980 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:24922546 C>A maps to NM_018958.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:24922546 C>A maps to NM_018958.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:90138747 G>T maps to NM_152259.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:90138747 G>T maps to NM_152259.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:226176061 T>G maps to NM_152608.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:226176061 T>G maps to NM_152608.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:151020973 C>A maps to NM_017860.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:151020973 C>A maps to NM_017860.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:140972590 G>T maps to ENST00000277549 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:140972590 G>T maps to ENST00000277549 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:1969333 C>G maps to NM_172364.4 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:1969333 C>G maps to NM_172364.4 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:134552465 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:134552465 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:30955325 C>A maps to ENST00000295055 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:30955325 C>A maps to ENST00000295055 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:25261484 G>T maps to NM_018272.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:25261484 G>T maps to NM_018272.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:7559188 T>C maps to ENST00000416109 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:7559188 T>C maps to ENST00000416109 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:227219082 T>G maps to ENST00000366766 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:227219082 T>G maps to ENST00000366766 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:64606194 A>G maps to NM_017525.2 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:64606194 A>G maps to NM_017525.2 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:58567502 G>T maps to NM_177980.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:58567502 G>T maps to NM_177980.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:63511298 G>C maps to NM_004361.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:63511298 G>C maps to NM_004361.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:61851500 C>A maps to NM_001796.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:61851500 C>A maps to NM_001796.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:26915966 G>A maps to NM_016279.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:26915966 G>A maps to NM_016279.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:34854815 G>C maps to NM_020180.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:34854815 G>C maps to NM_020180.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:134278165 T>C maps to NM_025180.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:134278165 T>C maps to NM_025180.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:184104631 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:184104631 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:233406158 G>A maps to NM_005199.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:233406158 G>A maps to NM_005199.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:154509357 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:154509357 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:99941252 G>T maps to NM_014361.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:99941252 G>T maps to NM_014361.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:99945011 T>C maps to NM_014361.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:99945011 T>C maps to NM_014361.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:125281943 G>T maps to NM_130773.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:125281943 G>T maps to NM_130773.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:75899097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:75899097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:121220514 G>A maps to NM_021110.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:121220514 G>A maps to NM_021110.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:189859296 G>T maps to NM_000090.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:189859296 G>T maps to NM_000090.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:189929365 G>T maps to NM_000393.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:189929365 G>T maps to NM_000393.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:61453143 C>A maps to NM_001853.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:61453143 C>A maps to NM_001853.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:47685847 G>A maps to NM_006587.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:47685847 G>A maps to NM_006587.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:125528161 C>A maps to NM_198148.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:125528161 C>A maps to NM_198148.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:2808658 G>T maps to NM_033225.5 S3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:2808658 G>T maps to NM_033225.5 S3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113988230 C>A maps to NM_198123.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113988230 C>A maps to NM_198123.1 E393*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-1676-01A-01D-0969-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-64-1676-01A-01D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:101892231 G>T maps to ENST00000360264 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:101892231 G>T maps to ENST00000360264 L1487L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-1676-01A-01D-0969-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-64-1676-01A-01D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:88885854 G>T maps to NM_152418.3 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:88885854 G>T maps to NM_152418.3 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:15983174 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:15983174 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:23018527 C>T maps to NM_182699.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:23018527 C>T maps to NM_182699.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:124364245 G>A maps to NM_207437.3 R2726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:124364245 G>A maps to NM_207437.3 R2726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:38758174 A>G maps to ENST00000327475 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:38758174 A>G maps to ENST00000327475 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:63084480 C>G maps to ENST00000371140 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:63084480 C>G maps to ENST00000371140 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:21768282 C>G maps to NM_003974.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:21768282 C>G maps to NM_003974.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:113515245 C>A maps to NM_004416.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:113515245 C>A maps to NM_004416.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:103128357 C>T maps to NM_001080463.1 L3502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:103128357 C>T maps to NM_001080463.1 L3502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:207528120 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:207528120 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:36381062 C>T maps to NM_012199.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:36381062 C>T maps to NM_012199.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:153609286 G>A maps to NM_000117.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:153609286 G>A maps to NM_000117.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:142566455 G>T maps to NM_004445.3 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:142566455 G>T maps to NM_004445.3 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:158531730 C>G maps to NM_020728.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:158531730 C>G maps to NM_020728.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:25744473 C>A maps to NM_152704.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:25744473 C>A maps to NM_152704.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:89772322 G>A maps to NM_014883.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:89772322 G>A maps to NM_014883.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:187077231 G>T maps to ENST00000356371 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:187077231 G>T maps to ENST00000356371 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:242402802 G>T maps to NM_014808.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:242402802 G>T maps to NM_014808.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:92620172 G>A maps to ENST00000298047 G4315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:92620172 G>A maps to ENST00000298047 G4315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:125109516 C>T maps to NM_001039112.2 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:125109516 C>T maps to NM_001039112.2 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:102378992 T>G maps to NM_175929.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:102378992 T>G maps to NM_175929.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:240255645 G>T maps to ENST00000406993 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:240255645 G>T maps to ENST00000406993 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:50045836 C>G maps to NM_175736.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:50045836 C>G maps to NM_175736.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:37744665 A>C maps to NM_014907.2 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:37744665 A>C maps to NM_014907.2 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:48584627 A>T maps to NM_015030.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:48584627 A>T maps to NM_015030.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:89523825 G>A maps to NM_002053.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:89523825 G>A maps to NM_002053.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:172163025 G>T maps to NM_198407.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:172163025 G>T maps to NM_198407.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:58604549 T>C maps to NM_145016.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:58604549 T>C maps to NM_145016.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:58605832 G>T maps to NM_145016.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:58605832 G>T maps to NM_145016.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:135428121 G>T maps to NM_153834.3 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:135428121 G>T maps to NM_153834.3 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131487639 G>T maps to NM_207364.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131487639 G>T maps to NM_207364.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:94134233 G>C maps to NM_016540.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:94134233 G>C maps to NM_016540.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:117128060 G>C maps to NM_148963.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:117128060 G>C maps to NM_148963.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:43436450 A>G maps to NM_015052.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:43436450 A>G maps to NM_015052.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:185959563 G>A maps to NM_031935.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:185959563 G>A maps to NM_031935.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:14248434 G>T maps to NM_006041.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:14248434 G>T maps to NM_006041.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:81585041 G>T maps to NM_172217.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:81585041 G>T maps to NM_172217.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43922292 C>T maps to NM_175882.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43922292 C>T maps to NM_175882.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182322937 G>A maps to NM_000885.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182322937 G>A maps to NM_000885.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:31309151 G>T maps to NM_001145808.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:31309151 G>T maps to NM_001145808.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:226822506 C>A maps to NM_002221.3 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:226822506 C>A maps to NM_002221.3 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:59970756 A>T maps to ENST00000356057 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:59970756 A>T maps to ENST00000356057 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110754217 G>T maps to NM_004978.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110754217 G>T maps to NM_004978.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:62044882 G>C maps to NM_172107.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:62044882 G>C maps to NM_172107.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:77727719 G>A maps to NM_023930.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:77727719 G>A maps to NM_023930.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43004446 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43004446 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:51901353 G>T maps to NM_032559.4 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:51901353 G>T maps to NM_032559.4 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31768508 C>T maps to NM_181599.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31768508 C>T maps to NM_181599.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31914062 G>T maps to ENST00000437381 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31914062 G>T maps to ENST00000437381 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:152759840 C>T maps to NM_178353.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:152759840 C>T maps to NM_178353.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:66083706 G>A maps to NM_002303.5 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:66083706 G>A maps to NM_002303.5 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:48653098 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:48653098 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:33886332 G>A maps to NM_005574.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:33886332 G>A maps to NM_005574.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:30254904 C>T maps to NM_002365.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:30254904 C>T maps to NM_002365.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:140969329 G>T maps to NM_138702.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:140969329 G>T maps to NM_138702.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:12491435 G>A maps to NM_018050.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:12491435 G>A maps to NM_018050.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43364127 G>A maps to ENST00000344686 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43364127 G>A maps to ENST00000344686 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:48248366 G>T maps to NM_002747.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:48248366 G>T maps to NM_002747.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:164466874 G>T maps to ENST00000514618 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:164466874 G>T maps to ENST00000514618 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:119727849 C>A maps to NM_006770.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:119727849 C>A maps to NM_006770.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:151134111 C>T maps to NM_053002.4 Q2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:151134111 C>T maps to NM_053002.4 Q2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:126776494 C>T maps to NM_032446.2 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:126776494 C>T maps to NM_032446.2 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:19288710 G>T maps to NM_001198695.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:19288710 G>T maps to NM_001198695.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:7612173 C>A maps to NM_019005.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:7612173 C>A maps to NM_019005.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:146576325 G>T maps to NM_172250.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:146576325 G>T maps to NM_172250.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:60064674 G>T maps to NM_148975.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:60064674 G>T maps to NM_148975.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:100678560 G>T maps to NM_001040105.1 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:100678560 G>T maps to NM_001040105.1 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:3248431 G>T maps to NM_015419.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:3248431 G>T maps to NM_015419.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23866763 C>A maps to NM_002471.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23866763 C>A maps to NM_002471.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:203053127 G>T maps to NM_002479.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:203053127 G>T maps to NM_002479.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:80246770 G>T maps to NM_032693.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:80246770 G>T maps to NM_032693.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:22849674 G>T maps to NM_004540.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:22849674 G>T maps to NM_004540.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:158494629 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:158494629 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:236192919 C>A maps to NM_002508.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:236192919 C>A maps to NM_002508.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:50744733 C>A maps to NM_022162.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:50744733 C>A maps to NM_022162.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153995617 C>T maps to NM_207308.2 Q1426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153995617 C>T maps to NM_207308.2 Q1426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:7531355 C>A maps to NM_198474.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:7531355 C>A maps to NM_198474.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:55735297 G>A maps to NM_001005491.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:55735297 G>A maps to NM_001005491.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123900721 C>A maps to ENST00000375021 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123900721 C>A maps to ENST00000375021 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:107332059 G>T maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:107332059 G>T maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:247835509 C>A maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:247835509 C>A maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:114090286 G>T maps to ENST00000374428 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:114090286 G>T maps to ENST00000374428 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123811223 C>T maps to NM_001001965.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123811223 C>T maps to NM_001001965.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:56380870 T>A maps to NM_001004740.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:56380870 T>A maps to NM_001004740.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:21108971 A>G maps to NM_001001968.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:21108971 A>G maps to NM_001001968.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123777158 C>T maps to NM_001005197.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123777158 C>T maps to NM_001005197.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:56511221 G>T maps to NM_001005284.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:56511221 G>T maps to NM_001005284.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:81905542 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:81905542 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:176738882 C>T maps to NM_020318.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:176738882 C>T maps to NM_020318.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:142537296 G>T maps to NM_013363.3 Y376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:142537296 G>T maps to NM_013363.3 Y376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:239165692 C>A maps to NM_022817.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:239165692 C>A maps to NM_022817.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:106513258 G>T maps to NM_002649.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:106513258 G>T maps to NM_002649.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:4934425 C>T maps to NM_002705.4 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:4934425 C>T maps to NM_002705.4 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:47087823 G>A maps to NM_005972.4 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:47087823 G>A maps to NM_005972.4 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:5294628 G>T maps to NM_144773.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:5294628 G>T maps to NM_144773.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:87701590 T>G maps to NM_080685.2 S1981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:87701590 T>G maps to NM_080685.2 S1981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:95412525 C>T maps to NM_012415.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:95412525 C>T maps to NM_012415.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:204128528 G>A maps to NM_000537.3 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:204128528 G>A maps to NM_000537.3 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:40705941 C>T maps to NM_012421.3 S1856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:40705941 C>T maps to NM_012421.3 S1856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:119207085 C>T maps to NM_032015.3 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:119207085 C>T maps to NM_032015.3 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:187416441 C>T maps to NM_001004312.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:187416441 C>T maps to NM_001004312.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:93004038 G>T maps to NM_175634.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:93004038 G>T maps to NM_175634.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:101704716 C>A maps to NM_001400.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:101704716 C>A maps to NM_001400.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:39556194 A>C maps to NM_006364.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:39556194 A>C maps to NM_006364.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:13912363 T>A maps to NM_025229.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:13912363 T>A maps to NM_025229.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:122631816 G>T maps to NM_001031702.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:122631816 G>T maps to NM_001031702.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:1719991 G>T maps to NM_005088.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:1719991 G>T maps to NM_005088.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:101944559 C>T maps to ENST00000306803 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:101944559 C>T maps to ENST00000306803 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:156784832 G>T maps to NM_001161441.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:156784832 G>T maps to NM_001161441.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56901118 G>A maps to NM_000339.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56901118 G>A maps to NM_000339.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:113456701 G>A maps to NM_003051.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:113456701 G>A maps to NM_003051.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62751942 G>A maps to NM_004790.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62751942 G>A maps to NM_004790.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:10027562 C>A maps to NM_001001290.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:10027562 C>A maps to NM_001001290.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:118174009 C>A maps to NM_173851.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:118174009 C>A maps to NM_173851.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75672393 C>A maps to NM_152697.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75672393 C>A maps to NM_152697.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:19445752 G>T maps to ENST00000395585 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:19445752 G>T maps to ENST00000395585 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:162661083 G>T maps to NM_001178015.1 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:162661083 G>T maps to NM_001178015.1 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:48504416 G>T maps to ENST00000417961 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:48504416 G>T maps to ENST00000417961 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21355422 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21355422 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:168096926 C>A maps to NM_003062.2 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:168096926 C>A maps to NM_003062.2 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:138586906 C>T maps to NM_001101677.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:138586906 C>T maps to NM_001101677.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:106960960 A>G maps to NM_014978.1 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:106960960 A>G maps to NM_014978.1 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158644392 A>T maps to NM_003126.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158644392 A>T maps to NM_003126.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:149486457 G>T maps to NM_198455.2 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:149486457 G>T maps to NM_198455.2 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:66812116 C>A maps to NM_001177880.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:66812116 C>A maps to NM_001177880.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:143141255 C>G maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:143141255 C>G maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:71604707 T>A maps to NM_000353.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:71604707 T>A maps to NM_000353.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:44555226 G>A maps to NM_145653.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:44555226 G>A maps to NM_145653.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:169648570 G>A maps to NM_003247.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:169648570 G>A maps to NM_003247.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:122755272 G>A maps to NM_001081550.1 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:122755272 G>A maps to NM_001081550.1 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:43779578 G>T maps to NM_005424.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:43779578 G>T maps to NM_005424.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:153692093 T>C maps to NM_145720.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:153692093 T>C maps to NM_145720.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:54214561 C>A maps to NM_014464.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:54214561 C>A maps to NM_014464.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:166935712 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:166935712 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:75387408 G>A maps to NM_138691.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:75387408 G>A maps to NM_138691.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:32962069 G>T maps to NM_207313.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:32962069 G>T maps to NM_207313.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:83417292 C>T maps to NM_001080506.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:83417292 C>T maps to NM_001080506.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:74902191 C>T maps to NM_001112808.2 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:74902191 C>T maps to NM_001112808.2 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:67190464 C>A maps to NM_003789.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:67190464 C>A maps to NM_003789.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:42166915 G>T maps to NM_001042646.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:42166915 G>T maps to NM_001042646.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248028077 G>A maps to NM_015431.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248028077 G>A maps to NM_015431.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77378051 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77378051 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:54586107 C>A maps to ENST00000260323 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:54586107 C>A maps to ENST00000260323 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:62304304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:62304304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:228771915 A>T maps to NM_178821.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:228771915 A>T maps to NM_178821.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:715996 G>A maps to NM_145294.4 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:715996 G>A maps to NM_145294.4 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:145274896 C>A maps to NM_014795.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:145274896 C>A maps to NM_014795.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:49559352 C>A maps to NM_015069.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:49559352 C>A maps to NM_015069.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:88965692 G>T maps to NM_181646.2 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:88965692 G>T maps to NM_181646.2 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:50121454 C>A maps to NM_007009.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:50121454 C>A maps to NM_007009.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:126180701 C>A maps to NM_025112.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:126180701 C>A maps to NM_025112.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:105948529 C>G maps to NM_015423.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:105948529 C>G maps to NM_015423.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:16225761 C>T maps to ENST00000399408 H1322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:16225761 C>T maps to ENST00000399408 H1322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:121175682 C>T maps to NM_000017.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:121175682 C>T maps to NM_000017.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:105419326 G>A maps to NM_138420.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:105419326 G>A maps to NM_138420.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:64935711 C>T maps to NM_004857.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:64935711 C>T maps to NM_004857.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:29498007 G>T maps to NM_004304.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:29498007 G>T maps to NM_004304.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:56204799 C>A maps to NM_052947.3 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:56204799 C>A maps to NM_052947.3 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:5922262 G>C maps to NM_001009941.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:5922262 G>C maps to NM_001009941.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:160141393 G>C maps to NM_144699.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:160141393 G>C maps to NM_144699.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:112600870 C>T maps to NM_001109662.2 K4193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:112600870 C>T maps to NM_001109662.2 K4193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:209956823 T>A maps to NM_152485.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:209956823 T>A maps to NM_152485.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:151859247 G>A maps to ENST00000367290 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:151859247 G>A maps to ENST00000367290 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:42678467 G>A maps to NM_000070.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:42678467 G>A maps to NM_000070.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:40902475 G>C maps to NM_170589.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:40902475 G>C maps to NM_170589.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:21751992 G>A maps to NM_004061.3 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:21751992 G>A maps to NM_004061.3 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:42552715 C>A maps to NM_000749.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:42552715 C>A maps to NM_000749.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:101978566 C>T maps to NM_001278.3 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:101978566 C>T maps to NM_001278.3 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:12274207 C>A maps to ENST00000342845 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:12274207 C>A maps to ENST00000342845 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:68549255 G>A maps to NM_001876.3 H445H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:68549255 G>A maps to NM_001876.3 H445H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:113883758 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:113883758 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:113897451 C>T maps to NM_001008895.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:113897451 C>T maps to NM_001008895.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:155001739 C>T maps to NM_144622.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:155001739 C>T maps to NM_144622.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:28934417 T>A maps to NM_001942.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:28934417 T>A maps to NM_001942.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:76818122 G>C maps to NM_001003892.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:76818122 G>C maps to NM_001003892.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:8934895 G>C maps to NM_001428.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:8934895 G>C maps to NM_001428.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:89660225 C>T maps to NM_014883.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:89660225 C>T maps to NM_014883.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:190195449 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:190195449 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:54806252 T>C maps to NM_001010872.1 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:54806252 T>C maps to NM_001010872.1 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:152323125 G>C maps to NM_001014342.2 S2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:152323125 G>C maps to NM_001014342.2 S2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:30949385 T>A maps to ENST00000327783 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:30949385 T>A maps to ENST00000327783 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:145038045 C>G maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:145038045 C>G maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:43016641 C>G maps to ENST00000458501 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:43016641 C>G maps to ENST00000458501 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:27565833 C>A maps to NM_152740.3 *337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:27565833 C>A maps to NM_152740.3 *337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:25726494 C>T maps to NM_170745.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:25726494 C>T maps to NM_170745.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:152190894 T>G maps to NM_001009931.1 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:152190894 T>G maps to NM_001009931.1 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:91144395 C>T maps to NM_001010987.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:91144395 C>T maps to NM_001010987.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:27457348 C>A maps to NM_181079.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:27457348 C>A maps to NM_181079.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:31477920 C>A maps to NM_144981.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:31477920 C>A maps to NM_144981.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:124665151 T>C maps to NM_001081675.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:124665151 T>C maps to NM_001081675.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:10599198 G>C maps to NM_213658.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:10599198 G>C maps to NM_213658.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:10583764 G>C maps to NM_002260.3 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:10583764 G>C maps to NM_002260.3 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:139847405 G>A maps to NM_178536.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:139847405 G>A maps to NM_178536.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:42360650 C>G maps to NM_152447.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:42360650 C>G maps to NM_152447.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:77745476 G>A maps to NM_001134745.1 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:77745476 G>A maps to NM_001134745.1 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:149013936 T>C maps to NM_005364.4 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:149013936 T>C maps to NM_005364.4 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:125580617 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:125580617 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:8966816 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:8966816 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:10409226 A>T maps to NM_005963.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:10409226 A>T maps to NM_005963.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr22:21377427 C>A maps to NM_005446.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr22:21377427 C>A maps to NM_005446.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:10695299 G>T maps to NM_017906.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:10695299 G>T maps to NM_017906.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:14645890 C>T maps to NM_002582.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:14645890 C>T maps to NM_002582.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:140236392 C>T maps to NM_018901.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:140236392 C>T maps to NM_018901.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:140481828 C>T maps to NM_018937.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:140481828 C>T maps to NM_018937.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:178762820 G>A maps to NM_016953.3 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:178762820 G>A maps to NM_016953.3 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:7077177 G>A maps to NM_001144831.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:7077177 G>A maps to NM_001144831.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:133848836 G>A maps to ENST00000395386 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:133848836 G>A maps to ENST00000395386 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:144994217 G>A maps to NM_201380.2 I3394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:144994217 G>A maps to NM_201380.2 I3394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:122334781 C>T maps to NM_001030059.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:122334781 C>T maps to NM_001030059.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:81112121 C>T maps to NM_005729.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:81112121 C>T maps to NM_005729.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:94733328 C>G maps to NM_058237.1 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:94733328 C>G maps to NM_058237.1 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:120650308 G>A maps to NM_001080855.1 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:120650308 G>A maps to NM_001080855.1 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:17699058 A>T maps to NM_001099218.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:17699058 A>T maps to NM_001099218.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:178745931 C>G maps to NM_152663.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:178745931 C>G maps to NM_152663.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:95091259 C>T maps to NM_014899.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:95091259 C>T maps to NM_014899.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:155230147 G>A maps to NM_005698.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:155230147 G>A maps to NM_005698.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:4116732 C>A maps to NM_152744.3 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:4116732 C>A maps to NM_152744.3 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:4198172 G>C maps to NM_152744.3 T1573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:4198172 G>C maps to NM_152744.3 T1573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:50350943 C>A maps to NM_020717.3 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:50350943 C>A maps to NM_020717.3 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:117050023 G>T maps to NM_001040455.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:117050023 G>T maps to NM_001040455.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:51633159 G>T maps to NM_014441.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:51633159 G>T maps to NM_014441.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:50819358 C>T maps to NM_003055.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:50819358 C>T maps to NM_003055.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:67473636 G>A maps to NM_005902.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:67473636 G>A maps to NM_005902.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:74046603 C>A maps to NM_014230.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:74046603 C>A maps to NM_014230.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:22354962 G>A maps to NM_003034.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:22354962 G>A maps to NM_003034.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:8007005 G>A maps to NM_031923.2 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:8007005 G>A maps to NM_031923.2 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:31129530 C>A maps to NM_007109.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:31129530 C>A maps to NM_007109.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:2290899 G>A maps to NM_003245.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:2290899 G>A maps to NM_003245.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:47221536 G>A maps to ENST00000394850 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:47221536 G>A maps to ENST00000394850 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:7692715 G>A maps to NM_020196.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:7692715 G>A maps to NM_020196.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:80608438 G>T maps to NM_032280.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:80608438 G>T maps to NM_032280.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:77619867 C>G maps to NM_024721.4 S893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:77619867 C>G maps to NM_024721.4 S893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:57646336 G>A maps to NM_052882.1 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:57646336 G>A maps to NM_052882.1 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:148801600 C>T maps to NM_001001661.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:148801600 C>T maps to NM_001001661.2 R454R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-64-1677-01A-01W-0928-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-64-1677-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:179076966 G>A maps to NM_007314.3 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:179076966 G>A maps to NM_007314.3 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:236882305 C>T maps to NM_001103.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:236882305 C>T maps to NM_001103.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:33576860 G>T maps to NM_030955.2 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:33576860 G>T maps to NM_030955.2 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:28212676 C>T maps to NM_006988.3 W528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:28212676 C>T maps to NM_006988.3 W528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:131795973 G>T maps to NM_001115.2 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:131795973 G>T maps to NM_001115.2 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:83349658 C>T maps to NM_004644.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:83349658 C>T maps to NM_004644.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:27106170 A>T maps to NM_006015.4 K1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:27106170 A>T maps to NM_006015.4 K1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:98512351 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:98512351 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:25264582 C>T maps to NM_001185085.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:25264582 C>T maps to NM_001185085.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160100251 G>T maps to NM_000702.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160100251 G>T maps to NM_000702.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:102751287 C>T maps to NM_017935.4 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:102751287 C>T maps to NM_017935.4 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:54417448 G>A maps to NM_130850.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:54417448 G>A maps to NM_130850.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:112744002 G>A maps to NM_001109662.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:112744002 G>A maps to NM_001109662.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:1953619 T>A maps to NM_172364.4 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:1953619 T>A maps to NM_172364.4 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:169023608 A>G maps to NM_017785.4 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:169023608 A>G maps to NM_017785.4 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:25562987 G>A maps to NM_001792.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:25562987 G>A maps to NM_001792.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:11219944 G>T maps to ENST00000409790 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:11219944 G>T maps to ENST00000409790 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:45495878 C>T maps to NM_001294.2 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:45495878 C>T maps to NM_001294.2 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:2775234 C>T maps to NM_019609.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:2775234 C>T maps to NM_019609.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr22:37329914 C>A maps to ENST00000262825 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr22:37329914 C>A maps to ENST00000262825 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:11098776 G>T maps to NM_001332.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:11098776 G>T maps to NM_001332.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:43166497 C>T maps to ENST00000354495 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:43166497 C>T maps to ENST00000354495 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:47810185 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:47810185 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:32678390 G>A maps to NM_001099434.1 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:32678390 G>A maps to NM_001099434.1 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:155156959 G>A maps to NM_017639.3 L2493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:155156959 G>A maps to NM_017639.3 L2493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:50563116 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:50563116 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:103908204 C>A maps to NM_001001711.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:103908204 C>A maps to NM_001001711.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:223177390 G>A maps to NM_032890.2 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:223177390 G>A maps to NM_032890.2 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:51829945 C>A maps to NM_001174116.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:51829945 C>A maps to NM_001174116.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:124297767 G>T maps to NM_207437.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:124297767 G>T maps to NM_207437.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:131671815 G>T maps to ENST00000355311 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:131671815 G>T maps to ENST00000355311 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:89456500 C>A maps to NM_005233.5 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:89456500 C>A maps to NM_005233.5 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:226016459 G>T maps to NM_001136018.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:226016459 G>T maps to NM_001136018.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:187625876 C>A maps to NM_177454.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:187625876 C>A maps to NM_177454.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:34148607 A>T maps to NM_203408.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:34148607 A>T maps to NM_203408.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:163082061 T>A maps to NM_004460.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:163082061 T>A maps to NM_004460.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:127597559 G>C maps to NM_001999.3 Y2744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:127597559 G>C maps to NM_001999.3 Y2744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:135440086 T>A maps to ENST00000443774 K54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:135440086 T>A maps to ENST00000443774 K54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:49393635 A>T maps to NM_001018071.3 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:49393635 A>T maps to NM_001018071.3 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:90024815 G>A maps to NM_002043.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:90024815 G>A maps to NM_002043.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:48413793 G>T maps to NM_016204.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:48413793 G>T maps to NM_016204.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:42063146 C>A maps to NM_000168.5 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:42063146 C>A maps to NM_000168.5 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:36246103 C>T maps to NM_001128227.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:36246103 C>T maps to NM_001128227.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:231403467 C>T maps to NM_014236.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:231403467 C>T maps to NM_014236.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:88780773 G>T maps to NM_001143831.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:88780773 G>T maps to NM_001143831.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:18380136 C>T maps to NM_005316.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:18380136 C>T maps to NM_005316.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:11401488 T>A maps to NM_005114.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:11401488 T>A maps to NM_005114.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:74759975 T>A maps to NM_013247.4 L414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:74759975 T>A maps to NM_013247.4 L414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:143129682 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:143129682 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:156812833 C>A maps to NM_014215.2 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:156812833 C>A maps to NM_014215.2 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:30837253 G>T maps to NM_006390.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:30837253 G>T maps to NM_006390.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:30843466 T>A maps to NM_006390.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:30843466 T>A maps to NM_006390.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:68596107 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:68596107 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:7659105 G>T maps to ENST00000256861 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:7659105 G>T maps to ENST00000256861 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:143586156 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:143586156 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:215792514 G>T maps to NM_016121.3 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:215792514 G>T maps to NM_016121.3 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:142639571 C>A maps to NM_000420.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:142639571 C>A maps to NM_000420.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:126061388 C>A maps to ENST00000377985 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:126061388 C>A maps to ENST00000377985 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:21016807 G>T maps to NM_020816.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:21016807 G>T maps to NM_020816.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:152648743 C>A maps to NM_178429.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:152648743 C>A maps to NM_178429.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:40399649 G>T maps to NM_020737.1 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:40399649 G>T maps to NM_020737.1 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:141116450 C>T maps to NM_018557.2 S3732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:141116450 C>T maps to NM_018557.2 S3732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:101597251 G>A maps to NM_024652.3 E1508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:101597251 G>A maps to NM_024652.3 E1508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:18956124 G>T maps to NM_147199.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:18956124 G>T maps to NM_147199.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:60558556 G>T maps to NM_206893.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:60558556 G>T maps to NM_206893.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:2254170 C>A maps to NM_006454.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:2254170 C>A maps to NM_006454.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:45299120 G>A maps to NM_002476.2 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:45299120 G>A maps to NM_002476.2 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:72197313 G>A maps to ENST00000424560 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:72197313 G>A maps to ENST00000424560 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:120381809 G>A maps to NM_001047980.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:120381809 G>A maps to NM_001047980.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:133541593 C>A maps to NM_207363.2 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:133541593 C>A maps to NM_207363.2 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70375175 C>T maps to NM_181303.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70375175 C>T maps to NM_181303.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70375181 C>T maps to NM_181303.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70375181 C>T maps to NM_181303.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70375184 C>T maps to NM_181303.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70375184 C>T maps to NM_181303.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:54314477 C>A maps to ENST00000391773 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:54314477 C>A maps to ENST00000391773 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:247597422 C>A maps to NM_004895.4 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:247597422 C>A maps to NM_004895.4 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:2954073 C>T maps to NM_003703.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:2954073 C>T maps to NM_003703.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:50885780 G>A maps to NM_007121.4 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:50885780 G>A maps to NM_007121.4 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:127300524 G>A maps to NM_033334.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:127300524 G>A maps to NM_033334.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:123518363 G>T maps to NM_001163278.1 R2139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:123518363 G>T maps to NM_001163278.1 R2139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:78412652 C>A maps to NM_001098816.2 E1669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:78412652 C>A maps to NM_001098816.2 E1669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:6807143 G>A maps to NM_001004489.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:6807143 G>A maps to NM_001004489.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:143633236 A>G maps to NM_001004685.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:143633236 A>G maps to NM_001004685.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:247752206 C>T maps to NM_001001915.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:247752206 C>T maps to NM_001001915.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:248402553 T>C maps to NM_017504.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:248402553 T>C maps to NM_017504.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:49974393 C>T maps to NM_001001955.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:49974393 C>T maps to NM_001001955.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:55322591 C>G maps to NM_001001920.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:55322591 C>G maps to NM_001001920.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:6023493 C>A maps to NM_001005179.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:6023493 C>A maps to NM_001005179.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:56128657 C>T maps to NM_001005205.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:56128657 C>T maps to NM_001005205.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:93862606 G>T maps to NM_015368.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:93862606 G>T maps to NM_015368.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:55721549 G>T maps to NM_001142763.1 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:55721549 G>T maps to NM_001142763.1 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:140563162 T>C maps to NM_020957.1 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:140563162 T>C maps to NM_020957.1 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:140736506 C>T maps to NM_018917.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:140736506 C>T maps to NM_018917.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:60646228 G>T maps to NM_194449.2 R1573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:60646228 G>T maps to NM_194449.2 R1573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:130839523 G>T maps to NM_004764.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:130839523 G>T maps to NM_004764.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:160901381 C>A maps to NM_007366.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:160901381 C>A maps to NM_007366.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:111427041 G>T maps to ENST00000312791 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:111427041 G>T maps to ENST00000312791 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:22325424 G>T maps to NM_018119.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:22325424 G>T maps to NM_018119.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:113518040 G>A maps to NM_002711.3 Q1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:113518040 G>A maps to NM_002711.3 Q1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:64699038 G>T maps to NM_006244.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:64699038 G>T maps to NM_006244.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:120112182 C>T maps to NM_006253.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:120112182 C>T maps to NM_006253.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:120112186 C>T maps to NM_006253.4 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:120112186 C>T maps to NM_006253.4 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:128186389 C>T maps to ENST00000409048 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:128186389 C>T maps to ENST00000409048 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:214170381 G>C maps to NM_002763.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:214170381 G>C maps to NM_002763.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:46873407 C>A maps to NM_182702.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:46873407 C>A maps to NM_182702.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:38873890 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:38873890 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:139115926 C>T maps to NM_181701.3 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:139115926 C>T maps to NM_181701.3 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:112671066 C>T maps to NM_001013734.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:112671066 C>T maps to NM_001013734.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:124754801 A>T maps to NM_019055.5 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:124754801 A>T maps to NM_019055.5 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr22:23401722 C>A maps to NM_014433.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr22:23401722 C>A maps to NM_014433.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:237664074 T>C maps to NM_001035.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:237664074 T>C maps to NM_001035.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:23909781 C>A maps to NM_014363.4 E2745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:23909781 C>A maps to NM_014363.4 E2745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:6463649 C>A maps to NM_001159576.1 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:6463649 C>A maps to NM_001159576.1 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:110448545 G>T maps to NM_006323.2 G1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:110448545 G>T maps to NM_006323.2 G1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:116728894 G>A maps to ENST00000445177 Q1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:116728894 G>A maps to ENST00000445177 Q1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:35918952 G>T maps to NM_052961.3 S820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:35918952 G>T maps to NM_052961.3 S820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:1240645 G>A maps to NM_182632.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:1240645 G>A maps to NM_182632.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:140335778 G>A maps to ENST00000452778 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:140335778 G>A maps to ENST00000452778 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:88416204 G>T maps to NM_004684.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:88416204 G>T maps to NM_004684.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:119554753 T>A maps to NM_194286.2 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:119554753 T>A maps to NM_194286.2 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:12785742 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:12785742 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:39997214 C>A maps to NM_025264.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:39997214 C>A maps to NM_025264.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:82242320 G>T maps to ENST00000376537 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:82242320 G>T maps to ENST00000376537 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:82336677 G>T maps to ENST00000376537 G653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:82336677 G>T maps to ENST00000376537 G653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:27262915 G>T maps to NM_017727.4 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:27262915 G>T maps to NM_017727.4 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:29927563 C>T maps to NM_016127.4 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:29927563 C>T maps to NM_016127.4 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:76061007 G>A maps to NM_001142640.1 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:76061007 G>A maps to NM_001142640.1 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:10920155 C>A maps to NM_199261.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:10920155 C>A maps to NM_199261.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:55032516 C>A maps to ENST00000357530 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:55032516 C>A maps to ENST00000357530 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:73235266 C>T maps to ENST00000419692 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:73235266 C>T maps to ENST00000419692 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:49691968 C>T maps to NM_017636.3 D605D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:49691968 C>T maps to NM_017636.3 D605D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:116617220 T>A maps to NM_014112.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:116617220 T>A maps to NM_014112.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:4924651 G>A maps to NM_016936.3 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:4924651 G>A maps to NM_016936.3 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:71555767 G>A maps to NM_020368.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:71555767 G>A maps to NM_020368.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:168101223 G>T maps to NM_152381.5 E1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:168101223 G>T maps to NM_152381.5 E1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:56436302 A>T maps to NM_052898.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:56436302 A>T maps to NM_052898.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:17221645 G>A maps to NM_022166.3 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:17221645 G>A maps to NM_022166.3 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:17228361 C>A maps to NM_022166.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:17228361 C>A maps to NM_022166.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:47271904 G>T maps to NM_003446.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:47271904 G>T maps to NM_003446.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:52869018 G>T maps to NM_001161425.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:52869018 G>T maps to NM_001161425.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:38033025 A>T maps to NM_199321.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:38033025 A>T maps to NM_199321.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:57935363 C>T maps to NM_007156.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:57935363 C>T maps to NM_007156.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:957720 C>T maps to NM_198576.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:957720 C>T maps to NM_198576.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr14:105412631 G>A maps to NM_138420.2 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr14:105412631 G>A maps to NM_138420.2 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:241451412 G>A maps to ENST00000401804 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:241451412 G>A maps to ENST00000401804 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr15:24922678 C>T maps to NM_018958.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr15:24922678 C>T maps to NM_018958.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:107013190 G>A maps to NM_006348.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:107013190 G>A maps to NM_006348.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr6:43184060 C>T maps to ENST00000354495 G2034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr6:43184060 C>T maps to ENST00000354495 G2034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr15:41224583 C>A maps to NM_019074.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr15:41224583 C>A maps to NM_019074.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:196664037 T>A maps to NM_018897.2 L3445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:196664037 T>A maps to NM_018897.2 L3445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:68802077 G>C maps to NM_182522.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:68802077 G>C maps to NM_182522.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr16:9858027 C>A maps to NM_000833.3 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr16:9858027 C>A maps to NM_000833.3 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:80677880 G>A maps to NM_001040708.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:80677880 G>A maps to NM_001040708.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr21:40778293 G>T maps to NM_152505.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr21:40778293 G>T maps to NM_152505.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr15:91449665 C>G maps to NM_006122.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr15:91449665 C>G maps to NM_006122.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:206628555 G>T maps to NM_201266.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:206628555 G>T maps to NM_201266.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:186413130 C>A maps to ENST00000340129 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:186413130 C>A maps to ENST00000340129 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr20:4680093 C>T maps to NM_001080123.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr20:4680093 C>T maps to NM_001080123.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr13:49076004 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr13:49076004 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:1159218 G>A maps to NM_016176.3 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:1159218 G>A maps to NM_016176.3 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:127785934 C>T maps to ENST00000464451 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:127785934 C>T maps to ENST00000464451 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:64534715 G>T maps to NM_201995.2 Y450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:64534715 G>T maps to NM_201995.2 Y450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:145640271 C>T maps to NM_130849.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:145640271 C>T maps to NM_130849.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:53071616 G>A maps to NM_014682.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:53071616 G>A maps to NM_014682.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr3:100009496 T>G maps to ENST00000394144 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr3:100009496 T>G maps to ENST00000394144 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr12:56811766 C>T maps to NM_003920.3 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr12:56811766 C>T maps to NM_003920.3 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:135215670 C>G maps to NM_030923.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:135215670 C>G maps to NM_030923.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr12:3047431 G>A maps to NM_001160408.1 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr12:3047431 G>A maps to NM_001160408.1 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr9:136671294 G>A maps to NM_001134398.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr9:136671294 G>A maps to NM_001134398.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:160139520 G>A maps to NM_001128212.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:160139520 G>A maps to NM_001128212.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:167850948 C>T maps to NM_001161661.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:167850948 C>T maps to NM_001161661.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:56895603 G>A maps to NM_144690.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:56895603 G>A maps to NM_144690.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:48256676 C>A maps to NM_032583.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:48256676 C>A maps to NM_032583.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:6306757 G>T maps to NM_133492.2 Y254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:6306757 G>T maps to NM_133492.2 Y254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:156964935 G>C maps to ENST00000430702 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:156964935 G>C maps to ENST00000430702 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:100009931 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:100009931 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:190554682 T>C maps to NM_144708.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:190554682 T>C maps to NM_144708.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:108153445 A>T maps to NM_000051.3 K1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:108153445 A>T maps to NM_000051.3 K1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:50244177 T>C maps to NM_006045.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:50244177 T>C maps to NM_006045.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:4790575 G>A maps to NM_139170.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:4790575 G>A maps to NM_139170.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:223567017 C>A maps to NM_152610.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:223567017 C>A maps to NM_152610.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:241536199 G>T maps to NM_023083.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:241536199 G>T maps to NM_023083.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:151677545 G>T maps to NM_007185.4 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:151677545 G>T maps to NM_007185.4 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:138219358 G>A maps to NM_024491.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:138219358 G>A maps to NM_024491.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:103907703 C>A maps to NM_001001711.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:103907703 C>A maps to NM_001001711.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:15742715 G>T maps to NM_004939.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:15742715 G>T maps to NM_004939.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:83170878 G>T maps to NM_001142699.1 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:83170878 G>T maps to NM_001142699.1 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:76503839 G>A maps to ENST00000389840 H1424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:76503839 G>A maps to ENST00000389840 H1424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:143055983 C>G maps to NM_001031690.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:143055983 C>G maps to NM_001031690.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:34150161 G>T maps to NM_203408.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:34150161 G>T maps to NM_203408.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:37537271 C>T maps to NM_012166.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:37537271 C>T maps to NM_012166.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:34072790 G>T maps to NM_139285.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:34072790 G>T maps to NM_139285.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:135428900 T>C maps to NM_153834.3 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:135428900 T>C maps to NM_153834.3 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:102516290 A>T maps to NM_021956.4 K878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:102516290 A>T maps to NM_021956.4 K878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:126085511 G>A maps to ENST00000377985 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:126085511 G>A maps to ENST00000377985 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:55331208 C>T maps to ENST00000355608 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:55331208 C>T maps to ENST00000355608 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:60913644 T>A maps to NM_005560.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:60913644 T>A maps to NM_005560.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:76372261 G>A maps to NM_001128922.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:76372261 G>A maps to NM_001128922.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:138697091 G>T maps to ENST00000370578 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:138697091 G>T maps to ENST00000370578 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:30408220 G>A maps to NM_033118.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:30408220 G>A maps to NM_033118.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:56466758 G>A maps to NM_176811.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:56466758 G>A maps to NM_176811.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:32453385 G>T maps to NM_013956.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:32453385 G>T maps to NM_013956.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:5968695 C>A maps to NM_001003443.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:5968695 C>A maps to NM_001003443.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:55904447 C>A maps to NM_001004064.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:55904447 C>A maps to NM_001004064.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:140176283 G>T maps to NM_018905.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:140176283 G>T maps to NM_018905.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:118386479 G>T maps to NM_005396.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:118386479 G>T maps to NM_005396.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:9305843 C>T maps to NM_002864.2 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:9305843 C>T maps to NM_002864.2 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:50272776 G>T maps to NM_004713.3 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:50272776 G>T maps to NM_004713.3 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:1559086 G>T maps to NM_006065.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:1559086 G>T maps to NM_006065.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:2337524 C>A maps to NM_152988.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:2337524 C>A maps to NM_152988.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:158605806 T>A maps to NM_003126.2 A1776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:158605806 T>A maps to NM_003126.2 A1776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:6478564 C>G maps to NM_033278.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:6478564 C>G maps to NM_033278.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:89531773 C>A maps to NM_020358.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:89531773 C>A maps to NM_020358.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:135756461 G>T maps to NM_025052.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:135756461 G>T maps to NM_025052.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:38343660 T>C maps to NM_006954.1 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:38343660 T>C maps to NM_006954.1 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:22804515 C>T maps to NM_015461.2 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:22804515 C>T maps to NM_015461.2 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109609685 G>T maps to NM_001093.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109609685 G>T maps to NM_001093.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109680289 C>T maps to NM_001093.3 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109680289 C>T maps to NM_001093.3 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109680381 G>T maps to NM_001093.3 P1721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109680381 G>T maps to NM_001093.3 P1721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33535097 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33535097 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:18776905 G>T maps to NM_001040272.4 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:18776905 G>T maps to NM_001040272.4 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:44148745 C>T maps to NM_001129.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:44148745 C>T maps to NM_001129.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:76198622 C>T maps to NM_001145526.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:76198622 C>T maps to NM_001145526.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:981167 G>A maps to NM_198576.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:981167 G>A maps to NM_198576.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:88292464 T>A maps to ENST00000395847 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:88292464 T>A maps to ENST00000395847 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:32878140 C>T maps to NM_000687.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:32878140 C>T maps to NM_000687.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:186333532 G>T maps to ENST00000273784 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:186333532 G>T maps to ENST00000273784 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:220098103 A>T maps to NM_001042410.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:220098103 A>T maps to NM_001042410.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:115361799 A>G maps to NM_173800.4 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:115361799 A>G maps to NM_173800.4 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:47607617 C>T maps to NM_006420.2 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:47607617 C>T maps to NM_006420.2 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:68962336 C>T maps to NM_001007231.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:68962336 C>T maps to NM_001007231.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:216213879 G>T maps to NM_004044.6 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:216213879 G>T maps to NM_004044.6 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:50226372 C>A maps to NM_024837.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:50226372 C>A maps to NM_024837.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:32222211 T>A maps to NM_001703.2 K76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:32222211 T>A maps to NM_001703.2 K76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:70049222 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:70049222 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:31599146 C>T maps to NM_080686.2 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:31599146 C>T maps to NM_080686.2 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:116670875 G>A maps to NM_152367.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:116670875 G>A maps to NM_152367.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:75055644 T>A maps to NM_001002912.4 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:75055644 T>A maps to NM_001002912.4 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:60538213 T>A maps to NM_152377.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:60538213 T>A maps to NM_152377.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:34596255 C>A maps to ENST00000373973 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:34596255 C>A maps to ENST00000373973 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:192516396 G>T maps to NM_178496.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:192516396 G>T maps to NM_178496.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:99746544 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:99746544 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:1994017 G>T maps to NM_172364.4 C396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:1994017 G>T maps to NM_172364.4 C396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:44630105 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:44630105 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158152740 A>T maps to NM_001766.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158152740 A>T maps to NM_001766.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:72667442 T>C maps to NM_005193.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:72667442 T>C maps to NM_005193.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:196887424 A>T maps to NM_006684.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:196887424 A>T maps to NM_006684.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:101978829 C>A maps to NM_001278.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:101978829 C>A maps to NM_001278.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:103548451 G>T maps to NM_080629.2 C61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:103548451 G>T maps to NM_080629.2 C61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:139788253 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:139788253 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:145634557 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:145634557 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:3265712 C>T maps to NM_033225.5 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:3265712 C>T maps to NM_033225.5 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206331182 T>G maps to ENST00000361052 *402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206331182 T>G maps to ENST00000361052 *402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:111785648 C>A maps to NM_015267.3 P1327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:111785648 C>A maps to NM_015267.3 P1327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:41386405 G>A maps to NM_000764.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:41386405 G>A maps to NM_000764.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:87530129 G>A maps to NM_006716.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:87530129 G>A maps to NM_006716.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:61077400 T>C maps to NM_001923.3 E811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:61077400 T>C maps to NM_001923.3 E811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:21730381 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:21730381 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:183584885 T>C maps to NM_018981.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:183584885 T>C maps to NM_018981.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:66992625 C>A maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:66992625 C>A maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:225761064 A>G maps to NM_014689.2 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:225761064 A>G maps to NM_014689.2 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:5788168 G>A maps to NM_020175.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:5788168 G>A maps to NM_020175.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:183888494 C>T maps to NM_004423.3 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:183888494 C>T maps to NM_004423.3 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:131666054 C>T maps to ENST00000355311 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:131666054 C>T maps to ENST00000355311 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:27364420 G>T maps to ENST00000458037 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:27364420 G>T maps to ENST00000458037 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:37865604 C>T maps to NM_004448.2 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:37865604 C>T maps to NM_004448.2 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:6318846 G>A maps to NM_000129.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:6318846 G>A maps to NM_000129.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:113773183 C>A maps to NM_000131.3 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:113773183 C>A maps to NM_000131.3 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:200183035 C>T maps to NM_001105517.1 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:200183035 C>T maps to NM_001105517.1 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:37576622 C>G maps to NM_030919.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:37576622 C>G maps to NM_030919.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:38274923 T>C maps to NM_001174067.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:38274923 T>C maps to NM_001174067.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:27949653 C>T maps to NM_005248.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:27949653 C>T maps to NM_005248.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:34191967 G>T maps to NM_025135.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:34191967 G>T maps to NM_025135.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:152279987 A>T maps to NM_002016.1 G2458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:152279987 A>T maps to NM_002016.1 G2458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:74670276 G>A maps to NM_003838.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:74670276 G>A maps to NM_003838.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:35260671 C>A maps to NM_002060.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:35260671 C>A maps to NM_002060.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:170521422 A>G maps to NM_152281.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:170521422 A>G maps to NM_152281.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:135485478 G>A maps to NM_153834.3 P2884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:135485478 G>A maps to NM_153834.3 P2884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:131487809 G>A maps to NM_198827.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:131487809 G>A maps to NM_198827.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:13906582 G>T maps to NM_000834.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:13906582 G>T maps to NM_000834.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:14804339 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:14804339 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:82937481 C>A maps to NM_001884.3 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:82937481 C>A maps to NM_001884.3 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:6305548 C>A maps to NM_001024598.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:6305548 C>A maps to NM_001024598.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:26158555 C>A maps to NM_138720.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:26158555 C>A maps to NM_138720.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27238026 A>C maps to NM_000522.4 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27238026 A>C maps to NM_000522.4 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27185360 G>C maps to NM_024014.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27185360 G>C maps to NM_024014.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:186395104 C>A maps to NM_000412.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:186395104 C>A maps to NM_000412.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70908241 G>T maps to NM_032821.2 I3637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70908241 G>T maps to NM_032821.2 I3637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:40271405 G>A maps to NM_021078.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:40271405 G>A maps to NM_021078.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:81188357 G>T maps to NM_018689.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:81188357 G>T maps to NM_018689.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:86568130 T>C maps to NM_001142749.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:86568130 T>C maps to NM_001142749.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:241712630 G>T maps to ENST00000373308 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:241712630 G>T maps to ENST00000373308 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:55263201 A>T maps to NM_015868.2 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:55263201 A>T maps to NM_015868.2 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:898277 G>A maps to NM_198317.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:898277 G>A maps to NM_198317.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:48688330 C>G maps to NM_001135629.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:48688330 C>G maps to NM_001135629.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53071970 C>T maps to NM_006121.3 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53071970 C>T maps to NM_006121.3 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:1651687 A>T maps to NM_001001480.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:1651687 A>T maps to NM_001001480.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:107696228 A>G maps to NM_007356.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:107696228 A>G maps to NM_007356.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:154182848 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:154182848 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:153177370 C>A maps to NM_001010857.1 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:153177370 C>A maps to NM_001010857.1 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:95557472 C>T maps to NM_005097.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:95557472 C>T maps to NM_005097.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:54760173 C>A maps to NM_001081442.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:54760173 C>A maps to NM_001081442.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:40399865 C>A maps to NM_020737.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:40399865 C>A maps to NM_020737.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:133881854 G>T maps to NM_144648.1 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:133881854 G>T maps to NM_144648.1 E515*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-5775-01A-01D-1625-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:2108972 G>A maps to NM_003550.2 S358S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-5775-01A-01D-1625-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:2108972 G>A maps to NM_003550.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:23889460 G>C maps to NM_019066.4 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:23889460 G>C maps to NM_019066.4 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:16177990 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:16177990 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:53471757 C>A maps to NM_012329.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:53471757 C>A maps to NM_012329.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:68773567 G>C maps to NM_145015.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:68773567 G>C maps to NM_145015.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:9062524 G>A maps to NM_024690.2 T8307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:9062524 G>A maps to NM_024690.2 T8307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:103348394 G>T maps to NM_001018116.1 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:103348394 G>T maps to NM_001018116.1 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:3229559 A>T maps to NM_015419.3 G2228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:3229559 A>T maps to NM_015419.3 G2228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:123456293 C>A maps to NM_053025.3 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:123456293 C>A maps to NM_053025.3 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:26436360 C>T maps to NM_017433.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:26436360 C>T maps to NM_017433.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:72208824 T>C maps to ENST00000424560 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:72208824 T>C maps to ENST00000424560 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:62850369 A>T maps to NM_004535.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:62850369 A>T maps to NM_004535.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:62853401 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:62853401 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:102731842 G>A maps to NM_032041.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:102731842 G>A maps to NM_032041.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:9807578 C>T maps to NM_016821.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:9807578 C>T maps to NM_016821.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:45799822 G>A maps to NM_001004297.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:45799822 G>A maps to NM_001004297.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:5989508 C>A maps to NM_001146033.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:5989508 C>A maps to NM_001146033.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:141619190 T>C maps to NM_001001656.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:141619190 T>C maps to NM_001001656.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:57886583 C>T maps to NM_001005211.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:57886583 C>T maps to NM_001005211.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103838231 C>A maps to NM_002553.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103838231 C>A maps to NM_002553.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:45893992 G>A maps to NM_145798.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:45893992 G>A maps to NM_145798.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:29617626 C>T maps to NM_183378.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:29617626 C>T maps to NM_183378.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:43552897 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:43552897 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:58207409 G>T maps to NM_001040429.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:58207409 G>T maps to NM_001040429.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140263226 C>A maps to NM_018904.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140263226 C>A maps to NM_018904.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140763011 G>A maps to NM_018920.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140763011 G>A maps to NM_018920.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140752015 G>A maps to NM_018924.2 Q685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140752015 G>A maps to NM_018924.2 Q685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:56139536 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:56139536 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:156883535 C>A maps to NM_001080471.1 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:156883535 C>A maps to NM_001080471.1 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:39537582 G>T maps to ENST00000398870 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:39537582 G>T maps to ENST00000398870 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:81925084 G>A maps to NM_002661.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:81925084 G>A maps to NM_002661.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:198950856 T>C maps to NM_006226.3 Y872Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:198950856 T>C maps to NM_006226.3 Y872Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:24767090 G>A maps to ENST00000379068 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:24767090 G>A maps to ENST00000379068 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:113300232 C>T maps to NM_019014.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:113300232 C>T maps to NM_019014.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:23509159 C>T maps to NM_020227.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:23509159 C>T maps to NM_020227.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:44553862 C>A maps to NM_001171603.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:44553862 C>A maps to NM_001171603.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:31157190 G>A maps to NM_173502.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:31157190 G>A maps to NM_173502.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43433837 A>G maps to NM_002783.2 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43433837 A>G maps to NM_002783.2 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:87081722 C>A maps to ENST00000276616 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:87081722 C>A maps to ENST00000276616 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:34803878 C>T maps to NM_001145521.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:34803878 C>T maps to NM_001145521.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:79348686 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:79348686 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103292157 A>T maps to ENST00000428762 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103292157 A>T maps to ENST00000428762 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:38963015 G>A maps to ENST00000296782 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:38963015 G>A maps to ENST00000296782 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:10480504 G>T maps to NM_178857.5 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:10480504 G>T maps to NM_178857.5 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:92762521 G>A maps to NM_152703.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:92762521 G>A maps to NM_152703.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:47460979 G>T maps to NM_012235.2 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:47460979 G>T maps to NM_012235.2 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:62018355 C>A maps to NM_000334.4 G1762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:62018355 C>A maps to NM_000334.4 G1762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:157820573 C>A maps to NM_003030.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:157820573 C>A maps to NM_003030.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:232579371 C>T maps to NM_020808.3 W1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:232579371 C>T maps to NM_020808.3 W1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:61113222 C>A maps to NM_005982.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:61113222 C>A maps to NM_005982.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:134050793 G>T maps to NM_006748.3 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:134050793 G>T maps to NM_006748.3 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:25813178 A>C maps to NM_005074.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:25813178 A>C maps to NM_005074.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:150657055 G>A maps to NM_001145017.1 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:150657055 G>A maps to NM_001145017.1 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:137484279 C>A maps to NM_004189.2 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:137484279 C>A maps to NM_004189.2 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:231090582 G>T maps to NM_007237.4 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:231090582 G>T maps to NM_007237.4 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:90670737 C>T maps to NM_020799.2 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:90670737 C>T maps to NM_020799.2 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:47685772 C>A maps to ENST00000371883 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:47685772 C>A maps to ENST00000371883 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:32818282 C>A maps to NM_000593.5 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:32818282 C>A maps to NM_000593.5 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:167592551 A>T maps to NM_001145121.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:167592551 A>T maps to NM_001145121.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:179561782 G>T maps to ENST00000444136 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:179561782 G>T maps to ENST00000444136 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43572138 C>T maps to NM_052955.2 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43572138 C>T maps to NM_052955.2 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:137988680 C>A maps to ENST00000272643 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:137988680 C>A maps to ENST00000272643 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:77715174 G>C maps to NM_020431.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:77715174 G>C maps to NM_020431.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:16070899 G>T maps to NM_001013641.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:16070899 G>T maps to NM_001013641.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:12248920 A>T maps to NM_001066.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:12248920 A>T maps to NM_001066.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:11363160 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:11363160 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:10920103 C>A maps to NM_199261.2 G384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:10920103 C>A maps to NM_199261.2 G384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:135781221 G>A maps to NM_000368.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:135781221 G>A maps to NM_000368.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:2696150 C>T maps to NM_025250.2 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:2696150 C>T maps to NM_025250.2 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:33491041 G>T maps to NM_173167.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:33491041 G>T maps to NM_173167.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:9613390 G>T maps to NM_153210.3 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:9613390 G>T maps to NM_153210.3 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:4431768 C>T maps to NM_138440.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:4431768 C>T maps to NM_138440.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:118477139 C>T maps to NM_006784.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:118477139 C>T maps to NM_006784.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:74652752 T>C maps to NM_032118.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:74652752 T>C maps to NM_032118.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:1989723 G>A maps to NM_005663.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:1989723 G>A maps to NM_005663.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:219754781 G>T maps to NM_025216.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:219754781 G>T maps to NM_025216.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:77768252 T>A maps to NM_024721.4 I3032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:77768252 T>A maps to NM_024721.4 I3032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:57286127 G>A maps to NM_001146326.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:57286127 G>A maps to NM_001146326.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:71512218 C>A maps to NM_006961.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:71512218 C>A maps to NM_006961.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58084848 C>T maps to NM_017879.1 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58084848 C>T maps to NM_017879.1 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:134494749 A>C maps to NM_152695.5 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:134494749 A>C maps to NM_152695.5 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:57012580 A>G maps to NM_001031623.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:57012580 A>G maps to NM_001031623.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58867549 G>A maps to NM_198458.1 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58867549 G>A maps to NM_198458.1 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:56586013 G>T maps to NM_018181.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:56586013 G>T maps to NM_018181.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:47775356 G>T maps to NM_007137.3 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:47775356 G>T maps to NM_007137.3 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:7568324 C>A maps to NM_145891.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:7568324 C>A maps to NM_145891.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:155030751 G>A maps to NM_207197.1 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:155030751 G>A maps to NM_207197.1 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:43858521 C>A maps to ENST00000389420 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:43858521 C>A maps to ENST00000389420 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136405801 C>A maps to ENST00000393061 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136405801 C>A maps to ENST00000393061 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:43248976 G>T maps to NM_000022.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:43248976 G>T maps to NM_000022.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3769637 C>A maps to NM_000683.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3769637 C>A maps to NM_000683.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:4829964 A>T maps to NM_018836.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:4829964 A>T maps to NM_018836.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:165118289 C>A maps to NM_012403.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:165118289 C>A maps to NM_012403.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:21251355 G>T maps to NM_000384.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:21251355 G>T maps to NM_000384.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:24981853 C>A maps to NM_001006634.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:24981853 C>A maps to NM_001006634.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:96789929 C>A maps to NM_001002036.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:96789929 C>A maps to NM_001002036.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:58024790 A>T maps to NM_001478.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:58024790 A>T maps to NM_001478.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:107524267 G>T maps to NM_001142568.1 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:107524267 G>T maps to NM_001142568.1 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:69093071 G>A maps to NM_014482.1 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:69093071 G>A maps to NM_014482.1 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:55803292 G>A maps to NM_001719.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:55803292 G>A maps to NM_001719.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:15724521 G>C maps to ENST00000382346 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:15724521 G>C maps to ENST00000382346 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:25148751 C>T maps to NM_001101339.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:25148751 C>T maps to NM_001101339.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:8092735 G>A maps to NM_017622.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:8092735 G>A maps to NM_017622.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:56728598 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:56728598 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:14763189 G>T maps to NM_032137.4 G489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:14763189 G>T maps to NM_032137.4 G489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:165715240 G>A maps to NM_144980.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:165715240 G>A maps to NM_144980.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:120629669 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:120629669 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:140850263 G>T maps to ENST00000277549 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:140850263 G>T maps to ENST00000277549 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:110551181 G>T maps to NM_015891.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:110551181 G>T maps to NM_015891.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:24487842 G>T maps to NM_006727.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:24487842 G>T maps to NM_006727.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:130550578 C>T maps to ENST00000373265 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:130550578 C>T maps to ENST00000373265 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48697760 T>A maps to NM_001407.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48697760 T>A maps to NM_001407.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:233391330 G>T maps to NM_000751.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:233391330 G>T maps to NM_000751.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:143036383 C>T maps to NM_000083.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:143036383 C>T maps to NM_000083.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:56021687 C>T maps to NM_030820.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:56021687 C>T maps to NM_030820.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:86590977 G>A maps to NM_152890.5 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:86590977 G>A maps to NM_152890.5 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48612108 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48612108 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:15531039 G>T maps to NM_005677.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:15531039 G>T maps to NM_005677.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113323374 C>A maps to NM_198123.1 E2573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113323374 C>A maps to NM_198123.1 E2573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:16982166 C>A maps to NM_001081.3 T1804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:16982166 C>A maps to NM_001081.3 T1804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41387974 G>T maps to NM_000764.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41387974 G>T maps to NM_000764.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:20000014 C>T maps to NM_001033553.1 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:20000014 C>T maps to NM_001033553.1 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:32430027 A>T maps to ENST00000357033 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:32430027 A>T maps to ENST00000357033 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:37665643 C>T maps to NM_005128.2 T2224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:37665643 C>T maps to NM_005128.2 T2224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:116485390 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:116485390 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:25754370 T>C maps to NM_021907.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:25754370 T>C maps to NM_021907.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:77079626 G>T maps to NM_001042573.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:77079626 G>T maps to NM_001042573.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:92511170 G>T maps to NM_173567.4 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:92511170 G>T maps to NM_173567.4 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:293212 C>G maps to NM_182705.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:293212 C>G maps to NM_182705.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:25744193 C>A maps to NM_152704.2 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:25744193 C>A maps to NM_152704.2 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:15928578 C>A maps to NM_012304.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:15928578 C>A maps to NM_012304.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:103384539 G>A maps to ENST00000331272 C266C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:103384539 G>A maps to ENST00000331272 C266C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:29237063 C>G maps to NM_005249.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:29237063 C>G maps to NM_005249.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:170224481 T>A maps to NM_014211.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:170224481 T>A maps to NM_014211.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:34889377 G>A maps to NM_001136006.1 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:34889377 G>A maps to NM_001136006.1 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:22820506 C>A maps to NM_020973.3 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:22820506 C>A maps to NM_020973.3 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:57430038 C>T maps to NM_080425.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:57430038 C>T maps to NM_080425.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:23437950 G>T maps to NM_002073.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:23437950 G>T maps to NM_002073.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:27333190 C>A maps to NM_005288.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:27333190 C>A maps to NM_005288.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:154147359 C>A maps to NM_001038705.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:154147359 C>A maps to NM_001038705.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10102597 G>C maps to NM_198182.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10102597 G>C maps to NM_198182.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:39888997 G>T maps to ENST00000310778 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:39888997 G>T maps to ENST00000310778 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36109806 G>T maps to NM_015302.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36109806 G>T maps to NM_015302.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:18687574 T>C maps to NM_178425.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:18687574 T>C maps to NM_178425.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:236727848 C>T maps to NM_018072.5 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:236727848 C>T maps to NM_018072.5 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:53642719 C>A maps to ENST00000276009 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:53642719 C>A maps to ENST00000276009 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:118624545 G>T maps to NM_152538.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:118624545 G>T maps to NM_152538.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:137325892 T>C maps to NM_014432.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:137325892 T>C maps to NM_014432.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:24463711 G>A maps to NM_021258.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:24463711 G>A maps to NM_021258.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55967070 C>A maps to NM_024710.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55967070 C>A maps to NM_024710.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:52825804 C>T maps to NM_002215.2 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:52825804 C>T maps to NM_002215.2 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:65323452 G>A maps to NM_002227.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:65323452 G>A maps to NM_002227.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:21319718 C>A maps to NM_021012.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:21319718 C>A maps to NM_021012.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:114188021 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:114188021 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:183273168 G>T maps to NM_130446.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:183273168 G>T maps to NM_130446.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:152732370 C>T maps to NM_001025231.1 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:152732370 C>T maps to NM_001025231.1 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107592471 G>A maps to NM_002291.2 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107592471 G>A maps to NM_002291.2 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:70618155 C>A maps to NM_017768.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:70618155 C>A maps to NM_017768.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131670678 G>C maps to NM_001127244.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131670678 G>C maps to NM_001127244.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:39893129 A>G maps to ENST00000361689 Q3378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:39893129 A>G maps to ENST00000361689 Q3378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:140992862 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:140992862 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39101765 A>T maps to NM_001042600.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39101765 A>T maps to NM_001042600.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:112323738 G>T maps to NM_139078.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:112323738 G>T maps to NM_139078.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:198571469 T>A maps to NM_138395.3 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:198571469 T>A maps to NM_138395.3 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:122486105 G>A maps to NM_032390.4 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:122486105 G>A maps to NM_032390.4 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:74689727 G>A maps to NM_006302.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:74689727 G>A maps to NM_006302.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:18955986 G>A maps to NM_147199.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:18955986 G>A maps to NM_147199.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:113563054 C>A maps to ENST00000189978 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:113563054 C>A maps to ENST00000189978 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:109318300 C>A maps to NM_015011.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:109318300 C>A maps to NM_015011.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:2027641 C>T maps to NM_003970.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:2027641 C>T maps to NM_003970.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:3600415 C>T maps to ENST00000448023 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:3600415 C>T maps to ENST00000448023 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:43656851 G>T maps to NM_182977.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:43656851 G>T maps to NM_182977.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:104190757 C>A maps to NM_001031701.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:104190757 C>A maps to NM_001031701.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:135333219 A>G maps to NM_015135.2 L1985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:135333219 A>G maps to NM_015135.2 L1985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:6898489 T>G maps to NM_207186.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:6898489 T>G maps to NM_207186.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:159505014 C>T maps to NM_001004469.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:159505014 C>T maps to NM_001004469.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:20692662 G>C maps to NM_001004480.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:20692662 G>C maps to NM_001004480.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:51516183 T>C maps to NM_001004703.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:51516183 T>C maps to NM_001004703.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:20215939 C>A maps to NM_172194.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:20215939 C>A maps to NM_172194.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:5841930 G>T maps to NM_001005174.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:5841930 G>T maps to NM_001005174.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:56020157 G>A maps to NM_001004747.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:56020157 G>A maps to NM_001004747.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:55873240 C>A maps to NM_001005200.1 C241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:55873240 C>A maps to NM_001005200.1 C241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:20216955 G>T maps to NM_015207.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:20216955 G>T maps to NM_015207.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:152554644 C>T maps to NM_002563.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:152554644 C>T maps to NM_002563.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:40564711 A>T maps to NM_020168.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:40564711 A>T maps to NM_020168.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:102285238 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:102285238 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140590431 G>T maps to NM_018932.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140590431 G>T maps to NM_018932.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140605137 C>T maps to NM_018934.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140605137 C>T maps to NM_018934.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140605155 A>G maps to NM_018934.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140605155 A>G maps to NM_018934.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140503637 C>T maps to NM_018938.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140503637 C>T maps to NM_018938.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140503766 C>T maps to NM_018938.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140503766 C>T maps to NM_018938.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140723758 G>A maps to NM_018916.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140723758 G>A maps to NM_018916.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140890661 A>G maps to NM_018915.2 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140890661 A>G maps to NM_018915.2 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:52733189 G>T maps to NM_052937.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:52733189 G>T maps to NM_052937.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:249211250 C>T maps to NM_170725.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:249211250 C>T maps to NM_170725.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49754273 C>A maps to NM_138733.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49754273 C>A maps to NM_138733.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:22880695 C>T maps to NM_005028.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:22880695 C>T maps to NM_005028.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:12475577 C>A maps to NM_015869.4 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:12475577 C>A maps to NM_015869.4 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220162047 G>T maps to NM_002846.3 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220162047 G>T maps to NM_002846.3 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:121652033 C>G maps to NM_002851.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:121652033 C>G maps to NM_002851.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:17701460 G>T maps to ENST00000395776 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:17701460 G>T maps to ENST00000395776 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49578777 G>T maps to NM_000324.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49578777 G>T maps to NM_000324.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:66833437 C>T maps to NM_014578.3 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:66833437 C>T maps to NM_014578.3 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39926287 G>T maps to NM_001020.4 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39926287 G>T maps to NM_001020.4 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:38980786 G>T maps to NM_000540.2 A1962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:38980786 G>T maps to NM_000540.2 A1962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:80194623 C>A maps to NM_001042423.1 C81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:80194623 C>A maps to NM_001042423.1 C81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:150846758 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:150846758 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:22680713 T>A maps to ENST00000376603 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:22680713 T>A maps to ENST00000376603 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220344799 A>T maps to NM_005876.4 T1760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220344799 A>T maps to NM_005876.4 T1760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220354289 G>A maps to NM_005876.4 R2850R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220354289 G>A maps to NM_005876.4 R2850R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:40364012 G>A maps to NM_012448.3 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:40364012 G>A maps to NM_012448.3 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:149884837 C>T maps to NM_014849.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:149884837 C>T maps to NM_014849.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:59560840 A>T maps to ENST00000393853 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:59560840 A>T maps to ENST00000393853 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:52896227 C>A maps to ENST00000398339 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:52896227 C>A maps to ENST00000398339 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:135390480 G>A maps to NM_000358.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:135390480 G>A maps to NM_000358.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:164394568 G>A maps to NM_032136.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:164394568 G>A maps to NM_032136.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:187004711 C>T maps to NM_003265.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:187004711 C>T maps to NM_003265.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:42866465 C>A maps to NM_001135099.1 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:42866465 C>A maps to NM_001135099.1 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:36511948 G>A maps to NM_145803.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:36511948 G>A maps to NM_145803.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:38225482 G>A maps to NM_003306.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:38225482 G>A maps to NM_003306.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:49693475 A>C maps to NM_017636.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:49693475 A>C maps to NM_017636.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:141955398 C>T maps to NM_001001317.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:141955398 C>T maps to NM_001001317.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:31770397 C>A maps to NM_020856.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:31770397 C>A maps to NM_020856.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:80749947 C>G maps to NM_003318.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:80749947 C>G maps to NM_003318.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:22864306 G>T maps to NM_052903.4 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:22864306 G>T maps to NM_052903.4 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:91489889 C>T maps to NM_018671.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:91489889 C>T maps to NM_018671.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:54617552 C>A maps to ENST00000404951 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:54617552 C>A maps to ENST00000404951 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36831323 G>A maps to NM_020917.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36831323 G>A maps to NM_020917.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:38246346 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:38246346 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52538394 G>A maps to NM_014650.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52538394 G>A maps to NM_014650.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:35273922 G>A maps to NM_014106.3 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:35273922 G>A maps to NM_014106.3 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52659498 G>A maps to NM_001102657.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52659498 G>A maps to NM_001102657.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:169792772 A>T maps to NM_003742.2 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:169792772 A>T maps to NM_003742.2 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:48121985 C>T maps to NM_033226.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:48121985 C>T maps to NM_033226.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:84651628 A>T maps to NM_207517.2 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:84651628 A>T maps to NM_207517.2 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:70903945 G>A maps to NM_001185054.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:70903945 G>A maps to NM_001185054.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:116064522 G>C maps to NM_001001936.1 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:116064522 G>C maps to NM_001001936.1 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:77816877 G>A maps to NM_001029870.1 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:77816877 G>A maps to NM_001029870.1 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:69409623 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:69409623 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:11197548 C>G maps to NM_013427.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:11197548 C>G maps to NM_013427.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:111927997 G>A maps to NM_001113511.1 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:111927997 G>A maps to NM_001113511.1 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:77284871 G>T maps to ENST00000355691 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:77284871 G>T maps to ENST00000355691 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:69454531 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:69454531 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:129246010 C>T maps to NM_003658.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:129246010 C>T maps to NM_003658.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:76740228 T>C maps to NM_024685.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:76740228 T>C maps to NM_024685.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:26508187 G>C maps to NM_001732.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:26508187 G>C maps to NM_001732.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:81579776 C>A maps to NM_000722.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:81579776 C>A maps to NM_000722.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:55582734 T>A maps to ENST00000436346 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:55582734 T>A maps to ENST00000436346 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:63529992 A>T maps to NM_004361.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:63529992 A>T maps to NM_004361.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:34180191 C>A maps to NM_022467.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:34180191 C>A maps to NM_022467.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:100518492 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:100518492 G>T did not map to a codon.
Multiple mappings detected for codon TCGA-64-5779-01A-01D-1625-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-64-5779-01A-01D-1625-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:33155721 G>C maps to NM_006371.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:33155721 G>C maps to NM_006371.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:3000044 G>T maps to NM_033225.5 L2061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:3000044 G>T maps to NM_033225.5 L2061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:46555803 T>C maps to NM_016593.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:46555803 T>C maps to NM_016593.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:6210908 C>T maps to ENST00000396741 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:6210908 C>T maps to ENST00000396741 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:169213029 C>A maps to NM_017631.5 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:169213029 C>A maps to NM_017631.5 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:11806088 T>C maps to NM_001372.3 S3820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:11806088 T>C maps to NM_001372.3 S3820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:56496091 T>C maps to ENST00000361203 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:56496091 T>C maps to ENST00000361203 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139158276 G>T maps to NM_015912.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139158276 G>T maps to NM_015912.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:34961517 G>T maps to NM_152631.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:34961517 G>T maps to NM_152631.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:29450054 C>G maps to NM_018099.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:29450054 C>G maps to NM_018099.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:44192963 C>T maps to NM_000162.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:44192963 C>T maps to NM_000162.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:74856164 C>T maps to ENST00000238018 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:74856164 C>T maps to ENST00000238018 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:167754670 G>A maps to NM_014498.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:167754670 G>A maps to NM_014498.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:136113698 A>C maps to NM_054021.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:136113698 A>C maps to NM_054021.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:173355837 A>G maps to ENST00000264106 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:173355837 A>G maps to ENST00000264106 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:35183406 G>T maps to NM_003024.2 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:35183406 G>T maps to NM_003024.2 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:147027965 G>T maps to NM_014790.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:147027965 G>T maps to NM_014790.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:17409335 G>A maps to NM_000525.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:17409335 G>A maps to NM_000525.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:29451057 T>A maps to NM_014939.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:29451057 T>A maps to NM_014939.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:200977968 G>T maps to NM_017596.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:200977968 G>T maps to NM_017596.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55341567 A>G maps to NM_013289.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55341567 A>G maps to NM_013289.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51361539 C>A maps to NM_001648.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51361539 C>A maps to NM_001648.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:52695777 C>A maps to NM_002284.3 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:52695777 C>A maps to NM_002284.3 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:46011576 G>A maps to NM_198688.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:46011576 G>A maps to NM_198688.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:107677873 T>C maps to NM_007356.2 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:107677873 T>C maps to NM_007356.2 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:33319596 G>A maps to NM_013975.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:33319596 G>A maps to NM_013975.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:108861555 A>C maps to NM_001098268.1 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:108861555 A>C maps to NM_001098268.1 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:40137020 C>A maps to NM_020929.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:40137020 C>A maps to NM_020929.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:41111392 C>T maps to ENST00000308370 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:41111392 C>T maps to ENST00000308370 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:56348549 C>T maps to NM_006785.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:56348549 C>T maps to NM_006785.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:42028380 A>T maps to ENST00000219905 K1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:42028380 A>T maps to ENST00000219905 K1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:57026478 C>T maps to NM_005372.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:57026478 C>T maps to NM_005372.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:68522175 A>G maps to NM_033281.5 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:68522175 A>G maps to NM_033281.5 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:68480779 G>T maps to NM_004923.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:68480779 G>T maps to NM_004923.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:9049833 C>T maps to NM_024690.2 W10599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:9049833 C>T maps to NM_024690.2 W10599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:71346871 C>A maps to NM_152291.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:71346871 C>A maps to NM_152291.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:3238370 C>A maps to NM_015419.3 P1785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:3238370 C>A maps to NM_015419.3 P1785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:105909740 G>A maps to NM_005746.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:105909740 G>A maps to NM_005746.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:32621580 C>A maps to NM_013956.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:32621580 C>A maps to NM_013956.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:228495020 C>G maps to NM_001098623.1 A4085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:228495020 C>G maps to NM_001098623.1 A4085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:167689181 C>A maps to NM_001122679.1 T2555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:167689181 C>A maps to NM_001122679.1 T2555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:123909453 G>C maps to NM_001004463.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:123909453 G>C maps to NM_001004463.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:31144137 T>A maps to NM_001173523.1 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:31144137 T>A maps to NM_001173523.1 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:13325782 C>A maps to NM_006214.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:13325782 C>A maps to NM_006214.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:95994066 G>T maps to ENST00000371380 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:95994066 G>T maps to ENST00000371380 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:31825663 A>G maps to NM_130852.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:31825663 A>G maps to NM_130852.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:47276567 G>A maps to NM_020820.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:47276567 G>A maps to NM_020820.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:95952240 G>T maps to NM_144707.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:95952240 G>T maps to NM_144707.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:45122458 C>T maps to ENST00000352766 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:45122458 C>T maps to ENST00000352766 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:40478081 G>T maps to NM_006503.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:40478081 G>T maps to NM_006503.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:192150555 G>T maps to NM_130782.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:192150555 G>T maps to NM_130782.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:196210726 G>A maps to NM_152617.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:196210726 G>A maps to NM_152617.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:78327865 C>T maps to NM_020914.4 S3591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:78327865 C>T maps to NM_020914.4 S3591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:125404009 G>T maps to NM_152553.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:125404009 G>T maps to NM_152553.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:21771690 T>A maps to NM_020366.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:21771690 T>A maps to NM_020366.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:21793122 A>T maps to NM_020366.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:21793122 A>T maps to NM_020366.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:99126614 G>C maps to NM_015179.3 V1033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:99126614 G>C maps to NM_015179.3 V1033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:51174545 G>T maps to ENST00000251020 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:51174545 G>T maps to ENST00000251020 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:67763154 G>T maps to NM_013257.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:67763154 G>T maps to NM_013257.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:232600633 C>A maps to NM_020808.3 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:232600633 C>A maps to NM_020808.3 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:101603527 G>T maps to NM_145913.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:101603527 G>T maps to NM_145913.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:40657159 G>T maps to NM_021097.2 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:40657159 G>T maps to NM_021097.2 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:228884870 A>G maps to NM_001142644.1 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:228884870 A>G maps to NM_001142644.1 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:9416180 G>A maps to NM_025106.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:9416180 G>A maps to NM_025106.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:53076547 G>A maps to NM_014682.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:53076547 G>A maps to NM_014682.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:22487121 G>T maps to NM_003034.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:22487121 G>T maps to NM_003034.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:191856009 C>A maps to NM_007315.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:191856009 C>A maps to NM_007315.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:40474405 G>A maps to NM_139276.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:40474405 G>A maps to NM_139276.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44555241 C>T maps to NM_145653.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44555241 C>T maps to NM_145653.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:121335209 G>A maps to NM_001033925.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:121335209 G>A maps to NM_001033925.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:35699424 G>A maps to NM_006289.3 Q2268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:35699424 G>A maps to NM_006289.3 Q2268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:130762586 C>T maps to NM_052913.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:130762586 C>T maps to NM_052913.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:123755299 G>T maps to NM_001013743.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:123755299 G>T maps to NM_001013743.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:18724956 T>C maps to NM_012109.2 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:18724956 T>C maps to NM_012109.2 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:69097024 C>A maps to NM_182502.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:69097024 C>A maps to NM_182502.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:69111383 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:69111383 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:74519630 G>T maps to NM_145052.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:74519630 G>T maps to NM_145052.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:11994733 G>T maps to NM_201402.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:11994733 G>T maps to NM_201402.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:177608441 G>A maps to NM_005429.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:177608441 G>A maps to NM_005429.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:100806507 C>T maps to NM_003378.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:100806507 C>T maps to NM_003378.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:85546999 G>T maps to NM_145172.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:85546999 G>T maps to NM_145172.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:47584879 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:47584879 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:207174291 G>T maps to NM_020923.1 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:207174291 G>T maps to NM_020923.1 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:840718 C>A maps to NM_024786.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:840718 C>A maps to NM_024786.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:32415137 C>A maps to NM_016107.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:32415137 C>A maps to NM_016107.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:50379320 G>T maps to NM_015896.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:50379320 G>T maps to NM_015896.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:85328122 G>A maps to NM_014630.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:85328122 G>A maps to NM_014630.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:40541580 C>G maps to NM_001005851.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:40541580 C>G maps to NM_001005851.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:148767931 G>A maps to NM_152411.3 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:148767931 G>A maps to NM_152411.3 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:58189889 G>T maps to NM_152677.2 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:58189889 G>T maps to NM_152677.2 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:169781253 G>T maps to NM_003742.2 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:169781253 G>T maps to NM_003742.2 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:150742372 G>T maps to ENST00000297504 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:150742372 G>T maps to ENST00000297504 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:48117861 T>A maps to NM_033226.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:48117861 T>A maps to NM_033226.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:89052317 G>A maps to NM_004827.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:89052317 G>A maps to NM_004827.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:119024757 C>T maps to NM_001142505.1 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:119024757 C>T maps to NM_001142505.1 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:47299959 C>A maps to NM_016428.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:47299959 C>A maps to NM_016428.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180257593 G>T maps to NM_032360.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180257593 G>T maps to NM_032360.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:31344624 C>A maps to NM_183377.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:31344624 C>A maps to NM_183377.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20487037 G>A maps to NM_001010845.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20487037 G>A maps to NM_001010845.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66328120 C>T maps to NM_001104.1 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66328120 C>T maps to NM_001104.1 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:38912023 G>T maps to NM_003816.2 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:38912023 G>T maps to NM_003816.2 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:130343101 G>T maps to NM_139055.2 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:130343101 G>T maps to NM_139055.2 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:28315711 C>T maps to NM_007038.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:28315711 C>T maps to NM_007038.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:45743058 C>T maps to NM_021116.2 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:45743058 C>T maps to NM_021116.2 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:31125053 C>T maps to ENST00000409489 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:31125053 C>T maps to ENST00000409489 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:112042823 A>G maps to NM_000677.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:112042823 A>G maps to NM_000677.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100151089 G>T maps to NM_006076.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100151089 G>T maps to NM_006076.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:978999 G>A maps to NM_198576.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:978999 G>A maps to NM_198576.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:29450488 C>A maps to NM_004304.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:29450488 C>A maps to NM_004304.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:29917833 A>T maps to NM_004304.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:29917833 A>T maps to NM_004304.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:112058741 C>A maps to NM_001113490.1 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:112058741 C>A maps to NM_001113490.1 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161192793 C>G maps to NM_001643.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161192793 C>G maps to NM_001643.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:148796290 C>T maps to NM_024605.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:148796290 C>T maps to NM_024605.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:100964151 G>T maps to NM_006828.2 I1993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:100964151 G>T maps to NM_006828.2 I1993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:54714393 G>C maps to NM_015941.2 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:54714393 G>C maps to NM_015941.2 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66114502 C>A maps to NM_006876.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66114502 C>A maps to NM_006876.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:17275960 G>T maps to NM_006317.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:17275960 G>T maps to NM_006317.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:31500658 C>A maps to ENST00000417556 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:31500658 C>A maps to ENST00000417556 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:136599484 C>A maps to NM_014739.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:136599484 C>A maps to NM_014739.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:70072551 G>A maps to NM_032735.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:70072551 G>A maps to NM_032735.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102201845 C>T maps to NM_182962.1 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102201845 C>T maps to NM_182962.1 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:61254451 G>C maps to NM_145017.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:61254451 G>C maps to NM_145017.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62439291 C>T maps to NM_001085372.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62439291 C>T maps to NM_001085372.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:95912350 G>T maps to NM_152592.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:95912350 G>T maps to NM_152592.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:24921211 C>A maps to NM_018958.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:24921211 C>A maps to NM_018958.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:24923341 C>A maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:24923341 C>A maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43333140 G>A maps to NM_152343.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43333140 G>A maps to NM_152343.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75037805 C>G maps to NM_001002912.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75037805 C>G maps to NM_001002912.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:35740726 A>G maps to ENST00000343811 F964F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:35740726 A>G maps to ENST00000343811 F964F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31671450 C>A maps to NM_182519.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31671450 C>A maps to NM_182519.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:8211785 G>T maps to NM_004054.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:8211785 G>T maps to NM_004054.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:43121602 C>A maps to NM_032806.4 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:43121602 C>A maps to NM_032806.4 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:5975559 T>A maps to ENST00000324058 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:5975559 T>A maps to ENST00000324058 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:89874755 C>G maps to NM_001039706.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:89874755 C>G maps to NM_001039706.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:12878739 A>C maps to NM_020844.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:12878739 A>C maps to NM_020844.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:74526691 G>A maps to NM_182505.3 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:74526691 G>A maps to NM_182505.3 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:86163131 C>T maps to NM_198584.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:86163131 C>T maps to NM_198584.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181620523 C>T maps to ENST00000357570 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181620523 C>T maps to ENST00000357570 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:40068256 G>A maps to NM_021096.3 V1531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:40068256 G>A maps to NM_021096.3 V1531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:54871257 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:54871257 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:7737719 G>T maps to NM_015215.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:7737719 G>T maps to NM_015215.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30883195 G>A maps to NM_001002259.1 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30883195 G>A maps to NM_001002259.1 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:11531871 G>T maps to NM_145045.4 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:11531871 G>T maps to NM_145045.4 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:74623567 C>T maps to ENST00000321288 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:74623567 C>T maps to ENST00000321288 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:8647023 G>A maps to NM_144681.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:8647023 G>A maps to NM_144681.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:156866173 C>A maps to NM_020307.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:156866173 C>A maps to NM_020307.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158152752 A>T maps to NM_001766.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158152752 A>T maps to NM_001766.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158326381 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158326381 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:160811392 C>A maps to NM_001166663.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:160811392 C>A maps to NM_001166663.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:60739345 C>A maps to NM_006725.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:60739345 C>A maps to NM_006725.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:19839112 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:19839112 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:37676280 A>G maps to NM_016507.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:37676280 A>G maps to NM_016507.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:40037170 G>T maps to NM_003718.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:40037170 G>T maps to NM_003718.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:46787141 C>T maps to NM_014246.1 W2064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:46787141 C>T maps to NM_014246.1 W2064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123877465 A>T maps to NM_007018.4 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123877465 A>T maps to NM_007018.4 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196881878 C>G maps to NM_006684.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196881878 C>G maps to NM_006684.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196967402 C>T maps to ENST00000367414 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196967402 C>T maps to ENST00000367414 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:87796048 T>A maps to NM_000735.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:87796048 T>A maps to NM_000735.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:102825901 C>A maps to NM_001177611.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:102825901 C>A maps to NM_001177611.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:140178588 C>A maps to NM_022131.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:140178588 C>A maps to NM_022131.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:99013597 G>A maps to NM_001298.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:99013597 G>A maps to NM_001298.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:41323781 C>A maps to NM_001843.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:41323781 C>A maps to NM_001843.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:2967316 A>T maps to NM_175607.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:2967316 A>T maps to NM_175607.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:147259349 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:147259349 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:148080825 C>A maps to NM_014141.5 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:148080825 C>A maps to NM_014141.5 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7838352 C>T maps to NM_001037144.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7838352 C>T maps to NM_001037144.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103348789 C>A maps to NM_080629.2 E1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103348789 C>A maps to NM_080629.2 E1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103444651 A>T maps to NM_080629.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103444651 A>T maps to NM_080629.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:101806848 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:101806848 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31294521 C>T maps to NM_053041.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31294521 C>T maps to NM_053041.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:130007239 C>A maps to NM_080385.4 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:130007239 C>A maps to NM_080385.4 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:126136902 C>A maps to NM_173689.5 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:126136902 C>A maps to NM_173689.5 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:75898354 G>T maps to NM_031461.5 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:75898354 G>T maps to NM_031461.5 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:153924737 G>A maps to NM_181715.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:153924737 G>A maps to NM_181715.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:113353817 C>A maps to NM_198123.1 R2180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:113353817 C>A maps to NM_198123.1 R2180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:120009269 T>A maps to NM_001145718.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:120009269 T>A maps to NM_001145718.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:11098737 C>A maps to NM_001332.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:11098737 C>A maps to NM_001332.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:15770035 G>A maps to NM_007272.2 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:15770035 G>A maps to NM_007272.2 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:83128555 T>A maps to NM_021118.1 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:83128555 T>A maps to NM_021118.1 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:105767800 C>A maps to NM_001340.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:105767800 C>A maps to NM_001340.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41512852 C>T maps to NM_000767.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41512852 C>T maps to NM_000767.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41522587 G>T maps to NM_000767.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41522587 G>T maps to NM_000767.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:96748757 C>T maps to NM_000771.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:96748757 C>T maps to NM_000771.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:47283691 C>G maps to NM_001099772.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:47283691 C>G maps to NM_001099772.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242689674 C>G maps to NM_152783.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242689674 C>G maps to NM_152783.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:59757933 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:59757933 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:39393457 G>A maps to NM_001343.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:39393457 G>A maps to NM_001343.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:59112624 C>T maps to NM_016651.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:59112624 C>T maps to NM_016651.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:103908011 C>A maps to NM_001001711.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:103908011 C>A maps to NM_001001711.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:115138454 C>A maps to ENST00000393274 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:115138454 C>A maps to ENST00000393274 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:21639421 C>T maps to NM_003777.3 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:21639421 C>T maps to NM_003777.3 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:128181689 G>A maps to NM_153330.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:128181689 G>A maps to NM_153330.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:183622483 G>A maps to NM_018981.1 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:183622483 G>A maps to NM_018981.1 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:94341978 G>A maps to NM_014597.4 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:94341978 G>A maps to NM_014597.4 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74783135 C>T maps to NM_001381.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74783135 C>T maps to NM_001381.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:63976266 G>T maps to NM_173812.4 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:63976266 G>T maps to NM_173812.4 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:105440264 G>T maps to NM_001385.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:105440264 G>T maps to NM_001385.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:33451049 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:33451049 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:95442508 G>T maps to NM_004411.4 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:95442508 G>T maps to NM_004411.4 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:43637771 G>A maps to NM_001159936.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:43637771 G>A maps to NM_001159936.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62378704 C>T maps to ENST00000278845 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62378704 C>T maps to ENST00000278845 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:132522602 G>T maps to ENST00000333577 E2093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:132522602 G>T maps to ENST00000333577 E2093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:89521733 C>G maps to NM_005233.5 Y937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:89521733 C>G maps to NM_005233.5 Y937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:66270132 G>T maps to NM_004439.5 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:66270132 G>T maps to NM_004439.5 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:144944967 C>A maps to NM_031308.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:144944967 C>A maps to NM_031308.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:212251643 G>T maps to NM_005235.2 R1139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:212251643 G>T maps to NM_005235.2 R1139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:159601638 T>C maps to NM_004453.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:159601638 T>C maps to NM_004453.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:453845 G>A maps to ENST00000315013 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:453845 G>A maps to ENST00000315013 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197024934 C>A maps to NM_001994.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197024934 C>A maps to NM_001994.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:139163633 C>A maps to NM_015912.3 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:139163633 C>A maps to NM_015912.3 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35719354 C>A maps to NM_152481.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35719354 C>A maps to NM_152481.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:150932773 C>A maps to NM_001447.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:150932773 C>A maps to NM_001447.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92526084 G>T maps to ENST00000298047 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92526084 G>T maps to ENST00000298047 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:39870664 G>T maps to NM_203301.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:39870664 G>T maps to NM_203301.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123535118 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123535118 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161479612 G>A maps to NM_001136219.1 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161479612 G>A maps to NM_001136219.1 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:6068531 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:6068531 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34081904 C>A maps to NM_025135.2 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34081904 C>A maps to NM_025135.2 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:152279700 G>T maps to NM_002016.1 S2554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:152279700 G>T maps to NM_002016.1 S2554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:28893580 G>A maps to NM_002019.4 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:28893580 G>A maps to NM_002019.4 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43313571 C>T maps to NM_005892.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43313571 C>T maps to NM_005892.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:79371324 G>T maps to NM_025074.6 E2099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:79371324 G>T maps to NM_025074.6 E2099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:14859202 T>C maps to ENST00000380880 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:14859202 T>C maps to ENST00000380880 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:49190936 C>T maps to NM_000145.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:49190936 C>T maps to NM_000145.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62400517 C>T maps to NM_198335.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62400517 C>T maps to NM_198335.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:9923092 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:9923092 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:8100385 G>T maps to NM_001002295.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:8100385 G>T maps to NM_001002295.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:61995230 G>T maps to NM_000515.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:61995230 G>T maps to NM_000515.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:56374810 G>T maps to NM_138736.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:56374810 G>T maps to NM_138736.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62476248 G>T maps to NM_012202.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62476248 G>T maps to NM_012202.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:170501309 G>A maps to NM_152281.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:170501309 G>A maps to NM_152281.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:217783677 C>A maps to NM_018040.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:217783677 C>A maps to NM_018040.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:122460065 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:122460065 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:120732756 C>T maps to NM_014619.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:120732756 C>T maps to NM_014619.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:9934798 G>T maps to NM_000833.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:9934798 G>T maps to NM_000833.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:9984902 G>T maps to NM_000833.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:9984902 G>T maps to NM_000833.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:51743226 G>A maps to NM_000839.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:51743226 G>A maps to NM_000839.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:106558346 A>G maps to ENST00000282249 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:106558346 A>G maps to ENST00000282249 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:50534960 C>T maps to NM_002112.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:50534960 C>T maps to NM_002112.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:197183363 G>T maps to NM_020760.1 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:197183363 G>T maps to NM_020760.1 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:28463680 G>A maps to NM_004667.4 C1994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:28463680 G>A maps to NM_004667.4 C1994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:186113374 A>T maps to NM_031935.2 T4665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:186113374 A>T maps to NM_031935.2 T4665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:12877044 G>C maps to NM_013312.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:12877044 G>C maps to NM_013312.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:27183049 C>A maps to NM_019102.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:27183049 C>A maps to NM_019102.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:26872993 T>A maps to NM_022081.4 K81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:26872993 T>A maps to NM_022081.4 K81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49657762 T>C maps to NM_002152.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49657762 T>C maps to NM_002152.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:13399540 G>T maps to NM_006042.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:13399540 G>T maps to NM_006042.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:21350616 G>T maps to NM_021002.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:21350616 G>T maps to NM_021002.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:50327637 G>A maps to ENST00000336089 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:50327637 G>A maps to ENST00000336089 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:117122230 A>G maps to NM_001542.2 D1059D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:117122230 A>G maps to NM_001542.2 D1059D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:5995117 C>T maps to NM_002189.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:5995117 C>T maps to NM_002189.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:76744337 C>T maps to NM_001563.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:76744337 C>T maps to NM_001563.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:15260576 C>T maps to NM_001031853.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:15260576 C>T maps to NM_001031853.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:95862155 G>C maps to NM_017864.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:95862155 G>C maps to NM_017864.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:173352312 G>T maps to ENST00000264106 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:173352312 G>T maps to ENST00000264106 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:46308662 C>A maps to NM_000211.3 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:46308662 C>A maps to NM_000211.3 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:4711403 G>T maps to ENST00000356617 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:4711403 G>T maps to ENST00000356617 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:106074327 C>A maps to NM_033397.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:106074327 C>A maps to NM_033397.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:133967449 G>T maps to NM_001105521.2 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:133967449 G>T maps to NM_001105521.2 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:23450580 C>A maps to NM_032876.4 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:23450580 C>A maps to NM_032876.4 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:84256461 G>T maps to NM_172347.2 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:84256461 G>T maps to NM_172347.2 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:90650806 C>A maps to NM_022054.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:90650806 C>A maps to NM_022054.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:133192463 C>A maps to NM_004519.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:133192463 C>A maps to NM_004519.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34753035 C>T maps to NM_020776.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34753035 C>T maps to NM_020776.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:73963349 G>T maps to NM_001008537.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:73963349 G>T maps to NM_001008537.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:39387721 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:39387721 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:18808308 G>T maps to NM_152375.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:18808308 G>T maps to NM_152375.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:117043380 G>A maps to NM_033495.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:117043380 G>A maps to NM_033495.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:21674823 C>A maps to NM_153270.1 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:21674823 C>A maps to NM_153270.1 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:84690772 G>T maps to NM_024731.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:84690772 G>T maps to NM_024731.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51483571 G>A maps to NM_005046.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51483571 G>A maps to NM_005046.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51507025 G>T maps to NM_012315.1 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51507025 G>T maps to NM_012315.1 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:38910702 G>A maps to NM_181534.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:38910702 G>A maps to NM_181534.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39521115 C>A maps to ENST00000394004 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39521115 C>A maps to ENST00000394004 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39535401 C>T maps to NM_021013.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39535401 C>T maps to NM_021013.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52994867 G>T maps to NM_080747.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52994867 G>T maps to NM_080747.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:31802903 C>A maps to NM_181600.1 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:31802903 C>A maps to NM_181600.1 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:31869265 C>A maps to NM_181610.1 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:31869265 C>A maps to NM_181610.1 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39316514 G>T maps to NM_032524.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39316514 G>T maps to NM_032524.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39394395 C>T maps to NM_031963.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39394395 C>T maps to NM_031963.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:52498520 C>A maps to NM_138417.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:52498520 C>A maps to NM_138417.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:77906790 G>A maps to NM_032808.5 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:77906790 G>A maps to NM_032808.5 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201869654 C>A maps to NM_012134.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201869654 C>A maps to NM_012134.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:82416771 T>C maps to ENST00000370717 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:82416771 T>C maps to ENST00000370717 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:62849168 G>T maps to ENST00000506720 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:62849168 G>T maps to ENST00000506720 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100176406 G>A maps to NM_002319.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100176406 G>A maps to NM_002319.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:42356334 G>A maps to NM_152447.3 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:42356334 G>A maps to NM_152447.3 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:141356322 C>A maps to NM_018557.2 V2357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:141356322 C>A maps to NM_018557.2 V2357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3887743 A>T maps to NM_020873.5 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3887743 A>T maps to NM_020873.5 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:151504189 C>A maps to NM_006439.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:151504189 C>A maps to NM_006439.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:141291416 C>T maps to NM_016249.3 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:141291416 C>T maps to NM_016249.3 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:161530848 G>T maps to NM_005922.2 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:161530848 G>T maps to NM_005922.2 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:49628331 G>A maps to NM_139049.1 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:49628331 G>A maps to NM_139049.1 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:98954083 C>T maps to ENST00000254898 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:98954083 C>T maps to ENST00000254898 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49959861 G>T maps to NM_001012300.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49959861 G>T maps to NM_001012300.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:151078260 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:151078260 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44641126 C>A maps to NM_004994.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44641126 C>A maps to NM_004994.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:84772675 G>T maps to NM_138409.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:84772675 G>T maps to NM_138409.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:822937 C>T maps to NM_001025190.1 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:822937 C>T maps to NM_001025190.1 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92715441 C>A maps to NM_005959.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92715441 C>A maps to NM_005959.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:26586718 G>T maps to NM_001135091.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:26586718 G>T maps to NM_001135091.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:9076552 G>T maps to NM_024690.2 P3631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:9076552 G>T maps to NM_024690.2 P3631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1095201 G>T maps to ENST00000441003 E2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1095201 G>T maps to ENST00000441003 E2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1274100 C>A maps to ENST00000447027 V5039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1274100 C>A maps to ENST00000447027 V5039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:42778786 G>A maps to NM_002463.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:42778786 G>A maps to NM_002463.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:15808818 C>T maps to NM_001040114.1 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:15808818 C>T maps to NM_001040114.1 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89916114 C>T maps to NM_005467.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89916114 C>T maps to NM_005467.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201777166 A>G maps to ENST00000367296 T1245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201777166 A>G maps to ENST00000367296 T1245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:106498469 G>T maps to NM_001004720.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:106498469 G>T maps to NM_001004720.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:124826398 G>A maps to NM_006312.4 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:124826398 G>A maps to NM_006312.4 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:152426642 G>A maps to NM_001164507.1 D5794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:152426642 G>A maps to NM_001164507.1 D5794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:24774646 C>T maps to NM_005382.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:24774646 C>T maps to NM_005382.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:55421014 C>G maps to NM_021191.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:55421014 C>G maps to NM_021191.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:52505471 C>A maps to NM_007361.3 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:52505471 C>A maps to NM_007361.3 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:201758086 A>T maps to NM_001136039.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:201758086 A>T maps to NM_001136039.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:7981664 C>G maps to NM_176821.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:7981664 C>G maps to NM_176821.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247592910 C>A maps to NM_004895.4 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247592910 C>A maps to NM_004895.4 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55450961 G>T maps to ENST00000446217 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55450961 G>T maps to ENST00000446217 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56466488 G>T maps to NM_176811.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56466488 G>T maps to NM_176811.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56244282 G>T maps to NM_176820.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56244282 G>T maps to NM_176820.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:156136233 C>A maps to NM_000910.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:156136233 C>A maps to NM_000910.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:32585596 G>A maps to NM_004495.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:32585596 G>A maps to NM_004495.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:212911977 C>T maps to NM_015471.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:212911977 C>T maps to NM_015471.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:229613446 C>T maps to NM_018230.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:229613446 C>T maps to NM_018230.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113400593 G>T maps to NM_006187.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113400593 G>T maps to NM_006187.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:29407950 C>T maps to NM_013941.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:29407950 C>T maps to NM_013941.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158576327 C>T maps to NM_001004478.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158576327 C>T maps to NM_001004478.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:107367419 C>A maps to NM_001004481.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:107367419 C>A maps to NM_001004481.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247751822 G>T maps to NM_001001915.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247751822 G>T maps to NM_001001915.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247752092 C>A maps to NM_001001915.1 C144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247752092 C>A maps to NM_001001915.1 C144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247769066 C>G maps to NM_001001914.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247769066 C>G maps to NM_001001914.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:29080107 G>T maps to NM_001005216.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:29080107 G>T maps to NM_001005216.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248343445 C>G maps to NM_001004688.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248343445 C>G maps to NM_001004688.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248402422 C>T maps to NM_017504.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248402422 C>T maps to NM_017504.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248789790 A>T maps to NM_001001964.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248789790 A>T maps to NM_001001964.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248569918 C>A maps to NM_030904.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248569918 C>A maps to NM_030904.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248551229 T>C maps to NM_001005471.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248551229 T>C maps to NM_001005471.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6007959 G>T maps to NM_001005173.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6007959 G>T maps to NM_001005173.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6008098 G>C maps to NM_001005173.2 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6008098 G>C maps to NM_001005173.2 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:59210994 G>T maps to NM_001004728.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:59210994 G>T maps to NM_001004728.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55761412 G>T maps to NM_003697.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55761412 G>T maps to NM_003697.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55944481 T>A maps to NM_001005492.1 L130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55944481 T>A maps to NM_001005492.1 L130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55595542 C>A maps to NM_001004739.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55595542 C>A maps to NM_001004739.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:56185387 G>A maps to NM_001004744.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:56185387 G>A maps to NM_001004744.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158687239 A>T maps to ENST00000368146 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158687239 A>T maps to ENST00000368146 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:26706329 C>T maps to NM_194248.2 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:26706329 C>T maps to NM_194248.2 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:241078727 G>T maps to NM_148961.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:241078727 G>T maps to NM_148961.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:121660768 C>T maps to NM_002560.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:121660768 C>T maps to NM_002560.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3593444 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3593444 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100155279 T>A maps to NM_017734.4 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100155279 T>A maps to NM_017734.4 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:142681452 C>A maps to NM_198504.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:142681452 C>A maps to NM_198504.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:206364737 G>T maps to ENST00000406610 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:206364737 G>T maps to ENST00000406610 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145060241 G>C maps to NM_032789.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145060241 G>C maps to NM_032789.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242077445 C>A maps to ENST00000358649 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242077445 C>A maps to ENST00000358649 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:134072089 A>C maps to NM_032961.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:134072089 A>C maps to NM_032961.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:141244260 C>A maps to NM_032420.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:141244260 C>A maps to NM_032420.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140237057 G>T maps to NM_018901.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140237057 G>T maps to NM_018901.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140558592 A>T maps to NM_019120.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140558592 A>T maps to NM_019120.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140769610 C>T maps to NM_003736.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140769610 C>T maps to NM_003736.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:78710912 C>T maps to NM_001190482.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:78710912 C>T maps to NM_001190482.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:183129073 C>A maps to NM_005019.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:183129073 C>A maps to NM_005019.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:7543246 C>A maps to NM_080662.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:7543246 C>A maps to NM_080662.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4851650 C>A maps to NM_005022.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4851650 C>A maps to NM_005022.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:100912824 C>A maps to NM_000926.4 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:100912824 C>A maps to NM_000926.4 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:64356527 C>T maps to NM_015153.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:64356527 C>T maps to NM_015153.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:32977014 G>A maps to NM_004572.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:32977014 G>A maps to NM_004572.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:30789750 C>T maps to NM_002657.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:30789750 C>T maps to NM_002657.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:171394594 C>A maps to NM_002662.3 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:171394594 C>A maps to NM_002662.3 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:155006 C>G maps to NM_052909.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:155006 C>G maps to NM_052909.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:145914457 T>C maps to NM_020353.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:145914457 T>C maps to NM_020353.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:102939073 G>T maps to NM_004279.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:102939073 G>T maps to NM_004279.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:133214628 G>A maps to ENST00000455752 A1886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:133214628 G>A maps to ENST00000455752 A1886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:132021505 C>A maps to NM_001083538.1 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:132021505 C>A maps to NM_001083538.1 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23816058 C>A maps to NM_013261.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23816058 C>A maps to NM_013261.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23833287 G>A maps to NM_013261.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23833287 G>A maps to NM_013261.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:81741467 G>T maps to NM_003625.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:81741467 G>T maps to NM_003625.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:46378244 G>A maps to NM_005400.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:46378244 G>A maps to NM_005400.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54403578 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54403578 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:120353853 C>A maps to NM_004248.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:120353853 C>A maps to NM_004248.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43523024 G>C maps to ENST00000306308 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43523024 G>C maps to ENST00000306308 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67943485 G>T maps to NM_006742.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67943485 G>T maps to NM_006742.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:23412034 G>A maps to NM_173495.2 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:23412034 G>A maps to NM_173495.2 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11579513 C>A maps to NM_020780.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11579513 C>A maps to NM_020780.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8499763 G>T maps to NM_002839.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8499763 G>T maps to NM_002839.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8518230 G>T maps to NM_002839.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8518230 G>T maps to NM_002839.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:128294834 C>A maps to ENST00000368210 G1387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:128294834 C>A maps to ENST00000368210 G1387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:15733635 C>T maps to NM_030667.1 Y1001Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:15733635 C>T maps to NM_030667.1 Y1001Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:57663633 C>G maps to ENST00000438036 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:57663633 C>G maps to ENST00000438036 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66039309 G>T maps to NM_030981.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66039309 G>T maps to NM_030981.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:4665603 T>C maps to NM_001130862.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:4665603 T>C maps to NM_001130862.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:160264502 C>T maps to NM_014247.2 H906H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:160264502 C>T maps to NM_014247.2 H906H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:82366731 T>A maps to NM_152545.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:82366731 T>A maps to NM_152545.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103163866 G>T maps to ENST00000428762 G2487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103163866 G>T maps to ENST00000428762 G2487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:117244364 C>A maps to NM_173560.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:117244364 C>A maps to NM_173560.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:72939586 C>A maps to NM_004296.4 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:72939586 C>A maps to NM_004296.4 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156354616 G>T maps to NM_020407.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156354616 G>T maps to NM_020407.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:18534822 G>C maps to NM_005406.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:18534822 G>C maps to NM_005406.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:33991969 G>C maps to NM_001036.3 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:33991969 G>C maps to NM_001036.3 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:136573483 G>T maps to NM_007101.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:136573483 G>T maps to NM_007101.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:28331560 G>T maps to NM_001024401.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:28331560 G>T maps to NM_001024401.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:12679983 C>T maps to NM_001112706.2 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:12679983 C>T maps to NM_001112706.2 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:166245430 C>A maps to NM_001040142.1 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:166245430 C>A maps to NM_001040142.1 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:177929538 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:177929538 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:4556014 C>A maps to NM_032108.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:4556014 C>A maps to NM_032108.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:26140370 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:26140370 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57367359 C>A maps to ENST00000403558 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57367359 C>A maps to ENST00000403558 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:40947908 G>A maps to NM_203344.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:40947908 G>A maps to NM_203344.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26938633 C>A maps to NM_001174103.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26938633 C>A maps to NM_001174103.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:130511548 G>A maps to NM_170600.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:130511548 G>A maps to NM_170600.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:17795575 G>T maps to NM_003026.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:17795575 G>T maps to NM_003026.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:164777758 G>T maps to NM_001041.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:164777758 G>T maps to NM_001041.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:87770177 C>A maps to NM_197965.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:87770177 C>A maps to NM_197965.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44671909 T>C maps to NM_001134771.1 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44671909 T>C maps to NM_001134771.1 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:98987860 G>A maps to NM_213611.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:98987860 G>A maps to NM_213611.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:47186733 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:47186733 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:8397903 C>T maps to ENST00000377479 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:8397903 C>T maps to ENST00000377479 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:108626830 C>A maps to NM_021815.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:108626830 C>A maps to NM_021815.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40397427 G>T maps to NM_021097.2 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40397427 G>T maps to NM_021097.2 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40656997 G>C maps to NM_021097.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40656997 G>C maps to NM_021097.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:20543243 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:20543243 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:72967156 C>T maps to NM_015110.3 Y1072Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:72967156 C>T maps to NM_015110.3 Y1072Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:122337652 T>C maps to ENST00000395451 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:122337652 T>C maps to ENST00000395451 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:101589248 G>A maps to NM_152628.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:101589248 G>A maps to NM_152628.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:97174271 G>A maps to NM_001034954.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:97174271 G>A maps to NM_001034954.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108366971 A>G maps to NM_001013031.1 Y1039Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108366971 A>G maps to NM_001013031.1 Y1039Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108923869 C>A maps to NM_001013031.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108923869 C>A maps to NM_001013031.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145101811 C>A maps to NM_198572.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145101811 C>A maps to NM_198572.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:149509062 G>A maps to NM_198455.2 R3206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:149509062 G>A maps to NM_198455.2 R3206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:53079445 C>T maps to NM_014682.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:53079445 C>T maps to NM_014682.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:146658823 G>A maps to NM_001112724.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:146658823 G>A maps to NM_001112724.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:147680373 G>T maps to NM_001127715.1 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:147680373 G>T maps to NM_001127715.1 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:223400985 G>T maps to NM_017982.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:223400985 G>T maps to NM_017982.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:135369515 C>T maps to NM_001143764.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:135369515 C>T maps to NM_001143764.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:46962008 C>T maps to NM_031912.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:46962008 C>T maps to NM_031912.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:229738094 A>T maps to NM_014409.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:229738094 A>T maps to NM_014409.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140698603 G>A maps to NM_005642.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140698603 G>A maps to NM_005642.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:118598073 T>C maps to NM_016281.3 E743E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:118598073 T>C maps to NM_016281.3 E743E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:38305108 G>A maps to ENST00000443402 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:38305108 G>A maps to ENST00000443402 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:1268366 G>T maps to NM_152228.1 G448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:1268366 G>T maps to NM_152228.1 G448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:179659918 A>G maps to ENST00000444136 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:179659918 A>G maps to ENST00000444136 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:133494433 C>T maps to NM_001063.3 C615C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:133494433 C>T maps to NM_001063.3 C615C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:35700301 G>A maps to NM_006289.3 I2182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:35700301 G>A maps to NM_006289.3 I2182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:105367360 C>G maps to NM_030788.2 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:105367360 C>G maps to NM_030788.2 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:10946029 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:10946029 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:129566542 C>A maps to NM_133448.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:129566542 C>A maps to NM_133448.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:15240918 A>T maps to NM_001004320.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:15240918 A>T maps to NM_001004320.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:123754006 C>T maps to NM_001013743.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:123754006 C>T maps to NM_001013743.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:109796453 C>A maps to NM_153015.1 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:109796453 C>A maps to NM_153015.1 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:209951492 G>A maps to NM_025228.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:209951492 G>A maps to NM_025228.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:202245492 T>A maps to NM_015049.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:202245492 T>A maps to NM_015049.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:140401412 C>A maps to NM_152616.4 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:140401412 C>A maps to NM_152616.4 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248039226 G>T maps to NM_015431.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248039226 G>T maps to NM_015431.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:72967970 G>A maps to NM_007332.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:72967970 G>A maps to NM_007332.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:142499757 G>T maps to ENST00000476941 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:142499757 G>T maps to ENST00000476941 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3474933 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3474933 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:54467178 G>C maps to NM_058163.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:54467178 G>C maps to NM_058163.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32829694 C>T maps to NM_052841.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32829694 C>T maps to NM_052841.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:166799737 C>G maps to NM_024753.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:166799737 C>G maps to NM_024753.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62502893 G>T maps to NM_173810.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62502893 G>T maps to NM_173810.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179443725 G>T maps to NM_133378.4 T20109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179443725 G>T maps to NM_133378.4 T20109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179622488 C>A maps to NM_133432.3 A3440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179622488 C>A maps to NM_133432.3 A3440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:47062971 C>G maps to NM_153280.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:47062971 C>G maps to NM_153280.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:49845455 G>A maps to NM_003335.2 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:49845455 G>A maps to NM_003335.2 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:10207065 G>T maps to NM_001105562.2 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:10207065 G>T maps to NM_001105562.2 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:19513692 G>A maps to ENST00000375267 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:19513692 G>A maps to ENST00000375267 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62444317 C>A maps to NM_015853.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62444317 C>A maps to NM_015853.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43531671 C>A maps to NM_173568.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43531671 C>A maps to NM_173568.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215956146 C>T maps to ENST00000366943 T3506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215956146 C>T maps to ENST00000366943 T3506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:57640628 A>T maps to NM_020903.2 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:57640628 A>T maps to NM_020903.2 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:22078011 C>A maps to NM_032236.5 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:22078011 C>A maps to NM_032236.5 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:117783871 G>T maps to NM_032334.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:117783871 G>T maps to NM_032334.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:108307696 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:108307696 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:135051580 C>A maps to NM_014468.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:135051580 C>A maps to NM_014468.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:79929504 C>A maps to ENST00000376646 S1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:79929504 C>A maps to ENST00000376646 S1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:122723132 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:122723132 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:95992120 G>T maps to ENST00000297954 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:95992120 G>T maps to ENST00000297954 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49360249 T>A maps to NM_003394.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49360249 T>A maps to NM_003394.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:30556124 G>C maps to NM_001011718.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:30556124 G>C maps to NM_001011718.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:41737149 G>A maps to ENST00000351589 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:41737149 G>A maps to ENST00000351589 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:135613822 G>A maps to NM_020863.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:135613822 G>A maps to NM_020863.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:77617294 G>T maps to NM_024721.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:77617294 G>T maps to NM_024721.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:136649857 G>C maps to NM_003413.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:136649857 G>C maps to NM_003413.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6953713 G>T maps to NM_013250.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6953713 G>T maps to NM_013250.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:146107493 C>T maps to NM_021061.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:146107493 C>T maps to NM_021061.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:64159472 G>T maps to NM_014951.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:64159472 G>T maps to NM_014951.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:31039147 G>C maps to NM_014717.1 T874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:31039147 G>C maps to NM_014717.1 T874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:37975730 C>T maps to NM_144694.1 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:37975730 C>T maps to NM_144694.1 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:53268920 A>G maps to NM_198457.2 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:53268920 A>G maps to NM_198457.2 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:58018005 G>A maps to NM_198542.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:58018005 G>A maps to NM_198542.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:48335364 C>T maps to NM_152701.3 S3008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:48335364 C>T maps to NM_152701.3 S3008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:94933551 A>T maps to ENST00000454898 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:94933551 A>T maps to ENST00000454898 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:51298091 C>T maps to NM_033068.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:51298091 C>T maps to NM_033068.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:185705146 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:185705146 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:35083386 A>T maps to NM_005159.4 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:35083386 A>T maps to NM_005159.4 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:36571809 G>T maps to NM_001177506.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:36571809 G>T maps to NM_001177506.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:241621966 C>A maps to NM_001102467.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:241621966 C>A maps to NM_001102467.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:50348098 T>A maps to NM_000486.5 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:50348098 T>A maps to NM_000486.5 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:123268938 A>T maps to NM_080928.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:123268938 A>T maps to NM_080928.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:28845863 A>T maps to NM_148414.1 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:28845863 A>T maps to NM_148414.1 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:60689437 G>A maps to NM_022893.3 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:60689437 G>A maps to NM_022893.3 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:128193339 C>T maps to NM_001004298.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:128193339 C>T maps to NM_001004298.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:81579741 C>T maps to NM_000722.2 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:81579741 C>T maps to NM_000722.2 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:40853443 C>T maps to NM_032587.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:40853443 C>T maps to NM_032587.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:116243866 C>A maps to NM_001232.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:116243866 C>A maps to NM_001232.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:3273913 C>T maps to NM_021938.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:3273913 C>T maps to NM_021938.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:170610314 A>T maps to NM_173872.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:170610314 A>T maps to NM_173872.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:147869450 C>A maps to NM_014141.5 S964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:147869450 C>A maps to NM_014141.5 S964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:48604562 G>T maps to NM_000094.3 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:48604562 G>T maps to NM_000094.3 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:113241098 G>T maps to NM_198123.1 S3617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:113241098 G>T maps to NM_198123.1 S3617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:6213365 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:6213365 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:230231655 C>A maps to NM_139072.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:230231655 C>A maps to NM_139072.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:131847495 A>T maps to NM_020438.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:131847495 A>T maps to NM_020438.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:128060611 G>A maps to NM_021937.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:128060611 G>A maps to NM_021937.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:46124785 C>A maps to NM_001193268.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:46124785 C>A maps to NM_001193268.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:154159112 C>T maps to NM_000132.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:154159112 C>T maps to NM_000132.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:91424921 C>T maps to NM_002569.2 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:91424921 C>T maps to NM_002569.2 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:127222088 C>T maps to NM_024523.5 W769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:127222088 C>T maps to NM_024523.5 W769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:67719579 G>A maps to NM_030819.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:67719579 G>A maps to NM_030819.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:46094524 C>A maps to NM_005282.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:46094524 C>A maps to NM_005282.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:114262224 G>A maps to ENST00000398283 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:114262224 G>A maps to ENST00000398283 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:197297865 A>C maps to NM_020760.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:197297865 A>C maps to NM_020760.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:161495341 C>T maps to NM_002155.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:161495341 C>T maps to NM_002155.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:100961628 G>A maps to NM_016247.2 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:100961628 G>A maps to NM_016247.2 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:233925274 C>A maps to ENST00000359570 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:233925274 C>A maps to ENST00000359570 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:41284240 C>T maps to NM_004700.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:41284240 C>T maps to NM_004700.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:34257576 G>T maps to NM_194313.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:34257576 G>T maps to NM_194313.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:52964527 G>T maps to NM_175053.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:52964527 G>T maps to NM_175053.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:26157197 G>T maps to NM_173699.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:26157197 G>T maps to NM_173699.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr14:75515968 C>A maps to NM_001040108.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr14:75515968 C>A maps to NM_001040108.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:48033415 A>G maps to NM_000179.2 K1240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:48033415 A>G maps to NM_000179.2 K1240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:32230131 C>A maps to NM_001040446.1 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:32230131 C>A maps to NM_001040446.1 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:10315770 G>T maps to NM_002472.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:10315770 G>T maps to NM_002472.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:130825793 G>A maps to NM_197956.3 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:130825793 G>A maps to NM_197956.3 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:148012568 G>A maps to ENST00000310701 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:148012568 G>A maps to ENST00000310701 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:28116371 G>T maps to NM_000275.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:28116371 G>T maps to NM_000275.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:107288952 C>A maps to NM_001001919.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:107288952 C>A maps to NM_001001919.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:57970804 A>T maps to NM_001004459.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:57970804 A>T maps to NM_001004459.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248263033 C>T maps to NM_175911.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248263033 C>T maps to NM_175911.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248737761 C>T maps to NM_001001821.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248737761 C>T maps to NM_001001821.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:55761522 G>T maps to NM_003697.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:55761522 G>T maps to NM_003697.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:29648338 C>T maps to NM_183378.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:29648338 C>T maps to NM_183378.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:74852991 A>G maps to NM_002704.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:74852991 A>G maps to NM_002704.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:74324813 T>A maps to NM_002766.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:74324813 T>A maps to NM_002766.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:39359958 G>A maps to NM_001195833.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:39359958 G>A maps to NM_001195833.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:101276265 A>C maps to NM_183419.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:101276265 A>C maps to NM_183419.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:165397964 G>T maps to NM_006917.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:165397964 G>T maps to NM_006917.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:92734861 A>G maps to NM_017654.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:92734861 A>G maps to NM_017654.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:246930494 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:246930494 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:9052128 C>A maps to NM_003966.2 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:9052128 C>A maps to NM_003966.2 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:38600928 G>A maps to NM_015073.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:38600928 G>A maps to NM_015073.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:108716301 G>A maps to NM_001013031.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:108716301 G>A maps to NM_001013031.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:113173789 C>T maps to ENST00000374463 W2070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:113173789 C>T maps to ENST00000374463 W2070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:56679853 G>T maps to ENST00000240361 Y484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:56679853 G>T maps to ENST00000240361 Y484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:31488201 C>A maps to NM_001042454.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:31488201 C>A maps to NM_001042454.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:11630123 G>A maps to ENST00000423059 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:11630123 G>A maps to ENST00000423059 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:6161857 G>T maps to NM_000552.3 C679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:6161857 G>T maps to NM_000552.3 C679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:167881063 G>T maps to NM_001161661.1 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:167881063 G>T maps to NM_001161661.1 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:77618440 C>A maps to NM_024721.4 Y706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:77618440 C>A maps to NM_024721.4 Y706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:50769535 T>A maps to NM_018197.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:50769535 T>A maps to NM_018197.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:30936247 C>T maps to NM_014717.1 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:30936247 C>T maps to NM_014717.1 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:67300881 T>C maps to ENST00000392677 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:67300881 T>C maps to ENST00000392677 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:3385071 C>T maps to NM_000049.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:3385071 C>T maps to NM_000049.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:10382278 G>A maps to NM_001001331.2 N1009N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:10382278 G>A maps to NM_001001331.2 N1009N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:153171454 C>A maps to NM_000054.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:153171454 C>A maps to NM_000054.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:83926568 G>A maps to NM_001717.3 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:83926568 G>A maps to NM_001717.3 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:50916416 C>A maps to NM_182554.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:50916416 C>A maps to NM_182554.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:57960334 A>G maps to NM_018168.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:57960334 A>G maps to NM_018168.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:34648809 T>C maps to ENST00000438749 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:34648809 T>C maps to ENST00000438749 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:175763779 C>A maps to ENST00000443967 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:175763779 C>A maps to ENST00000443967 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:42950013 G>A maps to NM_001099858.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:42950013 G>A maps to NM_001099858.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:181480553 G>A maps to ENST00000357570 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:181480553 G>A maps to ENST00000357570 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:110496261 A>G maps to NM_014289.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:110496261 A>G maps to NM_014289.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:37964343 C>T maps to NM_152243.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:37964343 C>T maps to NM_152243.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:24537698 C>A maps to NM_006727.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:24537698 C>A maps to NM_006727.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:73270727 C>A maps to ENST00000398860 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:73270727 C>A maps to ENST00000398860 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:6208957 G>A maps to NM_015557.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:6208957 G>A maps to NM_015557.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:1427296 C>A maps to NM_014461.2 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:1427296 C>A maps to NM_014461.2 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:106898753 C>A maps to NM_006348.3 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:106898753 C>A maps to NM_006348.3 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:19087068 G>T maps to NM_016138.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:19087068 G>T maps to NM_016138.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:211473090 A>G maps to NM_001122633.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:211473090 A>G maps to NM_001122633.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:4168421 G>A maps to NM_032607.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:4168421 G>A maps to NM_032607.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:34312506 G>A maps to ENST00000373381 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:34312506 G>A maps to ENST00000373381 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:114186032 G>A maps to NM_198123.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:114186032 G>A maps to NM_198123.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:149101917 C>A maps to NM_001013845.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:149101917 C>A maps to NM_001013845.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:115593060 A>G maps to NM_001017978.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:115593060 A>G maps to NM_001017978.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:19033421 C>T maps to NM_019070.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:19033421 C>T maps to NM_019070.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:4857037 G>T maps to NM_053013.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:4857037 G>T maps to NM_053013.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:154158392 G>T maps to NM_000132.3 I1224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:154158392 G>T maps to NM_000132.3 I1224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:17643133 G>T maps to ENST00000335393 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:17643133 G>T maps to ENST00000335393 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:92531938 C>G maps to ENST00000298047 Y1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:92531938 C>G maps to ENST00000298047 Y1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:92623915 C>A maps to ENST00000298047 S4469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:92623915 C>A maps to ENST00000298047 S4469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:128496847 C>A maps to NM_001458.4 I2478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:128496847 C>A maps to NM_001458.4 I2478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr13:39454486 C>T maps to NM_207361.4 R3025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr13:39454486 C>T maps to NM_207361.4 R3025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:167728077 T>C maps to NM_014498.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:167728077 T>C maps to NM_014498.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:89920949 G>T maps to NM_032119.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:89920949 G>T maps to NM_032119.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:104335779 G>T maps to NM_133445.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:104335779 G>T maps to NM_133445.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:23421767 T>C maps to NM_017815.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:23421767 T>C maps to NM_017815.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:124731953 G>A maps to NM_020733.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:124731953 G>A maps to NM_020733.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:28424342 T>C maps to NM_004667.4 T2988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:28424342 T>C maps to NM_004667.4 T2988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:151164069 C>T maps to NM_178822.4 V1233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:151164069 C>T maps to NM_178822.4 V1233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:219920174 G>A maps to NM_002181.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:219920174 G>A maps to NM_002181.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:48726110 G>A maps to ENST00000395509 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:48726110 G>A maps to ENST00000395509 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:20167605 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:20167605 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:43907003 T>C maps to NM_015284.2 G1589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:43907003 T>C maps to NM_015284.2 G1589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:53189526 G>T maps to ENST00000309505 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:53189526 G>T maps to ENST00000309505 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:52761048 C>T maps to NM_002283.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:52761048 C>T maps to NM_002283.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:151899873 A>G maps to NM_005367.5 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:151899873 A>G maps to NM_005367.5 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:135318498 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:135318498 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:12976792 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:12976792 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:38192395 G>A maps to NM_014815.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:38192395 G>A maps to NM_014815.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:50331753 C>T maps to NM_030973.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:50331753 C>T maps to NM_030973.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:129904903 T>A maps to NM_002417.4 K1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:129904903 T>A maps to NM_002417.4 K1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:151962196 G>T maps to ENST00000355193 C370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:151962196 G>T maps to ENST00000355193 C370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:9021115 C>A maps to NM_024690.2 E12403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:9021115 C>A maps to NM_024690.2 E12403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:74716537 G>A maps to NM_006656.5 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:74716537 G>A maps to NM_006656.5 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:105132285 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:105132285 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:105189910 T>C maps to NM_198465.2 Y1369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:105189910 T>C maps to NM_198465.2 Y1369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:28326972 C>A maps to NM_000275.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:28326972 C>A maps to NM_000275.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:50946022 G>A maps to NM_018245.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:50946022 G>A maps to NM_018245.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:248757057 G>T maps to NM_001004693.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:248757057 G>T maps to NM_001004693.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:55433034 G>C maps to NM_001004704.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:55433034 G>C maps to NM_001004704.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:5221795 G>T maps to NM_001004760.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:5221795 G>T maps to NM_001004760.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:5173254 G>A maps to NM_012375.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:5173254 G>A maps to NM_012375.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:97868643 G>T maps to NM_001005514.1 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:97868643 G>T maps to NM_001005514.1 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:31864557 C>A maps to NM_001191057.1 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:31864557 C>A maps to NM_001191057.1 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:64394678 T>C maps to NM_015153.2 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:64394678 T>C maps to NM_015153.2 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:133256575 T>C maps to ENST00000455752 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:133256575 T>C maps to ENST00000455752 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:55716907 G>T maps to NM_002842.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:55716907 G>T maps to NM_002842.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:141259373 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:141259373 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:49463562 C>A maps to NM_144593.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:49463562 C>A maps to NM_144593.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:38145110 T>C maps to NM_001034853.1 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:38145110 T>C maps to NM_001034853.1 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:27428247 G>T maps to NM_003047.3 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:27428247 G>T maps to NM_003047.3 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:168098447 G>T maps to NM_003062.2 G1294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:168098447 G>T maps to NM_003062.2 G1294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:157053464 G>A maps to NM_178424.1 D715D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:157053464 G>A maps to NM_178424.1 D715D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:38831003 C>A maps to NM_006068.3 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:38831003 C>A maps to NM_006068.3 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:7592604 C>T maps to NM_018081.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:7592604 C>T maps to NM_018081.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:128957763 G>A maps to NM_016032.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:128957763 G>A maps to NM_016032.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:58452537 A>T maps to NM_005773.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:58452537 A>T maps to NM_005773.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:94544949 C>A maps to NM_000350.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:94544949 C>A maps to NM_000350.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150739142 G>T maps to ENST00000297504 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150739142 G>T maps to ENST00000297504 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:95862947 G>A maps to NM_005845.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:95862947 G>A maps to NM_005845.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:76216216 A>T maps to ENST00000370834 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:76216216 A>T maps to ENST00000370834 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236918344 C>T maps to NM_001103.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236918344 C>T maps to NM_001103.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:58957350 G>C maps to NM_001110.2 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:58957350 G>C maps to NM_001110.2 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:24359023 G>T maps to ENST00000380789 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:24359023 G>T maps to ENST00000380789 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:33588900 C>A maps to NM_030955.2 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:33588900 C>A maps to NM_030955.2 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131812782 C>T maps to NM_001115.2 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131812782 C>T maps to NM_001115.2 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131955632 G>C maps to NM_001115.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131955632 G>C maps to NM_001115.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:77894746 C>G maps to NM_014913.3 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:77894746 C>G maps to NM_014913.3 S484*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-67-3771-01A-01D-1040-01. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-67-3771-01A-01D-1040-01. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105408230 G>A maps to NM_138420.2 D4519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105408230 G>A maps to NM_138420.2 D4519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105416867 C>G maps to NM_138420.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105416867 C>G maps to NM_138420.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62294196 C>A maps to NM_001620.1 G2564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62294196 C>A maps to NM_001620.1 G2564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:106968727 G>A maps to NM_001624.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:106968727 G>A maps to NM_001624.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:4747356 T>C maps to NM_006422.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:4747356 T>C maps to NM_006422.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:3726107 G>A maps to ENST00000403787 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:3726107 G>A maps to ENST00000403787 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:104120404 G>T maps to NM_020978.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:104120404 G>T maps to NM_020978.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:241439488 C>A maps to ENST00000401804 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:241439488 C>A maps to ENST00000401804 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:73962874 A>C maps to NM_032217.3 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:73962874 A>C maps to NM_032217.3 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:165118605 G>A maps to NM_012403.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:165118605 G>A maps to NM_012403.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:90346961 G>A maps to NM_001150.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:90346961 G>A maps to NM_001150.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:83332600 C>A maps to NM_004644.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:83332600 C>A maps to NM_004644.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:2121256 G>A maps to ENST00000355272 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:2121256 G>A maps to ENST00000355272 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:129996685 G>A maps to NM_001642.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:129996685 G>A maps to NM_001642.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:21234951 T>C maps to NM_000384.2 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:21234951 T>C maps to NM_000384.2 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:32103261 C>A maps to NM_018287.5 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:32103261 C>A maps to NM_018287.5 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:42407923 G>T maps to NM_199002.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:42407923 G>T maps to NM_199002.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:32848287 G>A maps to NM_001672.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:32848287 G>A maps to NM_001672.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:96809569 C>A maps to NM_018036.5 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:96809569 C>A maps to NM_018036.5 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160098581 C>A maps to NM_000702.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160098581 C>A maps to NM_000702.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:90029005 C>T maps to ENST00000428670 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:90029005 C>T maps to ENST00000428670 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36053417 G>T maps to NM_000704.2 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36053417 G>T maps to NM_000704.2 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110030426 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110030426 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57744833 G>T maps to NM_001015878.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57744833 G>T maps to NM_001015878.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:69640529 A>G maps to NM_001704.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:69640529 A>G maps to NM_001704.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:58786578 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:58786578 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:49458379 C>T maps to NM_198799.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:49458379 C>T maps to NM_198799.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:165491238 A>G maps to NM_000055.2 N580N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:165491238 A>G maps to NM_000055.2 N580N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:136594295 G>A maps to NM_014739.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:136594295 G>A maps to NM_014739.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:135570316 C>G maps to NM_001727.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:135570316 C>G maps to NM_001727.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:49690544 G>T maps to NM_003458.3 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:49690544 G>T maps to NM_003458.3 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:111395636 C>T maps to NM_004336.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:111395636 C>T maps to NM_004336.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:111425234 G>C maps to NM_004336.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:111425234 G>C maps to NM_004336.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72541682 G>T maps to NM_152710.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72541682 G>T maps to NM_152710.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156384529 C>G maps to ENST00000357975 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156384529 C>G maps to ENST00000357975 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:228363177 A>G maps to NM_001010867.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:228363177 A>G maps to NM_001010867.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:18445978 G>C maps to NM_001099407.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:18445978 G>C maps to NM_001099407.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:31901507 G>A maps to ENST00000437789 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:31901507 G>A maps to ENST00000437789 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:228497783 C>A maps to NM_020161.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:228497783 C>A maps to NM_020161.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:192516993 G>A maps to NM_178496.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:192516993 G>A maps to NM_178496.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:184801038 G>C maps to NM_001025266.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:184801038 G>C maps to NM_001025266.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:81504333 G>A maps to ENST00000508675 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:81504333 G>A maps to ENST00000508675 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:144124452 C>A maps to NM_173687.2 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:144124452 C>A maps to NM_173687.2 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:122526106 G>T maps to NM_001167940.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:122526106 G>T maps to NM_001167940.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:200730087 C>G maps to ENST00000236925 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:200730087 C>G maps to ENST00000236925 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:230910378 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:230910378 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:65793535 G>C maps to NM_053054.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:65793535 G>C maps to NM_053054.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:119170449 G>T maps to NM_005188.2 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:119170449 G>T maps to NM_005188.2 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57732051 C>G maps to NM_032269.5 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57732051 C>G maps to NM_032269.5 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57761224 G>A maps to NM_032269.5 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57761224 G>A maps to NM_032269.5 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:18513561 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:18513561 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:52439603 G>C maps to NM_031290.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:52439603 G>C maps to NM_031290.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:130899922 G>A maps to NM_207310.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:130899922 G>A maps to NM_207310.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64120218 C>T maps to NM_032251.5 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64120218 C>T maps to NM_032251.5 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:99997441 C>T maps to NM_005190.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:99997441 C>T maps to NM_005190.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:46401301 C>A maps to NM_001123041.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:46401301 C>A maps to NM_001123041.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:117552697 A>T maps to NM_004258.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:117552697 A>T maps to NM_004258.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:35823738 G>T maps to NM_001771.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:35823738 G>T maps to NM_001771.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:73991924 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:73991924 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:149999766 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:149999766 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:4892411 G>T maps to ENST00000328908 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:4892411 G>T maps to ENST00000328908 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:179983408 G>A maps to NM_014810.4 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:179983408 G>A maps to NM_014810.4 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:67034818 C>G maps to ENST00000326686 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:67034818 C>G maps to ENST00000326686 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:201994632 A>C maps to NM_001127183.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:201994632 A>C maps to NM_001127183.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:61763056 G>T maps to NM_017780.2 E1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:61763056 G>T maps to NM_017780.2 E1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:87302614 T>C maps to NM_014043.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:87302614 T>C maps to NM_014043.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:105150923 C>T maps to NM_018413.5 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:105150923 C>T maps to NM_018413.5 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:31538716 G>A maps to NM_012131.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:31538716 G>A maps to NM_012131.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:38724114 G>T maps to NM_175060.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:38724114 G>T maps to NM_175060.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14710888 C>G maps to ENST00000417570 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14710888 C>G maps to ENST00000417570 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:10288574 G>A maps to NM_138809.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:10288574 G>A maps to NM_138809.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:103440439 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:103440439 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:86578264 T>C maps to NM_152890.5 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:86578264 T>C maps to NM_152890.5 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:110817206 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:110817206 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61461737 C>T maps to NM_001853.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61461737 C>T maps to NM_001853.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:57490420 G>C maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:57490420 G>C maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:109055931 T>C maps to ENST00000420959 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:109055931 T>C maps to ENST00000420959 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:30232607 G>C maps to NM_032609.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:30232607 G>C maps to NM_032609.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:28848854 C>T maps to NM_182898.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:28848854 C>T maps to NM_182898.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149433913 C>A maps to NM_005211.3 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149433913 C>A maps to NM_005211.3 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:1422834 C>T maps to NM_001161530.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:1422834 C>T maps to NM_001161530.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:114185957 G>A maps to NM_198123.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:114185957 G>A maps to NM_198123.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:11082808 G>T maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:11082808 G>T maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150772098 C>T maps to NM_000396.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150772098 C>T maps to NM_000396.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:101671404 C>T maps to ENST00000360264 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:101671404 C>T maps to ENST00000360264 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143955875 T>A maps to ENST00000377675 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143955875 T>A maps to ENST00000377675 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143995832 A>G maps to NM_000498.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143995832 A>G maps to NM_000498.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:75014928 C>G maps to NM_000499.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:75014928 C>G maps to NM_000499.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:94828348 C>T maps to NM_183374.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:94828348 C>T maps to NM_183374.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99318001 G>A maps to ENST00000292414 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99318001 G>A maps to ENST00000292414 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:15756551 C>G maps to NM_000896.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:15756551 C>G maps to NM_000896.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61106637 G>A maps to NM_015533.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61106637 G>A maps to NM_015533.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:125298589 C>A maps to NM_001013628.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:125298589 C>A maps to NM_001013628.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160209913 G>C maps to NM_015726.3 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160209913 G>C maps to NM_015726.3 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:36699914 C>G maps to NM_004734.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:36699914 C>G maps to NM_004734.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:118579309 G>A maps to NM_006773.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:118579309 G>A maps to NM_006773.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:49936491 C>T maps to NM_001037729.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:49936491 C>T maps to NM_001037729.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:142190927 G>T maps to NM_014957.2 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:142190927 G>T maps to NM_014957.2 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:32217560 G>A maps to NM_001136029.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:32217560 G>A maps to NM_001136029.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:2209549 G>A maps to NM_145177.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:2209549 G>A maps to NM_145177.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:96220165 C>T maps to NM_006729.4 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:96220165 C>T maps to NM_006729.4 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:60590251 C>A maps to NM_001042517.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:60590251 C>A maps to NM_001042517.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:32383265 T>C maps to ENST00000357033 T1632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:32383265 T>C maps to ENST00000357033 T1632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:78340325 G>A maps to NM_013391.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:78340325 G>A maps to NM_013391.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:196664136 T>A maps to NM_018897.2 P3412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:196664136 T>A maps to NM_018897.2 P3412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:51392311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:51392311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:286582 G>C maps to NM_203447.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:286582 G>C maps to NM_203447.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:113286151 A>T maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:113286151 A>T maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:29126354 G>C maps to NM_001943.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:29126354 G>C maps to NM_001943.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:28993525 C>A maps to NM_001134453.1 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:28993525 C>A maps to NM_001134453.1 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:32438300 C>T maps to NM_001390.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:32438300 C>T maps to NM_001390.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:76111921 T>C maps to NM_020892.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:76111921 T>C maps to NM_020892.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:45397882 C>G maps to NM_014080.4 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:45397882 C>G maps to NM_014080.4 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:73993666 G>A maps to NM_003584.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:73993666 G>A maps to NM_003584.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:44703734 G>A maps to NM_022076.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:44703734 G>A maps to NM_022076.3 A119A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-67-3771-01A-01D-1040-01. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:241500166 C>G maps to NM_001033575.1 V22V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-67-3771-01A-01D-1040-01. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:241500166 C>G maps to NM_001033575.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:103106398 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:103106398 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:128060644 C>T maps to NM_021937.3 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:128060644 C>T maps to NM_021937.3 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:36194190 A>G maps to NM_030636.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:36194190 A>G maps to NM_030636.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:55259500 C>T maps to NM_005228.3 I853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:55259500 C>T maps to NM_005228.3 I853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:184039091 C>T maps to NM_001194947.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:184039091 C>T maps to NM_001194947.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:184044713 C>G maps to NM_001194947.1 S1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:184044713 C>G maps to NM_001194947.1 S1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:23762244 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:23762244 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:39990939 G>A maps to NM_052846.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:39990939 G>A maps to NM_052846.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:97605317 C>T maps to NM_001098175.1 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:97605317 C>T maps to NM_001098175.1 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132546779 C>T maps to ENST00000333577 V2706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132546779 C>T maps to ENST00000333577 V2706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:62141441 C>A maps to NM_001433.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:62141441 C>A maps to NM_001433.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:40194758 C>T maps to NM_005239.4 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:40194758 C>T maps to NM_005239.4 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:18284946 G>A maps to NM_001145127.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:18284946 G>A maps to NM_001145127.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:169528469 C>T maps to ENST00000367796 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:169528469 C>T maps to ENST00000367796 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:14563218 G>C maps to NM_031453.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:14563218 G>C maps to NM_031453.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:20879648 G>A maps to NM_207334.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:20879648 G>A maps to NM_207334.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45644331 C>G maps to NM_020937.2 S792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45644331 C>G maps to NM_020937.2 S792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150774062 C>T maps to NM_006712.3 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150774062 C>T maps to NM_006712.3 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150924903 C>A maps to NM_001447.2 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150924903 C>A maps to NM_001447.2 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:15936691 C>T maps to NM_012304.3 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:15936691 C>T maps to NM_012304.3 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157551322 G>T maps to NM_031282.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157551322 G>T maps to NM_031282.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:114879139 C>A maps to NM_020177.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:114879139 C>A maps to NM_020177.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:97368992 C>T maps to NM_001113382.1 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:97368992 C>T maps to NM_001113382.1 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:13702485 T>A maps to NM_018027.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:13702485 T>A maps to NM_018027.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:31089992 C>T maps to NM_031894.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:31089992 C>T maps to NM_031894.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:27765257 A>T maps to NM_033223.4 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:27765257 A>T maps to NM_033223.4 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:89888773 G>A maps to NM_002042.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:89888773 G>A maps to NM_002042.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:49611951 C>T maps to NM_002044.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:49611951 C>T maps to NM_002044.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:89917435 C>T maps to NM_003774.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:89917435 C>T maps to NM_003774.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:34117953 C>A maps to NM_016631.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:34117953 C>A maps to NM_016631.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:48428802 C>T maps to NM_004962.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:48428802 C>T maps to NM_004962.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:63930052 T>C maps to NM_003878.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:63930052 T>C maps to NM_003878.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:61959223 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:61959223 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40344577 C>T maps to NM_032484.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40344577 C>T maps to NM_032484.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31011703 C>T maps to NM_000823.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31011703 C>T maps to NM_000823.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:35227415 C>G maps to NM_153212.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:35227415 C>G maps to NM_153212.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:121747077 G>T maps to NM_005270.4 G1196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:121747077 G>T maps to NM_005270.4 G1196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52324414 C>G maps to NM_145262.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52324414 C>G maps to NM_145262.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:1930450 A>T maps to NM_001500.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:1930450 A>T maps to NM_001500.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:127651447 C>A maps to NM_002077.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:127651447 C>A maps to NM_002077.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:42478466 C>T maps to NM_001002909.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:42478466 C>T maps to NM_001002909.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:135431522 C>T maps to NM_153834.3 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:135431522 C>T maps to NM_153834.3 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:26533739 C>T maps to NM_001145168.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:26533739 C>T maps to NM_001145168.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:47684540 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:47684540 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:25464888 C>A maps to NM_020752.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:25464888 C>A maps to NM_020752.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:241569593 C>T maps to NM_001195381.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:241569593 C>T maps to NM_001195381.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:27720713 C>T maps to NM_005281.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:27720713 C>T maps to NM_005281.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:46094343 C>A maps to NM_005282.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:46094343 C>A maps to NM_005282.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:54456043 G>A maps to NM_001008397.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:54456043 G>A maps to NM_001008397.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:13717312 G>T maps to NM_000834.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:13717312 G>T maps to NM_000834.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:156482497 A>G maps to NM_001173393.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:156482497 A>G maps to NM_001173393.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:18631182 C>T maps to NM_178425.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:18631182 C>T maps to NM_178425.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:149858700 G>C maps to NM_003517.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:149858700 G>C maps to NM_003517.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:26545529 A>G maps to NM_006353.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:26545529 A>G maps to NM_006353.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:38796435 C>A maps to NM_138394.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:38796435 C>A maps to NM_138394.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18327040 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18327040 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:63235915 C>A maps to NM_054108.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:63235915 C>A maps to NM_054108.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:22040785 G>T maps to NM_021624.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:22040785 G>T maps to NM_021624.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:161495728 C>A maps to NM_002155.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:161495728 C>A maps to NM_002155.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:656539 C>A maps to NM_148959.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:656539 C>A maps to NM_148959.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:203653589 G>A maps to NM_138468.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:203653589 G>A maps to NM_138468.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:315103 G>T maps to ENST00000328221 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:315103 G>T maps to ENST00000328221 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:42176905 G>T maps to NM_001556.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:42176905 G>T maps to NM_001556.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:48156474 G>A maps to NM_002204.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:48156474 G>A maps to NM_002204.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:20371503 G>T maps to NM_002214.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:20371503 G>T maps to NM_002214.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:26553191 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:26553191 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:39681166 G>C maps to NM_002276.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:39681166 G>C maps to NM_002276.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:155555775 C>A maps to NM_002239.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:155555775 C>A maps to NM_002239.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:78651441 C>G maps to NM_001161352.1 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:78651441 C>G maps to NM_001161352.1 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:24035814 C>T maps to NM_001142730.1 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:24035814 C>T maps to NM_001142730.1 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:141318257 C>T maps to NM_014773.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:141318257 C>T maps to NM_014773.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:197408179 G>T maps to NM_014687.1 C750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:197408179 G>T maps to NM_014687.1 C750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:42293844 G>A maps to NM_015058.1 R1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:42293844 G>A maps to NM_015058.1 R1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72292390 C>A maps to NM_014431.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72292390 C>A maps to NM_014431.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:5743004 A>C maps to ENST00000414202 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:5743004 A>C maps to ENST00000414202 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:16359916 C>T maps to NM_024704.4 Q910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:16359916 C>T maps to NM_024704.4 Q910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:21036153 G>A maps to NM_020816.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:21036153 G>A maps to NM_020816.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:39092741 C>A maps to NM_015515.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:39092741 C>A maps to NM_015515.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53010125 G>A maps to NM_175068.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53010125 G>A maps to NM_175068.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:145537166 G>A maps to NM_020117.9 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:145537166 G>A maps to NM_020117.9 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:136570071 G>T maps to NM_002299.2 S721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:136570071 G>T maps to NM_002299.2 S721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:75609536 G>T maps to NM_001001933.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:75609536 G>T maps to NM_001001933.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:151520207 A>C maps to NM_006726.3 P1999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:151520207 A>C maps to NM_006726.3 P1999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:42355848 T>A maps to NM_152447.3 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:42355848 T>A maps to NM_152447.3 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:194080146 G>T maps to NM_001135057.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:194080146 G>T maps to NM_001135057.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:7231810 G>T maps to NM_001105581.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:7231810 G>T maps to NM_001105581.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:76372110 C>A maps to NM_001128922.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:76372110 C>A maps to NM_001128922.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:70639172 T>A maps to NM_017768.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:70639172 T>A maps to NM_017768.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:86057621 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:86057621 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:32529941 C>A maps to NM_012322.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:32529941 C>A maps to NM_012322.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:143784659 A>G maps to ENST00000292430 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:143784659 A>G maps to ENST00000292430 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:30918541 G>T maps to NM_183058.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:30918541 G>T maps to NM_183058.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:140995103 C>A maps to NM_005462.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:140995103 C>A maps to NM_005462.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:12028688 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:12028688 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:112406906 T>C maps to NM_001085377.1 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:112406906 T>C maps to NM_001085377.1 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113719263 C>T maps to NM_001112732.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113719263 C>T maps to NM_001112732.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:3294474 G>C maps to NM_000243.2 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:3294474 G>C maps to NM_000243.2 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:89449994 C>A maps to NM_005928.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:89449994 C>A maps to NM_005928.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:74740467 C>T maps to NM_024311.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:74740467 C>T maps to NM_024311.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:39884737 G>T maps to NM_001098270.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:39884737 G>T maps to NM_001098270.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:1565852 C>G maps to NM_080875.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:1565852 C>G maps to NM_080875.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:129903115 T>A maps to NM_002417.4 K2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:129903115 T>A maps to NM_002417.4 K2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:2535349 C>T maps to NM_033467.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:2535349 C>T maps to NM_033467.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:61201637 A>T maps to NM_002431.3 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:61201637 A>T maps to NM_002431.3 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108778672 C>T maps to NM_014429.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108778672 C>T maps to NM_014429.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:11297962 C>A maps to NM_004958.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:11297962 C>A maps to NM_004958.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9072072 C>A maps to NM_024690.2 E5125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9072072 C>A maps to NM_024690.2 E5125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1025313 G>T maps to NM_005961.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1025313 G>T maps to NM_005961.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50945489 C>A maps to NM_004533.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50945489 C>A maps to NM_004533.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:16143377 C>T maps to NM_013262.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:16143377 C>T maps to NM_013262.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:27441091 G>A maps to NM_078471.3 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:27441091 G>A maps to NM_078471.3 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:24401951 G>A maps to ENST00000330966 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:24401951 G>A maps to ENST00000330966 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:41834583 C>T maps to NM_006766.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:41834583 C>T maps to NM_006766.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:115769465 A>T maps to NM_022569.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:115769465 A>T maps to NM_022569.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:11185640 T>A maps to NM_006403.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:11185640 T>A maps to NM_006403.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:45004704 A>T maps to NM_001145107.1 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:45004704 A>T maps to NM_001145107.1 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:124676441 G>T maps to NM_001040214.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:124676441 G>T maps to NM_001040214.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247599346 C>A maps to NM_004895.4 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247599346 C>A maps to NM_004895.4 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56382249 G>A maps to NM_134444.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56382249 G>A maps to NM_134444.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56544114 G>C maps to NM_153447.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56544114 G>C maps to NM_153447.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:117660522 T>A maps to ENST00000338101 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:117660522 T>A maps to ENST00000338101 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:26941597 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:26941597 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:89184979 G>A maps to NM_016931.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:89184979 G>A maps to NM_016931.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:100934573 G>A maps to ENST00000392986 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:100934573 G>A maps to ENST00000392986 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61386224 C>A maps to NM_002531.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61386224 C>A maps to NM_002531.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:61386116 C>T maps to NM_002531.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:61386116 C>T maps to NM_002531.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205696876 G>A maps to NM_022731.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205696876 G>A maps to NM_022731.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:34263447 C>G maps to NM_006703.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:34263447 C>G maps to NM_006703.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:123556155 G>A maps to NM_001163278.1 D1479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:123556155 G>A maps to NM_001163278.1 D1479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:193364865 A>G maps to NM_130837.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:193364865 A>G maps to NM_130837.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:6897967 C>T maps to NM_207186.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:6897967 C>T maps to NM_207186.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:22102530 G>A maps to NM_001005466.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:22102530 G>A maps to NM_001005466.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57995948 C>T maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57995948 C>T maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247835785 A>G maps to NM_001005487.1 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247835785 A>G maps to NM_001005487.1 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:247695645 G>T maps to NM_198074.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:247695645 G>T maps to NM_198074.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:248436951 C>G maps to NM_001004695.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:248436951 C>G maps to NM_001004695.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:248551235 G>T maps to NM_001005471.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:248551235 G>T maps to NM_001005471.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:180581965 C>A maps to NM_206880.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:180581965 C>A maps to NM_206880.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:20482536 C>A maps to NM_001004712.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:20482536 C>A maps to NM_001004712.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:97868842 C>G maps to NM_001005514.1 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:97868842 C>G maps to NM_001005514.1 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:55703084 G>A maps to NM_006637.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:55703084 G>A maps to NM_006637.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:55681455 G>A maps to NM_001001960.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:55681455 G>A maps to NM_001001960.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247875709 T>A maps to NM_001005286.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247875709 T>A maps to NM_001005286.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:124294221 G>T maps to NM_001005196.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:124294221 G>T maps to NM_001005196.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:125286263 G>C maps to NM_022776.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:125286263 G>C maps to NM_022776.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:2451330 C>T maps to ENST00000425477 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:2451330 C>T maps to ENST00000425477 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:108576015 C>A maps to NM_005443.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:108576015 C>A maps to NM_005443.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:140864841 G>T maps to NM_018928.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:140864841 G>T maps to NM_018928.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:56140120 C>G maps to NM_002591.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:56140120 C>G maps to NM_002591.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31793151 A>T maps to NM_001191057.1 L659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31793151 A>T maps to NM_001191057.1 L659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:44006402 G>A maps to NM_198850.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:44006402 G>A maps to NM_198850.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:230020566 C>G maps to NM_017933.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:230020566 C>G maps to NM_017933.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:94330993 A>G maps to NM_152431.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:94330993 A>G maps to NM_152431.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:47882628 C>A maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:47882628 C>A maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:2164412 C>A maps to NM_001009944.2 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:2164412 C>A maps to NM_001009944.2 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:14766511 G>C maps to NM_003561.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:14766511 G>C maps to NM_003561.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:68289810 G>A maps to NM_012320.3 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:68289810 G>A maps to NM_012320.3 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:48578087 G>A maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:48578087 G>A maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:17053069 A>T maps to NM_001144382.1 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:17053069 A>T maps to NM_001144382.1 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:171395479 G>A maps to NM_002662.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:171395479 G>A maps to NM_002662.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:49357335 C>G maps to NM_020904.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:49357335 C>G maps to NM_020904.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39914253 C>T maps to NM_022835.2 Q854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39914253 C>T maps to NM_022835.2 Q854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:93163940 C>T maps to NM_001004330.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:93163940 C>T maps to NM_001004330.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128610523 T>A maps to NM_004805.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128610523 T>A maps to NM_004805.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:53103546 C>T maps to NM_182595.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:53103546 C>T maps to NM_182595.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:122263422 T>A maps to NM_001030059.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:122263422 T>A maps to NM_001030059.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:110977722 G>A maps to NM_139283.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:110977722 G>A maps to NM_139283.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:48758545 A>C maps to NM_005710.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:48758545 A>C maps to NM_005710.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:203455882 C>T maps to NM_201348.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:203455882 C>T maps to NM_201348.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:148582161 G>T maps to NM_138364.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:148582161 G>T maps to NM_138364.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113955198 C>T maps to NM_012455.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113955198 C>T maps to NM_012455.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:43530536 G>A maps to ENST00000306308 H2H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:43530536 G>A maps to ENST00000306308 H2H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50360332 C>T maps to NM_017432.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50360332 C>T maps to NM_017432.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31425211 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31425211 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64518938 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64518938 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:100152725 T>A maps to NM_032709.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:100152725 T>A maps to NM_032709.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40280323 C>A maps to NM_201434.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40280323 C>A maps to NM_201434.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:51663463 T>C maps to NM_015106.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:51663463 T>C maps to NM_015106.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:17699744 G>A maps to ENST00000395776 R1161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:17699744 G>A maps to ENST00000395776 R1161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:99273624 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:99273624 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:57346019 T>A maps to NM_003708.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:57346019 T>A maps to NM_003708.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:8425881 G>A maps to NM_012102.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:8425881 G>A maps to NM_012102.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:175957453 G>A maps to NM_022457.5 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:175957453 G>A maps to NM_022457.5 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14077444 C>T maps to NM_002918.4 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14077444 C>T maps to NM_002918.4 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:63189699 C>T maps to NM_003835.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:63189699 C>T maps to NM_003835.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:19955397 C>G maps to ENST00000255006 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:19955397 C>G maps to ENST00000255006 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:30304986 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:30304986 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:116949478 C>T maps to NM_001010892.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:116949478 C>T maps to NM_001010892.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:187088746 T>C maps to NM_022147.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:187088746 T>C maps to NM_022147.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:33292343 C>G maps to NM_022753.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:33292343 C>G maps to NM_022753.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:38770044 T>C maps to NM_006514.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:38770044 T>C maps to NM_006514.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:20403999 G>A maps to NM_001006946.1 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:20403999 G>A maps to NM_001006946.1 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:80546043 A>G maps to NM_006379.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:80546043 A>G maps to NM_006379.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:61305165 G>A maps to NM_002974.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:61305165 G>A maps to NM_002974.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156776987 G>A maps to NM_001161441.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156776987 G>A maps to NM_001161441.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:110048968 C>G maps to NM_001099289.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:110048968 C>G maps to NM_001099289.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:157820535 G>T maps to NM_003030.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:157820535 G>T maps to NM_003030.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:52147284 C>A maps to NM_001098612.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:52147284 C>A maps to NM_001098612.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:54603802 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:54603802 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:6606403 G>T maps to NM_177550.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:6606403 G>T maps to NM_177550.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27481774 G>T maps to NM_003459.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27481774 G>T maps to NM_003459.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:42024920 A>G maps to NM_006345.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:42024920 A>G maps to NM_006345.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:10967705 T>C maps to NM_014229.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:10967705 T>C maps to NM_014229.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:168137972 G>A maps to NM_003062.2 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:168137972 G>A maps to NM_003062.2 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:43881763 C>A maps to NM_003064.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:43881763 C>A maps to NM_003064.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:2718233 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:2718233 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:18856972 T>C maps to ENST00000389467 K1999K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:18856972 T>C maps to ENST00000389467 K1999K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:158342654 G>T maps to NM_016224.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:158342654 G>T maps to NM_016224.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:31324728 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:31324728 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:9416303 G>C maps to NM_025106.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:9416303 G>C maps to NM_025106.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:100231419 A>G maps to NM_005668.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:100231419 A>G maps to NM_005668.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14939209 C>T maps to NM_001193424.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14939209 C>T maps to NM_001193424.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:149882450 G>A maps to NM_014849.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:149882450 G>A maps to NM_014849.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:40851704 C>A maps to NM_020783.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:40851704 C>A maps to NM_020783.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:7056720 A>C maps to NM_152293.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:7056720 A>C maps to NM_152293.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:33272865 G>A maps to NM_172208.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:33272865 G>A maps to NM_172208.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:234593466 G>A maps to NM_005646.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:234593466 G>A maps to NM_005646.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:27809296 G>A maps to ENST00000409980 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:27809296 G>A maps to ENST00000409980 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:120916425 C>T maps to NM_152715.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:120916425 C>T maps to NM_152715.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:235612019 A>C maps to NM_003193.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:235612019 A>C maps to NM_003193.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:152057926 G>T maps to NM_001008536.1 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:152057926 G>T maps to NM_001008536.1 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149749092 G>A maps to ENST00000451292 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149749092 G>A maps to ENST00000451292 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:46620583 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:46620583 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:30704583 C>T maps to NM_031271.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:30704583 C>T maps to NM_031271.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:56681598 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:56681598 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:157158441 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:157158441 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:11485702 T>A maps to ENST00000423059 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:11485702 T>A maps to ENST00000423059 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:35719610 C>T maps to NM_006289.3 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:35719610 C>T maps to NM_006289.3 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52257046 C>A maps to ENST00000494383 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52257046 C>A maps to ENST00000494383 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:19381246 G>A maps to NM_001001524.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:19381246 G>A maps to NM_001001524.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:126137060 G>T maps to NM_052907.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:126137060 G>T maps to NM_052907.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:130762589 C>A maps to NM_052913.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:130762589 C>A maps to NM_052913.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:69096967 G>A maps to NM_007114.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:69096967 G>A maps to NM_007114.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:6521751 G>C maps to ENST00000355862 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:6521751 G>C maps to ENST00000355862 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1862434 A>T maps to ENST00000381906 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1862434 A>T maps to ENST00000381906 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:5399079 C>A maps to NM_001080495.2 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:5399079 C>A maps to NM_001080495.2 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:218713784 T>A maps to NM_022648.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:218713784 T>A maps to NM_022648.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:47343136 G>T maps to NM_022748.11 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:47343136 G>T maps to NM_022748.11 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:32017940 C>A maps to ENST00000375244 L3091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:32017940 C>A maps to ENST00000375244 L3091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:1418260 A>G maps to NM_000547.5 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:1418260 A>G maps to NM_000547.5 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:1306298 C>A maps to NM_012217.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:1306298 C>A maps to NM_012217.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:72734211 C>T maps to NM_178125.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:72734211 C>T maps to NM_178125.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:38266181 A>T maps to NM_003306.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:38266181 A>T maps to NM_003306.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:135651314 G>T maps to NM_020389.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:135651314 G>T maps to NM_020389.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:73213553 C>T maps to ENST00000419692 Q897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:73213553 C>T maps to ENST00000419692 Q897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:31769447 A>G maps to NM_020856.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:31769447 A>G maps to NM_020856.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:39161448 G>T maps to ENST00000301819 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:39161448 G>T maps to ENST00000301819 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113286317 A>T maps to NM_153712.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113286317 A>T maps to NM_153712.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179451992 G>T maps to NM_133378.4 T18747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179451992 G>T maps to NM_133378.4 T18747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:72233615 A>T maps to NM_032646.5 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:72233615 A>T maps to NM_032646.5 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:57958296 T>G maps to NM_016261.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:57958296 T>G maps to NM_016261.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:4186204 C>T maps to NM_003342.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:4186204 C>T maps to NM_003342.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:90039432 G>A maps to NM_016021.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:90039432 G>A maps to NM_016021.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19491399 G>C maps to ENST00000375267 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19491399 G>C maps to ENST00000375267 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:26612442 G>A maps to NM_183008.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:26612442 G>A maps to NM_183008.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:70070362 A>G maps to NM_001073.1 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:70070362 A>G maps to NM_001073.1 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:35541201 C>A maps to ENST00000416672 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:35541201 C>A maps to ENST00000416672 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:50835934 C>A maps to ENST00000456636 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:50835934 C>A maps to ENST00000456636 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:11505372 G>T maps to NM_001080491.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:11505372 G>T maps to NM_001080491.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:155130183 C>A maps to NM_005638.5 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:155130183 C>A maps to NM_005638.5 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:155171560 C>T maps to NM_005638.5 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:155171560 C>T maps to NM_005638.5 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:42259419 C>T maps to ENST00000417062 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:42259419 C>T maps to ENST00000417062 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:49842402 G>T maps to NM_198570.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:49842402 G>T maps to NM_198570.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:128471545 C>T maps to NM_018383.4 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:128471545 C>T maps to NM_018383.4 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:122396298 C>T maps to NM_144668.4 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:122396298 C>T maps to NM_144668.4 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:228109548 G>A maps to NM_003395.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:228109548 G>A maps to NM_003395.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:75265291 C>T maps to NM_019589.2 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:75265291 C>T maps to NM_019589.2 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36205666 C>T maps to NM_014383.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36205666 C>T maps to NM_014383.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62519744 G>A maps to NM_024784.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62519744 G>A maps to NM_024784.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:145156846 A>T maps to NM_014795.3 L636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:145156846 A>T maps to NM_014795.3 L636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:77768222 C>T maps to NM_024721.4 I3022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:77768222 C>T maps to NM_024721.4 I3022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:77762557 A>C maps to NM_024721.4 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:77762557 A>C maps to NM_024721.4 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:178358865 A>G maps to NM_030613.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:178358865 A>G maps to NM_030613.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39898381 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39898381 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:136649680 G>A maps to NM_003413.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:136649680 G>A maps to NM_003413.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:28213202 C>T maps to NM_019110.3 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:28213202 C>T maps to NM_019110.3 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:28056878 G>A maps to NM_003447.3 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:28056878 G>A maps to NM_003447.3 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:38126614 C>T maps to NM_021045.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:38126614 C>T maps to NM_021045.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:24310355 C>G maps to NM_203282.2 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:24310355 C>G maps to NM_203282.2 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:22842567 G>A maps to NM_080764.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:22842567 G>A maps to NM_080764.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:28963356 C>T maps to NM_001010877.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:28963356 C>T maps to NM_001010877.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:32354771 G>A maps to ENST00000375200 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:32354771 G>A maps to ENST00000375200 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57910782 C>G maps to NM_001172773.1 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57910782 C>G maps to NM_001172773.1 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:2832299 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:2832299 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55993189 C>T maps to NM_033113.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55993189 C>T maps to NM_033113.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:12502557 C>A maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:12502557 C>A maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:32031983 T>A maps to NM_001137674.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:32031983 T>A maps to NM_001137674.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:32032067 T>A maps to NM_001137674.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:32032067 T>A maps to NM_001137674.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:47886917 G>C maps to NM_021035.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:47886917 G>C maps to NM_021035.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:99662083 G>A maps to NM_145914.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:99662083 G>A maps to NM_145914.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:33140659 G>T maps to NM_032139.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:33140659 G>T maps to NM_032139.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:112998716 G>A maps to ENST00000273395 E690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:112998716 G>A maps to ENST00000273395 E690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:2987386 C>T maps to NM_032415.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:2987386 C>T maps to NM_032415.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:16612579 C>T maps to NM_014695.1 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:16612579 C>T maps to NM_014695.1 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:48613127 G>A maps to NM_000094.3 F1970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:48613127 G>A maps to NM_000094.3 F1970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:20108149 C>G maps to NM_001033553.1 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:20108149 C>G maps to NM_001033553.1 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:11665120 C>T maps to NM_032377.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:11665120 C>T maps to NM_032377.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chrX:71427305 C>T maps to NM_017669.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chrX:71427305 C>T maps to NM_017669.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr5:154270921 A>G maps to NM_015465.3 L1381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr5:154270921 A>G maps to NM_015465.3 L1381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:12977660 C>T maps to ENST00000429247 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:12977660 C>T maps to ENST00000429247 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:90650621 C>T maps to NM_022054.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:90650621 C>T maps to NM_022054.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:40004381 G>A maps to NM_152467.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:40004381 G>A maps to NM_152467.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:209797335 G>C maps to NM_000228.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:209797335 G>C maps to NM_000228.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr22:33777943 G>A maps to NM_133642.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr22:33777943 G>A maps to NM_133642.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:30748248 G>C maps to NM_005204.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:30748248 G>C maps to NM_005204.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:30748320 G>C maps to NM_005204.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:30748320 G>C maps to NM_005204.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:47958077 G>C maps to ENST00000426837 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:47958077 G>C maps to ENST00000426837 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr13:109779803 G>A maps to NM_015011.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr13:109779803 G>A maps to NM_015011.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:92090699 T>C maps to NM_016023.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:92090699 T>C maps to NM_016023.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:159499084 C>T maps to NM_003628.3 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:159499084 C>T maps to NM_003628.3 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:118228713 T>C maps to NM_001011709.2 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:118228713 T>C maps to NM_001011709.2 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:43197328 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:43197328 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:30655228 G>A maps to NM_001009552.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:30655228 G>A maps to NM_001009552.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr20:5294751 G>A maps to NM_144773.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr20:5294751 G>A maps to NM_144773.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr15:39881467 C>T maps to NM_003246.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr15:39881467 C>T maps to NM_003246.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:132585012 C>T maps to ENST00000437532 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:132585012 C>T maps to ENST00000437532 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:34826854 C>T maps to NM_017754.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:34826854 C>T maps to NM_017754.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:131792869 G>A maps to NM_001115.2 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:131792869 G>A maps to NM_001115.2 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr14:105416018 G>A maps to NM_138420.2 G1923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr14:105416018 G>A maps to NM_138420.2 G1923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:176857322 G>T maps to ENST00000281881 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:176857322 G>T maps to ENST00000281881 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:21991044 C>T maps to NM_152612.2 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:21991044 C>T maps to NM_152612.2 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:62544478 G>C maps to NM_001786.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:62544478 G>C maps to NM_001786.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:2944625 G>T maps to NM_033225.5 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:2944625 G>T maps to NM_033225.5 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:111746137 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:111746137 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:34883583 A>G maps to NM_001136006.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:34883583 A>G maps to NM_001136006.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:74526921 G>A maps to NM_012201.5 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:74526921 G>A maps to NM_012201.5 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:123489403 G>T maps to ENST00000456860 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:123489403 G>T maps to ENST00000456860 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:38066034 G>A maps to NM_001165958.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:38066034 G>A maps to NM_001165958.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:80399754 G>A maps to NM_173620.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:80399754 G>A maps to NM_173620.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:71946218 C>T maps to NM_001567.3 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:71946218 C>T maps to NM_001567.3 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:75936793 G>T maps to NM_006633.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:75936793 G>T maps to NM_006633.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:2749784 C>A maps to NM_033267.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:2749784 C>A maps to NM_033267.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:55144062 C>T maps to ENST00000427581 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:55144062 C>T maps to ENST00000427581 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:133812254 C>T maps to NM_144648.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:133812254 C>T maps to NM_144648.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:33572577 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:33572577 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:39760729 G>T maps to ENST00000361689 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:39760729 G>T maps to ENST00000361689 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:128391815 G>A maps to ENST00000389524 Q1834Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:128391815 G>A maps to ENST00000389524 Q1834Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr13:36129237 A>T maps to ENST00000400445 A2307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr13:36129237 A>T maps to ENST00000400445 A2307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:140256556 C>A maps to NM_018903.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:140256556 C>A maps to NM_018903.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:5522563 A>C maps to NM_025239.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:5522563 A>C maps to NM_025239.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:132193284 C>A maps to NM_020911.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:132193284 C>A maps to NM_020911.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:45075717 C>T maps to NM_001198721.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:45075717 C>T maps to NM_001198721.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:44030341 C>T maps to NM_152470.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:44030341 C>T maps to NM_152470.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:4327148 C>A maps to ENST00000314714 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:4327148 C>A maps to ENST00000314714 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:234835265 G>A maps to NM_024080.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:234835265 G>A maps to NM_024080.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:94818287 T>C maps to NM_014639.3 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:94818287 T>C maps to NM_014639.3 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:83775391 C>A maps to NM_198920.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:83775391 C>A maps to NM_198920.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:82815768 T>C maps to NM_004385.4 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:82815768 T>C maps to NM_004385.4 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:175437100 T>A maps to NM_003387.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:175437100 T>A maps to NM_003387.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:23547388 C>G maps to NM_014977.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:23547388 C>G maps to NM_014977.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:125877378 C>A maps to ENST00000273450 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:125877378 C>A maps to ENST00000273450 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:41554285 A>T maps to ENST00000415018 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:41554285 A>T maps to ENST00000415018 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr18:31323435 T>A maps to NM_030632.1 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr18:31323435 T>A maps to NM_030632.1 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:23985106 C>A maps to NM_017552.1 V1122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:23985106 C>A maps to NM_017552.1 V1122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:64879031 G>A maps to NM_013265.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:64879031 G>A maps to NM_013265.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76826612 G>A maps to ENST00000360841 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76826612 G>A maps to ENST00000360841 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:40054002 G>T maps to NM_032221.3 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:40054002 G>T maps to NM_032221.3 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:105833975 G>A maps to NM_000494.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:105833975 G>A maps to NM_000494.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:110827060 A>T maps to NM_001845.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:110827060 A>T maps to NM_001845.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:107408254 G>T maps to NM_033641.2 P1274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:107408254 G>T maps to NM_033641.2 P1274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:2975963 A>G maps to NM_033225.5 H2129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:2975963 A>G maps to NM_033225.5 H2129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:120008918 G>T maps to NM_001145718.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:120008918 G>T maps to NM_001145718.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr18:28908186 A>T maps to NM_001942.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr18:28908186 A>T maps to NM_001942.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:80037126 G>A maps to NM_004104.4 V2476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:80037126 G>A maps to NM_004104.4 V2476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:13649599 G>T maps to NM_001165035.1 G449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:13649599 G>T maps to NM_001165035.1 G449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:31178570 G>T maps to NM_024572.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:31178570 G>T maps to NM_024572.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:52762755 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:52762755 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr15:89422462 G>A maps to NM_178232.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr15:89422462 G>A maps to NM_178232.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:39330765 A>G maps to ENST00000221419 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:39330765 A>G maps to ENST00000221419 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:133789731 G>A maps to NM_014987.1 D1296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:133789731 G>A maps to NM_014987.1 D1296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:29973553 G>T maps to NM_014271.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:29973553 G>T maps to NM_014271.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr21:46047657 T>A maps to NM_198690.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr21:46047657 T>A maps to NM_198690.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr7:107569579 G>A maps to NM_002291.2 Q1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr7:107569579 G>A maps to NM_002291.2 Q1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:132641791 C>T maps to NM_015529.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:132641791 C>T maps to NM_015529.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:18257857 C>T maps to NM_000015.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:18257857 C>T maps to NM_000015.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:233839372 C>T maps to NM_019850.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:233839372 C>T maps to NM_019850.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:20404499 C>A maps to NM_001004063.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:20404499 C>A maps to NM_001004063.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:55563900 G>T maps to NM_001004735.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:55563900 G>T maps to NM_001004735.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:201814322 A>C maps to NM_006190.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:201814322 A>C maps to NM_006190.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:49454054 C>T maps to NM_003785.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:49454054 C>T maps to NM_003785.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:99663202 T>A maps to NM_001184880.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:99663202 T>A maps to NM_001184880.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:140261960 C>T maps to NM_018904.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:140261960 C>T maps to NM_018904.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:239186472 G>A maps to NM_022817.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:239186472 G>A maps to NM_022817.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:89183866 G>C maps to NM_152542.3 Y333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:89183866 G>C maps to NM_152542.3 Y333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:80388725 A>C maps to NM_006909.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:80388725 A>C maps to NM_006909.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:127818228 T>A maps to NM_173690.4 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:127818228 T>A maps to NM_173690.4 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:430711 C>A maps to NM_012435.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:430711 C>A maps to NM_012435.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:35922940 G>T maps to NM_052961.3 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:35922940 G>T maps to NM_052961.3 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:92918920 C>A maps to NM_152313.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:92918920 C>A maps to NM_152313.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:44891009 G>C maps to NM_025137.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:44891009 G>C maps to NM_025137.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:1220370 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:1220370 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:48700725 G>A maps to NM_199203.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:48700725 G>A maps to NM_199203.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:34802158 C>T maps to NM_017754.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:34802158 C>T maps to NM_017754.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:228750067 A>T maps to NM_178821.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:228750067 A>T maps to NM_178821.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:21991281 A>G maps to NM_003423.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:21991281 A>G maps to NM_003423.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:37383368 C>A maps to NM_001171979.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:37383368 C>A maps to NM_001171979.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:111617358 C>A maps to NM_006686.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:111617358 C>A maps to NM_006686.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:29280310 G>T maps to ENST00000394782 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:29280310 G>T maps to ENST00000394782 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:247014497 C>A maps to ENST00000428671 E1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:247014497 C>A maps to ENST00000428671 E1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:113351657 G>T maps to NM_025144.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:113351657 G>T maps to NM_025144.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:25408817 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:25408817 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:114278500 C>A maps to NM_001148.4 P2909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:114278500 C>A maps to NM_001148.4 P2909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:99053023 C>A maps to NM_181861.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:99053023 C>A maps to NM_181861.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:7803639 C>A maps to NM_001644.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:7803639 C>A maps to NM_001644.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:1748716 C>A maps to NM_001171038.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:1748716 C>A maps to NM_001171038.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:11038726 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:11038726 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:165548103 C>A maps to NM_000055.2 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:165548103 C>A maps to NM_000055.2 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:42235287 G>T maps to NM_024032.3 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:42235287 G>T maps to NM_024032.3 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:36786291 C>A maps to NM_001162530.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:36786291 C>A maps to NM_001162530.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:154172962 A>T maps to NM_001010979.1 L59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:154172962 A>T maps to NM_001010979.1 L59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:150027822 T>C maps to NM_138434.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:150027822 T>C maps to NM_138434.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:57347231 C>T maps to NM_000562.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:57347231 C>T maps to NM_000562.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:74526698 C>T maps to NM_182505.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:74526698 C>T maps to NM_182505.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:219896376 C>A maps to NM_194302.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:219896376 C>A maps to NM_194302.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:42586929 C>T maps to NM_000749.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:42586929 C>T maps to NM_000749.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:24976665 G>T maps to NM_001836.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:24976665 G>T maps to NM_001836.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:72183516 G>T maps to NM_018235.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:72183516 G>T maps to NM_018235.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:27003954 G>T maps to NM_001887.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:27003954 G>T maps to NM_001887.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:1407712 C>T maps to NM_001161530.1 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:1407712 C>T maps to NM_001161530.1 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:72361996 G>T maps to NM_019885.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:72361996 G>T maps to NM_019885.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:30633458 G>A maps to NM_003587.4 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:30633458 G>A maps to NM_003587.4 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:122693020 T>A maps to NM_019887.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:122693020 T>A maps to NM_019887.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:124330218 G>T maps to NM_207437.3 V1693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:124330218 G>T maps to NM_207437.3 V1693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:73360772 G>T maps to NM_012074.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:73360772 G>T maps to NM_012074.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:28983406 C>T maps to NM_001134453.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:28983406 C>T maps to NM_001134453.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:64082369 C>A maps to NM_004451.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:64082369 C>A maps to NM_004451.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:169493095 A>T maps to ENST00000367796 Y1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:169493095 A>T maps to ENST00000367796 Y1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:37580962 T>C maps to NM_030919.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:37580962 T>C maps to NM_030919.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:92257848 C>T maps to ENST00000298047 Y1114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:92257848 C>T maps to ENST00000298047 Y1114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:17895734 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:17895734 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:35940867 C>A maps to NM_005306.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:35940867 C>A maps to NM_005306.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:240370520 C>A maps to ENST00000406993 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:240370520 C>A maps to ENST00000406993 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:89402587 A>G maps to NM_153696.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:89402587 A>G maps to NM_153696.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:52249722 G>T maps to NM_002029.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:52249722 G>T maps to NM_002029.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:57790734 C>A maps to NM_152687.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:57790734 C>A maps to NM_152687.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:36484369 C>T maps to ENST00000398597 E1695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:36484369 C>T maps to ENST00000398597 E1695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:31598244 G>A maps to NM_015382.2 S1444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:31598244 G>A maps to NM_015382.2 S1444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:27114999 G>A maps to NM_080596.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:27114999 G>A maps to NM_080596.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:298709 G>A maps to NM_001025295.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:298709 G>A maps to NM_001025295.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:121107308 G>T maps to NM_002193.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:121107308 G>T maps to NM_002193.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:39513403 A>C maps to NM_145027.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:39513403 A>C maps to NM_145027.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:34046466 G>A maps to NM_133642.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:34046466 G>A maps to NM_133642.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:118109471 G>T maps to NM_001031855.1 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:118109471 G>T maps to NM_001031855.1 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:33411921 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:33411921 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:4635146 T>G maps to NM_001001683.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:4635146 T>G maps to NM_001001683.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:151944985 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:151944985 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:56667669 C>T maps to NM_176870.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:56667669 C>T maps to NM_176870.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:113530297 G>A maps to ENST00000189978 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:113530297 G>A maps to ENST00000189978 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10401160 C>A maps to NM_005963.3 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10401160 C>A maps to NM_005963.3 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10450850 G>A maps to NM_017534.5 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10450850 G>A maps to NM_017534.5 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:123337558 G>T maps to NM_053025.3 P1809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:123337558 G>T maps to NM_053025.3 P1809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:50862783 C>A maps to NM_004851.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:50862783 C>A maps to NM_004851.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:21120446 A>C maps to ENST00000430741 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:21120446 A>C maps to ENST00000430741 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:91937843 C>T maps to NM_022351.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:91937843 C>T maps to NM_022351.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:71359233 G>T maps to NM_001013627.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:71359233 G>T maps to NM_001013627.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:36332707 G>A maps to NM_004646.3 N908N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:36332707 G>A maps to NM_004646.3 N908N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:88476289 G>A maps to NM_001012338.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:88476289 G>A maps to NM_001012338.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:102895771 C>A maps to NM_031438.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:102895771 C>A maps to NM_031438.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:5142214 G>T maps to NM_001005222.2 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:5142214 G>T maps to NM_001005222.2 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:55904333 G>T maps to NM_001004064.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:55904333 G>T maps to NM_001004064.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:127253551 G>T maps to NM_006193.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:127253551 G>T maps to NM_006193.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:19681571 C>G maps to NM_025245.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:19681571 C>G maps to NM_025245.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:186423471 C>A maps to NM_014476.4 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:186423471 C>A maps to NM_014476.4 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:76425197 G>A maps to NM_007350.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:76425197 G>A maps to NM_007350.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:68981371 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:68981371 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:139216786 C>T maps to NM_032289.2 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:139216786 C>T maps to NM_032289.2 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:41306788 C>T maps to ENST00000373198 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:41306788 C>T maps to ENST00000373198 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:58381435 C>T maps to NM_017771.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:58381435 C>T maps to NM_017771.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:79314023 G>T maps to NM_006507.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:79314023 G>T maps to NM_006507.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:228871752 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:228871752 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:113314633 G>A maps to NM_001143854.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:113314633 G>A maps to NM_001143854.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:39709668 T>A maps to NM_000967.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:39709668 T>A maps to NM_000967.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:99125988 G>A maps to NM_015179.3 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:99125988 G>A maps to NM_015179.3 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:237895441 G>T maps to NM_001035.2 E3678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:237895441 G>T maps to NM_001035.2 E3678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:234217806 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:234217806 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38622837 G>A maps to NM_001099404.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38622837 G>A maps to NM_001099404.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:171849421 G>A maps to NM_001017995.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:171849421 G>A maps to NM_001017995.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:232538194 G>T maps to NM_020808.3 T1655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:232538194 G>T maps to NM_020808.3 T1655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:232601022 C>A maps to NM_020808.3 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:232601022 C>A maps to NM_020808.3 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:48500059 C>T maps to NM_000338.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:48500059 C>T maps to NM_000338.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:127520533 T>C maps to NM_001046.2 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:127520533 T>C maps to NM_001046.2 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:51621444 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:51621444 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:48865285 C>A maps to NM_019073.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:48865285 C>A maps to NM_019073.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:94999695 A>T maps to NM_031952.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:94999695 A>T maps to NM_031952.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:57677864 C>T maps to ENST00000506738 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:57677864 C>T maps to ENST00000506738 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:130068227 G>T maps to NM_021978.3 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:130068227 G>T maps to NM_021978.3 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:52556664 C>T maps to NM_015136.2 A2235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:52556664 C>T maps to NM_015136.2 A2235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:104096984 C>A maps to NM_017564.9 I1258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:104096984 C>A maps to NM_017564.9 I1258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:223536631 G>A maps to NM_017982.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:223536631 G>A maps to NM_017982.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:152640090 C>T maps to NM_182961.2 R5432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:152640090 C>T maps to NM_182961.2 R5432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:212977678 C>T maps to NM_001146171.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:212977678 C>T maps to NM_001146171.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:52972282 T>A maps to NM_018676.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:52972282 T>A maps to NM_018676.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:108536210 G>A maps to NM_018112.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:108536210 G>A maps to NM_018112.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:175335275 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:175335275 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:50636318 G>T maps to NM_025204.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:50636318 G>T maps to NM_025204.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:142503760 A>T maps to ENST00000476941 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:142503760 A>T maps to ENST00000476941 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:82833849 A>T maps to NM_004385.4 I1676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:82833849 A>T maps to NM_004385.4 I1676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:54636700 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:54636700 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:61053873 G>T maps to NM_152718.2 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:61053873 G>T maps to NM_152718.2 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:54398638 G>T maps to NM_015285.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:54398638 G>T maps to NM_015285.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168103075 C>A maps to NM_152381.5 S1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168103075 C>A maps to NM_152381.5 S1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168104597 C>T maps to NM_152381.5 H2232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168104597 C>T maps to NM_152381.5 H2232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:114070510 G>A maps to NM_001164342.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:114070510 G>A maps to NM_001164342.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:145274905 C>A maps to NM_014795.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:145274905 C>A maps to NM_014795.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:77766815 C>A maps to NM_024721.4 G2553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:77766815 C>A maps to NM_024721.4 G2553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:44932852 G>T maps to NM_014518.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:44932852 G>T maps to NM_014518.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:9578056 C>T maps to NM_152476.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:9578056 C>T maps to NM_152476.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:11833619 C>G maps to NM_001080493.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:11833619 C>G maps to NM_001080493.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:23543379 C>A maps to NM_003430.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:23543379 C>A maps to NM_003430.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:16256970 C>A maps to NM_001171.5 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:16256970 C>A maps to NM_001171.5 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:132402829 G>A maps to NM_017873.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:132402829 G>A maps to NM_017873.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:76872167 A>G maps to NM_000489.3 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:76872167 A>G maps to NM_000489.3 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:42744679 T>G maps to NM_001145080.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:42744679 T>G maps to NM_001145080.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:227223258 A>C maps to ENST00000366766 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:227223258 A>C maps to ENST00000366766 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:47548003 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:47548003 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:56724546 C>T maps to NM_018261.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:56724546 C>T maps to NM_018261.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:88898417 G>A maps to NM_000512.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:88898417 G>A maps to NM_000512.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:42988814 G>A maps to NM_002055.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:42988814 G>A maps to NM_002055.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:104749672 A>G maps to NM_182931.2 Q1251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:104749672 A>G maps to NM_182931.2 Q1251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:100678180 T>C maps to NM_001040105.1 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:100678180 T>C maps to NM_001040105.1 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr18:47462674 C>G maps to NM_001080467.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr18:47462674 C>G maps to NM_001080467.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:55846626 T>G maps to NM_054105.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:55846626 T>G maps to NM_054105.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:140189051 T>C maps to NM_018907.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:140189051 T>C maps to NM_018907.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:140209754 G>A maps to NM_018909.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:140209754 G>A maps to NM_018909.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:28264603 G>A maps to NM_032507.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:28264603 G>A maps to NM_032507.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:28264609 G>A maps to NM_032507.3 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:28264609 G>A maps to NM_032507.3 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:18279607 C>T maps to NM_005027.2 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:18279607 C>T maps to NM_005027.2 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:12835748 T>C maps to NM_001080830.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:12835748 T>C maps to NM_001080830.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:43575999 A>G maps to NM_031246.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:43575999 A>G maps to NM_031246.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:99337938 T>C maps to NM_001100426.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:99337938 T>C maps to NM_001100426.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:103202291 T>G maps to ENST00000428762 S1773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:103202291 T>G maps to ENST00000428762 S1773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:301808 A>G maps to NM_003044.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:301808 A>G maps to NM_003044.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:53805022 G>A maps to NM_138473.2 *786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:53805022 G>A maps to NM_138473.2 *786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:220412408 G>A maps to NM_001005209.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:220412408 G>A maps to NM_001005209.1 V116V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-67-6215-01A-11D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-67-6215-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:48941170 G>A maps to NM_005749.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:48941170 G>A maps to NM_005749.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:42231108 G>A maps to NM_033502.2 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:42231108 G>A maps to NM_033502.2 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:68506907 G>A maps to NM_018227.5 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:68506907 G>A maps to NM_018227.5 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:255921 A>T maps to NM_006624.4 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:255921 A>T maps to NM_006624.4 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:57935081 G>T maps to NM_007156.4 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:57935081 G>T maps to NM_007156.4 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:22068750 G>A maps to NM_005691.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:22068750 G>A maps to NM_005691.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chrX:110961490 A>G maps to NM_001099922.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chrX:110961490 A>G maps to NM_001099922.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:90220045 C>T maps to NM_004938.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:90220045 C>T maps to NM_004938.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:132996390 G>A maps to NM_015137.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:132996390 G>A maps to NM_015137.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr15:89824489 C>T maps to NM_001113378.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr15:89824489 C>T maps to NM_001113378.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:74646702 A>G maps to NM_000859.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:74646702 A>G maps to NM_000859.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr19:54780706 G>A maps to ENST00000391747 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr19:54780706 G>A maps to ENST00000391747 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:105509339 G>A maps to NM_013437.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:105509339 G>A maps to NM_013437.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:57128023 T>A maps to NM_000946.2 K384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:57128023 T>A maps to NM_000946.2 K384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:49095082 C>A maps to NM_198880.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:49095082 C>A maps to NM_198880.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr10:64000898 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr10:64000898 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:1675166 G>A maps to NM_002615.4 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:1675166 G>A maps to NM_002615.4 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:47103746 T>A maps to NM_014159.6 K2067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:47103746 T>A maps to NM_014159.6 K2067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr15:64717778 G>T maps to NM_016213.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr15:64717778 G>T maps to NM_016213.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:216419956 G>A maps to ENST00000366943 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:216419956 G>A maps to ENST00000366943 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:18622296 C>A maps to NM_001040272.4 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:18622296 C>A maps to NM_001040272.4 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:46604836 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:46604836 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2114282 C>T maps to ENST00000355272 E814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2114282 C>T maps to ENST00000355272 E814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115313 C>T maps to ENST00000355272 K751K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115313 C>T maps to ENST00000355272 K751K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115340 C>T maps to ENST00000355272 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115340 C>T maps to ENST00000355272 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115385 C>T maps to ENST00000355272 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115385 C>T maps to ENST00000355272 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2120871 C>T maps to ENST00000355272 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2120871 C>T maps to ENST00000355272 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:46243559 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:46243559 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:50271824 G>A maps to NM_024837.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:50271824 G>A maps to NM_024837.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:32198201 C>T maps to NM_001703.2 V1212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:32198201 C>T maps to NM_001703.2 V1212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:102839312 C>T maps to NM_017935.4 H391H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:102839312 C>T maps to NM_017935.4 H391H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:56389901 C>A maps to NM_004758.2 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:56389901 C>A maps to NM_004758.2 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:181726249 G>T maps to ENST00000357570 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:181726249 G>T maps to ENST00000357570 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:6188907 G>A maps to NM_015557.2 D1203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:6188907 G>A maps to NM_015557.2 D1203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:205035634 G>A maps to NM_005076.3 W628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:205035634 G>A maps to NM_005076.3 W628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:101814131 G>T maps to NM_001308.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:101814131 G>T maps to NM_001308.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:64508784 C>A maps to NM_022048.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:64508784 C>A maps to NM_022048.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:144909296 A>G maps to NM_004709.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:144909296 A>G maps to NM_004709.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:170599212 G>T maps to NM_005618.3 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:170599212 G>T maps to NM_005618.3 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:45444640 C>T maps to NM_175940.1 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:45444640 C>T maps to NM_175940.1 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:158223454 C>T maps to NM_024007.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:158223454 C>T maps to NM_024007.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:205588202 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:205588202 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:94066482 G>T maps to NM_004440.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:94066482 G>T maps to NM_004440.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:153678636 C>T maps to NM_004699.2 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:153678636 C>T maps to NM_004699.2 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:40434112 G>T maps to NM_003890.2 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:40434112 G>T maps to NM_003890.2 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:42635329 C>T maps to NM_001466.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:42635329 C>T maps to NM_001466.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:121413584 C>A maps to ENST00000393667 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:121413584 C>A maps to ENST00000393667 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:120690597 C>T maps to NM_014619.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:120690597 C>T maps to NM_014619.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:31779551 C>T maps to NM_005527.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:31779551 C>T maps to NM_005527.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:31719732 C>A maps to NM_006644.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:31719732 C>A maps to NM_006644.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:124377364 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:124377364 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:53072008 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:53072008 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:141291002 C>G maps to NM_016249.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:141291002 C>G maps to NM_016249.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:51562319 A>T maps to NM_002443.2 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:51562319 A>T maps to NM_002443.2 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:9046893 A>G maps to NM_024690.2 T11579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:9046893 A>G maps to NM_024690.2 T11579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:9063967 A>C maps to NM_024690.2 A7826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:9063967 A>C maps to NM_024690.2 A7826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:161179959 G>T maps to NM_004550.4 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:161179959 G>T maps to NM_004550.4 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:21594951 C>A maps to NM_006157.3 C793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:21594951 C>A maps to NM_006157.3 C793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:3006782 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:3006782 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:5565817 T>A maps to NM_001005289.1 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:5565817 T>A maps to NM_001005289.1 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140222228 G>A maps to NM_018911.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140222228 G>A maps to NM_018911.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140590350 G>A maps to NM_018932.3 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140590350 G>A maps to NM_018932.3 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140529990 G>A maps to NM_018939.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140529990 G>A maps to NM_018939.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:144991016 G>A maps to NM_201380.2 P4461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:144991016 G>A maps to NM_201380.2 P4461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr14:30100002 G>A maps to NM_002742.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr14:30100002 G>A maps to NM_002742.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:52442780 T>C maps to NM_002867.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:52442780 T>C maps to NM_002867.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:38770308 C>G maps to NM_006514.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:38770308 C>G maps to NM_006514.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:3991445 C>T maps to NM_152744.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:3991445 C>T maps to NM_152744.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:57613682 C>A maps to NM_016045.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:57613682 C>A maps to NM_016045.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:152804279 G>T maps to NM_182961.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:152804279 G>T maps to NM_182961.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:37250727 G>A maps to NM_017772.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:37250727 G>A maps to NM_017772.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:114837317 C>T maps to NM_000192.3 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:114837317 C>T maps to NM_000192.3 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:1604798 C>A maps to NM_024600.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:1604798 C>A maps to NM_024600.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:1272751 G>T maps to NM_012467.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:1272751 G>T maps to NM_012467.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:116631633 C>A maps to NM_014112.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:116631633 C>A maps to NM_014112.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142583207 C>T maps to NM_018646.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142583207 C>T maps to NM_018646.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:129063424 C>G maps to NM_006649.3 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:129063424 C>G maps to NM_006649.3 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:144557622 G>A maps to NM_015117.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:144557622 G>A maps to NM_015117.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:97054748 G>T maps to NM_194320.2 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:97054748 G>T maps to NM_194320.2 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:52193559 A>G maps to NM_006526.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:52193559 A>G maps to NM_006526.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:44635940 C>T maps to NM_013362.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:44635940 C>T maps to NM_013362.2 R392*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-67-6217-01A-11D-1753-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-67-6217-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:52003546 G>T maps to NM_032750.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:52003546 G>T maps to NM_032750.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:27281273 C>T maps to NM_021831.5 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:27281273 C>T maps to NM_021831.5 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:33292073 G>A maps to NM_004274.4 A1685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:33292073 G>A maps to NM_004274.4 A1685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:150786622 G>T maps to NM_001668.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:150786622 G>T maps to NM_001668.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:119249651 G>T maps to ENST00000313400 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:119249651 G>T maps to ENST00000313400 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118770824 T>C maps to NM_182557.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118770824 T>C maps to NM_182557.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:36147456 C>T maps to NM_006698.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:36147456 C>T maps to NM_006698.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:77804247 C>A maps to NM_024805.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:77804247 C>A maps to NM_024805.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:1013255 G>T maps to NM_001033026.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:1013255 G>T maps to NM_001033026.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:60456395 C>A maps to NM_152377.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:60456395 C>A maps to NM_152377.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:63618489 G>A maps to NM_001218.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:63618489 G>A maps to NM_001218.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:48696098 G>A maps to NM_018896.3 T1837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:48696098 G>A maps to NM_018896.3 T1837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:191098711 C>A maps to NM_178335.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:191098711 C>A maps to NM_178335.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:63548006 C>A maps to NM_004361.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:63548006 C>A maps to NM_004361.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:19996169 C>T maps to NM_172241.2 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:19996169 C>T maps to NM_172241.2 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:47611774 G>T maps to NM_001010969.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:47611774 G>T maps to NM_001010969.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:62496388 C>A maps to NM_004396.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:62496388 C>A maps to NM_004396.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:61513658 G>T maps to NM_033081.2 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:61513658 G>T maps to NM_033081.2 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:38919258 C>A maps to ENST00000327475 T4126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:38919258 C>A maps to ENST00000327475 T4126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:11696839 G>T maps to NM_001372.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:11696839 G>T maps to NM_001372.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:117391952 C>A maps to NM_020693.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:117391952 C>A maps to NM_020693.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:28934606 G>T maps to NM_001942.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:28934606 G>T maps to NM_001942.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:152914961 C>A maps to NM_001395.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:152914961 C>A maps to NM_001395.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:102457985 C>A maps to NM_001376.4 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:102457985 C>A maps to NM_001376.4 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:131640455 C>A maps to ENST00000355311 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:131640455 C>A maps to ENST00000355311 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:21925120 C>A maps to ENST00000265800 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:21925120 C>A maps to ENST00000265800 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:96253167 G>A maps to NM_001130140.1 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:96253167 G>A maps to NM_001130140.1 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:74485057 C>A maps to NM_016014.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:74485057 C>A maps to NM_016014.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:114257387 C>A maps to NM_012184.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:114257387 C>A maps to NM_012184.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:53967937 C>A maps to NM_001080432.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:53967937 C>A maps to NM_001080432.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:62397857 G>A maps to NM_198335.2 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:62397857 G>A maps to NM_198335.2 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:130117711 C>A maps to NM_032293.4 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:130117711 C>A maps to NM_032293.4 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:123342905 G>T maps to NM_003959.1 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:123342905 G>T maps to NM_003959.1 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:35556223 G>T maps to NM_182983.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:35556223 G>T maps to NM_182983.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:148884897 C>A maps to NM_032383.3 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:148884897 C>A maps to NM_032383.3 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:22202132 G>T maps to NM_005529.5 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:22202132 G>T maps to NM_005529.5 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118918522 G>T maps to NM_001130991.1 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118918522 G>T maps to NM_001130991.1 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:33374157 C>A maps to NM_002263.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:33374157 C>A maps to NM_002263.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:21334729 A>G maps to NM_018847.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:21334729 A>G maps to NM_018847.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:51361823 C>T maps to NM_001648.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:51361823 C>T maps to NM_001648.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:100176068 C>A maps to NM_002319.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:100176068 C>A maps to NM_002319.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:75017916 C>T maps to NM_000428.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:75017916 C>T maps to NM_000428.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:50904624 G>T maps to NM_198794.1 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:50904624 G>T maps to NM_198794.1 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:116675498 C>A maps to NM_015335.4 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:116675498 C>A maps to NM_015335.4 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:129905597 G>A maps to NM_002417.4 D1502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:129905597 G>A maps to NM_002417.4 D1502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:60567349 G>T maps to NM_206893.3 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:60567349 G>T maps to NM_206893.3 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr13:77900736 C>A maps to NM_015057.4 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr13:77900736 C>A maps to NM_015057.4 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:130947504 C>A maps to NM_024800.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:130947504 C>A maps to NM_024800.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:129744407 G>T maps to NM_006165.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:129744407 G>T maps to NM_006165.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:34269477 C>A maps to NM_001164749.1 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:34269477 C>A maps to NM_001164749.1 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:131748907 C>A maps to NM_015354.1 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:131748907 C>A maps to NM_015354.1 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:48266804 C>A maps to NM_001004727.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:48266804 C>A maps to NM_001004727.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:52847369 G>T maps to NM_004153.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:52847369 G>T maps to NM_004153.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:93913370 C>A maps to NM_015368.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:93913370 C>A maps to NM_015368.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:140625382 G>T maps to NM_018935.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:140625382 G>T maps to NM_018935.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:140798769 C>T maps to NM_018927.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:140798769 C>T maps to NM_018927.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:129289674 G>T maps to NM_015103.2 S1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:129289674 G>T maps to NM_015103.2 S1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:167358910 C>A maps to NM_002697.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:167358910 C>A maps to NM_002697.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:30529794 C>A maps to NM_025263.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:30529794 C>A maps to NM_025263.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:139215321 C>A maps to NM_032289.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:139215321 C>A maps to NM_032289.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:204128651 G>A maps to NM_000537.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:204128651 G>A maps to NM_000537.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:29837624 G>A maps to NM_021026.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:29837624 G>A maps to NM_021026.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:156144921 C>A maps to NM_022367.3 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:156144921 C>A maps to NM_022367.3 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:37951863 C>A maps to ENST00000223214 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:37951863 C>A maps to ENST00000223214 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:25264736 C>A maps to NM_001039948.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:25264736 C>A maps to NM_001039948.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:170078421 G>A maps to NM_005414.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:170078421 G>A maps to NM_005414.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:26817799 C>A maps to NM_001145975.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:26817799 C>A maps to NM_001145975.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:160858112 G>T maps to ENST00000392145 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:160858112 G>T maps to ENST00000392145 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:74625693 T>A maps to NM_018414.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:74625693 T>A maps to NM_018414.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:43893701 A>G maps to NM_153700.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:43893701 A>G maps to NM_153700.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:47921471 C>A maps to NM_170685.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:47921471 C>A maps to NM_170685.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:179620181 C>A maps to ENST00000444136 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:179620181 C>A maps to ENST00000444136 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:102904477 G>T maps to NM_014844.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:102904477 G>T maps to NM_014844.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:155175048 C>A maps to NM_007112.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:155175048 C>A maps to NM_007112.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:226841 G>T maps to NM_005131.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:226841 G>T maps to NM_005131.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:35852957 C>A maps to NM_001042590.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:35852957 C>A maps to NM_001042590.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:189582070 C>A maps to NM_003722.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:189582070 C>A maps to NM_003722.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:3726115 C>A maps to NM_016292.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:3726115 C>A maps to NM_016292.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:122653833 C>A maps to NM_032873.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:122653833 C>A maps to NM_032873.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:100866350 C>T maps to NM_017890.3 L3603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:100866350 C>T maps to NM_017890.3 L3603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:118474228 G>T maps to ENST00000441406 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:118474228 G>T maps to ENST00000441406 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:68248115 C>A maps to NM_015346.3 T1501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:68248115 C>A maps to NM_015346.3 T1501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:20698212 C>T maps to NM_001163941.1 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:20698212 C>T maps to NM_001163941.1 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:48261805 C>T maps to NM_032583.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:48261805 C>T maps to NM_032583.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:18152599 G>A maps to NM_030812.2 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:18152599 G>A maps to NM_030812.2 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:8018292 A>G maps to ENST00000380149 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:8018292 A>G maps to ENST00000380149 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:50271904 C>A maps to NM_024837.2 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:50271904 C>A maps to NM_024837.2 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:26452056 A>C maps to NM_006994.4 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:26452056 A>C maps to NM_006994.4 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:24923218 C>A maps to NM_018958.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:24923218 C>A maps to NM_018958.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:120221510 G>C maps to NM_001170330.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:120221510 G>C maps to NM_001170330.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:57347291 G>A maps to NM_000562.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:57347291 G>A maps to NM_000562.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:151509761 C>T maps to NM_020770.2 Y1184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:151509761 C>T maps to NM_020770.2 Y1184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:7803212 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:7803212 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:122862307 G>A maps to ENST00000302528 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:122862307 G>A maps to ENST00000302528 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:95368679 G>A maps to NM_001839.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:95368679 G>A maps to NM_001839.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:135080501 G>C maps to NM_001190850.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:135080501 G>C maps to NM_001190850.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:189856211 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:189856211 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr21:47410955 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr21:47410955 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:46332679 C>G maps to ENST00000288400 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:46332679 C>G maps to ENST00000288400 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:111776135 C>A maps to NM_015267.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:111776135 C>A maps to NM_015267.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:118678384 T>C maps to NM_022101.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:118678384 T>C maps to NM_022101.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:156746825 C>T maps to ENST00000442283 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:156746825 C>T maps to ENST00000442283 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:104427646 G>T maps to NM_015420.6 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:104427646 G>T maps to NM_015420.6 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:36778974 G>C maps to NM_033403.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:36778974 G>C maps to NM_033403.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:221879755 G>A maps to NM_007207.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:221879755 G>A maps to NM_007207.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:205589515 C>A maps to NM_001973.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:205589515 C>A maps to NM_001973.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:205589654 C>T maps to NM_001973.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:205589654 C>T maps to NM_001973.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:6937292 G>T maps to ENST00000381407 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:6937292 G>T maps to ENST00000381407 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:69695690 T>A maps to NM_001193363.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:69695690 T>A maps to NM_001193363.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:94818034 C>T maps to NM_019053.4 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:94818034 C>T maps to NM_019053.4 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:97082699 G>T maps to NM_017561.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:97082699 G>T maps to NM_017561.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:190068140 G>T maps to NM_199051.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:190068140 G>T maps to NM_199051.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:45644915 C>T maps to NM_020937.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:45644915 C>T maps to NM_020937.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:32097283 G>A maps to NM_022110.3 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:32097283 G>A maps to NM_022110.3 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:89405071 G>T maps to NM_153696.2 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:89405071 G>T maps to NM_153696.2 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:45973885 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:45973885 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:4798714 G>A maps to ENST00000450194 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:4798714 G>A maps to ENST00000450194 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:161277867 C>T maps to NM_001127648.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:161277867 C>T maps to NM_001127648.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:105517990 G>A maps to NM_013345.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:105517990 G>A maps to NM_013345.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:105483078 C>T maps to NM_000829.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:105483078 C>T maps to NM_000829.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:13906489 G>A maps to NM_000834.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:13906489 G>A maps to NM_000834.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:7503363 G>C maps to NM_181874.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:7503363 G>C maps to NM_181874.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:245023748 G>C maps to NM_031844.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:245023748 G>C maps to NM_031844.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:132439556 G>T maps to NM_002154.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:132439556 G>T maps to NM_002154.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:132439654 G>A maps to NM_002154.3 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:132439654 G>A maps to NM_002154.3 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr21:35229121 C>T maps to NM_003024.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr21:35229121 C>T maps to NM_003024.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:26961559 G>A maps to NM_014680.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:26961559 G>A maps to NM_014680.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:6863503 C>T maps to NM_014743.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:6863503 C>T maps to NM_014743.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:24722074 C>T maps to NM_019590.3 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:24722074 C>T maps to NM_019590.3 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:18376263 G>A maps to NM_001145304.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:18376263 G>A maps to NM_001145304.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:113388994 C>T maps to NM_001009899.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:113388994 C>T maps to NM_001009899.2 L44L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-73-4658-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:115560691 T>A maps to NM_002338.3 R307*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-73-4658-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:115560691 T>A maps to NM_002338.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:102763814 G>T maps to NM_032429.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:102763814 G>T maps to NM_032429.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:151935328 C>A maps to NM_005362.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:151935328 C>A maps to NM_005362.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:37242562 C>G maps to NM_170675.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:37242562 C>G maps to NM_170675.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118359360 C>T maps to NM_001197104.1 F1455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118359360 C>T maps to NM_001197104.1 F1455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:49927460 C>A maps to NM_002447.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:49927460 C>A maps to NM_002447.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:10404794 C>A maps to NM_005963.3 E1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:10404794 C>A maps to NM_005963.3 E1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:112528569 T>A maps to NM_024953.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:112528569 T>A maps to NM_024953.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:175184874 C>G maps to NM_207015.2 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:175184874 C>G maps to NM_207015.2 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:29559716 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:29559716 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:103950040 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:103950040 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:236212120 G>A maps to NM_002508.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:236212120 G>A maps to NM_002508.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:124979453 C>A maps to NM_001040214.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:124979453 C>A maps to NM_001040214.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:56482062 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:56482062 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:49424448 G>A maps to NM_006184.5 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:49424448 G>A maps to NM_006184.5 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:24878022 G>T maps to NM_025081.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:24878022 G>T maps to NM_025081.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:124030090 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:124030090 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:9968408 G>A maps to NM_058164.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:9968408 G>A maps to NM_058164.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:46032613 C>A maps to NM_001017989.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:46032613 C>A maps to NM_001017989.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:29407926 G>A maps to NM_013941.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:29407926 G>A maps to NM_013941.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158435884 C>T maps to NM_001004473.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158435884 C>T maps to NM_001004473.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158436016 C>A maps to NM_001004473.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158436016 C>A maps to NM_001004473.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:180582568 C>G maps to NM_206880.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:180582568 C>G maps to NM_206880.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:78216424 C>G maps to NM_198333.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:78216424 C>G maps to NM_198333.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:141243093 C>T maps to NM_032420.2 Q934Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:141243093 C>T maps to NM_032420.2 Q934Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:141243968 C>A maps to NM_032420.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:141243968 C>A maps to NM_032420.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:67802359 C>A maps to NM_203487.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:67802359 C>A maps to NM_203487.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:144865912 G>A maps to NM_014644.4 F1889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:144865912 G>A maps to NM_014644.4 F1889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:249212111 G>C maps to NM_170725.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:249212111 G>C maps to NM_170725.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:129767549 C>T maps to NM_199320.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:129767549 C>T maps to NM_199320.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:209142379 C>T maps to NM_015040.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:209142379 C>T maps to NM_015040.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:15425672 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:15425672 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:94316681 G>A maps to NM_152431.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:94316681 G>A maps to NM_152431.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:2153582 G>T maps to NM_001009944.2 L2825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:2153582 G>T maps to NM_001009944.2 L2825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:3328443 C>T maps to NM_022114.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:3328443 C>T maps to NM_022114.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:109367851 C>G maps to NM_006267.4 S469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:109367851 C>G maps to NM_006267.4 S469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:21636333 G>A maps to NM_032941.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:21636333 G>A maps to NM_032941.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:104955057 C>T maps to NM_001100117.2 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:104955057 C>T maps to NM_001100117.2 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:122338096 T>A maps to NM_139175.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:122338096 T>A maps to NM_139175.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:237886465 C>T maps to NM_001035.2 Y3531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:237886465 C>T maps to NM_001035.2 Y3531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:23803930 G>A maps to NM_002970.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:23803930 G>A maps to NM_002970.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:134023903 C>T maps to NM_021982.1 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:134023903 C>T maps to NM_021982.1 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:92899089 T>A maps to NM_152313.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:92899089 T>A maps to NM_152313.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:23243286 G>A maps to NM_001126106.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:23243286 G>A maps to NM_001126106.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:135098877 G>A maps to NM_001042537.1 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:135098877 G>A maps to NM_001042537.1 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:74915501 T>A maps to NM_007256.4 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:74915501 T>A maps to NM_007256.4 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:186544287 G>A maps to ENST00000355634 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:186544287 G>A maps to ENST00000355634 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:1828176 G>A maps to NM_080861.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:1828176 G>A maps to NM_080861.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:149519224 C>T maps to NM_198455.2 P4347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:149519224 C>T maps to NM_198455.2 P4347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:89793972 G>A maps to ENST00000433102 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:89793972 G>A maps to ENST00000433102 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:159463124 G>T maps to NM_054114.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:159463124 G>T maps to NM_054114.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:19027865 C>A maps to NM_024847.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:19027865 C>A maps to NM_024847.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:45028842 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:45028842 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:113176787 G>A maps to NM_006322.4 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:113176787 G>A maps to NM_006322.4 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118263479 G>T maps to NM_004788.2 E989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118263479 G>T maps to NM_004788.2 E989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:229773572 C>T maps to NM_014777.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:229773572 C>T maps to NM_014777.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:129060312 C>T maps to NM_006649.3 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:129060312 C>T maps to NM_006649.3 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:190993091 C>A maps to NM_198152.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:190993091 C>A maps to NM_198152.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:107315989 G>T maps to NM_001170553.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:107315989 G>T maps to NM_001170553.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:85707200 C>A maps to NM_014991.4 V1331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:85707200 C>A maps to NM_014991.4 V1331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:85559236 C>G maps to NM_145172.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:85559236 C>G maps to NM_145172.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:228786186 C>T maps to NM_178821.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:228786186 C>T maps to NM_178821.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38415992 G>T maps to NM_005108.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38415992 G>T maps to NM_005108.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:21706451 G>A maps to NM_024697.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:21706451 G>A maps to NM_024697.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:44775990 A>G maps to NM_145044.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:44775990 A>G maps to NM_145044.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:64967176 C>A maps to NM_015042.1 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:64967176 C>A maps to NM_015042.1 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:53276 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:53276 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:69347565 C>A maps to NM_001130004.1 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:69347565 C>A maps to NM_001130004.1 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:33561188 A>T maps to NM_030955.2 P1356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:33561188 A>T maps to NM_030955.2 P1356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:131916287 C>T maps to NM_001115.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:131916287 C>T maps to NM_001115.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:100239266 A>T maps to NM_000668.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:100239266 A>T maps to NM_000668.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:37823765 C>A maps to NM_000025.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:37823765 C>A maps to NM_000025.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:45823075 A>G maps to NM_001025356.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:45823075 A>G maps to NM_001025356.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:108160400 A>T maps to NM_000051.3 R1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:108160400 A>T maps to NM_000051.3 R1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:103761773 C>A maps to NM_024541.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:103761773 C>A maps to NM_024541.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:95910831 G>C maps to NM_152592.3 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:95910831 G>C maps to NM_152592.3 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:1162052 C>T maps to NM_018354.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:1162052 C>T maps to NM_018354.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:201030556 C>T maps to NM_000069.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:201030556 C>T maps to NM_000069.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:74709987 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:74709987 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:46521385 C>T maps to NM_001080402.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:46521385 C>T maps to NM_001080402.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:21878144 G>A maps to NM_001170629.1 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:21878144 G>A maps to NM_001170629.1 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:5903618 C>T maps to NM_001819.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:5903618 C>T maps to NM_001819.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:3078941 A>T maps to NM_175607.1 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:3078941 A>T maps to NM_175607.1 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:3685150 C>A maps to ENST00000418971 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:3685150 C>A maps to ENST00000418971 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:3072115 A>T maps to NM_033225.5 C1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:3072115 A>T maps to NM_033225.5 C1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:158272581 C>A maps to NM_004288.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:158272581 C>A maps to NM_004288.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:125685796 C>T maps to NM_178470.4 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:125685796 C>T maps to NM_178470.4 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:162902122 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:162902122 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:174869877 G>A maps to NM_000794.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:174869877 G>A maps to NM_000794.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:35386511 C>A maps to NM_001145315.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:35386511 C>A maps to NM_001145315.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:40023400 G>A maps to NM_152361.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:40023400 G>A maps to NM_152361.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:23701600 G>A maps to ENST00000359598 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:23701600 G>A maps to ENST00000359598 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:129206318 G>A maps to NM_001127197.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:129206318 G>A maps to NM_001127197.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:242042435 C>A maps to NM_006027.4 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:242042435 C>A maps to NM_006027.4 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:197019869 G>A maps to NM_001994.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:197019869 G>A maps to NM_001994.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:14746968 C>A maps to ENST00000380880 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:14746968 C>A maps to ENST00000380880 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:39435641 G>T maps to NM_207361.4 E2532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:39435641 G>T maps to NM_207361.4 E2532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:46099326 C>A maps to NM_173536.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:46099326 C>A maps to NM_173536.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:35045110 T>G maps to NM_020660.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:35045110 T>G maps to NM_020660.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:57864592 C>T maps to NM_005269.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:57864592 C>T maps to NM_005269.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:27212600 C>A maps to NM_018066.3 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:27212600 C>A maps to NM_018066.3 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:23667393 T>A maps to ENST00000414299 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:23667393 T>A maps to ENST00000414299 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:152188192 G>C maps to NM_001009931.1 S1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:152188192 G>C maps to NM_001009931.1 S1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:21187443 G>A maps to NM_021068.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:21187443 G>A maps to NM_021068.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:7774332 C>A maps to NM_002216.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:7774332 C>A maps to NM_002216.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160851994 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160851994 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:5155109 C>A maps to NM_002234.2 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:5155109 C>A maps to NM_002234.2 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:7801873 T>A maps to NM_012311.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:7801873 T>A maps to NM_012311.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:53012211 G>A maps to NM_175068.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:53012211 G>A maps to NM_175068.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:52778967 G>T maps to NM_033045.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:52778967 G>T maps to NM_033045.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:95517963 T>C maps to NM_005097.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:95517963 T>C maps to NM_005097.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:35297910 C>G maps to NM_005568.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:35297910 C>G maps to NM_005568.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:28143300 A>G maps to NM_153371.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:28143300 A>G maps to NM_153371.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:101523839 A>T maps to NM_024652.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:101523839 A>T maps to NM_024652.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:185191200 G>T maps to NM_004721.3 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:185191200 G>T maps to NM_004721.3 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:132325240 C>A maps to NM_016155.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:132325240 C>A maps to NM_016155.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:56369781 G>T maps to NM_134444.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:56369781 G>T maps to NM_134444.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:44571765 C>A maps to NM_013389.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:44571765 C>A maps to NM_013389.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:37370995 C>A maps to NM_153485.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:37370995 C>A maps to NM_153485.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:20692479 A>T maps to NM_001004480.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:20692479 A>T maps to NM_001004480.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:248525193 G>A maps to NM_001004696.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:248525193 G>A maps to NM_001004696.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:21623953 C>T maps to NM_001004731.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:21623953 C>T maps to NM_001004731.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:247876018 G>T maps to NM_001005286.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:247876018 G>T maps to NM_001005286.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:76779953 A>G maps to NM_020841.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:76779953 A>G maps to NM_020841.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:30723874 C>A maps to NM_001173523.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:30723874 C>A maps to NM_001173523.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:140263145 C>A maps to NM_018904.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:140263145 C>A maps to NM_018904.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:145580563 A>G maps to NM_006099.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:145580563 A>G maps to NM_006099.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:105395256 G>A maps to NM_138790.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:105395256 G>A maps to NM_138790.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:113518008 A>G maps to NM_002711.3 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:113518008 A>G maps to NM_002711.3 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:133758919 G>A maps to ENST00000455566 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:133758919 G>A maps to ENST00000455566 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:129817145 C>T maps to NM_020228.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:129817145 C>T maps to NM_020228.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48690419 C>A maps to NM_006904.6 E3956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48690419 C>A maps to NM_006904.6 E3956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48762046 C>G maps to NM_006904.6 L2340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48762046 C>G maps to NM_006904.6 L2340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:79384740 G>C maps to NM_138937.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:79384740 G>C maps to NM_138937.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:90020438 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:90020438 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:37336423 T>C maps to NM_003958.3 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:37336423 T>C maps to NM_003958.3 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:17896177 T>A maps to ENST00000381272 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:17896177 T>A maps to ENST00000381272 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:104129312 G>A maps to NM_017564.9 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:104129312 G>A maps to NM_017564.9 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:17747667 G>T maps to NM_003473.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:17747667 G>T maps to NM_003473.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:149882196 G>A maps to NM_014849.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:149882196 G>A maps to NM_014849.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:114841687 C>A maps to NM_000192.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:114841687 C>A maps to NM_000192.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:20857776 T>A maps to NM_007110.4 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:20857776 T>A maps to NM_007110.4 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:156378553 C>T maps to NM_138379.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:156378553 C>T maps to NM_138379.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:120476415 T>A maps to NM_138554.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:120476415 T>A maps to NM_138554.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:175304874 G>A maps to NM_003285.2 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:175304874 G>A maps to NM_003285.2 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:80720674 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:80720674 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:93314 A>G maps to NM_177987.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:93314 A>G maps to NM_177987.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:139609687 C>A maps to ENST00000358430 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:139609687 C>A maps to ENST00000358430 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:109937519 G>T maps to NM_183415.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:109937519 G>T maps to NM_183415.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:203764279 G>A maps to NM_018256.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:203764279 G>A maps to NM_018256.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:134232986 G>T maps to NM_003882.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:134232986 G>T maps to NM_003882.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:184205515 A>T maps to ENST00000448232 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:184205515 A>T maps to ENST00000448232 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:64814178 G>T maps to NM_007235.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:64814178 G>T maps to NM_007235.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:21875363 C>G maps to NM_206923.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:21875363 C>G maps to NM_206923.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:182026434 C>G maps to NM_001009992.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:182026434 C>G maps to NM_001009992.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:57217623 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:57217623 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:215862466 A>T maps to NM_173076.2 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:215862466 A>T maps to NM_173076.2 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70823471 C>A maps to NM_052957.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70823471 C>A maps to NM_052957.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70832807 G>C maps to NM_052957.4 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70832807 G>C maps to NM_052957.4 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:20491953 G>A maps to NM_001010845.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:20491953 G>A maps to NM_001010845.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:20554524 C>T maps to NM_182617.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:20554524 C>T maps to NM_182617.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:7857262 G>A maps to NM_001134647.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:7857262 G>A maps to NM_001134647.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:112024257 C>A maps to NM_001113490.1 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:112024257 C>A maps to NM_001113490.1 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:76845334 T>A maps to NM_000489.3 T2062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:76845334 T>A maps to NM_000489.3 T2062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:79165039 G>T maps to ENST00000269392 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:79165039 G>T maps to ENST00000269392 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:55814217 C>A maps to NM_032430.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:55814217 C>A maps to NM_032430.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:100613364 G>T maps to NM_000061.2 Y345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:100613364 G>T maps to NM_000061.2 Y345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:133100439 G>T maps to NM_052831.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:133100439 G>T maps to NM_052831.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:151869437 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:151869437 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:7586275 C>A maps to ENST00000416109 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:7586275 C>A maps to ENST00000416109 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:24201957 C>T maps to NM_001841.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:24201957 C>T maps to NM_001841.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:113651093 G>A maps to NM_198123.1 D1119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:113651093 G>A maps to NM_198123.1 D1119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:11159797 G>T maps to NM_001332.2 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:11159797 G>T maps to NM_001332.2 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42825783 C>T maps to NM_145663.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42825783 C>T maps to NM_145663.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:395292 G>A maps to NM_014974.2 H1029H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:395292 G>A maps to NM_014974.2 H1029H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:63974595 G>T maps to NM_173812.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:63974595 G>T maps to NM_173812.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:73480296 C>T maps to ENST00000358929 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:73480296 C>T maps to ENST00000358929 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:216850420 G>A maps to NM_001438.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:216850420 G>A maps to NM_001438.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:12722576 T>C maps to ENST00000429478 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:12722576 T>C maps to ENST00000429478 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:8111434 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:8111434 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:25887710 T>A maps to NM_020752.2 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:25887710 T>A maps to NM_020752.2 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:53607797 T>A maps to ENST00000276009 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:53607797 T>A maps to ENST00000276009 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:117150687 G>T maps to NM_001542.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:117150687 G>T maps to NM_001542.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:41739732 C>T maps to NM_002192.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:41739732 C>T maps to NM_002192.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:234106842 C>T maps to ENST00000359570 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:234106842 C>T maps to ENST00000359570 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:18113213 A>G maps to NM_002252.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:18113213 A>G maps to NM_002252.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:7752152 G>T maps to NM_001080424.1 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:7752152 G>T maps to NM_001080424.1 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:117033332 T>C maps to NM_033495.3 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:117033332 T>C maps to NM_033495.3 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:10665776 T>G maps to NM_023008.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:10665776 T>G maps to NM_023008.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:46067169 C>A maps to NM_198692.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:46067169 C>A maps to NM_198692.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:42109165 G>T maps to NM_001128608.1 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:42109165 G>T maps to NM_001128608.1 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:220791807 G>T maps to NM_018650.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:220791807 G>T maps to NM_018650.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:38179413 G>A maps to NM_014815.3 G740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:38179413 G>A maps to NM_014815.3 G740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:116339806 A>G maps to NM_001127500.1 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:116339806 A>G maps to NM_001127500.1 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:71359764 C>T maps to NM_001013627.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:71359764 C>T maps to NM_001013627.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:55110822 C>A maps to NM_001005274.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:55110822 C>A maps to NM_001005274.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:49974726 C>A maps to NM_001001955.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:49974726 C>A maps to NM_001001955.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:48328453 C>A maps to NM_001004725.1 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:48328453 C>A maps to NM_001004725.1 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:56128012 T>A maps to NM_001005205.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:56128012 T>A maps to NM_001005205.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:4900090 C>A maps to NM_020144.4 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:4900090 C>A maps to NM_020144.4 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:140562313 C>A maps to NM_020957.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:140562313 C>A maps to NM_020957.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:96762281 C>A maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:96762281 C>A maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:151152181 C>A maps to NM_001029884.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:151152181 C>A maps to NM_001029884.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39907023 C>T maps to NM_022835.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39907023 C>T maps to NM_022835.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:49127099 G>T maps to NM_033215.4 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:49127099 G>T maps to NM_033215.4 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:135721503 A>G maps to NM_002718.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:135721503 A>G maps to NM_002718.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:64875259 G>A maps to NM_015342.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:64875259 G>A maps to NM_015342.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:151261297 C>A maps to NM_016203.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:151261297 C>A maps to NM_016203.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:84233921 C>A maps to NM_153362.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:84233921 C>A maps to NM_153362.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:43262241 G>T maps to NM_182707.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:43262241 G>T maps to NM_182707.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:98209231 C>A maps to NM_000264.3 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:98209231 C>A maps to NM_000264.3 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:131127757 C>T maps to NM_014369.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:131127757 C>T maps to NM_014369.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:121682659 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:121682659 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:20577614 A>G maps to ENST00000360790 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:20577614 A>G maps to ENST00000360790 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:122338099 C>A maps to NM_139175.1 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:122338099 C>A maps to NM_139175.1 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:193794 G>T maps to NM_145651.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:193794 G>T maps to NM_145651.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:75187324 T>C maps to NM_001039573.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:75187324 T>C maps to NM_001039573.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:171765672 C>T maps to NM_001017995.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:171765672 C>T maps to NM_001017995.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:19550263 G>T maps to NM_020344.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:19550263 G>T maps to NM_020344.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:31498857 C>T maps to ENST00000431354 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:31498857 C>T maps to ENST00000431354 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:2656196 G>T maps to NM_015295.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:2656196 G>T maps to NM_015295.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:45307668 A>G maps to NM_020826.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:45307668 A>G maps to NM_020826.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:763397 C>T maps to NM_006755.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:763397 C>T maps to NM_006755.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:122635133 C>T maps to NM_016945.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:122635133 C>T maps to NM_016945.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:102864327 A>G maps to NM_032926.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:102864327 A>G maps to NM_032926.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:169641916 G>T maps to NM_003247.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:169641916 G>T maps to NM_003247.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:15599800 C>A maps to NM_001004320.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:15599800 C>A maps to NM_001004320.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:175336416 A>T maps to NM_003285.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:175336416 A>T maps to NM_003285.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:179575398 C>A maps to NM_133378.4 V8231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:179575398 C>A maps to NM_133378.4 V8231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:6496230 G>A maps to NM_006087.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:6496230 G>A maps to NM_006087.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:337650 G>A maps to NM_003441.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:337650 G>A maps to NM_003441.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:185798421 C>A maps to NM_194250.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:185798421 C>A maps to NM_194250.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:160199278 A>G maps to NM_005891.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:160199278 A>G maps to NM_005891.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:28306898 G>T maps to NM_007038.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:28306898 G>T maps to NM_007038.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:64447677 G>T maps to NM_197941.2 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:64447677 G>T maps to NM_197941.2 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:7695930 C>A maps to NM_020546.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:7695930 C>A maps to NM_020546.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:33046385 G>T maps to NM_004274.4 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:33046385 G>T maps to NM_004274.4 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:34985811 C>A maps to NM_015245.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:34985811 C>A maps to NM_015245.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:21262122 G>T maps to NM_145865.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:21262122 G>T maps to NM_145865.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:81926684 C>T maps to NM_145869.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:81926684 C>T maps to NM_145869.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:115351450 T>A maps to NM_173800.4 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:115351450 T>A maps to NM_173800.4 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:156910212 A>C maps to NM_198236.1 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:156910212 A>C maps to NM_198236.1 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154319196 G>T maps to NM_020452.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154319196 G>T maps to NM_020452.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:70808255 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:70808255 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:79945591 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:79945591 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:35749390 C>T maps to ENST00000343811 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:35749390 C>T maps to ENST00000343811 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:119217732 G>A maps to NM_016589.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:119217732 G>A maps to NM_016589.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54466458 G>T maps to NM_031895.5 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54466458 G>T maps to NM_031895.5 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:7792505 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:7792505 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:115481471 C>T maps to NM_033338.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:115481471 C>T maps to NM_033338.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:56420276 G>T maps to NM_001080433.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:56420276 G>T maps to NM_001080433.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:50094665 G>A maps to NM_033031.2 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:50094665 G>A maps to NM_033031.2 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:109810585 C>T maps to NM_001408.2 V2074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:109810585 C>T maps to NM_001408.2 V2074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:55893497 G>A maps to NM_001143685.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:55893497 G>A maps to NM_001143685.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:26515943 G>T maps to ENST00000374253 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:26515943 G>T maps to ENST00000374253 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:51258589 G>A maps to ENST00000395542 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:51258589 G>A maps to ENST00000395542 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:83226623 T>A maps to ENST00000261723 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:83226623 T>A maps to ENST00000261723 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:19996924 T>A maps to NM_172241.2 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:19996924 T>A maps to NM_172241.2 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:80831225 T>A maps to ENST00000402739 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:80831225 T>A maps to ENST00000402739 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:15734083 G>T maps to NM_007253.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:15734083 G>T maps to NM_007253.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:27840858 A>G maps to ENST00000435845 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:27840858 A>G maps to ENST00000435845 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:61511534 C>G maps to NM_006133.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:61511534 C>G maps to NM_006133.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:176885478 G>A maps to ENST00000393565 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:176885478 G>A maps to ENST00000393565 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:125299019 G>T maps to NM_001013628.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:125299019 G>T maps to NM_001013628.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:110714064 C>A maps to NM_003649.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:110714064 C>A maps to NM_003649.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:7705028 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:7705028 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:11865410 T>A maps to NM_001372.3 T4357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:11865410 T>A maps to NM_001372.3 T4357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:100829883 C>A maps to NM_001031723.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:100829883 C>A maps to NM_001031723.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:99481646 T>A maps to ENST00000428223 K1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:99481646 T>A maps to ENST00000428223 K1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:21769796 C>T maps to NM_003974.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:21769796 C>T maps to NM_003974.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:28736035 C>A maps to NM_024421.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:28736035 C>A maps to NM_024421.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:184663204 C>A maps to NM_025191.3 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:184663204 C>A maps to NM_025191.3 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:141542157 G>A maps to NM_012154.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:141542157 G>A maps to NM_012154.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:134911493 G>T maps to NM_004441.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:134911493 G>T maps to NM_004441.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:618724 C>A maps to NM_207332.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:618724 C>A maps to NM_207332.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:239039106 C>A maps to NM_194312.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:239039106 C>A maps to NM_194312.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:72182001 A>C maps to NM_000503.4 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:72182001 A>C maps to NM_000503.4 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:35075049 T>A maps to NM_004629.1 K504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:35075049 T>A maps to NM_004629.1 K504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:150921909 C>A maps to NM_001447.2 A2926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:150921909 C>A maps to NM_001447.2 A2926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:137793018 G>T maps to NM_004114.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:137793018 G>T maps to NM_004114.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:12735848 G>T maps to ENST00000429478 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:12735848 G>T maps to ENST00000429478 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:81390511 G>T maps to NM_022041.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:81390511 G>T maps to NM_022041.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:99771578 G>A maps to NM_152742.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:99771578 G>A maps to NM_152742.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:93879810 C>T maps to NM_005708.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:93879810 C>T maps to NM_005708.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:94956173 C>T maps to NM_199243.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:94956173 C>T maps to NM_199243.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:57389007 C>A maps to NM_007264.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:57389007 C>A maps to NM_007264.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:32796424 G>T maps to NM_004964.2 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:32796424 G>T maps to NM_004964.2 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:63943545 G>T maps to ENST00000261887 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:63943545 G>T maps to ENST00000261887 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:71005912 C>T maps to NM_025130.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:71005912 C>T maps to NM_025130.3 L318L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-73-4666-01A-01D-1265-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-73-4666-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:994667 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:994667 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:41143095 C>A maps to NM_001080444.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:41143095 C>A maps to NM_001080444.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:75902106 C>T maps to NM_006633.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:75902106 C>T maps to NM_006633.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:21319604 G>A maps to NM_021012.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:21319604 G>A maps to NM_021012.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:8919173 C>G maps to NM_020738.2 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:8919173 C>G maps to NM_020738.2 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:154395530 G>T maps to NM_001099293.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:154395530 G>T maps to NM_001099293.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:55349046 T>G maps to NM_012314.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:55349046 T>G maps to NM_012314.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:123072256 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:123072256 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:53040626 A>G maps to NM_000423.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:53040626 A>G maps to NM_000423.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:141004718 G>A maps to NM_018557.2 N4420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:141004718 G>A maps to NM_018557.2 N4420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:20198852 G>A maps to NM_182762.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:20198852 G>A maps to NM_182762.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:43603415 A>T maps to NM_000240.2 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:43603415 A>T maps to NM_000240.2 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:13885061 C>T maps to NM_000529.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:13885061 C>T maps to NM_000529.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:179096184 C>A maps to NM_033540.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:179096184 C>A maps to NM_033540.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:4727536 C>G maps to NM_015246.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:4727536 C>G maps to NM_015246.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:4731567 A>C maps to NM_015246.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:4731567 A>C maps to NM_015246.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9064675 A>G maps to NM_024690.2 P7590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9064675 A>G maps to NM_024690.2 P7590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:42807912 C>A maps to NM_001144925.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:42807912 C>A maps to NM_001144925.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:3241310 A>T maps to NM_015419.3 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:3241310 A>T maps to NM_015419.3 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:26465694 G>A maps to NM_017433.4 Q1453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:26465694 G>A maps to NM_017433.4 Q1453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:1926807 G>T maps to ENST00000399161 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:1926807 G>T maps to ENST00000399161 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:89883720 C>T maps to NM_005467.3 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:89883720 C>T maps to NM_005467.3 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:66850921 G>A maps to ENST00000359087 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:66850921 G>A maps to ENST00000359087 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:15555759 C>A maps to NM_015909.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:15555759 C>A maps to NM_015909.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:151771874 G>T maps to NM_020167.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:151771874 G>T maps to NM_020167.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:156752720 C>A maps to NM_138400.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:156752720 C>A maps to NM_138400.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:34818137 G>T maps to NM_207172.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:34818137 G>T maps to NM_207172.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:47808066 T>C maps to NM_015231.1 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:47808066 T>C maps to NM_015231.1 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:78412989 C>T maps to NM_001098816.2 G1556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:78412989 C>T maps to NM_001098816.2 G1556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:22102443 G>A maps to NM_001005466.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:22102443 G>A maps to NM_001005466.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:158368638 C>A maps to NM_001004475.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:158368638 C>A maps to NM_001004475.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248059634 C>A maps to NM_001001957.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248059634 C>A maps to NM_001001957.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154918706 C>T maps to NM_020524.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154918706 C>T maps to NM_020524.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140562562 G>T maps to NM_020957.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140562562 G>T maps to NM_020957.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140563489 C>T maps to NM_020957.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140563489 C>T maps to NM_020957.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140563648 C>A maps to NM_020957.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140563648 C>A maps to NM_020957.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:173429788 G>T maps to ENST00000392571 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:173429788 G>T maps to ENST00000392571 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:7890001 C>T maps to ENST00000377532 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:7890001 C>T maps to ENST00000377532 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:58348439 G>T maps to NM_080672.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:58348439 G>T maps to NM_080672.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:63342428 T>C maps to NM_001128203.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:63342428 T>C maps to NM_001128203.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:43194109 G>A maps to NM_133373.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:43194109 G>A maps to NM_133373.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:204214838 G>T maps to ENST00000367191 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:204214838 G>T maps to ENST00000367191 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:12009870 G>T maps to ENST00000376369 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:12009870 G>T maps to ENST00000376369 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152226623 C>A maps to NM_013364.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152226623 C>A maps to NM_013364.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:23521213 C>A maps to NM_020227.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:23521213 C>A maps to NM_020227.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:94203693 G>T maps to NM_178013.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:94203693 G>T maps to NM_178013.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:138724773 C>A maps to NM_001134659.1 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:138724773 C>A maps to NM_001134659.1 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:139216500 G>T maps to NM_032289.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:139216500 G>T maps to NM_032289.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:71054796 G>T maps to NM_002849.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:71054796 G>T maps to NM_002849.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:121680904 C>A maps to NM_002851.2 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:121680904 C>A maps to NM_002851.2 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:66274075 C>T maps to ENST00000451741 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:66274075 C>T maps to ENST00000451741 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:4876111 C>A maps to NM_018059.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:4876111 C>A maps to NM_018059.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:170305132 T>C maps to NM_022897.3 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:170305132 T>C maps to NM_022897.3 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:34240589 T>A maps to NM_001198838.1 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:34240589 T>A maps to NM_001198838.1 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:23907730 T>A maps to NM_014363.4 T3428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:23907730 T>A maps to NM_014363.4 T3428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:7214468 C>A maps to NM_001018039.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:7214468 C>A maps to NM_001018039.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:121634150 A>G maps to NM_021082.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:121634150 A>G maps to NM_021082.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:128633818 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:128633818 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:121429317 C>T maps to NM_003105.5 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:121429317 C>T maps to NM_003105.5 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:44876525 G>A maps to NM_025137.3 A1784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:44876525 G>A maps to NM_025137.3 A1784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:65266573 C>A maps to ENST00000389723 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:65266573 C>A maps to ENST00000389723 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:9281902 C>A maps to NM_004853.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:9281902 C>A maps to NM_004853.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:234599595 T>C maps to NM_005646.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:234599595 T>C maps to NM_005646.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:114026902 C>T maps to ENST00000481065 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:114026902 C>T maps to ENST00000481065 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:1604882 C>A maps to NM_024600.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:1604882 C>A maps to NM_024600.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:180659676 C>T maps to NM_033549.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:180659676 C>T maps to NM_033549.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:189065201 C>T maps to NM_178556.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:189065201 C>T maps to NM_178556.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:231672974 T>G maps to NM_005999.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:231672974 T>G maps to NM_005999.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:75072313 T>A maps to NM_145170.3 K404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:75072313 T>A maps to NM_145170.3 K404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:16859726 T>A maps to NM_018360.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:16859726 T>A maps to NM_018360.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:52923869 T>A maps to NM_020784.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:52923869 T>A maps to NM_020784.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:86278911 C>A maps to NM_013438.4 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:86278911 C>A maps to NM_013438.4 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:31747921 G>A maps to NM_006295.2 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:31747921 G>A maps to NM_006295.2 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42032774 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42032774 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154988887 C>G maps to ENST00000417934 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154988887 C>G maps to ENST00000417934 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:68219063 G>A maps to NM_015346.3 P2456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:68219063 G>A maps to NM_015346.3 P2456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9677223 C>A maps to NM_001008727.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9677223 C>A maps to NM_001008727.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:57931867 G>A maps to NM_006959.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:57931867 G>A maps to NM_006959.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:178506303 C>T maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:178506303 C>T maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:28206277 C>G maps to NM_018660.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:28206277 C>G maps to NM_018660.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:97920260 C>T maps to NM_014803.3 T1394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:97920260 C>T maps to NM_014803.3 T1394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:56114113 G>T maps to NM_153219.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:56114113 G>T maps to NM_153219.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:91382453 C>A maps to NM_201269.1 R1295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:91382453 C>A maps to NM_201269.1 R1295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58549359 G>T maps to NM_182572.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58549359 G>T maps to NM_182572.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:61562711 C>T maps to NM_000789.3 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:61562711 C>T maps to NM_000789.3 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:77398153 T>A maps to NM_199355.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:77398153 T>A maps to NM_199355.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:43823487 C>A maps to ENST00000389420 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:43823487 C>A maps to ENST00000389420 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:4228884 G>T maps to NM_000678.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:4228884 G>T maps to NM_000678.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:78807395 C>T maps to NM_001013619.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:78807395 C>T maps to NM_001013619.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:33122399 C>A maps to NM_032139.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:33122399 C>A maps to NM_032139.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:14851732 A>T maps to NM_001145029.1 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:14851732 A>T maps to NM_001145029.1 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:97784158 G>T maps to NM_001164315.1 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:97784158 G>T maps to NM_001164315.1 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:119133763 T>A maps to NM_020754.2 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:119133763 T>A maps to NM_020754.2 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:8221892 C>A maps to NM_173728.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:8221892 C>A maps to NM_173728.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:48543553 C>A maps to NM_024095.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:48543553 C>A maps to NM_024095.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:87153746 A>T maps to NM_152565.1 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:87153746 A>T maps to NM_152565.1 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:30698502 G>T maps to NM_206866.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:30698502 G>T maps to NM_206866.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:101946660 G>T maps to NM_032930.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:101946660 G>T maps to NM_032930.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:72588361 C>T maps to NM_152460.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:72588361 C>T maps to NM_152460.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:22964186 C>A maps to NM_015991.2 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:22964186 C>A maps to NM_015991.2 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:99891161 C>T maps to NM_032359.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:99891161 C>T maps to NM_032359.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:120767203 G>T maps to NM_024913.4 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:120767203 G>T maps to NM_024913.4 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:2794991 C>A maps to NM_199460.2 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:2794991 C>A maps to NM_199460.2 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:40066859 C>A maps to NM_021096.3 I1480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:40066859 C>A maps to NM_021096.3 I1480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:180381774 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:180381774 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:52439525 G>A maps to NM_031290.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:52439525 G>A maps to NM_031290.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:14140071 G>A maps to NM_001007530.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:14140071 G>A maps to NM_001007530.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:196645148 T>C maps to NM_000186.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:196645148 T>C maps to NM_000186.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:202025624 C>T maps to NM_001127183.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:202025624 C>T maps to NM_001127183.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:61767074 G>A maps to NM_017780.2 W2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:61767074 G>A maps to NM_017780.2 W2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:76481990 T>A maps to NM_033401.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:76481990 T>A maps to NM_033401.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:121267477 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:121267477 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:198327272 C>T maps to NM_025147.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:198327272 C>T maps to NM_025147.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:207814374 A>T maps to NM_173077.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:207814374 A>T maps to NM_173077.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:29103812 G>C maps to NM_031311.3 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:29103812 G>C maps to NM_031311.3 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:43274040 C>A maps to ENST00000449267 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:43274040 C>A maps to ENST00000449267 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:36091256 A>T maps to NM_173695.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:36091256 A>T maps to NM_173695.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:126215447 C>G maps to NM_014026.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:126215447 C>G maps to NM_014026.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197643290 T>C maps to NM_001195215.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197643290 T>C maps to NM_001195215.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:11622803 C>A maps to NM_001372.3 Y1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:11622803 C>A maps to NM_001372.3 Y1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:183601113 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:183601113 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:28713982 T>A maps to NM_024421.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:28713982 T>A maps to NM_024421.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:56425221 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:56425221 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107216864 A>T maps to NM_181581.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107216864 A>T maps to NM_181581.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:167088686 G>T maps to NM_001080426.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:167088686 G>T maps to NM_001080426.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:99976701 C>T maps to NM_015904.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:99976701 C>T maps to NM_015904.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:132476771 G>T maps to ENST00000333577 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:132476771 G>T maps to ENST00000333577 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29524530 C>T maps to NM_016570.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29524530 C>T maps to NM_016570.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:128360369 G>A maps to NM_001143820.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:128360369 G>A maps to NM_001143820.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197029535 G>T maps to NM_001994.2 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197029535 G>T maps to NM_001994.2 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:31435744 T>C maps to NM_001135812.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:31435744 T>C maps to NM_001135812.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:67574537 T>C maps to NM_001193523.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:67574537 T>C maps to NM_001193523.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:207135747 G>T maps to NM_001170631.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:207135747 G>T maps to NM_001170631.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:117711079 G>T maps to NM_001164831.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:117711079 G>T maps to NM_001164831.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:25405909 G>T maps to NM_021067.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:25405909 G>T maps to NM_021067.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:141904808 C>A maps to NM_001039547.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:141904808 C>A maps to NM_001039547.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:37282789 C>A maps to NM_000831.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:37282789 C>A maps to NM_000831.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:156715005 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:156715005 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:55128553 C>T maps to NM_001526.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:55128553 C>T maps to NM_001526.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:27775344 C>A maps to NM_003519.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:27775344 C>A maps to NM_003519.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:190345226 C>T maps to NM_002182.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:190345226 C>T maps to NM_002182.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:227660835 C>A maps to NM_005544.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:227660835 C>A maps to NM_005544.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:44177088 T>A maps to NM_198353.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:44177088 T>A maps to NM_198353.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:44108913 C>A maps to NM_015443.3 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:44108913 C>A maps to NM_015443.3 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:117053461 A>G maps to NM_002269.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:117053461 A>G maps to NM_002269.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:60892741 C>A maps to NM_005560.3 L2444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:60892741 C>A maps to NM_005560.3 L2444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107696156 A>T maps to NM_007356.2 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107696156 A>T maps to NM_007356.2 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107718761 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107718761 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:180243318 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:180243318 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55143452 C>A maps to ENST00000427581 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55143452 C>A maps to ENST00000427581 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55175786 C>A maps to ENST00000391733 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55175786 C>A maps to ENST00000391733 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:70411411 C>A maps to NM_018368.3 G336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:70411411 C>A maps to NM_018368.3 G336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:141641432 T>A maps to NM_018557.2 A1374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:141641432 T>A maps to NM_018557.2 A1374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:30377038 A>G maps to ENST00000327564 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:30377038 A>G maps to ENST00000327564 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:235973132 G>T maps to NM_000081.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:235973132 G>T maps to NM_000081.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:91257067 C>A maps to NM_145331.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:91257067 C>A maps to NM_145331.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:54824012 C>A maps to ENST00000371389 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:54824012 C>A maps to ENST00000371389 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:94253648 C>T maps to NM_024717.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:94253648 C>T maps to NM_024717.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:42032401 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:42032401 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:222805591 G>A maps to NM_198551.2 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:222805591 G>A maps to NM_198551.2 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:93649560 G>A maps to NM_022151.4 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:93649560 G>A maps to NM_022151.4 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:20235959 C>T maps to ENST00000414242 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:20235959 C>T maps to ENST00000414242 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84765080 C>A maps to NM_138409.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84765080 C>A maps to NM_138409.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:130884363 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:130884363 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:21494265 G>A maps to NM_002509.2 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:21494265 G>A maps to NM_002509.2 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3613764 A>G maps to ENST00000448023 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3613764 A>G maps to ENST00000448023 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:54304613 C>A maps to ENST00000391773 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:54304613 C>A maps to ENST00000391773 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:43653136 G>T maps to NM_182977.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:43653136 G>T maps to NM_182977.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:887453 C>G maps to NM_015658.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:887453 C>G maps to NM_015658.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:117703231 C>A maps to ENST00000338101 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:117703231 C>A maps to ENST00000338101 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107832197 G>C maps to ENST00000379032 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107832197 G>C maps to ENST00000379032 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:50280502 G>T maps to ENST00000404971 S1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:50280502 G>T maps to ENST00000404971 S1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:39987051 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:39987051 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:123780637 G>A maps to NM_001163278.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:123780637 G>A maps to NM_001163278.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:183675776 T>A maps to NM_001080477.1 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:183675776 T>A maps to NM_001080477.1 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:123909147 G>T maps to NM_001004463.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:123909147 G>T maps to NM_001004463.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:247654578 C>A maps to NM_001004698.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:247654578 C>A maps to NM_001004698.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:51515838 C>A maps to NM_001004703.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:51515838 C>A maps to NM_001004703.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:4945494 G>T maps to NM_001005237.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:4945494 G>T maps to NM_001005237.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:99961557 G>T maps to ENST00000457907 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:99961557 G>T maps to ENST00000457907 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:140237759 G>C maps to NM_018901.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:140237759 G>C maps to NM_018901.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:140553858 C>A maps to NM_018940.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:140553858 C>A maps to NM_018940.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:82584906 C>A maps to NM_033026.5 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:82584906 C>A maps to NM_033026.5 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:207110896 C>T maps to NM_002644.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:207110896 C>T maps to NM_002644.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:51897942 C>A maps to NM_138694.3 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:51897942 C>A maps to NM_138694.3 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:114874742 T>A maps to NM_001136025.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:114874742 T>A maps to NM_001136025.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50905994 A>T maps to ENST00000391817 K323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50905994 A>T maps to ENST00000391817 K323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:57857036 G>A maps to NM_000938.1 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:57857036 G>A maps to NM_000938.1 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:14542914 C>A maps to ENST00000444806 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:14542914 C>A maps to ENST00000444806 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:23527681 G>T maps to NM_020227.2 E829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:23527681 G>T maps to NM_020227.2 E829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:54629928 G>T maps to NM_015629.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:54629928 G>T maps to NM_015629.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:142459633 G>A maps to ENST00000486171 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:142459633 G>A maps to ENST00000486171 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:151237895 C>T maps to ENST00000368881 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:151237895 C>T maps to ENST00000368881 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:29708381 G>C maps to NM_014298.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:29708381 G>C maps to NM_014298.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:43609931 A>G maps to NM_020975.4 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:43609931 A>G maps to NM_020975.4 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:108488461 C>A maps to NM_182588.2 Y1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:108488461 C>A maps to NM_182588.2 Y1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:45088459 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:45088459 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:47120295 C>A maps to NM_080746.2 *215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:47120295 C>A maps to NM_080746.2 *215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:155911748 G>A maps to NM_181885.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:155911748 G>A maps to NM_181885.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:237754043 G>A maps to NM_001035.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:237754043 G>A maps to NM_001035.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:237947111 G>T maps to NM_001035.2 E4034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:237947111 G>T maps to NM_001035.2 E4034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:34016337 C>G maps to NM_001036.3 A2291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:34016337 C>G maps to NM_001036.3 A2291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:152043242 C>A maps to NM_001009555.3 *791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:152043242 C>A maps to NM_001009555.3 *791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:60711283 C>T maps to NM_016582.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:60711283 C>T maps to NM_016582.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:10022984 G>A maps to NM_020041.2 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:10022984 G>A maps to NM_020041.2 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:73826771 G>A maps to NM_014767.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:73826771 G>A maps to NM_014767.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:45800476 G>A maps to NM_018079.4 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:45800476 G>A maps to NM_018079.4 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:2812487 T>C maps to NM_016333.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:2812487 T>C maps to NM_016333.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:113098588 G>T maps to NM_017744.4 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:113098588 G>T maps to NM_017744.4 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:56750037 T>A maps to NM_005419.3 K55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:56750037 T>A maps to NM_005419.3 K55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:134925269 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:134925269 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:57244381 G>T maps to NM_001001433.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:57244381 G>T maps to NM_001001433.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3076160 C>A maps to NM_024339.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3076160 C>A maps to NM_024339.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:52971466 C>T maps to NM_018676.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:52971466 C>T maps to NM_018676.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:43783063 C>A maps to NM_005424.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:43783063 C>A maps to NM_005424.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:102323342 G>A maps to NM_052932.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:102323342 G>A maps to NM_052932.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:159158781 G>T maps to NM_018342.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:159158781 G>T maps to NM_018342.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:123754036 G>T maps to NM_001013743.1 C162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:123754036 G>T maps to NM_001013743.1 C162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:67940628 G>C maps to NM_182526.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:67940628 G>C maps to NM_182526.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:135583166 C>A maps to NM_020389.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:135583166 C>A maps to NM_020389.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:144695113 C>T maps to NM_003313.3 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:144695113 C>T maps to NM_003313.3 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:55253432 C>A maps to NM_001114108.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:55253432 C>A maps to NM_001114108.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:179395552 G>T maps to NM_133378.4 A32695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:179395552 G>T maps to NM_133378.4 A32695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:179565845 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:179565845 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:190903800 G>T maps to ENST00000248151 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:190903800 G>T maps to ENST00000248151 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:10166581 A>G maps to NM_001105562.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:10166581 A>G maps to NM_001105562.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:192998664 T>A maps to ENST00000367450 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:192998664 T>A maps to ENST00000367450 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:100452830 G>A maps to NM_015054.1 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:100452830 G>A maps to NM_015054.1 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:33481606 C>A maps to NM_173167.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:33481606 C>A maps to NM_173167.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:74927608 C>A maps to NM_030581.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:74927608 C>A maps to NM_030581.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:100349611 C>A maps to ENST00000349350 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:100349611 C>A maps to ENST00000349350 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:46559509 T>A maps to ENST00000242848 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:46559509 T>A maps to ENST00000242848 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31072580 C>A maps to NM_001172669.1 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31072580 C>A maps to NM_001172669.1 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:53958198 G>A maps to NM_001008401.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:53958198 G>A maps to NM_001008401.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:22574548 G>C maps to NM_001098626.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:22574548 G>C maps to NM_001098626.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:102181146 T>A maps to NM_175056.1 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:102181146 T>A maps to NM_175056.1 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:9251202 C>T maps to NM_000014.4 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:9251202 C>T maps to NM_000014.4 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:204259425 G>A maps to ENST00000295851 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:204259425 G>A maps to ENST00000295851 R194R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-73-4670-01A-01D-1265-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-73-4670-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:77817956 C>A maps to NM_024079.4 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:77817956 C>A maps to NM_024079.4 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:21232871 C>A maps to NM_000384.2 E2290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:21232871 C>A maps to NM_000384.2 E2290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:33443782 G>T maps to NM_004925.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:33443782 G>T maps to NM_004925.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:156911686 C>A maps to NM_198236.1 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:156911686 C>A maps to NM_198236.1 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197112094 C>T maps to NM_018136.4 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197112094 C>T maps to NM_018136.4 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:96799186 G>A maps to NM_001002036.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:96799186 G>A maps to NM_001002036.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:87126053 G>T maps to NM_152565.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:87126053 G>T maps to NM_152565.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:52442491 G>A maps to NM_004656.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:52442491 G>A maps to NM_004656.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:33185911 T>C maps to NM_198428.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:33185911 T>C maps to NM_198428.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:80982856 G>C maps to NM_183050.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:80982856 G>C maps to NM_183050.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:63586355 C>A maps to NM_138471.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:63586355 C>A maps to NM_138471.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:112708246 C>A maps to NM_001109662.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:112708246 C>A maps to NM_001109662.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:61854976 G>T maps to NM_001796.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:61854976 G>T maps to NM_001796.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:38724596 C>A maps to NM_175060.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:38724596 C>A maps to NM_175060.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:154254902 C>A maps to NM_004779.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:154254902 C>A maps to NM_004779.4 G261G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-73-4670-01A-01D-1265-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-73-4670-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:110827078 C>G maps to NM_001845.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:110827078 C>G maps to NM_001845.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:11364946 C>G maps to NM_001332.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:11364946 C>G maps to NM_001332.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:16948340 C>T maps to NM_001081.3 R2591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:16948340 C>T maps to NM_001081.3 R2591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:40498350 T>C maps to NM_144970.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:40498350 T>C maps to NM_144970.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:61084006 C>A maps to NM_001923.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:61084006 C>A maps to NM_001923.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:39088701 T>A maps to NM_198963.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:39088701 T>A maps to NM_198963.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:205156671 C>A maps to NM_015375.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:205156671 C>A maps to NM_015375.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:21205815 C>A maps to NM_001198801.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:21205815 C>A maps to NM_001198801.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:720163 C>T maps to NM_022772.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:720163 C>T maps to NM_022772.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:94594582 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:94594582 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:59059079 G>T maps to NM_147189.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:59059079 G>T maps to NM_147189.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:89709021 C>A maps to NM_014883.2 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:89709021 C>A maps to NM_014883.2 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153677049 C>A maps to NM_004699.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153677049 C>A maps to NM_004699.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:92086456 C>T maps to ENST00000298047 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:92086456 C>T maps to ENST00000298047 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:89402665 T>C maps to NM_153696.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:89402665 T>C maps to NM_153696.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:151821479 C>T maps to NM_018558.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:151821479 C>T maps to NM_018558.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:174169579 A>G maps to NM_017423.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:174169579 A>G maps to NM_017423.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57415373 C>T maps to NM_016592.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57415373 C>T maps to NM_016592.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:37780618 G>T maps to NM_181791.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:37780618 G>T maps to NM_181791.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:71142368 C>T maps to ENST00000439900 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:71142368 C>T maps to ENST00000439900 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:32975901 C>T maps to NM_002119.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:32975901 C>T maps to NM_002119.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:150154607 G>T maps to NM_005342.2 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:150154607 G>T maps to NM_005342.2 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:21984808 T>A maps to NM_005144.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:21984808 T>A maps to NM_005144.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:21206910 G>A maps to NM_002171.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:21206910 G>A maps to NM_002171.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130416667 C>G maps to NM_001170961.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130416667 C>G maps to NM_001170961.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153278821 G>T maps to NM_001569.3 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153278821 G>T maps to NM_001569.3 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:18546131 G>T maps to NM_016368.4 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:18546131 G>T maps to NM_016368.4 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:5155013 G>T maps to NM_002234.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:5155013 G>T maps to NM_002234.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:8784096 G>T maps to ENST00000456698 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:8784096 G>T maps to ENST00000456698 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:5463748 A>T maps to NM_015325.1 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:5463748 A>T maps to NM_015325.1 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:57181920 G>A maps to NM_020722.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:57181920 G>A maps to NM_020722.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:72298676 G>T maps to NM_014431.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:72298676 G>T maps to NM_014431.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:94067066 G>A maps to ENST00000393153 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:94067066 G>A maps to ENST00000393153 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:104123945 C>T maps to ENST00000445352 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:104123945 C>T maps to ENST00000445352 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:99771932 T>C maps to NM_014839.4 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:99771932 T>C maps to NM_014839.4 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:60821815 C>T maps to NM_152598.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:60821815 C>T maps to NM_152598.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:164507068 G>A maps to ENST00000514618 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:164507068 G>A maps to ENST00000514618 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:138708395 C>A maps to ENST00000370578 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:138708395 C>A maps to ENST00000370578 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:881703 T>C maps to NM_005481.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:881703 T>C maps to NM_005481.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:42058760 C>T maps to ENST00000219905 L2876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:42058760 C>T maps to ENST00000219905 L2876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:73020021 G>A maps to NM_032951.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:73020021 G>A maps to NM_032951.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:28196354 C>A maps to NM_002430.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:28196354 C>A maps to NM_002430.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:76349324 T>C maps to NM_002440.2 D642D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:76349324 T>C maps to NM_002440.2 D642D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:81101729 C>T maps to NM_002469.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:81101729 C>T maps to NM_002469.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:178257372 G>C maps to NM_018248.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:178257372 G>C maps to NM_018248.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:16349578 C>A maps to ENST00000263012 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:16349578 C>A maps to ENST00000263012 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:123518549 G>T maps to NM_001163278.1 V2077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:123518549 G>T maps to NM_001163278.1 V2077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:123538979 G>A maps to NM_001163278.1 N1764N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:123538979 G>A maps to NM_001163278.1 N1764N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:183696201 A>C maps to NM_001080477.1 R1734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:183696201 A>C maps to NM_001080477.1 R1734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130678553 G>T maps to NM_001004486.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130678553 G>T maps to NM_001004486.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:248129592 G>A maps to NM_001004491.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:248129592 G>A maps to NM_001004491.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:98188518 C>A maps to NM_001004736.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:98188518 C>A maps to NM_001004736.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26705388 G>A maps to NM_194248.2 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26705388 G>A maps to NM_194248.2 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:30723097 C>A maps to NM_001173523.1 C18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:30723097 C>A maps to NM_001173523.1 C18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:6386988 C>T maps to NM_031220.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:6386988 C>T maps to NM_031220.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:51613440 C>T maps to NM_138694.3 V2991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:51613440 C>T maps to NM_138694.3 V2991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:20249234 G>T maps to NM_014589.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:20249234 G>T maps to NM_014589.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:150131408 G>A maps to ENST00000443480 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:150131408 G>A maps to ENST00000443480 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:208390424 C>A maps to NM_025179.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:208390424 C>A maps to NM_025179.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153039399 C>A maps to NM_005393.2 V1122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153039399 C>A maps to NM_005393.2 V1122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:36260887 G>A maps to ENST00000457797 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:36260887 G>A maps to ENST00000457797 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:79784816 C>A maps to NM_007055.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:79784816 C>A maps to NM_007055.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:46611142 C>T maps to NM_001001928.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:46611142 C>T maps to NM_001001928.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:203012562 G>C maps to ENST00000367238 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:203012562 G>C maps to ENST00000367238 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:18763816 C>A maps to NM_032781.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:18763816 C>A maps to NM_032781.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158913668 C>T maps to NM_152501.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158913668 C>T maps to NM_152501.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:238820226 C>T maps to NM_005855.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:238820226 C>T maps to NM_005855.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:53503960 A>G maps to NM_005611.3 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:53503960 A>G maps to NM_005611.3 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:63747807 C>A maps to NM_020663.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:63747807 C>A maps to NM_020663.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:159572981 G>T maps to ENST00000440678 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:159572981 G>T maps to ENST00000440678 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237604626 G>A maps to NM_001035.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237604626 G>A maps to NM_001035.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237870569 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237870569 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33603216 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33603216 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:200246415 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:200246415 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:50148668 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:50148668 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:52200402 G>T maps to NM_014191.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:52200402 G>T maps to NM_014191.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:4167082 A>G maps to NM_152744.3 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:4167082 A>G maps to NM_152744.3 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:7214463 G>T maps to NM_001018039.1 S715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:7214463 G>T maps to NM_001018039.1 S715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45557791 C>T maps to NM_004212.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45557791 C>T maps to NM_004212.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:220088834 T>A maps to NM_018713.2 K472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:220088834 T>A maps to NM_018713.2 K472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:32417449 G>A maps to NM_001193513.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:32417449 G>A maps to NM_001193513.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:69158526 G>T maps to NM_018656.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:69158526 G>T maps to NM_018656.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:42336629 C>A maps to NM_000342.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:42336629 C>A maps to NM_000342.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:51363264 G>T maps to NM_018967.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:51363264 G>T maps to NM_018967.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:106916928 A>T maps to NM_014978.1 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:106916928 A>T maps to NM_014978.1 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:99920542 C>A maps to NM_014467.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:99920542 C>A maps to NM_014467.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:132910780 T>A maps to NM_003967.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:132910780 T>A maps to NM_003967.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:48399785 C>A maps to NM_002536.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:48399785 C>A maps to NM_002536.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:67818086 G>A maps to NM_006019.3 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:67818086 G>A maps to NM_006019.3 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:79355629 C>T maps to NM_003248.4 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:79355629 C>T maps to NM_003248.4 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:122765636 T>A maps to NM_001081550.1 K795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:122765636 T>A maps to NM_001081550.1 K795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:38245465 G>C maps to NM_003250.5 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:38245465 G>C maps to NM_003250.5 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:68930430 G>T maps to NM_207407.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:68930430 G>T maps to NM_207407.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:1278755 A>T maps to ENST00000445910 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:1278755 A>T maps to ENST00000445910 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:12880877 G>A maps to NM_021643.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:12880877 G>A maps to NM_021643.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:116038541 C>T maps to NM_198496.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:116038541 C>T maps to NM_198496.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:54280509 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:54280509 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:5993694 G>T maps to NM_015253.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:5993694 G>T maps to NM_015253.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:168098401 C>A maps to NM_152381.5 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:168098401 C>A maps to NM_152381.5 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:28116493 A>G maps to NM_006298.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:28116493 A>G maps to NM_006298.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:57723653 A>T maps to NM_003417.4 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:57723653 A>T maps to NM_003417.4 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:185802438 T>C maps to NM_194250.1 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:185802438 T>C maps to NM_194250.1 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57768207 G>T maps to NM_178457.1 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57768207 G>T maps to NM_178457.1 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:57934537 C>A maps to NM_007156.4 G773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:57934537 C>A maps to NM_007156.4 G773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:132051637 C>T maps to NM_001115.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:132051637 C>T maps to NM_001115.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:46231200 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:46231200 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:19190565 C>A maps to NM_001100420.1 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:19190565 C>A maps to NM_001100420.1 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:40937761 G>T maps to NM_000587.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:40937761 G>T maps to NM_000587.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:183884763 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:183884763 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:102999640 G>T maps to NM_001080463.1 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:102999640 G>T maps to NM_001080463.1 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:50941261 G>A maps to NM_007051.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:50941261 G>A maps to NM_007051.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:162577479 A>G maps to NM_020116.3 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:162577479 A>G maps to NM_020116.3 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:33373333 G>C maps to NM_005734.3 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:33373333 G>C maps to NM_005734.3 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:46313396 G>A maps to NM_000211.3 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:46313396 G>A maps to NM_000211.3 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:51330320 G>A maps to NM_017509.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:51330320 G>A maps to NM_017509.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:73566507 C>T maps to NM_001031803.1 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:73566507 C>T maps to NM_001031803.1 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:168833634 T>A maps to NM_004991.3 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:168833634 T>A maps to NM_004991.3 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:9073700 G>T maps to NM_024690.2 S4582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:9073700 G>T maps to NM_024690.2 S4582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:201777623 G>T maps to ENST00000367296 S1308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:201777623 G>T maps to ENST00000367296 S1308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:24839713 G>A maps to NM_001136022.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:24839713 G>A maps to NM_001136022.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:55493671 C>A maps to NM_017852.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:55493671 C>A maps to NM_017852.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:47283258 G>A maps to NM_005693.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:47283258 G>A maps to NM_005693.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:248551784 G>T maps to NM_001005471.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:248551784 G>T maps to NM_001005471.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:179248904 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:179248904 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:57327009 T>A maps to NM_006210.2 K934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:57327009 T>A maps to NM_006210.2 K934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:6380271 C>A maps to NM_181876.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:6380271 C>A maps to NM_181876.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:43382251 T>C maps to NM_006905.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:43382251 T>C maps to NM_006905.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:125148923 C>T maps to NM_000962.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:125148923 C>T maps to NM_000962.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:125498171 G>A maps to NM_007218.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:125498171 G>A maps to NM_007218.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:3627798 G>C maps to NM_001011.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:3627798 G>C maps to NM_001011.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:51165488 C>T maps to ENST00000391814 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:51165488 C>T maps to ENST00000391814 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:183486888 G>A maps to ENST00000367537 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:183486888 G>A maps to ENST00000367537 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:64653213 C>A maps to NM_182914.2 R5877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:64653213 C>A maps to NM_182914.2 R5877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:186329116 A>C maps to NM_003292.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:186329116 A>C maps to NM_003292.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:52519938 A>C maps to NM_025040.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:52519938 A>C maps to NM_025040.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156946816 C>T maps to NM_198236.1 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156946816 C>T maps to NM_198236.1 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:66113530 G>T maps to NM_006876.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:66113530 G>T maps to NM_006876.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:75037334 G>A maps to NM_001002912.4 A1353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:75037334 G>A maps to NM_001002912.4 A1353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:95578530 G>A maps to NM_177438.2 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:95578530 G>A maps to NM_177438.2 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:32613909 T>C maps to ENST00000357033 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:32613909 T>C maps to ENST00000357033 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:42552611 T>C maps to NM_019063.3 H720H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:42552611 T>C maps to NM_019063.3 H720H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:13679130 C>A maps to NM_001165035.1 Y1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:13679130 C>A maps to NM_001165035.1 Y1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:121942892 C>T maps to NM_001024613.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:121942892 C>T maps to NM_001024613.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:65652446 C>A maps to NM_198897.1 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:65652446 C>A maps to NM_198897.1 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:14848693 A>G maps to ENST00000380880 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:14848693 A>G maps to ENST00000380880 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:24432686 C>T maps to NM_006277.2 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:24432686 C>T maps to NM_006277.2 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:138554408 T>C maps to NM_001164665.1 V1550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:138554408 T>C maps to NM_001164665.1 V1550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:60907677 C>A maps to NM_005560.3 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:60907677 C>A maps to NM_005560.3 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:95715323 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:95715323 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:47600917 T>A maps to NM_001113498.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:47600917 T>A maps to NM_001113498.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr12:123687367 G>A maps to NM_022782.2 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr12:123687367 G>A maps to NM_022782.2 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:3239234 G>A maps to NM_015419.3 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:3239234 G>A maps to NM_015419.3 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:248737470 G>A maps to NM_001001821.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:248737470 G>A maps to NM_001001821.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:21109019 C>A maps to NM_001001968.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:21109019 C>A maps to NM_001001968.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:57947392 G>T maps to NM_001005212.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:57947392 G>T maps to NM_001005212.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:176738759 A>G maps to NM_020318.2 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:176738759 A>G maps to NM_020318.2 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:4705262 T>C maps to NM_012409.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:4705262 T>C maps to NM_012409.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:30890169 C>T maps to NM_013357.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:30890169 C>T maps to NM_013357.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:36159050 G>A maps to NM_194301.2 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:36159050 G>A maps to NM_194301.2 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:94747221 T>A maps to NM_203390.2 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:94747221 T>A maps to NM_203390.2 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:47158224 G>A maps to NM_014159.6 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:47158224 G>A maps to NM_014159.6 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:38787101 G>A maps to NM_003079.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:38787101 G>A maps to NM_003079.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:112228538 G>A maps to ENST00000391338 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:112228538 G>A maps to ENST00000391338 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:64449506 C>T maps to NM_182914.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:64449506 C>T maps to NM_182914.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:105883920 T>C maps to NM_004257.4 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:105883920 T>C maps to NM_004257.4 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142605735 A>G maps to NM_019841.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142605735 A>G maps to NM_019841.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:34802532 C>T maps to NM_017754.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:34802532 C>T maps to NM_017754.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:234394526 C>T maps to NM_018218.2 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:234394526 C>T maps to NM_018218.2 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:238053779 A>T maps to NM_021186.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:238053779 A>T maps to NM_021186.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:45743341 C>T maps to NM_021116.2 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:45743341 C>T maps to NM_021116.2 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:243663045 T>G maps to NM_181690.1 *466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:243663045 T>G maps to NM_181690.1 *466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:77409634 C>T maps to NM_003664.3 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:77409634 C>T maps to NM_003664.3 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:69002464 C>A maps to NM_001007231.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:69002464 C>A maps to NM_001007231.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:80971347 G>A maps to NM_152446.3 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:80971347 G>A maps to NM_152446.3 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:219824751 G>T maps to NM_003936.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:219824751 G>T maps to NM_003936.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:196794713 G>T maps to NM_002113.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:196794713 G>T maps to NM_002113.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:70793066 T>A maps to NM_016468.5 K102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:70793066 T>A maps to NM_016468.5 K102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:130025023 C>G maps to NM_001868.2 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:130025023 C>G maps to NM_001868.2 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:125685454 G>T maps to NM_178470.4 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:125685454 G>T maps to NM_178470.4 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:34500816 G>T maps to NM_012144.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:34500816 G>T maps to NM_012144.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:186299260 A>G maps to NM_016306.4 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:186299260 A>G maps to NM_016306.4 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:62175544 C>T maps to NM_001433.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:62175544 C>T maps to NM_001433.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:89874754 C>A maps to NM_000135.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:89874754 C>A maps to NM_000135.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:10106487 C>T maps to NM_033084.3 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:10106487 C>T maps to NM_033084.3 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:92531674 A>T maps to ENST00000298047 A1832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:92531674 A>T maps to ENST00000298047 A1832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:54497131 G>T maps to NM_004463.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:54497131 G>T maps to NM_004463.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:72756837 G>T maps to NM_003602.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:72756837 G>T maps to NM_003602.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:114271722 T>A maps to NM_148898.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:114271722 T>A maps to NM_148898.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:70503107 G>A maps to NM_145059.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:70503107 G>A maps to NM_145059.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:46043114 C>A maps to NM_173536.3 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:46043114 C>A maps to NM_173536.3 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr21:34117918 G>A maps to NM_016631.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr21:34117918 G>A maps to NM_016631.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:44189440 C>T maps to NM_000162.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:44189440 C>T maps to NM_000162.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:135431774 C>T maps to NM_153834.3 D1970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:135431774 C>T maps to NM_153834.3 D1970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:131486900 G>T maps to NM_207364.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:131486900 G>T maps to NM_207364.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:43882165 G>A maps to NM_001098204.1 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:43882165 G>A maps to NM_001098204.1 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:118824885 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:118824885 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:65702514 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:65702514 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:137323090 C>T maps to NM_014432.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:137323090 C>T maps to NM_014432.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:10602718 T>A maps to NM_203500.1 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:10602718 T>A maps to NM_203500.1 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:2597327 G>A maps to NM_015229.3 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:2597327 G>A maps to NM_015229.3 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:118222822 C>A maps to NM_020721.1 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:118222822 C>A maps to NM_020721.1 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:55294944 G>A maps to ENST00000291633 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:55294944 G>A maps to ENST00000291633 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:55467748 G>C maps to NM_018697.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:55467748 G>C maps to NM_018697.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:169701311 G>T maps to NM_005565.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:169701311 G>T maps to NM_005565.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:129905762 A>G maps to NM_002417.4 S1447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:129905762 A>G maps to NM_002417.4 S1447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:86437739 C>T maps to NM_016622.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:86437739 C>T maps to NM_016622.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:158468324 C>T maps to NM_017760.5 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:158468324 C>T maps to NM_017760.5 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:45209815 G>T maps to NM_001145107.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:45209815 G>T maps to NM_001145107.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:44579149 C>T maps to NM_013389.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:44579149 C>T maps to NM_013389.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:156834151 C>A maps to NM_002529.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:156834151 C>A maps to NM_002529.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:56875615 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:56875615 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:5443900 G>A maps to NM_001004757.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:5443900 G>A maps to NM_001004757.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:3591920 T>A maps to ENST00000435558 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:3591920 T>A maps to ENST00000435558 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:205986567 C>T maps to ENST00000406610 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:205986567 C>T maps to ENST00000406610 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:140216112 G>T maps to NM_018910.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:140216112 G>T maps to NM_018910.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:140574290 C>T maps to NM_018930.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:140574290 C>T maps to NM_018930.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:71114207 G>A maps to NM_021965.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:71114207 G>A maps to NM_021965.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:32130714 T>G maps to NM_138717.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:32130714 T>G maps to NM_138717.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:68882017 G>T maps to NM_138964.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:68882017 G>T maps to NM_138964.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:8339046 C>A maps to NM_002839.3 E1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:8339046 C>A maps to NM_002839.3 E1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:1668736 G>T maps to NM_012293.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:1668736 G>T maps to NM_012293.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:37735014 A>T maps to NM_001002814.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:37735014 A>T maps to NM_001002814.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:173953757 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:173953757 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:59483585 C>T maps to NM_173557.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:59483585 C>T maps to NM_173557.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:115783391 G>A maps to ENST00000257414 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:115783391 G>A maps to ENST00000257414 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:72138120 A>G maps to NM_015556.1 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:72138120 A>G maps to NM_015556.1 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:139742047 G>T maps to ENST00000507527 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:139742047 G>T maps to ENST00000507527 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:228882329 G>T maps to NM_001142644.1 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:228882329 G>T maps to NM_001142644.1 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:228884753 G>T maps to NM_001142644.1 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:228884753 G>T maps to NM_001142644.1 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:53079523 C>T maps to NM_014682.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:53079523 C>T maps to NM_014682.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:52546616 G>T maps to NM_015136.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:52546616 G>T maps to NM_015136.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:33194356 C>A maps to NM_015551.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:33194356 C>A maps to NM_015551.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:46961993 C>A maps to NM_031912.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:46961993 C>A maps to NM_031912.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:44560051 C>A maps to NM_016427.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:44560051 C>A maps to NM_016427.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65194245 A>G maps to NM_001010874.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65194245 A>G maps to NM_001010874.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:50791329 C>T maps to ENST00000263046 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:50791329 C>T maps to ENST00000263046 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:64202607 G>A maps to NM_014254.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:64202607 G>A maps to NM_014254.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:22880393 A>G maps to NM_003842.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:22880393 A>G maps to NM_003842.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:175334161 C>A maps to NM_003285.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:175334161 C>A maps to NM_003285.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:117660812 C>T maps to NM_025188.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:117660812 C>T maps to NM_025188.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:135278198 C>A maps to NM_007344.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:135278198 C>A maps to NM_007344.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:33639781 C>T maps to NM_173479.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:33639781 C>T maps to NM_173479.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:62421978 C>T maps to NM_025224.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:62421978 C>T maps to NM_025224.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:27419485 C>A maps to NM_007149.2 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:27419485 C>A maps to NM_007149.2 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:22805481 G>A maps to NM_015461.2 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:22805481 G>A maps to NM_015461.2 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:80789580 G>A maps to NM_024702.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:80789580 G>A maps to NM_024702.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:134427883 G>T maps to NM_007131.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:134427883 G>T maps to NM_007131.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:149545229 G>T maps to NM_001099220.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:149545229 G>T maps to NM_001099220.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:6324698 C>T maps to NM_007274.3 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:6324698 C>T maps to NM_007274.3 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:128983510 C>T maps to NM_133638.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:128983510 C>T maps to NM_133638.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:198051746 C>A maps to NM_001195144.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:198051746 C>A maps to NM_001195144.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:3002443 C>G maps to NM_004042.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:3002443 C>G maps to NM_004042.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:1391253 G>T maps to NM_001039211.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:1391253 G>T maps to NM_001039211.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:160093740 G>C maps to NM_000702.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:160093740 G>C maps to NM_000702.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:136597096 T>G maps to NM_014739.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:136597096 T>G maps to NM_014739.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:29830978 G>A maps to NM_024516.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:29830978 G>A maps to NM_024516.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:170934302 G>T maps to NM_001163629.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:170934302 G>T maps to NM_001163629.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:90573713 C>T maps to NM_012115.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:90573713 C>T maps to NM_012115.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:16593878 A>G maps to NM_014695.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:16593878 A>G maps to NM_014695.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:88104802 C>A maps to NM_001195308.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:88104802 C>A maps to NM_001195308.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr13:53036657 A>T maps to NM_001098525.1 K422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr13:53036657 A>T maps to NM_001098525.1 K422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:137646163 G>T maps to NM_000093.3 G607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:137646163 G>T maps to NM_000093.3 G607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:65509419 T>A maps to NM_004820.3 K434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:65509419 T>A maps to NM_004820.3 K434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:124311322 C>G maps to NM_207437.3 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:124311322 C>G maps to NM_207437.3 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:26501588 C>T maps to NM_001197293.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:26501588 C>T maps to NM_001197293.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:132982804 G>C maps to NM_015137.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:132982804 G>C maps to NM_015137.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:124195476 C>G maps to NM_032899.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:124195476 C>G maps to NM_032899.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:127728882 G>A maps to NM_001999.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:127728882 G>A maps to NM_001999.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:1611204 G>A maps to NM_001453.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:1611204 G>A maps to NM_001453.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:69965137 G>A maps to NM_006654.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:69965137 G>A maps to NM_006654.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:3879428 C>T maps to NM_001042413.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:3879428 C>T maps to NM_001042413.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:97247415 T>A maps to NM_030784.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:97247415 T>A maps to NM_030784.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:46943705 C>T maps to NM_133443.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:46943705 C>T maps to NM_133443.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:27483124 C>T maps to NM_001520.3 K1490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:27483124 C>T maps to NM_001520.3 K1490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:43592281 G>A maps to NM_019096.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:43592281 G>A maps to NM_019096.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:145039891 T>C maps to NM_002099.6 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:145039891 T>C maps to NM_002099.6 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:27147767 G>A maps to NM_153631.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:27147767 G>A maps to NM_153631.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:107975899 G>T maps to NM_003604.2 P1225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:107975899 G>T maps to NM_003604.2 P1225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:155711658 C>G maps to NM_002239.2 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:155711658 C>G maps to NM_002239.2 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr20:36856551 G>A maps to NM_001029864.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr20:36856551 G>A maps to NM_001029864.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr22:34157356 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr22:34157356 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:3701698 G>T maps to NM_020710.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:3701698 G>T maps to NM_020710.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:1940362 C>A maps to NM_001163926.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:1940362 C>A maps to NM_001163926.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:39090622 G>C maps to NM_001042600.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:39090622 G>C maps to NM_001042600.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:57910303 A>G maps to NM_004990.2 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:57910303 A>G maps to NM_004990.2 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:90365609 C>G maps to NM_014611.1 L5121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:90365609 C>G maps to NM_014611.1 L5121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:116412044 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:116412044 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:131557475 C>A maps to NM_002412.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:131557475 C>A maps to NM_002412.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:59949119 G>A maps to NM_152852.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:59949119 G>A maps to NM_152852.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:10426899 G>T maps to NM_017534.5 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:10426899 G>T maps to NM_017534.5 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:10535213 A>G maps to NM_002470.2 T1692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:10535213 A>G maps to NM_002470.2 T1692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:55594984 C>T maps to NM_001004739.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:55594984 C>T maps to NM_001004739.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:3802230 G>A maps to NM_002558.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:3802230 G>A maps to NM_002558.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:90690800 C>A maps to NM_080832.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:90690800 C>A maps to NM_080832.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140432183 C>A maps to NM_013340.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140432183 C>A maps to NM_013340.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140788221 A>T maps to NM_018926.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140788221 A>T maps to NM_018926.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:47882625 C>T maps to NM_138295.3 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:47882625 C>T maps to NM_138295.3 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:102494219 C>G maps to ENST00000451606 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:102494219 C>G maps to ENST00000451606 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:43359836 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:43359836 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:104314735 G>A maps to NM_019592.5 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:104314735 G>A maps to NM_019592.5 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:60168855 T>C maps to NM_004731.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:60168855 T>C maps to NM_004731.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:176825193 G>A maps to NM_003052.4 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:176825193 G>A maps to NM_003052.4 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:220337807 G>A maps to NM_005876.4 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:220337807 G>A maps to NM_005876.4 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr20:57242592 A>G maps to NM_001001433.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr20:57242592 A>G maps to NM_001001433.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:50384657 G>T maps to NM_024682.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:50384657 G>T maps to NM_024682.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:152060547 G>A maps to NM_001008536.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:152060547 G>A maps to NM_001008536.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:105924095 G>A maps to NM_004257.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:105924095 G>A maps to NM_004257.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:169650864 C>A maps to NM_003247.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:169650864 C>A maps to NM_003247.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:52486122 G>A maps to NM_003280.2 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:52486122 G>A maps to NM_003280.2 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:189063533 G>A maps to NM_178556.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:189063533 G>A maps to NM_178556.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:10755668 C>T maps to NM_173683.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:10755668 C>T maps to NM_173683.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:50070835 A>G maps to NM_007009.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:50070835 A>G maps to NM_007009.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:109678884 C>T maps to NM_001093.3 I1607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:109678884 C>T maps to NM_001093.3 I1607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:17378832 C>T maps to NM_001621.4 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:17378832 C>T maps to NM_001621.4 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:73956684 T>C maps to NM_032217.3 L2220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:73956684 T>C maps to NM_032217.3 L2220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:138844208 T>A maps to NM_173694.4 K854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:138844208 T>A maps to NM_173694.4 K854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:58022665 G>A maps to NM_001478.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:58022665 G>A maps to NM_001478.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:37180986 G>A maps to NM_023073.3 Q1848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:37180986 G>A maps to NM_023073.3 Q1848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:27459322 C>A maps to NM_004341.3 R1416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:27459322 C>A maps to NM_004341.3 R1416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:205496950 C>T maps to NM_212503.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:205496950 C>T maps to NM_212503.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:120142200 G>A maps to ENST00000392521 Y1757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:120142200 G>A maps to ENST00000392521 Y1757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:121929697 G>A maps to NM_014618.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:121929697 G>A maps to NM_014618.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:50136331 G>T maps to NM_001013742.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:50136331 G>T maps to NM_001013742.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:63411834 A>T maps to NM_152424.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:63411834 A>T maps to NM_152424.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:131520208 G>A maps to NM_001105195.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:131520208 G>A maps to NM_001105195.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:75537607 C>G maps to NM_024643.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:75537607 C>G maps to NM_024643.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:50513041 A>G maps to NM_022116.3 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:50513041 A>G maps to NM_022116.3 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:86088907 C>G maps to NM_013231.4 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:86088907 C>G maps to NM_013231.4 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:143921918 C>A maps to NM_002066.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:143921918 C>A maps to NM_002066.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:57389031 G>A maps to NM_007264.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:57389031 G>A maps to NM_007264.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:28377244 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:28377244 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:2461330 C>T maps to NM_001010926.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:2461330 C>T maps to NM_001010926.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:84216630 G>A maps to NM_006665.5 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:84216630 G>A maps to NM_006665.5 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:155233497 G>T maps to NM_002186.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:155233497 G>T maps to NM_002186.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:123258168 A>T maps to NM_015312.3 R4048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:123258168 A>T maps to NM_015312.3 R4048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:55146164 C>A maps to ENST00000427581 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:55146164 C>A maps to ENST00000427581 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:28319113 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:28319113 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:110791169 C>G maps to NM_198506.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:110791169 C>G maps to NM_198506.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:119670167 C>A maps to NM_005907.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:119670167 C>A maps to NM_005907.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:10393427 A>G maps to NM_170784.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:10393427 A>G maps to NM_170784.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:3108180 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:3108180 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:65308839 A>G maps to NM_139242.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:65308839 A>G maps to NM_139242.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:195487839 A>T maps to NM_018406.5 Y4921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:195487839 A>T maps to NM_018406.5 Y4921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:81110974 G>T maps to NM_005593.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:81110974 G>T maps to NM_005593.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:101756964 G>T maps to NM_052867.2 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:101756964 G>T maps to NM_052867.2 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:113076266 G>A maps to ENST00000316851 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:113076266 G>A maps to ENST00000316851 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:2616503 G>A maps to NM_006101.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:2616503 G>A maps to NM_006101.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:203465261 T>C maps to NM_014359.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:203465261 T>C maps to NM_014359.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:55371129 A>T maps to NM_001004700.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:55371129 A>T maps to NM_001004700.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:22369228 T>C maps to NM_001004719.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:22369228 T>C maps to NM_001004719.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:6191451 G>A maps to NM_001004052.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:6191451 G>A maps to NM_001004052.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:56510969 G>C maps to NM_001005284.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:56510969 G>C maps to NM_001005284.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:140811193 C>T maps to NM_003735.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:140811193 C>T maps to NM_003735.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:140731740 G>T maps to NM_018922.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:140731740 G>T maps to NM_018922.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:82580372 C>A maps to NM_033026.5 T3177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:82580372 C>A maps to NM_033026.5 T3177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:18524164 T>A maps to NM_004570.4 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:18524164 T>A maps to NM_004570.4 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:103339272 A>G maps to NM_013274.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:103339272 A>G maps to NM_013274.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:11508472 C>A maps to NM_005039.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:11508472 C>A maps to NM_005039.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:151372616 G>T maps to NM_016203.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:151372616 G>T maps to NM_016203.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:33764040 C>T maps to NM_006404.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:33764040 C>T maps to NM_006404.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:23511886 C>A maps to NM_001099780.1 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:23511886 C>A maps to NM_001099780.1 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:62164020 C>T maps to NM_005975.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:62164020 C>T maps to NM_005975.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:103275984 C>A maps to ENST00000428762 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:103275984 C>A maps to ENST00000428762 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:48058842 C>T maps to NM_153618.1 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:48058842 C>T maps to NM_153618.1 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:42643041 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:42643041 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:156238163 G>C maps to NM_015327.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:156238163 G>C maps to NM_015327.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:34926906 T>C maps to NM_138927.1 Y1790Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:34926906 T>C maps to NM_138927.1 Y1790Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:1278791 G>A maps to NM_198253.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:1278791 G>A maps to NM_198253.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:24828155 A>G maps to NM_014494.2 P1617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:24828155 A>G maps to NM_014494.2 P1617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:82834299 T>C maps to NM_004385.4 R1826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:82834299 T>C maps to NM_004385.4 R1826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:100514084 A>G maps to NM_017890.3 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:100514084 A>G maps to NM_017890.3 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:85561660 G>A maps to NM_145172.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:85561660 G>A maps to NM_145172.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:38121741 C>A maps to NM_021045.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:38121741 C>A maps to NM_021045.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:58862862 C>A maps to NM_130786.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:58862862 C>A maps to NM_130786.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:3655285 G>T maps to NM_025220.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:3655285 G>T maps to NM_025220.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:236957736 C>T maps to NM_001037131.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:236957736 C>T maps to NM_001037131.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:85677632 G>A maps to NM_006982.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:85677632 G>A maps to NM_006982.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:41572556 G>A maps to ENST00000415018 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:41572556 G>A maps to ENST00000415018 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:52284752 C>A maps to NM_182608.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:52284752 C>A maps to NM_182608.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:197872648 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:197872648 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:77409607 T>A maps to NM_003664.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:77409607 T>A maps to NM_003664.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:58524942 C>T maps to NM_006380.2 *586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:58524942 C>T maps to NM_006380.2 *586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:25235822 C>T maps to NM_001169.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:25235822 C>T maps to NM_001169.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:68179363 C>A maps to NM_006421.3 G592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:68179363 C>A maps to NM_006421.3 G592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:93761926 G>A maps to NM_182896.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:93761926 G>A maps to NM_182896.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:215595193 C>A maps to NM_000465.2 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:215595193 C>A maps to NM_000465.2 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:107391908 G>A maps to NM_001080450.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:107391908 G>A maps to NM_001080450.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:60549173 T>A maps to NM_001080512.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:60549173 T>A maps to NM_001080512.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:76121287 G>A maps to NM_007176.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:76121287 G>A maps to NM_007176.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:34378462 C>A maps to NM_015476.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:34378462 C>A maps to NM_015476.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:185153462 A>G maps to NM_001105518.1 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:185153462 A>G maps to NM_001105518.1 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:156704033 G>C maps to NM_015997.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:156704033 G>C maps to NM_015997.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:744287 G>A maps to NM_033409.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:744287 G>A maps to NM_033409.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:124251333 G>C maps to NM_032847.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:124251333 G>C maps to NM_032847.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:39315948 G>T maps to NM_001737.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:39315948 G>T maps to NM_001737.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:86249254 G>A maps to NM_001738.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:86249254 G>A maps to NM_001738.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:122003878 C>A maps to NM_001178065.1 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:122003878 C>A maps to NM_001178065.1 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119528 C>T maps to NM_001080850.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119528 C>T maps to NM_001080850.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:126152007 C>A maps to ENST00000505024 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:126152007 C>A maps to ENST00000505024 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:63898445 C>A maps to NM_145036.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:63898445 C>A maps to NM_145036.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100598747 G>T maps to NM_019083.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100598747 G>T maps to NM_019083.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:41822728 C>T maps to NM_052848.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:41822728 C>T maps to NM_052848.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7548877 A>T maps to ENST00000416109 C631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7548877 A>T maps to ENST00000416109 C631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:117078850 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:117078850 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:64981814 T>C maps to NM_001797.2 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:64981814 T>C maps to NM_001797.2 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:59221444 C>A maps to NM_031891.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:59221444 C>A maps to NM_031891.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:202700487 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:202700487 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:81053853 G>C maps to NM_001100624.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:81053853 G>C maps to NM_001100624.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:243327604 T>C maps to NM_014812.2 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:243327604 T>C maps to NM_014812.2 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:87040314 C>G maps to ENST00000263723 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:87040314 C>G maps to ENST00000263723 L520L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-75-5126-01A-01D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-75-5126-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:209007475 G>A maps to NM_005210.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:209007475 G>A maps to NM_005210.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:75974657 G>T maps to NM_001897.4 A1642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:75974657 G>T maps to NM_001897.4 A1642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:166535348 G>T maps to ENST00000409420 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:166535348 G>T maps to ENST00000409420 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:23420936 G>T maps to NM_138283.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:23420936 G>T maps to NM_138283.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:66333335 G>A maps to NM_003793.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:66333335 G>A maps to NM_003793.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:36091443 G>T maps to NM_173695.2 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:36091443 G>T maps to NM_173695.2 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:125298988 G>T maps to NM_001013628.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:125298988 G>T maps to NM_001013628.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:36401821 C>A maps to NM_004734.4 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:36401821 C>A maps to NM_004734.4 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:23678455 G>T maps to NM_032486.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:23678455 G>T maps to NM_032486.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:110714394 G>C maps to NM_003649.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:110714394 G>C maps to NM_003649.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:32492479 G>A maps to NM_014314.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:32492479 G>A maps to NM_014314.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:14775747 A>T maps to NM_004080.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:14775747 A>T maps to NM_004080.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7736528 G>A maps to NM_020877.2 K4373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7736528 G>A maps to NM_020877.2 K4373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:65864514 G>A maps to ENST00000371069 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:65864514 G>A maps to ENST00000371069 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:37661498 T>C maps to NM_005128.2 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:37661498 T>C maps to NM_005128.2 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:41539174 T>G maps to NM_001389.3 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:41539174 T>G maps to NM_001389.3 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:41684034 C>A maps to NM_001389.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:41684034 C>A maps to NM_001389.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:103057206 A>T maps to NM_001080463.1 V2290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:103057206 A>T maps to NM_001080463.1 V2290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6903851 C>T maps to ENST00000381407 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6903851 C>T maps to ENST00000381407 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:83381179 G>A maps to NM_021204.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:83381179 G>A maps to NM_021204.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:47601118 G>A maps to ENST00000426238 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:47601118 G>A maps to ENST00000426238 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:66356383 A>G maps to NM_004439.5 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:66356383 A>G maps to NM_004439.5 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:97167455 C>A maps to NM_001080448.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:97167455 C>A maps to NM_001080448.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:37034181 C>G maps to NM_014805.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:37034181 C>G maps to NM_014805.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:68268005 G>C maps to NM_024939.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:68268005 G>C maps to NM_024939.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:201853121 G>C maps to NM_173822.3 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:201853121 G>C maps to NM_173822.3 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:139163753 A>T maps to NM_015912.3 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:139163753 A>T maps to NM_015912.3 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:37029545 T>A maps to NM_001013736.2 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:37029545 T>A maps to NM_001013736.2 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:177249712 C>T maps to NM_021165.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:177249712 C>T maps to NM_021165.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:37580295 C>T maps to NM_030919.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:37580295 C>T maps to NM_030919.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10105579 G>T maps to NM_033084.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10105579 G>T maps to NM_033084.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:126373661 G>T maps to NM_024582.4 E3831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:126373661 G>T maps to NM_024582.4 E3831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127595410 G>T maps to NM_001999.3 I2825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127595410 G>T maps to NM_001999.3 I2825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127648324 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127648324 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:109724461 G>T maps to NM_213596.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:109724461 G>T maps to NM_213596.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:30433373 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:30433373 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:180667012 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:180667012 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:46053638 C>A maps to NM_173536.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:46053638 C>A maps to NM_173536.3 L311L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-75-5126-01A-01D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-75-5126-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:150389658 G>A maps to NM_015660.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:150389658 G>A maps to NM_015660.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:150174462 G>A maps to NM_175571.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:150174462 G>A maps to NM_175571.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:42085016 C>A maps to NM_000168.5 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:42085016 C>A maps to NM_000168.5 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:32126341 C>G maps to NM_022130.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:32126341 C>G maps to NM_022130.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:135455156 G>A maps to NM_153834.3 R2570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:135455156 G>A maps to NM_153834.3 R2570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815043 G>A maps to NM_006143.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815043 G>A maps to NM_006143.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815115 G>A maps to NM_006143.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815115 G>A maps to NM_006143.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815159 G>A maps to NM_006143.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815159 G>A maps to NM_006143.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:94377046 C>A maps to NM_001510.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:94377046 C>A maps to NM_001510.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:114279888 G>A maps to ENST00000398283 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:114279888 G>A maps to ENST00000398283 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:65480009 G>A maps to NM_138737.3 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:65480009 G>A maps to NM_138737.3 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:65480069 C>A maps to NM_138737.3 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:65480069 C>A maps to NM_138737.3 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:33308506 C>T maps to NM_005734.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:33308506 C>T maps to NM_005734.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:148791110 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:148791110 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:186141244 G>T maps to NM_031935.2 E5266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:186141244 G>T maps to NM_031935.2 E5266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:35661014 C>T maps to NM_001003681.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:35661014 C>T maps to NM_001003681.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:162900477 G>A maps to NM_001142556.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:162900477 G>A maps to NM_001142556.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:63256904 G>C maps to NM_000524.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:63256904 G>C maps to NM_000524.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:113775683 G>A maps to NM_006028.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:113775683 G>A maps to NM_006028.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:38835502 C>A maps to NM_153692.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:38835502 C>A maps to NM_153692.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:3137636 G>T maps to NM_002111.6 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:3137636 G>T maps to NM_002111.6 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:130417005 G>A maps to NM_001170961.1 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:130417005 G>A maps to NM_001170961.1 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:61923141 C>T maps to NM_001134779.1 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:61923141 C>T maps to NM_001134779.1 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:237272521 G>A maps to ENST00000457693 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:237272521 G>A maps to ENST00000457693 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:44223192 G>A maps to NM_019612.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:44223192 G>A maps to NM_019612.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:182339986 G>T maps to NM_000885.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:182339986 G>T maps to NM_000885.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:31277364 C>A maps to NM_001145808.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:31277364 C>A maps to NM_001145808.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:75434878 A>T maps to ENST00000341669 *630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:75434878 A>T maps to ENST00000341669 *630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:8785984 G>T maps to ENST00000456698 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:8785984 G>T maps to ENST00000456698 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:226446721 C>A maps to NM_020864.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:226446721 C>A maps to NM_020864.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:21334825 G>A maps to NM_018847.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:21334825 G>A maps to NM_018847.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:46000335 G>A maps to NM_198694.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:46000335 G>A maps to NM_198694.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:31973474 C>T maps to NM_181620.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:31973474 C>T maps to NM_181620.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:60889908 G>A maps to NM_005560.3 A2714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:60889908 G>A maps to NM_005560.3 A2714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:136555642 C>A maps to NM_002299.2 T1644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:136555642 C>A maps to NM_002299.2 T1644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43215926 C>T maps to NM_022356.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43215926 C>T maps to NM_022356.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:105474274 G>T maps to NM_001004317.2 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:105474274 G>T maps to NM_001004317.2 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:13183414 G>T maps to NM_001136561.2 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:13183414 G>T maps to NM_001136561.2 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100174740 C>A maps to NM_002319.3 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100174740 C>A maps to NM_002319.3 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:141474374 G>T maps to NM_018557.2 T1923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:141474374 G>T maps to NM_018557.2 T1923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57588393 C>T maps to NM_002332.2 F2701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57588393 C>T maps to NM_002332.2 F2701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57590050 C>A maps to NM_002332.2 I2961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57590050 C>A maps to NM_002332.2 I2961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:102763280 G>A maps to NM_032429.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:102763280 G>A maps to NM_032429.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:30254209 A>C maps to NM_002365.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:30254209 A>C maps to NM_002365.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:36640514 C>T maps to NM_018067.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:36640514 C>T maps to NM_018067.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:66055637 G>C maps to NM_001164664.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:66055637 G>C maps to NM_001164664.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:149247497 G>T maps to ENST00000404807 E1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:149247497 G>T maps to ENST00000404807 E1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119183320 C>A maps to NM_006500.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119183320 C>A maps to NM_006500.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:138713552 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:138713552 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:129913971 C>A maps to NM_002417.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:129913971 C>A maps to NM_002417.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:104749462 C>G maps to NM_182931.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:104749462 C>G maps to NM_182931.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6222227 C>A maps to NM_005934.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6222227 C>A maps to NM_005934.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220970053 G>T maps to NM_022746.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220970053 G>T maps to NM_022746.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:18194907 C>A maps to NM_054032.3 C35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:18194907 C>A maps to NM_054032.3 C35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:72754967 C>T maps to NM_005098.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:72754967 C>T maps to NM_005098.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:128393796 C>A maps to ENST00000389524 A1982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:128393796 C>A maps to ENST00000389524 A1982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:1926883 G>A maps to ENST00000399161 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:1926883 G>A maps to ENST00000399161 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:89896520 T>C maps to NM_005467.3 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:89896520 T>C maps to NM_005467.3 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:97031790 C>T maps to NM_015341.3 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:97031790 C>T maps to NM_015341.3 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:69724897 G>A maps to NM_138713.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:69724897 G>A maps to NM_138713.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:173998674 C>G maps to NM_014932.2 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:173998674 C>G maps to NM_014932.2 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56424210 C>T maps to NM_176810.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56424210 C>T maps to NM_176810.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:7070901 G>T maps to NM_176822.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:7070901 G>T maps to NM_176822.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:247588856 G>C maps to NM_004895.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:247588856 G>C maps to NM_004895.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56244353 T>C maps to NM_176820.2 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56244353 T>C maps to NM_176820.2 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:96099594 C>T maps to NM_022451.9 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:96099594 C>T maps to NM_022451.9 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:30475651 C>T maps to NM_006092.2 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:30475651 C>T maps to NM_006092.2 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:50745463 C>T maps to NM_022162.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:50745463 C>T maps to NM_022162.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:170819786 G>T maps to NM_002520.6 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:170819786 G>T maps to NM_002520.6 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:129350355 C>A maps to ENST00000393231 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:129350355 C>A maps to ENST00000393231 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:57970864 C>A maps to NM_001004459.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:57970864 C>A maps to NM_001004459.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:27879653 G>T maps to NM_033057.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:27879653 G>T maps to NM_033057.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:56247936 T>A maps to NM_001004707.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:56247936 T>A maps to NM_001004707.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20444456 C>A maps to NM_001005486.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20444456 C>A maps to NM_001005486.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55405904 C>T maps to NM_001004124.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55405904 C>T maps to NM_001004124.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55703123 C>A maps to NM_006637.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55703123 C>A maps to NM_006637.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55860791 C>A maps to NM_001003750.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55860791 C>A maps to NM_001003750.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:58209169 G>C maps to NM_001040429.2 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:58209169 G>C maps to NM_001040429.2 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:61986226 C>A maps to NM_022843.3 G669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:61986226 C>A maps to NM_022843.3 G669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140166213 G>A maps to NM_018900.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140166213 G>A maps to NM_018900.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140207687 C>A maps to NM_018909.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140207687 C>A maps to NM_018909.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140209901 C>A maps to NM_018909.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140209901 C>A maps to NM_018909.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140433274 G>A maps to NM_013340.2 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140433274 G>A maps to NM_013340.2 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140755008 C>G maps to NM_018919.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140755008 C>G maps to NM_018919.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:76709007 C>T maps to NM_003719.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:76709007 C>T maps to NM_003719.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:153270488 C>T maps to NM_052891.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:153270488 C>T maps to NM_052891.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:71701198 C>A maps to NM_015020.2 G556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:71701198 C>A maps to NM_015020.2 G556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:171395354 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:171395354 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:50724455 G>T maps to NM_012401.2 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:50724455 G>T maps to NM_012401.2 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:129284182 C>A maps to NM_015103.2 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:129284182 C>A maps to NM_015103.2 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:22330211 C>T maps to NM_018119.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:22330211 C>T maps to NM_018119.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:12887652 G>A maps to NM_001146344.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:12887652 G>A maps to NM_001146344.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:47265956 C>A maps to NM_020820.3 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:47265956 C>A maps to NM_020820.3 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:32117103 G>T maps to NM_030651.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:32117103 G>T maps to NM_030651.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:31095548 G>A maps to NM_001039503.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:31095548 G>A maps to NM_001039503.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:112891115 T>C maps to ENST00000392596 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:112891115 T>C maps to ENST00000392596 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:198668739 C>T maps to ENST00000271610 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:198668739 C>T maps to ENST00000271610 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:8507348 G>A maps to NM_002839.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:8507348 G>A maps to NM_002839.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:45389235 G>A maps to NM_001042724.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:45389235 G>A maps to NM_001042724.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:52336216 C>G maps to NM_144651.4 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:52336216 C>G maps to NM_144651.4 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:53487409 C>T maps to NM_005611.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:53487409 C>T maps to NM_005611.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103194237 G>T maps to ENST00000428762 I1946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103194237 G>T maps to ENST00000428762 I1946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103363605 A>G maps to ENST00000428762 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103363605 A>G maps to ENST00000428762 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:32589120 C>A maps to NM_001098527.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:32589120 C>A maps to NM_001098527.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:21052078 T>A maps to NM_145250.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:21052078 T>A maps to NM_145250.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:141457358 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:141457358 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:42851244 C>T maps to NM_198486.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:42851244 C>T maps to NM_198486.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:149826405 G>A maps to NM_005617.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:149826405 G>A maps to NM_005617.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100732077 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100732077 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:38931491 T>C maps to NM_000540.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:38931491 T>C maps to NM_000540.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:10625651 G>A maps to NM_001166215.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:10625651 G>A maps to NM_001166215.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:153835563 G>T maps to NM_024632.5 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:153835563 G>T maps to NM_024632.5 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:78167669 C>T maps to NM_144777.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:78167669 C>T maps to NM_144777.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:62186608 C>G maps to NM_003357.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:62186608 C>G maps to NM_003357.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:166900550 C>T maps to NM_001165963.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:166900550 C>T maps to NM_001165963.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:38592195 G>A maps to NM_001099404.1 Y1889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:38592195 G>A maps to NM_001099404.1 Y1889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:6483727 C>A maps to NM_001159576.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:6483727 C>A maps to NM_001159576.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:144874230 C>A maps to NM_182706.3 T1529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:144874230 C>A maps to NM_182706.3 T1529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:42533252 C>A maps to NM_015559.2 A1316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:42533252 C>A maps to NM_015559.2 A1316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:47161675 C>A maps to NM_014159.6 E1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:47161675 C>A maps to NM_014159.6 E1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:77471963 G>A maps to NM_024776.2 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:77471963 G>A maps to NM_024776.2 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:148406268 C>T maps to NM_024577.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:148406268 C>T maps to NM_024577.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:157820468 G>A maps to NM_003030.4 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:157820468 G>A maps to NM_003030.4 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:49938489 A>G maps to NM_020309.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:49938489 A>G maps to NM_020309.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:50820237 G>T maps to NM_003055.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:50820237 G>T maps to NM_003055.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:33947354 C>A maps to NM_016180.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:33947354 C>A maps to NM_016180.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:142228199 G>C maps to NM_001080431.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:142228199 G>C maps to NM_001080431.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:21422676 T>A maps to NM_134431.3 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:21422676 T>A maps to NM_134431.3 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:41486212 G>C maps to NM_144990.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:41486212 G>C maps to NM_144990.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:98781169 C>A maps to NM_003061.2 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:98781169 C>A maps to NM_003061.2 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:214215335 G>T maps to NM_024532.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:214215335 G>T maps to NM_024532.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:107460127 G>T maps to NM_001142351.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:107460127 G>T maps to NM_001142351.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37096800 G>C maps to NM_003162.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37096800 G>C maps to NM_003162.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:120998689 G>T maps to NM_005422.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:120998689 G>T maps to NM_005422.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841880 G>C maps to NM_007110.4 S2187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841880 G>C maps to NM_007110.4 S2187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20843946 G>A maps to NM_007110.4 V2110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20843946 G>A maps to NM_007110.4 V2110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:30694317 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:30694317 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:95231009 T>A maps to NM_014305.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:95231009 T>A maps to NM_014305.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:32492987 G>A maps to NM_003253.2 Q1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:32492987 G>A maps to NM_003253.2 Q1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:167020571 C>T maps to ENST00000507499 Q957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:167020571 C>T maps to ENST00000507499 Q957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:35704722 G>A maps to NM_006289.3 P1941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:35704722 G>A maps to NM_006289.3 P1941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:98446203 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:98446203 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:129822343 G>T maps to NM_133448.2 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:129822343 G>T maps to NM_133448.2 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:44107258 C>T maps to NM_018426.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:44107258 C>T maps to NM_018426.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:68846406 C>T maps to NM_139075.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:68846406 C>T maps to NM_139075.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103290629 C>A maps to ENST00000376052 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103290629 C>A maps to ENST00000376052 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:123675734 C>G maps to NM_001190945.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:123675734 C>G maps to NM_001190945.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:230661451 G>C maps to ENST00000389044 S1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:230661451 G>C maps to ENST00000389044 S1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:234878913 C>A maps to NM_024080.4 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:234878913 C>A maps to NM_024080.4 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:231700290 G>A maps to NM_005999.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:231700290 G>A maps to NM_005999.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:76330043 G>T maps to NM_015072.4 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:76330043 G>T maps to NM_015072.4 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:132237811 G>A maps to NM_080386.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:132237811 G>A maps to NM_080386.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:57599126 G>A maps to NM_030773.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:57599126 G>A maps to NM_030773.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:54307661 G>T maps to ENST00000260323 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:54307661 G>T maps to ENST00000260323 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:75852455 G>T maps to NM_003369.3 *700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:75852455 G>T maps to NM_003369.3 *700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:87018165 G>A maps to NM_016206.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:87018165 G>A maps to NM_016206.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:53770282 C>A maps to NM_173857.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:53770282 C>A maps to NM_173857.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:133072640 T>A maps to NM_004665.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:133072640 T>A maps to NM_004665.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:62202475 G>C maps to NM_020821.2 S2915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:62202475 G>C maps to NM_020821.2 S2915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:113128134 A>G maps to NM_001164496.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:113128134 A>G maps to NM_001164496.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:54358457 C>T maps to NM_015285.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:54358457 C>T maps to NM_015285.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:40948568 G>C maps to NM_032387.4 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:40948568 G>C maps to NM_032387.4 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:168108196 C>A maps to NM_152381.5 S3432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:168108196 C>A maps to NM_152381.5 S3432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:41282318 G>T maps to NM_022098.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:41282318 G>T maps to NM_022098.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:135744682 A>G maps to NM_025052.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:135744682 A>G maps to NM_025052.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100364792 G>T maps to ENST00000349350 G1591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100364792 G>T maps to ENST00000349350 G1591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:167016161 C>A maps to ENST00000307529 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:167016161 C>A maps to ENST00000307529 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:77912981 G>T maps to NM_152694.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:77912981 G>T maps to NM_152694.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:135614083 C>A maps to NM_020863.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:135614083 C>A maps to NM_020863.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72004835 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72004835 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:40758301 A>G maps to NM_005857.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:40758301 A>G maps to NM_005857.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:58216287 A>T maps to NM_001085384.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:58216287 A>T maps to NM_001085384.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:21720246 G>T maps to NM_001001415.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:21720246 G>T maps to NM_001001415.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:5085606 C>A maps to NM_032530.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:5085606 C>A maps to NM_032530.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:185801019 C>A maps to NM_194250.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:185801019 C>A maps to NM_194250.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:87168582 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:87168582 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:35578664 C>A maps to NM_198834.1 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:35578664 C>A maps to NM_198834.1 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr21:46603319 C>T maps to NM_015833.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr21:46603319 C>T maps to NM_015833.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:4736588 G>C maps to NM_006422.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:4736588 G>C maps to NM_006422.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:101075567 G>A maps to NM_006828.2 R1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:101075567 G>A maps to NM_006828.2 R1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:53793227 C>A maps to NM_033341.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:53793227 C>A maps to NM_033341.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:78317042 C>T maps to NM_032024.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:78317042 C>T maps to NM_032024.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:75078488 G>C maps to NM_001002912.4 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:75078488 G>C maps to NM_001002912.4 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:53883844 G>T maps to ENST00000514921 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:53883844 G>T maps to ENST00000514921 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:181702857 C>T maps to ENST00000357570 D1078D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:181702857 C>T maps to ENST00000357570 D1078D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:49704163 C>A maps to NM_001190986.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:49704163 C>A maps to NM_001190986.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:15733987 C>A maps to NM_007253.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:15733987 C>A maps to NM_007253.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:100672122 G>A maps to NM_001918.2 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:100672122 G>A maps to NM_001918.2 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:100185117 G>A maps to NM_001013660.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:100185117 G>A maps to NM_001013660.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:49190831 G>T maps to NM_000145.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:49190831 G>T maps to NM_000145.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:9850261 C>A maps to NM_201433.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:9850261 C>A maps to NM_201433.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:27140485 T>C maps to NM_006735.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:27140485 T>C maps to NM_006735.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:27445755 G>T maps to NM_181079.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:27445755 G>T maps to NM_181079.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:39538480 G>T maps to NM_021013.3 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:39538480 G>T maps to NM_021013.3 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:53201582 G>T maps to NM_002272.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:53201582 G>T maps to NM_002272.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:113907095 C>A maps to NM_022363.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:113907095 C>A maps to NM_022363.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:18145250 G>C maps to NM_004140.3 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:18145250 G>C maps to NM_004140.3 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:133824233 C>T maps to NM_144648.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:133824233 C>T maps to NM_144648.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:7014863 G>T maps to NM_201650.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:7014863 G>T maps to NM_201650.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:71491581 C>A maps to NM_005909.3 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:71491581 C>A maps to NM_005909.3 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:92714982 C>A maps to NM_005959.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:92714982 C>A maps to NM_005959.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:1264034 C>A maps to ENST00000447027 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:1264034 C>A maps to ENST00000447027 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:10544689 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:10544689 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:30408289 A>T maps to NM_033118.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:30408289 A>T maps to NM_033118.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:183713935 G>T maps to NM_001080477.1 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:183713935 G>T maps to NM_001080477.1 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:9204165 G>T maps to ENST00000305465 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:9204165 G>T maps to ENST00000305465 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:6806405 C>A maps to NM_001004489.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:6806405 C>A maps to NM_001004489.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:248569558 A>G maps to NM_030904.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:248569558 A>G maps to NM_030904.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:73008273 G>T maps to NM_004154.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:73008273 G>T maps to NM_004154.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:124487351 C>T maps to NM_052959.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:124487351 C>T maps to NM_052959.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:140764229 G>C maps to NM_018920.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:140764229 G>C maps to NM_018920.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:82876986 G>T maps to NM_015885.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:82876986 G>T maps to NM_015885.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:144877095 G>T maps to NM_014644.4 R1531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:144877095 G>T maps to NM_014644.4 R1531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:161087768 C>A maps to NM_012394.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:161087768 C>A maps to NM_012394.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:41712180 G>A maps to NM_002630.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:41712180 G>A maps to NM_002630.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:59828460 T>A maps to NM_176787.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:59828460 T>A maps to NM_176787.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:18272853 G>T maps to NM_005027.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:18272853 G>T maps to NM_005027.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8731975 C>A maps to NM_001010855.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8731975 C>A maps to NM_001010855.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:16287666 C>T maps to NM_001136213.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:16287666 C>T maps to NM_001136213.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:58514536 G>A maps to NM_006242.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:58514536 G>A maps to NM_006242.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:4705532 C>T maps to NM_012409.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:4705532 C>T maps to NM_012409.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:30889895 G>T maps to NM_013357.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:30889895 G>T maps to NM_013357.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:42965886 C>G maps to NM_178491.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:42965886 C>G maps to NM_178491.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:25251514 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:25251514 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:51159380 C>A maps to NM_001080420.1 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:51159380 C>A maps to NM_001080420.1 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:164780203 G>T maps to NM_001041.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:164780203 G>T maps to NM_001041.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:99340561 A>T maps to NM_005073.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:99340561 A>T maps to NM_005073.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:10277674 C>A maps to NM_130811.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:10277674 C>A maps to NM_130811.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:64491114 C>T maps to NM_020762.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:64491114 C>T maps to NM_020762.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:4104600 A>T maps to NM_003156.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:4104600 A>T maps to NM_003156.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:7006647 G>T maps to NM_001113361.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:7006647 G>T maps to NM_001113361.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:97440279 C>T maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:97440279 C>T maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:169648564 C>A maps to NM_003247.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:169648564 C>A maps to NM_003247.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:189063557 C>G maps to NM_178556.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:189063557 C>G maps to NM_178556.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:38237653 T>C maps to NM_003306.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:38237653 T>C maps to NM_003306.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:63992968 A>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:63992968 A>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:11345794 G>T maps to NM_013319.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:11345794 G>T maps to NM_013319.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:33497246 C>G maps to NM_173167.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:33497246 C>G maps to NM_173167.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:74687009 G>C maps to ENST00000393972 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:74687009 G>C maps to ENST00000393972 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:71036272 C>A maps to NM_022479.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:71036272 C>A maps to NM_022479.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:52844155 A>G maps to NM_130775.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:52844155 A>G maps to NM_130775.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:19177404 C>T maps to NM_019028.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:19177404 C>T maps to NM_019028.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:30936031 C>A maps to NM_014717.1 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:30936031 C>A maps to NM_014717.1 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:247201595 C>A maps to NM_033213.3 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:247201595 C>A maps to NM_033213.3 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:3681249 C>T maps to NM_004314.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:3681249 C>T maps to NM_004314.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr16:3647556 T>C maps to NM_032444.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr16:3647556 T>C maps to NM_032444.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:95665043 C>T maps to NM_004411.4 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:95665043 C>T maps to NM_004411.4 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:150890398 G>T maps to NM_033085.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:150890398 G>T maps to NM_033085.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr21:34897280 G>A maps to NM_001136006.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr21:34897280 G>A maps to NM_001136006.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:6942528 T>C maps to NM_001004684.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:6942528 T>C maps to NM_001004684.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:44086228 G>A maps to NM_002840.3 E1781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:44086228 G>A maps to NM_002840.3 E1781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr3:157817684 A>G maps to NM_003030.4 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr3:157817684 A>G maps to NM_003030.4 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:45555436 G>A maps to NM_004212.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:45555436 G>A maps to NM_004212.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:39874028 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:39874028 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:5427960 G>A maps to NM_001080495.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:5427960 G>A maps to NM_001080495.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr19:10478969 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr19:10478969 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr14:105413948 G>A maps to NM_138420.2 S2613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr14:105413948 G>A maps to NM_138420.2 S2613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr3:89456470 G>A maps to NM_005233.5 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr3:89456470 G>A maps to NM_005233.5 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr10:75550012 C>T maps to NM_015037.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr10:75550012 C>T maps to NM_015037.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:25175975 C>T maps to ENST00000380963 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:25175975 C>T maps to ENST00000380963 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:6022726 G>A maps to NM_152611.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:6022726 G>A maps to NM_152611.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:44579719 G>A maps to NM_013389.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:44579719 G>A maps to NM_013389.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:9546620 G>A maps to NM_177990.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:9546620 G>A maps to NM_177990.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:14766484 C>T maps to NM_003561.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:14766484 C>T maps to NM_003561.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:153697418 G>T maps to NM_017514.3 P1485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:153697418 G>T maps to NM_017514.3 P1485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:71482750 C>A maps to NM_145911.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:71482750 C>A maps to NM_145911.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:64748737 T>G maps to NM_197941.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:64748737 T>G maps to NM_197941.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr13:31540435 C>T maps to NM_152325.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr13:31540435 C>T maps to NM_152325.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:37430152 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:37430152 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr9:34093434 G>T maps to NM_015397.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr9:34093434 G>T maps to NM_015397.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr12:31566416 G>T maps to NM_144973.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr12:31566416 G>T maps to NM_144973.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr6:76023513 A>G maps to NM_015687.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr6:76023513 A>G maps to NM_015687.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:91870325 A>T maps to NM_194456.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:91870325 A>T maps to NM_194456.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:66400348 C>T maps to NM_001164664.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:66400348 C>T maps to NM_001164664.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:116412023 C>G maps to NM_001127500.1 Y1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:116412023 C>G maps to NM_001127500.1 Y1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:5363848 A>G maps to NM_001005567.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:5363848 A>G maps to NM_001005567.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:62519813 G>A maps to NM_024784.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:62519813 G>A maps to NM_024784.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:35476083 G>A maps to NM_007167.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:35476083 G>A maps to NM_007167.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:44933923 C>G maps to NM_014518.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:44933923 C>G maps to NM_014518.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:156915333 G>T maps to ENST00000430702 S832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:156915333 G>T maps to ENST00000430702 S832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171501585 A>G maps to ENST00000392078 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171501585 A>G maps to ENST00000392078 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:137717826 C>A maps to NM_001002026.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:137717826 C>A maps to NM_001002026.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:3059238 C>A maps to NM_033225.5 G1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:3059238 C>A maps to NM_033225.5 G1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:21167520 C>A maps to NM_001198801.1 E1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:21167520 C>A maps to NM_001198801.1 E1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:122723065 G>T maps to NM_001034194.1 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:122723065 G>T maps to NM_001034194.1 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:78389002 G>A maps to NM_173627.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:78389002 G>A maps to NM_173627.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:74032774 G>C maps to NM_032380.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:74032774 G>C maps to NM_032380.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:154876112 C>T maps to NM_024012.2 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:154876112 C>T maps to NM_024012.2 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:75979700 A>T maps to NM_006633.2 I1288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:75979700 A>T maps to NM_006633.2 I1288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:86373687 C>T maps to ENST00000393205 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:86373687 C>T maps to ENST00000393205 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:10212754 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:10212754 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:55944911 G>A maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:55944911 G>A maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:21064218 G>A maps to NM_058004.2 R1992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:21064218 G>A maps to NM_058004.2 R1992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:208252775 T>A maps to NM_025179.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:208252775 T>A maps to NM_025179.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr13:38154714 T>C maps to NM_006475.2 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr13:38154714 T>C maps to NM_006475.2 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:237817701 C>T maps to NM_001035.2 A2651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:237817701 C>T maps to NM_001035.2 A2651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:34123252 C>T maps to NM_001036.3 V3808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:34123252 C>T maps to NM_001036.3 V3808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:35086068 C>A maps to NM_001093728.1 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:35086068 C>A maps to NM_001093728.1 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:26936822 G>A maps to NM_003595.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:26936822 G>A maps to NM_003595.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:100380095 G>A maps to NM_139246.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:100380095 G>A maps to NM_139246.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:35965590 C>T maps to NM_152404.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:35965590 C>T maps to NM_152404.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:36038118 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:36038118 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:21843106 A>G maps to ENST00000434536 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:21843106 A>G maps to ENST00000434536 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:44419175 A>G maps to NM_003425.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:44419175 A>G maps to NM_003425.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:31087947 C>T maps to NM_014699.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:31087947 C>T maps to NM_014699.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:40772844 C>T maps to NM_033160.5 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:40772844 C>T maps to NM_033160.5 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr14:105414089 C>A maps to NM_138420.2 L2566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr14:105414089 C>A maps to NM_138420.2 L2566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:6063223 G>T maps to NM_006303.3 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:6063223 G>T maps to NM_006303.3 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:29456481 A>G maps to NM_004304.3 H812H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:29456481 A>G maps to NM_004304.3 H812H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:27057726 C>T maps to NM_006015.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:27057726 C>T maps to NM_006015.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:171510841 C>T maps to ENST00000392078 R1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:171510841 C>T maps to ENST00000392078 R1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:143999136 G>T maps to NM_000498.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:143999136 G>T maps to NM_000498.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:1497386 C>A maps to ENST00000357934 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:1497386 C>A maps to ENST00000357934 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:116757413 G>T maps to NM_013352.2 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:116757413 G>T maps to NM_013352.2 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:32918371 T>C maps to NM_006120.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:32918371 T>C maps to NM_006120.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:159900161 C>T maps to NM_001135050.1 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:159900161 C>T maps to NM_001135050.1 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:42814997 G>A maps to NM_020433.4 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:42814997 G>A maps to NM_020433.4 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:73849191 T>C maps to NM_004770.2 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:73849191 T>C maps to NM_004770.2 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:149901146 C>A maps to NM_003828.2 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:149901146 C>A maps to NM_003828.2 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:72433188 G>A maps to NM_021963.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:72433188 G>A maps to NM_021963.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:44733542 C>T maps to ENST00000444676 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:44733542 C>T maps to ENST00000444676 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:140502488 A>G maps to NM_018938.2 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:140502488 A>G maps to NM_018938.2 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:145021124 C>T maps to NM_001198832.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:145021124 C>T maps to NM_001198832.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:32754214 C>T maps to NM_001098535.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:32754214 C>T maps to NM_001098535.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:5335487 T>A maps to NM_006911.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:5335487 T>A maps to NM_006911.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:154942830 G>A maps to NM_001130040.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:154942830 G>A maps to NM_001130040.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:49832626 G>A maps to NM_003068.3 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:49832626 G>A maps to NM_003068.3 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:152510397 G>A maps to NM_182961.2 L7764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:152510397 G>A maps to NM_182961.2 L7764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:70598122 A>G maps to ENST00000449580 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:70598122 A>G maps to ENST00000449580 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:41497017 C>T maps to NM_017886.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:41497017 C>T maps to NM_017886.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr15:35274618 G>T maps to NM_014106.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr15:35274618 G>T maps to NM_014106.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:204259512 C>G maps to ENST00000295851 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:204259512 C>G maps to ENST00000295851 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:161575191 C>A maps to NM_020133.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:161575191 C>A maps to NM_020133.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:55033652 G>T maps to NM_014481.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:55033652 G>T maps to NM_014481.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:58946044 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:58946044 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:32937422 C>A maps to NM_000059.3 S2695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:32937422 C>A maps to NM_000059.3 S2695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:93788544 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:93788544 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:26448953 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:26448953 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:85724261 T>C maps to NM_198077.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:85724261 T>C maps to NM_198077.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:19165869 C>T maps to NM_001100420.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:19165869 C>T maps to NM_001100420.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:17539604 G>T maps to NM_006366.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:17539604 G>T maps to NM_006366.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:38858711 G>T maps to NM_021185.4 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:38858711 G>T maps to NM_021185.4 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:80274795 G>A maps to NM_006137.6 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:80274795 G>A maps to NM_006137.6 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:66945139 C>A maps to NM_004062.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:66945139 C>A maps to NM_004062.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:64172378 G>A maps to NM_021153.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:64172378 G>A maps to NM_021153.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:25543367 G>T maps to NM_001792.3 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:25543367 G>T maps to NM_001792.3 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:6194813 G>T maps to NM_015557.2 C992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:6194813 G>T maps to NM_015557.2 C992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:10150959 G>A maps to NM_016509.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:10150959 G>A maps to NM_016509.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:348116 G>C maps to NM_130386.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:348116 G>C maps to NM_130386.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129950738 G>A maps to NM_016352.3 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129950738 G>A maps to NM_016352.3 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:19297442 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:19297442 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:25044511 C>A maps to NM_001911.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:25044511 C>A maps to NM_001911.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:36122644 C>A maps to NM_173695.2 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:36122644 C>A maps to NM_173695.2 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:39390614 G>A maps to NM_001343.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:39390614 G>A maps to NM_001343.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:32305734 C>A maps to ENST00000357033 T2067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:32305734 C>A maps to ENST00000357033 T2067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:32407764 C>T maps to ENST00000357033 K1457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:32407764 C>T maps to ENST00000357033 K1457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:111368559 C>A maps to ENST00000428084 E1900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:111368559 C>A maps to ENST00000428084 E1900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:34396239 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:34396239 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:119604044 C>T maps to NM_001426.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:119604044 C>T maps to NM_001426.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:176948096 A>T maps to NM_001080458.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:176948096 A>T maps to NM_001080458.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:34962612 T>A maps to NM_152631.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:34962612 T>A maps to NM_152631.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:92531206 C>A maps to ENST00000298047 Y1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:92531206 C>A maps to ENST00000298047 Y1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:127641203 T>C maps to NM_001999.3 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:127641203 T>C maps to NM_001999.3 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:101153695 G>A maps to NM_001029860.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:101153695 G>A maps to NM_001029860.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:63927973 C>A maps to NM_003878.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:63927973 C>A maps to NM_003878.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:85904648 C>G maps to ENST00000436406 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:85904648 C>G maps to ENST00000436406 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:132887865 G>T maps to NM_001164617.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:132887865 G>T maps to NM_001164617.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:93837764 A>G maps to NM_001098672.1 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:93837764 A>G maps to NM_001098672.1 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:33209283 G>A maps to ENST00000374956 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:33209283 G>A maps to ENST00000374956 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:64968212 G>C maps to NM_032776.1 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:64968212 G>C maps to NM_032776.1 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:73848768 A>T maps to NM_004770.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:73848768 A>T maps to NM_004770.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:138670654 C>T maps to ENST00000298480 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:138670654 C>T maps to ENST00000298480 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:13215866 C>T maps to NM_020853.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:13215866 C>T maps to NM_020853.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:91497558 G>T maps to ENST00000416354 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:91497558 G>T maps to ENST00000416354 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:39751209 C>T maps to ENST00000395670 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:39751209 C>T maps to ENST00000395670 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:52685240 G>T maps to NM_002281.3 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:52685240 G>T maps to NM_002281.3 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:31744438 G>T maps to NM_181621.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:31744438 G>T maps to NM_181621.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:64737912 G>T maps to NM_031206.4 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:64737912 G>T maps to NM_031206.4 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:66850108 G>T maps to NM_207338.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:66850108 G>T maps to NM_207338.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:201915291 G>T maps to NM_012134.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:201915291 G>T maps to NM_012134.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:82416125 G>A maps to ENST00000370717 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:82416125 G>A maps to ENST00000370717 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:150327361 T>C maps to NM_194317.3 *172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:150327361 T>C maps to NM_194317.3 *172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35791290 G>T maps to NM_002361.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35791290 G>T maps to NM_002361.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:56411567 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:56411567 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:19379643 C>A maps to NM_001001671.3 R1249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:19379643 C>A maps to NM_001001671.3 R1249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:47346707 A>C maps to NM_001113498.2 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:47346707 A>C maps to NM_001113498.2 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:129906386 T>C maps to NM_002417.4 E1239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:129906386 T>C maps to NM_002417.4 E1239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:50572450 G>T maps to NM_018995.2 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:50572450 G>T maps to NM_018995.2 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:86582140 C>A maps to NM_001159377.1 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:86582140 C>A maps to NM_001159377.1 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:74183110 G>T maps to NM_001123226.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:74183110 G>T maps to NM_001123226.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:100676469 A>C maps to NM_001040105.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:100676469 A>C maps to NM_001040105.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:10417164 G>T maps to NM_005963.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:10417164 G>T maps to NM_005963.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:10366241 G>T maps to NM_017533.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:10366241 G>T maps to NM_017533.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:73928032 C>A maps to NM_016347.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:73928032 C>A maps to NM_016347.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:68224794 G>T maps to NM_173165.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:68224794 G>T maps to NM_173165.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:3614681 T>G maps to ENST00000448023 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:3614681 T>G maps to ENST00000448023 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:284493 C>T maps to NM_138329.1 Q798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:284493 C>T maps to NM_138329.1 Q798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:30326433 G>T maps to NM_000475.4 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:30326433 G>T maps to NM_000475.4 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:88483958 G>A maps to NM_001012338.1 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:88483958 G>A maps to NM_001012338.1 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:113416335 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:113416335 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:228412409 G>T maps to NM_001098623.1 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:228412409 G>T maps to NM_001098623.1 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:132290113 G>T maps to NM_002545.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:132290113 G>T maps to NM_002545.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:125288840 G>A maps to ENST00000359439 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:125288840 G>A maps to ENST00000359439 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:29430206 C>T maps to NM_030883.3 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:29430206 C>T maps to NM_030883.3 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:248616418 C>A maps to NM_001004136.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:248616418 C>A maps to NM_001004136.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:20296383 G>A maps to NM_001004723.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:20296383 G>A maps to NM_001004723.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:56128007 G>T maps to NM_001005205.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:56128007 G>T maps to NM_001005205.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:76788491 C>T maps to NM_020841.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:76788491 C>T maps to NM_020841.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:78216520 C>A maps to NM_198333.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:78216520 C>A maps to NM_198333.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:140175014 G>T maps to NM_018905.2 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:140175014 G>T maps to NM_018905.2 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:140589645 C>T maps to NM_018932.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:140589645 C>T maps to NM_018932.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:67269492 C>A maps to NM_004910.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:67269492 C>A maps to NM_004910.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:46615709 G>A maps to NM_001001928.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:46615709 G>A maps to NM_001001928.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:35068323 C>T maps to NM_000949.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:35068323 C>T maps to NM_000949.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:18067063 A>G maps to NM_175886.2 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:18067063 A>G maps to NM_175886.2 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:75815559 G>A maps to NM_002833.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:75815559 G>A maps to NM_002833.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:119508808 T>C maps to NM_203285.1 *459W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:119508808 T>C maps to NM_203285.1 *459W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:192545460 G>T maps to NM_002922.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:192545460 G>T maps to NM_002922.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:192547460 C>A maps to NM_002922.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:192547460 C>A maps to NM_002922.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:10470794 C>G maps to NM_178857.5 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:10470794 C>G maps to NM_178857.5 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:77378975 T>C maps to NM_198467.2 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:77378975 T>C maps to NM_198467.2 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:33603290 G>T maps to NM_001036.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:33603290 G>T maps to NM_001036.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:129867261 C>A maps to NM_144643.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:129867261 C>A maps to NM_144643.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:166898801 C>A maps to NM_001165963.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:166898801 C>A maps to NM_001165963.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:165970388 A>G maps to NM_006922.3 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:165970388 A>G maps to NM_006922.3 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:142596979 T>A maps to NM_001009609.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:142596979 T>A maps to NM_001009609.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:56212670 G>A maps to NM_024592.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:56212670 G>A maps to NM_024592.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:23711940 G>T maps to NM_003155.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:23711940 G>T maps to NM_003155.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:60584200 T>C maps to NM_003185.3 K597K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:60584200 T>C maps to NM_003185.3 K597K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:115971636 G>A maps to NM_198795.1 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:115971636 G>A maps to NM_198795.1 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:50696701 C>T maps to NM_172238.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:50696701 C>T maps to NM_172238.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:120476447 C>A maps to NM_138554.3 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:120476447 C>A maps to NM_138554.3 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:105360983 G>A maps to NM_030788.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:105360983 G>A maps to NM_030788.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:368839 G>A maps to ENST00000422053 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:368839 G>A maps to ENST00000422053 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:96260874 A>G maps to NM_138800.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:96260874 A>G maps to NM_138800.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:14507305 G>T maps to NM_007118.2 L2896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:14507305 G>T maps to NM_007118.2 L2896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:116632270 C>T maps to NM_014112.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:116632270 C>T maps to NM_014112.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:135797348 C>A maps to NM_000368.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:135797348 C>A maps to NM_000368.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:107018415 C>A maps to NM_198057.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:107018415 C>A maps to NM_198057.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:3200659 C>A maps to ENST00000398659 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:3200659 C>A maps to ENST00000398659 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:75029451 C>A maps to NM_145170.3 E1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:75029451 C>A maps to NM_145170.3 E1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:179614226 T>C maps to ENST00000375038 V4302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:179614226 T>C maps to ENST00000375038 V4302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:11505454 G>T maps to NM_001080491.2 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:11505454 G>T maps to NM_001080491.2 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:6182794 G>T maps to NM_000552.3 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:6182794 G>T maps to NM_000552.3 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:128890489 C>G maps to NM_003399.5 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:128890489 C>G maps to NM_003399.5 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:112927871 G>T maps to NM_022828.3 G1403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:112927871 G>T maps to NM_022828.3 G1403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:141163938 C>T maps to NM_001080412.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:141163938 C>T maps to NM_001080412.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:247319987 A>G maps to NM_003431.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:247319987 A>G maps to NM_003431.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:244218617 G>A maps to NM_205768.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:244218617 G>A maps to NM_205768.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:8577563 G>T maps to NM_001146175.1 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:8577563 G>T maps to NM_001146175.1 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:22804889 G>A maps to NM_015461.2 Q998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:22804889 G>A maps to NM_015461.2 Q998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:53007906 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:53007906 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:22292160 T>A maps to NM_152577.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:22292160 T>A maps to NM_152577.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:30581632 G>A maps to NM_145271.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:30581632 G>A maps to NM_145271.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr15:90167026 A>C maps to NM_152259.3 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr15:90167026 A>C maps to NM_152259.3 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr22:37888519 C>A maps to NM_014550.3 A891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr22:37888519 C>A maps to NM_014550.3 A891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:65660406 C>A maps to NM_005438.3 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:65660406 C>A maps to NM_005438.3 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr6:131944568 A>G maps to ENST00000403834 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr6:131944568 A>G maps to ENST00000403834 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr22:45309827 C>T maps to NM_138415.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr22:45309827 C>T maps to NM_138415.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:231222645 C>T maps to NM_138402.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:231222645 C>T maps to NM_138402.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:65268072 C>T maps to ENST00000389723 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:65268072 C>T maps to ENST00000389723 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chrX:9661223 C>T maps to NM_005647.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chrX:9661223 C>T maps to NM_005647.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:117784511 G>A maps to ENST00000413475 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:117784511 G>A maps to ENST00000413475 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:105410750 C>A maps to NM_138420.2 G3679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:105410750 C>A maps to NM_138420.2 G3679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:160049493 G>T maps to NM_025153.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:160049493 G>T maps to NM_025153.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:56553687 C>A maps to NM_031885.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:56553687 C>A maps to NM_031885.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:80001217 G>T maps to NM_153252.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:80001217 G>T maps to NM_153252.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47179381 T>A maps to NM_001003677.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47179381 T>A maps to NM_001003677.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:192635484 G>T maps to NM_178496.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:192635484 G>T maps to NM_178496.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:149633052 G>A maps to NM_015981.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:149633052 G>A maps to NM_015981.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:7737752 C>A maps to NM_015215.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:7737752 C>A maps to NM_015215.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156290752 G>C maps to NM_005998.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156290752 G>C maps to NM_005998.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:72250893 G>T maps to NM_032649.5 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:72250893 G>T maps to NM_032649.5 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:72180860 G>T maps to NM_018235.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:72180860 G>T maps to NM_018235.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:117027202 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:117027202 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:74428032 T>A maps to NM_182476.1 L350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:74428032 T>A maps to NM_182476.1 L350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr21:44592263 C>A maps to NM_000394.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr21:44592263 C>A maps to NM_000394.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:113331069 A>T maps to NM_198123.1 C2452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:113331069 A>T maps to NM_198123.1 C2452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:118502309 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:118502309 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:7572276 C>A maps to NM_004415.2 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:7572276 C>A maps to NM_004415.2 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:113773000 C>A maps to NM_000131.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:113773000 C>A maps to NM_000131.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:126370480 C>T maps to NM_024582.4 A2770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:126370480 C>T maps to NM_024582.4 A2770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:125107212 T>C maps to NM_001039112.2 C1543C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:125107212 T>C maps to NM_001039112.2 C1543C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:216262477 C>A maps to NM_212482.1 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:216262477 C>A maps to NM_212482.1 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:106558442 C>A maps to ENST00000282249 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:106558442 C>A maps to ENST00000282249 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:93822026 C>A maps to NM_001098672.1 Y729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:93822026 C>A maps to NM_001098672.1 Y729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:91851285 T>C maps to NM_001017975.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:91851285 T>C maps to NM_001017975.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:37838715 G>A maps to NM_181786.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:37838715 G>A maps to NM_181786.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:26875275 T>C maps to NM_022081.4 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:26875275 T>C maps to NM_022081.4 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:209961968 C>A maps to NM_006147.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:209961968 C>A maps to NM_006147.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:24006106 C>A maps to NM_030624.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:24006106 C>A maps to NM_030624.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:62897171 A>T maps to ENST00000506720 I1145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:62897171 A>T maps to ENST00000506720 I1145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:74734526 G>A maps to NM_024311.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:74734526 G>A maps to NM_024311.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:16694646 C>T maps to NM_012334.2 Q1211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:16694646 C>T maps to NM_012334.2 Q1211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:27425146 A>T maps to NM_078471.3 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:27425146 A>T maps to NM_078471.3 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:42083114 C>T maps to NM_153006.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:42083114 C>T maps to NM_153006.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:21494244 G>C maps to NM_002509.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:21494244 G>C maps to NM_002509.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:55135508 G>A maps to NM_001005275.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:55135508 G>A maps to NM_001005275.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:57268455 C>T maps to NM_021728.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:57268455 C>T maps to NM_021728.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:140249914 C>T maps to NM_018902.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:140249914 C>T maps to NM_018902.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:28815702 A>G maps to NM_023923.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:28815702 A>G maps to NM_023923.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:33832750 A>T maps to ENST00000419414 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:33832750 A>T maps to ENST00000419414 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:27240043 T>A maps to NM_001033561.1 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:27240043 T>A maps to NM_001033561.1 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:25151776 T>C maps to NM_001008496.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:25151776 T>C maps to NM_001008496.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:65208724 G>A maps to ENST00000394691 K830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:65208724 G>A maps to ENST00000394691 K830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:7622060 G>T maps to NM_001166111.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:7622060 G>T maps to NM_001166111.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:76794372 C>A maps to NM_006239.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:76794372 C>A maps to NM_006239.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:570479 C>T maps to NM_014700.3 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:570479 C>T maps to NM_014700.3 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:134459979 G>A maps to NM_198679.1 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:134459979 G>A maps to NM_198679.1 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:5300118 T>C maps to NM_134441.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:5300118 T>C maps to NM_134441.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:11118586 G>T maps to NM_001128849.1 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:11118586 G>T maps to NM_001128849.1 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:43585153 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:43585153 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:43779440 T>C maps to ENST00000330266 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:43779440 T>C maps to ENST00000330266 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:154626146 C>T maps to NM_003264.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:154626146 C>T maps to NM_003264.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:129370422 C>A maps to NM_001017395.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:129370422 C>A maps to NM_001017395.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:166009710 G>A maps to NM_001100389.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:166009710 G>A maps to NM_001100389.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:76823388 C>A maps to NM_025090.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:76823388 C>A maps to NM_025090.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:142152623 A>G maps to NM_014487.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:142152623 A>G maps to NM_014487.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:25667035 G>T maps to NM_015655.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:25667035 G>T maps to NM_015655.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:12739911 C>G maps to NM_153358.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:12739911 C>G maps to NM_153358.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:22952000 C>T maps to ENST00000397104 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:22952000 C>T maps to ENST00000397104 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:109698351 C>A maps to NM_001093.3 P2188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:109698351 C>A maps to NM_001093.3 P2188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:167815047 C>G maps to NM_018417.4 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:167815047 C>G maps to NM_018417.4 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:1412654 T>C maps to NM_031921.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:1412654 T>C maps to NM_031921.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chrX:76874342 G>T maps to NM_000489.3 T1793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chrX:76874342 G>T maps to NM_000489.3 T1793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:76555039 C>A maps to NM_033401.3 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:76555039 C>A maps to NM_033401.3 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:48542535 C>T maps to NM_015030.1 K2043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:48542535 C>T maps to NM_015030.1 K2043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr9:101052877 G>C maps to NM_005458.7 V938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr9:101052877 G>C maps to NM_005458.7 V938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chrX:101970072 A>G maps to NM_138437.5 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chrX:101970072 A>G maps to NM_138437.5 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:5021827 C>T maps to NM_000217.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:5021827 C>T maps to NM_000217.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:1278884 C>T maps to ENST00000447027 F5468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:1278884 C>T maps to ENST00000447027 F5468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:56380558 G>A maps to NM_001004740.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:56380558 G>A maps to NM_001004740.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr7:102087126 G>A maps to NM_032831.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr7:102087126 G>A maps to NM_032831.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr13:28855450 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr13:28855450 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:178969105 G>A maps to NM_001077197.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:178969105 G>A maps to NM_001077197.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:95403998 G>A maps to NM_012415.2 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:95403998 G>A maps to NM_012415.2 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:4829783 G>A maps to NM_144605.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:4829783 G>A maps to NM_144605.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:95056450 G>T maps to NM_000624.4 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:95056450 G>T maps to NM_000624.4 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:51501051 A>G maps to NM_005653.4 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:51501051 A>G maps to NM_005653.4 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:72815929 C>T maps to NM_017728.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:72815929 C>T maps to NM_017728.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:32456381 G>C maps to NM_024426.4 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:32456381 G>C maps to NM_024426.4 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:52703521 G>T maps to NM_004799.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:52703521 G>T maps to NM_004799.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:48314883 C>G maps to NM_152701.3 S1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:48314883 C>G maps to NM_152701.3 S1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:123419911 G>A maps to NM_203444.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:123419911 G>A maps to NM_203444.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:134131718 G>T maps to NM_014384.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:134131718 G>T maps to NM_014384.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:100672249 C>A maps to NM_139057.2 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:100672249 C>A maps to NM_139057.2 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:112028428 C>T maps to NM_020683.6 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:112028428 C>T maps to NM_020683.6 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:135263562 C>A maps to NM_022568.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:135263562 C>A maps to NM_022568.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:233246045 C>T maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:233246045 C>T maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:46455070 G>A maps to ENST00000458649 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:46455070 G>A maps to ENST00000458649 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:39358205 G>T maps to NM_001193289.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:39358205 G>T maps to NM_001193289.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:127231283 C>T maps to NM_001662.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:127231283 C>T maps to NM_001662.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:11187695 G>T maps to NM_013427.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:11187695 G>T maps to NM_013427.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:57867884 G>T maps to ENST00000393797 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:57867884 G>T maps to ENST00000393797 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:176845700 G>A maps to ENST00000281881 C1153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:176845700 G>A maps to ENST00000281881 C1153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:171504669 G>T maps to ENST00000392078 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:171504669 G>T maps to ENST00000392078 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:75269173 A>T maps to NM_001170714.1 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:75269173 A>T maps to NM_001170714.1 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:187447127 G>T maps to NM_001706.4 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:187447127 G>T maps to NM_001706.4 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:5788305 A>G maps to NM_017782.4 Q974Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:5788305 A>G maps to NM_017782.4 Q974Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:219890791 G>A maps to NM_194302.2 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:219890791 G>A maps to NM_194302.2 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:158325707 C>A maps to NM_030893.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:158325707 C>A maps to NM_030893.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:48650523 G>A maps to NM_005195.3 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:48650523 G>A maps to NM_005195.3 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:143043747 C>A maps to NM_000083.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:143043747 C>A maps to NM_000083.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:238261227 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:238261227 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:145622833 C>A maps to NM_013291.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:145622833 C>A maps to NM_013291.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:186257350 A>T maps to NM_017541.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:186257350 A>T maps to NM_017541.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:37333577 C>A maps to ENST00000262825 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:37333577 C>A maps to ENST00000262825 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:19997689 A>G maps to NM_172241.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:19997689 A>G maps to NM_172241.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35060506 C>T maps to ENST00000339266 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35060506 C>T maps to ENST00000339266 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:70202765 G>A maps to NM_001080449.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:70202765 G>A maps to NM_001080449.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:108213679 C>G maps to NM_012328.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:108213679 C>G maps to NM_012328.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:674400 G>T maps to ENST00000319815 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:674400 G>T maps to ENST00000319815 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:6196056 T>C maps to NM_000129.3 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:6196056 T>C maps to NM_000129.3 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:30041830 C>A maps to NM_031478.4 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:30041830 C>A maps to NM_031478.4 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:50979146 C>T maps to ENST00000391816 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:50979146 C>T maps to ENST00000391816 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:126372403 G>T maps to NM_024582.4 V3411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:126372403 G>T maps to NM_024582.4 V3411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:8211047 C>A maps to NM_032447.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:8211047 C>A maps to NM_032447.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:152328506 C>A maps to NM_001014342.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:152328506 C>A maps to NM_001014342.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:46014652 C>A maps to NM_024513.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:46014652 C>A maps to NM_024513.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:241569992 G>A maps to NM_001195381.1 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:241569992 G>A maps to NM_001195381.1 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:146720433 G>C maps to NM_000838.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:146720433 G>C maps to NM_000838.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:122641477 G>A maps to NM_005328.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:122641477 G>A maps to NM_005328.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:152190972 G>T maps to NM_001009931.1 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:152190972 G>T maps to NM_001009931.1 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:92616927 C>A maps to NM_019859.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:92616927 C>A maps to NM_019859.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:209104695 C>A maps to NM_005896.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:209104695 C>A maps to NM_005896.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:160063848 G>T maps to NM_052868.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:160063848 G>T maps to NM_052868.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:122657104 G>A maps to NM_001014336.1 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:122657104 G>A maps to NM_001014336.1 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62416482 C>A maps to NM_030628.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62416482 C>A maps to NM_030628.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:48309123 T>A maps to NM_001080394.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:48309123 T>A maps to NM_001080394.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:73495346 C>A maps to ENST00000375248 R1371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:73495346 C>A maps to ENST00000375248 R1371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:57972079 C>A maps to NM_004984.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:57972079 C>A maps to NM_004984.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:87743081 C>A maps to NM_017566.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:87743081 C>A maps to NM_017566.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:6655583 C>A maps to NM_014851.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:6655583 C>A maps to NM_014851.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:127894470 C>A maps to NM_000230.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:127894470 C>A maps to NM_000230.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:101464887 G>C maps to NM_024652.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:101464887 G>C maps to NM_024652.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:39852908 C>T maps to ENST00000361689 Q2737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:39852908 C>T maps to ENST00000361689 Q2737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:39888161 C>A maps to NM_017592.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:39888161 C>A maps to NM_017592.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:141738390 C>A maps to ENST00000475668 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:141738390 C>A maps to ENST00000475668 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:19345791 C>T maps to NM_020774.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:19345791 C>T maps to NM_020774.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:10267795 G>T maps to NM_003802.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:10267795 G>T maps to NM_003802.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:123458824 G>A maps to NM_053025.3 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:123458824 G>A maps to NM_053025.3 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:40104286 C>T maps to NM_018177.3 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:40104286 C>T maps to NM_018177.3 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15330451 C>A maps to NM_015909.2 E2170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15330451 C>A maps to NM_015909.2 E2170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15496519 G>T maps to NM_015909.2 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15496519 G>T maps to NM_015909.2 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:148012506 C>A maps to ENST00000310701 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:148012506 C>A maps to ENST00000310701 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:29881764 C>A maps to NM_021076.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:29881764 C>A maps to NM_021076.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:46128596 C>T maps to ENST00000362042 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:46128596 C>T maps to ENST00000362042 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:42675153 G>T maps to NM_005385.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:42675153 G>T maps to NM_005385.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:134073548 T>C maps to ENST00000451030 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:134073548 T>C maps to ENST00000451030 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62568673 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62568673 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228557765 C>T maps to NM_001098623.1 F6697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228557765 C>T maps to NM_001098623.1 F6697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:167674282 C>A maps to NM_001122679.1 P2104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:167674282 C>A maps to NM_001122679.1 P2104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:7530833 C>A maps to NM_198474.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:7530833 C>A maps to NM_198474.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:248005038 G>A maps to NM_001001959.1 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:248005038 G>A maps to NM_001001959.1 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:134071513 G>T maps to NM_032961.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:134071513 G>T maps to NM_032961.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140554463 C>A maps to NM_018940.2 S683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140554463 C>A maps to NM_018940.2 S683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140802146 C>A maps to NM_018914.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140802146 C>A maps to NM_018914.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140735711 T>A maps to NM_018917.2 Y315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140735711 T>A maps to NM_018917.2 Y315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:31917642 A>G maps to NM_001191057.1 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:31917642 A>G maps to NM_001191057.1 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:110523009 A>T maps to ENST00000426474 P3801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:110523009 A>T maps to ENST00000426474 P3801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:37547131 G>T maps to NM_015568.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:37547131 G>T maps to NM_015568.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:35554834 T>G maps to NM_017917.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:35554834 T>G maps to NM_017917.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:48064291 G>T maps to NM_206962.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:48064291 G>T maps to NM_206962.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:43698708 G>C maps to NM_002780.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:43698708 G>C maps to NM_002780.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:47028897 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:47028897 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:74473791 C>A maps to NM_024599.5 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:74473791 C>A maps to NM_024599.5 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:104973291 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:104973291 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:21502072 G>T maps to NM_001012264.3 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:21502072 G>T maps to NM_001012264.3 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:237789030 C>A maps to NM_001035.2 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:237789030 C>A maps to NM_001035.2 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:33955136 C>A maps to NM_001036.3 S1802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:33955136 C>A maps to NM_001036.3 S1802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:128712557 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:128712557 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:100572477 A>G maps to NM_194292.1 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:100572477 A>G maps to NM_194292.1 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:62043557 G>T maps to NM_000334.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:62043557 G>T maps to NM_000334.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:144876105 C>T maps to NM_182706.3 K1291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:144876105 C>T maps to NM_182706.3 K1291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:6755293 G>T maps to NM_005490.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:6755293 G>T maps to NM_005490.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:21050588 C>T maps to ENST00000444387 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:21050588 C>T maps to ENST00000444387 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:152065388 C>A maps to NM_001009555.3 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:152065388 C>A maps to NM_001009555.3 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:6981811 G>T maps to NM_032641.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:6981811 G>T maps to NM_032641.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:46326728 G>C maps to NM_004819.2 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:46326728 G>C maps to NM_004819.2 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:33273030 G>T maps to NM_172208.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:33273030 G>T maps to NM_172208.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:114793672 G>T maps to NM_000192.3 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:114793672 G>T maps to NM_000192.3 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:65147239 G>T maps to NM_001010874.4 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:65147239 G>T maps to NM_001010874.4 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:151820279 G>A maps to NM_182578.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:151820279 G>A maps to NM_182578.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:40661418 C>T maps to ENST00000454349 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:40661418 C>T maps to ENST00000454349 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:179592312 T>A maps to NM_133378.4 T5420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:179592312 T>A maps to NM_133378.4 T5420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:154530852 G>A maps to NM_017582.6 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:154530852 G>A maps to NM_017582.6 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:96601612 G>A maps to NM_020121.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:96601612 G>A maps to NM_020121.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:234590852 C>T maps to NM_019077.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:234590852 C>T maps to NM_019077.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:151149151 G>T maps to ENST00000354473 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:151149151 G>T maps to ENST00000354473 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:113119470 G>T maps to NM_001164496.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:113119470 G>T maps to NM_001164496.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:28213079 G>T maps to NM_019110.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:28213079 G>T maps to NM_019110.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:123597328 G>A maps to NM_003455.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:123597328 G>A maps to NM_003455.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:145999006 C>A maps to NM_030580.3 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:145999006 C>A maps to NM_030580.3 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:12461716 C>A maps to NM_030824.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:12461716 C>A maps to NM_030824.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:48319267 G>A maps to NM_152701.3 W2826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:48319267 G>A maps to NM_152701.3 W2826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150748262 C>A maps to NM_020321.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150748262 C>A maps to NM_020321.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:229567266 G>T maps to NM_001100.3 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:229567266 G>T maps to NM_001100.3 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7690889 G>T maps to NM_020546.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7690889 G>T maps to NM_020546.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:88029352 C>T maps to NM_001166693.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:88029352 C>T maps to NM_001166693.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:147919202 T>A maps to NM_002025.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:147919202 T>A maps to NM_002025.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:230846485 G>A maps to NM_000029.3 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:230846485 G>A maps to NM_000029.3 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:29551273 C>G maps to NM_004304.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:29551273 C>G maps to NM_004304.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:73659340 G>T maps to NM_015120.4 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:73659340 G>T maps to NM_015120.4 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:33520747 A>T maps to NM_152462.2 Y193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:33520747 A>T maps to NM_152462.2 Y193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:108334268 G>C maps to NM_001146.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:108334268 G>C maps to NM_001146.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:27306604 A>G maps to NM_014915.2 C1444C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:27306604 A>G maps to NM_014915.2 C1444C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:117876163 A>T maps to ENST00000357099 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:117876163 A>T maps to ENST00000357099 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:43618385 T>A maps to NM_018075.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:43618385 T>A maps to NM_018075.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:36587461 G>T maps to ENST00000332987 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:36587461 G>T maps to ENST00000332987 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:143913137 A>T maps to NM_018460.3 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:143913137 A>T maps to NM_018460.3 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:130219646 G>C maps to NM_144967.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:130219646 G>C maps to NM_144967.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:98985701 C>A maps to NM_005720.2 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:98985701 C>A maps to NM_005720.2 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:119858332 G>T maps to ENST00000313400 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:119858332 G>T maps to ENST00000313400 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:31325022 C>A maps to NM_030632.1 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:31325022 C>A maps to NM_030632.1 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:64756756 G>T maps to NM_138456.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:64756756 G>T maps to NM_138456.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98743639 A>G maps to NM_015652.2 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98743639 A>G maps to NM_015652.2 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6231319 C>A maps to NM_173525.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6231319 C>A maps to NM_173525.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:39586280 G>T maps to NM_025138.3 S884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:39586280 G>T maps to NM_025138.3 S884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:3802817 G>T maps to NM_018347.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:3802817 G>T maps to NM_018347.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:56728612 A>T maps to NM_178456.2 K28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:56728612 A>T maps to NM_178456.2 K28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2022272 G>T maps to NM_172364.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2022272 G>T maps to NM_172364.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27446490 G>A maps to NM_004341.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27446490 G>A maps to NM_004341.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33424516 T>A maps to NM_032816.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33424516 T>A maps to NM_032816.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:78013807 T>C maps to NM_017950.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:78013807 T>C maps to NM_017950.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:66479314 G>A maps to NM_005582.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:66479314 G>A maps to NM_005582.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:103442277 G>A maps to NM_006035.3 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:103442277 G>A maps to NM_006035.3 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:24487954 G>A maps to NM_006727.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:24487954 G>A maps to NM_006727.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:92244465 C>T maps to NM_001145306.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:92244465 C>T maps to NM_001145306.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:42213866 C>T maps to NM_004363.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:42213866 C>T maps to NM_004363.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:34855076 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:34855076 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:184105190 C>A maps to NM_003741.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:184105190 C>A maps to NM_003741.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:61978134 C>T maps to NM_000744.5 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:61978134 C>T maps to NM_000744.5 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3063923 G>A maps to NM_020982.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3063923 G>A maps to NM_020982.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:62212448 C>A maps to NM_173519.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:62212448 C>A maps to NM_173519.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:94039099 T>C maps to NM_000089.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:94039099 T>C maps to NM_000089.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:86200647 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:86200647 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:75950954 C>A maps to NM_001865.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:75950954 C>A maps to NM_001865.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:9768830 G>T maps to ENST00000383832 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:9768830 G>T maps to ENST00000383832 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34090211 C>T maps to ENST00000373381 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34090211 C>T maps to ENST00000373381 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:11732328 C>A maps to NM_001332.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:11732328 C>A maps to NM_001332.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:16980991 T>C maps to NM_001081.3 E1901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:16980991 T>C maps to NM_001081.3 E1901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:43014776 C>T maps to NM_001168370.1 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:43014776 C>T maps to NM_001168370.1 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:96609672 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:96609672 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57480985 G>A maps to ENST00000371231 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57480985 G>A maps to ENST00000371231 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:27999165 C>A maps to NM_001017930.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:27999165 C>A maps to NM_001017930.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6644757 C>A maps to NM_003737.2 E2717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6644757 C>A maps to NM_003737.2 E2717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:38095614 G>C maps to NM_001164232.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:38095614 G>C maps to NM_001164232.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:14797348 T>A maps to NM_004080.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:14797348 T>A maps to NM_004080.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:21766920 G>T maps to NM_003974.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:21766920 G>T maps to NM_003974.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:37572691 G>A maps to NM_005128.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:37572691 G>A maps to NM_005128.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:1825091 C>T maps to NM_001010865.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:1825091 C>T maps to NM_001010865.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:111531406 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:111531406 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:89445101 C>A maps to NM_005233.5 Y474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:89445101 C>A maps to NM_005233.5 Y474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:5624460 C>A maps to NM_147127.4 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:5624460 C>A maps to NM_147127.4 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:131520776 G>T maps to NM_001105195.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:131520776 G>T maps to NM_001105195.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:184764796 C>A maps to NM_052966.2 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:184764796 C>A maps to NM_052966.2 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:175528580 G>T maps to NM_001079529.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:175528580 G>T maps to NM_001079529.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:166039590 G>T maps to NM_001017961.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:166039590 G>T maps to NM_001017961.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:86089576 C>A maps to NM_013231.4 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:86089576 C>A maps to NM_013231.4 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:126142943 C>A maps to NM_017547.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:126142943 C>A maps to NM_017547.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:44198063 C>T maps to NM_032892.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:44198063 C>T maps to NM_032892.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:127239487 C>A maps to NM_020369.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:127239487 C>A maps to NM_020369.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:34117198 A>G maps to NM_016631.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:34117198 A>G maps to NM_016631.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233621022 C>A maps to ENST00000373566 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233621022 C>A maps to ENST00000373566 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:110146651 G>T maps to NM_005272.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:110146651 G>T maps to NM_005272.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:167728112 C>A maps to NM_014498.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:167728112 C>A maps to NM_014498.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:176622817 G>T maps to NM_005277.3 C46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:176622817 G>T maps to NM_005277.3 C46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:25886723 C>A maps to NM_020752.2 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:25886723 C>A maps to NM_020752.2 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150345291 C>A maps to NM_004224.3 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150345291 C>A maps to NM_004224.3 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:31045362 G>C maps to ENST00000327783 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:31045362 G>C maps to ENST00000327783 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:104499661 G>T maps to NM_133445.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:104499661 G>T maps to NM_133445.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:86415917 C>G maps to NM_000840.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:86415917 C>G maps to NM_000840.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:74004250 A>T maps to NM_016328.2 K813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:74004250 A>T maps to NM_016328.2 K813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:54326300 A>T maps to NM_002104.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:54326300 A>T maps to NM_002104.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:46808500 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:46808500 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:143080986 G>A maps to NM_006734.3 P2146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:143080986 G>A maps to NM_006734.3 P2146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:46703289 C>G maps to NM_024017.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:46703289 C>G maps to NM_024017.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:3176789 C>T maps to NM_002111.6 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:3176789 C>T maps to NM_002111.6 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:71948809 G>C maps to NM_001567.3 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:71948809 G>C maps to NM_001567.3 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:60003897 A>T maps to NM_020748.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:60003897 A>T maps to NM_020748.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:54802717 G>A maps to NM_002205.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:54802717 G>A maps to NM_002205.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:20421492 C>T maps to NM_002214.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:20421492 C>T maps to NM_002214.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:7683888 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:7683888 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:202887328 C>A maps to NM_021633.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:202887328 C>A maps to NM_021633.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:39597002 C>A maps to NM_006771.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:39597002 C>A maps to NM_006771.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:31964946 G>A maps to ENST00000399871 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:31964946 G>A maps to ENST00000399871 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55143584 C>T maps to ENST00000427581 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55143584 C>T maps to ENST00000427581 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:54760610 C>T maps to NM_001081442.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:54760610 C>T maps to NM_001081442.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:197703558 C>A maps to NM_001136049.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:197703558 C>A maps to NM_001136049.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:194081121 A>G maps to NM_001135057.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:194081121 A>G maps to NM_001135057.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:70291428 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:70291428 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:80529978 C>G maps to NM_178839.4 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:80529978 C>G maps to NM_178839.4 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:47330185 A>T maps to NM_003682.3 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:47330185 A>T maps to NM_003682.3 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:95713750 C>T maps to NM_002371.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:95713750 C>T maps to NM_002371.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:48252468 G>T maps to NM_002747.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:48252468 G>T maps to NM_002747.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:74701953 C>A maps to NM_001025101.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:74701953 C>A maps to NM_001025101.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:41988780 G>T maps to ENST00000219905 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:41988780 G>T maps to ENST00000219905 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:129913426 T>C maps to NM_002417.4 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:129913426 T>C maps to NM_002417.4 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:23812449 G>T maps to NM_005664.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:23812449 G>T maps to NM_005664.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:18194988 C>A maps to NM_054032.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:18194988 C>A maps to NM_054032.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:10231407 G>A maps to NM_003802.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:10231407 G>A maps to NM_003802.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55417574 C>T maps to NM_004829.5 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55417574 C>T maps to NM_004829.5 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156640298 C>A maps to NM_006617.1 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156640298 C>A maps to NM_006617.1 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233745955 G>T maps to NM_019850.2 C614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233745955 G>T maps to NM_019850.2 C614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:25507046 G>A maps to NM_025176.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:25507046 G>A maps to NM_025176.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:24786968 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:24786968 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:247582215 C>A maps to NM_004895.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:247582215 C>A maps to NM_004895.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:36330256 G>A maps to NM_004646.3 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:36330256 G>A maps to NM_004646.3 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32712583 C>A maps to ENST00000265074 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32712583 C>A maps to ENST00000265074 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:110255339 T>C maps to NM_032869.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:110255339 T>C maps to NM_032869.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:102334689 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:102334689 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:228399597 G>T maps to NM_001098623.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:228399597 G>T maps to NM_001098623.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:183603129 G>T maps to NM_001080477.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:183603129 G>T maps to NM_001080477.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123894351 C>T maps to NM_001001953.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123894351 C>T maps to NM_001001953.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248004726 G>A maps to NM_001001959.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248004726 G>A maps to NM_001001959.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:247614513 T>A maps to NM_001004492.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:247614513 T>A maps to NM_001004492.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:48238556 T>C maps to NM_001005470.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:48238556 T>C maps to NM_001005470.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59271728 T>C maps to NM_001004706.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59271728 T>C maps to NM_001004706.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59283101 C>A maps to NM_001004711.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59283101 C>A maps to NM_001004711.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97806522 T>G maps to NM_054106.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97806522 T>G maps to NM_054106.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97852014 C>A maps to NM_001005338.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97852014 C>A maps to NM_001005338.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:56258012 G>T maps to NM_001005282.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:56258012 G>T maps to NM_001005282.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158669515 A>T maps to NM_001005279.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158669515 A>T maps to NM_001005279.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:56127835 C>G maps to NM_001005205.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:56127835 C>G maps to NM_001005205.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:48921693 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:48921693 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:141618890 C>T maps to NM_001001656.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:141618890 C>T maps to NM_001001656.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:4190607 G>T maps to NM_177998.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:4190607 G>T maps to NM_177998.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:101721761 T>A maps to NM_002568.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:101721761 T>A maps to NM_002568.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56720555 G>A maps to NM_001127460.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56720555 G>A maps to NM_001127460.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:118950339 C>A maps to NM_002581.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:118950339 C>A maps to NM_002581.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:70056646 T>A maps to NM_022129.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:70056646 T>A maps to NM_022129.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:91873527 A>G maps to NM_032968.3 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:91873527 A>G maps to NM_032968.3 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:55582280 G>T maps to NM_001142763.1 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:55582280 G>T maps to NM_001142763.1 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:55944962 A>T maps to NM_001142763.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:55944962 A>T maps to NM_001142763.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:58207234 C>T maps to NM_001040429.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:58207234 C>T maps to NM_001040429.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:140503841 G>A maps to NM_018938.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:140503841 G>A maps to NM_018938.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:140712359 C>G maps to NM_018912.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:140712359 C>G maps to NM_018912.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:56755249 C>T maps to NM_021255.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:56755249 C>T maps to NM_021255.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:57353893 G>T maps to NM_001135690.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:57353893 G>T maps to NM_001135690.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:8169550 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:8169550 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:106508032 C>A maps to NM_002649.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:106508032 C>A maps to NM_002649.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:47882628 C>T maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:47882628 C>T maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:9360750 C>T maps to NM_001172646.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:9360750 C>T maps to NM_001172646.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41382475 T>C maps to NM_001005473.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41382475 T>C maps to NM_001005473.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:4517572 C>T maps to NM_001080400.1 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:4517572 C>T maps to NM_001080400.1 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:108155041 T>A maps to NM_015723.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:108155041 T>A maps to NM_015723.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:35065589 C>G maps to NM_000949.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:35065589 C>G maps to NM_000949.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:10387129 G>T maps to NM_198464.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:10387129 G>T maps to NM_198464.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:214557622 T>A maps to NM_005401.4 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:214557622 T>A maps to NM_005401.4 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:71016261 C>A maps to NM_001109754.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:71016261 C>A maps to NM_001109754.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:29587413 A>C maps to NM_005704.4 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:29587413 A>C maps to NM_005704.4 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:121624101 G>T maps to NM_002851.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:121624101 G>T maps to NM_002851.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:1652062 C>G maps to NM_012293.1 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:1652062 C>G maps to NM_012293.1 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:4776564 G>T maps to NM_014737.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:4776564 G>T maps to NM_014737.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151314766 C>T maps to NM_000449.3 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151314766 C>T maps to NM_000449.3 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:56390278 C>A maps to NM_022841.5 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:56390278 C>A maps to NM_022841.5 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:3441278 G>C maps to NM_198229.2 A1404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:3441278 G>C maps to NM_198229.2 A1404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:43161677 G>A maps to ENST00000352483 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:43161677 G>A maps to ENST00000352483 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:78357709 C>G maps to NM_020914.4 L4817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:78357709 C>G maps to NM_020914.4 L4817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:5752386 G>A maps to NM_207111.2 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:5752386 G>A maps to NM_207111.2 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:124745496 G>A maps to NM_022370.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:124745496 G>A maps to NM_022370.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:10466456 G>A maps to NM_178857.5 P1717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:10466456 G>A maps to NM_178857.5 P1717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:159493973 T>C maps to ENST00000440678 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:159493973 T>C maps to ENST00000440678 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:166856286 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:166856286 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:167055685 G>C maps to ENST00000303354 V1822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:167055685 G>C maps to ENST00000303354 V1822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:9227043 C>G maps to NM_003966.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:9227043 C>G maps to NM_003966.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:19427360 C>A maps to NM_172231.2 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:19427360 C>A maps to NM_172231.2 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:46355640 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:46355640 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51918204 G>T maps to NM_033130.4 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51918204 G>T maps to NM_033130.4 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51958819 G>T maps to NM_014442.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51958819 G>T maps to NM_014442.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:44845962 G>T maps to NM_173354.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:44845962 G>T maps to NM_173354.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:56904029 C>T maps to NM_000339.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:56904029 C>T maps to NM_000339.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:107676119 C>A maps to NM_017515.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:107676119 C>A maps to NM_017515.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:18270267 G>T maps to NM_001145195.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:18270267 G>T maps to NM_001145195.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:205628457 G>A maps to NM_033102.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:205628457 G>A maps to NM_033102.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33355538 C>T maps to NM_014270.4 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33355538 C>T maps to NM_014270.4 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:103299839 C>T maps to NM_003048.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:103299839 C>T maps to NM_003048.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:143271263 G>T maps to NM_173653.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:143271263 G>T maps to NM_173653.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:133672505 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:133672505 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:168098300 G>T maps to NM_003062.2 C1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:168098300 G>T maps to NM_003062.2 C1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2751312 C>T maps to NM_015295.2 I1401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2751312 C>T maps to NM_015295.2 I1401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2303979 C>A maps to NM_013321.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2303979 C>A maps to NM_013321.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:107005407 G>T maps to NM_014978.1 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:107005407 G>T maps to NM_014978.1 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:231067406 G>C maps to NM_080424.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:231067406 G>C maps to NM_080424.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:136078060 C>T maps to NM_005862.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:136078060 C>T maps to NM_005862.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:47746386 T>A maps to NM_001048166.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:47746386 T>A maps to NM_001048166.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:133106582 C>A maps to NM_174937.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:133106582 C>A maps to NM_174937.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:97862144 C>G maps to ENST00000379795 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:97862144 C>G maps to ENST00000379795 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:4310142 G>T maps to NM_003223.2 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:4310142 G>T maps to NM_003223.2 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:70451748 C>A maps to NM_022173.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:70451748 C>A maps to NM_022173.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:82340022 G>T maps to ENST00000376537 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:82340022 G>T maps to ENST00000376537 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66061838 C>A maps to NM_153266.3 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66061838 C>A maps to NM_153266.3 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:7993220 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:7993220 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:175106084 C>A maps to NM_022093.1 R1186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:175106084 C>A maps to NM_022093.1 R1186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:209951495 G>A maps to NM_025228.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:209951495 G>A maps to NM_025228.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:141370269 C>A maps to NM_031466.5 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:141370269 C>A maps to NM_031466.5 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:41196630 C>A maps to NM_198153.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:41196630 C>A maps to NM_198153.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:4406604 G>A maps to NM_003141.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:4406604 G>A maps to NM_003141.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:51872087 C>A maps to NM_173485.5 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:51872087 C>A maps to NM_173485.5 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179391981 G>C maps to NM_133378.4 G33343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179391981 G>C maps to NM_133378.4 G33343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179467006 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179467006 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:43857643 C>T maps to NM_018961.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:43857643 C>T maps to NM_018961.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:122647788 C>T maps to NM_032873.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:122647788 C>T maps to NM_032873.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:76168612 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:76168612 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:35310541 T>C maps to ENST00000396787 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:35310541 T>C maps to ENST00000396787 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:58366862 C>T maps to NM_001130480.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:58366862 C>T maps to NM_001130480.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:61026548 A>G maps to NM_152718.2 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:61026548 A>G maps to NM_152718.2 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:117959579 G>T maps to NM_173798.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:117959579 G>T maps to NM_173798.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:77616592 C>A maps to NM_024721.4 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:77616592 C>A maps to NM_024721.4 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:68217814 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:68217814 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:9581104 A>G maps to NM_152476.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:9581104 A>G maps to NM_152476.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:182026578 C>A maps to NM_001009992.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:182026578 C>A maps to NM_001009992.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:113955153 G>A maps to NM_007136.3 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:113955153 G>A maps to NM_007136.3 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:57768488 C>A maps to NM_178457.1 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:57768488 C>A maps to NM_178457.1 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:21215359 G>C maps to NM_003460.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:21215359 G>C maps to NM_003460.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:45506069 T>A maps to NM_020883.1 K584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:45506069 T>A maps to NM_020883.1 K584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:89659581 C>A maps to NM_152924.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:89659581 C>A maps to NM_152924.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:2938382 C>T maps to NM_080431.4 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:2938382 C>T maps to NM_080431.4 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:978963 C>G maps to NM_198576.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:978963 C>G maps to NM_198576.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:29551312 G>A maps to NM_004304.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:29551312 G>A maps to NM_004304.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:193210949 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:193210949 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:99641942 C>T maps to NM_138576.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:99641942 C>T maps to NM_138576.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:28576108 C>A maps to NM_000386.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:28576108 C>A maps to NM_000386.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:128774401 C>T maps to NM_145013.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:128774401 C>T maps to NM_145013.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:24923530 C>T maps to NM_018958.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:24923530 C>T maps to NM_018958.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:34663080 C>T maps to NM_001134734.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:34663080 C>T maps to NM_001134734.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:61689617 G>T maps to NM_001796.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:61689617 G>T maps to NM_001796.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:45671387 G>A maps to NM_003654.4 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:45671387 G>A maps to NM_003654.4 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:16358737 G>T maps to NM_004070.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:16358737 G>T maps to NM_004070.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:65447221 C>T maps to NM_006660.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:65447221 C>T maps to NM_006660.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:2778832 C>A maps to NM_019609.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:2778832 C>A maps to NM_019609.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:113363402 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:113363402 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:51535049 G>A maps to NM_031226.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:51535049 G>A maps to NM_031226.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:110653617 A>G maps to ENST00000358070 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:110653617 A>G maps to ENST00000358070 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:15953186 C>T maps to NM_032341.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:15953186 C>T maps to NM_032341.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:23019677 G>T maps to NM_182699.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:23019677 G>T maps to NM_182699.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:14378176 G>C maps to NM_004080.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:14378176 G>C maps to NM_004080.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:186299185 G>A maps to NM_016306.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:186299185 G>A maps to NM_016306.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:30021432 G>T maps to NM_003586.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:30021432 G>T maps to NM_003586.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:33449608 T>C maps to NM_024025.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:33449608 T>C maps to NM_024025.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:38448409 A>T maps to ENST00000354891 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:38448409 A>T maps to ENST00000354891 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:6266992 G>C maps to NM_000129.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:6266992 G>C maps to NM_000129.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:8138146 G>A maps to NM_032447.3 C2579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:8138146 G>A maps to NM_032447.3 C2579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:49170213 C>A maps to NM_004476.1 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:49170213 C>A maps to NM_004476.1 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26864297 G>A maps to NM_003593.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26864297 G>A maps to NM_003593.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:49210067 G>T maps to NM_000145.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:49210067 G>T maps to NM_000145.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:112024100 T>A maps to NM_153047.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:112024100 T>A maps to NM_153047.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:61040521 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:61040521 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:58006845 C>G maps to NM_001111270.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:58006845 C>G maps to NM_001111270.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:129360513 G>T maps to ENST00000442111 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:129360513 G>T maps to ENST00000442111 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:66788001 C>G maps to ENST00000359742 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:66788001 C>G maps to ENST00000359742 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:41055875 A>T maps to ENST00000296803 L334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:41055875 A>T maps to ENST00000296803 L334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:40148228 C>T maps to NM_016257.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:40148228 C>T maps to NM_016257.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:131102211 G>T maps to NM_033416.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:131102211 G>T maps to NM_033416.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:5020915 G>A maps to NM_000217.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:5020915 G>A maps to NM_000217.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:163302908 C>T maps to NM_033272.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:163302908 C>T maps to NM_033272.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:72300886 G>T maps to NM_014431.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:72300886 G>T maps to NM_014431.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:72351373 C>A maps to NM_153209.3 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:72351373 C>A maps to NM_153209.3 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:124658212 A>T maps to NM_001081675.2 C504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:124658212 A>T maps to NM_001081675.2 C504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:52962031 G>A maps to NM_175053.3 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:52962031 G>A maps to NM_175053.3 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:107703284 G>T maps to NM_007356.2 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:107703284 G>T maps to NM_007356.2 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:153177437 C>G maps to NM_001010857.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:153177437 C>G maps to NM_001010857.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:205389622 G>A maps to ENST00000367153 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:205389622 G>A maps to ENST00000367153 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:55107954 A>G maps to NM_006863.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:55107954 A>G maps to NM_006863.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:133637537 C>T maps to ENST00000250173 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:133637537 C>T maps to ENST00000250173 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:90400996 C>G maps to NM_001134479.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:90400996 C>G maps to NM_001134479.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:68688211 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:68688211 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:43607849 C>T maps to NM_001003690.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:43607849 C>T maps to NM_001003690.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:166959002 C>A maps to NM_032858.1 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:166959002 C>A maps to NM_032858.1 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:30676134 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:30676134 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:158527040 C>T maps to NM_022736.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:158527040 C>T maps to NM_022736.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr22:43870628 C>G maps to NM_001044370.1 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr22:43870628 C>G maps to NM_001044370.1 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:1915811 G>A maps to ENST00000399161 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:1915811 G>A maps to ENST00000399161 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:15701344 G>C maps to NM_015909.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:15701344 G>C maps to NM_015909.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:204943310 G>T maps to ENST00000367172 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:204943310 G>T maps to ENST00000367172 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:15141369 G>A maps to NM_173474.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:15141369 G>A maps to NM_173474.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:133051266 G>T maps to ENST00000262283 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:133051266 G>T maps to ENST00000262283 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:137814806 C>T maps to NM_175747.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:137814806 C>T maps to NM_175747.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:21623230 G>A maps to NM_001004731.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:21623230 G>A maps to NM_001004731.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:56128573 T>A maps to NM_001005205.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:56128573 T>A maps to NM_001005205.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:38287588 G>T maps to NM_005109.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:38287588 G>T maps to NM_005109.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:112899607 C>G maps to NM_007203.4 S595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:112899607 C>G maps to NM_007203.4 S595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:25017844 T>A maps to NM_006437.3 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:25017844 T>A maps to NM_006437.3 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:140237381 G>A maps to NM_018901.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:140237381 G>A maps to NM_018901.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:204197887 C>T maps to ENST00000367191 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:204197887 C>T maps to ENST00000367191 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:138763204 C>G maps to NM_001134657.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:138763204 C>G maps to NM_001134657.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:52781430 G>T maps to NM_000956.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:52781430 G>T maps to NM_000956.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:61471409 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:61471409 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:5997178 G>A maps to NM_000635.3 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:5997178 G>A maps to NM_000635.3 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:33264241 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:33264241 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:59483392 G>A maps to NM_173557.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:59483392 G>A maps to NM_173557.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:11332365 A>G maps to NM_004850.3 P1357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:11332365 A>G maps to NM_004850.3 P1357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:12683869 G>A maps to NM_001112706.2 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:12683869 G>A maps to NM_001112706.2 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:122645423 G>T maps to NM_001031702.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:122645423 G>T maps to NM_001031702.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:48244786 G>A maps to NM_000023.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:48244786 G>A maps to NM_000023.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:436422 C>T maps to NM_012435.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:436422 C>T maps to NM_012435.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:113420520 C>T maps to NM_005415.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:113420520 C>T maps to NM_005415.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:53409447 C>A maps to NM_006306.2 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:53409447 C>A maps to NM_006306.2 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:51465645 C>A maps to NM_018967.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:51465645 C>A maps to NM_018967.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:104149162 C>G maps to NM_017564.9 G2266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:104149162 C>G maps to NM_017564.9 G2266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:67942346 G>T maps to NM_001142503.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:67942346 G>T maps to NM_001142503.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:57501992 G>A maps to NM_003153.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:57501992 G>A maps to NM_003153.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:5461852 C>T maps to NM_018401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:5461852 C>T maps to NM_018401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:33560220 C>A maps to NM_198992.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:33560220 C>A maps to NM_198992.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:51135966 G>T maps to NM_001160329.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:51135966 G>T maps to NM_001160329.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:173176417 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:173176417 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:1316877 T>C maps to ENST00000382211 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:1316877 T>C maps to ENST00000382211 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:179568919 G>T maps to NM_133378.4 T8815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:179568919 G>T maps to NM_133378.4 T8815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:145651591 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:145651591 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:38189080 C>T maps to NM_023034.1 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:38189080 C>T maps to NM_023034.1 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:46543168 C>A maps to ENST00000242848 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:46543168 C>A maps to ENST00000242848 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:52991904 C>T maps to NM_001009881.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:52991904 C>T maps to NM_001009881.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:36883978 G>T maps to NM_133466.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:36883978 G>T maps to NM_133466.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:43323187 G>A maps to NM_014345.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:43323187 G>A maps to NM_014345.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:27368574 T>C maps to NM_001076781.1 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:27368574 T>C maps to NM_001076781.1 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:21214497 T>C maps to NM_003460.1 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:21214497 T>C maps to NM_003460.1 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:145770789 C>A maps to NM_025251.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:145770789 C>A maps to NM_025251.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:64673895 C>A maps to ENST00000421419 R1031R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:64673895 C>A maps to ENST00000421419 R1031R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:185552920 G>A maps to NM_032991.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:185552920 G>A maps to NM_032991.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:62289212 C>T maps to NM_173519.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:62289212 C>T maps to NM_173519.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:14110403 C>T maps to NM_001303.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:14110403 C>T maps to NM_001303.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:41704793 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:41704793 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:20013765 G>A maps to NM_001033553.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:20013765 G>A maps to NM_001033553.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:52416425 G>A maps to ENST00000273600 A2632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:52416425 G>A maps to ENST00000273600 A2632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:96533505 G>T maps to NM_001080448.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:96533505 G>T maps to NM_001080448.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:27840113 C>A maps to NM_001109763.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:27840113 C>A maps to NM_001109763.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:8307712 T>C maps to NM_053044.3 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:8307712 T>C maps to NM_053044.3 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:173344443 G>A maps to ENST00000264106 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:173344443 G>A maps to ENST00000264106 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr10:118969398 G>A maps to NM_181840.1 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr10:118969398 G>A maps to NM_181840.1 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:52862851 C>T maps to NM_173086.4 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:52862851 C>T maps to NM_173086.4 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:53169353 C>T maps to NM_015848.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:53169353 C>T maps to NM_015848.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:60904065 G>C maps to NM_005560.3 L1427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:60904065 G>C maps to NM_005560.3 L1427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:107600229 G>A maps to NM_002291.2 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:107600229 G>A maps to NM_002291.2 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr21:47685863 G>T maps to NM_003906.3 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr21:47685863 G>T maps to NM_003906.3 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:90381975 G>T maps to NM_014611.1 S4579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:90381975 G>T maps to NM_014611.1 S4579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:313563 C>A maps to NM_017550.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:313563 C>A maps to NM_017550.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:18052869 C>T maps to ENST00000205890 D2396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:18052869 C>T maps to ENST00000205890 D2396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:15935792 T>G maps to ENST00000395857 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:15935792 T>G maps to ENST00000395857 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:29528173 T>C maps to NM_001042492.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:29528173 T>C maps to NM_001042492.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:22102424 G>A maps to NM_001005466.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:22102424 G>A maps to NM_001005466.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr13:61987634 G>A maps to NM_022843.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr13:61987634 G>A maps to NM_022843.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:44157302 T>A maps to NM_006230.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:44157302 T>A maps to NM_006230.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:43523197 C>A maps to ENST00000449000 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:43523197 C>A maps to ENST00000449000 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr13:48941719 C>T maps to NM_000321.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr13:48941719 C>T maps to NM_000321.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:161223814 C>A maps to NM_016836.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:161223814 C>A maps to NM_016836.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:16411655 T>C maps to NM_015150.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:16411655 T>C maps to NM_015150.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:159572993 A>T maps to ENST00000440678 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:159572993 A>T maps to ENST00000440678 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:109764083 C>T maps to NM_003080.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:109764083 C>T maps to NM_003080.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:26905477 G>A maps to NM_006461.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:26905477 G>A maps to NM_006461.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:144337279 C>T maps to NM_001009614.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:144337279 C>T maps to NM_001009614.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr9:35102813 G>A maps to NM_013442.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr9:35102813 G>A maps to NM_013442.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:106967750 G>A maps to NM_001163436.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:106967750 G>A maps to NM_001163436.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:11464414 G>C maps to ENST00000423059 Y1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:11464414 G>C maps to ENST00000423059 Y1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:49335337 A>T maps to NM_003363.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:49335337 A>T maps to NM_003363.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:35884084 G>T maps to NM_005095.2 E1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:35884084 G>T maps to NM_005095.2 E1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr18:74587575 C>T maps to NM_007345.3 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr18:74587575 C>T maps to NM_007345.3 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:8873338 C>A maps to NM_001127448.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:8873338 C>A maps to NM_001127448.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:22035726 G>T maps to NM_005691.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:22035726 G>T maps to NM_005691.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:58503018 C>A maps to NM_003500.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:58503018 C>A maps to NM_003500.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:185709867 T>C maps to NM_001995.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:185709867 T>C maps to NM_001995.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33630890 T>A maps to NM_030955.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33630890 T>A maps to NM_030955.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161161349 C>A maps to NM_005099.4 G698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161161349 C>A maps to NM_005099.4 G698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161166466 G>T maps to NM_005099.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161166466 G>T maps to NM_005099.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:64672372 G>T maps to NM_182920.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:64672372 G>T maps to NM_182920.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:105409322 G>T maps to NM_138420.2 S4155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:105409322 G>T maps to NM_138420.2 S4155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:86278313 C>A maps to NM_006738.4 P2462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:86278313 C>A maps to NM_006738.4 P2462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:97388189 C>A maps to NM_002860.3 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:97388189 C>A maps to NM_002860.3 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:29519815 G>T maps to NM_004304.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:29519815 G>T maps to NM_004304.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:85383196 G>T maps to NM_020778.4 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:85383196 G>T maps to NM_020778.4 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:112021836 C>A maps to NM_001113490.1 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:112021836 C>A maps to NM_001113490.1 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:41552782 C>G maps to ENST00000415018 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:41552782 C>G maps to ENST00000415018 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:114279595 C>A maps to NM_001148.4 P3274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:114279595 C>A maps to NM_001148.4 P3274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27389138 G>T maps to NM_014915.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27389138 G>T maps to NM_014915.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:201477352 C>A maps to NM_001159.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:201477352 C>A maps to NM_001159.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:201534296 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:201534296 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:57036508 G>T maps to NM_153360.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:57036508 G>T maps to NM_153360.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154295569 G>T maps to NM_080429.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154295569 G>T maps to NM_080429.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:47570223 C>A maps to NM_006420.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:47570223 C>A maps to NM_006420.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:142513548 C>A maps to NM_015071.4 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:142513548 C>A maps to NM_015071.4 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:119134030 C>A maps to NM_020754.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:119134030 C>A maps to NM_020754.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:128839602 G>T maps to NM_001142685.1 P1821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:128839602 G>T maps to NM_001142685.1 P1821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:57377509 G>T maps to ENST00000360096 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:57377509 G>T maps to ENST00000360096 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:94891011 A>T maps to NM_198150.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:94891011 A>T maps to NM_198150.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:197102651 C>T maps to NM_018136.4 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:197102651 C>T maps to NM_018136.4 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:31021249 C>A maps to ENST00000375687 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:31021249 C>A maps to ENST00000375687 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161762109 C>A maps to NM_007348.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161762109 C>A maps to NM_007348.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161823064 C>A maps to NM_007348.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161823064 C>A maps to NM_007348.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:234178660 C>A maps to ENST00000392018 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:234178660 C>A maps to ENST00000392018 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160145942 C>A maps to NM_144699.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160145942 C>A maps to NM_144699.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:119509272 G>T maps to NM_001142447.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:119509272 G>T maps to NM_001142447.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52515215 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52515215 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:63968679 C>A maps to NM_001177387.1 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:63968679 C>A maps to NM_001177387.1 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:31858869 G>A maps to NM_194318.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:31858869 G>A maps to NM_194318.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57009182 C>A maps to NM_013449.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57009182 C>A maps to NM_013449.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:70049061 G>A maps to NM_032735.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:70049061 G>A maps to NM_032735.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:112638547 G>A maps to NM_001109662.2 R2649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:112638547 G>A maps to NM_001109662.2 R2649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:76620802 C>A maps to NM_017926.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:76620802 C>A maps to NM_017926.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:65890719 G>A maps to ENST00000420799 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:65890719 G>A maps to ENST00000420799 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:67698918 G>T maps to NM_032140.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:67698918 G>T maps to NM_032140.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:8092891 C>A maps to NM_017622.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:8092891 C>A maps to NM_017622.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156314497 G>T maps to NM_144627.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156314497 G>T maps to NM_144627.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:31672737 C>A maps to NM_182519.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:31672737 C>A maps to NM_182519.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:742373 G>A maps to NM_033409.3 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:742373 G>A maps to NM_033409.3 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:11723708 C>A maps to NM_001143948.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:11723708 C>A maps to NM_001143948.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100087212 C>A maps to ENST00000423930 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100087212 C>A maps to ENST00000423930 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:124243669 C>A maps to NM_032847.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:124243669 C>A maps to NM_032847.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:139740033 C>A maps to NM_001080482.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:139740033 C>A maps to NM_001080482.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:58236700 G>T maps to NM_000717.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:58236700 G>T maps to NM_000717.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:2788764 G>T maps to NM_199460.2 V1797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:2788764 G>T maps to NM_199460.2 V1797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27463195 C>A maps to NM_004341.3 R1854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27463195 C>A maps to NM_004341.3 R1854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27465514 G>T maps to NM_004341.3 G2084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27465514 G>T maps to NM_004341.3 G2084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:91090602 C>A maps to NM_004929.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:91090602 C>A maps to NM_004929.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:64950963 G>T maps to NM_005186.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:64950963 G>T maps to NM_005186.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:42676730 C>T maps to NM_000070.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:42676730 C>T maps to NM_000070.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:92905526 C>A maps to NM_017667.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:92905526 C>A maps to NM_017667.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159858267 G>T maps to NM_012337.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159858267 G>T maps to NM_012337.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:37007249 C>A maps to NM_003914.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:37007249 C>A maps to NM_003914.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:54528248 C>A maps to NM_021147.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:54528248 C>A maps to NM_021147.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:46415413 C>A maps to NM_001100168.1 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:46415413 C>A maps to NM_001100168.1 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158261956 G>T maps to NM_001765.2 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158261956 G>T maps to NM_001765.2 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158262416 C>A maps to NM_001765.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158262416 C>A maps to NM_001765.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:45127318 G>T maps to NM_022842.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:45127318 G>T maps to NM_022842.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:19747252 C>A maps to NM_004934.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:19747252 C>A maps to NM_004934.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:25457371 G>T maps to NM_018451.3 S1320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:25457371 G>T maps to NM_018451.3 S1320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:123907180 C>A maps to NM_007018.4 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:123907180 C>A maps to NM_007018.4 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:55880440 G>A maps to NM_001143685.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:55880440 G>A maps to NM_001143685.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40033673 C>A maps to NM_032221.3 A2569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40033673 C>A maps to NM_032221.3 A2569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40049531 C>A maps to NM_032221.3 G1915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40049531 C>A maps to NM_032221.3 G1915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:61773533 C>A maps to NM_017780.2 P2560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:61773533 C>A maps to NM_017780.2 P2560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:122286255 G>T maps to NM_015282.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:122286255 G>T maps to NM_015282.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:23444922 G>T maps to NM_153603.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:23444922 G>T maps to NM_153603.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:48629361 A>T maps to NM_000094.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:48629361 A>T maps to NM_000094.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:47746497 G>T maps to NM_006587.2 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:47746497 G>T maps to NM_006587.2 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:69011815 C>A maps to NM_006091.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:69011815 C>A maps to NM_006091.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:46679111 G>T maps to NM_001872.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:46679111 G>T maps to NM_001872.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:87027875 C>A maps to NM_001143935.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:87027875 C>A maps to NM_001143935.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153924903 G>T maps to NM_181715.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153924903 G>T maps to NM_181715.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:166533019 C>A maps to ENST00000409420 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:166533019 C>A maps to ENST00000409420 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:77470358 C>A maps to NM_004715.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:77470358 C>A maps to NM_004715.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:119672568 C>A maps to NM_003588.3 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:119672568 C>A maps to NM_003588.3 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:42917185 G>C maps to NM_004391.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:42917185 G>C maps to NM_004391.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155708001 C>A maps to NM_004632.3 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155708001 C>A maps to NM_004632.3 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155001741 G>T maps to NM_144622.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155001741 G>T maps to NM_144622.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153910246 G>T maps to NM_014856.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153910246 G>T maps to NM_014856.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31540671 G>T maps to NM_144973.3 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31540671 G>T maps to NM_144973.3 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220284977 G>T maps to NM_001927.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220284977 G>T maps to NM_001927.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:24585974 G>C maps to NM_001358.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:24585974 G>C maps to NM_001358.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:72130759 G>T maps to NM_014003.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:72130759 G>T maps to NM_014003.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:39090539 G>T maps to NM_198963.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:39090539 G>T maps to NM_198963.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:32472825 C>A maps to ENST00000357033 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:32472825 C>A maps to ENST00000357033 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:124274523 G>T maps to NM_207437.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:124274523 G>T maps to NM_207437.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:76503451 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:76503451 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:11778438 C>A maps to NM_001372.3 G3472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:11778438 C>A maps to NM_001372.3 G3472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:69571281 C>A maps to NM_021800.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:69571281 C>A maps to NM_021800.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:9785071 G>A maps to NM_000798.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:9785071 G>A maps to NM_000798.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:345853 G>T maps to ENST00000457386 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:345853 G>T maps to ENST00000457386 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:102483805 C>T maps to NM_001376.4 P2714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:102483805 C>T maps to NM_001376.4 P2714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150484962 C>A maps to ENST00000369049 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150484962 C>A maps to ENST00000369049 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:236645687 G>T maps to NM_145861.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:236645687 G>T maps to NM_145861.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:107521058 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:107521058 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:144942171 G>T maps to NM_031308.1 P1750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:144942171 G>T maps to NM_031308.1 P1750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:56491619 C>A maps to NM_001982.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:56491619 C>A maps to NM_001982.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:51048294 G>T maps to NM_007051.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:51048294 G>T maps to NM_007051.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:51863824 G>T maps to NM_001005751.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:51863824 G>T maps to NM_001005751.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:47919964 G>T maps to NM_018232.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:47919964 G>T maps to NM_018232.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:37027523 C>A maps to NM_001013736.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:37027523 C>A maps to NM_001013736.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:43629293 G>T maps to NM_001145196.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:43629293 G>T maps to NM_001145196.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:43630578 T>A maps to NM_001145196.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:43630578 T>A maps to NM_001145196.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:187518024 G>T maps to ENST00000260147 P4226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:187518024 G>T maps to ENST00000260147 P4226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:187541781 C>A maps to ENST00000260147 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:187541781 C>A maps to ENST00000260147 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:150943132 T>G maps to NM_001447.2 A1109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:150943132 T>G maps to NM_001447.2 A1109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157665122 G>T maps to NM_052939.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157665122 G>T maps to NM_052939.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159779905 C>A maps to NM_001004310.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159779905 C>A maps to NM_001004310.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:60125888 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:60125888 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:155526027 C>A maps to ENST00000407946 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:155526027 C>A maps to ENST00000407946 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152325409 C>A maps to NM_001014342.2 G1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152325409 C>A maps to NM_001014342.2 G1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:147063137 C>T maps to NM_152578.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:147063137 C>T maps to NM_152578.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:159646575 C>A maps to NM_032532.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:159646575 C>A maps to NM_032532.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:54145823 C>A maps to NM_001080432.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:54145823 C>A maps to NM_001080432.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:31200999 G>T maps to NM_004960.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:31200999 G>T maps to NM_004960.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151070419 G>T maps to NM_144618.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151070419 G>T maps to NM_144618.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:161119184 T>A maps to NM_000811.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:161119184 T>A maps to NM_000811.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:130149546 C>A maps to NM_032293.4 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:130149546 C>A maps to NM_032293.4 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:79117223 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:79117223 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76982253 G>T maps to ENST00000376217 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76982253 G>T maps to ENST00000376217 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:121768116 G>T maps to NM_000165.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:121768116 G>T maps to NM_000165.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:113935463 C>A maps to NM_020918.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:113935463 C>A maps to NM_020918.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:157427749 C>A maps to NM_000408.4 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:157427749 C>A maps to NM_000408.4 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:46977421 G>T maps to ENST00000283297 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:46977421 G>T maps to ENST00000283297 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:131487495 C>A maps to NM_207364.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:131487495 C>A maps to NM_207364.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:89933561 G>T maps to NM_032119.3 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:89933561 G>T maps to NM_032119.3 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:7620332 C>T maps to NM_181874.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:7620332 C>T maps to NM_181874.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:108635058 C>A maps to NM_005459.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:108635058 C>A maps to NM_005459.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:52216703 G>T maps to NM_001523.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:52216703 G>T maps to NM_001523.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:48191904 G>T maps to NM_015401.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:48191904 G>T maps to NM_015401.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:31604166 C>A maps to NM_015382.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:31604166 C>A maps to NM_015382.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:12015887 C>A maps to NM_002114.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:12015887 C>A maps to NM_002114.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:71103614 C>A maps to ENST00000439900 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:71103614 C>A maps to ENST00000439900 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:42761350 C>A maps to NM_032410.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:42761350 C>A maps to NM_032410.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:27148286 G>T maps to NM_153631.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:27148286 G>T maps to NM_153631.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:63327590 C>A maps to NM_017878.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:63327590 C>A maps to NM_017878.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152188170 G>T maps to NM_001009931.1 G1978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152188170 G>T maps to NM_001009931.1 G1978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:3728878 C>A maps to NM_052970.4 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:3728878 C>A maps to NM_052970.4 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:183818363 C>A maps to NM_182589.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:183818363 C>A maps to NM_182589.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:102796284 C>A maps to NM_000618.3 *154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:102796284 C>A maps to NM_000618.3 *154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:46627155 G>T maps to NM_207393.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:46627155 G>T maps to NM_207393.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:27374556 A>G maps to NM_000418.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:27374556 A>G maps to NM_000418.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153640109 C>A maps to NM_004515.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153640109 C>A maps to NM_004515.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:100961604 C>A maps to NM_016247.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:100961604 C>A maps to NM_016247.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:62261223 A>T maps to NM_176877.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:62261223 A>T maps to NM_176877.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:41729271 G>T maps to NM_002192.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:41729271 G>T maps to NM_002192.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57849973 C>A maps to NM_031479.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57849973 C>A maps to NM_031479.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145533109 G>A maps to NM_003637.3 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145533109 G>A maps to NM_003637.3 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:161052000 G>T maps to NM_000888.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:161052000 G>T maps to NM_000888.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160849190 C>A maps to NM_017625.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160849190 C>A maps to NM_017625.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:26868351 C>A maps to NM_002223.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:26868351 C>A maps to NM_002223.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:147019227 C>A maps to NM_014790.3 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:147019227 C>A maps to NM_014790.3 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:64950683 G>C maps to NM_032776.1 A2087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:64950683 G>C maps to NM_032776.1 A2087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153949470 C>A maps to NM_006694.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153949470 C>A maps to NM_006694.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:124160830 A>T maps to NM_001024660.3 K1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:124160830 A>T maps to NM_001024660.3 K1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:47989687 G>T maps to NM_004975.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:47989687 G>T maps to NM_004975.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:61601588 C>A maps to NM_030779.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:61601588 C>A maps to NM_030779.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32503441 T>A maps to NM_006559.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32503441 T>A maps to NM_006559.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:42823607 G>T maps to NM_015349.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:42823607 G>T maps to NM_015349.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:35906653 G>T maps to NM_024874.4 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:35906653 G>T maps to NM_024874.4 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:27720168 G>A maps to NM_015202.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:27720168 G>A maps to NM_015202.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:36869263 G>T maps to NM_001029864.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:36869263 G>T maps to NM_001029864.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:10327559 G>A maps to ENST00000377086 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:10327559 G>A maps to ENST00000377086 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:149857287 G>T maps to NM_004522.1 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:149857287 G>T maps to NM_004522.1 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55331450 G>A maps to ENST00000355608 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55331450 G>A maps to ENST00000355608 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:39593786 G>A maps to NM_006771.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:39593786 G>A maps to NM_006771.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:118199276 C>A maps to ENST00000339824 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:118199276 C>A maps to ENST00000339824 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:45436076 G>T maps to NM_015340.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:45436076 G>T maps to NM_015340.3 T44T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-91-6836-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:40777864 C>T maps to ENST00000415847 T28T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-91-6836-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:40777864 C>T maps to ENST00000415847 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21788498 G>A maps to NM_002300.6 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21788498 G>A maps to NM_002300.6 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:25005380 G>T maps to NM_018176.3 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:25005380 G>T maps to NM_018176.3 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:51885705 C>A maps to NM_030657.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:51885705 C>A maps to NM_030657.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:97405753 A>T maps to NM_001142292.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:97405753 A>T maps to NM_001142292.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:201915288 C>A maps to NM_012134.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:201915288 C>A maps to NM_012134.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:97823727 C>A maps to NM_014916.3 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:97823727 C>A maps to NM_014916.3 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1489937 G>T maps to NM_024830.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1489937 G>T maps to NM_024830.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:58318705 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:58318705 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:155670221 G>T maps to NM_004744.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:155670221 G>T maps to NM_004744.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24530800 G>T maps to NM_138360.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24530800 G>T maps to NM_138360.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:169557829 T>C maps to NM_024727.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:169557829 T>C maps to NM_024727.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76372165 C>A maps to NM_001128922.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76372165 C>A maps to NM_001128922.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:40136343 G>T maps to NM_020929.1 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:40136343 G>T maps to NM_020929.1 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:33572564 C>A maps to ENST00000354476 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:33572564 C>A maps to ENST00000354476 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:4283516 C>T maps to NM_017816.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:4283516 C>T maps to NM_017816.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:15918145 C>A maps to ENST00000310348 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:15918145 C>A maps to ENST00000310348 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:26212817 G>T maps to NM_173523.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:26212817 G>T maps to NM_173523.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:21217466 C>A maps to NM_145109.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:21217466 C>A maps to NM_145109.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:47912406 G>T maps to ENST00000426837 R2064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:47912406 G>T maps to ENST00000426837 R2064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:20070998 G>T maps to NM_001168465.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:20070998 G>T maps to NM_001168465.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:87080527 C>A maps to NM_138982.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:87080527 C>A maps to NM_138982.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:164506982 C>T maps to ENST00000514618 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:164506982 C>T maps to ENST00000514618 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:71668180 G>T maps to NM_052858.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:71668180 G>T maps to NM_052858.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:116424998 C>A maps to NM_015335.4 T1343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:116424998 C>A maps to NM_015335.4 T1343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:64574663 C>A maps to NM_130804.2 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:64574663 C>A maps to NM_130804.2 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237024486 C>A maps to NM_000254.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237024486 C>A maps to NM_000254.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:9017373 G>T maps to NM_024690.2 T12650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:9017373 G>T maps to NM_024690.2 T12650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:10206530 C>T maps to NM_003802.2 K1883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:10206530 C>T maps to NM_003802.2 K1883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:123419313 C>A maps to NM_053025.3 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:123419313 C>A maps to NM_053025.3 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57432272 C>A maps to NM_005379.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57432272 C>A maps to NM_005379.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76873963 C>A maps to NM_000260.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76873963 C>A maps to NM_000260.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:59668090 C>A maps to NM_199290.3 G151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:59668090 C>A maps to NM_199290.3 G151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:16892188 G>T maps to NM_017940.3 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:16892188 G>T maps to NM_017940.3 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:24985566 C>A maps to NM_003743.4 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:24985566 C>A maps to NM_003743.4 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:46262883 C>A maps to NM_181659.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:46262883 C>A maps to NM_181659.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:115891728 C>A maps to NM_022569.1 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:115891728 C>A maps to NM_022569.1 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:152499150 A>C maps to NM_001164507.1 Y2770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:152499150 A>C maps to NM_001164507.1 Y2770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:152554105 C>T maps to NM_001164507.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:152554105 C>T maps to NM_001164507.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:97311449 G>T maps to NM_001135175.1 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:97311449 G>T maps to NM_001135175.1 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:11190424 G>T maps to NM_006403.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:11190424 G>T maps to NM_006403.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:127089650 G>T maps to NM_001166171.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:127089650 G>T maps to NM_001166171.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:44917198 C>A maps to NM_001145107.1 G675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:44917198 C>A maps to NM_001145107.1 G675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156641483 C>A maps to NM_006617.1 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156641483 C>A maps to NM_006617.1 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:25761682 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:25761682 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161088668 C>A maps to NM_005600.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161088668 C>A maps to NM_005600.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:6008260 C>A maps to NM_015102.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:6008260 C>A maps to NM_015102.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15045797 A>G maps to NM_006985.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15045797 A>G maps to NM_006985.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:11907171 G>T maps to NM_006172.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:11907171 G>T maps to NM_006172.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:132177685 C>A maps to NM_001144058.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:132177685 C>A maps to NM_001144058.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:132180090 C>A maps to NM_001144058.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:132180090 C>A maps to NM_001144058.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:205687461 G>T maps to NM_022731.4 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:205687461 G>T maps to NM_022731.4 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37292070 C>T maps to NM_153485.1 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37292070 C>T maps to NM_153485.1 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:47826138 C>A maps to NM_015231.1 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:47826138 C>A maps to NM_015231.1 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:136081313 G>T maps to NM_014581.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:136081313 G>T maps to NM_014581.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:167420137 C>A maps to NM_001122679.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:167420137 C>A maps to NM_001122679.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:127572396 C>A maps to NM_182487.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:127572396 C>A maps to NM_182487.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:13154490 G>T maps to NM_021980.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:13154490 G>T maps to NM_021980.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:55322786 C>G maps to NM_001001920.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:55322786 C>G maps to NM_001001920.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:59245021 G>T maps to NM_001004705.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:59245021 G>T maps to NM_001004705.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:56310559 G>T maps to NM_001005245.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:56310559 G>T maps to NM_001005245.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:56020493 T>A maps to NM_001004747.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:56020493 T>A maps to NM_001004747.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:247875556 G>T maps to NM_001005286.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:247875556 G>T maps to NM_001005286.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:9236945 T>C maps to NM_001001958.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:9236945 T>C maps to NM_001001958.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:58111705 C>A maps to NM_006812.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:58111705 C>A maps to NM_006812.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:149916537 C>A maps to NM_020205.2 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:149916537 C>A maps to NM_020205.2 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:149931639 G>T maps to NM_020205.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:149931639 G>T maps to NM_020205.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:42990263 G>T maps to NM_148962.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:42990263 G>T maps to NM_148962.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:101724685 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:101724685 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:127255044 A>T maps to NM_006193.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:127255044 A>T maps to NM_006193.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:136048787 C>A maps to NM_001178014.1 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:136048787 C>A maps to NM_001178014.1 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:138451366 C>A maps to NM_019035.3 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:138451366 C>A maps to NM_019035.3 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:141244218 G>A maps to NM_032420.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:141244218 G>A maps to NM_032420.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:78547385 C>A maps to NM_001190482.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:78547385 C>A maps to NM_001190482.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:20522728 G>T maps to NM_000921.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:20522728 G>T maps to NM_000921.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:119044269 G>A maps to NM_173791.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:119044269 G>A maps to NM_173791.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:24344109 G>T maps to NM_199346.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:24344109 G>T maps to NM_199346.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7138982 G>T maps to NM_024297.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7138982 G>T maps to NM_024297.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:85685774 G>T maps to ENST00000393343 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:85685774 G>T maps to ENST00000393343 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:106509118 C>A maps to NM_002649.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:106509118 C>A maps to NM_002649.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:94316699 C>A maps to NM_152431.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:94316699 C>A maps to NM_152431.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:2155466 C>A maps to NM_001009944.2 R2624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:2155466 C>A maps to NM_001009944.2 R2624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:8639184 T>C maps to NM_015192.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:8639184 T>C maps to NM_015192.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:81942092 G>T maps to NM_002661.2 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:81942092 G>T maps to NM_002661.2 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:17051809 C>A maps to NM_001144382.1 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:17051809 C>A maps to NM_001144382.1 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:208218556 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:208218556 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:94542932 C>T maps to NM_005761.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:94542932 C>T maps to NM_005761.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:46997189 G>T maps to NM_020709.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:46997189 G>T maps to NM_020709.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151381038 G>T maps to NM_015100.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151381038 G>T maps to NM_015100.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:79741203 G>T maps to NM_007055.3 S1291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:79741203 G>T maps to NM_007055.3 S1291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:51589812 G>A maps to NM_002702.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:51589812 G>A maps to NM_002702.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:27832503 C>A maps to NM_003622.3 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:27832503 C>A maps to NM_003622.3 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:4934020 C>A maps to NM_002705.4 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:4934020 C>A maps to NM_002705.4 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:12941826 G>T maps to ENST00000376192 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:12941826 G>T maps to ENST00000376192 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:5282850 G>T maps to NM_144773.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:5282850 G>T maps to NM_144773.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150298243 C>A maps to NM_004698.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150298243 C>A maps to NM_004698.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:126860496 G>T maps to ENST00000330542 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:126860496 G>T maps to ENST00000330542 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:2871422 A>G maps to NM_006799.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:2871422 A>G maps to NM_006799.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151373828 C>A maps to NM_002796.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151373828 C>A maps to NM_002796.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151239725 C>A maps to ENST00000368881 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151239725 C>A maps to ENST00000368881 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:45297681 C>A maps to NM_003738.4 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:45297681 C>A maps to NM_003738.4 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27687284 G>T maps to NM_001034842.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27687284 G>T maps to NM_001034842.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:157931163 C>A maps to NM_002847.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:157931163 C>A maps to NM_002847.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:27042266 C>T maps to NM_001144943.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:27042266 C>T maps to NM_001144943.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72741443 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72741443 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220326682 G>T maps to ENST00000358951 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220326682 G>T maps to ENST00000358951 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220332760 A>T maps to ENST00000358951 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220332760 A>T maps to ENST00000358951 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28920081 C>A maps to NM_024816.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28920081 C>A maps to NM_024816.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100961445 C>A maps to NM_022777.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100961445 C>A maps to NM_022777.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109352196 G>T maps to NM_006267.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109352196 G>T maps to NM_006267.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:5925685 C>A maps to NM_007322.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:5925685 C>A maps to NM_007322.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:205070737 G>T maps to NM_005057.3 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:205070737 G>T maps to NM_005057.3 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:24578601 G>T maps to NM_006910.4 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:24578601 G>T maps to NM_006910.4 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:125621031 C>A maps to NM_001100588.1 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:125621031 C>A maps to NM_001100588.1 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:57797279 C>A maps to NM_005612.4 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:57797279 C>A maps to NM_005612.4 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:186522424 C>A maps to NM_181573.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:186522424 C>A maps to NM_181573.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:107144438 G>T maps to ENST00000357881 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:107144438 G>T maps to ENST00000357881 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151315027 G>T maps to NM_000449.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151315027 G>T maps to NM_000449.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:116279873 G>C maps to NM_144488.4 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:116279873 G>C maps to NM_144488.4 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:105260982 G>A maps to NM_001100117.2 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:105260982 G>A maps to NM_001100117.2 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150444216 G>T maps to NM_015203.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150444216 G>T maps to NM_015203.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:78899231 G>T maps to NM_020761.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:78899231 G>T maps to NM_020761.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:45107883 T>G maps to NM_015056.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:45107883 T>G maps to NM_015056.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:67776805 C>A maps to NM_173630.3 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:67776805 C>A maps to NM_173630.3 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237947923 C>A maps to NM_001035.2 G4304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237947923 C>A maps to NM_001035.2 G4304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:192701172 C>A maps to NM_004657.5 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:192701172 C>A maps to NM_004657.5 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:139370618 C>A maps to NM_014866.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:139370618 C>A maps to NM_014866.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145115871 C>A maps to NM_004892.4 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145115871 C>A maps to NM_004892.4 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:110452554 G>T maps to NM_006323.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:110452554 G>T maps to NM_006323.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:13830920 C>A maps to NM_025229.1 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:13830920 C>A maps to NM_025229.1 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151339213 G>T maps to ENST00000435071 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151339213 G>T maps to ENST00000435071 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156144921 C>A maps to NM_022367.3 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156144921 C>A maps to NM_022367.3 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:132101158 G>T maps to NM_001098811.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:132101158 G>T maps to NM_001098811.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:45574079 C>A maps to NM_007056.2 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:45574079 C>A maps to NM_007056.2 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:36946214 G>T maps to NM_001101341.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:36946214 G>T maps to NM_001101341.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:152096010 G>T maps to NM_001009555.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:152096010 G>T maps to NM_001009555.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:84286885 G>A maps to ENST00000434347 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:84286885 G>A maps to ENST00000434347 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:51123020 C>T maps to NM_001080420.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:51123020 C>T maps to NM_001080420.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:38572537 C>A maps to NM_015073.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:38572537 C>A maps to NM_015073.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:1559270 G>T maps to NM_006065.3 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:1559270 G>T maps to NM_006065.3 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:46262149 G>A maps to NM_003726.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:46262149 G>A maps to NM_003726.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131115779 G>T maps to NM_005094.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131115779 G>T maps to NM_005094.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:44979442 C>A maps to NM_173179.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:44979442 C>A maps to NM_173179.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33947309 G>T maps to NM_016180.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33947309 G>T maps to NM_016180.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220493251 C>A maps to NM_201574.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220493251 C>A maps to NM_201574.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:51890824 G>T maps to NM_001039960.1 E1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:51890824 G>T maps to NM_001039960.1 E1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:139740436 C>A maps to ENST00000507527 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:139740436 C>A maps to ENST00000507527 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:35467931 G>T maps to NM_006933.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:35467931 G>T maps to NM_006933.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1217011 C>T maps to NM_001003841.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1217011 C>T maps to NM_001003841.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21054389 C>A maps to NM_019844.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21054389 C>A maps to NM_019844.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156222250 G>T maps to NM_015327.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156222250 G>T maps to NM_015327.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:88405947 C>T maps to NM_198274.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:88405947 C>T maps to NM_198274.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:7987215 C>A maps to NM_003083.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:7987215 C>A maps to NM_003083.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:108439444 G>T maps to NM_001013031.1 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:108439444 G>T maps to NM_001013031.1 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:89764656 G>T maps to NM_152339.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:89764656 G>T maps to NM_152339.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:78021717 G>T maps to NM_004863.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:78021717 G>T maps to NM_004863.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:126015632 G>T maps to NM_003129.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:126015632 G>T maps to NM_003129.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:24979111 C>A maps to NM_005839.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:24979111 C>A maps to NM_005839.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:53071669 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:53071669 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:76779641 C>A maps to NM_152996.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:76779641 C>A maps to NM_152996.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:17369044 T>A maps to NM_001004470.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:17369044 T>A maps to NM_001004470.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:27010601 C>G maps to ENST00000382009 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:27010601 C>G maps to ENST00000382009 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:171488251 C>T maps to NM_005990.3 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:171488251 C>T maps to NM_005990.3 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29820929 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29820929 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155837813 G>A maps to NM_152280.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155837813 G>A maps to NM_152280.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:132874616 G>T maps to NM_053278.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:132874616 G>T maps to NM_053278.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:1729566 A>T maps to NM_006342.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:1729566 A>T maps to NM_006342.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:120807871 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:120807871 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150471510 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150471510 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:104380777 G>T maps to NM_003211.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:104380777 G>T maps to NM_003211.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:90446934 C>T maps to NM_018319.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:90446934 C>T maps to NM_018319.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:114044341 C>A maps to NM_058222.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:114044341 C>A maps to NM_058222.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56688568 G>T maps to ENST00000240361 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56688568 G>T maps to ENST00000240361 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:155619653 T>C maps to NM_016020.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:155619653 T>C maps to NM_016020.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:12938643 C>T maps to ENST00000311912 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:12938643 C>T maps to ENST00000311912 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24679974 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24679974 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29911707 C>A maps to NM_001193451.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29911707 C>A maps to NM_001193451.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:83289718 C>A maps to NM_152588.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:83289718 C>A maps to NM_152588.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:201332476 G>T maps to ENST00000421663 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:201332476 G>T maps to ENST00000421663 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:3724426 C>A maps to NM_016292.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:3724426 C>A maps to NM_016292.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:114466307 G>T maps to NM_018700.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:114466307 G>T maps to NM_018700.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:176078804 C>A maps to NM_012171.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:176078804 C>A maps to NM_012171.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:91077092 G>T maps to NM_001010854.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:91077092 G>T maps to NM_001010854.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:76330169 C>A maps to NM_015072.4 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:76330169 C>A maps to NM_015072.4 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179554579 G>T maps to NM_133378.4 P9358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179554579 G>T maps to NM_133378.4 P9358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179605488 G>T maps to NM_133437.3 S3986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179605488 G>T maps to NM_133437.3 S3986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72246133 G>T maps to NM_032646.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72246133 G>T maps to NM_032646.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:94013 G>T maps to NM_177987.2 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:94013 G>T maps to NM_177987.2 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154229621 C>A maps to NM_014847.3 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154229621 C>A maps to NM_014847.3 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:125397359 C>A maps to NM_021009.5 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:125397359 C>A maps to NM_021009.5 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161127931 G>T maps to NM_016406.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161127931 G>T maps to NM_016406.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:35955883 C>A maps to NM_152404.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:35955883 C>A maps to NM_152404.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:19699553 G>C maps to NM_014683.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:19699553 G>C maps to NM_014683.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:19720107 C>A maps to NM_014683.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:19720107 C>A maps to NM_014683.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:20906348 C>A maps to ENST00000455117 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:20906348 C>A maps to ENST00000455117 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:23080431 T>A maps to NM_020718.3 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:23080431 T>A maps to NM_020718.3 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:58259004 G>T maps to NM_032582.3 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:58259004 G>T maps to NM_032582.3 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:61447537 G>T maps to NM_014709.3 R2652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:61447537 G>T maps to NM_014709.3 R2652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56051992 G>T maps to NM_007146.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56051992 G>T maps to NM_007146.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:37035793 G>T maps to NM_053276.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:37035793 G>T maps to NM_053276.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52293448 A>T maps to NM_052950.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52293448 A>T maps to NM_052950.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:13916468 G>C maps to NM_004625.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:13916468 G>C maps to NM_004625.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:108642020 G>T maps to ENST00000261400 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:108642020 G>T maps to ENST00000261400 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:69922134 C>A maps to NM_007014.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:69922134 C>A maps to NM_007014.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:32902874 G>T maps to NM_001040436.1 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:32902874 G>T maps to NM_001040436.1 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:32908082 C>A maps to NM_001040436.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:32908082 C>A maps to NM_001040436.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27412569 C>A maps to NM_139312.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27412569 C>A maps to NM_139312.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154987588 G>T maps to ENST00000417934 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154987588 G>T maps to ENST00000417934 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:38120041 C>A maps to NM_021943.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:38120041 C>A maps to NM_021943.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:77690581 C>A maps to NM_024721.4 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:77690581 C>A maps to NM_024721.4 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:68597523 G>T maps to NM_133458.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:68597523 G>T maps to NM_133458.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:28217606 G>T maps to NM_019110.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:28217606 G>T maps to NM_019110.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:44807179 G>A maps to NM_031449.3 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:44807179 G>A maps to NM_031449.3 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:23688527 G>T maps to NM_001077195.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:23688527 G>T maps to NM_001077195.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:247492766 G>T maps to NM_032752.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:247492766 G>T maps to NM_032752.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:99521410 C>A maps to NM_014930.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:99521410 C>A maps to NM_014930.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:31039466 C>A maps to NM_014717.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:31039466 C>A maps to NM_014717.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:57768083 A>T maps to NM_178457.1 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:57768083 A>T maps to NM_178457.1 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:22939009 G>T maps to ENST00000397104 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:22939009 G>T maps to ENST00000397104 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:45486329 G>T maps to NM_020883.1 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:45486329 G>T maps to NM_020883.1 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:35693143 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:35693143 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:111691237 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:111691237 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:236908166 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:236908166 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:42850110 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:42850110 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:5239415 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:5239415 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:147891533 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:147891533 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:141333839 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:141333839 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:6337462 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:6337462 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:243788173 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:243788173 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:41526167 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:41526167 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:3391184 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:3391184 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:7532077 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:7532077 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:131797797 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:131797797 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:109233493 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:109233493 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:160129069 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:160129069 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:50279568 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:50279568 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:48488522 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:48488522 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:31669837 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:31669837 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:23603508 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:23603508 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:60475333 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:60475333 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:43806917 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:43806917 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:81967851 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:81967851 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:7861541 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:7861541 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:105692281 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:105692281 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:100615031 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:100615031 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:64070922 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:64070922 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:77888947 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:77888947 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:34385559 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:34385559 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:13645086 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:13645086 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:178489436 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:178489436 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:10536778 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:10536778 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:67404638 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:67404638 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:53781536 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:53781536 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:128457971 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:128457971 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:32687783 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:32687783 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:2499481 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:2499481 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:33266099 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:33266099 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:111441856 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:111441856 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:111342567 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:111342567 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:24505405 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:24505405 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:90708878 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:90708878 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:51986167 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:51986167 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:122737583 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:122737583 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:92818630 C>A maps to NM_001025233.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:92818630 C>A maps to NM_001025233.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:87680186 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:87680186 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:246797931 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:246797931 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:1414442 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:1414442 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:103404445 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:103404445 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:48267567 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:48267567 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:139662109 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:139662109 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:109861881 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:109861881 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr13:110866241 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr13:110866241 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:74416828 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:74416828 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:28778671 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:28778671 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:70904861 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:70904861 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:48993902 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:48993902 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:37652909 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:37652909 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15626342 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15626342 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:50592284 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:50592284 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:114449870 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:114449870 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:7093986 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:7093986 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:79584086 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:79584086 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:58196649 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:58196649 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:117744480 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:117744480 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:50757035 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:50757035 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:71892549 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:71892549 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:158422407 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:158422407 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:233347809 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:233347809 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:187084173 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:187084173 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:175525843 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:175525843 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:129099250 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:129099250 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:58468285 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:58468285 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:33420147 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:33420147 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:154956052 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:154956052 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr13:28592863 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr13:28592863 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:240334611 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:240334611 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:49450413 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:49450413 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:197500908 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:197500908 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:46314441 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:46314441 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:1960872 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:1960872 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:30885980 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:30885980 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:20329819 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:20329819 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:132863625 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:132863625 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:28499528 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:28499528 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:10099003 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:10099003 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:37315868 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:37315868 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:13764832 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:13764832 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:104385809 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:104385809 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:89422057 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:89422057 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:87380942 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:87380942 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:204824218 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:204824218 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:163167476 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:163167476 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:21350973 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:21350973 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:27670356 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:27670356 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:52054118 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:52054118 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:190347360 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:190347360 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:1881899 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:1881899 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:24428073 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:24428073 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:142641548 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:142641548 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:43888541 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:43888541 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:57187350 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:57187350 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:43010182 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:43010182 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:200957784 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:200957784 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:57966318 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:57966318 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:40003691 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:40003691 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:30755913 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:30755913 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:165180079 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:165180079 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:25610439 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:25610439 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:53764516 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:53764516 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:70446280 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:70446280 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:33335900 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:33335900 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:74992708 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:74992708 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:26080121 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:26080121 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:43702884 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:43702884 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:71501079 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:71501079 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:99016071 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:99016071 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:13884608 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:13884608 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:126784719 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:126784719 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:15651973 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:15651973 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:28308926 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:28308926 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:1977657 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:1977657 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:56660199 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:56660199 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:121458854 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:121458854 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:32229772 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:32229772 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:26351347 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:26351347 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:95121451 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:95121451 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:95137203 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:95137203 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:89910922 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:89910922 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:52481178 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:52481178 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:173993350 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:173993350 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:104174050 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:104174050 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:154030837 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:154030837 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:123787311 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:123787311 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:50946144 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:50946144 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:3819546 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:3819546 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:176769066 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:176769066 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:55129753 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:55129753 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:152624921 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:152624921 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:47697717 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:47697717 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:22147483 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:22147483 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:8720887 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:8720887 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:208213272 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:208213272 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:121213343 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:121213343 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:76793377 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:76793377 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:242098538 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:242098538 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:131885507 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:131885507 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:156761674 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:156761674 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43698861 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43698861 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43412071 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43412071 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:9304935 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:9304935 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:49069462 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:49069462 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:85776839 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:85776839 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:114404164 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:114404164 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:63681310 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:63681310 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:103202195 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:103202195 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:183675639 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:183675639 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:105173186 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:105173186 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:79793824 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:79793824 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:39305208 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:39305208 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:107031107 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:107031107 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:55200230 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:55200230 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:67684535 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:67684535 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:93088146 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:93088146 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:33873623 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:33873623 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:127905021 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:127905021 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:129925072 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:129925072 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:167144878 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:167144878 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:23224088 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:23224088 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:144885745 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:144885745 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:76892495 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:76892495 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:4215260 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:4215260 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:13856518 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:13856518 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:94924519 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:94924519 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:2765323 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:2765323 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:160718357 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:160718357 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:34610758 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:34610758 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:131647849 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:131647849 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:118596812 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:118596812 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:135112286 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:135112286 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:168176449 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:168176449 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:220338411 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:220338411 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:2807380 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:2807380 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:80738413 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:80738413 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:80769406 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:80769406 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:182760623 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:182760623 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:149495276 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:149495276 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:4025385 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:4025385 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:34004173 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:34004173 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:70608724 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chrX:70608724 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:65146828 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:65146828 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:4312297 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:4312297 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:29945180 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:29945180 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:38242897 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:38242897 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:44403454 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:44403454 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:15427302 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:15427302 G>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:19698599 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:19698599 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:150410426 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:150410426 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:53024707 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:53024707 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:35723404 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:35723404 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:144444876 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:144444876 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr13:19997122 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr13:19997122 T>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:10944558 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:10944558 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:30370041 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:30370041 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:28876956 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:28876956 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:72938099 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:72938099 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:81498718 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:81498718 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:94839404 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:94839404 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:40766498 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:40766498 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:71905130 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:71905130 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:43838766 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr21:43838766 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:74387719 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:74387719 A>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:1273141 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:1273141 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:113700071 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:113700071 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:77919801 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:77919801 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:100733411 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:100733411 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:12428681 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:12428681 C>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:123995131 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:123995131 C>G did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:61049183 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:61049183 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:122405847 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:122405847 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:228786283 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:228786283 A>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:56362865 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:56362865 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:6628083 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:6628083 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:3451892 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:3451892 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:52976587 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:52976587 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:85341291 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:85341291 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:50070680 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:50070680 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:52580286 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:52580286 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:9021844 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:9021844 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:9248128 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:9248128 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:8870075 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:8870075 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:150916358 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:150916358 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:89415155 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:89415155 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:74042271 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:74042271 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20548857 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20548857 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20448523 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20448523 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:64780684 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:64780684 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:96871084 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:96871084 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:33294033 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:33294033 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:40741334 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:40741334 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:5128064 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:5128064 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:202352273 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:202352273 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:40895190 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:40895190 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:27369607 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:27369607 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:228285784 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:228285784 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:30938485 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:30938485 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:11312821 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:11312821 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:17933142 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:17933142 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:177190269 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:177190269 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:62139608 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:62139608 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:32093855 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:32093855 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:203689889 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:203689889 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:154304211 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:154304211 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:379829 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:379829 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:48263365 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:48263365 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:11038749 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:11038749 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:11047628 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:11047628 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:11049483 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:11049483 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:18238751 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:18238751 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:32841391 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:32841391 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:36938801 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:36938801 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:116628764 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:116628764 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:134754367 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:134754367 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:6231939 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:6231939 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:88374098 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:88374098 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:45374762 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:45374762 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr18:51892229 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr18:51892229 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:178489755 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:178489755 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:37125559 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:37125559 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:41160202 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:41160202 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:165714064 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:165714064 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:165715840 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:165715840 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:57351891 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:57351891 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:96064464 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:96064464 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:27918182 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:27918182 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:86571449 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:86571449 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:159162338 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:159162338 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:24897314 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:24897314 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18513265 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18513265 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:126135137 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:126135137 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:85606472 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:85606472 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:78083006 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:78083006 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:7805560 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:7805560 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:174228251 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:174228251 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:17669445 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:17669445 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:55886646 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:55886646 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:67035549 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:67035549 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:49539681 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:49539681 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:126485327 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:126485327 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:203148403 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:203148403 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:125797914 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:125797914 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:7830366 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:7830366 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:201726364 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:201726364 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:62411996 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:62411996 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:99008298 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:99008298 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:17395094 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:17395094 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:125521482 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:125521482 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:103491750 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:103491750 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:47541581 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:47541581 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:130361755 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:130361755 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:68430093 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:68430093 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:197411254 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:197411254 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:34191212 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:34191212 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:113648998 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:113648998 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:96827274 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:96827274 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:42027797 C>T maps to ENST00000439847 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:42027797 C>T maps to ENST00000439847 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:99457660 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:99457660 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:72063034 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:72063034 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:43111524 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:43111524 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:19038920 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:19038920 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:6794175 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:6794175 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:29978207 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:29978207 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:100646343 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:100646343 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:120941886 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:120941886 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:234360761 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:234360761 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:172966463 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:172966463 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:53930232 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:53930232 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:76567764 G>T maps to ENST00000389840 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:76567764 G>T maps to ENST00000389840 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:11805969 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:11805969 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:77423506 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:77423506 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:74899556 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:74899556 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:36320641 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:36320641 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44168669 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44168669 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:120605877 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:120605877 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:23111645 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:23111645 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:37868023 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:37868023 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:6182452 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:6182452 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:57421224 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:57421224 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:201931712 A>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:201931712 A>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:74091818 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:74091818 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:62628502 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:62628502 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:95773621 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:95773621 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:17726036 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:17726036 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:60718285 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:60718285 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21553833 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21553833 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:142469693 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:142469693 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:49227604 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:49227604 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:31090139 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:31090139 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:144359060 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:144359060 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:29541892 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:29541892 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:26534842 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:26534842 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:19611893 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:19611893 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:135865098 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:135865098 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:179765435 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:179765435 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:179765469 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:179765469 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:73237910 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:73237910 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:133368075 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:133368075 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:155764976 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:155764976 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20084938 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20084938 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:95271296 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:95271296 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:19012896 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:19012896 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:30959668 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:30959668 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:88323945 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:88323945 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:178424906 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:178424906 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:145034896 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:145034896 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:54401487 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:54401487 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:28413405 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:28413405 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:75187578 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:75187578 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:71020805 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:71020805 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:177632763 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:177632763 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:22178776 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:22178776 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:147845313 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:147845313 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:70893943 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:70893943 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:91067140 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:91067140 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:47121274 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:47121274 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:113819952 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:113819952 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:15198537 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:15198537 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:118860656 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:118860656 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:20348898 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:20348898 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:30783691 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:30783691 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:30509425 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:30509425 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31392130 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31392130 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:65325707 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:65325707 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:19322620 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:19322620 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:6417151 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:6417151 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:94048431 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:94048431 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:30915257 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:30915257 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:53166439 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:53166439 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:25948904 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:25948904 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:42162153 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:42162153 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:36993139 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:36993139 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:22150747 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:22150747 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:38264753 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:38264753 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18394414 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18394414 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:75602949 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:75602949 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:54818625 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:54818625 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:54756139 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:54756139 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:5694280 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:5694280 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161027466 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161027466 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:133948535 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:133948535 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:66436827 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:66436827 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:196386523 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:196386523 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:79985706 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:79985706 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:90152310 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:90152310 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:166959143 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:166959143 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:136901579 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:136901579 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:10426692 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:10426692 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:160585776 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:160585776 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:58149710 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:58149710 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:13251195 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:13251195 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:112751737 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:112751737 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:132396293 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:132396293 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:4730184 A>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:4730184 A>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:154009731 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:154009731 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:24705103 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:24705103 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:41328101 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:41328101 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:819648 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:819648 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:64897085 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:64897085 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:11194589 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:11194589 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:48597185 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:48597185 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10405337 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10405337 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:123456176 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:123456176 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:52553357 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:52553357 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:12661231 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:12661231 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:95082778 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:95082778 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:164061565 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:164061565 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:72769926 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:72769926 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:78512104 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:78512104 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:183791691 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:183791691 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:204917936 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:204917936 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:104159991 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:104159991 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:173323001 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:173323001 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:151777532 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:151777532 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:43704592 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:43704592 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:33473884 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:33473884 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:117696827 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:117696827 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:155761073 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:155761073 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:132423265 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:132423265 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:103541716 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:103541716 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:102895640 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:102895640 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:228494001 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:228494001 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:50959843 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:50959843 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:74079268 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:74079268 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:248247346 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:248247346 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:122079562 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:122079562 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:3593567 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:3593567 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:23792381 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:23792381 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:52661507 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:52661507 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:70314809 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:70314809 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:56360355 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:56360355 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20386368 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20386368 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:35093360 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:35093360 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:3642712 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:3642712 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:33021746 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:33021746 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:160806344 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:160806344 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:64026280 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:64026280 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161173311 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161173311 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:145913108 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:145913108 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:44531073 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:44531073 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:94603507 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:94603507 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44276816 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44276816 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:44116295 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:44116295 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:38162190 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:38162190 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:35393440 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:35393440 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:75206338 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:75206338 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:32123308 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:32123308 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:69002765 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:69002765 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:102047967 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:102047967 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:20486125 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:20486125 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:45110460 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:45110460 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:36467788 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:36467788 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:228005253 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:228005253 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:11585378 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:11585378 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:48131008 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:48131008 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:3001865 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:3001865 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:198721699 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:198721699 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:55711566 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:55711566 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:29642074 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:29642074 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:121684367 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:121684367 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:20457961 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:20457961 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:2901470 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:2901470 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:179564830 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:179564830 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:46293310 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:46293310 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:79384952 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:79384952 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:79253766 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:79253766 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:79254103 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:79254103 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:92846256 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:92846256 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:81574062 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:81574062 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:45480162 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:45480162 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:32332698 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:32332698 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:237663944 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:237663944 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:78146328 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:78146328 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:159614440 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:159614440 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:167142802 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:167142802 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:74707314 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:74707314 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:95029669 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:95029669 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:95056655 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:95056655 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:37412860 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:37412860 T>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:84245578 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:84245578 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52033902 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52033902 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:60714393 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:60714393 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:100796556 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:100796556 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:44983626 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:44983626 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:46592315 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:46592315 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:62656233 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:62656233 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:42340146 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:42340146 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:27465718 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:27465718 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:27498175 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:27498175 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:55703416 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:55703416 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:70585056 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:70585056 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:101748938 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:101748938 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:98823917 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:98823917 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:50480786 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:50480786 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:106974166 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:106974166 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:39281973 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:39281973 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:22700145 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:22700145 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:34507189 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:34507189 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:220330714 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:220330714 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:147488427 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:147488427 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:55658604 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:55658604 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:131329001 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:131329001 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:9097847 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:9097847 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:187387108 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:187387108 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:48214518 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chrX:48214518 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:104096857 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:104096857 C>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:55853578 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:55853578 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:152655122 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:152655122 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:234595079 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:234595079 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:55895775 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:55895775 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:97870672 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:97870672 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:43552186 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:43552186 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:133948142 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:133948142 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:32825387 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:32825387 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:105360724 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:105360724 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:125833841 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:125833841 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:111794426 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:111794426 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:175097112 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:175097112 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:175375920 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:175375920 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:218686681 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:218686681 G>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:47463612 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:47463612 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:25642556 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:25642556 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:154166049 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:154166049 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:1488718 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:1488718 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:10922018 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:10922018 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:10942680 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:10942680 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:42230896 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:42230896 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:14471393 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:14471393 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:72967642 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:72967642 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:45815243 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:45815243 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:45821807 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:45821807 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:104681197 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:104681197 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:162567547 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:162567547 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:44443865 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:44443865 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:39771867 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:39771867 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:109926479 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:109926479 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:10239469 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:10239469 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:26629268 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:26629268 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:64069454 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:64069454 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20348851 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:20348851 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:96106166 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:96106166 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:62783189 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:62783189 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:113688668 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:113688668 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:144719264 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:144719264 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:144719291 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:144719291 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:2846969 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:2846969 A>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:42321607 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:42321607 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:36590593 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:36590593 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:67299653 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:67299653 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:38416674 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:38416674 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:32410791 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:32410791 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:111628166 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:111628166 T>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21558620 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21558620 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:64239686 A>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:64239686 A>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:21467188 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:21467188 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:21588788 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:21588788 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:32847438 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:32847438 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:53218913 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:53218913 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52627139 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52627139 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:81599368 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:81599368 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:44279285 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:44279285 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:2376380 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:2376380 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:109617932 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:109617932 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:108016772 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:108016772 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:87792284 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:87792284 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:24207289 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:24207289 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:39627141 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:39627141 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:1599056 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:1599056 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:45699469 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:45699469 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:7804814 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:7804814 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:40759086 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:40759086 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:86801145 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:86801145 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:86823105 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:86823105 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:116838846 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:116838846 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:110173097 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:110173097 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:74019916 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:74019916 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:92680174 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:92680174 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:101430688 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:101430688 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:101433708 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:101433708 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:101433906 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:101433906 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:150503932 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:150503932 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:32917841 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:32917841 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:86898878 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:86898878 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:11316664 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:11316664 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:66352734 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:66352734 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:150714101 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:150714101 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:10419886 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:10419886 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:63554792 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:63554792 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79166470 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79166470 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:72880867 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:72880867 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:11407581 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:11407581 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:36336970 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:36336970 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1472753 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1472753 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56403171 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56403171 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:16745716 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:16745716 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:73472616 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:73472616 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:118425378 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:118425378 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:62461563 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:62461563 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:2280965 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:2280965 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:231474383 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:231474383 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:60463538 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:60463538 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:156902557 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:156902557 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:34622569 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:34622569 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:40234472 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:40234472 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:2593886 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:2593886 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:25176553 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:25176553 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:34379747 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:34379747 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:140809009 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:140809009 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:141010275 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:141010275 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:2704936 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:2704936 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:181680016 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:181680016 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:54481547 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:54481547 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:54481549 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:54481549 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:46930138 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:46930138 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:134074269 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:134074269 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:110492303 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:110492303 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:15260163 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:15260163 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:75784884 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:75784884 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:122002502 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:122002502 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:14034500 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:14034500 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:42931197 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:42931197 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:110595085 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:110595085 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:74623140 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:74623140 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:119960725 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:119960725 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:45943392 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:45943392 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:837378 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:837378 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:80302010 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:80302010 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:21817017 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:21817017 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:21817021 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:21817021 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:68714850 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:68714850 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43093465 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43093465 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:6172548 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:6172548 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:82670558 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:82670558 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:23766504 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:23766504 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:136623174 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:136623174 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:61982413 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:61982413 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:154541835 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:154541835 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:14703195 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:14703195 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:7830188 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:7830188 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:123319370 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:123319370 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:87660203 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:87660203 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:87671610 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:87671610 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:224927215 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:224927215 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:74570184 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:74570184 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:165556061 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:165556061 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:33139749 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:33139749 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:33142404 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:33142404 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:75823502 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:75823502 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:48275259 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:48275259 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:109767252 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:109767252 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:116956462 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:116956462 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:48629265 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:48629265 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:149459215 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:149459215 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:47453592 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:47453592 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:93840945 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:93840945 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:211437941 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:211437941 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:197169701 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:197169701 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:122741924 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:122741924 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:99799917 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:99799917 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:35320561 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:35320561 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:36965932 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:36965932 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:99370100 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:99370100 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:16025236 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:16025236 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:16000217 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:16000217 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:59405180 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:59405180 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:59793590 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:59793590 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:57476974 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:57476974 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:3961335 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:3961335 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:155176939 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:155176939 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:169294998 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:169294998 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:137154235 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:137154235 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:79950396 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:79950396 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:40256701 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:40256701 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:182850643 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:182850643 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:47969891 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:47969891 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:55621588 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:55621588 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:13793972 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:13793972 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:109050529 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:109050529 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:41559768 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:41559768 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:42080836 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:42080836 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:80577306 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:80577306 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:110925517 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:110925517 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:140729016 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:140729016 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:53400345 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:53400345 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:73455692 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:73455692 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:80631255 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:80631255 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:120594881 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:120594881 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:120613782 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:120613782 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:142567014 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:142567014 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:51937459 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:51937459 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:61083937 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:61083937 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:86215677 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:86215677 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:128358753 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:128358753 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:127697496 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:127697496 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:127728738 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:127728738 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:55233597 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:55233597 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:125052357 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:125052357 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:84603940 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:84603940 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:58120279 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:58120279 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:33357124 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:33357124 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:146680353 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:146680353 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:14748735 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:14748735 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:131233312 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:131233312 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:49393810 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:49393810 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:17446951 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:17446951 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:230378929 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:230378929 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:53378979 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:53378979 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:120578933 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:120578933 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:118461088 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:118461088 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:167761352 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:167761352 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:37696651 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:37696651 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:113638906 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:113638906 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:11737792 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:11737792 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:31061955 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:31061955 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:74227164 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:74227164 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:25077021 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:25077021 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:45267020 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:45267020 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:236746280 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:236746280 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:73964836 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:73964836 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:65408431 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:65408431 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:42738902 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:42738902 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:29691943 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:29691943 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:221055380 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:221055380 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:21072172 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:21072172 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:60791982 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:60791982 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:14891689 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:14891689 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:70993477 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:70993477 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:190327005 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:190327005 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:66628922 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:66628922 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:66628926 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:66628926 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:50689297 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:50689297 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:182363663 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:182363663 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:73746101 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:73746101 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:124485039 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:124485039 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:20441335 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:20441335 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:52833112 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:52833112 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:41706686 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:41706686 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:156009594 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:156009594 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:70760879 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:70760879 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:36721882 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:36721882 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:493004 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:493004 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:26942854 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:26942854 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:70125489 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:70125489 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:94041585 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:94041585 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:61315480 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:61315480 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:44839183 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:44839183 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:10327433 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:10327433 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:55275190 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:55275190 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:126070626 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:126070626 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:51379646 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:51379646 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:39633998 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:39633998 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:52755389 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:52755389 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:119565407 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:119565407 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:36120152 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:36120152 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:71978709 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:71978709 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:25452334 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:25452334 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:70488726 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:70488726 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:42114657 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:42114657 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:239064 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:239064 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:166960796 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:166960796 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:151283364 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:151283364 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:47670108 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:47670108 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:60028435 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:60028435 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:103353305 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:103353305 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:50512859 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:50512859 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:50515228 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:50515228 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:47075247 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:47075247 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:108822892 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:108822892 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56356599 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56356599 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:60767429 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:60767429 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:27907985 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:27907985 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:65813541 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:65813541 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:11290881 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:11290881 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:17507276 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:17507276 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1155304 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1155304 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:102060673 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:102060673 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:23901794 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:23901794 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:46904659 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:46904659 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:128390967 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:128390967 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:47045902 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:47045902 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:32460360 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:32460360 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:54318364 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:54318364 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:56463806 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:56463806 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:50753626 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:50753626 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:200014482 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:200014482 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:18770802 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:18770802 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:33102146 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:33102146 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:45563670 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:45563670 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229600667 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229600667 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153968136 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153968136 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:101615491 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:101615491 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:228492381 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:228492381 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:167631742 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:167631742 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:161990088 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:161990088 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:248247309 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:248247309 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:248524833 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:248524833 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:58126655 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:58126655 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:179253666 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:179253666 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:3593190 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:3593190 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:24580289 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:24580289 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:20704804 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:20704804 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:76713966 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:76713966 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:64335186 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:64335186 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:169899542 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:169899542 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:111637860 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:111637860 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:532896 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:532896 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:18552546 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:18552546 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:8678570 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:8678570 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:131878805 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:131878805 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:42207609 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:42207609 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:133220711 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:133220711 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:86272898 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:86272898 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:113310459 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:113310459 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:18455926 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:18455926 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:146085939 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:146085939 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:91512929 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:91512929 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:91517755 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:91517755 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:14096546 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:14096546 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:84610228 C>G maps to NM_182948.2 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:84610228 C>G maps to NM_182948.2 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:24225900 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:24225900 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:61924530 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:61924530 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:141540758 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:141540758 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:10389130 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:10389130 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43372790 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43372790 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43545391 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43545391 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43262022 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43262022 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:102989142 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:102989142 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:231951951 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:231951951 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:184022009 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:184022009 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:11575321 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:11575321 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:27293394 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:27293394 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:180159463 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:180159463 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:180159811 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:180159811 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:170341164 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:170341164 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:173678840 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:173678840 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:178442406 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:178442406 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15571844 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15571844 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:80521429 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:80521429 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:391275 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:391275 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:79348662 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:79348662 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:3416625 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:3416625 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:104928553 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:104928553 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:104987540 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:104987540 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:18399743 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:18399743 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:42743111 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:42743111 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:6272204 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:6272204 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:66797175 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:66797175 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:26872623 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:26872623 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:99150637 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:99150637 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:159566390 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:159566390 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:39018548 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:39018548 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34117911 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34117911 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153516468 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153516468 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:100717493 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:100717493 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:50210530 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:50210530 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:4308336 G>A maps to ENST00000420750 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:4308336 G>A maps to ENST00000420750 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:10347471 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:10347471 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:177910912 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:177910912 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:122632546 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:122632546 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:196611992 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:196611992 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:43150550 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:43150550 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:27297073 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:27297073 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:7239386 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:7239386 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:73267910 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:73267910 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:67099860 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:67099860 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:2246984 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:2246984 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:3527579 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:3527579 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:113326904 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:113326904 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:1917938 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:1917938 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:160722055 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:160722055 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:51386500 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:51386500 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:51386718 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:51386718 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:51389288 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:51389288 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:37198813 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:37198813 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:46644291 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:46644291 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:44984528 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:44984528 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:18250888 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:18250888 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:10975882 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:10975882 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:168112681 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:168112681 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:168620626 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:168620626 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:51363053 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:51363053 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:125176075 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:125176075 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:151051017 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:151051017 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:49131870 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:49131870 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:32262456 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:32262456 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:234959605 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:234959605 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:55648409 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:55648409 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:30733730 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:30733730 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:99911965 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chrX:99911965 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:75894604 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:75894604 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:149523944 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:149523944 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:36546003 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:36546003 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:17726589 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:17726589 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:68447242 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:68447242 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:56745373 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:56745373 A>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:171481837 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:171481837 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:23749977 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:23749977 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:147556516 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:147556516 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:4452509 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:4452509 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:31590749 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:31590749 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:38104847 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:38104847 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:74181383 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:74181383 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:64895306 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:64895306 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:98155852 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:98155852 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:5748091 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:5748091 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:29911606 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:29911606 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:66355145 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:66355145 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:175292367 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:175292367 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:179870362 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:179870362 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:10973828 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:10973828 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:72667456 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:72667456 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:142569270 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:142569270 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:50487530 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:50487530 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:40764084 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:40764084 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:134229389 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:134229389 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:37936446 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:37936446 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:4192813 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:4192813 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:33510401 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:33510401 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229783583 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229783583 T>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:61459535 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:61459535 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:55471734 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:55471734 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:39274581 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:39274581 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:10084554 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:10084554 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:158662677 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:158662677 A>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:124152956 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:124152956 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:112375622 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:112375622 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:38134076 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:38134076 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:44584992 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:44584992 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:28218358 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:28218358 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:44752307 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:44752307 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:85342528 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:85342528 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:60636957 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:60636957 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:7382880 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:7382880 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:7680786 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:7680786 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8982313 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8982313 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8994176 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8994176 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:9260365 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:9260365 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:67197467 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:67197467 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:48349529 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:48349529 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:48415950 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:48415950 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:67016491 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:67016491 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:87215003 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:87215003 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:20668258 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:20668258 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:20698650 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:20698650 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:150731542 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:150731542 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:48210805 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:48210805 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:48138952 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:48138952 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:183639208 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:183639208 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:22004997 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:22004997 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:30545358 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:30545358 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:119027492 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:119027492 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:112194109 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:112194109 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:128598520 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:128598520 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:89382422 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:89382422 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:27508850 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:27508850 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:32365530 A>T maps to ENST00000430493 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:32365530 A>T maps to ENST00000430493 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:19423791 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:19423791 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:61568154 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:61568154 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:131296200 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:131296200 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20681340 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20681340 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20498057 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20498057 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20563432 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20563432 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20429667 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:20429667 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:81568761 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:81568761 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:2939409 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:2939409 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:158397545 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:158397545 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:158399172 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:158399172 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:156899203 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:156899203 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:87746189 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:87746189 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:87755087 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:87755087 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:207435396 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:207435396 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:39613230 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:39613230 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:39624856 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:39624856 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:43833652 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:43833652 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:43945607 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:43945607 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:161167709 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:161167709 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:18635881 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:18635881 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:18681697 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:18681697 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:154561803 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:154561803 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:123021809 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:123021809 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:131826196 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:131826196 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:67352471 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:67352471 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:3517827 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:3517827 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:147967295 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:147967295 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:148044517 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:148044517 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:74368756 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:74368756 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:88767358 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:88767358 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:236708168 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:236708168 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:76355662 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:76355662 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41456633 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41456633 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:35040922 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:35040922 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:129050056 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:129050056 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:427839 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:427839 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:55187279 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:55187279 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:55189394 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:55189394 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:137732498 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:137732498 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:19611483 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:19611483 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:74551585 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:74551585 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:29551361 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:29551361 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:233322137 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:233322137 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53817999 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53817999 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:865662 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:865662 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41557132 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41557132 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41558045 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41558045 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41585607 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:41585607 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:91974259 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:91974259 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:241439814 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:241439814 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:74026834 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:74026834 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:27355367 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:27355367 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:55489117 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:55489117 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:99548046 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:99548046 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:26538271 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:26538271 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:26612913 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:26612913 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:39355503 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:39355503 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:21255455 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:21255455 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:36052631 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:36052631 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:57271996 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:57271996 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:115336644 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:115336644 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:141041470 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:141041470 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:99019107 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:99019107 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:69053053 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:69053053 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45245090 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45245090 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:56785316 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:56785316 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:46285545 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:46285545 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:46289927 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:46289927 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:57390052 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:57390052 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:232141332 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:232141332 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:35724521 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:35724521 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:42249397 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:42249397 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:101173670 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:101173670 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:104561840 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:104561840 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:133365012 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:133365012 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:31314265 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:31314265 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124413898 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124413898 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:81354220 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:81354220 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:96756721 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:96756721 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:242598666 G>T maps to ENST00000425239 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:242598666 G>T maps to ENST00000425239 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:113470274 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:113470274 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:141626185 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:141626185 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138429862 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138429862 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:198509679 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:198509679 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:42554680 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:42554680 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:42588498 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:42588498 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:26413609 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:26413609 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:50225012 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:50225012 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:117094015 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:117094015 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:117221379 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:117221379 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:142204129 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:142204129 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:110033151 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:110033151 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:42275572 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:42275572 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:69900704 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:69900704 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:32756304 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:32756304 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:99573495 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:99573495 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:31891837 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:31891837 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:376377 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:376377 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:11098883 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:11098883 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:129171313 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:129171313 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:78423814 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:78423814 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51696464 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51696464 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:34091681 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:34091681 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:31611277 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:31611277 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:36940271 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:36940271 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:140501432 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:140501432 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32960194 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32960194 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50170588 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50170588 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50180892 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50180892 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:15732623 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:15732623 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:108045419 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:108045419 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:26507074 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:26507074 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:180432207 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:180432207 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:81841800 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:81841800 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:8938817 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:8938817 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93268771 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93268771 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:82824650 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:82824650 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:40110667 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:40110667 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:112600731 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:112600731 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:90263536 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:90263536 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:36906400 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:36906400 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:36910901 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:36910901 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:49433191 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:49433191 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:7158124 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:7158124 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:263128 G>A maps to NM_001013672.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:263128 G>A maps to NM_001013672.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51767523 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51767523 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:77042886 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:77042886 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:170955687 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:170955687 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:247719785 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:247719785 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:226187094 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:226187094 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:31876461 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:31876461 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:20234371 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:20234371 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46046971 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46046971 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46057232 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46057232 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:194947588 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:194947588 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:8671511 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:8671511 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:71027332 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:71027332 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:146617867 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:146617867 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:36226715 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:36226715 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:93929838 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:93929838 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:172512763 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:172512763 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32334094 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32334094 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:88154672 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:88154672 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:118805094 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:118805094 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:36294978 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:36294978 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:42971828 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:42971828 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:57420642 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:57420642 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:49985311 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:49985311 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:49986503 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:49986503 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124232295 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124232295 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124249310 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124249310 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:139929086 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:139929086 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:4618940 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:4618940 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:49713159 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:49713159 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:63619259 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:63619259 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:86250403 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:86250403 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:86389283 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:86389283 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:67226160 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:67226160 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:65142537 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:65142537 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53756215 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53756215 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53834230 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53834230 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:181726301 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:181726301 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:81611852 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:81611852 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:81689892 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:81689892 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:1949896 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:1949896 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:1995214 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:1995214 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:18827335 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:18827335 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:24366099 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:24366099 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:86063475 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:86063475 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:62485003 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:62485003 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:7342414 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:7342414 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:7355419 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:7355419 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:91094978 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:91094978 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:71417233 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:71417233 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:14992805 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:14992805 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:46939475 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:46939475 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:93116193 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:93116193 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:105217930 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:105217930 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:71571323 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:71571323 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:71571364 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:71571364 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:7202100 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:7202100 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:7811133 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:7811133 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:67675865 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:67675865 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:64977756 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:64977756 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2951725 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2951725 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2976597 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2976597 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:105010531 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:105010531 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3026714 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3026714 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3047863 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3047863 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:104972165 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:104972165 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:104815445 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:104815445 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:104817988 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:104817988 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:121981262 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:121981262 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:57107101 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:57107101 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:57115197 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:57115197 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:33417012 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:33417012 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179718047 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179718047 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179733832 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179733832 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:63957744 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:63957744 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:128758526 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:128758526 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:191087847 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:191087847 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:111290844 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:111290844 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:132287374 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:132287374 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:28605393 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:28605393 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8127167 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8127167 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49110579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49110579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:55783207 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:55783207 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43857712 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43857712 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43859776 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43859776 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158300905 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158300905 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158324492 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158324492 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:35837279 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:35837279 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:72608711 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:72608711 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:72578326 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:72578326 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:118223283 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:118223283 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:60781205 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:60781205 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:100961532 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:100961532 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:227300340 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:227300340 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:71281532 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:71281532 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:174232055 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:174232055 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:24509958 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:24509958 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:21756058 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:21756058 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:21883979 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:21883979 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:95177970 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:95177970 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:59170181 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:59170181 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:59217506 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:59217506 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44845432 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44845432 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:25585755 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:25585755 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:62055383 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:62055383 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:85970621 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:85970621 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:105663037 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:105663037 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:49836285 G>T maps to NM_001007540.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:49836285 G>T maps to NM_001007540.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:40085425 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:40085425 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:46058713 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:46058713 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:21065226 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:21065226 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:36642770 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:36642770 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:125873990 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:125873990 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:139866669 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:139866669 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:4703735 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:4703735 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:104060923 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:104060923 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:117257897 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:117257897 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:131186559 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:131186559 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:182423171 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:182423171 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:49535343 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:49535343 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:49539625 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:49539625 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50835856 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50835856 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50857732 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50857732 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50863407 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:50863407 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:6209507 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:6209507 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:6215811 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:6215811 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:402156 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:402156 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:439901 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:439901 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:19632482 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:19632482 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:109964795 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:109964795 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:175622859 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:175622859 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:61990855 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:61990855 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:78917434 C>A maps to ENST00000412074 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:78917434 C>A maps to ENST00000412074 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:101022960 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:101022960 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:105151597 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:105151597 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:69167643 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:69167643 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:46786656 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:46786656 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:86894088 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:86894088 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:86921273 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:86921273 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:143028258 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:143028258 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:49778053 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:49778053 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:96212831 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:96212831 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:14694030 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:14694030 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10226077 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10226077 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8687229 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8687229 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8612116 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8612116 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:73811374 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:73811374 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:95663069 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:95663069 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:1325075 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:1325075 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:140123633 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:140123633 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:41337685 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:41337685 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:205031439 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:205031439 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:3083930 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:3083930 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:125547435 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:125547435 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:40293978 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:40293978 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:103399944 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:103399944 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:121267699 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:121267699 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:121295854 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:121295854 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:101832184 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:101832184 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46888095 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46888095 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46898157 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:46898157 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:61943433 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:61943433 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:139838845 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:139838845 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:177679622 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:177679622 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:116984440 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:116984440 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:117012823 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:117012823 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48379224 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48379224 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:189858693 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:189858693 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:110833578 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:110833578 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:227954710 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:227954710 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:10099903 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:10099903 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:130289603 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:130289603 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48606801 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48606801 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48629272 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48629272 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:3665310 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:3665310 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:22607349 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:22607349 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:76112042 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:76112042 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:99819232 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:99819232 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:83224529 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:83224529 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:39161626 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:39161626 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:12897539 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:12897539 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:9581906 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:9581906 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:137613182 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:137613182 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:30695456 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:30695456 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:5827413 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:5827413 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:5853113 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:5853113 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17183312 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17183312 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:153925975 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:153925975 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:115276248 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:115276248 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:37332547 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:37332547 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:4645292 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:4645292 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:114186167 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:114186167 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:23549097 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:23549097 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:11117511 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:11117511 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:11397015 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:11397015 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:25043875 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:25043875 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:150779314 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:150779314 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:70255877 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:70255877 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:43164070 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:43164070 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:111744653 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:111744653 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:49032793 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:49032793 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:49052636 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:49052636 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:78527108 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:78527108 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:105879768 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:105879768 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:70326515 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:70326515 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:37651346 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:37651346 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15763585 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15763585 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:20140021 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:20140021 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:58514662 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:58514662 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:72050029 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:72050029 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:109288031 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:109288031 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:100676589 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:100676589 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:69585058 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:69585058 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:168025549 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:168025549 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:50742069 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:50742069 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:162745351 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:162745351 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:70398905 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:70398905 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:15760264 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:15760264 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:33055089 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:33055089 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:19077011 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:19077011 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:185969721 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:185969721 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:137406806 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:137406806 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:50129633 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:50129633 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54585878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54585878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:39074227 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:39074227 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:387304 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:387304 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153993989 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153993989 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:83180435 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:83180435 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:83878158 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:83878158 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:84028239 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:84028239 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:79565392 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:79565392 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:79576623 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:79576623 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:35369812 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:35369812 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:101194827 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:101194827 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:46972666 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:46972666 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:86815333 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:86815333 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:124325846 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:124325846 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:21789246 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:21789246 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:57505352 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:57505352 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21045249 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21045249 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:196746482 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:196746482 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:196859618 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:196859618 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:38795909 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:38795909 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:34512326 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:34512326 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:157174882 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:157174882 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:132219599 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:132219599 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:132235540 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:132235540 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:22048629 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:22048629 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:131001613 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:131001613 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:10934370 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:10934370 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:220238937 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:220238937 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:169145852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:169145852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:67425124 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:67425124 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:73219914 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:73219914 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:116485341 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:116485341 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:154677480 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:154677480 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:109027976 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:109027976 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:7867598 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:7867598 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:54137694 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:54137694 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:41561184 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:41561184 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:167086535 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:167086535 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57678863 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:57678863 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1275301 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1275301 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:71753138 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:71753138 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:71816908 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:71816908 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:74912286 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:74912286 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:41946714 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:41946714 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:78493459 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:78493459 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:62127097 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:62127097 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:28410127 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:28410127 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:82422982 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:82422982 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:13642112 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:13642112 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32135777 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32135777 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:38338725 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:38338725 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:38407276 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:38407276 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:55214219 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:55214219 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:110915779 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:110915779 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:137802345 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:137802345 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31855785 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31855785 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:37374720 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:37374720 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:186501345 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:186501345 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:186504800 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:186504800 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:99806243 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:99806243 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:184043037 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:184043037 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:37172660 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:37172660 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:79357396 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:79357396 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:132201184 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:132201184 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:132470974 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:132470974 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:132476069 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:132476069 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:132535319 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:132535319 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:131215587 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:131215587 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:5406746 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:5406746 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:111595538 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:111595538 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:222307543 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:222307543 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:134898591 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:134898591 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15341720 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15341720 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:110294415 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:110294415 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:37868063 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:37868063 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:212495162 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:212495162 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:103506510 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:103506510 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54280876 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54280876 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:76523755 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:76523755 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:22837316 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:22837316 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:74015577 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:74015577 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:140249227 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:140249227 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:67223469 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:67223469 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:57688934 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:57688934 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:72129172 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:72129172 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160968655 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160968655 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:61632456 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:61632456 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:14687519 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:14687519 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:47529466 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:47529466 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:139180118 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:139180118 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:177167640 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:177167640 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:15831172 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:15831172 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30038200 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30038200 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:93396968 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:93396968 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:78277406 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:78277406 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:29460818 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:29460818 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45939455 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45939455 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:127616078 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:127616078 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8201466 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:8201466 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:5947986 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:5947986 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48423158 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48423158 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:123526796 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:123526796 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157771231 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157771231 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157771491 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157771491 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157737467 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157737467 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157665423 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:157665423 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124978580 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:124978580 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:125325644 G>T maps to ENST00000392709 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:125325644 G>T maps to ENST00000392709 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:36981294 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:36981294 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:137715147 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:137715147 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:167447482 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:167447482 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:176519787 G>T maps to ENST00000377207 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:176519787 G>T maps to ENST00000377207 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:34092554 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:34092554 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:34092556 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:34092556 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:34322885 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:34322885 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:72470125 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:72470125 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:84604787 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:84604787 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153588028 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153588028 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:58062736 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:58062736 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128489090 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128489090 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128494825 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128494825 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:28893702 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:28893702 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240307230 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240307230 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240492338 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240492338 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240497358 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240497358 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:171221522 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:171221522 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:171168446 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:171168446 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:171177856 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:171177856 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:147022057 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:147022057 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:159618733 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:159618733 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:159651150 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:159651150 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:89405206 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:89405206 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:26857694 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:26857694 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:71008618 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:71008618 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:14747249 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:14747249 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:85913603 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:85913603 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:85926727 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:85926727 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:131214010 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:131214010 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:49376599 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:49376599 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32868764 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32868764 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:132939707 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:132939707 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:162459313 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:162459313 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:61902561 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:61902561 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:71686179 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:71686179 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:43871372 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:43871372 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:117711948 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:117711948 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:161117145 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:161117145 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:26806344 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:26806344 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1956517 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:1956517 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:46099195 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:46099195 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:89913273 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:89913273 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:26569878 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:26569878 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:158152844 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:158152844 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51752152 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:51752152 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:74963219 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:74963219 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:42644221 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:42644221 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:115439561 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:115439561 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114551167 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114551167 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9821264 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9821264 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9837475 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9837475 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9846423 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9846423 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:8100192 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:8100192 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:153800324 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:153800324 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:89476450 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:89476450 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:109066017 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:109066017 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120599242 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120599242 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120628062 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:120628062 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:10586722 C>T maps to NM_145655.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:10586722 C>T maps to NM_145655.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:72611835 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:72611835 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:74865577 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:74865577 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:69646189 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:69646189 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:23494215 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:23494215 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:42465575 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:42465575 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:42467043 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:42467043 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:42468122 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:42468122 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:86399574 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:86399574 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:134147855 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:134147855 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:134163120 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:134163120 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:75785216 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:75785216 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:92756865 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:92756865 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:151304010 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:151304010 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:14625416 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:14625416 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:102977232 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:102977232 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183909680 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183909680 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183920377 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183920377 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183942643 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183942643 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:155628451 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:155628451 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:155649696 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:155649696 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:11867256 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:11867256 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:37402900 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:37402900 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:72957469 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:72957469 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135469825 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135469825 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135485334 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135485334 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135487777 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135487777 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:47678336 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:47678336 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:22436932 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:22436932 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:4937714 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:4937714 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:117127520 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:117127520 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:176026852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:176026852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:123471264 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:123471264 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:152870272 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:152870272 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:158282138 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:158282138 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:72851273 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:72851273 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:126249333 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:126249333 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:48954148 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:48954148 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:38065180 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:38065180 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:119635055 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:119635055 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:52662462 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:52662462 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:74119613 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:74119613 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:156634167 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:156634167 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:127451548 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:127451548 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54401521 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:54401521 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:25077439 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:25077439 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:5255521 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:5255521 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:121376321 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:121376321 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:73659810 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:73659810 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:55120259 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:55120259 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48188755 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48188755 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:41058150 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:41058150 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:43505958 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:43505958 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93796926 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93796926 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93800624 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93800624 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93839146 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:93839146 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:63930836 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:63930836 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:28389205 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:28389205 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:91793929 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:91793929 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:81346532 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:81346532 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:210797045 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:210797045 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:46808465 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:46808465 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:114514363 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:114514363 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:33360518 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:33360518 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:26216314 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:26216314 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:176317465 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:176317465 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:71009879 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:71009879 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31248806 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31248806 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186062559 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186062559 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186120273 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186120273 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:55406844 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:55406844 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:27168602 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:27168602 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:54422765 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:54422765 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:162766533 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:162766533 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:119987818 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:119987818 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30998104 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30998104 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:22199988 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:22199988 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135592433 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:135592433 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:183770790 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:183770790 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:183773092 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:183773092 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:3211513 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:3211513 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:209104019 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:209104019 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:25699238 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:25699238 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65686621 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65686621 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:47117224 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:47117224 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:47118891 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:47118891 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160461833 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160461833 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:45931684 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:45931684 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:118648856 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:118648856 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:117150556 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:117150556 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:37995690 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:37995690 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:52051333 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:52051333 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53883600 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:53883600 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:103012980 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:103012980 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:29959651 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:29959651 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67705856 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67705856 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:3118363 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:3118363 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:155233586 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:155233586 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:166904517 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:166904517 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:111161578 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:111161578 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128033138 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128033138 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:6760615 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:6760615 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:30795469 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:30795469 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:143114396 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:143114396 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:121557177 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:121557177 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:5231741 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:5231741 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:62417534 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:62417534 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:12944233 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:12944233 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:3601188 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:3601188 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:145538884 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:145538884 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:42457233 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:42457233 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:56088217 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:56088217 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:56097046 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:56097046 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30495129 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:30495129 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:187541903 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:187541903 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:73727092 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:73727092 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:124528085 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:124528085 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:20438361 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:20438361 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160853327 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160853327 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:24525022 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:24525022 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:65339032 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:65339032 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:6082118 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:6082118 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:134014359 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:134014359 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:124237356 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:124237356 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49944156 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49944156 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:163241507 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:163241507 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:128708957 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:128708957 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:155711145 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:155711145 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:118960624 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:118960624 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:78649329 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:78649329 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:154794757 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:154794757 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:44133383 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:44133383 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:136637777 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:136637777 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:8829121 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:8829121 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:105543556 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:105543556 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:109714466 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:109714466 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:94120418 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:94120418 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:226378081 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:226378081 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138593714 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138593714 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44819545 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44819545 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44869648 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44869648 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57969238 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57969238 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:149806318 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:149806318 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:44569348 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:44569348 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87742112 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:87742112 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:30350628 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:30350628 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:900323 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:900323 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:173685209 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:173685209 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18780068 C>T maps to ENST00000431920 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18780068 C>T maps to ENST00000431920 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51412841 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51412841 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10541489 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10541489 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:123041815 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:123041815 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:123070120 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:123070120 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:39775828 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:39775828 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53039429 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53039429 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53184899 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53184899 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53201414 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53201414 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53004691 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53004691 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52965274 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52965274 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52825466 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52825466 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:39726287 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:39726287 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:45960050 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:45960050 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:32127866 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:32127866 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153132064 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153132064 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:130454909 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:130454909 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:55025396 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:55025396 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129370953 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129370953 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129478690 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129478690 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129571508 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129571508 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129582043 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129582043 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129759732 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:129759732 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:209824132 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:209824132 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:107732064 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:107732064 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183100546 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183100546 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183197878 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:183197878 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:133927852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:133927852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:154169792 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:154169792 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:50824401 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:50824401 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:145508724 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:145508724 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:46721267 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:46721267 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:18467700 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:18467700 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:54968891 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:54968891 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:52246794 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:52246794 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:6948075 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:6948075 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:66036120 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:66036120 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:66043466 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:66043466 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:35297817 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:35297817 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:48646672 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:48646672 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55112133 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55112133 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55146830 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55146830 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55177840 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55177840 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:73535414 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:73535414 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:31664205 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:31664205 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:27523282 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:27523282 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:73569075 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:73569075 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:73571095 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:73571095 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49504187 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:49504187 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:76375184 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:76375184 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165322267 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165322267 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160963585 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160963585 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160968736 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160968736 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161032521 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161032521 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161087474 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161087474 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:1481215 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:1481215 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:211956547 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:211956547 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:81969160 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:81969160 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:62845249 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:62845249 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:155665438 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:155665438 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:151344439 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:151344439 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141116546 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141116546 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141267671 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141267671 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141294119 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141294119 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141440996 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:141440996 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57571100 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57571100 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:170055469 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:170055469 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:170081743 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:170081743 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:46907541 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:46907541 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:99798492 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:99798492 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:26751993 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:26751993 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:52883213 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:52883213 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:70460341 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:70460341 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:70502016 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:70502016 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:40693139 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:40693139 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:96415877 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:96415877 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:160706773 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:160706773 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:150064990 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:150064990 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2257491 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2257491 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:151284098 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:151284098 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:79082778 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:79082778 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:118041957 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:118041957 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:75648218 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:75648218 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242161976 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242161976 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242162003 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242162003 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:136977653 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:136977653 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:136681825 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:136681825 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:136686837 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:136686837 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:52351035 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:52351035 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:1812585 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:1812585 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:50685559 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:50685559 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:165110214 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:165110214 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:119729004 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:119729004 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:119734901 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:119734901 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:119740004 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:119740004 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57881834 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57881834 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:66406070 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:66406070 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:3778467 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:3778467 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:65544193 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:65544193 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31495958 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31495958 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:112478885 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:112478885 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:138679030 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:138679030 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:35808695 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:35808695 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:136630465 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:136630465 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:207621881 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:207621881 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:90442243 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:90442243 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:150908499 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:150908499 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:6554903 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:6554903 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:19258351 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:19258351 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:156444856 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:156444856 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:3518972 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:3518972 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:15725504 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:15725504 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:46806710 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:46806710 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:28135248 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:28135248 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8804349 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:8804349 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:179104472 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:179104472 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:158524935 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:158524935 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:158526892 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:158526892 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:103353314 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:103353314 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:141756745 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:141756745 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:88424344 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:88424344 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165620222 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165620222 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:12341400 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:12341400 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:40827565 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:40827565 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:151902374 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:151902374 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:152012125 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:152012125 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:2535504 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:2535504 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:75431351 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:75431351 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:29638038 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:29638038 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:77228147 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:77228147 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:37742246 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:37742246 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:13109920 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:13109920 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:60754626 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:60754626 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:27876882 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:27876882 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:60558591 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:60558591 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:15967520 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:15967520 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:30645128 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:30645128 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:30658257 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:30658257 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:29598794 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:29598794 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:30062172 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:30062172 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:177193184 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:177193184 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:9018238 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:9018238 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:1085877 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:1085877 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:1099679 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:1099679 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:1101704 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:1101704 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:1373030 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:1373030 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:67479099 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:67479099 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:42302338 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:42302338 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:47367732 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:47367732 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:77625304 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:77625304 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:81102489 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:81102489 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15892573 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15892573 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:23862066 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:23862066 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:33568208 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:33568208 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:36696850 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:36696850 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:211159215 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:211159215 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:44179507 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:44179507 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:16761731 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:16761731 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:109699139 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:109699139 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:27419579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:27419579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:26400909 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:26400909 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57430239 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57430239 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:45010693 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:45010693 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:76869482 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:76869482 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:76900537 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:76900537 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:128353999 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:128353999 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:95088794 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:95088794 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:2072038 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:2072038 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:24417264 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:24417264 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:30260039 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:30260039 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:76857249 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:76857249 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101712382 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101712382 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101717918 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101717918 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101756828 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101756828 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101763039 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:101763039 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:17826561 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:17826561 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50960103 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50960103 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48716971 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:48716971 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:132984886 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:132984886 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:119026343 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:119026343 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:240951012 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:240951012 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:124910369 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:124910369 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:97338932 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:97338932 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:32572860 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:32572860 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:47605769 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:47605769 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:21098858 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:21098858 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:152524438 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:152524438 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:178272479 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:178272479 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:27233851 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:27233851 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:52787572 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:52787572 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:47163109 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:47163109 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:124676271 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:124676271 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:1037895 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:1037895 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:173998183 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:173998183 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:57099104 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:57099104 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:56422990 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:56422990 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:7060937 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:7060937 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:5424834 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:5424834 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:14951534 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:14951534 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:26087295 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:26087295 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:150696467 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:150696467 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:69334909 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:69334909 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:101606698 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:101606698 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:106888661 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:106888661 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:35801590 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:35801590 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:107822223 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:107822223 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:33481479 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:33481479 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:206631689 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:206631689 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:79117521 G>A maps to ENST00000330071 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:79117521 G>A maps to ENST00000330071 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:18764284 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:18764284 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104186773 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104186773 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:132184659 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:132184659 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:132204891 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:132204891 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9124292 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:9124292 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:88679077 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:88679077 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:106477482 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:106477482 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:32068651 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:32068651 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:44507862 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:44507862 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3781910 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:3781910 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:25901256 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:25901256 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:62572874 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:62572874 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:101093961 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:101093961 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:228491720 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:228491720 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:17339817 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:17339817 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:48894768 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:48894768 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:167181954 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:167181954 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:183713385 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:183713385 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:53625102 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:53625102 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:114522081 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:114522081 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:67290999 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:67290999 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:29343070 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:29343070 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:247836344 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:247836344 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3337146 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3337146 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:143632309 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:143632309 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248166656 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248166656 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248166730 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248166730 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248458922 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248458922 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248458994 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248458994 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248524793 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248524793 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248059919 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:248059919 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:102345914 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:102345914 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:4945677 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:4945677 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:6816981 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:6816981 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:60848468 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:60848468 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:45885788 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:45885788 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:38922039 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:38922039 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21690436 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21690436 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21737752 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21737752 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:26680811 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:26680811 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:29617679 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:29617679 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:107710015 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:107710015 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3806696 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3806696 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17720678 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17720678 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:734061 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:734061 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:56711295 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:56711295 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:108576140 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:108576140 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161990328 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161990328 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:162474996 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:162474996 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:162989901 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:162989901 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:122353847 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:122353847 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:44527327 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:44527327 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:150840307 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:150840307 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:36966732 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:36966732 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:18961072 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:18961072 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47359929 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47359929 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:134071189 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:134071189 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:91368704 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:91368704 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:91369354 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:91369354 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140177023 G>T maps to NM_031495.1 *825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:140177023 G>T maps to NM_031495.1 *825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:36895939 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:36895939 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47832710 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:47832710 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:65402379 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:65402379 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:71489743 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:71489743 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:95748018 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:95748018 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:33866568 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:33866568 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:178592736 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:178592736 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31792856 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31792856 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31887550 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:31887550 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:72308501 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:72308501 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:76587070 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:76587070 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:76627129 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:76627129 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:149504983 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:149504983 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:335743 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:335743 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15126926 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15126926 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15224348 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:15224348 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:69508376 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:69508376 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:31847887 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:31847887 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:31847889 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:31847889 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:41957327 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:41957327 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:152629136 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:152629136 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:179754550 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:179754550 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:6268372 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:6268372 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:197784945 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:197784945 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:97847137 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:97847137 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:77372918 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:77372918 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:74058428 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:74058428 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:96416859 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:96416859 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60570142 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60570142 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60639710 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:60639710 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:99344714 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:99344714 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65112218 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:65112218 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:35091220 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:35091220 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:39637787 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:39637787 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:8814702 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:8814702 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:8706525 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:8706525 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:209209792 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:209209792 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57994484 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:57994484 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:71404111 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:71404111 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:15408251 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:15408251 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:47897494 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:47897494 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:125298882 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:125298882 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:201289367 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:201289367 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:201297977 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:201297977 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:20474572 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:20474572 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:28754963 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:28754963 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:28805084 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:28805084 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:96025810 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:96025810 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:96058057 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:96058057 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:81916771 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:81916771 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:4722216 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:4722216 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:105396255 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:105396255 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242511373 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242511373 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242540452 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:242540452 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145008695 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145008695 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145008750 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145008750 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145028016 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:145028016 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:131949243 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:131949243 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:43535873 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:43535873 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161123263 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161123263 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161160297 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:161160297 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:208200697 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:208200697 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153696944 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:153696944 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160234488 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160234488 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:118364827 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:118364827 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:133241099 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:133241099 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:74848199 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:74848199 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:2195096 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:2195096 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:38355307 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:38355307 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:87322486 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:87322486 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:18796963 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:18796963 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:81741173 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:81741173 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:27745620 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:27745620 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:202394512 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:202394512 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:62192884 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:62192884 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:24196716 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:24196716 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:48084333 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:48084333 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:93615550 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:93615550 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:93617217 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:93617217 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:113825799 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:113825799 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32118112 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:32118112 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:31157041 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:31157041 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:228004075 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:228004075 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:46784391 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:46784391 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10387227 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10387227 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43343330 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43343330 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43575650 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43575650 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43259085 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43259085 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43349342 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43349342 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43757745 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43757745 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43773391 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:43773391 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:40477036 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:40477036 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:125140093 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:125140093 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:209357889 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:209357889 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:62162089 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:62162089 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:232577907 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:232577907 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:8524866 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:8524866 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:129854558 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:129854558 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55708389 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:55708389 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:157931305 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:157931305 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:121676790 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:121676790 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:121693934 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:121693934 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:130478319 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:130478319 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:130478321 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:130478321 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:119549086 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:119549086 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:144687782 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:144687782 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:174363349 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:174363349 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:76251967 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:76251967 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:37163978 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:37163978 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:131080175 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:131080175 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:167921538 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:167921538 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:86672976 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:86672976 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114766478 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114766478 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114782838 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114782838 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114784224 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114784224 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114789878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:114789878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:178414537 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:178414537 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:179546203 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:179546203 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:64503150 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:64503150 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17736358 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:17736358 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:141018054 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:141018054 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:103368500 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:103368500 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30060866 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30060866 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30060897 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:30060897 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:204136807 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:204136807 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:100052451 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:100052451 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:176118074 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:176118074 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:24036525 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:24036525 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:101075089 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:101075089 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240933204 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:240933204 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:182635923 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:182635923 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:63156637 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:63156637 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:130892064 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:130892064 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:104672413 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:104672413 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:104928901 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:104928901 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:43386831 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:43386831 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:3085385 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:3085385 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:87085158 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:87085158 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:87400063 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:87400063 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:88013511 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:88013511 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:49738206 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:49738206 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:141868776 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:141868776 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:30318347 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:30318347 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:25419088 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:25419088 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:101299592 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:101299592 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:78328161 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:78328161 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:78363552 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:78363552 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:78683299 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:78683299 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:77645927 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:77645927 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10473839 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10473839 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10480765 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10480765 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:68896884 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:68896884 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:17973500 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:17973500 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:8704487 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:8704487 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:45241097 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:45241097 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:7247516 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:7247516 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:99133322 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:99133322 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:6006406 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:6006406 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:6836426 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:6836426 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:43624470 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:43624470 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:109001229 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:109001229 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:157993768 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:157993768 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:123011384 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:123011384 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:179003934 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:179003934 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:93026759 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:93026759 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32339337 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32339337 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32352590 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:32352590 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137313434 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:137313434 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:33162716 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:33162716 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165414137 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:165414137 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:237620099 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:237620099 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:34105629 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:34105629 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:153362551 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:153362551 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:45781031 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:45781031 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:134983642 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:134983642 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:134991277 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:134991277 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:75146478 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:75146478 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:52011537 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:52011537 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:38781224 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:38781224 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:118037852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:118037852 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52139888 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:52139888 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:100660956 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:100660956 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:50319517 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:50319517 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:243456366 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:243456366 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:243471205 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:243471205 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:111957820 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:111957820 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:71335116 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:71335116 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:71348584 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:71348584 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:122645183 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:122645183 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:115813643 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:115813643 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:48060964 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:48060964 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48440264 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:48440264 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:42393003 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:42393003 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:35841909 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:35841909 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61223252 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61223252 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61228252 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61228252 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61307105 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61307105 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:2953083 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:2953083 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61463707 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:61463707 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:224842165 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:224842165 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:167540928 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:167540928 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:38446451 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:38446451 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:70564529 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:70564529 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:19142076 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:19142076 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:166733690 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:166733690 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:120920406 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:120920406 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:13959862 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:13959862 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67126300 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67126300 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67205271 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:67205271 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:223317264 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:223317264 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:2759330 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:2759330 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:19192394 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:19192394 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:21052589 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:21052589 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:84286743 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:84286743 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:87208779 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:87208779 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:96324040 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:96324040 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:601697 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:601697 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51960688 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51960688 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:100911440 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:100911440 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:38095500 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:38095500 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:38600699 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:38600699 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:1517712 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:1517712 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:39371597 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:39371597 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160580638 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160580638 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160594107 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:160594107 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:103703536 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:103703536 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:127522367 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:127522367 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:56938512 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:56938512 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44675156 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44675156 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:135390715 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:135390715 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:43247779 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:43247779 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:61432491 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:61432491 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15075227 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:15075227 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:53556223 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:53556223 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160670242 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:160670242 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:92909197 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:92909197 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:113758050 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:113758050 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:95799302 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:95799302 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:18062750 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:18062750 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:107431448 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:107431448 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:9836764 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:9836764 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:9987247 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:9987247 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:68399054 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:68399054 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44983639 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44983639 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:79244679 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:79244679 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:61447791 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:61447791 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:84063087 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:84063087 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31833994 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:31833994 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:162761160 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:162761160 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18004488 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18004488 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:101555861 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:101555861 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:85285974 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:85285974 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:20639474 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:20639474 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:74842613 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:74842613 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:20493586 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:20493586 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:20618453 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:20618453 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168134923 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168134923 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168150088 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168150088 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168199769 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168199769 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168201429 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:168201429 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:47721865 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:47721865 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45768188 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:45768188 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:70460997 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:70460997 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:246078724 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:246078724 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:246672461 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:246672461 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:65618894 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:65618894 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:36748842 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:36748842 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:97170584 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:97170584 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:106802768 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:106802768 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:16133312 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:16133312 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:231112621 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:231112621 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:142605326 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:142605326 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:172631396 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:172631396 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:133715239 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:133715239 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:48901969 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:48901969 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:35774234 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:35774234 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:35807450 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:35807450 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44171508 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44171508 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:55910524 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:55910524 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:32267220 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:32267220 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55648316 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55648316 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55653336 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55653336 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55653338 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55653338 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55659224 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:55659224 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158618161 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:158618161 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:45646909 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:45646909 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:45646912 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:45646912 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:35468639 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:35468639 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:35468641 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:35468641 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:104785766 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:104785766 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:133538672 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:133538672 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:149509778 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:149509778 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:48123043 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:48123043 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:48046183 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:48046183 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:107422991 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:107422991 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104015987 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104015987 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104099528 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104099528 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104122870 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:104122870 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:99795006 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:99795006 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:33686830 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:33686830 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:110842998 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:110842998 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:47734825 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:47734825 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:171479897 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:171479897 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:23808850 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:23808850 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:134041648 T>A maps to ENST00000368625 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:134041648 T>A maps to ENST00000368625 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:80577012 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:80577012 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:39564697 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:39564697 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10786571 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:10786571 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:70540210 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:70540210 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:70620590 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:70620590 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:27005251 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:27005251 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:27017259 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:27017259 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:149879433 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:149879433 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:75576773 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:75576773 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:109306215 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:109306215 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:10906328 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:10906328 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:32909545 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:32909545 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:152711598 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:152711598 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:66797763 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:66797763 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51132539 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:51132539 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:85456885 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:85456885 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:85468566 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:85468566 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:39813911 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:39813911 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:123989797 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:123989797 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:35797730 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:35797730 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:29990034 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:29990034 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:118599962 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:118599962 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:77923504 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:77923504 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:9684331 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:9684331 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:134303864 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:134303864 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:145883575 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:145883575 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:89965308 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:89965308 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:124171698 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:124171698 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:90485645 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:90485645 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:24666673 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:24666673 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:154520069 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:154520069 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:179558218 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:179558218 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:179619969 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:179619969 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:46663753 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:46663753 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:3120264 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:3120264 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53449056 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:53449056 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44943246 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44943246 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:56711823 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:56711823 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:133973163 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:133973163 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:133995687 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:133995687 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:122758526 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:122758526 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:122760537 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:122760537 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:121337348 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:121337348 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:32585806 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:32585806 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:32825348 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:32825348 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:156381394 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:156381394 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:82319825 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:82319825 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:62989841 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:62989841 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:19474773 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:19474773 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:193044447 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:193044447 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:32957255 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:32957255 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36038151 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36038151 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36236459 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:36236459 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:72094843 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:72094843 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:74331501 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:74331501 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:54259011 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:54259011 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:29927086 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:29927086 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:424492 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:424492 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:19701474 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:19701474 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:22881807 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:22881807 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44455853 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:44455853 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:74663916 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:74663916 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:74716288 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:74716288 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:175097674 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:175097674 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128622269 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128622269 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128629891 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:128629891 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:5364052 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:5364052 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:175332036 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:175332036 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:175333980 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:175333980 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:38641290 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:38641290 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:189590798 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:189590798 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:144344906 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:144344906 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:1507878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:1507878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:127294544 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:127294544 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186295042 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:186295042 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:36518590 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:36518590 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:41196845 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:41196845 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:73012839 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:73012839 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:4409788 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:4409788 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:5740814 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:5740814 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138235711 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:138235711 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:28889579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:28889579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:230701511 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:230701511 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:5922756 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:5922756 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:45825682 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr21:45825682 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:49703733 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:49703733 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:77407755 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:77407755 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:77442873 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:77442873 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:50854096 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:50854096 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:234851148 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:234851148 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:234904816 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:234904816 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:110230344 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:110230344 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:98596554 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:98596554 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:99721955 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:99721955 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:46649793 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:46649793 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:219611006 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:219611006 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50485772 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:50485772 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179500110 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179500110 T>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179597927 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179597927 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179635846 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:179635846 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2687692 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:2687692 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:5442723 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:5442723 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:37890183 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:37890183 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:37905092 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:37905092 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:41865771 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:41865771 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:70980054 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:70980054 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18685980 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:18685980 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:122653622 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:122653622 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:74738689 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:74738689 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:43352416 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:43352416 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:42656208 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:42656208 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:54793233 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:54793233 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:35425772 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:35425772 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:35543997 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:35543997 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:35624701 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:35624701 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:48146927 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:48146927 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:126222749 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:126222749 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:215807696 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:215807696 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:215823925 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:215823925 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:27664408 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:27664408 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:132620471 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:132620471 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:161133470 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:161133470 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:76794347 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:76794347 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:5041120 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:5041120 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:41047385 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:41047385 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:41055725 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrX:41055725 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrY:14833970 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chrY:14833970 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:72874776 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:72874776 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:144719294 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:144719294 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:145172050 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:145172050 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:75718701 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:75718701 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:70815928 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:70815928 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:30889141 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr6:30889141 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:118896282 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:118896282 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:17278463 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:17278463 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:79971822 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:79971822 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:100245268 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:100245268 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:91549108 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:91549108 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:53007778 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:53007778 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:118533307 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:118533307 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:54545340 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:54545340 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:61045798 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:61045798 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:42205006 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr22:42205006 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:73101310 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:73101310 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:122660513 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:122660513 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:78587946 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr15:78587946 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:241953763 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:241953763 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:54688165 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:54688165 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:33663230 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:33663230 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:141430061 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:141430061 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:84352935 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:84352935 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:43739420 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:43739420 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:96054483 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr9:96054483 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:102238744 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:102238744 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:118480495 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr12:118480495 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:184181990 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:184181990 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10782406 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr8:10782406 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:152373291 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:152373291 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:44244334 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:44244334 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:135756663 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:135756663 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:167033484 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:167033484 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:111312387 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:111312387 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:47584716 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:47584716 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:129688777 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr7:129688777 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:52961255 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:52961255 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:825152 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr5:825152 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:145162654 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr2:145162654 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:3816657 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:3816657 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:73464511 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr14:73464511 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:147131114 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:147131114 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:25264434 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:25264434 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:123601051 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr11:123601051 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:22153618 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:22153618 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:53368654 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:53368654 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:64429927 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:64429927 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:37580120 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:37580120 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:9643517 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:9643517 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:21587847 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:21587847 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:4815410 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:4815410 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44751713 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr3:44751713 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:22902178 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr18:22902178 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:64809 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr4:64809 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:52399822 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr19:52399822 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:227826878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr1:227826878 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:115089270 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr13:115089270 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57765978 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57765978 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57771064 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr20:57771064 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:34842744 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:34842744 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21210995 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr16:21210995 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:58117793 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr10:58117793 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3917579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3917579 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3975802 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1265-08 chr17:3975802 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:7680727 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:7680727 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:220085072 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:220085072 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:150746513 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:150746513 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:131329710 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:131329710 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:5239102 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:5239102 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:105271222 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:105271222 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:71388389 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:71388389 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:92680839 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:92680839 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:39410435 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:39410435 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:109249195 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:109249195 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:161928471 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:161928471 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:77271195 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:77271195 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:77108008 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:77108008 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr21:11049501 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr21:11049501 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:29571556 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:29571556 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:115917244 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:115917244 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:121411926 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:121411926 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:151789410 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:151789410 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:86386485 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:86386485 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:27459778 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:27459778 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:35855134 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:35855134 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:37962885 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:37962885 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:24493113 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:24493113 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:105653217 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:105653217 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:33267930 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:33267930 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:136623312 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:136623312 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:65497553 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:65497553 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:150909127 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:150909127 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:57996563 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:57996563 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:95368590 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:95368590 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:238243545 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:238243545 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:50313908 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:50313908 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:30721668 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:30721668 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:46846902 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:46846902 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:41969837 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:41969837 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:2813347 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:2813347 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:114388913 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:114388913 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:23432391 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:23432391 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:23805984 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:23805984 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:20134956 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:20134956 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:72278736 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:72278736 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:6913942 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:6913942 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:186006462 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:186006462 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:42729598 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:42729598 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:42729679 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:42729679 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:60554833 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:60554833 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:51086652 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:51086652 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:436608 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:436608 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:231858457 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:231858457 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:124392869 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:124392869 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:71791120 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:71791120 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:93253030 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:93253030 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:56488355 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:56488355 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:61624390 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:61624390 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:139255165 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:139255165 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:175528433 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:175528433 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:128371178 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:128371178 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:213036938 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:213036938 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:146676268 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:146676268 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:49196358 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:49196358 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:31199640 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:31199640 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:69581805 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:69581805 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:57485280 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:57485280 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:66975143 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:66975143 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:132841831 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:132841831 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:73617827 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:73617827 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:27147493 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:27147493 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:114405780 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:114405780 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:63257559 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:63257559 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:118422913 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:118422913 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:37533446 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr22:37533446 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:201843199 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:201843199 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:77944898 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:77944898 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:124515195 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:124515195 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:73531145 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:73531145 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:49934648 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:49934648 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:196458831 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:196458831 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:55325132 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:55325132 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:39140014 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:39140014 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:60911315 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr20:60911315 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:107601972 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:107601972 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:99380524 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:99380524 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:151826923 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:151826923 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:30349930 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:30349930 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:42103009 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:42103009 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:1216416 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:1216416 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:10303574 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:10303574 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:52606126 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:52606126 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:6638876 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:6638876 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:36339101 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:36339101 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:37327888 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:37327888 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:22332775 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:22332775 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:25067943 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr13:25067943 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:55599953 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:55599953 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:66637674 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:66637674 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:178883207 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:178883207 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:144860000 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:144860000 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:119044991 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:119044991 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:114246797 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:114246797 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:209219393 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:209219393 T>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:130851854 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:130851854 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:73372728 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:73372728 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:145918799 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:145918799 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:98268934 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:98268934 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:99341344 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:99341344 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:38901507 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:38901507 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:114362368 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:114362368 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:25729033 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:25729033 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:78324033 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:78324033 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:45088522 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:45088522 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:33603317 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:33603317 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:194333 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:194333 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:18259506 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chrX:18259506 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:108076718 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:108076718 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:91995955 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:91995955 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:157823826 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:157823826 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:25914762 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:25914762 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:37198700 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:37198700 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:58710187 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:58710187 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:21069234 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:21069234 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:168176727 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:168176727 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:118539501 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:118539501 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:89603222 G>T maps to NM_199367.1 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:89603222 G>T maps to NM_199367.1 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:66476530 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:66476530 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:206610484 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:206610484 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:149480792 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:149480792 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:45274335 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:45274335 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:3568739 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:3568739 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:145857962 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:145857962 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:106708349 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:106708349 T>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:106708376 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:106708376 G>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:71457099 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:71457099 A>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:98129784 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:98129784 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:12164593 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:12164593 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:3543891 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:3543891 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr21:10921839 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr21:10921839 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:141285634 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:141285634 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248039182 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248039182 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:73213256 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr9:73213256 A>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:2433605 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:2433605 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:142630622 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:142630622 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:80746172 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:80746172 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:126229454 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:126229454 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:85868038 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:85868038 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:82838146 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:82838146 C>G did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:86734732 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:86734732 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:125007094 A>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:125007094 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:41131098 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:41131098 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:121718104 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:121718104 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:107571866 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:107571866 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:123430862 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:123430862 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:48119700 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:48119700 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:19263384 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:19263384 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:67692307 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:67692307 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:19435084 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:19435084 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:19446452 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:19446452 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:32424684 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:32424684 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:78392423 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:78392423 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:132002590 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:132002590 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:178358703 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:178358703 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:109671949 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:109671949 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:15469931 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:15469931 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:58247322 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:58247322 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:102100301 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:102100301 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:112625796 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:112625796 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:99640699 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:99640699 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:4779939 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:4779939 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:124724862 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:124724862 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:150502605 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:150502605 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:64224324 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:64224324 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:36541432 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:36541432 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:35235360 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:35235360 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:36272254 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:36272254 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:34625716 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:34625716 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:52541043 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:52541043 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:42416782 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:42416782 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:354474 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:354474 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:107420644 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:107420644 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:40492619 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:40492619 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:45928261 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:45928261 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:90128894 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:90128894 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:44237004 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:44237004 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:55161184 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:55161184 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:89927176 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:89927176 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:50212230 T>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:50212230 T>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:181759694 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:181759694 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:65052055 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:65052055 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:94772533 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:94772533 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:94818717 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:94818717 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:99962097 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:99962097 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:10503745 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:10503745 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:202687729 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:202687729 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:100416448 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:100416448 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:34082305 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:34082305 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:50830337 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:50830337 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:50901651 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:50901651 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:233404295 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:233404295 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:155234394 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:155234394 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:205041748 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:205041748 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:146825954 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:146825954 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:189854794 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:189854794 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:10108654 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:10108654 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:28766190 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:28766190 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:34189950 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:34189950 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:80223452 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:80223452 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:11564972 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:11564972 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:16955721 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:16955721 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:23945585 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:23945585 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:52788038 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:52788038 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:121019197 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:121019197 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:137076123 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:137076123 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:137128893 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:137128893 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:49447490 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:49447490 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:182852798 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:182852798 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:3977813 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:3977813 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:98088416 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:98088416 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:46956784 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:46956784 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:65766817 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:65766817 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:183855276 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:183855276 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:120570027 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:120570027 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:55591234 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:55591234 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:45867915 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:45867915 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:62130598 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:62130598 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:93113126 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:93113126 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:6266699 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:6266699 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:96215111 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:96215111 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:93159717 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:93159717 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:45490358 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:45490358 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:207634984 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:207634984 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:92357436 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:92357436 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:108133868 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:108133868 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:84603710 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:84603710 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:28903893 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:28903893 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:12601556 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:12601556 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:120115918 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:120115918 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:117712383 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:117712383 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:78085901 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:78085901 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:160972191 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:160972191 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:42621683 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:42621683 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:30662099 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:30662099 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153831141 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153831141 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:120607838 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:120607838 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:5855242 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:5855242 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:5539549 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:5539549 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:24475327 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:24475327 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:64056844 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:64056844 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:37271695 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:37271695 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:13769644 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:13769644 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:130760992 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:130760992 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:33523459 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:33523459 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:33523461 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:33523461 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:27487749 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:27487749 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:242192194 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:242192194 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:124793376 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:124793376 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:97195132 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:97195132 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:176323030 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:176323030 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:100249800 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:100249800 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:38839334 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:38839334 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:52883107 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:52883107 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:22010466 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:22010466 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:15261953 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:15261953 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153713682 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153713682 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:2632919 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:2632919 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:145525060 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:145525060 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:15561226 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:15561226 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:9552680 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:9552680 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:52848160 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:52848160 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:123947014 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:123947014 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:170366205 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:170366205 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:58896210 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:58896210 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:45730301 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:45730301 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:52628895 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:52628895 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:129601109 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:129601109 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:112437003 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:112437003 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:112522901 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:112522901 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:189675647 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:189675647 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:40197356 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:40197356 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:54751041 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:54751041 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr21:15558462 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr21:15558462 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:197703464 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:197703464 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:23191184 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:23191184 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:43604478 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:43604478 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:35803290 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:35803290 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:186968385 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:186968385 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:6378736 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:6378736 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:47912845 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:47912845 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:46777133 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:46777133 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:141765660 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:141765660 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:44644770 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:44644770 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:43831154 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:43831154 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:151420808 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:151420808 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:68483452 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:68483452 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:100518414 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:100518414 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:15813431 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:15813431 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:50720867 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:50720867 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:23858485 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:23858485 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:123366000 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:123366000 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:95365554 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:95365554 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:35873087 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:35873087 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:95062097 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:95062097 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:2944169 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:2944169 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:89133581 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:89133581 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:32780751 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:32780751 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:84118467 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:84118467 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:104866517 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:104866517 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:69082674 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:69082674 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:47776232 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:47776232 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:247615309 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:247615309 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:248366368 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:248366368 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:21747191 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:21747191 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:72921879 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:72921879 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:40035230 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:40035230 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:25052096 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:25052096 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:72288642 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:72288642 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:144902974 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:144902974 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:58330097 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:58330097 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:9782274 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:9782274 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:42036399 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:42036399 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:28766142 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:28766142 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:43159971 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:43159971 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:70185239 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:70185239 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:52719223 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:52719223 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:307652 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chrX:307652 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:11035556 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:11035556 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:3701557 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:3701557 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:10390336 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:10390336 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:97342401 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:97342401 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:220164553 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:220164553 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:144902888 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:144902888 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:34240420 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:34240420 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:73554903 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:73554903 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:50098364 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:50098364 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:49462657 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:49462657 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:152021754 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:152021754 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:78857324 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:78857324 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:32366241 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:32366241 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:33941469 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:33941469 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:151138583 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:151138583 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:75526063 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:75526063 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:91949685 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:91949685 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:94909286 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:94909286 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:198269789 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:198269789 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:67101731 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:67101731 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:132160137 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:132160137 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:43329694 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:43329694 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:19566232 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:19566232 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:234367567 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:234367567 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:40402033 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:40402033 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:130918864 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:130918864 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:16010476 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:16010476 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:152944716 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:152944716 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:158596511 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:158596511 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:8720468 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:8720468 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:120760696 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:120760696 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:108869109 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:108869109 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:40850211 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:40850211 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:47921422 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:47921422 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:47925474 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:47925474 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:168266909 T>C maps to ENST00000441464 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:168266909 T>C maps to ENST00000441464 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:92249554 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:92249554 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:114849309 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:114849309 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:44253685 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:44253685 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:43471446 G>T maps to ENST00000454762 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:43471446 G>T maps to ENST00000454762 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:66551168 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:66551168 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:82324520 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:82324520 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:82324528 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:82324528 A>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:114164515 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr13:114164515 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:75621695 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:75621695 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:55889573 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:55889573 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:29811575 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:29811575 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:26668548 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:26668548 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175063093 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175063093 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175325655 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175325655 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:144345874 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:144345874 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr21:10934005 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr21:10934005 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:142626485 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:142626485 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:75036903 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:75036903 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:21644064 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:21644064 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:138836748 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:138836748 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:234663813 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:234663813 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:70462175 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:70462175 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:77910744 T>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:77910744 T>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:62176561 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:62176561 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:184633342 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:184633342 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:85630297 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:85630297 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:43752328 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:43752328 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:25370865 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:25370865 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:77599974 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:77599974 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:50705466 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:50705466 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:38108109 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:38108109 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:9583938 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:9583938 T>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:9771349 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:9771349 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:64970195 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:64970195 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:12785995 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:12785995 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:87173392 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:87173392 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:43707972 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:43707972 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:119029524 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:119029524 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:100617485 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:100617485 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:179102286 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:179102286 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7245800 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7245800 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:15063969 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:15063969 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:40054106 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:40054106 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:20487118 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:20487118 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:66329719 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:66329719 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:24254777 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:24254777 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:148039859 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:148039859 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:106987152 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:106987152 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:55035569 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:55035569 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:125877522 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:125877522 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:165636478 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:165636478 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:33520261 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:33520261 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:115222180 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:115222180 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:110169255 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:110169255 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:140075171 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:140075171 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:41548120 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:41548120 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:92678498 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:92678498 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:37506818 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:37506818 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:69379399 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:69379399 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:83333004 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:83333004 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:116692767 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:116692767 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:24979909 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:24979909 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:130215906 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:130215906 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:3007789 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:3007789 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:32087557 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:32087557 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:107380531 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:107380531 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108122516 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108122516 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:160047238 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:160047238 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:119510426 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:119510426 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:130713028 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:130713028 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:36046248 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:36046248 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:176049378 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:176049378 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:198509684 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:198509684 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77218099 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77218099 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77284980 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77284980 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:50193541 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:50193541 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:117704360 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:117704360 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:76845434 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:76845434 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:32591089 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:32591089 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:31834962 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:31834962 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:11039180 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:11039180 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:79419697 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:79419697 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:60566395 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:60566395 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:36158974 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:36158974 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:22053223 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:22053223 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:41203206 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:41203206 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:1471119 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:1471119 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:17515090 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:17515090 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:26468136 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:26468136 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:103696402 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:103696402 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:39596314 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:39596314 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:76548499 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:76548499 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7330845 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7330845 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:13612658 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:13612658 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:156264477 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:156264477 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:34564065 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:34564065 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:26637393 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:26637393 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:74041467 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:74041467 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:10145907 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:10145907 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:113468319 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:113468319 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:164435355 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:164435355 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159928755 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159928755 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:71099958 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:71099958 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:170155235 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:170155235 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:40193522 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:40193522 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:2613738 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:2613738 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:201042862 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:201042862 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:81964609 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:81964609 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:81978765 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:81978765 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:1994280 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:1994280 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:54515479 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:54515479 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:62502332 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:62502332 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:57103003 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:57103003 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:133378822 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:133378822 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:159860504 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:159860504 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:32724363 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:32724363 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169015590 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169015590 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:43865556 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:43865556 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:28948465 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:28948465 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:121828007 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:121828007 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:99296850 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:99296850 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:59170466 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:59170466 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:61890959 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:61890959 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:176017224 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:176017224 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:20722601 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:20722601 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:22332065 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:22332065 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:104066134 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:104066134 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:104104107 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:104104107 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:100365073 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:100365073 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:151996242 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:151996242 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:50856529 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:50856529 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:126485924 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:126485924 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:23766947 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:23766947 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:40355910 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:40355910 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:154542141 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:154542141 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:143017054 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:143017054 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:170557249 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:170557249 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:73800977 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:73800977 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:62289042 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:62289042 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87755644 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87755644 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:147336049 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:147336049 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:76513238 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:76513238 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:103449750 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:103449750 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:103479952 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:103479952 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:121209920 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:121209920 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:121216169 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:121216169 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:101796805 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:101796805 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:94057221 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:94057221 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:139648979 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:139648979 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:48605908 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:48605908 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:48628840 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:48628840 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:166326329 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:166326329 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:207871333 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:207871333 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:153923726 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:153923726 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:70800002 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:70800002 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:100075537 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:100075537 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:56078429 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:56078429 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:77513612 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:77513612 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:105768051 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:105768051 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:96698260 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:96698260 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:61498688 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:61498688 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:106119585 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:106119585 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:50589496 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:50589496 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:38884179 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:38884179 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:70670280 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:70670280 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:169353734 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:169353734 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:19296313 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:19296313 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:31540728 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:31540728 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:32188127 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:32188127 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:99359589 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:99359589 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:169938081 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:169938081 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:47879066 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:47879066 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:154001248 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:154001248 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:108124769 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:108124769 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7094194 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7094194 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:124377524 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:124377524 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7701347 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7701347 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:32871527 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:32871527 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169474590 C>A maps to NM_004946.2 Y1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169474590 C>A maps to NM_004946.2 Y1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:99554494 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:99554494 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:67406371 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:67406371 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:154172173 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:154172173 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:71892479 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:71892479 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:82520721 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:82520721 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:55240876 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:55240876 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:117658942 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:117658942 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:132148857 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:132148857 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:89478172 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:89478172 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:97202954 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:97202954 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:97329563 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:97329563 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:56495882 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:56495882 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:56044362 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:56044362 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:5746826 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:5746826 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:45731046 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:45731046 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:113803178 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:113803178 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160970595 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160970595 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:154090220 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:154090220 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:17644371 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:17644371 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:129104017 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:129104017 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:79698011 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:79698011 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:24380715 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:24380715 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:49225332 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:49225332 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:67666416 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:67666416 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87516523 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87516523 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:45657133 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:45657133 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:8167875 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:8167875 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:161479907 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:161479907 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:137805416 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:137805416 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:157772483 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:157772483 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:137785276 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:137785276 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:71012400 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:71012400 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:108337292 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:108337292 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153593924 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153593924 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:14813121 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:14813121 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:12734133 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:12734133 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:101147902 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:101147902 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:47428052 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:47428052 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:35741094 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:35741094 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:179752006 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:179752006 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:23502982 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:23502982 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:46173867 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:46173867 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:53986456 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:53986456 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:131943654 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:131943654 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:231401299 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:231401299 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:155737190 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:155737190 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:117753607 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:117753607 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:37794931 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:37794931 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:20329501 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:20329501 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:113917213 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:113917213 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:94958470 A>T maps to ENST00000428510 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:94958470 A>T maps to ENST00000428510 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:110087021 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:110087021 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:31023387 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:31023387 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:104449551 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:104449551 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:48847299 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:48847299 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:42355413 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:42355413 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:106694735 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:106694735 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:106849509 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:106849509 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:14827804 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:14827804 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:145032615 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:145032615 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:115338349 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:115338349 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:7915016 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:7915016 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:135318511 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:135318511 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:240097962 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:240097962 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:80399860 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:80399860 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:91818924 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:91818924 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:228645526 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:228645526 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:185986323 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:185986323 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:120293371 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:120293371 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:121434313 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:121434313 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:41812557 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:41812557 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:245018955 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:245018955 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:42823401 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:42823401 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:46804457 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:46804457 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:97226625 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:97226625 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:119977628 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:119977628 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:118460382 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:118460382 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:183754159 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:183754159 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:123508324 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:123508324 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:148579885 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:148579885 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:37159883 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:37159883 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:118648841 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:118648841 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:18740134 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:18740134 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153780354 C>A maps to NM_001099856.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153780354 C>A maps to NM_001099856.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:142640614 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:142640614 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:1460545 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:1460545 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:62593774 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:62593774 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:105048088 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:105048088 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:15261952 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:15261952 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:121491395 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:121491395 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:51895638 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:51895638 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:31373540 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:31373540 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:46330569 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:46330569 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:42137529 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:42137529 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:211035280 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:211035280 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:78646789 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:78646789 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:196288761 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:196288761 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:196296074 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:196296074 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108351865 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108351865 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:5070976 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:5070976 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:10602234 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:10602234 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:105514227 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:105514227 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:123140464 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:123140464 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:61331222 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:61331222 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:72337970 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:72337970 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:241725746 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:241725746 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:200945834 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:200945834 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55346504 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55346504 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:36357498 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:36357498 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:51377940 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:51377940 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:51380060 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:51380060 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:53045305 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:53045305 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:52910835 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:52910835 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:52646151 C>T maps to ENST00000257935 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:52646151 C>T maps to ENST00000257935 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:118105260 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:118105260 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:54868259 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:54868259 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:6986439 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:6986439 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:129649593 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:129649593 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:211336396 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:211336396 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:98837175 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:98837175 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:18395711 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:18395711 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:48950748 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:48950748 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:54778966 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:54778966 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:109297055 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:109297055 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:165179842 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:165179842 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:151411966 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:151411966 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:71193204 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:71193204 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:37114277 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:37114277 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:1905042 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:1905042 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:242746 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:242746 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:1316332 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:1316332 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77086274 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77086274 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:47908589 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:47908589 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:183535699 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:183535699 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:6296379 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:6296379 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:47504081 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:47504081 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:86160920 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:86160920 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:220978312 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:220978312 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:71376642 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:71376642 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:60230297 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:60230297 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:60059881 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:60059881 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:59947444 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:59947444 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:60482611 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:60482611 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:21811755 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:21811755 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:47653149 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:47653149 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:11174137 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:11174137 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:30630352 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:30630352 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:15813417 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:15813417 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10206385 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10206385 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:50721153 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:50721153 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10424852 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10424852 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10426620 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10426620 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:23888294 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:23888294 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:36708077 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:36708077 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:44179469 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:44179469 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:109518438 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:109518438 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:109699388 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:109699388 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:27438409 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:27438409 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:57435355 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:57435355 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:52613418 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:52613418 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:95126071 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:95126071 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:2027543 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:2027543 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:78592348 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:78592348 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:41346272 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:41346272 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:119115453 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:119115453 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:140213592 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:140213592 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:178274884 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:178274884 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:52509169 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:52509169 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:63768797 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:63768797 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55452722 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55452722 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:151783844 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:151783844 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:34204395 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:34204395 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:79564457 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:79564457 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:206617503 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:206617503 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:79180974 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:79180974 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:59502546 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:59502546 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:6609899 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:6609899 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:88417663 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:88417663 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:248247842 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:248247842 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:51515236 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:51515236 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:22332707 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:22332707 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:24903000 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:24903000 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:45890823 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:45890823 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:161215025 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:161215025 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:17398018 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:17398018 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:110459868 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:110459868 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:9560736 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:9560736 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:37014884 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:37014884 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:31822197 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:31822197 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:101121722 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:101121722 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:91369309 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:91369309 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:140552336 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:140552336 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:140874354 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:140874354 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:120388541 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:120388541 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:71518827 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:71518827 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:24593480 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:24593480 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:59726226 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:59726226 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:15125478 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:15125478 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:7354786 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:7354786 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:52831752 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:52831752 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77380233 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77380233 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:11022895 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:11022895 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:71915535 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:71915535 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:85737452 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:85737452 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:138461381 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:138461381 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:28718958 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:28718958 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:64023162 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:64023162 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:93131351 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:93131351 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:43970956 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:43970956 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:68615505 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:68615505 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153039214 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153039214 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:94641609 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:94641609 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:6048745 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:6048745 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:118199089 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:118199089 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:24806705 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:24806705 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:39247225 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:39247225 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:73933309 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:73933309 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:11188919 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:11188919 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:69015184 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:69015184 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:57144460 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:57144460 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:151261006 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:151261006 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:48080565 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:48080565 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:141537549 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:141537549 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:10389061 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:10389061 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:43348610 G>A maps to ENST00000449000 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:43348610 G>A maps to ENST00000449000 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:43430240 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:43430240 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:54127177 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:54127177 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:11574330 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:11574330 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:8527332 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:8527332 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:129839290 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:129839290 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:40789928 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:40789928 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:121693794 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:121693794 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:31439145 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:31439145 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:87847405 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:87847405 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:178858872 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:178858872 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:67763765 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:67763765 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:167933891 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:167933891 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:33745417 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:33745417 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:129536368 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:129536368 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:135961335 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:135961335 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:17151832 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:17151832 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:114320702 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:114320702 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:49578634 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:49578634 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:156346991 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:156346991 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:62631914 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:62631914 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:123983918 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:123983918 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:104948733 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:104948733 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:84563751 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:84563751 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:73811156 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:73811156 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:30313516 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:30313516 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:45098067 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:45098067 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:94484941 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:94484941 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:26887124 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:26887124 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:26898593 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:26898593 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:5984565 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:5984565 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:93026723 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:93026723 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159493818 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159493818 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:33163823 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:33163823 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:152005092 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:152005092 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:108070754 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:108070754 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:38798141 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:38798141 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:123504805 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:123504805 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:38662465 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:38662465 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:50053135 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:50053135 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:161310483 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:161310483 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:161332331 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:161332331 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:4002485 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:4002485 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:84702464 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:84702464 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:4551003 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:4551003 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:48022592 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:48022592 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:185339768 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:185339768 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:94912610 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:94912610 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:61568873 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:61568873 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:99865537 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:99865537 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:37425822 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:37425822 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:67710698 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:67710698 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:123503937 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:123503937 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:601505 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:601505 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164700715 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164700715 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164700882 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164700882 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164738907 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164738907 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160722828 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160722828 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:103718087 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:103718087 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:25813477 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:25813477 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119012798 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119012798 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:92401798 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:92401798 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:118174143 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:118174143 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:47380576 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:47380576 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:145638798 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:145638798 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:44508763 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:44508763 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:19480963 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:19480963 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:24888525 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:24888525 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:67289213 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:67289213 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:21036659 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:21036659 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:21196528 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:21196528 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:45395558 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:45395558 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:2097337 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:2097337 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:53423084 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:53423084 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:53440454 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:53440454 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:130912840 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:130912840 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:71255576 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:71255576 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:55913979 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:55913979 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:73824035 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:73824035 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:158622904 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:158622904 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:57333787 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:57333787 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:109205138 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:109205138 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:48126273 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:48126273 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:123183917 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:123183917 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:56743828 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:56743828 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:146752641 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:146752641 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:44237641 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:44237641 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:95840307 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:95840307 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:64676861 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:64676861 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:30864562 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:30864562 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:97363481 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:97363481 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:57406246 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:57406246 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:123975000 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:123975000 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:1733066 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:1733066 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77387316 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77387316 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77395236 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:77395236 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:47685388 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:47685388 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153641775 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:153641775 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:9660311 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:9660311 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:62703649 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:62703649 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:52943003 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:52943003 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:53018001 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:53018001 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:33094289 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:33094289 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:104492516 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:104492516 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:20857350 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:20857350 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:20869771 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:20869771 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:132350995 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:132350995 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66639602 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66639602 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:15424944 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:15424944 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:136384204 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:136384204 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:24523589 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:24523589 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:68935752 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:68935752 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:122075622 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:122075622 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:10916333 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:10916333 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:10971591 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:10971591 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:108549714 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:108549714 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:41250566 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:41250566 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:140419869 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:140419869 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:55032362 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:55032362 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:4626874 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:4626874 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:72967562 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:72967562 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:45819255 A>T maps to ENST00000397932 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:45819255 A>T maps to ENST00000397932 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:73253967 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:73253967 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:2134790 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:2134790 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:176084784 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:176084784 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:72218551 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:72218551 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:96622633 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:96622633 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:115597058 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:115597058 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100451548 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100451548 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100453574 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100453574 A>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:97247897 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:97247897 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:21991822 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:21991822 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:41048421 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:41048421 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:144744613 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:144744613 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:6773060 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:6773060 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:108152625 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:108152625 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:118896173 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:118896173 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:101185340 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:101185340 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:53008883 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:53008883 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:14943702 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:14943702 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:110439830 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:110439830 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:117480357 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:117480357 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:116962942 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:116962942 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:32414197 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:32414197 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:184114710 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:184114710 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87439717 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87439717 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87479134 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:87479134 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:217070014 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:217070014 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:88666114 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:88666114 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:128946886 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:128946886 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:57649749 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:57649749 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:70471213 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:70471213 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:42898741 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:42898741 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11894232 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11894232 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11894236 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11894236 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:111976277 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:111976277 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:44589558 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:44589558 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:44541550 C>A maps to ENST00000436261 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:44541550 C>A maps to ENST00000436261 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:134481011 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chrX:134481011 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:53451 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:53451 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:38200827 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:38200827 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:64821725 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:64821725 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:52521541 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:52521541 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66797594 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66797594 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:7715153 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:7715153 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:67148167 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:67148167 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:89018789 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:89018789 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20476766 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20476766 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20551900 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20551900 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:127708204 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:127708204 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:136282576 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:136282576 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:77354870 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:77354870 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:33585817 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:33585817 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:100217875 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:100217875 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:87531206 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:87531206 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:4745054 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:4745054 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:91632582 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:91632582 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:54230834 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:54230834 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:5672773 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:5672773 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:99059099 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:99059099 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:21224557 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:21224557 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:115361595 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:115361595 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:69045160 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:69045160 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:131803547 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:131803547 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:23250785 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:23250785 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:234201864 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:234201864 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:64665698 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:64665698 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:203669174 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:203669174 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:35814401 G>T maps to NM_001141972.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:35814401 G>T maps to NM_001141972.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:117704367 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:117704367 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:79171722 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:79171722 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:59961003 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:59961003 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:40630278 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:40630278 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:79999807 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:79999807 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:33566048 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:33566048 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:64722101 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:64722101 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:15661932 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:15661932 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:182869053 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:182869053 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:12815788 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:12815788 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:178490350 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:178490350 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:27880985 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:27880985 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:2742683 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:2742683 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:181707612 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:181707612 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:48681720 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:48681720 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:55003940 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:55003940 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:2963093 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:2963093 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:2978555 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:2978555 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:104903741 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:104903741 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:202131578 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:202131578 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:116247744 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:116247744 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:130899686 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:130899686 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:85568542 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:85568542 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:73479684 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:73479684 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:17076271 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:17076271 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:28948702 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:28948702 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:15818313 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:15818313 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:2404475 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:2404475 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:2635784 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:2635784 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:49860297 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:49860297 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:19473315 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:19473315 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:73548818 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:73548818 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:81056524 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:81056524 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:196946659 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:196946659 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:196694523 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:196694523 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:202002425 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:202002425 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:126485665 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:126485665 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:53276708 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:53276708 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:175622650 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:175622650 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:75563007 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:75563007 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100877769 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100877769 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10167428 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10167428 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:108685533 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:108685533 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:87683356 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:87683356 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:179991786 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:179991786 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:41303989 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:41303989 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:74344239 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:74344239 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:146536793 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:146536793 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:103354040 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:103354040 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:103379180 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:103379180 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:103427519 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:103427519 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:139614415 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:139614415 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:189854959 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:189854959 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:189861881 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:189861881 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:111153943 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:111153943 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:47410820 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:47410820 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:4408120 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:4408120 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:98309399 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:98309399 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:51014841 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:51014841 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:28844165 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:28844165 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:88713265 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:88713265 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:94836569 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:94836569 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:72147227 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:72147227 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:50942620 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:50942620 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:53570349 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:53570349 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:15964984 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:15964984 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:50016192 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:50016192 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:42739584 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:42739584 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:128841102 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:128841102 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:118969217 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:118969217 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:18007330 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:18007330 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:56471079 A>G maps to ENST00000361203 T2571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:56471079 A>G maps to ENST00000361203 T2571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:57669872 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:57669872 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:103191725 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:103191725 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:71795524 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:71795524 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:77419216 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:77419216 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:158266892 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:158266892 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:131665591 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:131665591 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67910949 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67910949 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67911319 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67911319 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:37415211 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:37415211 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:42531597 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:42531597 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:14875214 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:14875214 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:222308420 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:222308420 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:97200414 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:97200414 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:226032756 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:226032756 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:212566538 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:212566538 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:5810098 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:5810098 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:176947277 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:176947277 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:133749315 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:133749315 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:44165920 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:44165920 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:97749674 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:97749674 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:110596154 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:110596154 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:129100268 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:129100268 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:152859975 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:152859975 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:223484532 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:223484532 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:16091770 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:16091770 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:15936486 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:15936486 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:17125723 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:17125723 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:128475756 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:128475756 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:109276197 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:109276197 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:80544224 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:80544224 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:79205793 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:79205793 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:66082911 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:66082911 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:101258800 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:101258800 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:161580588 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:161580588 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:31154838 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:31154838 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:31215590 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:31215590 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:62400264 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:62400264 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:5827421 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:5827421 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:85781124 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:85781124 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:27905963 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:27905963 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:52402861 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:52402861 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:37901388 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:37901388 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:37346035 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:37346035 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:52713847 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:52713847 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:42355397 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:42355397 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:156643012 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:156643012 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:240097977 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:240097977 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:75221202 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:75221202 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:176315902 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:176315902 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:120298350 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:120298350 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:1080587 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:1080587 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:76463820 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:76463820 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:70995854 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:70995854 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:30193152 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:30193152 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:1499840 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:1499840 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:143235947 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:143235947 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:59975835 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:59975835 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:47488231 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:47488231 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:63955733 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:63955733 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:54780412 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:54780412 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:211035407 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:211035407 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:170159685 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:170159685 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:43378632 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:43378632 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:62076577 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:62076577 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:114155911 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:114155911 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:1369426 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:1369426 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:200943164 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:200943164 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:45220379 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:45220379 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:55281413 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:55281413 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:55270250 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:55270250 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:70535586 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:70535586 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10584685 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10584685 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10560231 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10560231 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10460673 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:10460673 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:53041647 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:53041647 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:52843063 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:52843063 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:34046287 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:34046287 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:71971888 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:71971888 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:55145224 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:55145224 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:161011909 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:161011909 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:197554102 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:197554102 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23344227 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23344227 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:141110652 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:141110652 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:142237927 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:142237927 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:40702894 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:40702894 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:41114292 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:41114292 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:99863099 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:99863099 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:35804023 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:35804023 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:75651769 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:75651769 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:75654157 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:75654157 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:56230817 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:56230817 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:60744607 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:60744607 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:60105567 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:60105567 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:76344973 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:76344973 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100695336 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100695336 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:26294575 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:26294575 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:192275911 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:192275911 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:62871863 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:62871863 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:76851518 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:76851518 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:45105227 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:45105227 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:47163341 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:47163341 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:24776160 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:24776160 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:65084483 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:65084483 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:57113061 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:57113061 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:6675687 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:6675687 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:150703844 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:150703844 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:161207898 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:161207898 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:32472117 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:32472117 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:2936903 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:2936903 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:154034177 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:154034177 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:45580628 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:45580628 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:28267586 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:28267586 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:50966403 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:50966403 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:67331625 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:67331625 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20483364 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20483364 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:55860776 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:55860776 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:3147661 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:3147661 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:29650550 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:29650550 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23240210 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23240210 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:52668614 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:52668614 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:47810810 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:47810810 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:66833285 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:66833285 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:120488143 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:120488143 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:149312168 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:149312168 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20373708 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20373708 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:197784556 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:197784556 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:58349575 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:58349575 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:96392139 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:96392139 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:50356527 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:50356527 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:47853456 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:47853456 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:47866868 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:47866868 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:9343695 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:9343695 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:39795097 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:39795097 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:131951236 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:131951236 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:44538119 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:44538119 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:113310159 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:113310159 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:57004311 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:57004311 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:60759219 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:60759219 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:63225838 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:63225838 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:127920339 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:127920339 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:23517870 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:23517870 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:120933462 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:120933462 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:57467239 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:57467239 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:54395924 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:54395924 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:48701459 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:48701459 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:36302982 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:36302982 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:109241694 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:109241694 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:170699561 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:170699561 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:43383758 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:43383758 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:53177705 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:53177705 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:220166165 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:220166165 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:220167286 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:220167286 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:40714509 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:40714509 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:226110140 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:226110140 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:144689069 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:144689069 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:21930620 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:21930620 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:24735806 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:24735806 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:4648104 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:4648104 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:95411502 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:95411502 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:86628287 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:86628287 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:114782653 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:114782653 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:113543701 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:113543701 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:173934331 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:173934331 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:118465910 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:118465910 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:155870155 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:155870155 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:94484652 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:94484652 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:136216154 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:136216154 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:166952375 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:166952375 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:123005860 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:123005860 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:39409050 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:39409050 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:12680150 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:12680150 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:75528691 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:75528691 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:84658569 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:84658569 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:101176516 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:101176516 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:407964 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:407964 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:43421948 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:43421948 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:1552324 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:1552324 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:21729743 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:21729743 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:25915957 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:25915957 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:22396177 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:22396177 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:103006516 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:103006516 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:85487953 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:85487953 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:26372277 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:26372277 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:1219833 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:1219833 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:40402081 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:40402081 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:74914094 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:74914094 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:98770955 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:98770955 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:169067091 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:169067091 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:2297596 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:2297596 A>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:167983617 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:167983617 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:167983776 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:167983776 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:2224939 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:2224939 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:48216749 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrX:48216749 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:92973238 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:92973238 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:220477818 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:220477818 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:8578923 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:8578923 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:24584422 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:24584422 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:46357803 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:46357803 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:46964082 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:46964082 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:64900726 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:64900726 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:1725332 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:1725332 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:52927127 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:52927127 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:15211832 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:15211832 T>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20871685 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20871685 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:155465667 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:155465667 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:166981070 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:166981070 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:63054225 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:63054225 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:126138084 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:126138084 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:48741559 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:48741559 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:101286988 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:101286988 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:152220648 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:152220648 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:12140163 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:12140163 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:43175188 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:43175188 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:1955112 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:1955112 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:62517463 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:62517463 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:144288332 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:144288332 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:103297229 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:103297229 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:20126702 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr13:20126702 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:10906859 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:10906859 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:30388636 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:30388636 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:36520016 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:36520016 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:117654811 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:117654811 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:55034987 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:55034987 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:14359322 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:14359322 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:72967854 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:72967854 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:99720656 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:99720656 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67858716 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67858716 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:75051833 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:75051833 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:46867263 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:46867263 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:158919875 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:158919875 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:104709746 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:104709746 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:171682217 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:171682217 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:35955675 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:35955675 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:132623373 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:132623373 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrY:15361646 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chrY:15361646 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:100587851 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:100587851 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:55429913 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:55429913 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:29136678 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:29136678 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:74943861 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:74943861 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:228786357 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:228786357 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:190331121 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:190331121 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:111633291 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:111633291 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:21856830 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:21856830 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:22853014 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:22853014 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:104192962 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:104192962 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:133732052 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:133732052 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:32368853 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:32368853 G>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:21465381 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:21465381 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:4815538 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:4815538 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:36963676 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:36963676 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:99161785 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:99161785 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:249150835 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:249150835 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:149191266 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:149191266 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:7568055 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:7568055 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:7721612 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:7721612 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53702499 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53702499 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125561190 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125561190 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125570872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125570872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151461987 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151461987 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170999802 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170999802 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74465186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74465186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41131380 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41131380 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70316517 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70316517 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121721541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121721541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121766401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121766401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:67151923 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:67151923 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:215855414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:215855414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107623879 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107623879 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94476981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94476981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94480051 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94480051 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94486714 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94486714 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94543453 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94543453 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94568723 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94568723 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:1049180 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:1049180 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101590218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101590218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101595814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101595814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183663612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183663612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74753294 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74753294 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150918649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150918649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119025668 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119025668 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119028882 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119028882 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119031128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119031128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44051585 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44051585 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44079424 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44079424 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51347343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51347343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51348419 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51348419 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25349167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25349167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25349250 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25349250 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116211363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116211363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116247664 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116247664 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116361541 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116361541 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116449973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116449973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47340507 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47340507 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35601976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35601976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109639333 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109639333 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109679098 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109679098 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109696759 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109696759 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109697924 C>A maps to ENST00000390027 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109697924 C>A maps to ENST00000390027 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112150497 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112150497 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132349207 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132349207 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:44074179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:44074179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61561146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61561146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23531580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23531580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73949479 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73949479 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78526850 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78526850 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:185678168 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:185678168 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:114164413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:114164413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20563422 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20563422 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7456920 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7456920 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33462828 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33462828 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33501514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33501514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33509527 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33509527 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33514886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33514886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:5567349 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:5567349 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179292281 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179292281 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:65469171 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:65469171 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42847299 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42847299 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127786953 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127786953 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155030277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155030277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156899277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156899277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87774841 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87774841 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:24188547 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:24188547 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:39627140 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:39627140 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120436569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120436569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120436575 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120436575 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3649674 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3649674 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:24304606 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:24304606 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38871462 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38871462 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33588684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33588684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136280139 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136280139 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72517709 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72517709 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5209168 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5209168 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:100591984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:100591984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:43837734 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:43837734 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136403559 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136403559 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136412041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136412041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136412143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136412143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:84659824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:84659824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143771636 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143771636 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143771688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143771688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140390509 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140390509 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167828960 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167828960 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7706729 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7706729 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7706845 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7706845 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25044359 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25044359 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25045317 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25045317 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25045338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25045338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70905810 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70905810 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:111879207 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:111879207 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100009830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100009830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100356327 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100356327 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186572532 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:186572532 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1895070 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:1895070 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:49530270 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:49530270 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73052903 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73052903 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67048184 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67048184 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40754857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40754857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116067732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116067732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88055580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88055580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:74321020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:74321020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88751941 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88751941 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88761426 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88761426 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:236715988 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:236715988 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150817254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150817254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150820810 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:150820810 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:178361415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:178361415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47713875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47713875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47727398 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47727398 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32149042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32149042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228389660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228389660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228416852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228416852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100356936 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100356936 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45402148 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45402148 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84465651 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84465651 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84515956 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84515956 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88207719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88207719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:109669074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:109669074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:109675706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:109675706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:306928 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:306928 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:17382697 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:17382697 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222867635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222867635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31583995 C>A maps to NM_004847.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31583995 C>A maps to NM_004847.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129289082 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129289082 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109395298 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109395298 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134133735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:134133735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:19596037 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:19596037 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49968902 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49968902 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97366500 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97366500 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75516227 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75516227 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105425511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105425511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105440653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105440653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112220839 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112220839 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67450271 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:67450271 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104192024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104192024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111724305 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111724305 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43919932 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43919932 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43919962 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43919962 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73835567 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73835567 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113298908 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113298908 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56191125 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56191125 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202173976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202173976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33997298 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33997298 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46450712 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46450712 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46569737 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46569737 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111214655 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111214655 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrY:6737958 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrY:6737958 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56396326 G>T maps to ENST00000314566 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56396326 G>T maps to ENST00000314566 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56397753 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56397753 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56401346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56401346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115222355 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115222355 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115237965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115237965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115238050 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115238050 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10524251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10524251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104120273 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:104120273 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:66247325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:66247325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:178820251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:178820251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:41573375 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:41573375 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114263081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:114263081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:62038690 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:62038690 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241421686 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241421686 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:16685204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:16685204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110467267 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110467267 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73950949 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:73950949 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:67951942 C>A maps to NM_001012419.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:67951942 C>A maps to NM_001012419.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:69385875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:69385875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:15749421 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:15749421 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37438482 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37438482 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37442624 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37442624 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37490288 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:37490288 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90327787 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90327787 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34934971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34934971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34985236 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:34985236 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21262182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21262182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101547071 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101547071 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36492212 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:36492212 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5687208 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:5687208 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26620391 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26620391 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26645925 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26645925 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26664713 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:26664713 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101381220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101381220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101381288 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101381288 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101430823 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101430823 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:45610210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:45610210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17444181 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17444181 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90346432 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90346432 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124693373 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124693373 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124705929 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124705929 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75775832 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75775832 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75784098 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75784098 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75139569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75139569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:47133420 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:47133420 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201476068 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201476068 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71768458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71768458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71779570 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71779570 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71789895 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71789895 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24035706 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24035706 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42022897 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42022897 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114438876 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114438876 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114444279 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114444279 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:40818033 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:40818033 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49719940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49719940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63579614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63579614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43345210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43345210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43351651 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43351651 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116693246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116693246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116693343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116693343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195298128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195298128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27425541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27425541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27425688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:27425688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32985883 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:32985883 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50368096 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50368096 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33384951 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:33384951 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:35182404 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:35182404 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:35236692 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:35236692 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72468960 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72468960 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:36134838 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:36134838 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61915271 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61915271 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47196537 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47196537 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:43195008 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:43195008 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68255556 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68255556 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47626695 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47626695 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30927634 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:30927634 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32103169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32103169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24873289 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24873289 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24886862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:24886862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6851026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6851026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94649690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94649690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94668294 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94668294 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119101094 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119101094 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36269274 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36269274 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:130219502 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:130219502 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:11243816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:11243816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7521144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7521144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155936553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155936553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111862090 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111862090 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157488112 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157488112 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157527236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157527236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93699264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93699264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232196452 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232196452 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80767306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80767306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80806773 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80806773 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80883864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80883864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80889561 C>A maps to ENST00000360062 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80889561 C>A maps to ENST00000360062 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127637454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127637454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74988357 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74988357 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:3028307 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:3028307 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3660796 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:3660796 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17919735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17919735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122944172 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122944172 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122945366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122945366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131124322 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131124322 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131172095 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:131172095 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123254505 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123254505 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123254676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123254676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123256401 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123256401 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123276849 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:123276849 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94419620 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:94419620 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132397749 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132397749 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:15272798 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:15272798 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:101127442 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:101127442 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:101215217 C>A maps to NM_006828.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:101215217 C>A maps to NM_006828.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:101312137 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:101312137 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37967891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37967891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1558100 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1558100 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1746672 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1746672 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62559431 C>A maps to NM_004318.3 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62559431 C>A maps to NM_004318.3 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62566106 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62566106 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62578154 G>T maps to NM_020164.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:62578154 G>T maps to NM_020164.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70188856 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70188856 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133364661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133364661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176853405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176853405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119495584 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119495584 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117021039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117021039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117066877 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117066877 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:89527401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:89527401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29157994 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29157994 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29158184 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:29158184 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81305476 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81305476 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:106682733 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:106682733 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11389564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11389564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:38536698 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:38536698 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47548635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47548635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47584083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47584083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113470339 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113470339 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113487137 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113487137 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113487145 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113487145 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113505553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113505553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25259550 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25259550 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25281354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25281354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193032625 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193032625 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116931439 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116931439 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116931469 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116931469 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116937654 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116937654 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116944300 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116944300 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110765311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110765311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110783019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110783019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:90021406 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:90021406 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84455950 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84455950 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84456224 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84456224 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57032830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57032830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124209156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124209156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124235630 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124235630 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138429846 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138429846 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138447611 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138447611 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44443690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44443690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172447760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172447760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:104078692 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:104078692 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:46739870 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:46739870 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52585478 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52585478 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:42588352 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:42588352 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154300272 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154300272 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154319243 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154319243 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50244098 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50244098 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77108116 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77108116 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3541652 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3541652 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:76920034 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:76920034 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:105516293 C>A maps to NM_020725.1 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:105516293 C>A maps to NM_020725.1 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74755195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74755195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:32590857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:32590857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:32957001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:32957001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31891623 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31891623 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:661115 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:661115 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44455899 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44455899 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48252817 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48252817 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29237834 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:29237834 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90642041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90642041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11039214 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11039214 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11047455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11047455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11047588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11047588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79384859 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79384859 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70048914 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70048914 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88039667 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88039667 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31605138 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31605138 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31655225 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31655225 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160261504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160261504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160319351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160319351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:33282636 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:33282636 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107262440 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107262440 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94033260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94033260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94057971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94057971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115110660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115110660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:49457138 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:49457138 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:25054872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:25054872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52402025 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52402025 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50170459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50170459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12240109 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12240109 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118778157 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118778157 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81303677 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81303677 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:112084439 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:112084439 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104004119 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:104004119 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:42127562 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:42127562 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:5023256 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:5023256 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:5024502 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:5024502 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:60273103 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:60273103 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:127806054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:127806054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32716654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32716654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43806939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43806939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40397955 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40397955 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22058767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22058767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55803262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55803262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55803507 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55803507 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88615774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88615774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:15540460 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:15540460 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140481244 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140481244 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41209029 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41209029 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41209053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41209053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92446420 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92446420 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28460061 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28460061 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28464174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28464174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125497060 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125497060 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34923181 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34923181 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1480406 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1480406 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62458044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62458044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122849898 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122849898 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83698853 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83698853 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:11899257 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:11899257 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:38560268 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:38560268 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:100629455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:100629455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26373569 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:26373569 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180326272 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180326272 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180335964 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180335964 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180374496 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180374496 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:111428054 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:111428054 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121596332 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121596332 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:77818365 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:77818365 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124458088 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124458088 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98708780 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98708780 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127451819 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127451819 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72538239 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72538239 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102749651 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102749651 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102750335 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102750335 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102750613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102750613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50255017 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:50255017 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103649150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103649150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103769080 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103769080 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103792948 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103792948 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8936548 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8936548 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47008696 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47008696 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124637008 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124637008 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122827327 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122827327 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:82625769 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:82625769 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64715017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64715017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32145285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32145285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:103695883 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:103695883 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121441937 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121441937 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112667464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112667464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112667480 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112667480 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31814874 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31814874 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110503740 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110503740 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113047463 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113047463 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75196925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75196925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40684142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40684142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76462221 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76462221 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76518303 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76518303 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49657717 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49657717 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49880331 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49880331 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:36911118 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:36911118 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90170140 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90170140 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40854950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40854950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67697236 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67697236 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89724635 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89724635 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4797309 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4797309 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89782845 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89782845 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30768780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30768780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8141674 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:8141674 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3725182 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3725182 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77802110 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77802110 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:71816024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:71816024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50658007 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50658007 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44252866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:44252866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34042969 G>T maps to NM_181435.4 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34042969 G>T maps to NM_181435.4 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24893029 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24893029 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:244640780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:244640780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:244641146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:244641146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231362598 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231362598 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75102192 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75102192 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:55174762 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:55174762 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185112461 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185112461 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154186893 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154186893 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150252031 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150252031 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156264495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156264495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60499358 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60499358 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60520855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60520855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:2519976 C>A maps to NM_001195737.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:2519976 C>A maps to NM_001195737.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172554947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172554947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35504626 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35504626 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18379290 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:18379290 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35743774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35743774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34618582 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:34618582 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61151480 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61151480 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31657612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31657612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31671168 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31671168 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31673804 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31673804 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3303351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3303351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3311343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3311343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:20246105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:20246105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31766111 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31766111 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31813169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31813169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:75929311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:75929311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74808787 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74808787 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74855396 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74855396 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210887614 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210887614 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242815431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242815431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:63349066 G>T maps to ENST00000448143 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:63349066 G>T maps to ENST00000448143 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:118869971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:118869971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:153202513 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:153202513 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57829596 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57829596 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113482050 C>A maps to NM_018392.4 G1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113482050 C>A maps to NM_018392.4 G1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:8456563 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:8456563 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113092392 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113092392 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:130030437 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:130030437 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184607718 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184607718 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3265715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3265715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159592735 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159592735 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123785673 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123785673 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:175740608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:175740608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36207259 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36207259 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43487242 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43487242 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172512928 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172512928 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37177822 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37177822 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37209553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37209553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37209647 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37209647 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37210710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37210710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37211523 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37211523 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37211576 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37211576 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37211646 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37211646 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37212402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37212402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41912151 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41912151 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41149261 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41149261 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41159144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41159144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41203155 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41203155 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165711422 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165711422 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165714121 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165714121 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30608231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30608231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30617329 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30617329 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:88140926 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:88140926 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127768640 G>T maps to NM_014702.4 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127768640 G>T maps to NM_014702.4 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127771069 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:127771069 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133091346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133091346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:107365610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:107365610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36296621 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36296621 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31735300 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31735300 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157744396 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:157744396 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35714983 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35714983 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31732171 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:31732171 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6631260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6631260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66420428 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66420428 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:120764297 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:120764297 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:47698471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:47698471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146279397 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:146279397 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:96281250 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:96281250 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:33371087 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:33371087 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22460188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22460188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35821587 G>T maps to ENST00000388950 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35821587 G>T maps to ENST00000388950 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:72459410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:72459410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:97535508 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:97535508 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114480648 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114480648 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77692144 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77692144 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136249588 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136249588 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150236103 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150236103 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:24573397 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:24573397 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121098501 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121098501 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21739955 C>A maps to NM_138644.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21739955 C>A maps to NM_138644.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21739988 C>A maps to NM_138644.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21739988 C>A maps to NM_138644.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21741482 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21741482 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:13355917 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:13355917 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140777374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140777374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140938409 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140938409 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140943631 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140943631 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2566927 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2566927 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2566951 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2566951 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2704972 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2704972 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181480500 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181480500 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181548363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181548363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181754812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:181754812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201054020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201054020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:81596885 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:81596885 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50421786 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50421786 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:54850940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:54850940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:54930707 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:54930707 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18439938 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18439938 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18550877 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18550877 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18629916 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18629916 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18828157 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:18828157 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:36962377 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:36962377 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:115080407 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:115080407 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:86061874 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:86061874 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27464101 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27464101 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7327197 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7327197 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7331566 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7331566 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91075316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:91075316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71416609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71416609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71423539 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71423539 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:14991413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:14991413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:14991439 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:14991439 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:14991659 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:14991659 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54115200 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54115200 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12595154 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12595154 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12833268 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12833268 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75597182 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75597182 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121687564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121687564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12872957 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12872957 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241533924 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241533924 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44140949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44140949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230921652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230921652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:55601418 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:55601418 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116528150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116528150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202052413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202052413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104970042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104970042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104819442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104819442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104872963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:104872963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116268049 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116268049 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43927552 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43927552 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26524749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:26524749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:38858084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:38858084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34482665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34482665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32194688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32194688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24897464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24897464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:172055 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:172055 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54651443 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54651443 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52834756 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52834756 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97779363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97779363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97779406 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97779406 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97791545 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97791545 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:66506184 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:66506184 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:55771001 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:55771001 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47787400 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47787400 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92987607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92987607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179730401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179730401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179733829 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179733829 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11531650 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11531650 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77265817 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77265817 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93687311 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93687311 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32670100 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32670100 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96284555 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96284555 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:78032793 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:78032793 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94794805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94794805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:191107224 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:191107224 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119937852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119937852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119966301 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:119966301 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120510563 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120510563 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49298070 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49298070 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32724388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32724388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32781645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:32781645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:91850749 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:91850749 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13800550 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13800550 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:28410104 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:28410104 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:118705617 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:118705617 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31110719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31110719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:26484701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:26484701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228681836 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228681836 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75398991 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75398991 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43388433 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43388433 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:37016254 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:37016254 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:122739342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:122739342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:59399708 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:59399708 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99991542 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:99991542 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43483887 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43483887 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2498850 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2498850 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97804126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:97804126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:208618260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:208618260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35819015 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35819015 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46414326 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46414326 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45943400 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45943400 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156286920 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156286920 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156303290 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156303290 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10254334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10254334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10261664 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10261664 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73476905 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73476905 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117556435 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117556435 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7591739 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7591739 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7592308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7592308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7637647 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7637647 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158227330 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158227330 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158147075 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158147075 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158324089 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158324089 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7806485 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7806485 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160808228 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160808228 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167408509 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:167408509 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204571368 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204571368 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47591992 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:47591992 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30366005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30366005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:72519048 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:72519048 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208062248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208062248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118175655 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118175655 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207956635 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207956635 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60780822 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60780822 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2632524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2632524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2637672 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2637672 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100963778 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100963778 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100983730 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100983730 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99285465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99285465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99285531 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99285531 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:115002432 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:115002432 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48219338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48219338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:137664147 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:137664147 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227204571 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227204571 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227239677 G>T maps to ENST00000366766 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:227239677 G>T maps to ENST00000366766 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64609240 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64609240 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:130695134 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:130695134 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22408188 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22408188 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44390561 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44390561 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38447948 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38447948 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:193205368 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:193205368 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25319757 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25319757 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45127073 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45127073 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45152350 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45152350 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24487726 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:24487726 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95164071 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95164071 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:59203688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:59203688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:25616620 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:25616620 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26881222 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:26881222 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:175995882 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:175995882 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:40087486 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:40087486 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205495446 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205495446 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58144427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58144427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31984923 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31984923 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123210125 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123210125 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123210146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123210146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:26978034 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:26978034 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130549102 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130549102 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36653579 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36653579 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14867462 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14867462 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125888401 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125888401 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85552944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:85552944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5165605 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5165605 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:4935692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:4935692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:42231241 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:42231241 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22310845 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22310845 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47493704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47493704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:11047418 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:11047418 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:11207430 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:11207430 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151681450 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151681450 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:3250888 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:3250888 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48664051 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48664051 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48668411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48668411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25039418 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25039418 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67862495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67862495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123880613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123880613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123921116 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123921116 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123935940 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123935940 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:56886803 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:56886803 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101443481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101443481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:89689869 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:89689869 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31912457 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31912457 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31912744 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31912744 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31915463 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31915463 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31919285 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31919285 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75446387 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75446387 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:196654149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:196654149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117149067 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117149067 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117230556 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117230556 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117246825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117246825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49551699 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49551699 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:93541624 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:93541624 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6690446 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6690446 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6700764 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6700764 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:6196481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:6196481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40141652 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40141652 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61736637 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:61736637 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53330837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53330837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53854642 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53854642 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125496653 C>A maps to ENST00000427383 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125496653 C>A maps to ENST00000427383 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125505458 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125505458 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125542637 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125542637 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133433246 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133433246 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111854262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111854262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:87276760 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:87276760 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:29252059 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:29252059 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184100394 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184100394 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78879052 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78879052 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78879059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78879059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154543651 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154543651 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:175246415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:175246415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:1270870 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:1270870 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:1270912 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:1270912 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120150953 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120150953 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120221888 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120221888 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113498328 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113498328 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46837705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46837705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:87025533 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:87025533 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:10174863 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:10174863 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:190120104 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:190120104 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10131676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10131676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70012106 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70012106 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70012277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70012277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10151706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:10151706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8610413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8610413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73732068 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73732068 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73770718 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73770718 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74919641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74919641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:95675702 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:95675702 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:68547165 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:68547165 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:140282722 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:140282722 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7289411 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7289411 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81694458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81694458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47945128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47945128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224804825 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:224804825 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97494519 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97494519 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32811353 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32811353 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135047596 G>T maps to ENST00000262563 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135047596 G>T maps to ENST00000262563 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:78641570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:78641570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:78740397 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:78740397 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99722529 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99722529 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:246823458 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:246823458 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3079024 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:3079024 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125285074 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125285074 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125521733 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:125521733 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:51097325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:51097325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230814821 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230814821 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46060731 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46060731 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46104130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46104130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116443138 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116443138 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103379283 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103379283 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103404580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103404580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103430981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103430981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103444352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103444352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103462590 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103462590 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103462605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103462605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103462617 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103462617 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491406 G>T maps to NM_080629.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491406 G>T maps to NM_080629.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491427 G>T maps to NM_080629.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:103491427 G>T maps to NM_080629.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75811639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:75811639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101767129 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101767129 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101801035 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101801035 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101804292 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101804292 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101817449 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101817449 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32150513 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32150513 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32154163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32154163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70812019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70812019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70850786 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70850786 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70850792 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70850792 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:94048769 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:94048769 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139809031 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139809031 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139809176 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:139809176 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:86241323 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:86241323 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:86622094 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:86622094 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116956755 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116956755 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116968012 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116968012 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116971898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116971898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7550681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:7550681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48391581 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48391581 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48391928 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48391928 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48392014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:48392014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189866244 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189866244 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110838915 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110838915 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110853280 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110853280 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110861831 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110861831 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110864675 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110864675 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110866226 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:110866226 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111084621 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111084621 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111134789 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111134789 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111141867 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:111141867 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227871902 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227871902 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227887117 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:227887117 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228012054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228012054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228012124 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228012124 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107408567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107408567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107408582 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107408582 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107446068 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:107446068 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189899917 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189899917 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189903964 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189903964 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189927516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189927516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238270461 C>A maps to NM_004369.3 E2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238270461 C>A maps to NM_004369.3 E2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130287481 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130287481 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48612691 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48612691 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48623243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48623243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48623717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48623717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70942269 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:70942269 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160259927 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160259927 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160287171 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160287171 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160287530 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160287530 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:139085678 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:139085678 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128979277 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:128979277 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49420857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49420857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54730970 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54730970 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54741864 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54741864 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198327493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198327493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120960671 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120960671 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47708694 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47708694 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47839876 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47839876 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100890427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100890427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69007444 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69007444 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129916430 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129916430 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129950861 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129950861 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17014450 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17014450 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46652842 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46652842 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56985502 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56985502 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87558912 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87558912 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:131300567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:131300567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36715910 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36715910 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:39118745 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:39118745 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:211513306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:211513306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68528980 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68528980 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:51009548 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:51009548 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:125639710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:125639710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207825963 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207825963 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207741404 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207741404 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207791613 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207791613 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:126132325 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:126132325 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65579988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65579988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35735279 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35735279 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:3860567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:3860567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35437438 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:35437438 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:36669731 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:36669731 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49806088 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49806088 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49815846 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49815846 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49815898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:49815898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:5837598 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:5837598 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86983829 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:86983829 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91178108 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91178108 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:27019153 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:27019153 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:26998002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:26998002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:208994427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:208994427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115282399 C>A maps to NM_001130523.1 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115282399 C>A maps to NM_001130523.1 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115282477 C>A maps to NM_001130523.1 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115282477 C>A maps to NM_001130523.1 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1407584 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1407584 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36937816 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36937816 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43657669 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43657669 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43657741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43657741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2965201 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2965201 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113421277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113421277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113649260 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113649260 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113988038 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113988038 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:38776981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:38776981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:480448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:480448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58200448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:58200448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31638715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31638715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31640091 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31640091 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47604065 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47604065 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47618217 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47618217 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68107602 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:68107602 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201453962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201453962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56679662 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56679662 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:56094478 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:56094478 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44778925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44778925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:111706127 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:111706127 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:11732233 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:11732233 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:16669277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:16669277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:16688679 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:16688679 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:41450443 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:41450443 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10789286 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10789286 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:15769843 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:15769843 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88042493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88042493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88059587 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:88059587 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66333128 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66333128 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65649026 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65649026 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117423036 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:117423036 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70267718 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70267718 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70277436 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70277436 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88776305 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88776305 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88776707 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88776707 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17107629 C>A maps to NM_001081.3 G1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17107629 C>A maps to NM_001081.3 G1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17171581 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:17171581 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148427128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148427128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148484065 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148484065 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:107949047 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:107949047 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43006229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43006229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:101713705 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:101713705 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:111701559 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:111701559 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124591777 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124591777 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64267654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64267654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64313946 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64313946 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101996735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:101996735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48993427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48993427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:49034539 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:49034539 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:49040029 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:49040029 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39306896 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39306896 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39306922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39306922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:18890885 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:18890885 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:44871562 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:44871562 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:74964656 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:74964656 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136873536 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136873536 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:75397413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:75397413 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156785980 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156785980 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74654079 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74654079 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96698376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96698376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96698395 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96698395 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41622079 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41622079 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60359523 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60359523 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60377371 C>A maps to NM_000775.2 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60377371 C>A maps to NM_000775.2 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60392199 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60392199 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99364651 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99364651 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99270341 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99270341 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:47398374 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:47398374 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:47611505 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:47611505 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:47611900 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:47611900 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:65508604 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:65508604 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:65508721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:65508721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:65508800 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:65508800 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:5021010 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:5021010 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:20013644 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:20013644 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:20137078 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:20137078 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:39856575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:39856575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124545835 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124545835 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39389293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:39389293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61510943 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61510943 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109281195 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109281195 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:90254516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:90254516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:90283440 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:90283440 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100787760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100787760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173823083 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173823083 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33289464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33289464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33289482 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33289482 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:121929358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:121929358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87507552 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87507552 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136517419 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136517419 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120125892 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120125892 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176893749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176893749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44096286 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44096286 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172314433 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172314433 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160213826 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160213826 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160236444 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160236444 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160250053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160250053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:43131524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:43131524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:43131581 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:43131581 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151153644 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151153644 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976373 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976373 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976606 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976606 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976658 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:14976658 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:183836578 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:183836578 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57926306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57926306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57926334 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57926334 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182678901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:182678901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114112451 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114112451 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114112462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114112462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114138408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114138408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:52744053 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:52744053 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61083926 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61083926 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47237821 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47237821 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162688776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162688776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70348757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70348757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70398349 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70398349 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49227044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49227044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49237681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49237681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135537684 G>T maps to NM_022779.7 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135537684 G>T maps to NM_022779.7 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:74114313 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:74114313 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12975087 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12975087 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35988774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35988774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124102273 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124102273 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35285903 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35285903 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:90021523 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:90021523 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30028468 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30028468 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18256723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18256723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18258175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18258175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197705200 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:197705200 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115144033 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115144033 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65962308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65962308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65995143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65995143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66064030 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66064030 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31576397 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31576397 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179326019 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179326019 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145541729 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145541729 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:14216427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:14216427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234375865 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234375865 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:54912107 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:54912107 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42643459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42643459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42793266 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42793266 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:137341150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:137341150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:137363287 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:137363287 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:137406906 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:137406906 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:55341813 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:55341813 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12628302 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12628302 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24464180 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24464180 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2185059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2185059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:24534408 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:24534408 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30627497 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30627497 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47883234 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47883234 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154010319 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154010319 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125470863 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:125470863 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72130711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72130711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72136901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72136901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72141522 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72141522 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:57676852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:57676852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39025411 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39025411 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39082149 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39082149 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182812577 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182812577 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182827649 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182827649 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122709022 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122709022 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140951489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140951489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:334262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:334262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:334266 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:334266 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:518346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:518346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66615829 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66615829 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66624308 G>T maps to NM_001143688.1 G878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66624308 G>T maps to NM_001143688.1 G878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231885661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231885661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40656366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40656366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11988466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11988466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:13072102 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:13072102 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197023987 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197023987 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071229 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071229 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071258 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071258 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071290 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:35071290 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172952653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172952653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172952697 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172952697 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172952992 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:172952992 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48051059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48051059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44685588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44685588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124359655 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124359655 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124384211 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124384211 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124385511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124385511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:32364032 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:32364032 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51830324 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51830324 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51830376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51830376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51837752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51837752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124285741 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124285741 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124293508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124293508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124364430 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124364430 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124416464 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124416464 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:21751285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:21751285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52393920 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52393920 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52396964 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52396964 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7704863 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7704863 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21098144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21098144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13700708 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13700708 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13754221 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13754221 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13844866 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13844866 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13862653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13862653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13885211 C>A maps to NM_001369.2 E957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:13885211 C>A maps to NM_001369.2 E957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196720498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:196720498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:11645664 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:11645664 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:11737936 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:11737936 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:11775166 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:11775166 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46990915 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46990915 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220150729 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220150729 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:157208696 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:157208696 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132229856 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132229856 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96394993 C>A maps to ENST00000360638 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96394993 C>A maps to ENST00000360638 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27503111 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27503111 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28527752 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28527752 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230271900 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230271900 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6530325 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6530325 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6593219 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6593219 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131010191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131010191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25468049 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:25468049 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31376560 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31376560 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220251722 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220251722 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44433761 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44433761 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94337580 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94337580 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128821644 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:128821644 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129200918 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129200918 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129200962 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129200962 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129209066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129209066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169111404 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169111404 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169116231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169116231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50900755 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50900755 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:111487006 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:111487006 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25232043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25232043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62923388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62923388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62939601 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62939601 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941283 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941283 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941288 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941288 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941632 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941632 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941817 C>A maps to ENST00000371140 G1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62941817 C>A maps to ENST00000371140 G1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62943252 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62943252 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62952937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62952937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62952994 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62952994 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62953155 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62953155 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62953162 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62953162 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62954514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62954514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62958346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62958346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62960179 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62960179 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99462606 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99462606 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67406182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:67406182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131846849 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131846849 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118972187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118972187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30919924 C>A maps to NM_080870.3 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30919924 C>A maps to NM_080870.3 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68021723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68021723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65113342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65113342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65113540 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65113540 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101479374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101479374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66253987 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66253987 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66259239 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66259239 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65804933 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65804933 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:109046937 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:109046937 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:63962989 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:63962989 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97700550 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97700550 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97770801 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97770801 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97771665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97771665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97771684 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97771684 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97771704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:97771704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116579914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:116579914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:28923572 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:28923572 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56362872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56362872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56469552 C>A maps to ENST00000361203 S3080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56469552 C>A maps to ENST00000361203 S3080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56481508 C>A maps to ENST00000281662 G2816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56481508 C>A maps to ENST00000281662 G2816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56481616 C>G maps to ENST00000281662 V2780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56481616 C>G maps to ENST00000281662 V2780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76111781 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76111781 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45452993 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45452993 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68100172 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68100172 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73994354 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73994354 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12630976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:12630976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183885865 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183885865 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102466513 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102466513 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102496075 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102496075 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102516707 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:102516707 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95705319 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95705319 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71762329 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71762329 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71801312 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71801312 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71883439 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71883439 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207527608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207527608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:137811219 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:137811219 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96258369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96258369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96264265 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96264265 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96293495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96293495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11590126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11590126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25890678 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:25890678 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43634549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43634549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43634573 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43634573 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150483715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150483715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236647456 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236647456 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74933011 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74933011 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33762499 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33762499 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184679498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:184679498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:83258968 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:83258968 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62128919 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62128919 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207025241 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:207025241 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144669068 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144669068 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:22088420 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:22088420 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:16948002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:16948002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52370297 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52370297 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52370336 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52370336 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52370802 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52370802 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:133014001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:133014001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:82523169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:82523169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38435391 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38435391 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38438424 G>T maps to ENST00000354891 G778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38438424 G>T maps to ENST00000354891 G778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41284336 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41284336 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65348033 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65348033 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64622337 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64622337 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42201869 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42201869 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140648607 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140648607 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140669535 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140669535 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125450107 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125450107 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65766798 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65766798 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40282411 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40282411 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36298206 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36298206 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2409095 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2409095 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:28734620 C>A maps to NM_003752.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:28734620 C>A maps to NM_003752.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8013306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8013306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7476265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7476265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53432295 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53432295 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184043518 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184043518 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184049156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184049156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:21191283 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:21191283 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170625369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170625369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:140046277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:140046277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201984467 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201984467 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34511530 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34511530 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205588945 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205588945 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:18555947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:18555947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37355455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37355455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37382195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37382195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45002261 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:45002261 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67236060 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67236060 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73450849 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73450849 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33725010 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33725010 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:101438975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:101438975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:2908841 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:2908841 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42508120 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42508120 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42515479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42515479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:89082465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:89082465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71503586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71503586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130579386 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130579386 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:8927383 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:8927383 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4860191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4860191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43839529 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43839529 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120592315 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120592315 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120592423 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:120592423 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:131971141 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:131971141 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150599747 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150599747 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150599779 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150599779 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40271886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40271886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110346715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110346715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27761002 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27761002 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27761605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27761605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132466549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132466549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132474713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132474713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132515713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132515713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132528715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132528715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132537798 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:132537798 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5394799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5394799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5445296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:5445296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43512916 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43512916 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47613677 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47613677 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:222299061 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:222299061 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134851493 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134851493 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134885868 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134885868 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134898668 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134898668 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100411206 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100411206 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92515841 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92515841 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11488618 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11488618 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220184414 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220184414 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16545161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16545161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43500569 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43500569 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43566007 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:43566007 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37868107 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37868107 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56490416 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56490416 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:212483885 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:212483885 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45872282 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45872282 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128047771 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128047771 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103518542 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103518542 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:8873824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:8873824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44804705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44804705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37601811 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37601811 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:23703246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:23703246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:23703499 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:23703499 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27633138 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27633138 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:47345541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:47345541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:64694332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:64694332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:103499427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:103499427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:158529733 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:158529733 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138174024 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138174024 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138187641 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:138187641 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:67636954 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:67636954 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204103846 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204103846 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:14028553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:14028553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36135542 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36135542 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185775133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185775133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36334397 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36334397 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93070858 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93070858 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93159514 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93159514 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:29696163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:29696163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:242015726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:242015726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:488929 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:488929 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:572731 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:572731 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67220844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67220844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67220920 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67220920 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:133692635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:133692635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:72968401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:72968401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11151012 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11151012 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99198329 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99198329 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133574661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133574661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:118849335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:118849335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28369003 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28369003 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133802460 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133802460 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148512508 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148512508 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159191726 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159191726 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160969214 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160969214 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6175141 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6175141 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6251210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6251210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154089933 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:154089933 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:51267281 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:51267281 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:51425533 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:51425533 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80451989 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80451989 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130742442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130742442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14609132 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14609132 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130279119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130279119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16483362 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16483362 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89660161 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89660161 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89744256 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89744256 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:53122827 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:53122827 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116603704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:116603704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74410986 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:74410986 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:75720277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:75720277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102697262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102697262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:119341101 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:119341101 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30915081 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30915081 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30931621 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30931621 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:29527101 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:29527101 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2661446 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2661446 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2733458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2733458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176965857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176965857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51892478 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:51892478 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46238945 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46238945 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46272913 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46272913 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46282104 C>A maps to ENST00000399588 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:46282104 C>A maps to ENST00000399588 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99691236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99691236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88950212 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88950212 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:10681657 G>T maps to NM_022068.2 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:10681657 G>T maps to NM_022068.2 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58629483 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58629483 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120892160 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120892160 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:34147940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:34147940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153676932 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153676932 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101504542 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101504542 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150971836 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150971836 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67578752 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67578752 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24849969 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24849969 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24873830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24873830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119418935 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119418935 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:212800057 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:212800057 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156592554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156592554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:40702783 C>A maps to NM_001083124.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:40702783 C>A maps to NM_001083124.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:40702807 G>T maps to NM_001083124.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:40702807 G>T maps to NM_001083124.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:38218329 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:38218329 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41029269 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41029269 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87516920 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87516920 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124206459 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:124206459 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37576657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37576657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37581169 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37581169 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33809835 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33809835 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89818498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89818498 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89877303 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89877303 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10115086 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10115086 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35424186 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35424186 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89837040 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89837040 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89856248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:89856248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127697133 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:127697133 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163099905 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163099905 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:5431201 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:5431201 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172629312 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:172629312 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170387058 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170387058 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7865975 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7865975 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:92403261 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:92403261 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48826181 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48826181 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48826188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48826188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48936741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48936741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127595026 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127595026 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127645124 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127645124 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33414689 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:33414689 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:15500757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:15500757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:417779 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:417779 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:171295540 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:171295540 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48423617 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48423617 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103433196 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103433196 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40399160 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40399160 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:157766844 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:157766844 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:157550072 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:157550072 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:159776463 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:159776463 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111747198 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111747198 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111749915 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:111749915 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:55247496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:55247496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:125033764 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:125033764 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:6075551 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:6075551 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:6077743 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:6077743 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:108516376 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:108516376 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91435284 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91435284 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:62356017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:62356017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155510472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155510472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32793113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:32793113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:95566330 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:95566330 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15937507 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15937507 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38275348 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38275348 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:59978143 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:59978143 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60133134 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60133134 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155533518 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155533518 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:153889117 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:153889117 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:153889301 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:153889301 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135290815 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135290815 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135292162 C>A maps to NM_001159699.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135292162 C>A maps to NM_001159699.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67264487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67264487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34322580 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34322580 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110112504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:110112504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:115946015 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:115946015 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72710811 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72710811 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152325910 C>A maps to NM_001014342.2 G1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152325910 C>A maps to NM_001014342.2 G1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327137 C>A maps to NM_001014342.2 G1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327137 C>A maps to NM_001014342.2 G1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327416 C>A maps to NM_001014342.2 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152327416 C>A maps to NM_001014342.2 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152329768 G>A maps to NM_001014342.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152329768 G>A maps to NM_001014342.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152279721 G>T maps to NM_002016.1 S2547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152279721 G>T maps to NM_002016.1 S2547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152280330 G>T maps to NM_002016.1 S2344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152280330 G>T maps to NM_002016.1 S2344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152280838 C>A maps to NM_002016.1 G2175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152280838 C>A maps to NM_002016.1 G2175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152281845 G>T maps to NM_002016.1 S1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152281845 G>T maps to NM_002016.1 S1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152283922 C>A maps to NM_002016.1 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152283922 C>A maps to NM_002016.1 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152284261 C>A maps to NM_002016.1 G1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152284261 C>A maps to NM_002016.1 G1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152288005 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152288005 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58097812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58097812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58111261 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58111261 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58131644 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:58131644 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27210304 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27210304 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28896902 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28896902 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28908127 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28908127 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:33129395 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:33129395 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:240334454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:240334454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:240497389 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:240497389 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171227148 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171227148 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171178104 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171178104 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171086230 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:171086230 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146661740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:146661740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216245442 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216245442 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216288857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:216288857 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94017905 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94017905 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94017976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:94017976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159772426 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159772426 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8196374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8196374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:42730881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:42730881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:89756866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:89756866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41193810 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:41193810 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:71008376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:71008376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41556477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41556477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126147299 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126147299 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:79360269 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:79360269 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39433359 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39433359 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168468029 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168468029 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13693897 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13693897 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13702586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13702586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:131231390 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:131231390 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:49450189 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:49450189 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:12728465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:12728465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120115768 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120115768 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53860431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:53860431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61898661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61898661 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61899011 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61899011 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61903711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61903711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37420816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37420816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37446173 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37446173 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133491915 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:133491915 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91419596 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91419596 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91420284 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91420284 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:71686198 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:71686198 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180666614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180666614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43871524 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43871524 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46016693 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46016693 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72850130 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72850130 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76584197 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76584197 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75611291 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75611291 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29574833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29574833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101216527 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101216527 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:151358164 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:151358164 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46099416 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:46099416 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:88411855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:88411855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230400933 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230400933 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230410328 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230410328 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62400643 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62400643 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81390378 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81390378 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36033785 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36033785 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:128111641 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:128111641 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130106484 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130106484 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130117520 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130117520 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130127564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130127564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:100972761 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:100972761 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:90102105 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:90102105 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153790466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153790466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153825738 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153825738 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35738743 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35738743 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35740419 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35740419 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22729232 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:22729232 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104129869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104129869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104136247 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104136247 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104141776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104141776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:237075142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:237075142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:38206262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:38206262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27728535 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27728535 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27729593 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27729593 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27729645 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27729645 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:53385690 C>A maps to NM_001498.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:53385690 C>A maps to NM_001498.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120578640 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120578640 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10586770 C>A maps to NM_145655.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10586770 C>A maps to NM_145655.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42891866 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42891866 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118430399 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118430399 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118441645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118441645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118449230 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118449230 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58009823 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58009823 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179728469 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179728469 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30536914 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30536914 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61958660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61958660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42688877 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42688877 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42711231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:42711231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233681759 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233681759 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233721466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:233721466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85712084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85712084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110390425 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110390425 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110418735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110418735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110426764 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110426764 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141896447 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141896447 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86368162 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86368162 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57860017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57860017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:42011896 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:42011896 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92712573 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92712573 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:131977676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:131977676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56868908 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56868908 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56872742 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56872742 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183942679 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183942679 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104391220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104391220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182354800 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182354800 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182354880 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182354880 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:1742986 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:1742986 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19741374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19741374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24702645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24702645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24705365 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24705365 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16290676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16290676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16290679 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:16290679 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:11868384 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:11868384 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57478859 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57478859 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231408018 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231408018 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102164743 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102164743 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121421285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121421285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167728521 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167728521 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167750293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:167750293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32126308 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32126308 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155724142 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155724142 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:170501496 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:170501496 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:45009577 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:45009577 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27223671 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27223671 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:132438717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:132438717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32180053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32180053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32181648 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32181648 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64702443 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64702443 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24445914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24445914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57595895 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57595895 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236368558 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236368558 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:25888237 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:25888237 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145583241 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145583241 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:95271913 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:95271913 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19049198 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19049198 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:90024368 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:90024368 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32159052 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32159052 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28499464 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28499464 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28473602 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:28473602 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:35500313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:35500313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:50663053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:50663053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165430255 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165430255 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11738118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11738118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10136570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10136570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30910083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:30910083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:9927956 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:9927956 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104448805 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104448805 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66786661 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66786661 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2990599 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2990599 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3015327 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3015327 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121156304 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121156304 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178408907 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:178408907 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13243846 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13243846 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119748792 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119748792 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124065183 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:124065183 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33524849 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33524849 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52657947 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52657947 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52661157 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52661157 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52764705 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52764705 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52767119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52767119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52698893 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52698893 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:106744322 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:106744322 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:110260052 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:110260052 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48960094 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48960094 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30879057 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:30879057 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73961364 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:73961364 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:74009453 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:74009453 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27509934 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27509934 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27560781 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27560781 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43591605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43591605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:1063171 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:1063171 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:106558232 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:106558232 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14781688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14781688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:44688623 G>T maps to NM_021927.2 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:44688623 G>T maps to NM_021927.2 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:145050254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:145050254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:145050334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:145050334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44887431 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44887431 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26426891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26426891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96386609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96386609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96387820 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96387820 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119923429 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119923429 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119923667 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119923667 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119929477 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119929477 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119935232 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119935232 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82937631 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82937631 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5274495 G>T maps to ENST00000380247 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5274495 G>T maps to ENST00000380247 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153222749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153222749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121376116 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121376116 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73624714 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73624714 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48673016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48673016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44641486 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44641486 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242186118 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242186118 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242194460 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242194460 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236715278 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236715278 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236729204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236729204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236735984 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236735984 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50118034 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50118034 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145268045 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145268045 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41004415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41004415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41045991 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41045991 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41061634 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41061634 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13140039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:13140039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31626366 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:31626366 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93220988 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93220988 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93237911 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:93237911 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43547583 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43547583 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43548526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43548526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96322493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:96322493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84347105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84347105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50615225 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50615225 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92826511 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:92826511 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124792234 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124792234 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124792258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124792258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64025226 C>A maps to ENST00000261887 G922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64025226 C>A maps to ENST00000261887 G922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28375620 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28375620 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28451352 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28451352 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28457544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28457544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28482335 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28482335 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89334196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89334196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91727995 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91727995 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91788778 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91788778 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91817085 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91817085 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222711961 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222711961 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222716772 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222716772 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222716837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222716837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100525402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100525402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100534150 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100534150 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102296023 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102296023 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118997601 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118997601 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119002712 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119002712 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75167545 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75167545 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75168611 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75168611 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25727106 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25727106 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27782126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27782126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149399062 G>T maps to NM_001024599.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149399062 G>T maps to NM_001024599.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:42041145 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:42041145 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:42041158 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:42041158 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71017216 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:71017216 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32781171 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32781171 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32713958 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32713958 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30136919 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30136919 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30147333 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30147333 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28828063 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:28828063 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186083019 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186083019 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186099757 G>T maps to NM_031935.2 G4387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186099757 G>T maps to NM_031935.2 G4387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186147778 C>A maps to NM_031935.2 S5392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186147778 C>A maps to NM_031935.2 S5392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:55363969 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:55363969 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43291366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43291366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:173473740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:173473740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:173531363 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:173531363 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:43058063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:43058063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:26240219 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:26240219 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86586564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:86586564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62489864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62489864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:245020882 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:245020882 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60328442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:60328442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27135562 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27135562 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27203141 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27203141 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27203506 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27203506 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:175443026 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:175443026 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:100183444 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:100183444 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18318292 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18318292 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84240458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:84240458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11276130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11276130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188354 G>T maps to NM_001009931.1 S1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188354 G>T maps to NM_001009931.1 S1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188412 C>A maps to NM_001009931.1 E1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188412 C>A maps to NM_001009931.1 E1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188471 G>T maps to NM_001009931.1 S1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188471 G>T maps to NM_001009931.1 S1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188481 C>A maps to NM_001009931.1 E1875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152188481 C>A maps to NM_001009931.1 E1875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152192303 C>A maps to NM_001009931.1 G601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152192303 C>A maps to NM_001009931.1 G601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:87380689 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:87380689 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:14248988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:14248988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209879317 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209879317 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43740345 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:43740345 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99060628 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99060628 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99060665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:99060665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119964425 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119964425 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119977696 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119977696 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128730587 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128730587 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64682710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64682710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31729843 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31729843 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135581732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135581732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:70898940 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:70898940 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124271608 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124271608 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124273607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:124273607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3148725 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3148725 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3174002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3174002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3214156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3214156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3221877 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:3221877 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:33318317 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:33318317 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:33370737 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:33370737 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:53579531 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:53579531 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70843861 C>A maps to NM_032821.2 G4902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70843861 C>A maps to NM_032821.2 G4902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94984783 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94984783 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94984986 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:94984986 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95049997 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95049997 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52883069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52883069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94267852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94267852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94269750 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:94269750 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2640266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2640266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6657810 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6657810 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163150048 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:163150048 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:112112790 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:112112790 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129168697 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129168697 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129188270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129188270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129195500 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:129195500 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:1604736 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:1604736 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:1607924 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:1607924 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27700048 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27700048 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118431719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118431719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21182197 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:21182197 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65622254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65622254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185364969 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185364969 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185393548 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:185393548 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160485346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160485346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160485395 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160485395 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160497066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160497066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:2154132 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:2154132 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:18618246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:18618246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:133801089 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:133801089 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:213878452 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:213878452 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56426575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56426575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:159713366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:159713366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:142643164 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:142643164 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81578183 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81578183 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9971529 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9971529 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207013177 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:207013177 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113590213 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113590213 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113780228 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113780228 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102967992 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102967992 T>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137325669 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137325669 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70690832 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70690832 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:79710480 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:79710480 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155231088 G>T maps to ENST00000369423 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155231088 G>T maps to ENST00000369423 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153638115 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153638115 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49062542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49062542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49064350 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49064350 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:76744547 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:76744547 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100947612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100947612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100964604 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100964604 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62288554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62288554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62365246 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62365246 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62586801 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62586801 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62613950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62613950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62614064 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62614064 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62626547 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62626547 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61909005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61909005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61909033 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61909033 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242648600 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242648600 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242664461 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242664461 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57843827 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57843827 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57849870 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57849870 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74682178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74682178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:134464017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:134464017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:134540259 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:134540259 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:1413160 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:1413160 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156821024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156821024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7122587 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7122587 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1542442 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1542442 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:212208783 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:212208783 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95885720 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:95885720 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44424085 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44424085 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44425814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44425814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44425869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44425869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24652580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24652580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24655402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24655402 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:30833615 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:30833615 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201823925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201823925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121547283 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121547283 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2618056 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2618056 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2638016 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2638016 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51936965 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51936965 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156513881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156513881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13094548 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13094548 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:275073 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:275073 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66611030 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66611030 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66628074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66628074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66638186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:66638186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:397058 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:397058 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85954950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85954950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76629126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76629126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32981728 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32981728 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33049888 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33049888 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33057837 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33057837 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33065685 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33065685 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33068380 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33068380 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33077564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33077564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2932918 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2932918 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2933246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:2933246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145527554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145527554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145528542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145528542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145542169 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145542169 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42461651 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42461651 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48166345 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48166345 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182347179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182347179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173341102 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173341102 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173344288 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173344288 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15561479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15561479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15600060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15600060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15649601 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15649601 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15650362 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15650362 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37523151 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37523151 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37544597 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37544597 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37626997 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37626997 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37627019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37627019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37627071 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37627071 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37627086 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37627086 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37792070 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:37792070 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31425990 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31425990 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3643081 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3643081 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30518009 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30518009 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30518029 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30518029 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31282265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31282265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31338114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31338114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:187495489 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:187495489 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33195922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33195922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:45367667 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:45367667 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124567129 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124567129 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:161025695 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:161025695 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20445621 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20445621 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7759490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7759490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7759494 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7759494 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7773736 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7773736 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52850878 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52850878 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52854043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52854043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52854059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52854059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7679542 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7679542 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156672852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156672852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160919967 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160919967 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3194562 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3194562 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226836355 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226836355 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33656981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33656981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35201848 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:35201848 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24471768 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24471768 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185267152 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:185267152 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128253483 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128253483 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6080571 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6080571 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6082076 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6082076 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134009665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134009665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134019080 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134019080 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139793703 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139793703 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139818800 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:139818800 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64960474 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64960474 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64981961 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64981961 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42806612 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42806612 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42806703 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42806703 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153949419 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153949419 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124414913 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:124414913 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62718687 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62718687 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62737140 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62737140 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62747171 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62747171 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75665561 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75665561 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57784860 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57784860 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57784894 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57784894 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170343490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170343490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170371267 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170371267 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155894767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155894767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211032767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211032767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211280739 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211280739 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:19432147 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:19432147 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103599650 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103599650 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20731758 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20731758 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20852066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20852066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:39213099 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:39213099 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:78651523 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:78651523 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154821733 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154821733 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73697372 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:73697372 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:138670518 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:138670518 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:24179573 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:24179573 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36438062 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36438062 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36454520 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:36454520 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:215751284 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:215751284 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103445646 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:103445646 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18207607 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:18207607 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44135020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44135020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:6984135 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:6984135 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55972113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55972113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142640567 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142640567 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142650839 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142650839 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142658817 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142658817 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32497292 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32497292 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:19563613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:19563613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197431393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197431393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6843760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6843760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35913725 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35913725 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35921580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35921580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35921600 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:35921600 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24554732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24554732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114246896 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:114246896 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43890039 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43890039 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43903433 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43903433 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43916549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43916549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85106474 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:85106474 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42245298 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42245298 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42265355 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:42265355 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46678776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46678776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19454555 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19454555 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5457888 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5457888 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105540963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:105540963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123155914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123155914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123277692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123277692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81241076 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81241076 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118242271 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118242271 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34753081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:34753081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113697681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113697681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113699484 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113699484 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113750414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113750414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113775215 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113775215 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113775329 C>A maps to ENST00000483766 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:113775329 C>A maps to ENST00000483766 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:5753310 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:5753310 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100088820 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100088820 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100090252 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100090252 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100119889 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100119889 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100133098 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100133098 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43450514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43450514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43496369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43496369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61308542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61308542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22475162 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22475162 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116857482 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116857482 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:17800165 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:17800165 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:29048449 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:29048449 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:44847316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:44847316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:44867707 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:44867707 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:16359409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:16359409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:91469084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:91469084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29809873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29809873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34242125 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:34242125 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45205602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45221697 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45221697 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45232750 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45232750 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57969416 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57969416 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57970172 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57970172 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57976425 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57976425 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32306970 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32306970 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32310069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:32310069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90188210 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90188210 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47308638 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47308638 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47308643 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47308643 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145692564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145692564 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7820780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7820780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55278483 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55278483 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158059454 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158059454 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66032567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66032567 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45854647 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45854647 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43027874 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43027874 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44569283 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44569283 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44588044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44588044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:110247958 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:110247958 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42986953 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42986953 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87748078 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87748078 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27950617 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27950617 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202880353 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202880353 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202894060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202894060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:30254760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:30254760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173726325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:173726325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:97512471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:97512471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183245830 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183245830 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88085009 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:88085009 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:241714356 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:241714356 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123046596 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123046596 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123087489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123087489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:45740593 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:45740593 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39084671 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39084671 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38854965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38854965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39644996 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:39644996 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52911841 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52911841 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52886396 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52886396 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52840964 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52840964 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52965652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52965652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53163321 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53163321 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53165034 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53165034 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52627410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52627410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52799580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52799580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52709078 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52709078 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52709133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52709133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117964814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:117964814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118034799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118034799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118034866 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118034866 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118293219 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118293219 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119190152 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:119190152 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:56117004 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:56117004 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134322394 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:134322394 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62677130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:62677130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6241338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6241338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6311631 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:6311631 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:71573929 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:71573929 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55021798 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55021798 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:7002393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:7002393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21413963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21413963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21444685 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21444685 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21469941 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21469941 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21470011 G>T maps to ENST00000416669 G1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21470011 G>T maps to ENST00000416669 G1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:112522776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:112522776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:60907802 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:60907802 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107564671 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107564671 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49158831 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49158831 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209789736 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209789736 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209795828 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209795828 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209796308 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209796308 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107717341 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107717341 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107717377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107717377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183104017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183104017 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119576410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:119576410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:34022202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:34022202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:863609 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:863609 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45517912 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45517912 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36989441 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36989441 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102986966 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102986966 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80223498 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80223498 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32751109 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:32751109 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46705123 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:46705123 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169694139 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169694139 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169715057 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169715057 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16504227 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16504227 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16504230 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16504230 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18497815 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18497815 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11230735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11230735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108999309 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108999309 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205350776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205350776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205388306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205388306 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33744901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33744901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52239480 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52239480 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38257949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:38257949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51447666 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51447666 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51450119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51450119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:39299311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:39299311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95518124 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95518124 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48956230 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48956230 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48956416 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:48956416 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48652998 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48652998 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:54780646 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:54780646 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:54783017 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:54783017 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41621149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41621149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41621180 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41621180 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41621187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41621187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45718325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45718325 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109297256 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109297256 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226420776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226420776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:58834716 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:58834716 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75116593 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75116593 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75116821 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75116821 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:57013410 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:57013410 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176778114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176778114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49504378 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49504378 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156476735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156476735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36136393 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36136393 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:76414307 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:76414307 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97833149 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:97833149 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100148512 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:100148512 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:96320691 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:96320691 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148008553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148008553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148008668 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148008668 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148009266 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148009266 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148009526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148009526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148009574 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148009574 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148011661 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148011661 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148016483 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148016483 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148021578 G>T maps to ENST00000310701 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148021578 G>T maps to ENST00000310701 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148024937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148024937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148024975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148024975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148251780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148251780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148251867 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148251867 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148252063 C>A maps to ENST00000369202 L4559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148252063 C>A maps to ENST00000369202 L4559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148342471 G>T maps to ENST00000369202 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148342471 G>T maps to ENST00000369202 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148344627 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148344627 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49227432 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49227432 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74762676 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74762676 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161032509 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161032509 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161032559 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161032559 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161032568 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161032568 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7086723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:7086723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211923212 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211923212 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:82446536 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:82446536 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:62449335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:62449335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11942922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11942922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56326365 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56326365 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104079803 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104079803 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11465624 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11465624 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99762248 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99762248 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99771170 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99771170 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155670385 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:155670385 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151198930 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151198930 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151344308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151344308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151509162 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151509162 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151749784 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151749784 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151837720 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:151837720 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197577311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197577311 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197577421 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:197577421 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100173281 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100173281 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:66430972 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:66430972 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:59279587 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:59279587 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:59307714 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:59307714 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170094719 C>A maps to NM_004525.2 E1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170094719 C>A maps to NM_004525.2 E1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170096089 G>T maps to NM_004525.2 S1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170096089 G>T maps to NM_004525.2 S1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170100043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170100043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170129354 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170129354 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44177772 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:44177772 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25452379 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25452379 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25452425 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25452425 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25479278 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:25479278 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99800098 C>A maps to ENST00000378906 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:99800098 C>A maps to ENST00000378906 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30372607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30372607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30374989 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30374989 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71211546 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71211546 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120053680 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120053680 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:70339302 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:70339302 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238628218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238628218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238642488 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238642488 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169546730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169546730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101552404 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101552404 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:40715099 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:40715099 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130217374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130217374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194362715 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194362715 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42113688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42113688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31765491 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31765491 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96397723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:96397723 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33484621 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:33484621 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46479418 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46479418 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46495759 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:46495759 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41796870 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41796870 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144178405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144178405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135635477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:135635477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6626706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:6626706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:56866571 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:56866571 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:56882372 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:56882372 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90347323 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90347323 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90348262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90348262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235918760 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235918760 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30900792 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30900792 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30900802 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30900802 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30901000 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30901000 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45868829 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45868829 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21335118 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:21335118 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:39910524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:39910524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:39950201 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:39950201 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1997451 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1997451 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2054097 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2054097 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2257752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2257752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47295459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47295459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47310873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47310873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:166960717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:166960717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:65342024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:65342024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114123292 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114123292 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114223973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114223973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:35801121 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:35801121 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:95715493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:95715493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:95826727 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:95826727 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118057394 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118057394 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118057531 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118057531 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139994081 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139994081 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91447374 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91447374 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12776049 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12776049 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:67921334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:67921334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7968795 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:7968795 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210557336 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:210557336 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161469335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161469335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161505487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161505487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161510314 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161510314 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136977662 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136977662 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30736647 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30736647 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102315027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102315027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102484489 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102484489 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102504456 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:102504456 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47912623 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:47912623 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183535837 G>T maps to NM_024871.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183535837 G>T maps to NM_024871.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75316801 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75316801 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75356083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75356083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136709479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136709479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:87080408 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:87080408 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:19286337 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:19286337 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:45923465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:45923465 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:45923481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:45923481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179675959 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:179675959 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42110095 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42110095 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:164449873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:164449873 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10397336 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10397336 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10407186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10407186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10417361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:10417361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63667290 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63667290 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63668165 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63668165 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63668248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63668248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63671429 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63671429 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:103918249 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:103918249 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57883622 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57883622 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12969265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12969265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46487610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46487610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:138644018 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:138644018 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47796169 C>A maps to NM_015845.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47796169 C>A maps to NM_015845.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37885950 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:37885950 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:41075799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:41075799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:100395558 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:100395558 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150550649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150550649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13201628 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13201628 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13240684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13240684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47656554 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:47656554 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52131396 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52131396 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52131504 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:52131504 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136620127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136620127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85486993 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85486993 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:94943226 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:94943226 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41617308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:41617308 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:63816225 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:63816225 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:68689163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:68689163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90405715 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90405715 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90428439 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90428439 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90529265 C>A maps to NM_014611.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:90529265 C>A maps to NM_014611.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153295725 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:153295725 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:29543233 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:29543233 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:116406686 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:116406686 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38209679 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:38209679 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134952770 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134952770 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156566490 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156566490 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66208008 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66208008 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123367658 C>A maps to ENST00000426959 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123367658 C>A maps to ENST00000426959 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:66795942 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:66795942 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:37188922 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:37188922 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:37391594 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:37391594 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:15725392 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:15725392 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46761090 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46761090 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:130143847 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:130143847 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128120649 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128120649 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116340356 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116340356 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116380181 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116380181 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170926665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170926665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196746550 G>T maps to NM_033316.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196746550 G>T maps to NM_033316.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:158539487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:158539487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:158542035 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:158542035 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24246122 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24246122 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205568146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205568146 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135093879 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135093879 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135120072 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135120072 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42041264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42041264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:140624702 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:140624702 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:39722172 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:39722172 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222806436 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222806436 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222822231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:222822231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41281377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41281377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:12380033 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:12380033 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31477540 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31477540 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24334382 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24334382 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129913347 C>A maps to NM_002417.4 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:129913347 C>A maps to NM_002417.4 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121134108 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121134108 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74725374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74725374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49415692 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49415692 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49436843 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49436843 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49448668 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49448668 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151879797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151879797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36219844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:36219844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:104750899 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:104750899 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168227016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168227016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168227036 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168227036 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168271187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:168271187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154878123 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:154878123 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23312643 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:23312643 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33834879 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33834879 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5012014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5012014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:55527231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:55527231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44641878 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44641878 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:90844455 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:90844455 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88703952 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:88703952 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99236754 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99236754 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:56757155 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:56757155 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39554814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39554814 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:39880756 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:39880756 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50581669 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50581669 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41960229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41960229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:28347385 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:28347385 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118128087 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118128087 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:94200970 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:94200970 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18956408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:18956408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:48350321 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:48350321 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59575154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59575154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:78830383 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:78830383 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68658899 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:68658899 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:26961077 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:26961077 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:131181805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:131181805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179311487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179311487 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3028374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:3028374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125047591 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125047591 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125047594 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125047594 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:72754863 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:72754863 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31708879 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31708879 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31711625 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31711625 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31726811 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31726811 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:830999 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:830999 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:65702341 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:65702341 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49721940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49721940 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155581965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155581965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56703837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56703837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56717793 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56717793 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105930747 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105930747 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42935967 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:42935967 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47640471 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47640471 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93545059 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93545059 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:66582167 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:66582167 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151277226 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151277226 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32243614 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32243614 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32249028 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32249028 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31234312 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31234312 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25848196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25848196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:92714596 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:92714596 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11174839 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:11174839 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30602511 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30602511 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30625710 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30625710 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30657965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:30657965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7869311 C>A maps to ENST00000514220 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:7869311 C>A maps to ENST00000514220 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236999048 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236999048 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237024422 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237024422 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100544041 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:100544041 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100678699 G>T maps to NM_001040105.1 G1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100678699 G>T maps to NM_001040105.1 G1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100684003 G>T maps to NM_001040105.1 G3103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100684003 G>T maps to NM_001040105.1 G3103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195492042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195492042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113510091 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:113510091 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29858995 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:29858995 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:42749089 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:42749089 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102045190 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102045190 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102053694 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102053694 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102060586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:102060586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241073462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241073462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15917209 G>T maps to NM_001040114.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15917209 G>T maps to NM_001040114.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108147315 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108147315 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108204142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108204142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108218211 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:108218211 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33565684 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33565684 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33574676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33574676 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33588044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:33588044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10307642 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:10307642 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:111348812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:111348812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56548541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56548541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56548655 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56548655 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56548822 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56548822 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56552297 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56552297 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46744471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46744471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169501223 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169501223 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16670609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16670609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16676118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16676118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16681659 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16681659 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16682154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16682154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16902668 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:16902668 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:18034051 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:18034051 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34869368 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34869368 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57430711 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57430711 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192265201 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192265201 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:45014851 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:45014851 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52605851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52605851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52662295 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52662295 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52664266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52664266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47398638 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:47398638 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76874070 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:76874070 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72118898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72118898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95095653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95095653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95155887 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95155887 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2005405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2005405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2027635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2027635 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2064087 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2064087 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24401773 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:24401773 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75399638 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75399638 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69957243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:69957243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:40204203 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:40204203 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:40208590 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:40208590 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1920933 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1920933 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89903369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89903369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191554888 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191554888 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191555075 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191555075 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57111832 C>A maps to NM_001113203.1 G1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57111832 C>A maps to NM_001113203.1 G1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71300605 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71300605 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101742366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101742366 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101797105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:101797105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76461137 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76461137 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76468012 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76468012 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:2985105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:2985105 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89618326 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:89618326 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:786223 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:786223 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:80438938 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:80438938 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:60747457 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:60747457 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:55273736 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:55273736 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34153784 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34153784 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34156161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34156161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34160886 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:34160886 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201778250 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201778250 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20117147 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20117147 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:78334227 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:78334227 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:15467850 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:15467850 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:15555626 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:15555626 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204055989 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:204055989 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:35743089 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:35743089 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:35864606 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:35864606 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148004530 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:148004530 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16891653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16891653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16893596 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16893596 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16893664 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16893664 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16894601 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16894601 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16895522 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16895522 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16902733 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16902733 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16908260 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16908260 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16913609 G>T maps to NM_017940.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16913609 G>T maps to NM_017940.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16914203 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16914203 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16914354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16914354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120385042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120385042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6631944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6631944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6637827 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6637827 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6640254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6640254 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134027982 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134027982 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97031610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97031610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97035277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:97035277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100405470 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100405470 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100405681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100405681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183529216 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183529216 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183533088 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:183533088 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:37260047 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:37260047 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54912403 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54912403 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54917095 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54917095 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232320344 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232320344 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232320639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:232320639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160327864 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160327864 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140100650 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140100650 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140100812 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140100812 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119148033 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:119148033 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152381137 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152381137 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152474773 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152474773 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152512622 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152512622 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152527442 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152527442 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152582040 C>A maps to NM_001164507.1 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152582040 C>A maps to NM_001164507.1 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84035979 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:84035979 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11233592 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:11233592 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75646554 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75646554 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11643409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:11643409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27387753 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27387753 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211842411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211842411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211843752 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:211843752 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52797415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52797415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52797445 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52797445 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73566931 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73566931 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73570437 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:73570437 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:70461330 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:70461330 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:70461514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:70461514 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:78383978 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:78383978 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61554413 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61554413 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61869713 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:61869713 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145668044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145668044 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129744367 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129744367 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129752608 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129752608 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129756178 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129756178 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47864825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:47864825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104529247 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104529247 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:47583612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:47583612 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39613236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:39613236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236189141 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:236189141 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51190420 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51190420 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99205574 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99205574 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36962208 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36962208 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37003463 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37003463 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37008701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37008701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37045704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:37045704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107528829 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107528829 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:63768767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:63768767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50642277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:50642277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:51874939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:51874939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33463262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33463262 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:173322331 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:173322331 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:56220275 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:56220275 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:49232951 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:49232951 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152127169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152127169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4519514 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4519514 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43624118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43624118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43700159 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:43700159 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30486532 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:30486532 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95086516 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95086516 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103918938 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103918938 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103919984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103919984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2949955 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2949955 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2953959 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2953959 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162313594 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162313594 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120460222 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120460222 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120467867 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120467867 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120467897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120467897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120478037 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120478037 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120478074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120478074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120506188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120506188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89133328 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:89133328 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69325368 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:69325368 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101591862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101591862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101592063 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101592063 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21121204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21121204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53900704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:53900704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110942421 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110942421 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132409976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:132409976 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15029263 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:15029263 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:21891541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:21891541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35805688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35805688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69745219 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69745219 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:24006381 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:24006381 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108492838 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108492838 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:149181303 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:149181303 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127316577 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127316577 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127316862 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127316862 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115348625 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115348625 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115350273 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115350273 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115365517 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:115365517 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27656741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27656741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27657334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27657334 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52260316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52260316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52303326 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52303326 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129348806 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129348806 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129348851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129348851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129348883 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129348883 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33469318 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33469318 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33502240 G>T maps to ENST00000374814 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33502240 G>T maps to ENST00000374814 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33552855 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:33552855 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206607864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206607864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206628354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:206628354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:78710242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:78710242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:79746622 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:79746622 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176694499 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176694499 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59498393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59498393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59506774 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:59506774 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27238204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27238204 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126194564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126194564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6600021 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6600021 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6607388 C>A maps to NM_017755.5 G478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6607388 C>A maps to NM_017755.5 G478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6631961 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:6631961 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72722393 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72722393 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40131357 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40131357 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:18770693 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:18770693 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104851235 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104851235 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156849214 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156849214 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:87285641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:87285641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:87486725 C>A maps to NM_001018065.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:87486725 C>A maps to NM_001018065.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205698645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205698645 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44507644 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44507644 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2290423 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2290423 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56473535 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56473535 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12215821 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12215821 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45563113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:45563113 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47869378 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:47869378 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131752317 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131752317 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154098952 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154098952 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13363376 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:13363376 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134039197 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134039197 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150059963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150059963 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56863058 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56863058 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56865977 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56865977 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25893507 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25893507 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67902386 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67902386 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101623758 C>A maps to NM_022053.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101623758 C>A maps to NM_022053.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:102337897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:102337897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101092932 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101092932 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228465451 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228465451 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:133061927 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:133061927 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28200297 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28200297 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28228481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28228481 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28235703 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28235703 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28272995 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:28272995 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128682490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128682490 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71068911 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:71068911 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10584188 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:10584188 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:198642 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:198642 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167673676 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167673676 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78369091 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78369091 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78369176 C>A maps to NM_001098816.2 E2746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:78369176 C>A maps to NM_001098816.2 E2746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44714001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44714001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44721296 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44721296 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56501025 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56501025 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56501060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56501060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56508897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:56508897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9798523 C>A maps to NM_016819.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9798523 C>A maps to NM_016819.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9807435 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9807435 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137815332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:137815332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193353349 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:193353349 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:67290430 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:67290430 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:67290511 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:67290511 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13175589 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13175589 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248166714 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248166714 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248185186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248185186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248247752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:248247752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180581925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180581925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180581937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180581937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:110629 T>A maps to ENST00000442916 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:110629 T>A maps to ENST00000442916 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:48285386 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:48285386 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6129006 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:6129006 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98072677 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:98072677 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:123625229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:123625229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201775998 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201775998 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201822096 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:201822096 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:31836401 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:31836401 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21946956 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21946956 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:24881818 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:24881818 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76853715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:76853715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:90933278 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:90933278 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21689962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:21689962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26680837 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26680837 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48792203 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48792203 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149915752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149915752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149936054 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149936054 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149949210 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149949210 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111957009 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:111957009 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41762153 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41762153 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41762191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41762191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41842750 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41842750 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41850112 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41850112 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41862852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:41862852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16313269 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16313269 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:107709761 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:107709761 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38263182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38263182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57114547 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57114547 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3592975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3592975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3592995 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:3592995 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121604063 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121604063 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121613175 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121613175 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151045735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:151045735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79805009 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:79805009 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56505369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56505369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73589872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73589872 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65984127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:65984127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105856249 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:105856249 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:81889153 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:81889153 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:110407033 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:110407033 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40564364 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:40564364 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:112687379 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:112687379 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100152358 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100152358 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100152394 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100152394 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56721087 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56721087 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56726503 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56726503 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28854542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28854542 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28866696 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:28866696 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:60998585 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:60998585 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176809302 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176809302 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119124851 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119124851 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108535393 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108535393 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108608174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:108608174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156213642 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156213642 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156216079 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156216079 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65553126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65553126 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65563257 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65563257 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226570717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:226570717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20815113 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20815113 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51978346 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51978346 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25034319 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25034319 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25058830 C>A maps to NM_006437.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:25058830 C>A maps to NM_006437.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72551923 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72551923 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72552027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72552027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242065571 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242065571 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125617210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125617210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125617218 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:125617218 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59410260 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:59410260 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:223066515 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:223066515 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:223085844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:223085844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114004296 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114004296 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52696091 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52696091 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:164532420 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:164532420 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154919796 G>T maps to ENST00000368460 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154919796 G>T maps to ENST00000368460 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:55665002 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:55665002 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140515005 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140515005 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140780153 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140780153 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113851420 G>T maps to ENST00000246505 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:113851420 G>T maps to ENST00000246505 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17869343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:17869343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:233397917 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:233397917 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17436937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17436937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78686658 G>T maps to NM_001190482.1 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:78686658 G>T maps to NM_001190482.1 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117100058 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117100058 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99002587 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99002587 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105197830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:105197830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:289066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:289066 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:289115 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:289115 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:289562 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:289562 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65421343 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65421343 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165844816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165844816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165895834 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:165895834 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178862660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:178862660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54964144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54964144 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54966319 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54966319 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72289409 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72289409 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72302299 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:72302299 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144854471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144854471 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144857763 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144857763 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144860029 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144860029 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144863292 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144863292 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144863464 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144863464 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144864120 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144864120 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144866011 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144866011 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144873858 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144873858 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144874654 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144874654 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144874725 C>A maps to NM_014644.4 E1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144874725 C>A maps to NM_014644.4 E1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144875939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144875939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144876074 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144876074 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144876081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144876081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144879083 C>A maps to NM_014644.4 G1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144879083 C>A maps to NM_014644.4 G1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144880708 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144880708 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144880777 C>A maps to NM_014644.4 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144880777 C>A maps to NM_014644.4 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144881483 C>A maps to NM_014644.4 E1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144881483 C>A maps to NM_014644.4 E1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144886376 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144886376 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144903020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144903020 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144904718 C>A maps to NM_014644.4 G865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144904718 C>A maps to NM_014644.4 G865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144916476 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144916476 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144916791 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144916791 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144922472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144922472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144922504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144922504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144931354 G>T maps to NM_001002811.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144931354 G>T maps to NM_001002811.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144952074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:144952074 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145015767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145015767 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145015779 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145015779 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145015828 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145015828 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120426968 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120426968 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149242652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149242652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136502474 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:136502474 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:540899 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:540899 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54257351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54257351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54342911 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54342911 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54348064 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54348064 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55144511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:55144511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149510023 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:149510023 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44037357 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44037357 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122829723 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:122829723 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20372021 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20372021 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22452032 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22452032 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33250145 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33250145 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33330112 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:33330112 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31725589 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31725589 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31840896 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:31840896 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32000403 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32000403 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32000437 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32000437 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32053866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32053866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32072245 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32072245 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32093220 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:32093220 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:73437060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:73437060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:73450057 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:73450057 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57324992 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:57324992 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66238700 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66238700 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:152600948 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:152600948 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143772254 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:143772254 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179605434 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:179605434 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42937741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42937741 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230459427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:230459427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153283034 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153283034 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153283064 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153283064 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74057888 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74057888 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:37841676 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:37841676 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:70993085 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:70993085 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13160541 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13160541 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13273173 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13273173 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33840785 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33840785 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169815014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169815014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169846463 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:169846463 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:11046377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:11046377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:11075435 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:11075435 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:45958024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:45958024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96418890 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96418890 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96439857 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:96439857 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120284385 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120284385 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:79728794 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:79728794 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:79735643 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:79735643 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:79787069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:79787069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18924583 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:18924583 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30762962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30762962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151282626 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151282626 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44426656 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44426656 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145585654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:145585654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26890795 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26890795 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98383163 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98383163 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:17140165 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:17140165 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:178937709 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:178937709 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46597411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46597411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130405027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130405027 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209214859 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209214859 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99936427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99936427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151196904 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151196904 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151214501 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151214501 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151214512 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151214512 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142829156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142829156 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142829164 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:142829164 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:3197737 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:3197737 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:111554158 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:111554158 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:130839037 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:130839037 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:94316570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:94316570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:47814706 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:47814706 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102048137 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102048137 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110455883 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110455883 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:51483834 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:51483834 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:159488198 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:159488198 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42373956 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42373956 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42377258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42377258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42379459 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42379459 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42282518 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42282518 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42302265 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42302265 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42437755 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42437755 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:20411377 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:20411377 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42040518 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42040518 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42046410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42046410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28851388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28851388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113825466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113825466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:8639429 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:8639429 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:8678220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:8678220 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:8731433 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:8731433 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:9388502 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:9388502 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:9417854 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:9417854 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219486408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219486408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95987300 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:95987300 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:39792299 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:39792299 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81902799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81902799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81902988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81902988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81914583 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81914583 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81967998 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:81967998 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155313957 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:155313957 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198953518 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198953518 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198953530 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198953530 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:199011361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:199011361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:17077377 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:17077377 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145000942 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145000942 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:19408153 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:19408153 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:19413966 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:19413966 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:131904133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:131904133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:39907168 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:39907168 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:65198342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:65198342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:172939 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67321998 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67321998 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6424662 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6424662 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93131327 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:93131327 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161123305 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161123305 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161123332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161123332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161133912 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:161133912 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:145795752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:145795752 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:103043295 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:103043295 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142395214 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:142395214 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208269330 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:208269330 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94613784 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:94613784 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72174280 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72174280 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74325792 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74325792 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74326810 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74326810 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219143206 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219143206 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219209459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219209459 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160225224 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160225224 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118350712 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:118350712 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:44342000 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:44342000 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42202579 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42202579 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50910169 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50910169 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133237959 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133237959 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44113657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44113657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121200665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121200665 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86325656 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86325656 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43487383 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:43487383 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:79745799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:79745799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106889754 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106889754 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106889764 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:106889764 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:22320705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:22320705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:629448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:629448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:630223 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:630223 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75070196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75070196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75070218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75070218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75104000 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75104000 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99153136 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:99153136 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43160022 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43160022 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43172566 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43172566 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43197511 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:43197511 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:16279383 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:16279383 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:16279386 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:16279386 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:120168852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:120168852 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:79177495 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:79177495 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:39503777 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:39503777 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57267739 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:57267739 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76812871 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:76812871 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70118226 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70118226 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70170837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70170837 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70170875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:70170875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:81762457 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:81762457 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7660930 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7660930 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159631850 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159631850 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170463579 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170463579 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43124891 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43124891 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43131613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43131613 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:63149005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:63149005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37518205 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:37518205 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54974717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:54974717 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:113517732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:113517732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242098610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242098610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6335257 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:6335257 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:133748076 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:133748076 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:320405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:320405 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:320602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:320602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103906387 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103906387 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103909790 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103909790 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103909830 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:103909830 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40539704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40539704 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40539727 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:40539727 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64868135 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:64868135 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77703519 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:77703519 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12943248 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12943248 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11421121 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11421121 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91527862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91527862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91527886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:91527886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129785797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:129785797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:121742299 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:121742299 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:90128267 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:90128267 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23509510 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23509510 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23517944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23517944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23523396 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:23523396 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64088414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64088414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57146355 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57146355 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:42853541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:42853541 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:57372240 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:57372240 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:57398077 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:57398077 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14218258 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14218258 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151263004 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151263004 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48788981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:48788981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:64738726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:64738726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:24226154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:24226154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53223879 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53223879 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6506242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6506242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6506388 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6506388 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6525369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:6525369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:2087417 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:2087417 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:54049908 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:54049908 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35084533 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35084533 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128184622 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128184622 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15989237 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:15989237 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16037267 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:16037267 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93605169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93605169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93611745 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:93611745 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37633012 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:37633012 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13647775 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13647775 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150298112 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150298112 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150319030 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150319030 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50026566 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50026566 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116048496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116048496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116053352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116053352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62614580 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62614580 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:1580231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:1580231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30663991 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30663991 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30665503 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30665503 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:170705118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:170705118 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:170705164 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:170705164 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2870948 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:2870948 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:86568961 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:86568961 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:25160899 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:25160899 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:25231243 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:25231243 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79465585 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79465585 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104164302 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104164302 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43352174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43352174 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43382025 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43382025 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43709763 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43709763 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43410972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43410972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43349187 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:43349187 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:35786519 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:35786519 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36070782 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:36070782 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151372053 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151372053 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127119289 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:127119289 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184026142 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184026142 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184026166 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184026166 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74338329 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:74338329 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24607485 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24607485 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24607508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:24607508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40986650 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40986650 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:54133721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:54133721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43577708 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43577708 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:803667 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:803667 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27692123 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27692123 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27702023 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27702023 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97316426 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97316426 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97342554 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97342554 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97345800 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97345800 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:479050 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:479050 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:89720898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:89720898 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:71437402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:71437402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40681972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:40681972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117484713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117484713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117516973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117516973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48164310 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48164310 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48166581 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48166581 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209271758 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209271758 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209307068 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209307068 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:28122981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:28122981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287550 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287550 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287681 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27287976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141799682 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141799682 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141843041 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:141843041 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:21026730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:21026730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:77240177 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:77240177 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:87725039 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:87725039 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214574984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214574984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:131126549 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:131126549 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:88934474 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:88934474 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120639799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120639799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:7888037 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:7888037 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8248135 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8248135 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8248188 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8248188 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40770544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40770544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40827807 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:40827807 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144902809 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144902809 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20494293 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20494293 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61180309 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61180309 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119545241 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119545241 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119545334 C>A maps to NM_203286.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119545334 C>A maps to NM_203286.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133277816 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:133277816 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25273025 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:25273025 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64517812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64517812 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158908131 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158908131 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49136498 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49136498 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:122290639 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:122290639 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:180158630 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:180158630 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136409251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:136409251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57652620 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57652620 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26257649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:26257649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73316393 C>A maps to NM_015470.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73316393 C>A maps to NM_015470.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8625002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:8625002 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153954987 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153954987 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156039363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156039363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56384599 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56384599 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73390692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73390692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205740507 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205740507 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:174245094 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:174245094 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125832745 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125832745 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120408553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:120408553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50388147 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50388147 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50400200 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50400200 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:8922997 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:8922997 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129853823 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129853823 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129854231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:129854231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170722846 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170722846 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109365616 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109365616 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109383778 G>T maps to NM_006267.4 E2262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:109383778 G>T maps to NM_006267.4 E2262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36262161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36262161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5928140 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5928140 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69045863 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:69045863 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:2866677 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:2866677 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:2888394 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:2888394 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:131351343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:131351343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134514004 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:134514004 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:160189264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:160189264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173825986 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173825986 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173861297 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173861297 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173881228 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:173881228 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22186674 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22186674 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22189976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22189976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22197435 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:22197435 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:130815192 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:130815192 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167932983 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:167932983 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114751070 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:114751070 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:85597586 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:85597586 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79265615 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79265615 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79284000 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79284000 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79293960 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79293960 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79356891 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:79356891 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33149529 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33149529 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:402910 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:402910 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51431520 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51431520 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114358355 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114358355 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114385128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114385128 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114395965 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114395965 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:145640531 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:145640531 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127964765 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:127964765 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55968423 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55968423 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238738166 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:238738166 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50000052 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50000052 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50095770 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:50095770 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135957354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:135957354 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65042525 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:65042525 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30402153 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30402153 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30402205 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30402205 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46190822 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:46190822 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:49077116 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:49077116 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:49096013 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:49096013 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63680132 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63680132 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31919870 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31919870 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34252754 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:34252754 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:110108400 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:110108400 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145737209 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145737209 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120337202 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120337202 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45540657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:45540657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:103205688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:103205688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73105466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:73105466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204125235 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204125235 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204126409 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:204126409 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:17040178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:17040178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:8716399 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:8716399 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85577865 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85577865 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111751559 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:111751559 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39306426 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39306426 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39306604 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39306604 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:34410462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:34410462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16399415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:16399415 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151318391 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151318391 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117199127 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117199127 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117215239 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:117215239 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19304682 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:19304682 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33260712 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33260712 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33261561 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33261561 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11529848 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11529848 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87220318 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87220318 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:153344536 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:153344536 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:192779454 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:192779454 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:192780735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:192780735 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116224229 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116224229 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:163122258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:163122258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:163122320 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:163122320 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:241032053 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:241032053 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:241094093 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:241094093 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182617448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182617448 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182617472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:182617472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75512935 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:75512935 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156337523 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156337523 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:25718645 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:25718645 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22863400 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22863400 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22868231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22868231 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8158906 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8158906 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:12812337 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:12812337 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38967396 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:38967396 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152273217 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152273217 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152308102 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:152308102 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123915051 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123915051 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33178832 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33178832 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:105195406 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:105195406 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155880203 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155880203 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87373677 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87373677 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87376972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87376972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87377178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87377178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87565627 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:87565627 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88016296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88016296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121002805 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121002805 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71701774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:71701774 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:33408499 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:33408499 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:33408630 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:33408630 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49728564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49728564 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49739860 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49739860 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10536613 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:10536613 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:7170214 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:7170214 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:158634770 C>A maps to NM_144726.2 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:158634770 C>A maps to NM_144726.2 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74161513 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74161513 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44036451 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:44036451 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42720663 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:42720663 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13978130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13978130 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:31600626 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:31600626 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1090136 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1090136 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1090523 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1090523 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117153071 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117153071 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156450962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156450962 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121855746 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:121855746 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32147345 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32147345 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32147365 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:32147365 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:89322377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:89322377 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:497921 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:497921 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90122286 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90122286 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241514396 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:241514396 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156024768 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156024768 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:78655872 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:78655872 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124747039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124747039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124765347 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124765347 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11354624 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:11354624 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:64516432 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:64516432 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:10480091 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:10480091 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41819614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41819614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92788947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92788947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:68910210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:68910210 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:21792749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:21792749 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113316875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:113316875 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88999638 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88999638 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8705919 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8705919 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8707142 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8707142 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101620805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:101620805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56510654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56510654 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136216030 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136216030 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120634838 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120634838 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33607051 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:33607051 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133136007 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133136007 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133138024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133138024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133138209 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:133138209 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81573494 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:81573494 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75111466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75111466 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167116243 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:167116243 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39452660 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39452660 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152129150 C>A maps to NM_001122965.1 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152129150 C>A maps to NM_001122965.1 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:78797060 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:78797060 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126074257 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126074257 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126081319 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:126081319 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110756682 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:110756682 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45094856 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45094856 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51971553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51971553 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67342484 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67342484 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77389030 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77389030 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77389069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77389069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77445833 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77445833 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55488966 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:55488966 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100733653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100733653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:93074797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:93074797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155294228 G>T maps to NM_001105205.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155294228 G>T maps to NM_001105205.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155297906 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155297906 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35559973 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35559973 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127820370 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127820370 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:38948293 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:38948293 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237659797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237659797 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237664106 C>A maps to NM_001035.2 S767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237664106 C>A maps to NM_001035.2 S767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237711746 G>T maps to NM_001035.2 G975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237711746 G>T maps to NM_001035.2 G975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237796784 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237796784 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34080395 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:34080395 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151955570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151955570 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151958750 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151958750 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153591313 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153591313 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153604355 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153604355 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153517084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:153517084 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10624475 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:10624475 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45785229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45785229 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234243553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:234243553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51175780 C>A maps to ENST00000251020 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:51175780 C>A maps to ENST00000251020 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:55243069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:55243069 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:44392061 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:44392061 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50845110 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50845110 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136573592 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136573592 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26715605 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:26715605 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109771945 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:109771945 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108930255 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108930255 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:148711263 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:148711263 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100591402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100591402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100598406 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:100598406 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66459195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66459195 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123782475 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123782475 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75142841 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:75142841 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155228554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155228554 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77095191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77095191 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:83582082 G>T maps to NM_024906.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:83582082 G>T maps to NM_024906.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78173905 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:78173905 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54231231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:54231231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51991478 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:51991478 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52011499 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:52011499 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38768564 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:38768564 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118037852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:118037852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165950853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:165950853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52106711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52106711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52115715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:52115715 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167142813 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167142813 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167142836 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:167142836 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151140557 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151140557 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6458206 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6458206 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:53458910 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:53458910 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120236376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:120236376 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:43654352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:43654352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9069645 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9069645 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9077490 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:9077490 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169822816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169822816 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:224437 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:224437 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:224653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:224653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4014196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4014196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4026736 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4026736 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4051710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4051710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4119053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:4119053 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:71335115 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:71335115 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10361016 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10361016 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:30890244 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:30890244 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42635869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42635869 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127788508 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:127788508 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108227863 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:108227863 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49292246 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49292246 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:13850881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:13850881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151338175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151338175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151340566 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151340566 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50646949 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50646949 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150329001 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:150329001 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:80433358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:80433358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:83029608 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:83029608 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:92008447 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:92008447 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:92065660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:92065660 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74906584 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74906584 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102739549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:102739549 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:9190353 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:9190353 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:9224774 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:9224774 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:47873517 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:47873517 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101231981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101231981 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13386746 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13386746 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110310616 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110310616 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110332154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:110332154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392318 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392318 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392378 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392378 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392399 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392399 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392438 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392438 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392442 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392571 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30392571 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30393023 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30393023 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30393267 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30393267 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242283121 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:242283121 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48284454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:48284454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:44953877 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:44953877 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:2838054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:2838054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:2953470 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:2953470 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100778918 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100778918 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:51918314 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:51918314 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57379151 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57379151 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109308672 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:109308672 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179974586 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179974586 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179982410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179982410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123875077 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123875077 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123888242 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:123888242 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135144971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135144971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64537898 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64537898 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:38433640 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:38433640 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24299059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:24299059 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198274414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198274414 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198274481 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:198274481 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70597743 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70597743 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7214723 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:7214723 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:70700477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:70700477 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1712287 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1712287 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1714229 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:1714229 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:174953630 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:174953630 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104486386 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104486386 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104492672 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104492672 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120917364 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:120917364 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:155756601 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:155756601 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:67155813 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:67155813 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:134619163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:134619163 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:134619374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:134619374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:134638642 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:134638642 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67710902 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:67710902 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:20202588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:20202588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72576681 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72576681 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72576694 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:72576694 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156778951 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156778951 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80409277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80409277 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2834706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:2834706 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:152065278 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:152065278 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19817688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:19817688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230955 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230955 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7535078 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7535078 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154936213 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154936213 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154940671 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154940671 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154940900 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154940900 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154940957 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154940957 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91666878 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:91666878 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49118152 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:49118152 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46637441 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:46637441 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:72897260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:72897260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77675420 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:77675420 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117063830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117063830 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:51917972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:51917972 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116731984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116731984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116827582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116827582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115318921 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115318921 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115321740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115321740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115322974 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115322974 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232629244 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232629244 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232629254 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232629254 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232629266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:232629266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1456799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1456799 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1460277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:1460277 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120741894 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120741894 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13611962 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:13611962 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164705042 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164705042 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164758909 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164758909 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164772961 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:164772961 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31928186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31928186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31928805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31928805 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31935218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31935218 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36152433 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36152433 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36168334 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36168334 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36168350 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36168350 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36168361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36168361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160720034 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160720034 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1698109 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1698109 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219250028 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219250028 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48559913 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:48559913 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127507380 G>T maps to NM_001046.2 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127507380 G>T maps to NM_001046.2 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43216924 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:43216924 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99339772 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99339772 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121631976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121631976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:22383760 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:22383760 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61594132 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:61594132 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169446342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:169446342 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116563528 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116563528 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116605582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116605582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160577123 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160577123 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95761237 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:95761237 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129505623 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129505623 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:18064054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:18064054 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128665795 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:128665795 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107406240 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107406240 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107314590 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107314590 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107336501 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107336501 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107336546 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107336546 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107355895 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:107355895 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:102993326 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:102993326 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92364119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:92364119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35980004 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35980004 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205896422 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:205896422 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:85461729 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:85461729 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45559641 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45559641 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8023632 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8023632 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:9064775 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:9064775 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130168358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:130168358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220088713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:220088713 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45779006 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:45779006 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:68398994 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:68398994 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32417549 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32417549 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32428276 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32428276 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101427372 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101427372 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101431275 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:101431275 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:118147512 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:118147512 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:118184931 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:118184931 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:112289543 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:112289543 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:234452305 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:234452305 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:234452310 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:234452310 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150712967 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:150712967 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:92881667 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:92881667 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124956084 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124956084 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140051274 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:140051274 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22265785 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:22265785 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56629298 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56629298 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95358112 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:95358112 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31832528 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31832528 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75805248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75805248 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33947240 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:33947240 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:19470343 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:19470343 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27900150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:27900150 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220501648 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220501648 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74481732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74481732 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74535119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74535119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27427525 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:27427525 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51853702 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51853702 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51890998 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51890998 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51901247 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51901247 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31498730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31498730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10976641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:10976641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:309776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:309776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:346234 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:346234 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49814631 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49814631 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1239727 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1239727 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11072822 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:11072822 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1394847 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1394847 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1421980 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1421980 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20658639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:20658639 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14489066 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:14489066 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44489886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44489886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170214304 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170214304 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68325090 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68325090 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111870133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:111870133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103274531 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103274531 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:481640 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:481640 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103128756 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:103128756 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48446827 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48446827 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21422475 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21422475 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21392123 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:21392123 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:20896339 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:20896339 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74873657 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74873657 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20597313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:20597313 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:168151409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:168151409 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57843781 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57843781 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57894890 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:57894890 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12421654 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12421654 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159834700 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:159834700 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128633690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128633690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56574718 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56574718 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56575421 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56575421 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:106876214 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:106876214 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:160141479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:160141479 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:17902253 C>A maps to ENST00000381272 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:17902253 C>A maps to ENST00000381272 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:55813742 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:55813742 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:18823222 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:18823222 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156221118 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156221118 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:130925202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:130925202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98634824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98634824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88367252 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88367252 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88390489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:88390489 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214504258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214504258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214504272 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:214504272 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:84301018 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:84301018 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139292741 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139292741 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139292886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139292886 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66782822 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:66782822 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70121108 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:70121108 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101825828 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:101825828 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41257208 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:41257208 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:46195088 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:46195088 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:46195174 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:46195174 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:51306855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:51306855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1079388 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1079388 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:86267634 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:86267634 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130748243 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130748243 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64448862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64448862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17943402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17943402 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99204005 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:99204005 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2314892 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:2314892 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179320534 G>T maps to NM_003101.4 G512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179320534 G>T maps to NM_003101.4 G512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186541124 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:186541124 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:107022042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:107022042 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121461688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:121461688 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7491672 C>A maps to ENST00000301597 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:7491672 C>A maps to ENST00000301597 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231033836 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231033836 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231042166 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231042166 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231042239 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:231042239 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124564186 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124564186 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:7721058 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:7721058 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118530715 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118530715 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118554808 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118554808 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118555043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118555043 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118581855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118581855 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118584391 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118584391 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118629271 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118629271 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118634484 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118634484 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118727658 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118727658 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35809979 G>T maps to NM_001039592.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35809979 G>T maps to NM_001039592.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35810560 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35810560 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:49059836 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:49059836 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:140785603 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:140785603 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172607352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172607352 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172694740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:172694740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:217842471 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:217842471 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48627844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:48627844 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:48764354 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:48764354 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:97327330 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:97327330 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:97328410 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:97328410 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44329765 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44329765 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49894062 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:49894062 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74680790 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:74680790 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177249275 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:177249275 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64938758 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64938758 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44046776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44046776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35644655 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35644655 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35646704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35646704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35692569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35692569 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35753641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35753641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35753708 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35753708 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35807388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:35807388 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220307882 C>A maps to ENST00000403148 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220307882 C>A maps to ENST00000403148 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220309293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220309293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44867082 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44867082 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89603194 C>A maps to NM_199367.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89603194 C>A maps to NM_199367.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228860209 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:228860209 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:229046273 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:229046273 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41145315 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41145315 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44354234 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44354234 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12535381 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:12535381 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4391071 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4391071 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:167663144 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:167663144 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1164119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1164119 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1164149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1164149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1165546 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1165546 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:47677604 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:47677604 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56862343 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56862343 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55648705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55648705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158593005 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158593005 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158646105 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:158646105 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131339362 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131339362 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131374142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131374142 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131390158 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131390158 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66467973 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66467973 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40996161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:40996161 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42166341 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42166341 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:65216669 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:65216669 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30720771 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30720771 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30731910 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30731910 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30736283 G>T maps to NM_006662.2 E1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30736283 G>T maps to NM_006662.2 E1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76028121 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:76028121 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:42271491 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:42271491 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206567047 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:206567047 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9068603 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9068603 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74068361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74068361 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100481897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100481897 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100484649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100484649 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100484662 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100484662 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:54692790 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:54692790 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109200059 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109200059 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109203437 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109203437 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57094834 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:57094834 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48054800 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:48054800 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:52681259 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:52681259 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130063999 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:130063999 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86108028 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86108028 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8717945 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8717945 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8751458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:8751458 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116869769 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116869769 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52553270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:52553270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:103988143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:103988143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57642346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:57642346 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136455362 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:136455362 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72470019 G>T maps to ENST00000308103 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:72470019 G>T maps to ENST00000308103 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66773575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:66773575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90683001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90683001 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90732886 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:90732886 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74086504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74086504 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74086516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:74086516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191849016 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191849016 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56749213 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56749213 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191894657 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:191894657 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47741177 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:47741177 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63965237 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63965237 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63967595 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:63967595 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220112891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:220112891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43659129 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:43659129 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23751788 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23751788 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23826427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:23826427 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219561685 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219561685 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219561736 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219561736 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219563260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219563260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:168986024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:168986024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27099303 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27099303 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74476179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:74476179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37121019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:37121019 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28148859 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28148859 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57251388 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:57251388 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:4509122 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:4509122 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31012231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31012231 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62594800 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:62594800 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118839547 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118839547 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53227293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:53227293 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:70515318 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:70515318 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:46288257 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:46288257 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:46294586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:46294586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:70620551 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:70620551 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31583400 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:31583400 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:45290658 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:45290658 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136221852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136221852 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136227926 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136227926 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95840306 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:95840306 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149879243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:149879243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:75469825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:75469825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58475154 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:58475154 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:33229815 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:33229815 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:33229953 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:33229953 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152443506 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152443506 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152497505 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152497505 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152541947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152541947 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152639204 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152639204 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152749322 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152749322 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152804179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:152804179 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:64632154 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:64632154 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33403262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33403262 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76166788 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76166788 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158505217 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158505217 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158509847 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158509847 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158515035 C>A maps to ENST00000367121 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:158515035 C>A maps to ENST00000367121 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35902687 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:35902687 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155850960 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155850960 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:51140462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:51140462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:37984776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:37984776 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1729301 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1729301 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1729400 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1729400 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61683635 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:61683635 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7056115 G>T maps to NM_152293.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:7056115 G>T maps to NM_152293.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93464153 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93464153 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93464196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93464196 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93470101 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93470101 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:8050982 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:8050982 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:100536677 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:100536677 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159464600 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159464600 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160005791 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:160005791 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118619454 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118619454 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118639060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118639060 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33272707 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33272707 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:234565803 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:234565803 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38305283 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38305283 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150460295 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150460295 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150464867 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:150464867 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:102194775 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:102194775 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11138518 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:11138518 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72243500 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72243500 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:77923485 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:77923485 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37281571 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:37281571 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78295580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78295580 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100971503 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100971503 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:36288288 C>A maps to NM_001123391.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:36288288 C>A maps to NM_001123391.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:75901835 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:75901835 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141543333 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:141543333 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235597464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235597464 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64889200 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:64889200 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:9665399 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:9665399 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124501369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124501369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119441614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119441614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:85448177 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:85448177 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:168262338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:168262338 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:115111950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:115111950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114837263 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:114837263 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62701108 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:62701108 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89973640 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89973640 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110354524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:110354524 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35088609 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35088609 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35088657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35088657 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160206778 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:160206778 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196018245 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:196018245 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124184369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124184369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179620249 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179620249 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100235688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100235688 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:3149650 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:3149650 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:65170856 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:65170856 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:10775827 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:10775827 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75690032 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:75690032 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1278711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:1278711 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35607431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35607431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56738122 C>A maps to ENST00000453538 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:56738122 C>A maps to ENST00000453538 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71215724 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71215724 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10398637 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10398637 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:50807825 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:50807825 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141762928 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:141762928 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:26891991 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:26891991 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:26892026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:26892026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100226820 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100226820 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195792517 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195792517 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:218607565 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:218607565 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:218610484 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:218610484 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101908910 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:101908910 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92182288 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:92182288 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2297662 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2297662 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134024063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134024063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134024072 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134024072 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134024083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:134024083 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:43783438 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:43783438 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:39885515 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:39885515 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169617847 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169617847 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169632297 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169632297 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169642134 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:169642134 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155171675 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155171675 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151847333 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151847333 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184093644 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184093644 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71633963 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:71633963 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:138414546 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:138414546 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39993167 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:39993167 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9412653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:9412653 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134118623 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:134118623 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121335172 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:121335172 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156378931 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:156378931 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76866911 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:76866911 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:82323202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:82323202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:171939237 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:171939237 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98164968 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98164968 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98273188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98273188 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:62948360 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:62948360 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63044429 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:63044429 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:102182629 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:102182629 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:102192016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:102192016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64880922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:64880922 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98336369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:98336369 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50156632 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50156632 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75404037 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75404037 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75436039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:75436039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81644234 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81644234 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81650667 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:81650667 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:38234534 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:38234534 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68936453 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68936453 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68952981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68952981 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93625809 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:93625809 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192815005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:192815005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41367757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41367757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41367801 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41367801 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41369358 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41369358 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112451149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:112451149 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:21101602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:21101602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1719958 C>G maps to NM_001127266.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1719958 C>G maps to NM_001127266.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159153962 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:159153962 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10725316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:10725316 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85828986 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:85828986 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135470766 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135470766 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135470988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135470988 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82373039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82373039 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159026387 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159026387 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159052282 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:159052282 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48700808 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48700808 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67261088 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67261088 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67261147 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67261147 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74300632 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74300632 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74304925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:74304925 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41956015 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:41956015 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:108521690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:108521690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12790022 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12790022 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12790101 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:12790101 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43423508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43423508 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44106169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44106169 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44115939 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44115939 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44119577 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:44119577 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46159627 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46159627 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156255802 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:156255802 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:700592 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:700592 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:700726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:700726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201115839 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:201115839 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69073387 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:69073387 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:98928050 C>A maps to NM_003276.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:98928050 C>A maps to NM_003276.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68928684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68928684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68935563 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:68935563 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51279190 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51279190 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51279216 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51279216 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:42852382 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:42852382 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117969826 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:117969826 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:2402075 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:2402075 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101769081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:101769081 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117810494 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117810494 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117819656 C>A maps to NM_002160.2 E1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117819656 C>A maps to NM_002160.2 E1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:60033894 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:60033894 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24234496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:24234496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117668091 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:117668091 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31544637 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:31544637 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170819208 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:170819208 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:122078235 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:122078235 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55653323 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55653323 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1947659 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1947659 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128632026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128632026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128696574 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:128696574 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40574201 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40574201 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40675948 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:40675948 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175293686 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175293686 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235291902 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:235291902 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:39078865 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:39078865 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:39725992 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:39725992 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:39750609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:39750609 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179887446 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179887446 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179833864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:179833864 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132569604 G>T maps to NM_014506.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:132569604 G>T maps to NM_014506.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42695510 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:42695510 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223990965 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:223990965 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44006793 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44006793 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:144380047 C>A maps to NM_022445.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:144380047 C>A maps to NM_022445.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35684614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35684614 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154130047 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154130047 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154143093 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154143093 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154144466 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154144466 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154144560 C>A maps to NM_153649.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154144560 C>A maps to NM_153649.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1500582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:1500582 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186306096 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186306096 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186315251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:186315251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65817443 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65817443 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11020831 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:11020831 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30369971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:30369971 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209936785 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209936785 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209953776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:209953776 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42218227 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42218227 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42260977 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42260977 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202275519 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:202275519 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45451941 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:45451941 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:123698760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:123698760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196407 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42196407 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42232416 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42232416 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126445537 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:126445537 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:12864694 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:12864694 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228584933 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:228584933 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:15501804 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:15501804 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119999068 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119999068 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114949553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:114949553 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27147598 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27147598 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117655923 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117655923 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117659385 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117659385 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55038462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:55038462 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5700419 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5700419 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5618154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5618154 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4624458 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:4624458 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32915265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:32915265 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31232256 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:31232256 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104415807 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104415807 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51475721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:51475721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:38155417 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:38155417 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14287183 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14287183 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14406167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14406167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14481328 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:14481328 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230662422 C>A maps to ENST00000389044 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230662422 C>A maps to ENST00000389044 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230679795 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:230679795 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:914575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:914575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64706416 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64706416 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64717701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64717701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100466063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100466063 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5921674 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5921674 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5922491 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5922491 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5923043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:5923043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28903984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:28903984 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:193045602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:193045602 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38213285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38213285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38320004 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38320004 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:101362221 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:101362221 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31362328 C>A maps to NM_002420.4 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:31362328 C>A maps to NM_002420.4 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49714393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:49714393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77354608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77354608 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77354615 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:77354615 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98495517 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98495517 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98567704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:98567704 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135779873 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135779873 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135786259 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:135786259 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67861339 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:67861339 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31107041 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:31107041 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:82280343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:82280343 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176079686 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:176079686 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115600263 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115600263 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115615684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:115615684 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58139474 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58139474 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43094585 G>T maps to ENST00000263802 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43094585 G>T maps to ENST00000263802 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231044804 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:231044804 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180322405 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:180322405 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75034161 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75034161 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39167027 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39167027 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39176550 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39176550 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34850236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:34850236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138818506 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138818506 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138818671 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138818671 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138857341 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:138857341 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32927861 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:32927861 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:46684264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:46684264 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47177419 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47177419 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47202024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47202024 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47202260 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47202260 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47233900 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:47233900 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644014 G>T maps to NM_003594.3 G1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644014 G>T maps to NM_003594.3 G1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644165 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644165 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644176 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117644176 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80722986 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:80722986 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219614690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219614690 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219618232 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:219618232 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113277824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:113277824 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179407457 C>A maps to NM_133378.4 G29807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179407457 C>A maps to NM_133378.4 G29807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179407786 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179407786 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179419011 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179419011 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179422363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179422363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179431750 C>A maps to NM_133378.4 G23802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179431750 C>A maps to NM_133378.4 G23802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179434543 C>A maps to NM_133378.4 G22871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179434543 C>A maps to NM_133378.4 G22871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179437710 G>T maps to NM_133378.4 S21815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179437710 G>T maps to NM_133378.4 S21815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179444866 C>A maps to NM_133378.4 G19815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179444866 C>A maps to NM_133378.4 G19815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179449605 C>A maps to NM_133378.4 G19020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179449605 C>A maps to NM_133378.4 G19020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179474393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179474393 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179516975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179516975 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179534396 C>A maps to ENST00000392423 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179534396 C>A maps to ENST00000392423 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179547401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179547401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179567276 C>A maps to NM_133378.4 G8869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179567276 C>A maps to NM_133378.4 G8869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179598285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179598285 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179634464 G>T maps to NM_133378.4 S2948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:179634464 G>T maps to NM_133378.4 S2948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:18566192 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:18566192 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89999796 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89999796 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40766251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:40766251 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43697356 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:43697356 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50662904 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:50662904 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151530015 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151530015 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151553370 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151553370 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35467939 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:35467939 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:15508190 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:15508190 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37889903 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:37889903 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104681043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:104681043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:662078 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:662078 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41862414 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:41862414 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:70976853 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:70976853 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162551000 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:162551000 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:47062492 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:47062492 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:138847263 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:138847263 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100008364 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100008364 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100008498 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:100008498 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99890624 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99890624 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99890830 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:99890830 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154231516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154231516 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43829501 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43829501 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122659786 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122659786 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122678896 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:122678896 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83669693 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83669693 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129519521 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129519521 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:1370411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:1370411 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154523382 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154523382 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154524175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:154524175 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76171551 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76171551 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76175705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:76175705 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202302314 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:202302314 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109935584 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109935584 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109936018 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109936018 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109936167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109936167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156956495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156956495 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156990914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156990914 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156990965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:156990965 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:10190526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:10190526 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4909016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:4909016 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42657417 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:42657417 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170871902 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:170871902 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103279261 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:103279261 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:171682399 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:171682399 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4454126 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:4454126 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13264048 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:13264048 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38924103 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38924103 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38924120 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38924120 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39507209 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:39507209 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128861626 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128861626 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128867165 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128867165 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128938653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128938653 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128944379 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:128944379 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96540243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:96540243 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64113444 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64113444 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69972833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:69972833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36066757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36066757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150290528 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:150290528 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41973284 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:41973284 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17738753 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:17738753 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35295659 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35295659 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35382335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35382335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33480040 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33480040 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33482538 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33482538 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33486246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:33486246 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73050875 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73050875 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73053374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:73053374 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:96106363 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:96106363 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12005932 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:12005932 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118975353 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118975353 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118975371 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:118975371 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:118913045 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:118913045 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97243410 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:97243410 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:29699111 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:29699111 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126226555 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126226555 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216074106 C>A maps to ENST00000366943 G2481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216074106 C>A maps to ENST00000366943 G2481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:196827 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:196827 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113683250 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113683250 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119228441 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:119228441 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109494637 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109494637 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61433127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61433127 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61528547 C>A maps to NM_014709.3 E1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:61528547 C>A maps to NM_014709.3 E1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77910563 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77910563 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6182559 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6182559 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6187532 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6187532 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11924418 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11924418 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11924924 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:11924924 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22056408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:22056408 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49335958 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49335958 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49335976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49335976 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49362114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49362114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49363041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49363041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120166480 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:120166480 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75302714 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75302714 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6971605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6971605 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:5038588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:5038588 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:8992340 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:8992340 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31195274 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:31195274 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129058692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:129058692 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52602503 G>T maps to NM_001004127.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52602503 G>T maps to NM_001004127.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101748912 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:101748912 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30200658 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:30200658 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144782493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144782493 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144835273 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:144835273 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:145148538 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:145148538 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7913445 G>T maps to NM_021995.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7913445 G>T maps to NM_021995.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7913586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:7913586 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70818631 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:70818631 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6575358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6575358 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155169335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:155169335 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116202213 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116202213 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136637187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:136637187 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75877757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:75877757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35060996 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35060996 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35062937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35062937 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35064133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:35064133 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:157081132 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:157081132 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42576893 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42576893 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:158824591 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:158824591 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4689186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:4689186 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51449949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:51449949 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:22599291 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:22599291 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79954853 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:79954853 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100115369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100115369 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100493780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:100493780 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:62283862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:62283862 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12416657 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:12416657 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2844580 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:2844580 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60906346 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:60906346 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38791757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38791757 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38869806 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38869806 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38908882 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:38908882 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33219258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33219258 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64120529 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64120529 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64196179 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:64196179 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151149077 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151149077 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151157964 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151157964 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184567055 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:184567055 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50512425 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:50512425 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117714968 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:117714968 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:98744679 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:98744679 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:215440558 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:215440558 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61050252 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61050252 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61050414 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:61050414 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:28822971 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:28822971 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119576012 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119576012 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119576064 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119576064 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119584866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119584866 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119619275 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119619275 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119627753 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119627753 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119628457 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:119628457 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14947417 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:14947417 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:42321583 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr22:42321583 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:70885851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:70885851 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170068296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:170068296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116093242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116093242 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:110446827 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:110446827 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118481202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118481202 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118482014 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118482014 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118488844 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118488844 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118493535 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118493535 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118494726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:118494726 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:76734014 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:76734014 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39119740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39119740 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39130836 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:39130836 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137005773 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137005773 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137019511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:137019511 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78587347 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:78587347 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85595853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85595853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43663195 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43663195 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54362445 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54362445 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54591353 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:54591353 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12781310 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:12781310 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151093346 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:151093346 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:33651445 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:33651445 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90270575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:90270575 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141427043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:141427043 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44184604 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44184604 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44236825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:44236825 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1976360 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1976360 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:175446013 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:175446013 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:863530 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:863530 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116918171 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:116918171 T>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30982417 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:30982417 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118481224 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:118481224 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108634114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:108634114 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184240641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:184240641 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87386274 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:87386274 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69965194 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:69965194 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149238698 C>A maps to NM_001168278.1 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:149238698 C>A maps to NM_001168278.1 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2670410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:2670410 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100444701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:100444701 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:21843258 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:21843258 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33246610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33246610 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183471853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183471853 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183490033 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:183490033 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66055236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:66055236 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44251788 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44251788 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135782157 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:135782157 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155646320 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:155646320 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100344372 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100344372 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48494754 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:48494754 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125680870 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:125680870 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33116182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:33116182 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203787833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:203787833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88666167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:88666167 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144623710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144623710 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47572266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47572266 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47597189 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:47597189 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129665943 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:129665943 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87447821 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87447821 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87493547 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87493547 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87493555 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87493555 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87493598 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:87493598 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88917949 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:88917949 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100000005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100000005 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:77222296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:77222296 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27158890 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:27158890 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128948611 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chrX:128948611 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:31610496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:31610496 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:31813071 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:31813071 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:145153942 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:145153942 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131502139 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131502139 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131517619 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131517619 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1195073 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1195073 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1197253 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:1197253 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80423420 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:80423420 A>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72017823 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:72017823 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72827108 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72827108 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:77775727 G>T maps to NM_024721.4 G3260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:77775727 G>T maps to NM_024721.4 G3260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42720182 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:42720182 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50713901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50713901 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50776544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:50776544 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:106440919 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:106440919 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:15127546 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:15127546 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:68217855 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:68217855 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52645973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52645973 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52719469 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:52719469 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140081808 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140081808 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:80961363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:80961363 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:81070999 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:81070999 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44796147 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:44796147 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:298270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:298270 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140482289 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:140482289 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6737454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:6737454 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:44619401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:44619401 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7023926 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:7023926 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:74620217 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:74620217 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116657652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:116657652 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89806515 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:89806515 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:111846877 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:111846877 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148903719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148903719 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:95842026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:95842026 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:142152562 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:142152562 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:38301203 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:38301203 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:38306363 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:38306363 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43127325 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43127325 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32332894 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:32332894 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64403732 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:64403732 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6778185 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6778185 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6787947 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6787947 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27368106 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:27368106 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46722593 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46722593 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58003607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58003607 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109701183 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:109701183 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99217143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99217143 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:32873351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:32873351 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135125214 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135125214 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135126328 C>A maps to NM_145806.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:135126328 C>A maps to NM_145806.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804988 C>A maps to NM_015461.2 G965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22804988 C>A maps to NM_015461.2 G965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805498 C>A maps to NM_015461.2 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805498 C>A maps to NM_015461.2 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805792 C>A maps to NM_015461.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22805792 C>A maps to NM_015461.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56601881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:56601881 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58196773 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58196773 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:37916891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:37916891 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64914944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64914944 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64968487 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64968487 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64973472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:64973472 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53217178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53217178 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116764850 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:116764850 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71660233 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:71660233 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91447950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91447950 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11609041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:11609041 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42950217 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:42950217 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58231721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:58231721 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:64004646 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:64004646 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30583427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30583427 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120168766 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:120168766 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:81733833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:81733833 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8327125 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:8327125 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30548619 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30548619 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30548730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:30548730 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148767440 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:148767440 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53983133 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53983133 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71913799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:71913799 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53156957 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:53156957 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:23567412 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:23567412 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:64853682 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:64853682 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:238053136 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:238053136 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:71532431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:71532431 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99654598 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:99654598 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45486260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45486260 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45501683 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:45501683 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113631218 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113631218 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126189668 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:126189668 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143079787 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:143079787 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:7383193 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:7383193 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44273573 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44273573 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:48547444 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:48547444 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:94473872 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:94473872 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:183695483 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:183695483 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:17424143 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:17424143 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:39973580 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:39973580 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119028870 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119028870 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:89679132 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:89679132 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:47264483 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:47264483 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:132036161 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:132036161 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6749202 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6749202 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:114171313 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:114171313 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69360495 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69360495 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:39695543 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:39695543 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:24261643 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:24261643 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:33637611 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:33637611 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:129030331 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:129030331 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:28305099 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:28305099 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:136402003 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:136402003 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:100242432 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:100242432 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:74357557 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:74357557 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:45402017 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:45402017 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:241813546 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:241813546 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:133990101 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:133990101 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:19610430 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:19610430 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:105250976 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:105250976 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:105268829 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:105268829 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:19554821 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:19554821 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:34179902 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:34179902 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:45939044 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:45939044 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:113279449 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:113279449 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:115218016 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:115218016 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:25398596 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:25398596 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:101775533 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:101775533 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:173616265 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:173616265 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:125599797 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:125599797 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:26663590 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:26663590 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:90328732 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:90328732 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:71772695 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:71772695 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:71823474 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:71823474 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:115202293 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:115202293 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:26785225 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:26785225 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:154295943 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:154295943 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:115361833 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:115361833 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:61917286 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:61917286 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:43236877 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:43236877 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156927398 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156927398 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:3396479 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:3396479 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:148988985 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:148988985 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:153575569 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:153575569 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:80767682 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:80767682 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:78260463 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:78260463 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:66381117 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:66381117 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:76943235 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:76943235 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:231133087 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:231133087 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:150873153 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:150873153 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:177138214 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:177138214 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:65554004 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:65554004 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:1544636 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:1544636 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:119187756 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:119187756 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:117067531 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:117067531 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:1431271 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:1431271 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:212788262 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:212788262 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64662438 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64662438 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64664988 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64664988 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:198505803 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:198505803 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:42617946 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:42617946 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:42628902 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:42628902 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:26108268 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:26108268 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:76870661 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:76870661 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:142238718 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:142238718 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:70163397 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:70163397 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:168725433 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:168725433 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:33244281 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:33244281 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:33113961 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:33113961 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:11038789 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:11038789 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:11049567 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:11049567 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64764503 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64764503 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156617003 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156617003 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:32800092 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:32800092 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:91341687 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:91341687 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:59970018 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:59970018 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:59974603 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:59974603 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:65960316 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:65960316 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:50359649 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:50359649 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:26411375 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:26411375 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:103766492 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:103766492 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:111750473 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:111750473 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:91670939 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:91670939 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:36911146 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:36911146 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:19612956 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:19612956 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:54893276 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:54893276 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:16628151 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:16628151 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:53686220 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:53686220 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:231488266 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:231488266 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:179417426 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:179417426 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:170965849 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:170965849 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75042514 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75042514 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34684394 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34684394 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:55111568 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:55111568 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:30602564 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:30602564 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:20140103 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:20140103 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3736093 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3736093 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:24400918 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:24400918 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:113554392 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:113554392 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:170652851 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:170652851 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:170653038 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:170653038 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:170653078 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:170653078 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:41149635 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:41149635 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32317650 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32317650 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:13470559 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:13470559 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:48035775 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:48035775 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:133092338 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:133092338 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31742460 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31742460 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:25182018 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:25182018 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:30185979 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:30185979 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:89897844 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:89897844 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:89934241 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:89934241 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:35825138 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:35825138 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:100673007 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:100673007 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:87970182 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:87970182 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:24434640 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:24434640 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:141007041 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:141007041 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:2704960 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:2704960 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:53765006 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:53765006 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:201030326 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:201030326 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152727401 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152727401 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:115069137 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:115069137 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:121701578 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:121701578 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:49898774 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:49898774 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:7151474 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:7151474 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:17426754 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:17426754 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:230931058 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:230931058 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:75672867 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:75672867 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:75699744 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:75699744 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:104951057 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:104951057 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:92174455 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:92174455 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:146289 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:146289 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:76916429 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:76916429 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:11545886 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:11545886 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:42965845 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:42965845 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:180378339 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:180378339 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118869065 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118869065 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:169018231 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:169018231 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:34311532 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:34311532 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:41908795 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:41908795 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156304792 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156304792 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:35831692 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:35831692 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72522226 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72522226 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:80300566 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:80300566 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49840113 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49840113 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157801727 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157801727 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:14518874 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:14518874 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:43828589 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:43828589 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214821964 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214821964 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214832168 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214832168 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:68492999 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:68492999 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:122717940 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:122717940 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:56846223 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:56846223 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:67040542 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:67040542 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:196879387 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:196879387 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:54997174 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:54997174 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:50824284 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:50824284 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:50830115 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:50830115 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:14158094 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:14158094 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:175673553 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:175673553 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:10996665 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:10996665 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:46812000 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:46812000 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:6979816 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:6979816 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:92814741 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:92814741 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:150644725 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:150644725 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:70738078 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:70738078 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:41303936 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:41303936 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:41418948 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:41418948 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:1262345 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:1262345 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:51258517 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:51258517 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:103548352 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:103548352 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:75890644 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:75890644 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:101749447 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:101749447 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:70866196 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:70866196 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:94051175 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:94051175 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:94056934 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:94056934 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:109774124 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:109774124 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:110830135 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:110830135 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:110844718 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:110844718 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111145439 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111145439 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111145469 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111145469 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:227976472 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:227976472 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:107834526 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:107834526 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:107434773 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:107434773 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:189898701 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:189898701 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47422667 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47422667 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:14502515 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:14502515 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:100893412 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:100893412 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:36145632 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:36145632 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:148604055 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:148604055 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:43910444 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:43910444 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:49704087 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:49704087 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:153925724 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:153925724 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34052630 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34052630 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34071590 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34071590 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:113420535 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:113420535 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:114186212 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:114186212 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:23545754 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:23545754 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:39771325 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:39771325 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:77489137 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:77489137 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:204735945 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:204735945 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:138253692 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:138253692 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:225364920 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:225364920 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:19955738 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:19955738 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:202936195 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:202936195 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:143994885 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:143994885 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:104591452 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:104591452 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:99293353 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:99293353 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:47403569 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:47403569 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:16008517 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:16008517 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:47433567 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:47433567 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59787179 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59787179 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59822119 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59822119 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:6474235 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:6474235 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:183836048 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:183836048 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:57939915 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:57939915 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:52758108 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:52758108 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:110544769 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:110544769 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:50563119 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:50563119 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:53525080 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:53525080 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61892811 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61892811 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:29845423 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:29845423 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:32215230 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:32215230 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40259974 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40259974 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:41597706 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:41597706 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:61686582 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:61686582 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:31986443 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:31986443 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:32632412 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:32632412 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:78340016 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:78340016 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:124398858 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:124398858 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:52433525 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:52433525 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:196922905 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:196922905 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:38885208 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:38885208 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:11604269 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:11604269 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186302439 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186302439 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62562427 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62562427 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:31379548 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:31379548 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:225738658 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:225738658 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:169508773 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:169508773 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:11348079 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:11348079 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:390697 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:390697 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:99534135 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:99534135 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:99602011 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:99602011 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:95782852 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:95782852 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:100509733 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:100509733 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:28728732 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:28728732 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120856087 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120856087 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120865273 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120865273 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:38597726 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:38597726 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:56368957 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:56368957 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:45408278 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:45408278 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:68110455 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:68110455 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:66770214 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:66770214 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:110576862 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:110576862 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:131762116 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:131762116 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:68921177 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:68921177 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:3765440 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:3765440 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:82533763 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:82533763 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:38438274 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:38438274 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:55259367 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:55259367 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:65767715 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:65767715 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:20152147 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:20152147 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:27591105 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:27591105 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:117658954 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:117658954 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:73608899 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:73608899 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:36901500 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:36901500 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:45022461 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:45022461 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:89131953 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:89131953 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:14730452 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:14730452 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:71498514 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:71498514 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:132190716 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:132190716 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:46107259 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:46107259 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:74453413 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:74453413 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:131216073 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:131216073 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:16551850 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:16551850 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:51874054 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:51874054 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:14013974 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:14013974 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:60240948 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:60240948 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:13935458 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:13935458 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:72211966 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:72211966 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:57337170 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:57337170 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:96071225 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:96071225 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:50290723 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:50290723 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:70527847 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:70527847 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:89950551 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:89950551 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:177474229 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:177474229 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:79629424 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:79629424 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:74130457 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:74130457 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:15325772 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:15325772 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:91760333 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:91760333 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:10695993 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:10695993 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:16793591 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:16793591 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:24849845 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:24849845 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:49227633 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:49227633 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:64365102 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:64365102 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:13669310 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:13669310 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:127627124 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:127627124 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:30677741 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:30677741 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:5966501 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:5966501 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:55765523 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:55765523 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:68691765 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:68691765 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:153303397 C>G maps to NM_001013415.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:153303397 C>G maps to NM_001013415.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:17865785 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:17865785 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:72651573 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:72651573 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157718260 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157718260 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157665806 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157665806 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157497837 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157497837 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:108386929 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:108386929 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:108388110 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:108388110 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:102375098 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:102375098 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:34192217 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:34192217 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:72743205 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:72743205 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:128478257 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:128478257 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:28891496 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:28891496 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49979647 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49979647 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:171244727 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:171244727 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:203224960 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:203224960 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:49175351 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:49175351 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:49204845 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:49204845 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:74671549 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:74671549 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:14859624 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:14859624 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47571437 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47571437 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:78095644 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:78095644 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:29588790 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:29588790 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:46973001 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:46973001 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:161520720 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:161520720 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89913038 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89913038 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:51759194 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:51759194 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:4848509 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:4848509 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:132683930 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:132683930 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69791917 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69791917 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:22707341 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:22707341 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:120585947 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:120585947 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:154304275 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:154304275 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:158399992 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:158399992 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:34935600 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:34935600 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61995646 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61995646 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:31015489 T>A maps to ENST00000434774 C327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:31015489 T>A maps to ENST00000434774 C327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:42468459 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:42468459 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:78557814 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:78557814 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:8099699 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:8099699 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:6554785 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:6554785 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:51693742 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:51693742 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:42079861 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:42079861 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:42153072 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:42153072 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:131964637 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:131964637 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:56869563 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:56869563 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:58605002 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:58605002 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:131019807 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:131019807 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:155755038 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:155755038 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:45101925 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:45101925 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42542095 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42542095 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:56526586 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:56526586 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:50498345 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:50498345 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:67227366 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:67227366 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:67577047 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:67577047 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:26534998 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:26534998 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:46849942 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:46849942 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:37686951 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:37686951 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:100349707 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:100349707 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:9714218 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:9714218 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:113638839 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:113638839 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:94547752 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:94547752 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:120823543 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:120823543 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:120831808 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:120831808 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:88780314 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:88780314 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:124072922 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:124072922 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52696929 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52696929 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:27489950 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:27489950 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:15621335 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:15621335 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:26507545 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:26507545 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:82940553 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:82940553 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:30687110 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:30687110 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42156374 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42156374 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:40998312 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:40998312 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:63978478 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:63978478 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:64004879 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:64004879 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:69699481 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:69699481 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:89393077 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:89393077 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:126080173 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:126080173 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:43047443 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:43047443 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:27565753 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:27565753 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:19371329 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:19371329 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:43292878 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:43292878 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:42829389 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:42829389 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:150681263 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:150681263 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:46654467 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:46654467 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:148858403 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:148858403 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18303899 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18303899 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18309599 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18309599 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186387598 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186387598 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:20838457 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:20838457 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:26043927 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:26043927 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:22192206 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:22192206 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:95042935 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:95042935 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:102813509 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:102813509 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:160454207 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:160454207 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:111640761 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:111640761 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:114242700 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:114242700 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52111411 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52111411 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:104440586 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:104440586 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:3132001 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:3132001 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:79673960 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:79673960 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:41740079 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:41740079 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:143129921 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:143129921 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156813377 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156813377 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:44432091 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:44432091 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:197616236 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:197616236 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:91010642 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:91010642 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156503677 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156503677 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156521477 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156521477 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:52218464 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:52218464 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42462773 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42462773 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:37778284 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:37778284 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:160968829 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:160968829 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:52852310 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:52852310 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:4699804 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:4699804 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:156009857 G>T maps to NM_172159.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:156009857 G>T maps to NM_172159.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:211034811 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:211034811 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:19491865 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:19491865 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:178978331 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:178978331 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:73900514 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:73900514 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:36644948 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:36644948 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:36766803 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:36766803 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:73056445 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:73056445 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:86713074 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:86713074 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:404667 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:404667 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:197409235 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:197409235 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:24508890 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:24508890 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:93943856 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:93943856 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:1377500 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:1377500 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:36888931 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:36888931 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:17987599 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:17987599 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:44846843 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:44846843 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:241725737 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:241725737 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:245766259 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:245766259 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:55354215 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:55354215 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:55593833 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:55593833 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:70413062 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:70413062 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:123055683 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:123055683 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:39674528 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:39674528 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:38855630 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:38855630 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52863094 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52863094 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52965007 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52965007 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52789734 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52789734 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119207873 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119207873 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:48963867 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:48963867 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:7038648 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:7038648 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:129637431 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:129637431 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:53286635 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:53286635 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:52250860 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:52250860 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:66101816 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:66101816 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63276525 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63276525 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:206776686 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:206776686 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:113906916 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:113906916 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:33886414 C>A maps to ENST00000411482 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:33886414 C>A maps to ENST00000411482 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:20826582 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:20826582 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:161032536 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:161032536 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:81968584 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:81968584 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:19805997 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:19805997 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:141771097 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:141771097 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:141777484 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:141777484 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:57578073 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:57578073 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:169996875 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:169996875 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:170068757 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:170068757 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:70300611 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:70300611 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:62457739 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:62457739 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:33487942 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:33487942 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:74977751 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:74977751 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:144178331 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:144178331 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:25004972 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:25004972 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:160783711 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:160783711 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:143846018 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:143846018 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:20926813 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:20926813 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:20193693 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:20193693 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:2255700 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:2255700 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:166962239 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:166962239 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:172935577 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:172935577 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:71202792 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:71202792 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:75316664 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:75316664 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:136710461 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:136710461 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:165110553 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:165110553 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:119727619 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:119727619 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186943003 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186943003 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3835102 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3835102 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:182733373 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:182733373 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:112403915 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:112403915 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:113656326 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:113656326 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:114619882 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:114619882 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:90459955 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:90459955 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:70346350 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:70346350 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:36632976 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:36632976 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:171765472 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:171765472 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119216360 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119216360 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:141767071 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:141767071 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:24455779 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:24455779 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:131155492 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:131155492 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:168311948 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:168311948 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:89086810 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:89086810 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:55519411 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:55519411 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:158817441 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:158817441 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:158817713 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:158817713 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:27358938 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:27358938 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:108778737 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:108778737 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:31329998 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:31329998 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:56355581 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:56355581 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:202557601 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:202557601 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:139065944 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:139065944 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:41344932 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:41344932 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:10603595 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:10603595 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:15998537 A>G maps to NM_002445.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:15998537 A>G maps to NM_002445.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:49928549 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:49928549 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:9739371 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:9739371 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:95598933 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:95598933 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:236998772 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:236998772 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9005265 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9005265 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:49425826 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:49425826 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10356736 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10356736 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:23882190 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:23882190 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10300326 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10300326 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:26355845 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:26355845 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:76602435 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:76602435 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:2027412 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:2027412 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62859385 T>A maps to ENST00000360149 *592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62859385 T>A maps to ENST00000360149 *592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:113442795 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:113442795 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:175436482 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:175436482 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:102029222 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:102029222 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:47996347 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:47996347 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:102884658 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:102884658 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6631988 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6631988 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:183536233 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:183536233 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:54912819 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:54912819 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21488033 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21488033 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:75563829 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:75563829 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:140216333 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:140216333 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:161180084 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:161180084 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:21435524 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:21435524 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152499880 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152499880 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:55992184 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:55992184 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:20869064 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:20869064 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:30057161 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:30057161 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101571195 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101571195 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101578129 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101578129 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:177576617 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:177576617 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:37027439 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:37027439 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:125144576 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:125144576 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:63768342 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:63768342 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:172661676 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:172661676 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:56419038 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:56419038 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:56531811 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:56531811 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:155718545 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:155718545 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:155728435 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:155728435 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:89182727 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:89182727 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:15026671 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:15026671 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:34889102 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:34889102 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:25264660 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:25264660 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:32620795 C>A maps to NM_001160004.1 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:32620795 C>A maps to NM_001160004.1 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:79270234 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:79270234 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:107961190 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:107961190 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:163297216 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:163297216 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69115506 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69115506 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69115782 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69115782 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:37328456 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:37328456 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:134008334 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:134008334 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28550292 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28550292 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:102337053 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:102337053 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:228492082 G>A maps to ENST00000366707 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:228492082 G>A maps to ENST00000366707 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:128724465 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:128724465 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:53602868 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:53602868 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:127563569 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:127563569 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:6890906 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:6890906 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248186219 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248186219 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:56232398 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:56232398 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:94505174 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:94505174 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:43545596 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:43545596 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:163736061 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:163736061 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:17634562 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:17634562 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:26300891 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:26300891 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:23652426 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:23652426 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:176525344 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:176525344 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:206118210 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:206118210 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:122354970 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:122354970 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:102541202 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:102541202 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47319564 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47319564 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:91238240 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:91238240 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47766212 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47766212 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47819833 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:47819833 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:71576129 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:71576129 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:101888090 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:101888090 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:195975268 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:195975268 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:165863890 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:165863890 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:178740727 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:178740727 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:14880519 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:14880519 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149510263 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149510263 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:122811414 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:122811414 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2646041 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2646041 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:74847080 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:74847080 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:99192099 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:99192099 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:197767539 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:197767539 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:28252036 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:28252036 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:153317627 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:153317627 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:47497967 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:47497967 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:106515262 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:106515262 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:8791420 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:8791420 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2169080 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2169080 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:51915254 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:51915254 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:9343455 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:9343455 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:43195900 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:43195900 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89872059 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89872059 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:118199316 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:118199316 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7618918 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7618918 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:84606346 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:84606346 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:133214483 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:133214483 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:86265794 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:86265794 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:134386703 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:134386703 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:38145670 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:38145670 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:43172403 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:43172403 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:76804053 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:76804053 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:28177046 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:28177046 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:3342545 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:3342545 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:57372236 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:57372236 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:57467043 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:57467043 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:84663367 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:84663367 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:169997969 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:169997969 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:53921600 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:53921600 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:20419023 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:20419023 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:36303207 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:36303207 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:93625104 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:93625104 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:113814286 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:113814286 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62612739 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62612739 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:43351977 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:43351977 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:127177790 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:127177790 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:52735431 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:52735431 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:142432292 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:142432292 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:198672410 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:198672410 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:8748050 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:8748050 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:48142857 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:48142857 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:31409384 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:31409384 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:110830862 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:110830862 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:1658155 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:1658155 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:10822728 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:10822728 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:29848853 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:29848853 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:220427266 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:220427266 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:155121290 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:155121290 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:34814883 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:34814883 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:79317611 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:79317611 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:4776435 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:4776435 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:173916442 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:173916442 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:76439534 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:76439534 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:79313657 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:79313657 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:103270660 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:103270660 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:85571880 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:85571880 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:85573369 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:85573369 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:43611892 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:43611892 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:176104033 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:176104033 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:3319857 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:3319857 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:241031871 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:241031871 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:241033459 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:241033459 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:63220916 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:63220916 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:107279814 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:107279814 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:130897049 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:130897049 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:105257016 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:105257016 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:40695231 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:40695231 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:87121887 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:87121887 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:177570877 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:177570877 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:3597827 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:3597827 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:30307363 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:30307363 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:88765943 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:88765943 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:185067545 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:185067545 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:117683689 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:117683689 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:68895424 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:68895424 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:53709055 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:53709055 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:133137758 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:133137758 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:55461875 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:55461875 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:166944944 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:166944944 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64137983 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:64137983 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:219457008 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:219457008 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:77394617 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:77394617 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:38095425 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:38095425 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:41771179 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:41771179 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:237872472 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:237872472 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:151958811 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:151958811 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:36014364 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:36014364 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:155228755 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:155228755 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:78187956 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:78187956 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:62186651 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:62186651 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:62011190 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:62011190 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:38764809 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:38764809 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:38938321 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:38938321 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:165971898 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:165971898 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6464864 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6464864 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:35195259 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:35195259 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:4248016 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:4248016 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:49319460 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:49319460 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:84644267 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:84644267 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:50224243 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:50224243 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:151107504 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:151107504 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:27296770 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:27296770 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:120917059 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:120917059 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:67145491 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:67145491 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:134496000 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:134496000 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:52066815 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:52066815 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:51200329 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:51200329 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:49159962 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:49159962 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:96303019 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:96303019 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:592020 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:592020 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:124508722 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:124508722 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:51958043 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:51958043 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:56359816 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:56359816 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:1629558 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:1629558 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:164793677 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:164793677 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:43246074 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:43246074 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:61444121 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:61444121 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49934225 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49934225 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:46936147 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:46936147 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:53571314 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:53571314 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63059220 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63059220 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:38359480 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:38359480 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:205884138 G>T maps to NM_134325.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:205884138 G>T maps to NM_134325.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:205892625 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:205892625 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:86894168 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:86894168 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:101376790 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:101376790 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:115924866 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:115924866 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:76084830 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:76084830 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3210489 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3210489 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:103300887 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:103300887 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:20525944 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:20525944 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:45755639 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:45755639 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:112350355 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:112350355 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:72938273 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:72938273 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:130930847 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:130930847 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:71227799 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:71227799 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:62552156 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:62552156 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:245912967 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:245912967 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:139275904 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:139275904 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:17885166 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:17885166 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:108377792 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:108377792 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:231405414 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:231405414 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:231152714 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:231152714 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:22675675 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:22675675 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:139308359 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:139308359 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:139310354 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:139310354 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:158580965 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:158580965 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:40995969 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:40995969 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:41026136 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:41026136 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:142735877 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:142735877 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2809748 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2809748 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:53079695 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:53079695 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186760357 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:186760357 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:104042689 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:104042689 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63962112 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63962112 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63965145 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:63965145 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:5400079 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:5400079 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:144508680 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:144508680 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44900534 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44900534 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:12232138 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:12232138 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:99945215 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:99945215 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:97362211 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:97362211 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120800458 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120800458 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:60588023 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:60588023 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:100038106 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:100038106 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:106091642 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:106091642 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:170880445 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:170880445 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:101396438 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:101396438 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:110354441 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:110354441 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:96152705 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:96152705 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:65155419 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:65155419 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:56688798 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:56688798 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:10419781 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:10419781 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:246727852 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:246727852 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:51565959 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:51565959 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:31485791 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:31485791 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:2375792 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:2375792 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:133931787 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:133931787 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:4686373 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:4686373 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:100169953 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:100169953 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:125811148 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:125811148 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:125835016 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:125835016 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:5737338 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:5737338 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52546791 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52546791 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:202984221 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:202984221 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:166009571 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:166009571 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:123755529 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:123755529 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:54275474 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:54275474 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:37470636 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:37470636 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6443189 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:6443189 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:9619186 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:9619186 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32040126 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32040126 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:42635069 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:42635069 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:42679795 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:42679795 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:42694332 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:42694332 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:113735128 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:113735128 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:1272109 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:1272109 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:49866482 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:49866482 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:42397214 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:42397214 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:15580878 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:15580878 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:154236943 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:154236943 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:6472481 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:6472481 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:67049305 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:67049305 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:100730379 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:100730379 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:193053900 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:193053900 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:98560089 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:98560089 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2127476 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2127476 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:71551313 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:71551313 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40095122 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40095122 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:89338911 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:89338911 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:117602820 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:117602820 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:80750060 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:80750060 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:84399140 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:84399140 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179659089 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179659089 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:63974014 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:63974014 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:54947233 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:54947233 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72248527 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72248527 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:68529667 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:68529667 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118243383 G>T maps to NM_004788.2 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118243383 G>T maps to NM_004788.2 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:10240058 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:10240058 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:19436749 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:19436749 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:76143516 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:76143516 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:70460845 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:70460845 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:70352501 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:70352501 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:41290950 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:41290950 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:17738837 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:17738837 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:24909187 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:24909187 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:24911379 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:24911379 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:18958434 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:18958434 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:18974851 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:18974851 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:216019484 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:216019484 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:132618663 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:132618663 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:55560836 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:55560836 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:113670247 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:113670247 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:61622306 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:61622306 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:41082707 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:41082707 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:30219710 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:30219710 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:82843743 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:82843743 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:133071117 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:133071117 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:79928818 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:79928818 A>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:100830882 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:100830882 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:62274821 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:62274821 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:62315919 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:62315919 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:53007964 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:53007964 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:150039851 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:150039851 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64171688 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64171688 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:26694626 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:26694626 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:177100851 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:177100851 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:117521235 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:117521235 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:122405863 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:122405863 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:134877935 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:134877935 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:141416175 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:141416175 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:1962885 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:1962885 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:970112 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:970112 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:95992261 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:95992261 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:25621263 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:25621263 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:52840317 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chrX:52840317 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:21823717 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:21823717 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:21827938 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:21827938 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:217039645 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:217039645 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:142103594 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:142103594 T>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:733067 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:733067 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:143543671 T>C maps to ENST00000508754 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:143543671 T>C maps to ENST00000508754 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:67432711 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:67432711 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:44986646 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:44986646 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:31791484 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:31791484 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:99110022 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:99110022 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:20579401 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:20579401 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:45927754 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:45927754 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:44621933 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:44621933 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:52076349 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:52076349 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:22255769 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:22255769 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:28964485 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:28964485 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:28971410 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:28971410 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7585854 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7585854 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:38407836 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:38407836 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62598957 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62598957 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:57901427 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:57901427 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9580446 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9580446 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:59080 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:59080 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:40998900 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:40998900 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:53960362 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:53960362 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:136268036 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:136268036 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:45508770 T>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:45508770 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:7680493 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:7680493 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:7726662 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:7726662 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:8991674 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:8991674 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:125570742 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:125570742 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:12776414 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:12776414 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:69709946 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:69709946 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:2331549 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:2331549 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:1053778 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:1053778 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:87199404 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:87199404 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:87340016 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:87340016 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:87043131 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:87043131 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:20698592 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:20698592 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:20698713 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:20698713 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:48167848 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:48167848 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48745767 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48745767 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:17457471 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:17457471 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:43707969 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:43707969 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:35501282 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:35501282 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:5568740 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:5568740 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:18153019 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:18153019 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:37400087 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:37400087 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:123317360 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:123317360 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:156889995 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:156889995 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:207408075 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:207408075 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:8656628 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:8656628 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:33614500 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:33614500 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:130275412 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:130275412 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:167844441 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:167844441 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:7626255 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:7626255 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:7690963 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:7690963 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:3055756 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:3055756 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:148715097 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:148715097 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:88048118 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:88048118 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:100623933 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:100623933 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150840703 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150840703 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:100361835 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:100361835 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:96904115 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:96904115 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:19866106 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:19866106 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:86251227 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:86251227 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:105290785 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:105290785 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:34175306 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:34175306 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:73786093 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:73786093 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:113346928 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:113346928 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:118071459 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:118071459 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:6360597 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:6360597 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:82905783 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:82905783 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:99837668 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:99837668 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:5687253 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:5687253 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:101477325 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:101477325 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:101477367 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:101477367 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:22272252 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:22272252 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:69330135 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:69330135 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:70015300 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:70015300 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:36571721 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:36571721 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:71808515 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:71808515 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:115230738 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:115230738 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:58430751 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:58430751 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:129959399 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:129959399 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156928510 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156928510 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:7511866 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:7511866 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:23297663 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:23297663 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:98951488 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:98951488 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:131128060 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:131128060 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155319423 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155319423 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124383044 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124383044 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:113485907 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:113485907 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:42471567 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:42471567 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:10452269 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:10452269 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:203671372 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:203671372 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:124235837 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:124235837 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:77119330 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:77119330 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:42274517 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:42274517 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:79163448 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:79163448 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:11039056 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:11039056 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:69665847 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:69665847 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:70065660 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:70065660 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:97935712 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:97935712 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:43315902 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:43315902 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:43318781 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:43318781 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:198621145 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:198621145 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:32859676 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:32859676 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:124090662 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:124090662 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:6231040 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:6231040 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124661391 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124661391 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:4639285 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:4639285 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:97082873 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:97082873 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:93100960 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:93100960 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:77297797 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:77297797 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:76463287 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:76463287 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:34647570 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:34647570 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:36993569 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:36993569 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:30503513 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:30503513 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:179339084 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:179339084 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:116669951 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:116669951 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:111890447 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:111890447 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:20226729 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:20226729 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:47716152 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:47716152 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:37469943 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:37469943 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:119232591 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:119232591 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:31962228 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:31962228 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:130030421 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:130030421 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:34558263 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:34558263 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:165714103 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:165714103 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:53989728 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:53989728 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31746723 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31746723 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:57422238 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:57422238 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:111808479 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:111808479 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:114454849 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:114454849 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:117405345 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:117405345 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:15593955 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:15593955 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:9009558 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:9009558 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:9019110 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:9019110 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:2711158 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:2711158 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:2711211 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:2711211 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:53766838 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:53766838 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:181452841 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:181452841 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:49074176 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:49074176 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48649535 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48649535 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48678634 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48678634 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1245922 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1245922 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18816462 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18816462 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:86062432 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:86062432 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:7341681 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:7341681 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:188225498 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:188225498 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:93065248 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:93065248 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:12870704 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:12870704 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:209776696 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:209776696 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:110820196 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:110820196 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:7528087 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:7528087 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:96064928 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:96064928 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:38861099 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:38861099 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:119146998 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:119146998 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:219869224 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:219869224 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:33444456 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:33444456 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:16594079 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:16594079 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:69458579 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:69458579 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:41907958 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:41907958 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:2485897 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:2485897 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:66367900 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:66367900 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:73478235 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:73478235 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158227157 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158227157 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158147035 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158147035 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158325959 G>T maps to ENST00000434258 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158325959 G>T maps to ENST00000434258 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:167402219 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:167402219 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:117302947 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:117302947 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:157806001 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:157806001 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:22078827 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:22078827 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:68835520 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:68835520 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:73462173 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:73462173 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:26885661 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:26885661 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:26885711 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:26885711 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:14139563 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:14139563 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:15794055 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:15794055 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:11047316 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:11047316 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:104061897 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:104061897 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:644704 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:644704 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131196680 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131196680 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:182403785 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:182403785 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:50830204 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:50830204 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:29095761 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:29095761 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:361434 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:361434 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:23767682 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:23767682 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:233394576 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:233394576 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1511718 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1511718 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:74447061 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:74447061 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:122794254 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:122794254 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:7303701 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:7303701 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:87951744 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:87951744 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:32767153 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:32767153 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:135048009 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:135048009 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:40950803 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:40950803 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:17466924 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:17466924 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:146997418 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:146997418 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:76509953 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:76509953 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:103399992 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:103399992 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:103461370 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:103461370 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121228555 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121228555 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121295870 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121295870 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121353529 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121353529 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:70851889 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:70851889 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48272059 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48272059 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:61937178 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:61937178 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:86307878 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:86307878 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:86426883 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:86426883 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:137677083 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:137677083 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:189933472 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:189933472 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:10091537 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:10091537 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:238271696 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:238271696 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:48623720 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:48623720 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:3665301 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:3665301 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130298511 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130298511 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:54744394 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:54744394 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:47765382 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:47765382 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24544504 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24544504 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211447319 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211447319 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211539551 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211539551 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:207782629 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:207782629 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:65579909 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:65579909 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:65592832 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:65592832 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:49700889 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:49700889 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:153924975 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:153924975 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:115269041 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:115269041 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:19315839 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:19315839 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113254027 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113254027 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113347731 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113347731 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113364582 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113364582 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113648988 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113648988 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166451768 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166451768 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:23729585 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:23729585 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:67650624 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:67650624 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:49018698 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:49018698 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:44873157 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:44873157 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:74963510 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:74963510 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:36163103 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:36163103 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:172398355 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:172398355 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:143958030 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:143958030 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:41533258 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:41533258 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:86047599 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:86047599 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:58522128 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:58522128 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:98600293 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:98600293 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:14976667 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:14976667 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:85787121 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:85787121 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:110725921 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:110725921 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:6783307 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:6783307 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179322514 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179322514 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:14620434 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:14620434 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137154482 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137154482 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:83344202 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:83344202 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:83525539 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:83525539 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:1581245 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:1581245 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:32868005 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:32868005 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:21048248 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:21048248 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:183624096 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:183624096 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:102965043 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:102965043 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44437721 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44437721 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:111484735 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:111484735 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:67266799 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:67266799 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:73159611 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:73159611 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:116538600 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:116538600 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:154684243 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:154684243 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:27148030 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:27148030 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:113890531 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:113890531 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:44010769 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:44010769 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:80584461 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:80584461 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71838327 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71838327 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:23544096 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:23544096 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:172474737 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:172474737 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:63206216 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:63206216 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:37368690 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:37368690 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:44090524 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:44090524 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:120630630 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:120630630 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:132515719 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:132515719 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:46609493 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:46609493 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:93965524 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:93965524 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100416022 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100416022 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:142560925 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:142560925 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100319085 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100319085 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14020370 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14020370 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14024783 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14024783 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:102814691 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:102814691 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:169487545 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:169487545 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:138612920 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:138612920 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:50291694 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:50291694 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50752225 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50752225 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:133923048 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:133923048 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:133923193 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:133923193 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:22985855 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:22985855 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:150396182 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:150396182 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:68194444 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:68194444 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:16734381 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:16734381 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:190203636 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:190203636 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128371246 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128371246 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:12049225 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:12049225 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:71507232 G>T maps to ENST00000416039 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:71507232 G>T maps to ENST00000416039 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:127653833 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:127653833 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:127664518 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:127664518 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:102614192 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:102614192 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:15500715 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:15500715 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:157718462 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:157718462 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:157489487 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:157489487 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:159778732 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:159778732 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:125029802 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:125029802 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:125058188 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:125058188 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:53326523 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:53326523 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:108387303 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:108387303 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:108388037 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:108388037 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:72483749 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:72483749 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:18650646 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:18650646 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:142469372 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:142469372 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128478308 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128478308 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128480747 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128480747 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:180043330 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:180043330 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:2977716 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:2977716 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:114269748 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:114269748 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:79403483 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:79403483 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:79403837 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:79403837 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:49217631 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:49217631 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:78432682 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:78432682 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:39169719 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:39169719 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:161292657 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:161292657 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:151560647 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:151560647 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:161520788 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:161520788 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:27586154 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:27586154 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:26581700 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:26581700 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:151800145 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:151800145 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:155158134 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:155158134 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:172735943 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:172735943 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:173301490 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:173301490 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:68455647 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:68455647 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:36033774 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:36033774 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:9828709 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:9828709 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:89657191 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:89657191 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44186252 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44186252 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:154284033 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:154284033 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:118030297 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:118030297 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:137593647 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:137593647 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:38880850 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:38880850 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150384080 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150384080 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150270150 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150270150 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:30714349 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:30714349 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:100656608 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:100656608 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:57859078 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:57859078 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:39033697 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:39033697 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:58606977 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:58606977 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:121386523 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:121386523 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:167747117 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:167747117 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155822977 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155822977 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:176622960 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:176622960 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:25701167 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:25701167 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:89933774 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:89933774 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:117150231 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:117150231 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:176026901 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:176026901 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:113634791 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:113634791 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:37903226 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:37903226 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:11765193 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:11765193 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:34007928 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:34007928 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:7348028 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:7348028 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:24323074 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:24323074 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:127453739 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:127453739 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156593564 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156593564 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50684600 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50684600 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:18684214 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:18684214 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:18975619 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:18975619 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:242192682 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:242192682 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:31789587 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:31789587 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:58120872 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:58120872 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:72639968 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:72639968 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:120389444 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:120389444 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:21801072 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:21801072 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:71103758 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:71103758 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:75113389 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:75113389 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:186077854 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:186077854 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12878324 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12878324 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:53619353 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:53619353 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:71012709 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:71012709 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:8167339 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:8167339 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:129225198 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:129225198 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:185407540 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:185407540 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:130413204 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:130413204 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:160061885 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:160061885 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:42166633 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:42166633 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:131995336 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:131995336 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:81582954 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:81582954 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:102997947 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:102997947 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:113875635 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:113875635 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:62504736 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:62504736 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:120595500 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:120595500 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:41740000 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:41740000 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:67677158 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:67677158 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:66638249 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:66638249 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:50679570 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:50679570 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:15760581 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:15760581 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:37627226 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:37627226 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31335939 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31335939 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31336247 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31336247 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52820931 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52820931 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:156649803 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:156649803 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152882227 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152882227 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:49247527 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:49247527 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:42747053 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:42747053 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:42730268 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:42730268 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:21305368 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:21305368 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:21698889 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:21698889 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:155566361 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:155566361 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154821909 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154821909 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:138606570 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:138606570 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:196398983 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:196398983 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:37453353 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:37453353 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155895870 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155895870 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:29454783 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:29454783 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:118228099 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:118228099 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:94039266 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:94039266 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:95505128 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:95505128 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:36868867 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:36868867 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:29809684 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:29809684 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168445705 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168445705 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:26174778 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:26174778 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55246700 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55246700 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:205312292 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:205312292 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:70293454 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:70293454 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:86877206 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:86877206 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:52911612 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:52911612 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:31852684 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:31852684 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:201352157 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:201352157 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:6975927 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:6975927 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:129723402 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:129723402 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:31212861 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:31212861 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:73631306 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:73631306 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:46716265 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:46716265 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:46724978 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:46724978 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:136564989 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:136564989 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:18487392 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:18487392 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2566616 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2566616 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55087674 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55087674 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55174923 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55174923 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:105404963 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:105404963 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:97832849 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:97832849 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150444308 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150444308 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:160998130 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:160998130 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:160998400 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:160998400 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:161025949 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:161025949 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:161027705 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:161027705 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:1490064 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:1490064 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:82446565 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:82446565 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:19813333 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:19813333 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:85982458 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:85982458 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:105507491 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:105507491 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141143690 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141143690 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141762873 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141762873 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:170024983 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:170024983 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:68193385 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:68193385 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:12336870 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:12336870 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:122676146 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:122676146 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:37163246 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:37163246 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:40657723 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:40657723 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:40671872 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:40671872 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:204586853 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:204586853 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:235901344 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:235901344 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:235901983 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:235901983 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:235938429 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:235938429 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:20199949 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:20199949 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2262451 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2262451 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:65344637 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:65344637 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:149671453 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:149671453 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:64566363 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:64566363 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:45927280 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:45927280 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:220777326 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:220777326 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:99019306 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:99019306 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:90387475 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:90387475 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:90491467 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:90491467 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:6378683 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:6378683 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:70348685 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:70348685 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:37576204 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:37576204 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:131902532 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:131902532 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:38187708 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:38187708 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:126667255 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:126667255 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:126674922 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:126674922 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:112779279 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:112779279 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:116381096 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:116381096 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141752053 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141752053 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14355354 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14355354 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:104722247 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:104722247 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:118363984 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:118363984 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:154884654 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:154884654 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:89087061 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:89087061 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50546715 C>A maps to ENST00000428564 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50546715 C>A maps to ENST00000428564 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:132693910 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:132693910 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71367019 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71367019 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:24689510 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:24689510 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:24705183 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:24705183 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:30439185 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:30439185 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18129790 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18129790 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60543015 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60543015 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:55709161 G>T maps to NM_170721.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:55709161 G>T maps to NM_170721.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:814222 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:814222 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:23399292 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:23399292 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49933885 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49933885 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:55473344 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:55473344 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:9009841 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:9009841 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:9019537 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:9019537 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100696198 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100696198 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:1082256 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:1082256 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:42762703 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:42762703 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:1289899 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:1289899 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:15893862 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:15893862 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10258328 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10258328 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:108173063 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:108173063 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10424586 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10424586 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10363237 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10363237 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:23866150 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:23866150 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:23896171 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:23896171 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:30418531 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:30418531 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:169498320 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:169498320 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:109704902 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:109704902 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:27401234 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:27401234 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:34862489 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:34862489 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:31094606 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:31094606 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:52609192 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:52609192 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:2021608 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:2021608 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:89868096 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:89868096 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:101727034 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:101727034 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:101944567 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:101944567 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:78552935 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:78552935 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152487557 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152487557 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:21555751 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:21555751 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:70416194 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:70416194 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:233759414 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:233759414 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:63769117 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:63769117 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:1037912 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:1037912 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:56416264 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:56416264 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:65731992 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:65731992 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14976434 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14976434 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14989538 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:14989538 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:26108257 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:26108257 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150698835 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150698835 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:155749816 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:155749816 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44575405 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44575405 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107871600 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107871600 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:131240573 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:131240573 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156849731 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156849731 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:162887141 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:162887141 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44467154 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44467154 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:229596336 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:229596336 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:50411470 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:50411470 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:101092311 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:101092311 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:8475302 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:8475302 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:228469925 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:228469925 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:28195734 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:28195734 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:50953623 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:50953623 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44736902 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:44736902 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:4945726 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:4945726 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:142749301 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:142749301 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141618564 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141618564 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:38280368 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:38280368 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:26687944 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:26687944 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3594361 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3594361 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3599032 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3599032 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:131539898 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:131539898 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:131543622 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:131543622 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:138454789 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:138454789 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:103260499 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:103260499 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:9520303 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:9520303 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:112694328 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:112694328 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:176679088 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:176679088 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:176739119 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:176739119 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:72543435 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:72543435 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:113993207 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:113993207 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:91368231 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:91368231 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:55586971 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:55586971 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:56367612 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:56367612 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:99605777 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:99605777 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:1483270 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:1483270 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:178879234 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:178879234 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:183032865 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:183032865 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31855491 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31855491 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:144922181 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:144922181 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:149247555 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:149247555 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:19375913 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:19375913 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:148701329 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:148701329 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:17412722 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:17412722 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:33953821 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:33953821 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:143792076 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:143792076 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:137146475 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:137146475 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:144074870 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:144074870 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:47489237 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:47489237 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:47630501 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:47630501 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151298721 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151298721 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:106507901 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:106507901 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110463174 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110463174 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110483283 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110483283 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:51892577 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:51892577 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:51892618 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:51892618 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155264022 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:155264022 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:63357419 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:63357419 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:186862043 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:186862043 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:59807826 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:59807826 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:84028934 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:84028934 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:81903901 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:81903901 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:75671408 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:75671408 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:95930864 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:95930864 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:38810806 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:38810806 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:132093203 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:132093203 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:155259 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:155259 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:131865972 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:131865972 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156183038 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156183038 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:160221981 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:160221981 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:184084659 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:184084659 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:75050745 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:75050745 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:124532500 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:124532500 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:130869561 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:130869561 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:7642304 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:7642304 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:159632047 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:159632047 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48221105 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48221105 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:111614262 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:111614262 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:43231008 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:43231008 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:43291759 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:43291759 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:173457094 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:173457094 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:23848546 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:23848546 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:3701126 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:3701126 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:9991808 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:9991808 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:27216584 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:27216584 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:43708534 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:43708534 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:43258365 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:43258365 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151373126 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151373126 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:89711766 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:89711766 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:89711768 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:89711768 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:71318472 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:71318472 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:71418572 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:71418572 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:40692537 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:40692537 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:7064445 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:7064445 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:44083586 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:44083586 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:62118377 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:62118377 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55696801 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55696801 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:40770817 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:40770817 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:29651668 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:29651668 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:58383463 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:58383463 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:100154819 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:100154819 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:42972165 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:42972165 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:174726137 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:174726137 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:66273868 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:66273868 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:12626587 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:12626587 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:41657437 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:41657437 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:48145151 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:48145151 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:22349557 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:22349557 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:130970734 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:130970734 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:65088401 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:65088401 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:31923093 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:31923093 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55559582 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55559582 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:79384547 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:79384547 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:79255421 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:79255421 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:103180971 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:103180971 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:103302072 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:103302072 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:8418092 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:8418092 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:73649989 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:73649989 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:16358230 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:16358230 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:240986599 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:240986599 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:90020723 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:90020723 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:33487163 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:33487163 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:12859163 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:12859163 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152289846 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152289846 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152322734 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152322734 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:43383068 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:43383068 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24807532 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24807532 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:87042851 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:87042851 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:21511111 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:21511111 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12923877 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12923877 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12923893 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12923893 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49739886 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49739886 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:25341403 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:25341403 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:78331230 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:78331230 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124764057 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124764057 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124764956 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124764956 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:69606 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:69606 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:39714362 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:39714362 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:35867090 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:35867090 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:39317234 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:39317234 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:110756483 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:110756483 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:4159366 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:4159366 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:45096558 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:45096558 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:108995372 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:108995372 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237604833 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237604833 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237663945 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237663945 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:134988004 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:134988004 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:130465631 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:130465631 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:44368650 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:44368650 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:44377227 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:44377227 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:44392409 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:44392409 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:153830578 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:153830578 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:9980643 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:9980643 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166229922 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166229922 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:75212738 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:75212738 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:30862425 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:30862425 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:177902464 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:177902464 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:169562817 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:169562817 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:83634611 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:83634611 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:83119340 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:83119340 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:9337789 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:9337789 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:48022843 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:48022843 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:55929610 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:55929610 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:56604505 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:56604505 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:35912231 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:35912231 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:61570584 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:61570584 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:167508116 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:167508116 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:50062843 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:50062843 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:26746906 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:26746906 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:30899729 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:30899729 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:102797063 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:102797063 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:67091480 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:67091480 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:67105414 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:67105414 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:57623457 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:57623457 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:46358214 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:46358214 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:50455138 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:50455138 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:51960653 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:51960653 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:164697234 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:164697234 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:46233745 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:46233745 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:160458756 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:160458756 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:43248288 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:43248288 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:25771137 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:25771137 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107355823 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107355823 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:92301298 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:92301298 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:92352885 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:92352885 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:92381932 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:92381932 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:155571805 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:155571805 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:25664258 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:25664258 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124950696 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124950696 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:140064333 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:140064333 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:57185131 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:57185131 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:31838833 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:31838833 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:76047831 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:76047831 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:42335195 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:42335195 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:32650024 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:32650024 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:20639564 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:20639564 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:40405779 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:40405779 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:40657457 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:40657457 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:484837 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:484837 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:21370274 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:21370274 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:20858876 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:20858876 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:70617540 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:70617540 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:56583119 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:56583119 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:18839540 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:18839540 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:71232740 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:71232740 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:71250144 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:71250144 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:246493914 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:246493914 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:10286934 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:10286934 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:127721576 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:127721576 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:51465848 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:51465848 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:26400481 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:26400481 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:70280995 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:70280995 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:130776629 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:130776629 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:65620492 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:65620492 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:158353192 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:158353192 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:186573904 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:186573904 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106602649 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106602649 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106675736 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106675736 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:121483622 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:121483622 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124561531 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:124561531 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:118570891 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:118570891 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:172737190 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:172737190 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:217822357 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:217822357 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:35753651 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:35753651 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:220326797 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:220326797 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:229046398 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:229046398 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:136448318 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:136448318 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158639387 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:158639387 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:45801737 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:45801737 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:60754169 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:60754169 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52544095 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52544095 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:104054168 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:104054168 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:36570494 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:36570494 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152992138 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152992138 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:191865766 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:191865766 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:220478855 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:220478855 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:242439725 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:242439725 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:134916818 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:134916818 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:57234643 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:57234643 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31004636 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31004636 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:53223376 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:53223376 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:70516996 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:70516996 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:70541705 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:70541705 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:109309472 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:109309472 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:12224791 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:12224791 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:152712314 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:152712314 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:64608872 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:64608872 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:9831303 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:9831303 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:99707758 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:99707758 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:118619030 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:118619030 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:9629176 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:9629176 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141672472 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141672472 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:27788318 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:27788318 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131553832 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131553832 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:47569086 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:47569086 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:100020825 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:100020825 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:36365183 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:36365183 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:75901996 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:75901996 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:9656354 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chrX:9656354 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:85446330 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:85446330 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:52943066 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:52943066 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:167794551 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:167794551 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:50786601 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:50786601 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:55204705 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:55204705 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:50696779 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:50696779 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:43552790 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:43552790 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:367049 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:367049 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:11633279 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:11633279 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:137917722 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:137917722 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:138169483 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:138169483 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:66641610 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:66641610 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:70342694 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:70342694 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52263594 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52263594 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:50152086 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:50152086 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:19485681 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:19485681 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:68901247 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:68901247 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:72786482 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:72786482 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:41369228 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:41369228 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:98409463 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:98409463 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60695108 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60695108 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:77685075 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:77685075 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29786290 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29786290 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29904591 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29904591 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:170784353 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:170784353 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:74819085 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:74819085 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12812374 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:12812374 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128696139 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:128696139 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:175355448 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:175355448 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:47468167 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:47468167 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:22318787 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:22318787 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:10998310 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:10998310 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:36513965 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:36513965 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:138266581 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:138266581 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:14369664 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:14369664 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:72948756 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:72948756 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:72975645 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:72975645 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:72983848 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:72983848 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130356637 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130356637 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:43227074 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:43227074 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:39178667 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:39178667 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:80732224 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:80732224 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50479756 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:50479756 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179451144 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179451144 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179495426 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179495426 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179516296 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179516296 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179550424 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179550424 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179647344 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179647344 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:5446825 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:5446825 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:15531374 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:15531374 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:48097132 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:48097132 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:138025394 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:138025394 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:44513508 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:44513508 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:69875591 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:69875591 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:34831772 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:34831772 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:33496791 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:33496791 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:176295409 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:176295409 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:167711389 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:167711389 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:36159321 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:36159321 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:126219000 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:126219000 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:55549429 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:55549429 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:17164019 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr21:17164019 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:36943631 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:36943631 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:133033072 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:133033072 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79835951 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79835951 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79955574 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79955574 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:145650094 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:145650094 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:38791934 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:38791934 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:38937679 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:38937679 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:70853506 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:70853506 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:71036264 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:71036264 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:118492582 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:118492582 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:241907651 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:241907651 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124442342 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124442342 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:1741802 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:1741802 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:32417980 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:32417980 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:167833146 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:167833146 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:79245432 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:79245432 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:31628595 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:31628595 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:183440025 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:183440025 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100395409 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100395409 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:99213630 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:99213630 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:106801184 G>T maps to ENST00000378472 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:106801184 G>T maps to ENST00000378472 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:147106586 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:147106586 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:58096447 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:58096447 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:57290677 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:57290677 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:58570602 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:58570602 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:219520857 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:219520857 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:6976879 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:6976879 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:21552285 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:21552285 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:178369898 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:178369898 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:57199974 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:57199974 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:22775073 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:22775073 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:123982289 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:123982289 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:91402966 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:91402966 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:182027223 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:182027223 T>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:53579878 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:53579878 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:53581252 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:53581252 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:149547489 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:149547489 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:22941891 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:22941891 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:238050951 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:238050951 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:15881309 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:15881309 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:58120016 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:58120016 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:70295153 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:70295153 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:96810319 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:96810319 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:114172843 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:114172843 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:957542 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:957542 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:8757755 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:8757755 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:55193448 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:55193448 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:39466618 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:39466618 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:183963614 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:183963614 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:99702844 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:99702844 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:150239099 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:150239099 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:130011389 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:130011389 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:57279959 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:57279959 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:101857000 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:101857000 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:77021320 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:77021320 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:176926733 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:176926733 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:50346691 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:50346691 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:171530076 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:171530076 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:6804900 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:6804900 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:8132566 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:8132566 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:60499391 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:60499391 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:241826584 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:241826584 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:69462752 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:69462752 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:167489116 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:167489116 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:2658899 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:2658899 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:3783731 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:3783731 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:95172174 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:95172174 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:47497087 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:47497087 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:233409065 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:233409065 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:844020 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:844020 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:121312846 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:121312846 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:101810163 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:101810163 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:94059740 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:94059740 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:107869613 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:107869613 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:36293445 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:36293445 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:128987333 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:128987333 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:153927293 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:153927293 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:67670777 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:67670777 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:36103395 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:36103395 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:58521833 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:58521833 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57926925 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57926925 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57926928 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57926928 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:38891651 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:38891651 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:120886367 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:120886367 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:137206552 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:137206552 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:57509259 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:57509259 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:236647287 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:236647287 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:43830183 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:43830183 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:10637632 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:10637632 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:112030805 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:112030805 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:44102532 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:44102532 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:133844424 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:133844424 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:57420904 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:57420904 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220043542 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220043542 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:47909351 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:47909351 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:24852877 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:24852877 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:150928850 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:150928850 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:44177838 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:44177838 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:5529990 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:5529990 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:135453790 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:135453790 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:145038170 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:145038170 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:50688260 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:50688260 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:813596 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:813596 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:93221713 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:93221713 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:63958712 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:63958712 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:26093248 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:26093248 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:27805722 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:27805722 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:68642539 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:68642539 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:9446814 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:9446814 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:187529056 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:187529056 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:7621668 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:7621668 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:128281393 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:128281393 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:39085177 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:39085177 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:127702909 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:127702909 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:123167987 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:123167987 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:61324716 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:61324716 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:149862005 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:149862005 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:39507673 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:39507673 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:36353525 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:36353525 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:53163419 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:53163419 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:27521160 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:27521160 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:100626007 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:100626007 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:12758246 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:12758246 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:39507344 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:39507344 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:47958731 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:47958731 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:63832037 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:63832037 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:5907028 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:5907028 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:30593106 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:30593106 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr21:42807646 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr21:42807646 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:109614064 A>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:109614064 A>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:20006165 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:20006165 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:112528434 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:112528434 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:24701523 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:24701523 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:101086825 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:101086825 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:87338474 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:87338474 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:150052877 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr6:150052877 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:101097623 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:101097623 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:248166560 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:248166560 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:20248373 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:20248373 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:74719204 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:74719204 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:56151210 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:56151210 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:67590321 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:67590321 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:151199725 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:151199725 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:102048819 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:102048819 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:18775902 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:18775902 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:113253278 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:113253278 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr21:43235955 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr21:43235955 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:97345600 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:97345600 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:62109952 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:62109952 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220172088 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220172088 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:96518630 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:96518630 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:156468277 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:156468277 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:237765272 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:237765272 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:134990415 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:134990415 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:27764654 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:27764654 T>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:28542582 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:28542582 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:481754 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:481754 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:62559099 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:62559099 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:127569612 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:127569612 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96954352 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96954352 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96954535 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96954535 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96955765 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96955765 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:12492471 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:12492471 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:26906505 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:26906505 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:26906891 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:26906891 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:88411707 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr4:88411707 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:89611236 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:89611236 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:41240754 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:41240754 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:66774545 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:66774545 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:23808897 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:23808897 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:46307603 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr20:46307603 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:39957425 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:39957425 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:64560011 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:64560011 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:60650571 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:60650571 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:140022503 C>G maps to ENST00000252100 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:140022503 C>G maps to ENST00000252100 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:129558264 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:129558264 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:239237472 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:239237472 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:234663632 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:234663632 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:58297003 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:58297003 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:151162736 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:151162736 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:224592296 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:224592296 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:109524335 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:109524335 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:109525146 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:109525146 C>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:1197890 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:1197890 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:129338801 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chrX:129338801 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:148875643 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:148875643 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:7568008 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:7568008 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:51355659 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:51355659 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:44073112 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:44073112 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:61560932 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:61560932 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:37395061 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:37395061 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:161161358 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:161161358 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:132232969 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:132232969 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:137708922 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:137708922 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:213173563 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:213173563 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:99703973 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:99703973 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:29385536 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:29385536 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:21227800 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:21227800 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:35177044 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:35177044 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:6500537 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:6500537 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:69015177 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:69015177 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:131785406 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:131785406 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:117067402 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:117067402 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:23632622 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:23632622 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:92447334 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:92447334 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:26406113 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:26406113 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:58711506 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:58711506 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:49907256 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:49907256 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:61150821 C>A maps to ENST00000370523 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:61150821 C>A maps to ENST00000370523 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:134344704 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:134344704 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr21:30437137 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr21:30437137 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:74493635 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:74493635 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:112648392 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:112648392 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:21884523 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:21884523 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:1636200 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:1636200 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:125769565 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:125769565 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:228141210 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:228141210 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:27021695 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:27021695 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10854003 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10854003 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:2967669 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:2967669 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:56090655 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:56090655 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:36397147 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:36397147 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:234345146 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:234345146 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:42734298 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:42734298 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:41224741 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:41224741 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:38821162 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:38821162 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr9:286374 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr9:286374 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:32455080 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:32455080 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:142566704 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:142566704 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:50681198 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:50681198 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:169495106 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:169495106 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:223507470 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:223507470 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:126320095 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:126320095 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:157789732 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:157789732 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:102520992 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:102520992 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:159672276 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:159672276 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:27573900 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:27573900 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:173233038 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:173233038 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:100973851 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:100973851 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:120582883 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:120582883 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:150727163 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:150727163 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:142732384 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:142732384 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:73944271 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:73944271 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:115344099 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:115344099 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:37835508 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:37835508 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:54404778 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:54404778 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:21978519 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:21978519 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:10385770 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:10385770 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:6054741 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:6054741 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:78768406 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:78768406 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:31340627 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:31340627 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:19389487 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:19389487 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:78704760 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:78704760 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:78850107 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:78850107 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:34787315 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:34787315 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:55367168 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:55367168 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:72301141 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:72301141 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:1896250 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:1896250 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:57803499 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:57803499 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55362608 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55362608 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:36353589 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:36353589 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:104145919 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:104145919 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:3827063 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:3827063 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:129781555 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:129781555 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:152573496 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:152573496 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:169690007 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:169690007 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:54772209 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:54772209 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:141459599 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:141459599 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:141771367 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:141771367 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:46910925 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:46910925 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:101601584 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:101601584 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:150325153 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:150325153 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:136633808 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:136633808 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:21903726 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:21903726 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:146545336 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:146545336 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:816832 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:816832 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:149907292 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:149907292 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:44179329 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:44179329 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:78522409 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:78522409 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:78582021 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:78582021 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:15448271 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:15448271 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:152410560 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:152410560 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:7079482 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:7079482 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:5947542 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:5947542 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:107824634 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:107824634 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:79175458 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:79175458 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:183992954 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:183992954 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:51065568 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:51065568 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:165863703 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:165863703 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:120549619 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:120549619 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:57334085 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:57334085 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:6257123 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:6257123 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:67576683 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:67576683 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:28823790 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:28823790 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:81924972 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:81924972 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:103041708 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:103041708 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:48457874 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:48457874 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:43550266 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:43550266 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:40558209 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:40558209 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:129780556 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:129780556 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:57472447 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:57472447 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:54408043 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:54408043 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:43359625 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:43359625 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:43697575 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:43697575 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:43674195 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:43674195 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:77317755 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:77317755 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:198703690 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:198703690 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55709949 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55709949 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:1687405 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:1687405 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:69061083 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:69061083 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:120342586 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:120342586 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:111752237 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:111752237 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:49583305 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:49583305 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:40245634 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:40245634 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:84563688 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:84563688 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:25374382 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:25374382 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:13978177 T>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:13978177 T>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:219536739 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:219536739 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:18548912 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:18548912 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:172395744 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:172395744 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:152023254 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:152023254 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237796725 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237796725 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237870137 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237870137 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:33992097 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:33992097 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:128922247 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chrX:128922247 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:28330265 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:28330265 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:165956738 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:165956738 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:10596035 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:10596035 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:4013979 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:4013979 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:39555225 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:39555225 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:18508361 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:18508361 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:52476382 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:52476382 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:242283101 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:242283101 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:149897704 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:149897704 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:129284064 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:129284064 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:308149 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:308149 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:21448520 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:21448520 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:101826598 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:101826598 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:64422274 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:64422274 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:231109863 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:231109863 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:32934107 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:32934107 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:59485385 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:59485385 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:56719996 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr15:56719996 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:10411642 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:10411642 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:2320933 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:2320933 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:79378184 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr5:79378184 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:371053 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:371053 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr21:32559571 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr21:32559571 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:76129380 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:76129380 C>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:72332678 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:72332678 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr21:45506568 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr21:45506568 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:3425784 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:3425784 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:46846244 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:46846244 T>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:29171840 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:29171840 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:190993145 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:190993145 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:49842190 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:49842190 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:71036197 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:71036197 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:52293266 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:52293266 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:67292371 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:67292371 T>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:54603281 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:54603281 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:22932207 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr18:22932207 C>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:12491137 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:12491137 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:56702189 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:56702189 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:1046442 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:1046442 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:147124512 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:147124512 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:74143931 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:74143931 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:136287522 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:136287522 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:5239671 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:5239671 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:46602441 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:46602441 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:31120329 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:31120329 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:86790879 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:86790879 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:4772769 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:4772769 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:77783986 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:77783986 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:77783988 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:77783988 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:56196187 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:56196187 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:74012896 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:74012896 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:51294664 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:51294664 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:161192882 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:161192882 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:68962476 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:68962476 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:17949409 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:17949409 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:155922402 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:155922402 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:97499141 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:97499141 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:3831393 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:3831393 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:8110860 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:8110860 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:69900822 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:69900822 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:235628936 C>T maps to ENST00000313984 *327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:235628936 C>T maps to ENST00000313984 *327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:11039131 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:11039131 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:69943123 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:69943123 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:70049173 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:70049173 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:61869893 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:61869893 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:66105333 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:66105333 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:93702080 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:93702080 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:16720843 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:16720843 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:82783570 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:82783570 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:58471746 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:58471746 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:169393968 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:169393968 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:170940730 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:170940730 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:92697129 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:92697129 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:55175476 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:55175476 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:46122225 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:46122225 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:33668478 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:33668478 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:49731115 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:49731115 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:140870355 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:140870355 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:48681815 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:48681815 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:81620634 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:81620634 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:18803320 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:18803320 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:44130000 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:44130000 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:188280539 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:188280539 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:93055954 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:93055954 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:223943127 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:223943127 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:2969503 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:2969503 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:115457382 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:115457382 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:219895375 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:219895375 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:92979152 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:92979152 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:49106051 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:49106051 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:34432749 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:34432749 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:50055773 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:50055773 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:43857966 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:43857966 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:118184375 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:118184375 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:535738 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:535738 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:24498637 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:24498637 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:25543582 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:25543582 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:123162869 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:123162869 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:109810124 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:109810124 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:49060555 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:49060555 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:117233360 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:117233360 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:7812155 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:7812155 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:72783309 G>T maps to NM_001039840.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:72783309 G>T maps to NM_001039840.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:136622960 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:136622960 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:27328453 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:27328453 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:1499151 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:1499151 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:36219570 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:36219570 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:140281838 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:140281838 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:87644950 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:87644950 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:39177504 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:39177504 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:230824386 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:230824386 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:139727920 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:139727920 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:189872190 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:189872190 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:125530732 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:125530732 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:207881716 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:207881716 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:3781736 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:3781736 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:149435007 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:149435007 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:31636451 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:31636451 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:88061182 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:88061182 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:119693909 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:119693909 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:107968499 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:107968499 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:111744578 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:111744578 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:83126379 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:83126379 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:50830430 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:50830430 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:50830432 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:50830432 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:143957315 G>T maps to ENST00000426487 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:143957315 G>T maps to ENST00000426487 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:96535106 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:96535106 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:6523594 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:6523594 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:109292268 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:109292268 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:16633689 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:16633689 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:42811534 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:42811534 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:176894941 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:176894941 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:100715502 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:100715502 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:125686609 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:125686609 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:55041977 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:55041977 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:74107366 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:74107366 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:19030528 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:19030528 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:169300988 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:169300988 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:117165722 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:117165722 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:24113954 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:24113954 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:39042905 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:39042905 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:31838261 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:31838261 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:51829082 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:51829082 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:6727752 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:6727752 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:25498279 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:25498279 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:220246036 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:220246036 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:117731319 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:117731319 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:89696933 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:89696933 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:162850028 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:162850028 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:174870191 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:174870191 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:113286121 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:113286121 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:167082838 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:167082838 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:77427621 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:77427621 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:57897520 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:57897520 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:3985483 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:3985483 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:13621270 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:13621270 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:71745746 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:71745746 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:100375677 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:100375677 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:14762137 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:14762137 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:66189811 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:66189811 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:220152741 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:220152741 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:95653541 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:95653541 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:27285493 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:27285493 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:66112530 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:66112530 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:184793596 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:184793596 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:220045999 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:220045999 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:30876531 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:30876531 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153735086 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153735086 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153740154 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153740154 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:85139057 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:85139057 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:187557735 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:187557735 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:102667817 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:102667817 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:121345491 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:121345491 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:161647045 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:161647045 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:125061725 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:125061725 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:39978384 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:39978384 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:71364201 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:71364201 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:128486326 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:128486326 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:49469794 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:49469794 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:96650971 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:96650971 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:111983190 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:111983190 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:47033556 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:47033556 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:89967796 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:89967796 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:104121693 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:104121693 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:89525149 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:89525149 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:72631443 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:72631443 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:76979736 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:76979736 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:13365945 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:13365945 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:30538723 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:30538723 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:6644574 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:6644574 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:58605720 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:58605720 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:150948568 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:150948568 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:65130898 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:65130898 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:37378684 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:37378684 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:96698022 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:96698022 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:27226999 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:27226999 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:27210846 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:27210846 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:66935842 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:66935842 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:3005808 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:3005808 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:3005818 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:3005818 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:119760365 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:119760365 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:33516593 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:33516593 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:52713653 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:52713653 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:14778521 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:14778521 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:144918639 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:144918639 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:18536023 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:18536023 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:28358496 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:28358496 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:210560771 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:210560771 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:186077557 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:186077557 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:100203146 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:100203146 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:25944656 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:25944656 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:3211508 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:3211508 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:94274975 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:94274975 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:206972207 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:206972207 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:104992802 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:104992802 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:6241677 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:6241677 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:1412843 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:1412843 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:78770838 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:78770838 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:31422282 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:31422282 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:6082073 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:6082073 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:6082076 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:6082076 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:61613002 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:61613002 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:196394950 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:196394950 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:84895173 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:84895173 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:20992909 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:20992909 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:72348837 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:72348837 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55290252 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55290252 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55272085 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55272085 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55272323 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55272323 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70281745 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70281745 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70456366 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70456366 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:91854968 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:91854968 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:53187744 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:53187744 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:52944033 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:52944033 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:31874501 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:31874501 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:25930941 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:25930941 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:54872461 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:54872461 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:129635774 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:129635774 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:107708661 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:107708661 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:225594241 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:225594241 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:16504593 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:16504593 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:18424598 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:18424598 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:66066916 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:66066916 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:148021472 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:148021472 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:148342290 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:148342290 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:82418778 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:82418778 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:141079782 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:141079782 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:116163901 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:116163901 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:55013425 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:55013425 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:148797198 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:148797198 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:21216885 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:21216885 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:45762187 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:45762187 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:18256518 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:18256518 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:47796221 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:47796221 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:98017263 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:98017263 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:6335060 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:6335060 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:49952854 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:49952854 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:116371663 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:116371663 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:106224775 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:106224775 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:17080453 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:17080453 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:60231747 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:60231747 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:10102508 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:10102508 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:149826537 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:149826537 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:17162059 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:17162059 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:7873740 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:7873740 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:110019128 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:110019128 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:15843973 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:15843973 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:10235578 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:10235578 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:108147248 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:108147248 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:10443452 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:10443452 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:109507930 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:109507930 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:109550504 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:109550504 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:27401670 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:27401670 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:8642128 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:8642128 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:17741218 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:17741218 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153197640 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153197640 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:105893627 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:105893627 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:201781871 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:201781871 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:78531251 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:78531251 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:100413657 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:100413657 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:54930661 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:54930661 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:1816033 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:1816033 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:42070893 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:42070893 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:119059435 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:119059435 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:32774718 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:32774718 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:115411724 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:115411724 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:152027284 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:152027284 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:152031271 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:152031271 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:17669289 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:17669289 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:154030965 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:154030965 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:101092850 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:101092850 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:21737754 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:21737754 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:47201707 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:47201707 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:34649298 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:34649298 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:150839404 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:150839404 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:91715530 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:91715530 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:53848678 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:53848678 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:178565766 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:178565766 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:183129157 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:183129157 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:119133731 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:119133731 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:73450068 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:73450068 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:47486893 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:47486893 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:16203296 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:16203296 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:25144804 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:25144804 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:42373658 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:42373658 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:113812391 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:113812391 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:8745781 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:8745781 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:67864298 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:67864298 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:150130987 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:150130987 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153036199 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153036199 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153039555 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:153039555 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:160221591 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:160221591 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:75103856 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:75103856 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:54974907 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:54974907 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:47265823 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:47265823 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:47276714 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:47276714 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:126887379 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:126887379 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:7435590 A>T maps to NM_001085382.1 L339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:7435590 A>T maps to NM_001085382.1 L339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:86357892 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:86357892 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:109371227 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:109371227 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:36271473 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:36271473 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:25621955 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:25621955 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:127979268 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:127979268 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:36164287 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:36164287 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:79314113 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:79314113 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:45529039 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:45529039 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:103270308 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:103270308 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:104671645 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:104671645 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:210867543 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:210867543 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:55475658 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:55475658 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:6820615 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:6820615 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:16635618 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:16635618 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:41767679 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:41767679 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:237608682 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:237608682 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:153520342 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:153520342 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:45784959 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:45784959 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:23932671 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:23932671 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:31191695 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:31191695 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:165948712 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:165948712 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:169701110 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:169701110 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:84657649 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:84657649 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:61160413 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr18:61160413 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:2769171 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:2769171 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:2829096 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:2829096 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:51215466 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:51215466 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:51123180 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:51123180 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:48511279 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:48511279 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:3669763 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:3669763 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:52034801 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:52034801 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:87476205 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:87476205 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:50489982 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:50489982 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:99086536 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:99086536 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:95202785 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:95202785 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:128851662 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:128851662 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:108389287 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:108389287 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:23818248 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:23818248 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:34206306 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:34206306 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:218023994 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:218023994 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:220353066 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:220353066 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:167675579 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:167675579 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:55648818 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:55648818 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:70856806 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:70856806 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:52546574 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:52546574 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:81837205 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:81837205 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:125474278 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:125474278 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:56136147 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:56136147 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:13030144 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:13030144 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:152470488 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:152470488 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:70608420 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:70608420 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:17446354 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:17446354 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:13325493 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:13325493 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:106083269 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:106083269 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:79278744 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:79278744 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:55208654 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:55208654 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:114290774 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:114290774 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:133941458 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:133941458 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:11419040 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:11419040 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:84206062 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:84206062 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:60598334 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:60598334 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:81628883 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:81628883 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:19475404 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:19475404 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:177019410 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:177019410 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:5748289 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:5748289 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:15470799 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:15470799 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:19687579 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:19687579 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:101277997 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:101277997 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:12198275 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:12198275 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:18206058 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:18206058 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:72372513 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:72372513 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:144344275 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:144344275 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:186308928 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:186308928 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:3427382 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:3427382 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:54467092 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:54467092 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:118974749 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:118974749 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:126220155 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:126220155 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:17517099 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:17517099 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:215844673 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:215844673 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:133316687 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:133316687 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:150572276 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:150572276 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:28872557 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:28872557 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:36581310 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:36581310 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:128888568 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:128888568 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:100386738 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:100386738 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:37354612 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:37354612 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:128962855 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chrX:128962855 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:106431024 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:106431024 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:3834765 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:3834765 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:38108173 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:38108173 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:22255607 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:22255607 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:99160441 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:99160441 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:21605966 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:21605966 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:135123551 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:135123551 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:57876405 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:57876405 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:81557433 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:81557433 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:53905467 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:53905467 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:22574229 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:22574229 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:238051639 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:238051639 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:238051836 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:238051836 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:49983224 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:49983224 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:58556757 G>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:58556757 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:9005035 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:9005035 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:94466730 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:94466730 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:229657240 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:229657240 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20685794 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20685794 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:101560335 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:101560335 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:50453795 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:50453795 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:156758098 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:156758098 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:44071762 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:44071762 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:44076893 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:44076893 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:73974830 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:73974830 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:70817760 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:70817760 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20471316 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20471316 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20430530 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20430530 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20451363 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20451363 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:35084279 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:35084279 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:236883599 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:236883599 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:98273825 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:98273825 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:156917528 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:156917528 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33595907 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33595907 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33641838 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33641838 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33881699 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33881699 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:5209202 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:5209202 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:64635301 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:64635301 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:84705801 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:84705801 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:131915977 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:131915977 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:132051587 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:132051587 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:31142996 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:31142996 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:70922829 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:70922829 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:3769779 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:3769779 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:67051309 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:67051309 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:58125462 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:58125462 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:50311572 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:50311572 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:241808246 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:241808246 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:241808787 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:241808787 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:143654648 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:143654648 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:117130608 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:117130608 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:105251011 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:105251011 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:45920274 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:45920274 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:56171049 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:56171049 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:233274208 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:233274208 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:104234118 C>T maps to NM_001008219.1 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:104234118 C>T maps to NM_001008219.1 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:111562850 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:111562850 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:110471813 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:110471813 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:37490349 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:37490349 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52281842 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52281842 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:197890024 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:197890024 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:36478689 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:36478689 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:101462131 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:101462131 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:45771746 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:45771746 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:69318113 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:69318113 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:72047595 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:72047595 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:159557684 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:159557684 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:10493732 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:10493732 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:116701619 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:116701619 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:64219733 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:64219733 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:36595485 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:36595485 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:25232972 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:25232972 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:115336379 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:115336379 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:35235334 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:35235334 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6876035 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6876035 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119112484 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119112484 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:27105436 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:27105436 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:80886055 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:80886055 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:35771055 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:35771055 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:123254504 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:123254504 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:100978645 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:100978645 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26839172 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26839172 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:62159784 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:62159784 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176934191 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176934191 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17327032 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17327032 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194147763 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194147763 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:152834702 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:152834702 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:130716648 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:130716648 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:667085 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:667085 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:40666087 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:40666087 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:70231465 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:70231465 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:33113436 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:33113436 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79430554 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79430554 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:69949001 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:69949001 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:70064119 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:70064119 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:72903482 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:72903482 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:52583431 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:52583431 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:18138475 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:18138475 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:45253504 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:45253504 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:53793906 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:53793906 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:22058732 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:22058732 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:31626597 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:31626597 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:36937288 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:36937288 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:65944153 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:65944153 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:50374055 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:50374055 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:36337045 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:36337045 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:79937888 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:79937888 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:107914416 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:107914416 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:61539443 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:61539443 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:103695874 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:103695874 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:57076089 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:57076089 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:45372553 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:45372553 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:58563715 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:58563715 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:60925283 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:60925283 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:73852261 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:73852261 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:74729845 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:74729845 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:20948749 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:20948749 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:244653794 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:244653794 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:200869433 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:200869433 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:12819148 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:12819148 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:57206347 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:57206347 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:57252711 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:57252711 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:35731303 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:35731303 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:37459131 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:37459131 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:14706638 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:14706638 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:43496006 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:43496006 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:165714964 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:165714964 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:109480314 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:109480314 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:151917458 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:151917458 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:39364587 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:39364587 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34382652 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34382652 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34401171 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34401171 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:13476085 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:13476085 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:53766832 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:53766832 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:181479549 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:181479549 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:201010573 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:201010573 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:54914902 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:54914902 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:55107417 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:55107417 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:37343026 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:37343026 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:86062197 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:86062197 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:86062312 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:86062312 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:93108584 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:93108584 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:110813915 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:110813915 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:44149081 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:44149081 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:42694166 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:42694166 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:116552118 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:116552118 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:71015815 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:71015815 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142985677 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142985677 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142988853 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142988853 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:119103471 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:119103471 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:33392058 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:33392058 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:13862618 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:13862618 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:139100940 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:139100940 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:41828653 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:41828653 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:75401181 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:75401181 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:34431160 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:34431160 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2506487 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2506487 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:62100261 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:62100261 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:28946890 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:28946890 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:47544175 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:47544175 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:72619715 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:72619715 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:35222538 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:35222538 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:207925394 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:207925394 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:24509641 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:24509641 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:64982667 G>T maps to ENST00000394156 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:64982667 G>T maps to ENST00000394156 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:21882678 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:21882678 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:68867466 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:68867466 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:59166402 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:59166402 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:61689332 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:61689332 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:61747893 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:61747893 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26905982 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26905982 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26988178 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26988178 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:40027945 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:40027945 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:125889438 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:125889438 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:51982016 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:51982016 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47499058 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47499058 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:11371045 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:11371045 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:72579803 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:72579803 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:122724330 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:122724330 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134280211 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134280211 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:55844394 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:55844394 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:126486080 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:126486080 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:73584500 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:73584500 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:29252201 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:29252201 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:110002764 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:110002764 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184106610 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184106610 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:120142046 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:120142046 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:120198708 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:120198708 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:143027814 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:143027814 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:143043956 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:143043956 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:1504332 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:1504332 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:139889750 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:139889750 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:29366549 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:29366549 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:10559967 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:10559967 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:1324023 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:1324023 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:45496194 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:45496194 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:87670062 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:87670062 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:87752011 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:87752011 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:58590675 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:58590675 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:246805167 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:246805167 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:74414577 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:74414577 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:99931811 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:99931811 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:147964247 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:147964247 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:125505040 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:125505040 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:125669150 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:125669150 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:51258798 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:51258798 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:71634930 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:71634930 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48274239 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48274239 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139642860 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139642860 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139838846 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139838846 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:86282600 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:86282600 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:116945371 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:116945371 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:116956583 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:116956583 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:7415222 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:7415222 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:48389269 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:48389269 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:111114600 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:111114600 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:189918981 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:189918981 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47409705 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47409705 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47545031 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47545031 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:238261290 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:238261290 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:47666999 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:47666999 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:166414460 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:166414460 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:87563526 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:87563526 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:89651112 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:89651112 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:211512573 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:211512573 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:50200733 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:50200733 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:1326949 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:1326949 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:5844794 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:5844794 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:37325609 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:37325609 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:34090637 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:34090637 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113249396 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113249396 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113348835 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113348835 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113599537 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113599537 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:23473739 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:23473739 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:11397028 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:11397028 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:70281043 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:70281043 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:16990392 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:16990392 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:48996896 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:48996896 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:47810943 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:47810943 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:105883728 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:105883728 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:202933913 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:202933913 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:7693861 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:7693861 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:42012969 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:42012969 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:1028167 C>A maps to ENST00000415893 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:1028167 C>A maps to ENST00000415893 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:39390450 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:39390450 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:14071858 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:14071858 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:50734290 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:50734290 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:114128670 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:114128670 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:169182256 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:169182256 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:126219750 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:126219750 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:197510275 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:197510275 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:9225134 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:9225134 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:50146660 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:50146660 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:41567677 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:41567677 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:61537158 C>T maps to NM_022105.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:61537158 C>T maps to NM_022105.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:35351023 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:35351023 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:46288026 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:46288026 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:52397185 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:52397185 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20952874 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20952874 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:21049073 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:21049073 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:11757755 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:11757755 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:96394795 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:96394795 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:28537038 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:28537038 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:67406110 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:67406110 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:37652538 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:37652538 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:162876716 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:162876716 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:74747217 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:74747217 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:174870122 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:174870122 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113281703 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113281703 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113288936 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113288936 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:28574488 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:28574488 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:117403063 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:117403063 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:4711895 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:4711895 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:109524267 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:109524267 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:67915483 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:67915483 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:128077254 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:128077254 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:28396154 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:28396154 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:16948122 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:16948122 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:19984597 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:19984597 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:55220428 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:55220428 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:110915768 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:110915768 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:34396263 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:34396263 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:34398173 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:34398173 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:65351611 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:65351611 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184038792 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184038792 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:27987004 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:27987004 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:48519418 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:48519418 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:43843781 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:43843781 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:40272052 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:40272052 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:139946603 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:139946603 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:131211390 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:131211390 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:89498603 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:89498603 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134670922 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134670922 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134851907 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134851907 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134967079 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:134967079 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:213291208 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:213291208 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:133502043 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:133502043 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:133692394 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:133692394 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:66115102 T>A maps to ENST00000370616 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:66115102 T>A maps to ENST00000370616 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:66115228 A>G maps to ENST00000370616 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:66115228 A>G maps to ENST00000370616 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:169500371 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:169500371 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:82392895 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:82392895 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:54162860 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:54162860 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:143056552 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:143056552 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:71138168 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:71138168 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139380381 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139380381 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:175488842 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:175488842 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:187625983 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:187625983 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:30921764 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:30921764 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:91549143 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:91549143 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:68587837 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:68587837 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:113264807 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:113264807 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:72109162 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:72109162 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:40705717 T>G maps to NM_001083124.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:40705717 T>G maps to NM_001083124.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:89831492 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:89831492 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:89821876 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:89821876 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:170394673 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:170394673 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:92569683 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:92569683 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126329537 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126329537 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126367446 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126367446 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:45960904 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:45960904 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48776241 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48776241 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:127644852 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:127644852 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:175158773 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:175158773 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17893781 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17893781 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:157670327 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:157670327 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:7344742 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:7344742 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76124322 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76124322 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:78395812 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:78395812 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128489168 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128489168 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128497098 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128497098 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:240334510 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:240334510 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:203322651 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:203322651 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:216288039 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:216288039 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27715495 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27715495 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:114284716 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:114284716 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:114299758 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:114299758 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:126139200 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:126139200 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:49409473 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:49409473 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:132556279 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:132556279 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:162402416 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:162402416 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:52781423 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:52781423 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:169764032 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:169764032 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:169764699 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:169764699 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:17468823 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:17468823 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:29549973 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:29549973 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:46314443 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:46314443 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:161116239 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:161116239 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:160761928 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:160761928 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:46066628 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:46066628 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:27772564 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:27772564 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26512675 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26512675 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:30886020 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:30886020 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:30953227 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:30953227 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:155115716 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:155115716 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:101011607 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:101011607 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:89573836 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:89573836 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:163212933 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:163212933 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:44187203 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:44187203 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:55099762 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:55099762 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:76928509 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:76928509 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:76982462 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:76982462 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:23499846 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:23499846 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:31013851 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:31013851 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:42467833 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:42467833 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:59597020 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:59597020 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150417045 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150417045 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150327049 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150327049 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:85715100 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:85715100 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:141932243 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:141932243 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:134244848 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:134244848 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:8099629 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:8099629 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:6606738 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:6606738 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:39053882 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:39053882 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151234797 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151234797 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:183933276 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:183933276 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:235779453 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:235779453 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:93536189 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:93536189 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:167761333 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:167761333 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21654938 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21654938 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117753474 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117753474 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:101165668 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:101165668 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:58756014 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:58756014 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:135435658 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:135435658 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:131605354 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:131605354 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:154145200 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:154145200 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:165404371 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:165404371 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:158142989 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:158142989 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:93511212 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:93511212 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:94344162 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:94344162 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:94377138 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:94377138 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:102372693 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:102372693 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:102483212 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:102483212 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:27474766 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:27474766 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:54857219 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:54857219 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:106698005 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:106698005 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:105198210 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:105198210 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:119929174 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:119929174 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:13540102 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:13540102 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:240111859 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:240111859 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:19015354 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:19015354 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:19015372 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:19015372 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:41045868 G>C maps to ENST00000296803 Y606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:41045868 G>C maps to ENST00000296803 Y606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:41070935 C>A maps to ENST00000296803 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:41070935 C>A maps to ENST00000296803 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:93839113 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:93839113 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79660634 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79660634 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42739588 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42739588 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:31245299 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:31245299 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:32918135 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:32918135 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33074437 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33074437 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:221054756 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:221054756 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:162902407 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:162902407 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:173531354 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:173531354 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:12875624 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:12875624 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:54428046 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:54428046 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:11276335 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:11276335 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:148731070 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:148731070 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:44217662 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:44217662 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:22211674 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:22211674 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113849820 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113849820 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113850013 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113850013 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:154863468 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:154863468 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:21186873 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:21186873 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27677165 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27677165 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:65621516 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:65621516 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:23508208 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:23508208 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:201195084 G>T maps to NM_001164586.1 A3540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:201195084 G>T maps to NM_001164586.1 A3540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:99008137 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:99008137 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50444526 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50444526 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50455012 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50455012 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:154422368 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:154422368 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:10791820 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:10791820 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76715291 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76715291 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:121107468 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:121107468 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:7267320 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:7267320 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:44432189 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:44432189 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:75948541 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:75948541 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:10251391 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:10251391 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:78786159 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:78786159 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:52223408 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:52223408 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31435571 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31435571 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:187487163 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:187487163 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31392967 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31392967 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:52813405 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:52813405 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:7785053 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:7785053 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:52863334 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:52863334 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:7679179 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:7679179 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:48832204 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:48832204 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:27056273 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:27056273 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:124153413 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:124153413 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:155893838 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:155893838 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:21305380 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:21305380 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:155711840 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:155711840 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:38822692 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:38822692 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36746651 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36746651 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:67354438 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:67354438 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142649456 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142649456 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142658593 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142658593 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:48424219 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:48424219 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:48459807 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:48459807 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:43896123 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:43896123 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:8777736 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:8777736 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34971832 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34971832 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44681699 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44681699 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:44889628 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:44889628 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:43004469 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:43004469 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:72346767 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:72346767 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:241684802 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:241684802 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4905590 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4905590 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:200969509 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:200969509 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55331551 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55331551 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55347304 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55347304 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43034678 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43034678 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:70413316 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:70413316 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:139164537 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:139164537 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:135012915 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:135012915 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:123054127 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:123054127 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:66033163 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:66033163 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:160231983 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:160231983 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:10673554 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:10673554 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:39594723 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:39594723 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:53001920 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:53001920 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52758012 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52758012 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31654362 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31654362 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119199120 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119199120 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119207714 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119207714 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6986081 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6986081 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:7026163 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:7026163 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:211301245 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:211301245 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:33777774 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:33777774 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:128990584 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:128990584 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:128990590 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:128990590 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:30457384 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:30457384 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152538379 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152538379 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:46705122 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:46705122 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:202274742 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:202274742 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:202275934 G>T maps to ENST00000487787 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:202275934 G>T maps to ENST00000487787 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:104309859 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:104309859 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:54733674 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:54733674 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55175172 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55175172 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:161010784 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:161010784 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:161021897 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:161021897 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:34654912 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:34654912 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:62897362 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:62897362 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:197581338 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:197581338 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100179905 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100179905 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:133868683 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:133868683 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141115484 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141115484 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141771401 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141771401 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:68216546 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:68216546 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194365489 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194365489 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47630706 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47630706 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47630708 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:47630708 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6497950 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6497950 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:41799190 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:41799190 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42445655 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42445655 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:39910298 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:39910298 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:166962129 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:166962129 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:140969829 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:140969829 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:51641312 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:51641312 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:54839520 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:54839520 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:71499716 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:71499716 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:21208332 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:21208332 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:12011083 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:12011083 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:114181760 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:114181760 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:46488513 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:46488513 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:31187961 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:31187961 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:151067806 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:151067806 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:60028129 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:60028129 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:48664594 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:48664594 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:88119487 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:88119487 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64574889 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64574889 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:82336978 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:82336978 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:141756801 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:141756801 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:74865024 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:74865024 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:135102758 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:135102758 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:19418492 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:19418492 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:1474409 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:1474409 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:50925376 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:50925376 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:40831401 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:40831401 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:37053460 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:37053460 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:20363642 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:20363642 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4965225 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4965225 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:62931365 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:62931365 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:132694183 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:132694183 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:123661342 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:123661342 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56348978 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56348978 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56353092 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56353092 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56355089 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56355089 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66204239 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66204239 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60561425 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60561425 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60561636 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60561636 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60269327 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60269327 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60170261 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60170261 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:47693792 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:47693792 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:120802650 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:120802650 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:56685901 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:56685901 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:124641010 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:124641010 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:8998799 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:8998799 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9027156 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9027156 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:42767730 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:42767730 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47361428 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47361428 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48443857 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48443857 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108178189 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108178189 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:10411637 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:10411637 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:10430129 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:10430129 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:23889039 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:23889039 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:169492397 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:169492397 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:16818320 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:16818320 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26219708 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26219708 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26243964 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26243964 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26465557 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26465557 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:24394529 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:24394529 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:89916045 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:89916045 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:164061308 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:164061308 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:201763727 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:201763727 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:16894764 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:16894764 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:16901191 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:16901191 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:71186019 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:71186019 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:124824777 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:124824777 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:124832359 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:124832359 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:119114990 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:119114990 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:152466263 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:152466263 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:130962247 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:130962247 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:182542477 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:182542477 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:29587340 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:29587340 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:204931403 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:204931403 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:41236591 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:41236591 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:103964407 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:103964407 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:42072749 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:42072749 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:236205612 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:236205612 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:51228416 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:51228416 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:63777549 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:63777549 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:160968013 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:160968013 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:15210429 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:15210429 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:43700437 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:43700437 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:203156053 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:203156053 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:32187891 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:32187891 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:120430234 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:120430234 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:155728184 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:155728184 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:62738220 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:62738220 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:132411690 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:132411690 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:107801018 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:107801018 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:78709847 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:78709847 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:135114691 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:135114691 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:102343778 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:102343778 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228466353 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228466353 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:8249254 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:8249254 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:44713895 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:44713895 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:102296164 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:102296164 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:2966340 C>A maps to ENST00000333466 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:2966340 C>A maps to ENST00000333466 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:29054079 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:29054079 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:248099959 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:248099959 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:55339562 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:55339562 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:58170885 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:58170885 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179247687 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179247687 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:146065661 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:146065661 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:38293722 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:38293722 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:34496379 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:34496379 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17586064 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17586064 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176679022 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176679022 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:118974271 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:118974271 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:122278544 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:122278544 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44587857 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44587857 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127253160 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127253160 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127253427 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127253427 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:91091045 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:91091045 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:91369066 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:91369066 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrY:5441469 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrY:5441469 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:55566949 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:55566949 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:56360516 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:56360516 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140180779 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140180779 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66638671 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66638671 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:20705459 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:20705459 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:144857555 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:144857555 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:58273272 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:58273272 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:149278101 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:149278101 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76704899 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76704899 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76707809 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76707809 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:176917951 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:176917951 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:70154663 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:70154663 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:15222080 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:15222080 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:73438908 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:73438908 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66235584 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66235584 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:61017554 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:61017554 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:41704542 T>C maps to ENST00000394278 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:41704542 T>C maps to ENST00000394278 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:71732162 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:71732162 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:31688259 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:31688259 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:77026747 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:77026747 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:81248837 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:81248837 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:51619798 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:51619798 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:20466627 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:20466627 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:8720963 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:8720963 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:9402201 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:9402201 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:9417851 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:9417851 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:242451548 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:242451548 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:43970131 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:43970131 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:57752455 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:57752455 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:208213452 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:208213452 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:131872378 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:131872378 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118199463 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118199463 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118231257 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118231257 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:7605695 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:7605695 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:140358737 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:140358737 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:37489453 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:37489453 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119367551 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119367551 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:81762454 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:81762454 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:81768260 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:81768260 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:57046779 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:57046779 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:161138211 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:161138211 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:146030090 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:146030090 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:131885480 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:131885480 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:102384057 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:102384057 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:102251586 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:102251586 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:11244934 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:11244934 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:129804795 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:129804795 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:23509758 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:23509758 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:57398090 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:57398090 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179315273 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179315273 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:116048718 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:116048718 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:42689395 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:42689395 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:170705132 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:170705132 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2870829 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2870829 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:152200229 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:152200229 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:227073438 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:227073438 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43520325 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43520325 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43766393 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43766393 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184022014 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184022014 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184024531 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184024531 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:74338329 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:74338329 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:54115800 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:54115800 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99050155 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99050155 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:98244223 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:98244223 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:11586582 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:11586582 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:97311865 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:97311865 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:78958395 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:78958395 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:131117298 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:131117298 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:18750584 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:18750584 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:18750643 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:18750643 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:198665831 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:198665831 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:8341568 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:8341568 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55713359 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:55713359 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:8252602 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:8252602 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:40710506 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:40710506 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:45535469 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:45535469 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:25262802 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:25262802 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:174274332 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:174274332 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:36264990 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:36264990 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:36301636 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:36301636 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:141230940 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:141230940 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:114766490 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:114766490 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:45487492 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:45487492 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:135958872 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:135958872 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:50031593 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:50031593 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:120342272 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:120342272 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:103183358 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:103183358 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:17070378 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:17070378 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:34395228 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:34395228 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:88056425 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:88056425 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:325381 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:325381 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:153332637 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:153332637 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:163122549 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:163122549 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:163131820 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:163131820 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:240933340 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:240933340 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:241093896 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:241093896 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:151200534 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:151200534 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:104949021 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:104949021 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:43385806 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:43385806 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:40503401 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:40503401 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:151766403 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:151766403 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:151331603 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:151331603 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:7164388 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:7164388 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:33413740 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:33413740 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:156437526 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:156437526 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56440117 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:56440117 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:124765293 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:124765293 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117631201 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117631201 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:66797087 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:66797087 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83319944 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83319944 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83375043 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83375043 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83389785 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83389785 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83411039 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:83411039 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:99153592 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:99153592 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:45111286 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:45111286 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48557177 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48557177 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:62294069 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:62294069 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:186915620 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:186915620 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:179023445 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:179023445 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:93074709 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:93074709 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:32360786 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:32360786 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39077918 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39077918 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237660117 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237660117 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237663981 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237663981 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237780849 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237780849 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237906993 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237906993 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:34156414 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:34156414 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:10334439 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:10334439 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:23939433 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:23939433 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:23942682 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:23942682 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:169650452 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:169650452 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44364490 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44364490 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:15889138 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:15889138 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:39959702 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:39959702 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:127730776 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:127730776 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:32976946 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:32976946 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:167279697 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:167279697 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:29980512 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:29980512 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:43610085 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:43610085 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:43610368 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:43610368 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4213691 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4213691 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:71394429 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:71394429 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:39512154 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:39512154 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:39524290 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:39524290 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:13971224 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:13971224 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:169582413 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:169582413 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84636060 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84636060 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84636062 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84636062 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84642164 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84642164 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84658586 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:84658586 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:74901547 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:74901547 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:55912144 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:55912144 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:94913018 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:94913018 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:95089858 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:95089858 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:2956007 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:2956007 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:70560647 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:70560647 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:67105429 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:67105429 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:17793601 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:17793601 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:51117879 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:51117879 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:49217219 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:49217219 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:72842267 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:72842267 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:113330061 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:113330061 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:117058277 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:117058277 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52000533 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52000533 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:51961665 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:51961665 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:103710527 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:103710527 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:1083817 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:1083817 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:1088989 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:1088989 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:121631822 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:121631822 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:63057611 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:63057611 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:38317613 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:38317613 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:129499694 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:129499694 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:128694752 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:128694752 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:40153758 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:40153758 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79233988 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79233988 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:103188930 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:103188930 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:108145380 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:108145380 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:75862335 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:75862335 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110734570 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110734570 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20636375 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20636375 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20674101 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20674101 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:23282656 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:23282656 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111901143 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111901143 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111997788 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111997788 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:103141364 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:103141364 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:135095603 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:135095603 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21377549 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21377549 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:133667910 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:133667910 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:33687453 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:33687453 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:20541056 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:20541056 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:168176692 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:168176692 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:37496634 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:37496634 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:71464616 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:71464616 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:11136920 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:11136920 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:106891870 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:106891870 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:96970650 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:96970650 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:2443697 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:2443697 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:25154989 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:25154989 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64802238 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64802238 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64803192 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:64803192 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:125223462 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:125223462 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:158358614 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:158358614 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:36767937 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:36767937 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:108337100 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:108337100 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:23818321 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:23818321 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:231175344 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:231175344 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:118512668 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:118512668 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:118727641 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:118727641 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:101195687 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:101195687 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:217822200 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:217822200 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:133714353 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:133714353 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:35753978 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:35753978 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:35792437 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:35792437 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:229046273 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:229046273 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:44171540 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:44171540 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:89911688 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:89911688 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158585296 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158585296 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158593040 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158593040 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158613331 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158613331 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158645887 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158645887 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158656229 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158656229 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:131346261 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:131346261 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:131356323 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:131356323 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:40995975 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:40995975 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:126015708 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:126015708 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:36028465 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:36028465 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:104767552 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:104767552 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26882065 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26882065 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:27957792 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:27957792 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:149522333 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:149522333 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:77093073 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:77093073 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:100231300 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:100231300 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:104105216 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:104105216 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:136183879 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:136183879 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:90672774 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:90672774 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:90703676 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:90703676 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:68443020 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:68443020 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:191937711 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:191937711 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:171488318 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:171488318 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219566747 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219566747 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:70945878 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:70945878 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:33327484 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:33327484 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:123988755 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:123988755 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:1742433 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:1742433 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:6969230 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:6969230 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:74179885 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:74179885 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15641926 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15641926 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:19751663 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:19751663 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:96178510 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:96178510 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:149777726 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:149777726 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:33065295 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:33065295 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:97444226 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:97444226 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:61084165 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:61084165 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:102891652 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:102891652 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:50686890 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:50686890 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:50696780 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:50696780 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100226010 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100226010 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:134029978 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:134029978 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79846106 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79846106 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:11581033 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:11581033 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:2560467 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:2560467 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:76116638 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:76116638 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:20096968 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:20096968 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:38228668 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:38228668 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:177019187 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:177019187 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:193048987 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:193048987 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:44374539 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:44374539 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:98452968 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:98452968 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:83416288 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:83416288 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150491001 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150491001 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:118404497 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:118404497 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:133771028 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:133771028 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:109665131 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:109665131 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:24646207 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:24646207 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:69084041 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:69084041 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:68829210 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:68829210 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:68708236 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:68708236 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:117979645 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:117979645 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:101266799 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:101266799 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:103599936 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:103599936 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:76079272 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:76079272 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175306626 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175306626 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175331702 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175331702 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175334110 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175334110 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:144150895 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:144150895 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:16199837 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:16199837 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:188956441 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:188956441 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10971740 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10971740 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10996117 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10996117 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:185655552 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:185655552 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:123685978 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:123685978 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:123698855 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:123698855 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228589723 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228589723 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189068531 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189068531 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189026198 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189026198 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:230664107 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:230664107 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:81468067 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:81468067 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:50250162 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:50250162 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:138832134 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:138832134 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179451622 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179451622 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179480254 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179480254 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179554792 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179554792 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179595570 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179595570 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179602946 T>A maps to NM_133378.4 K3501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179602946 T>A maps to NM_133378.4 K3501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:29178441 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:29178441 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:19753411 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:19753411 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:18566031 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:18566031 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:43838477 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:43838477 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:118257069 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:118257069 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:10239430 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:10239430 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:11333505 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:11333505 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:4921031 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:4921031 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:26644338 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:26644338 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:59337527 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:59337527 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:96665455 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:96665455 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:234656592 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:234656592 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70073981 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70073981 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70156571 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70156571 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70160199 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70160199 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346633 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346633 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17769094 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17769094 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:33479736 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:33479736 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:33501252 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:33501252 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:21974221 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:21974221 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43921479 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43921479 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216363520 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216363520 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216420663 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216420663 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:76720767 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:76720767 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:84774031 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:84774031 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113725189 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113725189 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:61632826 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:61632826 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:85868248 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:85868248 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:30213132 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:30213132 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:79820889 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:79820889 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:118519905 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:118519905 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6126085 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6126085 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:85645514 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:85645514 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:118481000 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:118481000 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:36579884 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:36579884 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:36595620 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:36595620 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:96082606 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:96082606 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228238281 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228238281 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:149245561 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:149245561 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:168108474 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:168108474 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:28110023 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:28110023 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:180804230 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:180804230 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43481020 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43481020 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:112929100 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:112929100 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100395325 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100395325 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:167031677 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:167031677 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:56189875 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:56189875 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:130166396 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:130166396 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:11846492 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:11846492 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:64196403 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chrX:64196403 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:87500788 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:87500788 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:31821623 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:31821623 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:145275039 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:145275039 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:106813152 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:106813152 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:45976694 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:45976694 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:30677105 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:30677105 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:44469496 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:44469496 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:244217027 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:244217027 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31906326 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31906326 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:38353107 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:38353107 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:178489011 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:178489011 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:49660021 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:49660021 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:109701434 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:109701434 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:44751544 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:44751544 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:37869882 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:37869882 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9724851 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9724851 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:53015761 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:53015761 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:53207689 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:53207689 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52505608 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52505608 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:56969678 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:56969678 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:144772324 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:144772324 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:9027479 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:9027479 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:67171023 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:67171023 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:183706310 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:183706310 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:25349308 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:25349308 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:48552028 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:48552028 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:35084558 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:35084558 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:52020172 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:52020172 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:156890362 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:156890362 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:178562884 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:178562884 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:7520759 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:7520759 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:31123988 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:31123988 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:233274217 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:233274217 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:101552329 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:101552329 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:144075971 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:144075971 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:18812849 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:18812849 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:23765384 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:23765384 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50434062 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50434062 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:160137040 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:160137040 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:42592738 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:42592738 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:33573433 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:33573433 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:156619803 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:156619803 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:11414364 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:11414364 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:1457239 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:1457239 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:580857 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:580857 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:124058701 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:124058701 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:122775269 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:122775269 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:73766334 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:73766334 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61151343 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61151343 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:45601989 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:45601989 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:23340416 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:23340416 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:27560171 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:27560171 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:15777826 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:15777826 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:86062538 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:86062538 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:71252896 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:71252896 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:160165581 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:160165581 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:63822402 C>A maps to NM_001037325.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:63822402 C>A maps to NM_001037325.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:107096270 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:107096270 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:130902637 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:130902637 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:35835906 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:35835906 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:62008827 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:62008827 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:24593347 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:24593347 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:73521841 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:73521841 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:55893612 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:55893612 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:87917455 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:87917455 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:74420313 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:74420313 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:189863364 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:189863364 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:107920681 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:107920681 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61468269 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61468269 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:1317370 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:1317370 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:1424474 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrX:1424474 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:37331634 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:37331634 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:10973544 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:10973544 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:15648321 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:15648321 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:87526731 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:87526731 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:155278315 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:155278315 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:151125167 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:151125167 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:2064593 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:2064593 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:6782268 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:6782268 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:32205477 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:32205477 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:182843887 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:182843887 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:25551436 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:25551436 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:116594354 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:116594354 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:71778332 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:71778332 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:71797159 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:71797159 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:34398196 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:34398196 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:48517685 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:48517685 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:89178848 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:89178848 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:14038471 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:14038471 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:75250343 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:75250343 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:169541370 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:169541370 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:62104241 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:62104241 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:190203679 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:190203679 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:125074046 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:125074046 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:125330617 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:125330617 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:128492560 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:128492560 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:28607903 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:28607903 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:172060984 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:172060984 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:42940030 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:42940030 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:41193966 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:41193966 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:132560673 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:132560673 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:132902930 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:132902930 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:49470929 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:49470929 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:29706370 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:29706370 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:44187448 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:44187448 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:137589714 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:137589714 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:85901134 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:85901134 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:42468601 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:42468601 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:88008863 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:88008863 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:6639472 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:6639472 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:180664967 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:180664967 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:37307560 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:37307560 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:36109978 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:36109978 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:19102702 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:19102702 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:50557758 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:50557758 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:28475373 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:28475373 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:35551241 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:35551241 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:118441193 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:118441193 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:71522922 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:71522922 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:51830588 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:51830588 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:68645274 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:68645274 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:99175840 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:99175840 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:75923174 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:75923174 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:182400097 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:182400097 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:133967581 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:133967581 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:215368239 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:215368239 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:58988557 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:58988557 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:72346801 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:72346801 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:70535679 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:70535679 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:17913271 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:17913271 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:169689826 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:169689826 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:126186508 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:126186508 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:75622430 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:75622430 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:197890335 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:197890335 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:27523567 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:27523567 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:73566412 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:73566412 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:62641357 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:62641357 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:70291568 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:70291568 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:41112286 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:41112286 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:21344035 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:21344035 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:144804159 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:144804159 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:45925992 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:45925992 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:45762239 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:45762239 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:37605235 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:37605235 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:169098911 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:169098911 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:42858892 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:42858892 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:23313756 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:23313756 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:156802313 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:156802313 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:108836919 A>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:108836919 A>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:108836923 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:108836923 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:123686675 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:123686675 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:18195826 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:18195826 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:60543032 A>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:60543032 A>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:124632246 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:124632246 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:10258397 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:10258397 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:10412763 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:10412763 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:1914136 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:1914136 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:101735285 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:101735285 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:132982107 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:132982107 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:54606217 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:54606217 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:150695562 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:150695562 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:170815074 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:170815074 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:11918590 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:11918590 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:84711185 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:84711185 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:247694783 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:247694783 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:41850031 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:41850031 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:121670210 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:121670210 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:100913260 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:100913260 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrY:5205717 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chrY:5205717 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:72307601 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:72307601 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:120528481 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:120528481 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:102781507 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:102781507 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:197757992 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:197757992 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:100909789 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:100909789 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:99358793 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:99358793 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:38468664 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr22:38468664 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:77660919 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:77660919 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:39593636 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:39593636 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81240979 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81240979 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:125255415 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:125255415 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:14766618 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:14766618 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:28856008 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:28856008 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:208234016 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:208234016 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:118199270 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:118199270 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50916946 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50916946 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:89199208 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:89199208 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:104170784 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:104170784 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:54115278 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:54115278 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:48164607 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:48164607 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr21:45534720 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr21:45534720 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:140125495 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:140125495 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:220373872 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:220373872 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:114392757 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:114392757 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:85608023 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:85608023 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:79350204 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:79350204 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:85572975 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:85572975 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:7404057 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:7404057 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:41772383 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr15:41772383 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:60194493 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:60194493 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:32356667 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:32356667 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:237801947 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:237801947 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:153517280 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:153517280 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:108923814 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:108923814 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:5046830 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:5046830 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:55914406 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:55914406 C>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:42618434 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:42618434 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:50057119 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:50057119 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:51957879 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:51957879 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:160589700 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:160589700 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:42336744 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:42336744 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:168187752 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:168187752 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:130910785 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:130910785 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:214794563 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:214794563 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:62173736 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:62173736 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:23598155 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:23598155 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:159184268 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:159184268 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:114837472 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:114837472 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:53303196 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:53303196 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:137999997 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:137999997 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:32043086 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:32043086 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:60694568 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:60694568 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:15430202 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:15430202 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:150422355 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:150422355 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:3648144 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:3648144 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:908066 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:908066 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:81448828 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:81448828 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:29173104 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr18:29173104 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:1364202 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:1364202 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:69535507 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:69535507 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:215822218 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:215822218 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr21:30422409 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr21:30422409 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr21:17135199 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr21:17135199 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:58348623 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:58348623 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:108313430 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:108313430 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:142468393 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:142468393 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085431 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085431 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085500 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085500 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085518 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085518 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:14942150 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:14942150 T>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:85717659 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:85717659 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:78142462 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:78142462 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:111667331 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:111667331 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:21851869 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:21851869 A>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:48437659 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:48437659 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:37356779 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:37356779 A>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:37917437 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:37917437 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:81571990 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:81571990 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:53905610 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:53905610 G>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:58849612 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:58849612 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:7759204 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:7759204 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:125587636 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:125587636 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:94506749 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:94506749 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:35766255 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:35766255 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:43214279 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:43214279 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:61558408 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:61558408 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23531552 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23531552 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:20551968 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:20551968 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:127782764 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:127782764 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:45719582 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:45719582 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:131922133 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:131922133 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:32878340 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:32878340 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:29754668 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:29754668 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:202172360 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:202172360 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:241494220 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:241494220 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:89356942 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:89356942 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:201466908 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:201466908 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:39496269 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:39496269 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:86915593 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:86915593 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:23257453 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:23257453 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:35833786 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:35833786 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:31326636 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:31326636 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:1396322 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:1396322 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:28913885 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:28913885 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:48253873 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:48253873 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:79411611 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:79411611 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:69772945 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:69772945 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:33543485 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:33543485 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:26465283 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:26465283 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:112677839 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:112677839 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:74189320 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:74189320 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:30977230 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:30977230 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:61150821 C>A maps to ENST00000370523 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:61150821 C>A maps to ENST00000370523 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:175740688 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:175740688 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:121544337 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:121544337 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:5952628 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:5952628 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:188247839 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:188247839 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:35904805 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:35904805 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:67116322 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:67116322 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:89434335 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:89434335 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:46982365 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:46982365 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:34689809 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:34689809 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:50094385 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:50094385 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158324501 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158324501 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:208061526 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:208061526 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:80091793 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:80091793 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:49842682 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:49842682 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:44640138 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:44640138 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:149938743 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:149938743 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:25616323 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:25616323 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:123907705 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:123907705 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:13100549 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:13100549 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:57015515 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:57015515 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:50835610 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:50835610 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:50870908 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:50870908 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:40079784 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:40079784 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:29252145 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:29252145 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:154519753 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:154519753 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:154520023 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:154520023 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:36216740 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:36216740 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:139675798 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:139675798 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:109971366 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:109971366 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:107827778 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:107827778 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:47407629 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:47407629 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:148596571 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:148596571 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:113358312 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:113358312 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:153880486 G>T maps to NM_172377.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:153880486 G>T maps to NM_172377.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:219266976 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:219266976 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:68535097 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:68535097 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:16970381 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:16970381 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:119669668 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:119669668 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:119677558 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:119677558 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:43164319 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:43164319 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:148627152 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:148627152 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:143956766 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:143956766 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:47609612 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:47609612 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:125686592 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:125686592 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:49230629 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:49230629 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:32205511 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:32205511 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:395456 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:395456 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:111863663 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:111863663 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:84256266 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:84256266 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:72297333 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:72297333 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:27502941 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:27502941 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:225635235 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:225635235 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:169504855 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:169504855 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:50756875 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:50756875 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:51393802 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:51393802 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:51393979 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:51393979 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:116226497 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:116226497 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:167064041 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:167064041 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:108405607 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:108405607 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:32266199 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:32266199 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:13641828 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:13641828 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:34419964 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:34419964 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:11565874 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:11565874 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:14854364 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:14854364 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:29342336 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:29342336 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:220193309 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:220193309 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:23713903 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:23713903 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:58919179 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:58919179 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:177163639 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:177163639 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:21955519 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:21955519 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:45605041 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:45605041 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:163045607 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:163045607 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:48936741 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:48936741 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:161476117 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:161476117 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:108282002 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:108282002 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:108370276 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:108370276 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:240492589 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:240492589 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:240555865 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:240555865 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:153471553 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:153471553 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:49204889 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:49204889 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:45971806 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:45971806 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:138664374 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:138664374 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:131264741 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:131264741 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:12692873 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:12692873 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:4307867 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:4307867 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:117712684 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:117712684 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:161292723 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:161292723 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:151128010 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:151128010 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:170236814 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:170236814 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:16261606 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:16261606 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:22748016 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:22748016 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:44184945 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:44184945 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:153670434 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:153670434 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:90604134 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:90604134 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:62250611 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:62250611 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:100384084 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:100384084 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:19028603 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:19028603 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:145731316 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:145731316 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:10099054 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:10099054 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:176868862 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:176868862 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:27840057 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:27840057 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:52630235 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:52630235 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:19063700 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:19063700 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:121376978 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:121376978 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:42738963 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:42738963 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:43029925 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:43029925 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:22191743 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:22191743 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:39735138 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:39735138 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:3117635 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:3117635 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:239079703 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:239079703 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:111127445 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:111127445 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:22020611 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:22020611 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:105181589 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:105181589 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:15561250 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:15561250 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:73750603 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:73750603 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:6058529 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:6058529 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:12902574 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:12902574 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:63448028 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:63448028 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:88654289 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:88654289 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:196197284 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:196197284 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:26965134 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:26965134 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:46690496 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:46690496 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:36352608 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:36352608 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:118298087 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:118298087 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:56125367 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:56125367 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:143799868 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:143799868 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:88445599 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:88445599 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:111914742 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:111914742 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55110826 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55110826 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:118140003 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:118140003 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:118148064 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:118148064 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:99753743 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:99753743 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:141267685 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:141267685 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:141771070 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:141771070 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:170044910 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:170044910 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:70339350 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:70339350 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:131678368 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:131678368 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:77748823 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:77748823 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:31675568 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:31675568 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:30900868 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:30900868 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:164466679 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:164466679 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:119744849 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:119744849 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:151148205 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:151148205 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:17616231 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:17616231 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:156437511 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:156437511 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:141734377 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:141734377 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:2258358 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:2258358 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:102742688 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:102742688 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23313504 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23313504 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:132636725 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:132636725 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:41891508 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:41891508 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:59837041 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:59837041 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:80071674 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:80071674 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:11850984 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:11850984 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23874717 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:23874717 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:56552539 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:56552539 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:1383806 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:1383806 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:26310613 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:26310613 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:90994911 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:90994911 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:4796314 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:4796314 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:152362825 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:152362825 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:45170984 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:45170984 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:5827012 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:5827012 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:6069588 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:6069588 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:5415752 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:5415752 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:888699 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:888699 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:26939562 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:26939562 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:69760296 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:69760296 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:105179070 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:105179070 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:50883610 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:50883610 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:93794944 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:93794944 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:107867646 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:107867646 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:167182131 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:167182131 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:59131884 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:59131884 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55606147 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55606147 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:121659799 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:121659799 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:131546278 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:131546278 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:56505443 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:56505443 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:169589277 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:169589277 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:6738754 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:6738754 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:70048876 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:70048876 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:164769159 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:164769159 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:91238180 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:91238180 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:55626669 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:55626669 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:55626691 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:55626691 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:56360534 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:56360534 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140569351 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140569351 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140569384 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140569384 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44575085 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44575085 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:144866023 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:144866023 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:122869312 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:122869312 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:95503803 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:95503803 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:230486646 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:230486646 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:37841676 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:37841676 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:41749303 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:41749303 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:18491576 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:18491576 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:106523402 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:106523402 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:22839533 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:22839533 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:3181347 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:3181347 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:131960326 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:131960326 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:132093276 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:132093276 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:23692541 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:23692541 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:133219372 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:133219372 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:133253293 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:133253293 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:23825897 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:23825897 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:57267740 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:57267740 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:35560258 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:35560258 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:102359503 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:102359503 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:129781910 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:129781910 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:106882435 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:106882435 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:27277593 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:27277593 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:9318049 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:9318049 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:76255262 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:76255262 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:68582177 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:68582177 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:85097215 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:85097215 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:48131964 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:48131964 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:48143889 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:48143889 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:53607809 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:53607809 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:167666236 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:167666236 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:3262873 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:3262873 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:107105338 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:107105338 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:121275211 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:121275211 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:72431618 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:72431618 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:73029201 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:73029201 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:182617464 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:182617464 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:74470328 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:74470328 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:104930639 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:104930639 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:43386669 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:43386669 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:87013130 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:87013130 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:87565662 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:87565662 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:196202057 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:196202057 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:79174587 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:79174587 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:18534672 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:18534672 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:117718355 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:117718355 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:113332508 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:113332508 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:55201710 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:55201710 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:92998231 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:92998231 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:35559070 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:35559070 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:76866633 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:76866633 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:166895907 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:166895907 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:110445849 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:110445849 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:97527281 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:97527281 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:2895551 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:2895551 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:65830393 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:65830393 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:65458162 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:65458162 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:48244689 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:48244689 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:13947821 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:13947821 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:52002984 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:52002984 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:52031190 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:52031190 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:78337371 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:78337371 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:119026636 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:119026636 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:79671815 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:79671815 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:57182384 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:57182384 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:10916587 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:10916587 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:103142687 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:103142687 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:70710968 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:70710968 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:128650514 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:128650514 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:144465745 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:144465745 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:47703820 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:47703820 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:46196269 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:46196269 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:106970799 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:106970799 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:231109675 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:231109675 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:97326790 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:97326790 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:35628756 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:35628756 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:73826607 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:73826607 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158621054 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158621054 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:41038430 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:41038430 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:42156073 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:42156073 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:62173472 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:62173472 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:104885241 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:104885241 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:107423431 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:107423431 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:52535330 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:52535330 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:102691002 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:102691002 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:136221851 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:136221851 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:152784406 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:152784406 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:7866630 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:7866630 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:159459135 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:159459135 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:32803143 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:32803143 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:141463881 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:141463881 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:100965522 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:100965522 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:106083497 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:106083497 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:102904350 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:102904350 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:27168458 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:27168458 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:1552598 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:1552598 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:69843950 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:69843950 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:43568988 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:43568988 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:133983960 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:133983960 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:79368069 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:79368069 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:88474959 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:88474959 T>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:86807185 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:86807185 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:10749747 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:10749747 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:109414924 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:109414924 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:62759682 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:62759682 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:42565650 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr15:42565650 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:35853118 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:35853118 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:43796839 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:43796839 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:37466468 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:37466468 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:170786811 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:170786811 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:218674734 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:218674734 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:154144373 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:154144373 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:10920031 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:10920031 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:123545115 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:123545115 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:73057027 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:73057027 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:25973184 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:25973184 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:189018443 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:189018443 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:73442941 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:73442941 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:99403429 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:99403429 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:159476455 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:159476455 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:47256255 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:47256255 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:54946636 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:54946636 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:2689475 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:2689475 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:19752291 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:19752291 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:662351 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr18:662351 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:154208957 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:154208957 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:118716965 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:118716965 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:216073297 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:216073297 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:87017637 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:87017637 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:150573588 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:150573588 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:36550988 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:36550988 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:190323434 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:190323434 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44207836 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44207836 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:69969912 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:69969912 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:52840354 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:52840354 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:111624701 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chrX:111624701 A>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:72030896 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:72030896 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:68236198 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:68236198 T>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:64442492 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:64442492 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:19976830 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:19976830 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:53321188 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:53321188 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:11976949 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:11976949 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:53352307 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:53352307 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:247150208 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:247150208 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:247171297 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:247171297 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:56702157 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:56702157 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:13939432 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:13939432 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:12776244 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:12776244 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:48141223 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:48141223 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:39998515 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:39998515 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:35605093 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:35605093 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:20486768 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:20486768 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:7475173 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:7475173 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:43777812 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:43777812 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:1881986 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:1881986 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:29400672 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:29400672 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:57274405 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:57274405 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:176853722 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:176853722 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:96798622 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:96798622 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:41937299 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:41937299 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:1800480 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:1800480 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:79027403 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:79027403 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:48888729 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:48888729 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:4430599 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:4430599 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:4446418 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:4446418 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:19663256 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:19663256 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:58504023 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:58504023 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:30502219 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:30502219 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:40955691 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:40955691 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:90498131 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:90498131 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:150235023 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:150235023 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:181620454 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:181620454 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201022460 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201022460 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201035571 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201035571 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:24373224 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:24373224 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:12833075 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:12833075 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:241537925 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:241537925 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38297883 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38297883 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:185550701 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:185550701 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:116310858 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:116310858 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:219878822 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:219878822 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:20796672 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:20796672 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:132288473 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:132288473 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:158262870 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:158262870 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:74002064 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:74002064 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:54606723 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:54606723 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:95158482 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:95158482 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:45024810 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:45024810 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:40192536 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:40192536 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:436355 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:436355 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:104851170 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:104851170 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:74443681 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:74443681 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:7883262 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:7883262 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:36508688 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:36508688 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:180001284 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:180001284 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:121208960 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:121208960 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:94027024 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:94027024 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:110831814 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:110831814 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:1321260 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:1321260 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:113240884 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:113240884 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:113529133 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:113529133 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:25044427 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:25044427 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:36958855 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:36958855 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:22925773 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:22925773 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:59789425 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:59789425 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:155708098 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:155708098 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:87514239 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:87514239 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:74594270 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:74594270 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:118572486 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:118572486 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:47852150 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:47852150 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:61538453 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:61538453 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:12944031 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:12944031 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:31241076 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:31241076 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:21904421 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:21904421 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:11568476 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:11568476 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:132225950 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:132225950 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:169507381 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:169507381 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:162875205 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:162875205 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:146777431 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:146777431 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:71797542 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:71797542 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:233349430 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:233349430 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:69250451 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:69250451 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:55218946 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:55218946 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:15777397 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:15777397 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:23721607 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:23721607 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:13733228 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:13733228 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:5955654 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:5955654 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:101146708 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:101146708 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:161514850 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:161514850 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:102379248 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:102379248 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:1018527 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:1018527 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:105977986 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:105977986 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:240351388 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:240351388 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:172003850 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:172003850 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:42647569 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:42647569 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:32660241 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:32660241 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:52781099 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:52781099 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:41055866 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:41055866 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:27723937 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:27723937 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:120565868 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:120565868 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:120582654 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:120582654 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:69649974 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:69649974 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:33448250 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:33448250 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:11872123 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:11872123 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:68610568 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:68610568 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:37317243 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:37317243 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:93305652 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:93305652 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:37902577 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:37902577 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:120489843 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:120489843 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:108935445 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:108935445 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:45304004 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:45304004 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:54674444 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:54674444 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:26236820 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:26236820 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:42814475 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:42814475 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118460382 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118460382 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:183777927 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:183777927 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:136700996 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:136700996 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:86393848 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:86393848 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:48148422 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:48148422 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:156644820 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:156644820 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:73879383 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:73879383 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:91483929 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:91483929 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:168443497 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:168443497 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:57969063 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:57969063 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:51446842 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:51446842 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38905418 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38905418 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:31973401 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:31973401 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201351969 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201351969 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:7080154 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:7080154 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:152659152 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:152659152 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:55142907 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:55142907 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:51890380 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:51890380 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:161022176 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:161022176 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:62641176 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:62641176 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:71152435 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:71152435 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:157174551 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:157174551 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:33499868 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:33499868 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:45956583 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:45956583 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:126754977 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:126754977 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:3424282 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:3424282 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr22:42150062 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr22:42150062 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:116403423 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:116403423 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:179225652 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:179225652 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:12229371 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:12229371 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:97685864 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:97685864 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:2268064 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:2268064 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:151734124 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:151734124 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:29881648 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:29881648 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:47872933 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:47872933 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:41949463 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:41949463 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:78152268 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:78152268 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:152467413 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:152467413 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:91937917 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:91937917 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:97331232 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:97331232 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:52678774 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:52678774 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:198222101 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:198222101 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:70417885 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:70417885 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:204982041 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:204982041 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:39622187 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:39622187 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:52521050 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:52521050 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:54318295 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:54318295 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:56459697 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:56459697 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:56223079 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:56223079 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:15174809 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:15174809 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:69320506 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:69320506 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:115357649 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:115357649 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:52343943 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:52343943 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:247694785 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:247694785 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:247768886 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:247768886 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248185238 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248185238 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248223816 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248223816 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:23777950 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:23777950 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:34663998 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:34663998 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:12549674 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:12549674 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:125648241 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:125648241 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:54967535 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:54967535 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:71404252 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:71404252 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:47853650 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:47853650 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:102056093 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:102056093 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:110424451 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:110424451 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:145464207 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:145464207 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:8639398 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:8639398 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:19126428 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:19126428 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:37295840 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:37295840 T>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118380435 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118380435 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118380791 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118380791 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:131195484 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:131195484 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:30818945 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:30818945 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:22328211 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:22328211 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:12458198 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:12458198 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:23510017 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:23510017 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:68989771 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:68989771 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:23847678 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:23847678 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6340269 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6340269 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:30103852 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:30103852 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:47194986 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:47194986 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:227073495 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:227073495 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:43348950 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:43348950 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:23713902 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:23713902 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:198703379 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:198703379 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:8406166 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:8406166 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:174190031 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:174190031 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:170679605 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:170679605 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:179541564 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:179541564 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:47046077 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:47046077 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:33167114 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:33167114 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:44013517 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr18:44013517 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:58296434 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:58296434 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:108995217 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:108995217 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:237730112 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:237730112 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:84791261 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:84791261 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:15870654 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:15870654 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:100553651 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:100553651 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:1110948 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:1110948 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:48055320 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:48055320 T>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:76385773 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:76385773 A>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:76385784 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:76385784 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:26131623 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:26131623 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:101957934 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:101957934 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:87195889 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:87195889 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:107427602 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:107427602 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:220091865 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:220091865 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:128844947 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:128844947 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:127638064 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:127638064 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:121427876 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:121427876 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:54723848 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:54723848 T>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:51128408 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:51128408 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:149691006 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr6:149691006 A>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:100531262 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:100531262 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:159860647 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:159860647 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:23723998 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:23723998 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:104464824 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:104464824 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:65146834 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:65146834 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:56657644 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:56657644 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:43584107 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:43584107 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:134144264 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:134144264 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:19068086 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:19068086 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:18047061 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:18047061 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:63362065 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:63362065 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6636247 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6636247 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:20077266 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:20077266 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:42235265 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:42235265 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:140922241 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:140922241 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:111195132 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chrX:111195132 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:3446928 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:3446928 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:3469327 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:3469327 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:94863596 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:94863596 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:192985377 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:192985377 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:96599450 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr13:96599450 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:61697853 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:61697853 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:54544177 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:54544177 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr22:42343202 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr22:42343202 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:128481891 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:128481891 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:69259707 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:69259707 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53302176 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53302176 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:52633939 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:52633939 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:55980292 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:55980292 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:8857884 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:8857884 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:48559903 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:48559903 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:67041215 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:67041215 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:20725490 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:20725490 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:107782550 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:107782550 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:47340514 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:47340514 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20494691 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20494691 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:24990220 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:24990220 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:42850576 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:42850576 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:207438026 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:207438026 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:207457501 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:207457501 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:175899296 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:175899296 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:72491971 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:72491971 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:72491984 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:72491984 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:64600954 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:64600954 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:50312004 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:50312004 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:32880130 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:32880130 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:4832174 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:4832174 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:85401848 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:85401848 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:220095979 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:220095979 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:99701402 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:99701402 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:39445310 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:39445310 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:16532020 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:16532020 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:155920587 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:155920587 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:111930027 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:111930027 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:35729480 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:35729480 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:119188075 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:119188075 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:119568147 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:119568147 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:72554621 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:72554621 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:3828756 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:3828756 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:3833794 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:3833794 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:73038508 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:73038508 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:87111176 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:87111176 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:55342314 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:55342314 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:50154291 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:50154291 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:31607271 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:31607271 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:52583306 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:52583306 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:197241021 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:197241021 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:16552885 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:16552885 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:112116862 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:112116862 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:112119673 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:112119673 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:26373429 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:26373429 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:41900000 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:41900000 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:31530894 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:31530894 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:76463278 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:76463278 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:44251710 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:44251710 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:182924620 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:182924620 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:35506113 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:35506113 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:63816015 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:63816015 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:143704282 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:143704282 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:71019980 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:71019980 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:123778412 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:123778412 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:40937556 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:40937556 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:181707462 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:181707462 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:201019909 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:201019909 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:159166575 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:159166575 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:110818339 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:110818339 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:3776860 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:3776860 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:7811207 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:7811207 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:41414906 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:41414906 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:104937554 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:104937554 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:74558911 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:74558911 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:6291760 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:6291760 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:34398439 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:34398439 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:24510015 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:24510015 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:49535638 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:49535638 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:93522312 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:93522312 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:120270670 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:120270670 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:43990111 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:43990111 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:33618827 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:33618827 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:73753443 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:73753443 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:33137742 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:33137742 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:121240844 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:121240844 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:139697352 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:139697352 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:110804879 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:110804879 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:107457579 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:107457579 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:137681069 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:137681069 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:125557673 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:125557673 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:197332893 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:197332893 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:1409523 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:1409523 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:3165023 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:3165023 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:114326756 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:114326756 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:80772927 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:80772927 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:69366815 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:69366815 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:70280995 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:70280995 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:49018910 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:49018910 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:71958966 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:71958966 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:143956359 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:143956359 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:59412671 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:59412671 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:176894216 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:176894216 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:155020757 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:155020757 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:38103231 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:38103231 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:15960223 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:15960223 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:44611348 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:44611348 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:115130322 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:115130322 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:50134349 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:50134349 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:42232263 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:42232263 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:84028204 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:84028204 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:124258687 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:124258687 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:38889055 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:38889055 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:132219568 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:132219568 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:40169225 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:40169225 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:27165080 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:27165080 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:71797245 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:71797245 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:69253204 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:69253204 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:93258594 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:93258594 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:44073793 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:44073793 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:65637870 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:65637870 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:140674014 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:140674014 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:8017407 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:8017407 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:71748935 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:71748935 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:73609260 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:73609260 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:89478377 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:89478377 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:158534099 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:158534099 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:93070820 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:93070820 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:66044839 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:66044839 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:46748236 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:46748236 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:124798725 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:124798725 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:15254715 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:15254715 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:126490203 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:126490203 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:8376462 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:8376462 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:150891345 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:150891345 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:17895112 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:17895112 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:68581899 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:68581899 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:4481879 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:4481879 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:128482832 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:128482832 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:43323119 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:43323119 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:79385787 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:79385787 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:49430249 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:49430249 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:155098506 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:155098506 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:230385027 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:230385027 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:19603055 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:19603055 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:27745265 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:27745265 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:10877357 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:10877357 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:120592760 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:120592760 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:42629316 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:42629316 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:42700124 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:42700124 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:150210470 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:150210470 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:129360767 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:129360767 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:6950712 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:6950712 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:58742246 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:58742246 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:47646626 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:47646626 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:154070093 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:154070093 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:6935351 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:6935351 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:11755151 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:11755151 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:87406922 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:87406922 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:33523481 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:33523481 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:6380767 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:6380767 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:129268252 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:129268252 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:15642846 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:15642846 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:81335167 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:81335167 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:81372292 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:81372292 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:32523303 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:32523303 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:21209347 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:21209347 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:81578200 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:81578200 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:143130291 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:143130291 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:9457804 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:9457804 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:2618034 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:2618034 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:12957348 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:12957348 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:66620647 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:66620647 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:173354046 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:173354046 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:30509283 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:30509283 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:7611608 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:7611608 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr21:35140005 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr21:35140005 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:63453935 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:63453935 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:96041064 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:96041064 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:178984519 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:178984519 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:196204945 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:196204945 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:5032781 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:5032781 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:6887884 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:6887884 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:55980996 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:55980996 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:24595993 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:24595993 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:34838703 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:34838703 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:36868869 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:36868869 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:26152410 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:26152410 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:154393370 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:154393370 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:39545819 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:39545819 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:33372020 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:33372020 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:51470294 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:51470294 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:53038772 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:53038772 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:7080192 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:7080192 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:145531364 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:145531364 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:189706960 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:189706960 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:73559550 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:73559550 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:82445497 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:82445497 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:151520060 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:151520060 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:141806918 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:141806918 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:3712373 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:3712373 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:114128316 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:114128316 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:35793623 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:35793623 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:39105149 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:39105149 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:36107042 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:36107042 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:22160347 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:22160347 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:60821965 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:60821965 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:217124506 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:217124506 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:12958029 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:12958029 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:47389130 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:47389130 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:204501200 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:204501200 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:70360811 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:70360811 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:15666575 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:15666575 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:2371201 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:2371201 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:42000107 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:42000107 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:31477728 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:31477728 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:10393065 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:10393065 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:100843502 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:100843502 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:48018306 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:48018306 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:68506069 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:68506069 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:30061950 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:30061950 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:9000040 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:9000040 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:9038555 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:9038555 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:9056167 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:9056167 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:195505432 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:195505432 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:1213452 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:1213452 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:23861607 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:23861607 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:26443668 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:26443668 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:76888587 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:76888587 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:128338274 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:128338274 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:71194085 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:71194085 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:78415665 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:78415665 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:15608699 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:15608699 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:46271153 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:46271153 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:20948799 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:20948799 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:41236555 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:41236555 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:278723 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:278723 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:120464236 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:120464236 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:115374526 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:115374526 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:44795248 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:44795248 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:27246709 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:27246709 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:40137418 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:40137418 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:37341366 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:37341366 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:55540847 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:55540847 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:21891859 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:21891859 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:26684426 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:26684426 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:26695369 G>T maps to ENST00000426958 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:26695369 G>T maps to ENST00000426958 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:73638538 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:73638538 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:9520104 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:9520104 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:169845378 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:169845378 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135202735 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135202735 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:25064614 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:25064614 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:150832576 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:150832576 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:56106372 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:56106372 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:120385414 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:120385414 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:149312256 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:149312256 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:34987994 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:34987994 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:39977928 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:39977928 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:8050971 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:8050971 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:7360575 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:7360575 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:13325586 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:13325586 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:99371247 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:99371247 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:178937195 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:178937195 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:106523626 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:106523626 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:102058640 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:102058640 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:96053176 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:96053176 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:161162461 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:161162461 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:190687365 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:190687365 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:140395108 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:140395108 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:24759999 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:24759999 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:19563596 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:19563596 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:42975333 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:42975333 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:91522251 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:91522251 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:129800717 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:129800717 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:6504416 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:6504416 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:73590755 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:73590755 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:43228126 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:43228126 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:43757876 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:43757876 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:23714090 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:23714090 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:18750955 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:18750955 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:44072343 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:44072343 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:119509625 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:119509625 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:64525443 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:64525443 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:50384011 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:50384011 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:141290442 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:141290442 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:33745388 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:33745388 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:33745454 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:33745454 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:49070637 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:49070637 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:103390111 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:103390111 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:176145169 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:176145169 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:74671948 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:74671948 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:151200590 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:151200590 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:62645706 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:62645706 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:45818414 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:45818414 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:104581001 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:104581001 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:66100963 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:66100963 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:21033224 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:21033224 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:40695490 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:40695490 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:31529111 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:31529111 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:79638912 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:79638912 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27829568 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27829568 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:48559231 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:48559231 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:109001581 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:109001581 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:71588534 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:71588534 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:237802269 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:237802269 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:33988746 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:33988746 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:34149856 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:34149856 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:153363207 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:153363207 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:155230303 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:155230303 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38753556 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38753556 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38835623 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38835623 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38961556 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38961556 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:10354102 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:10354102 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:35903123 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:35903123 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:61326621 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:61326621 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:2895573 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:2895573 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:35656880 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:35656880 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:73215339 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:73215339 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:164785377 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:164785377 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:119013908 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:119013908 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:119015284 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:119015284 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38348709 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:38348709 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:160668333 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:160668333 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:153934659 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:153934659 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:26692556 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:26692556 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:20648250 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:20648250 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:168127706 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:168127706 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:56563738 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:56563738 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:38005679 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:38005679 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:107005444 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:107005444 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:151045788 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:151045788 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:172633999 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:172633999 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:64938718 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:64938718 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:158647681 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:158647681 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:65268579 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:65268579 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:45983410 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:45983410 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:45983412 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:45983412 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:206619342 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:206619342 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:104078704 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:104078704 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:108863861 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:108863861 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:31590614 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:31590614 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:12112029 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:12112029 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:117074380 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:117074380 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:1282454 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:1282454 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:70127483 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chrX:70127483 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:56661723 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:56661723 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:29932482 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:29932482 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:138169139 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:138169139 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:75263628 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:75263628 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:202991942 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:202991942 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:118403400 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:118403400 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:111775991 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:111775991 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:57068011 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:57068011 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:47479349 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:47479349 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:20077248 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:20077248 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:42265230 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:42265230 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:41198005 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:41198005 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:55032997 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:55032997 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:14363743 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:14363743 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:49717253 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:49717253 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:31318337 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:31318337 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:98478713 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:98478713 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:141957558 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:141957558 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:112397334 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:112397334 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:40818305 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:40818305 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135103495 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135103495 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:56174084 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:56174084 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:138978324 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:138978324 T>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:3095892 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:3095892 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:19443985 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:19443985 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:128877778 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:128877778 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr21:43539055 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr21:43539055 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20355554 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20355554 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:17517198 C>A maps to NM_153676.3 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:17517198 C>A maps to NM_153676.3 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:216246127 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:216246127 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:216258243 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:216258243 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:61441858 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:61441858 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:5038328 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:5038328 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:5038334 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:5038334 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:9010501 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:9010501 A>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:144719329 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:144719329 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:33235810 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:33235810 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:119576064 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:119576064 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27241891 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27241891 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:203748525 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:203748525 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:124448858 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:124448858 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:46549341 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:46549341 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:88675166 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:88675166 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:57647585 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:57647585 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:45976742 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:45976742 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:45131752 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr20:45131752 A>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:116812462 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:116812462 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:16458527 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:16458527 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:56973648 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:56973648 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:53878904 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:53878904 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:67047391 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:67047391 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:226342569 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:226342569 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:8401196 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:8401196 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:47756108 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:47756108 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:42580199 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:42580199 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:58929101 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:58929101 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:42254861 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:42254861 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:54054593 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:54054593 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:31734593 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:31734593 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:179737050 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:179737050 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:635747 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:635747 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:29252792 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:29252792 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:201718234 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:201718234 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr12:107395460 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr12:107395460 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:96826846 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:96826846 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:126201272 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:126201272 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:82519615 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:82519615 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:133923351 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:133923351 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:54482917 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:54482917 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:171086166 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:171086166 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:71037258 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:71037258 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:158990341 T>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:158990341 T>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:212156260 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:212156260 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:49245653 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:49245653 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:108298118 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:108298118 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:158057682 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:158057682 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:108798503 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:108798503 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:226485580 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:226485580 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:148253043 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:148253043 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:34655544 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:34655544 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:77975213 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:77975213 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:61759286 T>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:61759286 T>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:86209276 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:86209276 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:72146615 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:72146615 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:80426850 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:80426850 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:133543373 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:133543373 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:204985748 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:204985748 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:101571896 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:101571896 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr14:26941468 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr14:26941468 A>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr16:138929 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr16:138929 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:50282122 G>A maps to ENST00000404971 R1300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:50282122 G>A maps to ENST00000404971 R1300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051197 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051197 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051223 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051223 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051405 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051405 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:149937910 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:149937910 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:36955481 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:36955481 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:28847855 A>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:28847855 A>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr13:38153922 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr13:38153922 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr9:85607699 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr9:85607699 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:1783184 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:1783184 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:103244323 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:103244323 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:93026724 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:93026724 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:39963160 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:39963160 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:26136165 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:26136165 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:116906562 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:116906562 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:25771134 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:25771134 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:118898334 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:118898334 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:36520524 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:36520524 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:36521152 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:36521152 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:204081959 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:204081959 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:168920200 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:168920200 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:67546469 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:67546469 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:100532458 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:100532458 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:150469203 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:150469203 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr21:32595948 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr21:32595948 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:171910262 T>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:171910262 T>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:33366801 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:33366801 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr20:62500838 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr20:62500838 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:180662119 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:180662119 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:907198 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:907198 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:101362143 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:101362143 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:98508635 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:98508635 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:158915971 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:158915971 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:68490651 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:68490651 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:20911332 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:20911332 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:99883803 T>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:99883803 T>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:99930832 A>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr6:99930832 A>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:158827187 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:158827187 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:150572260 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chrX:150572260 C>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:1118260 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:1118260 T>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089200 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089200 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089301 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089301 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089562 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089562 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089570 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:124089570 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:21826966 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:21826966 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:217057282 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:217057282 A>G did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr20:62598682 T>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr20:62598682 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:169792945 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:169792945 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:150741344 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:150741344 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:183699469 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:183699469 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:44080050 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:44080050 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:100523793 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:100523793 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:179087718 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:179087718 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:35512710 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:35512710 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:132337646 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:132337646 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:128598333 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:128598333 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:31416021 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:31416021 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:58514508 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:58514508 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:111559374 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:111559374 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:236889398 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:236889398 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:38519471 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:38519471 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:128018970 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:128018970 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:24339837 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:24339837 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:33751437 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:33751437 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:178700127 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:178700127 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:64506369 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:64506369 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:7757549 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:7757549 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:148715349 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:148715349 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:237029158 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:237029158 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:141301114 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:141301114 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:84509319 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:84509319 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:178307021 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:178307021 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:8765448 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:8765448 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:129270749 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:129270749 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:5045732 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:5045732 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:4879574 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:4879574 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:56165370 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:56165370 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:46719922 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:46719922 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:61822846 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:61822846 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:54535093 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:54535093 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:241494190 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:241494190 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:110463652 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:110463652 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:37451563 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:37451563 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:98175379 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:98175379 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:98177268 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:98177268 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:22292024 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:22292024 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:36616174 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:36616174 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:68753905 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:68753905 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:115351521 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:115351521 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:47626979 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:47626979 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:143959822 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:143959822 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:11315278 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:11315278 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:219099134 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:219099134 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:75001025 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:75001025 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:66941636 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:66941636 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:76398012 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:76398012 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:53927316 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:53927316 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:62538883 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:62538883 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:79937132 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:79937132 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:25991575 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:25991575 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:23977765 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:23977765 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:124413409 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:124413409 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:161821407 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:161821407 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:11372737 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:11372737 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:220085429 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:220085429 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:47574326 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:47574326 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:113530299 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:113530299 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:10904612 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:10904612 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:54708071 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:54708071 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:77243646 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:77243646 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:77090115 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:77090115 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:142186744 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:142186744 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:153171940 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:153171940 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:373572 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:373572 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:32204347 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:32204347 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:134312223 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:134312223 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:31656112 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:31656112 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:160240092 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:160240092 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:45250729 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:45250729 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:22615510 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:22615510 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:105695288 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:105695288 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:128153106 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:128153106 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:82783569 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:82783569 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:40078649 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:40078649 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:60592583 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:60592583 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:40678796 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:40678796 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:36910350 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:36910350 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:36983293 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:36983293 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:35238191 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:35238191 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:20234277 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:20234277 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:197673870 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:197673870 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:170506008 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:170506008 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:41911006 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:41911006 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:41149635 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:41149635 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:97627244 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:97627244 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:40909772 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:40909772 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142637342 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142637342 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:89884649 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:89884649 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:57395349 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:57395349 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:38374039 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:38374039 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:39288821 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:39288821 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:132594138 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:132594138 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:2787106 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:2787106 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:1910186 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:1910186 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:36962328 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:36962328 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:86063597 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:86063597 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159161886 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159161886 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44130809 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44130809 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:7737547 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:7737547 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:7796974 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:7796974 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:134344817 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:134344817 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:68609887 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:68609887 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:94818048 C>A maps to ENST00000393113 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:94818048 C>A maps to ENST00000393113 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:128757781 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:128757781 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:150578764 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:150578764 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:91825946 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:91825946 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34207224 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34207224 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:95894998 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:95894998 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:33288464 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:33288464 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7525911 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7525911 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:66492276 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:66492276 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158152620 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158152620 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158153981 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158153981 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158325577 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158325577 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:15826650 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:15826650 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157805483 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157805483 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:100843033 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:100843033 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:227182455 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:227182455 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:227381438 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:227381438 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:64851366 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:64851366 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:64982073 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:64982073 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:83781881 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:83781881 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:59206529 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:59206529 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:73405794 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:73405794 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:60499638 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:60499638 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31299541 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31299541 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:85970713 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:85970713 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:202698761 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:202698761 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:50856905 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:50856905 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43098786 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43098786 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:15813957 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:15813957 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:46807706 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:46807706 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:104068461 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:104068461 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:214781946 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:214781946 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49552059 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49552059 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49533388 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49533388 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:7798887 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:7798887 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:87295083 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:87295083 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:41562880 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:41562880 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:10988996 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:10988996 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:143018993 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:143018993 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:37859217 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:37859217 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:11660684 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:11660684 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:146741175 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:146741175 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:33143539 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:33143539 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:75848325 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:75848325 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70850768 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70850768 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70894574 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70894574 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:94041442 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:94041442 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:139638524 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:139638524 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189858670 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189858670 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189863489 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189863489 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:107849871 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:107849871 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:3652161 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:3652161 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:62363160 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:62363160 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:18899888 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:18899888 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:36642524 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:36642524 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:129913067 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:129913067 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:130002885 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:130002885 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:93897333 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:93897333 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:46338850 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:46338850 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152384753 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152384753 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:107393681 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:107393681 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:25623958 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:25623958 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:25597355 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:25597355 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:2876252 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:2876252 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:113293345 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:113293345 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:113585678 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:113585678 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:67976535 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:67976535 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:80333353 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:80333353 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:117431173 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:117431173 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:101459240 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:101459240 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:107274537 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:107274537 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:51504814 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:51504814 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:219677899 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:219677899 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:41382306 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:41382306 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:96534729 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:96534729 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160249707 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160249707 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160249729 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160249729 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:34614162 T>C maps to NM_024348.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:34614162 T>C maps to NM_024348.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:115147478 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:115147478 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:19305277 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:19305277 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179325638 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179325638 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:234299160 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:234299160 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:11985968 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:11985968 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:83502075 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:83502075 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:83525933 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:83525933 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124357565 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124357565 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:46287457 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:46287457 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:118479674 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:118479674 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:11659783 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:11659783 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:11784759 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:11784759 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:172376983 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:172376983 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:169141004 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:169141004 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:51393402 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:51393402 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:51395332 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:51395332 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:67365536 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:67365536 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:116226051 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:116226051 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:154143448 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:154143448 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:63987979 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:63987979 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:64045734 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:64045734 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:134010509 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:134010509 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:105440153 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:105440153 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56380133 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56380133 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56510807 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56510807 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:45412679 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:45412679 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57678937 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57678937 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71797198 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71797198 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:77449520 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:77449520 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:65824403 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:65824403 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:62129203 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:62129203 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:13641931 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:13641931 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:6066318 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:6066318 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:141567356 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:141567356 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:8014289 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:8014289 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:184043631 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:184043631 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:36895150 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:36895150 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:132530138 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:132530138 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:112030809 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:112030809 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97329608 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97329608 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:220152724 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:220152724 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:220184449 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:220184449 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216824131 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216824131 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:22826627 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:22826627 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:576739 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:576739 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:464529 A>T maps to ENST00000503889 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:464529 A>T maps to ENST00000503889 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:72234361 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:72234361 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:45811773 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:45811773 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:113797982 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:113797982 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:51210243 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:51210243 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:86150651 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:86150651 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:10671679 A>G maps to NM_022068.2 L2701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:10671679 A>G maps to NM_022068.2 L2701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:10696599 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:10696599 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:137677474 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:137677474 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:150980931 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:150980931 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:78280764 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:78280764 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:163066508 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:163066508 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:187538096 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:187538096 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:127599052 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:127599052 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8151215 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8151215 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:48045892 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:48045892 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159272705 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159272705 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157490786 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157490786 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157497281 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157497281 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157513946 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:157513946 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:124987588 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:124987588 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:124988028 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:124988028 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:108436297 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:108436297 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:155510805 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:155510805 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:14942493 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:14942493 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:191861948 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:191861948 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:153889279 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:153889279 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:34288914 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:34288914 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:180047312 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:180047312 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:240306044 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:240306044 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:89421662 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:89421662 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:126141285 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:126141285 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:79360288 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:79360288 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:132763451 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:132763451 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49469499 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49469499 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:144361102 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:144361102 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161495168 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161495168 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161576502 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161576502 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:26506630 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:26506630 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:4830144 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:4830144 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:36033823 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:36033823 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34077351 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34077351 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34079359 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34079359 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:9885007 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:9885007 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111845683 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111845683 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:55192316 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:55192316 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:42719540 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:42719540 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:121745674 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:121745674 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:9739825 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:9739825 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20337583 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20337583 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:33603359 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:33603359 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:47684470 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:47684470 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:90281423 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:90281423 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:7456679 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:7456679 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:119748273 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:119748273 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:30565730 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:30565730 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:106695502 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:106695502 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:106697259 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:106697259 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:14809564 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:14809564 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:108931124 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:108931124 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:140053967 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:140053967 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:17160600 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:17160600 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5289935 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5289935 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:239990375 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:239990375 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:18869183 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:18869183 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:26020627 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:26020627 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:27839641 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:27839641 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:71146054 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:71146054 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152195502 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152195502 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:56540080 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:56540080 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148839552 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148839552 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148842438 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148842438 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148842444 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148842444 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:31714296 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:31714296 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:53653001 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:53653001 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:10403931 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:10403931 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:8822263 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:8822263 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:27708431 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:27708431 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:23509788 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:23509788 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:160482399 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:160482399 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:118624667 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:118624667 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124754316 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124754316 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:110303632 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:110303632 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:76728356 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:76728356 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:143324216 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:143324216 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:182399687 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:182399687 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:15726136 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:15726136 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:37555472 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:37555472 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:31435412 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:31435412 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:187501010 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:187501010 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:54823577 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:54823577 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:156671558 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:156671558 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:231740323 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:231740323 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:41243685 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:41243685 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:17949216 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:17949216 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:147028043 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:147028043 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:20113628 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:20113628 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:21919585 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:21919585 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:88658478 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:88658478 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:2594025 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:2594025 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:36703264 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:36703264 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:36746673 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:36746673 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:202777822 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:202777822 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:55964016 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:55964016 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142638513 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142638513 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:6513540 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:6513540 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:97275399 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:97275399 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:43493838 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:43493838 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:241686785 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:241686785 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:34259738 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:34259738 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:7804403 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:7804403 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55268523 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55268523 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55278410 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55278410 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158059484 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158059484 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:27950465 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:27950465 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:38933679 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:38933679 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:52758716 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:52758716 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:60907576 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:60907576 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:50822677 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:50822677 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152659292 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152659292 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:153177534 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:153177534 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:189700803 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:189700803 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:66085594 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:66085594 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:71929008 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:71929008 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55086081 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55086081 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54745776 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54745776 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:161014926 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:161014926 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:141232925 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:141232925 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57574277 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57574277 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:46889780 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:46889780 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:46479405 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:46479405 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:151137500 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:151137500 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:39902136 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:39902136 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148664880 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:148664880 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:78131119 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:78131119 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:172930253 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:172930253 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:39100386 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:39100386 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:22142806 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:22142806 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:119752127 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:119752127 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57881805 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57881805 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:70892348 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:70892348 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:138713451 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:138713451 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:150908776 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:150908776 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:118535547 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:118535547 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:88056780 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:88056780 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:126769301 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:126769301 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:135206205 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:135206205 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:20246067 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:20246067 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:30602062 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:30602062 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34964585 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34964585 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:39421871 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:39421871 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19585097 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19585097 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:47698046 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:47698046 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:47748973 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:47748973 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:56703924 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:56703924 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:38287772 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:38287772 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:151420976 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:151420976 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:149902484 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:149902484 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:30659788 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:30659788 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8968992 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8968992 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9018635 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9018635 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9018639 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9018639 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:1082525 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:1082525 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:1154330 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:1154330 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:1289699 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:1289699 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:153027164 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:153027164 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:108205245 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:108205245 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10419235 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10419235 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10446926 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10446926 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10356685 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10356685 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:23885630 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:23885630 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10299851 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:10299851 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:111349025 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:111349025 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:46901261 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:46901261 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57440632 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57440632 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:26285527 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:26285527 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:171092686 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:171092686 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:120107117 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:120107117 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:30260255 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:30260255 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:78334813 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:78334813 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:15542242 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:15542242 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:113102575 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:113102575 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:113133595 C>A maps to ENST00000397960 Y744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:113133595 C>A maps to ENST00000397960 Y744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:22910111 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:22910111 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:133668777 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:133668777 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:140402551 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:140402551 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:91967706 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:91967706 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:84028175 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:84028175 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:55989596 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:55989596 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:44915986 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:44915986 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:29647377 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:29647377 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:77208721 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:77208721 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:47864701 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:47864701 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:65108278 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:65108278 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:183221974 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:183221974 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:2635346 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:2635346 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:150704097 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:150704097 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:32178752 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:32178752 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:155743747 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:155743747 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:69339749 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:69339749 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:45691031 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:45691031 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:110937163 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:110937163 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:5933435 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:5933435 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:9005042 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:9005042 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:50847352 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:50847352 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:79117752 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:79117752 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:88679281 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:88679281 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:34360148 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:34360148 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:163297402 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:163297402 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:73754026 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:73754026 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:102343811 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:102343811 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:105642414 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:105642414 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:123838840 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:123838840 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:4470542 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:4470542 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6816948 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6816948 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:76853518 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:76853518 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:26695257 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:26695257 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:161780909 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:161780909 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:44547344 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:44547344 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:56367779 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:56367779 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:93024134 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:93024134 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:71570409 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:71570409 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:56447104 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:56447104 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:165746506 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:165746506 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:650003 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:650003 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:103780654 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:103780654 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:148701309 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:148701309 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20410371 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20410371 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:239171017 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:239171017 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7360449 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7360449 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:137146272 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:137146272 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:58348257 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:58348257 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:22095521 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:22095521 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:45312563 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:45312563 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:56151239 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:56151239 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:155261543 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:155261543 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:33021743 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:33021743 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:43196462 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:43196462 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:23690773 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:23690773 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:208234016 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:208234016 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:118359481 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:118359481 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:118199316 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:118199316 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:118199420 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:118199420 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:44280244 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:44280244 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:140400280 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:140400280 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:89896388 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:89896388 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:53104301 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:53104301 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:38138548 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:38138548 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:131873297 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:131873297 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:94640767 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:94640767 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:23522321 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:23522321 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:69104501 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:69104501 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:20414665 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:20414665 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:95953845 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:95953845 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:13629018 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:13629018 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43348324 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43348324 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352054 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352054 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352069 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352069 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352144 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352144 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352203 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352203 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352358 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43352358 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43520003 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43520003 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43579857 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43579857 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43583711 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43583711 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43600833 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:43600833 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:53175553 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:53175553 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:123589224 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:123589224 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:807773 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:807773 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:112883985 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:112883985 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:18750418 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:18750418 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:18765020 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:18765020 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:8528583 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:8528583 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:48181432 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:48181432 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:15718718 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:15718718 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:121701104 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:121701104 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:130845994 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:130845994 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:79312550 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:79312550 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:64502895 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:64502895 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:79348488 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:79348488 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:79349012 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:79349012 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:103136361 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:103136361 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:8568611 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:8568611 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:111751001 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:111751001 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:198511067 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:198511067 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:3418611 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:3418611 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:241094013 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:241094013 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:241161740 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:241161740 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:104664377 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:104664377 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:105026022 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:105026022 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:67690053 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:67690053 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31529070 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31529070 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:141889040 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:141889040 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:30315513 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:30315513 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:55462537 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:55462537 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:20222058 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:20222058 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:99138989 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:99138989 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:100746893 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:100746893 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:67871250 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:67871250 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92999101 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92999101 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237608945 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237608945 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237906877 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237906877 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237993982 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:237993982 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:33941531 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:33941531 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:45763597 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:45763597 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73663573 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73663573 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:41514591 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:41514591 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:6465098 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:6465098 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:9081066 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:9081066 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:35205484 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:35205484 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:243419401 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:243419401 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:4215483 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:4215483 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:12185049 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:12185049 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:12185209 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:12185209 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:13830991 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:13830991 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:169560753 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:169560753 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:9054072 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:9054072 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:150919301 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:150919301 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:22019267 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:22019267 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:14166484 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:14166484 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:134618281 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:134618281 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:134619638 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:134619638 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:2265146 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:2265146 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:91727547 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:91727547 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:100838169 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:100838169 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:100901732 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:100901732 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:46247887 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:46247887 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:31933554 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:31933554 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:31935477 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:31935477 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:122811980 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:122811980 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:6591059 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:6591059 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:61597756 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:61597756 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:119012871 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:119012871 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:50820452 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:50820452 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:36686152 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:36686152 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:38307746 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:38307746 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:19785892 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:19785892 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:95906670 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:95906670 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:107427425 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:107427425 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92301240 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92301240 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92375832 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92375832 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:205902066 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:205902066 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:44197569 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:44197569 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:105238409 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:105238409 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:57193674 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:57193674 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:75699661 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:75699661 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:42337924 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:42337924 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:72400177 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:72400177 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111860041 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111860041 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111962756 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111962756 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:103299661 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:103299661 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:48471963 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:48471963 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:143223109 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:143223109 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:156237152 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:156237152 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:130930349 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:130930349 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:10286856 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:10286856 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:46195105 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:46195105 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:51569418 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:51569418 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:51617037 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:51617037 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:601109 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:601109 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:186578534 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:186578534 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:108338836 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:108338836 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:108427396 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:108427396 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:106802765 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:106802765 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:121393465 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:121393465 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:24102628 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:24102628 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:85029553 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:85029553 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:3397853 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:3397853 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:55909775 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:55909775 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:55648774 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:55648774 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158597409 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158597409 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158604297 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158604297 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158621340 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158621340 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158623306 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158623306 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158644315 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158644315 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:54876660 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:54876660 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:45619976 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:45619976 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:76019341 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:76019341 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:149495279 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:149495279 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:66784985 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:66784985 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:172750444 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:172750444 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:23823297 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:23823297 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:16052989 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:16052989 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:125467106 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:125467106 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:130442360 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:130442360 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:130442370 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:130442370 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:120840406 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:120840406 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:4459501 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:4459501 T>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:136199368 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:136199368 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:75469876 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:75469876 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:75591496 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:75591496 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:152804076 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:152804076 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:7324167 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:7324167 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34151073 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:34151073 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:9991595 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:9991595 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:23906842 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:23906842 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:118684079 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:118684079 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:106083825 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:106083825 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:55906967 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:55906967 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:85469918 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:85469918 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152057309 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152057309 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:104491049 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:104491049 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:30695586 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:30695586 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:2291163 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:2291163 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:30753087 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:30753087 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:50146436 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:50146436 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:112369361 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:112369361 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:150501974 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:150501974 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111769715 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111769715 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:29670308 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:29670308 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:42267770 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:42267770 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:217724870 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:217724870 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:175355156 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:175355156 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:144345051 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:144345051 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:10914518 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:10914518 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:41204199 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:41204199 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:228595872 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:228595872 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:140407475 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:140407475 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:14387460 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:14387460 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:193029185 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:193029185 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:101347343 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:101347343 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142625145 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142625145 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142626067 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142626067 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142572148 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:142572148 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:98562187 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:98562187 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:143435961 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:143435961 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179463211 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179463211 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179473796 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179473796 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54941974 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54941974 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:10197323 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:10197323 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19503936 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19503936 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:18596856 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:18596856 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:114676854 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:114676854 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:69968458 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:69968458 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:33482220 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:33482220 T>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:96090582 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:96090582 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:24916321 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:24916321 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:215807774 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:215807774 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216051287 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216051287 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:120189601 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:120189601 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:5044682 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:5044682 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:8988719 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:8988719 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:77896580 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:77896580 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:108116940 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:108116940 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:101188929 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:101188929 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:247419369 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:247419369 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:12566863 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:12566863 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:61082737 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:61082737 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:122624730 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:122624730 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:100950239 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:100950239 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:66446809 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:66446809 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:102239782 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:102239782 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:128881742 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chrX:128881742 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:17232155 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:17232155 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:183474512 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:183474512 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:155631237 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:155631237 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:98349494 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:98349494 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:138768511 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:138768511 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:52903848 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:52903848 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:122968120 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:122968120 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:6621323 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:6621323 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44896372 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44896372 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44901290 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44901290 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:147120724 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:147120724 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52076427 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52076427 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:71512969 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:71512969 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6962757 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6962757 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57862887 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57862887 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57908263 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57908263 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58046691 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58046691 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9585953 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9585953 G>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56901654 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56901654 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:16458776 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:16458776 C>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:20829314 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:20829314 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:11608977 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:11608977 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:124496641 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:124496641 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:8325042 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:8325042 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:38160022 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:38160022 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:53455906 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:53455906 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:53156107 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:53156107 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:53157380 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:53157380 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:21209281 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:21209281 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:102188063 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:102188063 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:135975242 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:135975242 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58563848 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58563848 C>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr4:123317613 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr4:123317613 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr13:42882828 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr13:42882828 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:133327571 G>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:133327571 G>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr11:134252532 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr11:134252532 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:88379988 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:88379988 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:48880077 C>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:48880077 C>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132597408 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132597408 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:7556474 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:7556474 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr5:21884284 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr5:21884284 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:151502366 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:151502366 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:11866265 T>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:11866265 T>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:224553426 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:224553426 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr7:146829727 G>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr7:146829727 G>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:43910795 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:43910795 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:59409859 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:59409859 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:72310144 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:72310144 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:23240068 A>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:23240068 A>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr6:152202017 T>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr6:152202017 T>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr15:93173583 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr15:93173583 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr13:99090190 C>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr13:99090190 C>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr13:29001830 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr13:29001830 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr6:42931215 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr6:42931215 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr4:94145937 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr4:94145937 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:77796078 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:77796078 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:6381547 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:6381547 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:66221766 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:66221766 T>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr15:78765428 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr15:78765428 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:94170865 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:94170865 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:209797106 G>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:209797106 G>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr5:169675886 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr5:169675886 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr11:56954646 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr11:56954646 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:60837499 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:60837499 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chrX:64951881 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chrX:64951881 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:21486709 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:21486709 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:204956836 A>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:204956836 A>C did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr10:102584289 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr10:102584289 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:207228016 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:207228016 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:18573849 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr12:18573849 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:127730674 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:127730674 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr6:34730287 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr6:34730287 C>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:220334105 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:220334105 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr15:43893570 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr15:43893570 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:102873662 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:102873662 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:39988359 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:39988359 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:194331816 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:194331816 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:77715254 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr14:77715254 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:111768942 G>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:111768942 G>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr21:45509830 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr21:45509830 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:37917015 G>A did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:37917015 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:85410631 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:85410631 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr14:58832049 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr14:58832049 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:180374507 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:180374507 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr10:124459310 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr10:124459310 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:113481806 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:113481806 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:71418844 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:71418844 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:85606316 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:85606316 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:46759223 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:46759223 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:67000100 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:67000100 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:122227630 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:122227630 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr13:111119376 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr13:111119376 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:14502760 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:14502760 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:61503737 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:61503737 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:678621 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:678621 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:19112460 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:19112460 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr12:51074575 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr12:51074575 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:134670939 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:134670939 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr20:820167 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr20:820167 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:73291523 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:73291523 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:14974722 A>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:14974722 A>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:72685745 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:72685745 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:58095235 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:58095235 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:29541768 T>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:29541768 T>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:7348142 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:7348142 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr12:21729048 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr12:21729048 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr12:104496729 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr12:104496729 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:31323939 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:31323939 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:185902972 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:185902972 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:120608221 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:120608221 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr10:64982075 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr10:64982075 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:141757913 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:141757913 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:60073817 T>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:60073817 T>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr14:57863603 T>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr14:57863603 T>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr8:24774550 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr8:24774550 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:52514139 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:52514139 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:101093944 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:101093944 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:108508778 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:108508778 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:56154502 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:56154502 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:86532786 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:86532786 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr20:41408950 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr20:41408950 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:101705710 C>T maps to ENST00000424264 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:101705710 C>T maps to ENST00000424264 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:134033091 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:134033091 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:50221133 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:50221133 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:35806793 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:35806793 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:220332257 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:220332257 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:30723535 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:30723535 A>G did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:36467467 T>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:36467467 T>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:7998481 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:7998481 G>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:74329727 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:74329727 A>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:18684356 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:18684356 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr13:96529417 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr13:96529417 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:150064244 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:150064244 T>C did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr8:196464 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr8:196464 C>A did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:135966606 C>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:135966606 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48349763 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48349763 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48431792 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48431792 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48545807 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48545807 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:66890270 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:66890270 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:16130470 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:16130470 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:150921269 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:150921269 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:35580412 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:35580412 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:124806909 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:124806909 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:31344537 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:31344537 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:44073119 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:44073119 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:140997112 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:140997112 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:6753872 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:6753872 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:185678668 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:185678668 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20648256 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20648256 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20548511 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20548511 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:7477088 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:7477088 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:5568415 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:5568415 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100606329 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100606329 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207436384 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207436384 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207451969 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207451969 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207457272 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207457272 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:72511078 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:72511078 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:5146669 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:5146669 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:100594282 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:100594282 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:100739681 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:100739681 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:77354873 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:77354873 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:128984682 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:128984682 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:84324456 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:84324456 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167803154 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167803154 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7717472 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7717472 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7743901 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7743901 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7784471 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7784471 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:161587510 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:161587510 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:178305791 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:178305791 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:16904561 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:16904561 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159042906 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159042906 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:4830051 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:4830051 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:4834405 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:4834405 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:33004658 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:33004658 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109385918 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109385918 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:134225785 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:134225785 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:137776451 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:137776451 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:116154499 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:116154499 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:97413147 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:97413147 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:24505041 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:24505041 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:95448589 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:95448589 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:45919679 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:45919679 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:38471727 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:38471727 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:38533893 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:38533893 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:875146 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:875146 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:41545643 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:41545643 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:113748370 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:113748370 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:114238830 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:114238830 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:114271283 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:114271283 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:190585553 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:190585553 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:54517680 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:54517680 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:139839058 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:139839058 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:26547292 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:26547292 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83331854 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83331854 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:39358626 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:39358626 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:129959491 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:129959491 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:11187940 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:11187940 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:17954075 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:17954075 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157014185 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157014185 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:18804767 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:18804767 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:28284090 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:28284090 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:101857062 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:101857062 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:35834138 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:35834138 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69489845 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69489845 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69499926 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69499926 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:2924773 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:2924773 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:76398058 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:76398058 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:132397453 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:132397453 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:62580764 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:62580764 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:176845591 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:176845591 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:29157987 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:29157987 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:161753748 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:161753748 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:96789103 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:96789103 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:7838158 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:7838158 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153664007 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153664007 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:67487351 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:67487351 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:77302207 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:77302207 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:76889980 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:76889980 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:182987452 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:182987452 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:373321 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:373321 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:11039168 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:11039168 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:143570375 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:143570375 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:69666724 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:69666724 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:70065868 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:70065868 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:33392558 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:33392558 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:104003907 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:104003907 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:70837173 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:70837173 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:76212683 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:76212683 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:98006724 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:98006724 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:69093719 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:69093719 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:112989920 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:112989920 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:36963003 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:36963003 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83687104 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83687104 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:15643551 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:15643551 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:26377085 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:26377085 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:103750512 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:103750512 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:134752354 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:134752354 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:76253420 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:76253420 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:86048379 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:86048379 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:112681596 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:112681596 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:47011990 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:47011990 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:57092055 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:57092055 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23567324 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23567324 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:36906362 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:36906362 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:32904698 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:32904698 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34195623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34195623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:30665157 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:30665157 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:4670146 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:4670146 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:22970729 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:22970729 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:228288677 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:228288677 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:60499069 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:60499069 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:20234188 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:20234188 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:10594455 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:10594455 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:20031058 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:20031058 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:241830950 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:241830950 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:170518665 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:170518665 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6678127 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6678127 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:196241862 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:196241862 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:113460894 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:113460894 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:81307718 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:81307718 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:98946951 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:98946951 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:99030524 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:99030524 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:164435321 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:164435321 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:165706972 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:165706972 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:151914467 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:151914467 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:57349119 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:57349119 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:98728713 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:98728713 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65120335 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65120335 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:140807750 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:140807750 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:141009867 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:141009867 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:49086870 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:49086870 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:81579549 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:81579549 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:174977925 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:174977925 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:188247863 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:188247863 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:44137733 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:44137733 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:44147611 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:44147611 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:42703406 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:42703406 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:110492381 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:110492381 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:75686949 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:75686949 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:3038591 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:3038591 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:41437555 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:41437555 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142988811 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142988811 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:70205359 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:70205359 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:15132406 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:15132406 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:42784570 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:42784570 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:191092809 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:191092809 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:113225515 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:113225515 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:46511610 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:46511610 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111290817 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111290817 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:86133560 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:86133560 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:32688966 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:32688966 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:75398948 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:75398948 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158152113 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158152113 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158324999 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158324999 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:35827308 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:35827308 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49838762 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49838762 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:60781145 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:60781145 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:14508152 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:14508152 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:100858667 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:100858667 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:21882776 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:21882776 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:21884277 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:21884277 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:19520995 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:19520995 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73544643 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73544643 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:58564269 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:58564269 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:58576533 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:58576533 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:31322998 A>T maps to NM_004932.2 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:31322998 A>T maps to NM_004932.2 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:61761188 G>T maps to ENST00000394178 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:61761188 G>T maps to ENST00000394178 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:61823217 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:61823217 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26890738 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26890738 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26902550 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26902550 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:4935707 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:4935707 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109807746 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109807746 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109810086 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109810086 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:100385101 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:100385101 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:131185653 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:131185653 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:31917946 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:31917946 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:196645093 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:196645093 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:87797820 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:87797820 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:4405994 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:4405994 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:50854543 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:50854543 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:57127244 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:57127244 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:146727414 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:146727414 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:93499634 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:93499634 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:7797418 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:7797418 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:175622430 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:175622430 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:43891506 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:43891506 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:80561793 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:80561793 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:143018979 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:143018979 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:14705930 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:14705930 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:36203044 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:36203044 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:140167590 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:140167590 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:140282639 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:140282639 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:36304086 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:36304086 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:10286380 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:10286380 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:87656938 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:87656938 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:21549942 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:21549942 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:2908648 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:2908648 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:100061782 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:100061782 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:125555950 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:125555950 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:121354611 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:121354611 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:101784314 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:101784314 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:70916802 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:70916802 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:48271877 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:48271877 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:139736815 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:139736815 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:139749905 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:139749905 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:109859043 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:109859043 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107864944 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107864944 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107433554 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107433554 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107447900 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:107447900 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:137622367 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:137622367 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:10096643 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:10096643 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:70976303 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:70976303 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:71003855 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:71003855 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:61458656 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:61458656 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:73923757 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:73923757 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:17119986 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:17119986 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207826952 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:207826952 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:211447451 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:211447451 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:186256438 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:186256438 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:1413186 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:1413186 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:61950711 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:61950711 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:61951014 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:61951014 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:34118078 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:34118078 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:34164249 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:34164249 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:34285976 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:34285976 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113259208 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113259208 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113347733 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113347733 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113648978 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113648978 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113657315 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:113657315 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:23473775 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:23473775 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:100093221 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:100093221 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:69281493 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:69281493 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:16996590 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:16996590 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:17089614 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:17089614 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:101502782 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:101502782 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:48996879 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:48996879 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:49040332 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:49040332 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:36089912 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:36089912 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:145689626 C>A maps to NM_001129888.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:145689626 C>A maps to NM_001129888.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:41515414 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:41515414 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:96609838 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:96609838 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135371431 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135371431 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:99457446 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:99457446 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:99363897 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:99363897 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47533118 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47533118 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:72133869 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:72133869 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:109292332 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:109292332 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:42824364 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:42824364 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:87514501 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:87514501 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:176894442 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:176894442 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:69541944 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:69541944 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:50994462 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:50994462 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:31695230 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:31695230 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:103907481 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:103907481 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:118583273 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:118583273 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:134683448 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:134683448 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:41202623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:41202623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:11831803 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:11831803 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:197659334 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:197659334 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:32200741 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:32200741 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:12677391 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:12677391 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:2209447 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:2209447 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:124330322 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:124330322 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:124402584 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:124402584 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:32632365 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:32632365 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:124416666 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:124416666 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:21042352 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:21042352 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:11737901 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:11737901 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:22217306 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:22217306 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65852407 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65852407 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:225662740 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:225662740 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:169098051 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:169098051 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:169138801 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:169138801 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:464109 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:464109 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:154519682 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:154519682 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:117309725 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:117309725 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:41683920 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:41683920 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:28986391 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:28986391 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:56472826 A>T maps to ENST00000361203 L1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:56472826 A>T maps to ENST00000361203 L1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:58959803 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:58959803 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:7133955 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:7133955 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:82126742 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:82126742 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71840559 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71840559 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:158223321 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:158223321 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:4236893 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:4236893 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:65637570 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:65637570 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:34419596 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:34419596 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:24089623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:24089623 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:140035960 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:140035960 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:73462780 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:73462780 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6898525 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6898525 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6921921 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6921921 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:77078167 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:77078167 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:132476983 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:132476983 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:21938045 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:21938045 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:21938456 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:21938456 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:32594622 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:32594622 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:89445176 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:89445176 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:89478185 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:89478185 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:66213940 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:66213940 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:66439850 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:66439850 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:134960227 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:134960227 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:37865978 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:37865978 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:19146257 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:19146257 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:6505713 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:6505713 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152382261 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152382261 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:66054070 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:66054070 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:46760789 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:46760789 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:154212799 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:154212799 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109103200 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109103200 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74490029 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74490029 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:45728739 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:45728739 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:135419168 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:135419168 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:29526294 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:29526294 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:68194706 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:68194706 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:62273610 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:62273610 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:46280911 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:46280911 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129083836 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129083836 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:34147932 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:34147932 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:190203493 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:190203493 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:131831426 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:131831426 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:38224702 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:38224702 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7862790 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:7862790 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:127704738 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:127704738 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:99322094 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:99322094 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:99365614 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:99365614 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:16577151 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:16577151 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:175180759 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:175180759 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:137808185 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:137808185 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157566159 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157566159 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:108523024 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:108523024 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:45603510 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:45603510 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:72708302 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:72708302 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:142500187 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:142500187 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:128497167 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:128497167 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:29001802 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:29001802 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:28608430 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:28608430 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:180048535 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:180048535 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:180058780 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:180058780 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:240492625 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:240492625 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:153492933 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:153492933 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:171310526 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:171310526 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:65417198 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:65417198 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:89395379 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:89395379 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:2974398 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:2974398 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:71161914 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:71161914 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:12708278 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:12708278 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:161309523 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:161309523 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:161528203 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:161528203 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:27725782 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:27725782 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:26582029 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:26582029 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:99764019 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:99764019 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:154996816 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:154996816 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:34648700 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:34648700 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:48650665 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:48650665 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:10877346 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:10877346 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:57976836 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:57976836 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74810382 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74810382 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:158402500 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:158402500 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:69565520 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:69565520 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:137609996 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:137609996 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:42467210 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:42467210 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:42688846 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:42688846 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30714282 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30714282 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:6535939 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:6535939 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:74537692 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:74537692 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:42018078 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:42018078 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:14599222 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:14599222 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56226146 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56226146 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56377893 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56377893 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:179138614 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:179138614 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:47284632 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:47284632 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121395672 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121395672 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20337592 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20337592 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:96688032 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:96688032 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:92560078 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:92560078 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:94958126 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:94958126 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:176561208 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:176561208 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:57596919 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:57596919 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:25701166 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:25701166 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:19028712 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:19028712 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:123431745 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:123431745 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:113604229 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:113604229 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:113638738 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:113638738 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:11696628 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:11696628 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:102649249 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:102649249 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:24664339 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:24664339 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:158256803 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:158256803 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:122562058 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:122562058 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:87406930 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:87406930 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:37319185 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:37319185 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:140059564 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:140059564 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:140059820 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:140059820 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:66788144 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:66788144 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:42895197 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:42895197 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27552212 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27552212 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:17449642 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:17449642 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:106856727 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:106856727 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:122629214 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:122629214 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:36113709 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:36113709 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:5247007 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:5247007 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:5248059 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:5248059 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:5275442 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:5275442 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153227638 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153227638 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121366028 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121366028 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:71787453 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:71787453 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:125621626 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:125621626 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:73980717 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:73980717 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:31852720 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:31852720 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:93247543 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:93247543 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:65414907 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:65414907 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:65474858 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:65474858 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:42734517 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:42734517 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:228645070 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:228645070 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:148782773 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:148782773 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:30138025 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:30138025 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:162918059 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:162918059 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:26044028 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:26044028 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:96743086 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:96743086 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:119981572 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:119981572 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:119987963 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:119987963 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:44949597 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:44949597 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:148839587 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:148839587 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:20398288 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:20398288 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:183770952 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:183770952 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:147830872 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:147830872 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:3240377 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:3240377 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:70884248 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:70884248 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:70955160 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:70955160 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21231731 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21231731 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21305308 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21305308 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27682469 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27682469 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:107937322 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:107937322 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:57939336 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:57939336 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:38414075 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:38414075 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:130407955 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:130407955 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:130412979 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:130412979 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:18735786 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:18735786 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:81578275 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:81578275 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:29959657 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:29959657 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:113887116 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:113887116 G>C did not map to a codon.
Alternatively spliced codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:105170249 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:105170249 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:143066973 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:143066973 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:123109247 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:123109247 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:15655808 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:15655808 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:3651108 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:3651108 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31391992 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31391992 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:9552597 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:9552597 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:7750927 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:7750927 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:52864567 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:52864567 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:78618037 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:78618037 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:4685791 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:4685791 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:146971352 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:146971352 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:153949633 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:153949633 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:62704055 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:62704055 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:39671147 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:39671147 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:78850048 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:78850048 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:113740081 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:113740081 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:138657095 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:138657095 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:196288557 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:196288557 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:196302955 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:196302955 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:36703228 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:36703228 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:136637766 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:136637766 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:48626235 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:48626235 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47183527 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47183527 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:27788218 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:27788218 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:8718688 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:8718688 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:138599508 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:138599508 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:168434740 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:168434740 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69549444 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69549444 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69549454 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69549454 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:55289927 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:55289927 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:55346479 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:55346479 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:202888818 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:202888818 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:166231975 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:166231975 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:97423826 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:97423826 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:187177113 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:187177113 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:160243950 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:160243950 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:117047555 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:117047555 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:32635432 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:32635432 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:52758189 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:52758189 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:52760631 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:52760631 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:39724159 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:39724159 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31743940 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31743940 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:32119525 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:32119525 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:32185574 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:32185574 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:143799612 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:143799612 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:108843691 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:108843691 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:107580393 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:107580393 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:107744881 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:107744881 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:133942246 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:133942246 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:152659669 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:152659669 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:46730496 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:46730496 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:136566001 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:136566001 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:136594094 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:136594094 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:16504243 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:16504243 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:40095186 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:40095186 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:54818641 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:54818641 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:81969165 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:81969165 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:99753461 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:99753461 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105502806 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105502806 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105521316 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105521316 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141113846 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141113846 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141115762 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141115762 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141533624 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141533624 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141571199 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:141571199 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:169995230 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:169995230 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:44201547 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:44201547 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:24537987 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:24537987 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:67384226 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:67384226 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:30354866 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:30354866 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70339275 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70339275 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70460377 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70460377 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70493758 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70493758 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70503627 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:70503627 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:238642499 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:238642499 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:24784927 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:24784927 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:150071022 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:150071022 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:14108200 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:14108200 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:151896672 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:151896672 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:151283159 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:151283159 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:35820218 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:35820218 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30269743 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:30269743 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:140984184 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:140984184 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:114092318 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:114092318 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:49019347 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:49019347 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103650919 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103650919 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:21208450 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:21208450 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:12011070 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:12011070 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:68061871 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:68061871 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:210517892 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:210517892 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:210574612 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:210574612 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:136709383 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:136709383 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:179696250 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:179696250 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:160623872 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:160623872 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:220823917 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:220823917 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3783286 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3783286 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:119180641 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:119180641 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:113742169 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:113742169 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:85412636 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:85412636 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:119738030 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:119738030 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:47600873 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:47600873 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:28134864 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:28134864 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:191354473 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:191354473 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141750291 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141750291 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:74928869 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:74928869 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:14294610 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:14294610 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:102667942 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:102667942 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:61201478 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:61201478 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:61263094 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:61263094 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:13112197 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:13112197 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:43870533 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:43870533 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:161275974 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:161275974 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:138119350 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:138119350 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:121444403 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:121444403 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:224822085 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:224822085 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:125047613 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:125047613 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:59945698 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:59945698 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:59949038 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:59949038 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62361566 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62361566 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21929999 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21929999 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:151256324 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:151256324 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:149867530 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:149867530 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:63564890 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:63564890 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9000264 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9000264 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9002237 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9002237 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9027166 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9027166 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:102053700 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:102053700 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:47374043 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:47374043 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:48441223 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:48441223 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10212799 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10212799 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:108110902 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:108110902 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10416163 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10416163 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10544584 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10544584 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10359122 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:10359122 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23852575 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23852575 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111357035 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111357035 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:46743599 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:46743599 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:109364924 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:109364924 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:109535357 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:109535357 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:192278935 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:192278935 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:31099936 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:31099936 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:26414544 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:26414544 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:47365453 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:47365453 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:76925116 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:76925116 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31131497 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31131497 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:1906742 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:1906742 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:1920953 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:1920953 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:175164984 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:175164984 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113103424 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113103424 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:71038944 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:71038944 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:126236445 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:126236445 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:119026355 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:119026355 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:21074852 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:21074852 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:152432388 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:152432388 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:130799235 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:130799235 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:21191310 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:21191310 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:73454191 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:73454191 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:70416244 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:70416244 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:70532851 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:70532851 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103978933 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103978933 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:220012364 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:220012364 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:71264712 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:71264712 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:236143999 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:236143999 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:52535717 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:52535717 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:51196185 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:51196185 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:5811758 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:5811758 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:7984701 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:7984701 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:247611816 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:247611816 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:26087292 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:26087292 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:33684703 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:33684703 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:44555306 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:44555306 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:182772962 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:182772962 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:34889355 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:34889355 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100897337 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100897337 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:2936918 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:2936918 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:59510517 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:59510517 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:6604575 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:6604575 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:93794753 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:93794753 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:86199333 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:86199333 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:107867584 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:107867584 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:88474542 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:88474542 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:17316821 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:17316821 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:110255542 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:110255542 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:37326089 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:37326089 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56857485 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56857485 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:101623683 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:101623683 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:133044418 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:133044418 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:133051385 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:133051385 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:123697730 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:123697730 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:70774510 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:70774510 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:10313197 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:10313197 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:193366712 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:193366712 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:67273738 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:67273738 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:74800784 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:74800784 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248166940 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248166940 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248247577 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248247577 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:56246910 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:56246910 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4945571 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4945571 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:56125442 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:56125442 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:24945965 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:24945965 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:26725344 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:26725344 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:4204166 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:4204166 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:56501118 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:56501118 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:43284824 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:43284824 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:39667177 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:39667177 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:9523182 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:9523182 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:112694416 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:112694416 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124487391 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124487391 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:39591296 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:39591296 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:162475079 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:162475079 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:226570899 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:226570899 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:44536469 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:44536469 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:91238287 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:91238287 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:91238334 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:91238334 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:55943076 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:55943076 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:56106295 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:56106295 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:36896467 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:36896467 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:105108401 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:105108401 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:233424943 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:233424943 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:165801670 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:165801670 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:165810022 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:165810022 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:20602564 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:20602564 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:149312180 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:149312180 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:122843222 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:122843222 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:15222117 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:15222117 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:119059605 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:119059605 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:22010351 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:22010351 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:216916161 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:216916161 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:42933311 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:42933311 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:54959907 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:54959907 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:58349708 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:58349708 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:96421774 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:96421774 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:79671399 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:79671399 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:111664220 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:111664220 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:77538338 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:77538338 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:98411165 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:98411165 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:39573208 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:39573208 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:57994096 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:57994096 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3639070 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3639070 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:27381757 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:27381757 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:119347880 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:119347880 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:48591897 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:48591897 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:8637753 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:8637753 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:219487611 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:219487611 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:96014437 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:96014437 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:198953564 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:198953564 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:4721278 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:4721278 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:132109566 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:132109566 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:23691659 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:23691659 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:145828018 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:145828018 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:103041281 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:103041281 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:146177841 C>T maps to ENST00000497985 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:146177841 C>T maps to ENST00000497985 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153698542 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153698542 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:131829859 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:131829859 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:131848871 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:131848871 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:129275045 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:129275045 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:74327365 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:74327365 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:108138059 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:108138059 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:116171082 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:116171082 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121179123 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121179123 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121203828 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121203828 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:134385639 C>T maps to ENST00000419118 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:134385639 C>T maps to ENST00000419118 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:134394064 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:134394064 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:134397673 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:134397673 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:94978133 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:94978133 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:94979581 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:94979581 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:19566157 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:19566157 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:16288033 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:16288033 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:31133881 C>A maps to ENST00000441888 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:31133881 C>A maps to ENST00000441888 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:46611057 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:46611057 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:27745099 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:27745099 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:27840525 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:27840525 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:37529179 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:37529179 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:48931380 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:48931380 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135164841 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135164841 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91524330 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91524330 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:23517985 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:23517985 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:47266761 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:47266761 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:49690330 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:49690330 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:106871988 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:106871988 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:36458869 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:36458869 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142457401 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142457401 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:18656783 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:18656783 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43244400 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43244400 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43411501 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43411501 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43421726 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43421726 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43600891 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:43600891 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:23751208 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:23751208 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103008534 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103008534 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:30807239 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:30807239 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:131116957 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:131116957 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:18759423 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:18759423 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8340219 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8340219 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8404420 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8404420 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8465428 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8465428 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:62204749 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:62204749 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:220161694 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:220161694 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:40827779 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:40827779 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:41100896 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:41100896 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:121623629 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:121623629 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:108079664 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:108079664 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:58398562 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:58398562 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:74276295 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:74276295 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:61471567 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:61471567 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:110950712 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:110950712 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:20114366 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:20114366 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:69036309 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:69036309 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:173850326 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:173850326 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113537594 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113537594 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:82348913 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:82348913 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53555177 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53555177 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:106361904 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:106361904 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:238730094 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:238730094 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167599652 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167599652 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79349046 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79349046 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79253731 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79253731 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:141018470 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:141018470 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103294529 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103294529 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103629476 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103629476 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153200916 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:153200916 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:43600683 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:43600683 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:240966166 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:240966166 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:25697056 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:25697056 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:130912695 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:130912695 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:8895380 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:8895380 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:104943645 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:104943645 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:66099705 C>A maps to ENST00000424433 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:66099705 C>A maps to ENST00000424433 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:87404327 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:87404327 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:41179412 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:41179412 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:25338207 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:25338207 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:2514676 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:2514676 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:77614330 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:77614330 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124742272 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124742272 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124766322 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124766322 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:60849022 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:60849022 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:77277351 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:77277351 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:117686135 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:117686135 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:92765688 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:92765688 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:38180392 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:38180392 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113266086 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113266086 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:118920823 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:118920823 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:66795621 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:66795621 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:39926418 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:39926418 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:78516404 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:78516404 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:55483307 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:55483307 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:62316828 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:62316828 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:60097101 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:60097101 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:186917318 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:186917318 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:70161319 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:70161319 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:71634198 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:71634198 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:155294587 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:155294587 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:237669978 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:237669978 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:237804304 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:237804304 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:44392383 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:44392383 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:128750981 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:128750981 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:9981216 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:9981216 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:75310398 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:75310398 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:78138068 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:78138068 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:54139939 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:54139939 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:193653 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:193653 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:159606465 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:159606465 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:38647681 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:38647681 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:38649768 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:38649768 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:139299457 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:139299457 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:18485209 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:18485209 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:12206454 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:12206454 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:151340866 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:151340866 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:84671659 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:84671659 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:84702465 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:84702465 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:47873462 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:47873462 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:13380846 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:13380846 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:26131588 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:26131588 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:61379773 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:61379773 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:61570573 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:61570573 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:28595550 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:28595550 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:30978810 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:30978810 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:27285168 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:27285168 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:65466073 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:65466073 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:132211390 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:132211390 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:48244640 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:48244640 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:67091695 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:67091695 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:67133273 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:67133273 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:80533931 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:80533931 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:51189750 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:51189750 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:154942390 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:154942390 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:117057192 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:117057192 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:51957402 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:51957402 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:38682755 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:38682755 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:164714443 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:164714443 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:54645369 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:54645369 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:44663864 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:44663864 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:34528408 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:34528408 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:122809070 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:122809070 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:45217715 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:45217715 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:135390247 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:135390247 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:43316360 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:43316360 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:60713986 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:60713986 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:113416316 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:113416316 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:38311831 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:38311831 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:19634609 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:19634609 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:107431828 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:107431828 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:92365064 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:92365064 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:44201299 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:44201299 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43395489 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43395489 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:32429010 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:32429010 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:42031438 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:42031438 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:25667959 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:25667959 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:47178311 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:47178311 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:18280025 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:18280025 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:21468866 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:21468866 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:190445201 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:190445201 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57185125 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57185125 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:108151294 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:108151294 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:10748843 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:10748843 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:75685474 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:75685474 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:75707765 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:75707765 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:162815077 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:162815077 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:150769254 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:150769254 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:85279674 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:85279674 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14509521 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14509521 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:40401923 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:40401923 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:173486576 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:173486576 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:21450296 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:21450296 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:98816304 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:98816304 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:128649850 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:128649850 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:2104285 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:2104285 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:72962986 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:72962986 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:183507601 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:183507601 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:130924962 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:130924962 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:19192363 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:19192363 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:108427575 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:108427575 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:121430370 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:121430370 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:16067944 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:16067944 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:214972994 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:214972994 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:118617342 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:118617342 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:123595018 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:123595018 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:142597120 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:142597120 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:52946137 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:52946137 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:88901609 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:88901609 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158605573 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158605573 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158609347 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:158609347 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:131375780 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:131375780 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:66475807 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:66475807 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:94817861 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:94817861 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:99905753 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:99905753 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:149490781 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:149490781 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53079701 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53079701 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:116862155 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:116862155 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:116869780 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:116869780 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:52546837 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:52546837 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:103984671 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:103984671 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:104082118 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:104082118 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:40452656 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:40452656 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:23768876 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:23768876 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:39540830 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:39540830 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:31404598 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:31404598 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:44237824 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:44237824 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:114864399 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:114864399 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:86328846 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:86328846 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152453417 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152453417 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152757290 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152757290 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152792680 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:152792680 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:99653999 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:99653999 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:202574944 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:202574944 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:222753218 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:222753218 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140698506 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140698506 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:61176637 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:61176637 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:62701011 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:62701011 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:145826845 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:145826845 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:96157704 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:96157704 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:124155735 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:124155735 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:104457448 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:104457448 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:53457100 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:53457100 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69945099 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:69945099 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:246704238 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:246704238 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:105883795 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:105883795 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:122802177 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:122802177 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:32590057 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:32590057 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:168169342 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:168169342 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:63031763 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:63031763 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83788526 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83788526 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:20027136 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:20027136 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129825326 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129825326 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129847656 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:129847656 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27261695 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27261695 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14177211 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14177211 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:92032572 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:92032572 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:24565468 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:24565468 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:24565682 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:24565682 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:154754353 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:154754353 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:68725405 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:68725405 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:68964770 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:68964770 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:101308534 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:101308534 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:12253927 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:12253927 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6667329 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:6667329 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:74669996 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:74669996 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113703897 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113703897 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113703918 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113703918 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113731173 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:113731173 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:68837975 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:68837975 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:20137990 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:20137990 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:10922028 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:10922028 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:111922371 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:111922371 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:49885556 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:49885556 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55033072 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55033072 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:72728364 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:72728364 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248031117 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248031117 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:122835847 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:122835847 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:73164369 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:73164369 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142625434 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142625434 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142626721 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142626721 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142630651 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142630651 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141957547 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141957547 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:81448887 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:81448887 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:71537908 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:71537908 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:43425762 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:43425762 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:38460489 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:38460489 A>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:135266239 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:135266239 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179543388 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179543388 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179554423 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179554423 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179658341 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179658341 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:72245640 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:72245640 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:19755784 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:19755784 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49388629 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49388629 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:15615366 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:15615366 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:52492897 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:52492897 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:113088318 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:113088318 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:154238971 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:154238971 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:83602680 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:83602680 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:64707452 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:64707452 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:35988534 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:35988534 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:6413469 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:6413469 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73057591 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73057591 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:35616771 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:35616771 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:215803337 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:215803337 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:215916492 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:215916492 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216595680 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216595680 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113679686 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113679686 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:76799372 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:76799372 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:106710471 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:106710471 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:108116590 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:108116590 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:108138974 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:108138974 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:177632897 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:177632897 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:41188325 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:41188325 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:38768138 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:38768138 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124006696 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:124006696 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:61032535 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:61032535 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:110429643 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:110429643 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:70885804 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:70885804 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:85716010 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:85716010 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:167217819 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:167217819 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:54349804 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:54349804 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:863590 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:863590 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:96000633 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:96000633 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:10062038 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:10062038 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:10094124 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:10094124 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:31573111 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:31573111 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168096498 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168096498 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168101658 G>T maps to NM_152381.5 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168101658 G>T maps to NM_152381.5 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:56367336 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:56367336 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:180772790 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:180772790 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:114120920 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:114120920 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:136652399 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:136652399 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:44797436 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:44797436 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:70462302 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chrX:70462302 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:22256392 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:22256392 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:133768686 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:133768686 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:53393591 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:53393591 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:32344879 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:32344879 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:53643420 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:53643420 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:37721333 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:37721333 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:21606239 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:21606239 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:28304793 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:28304793 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:57194476 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:57194476 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:44101004 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:44101004 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:48370424 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:48370424 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9585017 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9585017 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:59181 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:59181 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:52633910 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:52633910 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:227842033 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:227842033 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:247163447 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:247163447 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:53950457 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:53950457 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34842458 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34842458 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:238049328 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:238049328 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:238053756 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:238053756 T>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58600231 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58600231 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58189270 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58189270 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:187694447 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:187694447 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:58118793 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:58118793 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:67020287 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:67020287 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:101603414 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:101603414 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:132378623 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:132378623 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:19446058 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:19446058 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:178548630 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:178548630 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:79082887 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:79082887 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:18906924 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:18906924 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:131916423 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:131916423 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:26000331 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:26000331 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:3057653 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:3057653 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:74363523 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:74363523 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:65656340 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:65656340 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:104116868 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:104116868 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:41574385 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:41574385 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:169105947 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:169105947 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:33933051 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:33933051 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:84306562 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:84306562 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:135789231 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:135789231 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:135861767 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:135861767 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:101858803 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:101858803 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:2878480 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:2878480 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:66937279 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:66937279 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:84487159 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:84487159 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:77296342 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:77296342 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:94087693 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:94087693 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:32862810 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:32862810 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:153171896 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:153171896 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:347264 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:347264 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:167889139 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:167889139 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:100615020 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:100615020 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:76463512 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:76463512 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:36906046 G>A maps to ENST00000310178 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:36906046 G>A maps to ENST00000310178 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:77042520 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:77042520 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:178482170 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:178482170 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr21:45945459 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr21:45945459 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:34584922 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:34584922 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:132382864 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:132382864 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:139707382 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:139707382 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:86158001 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:86158001 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:71411469 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:71411469 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:73478597 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:73478597 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:38447621 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:38447621 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:60503224 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:60503224 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:80718410 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:80718410 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:29407609 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:29407609 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:109937256 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:109937256 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:26864010 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:26864010 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:12264485 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:12264485 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:10147895 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:10147895 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40845265 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40845265 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:101749532 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:101749532 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:101784478 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:101784478 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr21:46899968 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr21:46899968 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:139701045 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:139701045 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:107823684 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:107823684 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:139076974 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:139076974 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:3215644 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:3215644 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:49701714 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:49701714 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:41265540 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:41265540 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:117423017 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:117423017 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:44871271 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:44871271 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:105879709 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:105879709 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:36163016 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:36163016 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:41597864 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:41597864 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:42524019 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:42524019 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:134711001 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:134711001 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:137284459 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:137284459 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:51115031 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:51115031 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:38127664 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:38127664 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:124357626 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:124357626 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:53930283 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:53930283 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56211606 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56211606 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:98088686 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:98088686 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:68036609 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:68036609 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:116593846 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:116593846 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:26439593 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:26439593 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:158139390 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:158139390 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:74923761 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:74923761 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:37256172 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:37256172 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:236388358 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:236388358 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:239025473 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:239025473 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:154124610 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:154124610 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:46221238 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:46221238 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:89849523 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:89849523 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:89858585 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:89858585 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:48757710 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:48757710 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:117365818 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:117365818 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:161682847 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:161682847 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:125079971 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:125079971 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:110048514 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:110048514 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:110048528 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:110048528 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:180057361 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:180057361 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:146676461 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:146676461 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:27184301 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:27184301 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:161580457 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:161580457 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:128121652 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:128121652 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:104119879 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:104119879 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:171811346 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:171811346 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:58752330 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:58752330 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:58757866 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:58757866 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:120702466 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:120702466 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:38128806 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:38128806 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:13256229 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:13256229 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:27565627 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:27565627 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:127447806 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:127447806 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:127453784 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:127453784 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:50684053 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:50684053 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:145235187 G>T maps to NM_032450.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:145235187 G>T maps to NM_032450.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:41065625 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:41065625 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:46823598 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:46823598 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:19319124 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:19319124 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:185931616 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:185931616 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:24140886 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:24140886 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:43043132 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:43043132 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:131803236 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:131803236 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr13:47408948 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr13:47408948 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:130415508 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:130415508 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:103053582 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:103053582 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:131100273 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:131100273 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:123151955 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:123151955 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:31421614 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:31421614 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:54781364 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:54781364 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:33644868 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:33644868 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:65309978 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:65309978 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:19492582 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:19492582 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:94046441 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:94046441 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:100013023 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:100013023 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:36850789 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:36850789 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:53042920 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:53042920 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:52647158 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:52647158 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr21:32253912 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr21:32253912 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:871317 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:871317 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:51885852 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:51885852 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:133948742 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:133948742 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:141739652 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:141739652 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:170032885 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:170032885 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:140953459 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:140953459 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:43656530 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:43656530 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:165111034 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:165111034 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:10407053 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:10407053 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:119738113 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:119738113 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:37622418 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:37622418 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:207610310 A>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:207610310 A>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:90320535 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:90320535 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:141727037 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:141727037 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:99291447 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:99291447 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:40859298 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:40859298 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:73013690 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:73013690 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:102592587 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:102592587 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:198400419 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:198400419 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:108746748 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:108746748 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:48325704 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:48325704 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:2027067 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:2027067 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:78520991 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:78520991 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:133636362 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:133636362 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:45269391 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:45269391 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:56520126 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:56520126 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:14989554 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:14989554 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:6670019 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:6670019 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:89068943 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:89068943 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:107937772 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:107937772 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:88474460 G>A maps to ENST00000343782 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:88474460 G>A maps to ENST00000343782 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:105643123 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:105643123 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:13779147 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:13779147 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:248167376 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:248167376 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:248247658 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:248247658 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:102345882 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:102345882 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:26697097 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:26697097 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:9524846 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:9524846 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:9543472 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:9543472 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:9546387 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:9546387 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:176680888 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:176680888 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:119139781 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:119139781 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:134075549 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:134075549 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:120432184 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:120432184 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:153095668 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:153095668 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:111941513 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:111941513 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:32058293 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:32058293 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:201286625 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:201286625 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:33021796 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:33021796 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:198966094 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:198966094 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:209614 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:209614 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:24948525 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:24948525 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:42825923 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:42825923 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:6383622 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:6383622 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:50128886 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:50128886 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:150867151 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:150867151 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:142460173 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:142460173 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:43348816 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:43348816 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:43707840 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:43707840 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:15470074 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:15470074 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:23751281 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:23751281 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:488415 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:488415 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:79002051 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:79002051 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:8113796 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:8113796 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:45368460 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:45368460 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:127975855 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:127975855 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:80364045 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:80364045 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:80381538 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:80381538 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr13:79943173 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr13:79943173 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:9808085 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:9808085 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:79313696 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:79313696 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:204126244 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:204126244 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:40613900 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:40613900 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:55609440 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:55609440 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:27050935 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:27050935 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56510422 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56510422 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:57247100 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:57247100 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:67860782 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:67860782 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:237494302 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:237494302 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:237666856 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:237666856 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:237850809 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:237850809 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:35532554 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:35532554 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:148761292 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:148761292 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:25669682 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:25669682 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:38791550 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:38791550 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:52168314 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:52168314 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:108197890 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:108197890 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:57369416 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:57369416 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:109309720 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:109309720 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:26707664 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:26707664 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:81371929 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:81371929 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:81318890 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:81318890 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:45192210 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:45192210 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:61414390 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:61414390 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:15075051 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:15075051 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:205897188 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:205897188 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:9129447 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:9129447 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:61519222 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:61519222 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:220495099 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:220495099 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:313936 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:313936 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:115574995 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:115574995 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:61303030 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:61303030 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:128582494 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:128582494 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:17912966 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:17912966 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:21989933 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:21989933 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:1690043 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:1690043 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:32372238 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:32372238 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:99918569 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:99918569 T>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:31805999 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:31805999 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:24993262 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:24993262 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:53028756 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:53028756 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:52555555 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:52555555 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110835457 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110835457 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:23823392 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:23823392 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:43625742 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:43625742 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:125902102 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:125902102 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:31659292 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:31659292 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:62591578 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:62591578 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:10964125 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:10964125 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:70607398 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:70607398 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:70678025 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:70678025 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:23895128 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:23895128 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:71601979 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:71601979 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:101666805 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:101666805 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:57539172 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:57539172 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:52896359 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:52896359 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:120998453 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:120998453 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:103064618 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:103064618 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:10400610 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:10400610 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:10407100 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:10407100 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:2427390 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:2427390 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:35725187 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:35725187 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:104232540 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:104232540 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:112856326 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:112856326 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:175372255 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:175372255 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:45808732 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:45808732 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:50955117 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:50955117 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:179585470 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:179585470 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:179586543 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:179586543 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:22853905 A>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:22853905 A>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:49850833 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:49850833 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:54707283 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:54707283 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:126236332 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:126236332 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:11976834 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:11976834 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:5033580 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:5033580 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40926773 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40926773 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110456856 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110456856 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:67340424 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:67340424 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:174052168 A>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:174052168 A>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:147120392 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:147120392 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:101166803 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chrX:101166803 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:2850497 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:2850497 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:57211258 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:57211258 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:16225546 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:16225546 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:148586758 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:148586758 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7125753 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7125753 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15059389 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15059389 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47266982 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47266982 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:38520135 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:38520135 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:58938102 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:58938102 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:207452045 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:207452045 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:33891833 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:33891833 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:72517684 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:72517684 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:100672098 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:100672098 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:43837563 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:43837563 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:64617236 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:64617236 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:202920270 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:202920270 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:1887258 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:1887258 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:10328197 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:10328197 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:49518511 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:49518511 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:100185431 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:100185431 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:100360619 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:100360619 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:74303030 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:74303030 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:87531380 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:87531380 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:78805810 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:78805810 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:178386181 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:178386181 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:6054642 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:6054642 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:4834457 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:4834457 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:96924382 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:96924382 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:55190107 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:55190107 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:134217843 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:134217843 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:4884564 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:4884564 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:165638719 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:165638719 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:34175351 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:34175351 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:233244765 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:233244765 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:44296804 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:44296804 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:56401629 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:56401629 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:110169245 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:110169245 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:38462116 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:38462116 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:38543366 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:38543366 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:104297219 T>C maps to NM_001008218.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:104297219 T>C maps to NM_001008218.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:2114392 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:2114392 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:43342303 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:43342303 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:115351167 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:115351167 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:63661775 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:63661775 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:27529351 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:27529351 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:176851966 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:176851966 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:119249596 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:119249596 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161816432 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161816432 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:25981179 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:25981179 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:25266549 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:25266549 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:119504509 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:119504509 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:3831505 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:3831505 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36043856 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36043856 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:57605302 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:57605302 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:26542830 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:26542830 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:50310656 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:50310656 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:69684793 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:69684793 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:215634075 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:215634075 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:171561143 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:171561143 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:25002633 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:25002633 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:56869346 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:56869346 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:61867855 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:61867855 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:28459953 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:28459953 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:37704292 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:37704292 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55813392 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55813392 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:26410035 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:26410035 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:180376778 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:180376778 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:56395575 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:56395575 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118423606 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118423606 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:112703646 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:112703646 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:97051522 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:97051522 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58711526 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58711526 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:60903805 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:60903805 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:34376526 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:34376526 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:8735878 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:8735878 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:3724724 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:3724724 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:73139188 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:73139188 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:200867634 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:200867634 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247712341 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247712341 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:12819156 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:12819156 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:35444784 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:35444784 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:3234357 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:3234357 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:31815323 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:31815323 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:63540352 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:63540352 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:6679342 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:6679342 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:81308394 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:81308394 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:41154926 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:41154926 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:165711595 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:165711595 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:35716273 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:35716273 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:40955402 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:40955402 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:99754178 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:99754178 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:120774022 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:120774022 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:89874906 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:89874906 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:67427970 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:67427970 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:2715845 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:2715845 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:181707570 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:181707570 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:181714586 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:181714586 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:86062750 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:86062750 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:159162340 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:159162340 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:71418848 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:71418848 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:188245399 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:188245399 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:188280511 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:188280511 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:7811039 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:7811039 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:2969712 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:2969712 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:116243769 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:116243769 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:68609549 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:68609549 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:57765052 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:57765052 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106214162 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106214162 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:77304923 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:77304923 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:32833292 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:32833292 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:85568569 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:85568569 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:57394571 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:57394571 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:74432908 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:74432908 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:74493580 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:74493580 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:7647634 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:7647634 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:158326776 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:158326776 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:41939153 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:41939153 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51729437 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51729437 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:135732339 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:135732339 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14492286 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14492286 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:19504461 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:19504461 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:21882850 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:21882850 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:59203894 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:59203894 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:202712280 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:202712280 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:85525671 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:85525671 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:5167502 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:5167502 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43098828 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43098828 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:17662299 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:17662299 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46794393 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46794393 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:50863503 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:50863503 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:14157830 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:14157830 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7797427 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7797427 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:133424566 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:133424566 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:203185975 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:203185975 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:440098 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:440098 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:23767578 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:23767578 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:184103973 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:184103973 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:32323089 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:32323089 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:26805826 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:26805826 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143043904 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143043904 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:16374725 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:16374725 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:6981534 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:6981534 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:95661000 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:95661000 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:140178651 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:140178651 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:19168200 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:19168200 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:19230159 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:19230159 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:123318798 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:123318798 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:87670872 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:87670872 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:74316355 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:74316355 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:70543060 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:70543060 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:103352647 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:103352647 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:32130906 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:32130906 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:116956755 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:116956755 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189856501 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189856501 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189871740 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189871740 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:227973109 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:227973109 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189917591 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189917591 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:47407629 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:47407629 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:68430097 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:68430097 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211457698 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211457698 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211512462 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211512462 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:65617369 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:65617369 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:17183670 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:17183670 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:3165785 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:3165785 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113267787 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113267787 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113650899 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113650899 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113697599 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113697599 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70822917 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70822917 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:23667701 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:23667701 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:80389589 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:80389589 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:11111211 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:11111211 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:117375300 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:117375300 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:117451048 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:117451048 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:17168734 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:17168734 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:17168737 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:17168737 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:225367912 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:225367912 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:48979369 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:48979369 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160194777 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160194777 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:118588359 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:118588359 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:125780517 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:125780517 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:55034893 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:55034893 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:29958067 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:29958067 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:238493 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:238493 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:3784373 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:3784373 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:196807847 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:196807847 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:83691445 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:83691445 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36003862 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36003862 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124268488 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124268488 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124383366 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124383366 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:76447033 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:76447033 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:38691264 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:38691264 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:132201288 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:132201288 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:132220238 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:132220238 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:65111562 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:65111562 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:116540088 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:116540088 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:162930441 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:162930441 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:168670162 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:168670162 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:28669613 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:28669613 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:56468158 T>C maps to ENST00000361203 A3456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:56468158 T>C maps to ENST00000361203 A3456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:15524603 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:15524603 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:45394260 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:45394260 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:57670487 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:57670487 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:96277239 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:96277239 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:158223225 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:158223225 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:33703793 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:33703793 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:57897532 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:57897532 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:93202759 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:93202759 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:60469359 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:60469359 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:19959641 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:19959641 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:55268109 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:55268109 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14882982 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14882982 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:77080395 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:77080395 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:111470658 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:111470658 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:111938996 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:111938996 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:66217098 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:66217098 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:66217325 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:66217325 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:133836378 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:133836378 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:66013923 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:66013923 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:14564106 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:14564106 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:137298212 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:137298212 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:29526432 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:29526432 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155223797 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155223797 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:113264772 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:113264772 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:116837190 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:116837190 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:10691085 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:10691085 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:177249518 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:177249518 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:25024082 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:25024082 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:49204076 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:49204076 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:10070423 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:10070423 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:45605797 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:45605797 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:150885994 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:150885994 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48818225 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48818225 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:127624375 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:127624375 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:127644817 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:127644817 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:127712285 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:127712285 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:117595936 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:117595936 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161692733 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161692733 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:34326841 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:34326841 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:180048334 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:180048334 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:171227363 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:171227363 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:146685224 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:146685224 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:49179694 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:49179694 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:41558172 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:41558172 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:79294093 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:79294093 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:48559138 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:48559138 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:32868712 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:32868712 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:96652194 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:96652194 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:39169740 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:39169740 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:101147817 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:101147817 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:151393488 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:151393488 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:26793425 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:26793425 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:46066406 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:46066406 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:90012059 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:90012059 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:88401001 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:88401001 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:31178381 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:31178381 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:230372546 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:230372546 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:9820476 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:9820476 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:81626990 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:81626990 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:154282030 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:154282030 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:42987729 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:42987729 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:55192147 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:55192147 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:34913228 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:34913228 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:69207974 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:69207974 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:93555329 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:93555329 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:121396084 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:121396084 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:132896978 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:132896978 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:132889903 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:132889903 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:47676027 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:47676027 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:80011139 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:80011139 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:123470185 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:123470185 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:105623601 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:105623601 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:87898571 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:87898571 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120732879 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120732879 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:112719870 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:112719870 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:15637948 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:15637948 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5592929 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5592929 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5602038 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5602038 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:104474503 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:104474503 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:18767421 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:18767421 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:18868675 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:18868675 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:41009953 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:41009953 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:31644053 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:31644053 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:89415295 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:89415295 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:72638744 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:72638744 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:118963794 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:118963794 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:186055283 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:186055283 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:186114498 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:186114498 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:43043116 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:43043116 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42814273 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42814273 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:148876275 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:148876275 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:60794654 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:60794654 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:119987982 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:119987982 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:128000852 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:128000852 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:31712456 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:31712456 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:88732481 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:88732481 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140034244 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140034244 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:114242484 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:114242484 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:113736304 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:113736304 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:103903795 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:103903795 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:39735415 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:39735415 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:166892080 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:166892080 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:76714944 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:76714944 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:242663120 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:242663120 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:15247163 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:15247163 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:128577740 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:128577740 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156504071 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156504071 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156504888 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156504888 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:78762865 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:78762865 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:85947999 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:85947999 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:13251397 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:13251397 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:37627074 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:37627074 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:31422369 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:31422369 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:3638334 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:3638334 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:31368273 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:31368273 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:20418641 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:20418641 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:26553054 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:26553054 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:185268722 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:185268722 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:39742498 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:39742498 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:30854434 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:30854434 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:15390180 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:15390180 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47597272 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47597272 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:48098389 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:48098389 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:75436823 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:75436823 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:119914621 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:119914621 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:211280525 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:211280525 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:128781126 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:128781126 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:215256634 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:215256634 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:34302604 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:34302604 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:6734941 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:6734941 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:75152409 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:75152409 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:27789145 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:27789145 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58955610 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58955610 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44794740 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44794740 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44794829 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44794829 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:108285290 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:108285290 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118699930 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118699930 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:176858036 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:176858036 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:17788230 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:17788230 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:29048653 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:29048653 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:16496343 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:16496343 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:241683326 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:241683326 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:10385929 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:10385929 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:4916933 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:4916933 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:132073046 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:132073046 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55284726 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55284726 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55270394 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55270394 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36347996 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36347996 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:87742852 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:87742852 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:27934198 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:27934198 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:173735508 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:173735508 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:52910815 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:52910815 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:52965671 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:52965671 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:52646151 C>T maps to ENST00000257935 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:52646151 C>T maps to ENST00000257935 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:32253872 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:32253872 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:31813082 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:31813082 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:32119527 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:32119527 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129637114 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129637114 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129781319 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129781319 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:112499257 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:112499257 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:60888685 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:60888685 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:133932536 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:133932536 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:30756238 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:30756238 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:138555138 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:138555138 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:138556211 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:138556211 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:49227148 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:49227148 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:81892405 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:81892405 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:82450530 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:82450530 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:39985904 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:39985904 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:155670386 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:155670386 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:151792627 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:151792627 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:59279770 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:59279770 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:170088133 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:170088133 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68157557 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68157557 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:122677576 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:122677576 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:127670725 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:127670725 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:70397084 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:70397084 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:70397308 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:70397308 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:76975798 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:76975798 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:33484576 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:33484576 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:160738873 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:160738873 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:4275961 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:4275961 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:4283636 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:4283636 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:39781941 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:39781941 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:1326671 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:1326671 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:166991136 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:166991136 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:54841038 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:54841038 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:78256628 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:78256628 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:77109369 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:77109369 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:43592151 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:43592151 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:19380753 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:19380753 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:161530729 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:161530729 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:87023014 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:87023014 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:42109705 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:42109705 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:217123991 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:217123991 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:43929930 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:43929930 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:85422307 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:85422307 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:118543086 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:118543086 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:3296479 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:3296479 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:37375945 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:37375945 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:47909679 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:47909679 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:119212732 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:119212732 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:74770937 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:74770937 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:141763283 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:141763283 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:141778753 G>C maps to ENST00000475668 V1932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:141778753 G>C maps to ENST00000475668 V1932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:4723303 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:4723303 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:12284014 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:12284014 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:185650300 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:185650300 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:151884726 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:151884726 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:44641814 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:44641814 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:62965392 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:62965392 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:48342066 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:48342066 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:36476416 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:36476416 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:55752273 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:55752273 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:242035204 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:242035204 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:64902464 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:64902464 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:56570405 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:56570405 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236992741 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236992741 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:3248466 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:3248466 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:203140495 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:203140495 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8464928 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8464928 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:15894003 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:15894003 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10265369 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10265369 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10316056 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10316056 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:123411573 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:123411573 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:16676117 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:16676117 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:18062438 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:18062438 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:27426586 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:27426586 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:192226894 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:192226894 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:171260965 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:171260965 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:171260985 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:171260985 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:1983683 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:1983683 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62854569 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62854569 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:78571144 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:78571144 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:16893021 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:16893021 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:19359718 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:19359718 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:54901761 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:54901761 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:183859678 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:183859678 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:115760748 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:115760748 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:16767139 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:16767139 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:72740196 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:72740196 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:211844727 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:211844727 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:77221373 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:77221373 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:77246995 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:77246995 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:34262602 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:34262602 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236187341 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236187341 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55508637 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55508637 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:56249155 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:56249155 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:50756677 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:50756677 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:79916179 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:79916179 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:89173818 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:89173818 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:108044601 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:108044601 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36336499 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36336499 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:34818225 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:34818225 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:73865936 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:73865936 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:73884559 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:73884559 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:132082104 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:132082104 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:96066710 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:96066710 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:88483994 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:88483994 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:88726814 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:88726814 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:17332892 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:17332892 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:71068125 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:71068125 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:72006572 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:72006572 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161987176 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161987176 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:27880153 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:27880153 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248138974 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248138974 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248262532 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248262532 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5509928 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5509928 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:4702913 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:4702913 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55563012 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55563012 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:38078965 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:38078965 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:21883563 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:21883563 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:76784448 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:76784448 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:29630545 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:29630545 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:41853476 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:41853476 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:66001222 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:66001222 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:51472518 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:51472518 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:75937541 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:75937541 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:150844444 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:150844444 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:102584321 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:102584321 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:91368618 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:91368618 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:56106071 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:56106071 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140593606 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140593606 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:167401997 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:167401997 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:5522721 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:5522721 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:165895890 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:165895890 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:165956913 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:165956913 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:31913060 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:31913060 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:15222122 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:15222122 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:152682148 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:152682148 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:54982527 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:54982527 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:133873658 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:133873658 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:133851901 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:133851901 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:99376648 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:99376648 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:85712360 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:85712360 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8792279 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8792279 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:27370471 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:27370471 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:25153863 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:25153863 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:47840160 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:47840160 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:47873916 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:47873916 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:47920244 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:47920244 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:137235148 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:137235148 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:51503503 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:51503503 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:51774351 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:51774351 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:64029379 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:64029379 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:219492735 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:219492735 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:198965944 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:198965944 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:131936091 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:131936091 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:96167116 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:96167116 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:131878738 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:131878738 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:94562909 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:94562909 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:6038961 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:6038961 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:160222067 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:160222067 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118355699 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118355699 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118305771 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118305771 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:44341906 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:44341906 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:74988160 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:74988160 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:842515 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:842515 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120186228 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120186228 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:37518059 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:37518059 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:146080892 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:146080892 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:102004305 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:102004305 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:23509887 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:23509887 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:68989580 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:68989580 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:57467225 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:57467225 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:31155183 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:31155183 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43699059 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43699059 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43674119 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43674119 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43520064 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43520064 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43579464 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43579464 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43765797 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43765797 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:67961107 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:67961107 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:35782000 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:35782000 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:86358164 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:86358164 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:29618377 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:29618377 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:119599299 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:119599299 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:45534839 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:45534839 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:3147060 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:3147060 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:136399363 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:136399363 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:56928423 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:56928423 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:87847003 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:87847003 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:135815727 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:135815727 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:135872732 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:135872732 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:114792813 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:114792813 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:53580773 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:53580773 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:79384668 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:79384668 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:73101739 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:73101739 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:43617487 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:43617487 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:111685008 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:111685008 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62707770 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62707770 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:72925145 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:72925145 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:105261641 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:105261641 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:21051953 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:21051953 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:3597783 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:3597783 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:153627775 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:153627775 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:170586191 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:170586191 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:8706808 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:8706808 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:166921634 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:166921634 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54705331 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54705331 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:87459368 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:87459368 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:93023354 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:93023354 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:49513734 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:49513734 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:237801617 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:237801617 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:34060758 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:34060758 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:34093079 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:34093079 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:5616088 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:5616088 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68312247 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68312247 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:62063820 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:62063820 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:166166776 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:166166776 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:38597356 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:38597356 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:83784651 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:83784651 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:12982489 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:12982489 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:84636097 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:84636097 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61223382 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61223382 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:2890821 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:2890821 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:65819817 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:65819817 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:30899392 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:30899392 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:22020820 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:22020820 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:1915457 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:1915457 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:164741643 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:164741643 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:219252211 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:219252211 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:56906185 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:56906185 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:124837602 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:124837602 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:20008162 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:20008162 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:20022501 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:20022501 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:43269799 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:43269799 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:62782032 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:62782032 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4837572 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4837572 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48426610 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48426610 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:41382520 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:41382520 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:103030857 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:103030857 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:128326162 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:128326162 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:85476166 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:85476166 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:8428396 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:8428396 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:124954892 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:124954892 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:336865 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:336865 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:40657513 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:40657513 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:72758058 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:72758058 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:2116105 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:2116105 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:128849109 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:128849109 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:28279968 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:28279968 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:42807600 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:42807600 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:10273678 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:10273678 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:10279776 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:10279776 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:139276234 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:139276234 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:90756854 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:90756854 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:25222225 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:25222225 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51465600 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51465600 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51465602 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51465602 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:107827659 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:107827659 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106675708 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106675708 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106937981 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106937981 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106959751 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106959751 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106983112 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:106983112 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:107022076 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:107022076 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:16505859 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:16505859 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:4863845 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:4863845 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:52946238 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:52946238 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:229046381 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:229046381 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:147211010 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:147211010 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:168155033 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:168155033 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:158609310 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:158609310 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:94800346 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:94800346 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:206567046 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:206567046 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:28004801 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:28004801 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:26377334 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:26377334 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:149508906 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:149508906 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:48206897 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:48206897 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:134478043 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:134478043 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:76771577 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:76771577 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:74526205 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:74526205 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:219562475 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:219562475 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:81862170 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:81862170 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:134931136 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:134931136 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:21831341 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:21831341 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:39966845 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:39966845 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:152529433 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:152529433 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:64599254 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:64599254 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55690318 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:55690318 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:75426078 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:75426078 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:166838564 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:166838564 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:234563601 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:234563601 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:13371104 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:13371104 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:45776159 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:45776159 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:162275686 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:162275686 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:85448063 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:85448063 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31008835 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31008835 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31019150 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31019150 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:115971458 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:115971458 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:115590855 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:115590855 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:133941468 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:133941468 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:72058475 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:72058475 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:171910452 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:171910452 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:154744017 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:154744017 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:83359551 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:83359551 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:12195759 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:12195759 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:93609353 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:93609353 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:175372820 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:175372820 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:175375869 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:175375869 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:128807309 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:128807309 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:65821896 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:65821896 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10910410 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10910410 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10971253 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10971253 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:30363836 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:30363836 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:239261685 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:239261685 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:141294173 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:141294173 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55034973 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55034973 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55035913 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55035913 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:165961172 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:165961172 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:92460139 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:92460139 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:116616040 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:116616040 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:16331613 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:16331613 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:142625176 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:142625176 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:122518947 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:122518947 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:113233281 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:113233281 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179647206 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179647206 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:151554080 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:151554080 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:43862835 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:43862835 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:23258708 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:23258708 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:59338119 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:59338119 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:234602663 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:234602663 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:234581479 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:234581479 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70066152 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70066152 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:26875597 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:26875597 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:96106530 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:96106530 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:35453318 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:35453318 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:17537869 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:17537869 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216221777 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216221777 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216363547 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216363547 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216424521 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216424521 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:17135380 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:17135380 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:58258062 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:58258062 T>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:95922550 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:95922550 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:5035823 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:5035823 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:52593028 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:52593028 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:101731764 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:101731764 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:144761744 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:144761744 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:101186344 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:101186344 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:37014215 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:37014215 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:79918000 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:79918000 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:100115082 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:100115082 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:42470889 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:42470889 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:97342550 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:97342550 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:97347467 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:97347467 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:54610348 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:54610348 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:27741612 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:27741612 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:122633523 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:122633523 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:128484485 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:128484485 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:80585242 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:80585242 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:33628484 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:33628484 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:32417709 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:32417709 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:184171163 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:184171163 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:168108518 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:168108518 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:56270116 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:56270116 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:56364859 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:56364859 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:135738352 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:135738352 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:100741125 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:100741125 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62420981 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62420981 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:111625388 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chrX:111625388 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:37304321 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:37304321 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:28476563 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:28476563 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:145157859 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:145157859 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:135615211 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:135615211 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:68222901 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:68222901 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:25268632 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:25268632 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:44946981 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:44946981 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58455276 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58455276 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54074758 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54074758 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:14132188 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:14132188 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53007832 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53007832 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53007838 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53007838 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:53281 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:53281 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:3493188 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:3493188 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58231741 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58231741 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58016901 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58016901 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:40553219 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:40553219 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:100866744 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:100866744 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:238051908 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:238051908 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58557211 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:58557211 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:58117947 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:58117947 T>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:38959518 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:38959518 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:18675908 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:18675908 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:230841596 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:230841596 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr12:124218406 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr12:124218406 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr19:1789737 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr19:1789737 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:21784477 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:21784477 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:22987945 A>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:22987945 A>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr12:96694171 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr12:96694171 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:85552876 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:85552876 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:78927767 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:78927767 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr13:111090844 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr13:111090844 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr21:47544501 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr21:47544501 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr22:37319416 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr22:37319416 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:158291127 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:158291127 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chrX:86087199 T>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chrX:86087199 T>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr5:140966597 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr5:140966597 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr14:80672112 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr14:80672112 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:67912193 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:67912193 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:22927331 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:22927331 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:212538080 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:212538080 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:119295857 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:119295857 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:37541160 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:37541160 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr22:32871328 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr22:32871328 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr19:45973795 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr19:45973795 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:150210545 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:150210545 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:56374945 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:56374945 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:28421941 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:28421941 A>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:145534982 T>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:145534982 T>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:121107518 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:121107518 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr12:66621891 T>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr12:66621891 T>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:150649480 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:150649480 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:233482121 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:233482121 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:109278677 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr2:109278677 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:48887525 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:48887525 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr22:42456898 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr22:42456898 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:47754125 T>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:47754125 T>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:131815341 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:131815341 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:34295149 T>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:34295149 T>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:115095150 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:115095150 G>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:118320120 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:118320120 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:43777198 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:43777198 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:98452828 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:98452828 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr21:43796589 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr21:43796589 G>C did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr17:17788166 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr17:17788166 C>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr18:74625670 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr18:74625670 C>G did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:57194476 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr7:57194476 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:31073699 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:31073699 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:111213350 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:111213350 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:109507606 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:109507606 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:109507917 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:109507917 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:195295723 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:195295723 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:9496287 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:9496287 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:219528121 C>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:219528121 C>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:59853989 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:59853989 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr4:113486302 T>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr4:113486302 T>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr9:131591150 A>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr9:131591150 A>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:14024150 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:14024150 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:57650381 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:57650381 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr8:101146304 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr8:101146304 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr4:158142086 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr4:158142086 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:22172820 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:22172820 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:22173764 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:22173764 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:160849220 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:160849220 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr16:57775497 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr16:57775497 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr12:55354767 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr12:55354767 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:8315893 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:8315893 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:70930878 A>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:70930878 A>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:138688029 A>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chrX:138688029 A>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:16979014 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:16979014 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr11:1154212 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr11:1154212 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:95211730 A>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:95211730 A>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:15984099 T>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:15984099 T>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr14:57269168 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr14:57269168 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:102780350 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:102780350 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr8:77896529 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr8:77896529 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:207241414 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:207241414 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr11:45970398 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr11:45970398 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:208219158 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:208219158 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr18:43591130 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr18:43591130 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:36255722 T>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:36255722 T>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:86676294 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:86676294 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:50146864 A>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:50146864 A>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:11448172 T>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:11448172 T>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr4:39457936 C>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr4:39457936 C>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr11:61976174 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr11:61976174 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:153839647 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:153839647 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr14:23816452 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr14:23816452 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr15:92663628 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr15:92663628 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr14:76232395 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr14:76232395 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:27745417 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:27745417 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:43665046 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr1:43665046 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr7:75988020 A>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr7:75988020 A>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:71654582 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:71654582 G>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:53913790 G>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:53913790 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:61843482 T>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:61843482 T>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:5963186 C>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:5963186 C>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr21:27372544 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr21:27372544 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:10863169 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:10863169 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:27742962 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:27742962 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:32972944 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:32972944 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:37210754 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:37210754 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:121481257 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:121481257 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:45015297 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:45015297 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:76513452 T>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:76513452 T>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:86488566 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:86488566 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:207867651 T>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:207867651 T>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:86983854 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:86983854 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:102013409 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:102013409 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:220251155 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:220251155 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:33455065 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:33455065 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:131761175 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:131761175 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:142568184 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:142568184 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:103474214 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:103474214 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:22824157 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:22824157 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:127636642 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:127636642 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:180057383 C>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:180057383 C>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:46050632 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:46050632 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:64952670 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:64952670 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr20:62062620 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr20:62062620 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:55258663 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:55258663 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:49170111 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:49170111 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:65639580 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:65639580 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587390 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587390 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587617 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587617 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587683 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:169587683 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:62851874 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:62851874 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:41958759 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:41958759 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr18:47581606 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr18:47581606 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:1913985 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:1913985 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:15468525 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:15468525 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:203167632 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:203167632 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:162337267 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:162337267 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr15:28141073 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr15:28141073 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:10312419 A>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:10312419 A>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:17594542 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:17594542 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:249207882 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:249207882 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:46005255 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:46005255 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:30336929 A>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:30336929 A>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr14:103167703 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr14:103167703 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:111751312 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:111751312 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:62020629 C>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:62020629 C>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:122658266 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:122658266 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr20:1456806 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr20:1456806 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:56906505 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:56906505 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:2940479 T>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:2940479 T>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:42077615 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:42077615 A>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr20:61300271 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr20:61300271 C>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:158592733 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:158592733 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:61034714 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:61034714 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:50063716 T>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:50063716 T>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:152220629 T>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:152220629 T>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:18512009 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:18512009 A>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17721034 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17721034 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17728679 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17728679 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17728694 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17728694 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:216061716 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:216061716 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:216462856 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:216462856 G>C did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:177632877 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:177632877 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:88924319 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:88924319 G>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:21512215 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:21512215 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:7457136 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:7457136 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:20423102 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:20423102 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:3053806 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:3053806 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:147985645 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:147985645 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:47736123 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:47736123 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:26463370 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:26463370 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:77473152 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:77473152 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:2838570 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:2838570 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:119583073 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:119583073 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:119738472 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:119738472 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:115894548 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:115894548 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:9496362 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:9496362 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:6694726 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:6694726 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:81884832 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:81884832 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:42949191 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:42949191 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:120906725 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:120906725 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:53835503 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:53835503 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:16608826 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:16608826 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:160802415 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:160802415 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:24535778 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:24535778 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:22654244 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:22654244 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:104068413 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:104068413 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:131356183 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:131356183 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:11113918 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:11113918 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:48273487 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:48273487 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:10091863 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:10091863 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr21:47422376 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr21:47422376 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr6:36712973 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr6:36712973 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:4646077 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:4646077 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:11236960 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:11236960 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr18:47809155 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr18:47809155 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:15655094 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:15655094 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:85816293 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:85816293 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:59893543 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:59893543 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:59894848 A>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:59894848 A>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:14722302 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:14722302 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:124399140 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:124399140 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:169446217 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:169446217 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:109027773 T>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:109027773 T>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:97771937 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:97771937 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:158522579 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:158522579 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:144663350 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:144663350 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:141554537 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:141554537 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:180057434 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:180057434 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:14748654 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:14748654 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:90151812 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:90151812 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:44693848 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:44693848 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:19015620 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:19015620 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:162894790 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:162894790 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:10268009 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:10268009 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:31374408 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:31374408 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:7658099 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:7658099 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:42162871 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:42162871 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:107698401 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:107698401 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:141806811 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:141806811 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:85521553 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:85521553 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:61771186 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:61771186 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:165111142 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:165111142 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:150266783 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:150266783 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:54377804 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:54377804 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:15853610 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:15853610 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:15878612 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:15878612 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr14:23900576 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr14:23900576 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:113078729 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:113078729 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:50753793 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:50753793 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:73012573 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:73012573 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:115410133 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:115410133 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:73230632 T>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:73230632 T>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:228528972 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:228528972 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248154592 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248154592 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:26703192 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:26703192 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:149931583 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:149931583 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:34649278 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:34649278 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:127255387 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:127255387 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:233152610 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:233152610 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr6:165752647 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr6:165752647 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:14840850 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:14840850 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:25145814 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:25145814 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:32996392 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:32996392 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:40582752 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:40582752 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:44333165 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:44333165 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:170336612 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:170336612 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:74660513 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:74660513 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr14:63735938 A>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr14:63735938 A>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:141832514 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:141832514 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:77626768 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:77626768 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:53672333 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:53672333 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:62325871 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:62325871 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:237942119 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:237942119 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:237961476 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:237961476 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:34032029 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:34032029 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:4833835 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:4833835 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:57379109 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:57379109 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:162381855 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:162381855 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:68410402 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:68410402 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:110740265 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:110740265 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:101811509 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:101811509 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:31324387 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:31324387 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:220333523 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:220333523 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:130059620 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:130059620 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:75445649 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:75445649 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:20082280 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:20082280 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:47342542 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:47342542 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:52472880 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:52472880 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:142467343 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:142467343 A>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:33593396 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:33593396 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:101346978 T>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:101346978 T>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:141952237 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:141952237 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:166770237 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:166770237 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:103300575 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:103300575 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:35991431 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:35991431 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:215932905 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:215932905 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:108315323 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:108315323 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr14:74712018 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr14:74712018 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:6076586 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:6076586 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:128522622 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:128522622 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:39107160 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:39107160 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:54319768 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:54319768 A>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:31587156 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:31587156 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:128896777 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chrX:128896777 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:167031670 A>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:167031670 A>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:138765054 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr7:138765054 T>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:77690782 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:77690782 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:44648688 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:44648688 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:22817466 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:22817466 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:56901663 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:56901663 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:53560 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:53560 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:64748456 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:64748456 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:111875951 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:111875951 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chrX:148035002 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chrX:148035002 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr13:26348923 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr13:26348923 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:26508055 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:26508055 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:36252915 A>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:36252915 A>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:100064481 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:100064481 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chrX:107455062 A>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chrX:107455062 A>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:36720781 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:36720781 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:41497168 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:41497168 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:63119566 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:63119566 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:33874319 C>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:33874319 C>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:180039940 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:180039940 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chrX:12734145 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chrX:12734145 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:29574823 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:29574823 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:178968421 T>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:178968421 T>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:66255198 A>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:66255198 A>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr13:101748110 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr13:101748110 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:64418217 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:64418217 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:9524932 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:9524932 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:9319496 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:9319496 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:43765861 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:43765861 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:64514591 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:64514591 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:179023687 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:179023687 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:124111369 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:124111369 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:39949723 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:39949723 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:121000974 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:121000974 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr21:45820278 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr21:45820278 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:135756276 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:135756276 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:7743312 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:7743312 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:8975129 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:8975129 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:44274314 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:44274314 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:17457560 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:17457560 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:153001551 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:153001551 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:119029079 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:119029079 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:116203902 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:116203902 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:148627519 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:148627519 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:108002606 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:108002606 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:23547281 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:23547281 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20432492 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20432492 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:127760257 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:127760257 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:39442036 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:39442036 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:156991373 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:156991373 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:135086590 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:135086590 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:33881629 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:33881629 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:18574395 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:18574395 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:100229036 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:100229036 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:147733750 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:147733750 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:45710772 G>C maps to NM_000658.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:45710772 G>C maps to NM_000658.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:77752575 A>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:77752575 A>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:49962165 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:49962165 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:56149384 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:56149384 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:21890739 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:21890739 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:861992 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:861992 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:92680672 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:92680672 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:75775888 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:75775888 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:6422484 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:6422484 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:176853380 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:176853380 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:119976439 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:119976439 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:31312118 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:31312118 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:96770691 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:96770691 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:113508589 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:113508589 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:55317825 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:55317825 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:117185869 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:117185869 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:134353399 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:134353399 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:133118799 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:133118799 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:83926180 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:83926180 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:220233190 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:220233190 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:105687944 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:105687944 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:1480314 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:1480314 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:60903779 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:60903779 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:761678 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:761678 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:99739830 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:99739830 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:39609961 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:39609961 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:38369846 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:38369846 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:136253183 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:136253183 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:135762987 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:135762987 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:140881221 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:140881221 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:81579840 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:81579840 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:54961829 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:54961829 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:30876304 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:30876304 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:139266126 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:139266126 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:15831068 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:15831068 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:43939727 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:43939727 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:74619186 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:74619186 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:3672289 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:3672289 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:75399117 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:75399117 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:30445968 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:30445968 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:7806657 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:7806657 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:111343303 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:111343303 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:45127661 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:45127661 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:21883403 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:21883403 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:21883729 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:21883729 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:58571840 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:58571840 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:31083790 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:31083790 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:25463592 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:25463592 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:117282459 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:117282459 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:37766777 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:37766777 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:6196404 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:6196404 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:40351529 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:40351529 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:1501604 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:1501604 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:95675664 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:95675664 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:33156986 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:33156986 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:121353457 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:121353457 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:107816960 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:107816960 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:107923873 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:107923873 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:207697444 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:207697444 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:113702320 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:113702320 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:114185911 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:114185911 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:24939541 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:24939541 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:56083587 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:56083587 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:57485695 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:57485695 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:11732183 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:11732183 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:143996108 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:143996108 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:58157624 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:58157624 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:96748520 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:96748520 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:135369242 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:135369242 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:16025513 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:16025513 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:242690868 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:242690868 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:47151527 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:47151527 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:53321514 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:53321514 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:49986888 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:49986888 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:52348058 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:52348058 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:47883281 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:47883281 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:47883285 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:47883285 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:233195546 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:233195546 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:13922153 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:13922153 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:225750594 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:225750594 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:99537888 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:99537888 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:56468297 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:56468297 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:30451817 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:30451817 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:48624437 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:48624437 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:57670746 A>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:57670746 A>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:137807202 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:137807202 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:108388618 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:108388618 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:150264619 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:150264619 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45453837 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45453837 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45454240 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45454240 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45454283 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45454283 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45454330 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45454330 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:23693510 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:23693510 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:37252838 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:37252838 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:73470539 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:73470539 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:73470872 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:73470872 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:120613724 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:120613724 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:132522727 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:132522727 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:94124583 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:94124583 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:553752 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:553752 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:135433359 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:135433359 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:1659090 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:1659090 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:124792344 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:124792344 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:127613568 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:127613568 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:102553703 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:102553703 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:6690003 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:6690003 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:186363939 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:186363939 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:128487938 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:128487938 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:180038191 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:180038191 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:171244387 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:171244387 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:147009968 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:147009968 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:172050860 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:172050860 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:114270118 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:114270118 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:52188614 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:52188614 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:4306147 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:4306147 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:4311812 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:4311812 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:161302737 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:161302737 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:46252672 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:46252672 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:46307790 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:46307790 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27222009 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27222009 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27778113 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27778113 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:26589660 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:26589660 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:173852452 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:173852452 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:115439808 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:115439808 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:89524015 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:89524015 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:89733264 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:89733264 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:10557655 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:10557655 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:69564887 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:69564887 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:150168024 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:150168024 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:33075832 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:33075832 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:56374523 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:56374523 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:150635916 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:150635916 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:94197388 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:94197388 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:80015085 T>C maps to ENST00000320548 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:80015085 T>C maps to ENST00000320548 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:51746354 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:51746354 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:38068850 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:38068850 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:110224423 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:110224423 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:14813796 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:14813796 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:148714026 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:148714026 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:25077800 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:25077800 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:60331646 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:60331646 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:118443278 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:118443278 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:137892116 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:137892116 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:118925048 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:118925048 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:112096171 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:112096171 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:68701168 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:68701168 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:111659382 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:111659382 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:104961570 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:104961570 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:102955526 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:102955526 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:24507391 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:24507391 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:41730175 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:41730175 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:9457802 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:9457802 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:3631521 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:3631521 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:146991753 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:146991753 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:27056324 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:27056324 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:170359554 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:170359554 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:156254344 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:156254344 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:155555205 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:155555205 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:62073745 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:62073745 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:73765389 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:73765389 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:36746009 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:36746009 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:24056721 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:24056721 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:6502739 G>A maps to NM_001100603.1 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:6502739 G>A maps to NM_001100603.1 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:32504101 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:32504101 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:136554826 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:136554826 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:27732802 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:27732802 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:36874533 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:36874533 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:44894106 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:44894106 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45221723 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45221723 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:69615734 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:69615734 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:55328840 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:55328840 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:27944937 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:27944937 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:186460132 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:186460132 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:39537531 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:39537531 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:52826759 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:52826759 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:32253334 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:32253334 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:42164642 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:42164642 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:17596902 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:17596902 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:136570529 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:136570529 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:226127790 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:226127790 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:75596465 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:75596465 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:55179522 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:55179522 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:54756036 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:54756036 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:96322462 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:96322462 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:62445432 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:62445432 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:814882 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:814882 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:47266876 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:47266876 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:141272151 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:141272151 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:170002193 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:170002193 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:33484715 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:33484715 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:25071478 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:25071478 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:148770566 T>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:148770566 T>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:144804231 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:144804231 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:10407151 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:10407151 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:51731343 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:51731343 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:21896314 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:21896314 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:126753236 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:126753236 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:74865077 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:74865077 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:90830582 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:90830582 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:108682508 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:108682508 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:7886680 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:7886680 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:3248478 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:3248478 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:42311238 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:42311238 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:10428421 A>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:10428421 A>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:56552227 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:56552227 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:123458743 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:123458743 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:24422046 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:24422046 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:89914910 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:89914910 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:78562461 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:78562461 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:36241793 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:36241793 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:19334760 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:19334760 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:170315721 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:170315721 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:21251017 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:21251017 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:5495386 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:5495386 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:204924235 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:204924235 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:236208674 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:236208674 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:156759123 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:156759123 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:32180889 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:32180889 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:66193355 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:66193355 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:45697056 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:45697056 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:110927764 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:110927764 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:179533763 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:179533763 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:72109776 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:72109776 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:115377391 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:115377391 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:107872664 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:107872664 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:46826610 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:46826610 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:88472300 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:88472300 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:88474496 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:88474496 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:73231416 T>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:73231416 T>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:57619574 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:57619574 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:228566573 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:228566573 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:50944251 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:50944251 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:102312369 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:102312369 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:20388745 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:20388745 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:21898822 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:21898822 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:24846358 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:24846358 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:41794715 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:41794715 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:103234147 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:103234147 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:118989846 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:118989846 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:3949444 G>A maps to ENST00000237841 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:3949444 G>A maps to ENST00000237841 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:125616279 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:125616279 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:33306380 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:33306380 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:33904006 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:33904006 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:133291385 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:133291385 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:130453045 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:130453045 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:75672092 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:75672092 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:113823137 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:113823137 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:20335970 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:20335970 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:118198995 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:118198995 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:74305271 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:74305271 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:19573208 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:19573208 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:19574137 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:19574137 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:167334831 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:167334831 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:44393938 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:44393938 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:37529398 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:37529398 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:47274825 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:47274825 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:50025043 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:50025043 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:44071153 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:44071153 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:128304169 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:128304169 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:121679718 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:121679718 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:21614097 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:21614097 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:220383683 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:220383683 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:24574723 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:24574723 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:10127964 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:10127964 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:110124866 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:110124866 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:79312774 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:79312774 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:79253990 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:79253990 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:18238705 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:18238705 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:198496053 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:198496053 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156347341 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156347341 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:87243321 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:87243321 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:48561883 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:48561883 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:55534940 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:55534940 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:101622874 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:101622874 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:45211118 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:45211118 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:77402091 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:77402091 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:6000521 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:6000521 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:12096809 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:12096809 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:237777327 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:237777327 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:237802301 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:237802301 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:153826468 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:153826468 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:6457989 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:6457989 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr22:43603967 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr22:43603967 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:24912020 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:24912020 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:83763284 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:83763284 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:9190585 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:9190585 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:94752419 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:94752419 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:23820833 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:23820833 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:146261793 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:146261793 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:147214981 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:147214981 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:147438077 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:147438077 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:1075352 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:1075352 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:22360242 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:22360242 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:92913839 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:92913839 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:92375684 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:92375684 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:8075339 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:8075339 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:140051039 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:140051039 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:165809378 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:165809378 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:47163034 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:47163034 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:1209044 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:1209044 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:55731727 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:55731727 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:21422396 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:21422396 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:2297588 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:2297588 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:108589326 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:108589326 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:106899351 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:106899351 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:50616995 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:50616995 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:231267473 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:231267473 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:147444942 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:147444942 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:147450048 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:147450048 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:168004473 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:168004473 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158596906 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158596906 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158606393 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158606393 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:130060248 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:130060248 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:68449283 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:68449283 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:68472000 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:68472000 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:4325382 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:4325382 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:81862181 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:81862181 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:180962672 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:180962672 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:70608073 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chrX:70608073 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:32797558 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:32797558 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:72243917 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:72243917 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:61041320 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:61041320 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:65155421 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:65155421 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45811758 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:45811758 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:95230922 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:95230922 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:2297706 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:2297706 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:39973442 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:39973442 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:165737915 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:165737915 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:52546782 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:52546782 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:100277484 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:100277484 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:23003528 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:23003528 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:75009674 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:75009674 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:10914483 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:10914483 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:185636260 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:185636260 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:112572952 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:112572952 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:141034234 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:141034234 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:142626749 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:142626749 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:179545113 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:179545113 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:157009539 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:157009539 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:42287475 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:42287475 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:196083731 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:196083731 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:96484917 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:96484917 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:70146101 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:70146101 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20346765 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20346765 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:121154854 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:121154854 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:35390129 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:35390129 T>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:35648137 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:35648137 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:126220025 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:126220025 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:216061724 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:216061724 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:76721750 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:76721750 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:144750709 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:144750709 C>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:177650638 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:177650638 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:2651342 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:2651342 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:61077469 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:61077469 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:14949688 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:14949688 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:109533962 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:109533962 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:65449065 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:65449065 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:11036358 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:11036358 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:77239689 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:77239689 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:67433379 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:67433379 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:1197218 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:1197218 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:57653931 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:57653931 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:44804117 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:44804117 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:47869172 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:47869172 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:136110947 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:136110947 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:49518759 T>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:49518759 T>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr8:22058877 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr8:22058877 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:55819994 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:55819994 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:30893796 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:30893796 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:49838947 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:49838947 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:6196777 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:6196777 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:5905581 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:5905581 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:8613239 G>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:8613239 G>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr9:101800820 G>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr9:101800820 G>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:98310005 A>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:98310005 A>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr22:38964289 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr22:38964289 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr5:83356394 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr5:83356394 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr13:32841289 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr13:32841289 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr13:102344857 A>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr13:102344857 A>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:113724909 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:113724909 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:148346484 A>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:148346484 A>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr7:141775938 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr7:141775938 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:108788347 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:108788347 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr17:8351822 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr17:8351822 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr14:52477577 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr14:52477577 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr6:124604065 G>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr6:124604065 G>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr16:50583305 A>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr16:50583305 A>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr5:6622252 A>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr5:6622252 A>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:156848860 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:156848860 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr2:239157635 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr2:239157635 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr7:47930103 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr7:47930103 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr6:51934409 G>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr6:51934409 G>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chrX:23704361 T>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chrX:23704361 T>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:43358218 A>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:43358218 A>C did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:50131117 T>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:50131117 T>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:113327772 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:113327772 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:45996280 C>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:45996280 C>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr22:50894057 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr22:50894057 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr17:46262233 A>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr17:46262233 A>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:121634658 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr3:121634658 C>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:72335676 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:72335676 C>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:1175043 T>G did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:1175043 T>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:20668463 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:20668463 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:32423608 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:32423608 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:32431848 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:32431848 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:96858463 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:96858463 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:109358673 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:109358673 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:109358771 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:109358771 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:73830544 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:73830544 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:31542083 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:31542083 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:30930956 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:30930956 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:155920410 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:155920410 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:42248103 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:42248103 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:212792563 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:212792563 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:193210832 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:193210832 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:79166230 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:79166230 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49464212 C>G maps to NM_004324.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49464212 C>G maps to NM_004324.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:27713961 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:27713961 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:30770953 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:30770953 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:40979810 T>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:40979810 T>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr13:111286884 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr13:111286884 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:207956597 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:207956597 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:64603383 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:64603383 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:88478638 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:88478638 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:93515689 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:93515689 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:71046607 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:71046607 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:177715113 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:177715113 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:87557201 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:87557201 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:34080077 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:34080077 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:41278226 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:41278226 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:41456777 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:41456777 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:6210315 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:6210315 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:172333469 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:172333469 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:14978650 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:14978650 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:197552178 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:197552178 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:32536067 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:32536067 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:32584084 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:32584084 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:196911986 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:196911986 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:102978309 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:102978309 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:100377659 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:100377659 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:41564288 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:41564288 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:70284908 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:70284908 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:89669034 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:89669034 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:80040600 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:80040600 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:161518127 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:161518127 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:33454045 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:33454045 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:190864557 T>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:190864557 T>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:190864559 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:190864559 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:13838428 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:13838428 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49469411 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49469411 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:16254292 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:16254292 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:81399217 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:81399217 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:3586441 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:3586441 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:122488842 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:122488842 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:73959045 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:73959045 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:105198403 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:105198403 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:80679679 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:80679679 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:222716811 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:222716811 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:75203021 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:75203021 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:33095817 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:33095817 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:33095824 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:33095824 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:174253150 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:174253150 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:46675090 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:46675090 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:88295806 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:88295806 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:160494682 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:160494682 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr21:34649199 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr21:34649199 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:90969500 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:90969500 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:24557598 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:24557598 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:416586 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:416586 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:29018158 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:29018158 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:137520898 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:137520898 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr13:70469330 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr13:70469330 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:53069426 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:53069426 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:52825904 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:52825904 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr21:32185279 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr21:32185279 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:169571506 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:169571506 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:80198598 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:80198598 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:70415832 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:70415832 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:919116 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:919116 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:62935741 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:62935741 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:141441259 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:141441259 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:151899778 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:151899778 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:151899794 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:151899794 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:4110459 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:4110459 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:68720467 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:68720467 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:126479003 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:126479003 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:62435265 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:62435265 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:171761064 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:171761064 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:40424303 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:40424303 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:102819957 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:102819957 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:108688495 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:108688495 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:55917332 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:55917332 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:56673300 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:56673300 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:56716967 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:56716967 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:23874990 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:23874990 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:78204271 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:78204271 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:160322032 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:160322032 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:45097418 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:45097418 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:56435825 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:56435825 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:5445167 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:5445167 A>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:100110954 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:100110954 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:206617757 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:206617757 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:104857815 G>C maps to ENST00000369853 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:104857815 G>C maps to ENST00000369853 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:154125454 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:154125454 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:31836440 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:31836440 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:23235720 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:23235720 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:95764807 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:95764807 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:54880299 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:54880299 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:137235436 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:137235436 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:204216608 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:204216608 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:45267705 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:45267705 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr20:31825442 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr20:31825442 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:42212826 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:42212826 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:75609616 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:75609616 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:43414551 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:43414551 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:43765802 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:43765802 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:14632423 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:14632423 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:74340978 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:74340978 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:120643514 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:120643514 A>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:31441351 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:31441351 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:108102816 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:108102816 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:180166486 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:180166486 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:85441892 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:85441892 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:25622027 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:25622027 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:53728648 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:53728648 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr13:48942592 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr13:48942592 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:94493097 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:94493097 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:23959311 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:23959311 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:23406338 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:23406338 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:155294808 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:155294808 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:139359058 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr9:139359058 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:30735372 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:30735372 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:30736438 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:30736438 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:30736453 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:30736453 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:22019332 T>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:22019332 T>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:160557533 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:160557533 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:107427165 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:107427165 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:107427401 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:107427401 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:153933325 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:153933325 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:1394835 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:1394835 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:68330751 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:68330751 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:128582536 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chrX:128582536 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:150936247 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:150936247 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:150936326 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:150936326 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:18882051 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:18882051 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:186168346 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:186168346 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:42150738 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:42150738 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:133480438 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr5:133480438 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:10769741 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:10769741 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:105913055 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:105913055 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:67261115 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:67261115 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:54497766 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:54497766 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:9537385 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:9537385 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:41118142 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:41118142 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:2122439 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr16:2122439 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:101750279 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:101750279 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88213131 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88213131 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88213362 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88213362 C>G did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:135741405 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:135741405 G>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:52903784 T>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:52903784 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9265196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9265196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:48438917 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:48438917 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:101578718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:101578718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:43759815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:43759815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:1342097 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:1342097 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:123033019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:123033019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:50307630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:50307630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:6908419 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:6908419 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:15755257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:15755257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:37447173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:37447173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:98190022 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:98190022 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:6032435 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:6032435 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:47024032 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:47024032 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:10691873 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:10691873 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:36369894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:36369894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:144162337 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:144162337 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:1871249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:1871249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:53522600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:53522600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:232127154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:232127154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:176952967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:176952967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25255611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25255611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:193185435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:193185435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr21:11057398 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr21:11057398 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chrX:152966487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chrX:152966487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:127818194 C>T maps to NM_139346.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:127818194 C>T maps to NM_139346.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:112677042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:112677042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:7053848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:7053848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:25149380 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:25149380 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:36950113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:36950113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:24105996 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:24105996 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:8689860 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:8689860 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:111831641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:111831641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:7832222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:7832222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:157731873 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:157731873 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:89901078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:89901078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:27927252 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:27927252 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:181498288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:181498288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:24324240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:24324240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr18:66419440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr18:66419440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:3672164 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:3672164 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:21883027 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:21883027 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:82769390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:82769390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:134276926 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:134276926 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:105815498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:105815498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:14080572 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:14080572 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:78349865 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:78349865 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:230272209 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:230272209 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:107217699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:107217699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:20490757 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:20490757 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:217243224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:217243224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:74097947 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:74097947 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:89865711 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:89865711 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:127606670 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:127606670 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9931117 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9931117 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:15927949 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:15927949 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:39433137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:39433137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:33044972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:33044972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:190871352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:190871352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:71319825 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:71319825 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:56045714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:56045714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:10877356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:10877356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:121685257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:121685257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:37317714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:37317714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:92826792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:92826792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:35551525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:35551525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:70980469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:70980469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:25762898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:25762898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:55204060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:55204060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:111034848 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:111034848 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:6068394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:6068394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:62704059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:62704059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:154539651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:154539651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:10355100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:10355100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9162483 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9162483 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:52708942 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:52708942 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:55085393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:55085393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:54782477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:54782477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:91170739 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:91170739 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:176778160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:176778160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:62778675 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:62778675 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:141115787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:141115787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:14239532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:14239532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:41888851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:41888851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:31473362 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:31473362 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:10317636 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:10317636 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:71305770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:71305770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:21330867 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:21330867 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:152520400 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:152520400 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:73541658 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:73541658 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:23946876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:23946876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:5415411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:5415411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:115406791 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:115406791 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:59548151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:59548151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:59548153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:59548153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:131722471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:131722471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:131809955 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:131809955 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:88770993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:88770993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:867248 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:867248 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:31720734 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:31720734 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25024011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25024011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25043947 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25043947 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chrX:91715541 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chrX:91715541 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:145004674 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:145004674 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:11022851 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:11022851 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:75737308 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:75737308 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr18:44426824 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr18:44426824 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:94318459 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:94318459 T>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:81941974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:81941974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:41313926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:41313926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:204274962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:204274962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:76812941 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:76812941 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:32130754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:32130754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:628278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:628278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:1582840 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:1582840 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:53839946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:53839946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:117472590 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:117472590 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr9:8486431 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr9:8486431 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:29939078 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:29939078 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:241519204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:241519204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:55534650 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:55534650 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:33134784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:33134784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:123065 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:123065 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr20:950979 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr20:950979 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:237895271 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:237895271 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:237994911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:237994911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:166142354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:166142354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:12208832 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:12208832 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr22:26611250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr22:26611250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:164730665 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:164730665 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:25676046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:25676046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44223912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44223912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44223959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44223959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44224621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44224621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:42334703 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:42334703 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:173523801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:173523801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:70623556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:70623556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:20533719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:20533719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:88327642 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:88327642 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr20:10277481 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr20:10277481 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:50892131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:50892131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:101589384 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:101589384 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:26906969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:26906969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:206577786 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:206577786 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:89791111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:89791111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:99885934 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:99885934 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:74477198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:74477198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:33194088 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:33194088 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:46965321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:46965321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:77922922 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:77922922 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:74173917 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:74173917 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:139543925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:139543925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:152079857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:152079857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:51504804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:51504804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr22:26899578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr22:26899578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:138314217 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:138314217 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:98205674 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:98205674 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:98205941 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:98205941 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:98206065 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:98206065 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:24680594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:24680594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:91760221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:91760221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:36899466 G>C maps to NM_014831.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:36899466 G>C maps to NM_014831.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:3448019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr17:3448019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:141954854 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr7:141954854 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:81422341 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:81422341 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:19492311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:19492311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:5412113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:5412113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:54586370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:54586370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:77830954 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:77830954 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:91546276 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:91546276 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:104177221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:104177221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:29643050 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:29643050 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:38145393 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:38145393 C>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:31927804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr16:31927804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr18:74092261 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr18:74092261 A>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:55039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:55039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:22362403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:22362403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:6403860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:6403860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:7383159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:7383159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:7568516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:7568516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:48741548 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:48741548 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:31672929 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:31672929 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:141002236 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:141002236 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:100591700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:100591700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:123071210 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:123071210 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:125826121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:125826121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:145916516 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:145916516 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:41545817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:41545817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:35212662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:35212662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:148894274 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:148894274 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:144313962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:144313962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:131687406 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:131687406 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:235459476 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:235459476 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:113464904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:113464904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:193071869 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:193071869 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:11047750 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:11047750 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:11068245 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:11068245 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:32207609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:32207609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:33573921 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:33573921 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:43293006 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:43293006 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:112740064 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:112740064 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:6809682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:6809682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:64732105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:64732105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:170927196 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:170927196 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:11880585 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:11880585 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:175735129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:175735129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:49088121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:49088121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:81634673 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:81634673 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:86115738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:86115738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:93113426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:93113426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:219892856 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:219892856 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:44815220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:44815220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:123156988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:123156988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:126485359 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:126485359 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:6186601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:6186601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:53265540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:53265540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:109919382 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:109919382 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:10191671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:10191671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:88249422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:88249422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr18:72223506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr18:72223506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:147914330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:147914330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:103487242 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:103487242 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:71697558 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:71697558 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:101759498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:101759498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:139819974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:139819974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:139856209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:139856209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:110844536 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:110844536 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:130311470 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:130311470 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:130318586 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:130318586 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:68900953 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:68900953 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:131623900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:131623900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:207804145 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:207804145 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:211527950 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:211527950 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:1715212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:1715212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:43777586 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:43777586 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:1321325 G>C maps to ENST00000381567 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:1321325 G>C maps to ENST00000381567 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:34190024 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:34190024 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:114388917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:114388917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:23807309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:23807309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:80101177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:80101177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:88029475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:88029475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:58712268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:58712268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:109292643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:109292643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:155218882 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:155218882 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:110734386 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:110734386 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:74125188 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:74125188 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:445247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:445247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:233127786 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:233127786 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:35069377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:35069377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:13885038 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:13885038 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:67012342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:67012342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:98092503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:98092503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:169122998 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:169122998 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:169135109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:169135109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:21738081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:21738081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:116497208 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:116497208 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:41521191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:41521191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:4708363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:4708363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:36327124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:36327124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:43995741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:43995741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:36910140 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:36910140 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:134852060 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:134852060 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:133722850 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:133722850 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:61028190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:61028190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:99697765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:99697765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:99042091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:99042091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:137778147 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:137778147 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:124872413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:124872413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:36978682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:36978682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:138140565 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:138140565 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:38285758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:38285758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:203175008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:203175008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:197483216 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:197483216 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:27184302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:27184302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:74838193 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:74838193 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:55192348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:55192348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:150757984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:150757984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:22415035 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:22415035 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:131621483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:131621483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:154071614 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:154071614 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:133214118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:133214118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:37899091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:37899091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:93365358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:93365358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:102483195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:102483195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:13769622 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:13769622 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:66800224 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:66800224 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:34029650 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:34029650 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:52630298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:52630298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:108708280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:108708280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:119935232 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:119935232 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:43505903 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:43505903 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:197086831 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:197086831 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:29797815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:29797815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:29797817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:29797817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:29797987 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:29797987 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:114010013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:114010013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:52112028 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:52112028 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:7231316 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:7231316 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:182359974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:182359974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:15689129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:15689129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:187532367 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:187532367 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:17937404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:17937404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:8591612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:8591612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:120382728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:120382728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:150649467 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:150649467 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:73879598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:73879598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:57190504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:57190504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:100137892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:100137892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:57961482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:57961482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:70549712 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:70549712 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:48681897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:48681897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:32127740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:32127740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:71238987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:71238987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:143742808 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:143742808 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:107591534 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:107591534 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:107745152 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:107745152 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:136555718 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:136555718 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:55142686 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:55142686 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:151793766 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:151793766 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:40498243 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:40498243 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:141092239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:141092239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:40788468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:40788468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:186943418 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:186943418 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:64575347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:64575347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:150438284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:150438284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:174538072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:174538072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:65813060 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:65813060 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:30421594 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:30421594 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:42817300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:42817300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:76602481 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:76602481 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:76780282 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:76780282 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:22696596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:22696596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:97330343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:97330343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:34243499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:34243499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:34790145 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:34790145 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:18757876 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:18757876 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:88735139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:88735139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:113396286 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:113396286 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:97616195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:97616195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:97619472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:97619472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:131235401 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:131235401 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:143771205 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:143771205 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:4665870 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:4665870 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:21702820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:21702820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:73979016 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:73979016 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:23792072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:23792072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:17699525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:17699525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:110342186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:110342186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:112816091 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:112816091 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:56128728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:56128728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:70180141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:70180141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:37839238 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:37839238 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:85782282 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:85782282 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:71549787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:71549787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:8708086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:8708086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:145796834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:145796834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:146311674 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:146311674 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:131841510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:131841510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:118236701 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:118236701 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:16287894 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:16287894 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:37518151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:37518151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:37531178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:37531178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:47262318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:47262318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:68872942 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:68872942 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:25147364 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:25147364 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:8500712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:8500712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:62110243 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:62110243 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:220162286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:220162286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:20663724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:20663724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:69047878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:69047878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:34240403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:34240403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:6146720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:6146720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:167658092 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:167658092 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:117237275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:117237275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:72435649 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:72435649 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:130912950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:130912950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:104928826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:104928826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:141832247 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:141832247 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:7226993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:7226993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:36171801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:36171801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:39002317 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:39002317 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:5595253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:5595253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:53460905 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:53460905 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:150263948 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:150263948 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:52067689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:52067689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:19666359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:19666359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:51160941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:51160941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:45192026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:45192026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:128362811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:128362811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:110741153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:110741153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:70530311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:70530311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:21032335 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:21032335 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:183485193 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:183485193 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:125179763 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:125179763 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:220345389 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:220345389 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:158612134 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:158612134 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:57094709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:57094709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:104118505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:104118505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:39964039 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:39964039 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:152555172 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:152555172 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:85457011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:85457011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr18:23807281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr18:23807281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:6998031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:6998031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:115117579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:115117579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:10411976 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:10411976 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:29932769 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:29932769 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:43774002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:43774002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:2575625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:2575625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:60697892 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:60697892 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:48867279 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:48867279 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:29982934 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:29982934 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:51361805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:51361805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:175372256 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:175372256 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:175536733 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:175536733 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:16197359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:16197359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:1488348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:1488348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:20068954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:20068954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:35827974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:35827974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:5949723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:5949723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:100469061 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:100469061 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:73236102 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:73236102 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:234839291 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:234839291 T>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:51629110 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr20:51629110 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr18:29178682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr18:29178682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:66532397 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:66532397 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:103316091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:103316091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:176335494 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:176335494 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:61433141 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:61433141 A>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:72868500 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:72868500 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:219294220 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:219294220 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:65418939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:65418939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:79985619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:79985619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:100423444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:100423444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:58313619 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:58313619 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:98846488 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:98846488 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:78229208 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:78229208 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:128901798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chrX:128901798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:77220632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:77220632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:135552764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:135552764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:267072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:267072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:37618015 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:37618015 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:12474455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:12474455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:4812490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:4812490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:59164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:59164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:99081328 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:99081328 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:94479895 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:94479895 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:17414501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:17414501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:73152073 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:73152073 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:81610621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:81610621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:64532752 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:64532752 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:70900435 T>C maps to NM_017488.3 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:70900435 T>C maps to NM_017488.3 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:12351046 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:12351046 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:49332849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:49332849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:105258814 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:105258814 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:58247365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:58247365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:6374124 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:6374124 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:38431762 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:38431762 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:61847893 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:61847893 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:115202460 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:115202460 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:24442009 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:24442009 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:144244726 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:144244726 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:46233322 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:46233322 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:109286138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:109286138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:23322838 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:23322838 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:119957752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:119957752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:120006961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:120006961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:47582535 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:47582535 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:25263342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:25263342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:193130415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:193130415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:36051577 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:36051577 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:7841881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:7841881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr21:11046744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr21:11046744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr21:11076094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr21:11076094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:22035125 T>C maps to ENST00000354870 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:22035125 T>C maps to ENST00000354870 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:13600497 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:13600497 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:33000698 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:33000698 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57252702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57252702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:62317135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:62317135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:81463317 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:81463317 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:93755718 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:93755718 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57406509 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57406509 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57420541 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57420541 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:98690875 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:98690875 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:77697979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:77697979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:2024143 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:2024143 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44647364 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44647364 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:92070852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:92070852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:70509454 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:70509454 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:33444400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:33444400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:44750365 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:44750365 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:227279519 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:227279519 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:21752442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:21752442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:19839213 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:19839213 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:61851229 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:61851229 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:26886245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:26886245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:37667754 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:37667754 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:123173548 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:123173548 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:80646391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:80646391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:135944035 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:135944035 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:214830825 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:214830825 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:93467812 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:93467812 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:136623208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:136623208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:10150760 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:10150760 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:62289354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:62289354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:99005960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:99005960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:3067779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:3067779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:147259418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:147259418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:75837949 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:75837949 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:71716656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:71716656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:86622109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:86622109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:70944768 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:70944768 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:27943883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:27943883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:46851445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:46851445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:1327820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:1327820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:10868260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:10868260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:34166387 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:34166387 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:80349124 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:80349124 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:80684165 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:80684165 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:49039978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:49039978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:16000636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:16000636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:59805209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:59805209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:50994154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:50994154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:24291343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:24291343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:126164227 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:126164227 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:5388596 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:5388596 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:107557189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:107557189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:7671591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:7671591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:13811940 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:13811940 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:115318676 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:115318676 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:102508275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:102508275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:83356067 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:83356067 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:16976123 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:16976123 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:110914643 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:110914643 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:233421263 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:233421263 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:33867097 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:33867097 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:7026684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:7026684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:89390871 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:89390871 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:66355977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:66355977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:56493859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:56493859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:15091205 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:15091205 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:66005980 A>G maps to ENST00000370616 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:66005980 A>G maps to ENST00000370616 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:139487411 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:139487411 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:150386938 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:150386938 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:127614989 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:127614989 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:161476436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:161476436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:137802910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:137802910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:157776928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:157776928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:102915626 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:102915626 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:72756928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:72756928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:171073163 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:171073163 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:146696266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:146696266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:159682106 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:159682106 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:190882076 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:190882076 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:13779740 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:13779740 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:32786356 T>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:32786356 T>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:78414387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:78414387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:173301432 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:173301432 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:173530779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:173530779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:128092249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:128092249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:69652879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:69652879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:69564981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:69564981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:42468091 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:42468091 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:59599305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:59599305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:121684802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:121684802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:102968323 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:102968323 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:129360406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:129360406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:129467671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:129467671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:100354499 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:100354499 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:11756633 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:11756633 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:105797708 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:105797708 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:10007564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:10007564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:126750298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:126750298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:42146405 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:42146405 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:45481729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:45481729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:41057161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:41057161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:197187401 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:197187401 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124789918 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124789918 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:186008790 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:186008790 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:115203868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:115203868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:70842024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:70842024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:140034409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:140034409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:104984383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:104984383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:79672799 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:79672799 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:187542042 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:187542042 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:124181324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:124181324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:19384040 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:19384040 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:178560795 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:178560795 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:133198301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:133198301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:7046799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:7046799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:79755385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:79755385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:21009106 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:21009106 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:55271926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:55271926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:55247198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:55247198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:56269681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:56269681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:39019874 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:39019874 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:54875809 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:54875809 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:7016371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:7016371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:209803305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:209803305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:71898226 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:71898226 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:48956191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:48956191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:105405173 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:105405173 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:11922253 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:11922253 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:25248780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:25248780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:40137871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:40137871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:52883221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:52883221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:40714829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:40714829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:77626152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:77626152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:185197887 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:185197887 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:30728324 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:30728324 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:162930317 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:162930317 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr22:36013167 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr22:36013167 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:13885540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:13885540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:47530404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:47530404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:47849044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:47849044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr22:42172022 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr22:42172022 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:151971647 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:151971647 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:14936917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:14936917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:59939617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:59939617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:120791214 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:120791214 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:120791217 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:120791217 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:120791547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:120791547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121530873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121530873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:135511238 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:135511238 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:153042833 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:153042833 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:10398022 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:10398022 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:31131491 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:31131491 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:31131648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:31131648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:78177091 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:78177091 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:78583738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:78583738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:133636224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:133636224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:103987461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:103987461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:44833114 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:44833114 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:126296134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:126296134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:93794788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:93794788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:132180159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:132180159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:106480500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:106480500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:37331768 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:37331768 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:22344709 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:22344709 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:52847600 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:52847600 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:117092868 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:117092868 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:38271070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:38271070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:734198 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:734198 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:75939641 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:75939641 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:36966730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:36966730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:55570301 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:55570301 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:55780295 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:55780295 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:165832097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:165832097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:20769351 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:20769351 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:178937677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:178937677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:209204901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:209204901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:130855617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:130855617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:110466857 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:110466857 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:119334785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:119334785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:8862172 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:8862172 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:81719545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:81719545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:22350515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:22350515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:23509378 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:23509378 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:68950605 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:68950605 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:69050645 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:69050645 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:8248265 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:8248265 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:31501753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:31501753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:220335660 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:220335660 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:220357364 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:220357364 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:4654860 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:4654860 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:131350976 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chrX:131350976 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:88240713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:88240713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr22:35947516 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr22:35947516 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:38900554 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:38900554 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:57379838 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:57379838 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:79384477 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:79384477 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:120336708 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:120336708 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:103322824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:103322824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:2330788 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:2330788 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:131187567 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:131187567 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:114986000 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:114986000 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:64381936 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:64381936 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:117704426 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:117704426 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:55533479 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:55533479 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:37009999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:37009999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:159493797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:159493797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:33865618 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:33865618 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:153533778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:153533778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:18128285 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:18128285 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:78176736 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:78176736 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:80447561 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:80447561 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:79469104 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:79469104 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:49231518 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:49231518 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124524959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124524959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:20002996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:20002996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:18250464 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:18250464 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:20676458 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:20676458 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:68321599 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:68321599 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:92669538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:92669538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:70743941 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:70743941 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:159841161 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:159841161 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:18840560 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:18840560 A>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:34725737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:34725737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121768025 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121768025 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:158596967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:158596967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104049006 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104049006 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104049363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104049363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:125467026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:125467026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:31667628 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:31667628 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:4065385 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:4065385 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:203071899 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:203071899 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:48152981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:48152981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:56700441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:56700441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:71447171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:71447171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:3006031 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:3006031 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr21:19698654 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr21:19698654 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:175088089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:175088089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179530191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179530191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179600189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179600189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:49578783 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:49578783 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:113208248 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:113208248 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:48075824 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:48075824 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:129474735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:129474735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:62446113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:62446113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:165860446 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:165860446 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:35401852 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:35401852 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:216419842 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:216419842 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:62783320 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:62783320 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:62212147 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:62212147 A>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:142468414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:142468414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:43507195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:43507195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:62521548 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:62521548 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:64439924 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:64439924 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:58948145 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:58948145 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:52909316 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:52909316 T>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:40553237 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:40553237 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:58119318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:58119318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr14:70926404 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr14:70926404 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:22297804 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:22297804 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr13:31782916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr13:31782916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:77305580 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:77305580 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr7:146864625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr7:146864625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr10:68992346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr10:68992346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr8:143998980 T>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr8:143998980 T>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:160194942 A>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:160194942 A>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr18:29104962 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr18:29104962 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr9:95274444 C>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr9:95274444 C>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:134646738 G>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:134646738 G>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:137304451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:137304451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:119641078 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:119641078 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr6:33052696 T>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr6:33052696 T>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr7:110785520 C>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr7:110785520 C>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:46671683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:46671683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:38682226 T>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:38682226 T>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr15:52250919 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr15:52250919 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:148752243 C>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:148752243 C>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr10:98113110 C>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr10:98113110 C>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:59210627 G>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:59210627 G>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:58094273 G>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:58094273 G>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr9:119038046 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr9:119038046 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr21:41292484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr21:41292484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:59064158 A>T maps to NM_001197218.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:59064158 A>T maps to NM_001197218.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:95430978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:95430978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:31422864 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:31422864 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr22:45754537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr22:45754537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr2:231204656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr2:231204656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr17:28887554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr17:28887554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:154145256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:154145256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:84386690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:84386690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr2:61522201 C>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr2:61522201 C>A did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:227884806 A>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr1:227884806 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:44269075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:44269075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:48119456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:48119456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:33840541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:33840541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:79083398 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:79083398 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:32846377 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:32846377 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:69366298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:69366298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47077906 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47077906 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47107975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47107975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:17958662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:17958662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:100978671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:100978671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:18195913 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:18195913 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:60559037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:60559037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:169351646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:169351646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:22058797 A>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:22058797 A>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:33677659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:33677659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:99183363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:99183363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:45253690 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:45253690 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:31674032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:31674032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:98761870 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:98761870 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:3738269 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:3738269 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:111849400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:111849400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:7252319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:7252319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:117311023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:117311023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:54424230 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:54424230 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:91978899 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:91978899 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:82689191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:82689191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:31322771 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:31322771 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:43087880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:43087880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:151678658 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:151678658 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:32366411 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:32366411 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:40339209 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:40339209 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:8286686 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:8286686 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:8613753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:8613753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:100207766 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:100207766 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139866385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139866385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:34117866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:34117866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:80801157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:80801157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:5018479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:5018479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:85559818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:85559818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:155298358 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:155298358 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:151114270 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:151114270 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:75501596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:75501596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:88577619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:88577619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:105393332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:105393332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr21:41559241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr21:41559241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:45390462 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:45390462 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:71864641 T>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:71864641 T>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:83512617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:83512617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:31483822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:31483822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:37302519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:37302519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:46125008 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:46125008 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:29442074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:29442074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:55991424 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:55991424 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:207097842 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:207097842 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139145142 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139145142 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:30872127 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:30872127 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:30922702 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:30922702 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:16740590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:16740590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:16793549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:16793549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:161512793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:161512793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:161691662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:161691662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:125010115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:125010115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:31050224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:31050224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:115369366 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:115369366 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:151228705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:151228705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:153190511 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:153190511 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:9934977 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:9934977 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:106558144 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:106558144 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:42518994 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:42518994 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:5284067 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:5284067 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:24130757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:24130757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:62490019 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:62490019 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:207010429 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:207010429 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:143052837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:143052837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:31374173 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr16:31374173 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:4650289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:4650289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:153949765 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:153949765 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:55332929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:55332929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr13:74339032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr13:74339032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:42985505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:42985505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:38974757 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:38974757 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:153130246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:153130246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:104309518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:104309518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:96440810 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:96440810 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:62862219 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:62862219 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:40491655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:40491655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:133686434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:133686434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:33196720 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:33196720 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:77708072 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:77708072 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:42108003 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:42108003 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:89179889 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:89179889 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:60167738 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:60167738 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:63473358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:63473358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:81102820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:81102820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:23855119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:23855119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:52689302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:52689302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:1921221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:1921221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:134076377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:134076377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:133636212 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:133636212 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:14088342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:14088342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:36953975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:36953975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:5964964 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:5964964 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:119534078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:119534078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:248569264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:248569264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:144992682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:144992682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:54975458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:54975458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:151280329 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:151280329 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:43239144 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:43239144 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:190738191 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:190738191 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:131191247 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:131191247 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:42825429 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:42825429 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:111636892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:111636892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47083779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47083779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:82549281 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:82549281 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:47296464 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:47296464 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:47339015 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:47339015 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:57350149 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:57350149 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:158007204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:158007204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:10823376 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:10823376 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:156038265 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:156038265 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:69036510 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:69036510 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:155477622 T>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:155477622 T>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:79314125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:79314125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:63186151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:63186151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:38959909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:38959909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr18:61310551 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr18:61310551 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:166748211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:166748211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:14166655 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:14166655 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:67199335 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:67199335 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:82398734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:82398734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:42026118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:42026118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:23608817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:23608817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:40366503 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:40366503 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:143344134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:143344134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr13:36743012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr13:36743012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:44175774 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:44175774 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:48053558 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chrX:48053558 A>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:186754530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:186754530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:76771501 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:76771501 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:104118498 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:104118498 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:3990996 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:3990996 A>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:113149456 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:113149456 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:93606169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:93606169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:125551264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:125551264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:59555912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:59555912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:133941452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:133941452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:137928196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:137928196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:56818761 T>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:56818761 T>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:60689191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:60689191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:122219127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:122219127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:150493669 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:150493669 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:175452956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:175452956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr13:103297088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr13:103297088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:73050688 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr12:73050688 C>G did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:30297565 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:30297565 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:5952455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:5952455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:143407587 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:143407587 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:143413087 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:143413087 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:99420217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:99420217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:43211857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:43211857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:113214915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:113214915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:35068468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:35068468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:37028642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:37028642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:159826193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:159826193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:98828387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:98828387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:100993180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:100993180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:128484355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr2:128484355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:116955437 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:116955437 T>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:32439236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:32439236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:138739820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:138739820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:52471688 A>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:52471688 A>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:37580043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:37580043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:57184329 G>C did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:57184329 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:7391114 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:7391114 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:32410082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:32410082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:108890892 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:108890892 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:33613396 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:33613396 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:7757304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:7757304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:76229551 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:76229551 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:6599346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:6599346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:4745324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:4745324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:125928431 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:125928431 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:113278104 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:113278104 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:110820966 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:110820966 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:108347559 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:108347559 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:26452941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:26452941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:29316286 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:29316286 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:135827683 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:135827683 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:231125835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:231125835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:40629590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:40629590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:33512165 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:33512165 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr22:18189499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr22:18189499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr22:32819567 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr22:32819567 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:38396216 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:38396216 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:103292247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:103292247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:103303561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:103303561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:33159248 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:33159248 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:40047343 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:40047343 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:58504036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:58504036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:185189666 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:185189666 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:53993124 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:53993124 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:74072699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:74072699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:39606001 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:39606001 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:38369845 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:38369845 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:140830909 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:140830909 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:209764642 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:209764642 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:111279954 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:111279954 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:89418694 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:89418694 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:74509675 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:74509675 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:58312295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:58312295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:159255857 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:159255857 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:159255859 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:159255859 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:15815418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:15815418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:12252056 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:12252056 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:48222381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:48222381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:22622960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:22622960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:82940445 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:82940445 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:73405744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:73405744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:73462463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:73462463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:90379503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:90379503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:196695577 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:196695577 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:136623175 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:136623175 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:87018364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:87018364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:90028035 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:90028035 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:57973720 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:57973720 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:70721134 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:70721134 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:125470811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:125470811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:230788297 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:230788297 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:103379122 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:103379122 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:70778246 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:70778246 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:139704449 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:139704449 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:107886555 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:107886555 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:107886562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:107886562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:189918216 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:189918216 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:115420693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:115420693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:207825710 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:207825710 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:113883894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:113883894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:155003250 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:155003250 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:85797609 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:85797609 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:70721801 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:70721801 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:185975736 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:185975736 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:137148401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:137148401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:127582470 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:127582470 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:387428 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:387428 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:162865188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:162865188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:56524487 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:56524487 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:44067854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:44067854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:109168427 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:109168427 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:24332233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:24332233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:59838937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:59838937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:240387897 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:240387897 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:240387905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:240387905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:79420850 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:79420850 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:79440871 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:79440871 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:14202525 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:14202525 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:69225851 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:69225851 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:162421034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:162421034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:80547838 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:80547838 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:93414781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:93414781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:92370016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:92370016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:92370030 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:92370030 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:122598989 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:122598989 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:102426347 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:102426347 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:106858149 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:106858149 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:5274360 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:5274360 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:186010096 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:186010096 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:26005308 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:26005308 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:111636889 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:111636889 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:9945189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:9945189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:103899610 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:103899610 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:104973879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:104973879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:102879475 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:102879475 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:91477523 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:91477523 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:39537906 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:39537906 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:53223944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:53223944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:52639507 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:52639507 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr18:6244410 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr18:6244410 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:129543643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:129543643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:16510018 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:16510018 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:197881777 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:197881777 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:38499603 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:38499603 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:41390057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:41390057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:62188762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:62188762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:44594666 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:44594666 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:24753656 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:24753656 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:87334524 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:87334524 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:49618333 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:49618333 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:165110910 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:165110910 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:88759877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:88759877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:107088752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chrX:107088752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:152077097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:152077097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:132649102 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:132649102 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:167743712 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:167743712 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:68660337 C>T maps to ENST00000447977 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:68660337 C>T maps to ENST00000447977 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:28002277 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:28002277 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:108118141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:108118141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:78457793 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:78457793 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:103865367 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:103865367 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:103865385 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:103865385 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:5481273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:5481273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:169319478 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:169319478 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:34312582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:34312582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:25894581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:25894581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:133328671 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:133328671 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:248223940 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:248223940 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:9560715 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:9560715 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:69615237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:69615237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:125616599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:125616599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:178575649 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:178575649 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:54943613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:54943613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:31926456 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:31926456 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:95222055 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:95222055 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:20333046 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:20333046 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:7650657 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:7650657 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:244857681 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:244857681 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:105741551 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:105741551 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:57509410 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:57509410 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:57512913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:57512913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:45947324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:45947324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:43348787 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:43348787 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:87638143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:87638143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:2848694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:2848694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:5273446 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:5273446 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:100152674 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:100152674 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:82705341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:82705341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:178861580 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:178861580 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:131007114 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:131007114 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:127982955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:127982955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:176092143 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:176092143 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:6073412 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:6073412 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:72699028 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:72699028 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:125403750 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:125403750 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:79736502 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:79736502 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:94488819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:94488819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:133137914 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:133137914 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:218458933 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:218458933 T>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:16801198 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:16801198 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:237758999 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:237758999 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:33767804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:33767804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:33789326 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:33789326 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:41582538 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:41582538 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:52059875 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:52059875 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:124509387 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:124509387 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:25921136 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:25921136 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:63175705 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:63175705 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:19604559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:19604559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:155551076 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:155551076 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:165793986 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:165793986 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:14509474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:14509474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:111860138 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:111860138 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:98773997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:98773997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:20600073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:20600073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:47705145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:47705145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:25156088 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr15:25156088 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:108430806 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:108430806 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:106976644 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr10:106976644 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:24414419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:24414419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:36903441 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:36903441 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:114640307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:114640307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:38625642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:38625642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:16164810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:16164810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:141619119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:141619119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:79378986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:79378986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:120199550 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:120199550 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:95603247 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:95603247 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:29785968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:29785968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:24233370 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:24233370 T>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:74864317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:74864317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:20068855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:20068855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:202276373 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:202276373 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:73169320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:73169320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:77365451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:77365451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:179528832 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:179528832 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:12709189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:12709189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:33466938 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:33466938 T>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:17834082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:17834082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:70638217 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:70638217 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:76772959 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:76772959 A>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:108634082 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:108634082 G>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:17431404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr16:17431404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:102100388 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:102100388 A>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:100006025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:100006025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:40408153 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr8:40408153 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:38089365 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:38089365 C>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:116663357 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:116663357 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:57828285 C>G did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr20:57828285 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:7176509 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:7176509 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:48244244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:48244244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:87222362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:87222362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:39967448 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:39967448 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:78474243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:78474243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:158443659 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:158443659 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:39442716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:39442716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:156917547 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:156917547 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:39128338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:39128338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:26716695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:26716695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:100160400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:100160400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:67517406 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:67517406 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:247068792 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:247068792 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:243809166 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:243809166 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:45937037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:45937037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:110824046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:110824046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:56637982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:56637982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:47756105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:47756105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:41008645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:41008645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:21239700 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:21239700 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:115348044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:115348044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:156921329 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:156921329 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:2930967 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:2930967 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:43668273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:43668273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:52511838 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:52511838 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:47233829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:47233829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:11077865 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:11077865 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:32202982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:32202982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:28970175 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:28970175 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:99723594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:99723594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:32480350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:32480350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:7880410 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:7880410 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:88614984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:88614984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:151015949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:151015949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:65955615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:65955615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:887436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:887436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:107848216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:107848216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:50916688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:50916688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:102558438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:102558438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:76549201 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:76549201 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:6919342 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:6919342 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:34192055 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:34192055 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:3716651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:3716651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:3716654 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:3716654 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:50985349 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:50985349 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:10200200 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:10200200 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:51770968 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:51770968 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:184404563 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:184404563 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:178491002 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:178491002 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:20234252 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:20234252 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:165714070 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:165714070 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:57417663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:57417663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:39342056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:39342056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:2702527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:2702527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:181728029 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:181728029 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:49084603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:49084603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:18690714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:18690714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:36976105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:36976105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:24358051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:24358051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:93063375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:93063375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:209773564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:209773564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:39234907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:39234907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:54573507 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:54573507 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:158261217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:158261217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:6923265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:6923265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:83251134 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:83251134 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:95207034 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:95207034 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:55857681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:55857681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:40066016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:40066016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:14710638 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:14710638 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:8688634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:8688634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:48262858 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:48262858 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:139869535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:139869535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:48603687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:48603687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:130002698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:130002698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:2824067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:2824067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:480641 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:480641 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:11365027 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:11365027 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:11365031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:11365031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:16656933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:16656933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:16669441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:16669441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:150778512 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:150778512 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:35351868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:35351868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:119694552 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:119694552 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:49033039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:49033039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:36156176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:36156176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:15760589 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:15760589 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:73404848 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:73404848 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:50278792 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:50278792 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:50589840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:50589840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:182673075 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:182673075 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:61079232 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:61079232 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:126389360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:126389360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:140259689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:140259689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:96194203 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:96194203 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:232978764 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:232978764 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:79579534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:79579534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:35365116 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:35365116 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:13777180 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:13777180 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:196892809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:196892809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:27502926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:27502926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:10904360 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:10904360 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:25456947 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:25456947 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:37652555 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:37652555 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:28584392 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:28584392 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:28602247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:28602247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:28609377 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:28609377 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:4711831 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:4711831 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:38427021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:38427021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:33867281 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:33867281 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:73474655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:73474655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:129837403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:129837403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:77707280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:77707280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:70052154 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:70052154 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:29973142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:29973142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:10067976 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:10067976 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:89826496 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:89826496 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:163030362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:163030362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:8148096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:8148096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:117365996 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:117365996 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:97053769 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:97053769 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:34289390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr18:34289390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:164469892 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:164469892 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:18158064 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:18158064 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:171308422 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:171308422 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:65417159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:65417159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31199707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31199707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:151183401 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:151183401 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:169763320 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:169763320 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:154997022 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:154997022 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:120578599 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:120578599 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:46180809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:46180809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:74542868 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:74542868 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:42219506 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:42219506 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:151239240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:151239240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:14625188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:14625188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:14675735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:14675735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:33620947 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:33620947 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:129519536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:129519536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:120685306 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:120685306 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:34029579 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:34029579 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:148727817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:148727817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:52671554 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:52671554 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:106698650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:106698650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:25077034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:25077034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:42156289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:42156289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:21679294 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:21679294 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:245025890 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:245025890 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:97357047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:97357047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:6659776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:6659776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:159023555 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:159023555 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:47121280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:47121280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:101017059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr3:101017059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:143045635 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:143045635 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:154488989 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:154488989 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:2624008 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:2624008 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:178464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:178464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:77944576 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:77944576 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:2927445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:2927445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31418758 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31418758 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31340628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31340628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31383514 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:31383514 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:147012123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:147012123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:133967359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:133967359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:120178581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:120178581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:49626890 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:49626890 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:40318172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:40318172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:78674527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:78674527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:215751282 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:215751282 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:55285229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:55285229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:241712219 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:241712219 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:25919378 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:25919378 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:64751151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:64751151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:150941017 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:150941017 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:40175359 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:40175359 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:74762633 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:74762633 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:40361176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:40361176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:141250323 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:141250323 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:141816379 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:141816379 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:170060848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:170060848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:140991500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:140991500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:65374053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:65374053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:36050415 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:36050415 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:165118929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:165118929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:10425416 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:10425416 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:119700032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:119700032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:7591267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:7591267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:41606653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:41606653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:106144913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:106144913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:60075690 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:60075690 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:60471564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:60471564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:60482420 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:60482420 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:10281857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:10281857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:63551364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:63551364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:63568697 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:63568697 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:7869174 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:7869174 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:7869176 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr5:7869176 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:109839044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:109839044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:81102559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:81102559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:23874811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:23874811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:27409243 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:27409243 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:192173214 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:192173214 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:101735073 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:101735073 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:22841151 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:22841151 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:54902456 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:54902456 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:71075092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:71075092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:21492344 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr14:21492344 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:144920986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:144920986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:32011636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:32011636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:32585407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:32585407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:131459578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:131459578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:131781322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:131781322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:131865426 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:131865426 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:113407866 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:113407866 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:228407093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:228407093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:10584121 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:10584121 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:123556574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:123556574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:27880160 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:27880160 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:69479508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:69479508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:40027511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:40027511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:31822171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:31822171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:30880150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:30880150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:233150373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:233150373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:101186011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:101186011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:20769150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:20769150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:144979864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:144979864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:145019126 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:145019126 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:45278883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:45278883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:25256644 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:25256644 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:201285875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:201285875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:103043496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:103043496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:118307842 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:118307842 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:7621332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:7621332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:2160807 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:2160807 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:63087826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:63087826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:11508045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:11508045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:45117275 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:45117275 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:24180751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:24180751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:27220549 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:27220549 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:43698422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:43698422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:43770525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:43770525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:198677228 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:198677228 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:8492773 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr9:8492773 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:157691584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:157691584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:38508134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:38508134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:49030606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:49030606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:103162399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:103162399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:106977042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:106977042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:109697917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:109697917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:241469866 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:241469866 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:73043627 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:73043627 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:42729061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:42729061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:117632128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:117632128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:10488498 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:10488498 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:75112573 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:75112573 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:78854114 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:78854114 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:16806278 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:16806278 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:34049896 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:34049896 A>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:134991603 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:134991603 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:166142435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:166142435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:53446051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:53446051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:55078368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:55078368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:9096219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:9096219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:100709315 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:100709315 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:158549328 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:158549328 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:52371081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:52371081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:28884762 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr16:28884762 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:80355586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:80355586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:51918954 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:51918954 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:46262016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:46262016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:25813485 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:25813485 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:95819102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:95819102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:18270454 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:18270454 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:32473200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:32473200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:48494619 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:48494619 T>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:127729486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:127729486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:70124410 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:70124410 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:106865068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:106865068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:106937999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr10:106937999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:231174514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:231174514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:158585250 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:158585250 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:158615233 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:158615233 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:99911872 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:99911872 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:2221100 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:2221100 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:74178572 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:74178572 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:59544829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr17:59544829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:50803998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr6:50803998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:114286075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr13:114286075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:134034482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:134034482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:2594030 T>C maps to ENST00000424949 Y645Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:2594030 T>C maps to ENST00000424949 Y645Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:91637855 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:91637855 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:133726340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:133726340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:151145934 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:151145934 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:175091725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:175091725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:175375318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:175375318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:175630268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:175630268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:42680196 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:42680196 G>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:60031402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:60031402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:113705574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:113705574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:72350260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:72350260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:10916508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:10916508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:10934929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:10934929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:5841449 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr11:5841449 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:111096877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:111096877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:51869910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr20:51869910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:31781350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:31781350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:115593214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:115593214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179474722 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179474722 A>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179481202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179481202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179543626 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179543626 T>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179659293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:179659293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:36399149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:36399149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:154241155 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:154241155 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:43846995 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr21:43846995 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:157000044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:157000044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:70360773 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:70360773 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:6833875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:6833875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:108412389 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:108412389 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:150049081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr1:150049081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:6121125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr12:6121125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:71036409 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:71036409 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:141408507 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr7:141408507 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:31572755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr2:31572755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:111398832 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chrX:111398832 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:30134463 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr22:30134463 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:146155945 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:146155945 T>C did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:146155977 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr8:146155977 G>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:56958442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr15:56958442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:62389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr4:62389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:56758180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z008-01A-01W-0746-08 chr19:56758180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:20492089 A>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:20492089 A>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:73179386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:73179386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr9:18769768 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr9:18769768 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr8:68179297 A>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr8:68179297 A>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:161928479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:161928479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:11037947 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:11037947 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:11072283 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:11072283 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr6:36294543 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr6:36294543 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:122054054 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:122054054 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:70050305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:70050305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:36122606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:36122606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:21115926 A>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:21115926 A>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:169435634 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:169435634 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr19:48525312 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr19:48525312 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr20:25198381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr20:25198381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:127654019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:127654019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:76979942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:76979942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:88258671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:88258671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:106697165 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:106697165 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr14:94581093 A>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr14:94581093 A>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:103892258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:103892258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr18:12028753 A>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr18:12028753 A>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:8937044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:8937044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:100271392 C>T maps to NM_152449.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:100271392 C>T maps to NM_152449.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:140984613 C>A maps to NM_177456.2 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chrX:140984613 C>A maps to NM_177456.2 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:86995577 A>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:86995577 A>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:60541122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:60541122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:30252343 T>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:30252343 T>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:13364775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:13364775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:145010291 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:145010291 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:86292632 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:86292632 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr20:37518012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr20:37518012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:3327915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:3327915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:87725143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:87725143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr12:113552598 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr12:113552598 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr14:24647921 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr14:24647921 T>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:151167619 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:151167619 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr17:30478171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr17:30478171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr22:50836242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr22:50836242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:145444332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:145444332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:22398081 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:22398081 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:103130769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:103130769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr12:21229255 A>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr12:21229255 A>G did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:77510309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:77510309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:202323422 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:202323422 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:120811526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:120811526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:48029979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:48029979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr9:73531956 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr9:73531956 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:69874468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:69874468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:241959736 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:241959736 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:178293396 A>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:178293396 A>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:54576 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:54576 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:215823181 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:215823181 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:87215072 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:87215072 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:87104551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:87104551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:220078714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:220078714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:223786245 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:223786245 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:20451030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:20451030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:127737769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:127737769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:33595921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:33595921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:100692721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:100692721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:123046445 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:123046445 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:70900203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:70900203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:112046028 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:112046028 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:159378206 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:159378206 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:7774450 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:7774450 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:7774739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:7774739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:236836989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:236836989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:47736296 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:47736296 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:35033368 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:35033368 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:129008293 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:129008293 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:106975408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:106975408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:49955802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:49955802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:29973498 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:29973498 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:118065006 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:118065006 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:73944296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:73944296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:118893527 C>T maps to NM_001105576.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:118893527 C>T maps to NM_001105576.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:1743014 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:1743014 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:177002041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:177002041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:119538063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:119538063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:160097377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:160097377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:32718662 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:32718662 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:69454532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:69454532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:66278093 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:66278093 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156616316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156616316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:70051350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:70051350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:34193561 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:34193561 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:95982154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:95982154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:41243326 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:41243326 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:180376335 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:180376335 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:50376117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:50376117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:33640004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:33640004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:5126576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:5126576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:13620999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:13620999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:50655822 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:50655822 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:154172103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:154172103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:154172859 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:154172859 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:34666016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:34666016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:31804875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:31804875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:40909773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:40909773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:121098792 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:121098792 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:55107632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:55107632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:54496523 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:54496523 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:46929830 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:46929830 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:219903372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:219903372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:17071756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:17071756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:17076111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:17076111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:67614468 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:67614468 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:15850125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:15850125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:54439309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:54439309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:21884133 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:21884133 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44845702 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44845702 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:122747998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:122747998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:27321926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:27321926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:67842098 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:67842098 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:85158368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:85158368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:73803342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:73803342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:29397157 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:29397157 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:57758211 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:57758211 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:108685615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:108685615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:57996798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:57996798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:21613413 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:21613413 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:70723392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:70723392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:41421796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:41421796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:3080703 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:3080703 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:107421846 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:107421846 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:130000899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:130000899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:27003782 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:27003782 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:113256560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:113256560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:113403103 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:113403103 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:79878802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:79878802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:117386171 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:117386171 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:219677163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:219677163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:42006574 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:42006574 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:91539817 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:91539817 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:110653090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:110653090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:38883819 A>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:38883819 A>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:31697449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:31697449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:14733849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:14733849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:185986569 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:185986569 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:72131546 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:72131546 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:83194498 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:83194498 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:38958221 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:38958221 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:21818510 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:21818510 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:117777354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:117777354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169188430 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169188430 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169494741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169494741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:21767486 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:21767486 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:27162814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:27162814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:76861637 T>A maps to ENST00000356369 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:76861637 T>A maps to ENST00000356369 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:55223444 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:55223444 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:110348347 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:110348347 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:66213935 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:66213935 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:66361296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:66361296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:142567863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:142567863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:14027984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:14027984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:62126569 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:62126569 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:44011413 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:44011413 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:6219259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:6219259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:159626016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:159626016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:159640739 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:159640739 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:50278642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:50278642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:14709773 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:14709773 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:35718769 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:35718769 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:10677894 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:10677894 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:177249497 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:177249497 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:78332176 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:78332176 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:150920037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:150920037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:15500922 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:15500922 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:27943686 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:27943686 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:34261338 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:34261338 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:113937203 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:113937203 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:78091365 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:78091365 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:27571916 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:27571916 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:97742982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:97742982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:13434726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:13434726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:1734039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:1734039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:113941419 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:113941419 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:132887384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:132887384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:100384182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:100384182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:113588523 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:113588523 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:40344528 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:40344528 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:158283915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:158283915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:93226001 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:93226001 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:66849136 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:66849136 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:130763645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:130763645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:44690189 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:44690189 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:21721683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:21721683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:125614246 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:125614246 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:58133653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:58133653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:65479925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:65479925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:186106103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:186106103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:43298587 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:43298587 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:76476134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:76476134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:83586583 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:83586583 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:63325806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:63325806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:148571703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:148571703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:35480202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:35480202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:156673103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:156673103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:35107303 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:35107303 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:110765572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:110765572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169984082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169984082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169994644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:169994644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:20884213 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:20884213 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:154821809 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:154821809 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:142649469 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:142649469 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:39413573 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:39413573 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:31988959 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:31988959 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:6244449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:6244449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:129077034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:129077034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:101024600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:101024600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:202276137 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:202276137 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:54783977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:54783977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156106682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156106682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:81968278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:81968278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:2940578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:2940578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:141083259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:141083259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:170029575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:170029575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:101566134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:101566134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:24750667 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:24750667 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:160771578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:160771578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:54841561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:54841561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:65455877 A>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:65455877 A>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:165109834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:165109834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:165109846 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:165109846 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:75686683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:75686683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:24437450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:24437450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:102562423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:102562423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:78830341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:78830341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:10631408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:10631408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:56660465 G>A maps to ENST00000330439 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:56660465 G>A maps to ENST00000330439 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:125716188 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:125716188 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:9009969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:9009969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:100701465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:100701465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:10248692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:10248692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:108188790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:108188790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:10317453 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:10317453 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:171259200 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:171259200 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:171264048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:171264048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:40054197 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:40054197 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:101735417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:101735417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:101736177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:101736177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:101936253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:101936253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:2975953 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:2975953 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:19649301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:19649301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:78334222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:78334222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:78521057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:78521057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:158444965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:158444965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:70423254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:70423254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:42805349 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:42805349 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:155774356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:155774356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:44556277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:44556277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:34701232 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:34701232 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:149020208 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:149020208 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:131221955 A>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:131221955 A>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:166854832 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:166854832 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:74678106 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:74678106 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:53603186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:53603186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:128414502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:128414502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:47762884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:47762884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248186175 G>T maps to ENST00000355281 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248186175 G>T maps to ENST00000355281 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:4870608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:4870608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:56125384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:56125384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179237001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179237001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:43552616 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:43552616 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:43552705 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:43552705 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:25670319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:25670319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:128551055 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:128551055 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:55877247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:55877247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:93038076 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:93038076 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:233231425 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:233231425 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:55153718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:55153718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:10468240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:10468240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:153277301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:153277301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:58342641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:58342641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:11076019 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:11076019 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:47621562 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:47621562 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:131476669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:131476669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:9434132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:9434132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:96025728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:96025728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:198840393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:198840393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:41313938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:41313938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:132093113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:132093113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:132110017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:132110017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:161160061 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:161160061 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:12017259 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:12017259 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:121265495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:121265495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:76797420 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:76797420 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:37547335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:37547335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:49138360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:49138360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:70981372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:70981372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:47350871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:47350871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:57264864 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:57264864 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:57504960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:57504960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:151478164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:151478164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:76077068 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:76077068 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:5295054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:5295054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:16019885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:16019885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:150298363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:150298363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:57256882 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:57256882 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:43699028 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:43699028 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:43674434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:43674434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:8454450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:8454450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:55693323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:55693323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:48161350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:48161350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:71056253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:71056253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:135975611 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:135975611 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:21936605 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:21936605 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:240934052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:240934052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:87513827 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:87513827 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:21387722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:21387722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:44036339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:44036339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:24620139 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:24620139 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:38934653 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:38934653 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:39014636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:39014636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237619804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237619804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:108917426 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:108917426 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:10024311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:10024311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:165986330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:165986330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:97531533 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:97531533 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:48057356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:48057356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:42387522 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:42387522 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:100780227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:100780227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:135144960 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:135144960 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:19413246 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:19413246 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:51153862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:51153862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:52115379 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:52115379 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:1538215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:1538215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:1616714 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:1616714 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:135366288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:135366288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:99362206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:99362206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:25850896 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:25850896 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:23425903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:23425903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:92405984 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:92405984 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:44199862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:44199862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:47170675 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:47170675 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:70756779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:70756779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:42338213 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:42338213 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:170214124 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:170214124 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:21196234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:21196234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:168620576 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:168620576 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:109763927 C>T maps to ENST00000458487 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:109763927 C>T maps to ENST00000458487 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:153043030 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:153043030 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:158618446 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:158618446 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:54706518 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:54706518 T>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:99797813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:99797813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:63971418 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:63971418 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:80553842 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:80553842 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:74472366 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:74472366 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:131293159 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:131293159 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:53218847 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:53218847 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:29821408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:29821408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:70100085 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chrX:70100085 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:169629822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:169629822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:167020230 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:167020230 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:35699474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:35699474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:103279069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:103279069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:202985298 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:202985298 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:12778340 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:12778340 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:29904488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:29904488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44453376 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44453376 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:38633802 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:38633802 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:44956346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:44956346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:209948413 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:209948413 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:30164655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:30164655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248039173 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248039173 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:29075410 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:29075410 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:72935021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:72935021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:31293949 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:31293949 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:31359917 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:31359917 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:77376483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:77376483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:31778522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:31778522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179599398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179599398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:75229832 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:75229832 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:34929515 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:34929515 T>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:70505335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:70505335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:69870916 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:69870916 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:70070414 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:70070414 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:17785596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:17785596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:145095346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:145095346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:213162021 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:213162021 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:6850672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:6850672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44237241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44237241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:75902506 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:75902506 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:44653714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:44653714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:43533814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:43533814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:47584915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:47584915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:822056 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:822056 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:57290618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:57290618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:22256492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:22256492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:38294398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:38294398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:227884503 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:227884503 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:40556393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:40556393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:23567626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:23567626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:215799048 A>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:215799048 A>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:128013632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:128013632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:167844342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:167844342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:73785980 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:73785980 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:101546485 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:101546485 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:195298085 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:195298085 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:58766459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:58766459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:58766464 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:58766464 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:80743378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:80743378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:45007531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:45007531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:171485163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:171485163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:81228076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:81228076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:67166313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:67166313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:7170188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:7170188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:11015011 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:11015011 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:57103020 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:57103020 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:34417409 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:34417409 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:28950156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:28950156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:96780713 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:96780713 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:125470734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:125470734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:125546111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:125546111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr21:47546166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr21:47546166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:84922826 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:84922826 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:2949194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:2949194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:100187686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:100187686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:58993052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:58993052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:16639578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:16639578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:12949015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:12949015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:66361036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:66361036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:216741577 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:216741577 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:133011660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:133011660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:126477763 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:126477763 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:49225422 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:49225422 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:157557525 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:157557525 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:102670439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:102670439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:240307571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:240307571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:101213958 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:101213958 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:31155176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:31155176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:118429177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:118429177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:46886012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:46886012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:47031074 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:47031074 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:11777374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:11777374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:21721760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:21721760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:183755623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:183755623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:67672763 A>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:67672763 A>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:37539521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:37539521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:156192752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:156192752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:163369873 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:163369873 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:178525287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:178525287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:202698064 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:202698064 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:43480872 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:43480872 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:168414495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:168414495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:53011808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:53011808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:118293229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:118293229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:133952807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:133952807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:141571191 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:141571191 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:144164577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:144164577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:24998286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:24998286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:117984982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:117984982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:21201649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:21201649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:71196919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:71196919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:46495682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:46495682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:15039253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:15039253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:31473306 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:31473306 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:31473311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:31473311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:14294919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:14294919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:36221204 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:36221204 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:21994380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:21994380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:52396219 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:52396219 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:17088232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:17088232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:29656389 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:29656389 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:10218922 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:10218922 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:40119677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:40119677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44694063 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44694063 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44698728 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44698728 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44698739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44698739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44698830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44698830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44699179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44699179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44699208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44699208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:75580842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:75580842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:63659723 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:63659723 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:104190851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:104190851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:134098161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:134098161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:28000704 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:28000704 T>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:9967462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:9967462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:248005230 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:248005230 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:56085679 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:56085679 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:72533706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:72533706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:59755911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:59755911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:39623310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:39623310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:186429772 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:186429772 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:585555 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:585555 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:49949766 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:49949766 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:131833510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:131833510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:113308767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:113308767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:91520118 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:91520118 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:57504623 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:57504623 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:54386561 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:54386561 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:43584664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:43584664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:23750810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:23750810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:121513485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr7:121513485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:174188230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:174188230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:114748890 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:114748890 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:176145159 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:176145159 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:78350035 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:78350035 A>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:35210731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:35210731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:177916908 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:177916908 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:164758645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:164758645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:33353017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:33353017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:20896220 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:20896220 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:70480271 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:70480271 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:96947383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:96947383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:7514298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:7514298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:62547463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr14:62547463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:125334233 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:125334233 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:74663902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:74663902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:38320024 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr13:38320024 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:16336798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:16336798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr21:43863571 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr21:43863571 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:19486547 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:19486547 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:59352015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:59352015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:5411987 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:5411987 G>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:17743757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:17743757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:13916382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:13916382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:32438144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:32438144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:17280535 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:17280535 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:38109783 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:38109783 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:44423960 A>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:44423960 A>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:238048917 T>C did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:238048917 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:29543604 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:29543604 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:156562006 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:156562006 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:64219810 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:64219810 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:72421640 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:72421640 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:42492084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:42492084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:10918798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:10918798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:17705802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr20:17705802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:30503187 A>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:30503187 A>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:122054129 C>A maps to ENST00000449022 G861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:122054129 C>A maps to ENST00000449022 G861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:114603622 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:114603622 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:93646449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:93646449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:57449784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:57449784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:19591362 A>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:19591362 A>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:25532323 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:25532323 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:42798318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:42798318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:25167432 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:25167432 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:24975496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr14:24975496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:58568041 A>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:58568041 A>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:35970090 A>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:35970090 A>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr13:106118625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr13:106118625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:91558499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:91558499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:134681055 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chrX:134681055 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:10277265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:10277265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:46860093 A>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:46860093 A>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:89708898 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:89708898 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:79817813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:79817813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:29463952 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:29463952 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr22:45927206 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr22:45927206 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:48808374 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:48808374 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:155210413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:155210413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:74566054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:74566054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:9765329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:9765329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:30006858 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr16:30006858 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:26197481 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr6:26197481 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:121507286 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:121507286 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:37523100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:37523100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:47162323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:47162323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:22150787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:22150787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:238664728 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:238664728 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr13:77732062 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr13:77732062 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:55992223 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:55992223 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:27062400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr17:27062400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:13418946 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:13418946 G>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:228487065 G>A maps to ENST00000366707 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:228487065 G>A maps to ENST00000366707 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:17172205 T>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:17172205 T>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:43702143 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr19:43702143 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:9317722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:9317722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:130791481 A>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:130791481 A>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:82366999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr4:82366999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:120337309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:120337309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:31511131 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr5:31511131 T>C did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:61310820 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr18:61310820 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:117052828 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr11:117052828 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:140080193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr7:140080193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:85279343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:85279343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:161198296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr1:161198296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:59739470 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr8:59739470 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:49723165 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr12:49723165 C>T did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:31330377 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr15:31330377 C>G did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:3341779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:3341779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:128482626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr2:128482626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:183454622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z012-01A-01W-0746-08 chr3:183454622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr16:48143225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr16:48143225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr16:16218886 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr16:16218886 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:116942252 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:116942252 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:160104081 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:160104081 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:111963131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:111963131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr21:11021234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr21:11021234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:70037662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:70037662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:31660963 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:31660963 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:140461835 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:140461835 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:13621023 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:13621023 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:21084245 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:21084245 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:33370941 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:33370941 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr19:13323628 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr19:13323628 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:56627804 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:56627804 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:45134660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:45134660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:122737111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:122737111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:43989732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:43989732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:189849415 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:189849415 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:40766821 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:40766821 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:16903055 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:16903055 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:16956107 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:16956107 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:49018923 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:49018923 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:167971652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:167971652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:49943141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:49943141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr22:37814680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr22:37814680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:40433762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:40433762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr20:25198247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr20:25198247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:29503581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:29503581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:152857939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:152857939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:191888532 A>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:191888532 A>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:151124083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:151124083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:49217096 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:49217096 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:49217109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:49217109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:150384737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:150384737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:14740912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:14740912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:93518458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:93518458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:108652435 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:108652435 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:119935415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:119935415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:18874928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:18874928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:89388133 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:89388133 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:47119870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:47119870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:117910273 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:117910273 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:201845341 C>A maps to ENST00000456707 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:201845341 C>A maps to ENST00000456707 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:121509137 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:121509137 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:28150402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:28150402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:120311802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:120311802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:64673656 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:64673656 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:123164128 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:123164128 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:44569573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:44569573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:10584684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:10584684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:119204020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:119204020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:6949081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr18:6949081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:209791196 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:209791196 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:12277610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:12277610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:56893508 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:56893508 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:9002619 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:9002619 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr14:48041100 A>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr14:48041100 A>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr11:66205600 A>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr11:66205600 A>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:30969917 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:30969917 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:16068205 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:16068205 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr11:20975126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr11:20975126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:212619088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:212619088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:33462262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:33462262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:107799862 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:107799862 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:32340427 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:32340427 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:97618117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:97618117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:167253011 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:167253011 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr9:112579564 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr9:112579564 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:206058068 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:206058068 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:162575076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:162575076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:144951954 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:144951954 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:197791346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:197791346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:28792818 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:28792818 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:171500401 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:171500401 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:160765697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:160765697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:103897464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:103897464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:57422986 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:57422986 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr14:30195742 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr14:30195742 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:22306481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:22306481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:155567375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:155567375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:29401680 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:29401680 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:77117803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:77117803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr9:91680559 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr9:91680559 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:164714141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:164714141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:168250218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:168250218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:22422100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:22422100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:182760601 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:182760601 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:53278847 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:53278847 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:136219175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:136219175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:67924984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chrX:67924984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:10045183 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:10045183 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr20:60582734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr20:60582734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:38301642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:38301642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:54214468 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr6:54214468 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr9:84268780 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr9:84268780 T>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:50149410 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:50149410 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:87521732 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:87521732 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:6522595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:6522595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr21:10973710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr21:10973710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:38211010 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:38211010 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:41308839 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:41308839 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:58345388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:58345388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:102240661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:102240661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:108629594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:108629594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr16:17333154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr16:17333154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr14:75249075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr14:75249075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:4323103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:4323103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:77235975 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:77235975 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:124483608 A>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:124483608 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:52610547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:52610547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:8805662 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:8805662 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:8862171 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:8862171 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:87323335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:87323335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:220074621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:220074621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153005520 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153005520 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:89738693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:89738693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:23078624 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:23078624 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:31351414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:31351414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:236881129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:236881129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:236917045 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:236917045 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:54494558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:54494558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:5191962 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:5191962 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:5237291 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:5237291 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:5263028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:5263028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:131812941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:131812941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:87974133 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:87974133 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:147967181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:147967181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:16840927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:16840927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:109668015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:109668015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:86205756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:86205756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:55050157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:55050157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:125651461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:125651461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:5129738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:5129738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:43919177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:43919177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:30076388 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:30076388 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:112590695 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:112590695 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:114269240 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:114269240 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:117864520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:117864520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:154295972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:154295972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47424583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47424583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:36128566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:36128566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:130217319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:130217319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:11505143 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:11505143 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:13387015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:13387015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:96795730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:96795730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:176953286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:176953286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:119366274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:119366274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:119802303 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:119802303 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:25265411 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:25265411 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:40659727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:40659727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:77298685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:77298685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:11021147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:11021147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:11048735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:11048735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:134353657 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:134353657 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:171493900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:171493900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:52611505 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:52611505 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:26237666 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:26237666 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:154334007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:154334007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:111368963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:111368963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:180482342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:180482342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:10342760 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:10342760 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:95884438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:95884438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:244769277 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:244769277 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:169771962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:169771962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:170964485 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:170964485 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:31654529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:31654529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:31811862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:31811862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:46002495 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:46002495 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:40966389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:40966389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:31736478 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:31736478 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:108524367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:108524367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:69612521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:69612521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:63632681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:63632681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181705571 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181705571 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181754789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181754789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:6979618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:6979618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110495140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110495140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:92070709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:92070709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:128432407 T>A maps to ENST00000464832 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:128432407 T>A maps to ENST00000464832 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:27606122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:27606122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:43866066 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:43866066 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:112063713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:112063713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:71062577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:71062577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:167410121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:167410121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:21883262 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:21883262 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:18668392 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:18668392 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:133302783 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:133302783 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:50863356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:50863356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:7806567 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:7806567 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:111854637 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:111854637 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:87294815 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:87294815 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:129327492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:129327492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:78415906 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:78415906 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:9920076 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:9920076 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:122205691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:122205691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:146182511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:146182511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:125623020 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:125623020 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:103388842 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:103388842 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:103398094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:103398094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:101830732 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:101830732 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:32156194 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:32156194 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:105831952 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:105831952 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:70637971 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:70637971 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:139869995 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:139869995 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:177669470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:177669470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:107478344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:107478344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:189950358 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:189950358 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:238266649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:238266649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:47746614 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:47746614 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:129914979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:129914979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:101829684 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:101829684 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:211515226 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:211515226 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:30695740 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:30695740 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:36666282 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:36666282 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:5827138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:5827138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:1407647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:1407647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:2975878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:2975878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:3226685 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:3226685 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:3266894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:3266894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:4078129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:4078129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:113317162 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:113317162 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:113326874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:113326874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:113358522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:113358522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:56078265 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:56078265 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:79647101 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:79647101 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:68317227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:68317227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:69343427 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:69343427 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:135370454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:135370454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:159660783 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:159660783 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:10683509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:10683509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:34089244 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:34089244 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:88884992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:88884992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:74594677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:74594677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:169167913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:169167913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:6794215 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:6794215 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:16118643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:16118643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:137293541 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:137293541 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:24760614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:24760614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:2300702 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:2300702 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:39038418 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:39038418 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:31227587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:31227587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:31241364 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:31241364 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:31366613 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:31366613 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:32767052 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:32767052 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:21784036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:21784036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11520630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11520630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11681983 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11681983 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:172021779 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:172021779 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:117762119 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:117762119 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:111409560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:111409560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:168693893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:168693893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:28607460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:28607460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:82126337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:82126337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:158440722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:158440722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:93170802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:93170802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:233431486 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:233431486 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:129208200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:129208200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:79470910 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:79470910 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:66286124 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:66286124 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:97185129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:97185129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:65288516 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:65288516 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:56467670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:56467670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:100511611 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:100511611 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:169513895 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:169513895 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:169529741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:169529741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:138613047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:138613047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:175526051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:175526051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:10690976 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:10690976 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:59102305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:59102305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:119419884 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:119419884 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:231155893 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:231155893 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:8380296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:8380296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:33827099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:33827099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:163029884 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:163029884 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:5750404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:5750404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:187557155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:187557155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:126319897 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:126319897 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:72317061 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:72317061 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:159777762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:159777762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:125072658 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:125072658 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:34174678 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:34174678 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:241663635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:241663635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:152331133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:152331133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:71364336 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:71364336 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:240306044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:240306044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:89405237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:89405237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:49179649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:49179649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:94039195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:94039195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:79447579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:79447579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:49345762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:49345762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:117712647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:117712647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:27334279 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:27334279 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:16254334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:16254334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:11424585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:11424585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:173150761 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:173150761 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:173883852 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:173883852 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:57348397 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:57348397 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:76954730 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:76954730 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:85777882 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:85777882 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:35222837 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:35222837 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:121742338 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:121742338 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:183924131 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:183924131 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:154070868 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:154070868 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:89943646 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:89943646 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:28473454 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:28473454 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:50672886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:50672886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:73389715 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:73389715 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:10102666 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:10102666 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:10009156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:10009156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:13839350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:13839350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:7348393 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:7348393 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:52766959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:52766959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:108695481 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:108695481 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:73624779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:73624779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:37297271 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:37297271 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:93258749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:93258749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:43283607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:43283607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:92824982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:92824982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:93834661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:93834661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:81346728 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:81346728 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:26217141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:26217141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:185959616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:185959616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:70097582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:70097582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:148842494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:148842494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:110630617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:110630617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:45930419 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:45930419 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:118647313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:118647313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:118647652 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:118647652 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:117146238 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:117146238 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:111661295 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:111661295 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:53886162 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:53886162 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:29325240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:29325240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:71940000 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:71940000 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:212126070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:212126070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:50686973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:50686973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:50689291 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:50689291 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:45363550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:45363550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:102140969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:102140969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:54779997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:54779997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:54817225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:54817225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:78616705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:78616705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:40705047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:40705047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:39778586 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:39778586 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:124165916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:124165916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:39129835 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:39129835 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:24173981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:24173981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:53223961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:53223961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:55968678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:55968678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:138530885 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:138530885 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:109742405 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:109742405 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:94369086 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:94369086 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:57970278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:57970278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:137065602 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:137065602 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:39521814 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:39521814 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:134337950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:134337950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153706442 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:153706442 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:107756443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:107756443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:36997830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:36997830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:54967458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:54967458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:51443006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:51443006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:95552818 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:95552818 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:71928839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:71928839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:148009746 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:148009746 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:141625150 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:141625150 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:141680486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:141680486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:141812560 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:141812560 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:169986951 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:169986951 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:12352941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:12352941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70493741 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70493741 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70524896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70524896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:238688020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:238688020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:77748755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:77748755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:43587334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:43587334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:91226180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:91226180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:20031405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:20031405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:165111429 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:165111429 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:217211355 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:217211355 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:138678653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:138678653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:126653765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:126653765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:66250170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:66250170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:74928873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:74928873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:108751517 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:108751517 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:24703430 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:24703430 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:28483646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:28483646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:59858030 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:59858030 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:7873437 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:7873437 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:124646921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:124646921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:113496751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:113496751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:128750408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:128750408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:10354556 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:10354556 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:109613873 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:109613873 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:101714311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:101714311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:101756874 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:101756874 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:101871789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:101871789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16893065 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16893065 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16904390 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16904390 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16908675 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16908675 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:113076547 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:113076547 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:54912573 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:54912573 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:133635592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:133635592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:35284997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:35284997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:4768110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:4768110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:152362881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:152362881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:91937933 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:91937933 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:8235113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:8235113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27243841 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27243841 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27256488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27256488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:170323053 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:170323053 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:170520372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:170520372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:45079576 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:45079576 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:204915742 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:204915742 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:13544251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:13544251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7063512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7063512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7079109 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7079109 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:120536820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:120536820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:120558251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:120558251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:69339114 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:69339114 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:72959098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:72959098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:36326482 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:36326482 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:32774640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:32774640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:47281926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:47281926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:119501719 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:119501719 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:119534324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:119534324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:129317416 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:129317416 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:83706965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:83706965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:84538917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:84538917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:50966335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:50966335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:64458816 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:64458816 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:79490339 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:79490339 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:18766373 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:18766373 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:131737741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:131737741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:69113303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:69113303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:97614338 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:97614338 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:128725063 A>T maps to ENST00000421568 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:128725063 A>T maps to ENST00000421568 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:124097238 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:124097238 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:95165729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:95165729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:29399822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:29399822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:5509780 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:5509780 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:125279149 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:125279149 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:32058816 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:32058816 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:29615066 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:29615066 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:34497108 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:34497108 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110274149 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110274149 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110385188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110385188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110439558 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:110439558 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:205496945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:205496945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:161954961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:161954961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:161973116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:161973116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:59405711 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:59405711 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:47217800 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:47217800 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:178862753 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:178862753 A>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:178862779 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:178862779 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:20769337 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:20769337 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:66831344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:66831344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:144938742 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:144938742 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:144999150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:144999150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:54256618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:54256618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:54751361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:54751361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:55156404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:55156404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:19372562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:19372562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:133548049 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:133548049 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:209215982 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:209215982 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:102058217 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:102058217 T>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:16847577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:16847577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:208842338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:208842338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:161132804 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:161132804 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:23700733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:23700733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:121168429 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:121168429 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:18800479 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:18800479 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7558198 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7558198 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:38743017 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:38743017 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:94745061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:94745061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:19651258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:19651258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:47268160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:47268160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:57512784 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:57512784 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:6341222 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:6341222 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:52898697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:52898697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:43579453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:43579453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:70930062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:70930062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:198710985 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:198710985 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:21598276 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:21598276 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:52555205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:52555205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:82698585 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:82698585 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:50393064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:50393064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:173855681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:173855681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:33749219 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:33749219 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:53586877 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:53586877 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:79349085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:79349085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:79255167 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:79255167 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:192127711 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:192127711 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:73003082 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:73003082 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:31422761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:31422761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:29617327 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:29617327 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:2314155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:2314155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:77286833 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:77286833 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:116951424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:116951424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:237753740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:237753740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:134988936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:134988936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:53831570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:53831570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:166021093 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:166021093 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:151140398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:151140398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:121692697 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:121692697 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:83764302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:83764302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:80380760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:80380760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:57373795 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:57373795 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:153912516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:153912516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:70709451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:70709451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:96318201 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:96318201 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:45228543 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:45228543 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:63141593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:63141593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:65147453 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:65147453 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:107334932 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:107334932 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:86902916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:86902916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:234271790 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:234271790 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:27889983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:27889983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:42337142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:42337142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:27423516 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:27423516 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:70148590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:70148590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:21349860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:21349860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:168149934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:168149934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:55825505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:55825505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:88384127 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:88384127 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:51613042 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:51613042 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:121460899 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:121460899 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:16424103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:16424103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:231135184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:231135184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:118583621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:118583621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:144337691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:144337691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16727086 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:16727086 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:48525055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:48525055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:229007135 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:229007135 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:91041517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:91041517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:167890888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:167890888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:155004531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:155004531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158582602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158582602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158582870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158582870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158612911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158612911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158620999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158620999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:48116851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:48116851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:53045902 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:53045902 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:81610724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr15:81610724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:104332672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:104332672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:114911475 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:114911475 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:75449123 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:75449123 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:10887381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:10887381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:33529652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:33529652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:99941661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:99941661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:13367595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:13367595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:26721782 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:26721782 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:70742092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:70742092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:92193447 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:92193447 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:2381127 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:2381127 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:134119193 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:134119193 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:100603497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:100603497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:3028691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:3028691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:133050234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:133050234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:56290700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:56290700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:68812123 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:68812123 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:68749615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:68749615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:10943070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:10943070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:45773845 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr21:45773845 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:142606564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:142606564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:98560206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:98560206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:143396531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:143396531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:3341645 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:3341645 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:84356271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:84356271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:109926162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:109926162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:34824254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:34824254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:4954524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:4954524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:17752413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:17752413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:35425583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:35425583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:216138947 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:216138947 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:23109056 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:23109056 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:5035673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:5035673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:49346141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:49346141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:101763433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:101763433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:31750278 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:31750278 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:108184207 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:108184207 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:108247572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:108247572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:133020254 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:133020254 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:133072676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:133072676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:107319547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:107319547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:167338172 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:167338172 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:74920407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:74920407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:68364641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:68364641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:971206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:971206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:108641627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:108641627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:31783030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:31783030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:31711784 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:31711784 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:106573779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:106573779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:4646875 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:4646875 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:22156215 A>G maps to NM_007153.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:22156215 A>G maps to NM_007153.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:38108283 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:38108283 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:152610220 G>A maps to ENST00000095634 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:152610220 G>A maps to ENST00000095634 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47306643 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chrX:47306643 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:38287063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:38287063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:37647296 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:37647296 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:37698042 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:37698042 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:59554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:59554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:63889 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:63889 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:227828711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:227828711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:106261 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:106261 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:102189414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:102189414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:9013458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:9013458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:87151644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:87151644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:87180011 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:87180011 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:20666135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:20666135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:101604246 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:101604246 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:48750508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:48750508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:95735305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:95735305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:22015838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:22015838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:44052163 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:44052163 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:89698858 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:89698858 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:148626007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:148626007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:35444173 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:35444173 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:89416276 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:89416276 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:32014678 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:32014678 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:229567936 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:229567936 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:100252833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:100252833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:236881118 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:236881118 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:236894644 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:236894644 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:43944676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:43944676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:87967183 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:87967183 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148048254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148048254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148055168 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148055168 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148059871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148059871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:87468522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:87468522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:49309820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:49309820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:186337577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:186337577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:8757302 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:8757302 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:58492792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:58492792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:41519228 T>A maps to ENST00000415018 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:41519228 T>A maps to ENST00000415018 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:92679870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:92679870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:99541605 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:99541605 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:101316170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:101316170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:100767180 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:100767180 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:90334394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:90334394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:36588326 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:36588326 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:143973044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:143973044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:69040775 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:69040775 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:11682954 G>A maps to ENST00000413512 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:11682954 G>A maps to ENST00000413512 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:156921172 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:156921172 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:135754058 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:135754058 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:157517493 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:157517493 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:35729196 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:35729196 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:35750436 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:35750436 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:69500515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:69500515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:66766618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:66766618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:95227368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:95227368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:176983667 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:176983667 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:120062087 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:120062087 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:107397075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:107397075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:77298314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:77298314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:77298316 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:77298316 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:63976116 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:63976116 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:32956875 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:32956875 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11039059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11039059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11044425 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11044425 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11059130 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11059130 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11059288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11059288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11071418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11071418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11074966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11074966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11075445 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:11075445 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:56531832 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:56531832 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:127512030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:127512030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:187442984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:187442984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:169352885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:169352885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:22051897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:22051897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:7861862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:7861862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:95894254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:95894254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154317507 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154317507 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:135570737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:135570737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:79936785 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:79936785 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:180326272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:180326272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:77818331 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:77818331 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:36680777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:36680777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:30834599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:30834599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:51769230 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:51769230 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:210004485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:210004485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:57202687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:57202687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:55174632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:55174632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:185195993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:185195993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:9510207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:9510207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:31660374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:31660374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:20232503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:20232503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:118870189 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:118870189 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:41158702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:41158702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:41159469 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:41159469 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:41164188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:41164188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:47872274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:47872274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:127898667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:127898667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:40889581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:40889581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:39285367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:39285367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:98643716 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:98643716 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:65117771 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:65117771 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:2764298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:2764298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:181480070 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:181480070 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:81589185 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:81589185 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:54537414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:54537414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:152830088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:152830088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:91075232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:91075232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:49899115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:49899115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:70490097 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:70490097 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:159281741 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:159281741 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:96292326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:96292326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:113213059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:113213059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:32632876 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:32632876 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:56491040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:56491040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:169023732 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:169023732 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:135738609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:135738609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:149984761 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:149984761 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:149984763 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:149984763 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:3782098 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:3782098 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:21802192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:21802192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:21883797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:21883797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:19483703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:19483703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:19483743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:19483743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44891151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44891151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44910756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44910756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:73200550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:73200550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:73498248 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:73498248 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:90400303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:90400303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:151678485 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:151678485 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:49440481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:49440481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:182514867 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:182514867 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:49551697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:49551697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:50824264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:50824264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:126449352 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:126449352 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:40081213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:40081213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125505256 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125505256 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:85158767 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:85158767 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:78917467 G>T maps to ENST00000412074 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:78917467 G>T maps to ENST00000412074 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:65501958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:65501958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:122215208 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:122215208 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:143020376 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:143020376 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:10168175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:10168175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:141643894 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:141643894 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:140151002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:140151002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:140178689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:140178689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:66600376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:66600376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:150911173 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:150911173 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:87606748 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:87606748 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:58391336 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:58391336 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:146997189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:146997189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:125545128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:125545128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:125655017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:125655017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:71716830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:71716830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:121238796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:121238796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:121292450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:121292450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:121295757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:121295757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:139872501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:139872501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:86453277 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:86453277 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:109810493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:109810493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:117063835 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:117063835 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:107405935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:107405935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:47546379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:47546379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:130279402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:130279402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:40773210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:40773210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:207830485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:207830485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:36692028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:36692028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:49825140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:49825140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:99655246 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:99655246 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:1414402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:1414402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:34261933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:34261933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:34403489 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:34403489 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:34617227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:34617227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:113243918 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:113243918 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:113259217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:113259217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57571069 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57571069 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:75396666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:75396666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:37652815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:37652815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:94836520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:94836520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:41532948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:41532948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:99319825 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:99319825 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:47395733 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:47395733 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16025516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16025516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16038330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16038330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:158291001 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:158291001 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:64320964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:64320964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:122017691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:122017691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:36383059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:36383059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:61077627 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:61077627 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:118162848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:118162848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:29845663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:29845663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:29978411 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:29978411 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:126288471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:126288471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:197641095 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:197641095 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:50131475 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:50131475 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:127578730 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:127578730 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:108178993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:108178993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:83445397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:83445397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:83497873 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:83497873 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:3580688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:3580688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:4492462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:4492462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:230456282 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:230456282 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:171821967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:171821967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:45670638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:45670638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:94344723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:94344723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:50824395 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:50824395 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:37650199 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:37650199 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:153959212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:153959212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:34985223 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:34985223 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:32970483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:32970483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:117428975 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:117428975 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:117553108 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:117553108 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:96239621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:96239621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:3775890 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:3775890 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:38458523 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:38458523 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:34395075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:34395075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:40226637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:40226637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:2414035 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:2414035 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:37052088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:37052088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:131186652 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:131186652 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:134670057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:134670057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:110304321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:110304321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:11159894 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:11159894 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:118819683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:118819683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:133767991 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:133767991 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:66013899 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:66013899 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:66104061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:66104061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:6248674 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:6248674 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154132395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154132395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154250902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154250902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:159650388 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:159650388 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:50288198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:50288198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:14601254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:14601254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153377263 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153377263 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54112422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54112422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:139255091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:139255091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:131829602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:131829602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:94391750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:94391750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:68119039 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:68119039 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:62415839 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:62415839 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:177155693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:177155693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:163037993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:163037993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:172633364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:172633364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:48782323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:48782323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:127668830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:127668830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:15769259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:15769259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:15937325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:15937325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:33772067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:33772067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:161559176 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:161559176 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:159777722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:159777722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:124982157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:124982157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:125022629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:125022629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125351302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125351302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:137939893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:137939893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:60814813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:60814813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:34179945 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:34179945 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:164468384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:164468384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:128479977 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:128479977 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:240497606 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:240497606 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:153259322 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:153259322 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:147088155 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:147088155 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:79207481 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:79207481 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:168476128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:168476128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:44282098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:44282098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:37744266 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:37744266 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:37445233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:37445233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153762747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153762747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:27138983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:27138983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153717033 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153717033 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:154875931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:154875931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:4870417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:4870417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:172986438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:172986438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:9823043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:9823043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:9901160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:9901160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:81578931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:81578931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:74837976 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:74837976 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:34025046 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:34025046 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153670676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153670676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:55266659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:55266659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:110429409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:110429409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:100658671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:100658671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:191819685 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:191819685 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:150760041 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:150760041 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:20327417 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:20327417 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:133087438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:133087438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:176777566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:176777566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:119935580 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:119935580 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:19045211 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:19045211 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:35501113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:35501113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:123489531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:123489531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:122387080 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:122387080 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:93743738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:93743738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:94436330 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:94436330 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:104390431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:104390431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:86493506 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:86493506 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:88386590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:88386590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:126085983 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:126085983 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:42620548 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:42620548 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:42620589 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:42620589 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:106697122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:106697122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:14827454 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:14827454 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:127447685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:127447685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:54327099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:54327099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:45353353 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:45353353 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:71787902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:71787902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:18633749 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:18633749 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:18819894 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:18819894 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:19018034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:19018034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:43477794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:43477794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:100689760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:100689760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:65419003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:65419003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:65486236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:65486236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:29864593 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:29864593 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:80371620 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:80371620 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:175110087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:175110087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:25881843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:25881843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:26044057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:26044057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:209874937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:209874937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:128744824 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:128744824 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:198358264 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:198358264 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:113865592 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:113865592 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153053075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153053075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:39847361 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:39847361 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148586154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:148586154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:21231728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:21231728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:21231826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:21231826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:112090930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:112090930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:99250728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:99250728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:46733026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:46733026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:130410304 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:130410304 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:104650770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:104650770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:104886210 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:104886210 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:68595781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:68595781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:3143586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:3143586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:120607860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:120607860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:30827040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:30827040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:15760934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:15760934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:31422328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:31422328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:187529043 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:187529043 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:7657931 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:7657931 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:24531440 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:24531440 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:111145888 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:111145888 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:211034961 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:211034961 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:163419839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:163419839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:169780837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:169780837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:169898704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:169898704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:215408510 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:215408510 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:44266873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:44266873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:53225783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:53225783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:142661268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:142661268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:47162395 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:47162395 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:42501194 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:42501194 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:94053360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:94053360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:94129094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:94129094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:43481290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:43481290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:8940714 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:8940714 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:69595840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:69595840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158047415 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158047415 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152733822 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152733822 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152733876 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152733876 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:38956214 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:38956214 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:39643456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:39643456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:39644762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:39644762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:52992581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:52992581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:39388596 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:39388596 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:35979474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:35979474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:129634380 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:129634380 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:209797176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:209797176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107710114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107710114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107746205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107746205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:64749019 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:64749019 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152785397 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152785397 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:46758668 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:46758668 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:111914782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:111914782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:54772799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:54772799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:55176015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:55176015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:41673201 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:41673201 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:27991567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:27991567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:27999277 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:27999277 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:28148447 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:28148447 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:36105364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:36105364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:148000717 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:148000717 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:118148389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:118148389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:118151703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:118151703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:74762947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:74762947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:42282593 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:42282593 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57535138 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57535138 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:76975738 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:76975738 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:115919134 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:115919134 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:115987159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:115987159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:75048589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:75048589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:114524285 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:114524285 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:160789240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:160789240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:45869893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:45869893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:140967444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:140967444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54839746 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54839746 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54841072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54841072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:67450501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:67450501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:128096650 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:128096650 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:87090214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:87090214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:60866032 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:60866032 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:220799553 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:220799553 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:149270531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:149270531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:138669856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:138669856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:138688009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:138688009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:85498861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:85498861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:49959502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:49959502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47573657 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47573657 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47669960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47669960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:37962293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:37962293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:66669969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:66669969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:135075487 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:135075487 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:102734849 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:102734849 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:13125039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:13125039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154022753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154022753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:43830879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:43830879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:59940731 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:59940731 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154294350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154294350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:92715525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:92715525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:11174960 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:11174960 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:9005307 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:9005307 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:9038483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:9038483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:100695327 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:100695327 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:1213753 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:1213753 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:49419137 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:49419137 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:102025748 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:102025748 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:77644746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:77644746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:10215524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:10215524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:10433078 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:10433078 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:45299668 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:45299668 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:109779931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:109779931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57422450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57422450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57433110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57433110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:26409802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:26409802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:171240416 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:171240416 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:40299729 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:40299729 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:78540112 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:78540112 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:148003800 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:148003800 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:16901320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:16901320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:41304235 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:41304235 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:149912380 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:149912380 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:115858749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:115858749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:119005826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:119005826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:21147149 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:21147149 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:20958065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:20958065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:29654663 C>T maps to NM_001042492.2 Q1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:29654663 C>T maps to NM_001042492.2 Q1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:41204675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:41204675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:71288402 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:71288402 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:183221759 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:183221759 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:183387497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:183387497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:56482459 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:56482459 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:114127525 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:114127525 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:31463017 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:31463017 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:6586684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:6586684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:162268141 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:162268141 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145283254 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145283254 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:120506171 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:120506171 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:120430555 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:120430555 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:89068996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:89068996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:89177466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:89177466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:102595772 C>T maps to NM_173199.1 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:102595772 C>T maps to NM_173199.1 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107790154 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107790154 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107866016 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:107866016 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:84447544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:84447544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:206628156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:206628156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:79200291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:79200291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:79423461 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:79423461 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:5588353 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:5588353 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:131717427 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:131717427 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:131836903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:131836903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:131865401 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:131865401 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132204934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132204934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:107979277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:107979277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:88525843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:88525843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:88667298 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:88667298 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:47857176 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:47857176 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:135323482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:135323482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:153965278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:153965278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101091848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101091848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101096622 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101096622 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101098122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101098122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:8651447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:8651447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123637366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123637366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123822529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123822529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:55143661 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:55143661 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132304818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132304818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132305911 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132305911 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132693026 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:132693026 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:133010615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:133010615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:67327528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:67327528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158549795 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158549795 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:247751498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:247751498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248138842 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248138842 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248247090 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248247090 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55405767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55405767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57797248 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57797248 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:43547709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:43547709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:110289542 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:110289542 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:110463775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:110463775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:9543475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:9543475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:39589521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:39589521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:97009235 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:97009235 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:150780099 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:150780099 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:102533824 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:102533824 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:71489975 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:71489975 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:99001132 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:99001132 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:178862194 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:178862194 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:31890119 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:31890119 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:66833804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:66833804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:144992376 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:144992376 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145020320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145020320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145025288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145025288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145026524 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:145026524 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:58317295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:58317295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:55087363 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:55087363 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:15586229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:15586229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:153283228 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:153283228 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:100920867 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:100920867 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:47632619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:47632619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:77469690 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:77469690 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125079257 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125079257 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125281796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:125281796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:159488547 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:159488547 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:8628659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:8628659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:198956914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:198956914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:18854509 A>G maps to ENST00000447925 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:18854509 A>G maps to ENST00000447925 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:18892441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:18892441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:19460890 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:19460890 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:132022462 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:132022462 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:181794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:181794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:68607710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:68607710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:103041172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:103041172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:131829785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:131829785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:94634547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:94634547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:74325120 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:74325120 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:89865358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:89865358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:43568548 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:43568548 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:62529220 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:62529220 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:132010917 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:132010917 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:75341300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:75341300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:7561476 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:7561476 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:160624697 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:160624697 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:182907613 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:182907613 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:146070865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:146070865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:146080908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:146080908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:6494117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:6494117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:77703498 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:77703498 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:12918836 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:12918836 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:14073346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:14073346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:23509998 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:23509998 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:23524381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:23524381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:69002765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:69002765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:69032570 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:69032570 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:57314488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:57314488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:57390334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:57390334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:61656302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:61656302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:61659324 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:61659324 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:53781120 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:53781120 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:43674240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:43674240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:43679646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:43679646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:43514501 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:43514501 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:98244370 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:98244370 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:71331710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:71331710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:64259010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:64259010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:214546292 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:214546292 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70966026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70966026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:40811963 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:40811963 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:41306426 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:41306426 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:45377032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:45377032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:100146711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:100146711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:9313806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:9313806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70150086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70150086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:69148360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:69148360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:46740391 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:46740391 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:85403833 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:85403833 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:5932407 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:5932407 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:112191376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:112191376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:173832213 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:173832213 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:28095802 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:28095802 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:23370873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:23370873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:155511071 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:155511071 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:106356256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:106356256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:65041461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:65041461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:241463958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:241463958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:46803612 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:46803612 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:119293344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:119293344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:40613016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:40613016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:87049386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:87049386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:87414190 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:87414190 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:196214491 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:196214491 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:90074094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:90074094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:90074096 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:90074096 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:201958760 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:201958760 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:61152119 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:61152119 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:41815413 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:41815413 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:53672395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:53672395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:100646601 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:100646601 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:153964362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:153964362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:83360758 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:83360758 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:83402985 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:83402985 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:108913117 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:108913117 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:108995950 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:108995950 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:36467135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:36467135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:134992424 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:134992424 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:128926857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:128926857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:78192076 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:78192076 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:53751767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:53751767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:41578781 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:41578781 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:18341952 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:18341952 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:166237054 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:166237054 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:62049694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:62049694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:144891924 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:144891924 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:177909874 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:177909874 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:18492937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:18492937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:169703588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:169703588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:169694798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:169694798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:169679512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:169679512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:61388401 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:61388401 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:26640579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:26640579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:102798281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:102798281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:156017842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:156017842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:13959701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:13959701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:14720489 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:14720489 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:67136544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:67136544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:52066854 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:52066854 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:40824152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:40824152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:148427379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:148427379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:38673054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:38673054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:1918275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:1918275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:164793807 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:164793807 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44672665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44672665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44684781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44684781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:42946264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:42946264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:121658135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:121658135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:92407400 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:92407400 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:128335249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:128335249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:45554361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:45554361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:32427237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:32427237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:118588147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:118588147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:58048190 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:58048190 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:58060566 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:58060566 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:140035026 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:140035026 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:84066906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:84066906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75911682 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75911682 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:33964167 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:33964167 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:74481739 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:74481739 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:10905395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:10905395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:28530394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:28530394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:20652074 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:20652074 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:40392213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:40392213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:40605836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:40605836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:70512597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:70512597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:21551341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:21551341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:144898834 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:144898834 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:142718956 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:142718956 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:128657043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:128657043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:21762043 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:21762043 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:88367252 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:88367252 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:51363078 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:51363078 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:108489682 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:108489682 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:106802913 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:106802913 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:39285803 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:39285803 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:214878641 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:214878641 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:49048027 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:49048027 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:123593575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:123593575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:140336709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:140336709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:140373582 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:140373582 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:144336735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:144336735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:142803584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:142803584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:44344259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:44344259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:35668653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:35668653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55648734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55648734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158580933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158580933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158580935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158580935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158597360 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158597360 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158645854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158645854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:31762850 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:31762850 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104079015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104079015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104126558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104126558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123204915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123204915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:168997078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:168997078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:31659274 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:31659274 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:37414643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:37414643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:223497484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:223497484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:113213736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:113213736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:113213738 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:113213738 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:12089791 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:12089791 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:152532592 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:152532592 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:75322460 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:75322460 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:75350574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:75350574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:160031288 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:160031288 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:142918955 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:142918955 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:186271887 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:186271887 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152060366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152060366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:3119871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:3119871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:11441644 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:11441644 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:156375422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:156375422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153524115 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:153524115 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:35699909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:35699909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:63073492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:63073492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:4675170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:4675170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:125955813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:125955813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:129617822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:129617822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:123756148 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:123756148 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:95628882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:95628882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154720959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:154720959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101769132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:101769132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:175306891 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:175306891 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:53038145 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:53038145 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:133375795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:133375795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:7579751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:7579751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:10969929 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr21:10969929 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:72774537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:72774537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:77403429 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:77403429 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:77403701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:77403701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234863910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234863910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234891488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234891488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:3427681 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:3427681 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:51722783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:51722783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:115601638 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:115601638 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:179530286 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:179530286 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:179586470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:179586470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:179658027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:179658027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:1198689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:1198689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:138023965 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:138023965 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:12704746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:12704746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:23309481 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:23309481 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:154528092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:154528092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:19443692 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:19443692 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:70460861 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:70460861 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:70505438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:70505438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:96091646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:96091646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:216259097 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:216259097 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:179399939 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:179399939 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:160393759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:160393759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:108315475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:108315475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:177648844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:177648844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:38044810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:38044810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:51457151 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:51457151 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:42415660 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:42415660 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:54362040 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:54362040 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:112385760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:112385760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54249933 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:54249933 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:69942787 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:69942787 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:31611314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:31611314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123022381 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:123022381 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:33422862 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:33422862 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:64250709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:64250709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:80604289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:80604289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:74725691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:74725691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:69259440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:69259440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:40720194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:40720194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:28194852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:28194852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:95841832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:95841832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:95843204 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:95843204 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:31047972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:31047972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:9408688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:9408688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:84523196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chrX:84523196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:37314166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:37314166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:13928234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:13928234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:113619167 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:113619167 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6656487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6656487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6761568 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6761568 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6940691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6940691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6947864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:6947864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7016004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7016004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7419150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7419150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7441485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7441485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7477029 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7477029 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7477049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7477049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7507945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:7507945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:48135382 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:48135382 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:100647945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:100647945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:124797417 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:124797417 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:31434958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:31434958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:31815744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:31815744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:31983864 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:31983864 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:32091999 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:32091999 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:40027871 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:40027871 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:40037982 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:40037982 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:131323978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:131323978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20559549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20559549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:18108507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:18108507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:155033230 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:155033230 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:120440199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:120440199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:24364912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:24364912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:33557615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:33557615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:33654978 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:33654978 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:33780979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:33780979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:5318482 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:5318482 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:129030719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:129030719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:136411974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:136411974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:7745424 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:7745424 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:7789699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:7789699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:159350365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:159350365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:87956516 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:87956516 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:86922417 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:86922417 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:87565042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:87565042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:49409775 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:49409775 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:4812649 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:4812649 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:33147383 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:33147383 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29419879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29419879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29575293 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29575293 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:30064750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:30064750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:202208753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:202208753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:71469727 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:71469727 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:9258956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:9258956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:9275399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:9275399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:73958110 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:73958110 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:100060778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:100060778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:99308361 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:99308361 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:99834689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:99834689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:5748389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:5748389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101259706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101259706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101400945 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101400945 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101470959 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101470959 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101504152 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:101504152 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:80828114 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:80828114 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:122589715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:122589715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36626016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36626016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:83360409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:83360409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:40820880 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:40820880 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:112060404 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:112060404 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:36369326 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:36369326 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:21250943 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:21250943 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:115309816 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:115309816 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:36084024 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:36084024 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:69033506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:69033506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:142470428 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:142470428 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:6851988 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:6851988 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:27100612 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:27100612 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:35751309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:35751309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:77021395 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:77021395 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:131087182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:131087182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:197053894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:197053894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:176845458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:176845458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119370211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119370211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119498708 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119498708 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119695573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119695573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119995265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:119995265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:120159796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:120159796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:124364425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:124364425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:96795796 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:96795796 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:47517774 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:47517774 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:10413445 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:10413445 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:10694849 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:10694849 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:10722643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:10722643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:130648809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:130648809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:154315239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:154315239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:3605949 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:3605949 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:142218311 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:142218311 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:63526065 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:63526065 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:11039310 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:11039310 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:11065633 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:11065633 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:70071472 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:70071472 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:215593792 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:215593792 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:160319574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:160319574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:56531478 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:56531478 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:99682653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:99682653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:96697933 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:96697933 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:12863231 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:12863231 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:70065377 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:70065377 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:70078454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:70078454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:34172048 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:34172048 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:112944693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:112944693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:112997243 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:112997243 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:32829762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:32829762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:107889141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:107889141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:108042479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:108042479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:72543289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:72543289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:103750202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:103750202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:93235149 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:93235149 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:49054433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:49054433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:110503493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:110503493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:49707284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:49707284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:49889064 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:49889064 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:5133042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:5133042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:30496724 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:30496724 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:18679133 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:18679133 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:77042825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:77042825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:169772495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:169772495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:162352896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:162352896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:9510177 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:9510177 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:9510591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:9510591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:8770720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:8770720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:58792283 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:58792283 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:37502163 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:37502163 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:98737855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:98737855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:118879940 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:118879940 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:149901268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:149901268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:40504878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:40504878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:40616761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:40616761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:40858287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:40858287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:120813340 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:120813340 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:140873142 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:140873142 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2662802 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2662802 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2665000 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2665000 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2665031 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2665031 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2724871 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:2724871 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:181670124 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:181670124 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:181707582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:181707582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:181708129 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:181708129 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:201054057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:201054057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:81898451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:81898451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:54458668 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:54458668 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:54810600 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:54810600 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:54914974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:54914974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:1909440 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:1909440 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:18751330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:18751330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:86061743 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:86061743 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:62449287 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:62449287 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:134527800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:134527800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:110571726 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:110571726 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:110711111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:110711111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:44147976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:44147976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:48733992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:48733992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:116260235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:116260235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121916203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121916203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121928069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121928069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:32194714 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:32194714 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:66480664 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:66480664 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:179748646 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:179748646 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:24821147 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:24821147 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:13104265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:13104265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:130898724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:130898724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:56496519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:56496519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:28461284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:28461284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:28473936 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:28473936 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:28549320 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:28549320 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:118696481 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:118696481 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:156877008 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:156877008 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158300374 G>T maps to ENST00000412358 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158300374 G>T maps to ENST00000412358 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:112653641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:112653641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:67533436 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:67533436 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:67588246 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:67588246 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:103474194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:103474194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:22829789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:22829789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:22833639 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:22833639 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:82759731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:82759731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:83324468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:83324468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:19565890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:19565890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:19612765 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:19612765 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:19980159 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:19980159 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:68776486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:68776486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:59108041 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:59108041 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:44899296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:44899296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:44926495 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:44926495 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:59886914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:59886914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:60363462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:60363462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:26922198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:26922198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:20821946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:20821946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:133681166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:133681166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:42314327 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:42314327 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:15807705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:15807705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:34960555 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:34960555 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:35007356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:35007356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:214828562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:214828562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:95107894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:95107894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:122736928 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:122736928 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:29329625 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:29329625 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:239591109 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:239591109 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:32332701 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:32332701 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:45905776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:45905776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:178060459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:178060459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:72144991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:72144991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:150670813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:150670813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:139739589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:139739589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:3565308 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:3565308 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:100537370 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:100537370 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:88117907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:88117907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:224927218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:224927218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:41195551 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:41195551 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:2468182 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:2468182 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:2978237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:2978237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:99667492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:99667492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:99995836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:99995836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:146002746 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:146002746 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:146712856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:146712856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:146753904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:146753904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:124791174 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:124791174 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:124999732 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:124999732 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:55933972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:55933972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:139809189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:139809189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:139867800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:139867800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:110084729 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:110084729 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:70942197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:70942197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:46779432 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:46779432 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:28752438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:28752438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:131476853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:131476853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:39112000 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:39112000 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:211513308 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:211513308 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125593233 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125593233 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125601808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125601808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125692081 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125692081 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125692083 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:125692083 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:197396500 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:197396500 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:2886768 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:2886768 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:3424005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:3424005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:4368263 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:4368263 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:34071435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:34071435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:34377421 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:34377421 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:113678761 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:113678761 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:113956185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:113956185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:113987987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:113987987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:114041778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:114041778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:39784960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:39784960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79610609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79610609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79786803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79786803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:80700009 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:80700009 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11078008 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11078008 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11082683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11082683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11117549 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11117549 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11653727 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11653727 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11780299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:11780299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:111481887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:111481887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:107208206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:107208206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:49049728 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:49049728 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:35985707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:35985707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:41660641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:41660641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:59682262 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:59682262 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:39840881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:39840881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:58357813 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:58357813 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:39388697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:39388697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:121993607 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:121993607 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:50292638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:50292638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31302431 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31302431 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31302433 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31302433 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:110655069 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:110655069 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:162637178 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:162637178 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:118121199 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:118121199 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:120940613 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:120940613 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:24748121 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:24748121 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:14898445 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:14898445 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:234372224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:234372224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:2300727 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:2300727 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:40662561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:40662561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:107956816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:107956816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:108169639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:108169639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:83390335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:83390335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:84250562 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:84250562 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:84391211 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:84391211 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:69669041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:69669041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:69721999 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:69721999 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:79552077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:79552077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:32862885 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:32862885 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:78349864 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:78349864 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:124263352 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:124263352 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:7644069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:7644069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:11572676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:11572676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:11812882 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:11812882 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:69565162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:69565162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:169148924 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:169148924 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:50925858 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:50925858 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:21738299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:21738299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:73274947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:73274947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:115200334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:115200334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:116390680 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:116390680 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:154374722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:154374722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:32943957 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:32943957 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:97671757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:97671757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:98115829 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:98115829 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:28651534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:28651534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117352587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117352587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117550477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117550477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117583434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117583434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:28935381 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:28935381 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:212229241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:212229241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:45393530 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:45393530 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:350918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:350918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:66761882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:66761882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:71912341 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:71912341 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:158334221 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:158334221 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:83288347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:83288347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:13609106 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:13609106 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:36352616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:36352616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:120801389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:120801389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:184039060 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:184039060 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:10825277 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:10825277 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:205595139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:205595139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36960774 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36960774 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36984302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36984302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36995141 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:36995141 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:37460859 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:37460859 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31757298 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31757298 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:34788912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:34788912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:5433878 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:5433878 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:38226927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:38226927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:96591409 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:96591409 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:96788174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:96788174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:96857822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:96857822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:97334108 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:97334108 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:134746771 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:134746771 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:134804250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:134804250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:134978134 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:134978134 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:51871532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:51871532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:212495003 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:212495003 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:53686207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:53686207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216944425 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216944425 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:44011457 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:44011457 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:128426689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:128426689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133363785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133363785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133589099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133589099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133676177 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133676177 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:72237742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:72237742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:66012243 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:66012243 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:66104864 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:66104864 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:50264505 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:50264505 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:50279503 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:50279503 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:175530843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:175530843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:108468377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:108468377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:179730858 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:179730858 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:179731554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:179731554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:99046852 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:99046852 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:30846899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:30846899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:29526165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:29526165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:29680828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:29680828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:29716863 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:29716863 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:18693116 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:18693116 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:91329689 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:91329689 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:62183032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:62183032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:10887366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:10887366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:29894559 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:29894559 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:29937532 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:29937532 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:177226596 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:177226596 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190067132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190067132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190336127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190336127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:54742822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:54742822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:13743205 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:13743205 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:92092229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:92092229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:127597348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:127597348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:127671312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:127671312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:97333605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:97333605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:117593557 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:117593557 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:161480055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:161480055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:124877249 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:124877249 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:14926390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:14926390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:95475117 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:95475117 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:95566221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:95566221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:192113496 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:192113496 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:137977822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:137977822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:170872011 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:170872011 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:59891823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:59891823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:58087886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:58087886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:76052685 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:76052685 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:240334551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:240334551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:240494069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:240494069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:49168532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:49168532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:90031149 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:90031149 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:71161868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:71161868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:113890380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:113890380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:14395486 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:14395486 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:49218859 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:49218859 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:35649124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:35649124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117725551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:117725551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:31048310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:31048310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:27159865 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:27159865 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:46066417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:46066417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:27700938 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:27700938 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:26540386 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:26540386 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:30896161 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:30896161 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:88319909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:88319909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:31307386 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:31307386 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:172939999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:172939999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:173899665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:173899665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:100975629 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:100975629 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:42428535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:42428535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:42699872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:42699872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:150175051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:150175051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:78578041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:78578041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:121730160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:121730160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:4074960 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:4074960 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:4867895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:4867895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:45017937 C>T maps to NM_054022.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:45017937 C>T maps to NM_054022.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:58753272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:58753272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20340559 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20340559 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:92444511 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:92444511 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20053199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20053199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20065933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20065933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:25736992 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:25736992 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:25857402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:25857402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:88473703 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:88473703 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:123469873 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:123469873 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:40370857 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:40370857 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:152961472 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:152961472 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:153028611 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:153028611 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:105725989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:105725989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:87791497 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:87791497 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:102304481 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:102304481 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:37285482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:37285482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:120479311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:120479311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:120488797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:120488797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:120790348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:120790348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:9960969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:9960969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:9966147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:9966147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:14085218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:14085218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:14097346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:14097346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:104459563 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:104459563 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:104477576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:104477576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:121085870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:121085870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:88306495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:88306495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:7436533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:7436533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:7484946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:7484946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:27936920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:27936920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:27972158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:27972158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:108623769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:108623769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:108712927 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:108712927 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:5338103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:5338103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:45498433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:45498433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:32087210 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:32087210 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:240267860 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:240267860 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:18722472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:18722472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:18748800 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:18748800 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:18816737 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:18816737 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:19021510 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:19021510 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:41039317 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:41039317 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:43284407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:43284407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:72637953 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:72637953 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:81334249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:81334249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:210733204 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:210733204 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:145629643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:145629643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:176316614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:176316614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31308991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31308991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:29796268 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:29796268 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:30147502 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:30147502 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:173491100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:173491100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:21725154 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:21725154 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:27169622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:27169622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:18312939 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:18312939 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:175103005 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:175103005 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:25933634 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:25933634 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:25944761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:25944761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:67203063 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:67203063 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:14891655 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:14891655 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:70896559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:70896559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:123516728 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:123516728 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:27679320 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:27679320 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:57919307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:57919307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51813677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51813677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:118623809 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:118623809 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:118714379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:118714379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:117172249 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:117172249 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:34658452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:34658452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:113736325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:113736325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31514851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31514851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:143051517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:143051517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:143209090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:143209090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:15257007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:15257007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:77655342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:77655342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:102879510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:102879510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:61847904 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:61847904 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:67768232 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:67768232 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:68600056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:68600056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:52223296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:52223296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:37539835 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:37539835 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:37544052 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:37544052 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:30524839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:30524839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:31336186 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:31336186 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:31344091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:31344091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:93428790 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:93428790 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:5041348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:5041348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:27081795 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:27081795 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:28084861 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:28084861 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:64950487 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:64950487 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:155972280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:155972280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:156097833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:156097833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:61615417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:61615417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:169988461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:169988461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:21625602 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:21625602 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:140631688 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:140631688 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:44283998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:44283998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:142642120 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:142642120 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:136637631 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:136637631 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:114158126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:114158126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:27764358 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:27764358 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:42266940 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:42266940 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:154504569 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:154504569 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:81192982 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:81192982 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:24574542 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:24574542 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:5729037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:5729037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:118854856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:118854856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:5962095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:5962095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:32326078 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:32326078 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:55246671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:55246671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158016080 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158016080 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158048854 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158048854 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:38953146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:38953146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:39191121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:39191121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129250735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129250735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129800122 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129800122 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:34007772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:34007772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:152636945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:152636945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:16617157 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:16617157 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:1827186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:1827186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:41649116 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:41649116 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:28411837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:28411837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:58799471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:58799471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:76399987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:76399987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:76412211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:76412211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:132120475 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:132120475 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:132120495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:132120495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:161027840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:161027840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:82024519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:82024519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:62903590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:62903590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:99374264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:99374264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:188122381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:188122381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:40365604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:40365604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:40415847 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:40415847 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:42190668 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:42190668 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:42206212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:42206212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133916685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133916685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133926838 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:133926838 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141079826 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141079826 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141143291 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141143291 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141159361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141159361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141747238 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:141747238 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:25448232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:25448232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:62893401 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:62893401 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:44400280 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:44400280 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:40164678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:40164678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:40174426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:40174426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:40648395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:40648395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:41035800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:41035800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:41453866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:41453866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:70249104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:70249104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:85596025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:85596025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:77392421 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:77392421 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:77715146 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:77715146 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115734313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115734313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115848476 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115848476 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:116110344 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:116110344 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:24910338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:24910338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:24993417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:24993417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31686699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31686699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:160734639 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:160734639 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:6595407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:6595407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:65449225 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:65449225 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:65449234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:65449234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:65623828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:65623828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:95916185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:95916185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:95980899 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:95980899 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:44043763 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:44043763 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:164880485 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:164880485 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:165153424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:165153424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:217130280 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:217130280 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220773255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220773255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220801441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220801441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:136603159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:136603159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:94161656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:94161656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:47573316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:47573316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:47955235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:47955235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:151126946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:151126946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:116431764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:116431764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:8807803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:8807803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:86545734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:86545734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:43210665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:43210665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:56267017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:56267017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:151975560 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:151975560 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:21957872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:21957872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:154820392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:154820392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158817773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:158817773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:62929269 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:62929269 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:108759094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:108759094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220948264 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220948264 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:59940031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:59940031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:55540910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:55540910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:10231180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:10231180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:9954743 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:9954743 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:65744245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:65744245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:47657033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:47657033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:151256886 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:151256886 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:29682828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:29682828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:81112298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:81112298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:23854033 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:23854033 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:23883425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:23883425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:23902508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:23902508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:46764711 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:46764711 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:30959713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:30959713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:26453729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:26453729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:26463597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:26463597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:137114032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:137114032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:175090484 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:175090484 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:101930560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:101930560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:102029558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:102029558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:102948554 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:102948554 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:54925442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:54925442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:134104064 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:134104064 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:71305458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:71305458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:132984864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:132984864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:160319870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:160319870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:115798994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:115798994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:115804842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:115804842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:161169573 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:161169573 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:27212574 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:27212574 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:198225543 A>T maps to ENST00000367383 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:198225543 A>T maps to ENST00000367383 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20930634 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20930634 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:21380191 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:21380191 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:45013690 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:45013690 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:45135754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:45135754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:68200993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:68200993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:103870628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:103870628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:173197165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:173197165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:173342986 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:173342986 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:32477418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:32477418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:247594709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:247594709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:56372701 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:56372701 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:31599587 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:31599587 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:33480886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:33480886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:33644123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:33644123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:34119017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:34119017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:34138643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:34138643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:34233417 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:34233417 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:25264720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:25264720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:119501727 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:119501727 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:142816443 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:142816443 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:52276266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:52276266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:31657801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:31657801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:32251693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:32251693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:32307799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:32307799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:32330011 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:32330011 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:83908287 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:83908287 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:84151203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:84151203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:84541972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:84541972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:50880392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:50880392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:79482856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:79482856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:79941033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:79941033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:123725003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:123725003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131308494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131308494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131341584 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131341584 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131597475 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131597475 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131727879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131727879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131795935 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131795935 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131863820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131863820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131866921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131866921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131876665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131876665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131999529 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:131999529 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132016465 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132016465 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132029350 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132029350 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132164452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132164452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:107712763 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:107712763 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:87599838 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:87599838 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:88445389 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:88445389 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:88483716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:88483716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:163295724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:163295724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:56785599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:56785599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:8650621 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:8650621 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:48909745 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:48909745 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:167054024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:167054024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:167416895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:167416895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:167645118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:167645118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132410604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132410604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132621940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:132621940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:6865180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:6865180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:143789230 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:143789230 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248220306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248220306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248225878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248225878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:117093843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:117093843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:58111180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:58111180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:163482452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:163482452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:9521520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:9521520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:169478986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:169478986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:169519567 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:169519567 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:176781401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:176781401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:118938422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:118938422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:52236511 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:52236511 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:34541538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:34541538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:36899660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:36899660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:37010193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:37010193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:91642708 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:91642708 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:91714784 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:91714784 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:30845111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:30845111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:67083037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:67083037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:183194264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:183194264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:14802531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:14802531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:144930943 T>C maps to NM_001002811.1 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:144930943 T>C maps to NM_001002811.1 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:149283769 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:149283769 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76679708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76679708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:95219057 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:95219057 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:95427329 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:95427329 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:28495445 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:28495445 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:31679641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:31679641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:102781462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:102781462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:41638332 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:41638332 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:152626234 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:152626234 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:97834635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:97834635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:71006715 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:71006715 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:100912647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:100912647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:28792380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:28792380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:96438820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:96438820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:53989450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:53989450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:111542023 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:111542023 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:111593362 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:111593362 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:77469356 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:77469356 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:229937921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:229937921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:65453694 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:65453694 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:47952642 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:47952642 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:42045148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:42045148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:8176416 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:8176416 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:198817943 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:198817943 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:16886918 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:16886918 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:30126941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:30126941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:43908222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:43908222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:131914658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:131914658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:131994149 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:131994149 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:28172050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:28172050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:38144928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:38144928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:16256757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:16256757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:39481805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:39481805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:81751067 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:81751067 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:27746434 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:27746434 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:7631348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:7631348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:170460773 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:170460773 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:25664611 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:25664611 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:146091237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:146091237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:146099442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:146099442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:146404593 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:146404593 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:47280290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:47280290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:47307481 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:47307481 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:186280449 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:186280449 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:57398408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:57398408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:57454095 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:57454095 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:94187269 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:94187269 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:24104039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:24104039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:54403757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:54403757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:53107133 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:53107133 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:119920662 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:119920662 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:7435643 C>T maps to NM_001085382.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:7435643 C>T maps to NM_001085382.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43706894 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43706894 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43552631 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43552631 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:27287676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:27287676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:88998587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:88998587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:70938456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:70938456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:10192599 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:10192599 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:8814404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:8814404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:8951530 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:8951530 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:9762499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:9762499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:61839409 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:61839409 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:41095496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:41095496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:41180798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:41180798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:41473280 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:41473280 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:52373872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:52373872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:52412431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:52412431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:52547931 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:52547931 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:100143857 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:100143857 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:107085367 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:107085367 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:131926799 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:131926799 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:121047413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:121047413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:20651906 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:20651906 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:85211380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:85211380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:85330045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:85330045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:85339871 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:85339871 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:170493025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:170493025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:22297931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:22297931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:79327416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:79327416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:48892150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:48892150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:46293014 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:46293014 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31855187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31855187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31888658 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:31888658 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79312457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79312457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79314140 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79314140 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:103183079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:103183079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:103521000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:103521000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:15321304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:15321304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:107072295 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:107072295 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:183661409 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:183661409 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:192127941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:192127941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:192307678 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:192307678 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:72600537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:72600537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:72701826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:72701826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:72932144 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:72932144 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:63872992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:63872992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:241319373 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:241319373 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:107224945 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:107224945 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:152299848 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:152299848 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:105259299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:105259299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:40500777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:40500777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:87998074 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:87998074 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:79250253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:79250253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:79815073 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:79815073 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:77112279 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:77112279 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:64516640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:64516640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:94473492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:94473492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:1764526 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:1764526 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:113213544 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:113213544 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:113319699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:113319699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:89003402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:89003402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:58296431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:58296431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:15159049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:15159049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:74659499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:74659499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237661785 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237661785 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237935268 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237935268 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237961261 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237961261 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237982713 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:237982713 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:148867325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:148867325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:158920738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:158920738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:159116722 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:159116722 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:38835651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:38835651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:243507639 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:243507639 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:71512679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:71512679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:54826848 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:54826848 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:108192697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:108192697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:53925865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:53925865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:74906262 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:74906262 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:122748401 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:122748401 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:115803246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:115803246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:17834815 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:17834815 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:17974486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:17974486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:17980910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:17980910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:94909715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:94909715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:94962654 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:94962654 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:61166540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:61166540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:37417780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:37417780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:26634370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:26634370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:70572394 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:70572394 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:7371810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:7371810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:56084222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:56084222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155372984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155372984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155457716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155457716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:23752432 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:23752432 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:52113678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:52113678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:52113682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:52113682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:84188715 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:84188715 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:84192041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:84192041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:148083879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:148083879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:70641890 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:70641890 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:50428440 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:50428440 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51655578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51655578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:138428619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:138428619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:71958799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:71958799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:122774737 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:122774737 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:43078266 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:43078266 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:43132621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:43132621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:43170840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:43170840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:22381078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:22381078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:100811775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:100811775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:20029102 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:20029102 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:3413547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:3413547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:19743168 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:19743168 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:92867705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:92867705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:37310568 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:37310568 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:92301721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:92301721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:35919322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:35919322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:40289662 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:40289662 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:40422402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:40422402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:118257383 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:118257383 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:92918594 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:92918594 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:61451574 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:61451574 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:54968639 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:54968639 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:18259030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:18259030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:18331871 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:18331871 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:162652365 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:162652365 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:32651168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:32651168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20645013 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20645013 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:173517435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:173517435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:142997325 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:142997325 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:143090913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:143090913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:21057584 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:21057584 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:20894176 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:20894176 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:92443604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:92443604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:101810595 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:101810595 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:98900037 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:98900037 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:168620361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:168620361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:168678598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:168678598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:164905176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:164905176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:70484218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:70484218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:246594924 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:246594924 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:227929581 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:227929581 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:25179383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:25179383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:25213217 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:25213217 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:51557424 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:51557424 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:51621608 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:51621608 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:51700112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:51700112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:1285283 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:1285283 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:17838900 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:17838900 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:65618420 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:65618420 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:17929495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:17929495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:186859994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:186859994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:108363619 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:108363619 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:108373736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:108373736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106847821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106847821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106916580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106916580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106916756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106916756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106989539 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:106989539 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:107021945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:107021945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:24179415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:24179415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:7721264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:7721264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:214208400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:214208400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:123593579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:123593579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:142598783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:142598783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:151049414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:151049414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:217822388 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:217822388 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:48791146 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:48791146 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:136426705 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:136426705 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:136816790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:136816790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:167919623 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:167919623 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:41026138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:41026138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:54759283 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:54759283 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:53124625 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:53124625 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:126284071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:126284071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:186792135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:186792135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:76951631 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:76951631 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:136196306 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:136196306 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:68442837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:68442837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:96859181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:96859181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:74601356 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:74601356 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:81850483 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:81850483 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:184910652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:184910652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:9181555 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:9181555 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:53150204 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:53150204 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:120899705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:120899705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:67621906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:67621906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:70540226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:70540226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:44222019 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:44222019 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:114849522 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:114849522 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:75559211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:75559211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:109316780 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:109316780 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:152534648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:152534648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:110018428 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:110018428 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:79508646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:79508646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:40850780 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:40850780 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:55685807 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:55685807 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:150463815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:150463815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:75947824 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:75947824 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:101706458 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:101706458 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:179292810 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:179292810 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:6812034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:6812034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:139525082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:139525082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:53107771 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:53107771 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:102842585 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:102842585 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:1264755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:1264755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43921999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43921999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43922302 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:43922302 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:56700455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:56700455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:50808084 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:50808084 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:133472218 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:133472218 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:3448044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:3448044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:133905131 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:133905131 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:11486086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:11486086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:11629892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:11629892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:11857829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:11857829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:137750929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:137750929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:137964804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:137964804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:121341670 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:121341670 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:156346441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:156346441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:63014829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:63014829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:63088552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:63088552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:38783508 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:38783508 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:120464668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:120464668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:120477084 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:120477084 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:98290159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:98290159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:38225073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:38225073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:44608094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:44608094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:44645921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:44645921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:130121532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:130121532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:42824381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:42824381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:55831594 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:55831594 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:15271377 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:15271377 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:15526593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:15526593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:68735589 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:68735589 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:83286348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:83286348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:66378672 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:66378672 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:74958126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:74958126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175054750 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175054750 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175365584 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175365584 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175652147 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175652147 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175674841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:175674841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:47390402 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:47390402 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:42546010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:42546010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:1278578 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:1278578 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:10917290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:10917290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:10971773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:10971773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:202277299 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:202277299 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:123734393 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:123734393 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72954071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72954071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:67061741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:67061741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:122869573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:122869573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:111312990 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:111312990 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:142574388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:142574388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:141957461 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:141957461 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:81441167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:81441167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:81462880 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:81462880 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:51621235 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:51621235 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:52024814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:52024814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:31076717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:31076717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:9307491 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:9307491 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:135252744 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:135252744 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:135252751 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:135252751 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:179500554 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:179500554 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:2698505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:2698505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:43826368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr21:43826368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:202300910 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:202300910 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:25585396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:25585396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:96635758 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr13:96635758 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:41878183 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:41878183 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:54708082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:54708082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:35504027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:35504027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:35542000 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:35542000 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216270755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216270755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216517892 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216517892 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216544416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:216544416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:18649935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:18649935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:219417702 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:219417702 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:234462924 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:234462924 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:15471023 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrY:15471023 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:106721104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:106721104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:77899618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:77899618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:108152602 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:108152602 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:36541077 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr20:36541077 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:117749225 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:117749225 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:70729445 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:70729445 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:71082457 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:71082457 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:100864249 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:100864249 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:170058357 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:170058357 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76734495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76734495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76745545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76745545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:113128406 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:113128406 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:1954928 C>T maps to ENST00000350915 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:1954928 C>T maps to ENST00000350915 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:32433121 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:32433121 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:31620328 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:31620328 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:10856264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:10856264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:11011182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:11011182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:14219366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:14219366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:27409635 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:27409635 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:151694422 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:151694422 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:22800355 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:22800355 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:111392648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:111392648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:111392780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chrX:111392780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72008544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72008544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57059326 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57059326 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57293506 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57293506 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:40600533 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:40600533 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:64393749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:64393749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:180626968 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:180626968 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:21782118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:21782118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:21811748 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:21811748 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:22109372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:22109372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:23693527 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:23693527 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:178373772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:178373772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:30886412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:30886412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:30957931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:30957931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:31044581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:31044581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:124003224 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:124003224 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:52627434 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:52627434 T>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:130206132 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:130206132 T>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:238048420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:238048420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:7191968 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:7191968 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:7331904 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:7331904 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:7383000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:7383000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:31808929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:31808929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:127812211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:127812211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:127833309 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:127833309 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:127846866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:127846866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:84363877 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:84363877 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:111890284 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:111890284 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:100453902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:100453902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:49019664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:49019664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:88387799 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:88387799 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:134216947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:134216947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:41522669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:41522669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:21228941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:21228941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:7803593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:7803593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135768071 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135768071 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135789373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135789373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:100879828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:100879828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:177133463 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:177133463 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:26029276 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:26029276 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:31294810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:31294810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:182598640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:182598640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:138880577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:138880577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:69808930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:69808930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:11052817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:11052817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:11077294 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:11077294 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:88048940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:88048940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:122791421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:122791421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:18222162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:18222162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:7786027 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:7786027 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:13614669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:13614669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:79999862 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:79999862 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:93792130 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:93792130 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:26467860 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:26467860 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:77700244 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:77700244 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:11420813 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:11420813 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:58483980 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:58483980 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:172537371 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:172537371 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:130164647 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:130164647 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:181650343 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:181650343 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:106112556 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:106112556 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:33255538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:33255538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:158300025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:158300025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:157811457 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:157811457 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:21941907 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:21941907 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:24488322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:24488322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:21882646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:21882646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:73511646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:73511646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:4892620 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:4892620 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:34864110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:34864110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:104107058 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:104107058 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:50901683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:50901683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:10155763 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:10155763 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:141330966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:141330966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:103400165 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:103400165 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:130300340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:130300340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:166325211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:166325211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:87563478 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:87563478 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:20987406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:20987406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:1414371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:1414371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:4757506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:4757506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:70803489 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:70803489 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:15994913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:15994913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:58114305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:58114305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:114138486 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:114138486 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:162688968 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:162688968 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:126663638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:126663638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:31737075 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:31737075 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:186024607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:186024607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:57650385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:57650385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:47974224 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:47974224 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:83357651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:83357651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:31719665 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:31719665 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:76498744 G>C maps to ENST00000389840 T1695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:76498744 G>C maps to ENST00000389840 T1695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:13754480 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:13754480 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:13758740 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:13758740 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:11550332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:11550332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:84876499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:84876499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:128788710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:128788710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:169443015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:169443015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:34994131 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:34994131 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:68921171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:68921171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:82523321 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:82523321 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:37284103 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:37284103 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:10641526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:10641526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:89521513 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:89521513 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:15822285 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:15822285 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:5285977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:5285977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:8154857 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:8154857 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:161559302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:161559302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:102454252 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:102454252 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:159817051 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:159817051 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:71461154 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:71461154 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:48564879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:48564879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:158408160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:158408160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:133353501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:133353501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:37370606 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:37370606 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:167058413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:167058413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:37389672 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:37389672 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:48832304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:48832304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:52216510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:52216510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:50546713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:50546713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:63926226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:63926226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:46812638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:46812638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:129236288 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:129236288 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:51828508 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:51828508 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:29442871 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:29442871 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:102964713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:102964713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:35871119 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:35871119 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:54776248 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:54776248 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:65310712 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:65310712 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:84256650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:84256650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:133317587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:133317587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:36766764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:36766764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:27610079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:27610079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:5429423 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:5429423 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:100127886 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:100127886 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:118708344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:118708344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:10394829 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:10394829 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:126824317 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:126824317 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:25398320 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:25398320 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:39661877 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:39661877 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:107692476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:107692476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:37489590 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:37489590 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:40098079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:40098079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:69171194 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:69171194 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:82188518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:82188518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:82372970 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:82372970 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:40493676 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:40493676 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:46908160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:46908160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:68688315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:68688315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:115765172 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:115765172 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:31682890 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:31682890 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:160691981 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:160691981 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:166962127 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:166962127 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:151283310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:151283310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:140992841 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:140992841 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:72723098 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:72723098 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:67452979 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:67452979 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:20044111 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:20044111 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135313654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135313654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:138711784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:138711784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:71059803 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:71059803 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:158815368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:158815368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:30490384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:30490384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:17075990 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:17075990 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:10605072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:10605072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:63615350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:63615350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:195461855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:195461855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:171034991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:171034991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:19462992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:19462992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:41341031 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:41341031 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:115856323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:115856323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:56148448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:56148448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:21451648 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:21451648 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:10729578 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:10729578 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:119535811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:119535811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:78887266 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:78887266 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:6616983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:6616983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:88679693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:88679693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:8641161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:8641161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:67291134 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:67291134 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:248099458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:248099458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:57957846 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:57957846 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:3803115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:3803115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:103298582 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:103298582 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:110344682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:110344682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:34661506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:34661506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:161980025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:161980025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:71502753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:71502753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:101983938 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:101983938 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:39975300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:39975300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:31725850 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:31725850 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:28266592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:28266592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:71933541 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:71933541 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:8741380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:8741380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:75676382 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:75676382 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:155467449 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:155467449 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:24753473 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:24753473 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:74331019 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:74331019 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:51800269 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:51800269 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:94708065 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:94708065 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:12920986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:12920986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:49032946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:49032946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:57257550 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:57257550 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:151487002 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:151487002 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:10390292 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:10390292 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:43679210 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:43679210 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:43527442 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:43527442 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:184024428 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:184024428 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:214576388 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:214576388 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:71158894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:71158894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:46736683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:46736683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:150079947 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:150079947 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135956612 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:135956612 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:79254793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:79254793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:79255222 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:79255222 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:79255402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:79255402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:103191754 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:103191754 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:17024251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:17024251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:73136188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:73136188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:25627383 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:25627383 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:42880127 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:42880127 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:96518690 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:96518690 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:5339752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:5339752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:87106024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:87106024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:87569616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:87569616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:7059209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:7059209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:11356109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:11356109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:68910070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:68910070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:113212623 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:113212623 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:172396314 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:172396314 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:187086402 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:187086402 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:34129203 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:34129203 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:243449735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:243449735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:177915689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:177915689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:156785512 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:156785512 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:84286808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:84286808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr20:44672118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr20:44672118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:36686112 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:36686112 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:107350426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:107350426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:118588052 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:118588052 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:48318327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:48318327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:76069437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:76069437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:158613237 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:158613237 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:64437112 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:64437112 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:133524895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:133524895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:38078428 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:38078428 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:48218338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:48218338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:52682430 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:52682430 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:74082518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:74082518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:81864818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:81864818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:31012517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:31012517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:75505735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:75505735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:113139413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:113139413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:29972699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:29972699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:64468491 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:64468491 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:34022389 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:34022389 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:2569755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:2569755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:79282168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:79282168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:10400916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:10400916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:50807859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:50807859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:43560194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:43560194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:165788711 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:165788711 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:103323537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:103323537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:193059330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:193059330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:125873314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:125873314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:125959302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:125959302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:129694578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:129694578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:62745023 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:62745023 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:15433713 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:15433713 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:129818490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:129818490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:54511289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:54511289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:29927123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:29927123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:19716379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:19716379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:76089666 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:76089666 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:18147925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:18147925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:42132946 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:42132946 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:72776996 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:72776996 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:120007907 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:120007907 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:189027931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:189027931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:170938408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:170938408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:36069063 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:36069063 A>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:84808875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:84808875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:75300681 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:75300681 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:87039756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:87039756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:6199417 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:6199417 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:95972522 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:95972522 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:10102710 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:10102710 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:67741158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chrX:67741158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:31791479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:31791479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:44101068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:44101068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:32873578 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:32873578 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:65051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:65051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:67358 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:67358 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:52633831 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:52633831 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:127011772 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:127011772 T>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:238048431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:238048431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:85149257 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr15:85149257 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:48396087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:48396087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:48734259 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:48734259 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:95727522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:95727522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:35634088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:35634088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:31676333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:31676333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:236906436 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:236906436 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:236906445 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:236906445 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:147855156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:147855156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:77984061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:77984061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:244006379 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:244006379 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:26620591 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:26620591 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:33391543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:33391543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:3028115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:3028115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:42474300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:42474300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:47118363 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:47118363 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:70227695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:70227695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11030639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11030639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11042994 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11042994 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11043891 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11043891 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11046418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11046418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11046911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11046911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11048509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:11048509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:72856980 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:72856980 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:73001917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:73001917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:34079867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:34079867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:32819843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:32819843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:140477739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:140477739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:81209333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:81209333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:247726865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:247726865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:34636318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:34636318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:9510544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:9510544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:23956424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:23956424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:27436172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:27436172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:93489583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:93489583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:120768587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:120768587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:57422711 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:57422711 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:140953511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:140953511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:81695887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:81695887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:188228027 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:188228027 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:93101847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:93101847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:2998223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:2998223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:85627343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:85627343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:32614717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:32614717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:68470997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:68470997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:74491051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:74491051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:7810116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:7810116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:51729383 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:51729383 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:227504936 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:227504936 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:21883731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:21883731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:44843314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:44843314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:18631448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:18631448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:45024465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:45024465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:100387151 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:100387151 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:55890526 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:55890526 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:143018393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:143018393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:31587488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:31587488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:10539296 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:10539296 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:87679505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:87679505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:224872687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:224872687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:17486953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:17486953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:51095388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:51095388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:103400557 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:103400557 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:139889973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:139889973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:74670575 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:74670575 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:107422443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:107422443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:125506586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:125506586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:159683209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:159683209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:151909134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:151909134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:37319242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:37319242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:143996674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:143996674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:96701515 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:96701515 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:60366602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:60366602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:65508616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:65508616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:85906204 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:85906204 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:85906210 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:85906210 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:50319209 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:50319209 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:6647085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:6647085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:126643099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:126643099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:30633123 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:30633123 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:39038462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:39038462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:96502844 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:96502844 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:11684546 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:11684546 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:11790373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:11790373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:169126490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:169126490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:116066788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:116066788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:28588511 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:28588511 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:325804 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:325804 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:57670676 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:57670676 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:102516550 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:102516550 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:131760397 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:131760397 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:67911566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:67911566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:13641859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:13641859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:37299161 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:37299161 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:129790500 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:129790500 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:185096295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:185096295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:60186676 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:60186676 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:72211809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:72211809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:139155210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:139155210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:179782861 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:179782861 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:29526829 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:29526829 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:62153760 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:62153760 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:137756722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:137756722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:110037826 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:110037826 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:240306914 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:240306914 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:240307249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:240307249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:216242738 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:216242738 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:159650818 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:159650818 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:27184975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:27184975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:16261169 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:16261169 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:173232985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:173232985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:120569843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:120569843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:16254988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:16254988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:132458592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:132458592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:10049097 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:10049097 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:14561793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:14561793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:108942952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:108942952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:156459916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:156459916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:18801911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:18801911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:50545730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:50545730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:30501153 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:30501153 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:21073987 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:21073987 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:26044200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:26044200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:18581011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:18581011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:206945576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:206945576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:207009976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:207009976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:31393053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:31393053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:35186419 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:35186419 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:124164920 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:124164920 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:163360881 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:163360881 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:196553117 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:196553117 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:36663726 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:36663726 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:42442348 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:42442348 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:57966310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:57966310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:55272036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:55272036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:55330200 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:55330200 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:52788707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:52788707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:138417021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:138417021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:43220688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:43220688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:35787140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:35787140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:55105821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:55105821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:51890698 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:51890698 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:90982214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:90982214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:141115515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:141115515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:101596964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:101596964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:77563361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:77563361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:56891273 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:56891273 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:27839404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:27839404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:140996708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:140996708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:75356119 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:75356119 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:165110848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:165110848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:48653922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:48653922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:116415239 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:116415239 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:10491269 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:10491269 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:89209555 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:89209555 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:20222514 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:20222514 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:62362133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:62362133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:149908041 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:149908041 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:23884538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:23884538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:26400945 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:26400945 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:76545529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:76545529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:1813025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:1813025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:41341941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:41341941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:21191364 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:21191364 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:26223438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:26223438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:47881041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:47881041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:71264675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:71264675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:124979588 T>A maps to ENST00000368416 C177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:124979588 T>A maps to ENST00000368416 C177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:142397239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:142397239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:103922041 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:103922041 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:120558251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:120558251 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:139232787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:139232787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:84744685 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:84744685 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:131550306 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:131550306 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:102512126 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:102512126 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:102512138 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:102512138 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:28171514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:28171514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:167646178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:167646178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:29394423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:29394423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:125562400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:125562400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:9523407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:9523407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:176811647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:176811647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:140189254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:140189254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:24690905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:24690905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:3147578 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:3147578 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:71825330 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:71825330 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:118495802 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:118495802 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:60996105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:60996105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:32017927 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:32017927 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:94320539 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:94320539 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:51798747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:51798747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:84569351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:84569351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:24766973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:24766973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:43259674 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:43259674 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:57328906 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:57328906 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:57499089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:57499089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:150867175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:150867175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43371375 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43371375 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43539893 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43539893 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43770581 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43770581 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:43609176 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:43609176 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:198668534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:198668534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:79255448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:79255448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:103123971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:103123971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:43617523 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:43617523 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:25632870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:25632870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:104672371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:104672371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:44030175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:44030175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:44989068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:44989068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:158015741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:158015741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:237446192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:237446192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:134978250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:134978250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:15882886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:15882886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:148795397 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:148795397 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:83601842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:83601842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:38760393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:38760393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:177906202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:177906202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:83636641 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:83636641 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:7239689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:7239689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:19251948 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:19251948 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:19818017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:19818017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:43405778 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:43405778 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:46214541 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:46214541 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:92949201 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:92949201 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:103029978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:103029978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:92352582 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:92352582 A>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:47162213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:47162213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:33591956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:33591956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:88367563 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:88367563 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:70129936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:70129936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:27596076 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:27596076 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:97197461 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:97197461 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:106675713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:106675713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:106960808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:106960808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:231363569 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:231363569 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:152944660 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:152944660 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:158626315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:158626315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:158637980 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:158637980 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:52674372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:52674372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:48045512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:48045512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:44988217 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:44988217 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:12187426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:12187426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:75313848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:75313848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:75991381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:75991381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:106116688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:106116688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:79279681 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:79279681 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:145887539 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:145887539 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:188349010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:188349010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:11418910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:11418910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:159174722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:159174722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:100274261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:100274261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:34854063 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:34854063 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:5359832 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:5359832 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:175521729 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:175521729 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:175644571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:175644571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:175676059 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:175676059 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:10973782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:10973782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:4406463 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:4406463 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:116454783 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:116454783 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:51599511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:51599511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:43212002 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:43212002 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:91252703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:91252703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:80749389 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:80749389 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:103331275 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:103331275 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:35954264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:35954264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:35542337 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:35542337 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:216260026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:216260026 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:144875802 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:144875802 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:82779262 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:82779262 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:158896408 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:158896408 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:76776239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:76776239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:15538417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:15538417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:30954382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:30954382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:78459049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:78459049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:167759884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:167759884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:75991302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:75991302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:74641833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:74641833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:147131356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:147131356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:70465444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chrX:70465444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:44619310 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:44619310 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:22270765 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:22270765 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:87914899 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr6:87914899 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:64395881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:64395881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:12386638 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:12386638 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:44752246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:44752246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:37917122 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:37917122 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:58322235 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:58322235 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:58337759 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:58337759 C>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:65590 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:65590 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:23938223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:23938223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:102182934 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:102182934 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:6992616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:6992616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:6992620 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:6992620 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:9033270 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:9033270 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:48218331 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:48218331 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:16302426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:16302426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:24157655 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:24157655 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:64628394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:64628394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:134212615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:134212615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:58531961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:58531961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:29519745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:29519745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:29520022 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:29520022 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:118074422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:118074422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:43601003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:43601003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:2109079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:2109079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr22:36653585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr22:36653585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:119943316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:119943316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:89997430 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:89997430 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr21:11064648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr21:11064648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr21:11074835 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr21:11074835 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:66296691 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:66296691 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:129173012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:129173012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:107886055 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:107886055 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:107916578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:107916578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:86055611 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:86055611 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:112665779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:112665779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:7249744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:7249744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:31676595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:31676595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:113554418 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:113554418 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:98480163 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:98480163 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:40656386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:40656386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:69374617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:69374617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:62751728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:62751728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:121708848 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:121708848 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:64973127 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:64973127 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:104900973 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:104900973 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:31571202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:31571202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:159854361 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:159854361 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:158301215 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:158301215 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:19473889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:19473889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:50830322 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:50830322 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:203185838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:203185838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr21:19331338 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr21:19331338 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:120147591 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:120147591 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:73769479 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:73769479 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:100129127 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:100129127 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:147938231 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:147938231 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:94041844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:94041844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:120105470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:120105470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:166325368 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:166325368 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:131337928 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:131337928 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:53567338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:53567338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:34427377 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:34427377 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:113276072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:113276072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:113363499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:113363499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:36447328 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:36447328 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:54656590 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:54656590 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:41519110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:41519110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109292651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109292651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:85087338 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:85087338 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:7697703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:7697703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:73675852 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:73675852 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:31452040 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:31452040 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:154375973 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:154375973 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:29121111 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:29121111 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:48385716 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:48385716 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:55238293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:55238293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:1213592 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:1213592 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:76929097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:76929097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:216944082 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:216944082 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:70284908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:70284908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:6185917 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:6185917 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:122121939 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:122121939 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:97957646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:97957646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:92120603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:92120603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:161692437 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:161692437 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:60718354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:60718354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:61119425 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:61119425 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:40059344 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:40059344 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:173657744 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:173657744 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:158366791 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:158366791 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:42465515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:42465515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:121769174 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:121769174 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:6604888 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:6604888 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:135455442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:135455442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:88388394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:88388394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:142965390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:142965390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:43351323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:43351323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:26273674 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:26273674 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:71025342 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:71025342 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:25641646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:25641646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:118730288 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:118730288 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:118851574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:118851574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:237316604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:237316604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:52824653 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:52824653 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:26748380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:26748380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:124149491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:124149491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:127702908 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:127702908 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:133381935 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:133381935 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:6911843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:6911843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:105521078 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:105521078 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:105521080 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:105521080 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:4918583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:4918583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:55544523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:55544523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:117064210 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:117064210 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr13:46716598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr13:46716598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:150444655 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:150444655 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:161007733 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:161007733 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:62168023 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:62168023 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:11824713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:11824713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:169995974 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:169995974 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:40637053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:40637053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:84182584 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:84182584 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:40660267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:40660267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:103673339 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:103673339 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:87028332 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:87028332 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:46429841 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:46429841 A>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:86323229 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:86323229 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:42861524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:42861524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:135185875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:135185875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:102457359 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:102457359 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:6710966 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:6710966 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:62365392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:62365392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:9027577 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:9027577 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:81112329 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:81112329 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:17308731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:17308731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:76732040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:76732040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:19650361 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:19650361 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:90995101 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:90995101 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:56510959 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:56510959 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:162184338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:162184338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:89162785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:89162785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:2940096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:2940096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:166712152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:166712152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:79006318 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:79006318 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:16729234 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:16729234 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:32195514 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:32195514 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:54837220 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:54837220 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:70190351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:70190351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:85712034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:85712034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:20364793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:20364793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:20415699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:20415699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:171362663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:171362663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:119367866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:119367866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:56989373 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:56989373 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:57266880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:57266880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:79380955 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:79380955 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:139215491 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:139215491 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:78834747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:78834747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:170821866 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:170821866 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:97307619 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:97307619 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:62017222 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:62017222 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:5183240 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:5183240 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:29639009 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:29639009 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:29771876 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:29771876 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:82752485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:82752485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:21997063 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:21997063 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:103404403 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:103404403 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:176012448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:176012448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:10501630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:10501630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:219445506 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:219445506 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:18291447 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:18291447 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:39422911 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:39422911 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:165950785 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:165950785 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:3426316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:3426316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:177969542 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:177969542 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:170169559 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:170169559 T>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:121621573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:121621573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:20619306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:20619306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:70406652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:70406652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:35038166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:35038166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:23805978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:23805978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:16032996 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:16032996 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:52946108 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr4:52946108 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:44174237 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:44174237 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:45616430 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:45616430 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109209759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109209759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr13:33751981 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr13:33751981 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:38256564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:38256564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:99608244 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:99608244 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:114841068 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr9:114841068 T>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:115455596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:115455596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:12173669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:12173669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:123781443 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:123781443 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:27849559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:27849559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:36356063 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:36356063 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:120973473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:120973473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:137534502 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:137534502 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:46990166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:46990166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:36066901 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:36066901 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:41759403 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:41759403 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:155149584 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chrX:155149584 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:78253725 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:78253725 G>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:114062454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:114062454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:45966409 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:45966409 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:72627695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:72627695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:12462769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:12462769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:123973646 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:123973646 T>C did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:71575082 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:71575082 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:22375804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:22375804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:43653141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:43653141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:66925423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:66925423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:87762153 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:87762153 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:84539715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:84539715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:123137356 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:123137356 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:100125327 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:100125327 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:67372797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:67372797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:26012818 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:26012818 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:87065971 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:87065971 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:50052696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:50052696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:129272692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:129272692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:134261846 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:134261846 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:137789995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:137789995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:38469435 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:38469435 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:104160473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:104160473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:5698895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:5698895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:101352868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:101352868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:40940039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:40940039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:144421429 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:144421429 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:43473995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:43473995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:32582784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:32582784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:155921419 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:155921419 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:111898473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:111898473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:70284861 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:70284861 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:177036702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:177036702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:119497181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:119497181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:123650943 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:123650943 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:85992334 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:85992334 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr21:11081297 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr21:11081297 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr21:11081307 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr21:11081307 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:102753975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:102753975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:34182745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:34182745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:45928365 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:45928365 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:112740210 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:112740210 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:73844654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:73844654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:126272291 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:126272291 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:99729009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:99729009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:151917798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:151917798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:181708192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:181708192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:201038377 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:201038377 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:55085888 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:55085888 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:86062822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:86062822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:228681921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:228681921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:34199359 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:34199359 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:61760955 G>T maps to ENST00000425507 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:61760955 G>T maps to ENST00000425507 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:61854757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:61854757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:26905930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:26905930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:43097500 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:43097500 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:17618882 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:17618882 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:122713857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:122713857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:29251994 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:29251994 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:120214776 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:120214776 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:74445431 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:74445431 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:139780042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:139780042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:57758639 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:57758639 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:6990107 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:6990107 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:88238980 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:88238980 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:41436290 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:41436290 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:74334748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:74334748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:147880867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:147880867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:125000025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:125000025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:106870996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:106870996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:101802743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:101802743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:94057500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:94057500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:139707043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:139707043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr21:47422371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr21:47422371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:131261682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:131261682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:9758689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:9758689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:211452941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:211452941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:125590393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:125590393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:28735774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:28735774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:3257092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:3257092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:25043761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:25043761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:148496482 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:148496482 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:105768117 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:105768117 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:90262461 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:90262461 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:35984346 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:35984346 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:117266458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:117266458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:14353594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:14353594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:11696812 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:11696812 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:172292455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:172292455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:29038272 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:29038272 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:4705492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:4705492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:25716036 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:25716036 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:42930008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:42930008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:140657118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:140657118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:51854720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:51854720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:76905571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:76905571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:5729243 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:5729243 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:65753506 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:65753506 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:66104667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:66104667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:139187541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:139187541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:15331089 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:15331089 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:135433136 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:135433136 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:179012884 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:179012884 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:40330628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:40330628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:102915436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:102915436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:60015626 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:60015626 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:58116291 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:58116291 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:52194797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:52194797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:12276035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:12276035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:47213260 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:47213260 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:26581330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:26581330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:109069518 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:109069518 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:111846712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:111846712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:102444221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:102444221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:175580429 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:175580429 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:32126857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:32126857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:176835413 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:176835413 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:22449197 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:22449197 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:87534205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:87534205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:88695981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:88695981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:240016681 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:240016681 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:73985885 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:73985885 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:42016974 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:42016974 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:29944499 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:29944499 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:36059378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:36059378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:22844853 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:22844853 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:124249155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:124249155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:185414479 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:185414479 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:117188926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:117188926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:113786662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:113786662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:29472453 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:29472453 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:29935734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:29935734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:120607778 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:120607778 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:128615245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:128615245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:30848602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:30848602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:15649499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:15649499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:7785097 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:7785097 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:26492256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:26492256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:124117371 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:124117371 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:178488998 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:178488998 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:142650430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:142650430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:114233786 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:114233786 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:24471288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:24471288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:108298113 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:108298113 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:173735541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:173735541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:7055979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:7055979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:90497581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:90497581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:156104970 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:156104970 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:82002233 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:82002233 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:78496206 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:78496206 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:21214933 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:21214933 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:48241648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:48241648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:94356766 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:94356766 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:126676044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:126676044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:28188268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:28188268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:168349198 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:168349198 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:102667962 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:102667962 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:76262570 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:76262570 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:237013865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:237013865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:77661807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:77661807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:10416883 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:10416883 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:26168280 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:26168280 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:72193499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:72193499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:48634239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:48634239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:13991250 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:13991250 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:20099034 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:20099034 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:36188728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:36188728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:16904448 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:16904448 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:158438168 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:158438168 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:84035363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:84035363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:204966248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:204966248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:77732641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:77732641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:63830987 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:63830987 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:169713331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:169713331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:100928837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:100928837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:102596525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:102596525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:76243173 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:76243173 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:80176218 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:80176218 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:87325896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:87325896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:133057853 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:133057853 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248138482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248138482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:58126570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:58126570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:76904573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:76904573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:17555340 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:17555340 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:35455828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:35455828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:67296794 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:67296794 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:290895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:290895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:165806001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:165806001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:178524775 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:178524775 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:66837970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:66837970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:144866542 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:144866542 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:76627405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:76627405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:31848203 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:31848203 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:58348251 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:58348251 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:85685739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:85685739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:65110437 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:65110437 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:142836316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:142836316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:94316458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:94316458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:81157417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:81157417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:51514061 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:51514061 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:9391818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:9391818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:95927479 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:95927479 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:131925725 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:131925725 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:57404488 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:57404488 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:169999059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:169999059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:24614788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:24614788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:8376866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:8376866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:44070746 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:44070746 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:17510851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:17510851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:82750818 T>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:82750818 T>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:73388762 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:73388762 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:76254797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:76254797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:150240954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:150240954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:34818994 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:34818994 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:109369413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:109369413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:29453094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:29453094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:192150408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:192150408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:40196974 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:40196974 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:182555969 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:182555969 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:63553343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:63553343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:78934011 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:78934011 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:92846454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:92846454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:83419509 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:83419509 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:4197385 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:4197385 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:33962576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:33962576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:33988395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:33988395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:55231117 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:55231117 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:35559121 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:35559121 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:166125284 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:166125284 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:52184303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:52184303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:167151250 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:167151250 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:110454961 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:110454961 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:44953885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:44953885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:95029771 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:95029771 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:52899846 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:52899846 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:70670211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:70670211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:70803431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:70803431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:124535205 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:124535205 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:113300169 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:113300169 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:43247993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr18:43247993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:35298233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:35298233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:160557014 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:160557014 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:131667364 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:131667364 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:71023483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:71023483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:46591667 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:46591667 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:1349413 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:1349413 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:130780050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:130780050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:24017224 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:24017224 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:24565123 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:24565123 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:52961110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:52961110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:55911011 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:55911011 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:158596607 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:158596607 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:158612346 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:158612346 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:158655167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:158655167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:99920695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:99920695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:48053731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chrX:48053731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:76774480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:76774480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:77074289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:77074289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:77510320 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:77510320 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:116637753 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:116637753 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:74080749 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:74080749 G>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:191898460 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:191898460 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:8513816 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:8513816 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:8513850 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:8513850 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:74477423 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:74477423 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:32591622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:32591622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:32591624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:32591624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:67925066 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:67925066 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:152631797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:152631797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:33545233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:33545233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:85409014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:85409014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:72312366 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:72312366 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:45821477 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:45821477 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:139565517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:139565517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:139565521 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:139565521 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:96178829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:96178829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:27169643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:27169643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:43777627 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:43777627 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:75446849 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:75446849 A>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:15405277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:15405277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:95691148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:95691148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:74874965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:74874965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:42398463 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:42398463 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:27151105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:27151105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:6472761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:6472761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:55035786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:55035786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:130363911 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:130363911 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179446578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179446578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179644621 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179644621 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:15542125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:15542125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:19484210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:19484210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:35965368 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:35965368 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:115585299 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:115585299 T>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:35588837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:35588837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:215931887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:215931887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:101197961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:101197961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:38857279 T>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:38857279 T>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:241904970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:241904970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:43496917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:43496917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:82373275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:82373275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:138713395 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:138713395 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:64425874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:64425874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:68358 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:68358 A>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:81564664 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:81564664 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:6497094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:6497094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:6920687 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:6920687 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:7388955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:7388955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:7441849 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:7441849 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125561191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125561191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:151452057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:151452057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:12776380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:12776380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:57239817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:57239817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:121763261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:121763261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:107643833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:107643833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:94545886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:94545886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67084303 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67084303 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67109922 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67109922 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67133424 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67133424 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:66988483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:66988483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:229657332 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:229657332 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169783460 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169783460 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169870030 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169870030 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169870100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169870100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87162112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87162112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87226481 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87226481 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74362046 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74362046 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:123434284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:123434284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:16161828 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:16161828 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:101553455 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:101553455 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:101571610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:101571610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:101611399 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:101611399 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:95723579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:95723579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:95724141 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:95724141 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17418607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17418607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:21997987 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:21997987 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89149161 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89149161 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44102562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44102562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100569679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100569679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100660497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100660497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100678774 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100678774 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:8079317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:8079317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:148586476 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:148586476 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:136137917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:136137917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:127398778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:127398778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35506664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35506664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35518988 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35518988 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35520717 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35520717 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35564823 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:35564823 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109614120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109614120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:128598333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:128598333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:195070549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:195070549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:180378591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:180378591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31366289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31366289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31438144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31438144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31460295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31460295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31593912 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31593912 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31779111 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31779111 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31831498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:31831498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32088566 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32088566 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32275199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32275199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:50471325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:50471325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15612861 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15612861 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76624645 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76624645 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125546224 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125546224 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:108924060 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:108924060 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:131313435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:131313435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:131324066 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:131324066 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20575839 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20575839 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20432564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20432564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:81579413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:81579413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18101139 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18101139 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:69429758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:69429758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:114684899 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:114684899 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52363985 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52363985 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:54401522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:54401522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:127763926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:127763926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:127806513 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:127806513 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:39494694 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:39494694 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:24357657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:24357657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:38961108 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:38961108 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33557731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33557731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33659969 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33659969 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33661942 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33661942 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33678843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33678843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:5242370 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:5242370 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:100802541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:100802541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:77465544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:77465544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:128983635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:128983635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:73188684 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:73188684 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:73275036 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:73275036 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:64452755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:64452755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:18486807 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:18486807 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:18528511 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:18528511 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:18680584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:18680584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:84637948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:84637948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:46591708 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:46591708 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:167791623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:167791623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7690797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7690797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7707972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7707972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:132022324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:132022324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:31124492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:31124492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:33549533 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:33549533 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:70847293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:70847293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:100203865 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:100203865 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:37214651 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:37214651 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203134369 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203134369 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:26705232 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:26705232 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:116146893 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:116146893 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147714612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147714612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147742058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147742058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147749601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147749601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147825719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147825719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147882229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147882229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147883300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147883300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148028726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148028726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148039688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148039688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:100454116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:100454116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:86801283 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:86801283 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:86875136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:86875136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:86915446 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:86915446 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87123734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87123734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87258527 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87258527 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87564380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87564380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49304769 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49304769 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49332701 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49332701 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49532639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49532639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49717160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:49717160 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:50031595 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:50031595 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:50307767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:50307767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230845572 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230845572 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35044961 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35044961 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:135750969 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:135750969 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:222867045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:222867045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:77985438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:77985438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:96953460 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:96953460 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:19813325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:19813325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:119048973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:119048973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:32911784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:32911784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134225908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134225908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134231708 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134231708 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134261935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134261935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134132817 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134132817 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137736396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137736396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:4873102 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:4873102 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:40771225 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:40771225 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:243946695 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:243946695 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:105262737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:105262737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:58257749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:58257749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:125850392 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:125850392 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110927880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110927880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110951802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110951802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29606489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29606489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29745231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29745231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29751156 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29751156 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29981422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29981422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30061486 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30061486 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30107767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30107767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30124112 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30124112 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:45936927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:45936927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:116835313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:116835313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:46450203 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:46450203 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:11318866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:11318866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:94534613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:94534613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:94535098 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:94535098 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:71389471 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:71389471 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:77270453 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:77270453 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:870667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:870667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:113970763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:113970763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:114238969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:114238969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:114252938 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:114252938 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:114257967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:114257967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61973135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61973135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:62039286 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:62039286 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:54559638 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:54559638 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:14767214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:14767214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:14809819 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:14809819 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113266733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113266733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:110475391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:110475391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:5919901 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:5919901 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:73942559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:73942559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:4222808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:4222808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:33108570 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:33108570 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:37414946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:37414946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:37447547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:37447547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:37506618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:37506618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:198051514 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:198051514 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:117880134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:117880134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:100100632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:100100632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:100234294 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:100234294 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99480022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99480022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99498988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99498988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:43428652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:43428652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5738832 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5738832 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5842067 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5842067 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5876090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5876090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5969295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5969295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26463846 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26463846 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26465274 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26465274 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26663423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26663423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101147639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101147639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101242233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101242233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101277946 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101277946 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45752950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45752950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45754296 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45754296 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:90347684 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:90347684 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:69252274 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:69252274 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:69468958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:69468958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:169049335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:169049335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40996509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40996509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:41001429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:41001429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:77321666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:77321666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:83360618 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:83360618 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:42020080 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:42020080 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99065529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99065529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:26759797 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:26759797 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:34922277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:34922277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:105583675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:105583675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:35152404 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:35152404 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:35165961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:35165961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:35166690 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:35166690 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:36135188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:36135188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:148802928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:148802928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:148958479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:148958479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:144473725 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:144473725 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119051104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119051104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:128948206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:128948206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:145830367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:145830367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:11308504 G>A maps to ENST00000380732 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:11308504 G>A maps to ENST00000380732 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:11315124 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:11315124 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120328719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120328719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42392152 G>A maps to NM_199002.1 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42392152 G>A maps to NM_199002.1 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:144076005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:144076005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135863100 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135863100 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:34622006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:34622006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100243501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100243501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:53503218 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:53503218 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:23320719 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:23320719 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:13329082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:13329082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:13341591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:13341591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:35730471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:35730471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69497147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69497147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:66786718 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:66786718 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:9472728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:9472728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95143492 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95143492 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176848357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176848357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176853628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176853628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176864007 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176864007 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176901536 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176901536 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176939225 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176939225 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176939640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176939640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176952550 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176952550 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177037245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177037245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119488437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119488437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119649990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119649990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119865779 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119865779 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:120062939 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:120062939 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:120170370 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:120170370 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:120176545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:120176545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:89527379 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:89527379 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176001187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176001187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161790825 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161790825 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:14629024 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:14629024 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112269126 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112269126 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107361948 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107361948 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10663549 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10663549 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10663552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10663552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:160042780 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:160042780 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138882415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138882415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138886867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138886867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160100118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160100118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160147209 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160147209 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:119510186 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:119510186 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36046324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36046324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:114309324 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:114309324 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:57037873 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:57037873 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:27099901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:27099901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40653194 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40653194 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77227268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77227268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:26112217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:26112217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:26153860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:26153860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:76872011 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:76872011 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:142170242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:142170242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:16399772 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:16399772 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:105505389 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:105505389 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:70107041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:70107041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:34158964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:34158964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:32957163 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:32957163 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69454540 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69454540 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69455837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:69455837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:63622194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:63622194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:168713747 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:168713747 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:71628066 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:71628066 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:47236785 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:47236785 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104197018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104197018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90781808 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90781808 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90809025 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90809025 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90845569 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90845569 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:69908775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:69908775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:70087810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:70087810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:97941390 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:97941390 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:134319563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:134319563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171494202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171494202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:33404384 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:33404384 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156615999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156615999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156627398 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156627398 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:58804519 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:58804519 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:58887691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:58887691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:59063627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:59063627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:60731921 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:60731921 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:60737232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:60737232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129146845 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129146845 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129162884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129162884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:96703406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:96703406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18221602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18221602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:101408746 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:101408746 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:78376478 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:78376478 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:60574817 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:60574817 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:51707518 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:51707518 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:32692567 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:32692567 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:96052781 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:96052781 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:203417613 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:203417613 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15564794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15564794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:16738329 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:16738329 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:16769547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:16769547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:36965662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:36965662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:140508806 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:140508806 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:28422528 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:28422528 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:66105606 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:66105606 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:36175014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:36175014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:116131769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:116131769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107755834 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107755834 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107761876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107761876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107782344 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107782344 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107790616 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107790616 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107833345 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107833345 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107938155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107938155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:92509963 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:92509963 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:77542851 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:77542851 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:77570223 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:77570223 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:77845871 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:77845871 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:33134973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:33134973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50255348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50255348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:103649263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:103649263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:128306651 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:128306651 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76197469 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76197469 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:4593624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:4593624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:33667226 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:33667226 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:6231905 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:6231905 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:71809095 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:71809095 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:36680754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:36680754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:103759986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:103759986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4629748 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4629748 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6811820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6811820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:97080383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:97080383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:57075666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:57075666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:80981523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:80981523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:91587192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:91587192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:76525231 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:76525231 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:100793355 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:100793355 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:103571470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:103571470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:37085423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:37085423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:13594425 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:13594425 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:31001809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:31001809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:15361730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:15361730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:15394124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:15394124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169654349 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169654349 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169801664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169801664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169385575 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169385575 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:231474050 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:231474050 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:179408901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:179408901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:179452371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:179452371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57221674 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57221674 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57224482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57224482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:75102278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:75102278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:109650805 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:109650805 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:184466788 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:184466788 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:54561086 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:54561086 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:60496015 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:60496015 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:34560505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:34560505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:20066231 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:20066231 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:20158270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:20158270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:31763134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:31763134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:46003086 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:46003086 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:33965215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:33965215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44599729 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44599729 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44893077 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44893077 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44981121 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:44981121 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:200802335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:200802335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:74803407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:74803407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:120097796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:120097796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:63665147 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:63665147 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:191013734 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:191013734 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119446826 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119446826 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:99868987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:99868987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:99895167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:99895167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:99896737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:99896737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:8766178 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:8766178 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:161065911 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:161065911 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:184866096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:184866096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:207300355 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:207300355 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:81849086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:81849086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:98515459 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:98515459 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:159969376 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:159969376 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:111100261 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:111100261 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:93708082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:93708082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:43042822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:43042822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:147281486 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:147281486 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41181976 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41181976 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41225881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41225881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:32291472 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:32291472 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:165722060 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:165722060 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:47989923 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:47989923 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:53995666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:53995666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:54115063 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:54115063 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133118322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133118322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:4087978 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:4087978 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:118986366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:118986366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:40788946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:40788946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:31747018 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:31747018 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120678263 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120678263 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120692598 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120692598 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120921532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120921532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:112521396 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:112521396 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:72518664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:72518664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135374724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135374724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:34415002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:34415002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5494395 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5494395 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:111820047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:111820047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:111856648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:111856648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71152153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71152153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:15906572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:15906572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:49916014 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:49916014 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50051526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50051526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50088815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50088815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50136919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50136919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:86207275 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:86207275 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150234528 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150234528 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2270282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2270282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2559113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2559113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2601298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2601298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2664747 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2664747 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2706312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2706312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2715584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2715584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2743572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2743572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2778400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2778400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:53633375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:53633375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:53695220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:53695220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181471247 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181471247 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181479055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181479055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181721515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181721515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181727256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:181727256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:201038391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:201038391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81985730 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81985730 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54484586 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54484586 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54629126 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54629126 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54804021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54804021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18822915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18822915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:37050289 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:37050289 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24366053 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24366053 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24372583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24372583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85303422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85303422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85309058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85309058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85709799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85709799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85801606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:85801606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:86063490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:86063490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:159151205 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:159151205 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:7341724 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:7341724 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:7374454 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:7374454 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54113366 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54113366 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46925905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46925905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:71499030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:71499030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:209775662 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:209775662 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:110593653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:110593653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6911427 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6911427 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179155688 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179155688 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30993163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:30993163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110490826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110490826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110497649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110497649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110512606 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110512606 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:75699432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:75699432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:78163504 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:78163504 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:104896878 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:104896878 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142989006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142989006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:104816277 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:104816277 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:104871292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:104871292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15834292 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15834292 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:54987700 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:54987700 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128446465 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128446465 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128455588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128455588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:24878390 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:24878390 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:96273930 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:96273930 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:96300045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:96300045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:180397268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:180397268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:113229206 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:113229206 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:111336646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:111336646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:529685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:529685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112346873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112346873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:28678679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:28678679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:118705498 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:118705498 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:6286793 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:6286793 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34417243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34417243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:50088817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:50088817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4408957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4408957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:159758092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:159758092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:35682040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:35682040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:7525911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:7525911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:66486116 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:66486116 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:66492260 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:66492260 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28943440 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28943440 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158224724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158224724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158325384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158325384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158325938 C>A maps to ENST00000434258 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158325938 C>A maps to ENST00000434258 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112058297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112058297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160808164 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160808164 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:72540715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:72540715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:208062438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:208062438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135728153 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135728153 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135741768 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135741768 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160681605 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160681605 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:111434103 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:111434103 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:111434202 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:111434202 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160523971 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160523971 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160549113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160549113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:121819381 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:121819381 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:111266911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:111266911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:2658655 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:2658655 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:54415613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:54415613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:3782491 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:3782491 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:21942555 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:21942555 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:65068859 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:65068859 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:21842442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:21842442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:22089288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:22089288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:22143127 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:22143127 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:22592920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:22592920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:82768466 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:82768466 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:82815221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:82815221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83066998 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83066998 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83373597 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83373597 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83600480 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83600480 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83601820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83601820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83798362 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:83798362 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:59170417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:59170417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44845304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44845304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44903952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44903952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:73193318 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:73193318 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:58562745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:58562745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:25570040 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:25570040 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:59951812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:59951812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:60005736 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:60005736 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:60089657 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:60089657 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:31316245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:31316245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26916050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26916050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26941620 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26941620 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90437814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90437814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90456378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90456378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90463857 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90463857 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90640115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:90640115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:202737161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:202737161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:47084198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:47084198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:50883004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:50883004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:50883051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:50883051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18662807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18662807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:21968295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:21968295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:5163640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:5163640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43097417 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43097417 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15807568 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15807568 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:151684115 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:151684115 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:35111822 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:35111822 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:104055615 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:104055615 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:104068941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:104068941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100401039 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100401039 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:95099681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:95099681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:13114265 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:13114265 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:34063668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:34063668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:138291769 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:138291769 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:182402975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:182402975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:196958233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:196958233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50863505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50863505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:132554374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:132554374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126464245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126464245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126503587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126503587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126598873 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126598873 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126645564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126645564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7797394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7797394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:40143379 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:40143379 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:384664 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:384664 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:384788 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:384788 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:431255 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:431255 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:87302705 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:87302705 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:29393177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:29393177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:102114047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:102114047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109963235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109963235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:62678648 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:62678648 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136578040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136578040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136597475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136597475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136623300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136623300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136651665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136651665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136670668 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:136670668 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:239590780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:239590780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:239595206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:239595206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:239868699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:239868699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:175622925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:175622925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:78858552 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:78858552 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:32360463 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:32360463 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:32365947 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:32365947 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:233409478 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:233409478 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:24608587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:24608587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:122166657 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:122166657 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:87021257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:87021257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:143016239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:143016239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:143043411 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:143043411 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10139557 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10139557 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10166218 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10166218 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49764795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49764795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:37919740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:37919740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7165757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7165757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8666294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8666294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8692085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8692085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8612996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8612996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154521490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154521490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36510058 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36510058 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36517247 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36517247 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29375544 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29375544 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:95676993 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:95676993 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:10522328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:10522328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:10542276 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:10542276 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:150661493 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:150661493 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:17524389 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:17524389 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:139697827 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:139697827 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:139862767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:139862767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:139924449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:139924449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:140122210 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:140122210 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:140165546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:140165546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:19220940 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:19220940 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:62213438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:62213438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:81618622 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:81618622 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:108684888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:108684888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:87670488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:87670488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:87670506 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:87670506 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:21544888 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:21544888 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:21568626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:21568626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:21591262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:21591262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:78666126 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:78666126 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:154251118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:154251118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:41383788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:41383788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100016661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100016661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100044200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100044200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100128137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100128137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100141998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100141998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100208267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100208267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100215899 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:100215899 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:1367351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:1367351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:1443274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:1443274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:145949724 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:145949724 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:147376604 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:147376604 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:147434471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:147434471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:147501689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:147501689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:39154048 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:39154048 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:76550691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:76550691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:76592331 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:76592331 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:124810044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:124810044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125021905 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125021905 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125105048 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125105048 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125141334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125141334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125142392 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125142392 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125276352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125276352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125340118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125340118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125460702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125460702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125470630 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125470630 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125470978 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125470978 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125501440 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125501440 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125528840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125528840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125530341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125530341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125620945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125620945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125623697 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125623697 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125641049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125641049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125655656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:125655656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:51092690 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:51092690 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230824388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230824388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107090583 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107090583 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:103343529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:103343529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:103491707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:103491707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33146839 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33146839 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:75800122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:75800122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:71697375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:71697375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:71716611 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:71716611 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101728634 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101728634 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:32148877 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:32148877 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:105809940 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:105809940 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:70897241 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:70897241 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:48281860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:48281860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:48281884 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:48281884 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:94043382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:94043382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:55925473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:55925473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:56031798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:56031798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139705967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139705967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:177665749 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:177665749 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:177672889 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:177672889 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109938328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109938328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110120594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110120594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:48372192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:48372192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:189851705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:189851705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:189867117 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:189867117 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:110865052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:110865052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:111026152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:111026152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107760788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107760788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107917677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107917677 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107938161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107938161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107938177 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107938177 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107938696 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107938696 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107417516 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107417516 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107442343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107442343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107471003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107471003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107471985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107471985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107509000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107509000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:130290614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:130290614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47765382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47765382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30199617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30199617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:69018152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:69018152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:4462499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:4462499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:46871592 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:46871592 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77155019 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77155019 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:130022143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:130022143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:93904938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:93904938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:166403610 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:166403610 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:175308317 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:175308317 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:131562013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:131562013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:131714019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:131714019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:39268100 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:39268100 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:211456786 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:211456786 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:211502641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:211502641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:8616234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:8616234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:207739292 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:207739292 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94266665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94266665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:197313646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:197313646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:197332706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:197332706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137567077 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137567077 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:28602052 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:28602052 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43849306 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43849306 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43893964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43893964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:36696409 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:36696409 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5859109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5859109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:17250763 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:17250763 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:86991233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:86991233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107415803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107415803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:209025468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:209025468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21305549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21305549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:115260764 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:115260764 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:115276831 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:115276831 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:19429518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:19429518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:2831873 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:2831873 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3047313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3047313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3177602 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3177602 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3293134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3293134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3377995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:3377995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:4368324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:4368324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:4645233 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:4645233 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:4715561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:4715561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34145913 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34145913 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34358534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34358534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34389594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34389594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34404996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34404996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34450003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34450003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34454444 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34454444 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34474324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:34474324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113569223 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113569223 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113725834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113725834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113727804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113727804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113882019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113882019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113933643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113933643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113935049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113935049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:114431623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:114431623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:68076868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:68076868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:23434023 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:23434023 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:126678347 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:126678347 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:67663239 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:67663239 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:79494921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:79494921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:79788509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:79788509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:79982892 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:79982892 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80217574 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80217574 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80302269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80302269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80323939 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80323939 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80333482 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80333482 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80361453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80361453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80608165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80608165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80686806 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80686806 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80812059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:80812059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:67726292 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:67726292 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:68040445 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:68040445 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:36450657 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:36450657 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11002388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11002388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11009692 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11009692 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11199785 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11199785 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11217553 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11217553 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11276534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11276534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11277949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11277949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11598257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11598257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11737718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11737718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11743703 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11743703 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11842044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:11842044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15764827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15764827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:25044273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:25044273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:117394266 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:117394266 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:16976652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:16976652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:16989130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:16989130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:16996134 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:16996134 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:111487328 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:111487328 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:64081302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:64081302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118675275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118675275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:105910589 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:105910589 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:36103707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:36103707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:36156594 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:36156594 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:61513309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:61513309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:51501053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:51501053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:96602529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:96602529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:41970491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:41970491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42010980 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42010980 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:47608040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:47608040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:16038213 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:16038213 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:15782722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:15782722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:15990136 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:15990136 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:187120037 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:187120037 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:47489374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:47489374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:65679288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:65679288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:48978938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:48978938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:6204488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:6204488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5016833 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5016833 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:59748547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:59748547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57476524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57476524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57526782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57526782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57536550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57536550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57857936 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57857936 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:58199501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:58199501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:58424573 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:58424573 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:39415705 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:39415705 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:86067836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:86067836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23043916 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23043916 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:61510956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:61510956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:106119296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:106119296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:10689799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:10689799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24587182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24587182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24588645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24588645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104455131 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104455131 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:172337379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:172337379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:168035032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:168035032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:27997189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:27997189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:55044628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:55044628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:155374482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:155374482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:115601365 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:115601365 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:95117825 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:95117825 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15960136 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:15960136 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134683486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134683486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:62500323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:62500323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:169195302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:169195302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:169206433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:169206433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:117925005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:117925005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:118095608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:118095608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:29993844 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:29993844 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11851646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11851646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:126304754 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:126304754 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:126322677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:126322677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:16177038 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:16177038 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:24758574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:24758574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:19112781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:19112781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14188952 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14188952 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14575819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14575819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14776482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14776482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14811363 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14811363 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14922237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:14922237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137097010 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137097010 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137271688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137271688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137442439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137442439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137445500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137445500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137472506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:137472506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:50165244 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:50165244 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24429017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24429017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24464147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24464147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:24541683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:24541683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:96319239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:96319239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:96634022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:96634022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:60635682 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:60635682 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153996927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153996927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154004884 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154004884 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38134217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38134217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:83525565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:83525565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:84379011 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:84379011 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:84731957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:84731957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:85118024 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:85118024 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:79626857 C>G maps to ENST00000372387 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:79626857 C>G maps to ENST00000372387 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:4176816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:4176816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:172950374 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:172950374 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31159960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31159960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31201074 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31201074 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31222431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31222431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31397152 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31397152 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31697744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31697744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31817010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31817010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31947413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:31947413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:32533497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:32533497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:32538849 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:32538849 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:33146312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:33146312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:46278329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:46278329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:991128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:991128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:124382671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:124382671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:21679076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:21679076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:21759819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:21759819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:52416608 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:52416608 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13811693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13811693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13845372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13845372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:38758296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:38758296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11640185 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11640185 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11644866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11644866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11672372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11672372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11687488 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11687488 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11819805 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11819805 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11819807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11819807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:33036538 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:33036538 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56217009 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56217009 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:65860521 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:65860521 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171875150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171875150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:172007639 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:172007639 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:31379385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:31379385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117639446 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117639446 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117701948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117701948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:128840847 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:128840847 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:129074635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:129074635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169335528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169335528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169445595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169445595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:111438883 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:111438883 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:111547502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:111547502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:111755433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:111755433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:325530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:325530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:67084494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:67084494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:67126444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:67126444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:118968926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:118968926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:101458157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:101458157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:115689084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:115689084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:115790980 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:115790980 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:116105598 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:116105598 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:116171639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:116171639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:116283729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:116283729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162902417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162902417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:153584823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:153584823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:153789296 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:153789296 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154172126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154172126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154172175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154172175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154242463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154242463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154266680 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154266680 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154371897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154371897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154375379 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154375379 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154619001 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154619001 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:109031276 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:109031276 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:64014965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:64014965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146780982 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146780982 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105393349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105393349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105464729 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105464729 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113287554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113287554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:113875065 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:113875065 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100509263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100509263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:28605690 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:28605690 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:42200958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:42200958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:116725069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:116725069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:45456913 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:45456913 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:12673022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:12673022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:167086460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:167086460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95616673 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95616673 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95686617 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95686617 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:103013847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:103013847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4700538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4700538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108329943 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108329943 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108392891 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108392891 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:15476048 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:15476048 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:158236645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:158236645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:158439748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:158439748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:183996159 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:183996159 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:95262813 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:95262813 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:139178313 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:139178313 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:65819741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:65819741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:68923350 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:68923350 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83479882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83479882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83525566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83525566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83542240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83542240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83549877 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:83549877 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:127934663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:127934663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:3736778 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:3736778 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:44209472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:44209472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:44062479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:44062479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:44062488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:44062488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:13624345 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:13624345 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:55107436 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:55107436 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:55234662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:55234662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110901366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110901366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110925816 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110925816 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34400234 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34400234 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:88892737 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:88892737 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:45316546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:45316546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:36521446 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:36521446 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24085945 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24085945 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:184035685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:184035685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:23736727 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:23736727 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:23776071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:23776071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:50595073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:50595073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129206479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129206479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:36934696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:36934696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:37052876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:37052876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:2909623 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:2909623 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:6924284 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:6924284 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:14757938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:14757938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:672784 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:672784 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43861289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43861289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43900673 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43900673 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43930299 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43930299 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129761812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129761812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:132552633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:132552633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5491194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5491194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5571953 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5571953 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5627939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5627939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:38185566 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:38185566 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:16474722 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:16474722 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:89462475 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:89462475 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66199883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66199883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66439634 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66439634 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66439645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66439645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:96846342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:96846342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:97064223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:97064223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:93965484 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:93965484 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134594411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134594411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134638790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134638790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134804668 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134804668 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134807932 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134807932 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134890319 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134890319 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43470754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:43470754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:212615489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:212615489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:213290880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:213290880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:55693534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:55693534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50725169 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50725169 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29496336 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29496336 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:39912160 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:39912160 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:39990641 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:39990641 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20865106 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20865106 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:62175663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:62175663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:217214362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:217214362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103498818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103498818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:11978545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:11978545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:12264149 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:12264149 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:36346502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:36346502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5742737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5742737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:133507509 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:133507509 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:133722169 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:133722169 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:72503299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:72503299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:72962078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:72962078 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:72181966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:72181966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:72229657 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:72229657 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:45617907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:45617907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:45633382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:45633382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:45811891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:45811891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133636821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133636821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133817553 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133817553 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:64587479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:64587479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:64983089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:64983089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:65096426 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:65096426 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169524261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169524261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169547044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169547044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154115830 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154115830 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154130236 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154130236 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:58589477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:58589477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:41714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:41714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:203560582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:203560582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:133906486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:133906486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:132241847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:132241847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:92960996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:92960996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139190691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139190691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139196896 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139196896 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139263360 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139263360 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139400070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:139400070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89972073 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89972073 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61012526 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61012526 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61030333 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61030333 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61115508 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:61115508 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:283053 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:283053 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:79834383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:79834383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:108105228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:108105228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:108339627 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:108339627 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11301400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11301400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:74095108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:74095108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:99045881 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:99045881 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29266512 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:29266512 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:119444599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:119444599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:91199558 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:91199558 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:92194933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:92194933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:92277972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:92277972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:68395348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:68395348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:68501852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:68501852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:62147535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:62147535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:68811717 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:68811717 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:88876744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:88876744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:10766308 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:10766308 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:10885976 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:10885976 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16794656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16794656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16818757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16818757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:114426198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:114426198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177214752 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177214752 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177223093 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177223093 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177232153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177232153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177242733 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177242733 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190223961 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190223961 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190370136 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190370136 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128365433 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128365433 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:124203854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:124203854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:54744459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:54744459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:54746727 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:54746727 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:33824396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:33824396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:9080238 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:9080238 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:89848996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:89848996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:5353248 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:5353248 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:5448295 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:5448295 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:223511717 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:223511717 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92143952 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92143952 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92384693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92384693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92384701 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92384701 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92396524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92396524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92530979 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92530979 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127670750 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127670750 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127680978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127680978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127710240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127710240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:102669028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:102669028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15552716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15552716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15552903 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15552903 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15596985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15596985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15628621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15628621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15664326 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15664326 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15693098 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15693098 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15725721 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15725721 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15789277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15789277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15821021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15821021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15847349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:15847349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:37515623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:37515623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:171408959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:171408959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:103431513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:103431513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161188843 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161188843 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161645598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161645598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161645851 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161645851 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161561219 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161561219 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:137776646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:137776646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157765807 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157765807 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157650606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157650606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157665030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157665030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157488179 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157488179 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157512393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:157512393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161692649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161692649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55222262 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55222262 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:124925229 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:124925229 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:125127589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:125127589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:108149488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:108149488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:108387795 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:108387795 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:44388351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:44388351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:137761107 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:137761107 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:137981473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:137981473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:137996186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:137996186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138152819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138152819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138219339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138219339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102521018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102521018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102810569 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102810569 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102826973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102826973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102853870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102853870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102922585 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102922585 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4543352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4543352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:38286870 G>T maps to ENST00000326296 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:38286870 G>T maps to ENST00000326296 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:59933751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:59933751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:60932278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:60932278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:61115165 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:61115165 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39974871 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39974871 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:33014217 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:33014217 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:108317568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:108317568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:60931672 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:60931672 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:142470561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:142470561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128495050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128495050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:50043861 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:50043861 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171234087 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171234087 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171172958 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:171172958 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203272657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203272657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147011975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:147011975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:22566232 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:22566232 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2981043 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2981043 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:114133012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:114133012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49109719 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49109719 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14746749 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14746749 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14779643 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14779643 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14824779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14824779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14859569 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14859569 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:13993573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:13993573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:14212023 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:14212023 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:14293453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:14293453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:44241533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:44241533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:52174734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:52174734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:131217353 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:131217353 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:131219861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:131219861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:37673500 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:37673500 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12277197 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12277197 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12296362 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12296362 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12308716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12308716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12712638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12712638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12738577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:12738577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30255430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30255430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:49293796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:49293796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:49295666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:49295666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:78432680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:78432680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:39149564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:39149564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153761371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153761371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153950176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153950176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101134182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101134182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:46305408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:46305408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151420158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151420158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151489000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151489000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151495710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151495710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151536590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151536590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151560553 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151560553 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47150893 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47150893 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47364304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47364304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:160757727 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:160757727 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:26828475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:26828475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:26952898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:26952898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:26998205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:26998205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151128295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151128295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:27573907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:27573907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151815233 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151815233 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:26513075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:26513075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49173870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49173870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:859181 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:859181 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:88361204 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:88361204 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:88421294 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:88421294 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101602508 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101602508 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:154769967 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:154769967 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:154865659 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:154865659 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31151388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31151388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31160550 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31160550 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31219302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31219302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:174239521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:174239521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:16168501 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:16168501 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:173508882 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:173508882 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:173779580 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:173779580 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:22827407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:22827407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:89660906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:89660906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163210119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163210119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:27745527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:27745527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120569256 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120569256 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120576452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120576452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:34041655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:34041655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:58007619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:58007619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34923459 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34923459 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:24615891 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:24615891 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:42453770 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:42453770 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:42468168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:42468168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:42653004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:42653004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150402904 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150402904 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150210323 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150210323 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:78548266 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:78548266 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:110390544 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:110390544 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:147236221 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:147236221 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:30712696 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:30712696 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100662592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100662592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:134147135 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:134147135 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:6540208 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:6540208 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:6589357 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:6589357 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:42152996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:42152996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:42153643 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:42153643 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:38653290 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:38653290 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39053331 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39053331 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102967357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102967357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56873057 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56873057 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:58606968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:58606968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:58607110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:58607110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220368605 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220368605 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220369569 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220369569 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220369660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220369660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:52433535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:52433535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:93350057 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:93350057 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:167728495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:167728495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:42513778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:42513778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:133033482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:133033482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:132438656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:132438656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:92182497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:92182497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:93518775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:93518775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:94186389 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:94186389 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:94726954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:94726954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63784347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63784347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:67510284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:67510284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135439690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:135439690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:22437113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:22437113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:22446766 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:22446766 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100374653 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:100374653 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:59897829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:59897829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20058628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:20058628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6311385 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6311385 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:25509870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:25509870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19013208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19013208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19028653 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19028653 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19063150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19063150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:40335220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:40335220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:11706501 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:11706501 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:10130809 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:10130809 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:24666012 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:24666012 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:153108415 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:153108415 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122492630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122492630 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122536999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122536999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:105836799 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:105836799 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87501396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87501396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87648463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87648463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87845157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87845157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87848265 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87848265 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87851595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:87851595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94137748 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94137748 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94247339 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94247339 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94446450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94446450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94615368 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:94615368 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:102276434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:102276434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:37298807 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:37298807 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:37397791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:37397791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120429024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120429024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120541278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120541278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13792234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13792234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13912999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13912999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:14013683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:14013683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:104385543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:104385543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:104498105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:104498105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48837589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48837589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:86442865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:86442865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88319766 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88319766 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88650988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88650988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:7611033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:7611033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:126547131 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:126547131 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:126645620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:126645620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:126793322 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:126793322 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:52616601 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:52616601 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:52764716 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:52764716 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:52858909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:52858909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:46724472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:46724472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42165652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42165652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:2748286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:2748286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:144961217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:144961217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152734593 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152734593 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5291159 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5291159 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:139715730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:139715730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45307300 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45307300 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45312809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45312809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45353851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45353851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45386400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45386400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45497391 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45497391 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45498182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:45498182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:48183456 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:48183456 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71766410 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71766410 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:18467245 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:18467245 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:18814393 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:18814393 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:18904920 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:18904920 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:83695396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:83695396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:73965077 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:73965077 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41012910 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41012910 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:197081908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:197081908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:197297729 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:197297729 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:124739621 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:124739621 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:65163942 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:65163942 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93837943 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93837943 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:28408159 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:28408159 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:28441169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:28441169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:69748292 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:69748292 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:193854615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:193854615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:120388388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:120388388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81350206 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81350206 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81366692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81366692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81386721 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81386721 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108096081 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108096081 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:191105884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:191105884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:62188848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:62188848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:75191315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:75191315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:114505837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:114505837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26282795 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26282795 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149858234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149858234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149858523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149858523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:42302738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:42302738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:71129169 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:71129169 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:70987149 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:70987149 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33063856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33063856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:148777615 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:148777615 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:185749697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:185749697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:185813030 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:185813030 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:186120568 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:186120568 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:66311520 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:66311520 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:173500689 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:173500689 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:173502653 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:173502653 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:173531368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:173531368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:83550449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:83550449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46636872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46636872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46640798 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46640798 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54401820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54401820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54405528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54405528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:133627708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:133627708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:100182428 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:100182428 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:100471828 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:100471828 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:100531300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:100531300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:6462288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:6462288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:25838357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:25838357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:25879680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:25879680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:26139027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:26139027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:114470770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:114470770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:96796081 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:96796081 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:96886934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:96886934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:209873306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:209873306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148802184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148802184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148839960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:148839960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113802089 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113802089 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:92502208 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:92502208 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:92523258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:92523258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:33326480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:33326480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:53589943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:53589943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:70943853 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:70943853 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:8253092 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:8253092 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:25672098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:25672098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:129200818 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:129200818 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:99288380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:99288380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:102813206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:102813206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:45956786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:45956786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:151162650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:151162650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:130413339 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:130413339 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:130455813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:130455813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:130532152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:130532152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18525381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18525381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18564064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18564064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18632402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:18632402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117883867 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117883867 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:142640523 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:142640523 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:113788843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:113788843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:102794102 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:102794102 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:28658309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:28658309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:29417484 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:29417484 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103882480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103882480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104026758 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104026758 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104274649 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104274649 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104478348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104478348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104651435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104651435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104761918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104761918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104761937 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104761937 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104772714 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104772714 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104857247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104857247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104893988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104893988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104950037 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:104950037 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:190251172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:190251172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:55159377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:55159377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:74670283 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:74670283 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:155232743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:155232743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110555309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110555309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110903734 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110903734 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:41735818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:41735818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30016794 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30016794 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:142990442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:142990442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:143008481 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:143008481 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:143066849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:143066849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:143709963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:143709963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:234076242 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:234076242 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:118859663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:118859663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:118861024 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:118861024 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:7132340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:7132340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:153723551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:153723551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:95839415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:95839415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:49765501 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:49765501 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:237317565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:237317565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:51884121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:51884121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:75932744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:75932744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:75973187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:75973187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156501196 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156501196 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156513046 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156513046 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156533300 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156533300 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:280206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:280206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153284804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153284804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:74424810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:74424810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:16158683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:16158683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145538812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145538812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:68698722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:68698722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:182350602 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:182350602 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:182390081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:182390081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56082566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56082566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:31384823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:31384823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70524765 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70524765 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53589336 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53589336 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20420460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20420460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20431150 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20431150 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20438416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20438416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54819310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54819310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7619006 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7619006 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:26664284 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:26664284 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:26797214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:26797214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33653825 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33653825 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:24557613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:24557613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:40702823 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:40702823 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:65323510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:65323510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6042552 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6042552 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39703622 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39703622 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123834413 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123834413 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123938364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123938364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123962560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123962560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123978853 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:123978853 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:124046704 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:124046704 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:124197278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:124197278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:62747121 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:62747121 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:62756858 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:62756858 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:44595746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:44595746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:85262309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:85262309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6145211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6145211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:73817043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:73817043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120006390 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120006390 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120377222 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:120377222 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:112436569 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:112436569 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210957202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210957202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210995516 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210995516 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:211171343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:211171343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150646203 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150646203 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63226117 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63226117 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63229079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63229079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:61611230 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:61611230 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163253231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163253231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163257146 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163257146 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163309489 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:163309489 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:19432257 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:19432257 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169931700 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169931700 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:170103269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:170103269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:20783569 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:20783569 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:20870957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:20870957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:21014940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:21014940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:21263433 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:21263433 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:39010030 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:39010030 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:21919616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:21919616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39282623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39282623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:215328002 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:215328002 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:215332511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:215332511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:140631447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:140631447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:79271156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:79271156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:178386964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:178386964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:178388809 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:178388809 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:178976720 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:178976720 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:41283726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:41283726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:73759979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:73759979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:196531188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:196531188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:36664778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:36664778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:143818764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:143818764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:103441632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:103441632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:7094490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:7094490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142639317 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142639317 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:62770195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:62770195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:27315014 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:27315014 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:141309688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:141309688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:71961472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:71961472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:46263280 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:46263280 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:46284077 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:46284077 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:5457979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:5457979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:84859506 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:84859506 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:34961295 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:34961295 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118220332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118220332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:24375160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:24375160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:86509993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:86509993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:93877559 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:93877559 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94079503 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94079503 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108284110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108284110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:138620436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:138620436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:44676666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:44676666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:233489728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:233489728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:73971598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:73971598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74137419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74137419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:39756765 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:39756765 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200952024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200952024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200993782 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200993782 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:86495427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:86495427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39328382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39328382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39411979 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:39411979 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:90188558 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:90188558 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7821016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7821016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55361984 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55361984 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55362007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55362007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36355655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36355655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126597777 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126597777 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126615967 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126615967 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158024971 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158024971 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158026813 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158026813 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:74479513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:74479513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126062785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126062785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:70456659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:70456659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:20805833 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:20805833 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:135020333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:135020333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53068774 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53068774 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39616153 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39616153 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53185453 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53185453 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52842879 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52842879 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52865660 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52865660 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52681595 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52681595 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:46011198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:46011198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:1651838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:1651838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:118021461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:118021461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:56118534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:56118534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:56134080 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:56134080 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:56138198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:56138198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134338143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:134338143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:41601246 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:41601246 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54867941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54867941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:6982614 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:6982614 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:7038531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:7038531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107684182 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107684182 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183181584 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183181584 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183186971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183186971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:119576889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:119576889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:64743930 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:64743930 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169362618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169362618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152538914 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152538914 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:25143619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:25143619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169724458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:169724458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:16512022 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:16512022 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:16587649 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:16587649 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109037535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109037535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33748821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33748821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:65971061 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:65971061 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:25007833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:25007833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:202204705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:202204705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111920122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111920122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104171816 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104171816 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104308261 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104308261 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104457344 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104457344 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54804265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54804265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55178382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55178382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55179315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55179315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:41404227 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:41404227 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:41469571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:41469571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:41691714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:41691714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128436462 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128436462 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:28291997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:28291997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:58805847 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:58805847 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:58812787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:58812787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:11647368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:11647368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:49005403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:49005403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:165192716 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:165192716 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:147966802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:147966802 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118116993 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118116993 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:160958712 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:160958712 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:81820212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:81820212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62445165 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62445165 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62641233 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62641233 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62641247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62641247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62812488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62812488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62873387 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62873387 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62894559 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:62894559 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:104048197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:104048197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:187998452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:187998452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:47279600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:47279600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:40530109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:40530109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36430219 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36430219 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:42345837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:42345837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:85994139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:85994139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:86000936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:86000936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141278850 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141278850 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141732747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141732747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141757836 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141757836 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141819871 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141819871 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141986698 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:141986698 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:142003427 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:142003427 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:170031642 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:170031642 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:170062156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:170062156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25344338 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25344338 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25460755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25460755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:26729887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:26729887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:40172505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:40172505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:40373734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:40373734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:40612817 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:40612817 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41070551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41070551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41304950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41304950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41418742 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41418742 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41450647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:41450647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70239412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70239412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70429783 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70429783 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:90128786 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:90128786 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:90369886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:90369886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:86042393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:86042393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:76998030 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:76998030 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:77598547 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:77598547 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115557123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115557123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115687979 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115687979 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115743041 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115743041 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115912591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:115912591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116001335 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116001335 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116002718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116002718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116007123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116007123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116163899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:116163899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:194383238 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:194383238 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31766221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31766221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:32528840 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:32528840 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:33572687 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:33572687 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:25030048 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:25030048 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:150237671 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:150237671 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:54978404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:54978404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:235878331 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:235878331 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:14606173 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:14606173 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:14957108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:14957108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:15240570 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:15240570 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:2078096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:2078096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151899835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151899835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151870279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:151870279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:51611412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:51611412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54837132 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54837132 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:77824077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:77824077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:78755083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:78755083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:114137053 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:114137053 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77126191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77126191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77134661 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:77134661 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:35804103 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:35804103 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:10782700 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:10782700 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:95817842 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:95817842 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149628275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149628275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:71482673 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:71482673 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:172945152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:172945152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:66773581 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:66773581 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67452856 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67452856 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67484336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67484336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67501725 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:67501725 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:185047085 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:185047085 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:56160464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:56160464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:61768925 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:61768925 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:64557475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:64557475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:206905120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:206905120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:16095726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:16095726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:16178021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:16178021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164449807 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164449807 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164458006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164458006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164534584 G>A maps to NM_017923.3 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164534584 G>A maps to NM_017923.3 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164852479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164852479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:220804250 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:220804250 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:63670794 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:63670794 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:186947811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:186947811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:186990520 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:186990520 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:187003887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:187003887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:82043560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:82043560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:97893161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:97893161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:20191746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:20191746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:20207112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:20207112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:84089845 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:84089845 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:13918291 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:13918291 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:182769855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:182769855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138735662 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:138735662 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:94289136 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:94289136 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:94903133 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:94903133 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47572431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47572431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47627910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47627910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47693719 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47693719 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47994457 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:47994457 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:48000814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:48000814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:48035912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:48035912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:48079329 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:48079329 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90457210 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:90457210 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169304453 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169304453 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:150819923 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:150819923 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:150881911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:150881911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:151131110 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:151131110 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70341092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70341092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70353111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70353111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:17616472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:17616472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:66458270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:66458270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:66491103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:66491103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:42177404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:42177404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:36597177 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:36597177 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:88759976 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:88759976 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:112725608 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:112725608 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:28179446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:28179446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56077938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56077938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:116372727 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:116372727 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8808316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:8808316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:40432948 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:40432948 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141725063 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141725063 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141775885 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141775885 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141782957 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141782957 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10829014 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:10829014 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107152672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107152672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:328042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:328042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:89296518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:89296518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:37832875 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:37832875 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:69983368 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:69983368 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:129908546 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:129908546 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:47042393 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:47042393 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:22006821 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:22006821 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:89261923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:89261923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:89285425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:89285425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:89324144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:89324144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102667238 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102667238 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102465521 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102465521 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102487413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102487413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102709159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102709159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102709770 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102709770 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102713390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102713390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102584380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:102584380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158813530 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158813530 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:56757334 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:56757334 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108710531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108710531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108751674 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108751674 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108818417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108818417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:106228601 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:106228601 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:220974931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:220974931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:13125614 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:13125614 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154020333 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154020333 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:202541738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:202541738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30410205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30410205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30561880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30561880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:60167843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:60167843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:59830232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:59830232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:47818185 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:47818185 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:55583563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:55583563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9948344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9948344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9958037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9958037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154294389 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154294389 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:135215526 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:135215526 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:151358402 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:151358402 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149764346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149764346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149767269 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149767269 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149775055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149775055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:9711260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:9711260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149877188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:149877188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:63616862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:63616862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7893137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7893137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7899048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:7899048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:29665970 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:29665970 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:29881343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:29881343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:29970103 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:29970103 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9015876 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9015876 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9024029 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9024029 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100696129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100696129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:195453533 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:195453533 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:4442370 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:4442370 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:67525020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:67525020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42331063 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42331063 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:48608813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:48608813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:15865158 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:15865158 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108160129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108160129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108183705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108183705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108211571 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:108211571 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23857154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23857154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23885063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23885063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23886621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23886621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23899881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:23899881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:211163080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:211163080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:111353394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:111353394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:109777410 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:109777410 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:109825486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:109825486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:57441513 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:57441513 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:192231500 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:192231500 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:171230625 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:171230625 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:52632271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:52632271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17743078 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17743078 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:95150190 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:95150190 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:24394881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:24394881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:120094539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:120094539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:39917378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:39917378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1890416 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1890416 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1891527 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1891527 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:2336219 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:2336219 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:89903352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:89903352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:71184604 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:71184604 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:71302929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:71302929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:101763590 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:101763590 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:101844187 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:101844187 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102011155 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:102011155 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:92928305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:92928305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:80438943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:80438943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55287670 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55287670 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:78417099 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:78417099 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:78479542 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:78479542 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:15560630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:15560630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:15700033 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:15700033 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:35998928 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:35998928 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:16907234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:16907234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:16913158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:16913158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:102726107 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:102726107 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:112890061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:112890061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113076155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113076155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54912552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54912552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54912555 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54912555 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54915040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54915040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:133652505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:133652505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:46268214 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:46268214 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:16029571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:16029571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:43833141 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:43833141 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:149895376 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:149895376 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:119115789 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:119115789 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:115838902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:115838902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:115997855 C>A maps to NM_022569.1 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:115997855 C>A maps to NM_022569.1 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:124910682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:124910682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4791497 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4791497 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152520920 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152520920 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152522930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152522930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152576799 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152576799 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:56036958 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:56036958 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:11227896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:11227896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:11238180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:11238180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:27233412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:27233412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:27279496 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:27279496 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:130889804 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:130889804 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20757994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20757994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:21422288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:21422288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:44951164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:44951164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45054186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45054186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45072543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45072543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45072792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45072792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45073001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45073001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45291177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:45291177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:70425711 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:70425711 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204814264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204814264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204953161 G>A maps to ENST00000367172 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204953161 G>A maps to ENST00000367172 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:50164288 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:50164288 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:61857767 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:61857767 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47853838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:47853838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:233834905 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:233834905 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25781054 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25781054 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17624937 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17624937 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17689834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17689834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17704904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17704904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17715172 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:17715172 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:236156730 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:236156730 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:52527136 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:52527136 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:63229159 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:63229159 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:63715873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:63715873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:173280773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:173280773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:173399089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:173399089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:5934821 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:5934821 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:6023309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:6023309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:57113415 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:57113415 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54301320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54301320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55492979 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55492979 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:247607261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:247607261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56379304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56379304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56390125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56390125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56552468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56552468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169169836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169169836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:151774922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:151774922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:43628499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:43628499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:43666813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:43666813 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:18562583 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:18562583 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:117705983 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:117705983 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:117749483 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:117749483 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26098071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26098071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26115621 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26115621 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26143921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26143921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169713351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169713351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:120505535 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:120505535 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:46475644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:46475644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:155721956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:155721956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:89293366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:89293366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34134381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34134381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34134586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34134586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34247819 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:34247819 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:21127807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:21127807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36333184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36333184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:182778212 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:182778212 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:182783995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:182783995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:32758833 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:32758833 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:32762042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:32762042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:32774762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:32774762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:34818042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:34818042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:100923147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:100923147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:115423526 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:115423526 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107825063 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107825063 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:83658164 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:83658164 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84219007 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84219007 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84267235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84267235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84399060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84399060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84462707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:84462707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2940242 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:2940242 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:105088019 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:105088019 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:50731521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:50731521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:51001025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:51001025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78641071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78641071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78701556 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78701556 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78844496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78844496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78945893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78945893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79013590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79013590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79065035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79065035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79110863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79110863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79158098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79158098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79189822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79189822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79274892 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79274892 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79276708 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79276708 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79359245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79359245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:80316082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:80316082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:80318073 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:80318073 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152031426 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:152031426 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:126179324 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:126179324 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:93794824 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:93794824 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:72722404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:72722404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18885333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18885333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:18768073 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:18768073 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:116506750 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:116506750 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5589056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5589056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131260546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131260546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131264628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131264628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131465772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131465772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131593379 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:131593379 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:132104221 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:132104221 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:107761409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:107761409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:107851589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:107851589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:108003040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:108003040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:87446582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:87446582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88533305 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88533305 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88600979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88600979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88679617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88679617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88792253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88792253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:10863033 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:10863033 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:44525473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:44525473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:163292090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:163292090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:13381836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:13381836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:106415551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:106415551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102339092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:102339092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:101095096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:101095096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:8578789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:8578789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:228437431 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:228437431 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133062303 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133062303 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:123597696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:123597696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:166712161 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:166712161 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:166915079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:166915079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167377222 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167377222 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167416760 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167416760 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167553738 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167553738 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167673614 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167673614 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:183112445 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:183112445 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:78369904 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:78369904 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:78402950 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:78402950 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:78712454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:78712454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:79003103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:79003103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70777183 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70777183 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161976080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161976080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:133392245 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:133392245 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:67537418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:67537418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153418610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153418610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:47791164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:47791164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:47793884 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:47793884 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29430729 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29430729 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248099392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248099392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248166364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248166364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248166366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248166366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248459020 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248459020 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248437311 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248437311 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22317852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22317852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22323770 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22323770 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22325351 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22325351 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22332625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22332625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22345537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22345537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22371610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22371610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22371655 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:22371655 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5375408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5375408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:4702687 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:4702687 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:201791390 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:201791390 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:76882856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:76882856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:52183203 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:52183203 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:77746654 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:77746654 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:32048160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:32048160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29597286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29597286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29624995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29624995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29640195 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29640195 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:107382352 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:107382352 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121605500 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121605500 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:20706532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:20706532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:163250821 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:163250821 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:163382515 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:163382515 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:34499333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:34499333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:17585919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:17585919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26298274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26298274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49456124 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49456124 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:103243770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:103243770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110202716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110202716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110214288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110214288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110226377 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110226377 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110226556 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110226556 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110245648 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110245648 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110251646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110251646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110295479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110295479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110296355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110296355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110313408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110313408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110366609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110366609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110437459 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:110437459 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9633440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9633440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9785005 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9785005 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:35462915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:35462915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56719269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56719269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93886945 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93886945 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:73733363 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:73733363 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:97002133 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:97002133 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176449938 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176449938 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176524941 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176524941 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176790613 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176790613 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:118979209 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:118979209 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:118998046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:118998046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119094058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:119094058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:205473623 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:205473623 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:205904798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:205904798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:206462562 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:206462562 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:34821385 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:34821385 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:162628562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:162628562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:162844441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:162844441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:139726278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:139726278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20824712 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20824712 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:150770144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:150770144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:102526345 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:102526345 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:102546499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:102546499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:102558148 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:102558148 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:70052057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:70052057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:164815007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:164815007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:91368384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:91368384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:55890549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:55890549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:55955662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:55955662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56138713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56138713 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56215500 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56215500 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56885406 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56885406 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56890007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:56890007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99605491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99605491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99632480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99632480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:30847910 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:30847910 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:30912484 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:30912484 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67591107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67591107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67751641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67751641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140201325 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140201325 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140501562 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140501562 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:36895192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:36895192 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:82748267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:82748267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:233359011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:233359011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:142537010 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:142537010 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:142539666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:142539666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100199975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100199975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:95759236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:95759236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24609798 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24609798 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24664348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24664348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5563101 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5563101 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:56448478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:56448478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:165807362 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:165807362 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:165870072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:165870072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:178544900 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:178544900 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:178769977 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:178769977 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54948754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:54948754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:72290461 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:72290461 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:14803501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:14803501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66289029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66289029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66346581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66346581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144865688 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144865688 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144879652 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144879652 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145024188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145024188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145034627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145034627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:58648418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:58648418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:59040431 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:59040431 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:59616956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:59616956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:149284812 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:149284812 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:76516733 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:76516733 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:44188982 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:44188982 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:103857489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:103857489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:122868726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:122868726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176924622 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176924622 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:31725589 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:31725589 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:31891702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:31891702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21996010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21996010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:41953078 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:41953078 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:179561108 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:179561108 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:179657906 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:179657906 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54972819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:54972819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:48509865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:48509865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230459517 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230459517 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230468428 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:230468428 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:97746489 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:97746489 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:12757457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:12757457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9074169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9074169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9082878 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9082878 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:22129320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:22129320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:22146406 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:22146406 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:22186303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:22186303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133849870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133849870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71873385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71873385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18944447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18944447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:118485237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:118485237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:151278898 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:151278898 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:85675630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:85675630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35093777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35093777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:111942084 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:111942084 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204394881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204394881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:18489401 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:18489401 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:18800727 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:18800727 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:39629594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:39629594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:8714342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:8714342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71409828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71409828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71463674 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:71463674 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142836420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142836420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:51550649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:51550649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:51670861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:51670861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125202289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125202289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125298877 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125298877 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:159405379 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:159405379 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:159497027 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:159497027 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119343811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119343811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160840670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160840670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:144364796 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:144364796 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:44161168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:44161168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:44169316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:44169316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:8189111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:8189111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:8436465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:8436465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9166481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9166481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9284865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9284865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9424526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:9424526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:95897448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:95897448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:96012740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:96012740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:39791045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:39791045 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:198990591 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:198990591 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41318564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41318564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41383192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:41383192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:18846019 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:18846019 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:40863851 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:40863851 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:16892602 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:16892602 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:131935960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:131935960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150130955 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150130955 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68608100 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68608100 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68608146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68608146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68610777 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68610777 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68622715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68622715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68623006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:68623006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:21209766 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:21209766 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49028244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:49028244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126733988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:126733988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:208310543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:208310543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153691597 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153691597 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:132053145 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:132053145 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:132075907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:132075907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94585777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94585777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94589137 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94589137 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:50369630 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:50369630 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:118215229 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:118215229 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:84617978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:84617978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24759679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24759679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24948462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:24948462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:133241173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:133241173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119373495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:119373495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120131112 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:120131112 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:39411054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:39411054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:122288183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:122288183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:12369710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:12369710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18797362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18797362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203043276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203043276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:27803203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:27803203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:42681186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:42681186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160560096 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160560096 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160598626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160598626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160631259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160631259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160714060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160714060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160747067 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:160747067 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52709087 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52709087 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52712021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52712021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146030290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146030290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146053335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146053335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146071440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146071440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146146796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146146796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146184010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146184010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146431114 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:146431114 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6330936 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6330936 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6377356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6377356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94665972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94665972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:74538503 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:74538503 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:23523167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:23523167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:23524339 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:23524339 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203455828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:203455828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:105736528 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:105736528 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47268149 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47268149 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47270133 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47270133 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47309362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47309362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47346133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47346133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:69002966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:69002966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:69095551 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:69095551 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:57512373 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:57512373 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94227765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94227765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57139960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:57139960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:23969382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:23969382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24124199 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24124199 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24212061 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24212061 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:46075911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:46075911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:46098939 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:46098939 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:46246076 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:46246076 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169953298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169953298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:6592606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:6592606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:48713329 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:48713329 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:53200610 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:53200610 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:53723654 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:53723654 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35092454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35092454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:75333132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:75333132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:119970400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:119970400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:37265415 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:37265415 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:86533797 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:86533797 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:86568131 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:86568131 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:228004851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:228004851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:18551467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:18551467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:113951399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:113951399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43359902 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43359902 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43362239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43362239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43383223 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43383223 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43383544 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43383544 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43519726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43519726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43571275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43571275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43601000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43601000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43310254 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:43310254 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162258002 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162258002 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:38137774 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:38137774 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43616659 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43616659 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99058102 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99058102 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:71331518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:71331518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:71440182 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:71440182 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:71478258 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:71478258 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:209302173 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:209302173 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:141851092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:141851092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:120567725 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:120567725 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:18762429 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:18762429 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:70938256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:70938256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:198687624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:198687624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:10155374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:10155374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:10554941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:10554941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8317809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8317809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8395557 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8395557 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8493143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8493143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8525181 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8525181 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8636688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8636688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8951383 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:8951383 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9196946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9196946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9262923 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9262923 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9369533 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9369533 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9889816 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9889816 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9913713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9913713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9918772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:9918772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:44069258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:44069258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55713709 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55713709 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:128718589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:128718589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:7712976 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:7712976 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:157907562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:157907562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:158038114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:158038114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220162838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220162838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220167628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220167628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220168429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220168429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:71056430 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:71056430 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:71191689 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:71191689 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:71213049 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:71213049 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:40838757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:40838757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:41407548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:41407548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:41680947 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:41680947 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:41741181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:41741181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:121548829 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:121548829 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:121679452 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:121679452 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:134230547 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:134230547 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:52433091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:52433091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1677190 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1677190 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:51376464 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:51376464 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9302229 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9302229 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9304977 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9304977 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9316560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:9316560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:140110928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:140110928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:52548897 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:52548897 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:13383065 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:13383065 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:9842271 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:9842271 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:23488967 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:23488967 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154489807 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154489807 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:52398828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:52398828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:229424454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:229424454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:229439418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:229439418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40283202 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40283202 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133558306 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133558306 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103068154 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103068154 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:174593863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:174593863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:174616585 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:174616585 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4655169 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4655169 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68739954 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68739954 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68837897 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68837897 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68841568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68841568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68841905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:68841905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:129819366 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:129819366 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:129853179 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:129853179 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:85731310 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:85731310 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40914581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:40914581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:170678788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:170678788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:36269348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:36269348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:36270227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:36270227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:112191256 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:112191256 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:2868962 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:2868962 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:21924209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:21924209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:22233809 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:22233809 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25246001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25246001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25578291 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25578291 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25602715 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25602715 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:85605390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:85605390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179546458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179546458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:80289786 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:80289786 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:33745847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:33745847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:38911480 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:38911480 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:48956146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:48956146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:205066365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:205066365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:127973496 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:127973496 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:36279434 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:36279434 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43941995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43941995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:26400296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:26400296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:173921287 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:173921287 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:31896149 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:31896149 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103251084 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103251084 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103292411 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103292411 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103383712 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103383712 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103389732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103389732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103488946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103488946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:8674867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:8674867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:3228776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:3228776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107002540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107002540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107071410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107071410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107075847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:107075847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183836624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183836624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183853076 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183853076 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:73155441 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:73155441 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:163122205 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:163122205 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:72541356 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:72541356 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:63840521 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:63840521 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240934325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240934325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240990495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240990495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241249264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241249264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:227819886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:227819886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63712784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63712784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63724399 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:63724399 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:33503469 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:33503469 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:33535115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:33535115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8158778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8158778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:12757515 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:12757515 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:130963621 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:130963621 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104764620 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104764620 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104959730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:104959730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105260457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105260457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43394306 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43394306 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:40572319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:40572319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:87056587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:87056587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:21359609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:21359609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:13977246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:13977246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:117109211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:117109211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:5675876 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:5675876 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:219529629 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:219529629 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:79293190 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:79293190 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:79384755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:79384755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77651200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77651200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77683989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77683989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:94426304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:94426304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:60948264 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:60948264 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:117708170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:117708170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:33136017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:33136017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113285673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113285673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:2001033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:2001033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:5000981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:5000981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:58024238 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:58024238 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:78831509 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:78831509 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:99161074 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:99161074 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:45107288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:45107288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:77524756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:77524756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:38090055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:38090055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:158092707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:158092707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:60298191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:60298191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:12140139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:12140139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87445640 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87445640 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92972767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92972767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:45454354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:45454354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:165374872 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:165374872 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:38993140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:38993140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237390211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237390211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237675161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237675161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237741472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237741472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237766465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237766465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237770981 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237770981 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237780951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237780951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237796813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237796813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237806494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237806494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:33673226 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:33673226 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:34018520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:34018520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:34030921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:34030921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:153411413 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:153411413 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134975684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134975684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134990451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134990451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:119278458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:119278458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:119545432 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:119545432 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:55104700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:55104700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128747112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128747112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:127733893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:127733893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:31103312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:31103312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:53745031 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:53745031 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:224464088 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:224464088 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:159164888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:159164888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:159289069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:159289069 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:12631983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:12631983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18265064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:18265064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:108041815 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:108041815 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38763740 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38763740 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:151140398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:151140398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:55062581 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:55062581 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:97614352 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:97614352 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1290950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1290950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26988674 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:26988674 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:3490774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:3490774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:3638165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:3638165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:71574828 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:71574828 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177913916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177913916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:122959690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:122959690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110370768 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:110370768 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:119659575 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:119659575 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:49296923 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:49296923 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169558605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169558605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169580661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169580661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:84671399 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:84671399 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:84727059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:84727059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9280605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9280605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9318534 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9318534 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9408196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9408196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9444010 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:9444010 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:115815593 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:115815593 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:115824041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:115824041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:115898689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:115898689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:47778995 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:47778995 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:196626785 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:196626785 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:101076389 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:101076389 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94961949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94961949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94940513 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:94940513 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:75283546 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:75283546 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42313901 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42313901 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42390262 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42390262 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150914935 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150914935 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135175951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135175951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:26708047 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:26708047 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7239434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7239434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7242324 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7242324 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7372811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:7372811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:46316031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:46316031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:120900552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:120900552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:155407979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:155407979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:155571121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:155571121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:155998090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:155998090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:14157928 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:14157928 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:14167208 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:14167208 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67124544 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67124544 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67153130 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67153130 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67196096 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67196096 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:123496225 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:123496225 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:82330200 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:82330200 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17619532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17619532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17738075 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17738075 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17778906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17778906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17779172 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:17779172 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:87212178 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:87212178 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19563888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19563888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19816685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19816685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19817750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:19817750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:109867960 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:109867960 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:110057157 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:110057157 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:148290496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:148290496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7530220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7530220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:91654537 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:91654537 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:113320533 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:113320533 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:51919745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:51919745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52033843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52033843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:38665131 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:38665131 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1551839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1551839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:13612255 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:13612255 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:164758955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:164758955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46217310 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:46217310 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:36168680 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:36168680 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160460598 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160460598 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160477401 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:160477401 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:51389661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:51389661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127503587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:127503587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43028609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43028609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43051676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43051676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43108986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43108986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43207392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:43207392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:99340885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:99340885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:60709175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:60709175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25845596 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25845596 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25756236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:25756236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:35411922 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:35411922 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:63080832 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:63080832 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:64326571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:64326571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:62965729 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:62965729 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:43267841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:43267841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:19561696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:19561696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:19666875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:19666875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:19705076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:19705076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:92846734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:92846734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95942837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:95942837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:48899902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:48899902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:37286418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:37286418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107314549 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:107314549 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103021547 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:103021547 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92289580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92289580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92382505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92382505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:128317190 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:128317190 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:44194485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:44194485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:9982957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:9982957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:32422591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:32422591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:118111181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:118111181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:8420860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:8420860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:118598582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:118598582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:234076773 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:234076773 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:234076775 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:234076775 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:234323841 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:234323841 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:61449209 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:61449209 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:61464327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:61464327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:70845749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:70845749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18282324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18282324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18282326 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:18282326 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:21467410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:21467410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33964153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:33964153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162497329 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162497329 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162666920 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162666920 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:72143111 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:72143111 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:72413457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:72413457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:72423423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:72423423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:27465744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:27465744 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:51857508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:51857508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26732955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:26732955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:32480276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:32480276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:32646506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:32646506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101584171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:101584171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:10966639 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:10966639 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:308149 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:308149 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:358935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:358935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:361040 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:361040 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:115577879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:115577879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:55735967 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:55735967 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20629213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20629213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:44466307 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:44466307 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:40449542 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:40449542 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:40666582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:40666582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:111921059 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:111921059 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:111921335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:111921335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:46494905 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:46494905 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143001211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143001211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143031320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143031320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143066244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143066244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143090311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143090311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143244882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143244882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143251552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143251552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143297288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143297288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143551138 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:143551138 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:21281913 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:21281913 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133740284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133740284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:101585308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:101585308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168093814 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168093814 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168119491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168119491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168244284 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168244284 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168271692 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168271692 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168271709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168271709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168364598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168364598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168719648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:168719648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:105765312 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:105765312 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:40878890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:40878890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56578914 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56578914 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:2673366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:2673366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:18861460 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:18861460 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183521245 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:183521245 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:169019394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:169019394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:49833118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:49833118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10265248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10265248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10286970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10286970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96963958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96963958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96964877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96964877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96967161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96967161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96971182 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:96971182 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:121757591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:121757591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1020895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1020895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1023059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:1023059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:75902890 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:75902890 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:2314979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:2314979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:107864127 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:107864127 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:108378050 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:108378050 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:108896200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:108896200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:7650573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:7650573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:7669158 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:7669158 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106486199 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106486199 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106635016 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106635016 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106679597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106679597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106976529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106976529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106983097 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:106983097 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:121383918 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:121383918 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204092358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204092358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:23728811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:23728811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:24180137 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:24180137 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:16398354 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:16398354 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:16407939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:16407939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:231109663 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:231109663 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53732306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53732306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:214332179 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:214332179 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:214740078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:214740078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:142597154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:142597154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:142597255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:142597255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:172714605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:172714605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:52940642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:52940642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:52948455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:52948455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:177114566 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:177114566 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169733934 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:169733934 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35779063 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35779063 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:12479593 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:12479593 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:136372139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:136372139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:167833962 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:167833962 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:13984195 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:13984195 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:14063672 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:14063672 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:139307869 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:139307869 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158588929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158588929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158596055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158596055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158606387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158606387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158617295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158617295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158624657 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158624657 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158636304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158636304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158641697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158641697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158644282 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158644282 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:65252706 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:65252706 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:65314563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:65314563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:13144886 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:13144886 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:206630302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:206630302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104844009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:104844009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126135990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126135990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99919964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99919964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:38013852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:38013852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:38031331 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:38031331 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:119496750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:119496750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:170663662 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:170663662 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:28004684 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:28004684 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48206583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48206583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:53181227 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:53181227 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:76779708 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:76779708 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:77012310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:77012310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:77378184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:77378184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:116797851 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:116797851 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:116797861 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:116797861 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:22386181 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:22386181 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:104071400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:104071400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:104099528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:104099528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:37369692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:37369692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:67933124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:67933124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56744318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:56744318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:74436591 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:74436591 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5378143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5378143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:99514065 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:99514065 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81888422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81888422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125477689 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:125477689 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:144468844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:144468844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:120889696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:120889696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:70515035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:70515035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:70515354 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:70515354 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:70615385 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:70615385 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:108881580 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:108881580 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:4458765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:4458765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:21838357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:21838357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:223395461 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:223395461 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:223396490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:223396490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149882374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149882374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:75450212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:75450212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:16754428 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:16754428 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:115523918 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:115523918 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:58448825 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:58448825 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:12195670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:12195670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64669776 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64669776 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64670556 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64670556 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64691776 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64691776 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43995877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43995877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:62482701 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:62482701 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79325088 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79325088 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79366700 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79366700 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79670677 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79670677 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79671384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:79671384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:7305508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:7305508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:7361774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:7361774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:7390234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:7390234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99945203 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99945203 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:149606639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:149606639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:30986938 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:30986938 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160051056 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160051056 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160053075 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160053075 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160076194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:160076194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:102215969 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:102215969 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:3568202 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:3568202 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:78352627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:78352627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:101667120 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:101667120 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:9464597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:9464597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:139571872 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:139571872 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:139657307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:139657307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:132964994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:132964994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:145851224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:145851224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:53114524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:53114524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:53303611 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:53303611 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:85454826 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:85454826 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152109528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152109528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:12835806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:12835806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:35448253 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:35448253 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:27124278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:27124278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20873431 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20873431 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20873518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20873518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:58010264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:58010264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:103065896 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:103065896 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107224268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:107224268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:141724188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:141724188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48890881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:48890881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:115610775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:115610775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133452173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133452173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:218607289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:218607289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101900581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:101900581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:2320396 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:2320396 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133898501 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133898501 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133925540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133925540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133929529 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133929529 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134034469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134034469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134068024 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134068024 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134072264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134072264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134143938 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134143938 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122760645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122760645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122803899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:122803899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:11468906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:11468906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:11611364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:11611364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:137755294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:137755294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:137917702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:137917702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:137946637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:137946637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:138003988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:138003988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24013735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24013735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24015485 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:24015485 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:134118958 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:134118958 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126163533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:126163533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71850789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71850789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153533560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153533560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153543398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:153543398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:70343636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:70343636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:82212244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:82212244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:171872530 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:171872530 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:98136416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:98136416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35698593 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35698593 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:19375383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:19375383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105351623 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105351623 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105362279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105362279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:30729760 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:30729760 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:75382852 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:75382852 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:95008662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:95008662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:69385775 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:69385775 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:132953389 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:132953389 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133004876 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:133004876 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:52894710 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:52894710 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:98413726 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:98413726 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125840454 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125840454 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125854413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125854413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:126051980 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:126051980 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:126128557 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:126128557 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129664639 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129664639 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129751114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129751114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129927791 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129927791 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:130240746 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:130240746 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32936980 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32936980 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:86806022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:86806022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109324809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109324809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109372496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109372496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109383936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:109383936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:216960647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:216960647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150489950 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:150489950 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:57472330 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:57472330 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15652591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15652591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15670840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:15670840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100349540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100349540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:16797242 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:16797242 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133745790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133745790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133771212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:133771212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:109797347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:109797347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:4292562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:4292562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154743472 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:154743472 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:69101827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:69101827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:68974186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:68974186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:19754740 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:19754740 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103216886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:103216886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29790069 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29790069 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29906107 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:29906107 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:66346898 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:66346898 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:23002546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:23002546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:170828672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:170828672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:171126784 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:171126784 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44452836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44452836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:74833588 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:74833588 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:75009442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:75009442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175105209 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175105209 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175108246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175108246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24831693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24831693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175324274 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175324274 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175331741 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175331741 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175355143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175355143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175418025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175418025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175427500 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175427500 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175579404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175579404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175650543 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175650543 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175655190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175655190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175670405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175670405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175673582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175673582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175680511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175680511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175690033 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175690033 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175698210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175698210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161211762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:161211762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25642490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:25642490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42635447 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42635447 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42694772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42694772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7577799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7577799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:144320468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:144320468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:188954194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:188954194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:186314888 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:186314888 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10907328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10907328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10908819 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10908819 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10909661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10909661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10965026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:10965026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:30366809 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:30366809 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:45513787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:45513787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123600183 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123600183 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123673596 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123673596 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123683475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123683475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:41196295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:41196295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:110108404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:110108404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:189063401 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:189063401 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:14203978 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:14203978 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:900482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:900482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100274613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:100274613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:49718100 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:49718100 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:122828401 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:122828401 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111097378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111097378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111121979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111121979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111299234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111299234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111300455 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111300455 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111309410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111309410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:135634081 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:135634081 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:31319016 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:31319016 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:73398834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:73398834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:73528288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:73528288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:74036787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:74036787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:77397218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:77397218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:3458209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:3458209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142616535 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142616535 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:98574417 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:98574417 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81449403 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81449403 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81514491 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81514491 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81558821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81558821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:51621566 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:51621566 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:51790928 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:51790928 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:51885966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:51885966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:31778492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:31778492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:31782273 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:31782273 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:50247791 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:50247791 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:67854913 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:67854913 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176083287 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176083287 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99888269 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:99888269 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:38517956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:38517956 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:3306701 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:3306701 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113234783 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:113234783 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156553319 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:156553319 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:94860305 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:94860305 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:15279462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:15279462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:47229730 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:47229730 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:91196634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:91196634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:9874677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:9874677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:76195105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:76195105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179538316 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179538316 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179580073 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179580073 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179580200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179580200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:18562488 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:18562488 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8087774 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8087774 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:35480559 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:35480559 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:48095876 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:48095876 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:37907505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:37907505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:19919782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:19919782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:89008049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:89008049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:44515894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:44515894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:70958576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:70958576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:68529552 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:68529552 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:99993550 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:99993550 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:43831299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:43831299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118708963 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:118708963 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:25589244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:25589244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:23578551 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:23578551 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:43244648 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:43244648 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42615819 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42615819 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26629459 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26629459 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26629461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26629461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:59338572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:59338572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128853220 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128853220 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128922460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128922460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:70505470 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:70505470 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35956044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35956044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35991142 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:35991142 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:41645925 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:41645925 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:41983563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:41983563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:17720641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:17720641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35382330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35382330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:54531975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:54531975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:96128002 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:96128002 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:96151786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:96151786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:35248739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:35248739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:12076966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:12076966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:215959900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:215959900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216015949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216015949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216074271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216074271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216241826 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216241826 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216318647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216318647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216338057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216338057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216542670 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:216542670 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:179499618 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:179499618 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:62790399 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:62790399 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109510056 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109510056 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:11959972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:11959972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:50831178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:50831178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:75258978 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:75258978 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:31221232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:31221232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129063621 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:129063621 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:75723451 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:75723451 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31749556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31749556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:77921643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:77921643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:108366399 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:108366399 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:82794681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:82794681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:82818168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:82818168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:77908844 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:77908844 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:37002617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:37002617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133020191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:133020191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:100481099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:100481099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:100729327 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:100729327 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:122747957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:122747957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:58311277 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:58311277 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:36570854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:36570854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:22142888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:22142888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:22155821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:22155821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:98784140 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:98784140 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:98797400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:98797400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6126258 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6126258 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:70875665 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:70875665 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:71134904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:71134904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:73100936 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:73100936 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:20180335 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:20180335 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:1147458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:1147458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117570607 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:117570607 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:167259783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:167259783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241876699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241876699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241943426 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241943426 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241947932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:241947932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:43652634 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:43652634 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:122396772 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:122396772 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:37657221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:37657221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:53901818 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:53901818 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67340310 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67340310 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:3551674 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:3551674 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:90286386 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:90286386 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43752414 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:43752414 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:175445905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:175445905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134217386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:134217386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:1006052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:1006052 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:49361603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:49361603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7606001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:7606001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:6021635 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:6021635 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167882158 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:167882158 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:78434609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:78434609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:79027502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:79027502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:87410496 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:87410496 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:168550200 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:168550200 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31589626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:31589626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:2726174 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:2726174 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:167892938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:167892938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:56079303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:56079303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11005323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11005323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11007919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:11007919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:128889424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:128889424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:128894632 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:128894632 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28118814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28118814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:180780737 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:180780737 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74629938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74629938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74629943 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74629943 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38401943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38401943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:57477260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:57477260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:155629349 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:155629349 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:173977840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:173977840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:167048599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:167048599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:114426659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:114426659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:114637325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:114637325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:197159121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:197159121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:45744075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:45744075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:45895362 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:45895362 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111406674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111406674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111407957 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111407957 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111424278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111424278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111625530 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:111625530 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100003987 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100003987 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74698891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:74698891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14566743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:14566743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:31629518 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:31629518 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:135568500 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:135568500 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77732740 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77732740 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:50768637 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:50768637 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:106399277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:106399277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:101167029 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:101167029 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:40696101 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:40696101 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:40721019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:40721019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70466193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70466193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70467980 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:70467980 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:35817102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:35817102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:58573179 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:58573179 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:44679333 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:44679333 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:74637128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:74637128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:38108688 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:38108688 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:53302005 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:53302005 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:53302290 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:53302290 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:14806577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:14806577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44579337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:44579337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:64298461 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:64298461 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:64311703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:64311703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:64415417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:64415417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:21464190 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:21464190 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:21853901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:21853901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:72516058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:72516058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:49559129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:49559129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134484691 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:134484691 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99226654 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99226654 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99230970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99230970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:57883089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:57883089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:57911285 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:57911285 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:37646122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:37646122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:64928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:64928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:58510764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:58510764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:46314695 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:46314695 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:46315483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chrX:46315483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:88677188 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:88677188 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:146831102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:146831102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52671121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52671121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:101833821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:101833821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:101941651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:101941651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:102104280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:102104280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:8991841 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:8991841 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:87035539 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:87035539 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:20792925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:20792925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:48138954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:48138954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:100471568 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:100471568 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:148577543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:148577543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:31587575 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:31587575 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:32338311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:32338311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:58516407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:58516407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:185683735 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:185683735 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:223806374 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:223806374 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:87816013 T>C maps to NM_021722.4 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:87816013 T>C maps to NM_021722.4 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:131912768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:131912768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:19610308 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:19610308 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:87957987 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:87957987 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:148068831 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:148068831 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:100690797 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:100690797 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:74316540 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:74316540 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:236750804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:236750804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:87412529 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:87412529 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:100349872 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:100349872 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:16904133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:16904133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:94586992 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:94586992 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:41591606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:41591606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:197878438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:197878438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:5808749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:5808749 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:101231843 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:101231843 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:51237795 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:51237795 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:43206657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:43206657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:148894064 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:148894064 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:144466422 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:144466422 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:119112157 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:119112157 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:42396214 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:42396214 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:80869072 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:80869072 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:150814756 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:150814756 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:77025165 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:77025165 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:155313627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:155313627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:1748886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:1748886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:176847249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:176847249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:119903435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:119903435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:25281144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:25281144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:54729954 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:54729954 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:46239518 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:46239518 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:11039630 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:11039630 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:88039566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:88039566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:134319465 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:134319465 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:33645039 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:33645039 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:91326037 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:91326037 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:15540368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:15540368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:112940758 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:112940758 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:140507907 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:140507907 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:50255128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:50255128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:61249737 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:61249737 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:111386747 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:111386747 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:14959634 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:14959634 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:97043855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:97043855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:97078524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:97078524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:31526710 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:31526710 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:47009931 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:47009931 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:30476238 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:30476238 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:62307738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:62307738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:14703251 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:14703251 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:74072763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:74072763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:74073204 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:74073204 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:24464369 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:24464369 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:140848420 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:140848420 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:2714782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:2714782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:36974666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:36974666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:86115949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:86115949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:7797238 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:7797238 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:44143771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:44143771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:31690714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:31690714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:197534688 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:197534688 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:49901201 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:49901201 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:49916135 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:49916135 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:119916764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:119916764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:111336665 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:111336665 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:158260704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:158260704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:44413374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:44413374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:24487731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:24487731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:21854914 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:21854914 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:19612752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:19612752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:19612754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:19612754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:59206469 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:59206469 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:25531983 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:25531983 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:90492455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:90492455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:30815605 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:30815605 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:42218707 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:42218707 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:34994297 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:34994297 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:196918789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:196918789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:57795357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:57795357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:57820831 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:57820831 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:175665067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:175665067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:109932108 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:109932108 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:90774104 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:90774104 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:8560234 C>A maps to NM_194284.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:8560234 C>A maps to NM_194284.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:123376819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:123376819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:87683090 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:87683090 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:95365109 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:95365109 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:205042108 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:205042108 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:125494978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:125494978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:75830862 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:75830862 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:101806954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:101806954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:70854180 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:70854180 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:94037113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:94037113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:139868024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:139868024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:7420261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:7420261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:7421150 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:7421150 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:111007802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:111007802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:228155615 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:228155615 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:10080476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:10080476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:10099655 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:10099655 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:48617272 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:48617272 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:109094896 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:109094896 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:131348493 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:131348493 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:207890734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:207890734 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:35733174 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:35733174 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:61987297 C>T maps to ENST00000450719 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:61987297 C>T maps to ENST00000450719 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:4236319 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:4236319 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:113568982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:113568982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:113648935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:113648935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:79878655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:79878655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:80819156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:80819156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:80831125 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:80831125 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:80831331 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:80831331 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:148494874 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:148494874 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:44873761 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:44873761 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:134907614 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:134907614 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:156753137 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:156753137 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:83126626 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:83126626 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:41597910 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:41597910 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:46598670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:46598670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:59002176 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:59002176 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:122022650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:122022650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:50196458 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:50196458 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:71889173 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:71889173 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:14964937 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:14964937 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:95131179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:95131179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:20987362 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:20987362 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:74104454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:74104454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:123048 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:123048 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:59934780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:59934780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:59983114 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:59983114 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:14724829 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:14724829 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:12133733 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:12133733 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:349041 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:349041 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:463823 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:463823 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:108124821 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:108124821 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:107558681 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:107558681 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:83445439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:83445439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:35989864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:35989864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:11550665 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:11550665 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:117817212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:117817212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:111503635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:111503635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:115948655 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:115948655 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:162902239 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:162902239 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:153659754 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:153659754 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:168683712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:168683712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:63962928 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:63962928 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:117319999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:117319999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71778302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71778302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:19253731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:19253731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:21216212 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:21216212 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:52380671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:52380671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:110864391 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:110864391 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:36315752 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:36315752 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:176064756 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:176064756 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:23732364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:23732364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:112013871 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:112013871 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:149447958 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:149447958 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:97185323 C>A maps to ENST00000514100 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:97185323 C>A maps to ENST00000514100 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:8075692 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:8075692 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:11972067 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:11972067 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:66102466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:66102466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:6191316 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:6191316 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:51805479 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:51805479 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:139269023 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:139269023 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:139424086 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:139424086 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:29206312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:29206312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:71992729 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:71992729 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:113269223 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:113269223 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:12040293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:12040293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:98983291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:98983291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48800964 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48800964 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48905059 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48905059 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:147781508 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:147781508 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:48420862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:48420862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:161696816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:161696816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:27956361 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:27956361 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:76028625 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:76028625 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:76029522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:76029522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:58095708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:58095708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:128492554 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:128492554 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:216288753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:216288753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:22562482 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:22562482 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:8195140 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:8195140 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:135439147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:135439147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:65167167 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:65167167 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:32792873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:32792873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:162380477 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:162380477 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:76580891 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:76580891 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:46967292 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:46967292 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:48652705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:48652705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:81692232 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:81692232 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:48426495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:48426495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:78509352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:78509352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:52723249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:52723249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:55527187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:55527187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:93982509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:93982509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:176883280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:176883280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:25510200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:25510200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:90398020 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:90398020 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:123474049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:123474049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:165378327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:165378327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:87721370 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:87721370 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:120668025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:120668025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13764923 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13764923 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:146686076 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:146686076 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13256245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13256245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:68863488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:68863488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:104480826 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:104480826 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:124792484 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:124792484 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:74014817 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:74014817 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:29855504 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:29855504 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:39329419 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:39329419 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:148871237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:148871237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:112108012 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:112108012 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:129175647 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:129175647 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:42223288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:42223288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:38612886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:38612886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:118647596 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:118647596 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:128041004 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:128041004 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:99187104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:99187104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:107979601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:107979601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:52177948 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:52177948 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:31429889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:31429889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:31372796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:31372796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:102144937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:102144937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:26835495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:26835495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:17949053 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:17949053 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:17762013 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:17762013 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:119914558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:119914558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:169894017 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:169894017 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:160017266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:160017266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:78704395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:78704395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:78785235 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:78785235 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:113822631 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:113822631 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:53244882 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:53244882 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:55956348 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:55956348 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:55360037 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:55360037 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:6511816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:6511816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:96973330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:96973330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:24037815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:24037815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:28981472 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:28981472 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:170024426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:170024426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36353214 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36353214 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:97423824 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:97423824 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:135025383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:135025383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:118020070 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:118020070 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:6020740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:6020740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:133914469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:133914469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:150939979 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:150939979 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:8326501 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:8326501 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:138415882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:138415882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:46704867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:46704867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:40196768 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:40196768 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:48647109 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:48647109 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54756655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54756655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:70423727 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:70423727 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:197762925 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:197762925 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:156096605 C>T maps to ENST00000392353 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:156096605 C>T maps to ENST00000392353 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:160999839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:160999839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:133861612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:133861612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:133916124 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:133916124 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:170013798 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:170013798 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:235897224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:235897224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:235971727 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:235971727 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:140984189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:140984189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:185135542 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:185135542 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:61714449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:61714449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:48181549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:48181549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:119727532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:119727532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:186951576 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:186951576 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:47800734 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:47800734 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:113668971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:113668971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:47136091 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:47136091 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:47530414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:47530414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:86185290 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:86185290 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:169230242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:169230242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:42139210 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:42139210 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:37390999 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:37390999 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:141721341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:141721341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:141734423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:141734423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:131081982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:131081982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:56231264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:56231264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:113237590 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:113237590 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:138111867 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:138111867 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:78806608 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:78806608 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:54681772 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:54681772 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:79952086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:79952086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:149896372 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:149896372 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:11307865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:11307865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:40362893 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:40362893 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48444034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48444034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:108174487 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:108174487 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:10302694 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:10302694 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:3277516 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:3277516 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:169496503 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:169496503 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71300476 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71300476 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:148556280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:148556280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:183556150 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:183556150 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:133632007 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:133632007 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:119115730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:119115730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:97345747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:97345747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:52667104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:52667104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36387459 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36387459 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:23946390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:23946390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:32181751 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:32181751 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:179533707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:179533707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:100897124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:100897124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:119511309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:119511309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:126213747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:126213747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:5585496 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:5585496 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:131296678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:131296678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:88472411 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:88472411 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:101091844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chrX:101091844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:8475640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:8475640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:132290255 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:132290255 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:6865592 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:6865592 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:9293602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:9293602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:24932097 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:24932097 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:77755597 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:77755597 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:3593335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:3593335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:150930959 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:150930959 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:103271367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:103271367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:119144873 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:119144873 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:55944843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:55944843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:165989832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:165989832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:145027808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:145027808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:41587853 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:41587853 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:179576976 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:179576976 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:48533759 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:48533759 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:64089163 A>T maps to NM_001172818.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:64089163 A>T maps to NM_001172818.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:131703586 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:131703586 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:21087247 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:21087247 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:77558314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:77558314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:110437293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:110437293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:74695502 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:74695502 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:28754911 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:28754911 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:133244362 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:133244362 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:86332735 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:86332735 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:38363746 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:38363746 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:44836290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:44836290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:170471028 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:170471028 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:170487258 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:170487258 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:37531501 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:37531501 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:94881458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:94881458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:11106550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:11106550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:121619505 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:121619505 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:121814175 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:121814175 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:81121207 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:81121207 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:150319031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:150319031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:126887354 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:126887354 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:214705576 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:214705576 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:8565347 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:8565347 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:44139746 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:44139746 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:3145052 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:3145052 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:66169873 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:66169873 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:128814159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:128814159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:40282249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:40282249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:174219849 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:174219849 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:66103431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:66103431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:110062507 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:110062507 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:36235862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:36235862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:63312000 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:63312000 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:80376334 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:80376334 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:79896447 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:79896447 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:43942957 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:43942957 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:26431951 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:26431951 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:46223458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:46223458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:77240682 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:77240682 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:68192032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:68192032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:137780257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:137780257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:79386020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:79386020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:108475318 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:108475318 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:118469085 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:118469085 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:35751036 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:35751036 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:163138280 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:163138280 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:241083728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:241083728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:156352689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:156352689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:25712124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:25712124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:72970293 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:72970293 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:33179844 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:33179844 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:125498036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:125498036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:158596135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:158596135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:55609136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:55609136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:35867181 A>T maps to ENST00000397161 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:35867181 A>T maps to ENST00000397161 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:213436183 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:213436183 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:237870118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:237870118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:33633014 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:33633014 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:78158622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:78158622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:31152506 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:31152506 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:141206714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:141206714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:110427450 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:110427450 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:156144518 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:156144518 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:132099162 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:132099162 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179996807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179996807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:7371329 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:7371329 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:246617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:246617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:51191453 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:51191453 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:52000270 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:52000270 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16974632 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16974632 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16974671 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16974671 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:31927196 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:31927196 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:160460894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:160460894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:45236116 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:45236116 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48414359 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:48414359 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:110083987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:110083987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:118078203 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:118078203 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:25678391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:25678391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:47173910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:47173910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:17412653 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:17412653 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:21229352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:21229352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:98634635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:98634635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:121748189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:121748189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:7665430 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:7665430 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55648408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55648408 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:158583760 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:158583760 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:158607815 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:158607815 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:41078200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:41078200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:65216420 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:65216420 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:65292044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:65292044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:31756636 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:31756636 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:9050014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:9050014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:33687210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:33687210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:23825086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:23825086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:57234759 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:57234759 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:25326212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:25326212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:149879872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:149879872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:7487997 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:7487997 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:162043604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:162043604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:38313146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:38313146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:38356519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:38356519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:13550314 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:13550314 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:74174179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:74174179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:67236237 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:67236237 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:115973389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:115973389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:104516027 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:104516027 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:138169159 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:138169159 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:82219961 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:82219961 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:63044764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:63044764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:52896104 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:52896104 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:129704047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:129704047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:129747002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:129747002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:83290436 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:83290436 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:171124467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:171124467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:218750092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:218750092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:17752187 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:17752187 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:39743990 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr20:39743990 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:43720707 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr15:43720707 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:144245790 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:144245790 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:10970142 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:10970142 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:141362712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:141362712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:54973412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:54973412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:189026490 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:189026490 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:122828337 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:122828337 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:142572638 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:142572638 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:3377369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:3377369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:3377390 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:3377390 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179391670 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179391670 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179592756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179592756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179592770 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179592770 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179629075 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:179629075 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:113007153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:113007153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:115057047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr13:115057047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:17552611 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:17552611 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:179470017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:179470017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:77919735 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:77919735 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:108309023 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:108309023 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:157099226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:157099226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:17277400 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:17277400 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:37002019 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:37002019 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:46696440 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:46696440 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:38767991 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:38767991 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:98858654 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:98858654 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:70875798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:70875798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:70965588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:70965588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:55504069 C>G maps to ENST00000442038 *130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:55504069 C>G maps to ENST00000442038 *130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:7606166 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:7606166 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:56216832 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:56216832 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:56305983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:56305983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:57465743 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:57465743 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:69198021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:69198021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:114004007 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:114004007 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:157915294 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:157915294 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:145182141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:145182141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:38087429 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:38087429 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:38120476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:38120476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:64429834 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:64429834 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:72628209 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:72628209 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:72628212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr18:72628212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:109704722 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:109704722 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:53280664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:53280664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71655660 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71655660 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:11608931 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:11608931 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:12016300 G>A maps to ENST00000429654 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:12016300 G>A maps to ENST00000429654 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:58016570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:58016570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:64853652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:64853652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:6390625 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:6390625 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:7286874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:7286874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:48467325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:48467325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:48568388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:48568388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:48659516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:48659516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:67102403 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:67102403 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:66921152 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:66921152 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:17448577 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:17448577 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:43621939 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:43621939 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:89052492 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:89052492 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7240170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7240170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:31517871 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:31517871 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:31716287 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:31716287 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:32074561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:32074561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:32410738 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:32410738 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:20635228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:20635228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:20429347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:20429347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:127857582 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:127857582 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:156918831 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:156918831 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:33825521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:33825521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:1650771 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:1650771 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:123121964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:123121964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:131803662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:131803662 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:31120330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:31120330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:70848260 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:70848260 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:147693319 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:147693319 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:147967367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:147967367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:100381087 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:100381087 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:222849664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:222849664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:56287184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:56287184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:21902973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:21902973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:114147537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:114147537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:54434778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:54434778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:129990725 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:129990725 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:142170497 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:142170497 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:128856791 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:128856791 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:53526520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:53526520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:66789690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:66789690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:120072979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:120072979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:120157846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:120157846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:23977656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:23977656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:176001205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:176001205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:27097450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:27097450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:172410780 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:172410780 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:50223306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:50223306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:69492669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:69492669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:56553552 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:56553552 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:60773525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:60773525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:32673740 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:32673740 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:7855021 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:7855021 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:86023488 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:86023488 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:103691529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:103691529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:97060782 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:97060782 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:30414692 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:30414692 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:74042110 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:74042110 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:85057888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:85057888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:41904406 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:41904406 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:169674876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:169674876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:88119527 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:88119527 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:121401862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:121401862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:35705732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:35705732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:39610244 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:39610244 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:69523585 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:69523585 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:49984196 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:49984196 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:9023450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:9023450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:181535976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:181535976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:181759711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:181759711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:54690661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:54690661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:85775706 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:85775706 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:134552431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:134552431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:44147421 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:44147421 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:110511782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:110511782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:110560130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:110560130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:44430574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:44430574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:64108005 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:64108005 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:37016254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:37016254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:56125831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:56125831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:150046100 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:150046100 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:21882882 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:21882882 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:22687183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:22687183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:95225534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:95225534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:23523665 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:23523665 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:59959333 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:59959333 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:92291329 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:92291329 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:17629268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:17629268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:49552053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:49552053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:170465548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:170465548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:78061959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:78061959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:77340699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:77340699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:7289952 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:7289952 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:19245910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:19245910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:88000028 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:88000028 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:17104210 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:17104210 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:146226729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:146226729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:147312997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:147312997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:39104434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:39104434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:125611431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:125611431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:71588464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:71588464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:121240415 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:121240415 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:121344785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:121344785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:101759425 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:101759425 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:101765656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:101765656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:32158315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:32158315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:56141451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:56141451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:130352402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:130352402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:56963927 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:56963927 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:131405751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:131405751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:122720617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:122720617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:113395910 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:113395910 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:113721314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:113721314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:67703108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:67703108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:67780017 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:67780017 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:67883609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:67883609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:69094120 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:69094120 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:16709759 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:16709759 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:45017512 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:45017512 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:134299333 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:134299333 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:57756983 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:57756983 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:52729952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:52729952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:53581141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:53581141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:103907500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:103907500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:49986846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:49986846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:19044761 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:19044761 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:137096841 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:137096841 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:51017225 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:51017225 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:32490479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:32490479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:78359375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:78359375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7660321 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7660321 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:21147482 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:21147482 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:13737633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:13737633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:129160163 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:129160163 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:111809819 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:111809819 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:67490756 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:67490756 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:116268761 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:116268761 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:109023522 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:109023522 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:105396387 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:105396387 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:105456384 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:105456384 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:117572677 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:117572677 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:42174561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:42174561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:32455177 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:32455177 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:68088648 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:68088648 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:76855255 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:76855255 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:46784712 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:46784712 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:83445169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:83445169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:23749044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:23749044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:33718923 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:33718923 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:129966411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:129966411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:96909642 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:96909642 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:134840050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:134840050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:43565987 T>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:43565987 T>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:39823036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:39823036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:7912613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:7912613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:66100702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:66100702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:139470987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:139470987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:35718801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:35718801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:57200990 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:57200990 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:68194302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:68194302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:190110888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:190110888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:190250612 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:190250612 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:54743434 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:54743434 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:29464193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:29464193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:150774525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:150774525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:150891686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:150891686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161563247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161563247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161680713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161680713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:125014505 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:125014505 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:34280962 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:34280962 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:60956422 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:60956422 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:240492905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:240492905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:52043523 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:52043523 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:37735539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:37735539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:12331436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:12331436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:31201807 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:31201807 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:35610224 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:35610224 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:112079996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:112079996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:77988798 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:77988798 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:46976422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:46976422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:47221638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:47221638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:161580088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:161580088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:27586217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:27586217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:151812343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:151812343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:154759229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:154759229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:51771257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:51771257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:173202495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:173202495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:173301305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:173301305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:173503356 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:173503356 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:44222279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:44222279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:13364942 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:13364942 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:131285502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:131285502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:131285736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:131285736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:131285779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:131285779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:175660994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:175660994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:57448652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:57448652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:235715383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:235715383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:171806361 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:171806361 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:133065546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:133065546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:176625502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:176625502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:22481510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:22481510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:165383518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:165383518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:87679773 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:87679773 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:93346792 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:93346792 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:94145719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:94145719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:94500269 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:94500269 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:31201794 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:31201794 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:31250661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:31250661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:13842390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:13842390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:126340071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:126340071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:144704708 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:144704708 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:127451561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:127451561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:134705048 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:134705048 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:39881466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:39881466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:29962833 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:29962833 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:173495990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:173495990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:173525213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:173525213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:41787191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:41787191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:100773177 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:100773177 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:11272195 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:11272195 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:18560334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:18560334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:41130053 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:41130053 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:133800867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:133800867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:35874707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:35874707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:57878618 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:57878618 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:76771175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:76771175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143039615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143039615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143626086 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143626086 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:118856410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:118856410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:16233801 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:16233801 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:31342907 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:31342907 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:15183791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:15183791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:156032439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:156032439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:20731842 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:20731842 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:21401794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:21401794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:21716105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:21716105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:155698053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:155698053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:39034610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:39034610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:215342704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:215342704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:36698421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:36698421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:19563900 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:19563900 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:55272499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:55272499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:55329628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:55329628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:126597385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:126597385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:204164501 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:204164501 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:44588212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:44588212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:32410820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:32410820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:118068540 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:118068540 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:209797434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:209797434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:152777523 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:152777523 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:16725236 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:16725236 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:104172636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:104172636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:28371566 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:28371566 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:90488326 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:90488326 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:96444445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:96444445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:156524933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:156524933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:135178228 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:135178228 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:62405330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:62405330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:59300725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:59300725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:141172805 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:141172805 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:142271600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:142271600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:41089837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:41089837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:70394369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:70394369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:101554685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:101554685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:116163717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:116163717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:33525458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:33525458 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:91502776 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:91502776 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:114536448 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:114536448 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:118065405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:118065405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:109049198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:109049198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:21208498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:21208498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:49634681 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:49634681 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:16077113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:16077113 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:164592633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:164592633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:217214872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:217214872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:45769479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:45769479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:98932715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:98932715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:74936668 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:74936668 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:154878147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:154878147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:135047162 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:135047162 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:108723573 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:108723573 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:151288042 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:151288042 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:92700343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:92700343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:29841809 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:29841809 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:123451650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:123451650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:26284353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr22:26284353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:2229062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:2229062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:78333902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:78333902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:15386636 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:15386636 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:148560547 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:148560547 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:103091023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:103091023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:112906097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:112906097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:17834752 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:17834752 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:149922710 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:149922710 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:55839415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:55839415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:55958348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:55958348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:70531932 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:70531932 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:204970211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:204970211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:26224037 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:26224037 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:129751594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:129751594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:236177010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:236177010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:32458250 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:32458250 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:56491084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:56491084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:162175441 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:162175441 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:27006964 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:27006964 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:50171357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:50171357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:50663799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:50663799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:78687934 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:78687934 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:79942990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:79942990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:132084640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:132084640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:156834336 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:156834336 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:56812513 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:56812513 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:819060 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:819060 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:79095140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:79095140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:15052158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:15052158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:31823044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:31823044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:32060222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:32060222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:103240577 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:103240577 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:77175291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:77175291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:119013311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:119013311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:206150171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:206150171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:206440511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:206440511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:161768848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:161768848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:162450227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:162450227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:14708509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:14708509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:233236774 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:233236774 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:167422591 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:167422591 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:105191996 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:105191996 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:95387120 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:95387120 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:73647837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:73647837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:216884140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:216884140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:153276263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:153276263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:77569752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:77569752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:22903325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:22903325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:6367253 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:6367253 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:51827273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:51827273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:33022023 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:33022023 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:20361462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:20361462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:28855911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:28855911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:41505007 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:41505007 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:242481246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:242481246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:100853593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:100853593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:131895690 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:131895690 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:132292889 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:132292889 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:94589144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:94589144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:72186355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:72186355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:82060472 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:82060472 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:11201407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:11201407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:133539666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:133539666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:15981093 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:15981093 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:27220922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:27220922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:142458571 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:142458571 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:113953244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:113953244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:43352067 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:43352067 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:36908932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:36908932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:1097852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:1097852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:8317960 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:8317960 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:8372140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:8372140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:71065709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:71065709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:40827613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:40827613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:158924982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:158924982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:25632054 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:25632054 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:103292314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:103292314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:73176926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:73176926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:107048232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:107048232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:72940560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:72940560 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:63735904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:63735904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:104930645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:104930645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:40411754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:40411754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:87131232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:87131232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:78940030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:78940030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:113216714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:113216714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:39052177 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:39052177 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237619798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237619798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237796719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237796719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237924653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237924653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:169656340 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:169656340 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:174292743 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:174292743 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:4285259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:4285259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:9320600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:9320600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:48022735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:48022735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:48056281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:48056281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:158571664 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:158571664 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:2900991 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:2900991 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:28595661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:28595661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:155752858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:155752858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:148392038 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:148392038 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:72190348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:72190348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:56903775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:56903775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:44686311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:44686311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:42940275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr18:42940275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:25779051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:25779051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:22362973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:22362973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:22381090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:22381090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:4871811 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:4871811 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:92279456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:92279456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:40392249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:40392249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:8422640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:8422640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75680243 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75680243 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75792494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75792494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:10881995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:10881995 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:55728469 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:55728469 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21457541 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21457541 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21471551 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21471551 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:20896345 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:20896345 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:20547748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:20547748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:95210561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:95210561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:246165821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:246165821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:246513284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:246513284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:227935376 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:227935376 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:84336992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:84336992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:70129594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:70129594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:121740647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:121740647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:51046155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:51046155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:51075443 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:51075443 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:23696395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:23696395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:24538803 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:24538803 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:101251338 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:101251338 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:151051274 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:151051274 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:52955247 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:52955247 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:35739980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:35739980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:168004243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:168004243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:121229394 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:121229394 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:119538564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:119538564 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:149523940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:149523940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:44383531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:44383531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:76940070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:76940070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:33838511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:33838511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:67882457 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:67882457 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:146747217 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:146747217 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:5080285 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:5080285 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:5251160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:5251160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:70707859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:70707859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:4297381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:4297381 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:91832547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:91832547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:114669264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:114669264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:30970572 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:30970572 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:33281882 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:33281882 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:13421540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:13421540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:17747524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:17747524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:151748213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:151748213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:133948136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:133948136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:2790327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:2790327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:82207139 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:82207139 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:109396830 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:109396830 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:100273807 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:100273807 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:64198004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:64198004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:226046846 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:226046846 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:109688956 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:109688956 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:109707985 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:109707985 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:109797366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:109797366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:100326298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:100326298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:101770132 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chrX:101770132 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:74880397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:74880397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:175457716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:175457716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:175661690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:175661690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:218670342 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:218670342 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:5949892 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:5949892 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:38396056 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:38396056 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:77438472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:77438472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:116605144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:116605144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:81450135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:81450135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:51601106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:51601106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:51895108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:51895108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:147645346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:147645346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:37924895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:37924895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:35998285 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:35998285 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:17779066 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:17779066 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:54586336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:54586336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:158964302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:158964302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:1599338 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:1599338 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:216380526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:216380526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:132631132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:132631132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:75301078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:75301078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:191018090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:191018090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:100921251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:100921251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:53961212 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:53961212 A>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:78570562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:78570562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:114117820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:114117820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:72929415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:72929415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:106794575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:106794575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:85306519 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:85306519 C>G did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:62489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:62489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:71607201 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:71607201 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:71607740 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:71607740 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:53747211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:53747211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:238053032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:238053032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:58121090 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:58121090 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:52601787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:52601787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:6189926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:6189926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:6507311 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:6507311 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7208737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7208737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7279780 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7279780 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7645463 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7645463 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7726692 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:7726692 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:9243156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:9243156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:44279794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:44279794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:67148330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:67148330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:94463734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:94463734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87151351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87151351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87174372 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87174372 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87225139 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87225139 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87079475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87079475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:48234167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:48234167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48750319 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48750319 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:17425970 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:17425970 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100630514 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100630514 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:35468401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:35468401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109644721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109644721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:32408695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:32408695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:8368600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:8368600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:20559628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:20559628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:229568718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:229568718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74143905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74143905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:236918232 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:236918232 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66322143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66322143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:158705315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:158705315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42849052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42849052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:38961282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:38961282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:5182435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:5182435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:100672148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:100672148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:73171795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:73171795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:64592817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:64592817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:18829642 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:18829642 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:84365063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:84365063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41211162 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41211162 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:7691157 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:7691157 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:7766938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:7766938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123051536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123051536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:49167444 G>A maps to ENST00000395210 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:49167444 G>A maps to ENST00000395210 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131826566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131826566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131848487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131848487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31121484 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31121484 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31126628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31126628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:116058987 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:116058987 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:87968820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:87968820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:74354298 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:74354298 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86823127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86823127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86898138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86898138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:49023512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:49023512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:27275818 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:27275818 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:228356187 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:228356187 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:143654709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:143654709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86087237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86087237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86182601 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:86182601 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:32841194 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:32841194 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:91570284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:91570284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:244006635 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:244006635 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:125831733 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:125831733 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:37569464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:37569464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73659252 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73659252 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:45940952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:45940952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:202591927 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:202591927 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71469744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71469744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:46565611 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:46565611 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:96350447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:96350447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:41525699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:41525699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:41573370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:41573370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:114282104 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:114282104 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:139928880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:139928880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:92020475 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:92020475 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:110450880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:110450880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:37434002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:37434002 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:37441083 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:37441083 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:82924431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:82924431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90327652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90327652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:99145089 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:99145089 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:26663651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:26663651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:22249139 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:22249139 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:45664173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:45664173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:45741769 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:45741769 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:36671635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:36671635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:10692320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:10692320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:83360477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:83360477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:21237474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:21237474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:115361548 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:115361548 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:121303518 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:121303518 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:86893182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:86893182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:69040399 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:69040399 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:11242396 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:11242396 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:11315212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:11315212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156938091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156938091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156943482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156943482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111896373 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111896373 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:23326111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:23326111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:100912656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:100912656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:35750657 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:35750657 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:69499971 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:69499971 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:3681681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:3681681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131072675 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131072675 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131285693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131285693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:101152680 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:101152680 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:62475441 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:62475441 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176857155 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176857155 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176934241 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176934241 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176954134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176954134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176992826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176992826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:177001569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:177001569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:120113322 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:120113322 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:108159696 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:108159696 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:138828080 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:138828080 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:193036719 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:193036719 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:160104463 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:160104463 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:160104887 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:160104887 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:42492806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:42492806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:130656228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:130656228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84486905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84486905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:43664207 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:43664207 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40666035 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40666035 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:104053310 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:104053310 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:77264820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:77264820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:42592798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:42592798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:50287513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:50287513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:76940403 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:76940403 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:28841175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:28841175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42274203 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42274203 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:69952101 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:69952101 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:58201311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:58201311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:63543566 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:63543566 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235613468 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235613468 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:47234048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:47234048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11021628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11021628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11022801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11022801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11028374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11028374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11069456 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:11069456 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:69758007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:69758007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:215661847 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:215661847 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:171553403 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:171553403 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:35262131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:35262131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:58887777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:58887777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:24995312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:24995312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41895496 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41895496 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:96706537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:96706537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:133118912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:133118912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:60562755 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:60562755 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:11400688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:11400688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:22615538 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:22615538 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:22053593 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:22053593 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:112989520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:112989520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:52549308 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:52549308 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:203274719 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:203274719 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127427050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127427050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105945884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105945884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:112642243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:112642243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:99183211 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:99183211 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8140618 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8140618 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:24892874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:24892874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170965730 G>A maps to NM_001163629.1 W474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170965730 G>A maps to NM_001163629.1 W474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247726815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247726815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12819150 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12819150 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:172520570 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:172520570 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:9496896 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:9496896 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31889240 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31889240 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:106690642 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:106690642 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:20939689 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:20939689 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:10282291 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:10282291 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:88824992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:88824992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:113506686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:113506686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:81844488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:81844488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:81849263 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:81849263 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:76489313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:76489313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:184605448 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:184605448 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:118823180 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:118823180 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:120918962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:120918962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:135601314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:135601314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:121093816 C>T maps to ENST00000453000 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:121093816 C>T maps to ENST00000453000 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:140818800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:140818800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:2723010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:2723010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:53806856 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:53806856 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181741407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181741407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181764221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181764221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:81591750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:81591750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:54186082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:54186082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:1996142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:1996142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:36983618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:36983618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:159163361 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:159163361 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:14989436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:14989436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:14989456 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:14989456 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:54113730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:54113730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:110565063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:110565063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:115451721 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:115451721 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:219897312 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:219897312 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57752493 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57752493 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49918188 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49918188 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:159846265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:159846265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42759544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42759544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:130898684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:130898684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:85568643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:85568643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:28496389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:28496389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:95902557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:95902557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:132084262 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:132084262 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:17076293 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:17076293 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158225693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158225693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:112666616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:112666616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51728953 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51728953 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:157802913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:157802913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:87042559 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:87042559 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:111289890 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:111289890 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:12238444 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:12238444 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:130695315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:130695315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:44394623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:44394623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:64981335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:64981335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:65023550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:65023550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:21883393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:21883393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:31305637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:31305637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:61689353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:61689353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:61760856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:61760856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:58145205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:58145205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:14861884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:14861884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:51723689 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:51723689 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:47508640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:47508640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:123907449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:123907449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:134281646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:134281646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:66995152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:66995152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:55883830 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:55883830 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:50863414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:50863414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:98234346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:98234346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:29535655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:29535655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7349313 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7349313 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:10995696 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:10995696 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7163585 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7163585 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:8687184 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:8687184 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:140265299 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:140265299 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:140283001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:140283001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:57728456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:57728456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:123375000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:123375000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:128889864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:128889864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57950085 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57950085 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57996430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57996430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:87644957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:87644957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:97492446 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:97492446 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:58592369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:58592369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:70732713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:70732713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54647369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54647369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40963009 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40963009 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:100012000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:100012000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:146471273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:146471273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:125261825 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:125261825 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103386017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103386017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103462501 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103462501 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:75855729 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:75855729 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105819325 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105819325 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105835930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105835930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:56141284 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:56141284 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:139815191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:139815191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:110828655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:110828655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111099269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111099269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:130346068 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:130346068 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:62362894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:62362894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:129986528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:129986528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:175303166 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:175303166 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:131415476 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:131415476 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:131434754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:131434754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:131442187 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:131442187 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:98310067 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:98310067 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:8609198 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:8609198 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207851646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207851646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207785241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207785241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84888143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84888143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84902406 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84902406 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84923003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:84923003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:5875060 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:5875060 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48343345 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48343345 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:25620800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:25620800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:1424459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:1424459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:19315276 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:19315276 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:4646079 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:4646079 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:114137841 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:114137841 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:58208453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:58208453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:68013470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:68013470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:68535300 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:68535300 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:11346431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:11346431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:44520905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:44520905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66332490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66332490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:16995969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:16995969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:17082984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:17082984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:43017637 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:43017637 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:50787290 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:50787290 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:50810273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:50810273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:143996347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:143996347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41355620 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41355620 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:42012139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:42012139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:187118620 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:187118620 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:86048043 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:86048043 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:20016140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:20016140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69551228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69551228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69551563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69551563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:98519389 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:98519389 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151153390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151153390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74592872 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74592872 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:31231556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:31231556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:38888172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:38888172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169294700 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169294700 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169343131 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169343131 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:29965003 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:29965003 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:29965935 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:29965935 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:29992974 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:29992974 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:126531882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:126531882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:32213405 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:32213405 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:14613812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:14613812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:14614254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:14614254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:169951986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:169951986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127579631 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127579631 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47882910 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47882910 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:37634777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:37634777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:111853271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:111853271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107542684 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107542684 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38136296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38136296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:69669171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:69669171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:124345566 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:124345566 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:124350111 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:124350111 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:124389722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:124389722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:124288394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:124288394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21014608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21014608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21093084 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21093084 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:13692088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:13692088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:13864750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:13864750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:38906523 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:38906523 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:11573177 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:11573177 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:66992528 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:66992528 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:65867629 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:65867629 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:172348135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:172348135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:169147344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:169147344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:169508805 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:169508805 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:320267 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:320267 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:320271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:320271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:37541463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:37541463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:44436150 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:44436150 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:116600096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:116600096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:154519682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:154519682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64038285 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64038285 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64057425 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64057425 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:113847805 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:113847805 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:113878554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:113878554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:42064612 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:42064612 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:76868737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:76868737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30439420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30439420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:57669618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:57669618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:95616612 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:95616612 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:71887921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:71887921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:96270220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:96270220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:158338040 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:158338040 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:139165413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:139165413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:207026893 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:207026893 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:144668877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:144668877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:133023167 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:133023167 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184043772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184043772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:33866919 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:33866919 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:23754650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:23754650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:11576946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:11576946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:43839686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:43839686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:43968753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:43968753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41545678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41545678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:97015539 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:97015539 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:97200309 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:97200309 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:134911333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:134911333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:134920106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:134920106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:220152159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:220152159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:20811534 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:20811534 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:103499260 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:103499260 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:157098233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:157098233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:72968241 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:72968241 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:45797731 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:45797731 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:187201546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:187201546 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:57515143 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:57515143 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:14816142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:14816142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:126111010 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:126111010 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:17654260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:17654260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:16478932 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:16478932 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:139185182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:139185182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:89658588 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:89658588 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30931398 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30931398 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:150387365 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:150387365 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:150399977 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:150399977 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:51877906 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:51877906 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:16787661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:16787661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:89877050 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:89877050 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:48905342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:48905342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127595038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127595038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127647202 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127647202 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127648640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127648640 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:15517928 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:15517928 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:15937334 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:15937334 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:161475671 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:161475671 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:50027725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:50027725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:159778347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:159778347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:125094489 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:125094489 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:125107432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:125107432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63987607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63987607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:108521893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:108521893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:102378929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:102378929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67272056 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67272056 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:15365209 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:15365209 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179334274 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179334274 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:142477707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:142477707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:33261733 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:33261733 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240308028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240308028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:147030163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:147030163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:49771827 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:49771827 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:71037286 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:71037286 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79102797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79102797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79238461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79238461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:116366241 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:116366241 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:69351424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:69351424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:49210405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:49210405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:49295687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:49295687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:37430910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:37430910 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:39261719 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:39261719 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:101377759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:101377759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:46099427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:46099427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:161520821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:161520821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:161569020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:161569020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:27636062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:27636062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:27722736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:27722736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:88450886 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:88450886 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:31215629 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:31215629 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:158156185 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:158156185 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69798014 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69798014 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69798084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69798084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:16264095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:16264095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:128067315 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:128067315 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:34900351 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:34900351 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:53370697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:53370697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:118413398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:118413398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:158366820 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:158366820 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:13420074 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:13420074 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61958353 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61958353 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:233671146 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:233671146 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:141901975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:141901975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:9765239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:9765239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:151274837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:151274837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48260031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48260031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58605705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58605705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58605716 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58605716 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62223857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62223857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:2802291 G>A maps to ENST00000407653 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:2802291 G>A maps to ENST00000407653 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:36246000 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:36246000 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:167026682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:167026682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:167054396 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:167054396 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:94086339 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:94086339 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:157367603 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:157367603 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:46988586 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:46988586 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:131514478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:131514478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47843940 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47843940 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:11774235 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:11774235 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:87676134 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:87676134 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:94516392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:94516392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:101878725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:101878725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:3011338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:3011338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:88582863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:88582863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:42895125 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:42895125 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:106039062 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:106039062 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:89984311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:89984311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:108635131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:108635131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:21733136 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:21733136 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:54403865 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:54403865 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:18675916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:18675916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:18816422 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:18816422 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:50540393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:50540393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:45472821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:45472821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:42734464 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:42734464 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30135771 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30135771 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:55364114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:55364114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:74646042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:74646042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:74647474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:74647474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:43292475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:43292475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:179044501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:179044501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67469788 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67469788 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:120050338 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:120050338 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:145532726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:145532726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:56553573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:56553573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:102550062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:102550062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:64682617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:64682617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:20385629 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:20385629 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113779909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113779909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:147929616 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:147929616 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:21441091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:21441091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:99465259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:99465259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:47120760 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:47120760 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:130410792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:130410792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:18704874 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:18704874 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37985578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37985578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37991414 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37991414 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:117875167 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:117875167 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:52109150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:52109150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:102642744 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:102642744 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:136674588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:136674588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:37529573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:37529573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:35874436 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:35874436 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:166904753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:166904753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4892927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4892927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30791744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30791744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:121550901 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:121550901 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156813304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156813304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7174522 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7174522 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:19701530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:19701530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:62072490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:62072490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:32981420 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:32981420 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42451937 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42451937 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:182360067 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:182360067 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:31424104 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:31424104 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:31336129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:31336129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123857392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123857392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124160707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124160707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40271500 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40271500 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:65486699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:65486699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7830954 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7830954 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:73819639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:73819639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:19190144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:19190144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:21485227 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:21485227 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:88658509 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:88658509 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:178546228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:178546228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:178560423 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:178560423 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:178978294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:178978294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:18112228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:18112228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67328198 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67328198 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:45768720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:45768720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:53240090 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:53240090 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:126085335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:126085335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:27789113 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:27789113 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:55356072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:55356072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:19446586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:19446586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:57139533 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:57139533 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:24762153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:24762153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94087357 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94087357 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94101079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94101079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94158367 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94158367 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94158369 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94158369 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:111585260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:111585260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:241689975 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:241689975 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:39581215 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:39581215 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170004720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170004720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55264077 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55264077 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55272228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55272228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55330260 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55330260 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55351291 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55351291 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:126319105 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:126319105 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:126587278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:126587278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:42986734 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:42986734 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:87782150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:87782150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51512619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51512619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:134981820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:134981820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:66033132 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:66033132 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:32631612 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:32631612 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45741487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45741487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39661805 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39661805 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:52708821 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:52708821 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:31744595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:31744595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39382868 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39382868 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:130373905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:130373905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:130413886 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:130413886 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:48962425 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:48962425 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:129571160 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:129571160 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:49159113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:49159113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:209800172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:209800172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:34046313 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:34046313 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:36995370 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:36995370 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:169689933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:169689933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:103870534 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:103870534 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:88441071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:88441071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153176982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153176982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:65634919 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:65634919 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54969197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54969197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:189682017 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:189682017 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:189687172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:189687172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:66031413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:66031413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:40195185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:40195185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:40200006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:40200006 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71974359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71974359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:180241233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:180241233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48668714 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48668714 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55106097 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55106097 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54799935 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54799935 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54783586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54783586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55177261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55177261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:50586216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:50586216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:58834725 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:58834725 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156100241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156100241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:132124472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:132124472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:148004979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:148004979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:62722053 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:62722053 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:62758161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:62758161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151412263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151412263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151729383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151729383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:25495465 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:25495465 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:46586800 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:46586800 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:70502325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:70502325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:70542016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:70542016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:169551048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:169551048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:130221255 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:130221255 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:115775891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:115775891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:116163700 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:116163700 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:255974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:255974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235950675 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235950675 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:39913053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:39913053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:119509841 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:119509841 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:43628481 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:43628481 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:172928627 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:172928627 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:67532303 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:67532303 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61769309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61769309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:39106963 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:39106963 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:47950522 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:47950522 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:32706834 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:32706834 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:164854127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:164854127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:220800171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:220800171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57881805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57881805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:20126578 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:20126578 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:94259619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:94259619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:16689249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:16689249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:15014502 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:15014502 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:37187051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:37187051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:29772462 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:29772462 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:60512534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:60512534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:18389200 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:18389200 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:89129074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:89129074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71785927 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71785927 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:108836922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:108836922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:37710286 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:37710286 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66206351 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66206351 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:36476729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:36476729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:179306651 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:179306651 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151733197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151733197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151733895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151733895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125042900 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125042900 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:56686793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:56686793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74435016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74435016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:31234282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:31234282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:63444360 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:63444360 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:11167223 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:11167223 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:7889565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:7889565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237016120 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237016120 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237026644 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237026644 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237026666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237026666 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:8998457 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:8998457 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9012758 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9012758 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:77773202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:77773202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81110805 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81110805 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:15835206 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:15835206 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10224828 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10224828 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:108209096 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:108209096 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10436511 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10436511 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10440956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10440956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10443488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10443488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:23902516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:23902516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:36680074 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:36680074 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:3253493 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:3253493 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:111353638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:111353638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:27414223 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:27414223 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26166212 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26166212 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26388534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26388534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:59528894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:59528894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:26500757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:26500757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:47365422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:47365422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:47432747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:47432747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:3089130 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:3089130 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:69956532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:69956532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:47900663 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:47900663 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62836859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62836859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:48585258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:48585258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:40144543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:40144543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:88628827 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:88628827 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:89903344 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:89903344 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:71201770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:71201770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:78334063 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:78334063 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:15608699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:15608699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:16935410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:16935410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:16942588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:16942588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113078159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113078159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:106509317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:106509317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:71060481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:71060481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:124884986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:124884986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55418210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55418210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55418213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55418213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:41318240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:41318240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:80122413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:80122413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:119059420 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:119059420 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:240933653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:240933653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152496660 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152496660 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152581592 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152581592 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152586091 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152586091 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:72740797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:72740797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:20965450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:20965450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:21306013 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:21306013 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:24845335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:24845335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:63769245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:63769245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56307302 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56307302 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56307652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56307652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56372973 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56372973 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30485748 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30485748 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:26115995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:26115995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:32166192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:32166192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:36339820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:36339820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:34874132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:34874132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:108508706 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:108508706 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:83992193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:83992193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:84446264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:84446264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:6007027 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:6007027 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64453030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64453030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:79276600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:79276600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:79947243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:79947243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:93795219 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:93795219 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:131720971 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:131720971 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:132123250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:132123250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:88575884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:88575884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:71747045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:71747045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:133044496 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:133044496 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:97616281 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:97616281 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:167642020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:167642020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:183652318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:183652318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:78431304 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:78431304 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:161953394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:161953394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125240298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125240298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248099477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248099477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248166473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248166473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248246906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248246906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248458929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248458929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:3323848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:3323848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22333005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22333005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:55682072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:55682072 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:31298756 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:31298756 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21771696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21771696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:146077053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:146077053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56506583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56506583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:101724570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:101724570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:55104099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:55104099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:55104113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:55104113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:6737822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:6737822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:97018783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:97018783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176740405 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176740405 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176801618 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:176801618 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:205986259 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:205986259 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:122269753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:122269753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:102562534 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:102562534 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:102562589 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:102562589 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:102566379 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:102566379 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:91368763 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:91368763 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:4972443 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:4972443 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:5205816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrY:5205816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:67748667 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:67748667 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:24568633 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:24568633 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:233353741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:233353741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:71570073 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:71570073 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66633599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66633599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31833886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31833886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31920546 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31920546 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31981118 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31981118 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:144866041 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:144866041 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:149311867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:149311867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:95394455 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:95394455 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:76640516 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:76640516 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:54879917 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:54879917 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:39918814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:39918814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:56645016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:56645016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8048329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8048329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:152682229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:152682229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7550710 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7550710 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:230459396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:230459396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:230486862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:230486862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:27240792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:27240792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:79707402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:79707402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:111631901 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:111631901 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44006030 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44006030 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:13336599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:13336599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:98392714 G>A maps to ENST00000371109 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:98392714 G>A maps to ENST00000371109 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8784870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8784870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:22828727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:22828727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:130842170 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:130842170 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:81145700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:81145700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:137243383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:137243383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:88959368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:88959368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51483814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51483814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51881203 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51881203 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:125299687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:125299687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:32945338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:32945338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:28829474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:28829474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96014175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96014175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96018494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96018494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:131955101 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:131955101 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:146323145 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:146323145 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:48464793 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:48464793 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:129281582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:129281582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190656498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190656498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190729093 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190729093 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:68389808 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:68389808 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7618739 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7618739 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:140374732 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:140374732 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:24721504 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:24721504 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:24761546 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:24761546 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:121017277 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:121017277 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:43211892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:43211892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:16287122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:16287122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:74853129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:74853129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:76812710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:76812710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81657180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81657180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81735155 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81735155 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81758914 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:81758914 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:82089986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:82089986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49632047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49632047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:4953796 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:4953796 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:146435095 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:146435095 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:146435113 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:146435113 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:135745968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:135745968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:135768022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:135768022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:63851086 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:63851086 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:244857803 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:244857803 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:23523498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:23523498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:186280778 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:186280778 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:57431367 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:57431367 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:57484090 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:57484090 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:57487234 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:57487234 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:49398152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:49398152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:49412550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:49412550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:23942895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:23942895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:23966451 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:23966451 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:24105637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:24105637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:24231530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:24231530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54387574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:54387574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:2006561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:2006561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:30115097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:30115097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:35069107 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:35069107 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:35069109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:35069109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:20413654 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:20413654 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:5283424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:5283424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:45583382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:45583382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:150316591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:150316591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:50029452 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:50029452 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:36424835 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:36424835 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:2763992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:2763992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:43375846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:43375846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:90735689 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:90735689 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54152905 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54152905 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:86333331 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:86333331 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:86363606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:86363606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:98242079 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:98242079 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:117492295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:117492295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:27288604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:27288604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:70946399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:70946399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:8523672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:8523672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:128312055 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:128312055 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:157366969 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:157366969 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40979254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40979254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:41090811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:41090811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:41630771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:41630771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:52384892 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:52384892 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64517793 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64517793 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:163876580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:163876580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:122291592 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:122291592 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136418791 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136418791 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136418804 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136418804 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:135851080 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:135851080 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:135884267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:135884267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:220427240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:220427240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:5271831 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:5271831 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:114390334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:114390334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:120428433 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:120428433 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:68935685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:68935685 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:95479851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:95479851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:20447415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:20447415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67763740 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:67763740 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:173782497 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:173782497 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:173879383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:173879383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:204312897 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:204312897 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63306869 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63306869 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63313775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63313775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:178414923 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:178414923 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:178423842 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:178423842 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:114400033 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:114400033 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:50107847 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:50107847 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:43940737 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:43940737 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:31887271 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:31887271 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:73647226 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:73647226 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:79312793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:79312793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:79385936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:79385936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:139238639 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:139238639 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:186507925 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:186507925 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:32596099 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:32596099 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:109693842 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:109693842 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:101117510 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:101117510 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:116277142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:116277142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:72751214 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:72751214 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:72944961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:72944961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240933568 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240933568 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240933889 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240933889 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:241083183 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:241083183 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:63173838 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:63173838 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:63174085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:63174085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:49574637 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:49574637 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:30538049 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:30538049 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:33482906 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:33482906 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:12800610 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:12800610 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105017427 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105017427 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105256933 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105256933 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105261113 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105261113 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:87096064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:87096064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:87315067 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:87315067 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:33410992 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:33410992 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:152130564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:152130564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90077750 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90077750 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90087610 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90087610 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:36466705 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:36466705 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237906993 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:237906993 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:33928133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:33928133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:92730577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:92730577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:153830578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:153830578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55748240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55748240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:100598281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:100598281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:200245282 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:200245282 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:158842266 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:158842266 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38951720 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38951720 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:9096193 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:9096193 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:100728091 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:100728091 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50266422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50266422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:71394402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:71394402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:30866363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:30866363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:121671720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:121671720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:13380834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:13380834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:55872909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:55872909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:242283118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:242283118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:42382124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:42382124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:150263590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:150263590 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:173881235 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:173881235 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:167182920 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:167182920 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:180013967 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:180013967 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:42281813 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:42281813 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:42281874 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:42281874 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:9515235 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:9515235 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:65474475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:65474475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48245234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48245234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:67108563 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:67108563 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:67109128 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:67109128 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:82331393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:82331393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:82369321 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:82369321 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:148388384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:148388384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:18233859 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:18233859 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:72822595 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:72822595 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51647653 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51647653 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51629226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:51629226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:36181811 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:36181811 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:51394077 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:51394077 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:48539033 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:48539033 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124854795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124854795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:25776764 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:25776764 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:22396297 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:22396297 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:119014664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:119014664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63066982 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63066982 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38317319 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38317319 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:116609590 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:116609590 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:19702037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:19702037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156170304 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:156170304 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107350489 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107350489 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:205886344 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:205886344 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153751427 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153751427 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:118147692 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:118147692 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:115923692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:115923692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:150677978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:150677978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:43963357 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:43963357 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:47182431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:47182431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69924954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:69924954 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:220505492 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:220505492 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:31498803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:31498803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:108618156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:108618156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:170216425 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:170216425 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:40342374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:40342374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:40438528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:40438528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:111873978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:111873978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:20890031 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:20890031 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:101599296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:101599296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33750095 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33750095 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168139249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168139249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168250561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168250561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:84453528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:84453528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105781739 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:105781739 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:47705005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:47705005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:17897307 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:17897307 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:70352838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:70352838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:70477402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:70477402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:88392938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:88392938 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:43381715 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:43381715 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:70121063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:70121063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:70123541 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:70123541 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:51095741 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:51095741 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:51314967 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:51314967 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:51664697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:51664697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:122161711 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:122161711 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:107005425 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:107005425 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:121347387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:121347387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:121414161 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:121414161 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:121448207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:121448207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:24661185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:24661185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:231331599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:231331599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:231367692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:231367692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:20826441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:20826441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:20826591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:20826591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:118530428 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:118530428 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:118634395 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:118634395 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:22676709 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:22676709 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:52825496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:52825496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:24585621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:24585621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:217934703 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:217934703 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:52917721 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:52917721 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:28986804 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:28986804 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4349545 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4349545 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:167655999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:167655999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:167658771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:167658771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153012867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153012867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153085329 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:153085329 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158618180 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158618180 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:45773988 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:45773988 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:45801719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:45801719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:45801958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:45801958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:30721879 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:30721879 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64505789 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64505789 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:112197007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:112197007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:28011470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:28011470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155981680 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155981680 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:53055628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:53055628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:74622256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:74622256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:74623084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:74623084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:104031752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:104031752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37815243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37815243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:191850244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:191850244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56740465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56740465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:191894686 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:191894686 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63967897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:63967897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:125465806 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:125465806 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:59549121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:59549121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:53076911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:53076911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:70513115 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:70513115 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:45021738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:45021738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:58461891 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:58461891 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:15219029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:15219029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:64635581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:64635581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:85422403 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:85422403 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:123976042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:123976042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61678724 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61678724 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29992975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29992975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29994047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29994047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:33455210 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:33455210 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:122634760 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:122634760 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:125527930 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:125527930 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:10318035 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:10318035 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:10318218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:10318218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:28887554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:28887554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:13288653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:13288653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:79278799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:79278799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:59543334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:59543334 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:139516552 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:139516552 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62703588 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62703588 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:145851018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:145851018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:134210429 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:134210429 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:134210518 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:134210518 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:133482070 T>C maps to ENST00000395029 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:133482070 T>C maps to ENST00000395029 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:104470693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:104470693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:12951948 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:12951948 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20858995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20858995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:75688084 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:75688084 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:92182367 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:92182367 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:2298207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:2298207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:2376131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:2376131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:133925224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:133925224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:24321530 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:24321530 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:24357993 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:24357993 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:24013154 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:24013154 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:114018392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:114018392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:70342661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:70342661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:82333934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:82333934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:166964633 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:166964633 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:81638859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:81638859 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140021705 G>A maps to ENST00000505086 *188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140021705 G>A maps to ENST00000505086 *188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:60687407 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:60687407 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:10018616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:10018616 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:44287725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:44287725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:159162564 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:159162564 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:202977008 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:202977008 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100270783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100270783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:94807630 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:94807630 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:28643835 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:28643835 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:68964803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:68964803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:170945763 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:170945763 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:171131190 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:171131190 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:9435688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:9435688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:218696382 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:218696382 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:25639968 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:25639968 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:224009296 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:224009296 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:144288447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:144288447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:186291609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:186291609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:20067055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:20067055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:10970462 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:10970462 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:10971896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:10971896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30366576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30366576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:202277617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:202277617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:17195665 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:17195665 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:110131135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:110131135 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:14293247 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:14293247 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:14390524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:14390524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:126329796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:126329796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:72975640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:72975640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:142611888 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:142611888 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:98565098 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:98565098 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:18541229 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:18541229 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:51610469 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:51610469 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:120480007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:120480007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:58140070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:58140070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:138833139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:138833139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:33037792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:33037792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:147737769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:147737769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:76201684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:76201684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179408910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179408910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179517628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179517628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179558564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179558564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179568767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179568767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179611123 C>A maps to ENST00000375038 E5337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179611123 C>A maps to ENST00000375038 E5337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:57594519 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:57594519 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22836189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22836189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:158910769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:158910769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:139568922 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:139568922 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:104742005 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:104742005 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109927831 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109927831 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:103372759 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:103372759 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134406103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134406103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70503718 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70503718 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70503722 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70503722 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:69874925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:69874925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70070020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70070020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:17785581 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:17785581 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33486594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33486594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33513715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33513715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:73053061 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:73053061 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:96222723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:96222723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:96222904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:96222904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:35579562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:35579562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:52605335 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:52605335 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:30205383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:30205383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:106761590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:106761590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:171678785 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:171678785 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:136804087 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:136804087 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:2652661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:2652661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12342739 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12342739 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:150064255 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:150064255 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184567654 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184567654 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:22128197 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:22128197 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124015772 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124015772 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:215278869 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:215278869 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:6058393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:6058393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:6140545 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:6140545 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:6145516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:6145516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:167254857 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:167254857 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74650565 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74650565 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:74999730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:74999730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:43664146 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:43664146 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190333383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190333383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:54603240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:54603240 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:25621390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:25621390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:128895081 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chrX:128895081 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:180775799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:180775799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44057907 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44057907 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:216986776 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:216986776 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:17292309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:17292309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:1268400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:1268400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46537854 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46537854 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46594532 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46594532 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:72863673 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:72863673 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:32397492 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:32397492 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:25264187 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:25264187 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:75184306 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:75184306 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:38107608 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:38107608 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:146112183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:146112183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:53302074 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:53302074 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:43433247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:43433247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:95841924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:95841924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:72352848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:72352848 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:44540960 C>T maps to ENST00000436261 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:44540960 C>T maps to ENST00000436261 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:57200096 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:57200096 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:22817172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:22817172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:38283490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:38283490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58262131 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58262131 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:68427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:68427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:35260599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:35260599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58499574 C>A maps to NM_025027.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58499574 C>A maps to NM_025027.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:20806809 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:20806809 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:71625916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:71625916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:81709417 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:81709417 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:101850233 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:101850233 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:71542448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:71542448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58556385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58556385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58556724 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58556724 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58564015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58564015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56832240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:56832240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:94505586 T>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:94505586 T>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr5:5237073 T>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr5:5237073 T>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:97694492 T>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:97694492 T>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:33138951 A>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:33138951 A>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr16:88776694 G>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr16:88776694 G>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr16:90020795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr16:90020795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:33173932 T>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:33173932 T>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr13:48953790 G>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr13:48953790 G>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:79350261 A>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:79350261 A>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:88773811 T>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:88773811 T>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr20:590587 G>A maps to NM_004609.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr20:590587 G>A maps to NM_004609.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:72935135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:72935135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:7102180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:7102180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:9264831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:9264831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:48349978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:48349978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:67290750 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:67290750 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:87179628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:87179628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:20698687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:20698687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:43621891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:43621891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:148610149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:148610149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:107781676 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:107781676 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:156787267 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:156787267 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:20563399 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:20563399 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:179291294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:179291294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:156917306 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:156917306 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:207395808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:207395808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:207424572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:207424572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33662248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33662248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33686503 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33686503 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33804064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33804064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33811737 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33811737 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:130331581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:130331581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:77323001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:77323001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7606704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7606704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7711770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7711770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7773316 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7773316 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:12367252 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:12367252 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:86726134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:86726134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:87572182 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:87572182 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:50312192 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:50312192 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:109677670 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:109677670 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:109859904 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:109859904 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:134225942 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:134225942 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:73635923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:73635923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33989620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33989620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33997333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33997333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:113267004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:113267004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:124714863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:124714863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:36763781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:36763781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:72410245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:72410245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:161022212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:161022212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:144068248 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:144068248 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:46298924 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:46298924 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:34627565 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:34627565 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:49017946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:49017946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:13407082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:13407082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:94927394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:94927394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:95141821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:95141821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176905589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176905589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176952052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176952052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176979454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176979454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:120169141 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:120169141 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:51207726 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:51207726 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:160059450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:160059450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:25262359 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:25262359 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:192997141 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:192997141 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:193081240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:193081240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160151863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160151863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:42416848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:42416848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:11078573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:11078573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:11096880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:11096880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:69984380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:69984380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:11413052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:11413052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:40397990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:40397990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:112962541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:112962541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:198621114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:198621114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:31627966 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:31627966 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:92433650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:92433650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:40607684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:40607684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26501499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26501499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56395575 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56395575 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:4594489 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:4594489 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:33622061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:33622061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:108302426 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:108302426 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:43363035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:43363035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:103346663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:103346663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:30873050 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:30873050 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:40829853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:40829853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:22987945 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:22987945 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:75086358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:75086358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:55134628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:55134628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:178489485 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:178489485 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:32790949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:32790949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:45598865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:45598865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:26644335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:26644335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:31964183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:31964183 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:100434813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:100434813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:172507768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:172507768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:165714109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:165714109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:39078266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:39078266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:170158817 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:170158817 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:40193667 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:40193667 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:86250681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:86250681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:201035343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:201035343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:159169501 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:159169501 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:27460508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:27460508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:44148426 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:44148426 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:110495772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:110495772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:105010673 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:105010673 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:104954312 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:104954312 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160160847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160160847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:105464724 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:105464724 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:219900483 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:219900483 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:109455613 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:109455613 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179710524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179710524 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:34324761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:34324761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:38457306 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:38457306 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:83430494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:83430494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:58571577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:58571577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:68720493 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:68720493 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:31287108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:31287108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:45033479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:45033479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:13096058 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:13096058 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:95286264 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:95286264 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:55844109 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:55844109 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:196918926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:196918926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:71570495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:71570495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:46765562 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:46765562 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:33663465 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:33663465 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:96229428 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:96229428 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:190127676 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:190127676 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:6979877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:6979877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:141331871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:141331871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:45922771 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:45922771 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:10594645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:10594645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:150644578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:150644578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:19245393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:19245393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:88365806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:88365806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:87669834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:87669834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:87680163 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:87680163 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:58608823 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:58608823 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:99632085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:99632085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:147014486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:147014486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:147097177 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:147097177 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:75892693 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:75892693 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:32119683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:32119683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:70850766 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:70850766 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:70875815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:70875815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:55939085 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:55939085 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:139889970 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:139889970 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:109820388 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:109820388 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:110222761 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:110222761 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:10103897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:10103897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47643886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47643886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47840027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47840027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:207886086 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:207886086 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:43907956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:43907956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:36692017 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:36692017 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:5853584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:5853584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:61950766 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:61950766 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114111192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114111192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114290946 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114290946 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114389118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114389118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:30910672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:30910672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:11564999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:11564999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:17169793 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:17169793 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:35938203 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:35938203 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:52774205 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:52774205 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:41395228 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:41395228 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:41518744 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:41518744 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:47515296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:47515296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:57973303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:57973303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:58771953 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:58771953 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:72131077 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:72131077 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10683614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10683614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:122012346 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:122012346 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:172314343 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:172314343 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:117853330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:117853330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:74596200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:74596200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:66033885 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:66033885 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:19370006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:19370006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:68943011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:68943011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:137359457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:137359457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:60707039 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:60707039 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:47924224 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:47924224 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:47961606 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:47961606 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:111909914 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:111909914 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:35989561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:35989561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:118479491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:118479491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:21659515 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:21659515 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:21723697 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:21723697 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:13701266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:13701266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:38754732 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:38754732 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:11514370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:11514370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:12989464 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:12989464 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:101654699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:101654699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:169423204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:169423204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:67365912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:67365912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:34982155 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:34982155 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:64045435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:64045435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:64045544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:64045544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:39448556 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:39448556 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:28956808 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:28956808 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:30451842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:30451842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:44703979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:44703979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:96285431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:96285431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:93285294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:93285294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:43995880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:43995880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:55268195 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:55268195 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:78109998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:78109998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:73474516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:73474516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:225702734 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:225702734 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:71497730 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:71497730 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:66439676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:66439676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:22915264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:22915264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:220205973 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:220205973 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:60240851 G>A maps to ENST00000426742 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:60240851 G>A maps to ENST00000426742 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:158178305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:158178305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:138191064 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:138191064 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:122731323 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:122731323 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:64567626 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:64567626 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:64814207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:64814207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:6160249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:6160249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:61065718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:61065718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:74409457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:74409457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:85135970 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:85135970 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7863199 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:7863199 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:127680324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:127680324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:100188003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:100188003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:153273504 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:153273504 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:157772057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:157772057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:157740548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:157740548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:157668026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:157668026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:159768574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:159768574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:159778369 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:159778369 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:102454330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:102454330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:59978162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:59978162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:34205812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:34205812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:60982675 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:60982675 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:142481001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:142481001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:240308544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:240308544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:171162463 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:171162463 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:29237974 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:29237974 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:190871010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:190871010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:168465831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:168465831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:131231469 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:131231469 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:32757013 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:32757013 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:53799835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:53799835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:101370110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:101370110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:161324515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:161324515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:97744291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:97744291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:110745617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:110745617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:89654509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:89654509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95262488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95262488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:61958528 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:61958528 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:42582563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:42582563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:3589995 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:3589995 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:147245699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:147245699 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:58604936 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:58604936 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:155615688 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:155615688 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:6952884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:6952884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:155784038 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:155784038 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:94611540 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:94611540 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:119957036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:119957036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123468936 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123468936 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123469694 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123469694 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:94416651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:94416651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:120838159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:120838159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:48855785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:48855785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:119748250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:119748250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:110211871 G>C maps to ENST00000369830 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:110211871 G>C maps to ENST00000369830 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:110198976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:110198976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:106842436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:106842436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:240097898 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:240097898 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:31856242 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:31856242 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:43563332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:43563332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:43581636 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:43581636 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:81366032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:81366032 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:191136790 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:191136790 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:71128268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:71128268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:176308278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:176308278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:32522358 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:32522358 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:186107182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:186107182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26545804 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26545804 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:70098867 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:70098867 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:42829231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:42829231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:46673519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:46673519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:100249960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:100249960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:26132919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:26132919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:122928360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:122928360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:70897627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:70897627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:71094280 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:71094280 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:68673759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:68673759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:29686656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:29686656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:29973109 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:29973109 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:207073584 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:207073584 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:39788989 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:39788989 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35876650 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35876650 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:110978089 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:110978089 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:111024330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:111024330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:62367222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:62367222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:201837745 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:201837745 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:91030664 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:91030664 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:78763030 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:78763030 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:128588437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:128588437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:85936526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:85936526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:50683307 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:50683307 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:145537866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:145537866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:6055930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:6055930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:120166284 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:120166284 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:163696182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:163696182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:20852134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:20852134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:215345552 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:215345552 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36698134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36698134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36768277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36768277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:53223191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:53223191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:62900946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:62900946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:123229063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:123229063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95507082 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95507082 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:5763882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:5763882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:20946564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:20946564 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:200973726 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:200973726 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:7829760 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:7829760 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:51533925 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:51533925 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:51322428 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:51322428 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:52794251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:52794251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:52757812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:52757812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:52698610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:52698610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:129250774 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:129250774 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:129805965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:129805965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:107732892 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:107732892 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:108999218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:108999218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:189691578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:189691578 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:48919067 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:48919067 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:48958238 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:48958238 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:28635256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:28635256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:18145076 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:18145076 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:197701874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:197701874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:165182621 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:165182621 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:148176198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:148176198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:62812909 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:62812909 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:188124212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:188124212 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:40439966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:40439966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:42220069 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:42220069 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:42355792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:42355792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:25232545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:25232545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:150164030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:150164030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141135676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141135676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141283651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141283651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141441492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141441492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:25098976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:25098976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:151304176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:151304176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:26211919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:26211919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:26073288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:26073288 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:68065132 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:68065132 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:102486714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:102486714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:48190904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:48190904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10423298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10423298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:182763142 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:182763142 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:90371105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:90371105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:131917628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:131917628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:41719205 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:41719205 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:15692478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:15692478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:86383168 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:86383168 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:53491504 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:53491504 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:154889819 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:154889819 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:102713682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:102713682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:67799810 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:67799810 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:18158600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:18158600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:24415198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:24415198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:60559881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:60559881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:68506351 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:68506351 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:74207358 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:74207358 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:100527853 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:100527853 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:9016504 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:9016504 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:49399586 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:49399586 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:49409508 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:49409508 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:42311267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:42311267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:23884724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:23884724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:26184658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:26184658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:171034772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:171034772 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:171458601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:171458601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:76841709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:76841709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:35622686 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:35622686 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:71082318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:71082318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:55421558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:55421558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:132980042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:132980042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:161180181 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:161180181 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:20699738 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:20699738 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:70417869 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:70417869 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:47156702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:47156702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:204873440 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:204873440 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:103534468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:103534468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:52511763 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:52511763 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:232392701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:232392701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:34095269 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:34095269 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:110883157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:110883157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:206641177 C>T maps to NM_018534.3 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:206641177 C>T maps to NM_018534.3 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:50850775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:50850775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:152037204 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:152037204 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:131350898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:131350898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:131723549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:131723549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:131818016 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:131818016 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:132098670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:132098670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:132187789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:132187789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:132205041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:132205041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:88576313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:88576313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:45553202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:45553202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:118015117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:118015117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:101623621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:101623621 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:228543939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:228543939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:95147853 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:95147853 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:15115234 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:15115234 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:53602861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:53602861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:88420996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:88420996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:125274124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:125274124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:55578880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:55578880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:56381040 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:56381040 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:57815807 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:57815807 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:58112602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:58112602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:76777906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:76777906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:21739469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:21739469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:20234285 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:20234285 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:17586047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:17586047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:6742739 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:6742739 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176501790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176501790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176608348 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176608348 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176779050 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:176779050 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:25024056 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:25024056 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:102522682 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:102522682 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:31823442 T>C maps to NM_001604.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:31823442 T>C maps to NM_001604.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:55780236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:55780236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:57024857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:57024857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:17290558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:17290558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:178635367 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:178635367 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:32282596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:32282596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:54954009 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:54954009 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156873716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156873716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:92120952 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:92120952 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:97891897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:97891897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:58248678 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:58248678 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:26881092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:26881092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:99964557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:99964557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:130839067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:130839067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:46680135 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:46680135 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:9453572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:9453572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:9457270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:9457270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:242355197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:242355197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:242355219 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:242355219 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:242511369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:242511369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:38803789 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:38803789 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:131831475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:131831475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:131947567 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:131947567 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:6031559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:6031559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:68385363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:68385363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:42210133 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:42210133 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:121212996 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:121212996 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:75552588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:75552588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:15013640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:15013640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:23814840 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:23814840 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:93389660 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:93389660 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:94740707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:94740707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:146087110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:146087110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:100056532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:100056532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:47248784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:47248784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:47412649 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:47412649 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:68950331 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:68950331 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:64132469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:64132469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:57420201 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:57420201 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:57480975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:57480975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:655855 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:655855 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:48805956 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:48805956 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:20529994 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:20529994 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:142459926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:142459926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:142460071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:142460071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:227079329 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:227079329 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:127174491 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:127174491 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:117505558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:117505558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:128298009 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:128298009 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:40730640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:40730640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:41180289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:41180289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:13386049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:13386049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:103136874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:103136874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:103163669 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:103163669 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:204126463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:204126463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:241083223 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:241083223 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:241262107 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:241262107 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:46793056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:46793056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:129247965 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:129247965 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:87016654 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:87016654 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:87896570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:87896570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:104323710 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:104323710 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:78710148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:78710148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:124757412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:124757412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:68898290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:68898290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:15162157 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:15162157 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:11940534 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:11940534 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:43892923 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:43892923 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:57264752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:57264752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:158178687 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:158178687 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:237617676 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:237617676 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:84791495 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:84791495 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:147885380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:147885380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:50854594 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:50854594 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:190157 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:190157 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:13856805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:13856805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:151339451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:151339451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:9356882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:9356882 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:122679798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:122679798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:13378429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:13378429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:95053669 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:95053669 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61377382 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61377382 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61468322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61468322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:51915549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:51915549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:26643920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:26643920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:26691845 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:26691845 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:36982410 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:36982410 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:120914477 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:120914477 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:40863652 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:40863652 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:148384188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:148384188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:91689955 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:91689955 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:100862013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:100862013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:164777879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:164777879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:54652277 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:54652277 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:42897147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:42897147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:19398753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:19398753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:37157254 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:37157254 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:108728432 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:108728432 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:128665812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:128665812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:85478467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:85478467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:9910057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:9910057 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:8421088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:8421088 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:170214315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:170214315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:40387814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:40387814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:143140228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:143140228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:20619042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:20619042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:128631000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:128631000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:24143087 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:24143087 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:130934012 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:130934012 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:96953035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:96953035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:1251324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:1251324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:1285283 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:1285283 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:99225508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:99225508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:23797266 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:23797266 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:231174838 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:231174838 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:144336801 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:144336801 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:123946203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:123946203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35641529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35641529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35800280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35800280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:44352466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:44352466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:14195159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:14195159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:14263409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:14263409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:158623220 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:158623220 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43141554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43141554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43146515 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43146515 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:9057433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:9057433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:38023951 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:38023951 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:74077293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:74077293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:40354610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:40354610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:171509830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:171509830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:23883093 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:23883093 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:7175687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:7175687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:31046141 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:31046141 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:75427516 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:75427516 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:113208109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:113208109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:10899006 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:10899006 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:7384965 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:7384965 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:100533133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chrX:100533133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:61369684 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:61369684 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:13374173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:13374173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:27375462 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:27375462 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:102916810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:102916810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:43920715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:43920715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:50808145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:50808145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:137912857 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:137912857 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:44403867 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:44403867 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:8889644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:8889644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:57466501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:57466501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:15427213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:15427213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:108522026 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:108522026 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:23058196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:23058196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:74701273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:74701273 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:175049229 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:175049229 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:175323466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:175323466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:80992707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:80992707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:186296840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:186296840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:41250491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:41250491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:72962972 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:72962972 A>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:101323841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:101323841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:98560276 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:98560276 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:81499214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:81499214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:51869992 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:51869992 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:113236794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:113236794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:138858533 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:138858533 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:15175153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:15175153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:91196222 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:91196222 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179493928 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179493928 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179522281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179522281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:37903123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:37903123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:165877065 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:165877065 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:36066761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:36066761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:43495965 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:43495965 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:33510435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:33510435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:126208047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:126208047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:216370092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:216370092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:179463224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:179463224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:17815374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:17815374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:49828097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:49828097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:6105470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:6105470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:42397320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:42397320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:85687332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:85687332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:44237255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:44237255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:32410742 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:32410742 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:10757076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:10757076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:42554666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:42554666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:98353330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:98353330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:16270074 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:16270074 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:16274777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:16274777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:31816207 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:31816207 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:106767144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:106767144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:123966330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:123966330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:57286983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:57286983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:57650107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:57650107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:44676160 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:44676160 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71743016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71743016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:21217085 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:21217085 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:44101198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:44101198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:27824138 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:27824138 T>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:37428162 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:37428162 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:125987817 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:125987817 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:56901330 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:56901330 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:60049 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:60049 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:66043 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:66043 A>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:238050024 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:238050024 T>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:238052829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:238052829 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:9248425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:9248425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:41107292 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:41107292 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:67178222 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:67178222 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48398819 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48398819 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:94505764 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:94505764 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:67255962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:67255962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:67266919 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:67266919 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:87174080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:87174080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183905812 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183905812 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100489474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100489474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100567508 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100567508 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100657874 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100657874 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:35598836 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:35598836 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:31914063 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:31914063 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:35084574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:35084574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:1569228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:1569228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:78391960 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:78391960 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:7724738 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:7724738 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31126478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31126478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:33559987 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:33559987 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:67366009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:67366009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:147925102 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:147925102 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:100185201 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:100185201 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:86697908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:86697908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:49208587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:49208587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:109674007 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:109674007 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:241814460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:241814460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:247061488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:247061488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:21331141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:21331141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:75540600 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:75540600 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:67433922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:67433922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:165667582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:165667582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:94597858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:94597858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:112025683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:112025683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:858756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:858756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:114199125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:114199125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:74039882 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:74039882 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:33110109 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:33110109 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:100169246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:100169246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:5886663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:5886663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:101436058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:101436058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:242130439 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:242130439 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:201468860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:201468860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:26800879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:26800879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21239531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21239531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:33402118 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:33402118 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:63661441 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:63661441 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:23292131 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:23292131 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:23297702 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:23297702 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:28284139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:28284139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:98509342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:98509342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:101152370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:101152370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:3905690 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:3905690 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:47582618 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:47582618 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:113532724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:113532724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:25273152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:25273152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:114309287 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:114309287 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:117061586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:117061586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:70254729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:70254729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:11028280 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:11028280 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:11066593 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:11066593 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:69665787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:69665787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:215610418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:215610418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:52612284 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:52612284 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:60866223 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:60866223 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:43297681 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:43297681 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:83937068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:83937068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:32940748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:32940748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55814610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55814610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:85933699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:85933699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:88391780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:88391780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:88420920 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:88420920 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:30847128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:30847128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:7743897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:7743897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:247719881 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:247719881 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:12819078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:12819078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:31885543 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:31885543 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:46096248 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:46096248 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:63379980 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:63379980 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:100451128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:100451128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:123776407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:123776407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:60455739 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:60455739 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:165715011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:165715011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:130182434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:130182434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:157731899 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:157731899 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:40193432 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:40193432 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31746729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31746729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:66407052 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:66407052 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:96271982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:96271982 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:115456524 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:115456524 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:49744786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:49744786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:49824822 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:49824822 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:65137393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:65137393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:140954101 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:140954101 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:181480415 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:181480415 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:181690871 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:181690871 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:81601041 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:81601041 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:86063858 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:86063858 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:85628501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:85628501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:41495960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:41495960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219883951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219883951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31682217 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31682217 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:24845698 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:24845698 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:191098602 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:191098602 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:119960636 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:119960636 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:119960832 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:119960832 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:86111670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:86111670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:46401147 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:46401147 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158262719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158262719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158324883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158324883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:7807760 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:7807760 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:35241795 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:35241795 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:60889386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:60889386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:103405934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:103405934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:65015828 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:65015828 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:21802585 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:21802585 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:61761176 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:61761176 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:125850909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:125850909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:15783362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:15783362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:179989051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:179989051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:31915912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:31915912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:87303013 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:87303013 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:26806832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:26806832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40225217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40225217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:141645881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:141645881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:10198303 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:10198303 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68547060 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68547060 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:81735232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:81735232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:87644856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:87644856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:74334798 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:74334798 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:124783391 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:124783391 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:125530304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:125530304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:125530722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:125530722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:75855982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:75855982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70875769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70875769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:139636167 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:139636167 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:189903891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:189903891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70964940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70964940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:71004377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:71004377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:69018087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:69018087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:129950928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:129950928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:83218103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:83218103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:83239915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:83239915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:175305869 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:175305869 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:197411436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:197411436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:25599991 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:25599991 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:3265389 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:3265389 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:4368304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:4368304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:4368308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:4368308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:34401647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:34401647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:34404287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:34404287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:113812549 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:113812549 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:23667548 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:23667548 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:80389759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:80389759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:11833518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:11833518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:43173729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:43173729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219028725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219028725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:40489798 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:40489798 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:41711805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:41711805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:37688632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:37688632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:59727527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:59727527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39824314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39824314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:121929280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:121929280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:43102104 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:43102104 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:155287805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:155287805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:151154060 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:151154060 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:118572236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:118572236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:115079500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:115079500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:100656027 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:100656027 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:80677415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:80677415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:468636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:468636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:96650428 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:96650428 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:124376665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:124376665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:21049054 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:21049054 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:21108871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:21108871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:4496796 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:4496796 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:78471019 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:78471019 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:220250827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:220250827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:225702445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:225702445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:73109546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:73109546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:154544609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:154544609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:64045614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:64045614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:113874678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:113874678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:100497570 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:100497570 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:117647490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:117647490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:311986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:311986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:95457509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:95457509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:103027574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:103027574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:103027576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:103027576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:150482376 C>A maps to ENST00000369049 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:150482376 C>A maps to ENST00000369049 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:184692836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:184692836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:78492185 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:78492185 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:38406349 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:38406349 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:64622370 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:64622370 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:40289270 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:40289270 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:32608337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:32608337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:8056512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:8056512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:37485936 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:37485936 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:111119296 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:111119296 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:143088545 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:143088545 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:96996376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:96996376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:19216679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:19216679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:56270545 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:56270545 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:157067533 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:157067533 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:242024097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:242024097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:45700707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:45700707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:96289346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:96289346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:139489308 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:139489308 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:177156386 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:177156386 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:108272982 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:108272982 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:79627399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:79627399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:124204260 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:124204260 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:170425785 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:170425785 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:112942695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:112942695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:127684912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:127684912 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:125131011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:125131011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:191861775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:191861775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:102902928 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:102902928 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:60133110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:60133110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:72714519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:72714519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:43318480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:43318480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153247050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153247050 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153488719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153488719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:146658948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:146658948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:79430249 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:79430249 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:13838332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:13838332 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:32783374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:32783374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:4323509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:4323509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:39169726 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:39169726 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:160753582 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:160753582 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:26961776 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:26961776 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:26589617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:26589617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:49157762 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:49157762 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9873132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9873132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9923275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9923275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:55224035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:55224035 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:25010972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:25010972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31016972 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:31016972 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:42628973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:42628973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:6553356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:6553356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:58601811 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:58601811 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:4873808 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:4873808 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:16247254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:16247254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:93539993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:93539993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:231406497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:231406497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:131019256 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:131019256 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155737110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155737110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:20334343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:20334343 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:96691483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:96691483 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:157426745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:157426745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:46856004 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:46856004 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:22414752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:22414752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:25886598 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:25886598 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:90074219 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:90074219 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:19873043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:19873043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:94454476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:94454476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:120687900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:120687900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:9923615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:9923615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:14553012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:14553012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:27802671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:27802671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:52622617 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:52622617 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:18748910 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:18748910 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:31597789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:31597789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:124792501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:124792501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:28459690 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:28459690 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:210715172 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:210715172 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:27578106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:27578106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:75171375 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:75171375 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:149858263 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:149858263 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:75104499 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:75104499 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:33095916 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:33095916 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:185815124 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:185815124 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:43299015 C>A maps to NM_002130.6 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:43299015 C>A maps to NM_002130.6 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:179047813 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:179047813 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:46636303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:46636303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:54403563 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:54403563 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:25741876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:25741876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:25741901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:25741901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:122471631 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:122471631 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:74757959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:74757959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48005077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48005077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:21209378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:21209378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:130410806 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:130410806 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:113535488 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:113535488 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:154437509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:154437509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:166925837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:166925837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:99193730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:99193730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:71940605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:71940605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:237253617 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:237253617 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:121536732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:121536732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:91016346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:91016346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:156510716 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:156510716 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:50679353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:50679353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68609578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68609578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:30492919 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:30492919 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124538576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124538576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:24484128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:24484128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:147009370 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:147009370 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124378442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124378442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:75436085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:75436085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:211032937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:211032937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:68171167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:68171167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39284542 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39284542 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39170171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39170171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:78918562 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:78918562 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:79154574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:79154574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:178978030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:178978030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:138648794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:138648794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:196458914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:196458914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:215759828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:215759828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:23397634 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:23397634 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155889691 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155889691 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:24398109 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:24398109 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:94066902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:94066902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:100053561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:100053561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:20926451 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:20926451 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:111585232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:111585232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:149853984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:149853984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39512553 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:39512553 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55284755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55284755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55255150 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55255150 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55270549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55270549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:10603247 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:10603247 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:38925931 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:38925931 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:52682307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:52682307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:129479507 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:129479507 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:129581799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:129581799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:46724987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:46724987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:18380275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:18380275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:48935911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:48935911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:41496509 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:41496509 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:118112439 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:118112439 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:160978733 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:160978733 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:47295727 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:47295727 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:170038132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:170038132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:52864179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:52864179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:25004875 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:25004875 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:14527930 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:14527930 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:15866483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:15866483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:166990295 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:166990295 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:65342807 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:65342807 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:77824487 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:77824487 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:77973370 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:77973370 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:71482762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:71482762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:161527751 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:161527751 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:36104166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:36104166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:57921445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:57921445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:94417211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:94417211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:47670032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:47670032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:68709048 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:68709048 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:131900173 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:131900173 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:42159103 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:42159103 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:95889042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:95889042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:47042366 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:47042366 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:151949530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:151949530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:21977376 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:21977376 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:89339534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:89339534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:56231218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:56231218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44645079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44645079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108819464 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108819464 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:56670473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:56670473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:56704487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:56704487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:86582040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:86582040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:100699663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:100699663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:195485922 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:195485922 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:74684145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:74684145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:203139615 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:203139615 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108158554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108158554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108179229 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108179229 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108212236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:108212236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:10426758 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:10426758 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:23884151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:23884151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:10305167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:10305167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:36708088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:36708088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:16670538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:16670538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:52645750 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:52645750 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:72195608 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:72195608 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:17742351 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:17742351 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:69955311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:69955311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:89903212 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:89903212 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:174777302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:174777302 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:78570898 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:78570898 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:16905277 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:16905277 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:16905279 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:16905279 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:120385042 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:120385042 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:54928368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:54928368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:133733462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:133733462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:23931340 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:23931340 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:97334180 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:97334180 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:20959282 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:20959282 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:21125784 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:21125784 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:45072973 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:45072973 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:74705505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:74705505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:204915660 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:204915660 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:125076565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:125076565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:63191351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:63191351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:32786463 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:32786463 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:34898865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:34898865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:107834656 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:107834656 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:206590916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:206590916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:44819127 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:44819127 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:131727981 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:131727981 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9066030 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9066030 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:88670298 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:88670298 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:101090889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:101090889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113354603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113354603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:161969893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:161969893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:193382644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:193382644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:132643465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:132643465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:248247389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:248247389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:22332440 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:22332440 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:55889755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:55889755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:57877013 C>T maps to ENST00000357944 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:57877013 C>T maps to ENST00000357944 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:241078846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:241078846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:32058089 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:32058089 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:9524929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:9524929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:9721971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:9721971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:124483028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:124483028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:39575843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:39575843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:176734713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:176734713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:176740339 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:176740339 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:162851312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:162851312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:102584615 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:102584615 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:36942389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:36942389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:91369419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:91369419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:55664981 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:55664981 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:233158233 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:233158233 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:66379145 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:66379145 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:103797616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:103797616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:55153525 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:55153525 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:148708855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:148708855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:13940301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:13940301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:31700410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:31700410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:41900184 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:41900184 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:65114325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:65114325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44047450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44047450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:18511588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:18511588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:142829447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:142829447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:15473960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:15473960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:51556978 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:51556978 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:201287685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:201287685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:74340459 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:74340459 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:121228643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:121228643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:19563547 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:19563547 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:39246892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:39246892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:122280405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:122280405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:81747224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:81747224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:30572713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:30572713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:45899587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:45899587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:129785791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:129785791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:186269352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:186269352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:57343117 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:57343117 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:68872883 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:68872883 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153512974 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153512974 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:50029565 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:50029565 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:120009916 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:120009916 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:36422578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:36422578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:2871298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:2871298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:43514676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:43514676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:1098706 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:1098706 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:86363712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:86363712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:16553327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:16553327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:28123113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:28123113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:232577106 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:232577106 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:6879552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:6879552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:70928552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:70928552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:70988238 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:70988238 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:8493158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:8493158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:40980620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:40980620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:41324901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:41324901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:52370306 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:52370306 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:27815929 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:27815929 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:174926949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:174926949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:174945134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:174945134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:5924713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:5924713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:22165306 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:22165306 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:22184649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:22184649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:80376117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:80376117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:53547560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:53547560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:155095106 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:155095106 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:235294907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:235294907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:103201970 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:103201970 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:103314408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:103314408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:204125604 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:204125604 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:73646354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:73646354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:240939343 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:240939343 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:104671990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:104671990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:3595450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:3595450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:18436163 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:18436163 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:30329834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:30329834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:18539771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:18539771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:34287500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:34287500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:55534163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:55534163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:66792022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:66792022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:10267474 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:10267474 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:123005116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:123005116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:37080576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:37080576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:237886375 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:237886375 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:237994084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:237994084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:33840248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:33840248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:18291031 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:18291031 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:134991014 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:134991014 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:71923802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:71923802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:18427807 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:18427807 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:78133839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:78133839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:38598636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:38598636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:97620540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:97620540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:71344884 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:71344884 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113867257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113867257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:49304082 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:49304082 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:169562974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:169562974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:9051936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:9051936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:9443460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:9443460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:47656820 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:47656820 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:48056589 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:48056589 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:167189324 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:167189324 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:37423644 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:37423644 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:155771454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:155771454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:14157874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:14157874 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:14412202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:14412202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67126086 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67126086 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67132979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67132979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:51172583 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:51172583 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:54639330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:54639330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:43219624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:43219624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:63129962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:63129962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:43267829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:43267829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113758556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113758556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:176823934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:176823934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:18266706 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:18266706 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:18266751 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:18266751 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:108098078 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:108098078 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:27444930 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:27444930 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:101577805 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:101577805 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:85267178 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:85267178 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:40402538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:40402538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:70612587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:70612587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:143567221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:143567221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:168222422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:168222422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:67402543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:67402543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:217281149 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:217281149 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:17851629 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:17851629 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:70490230 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:70490230 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:31491116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:31491116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:245961706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:245961706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:1285283 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:1285283 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:158288492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:158288492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:36767891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:36767891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:106563414 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:106563414 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:106602541 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:106602541 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:45345433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:45345433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:231112562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:231112562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:231177522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:231177522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:214878901 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:214878901 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:220326529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:220326529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44171163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44171163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158609218 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158609218 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:74056563 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:74056563 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:35837143 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:35837143 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:92977388 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:92977388 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104062571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104062571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104122591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104122591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:136456018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:136456018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:90672781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:90672781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219562166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219562166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:47228503 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:47228503 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:223395384 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:223395384 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:223402471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:223402471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:10929890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:10929890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:58444044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:58444044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:32933862 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:32933862 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:33376545 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:33376545 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:64574334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:64574334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:62536253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:62536253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:79747443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:79747443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:7464822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:7464822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:32803312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:32803312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:47308178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr22:47308178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:100965843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:100965843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:100995869 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:100995869 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:141600072 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:141600072 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:119441573 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:119441573 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:97447339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:97447339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:133475541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:133475541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:41847731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:41847731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:218591991 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:218591991 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:133975528 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:133975528 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:20750213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:20750213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:2573091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:2573091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:2578060 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:2578060 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:81660484 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:81660484 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:38229762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:38229762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:129822150 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:129822150 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:32959943 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:32959943 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:15267197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:15267197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:194313774 C>A maps to ENST00000273580 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:194313774 C>A maps to ENST00000273580 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100295666 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:100295666 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:117945612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:117945612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:111794161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:111794161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:7454311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:7454311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175295678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175295678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175372212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175372212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175454459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175454459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175650434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:175650434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:47467811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:47467811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113728634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113728634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:21500274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:21500274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:41197098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:41197098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:138262370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:138262370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:30071103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:30071103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:72732811 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:72732811 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:248039827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:248039827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:72965845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:72965845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:73408553 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:73408553 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:144698595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:144698595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:179472430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:179472430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:37898426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:37898426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:19452859 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:19452859 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:103298028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:103298028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:19705047 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:19705047 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:54589932 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:54589932 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:96171477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:96171477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:126216851 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:126216851 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:215800754 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:215800754 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:215901278 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:215901278 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:197563 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:197563 T>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:6967788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:6967788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:8993065 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:8993065 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:101740176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:101740176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:155119299 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:155119299 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:108115927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:108115927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219288979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:219288979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:2639782 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:2639782 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:133072720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:133072720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:79867357 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:79867357 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:100149105 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:100149105 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:38869769 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:38869769 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98750228 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98750228 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98823107 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98823107 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:119659559 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:119659559 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:27151523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:27151523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:55423644 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:55423644 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:177050045 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:177050045 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:177063244 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:177063244 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:76728892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:76728892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:48934034 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:48934034 T>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44108745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:44108745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:78859646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:78859646 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:100182926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chrX:100182926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:74075703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:74075703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:68232826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:68232826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:147113616 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:147113616 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:5012680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:5012680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:44770583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:44770583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:64382826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:64382826 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:49798424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:49798424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:44751539 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:44751539 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52955183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52955183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:31041623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:31041623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:48310755 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:48310755 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:67947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:67947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:56969410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:56969410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:227894188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:227894188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:55991074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:55991074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:146791339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:146791339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:6417313 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:6417313 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:6484276 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:6484276 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:6569958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:6569958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:7138734 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:7138734 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:7176391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:7176391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8975979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8975979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9222544 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9222544 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:41107742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:41107742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:105962338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:105962338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48285073 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48285073 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48288996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48288996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48352832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48352832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48545802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48545802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94502166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94502166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94521032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94521032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94553394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94553394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67080686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67080686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67098977 T>A maps to NM_080284.2 K958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67098977 T>A maps to NM_080284.2 K958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67130983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67130983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:66878642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:66878642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:66902051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:66902051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67004493 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67004493 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67022355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67022355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169791964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169791964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169826477 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169826477 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87144767 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87144767 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87146092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87146092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87150936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87150936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87170519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87170519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87170601 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87170601 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87074147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87074147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87104813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87104813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:20706407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:20706407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150737524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150737524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:123414454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:123414454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:48201678 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:48201678 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:48117461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:48117461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:48138317 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:48138317 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101590299 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101590299 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48734621 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48734621 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:95723835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:95723835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:17419840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:17419840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21957991 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21957991 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21965127 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21965127 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74760069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74760069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150912581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150912581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150920971 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150920971 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150920999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150920999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:51355442 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:51355442 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:43744130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:43744130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100527186 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100527186 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100530060 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100530060 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100554508 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100554508 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100569621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100569621 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100630785 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100630785 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179081425 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179081425 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211057677 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211057677 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76208925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76208925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76210389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76210389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89386933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89386933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:195027168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:195027168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:195029511 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:195029511 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15082104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15082104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31351762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31351762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31352337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31352337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31421188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31421188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31565679 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31565679 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31585618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31585618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31618337 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31618337 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31652780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31652780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31705453 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31705453 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31827362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31827362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31881790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31881790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32102601 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32102601 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32102720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32102720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55072769 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55072769 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55081928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55081928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80639813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80639813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:8372792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:8372792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6187494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6187494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:114176518 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:114176518 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20559515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20559515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:33464092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:33464092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:69376404 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:69376404 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:236922966 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:236922966 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66321681 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66321681 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158595115 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158595115 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:39508585 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:39508585 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156851968 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156851968 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156889932 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156889932 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:39602146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:39602146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:39016088 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:39016088 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8654052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8654052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8668561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8668561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33614246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33614246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33648770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33648770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33665989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33665989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33672270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33672270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33815898 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33815898 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:136298372 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:136298372 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100673390 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100673390 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100871000 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100871000 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:128920764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:128920764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43769736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43769736 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43826340 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43826340 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43862299 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43862299 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43884263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:43884263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:178541397 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:178541397 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:178554938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:178554938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:18657595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:18657595 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84359096 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84359096 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84373111 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84373111 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84408941 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84408941 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84660024 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84660024 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84676631 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84676631 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:46591510 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:46591510 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1622345 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1622345 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1667988 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1667988 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:140379228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:140379228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167803365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167803365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167815159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167815159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167829162 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167829162 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:7698553 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:7698553 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:7804839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:7804839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:25045373 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:25045373 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24791134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24791134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24791485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24791485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24794887 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24794887 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:131902039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:131902039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:111880291 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:111880291 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100205396 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100205396 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100207909 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100207909 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100242641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100242641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:67356584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:67356584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:76104248 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:76104248 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:112028471 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:112028471 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:26074938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:26074938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44153187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44153187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:148679972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:148679972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:147919380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:147919380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:100444956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:100444956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74361152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74361152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74309265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74309265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74315229 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74315229 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58126859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58126859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:86725558 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:86725558 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:86823291 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:86823291 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87135800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87135800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87182479 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87182479 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87235391 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87235391 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87437825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87437825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87572166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:87572166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47681649 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47681649 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49290405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49290405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49442412 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49442412 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49464573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49464573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49575805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49575805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49947088 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:49947088 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161557462 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161557462 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148458771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148458771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:424175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:424175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:222867506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:222867506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143486447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143486447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143654271 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143654271 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:26672494 C>A maps to NM_001039775.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:26672494 C>A maps to NM_001039775.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:4832305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:4832305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:77784043 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:77784043 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:91645287 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:91645287 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109954559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109954559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:134131867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:134131867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:4932285 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:4932285 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19597087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19597087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:55041504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:55041504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:104187072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:104187072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29445298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29445298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29867887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29867887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:30072493 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:30072493 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7979125 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7979125 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6913861 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6913861 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:233321599 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:233321599 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:113362409 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:113362409 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85366382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85366382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46725215 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46725215 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46534123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46534123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56417037 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56417037 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:118076485 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:118076485 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:38424286 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:38424286 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:104234062 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:104234062 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:112625738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:112625738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:108367415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:108367415 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41513327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41513327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41519213 G>T maps to ENST00000415018 L1908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41519213 G>T maps to ENST00000415018 L1908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41591282 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41591282 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41665476 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41665476 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:114266928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:114266928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65212124 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65212124 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:72848695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:72848695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74014778 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74014778 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37414840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37414840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37422767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37422767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37423100 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37423100 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37433997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37433997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37451509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:37451509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:94031052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:94031052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98177029 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98177029 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:197990267 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:197990267 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:100169282 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:100169282 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:99166694 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:99166694 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:5747266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:5747266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:5801777 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:5801777 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45663409 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45663409 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:242162554 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:242162554 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:46159185 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:46159185 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:47037055 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:47037055 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:47092608 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:47092608 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36677628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36677628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36734495 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36734495 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29727687 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29727687 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29735198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29735198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33977323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33977323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33997830 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33997830 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:42027722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:42027722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51237099 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51237099 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72046046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72046046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:29368377 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:29368377 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26781333 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26781333 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26848942 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26848942 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:116691564 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:116691564 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45452236 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45452236 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:116703473 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:116703473 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45409791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45409791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45412582 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45412582 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:27425353 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:27425353 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:33385506 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:33385506 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115327724 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115327724 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115346607 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115346607 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115350325 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115350325 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:35978530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:35978530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:36150174 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:36150174 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:141044447 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:141044447 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68226678 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68226678 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:148823165 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:148823165 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144179628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144179628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144329407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144329407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144344512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144344512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144344605 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144344605 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144467602 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:144467602 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110462453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110462453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110505891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110505891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128932359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128932359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128947483 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128947483 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36269542 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36269542 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36276428 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36276428 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130217302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130217302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:11316436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:11316436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:8216577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:8216577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:56788997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:56788997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34627680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34627680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:48998964 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:48998964 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:137989095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:137989095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:35729176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:35729176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:66303863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:66303863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104638360 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104638360 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:23759549 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:23759549 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150883751 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150883751 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5690476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5690476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76384630 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76384630 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:95143523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:95143523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:101215275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:101215275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:62430000 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:62430000 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:62559277 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:62559277 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:62602341 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:62602341 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133359186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133359186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176833057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176833057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176847249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176847249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176863990 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176863990 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176883690 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176883690 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176900222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176900222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176927330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176927330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176977998 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176977998 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119526273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119526273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119748288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119748288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119837790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119837790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119879670 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119879670 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119909769 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:119909769 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:120063984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:120063984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:120100666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:120100666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:120115356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:120115356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31230325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31230325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31305438 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31305438 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31306800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31306800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31306910 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:31306910 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:117024925 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:117024925 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:96758239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:96758239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:106634246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:106634246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150720432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150720432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:216195133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:216195133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108098692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108098692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:25932589 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:25932589 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47537489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47537489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47574025 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47574025 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:113526214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:113526214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:113527470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:113527470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19756676 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19756676 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17331102 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17331102 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:193210604 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:193210604 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:116943369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:116943369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:42489949 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:42489949 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160143214 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160143214 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:119504439 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:119504439 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10428293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10428293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10689068 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10689068 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10689618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10689618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203690706 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203690706 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36053976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36053976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40673155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40673155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124209427 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124209427 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:87155212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:87155212 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:71190181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:71190181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:104078759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:104078759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:10911863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:10911863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26411084 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26411084 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26417365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26417365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26424473 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26424473 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26477558 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:26477558 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154321235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154321235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:50399199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:50399199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:50346333 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:50346333 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:76906391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:76906391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:105447455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:105447455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:69871191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:69871191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70107688 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70107688 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:3065348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:3065348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:69454623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:69454623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63545567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63545567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235611628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235611628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:31843329 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:31843329 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47236185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47236185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47237780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47237780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:30701773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:30701773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90704633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90704633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90778719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90778719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:33257015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:33257015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11047606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11047606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11050981 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11050981 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11067159 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11067159 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11067161 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11067161 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11094574 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:11094574 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69483648 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69483648 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69511371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69511371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69666447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69666447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:102946313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:102946313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:91182816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:91182816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:27114953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:27114953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94107968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94107968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:58757069 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:58757069 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:99708626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:99708626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51717923 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51717923 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:32836450 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:32836450 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36147140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36147140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:97967482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:97967482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:43830764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:43830764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:69092670 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:69092670 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7791715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7791715 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:55748465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:55748465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96025724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96025724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:43293749 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:43293749 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16451688 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16451688 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16789456 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16789456 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112999847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112999847 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31624176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31624176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31627894 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31627894 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36954949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36954949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15383964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15383964 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:28352282 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:28352282 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:36334992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:36334992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107886967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107886967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:108004203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:108004203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124066898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124066898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38255914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38255914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:26411914 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:26411914 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:26444083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:26444083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:180430645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:180430645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40512980 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40512980 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:16705173 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:16705173 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:96955474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:96955474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:72531448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:72531448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:128114358 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:128114358 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:128326954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:128326954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33583362 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33583362 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111154753 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111154753 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:82824650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:82824650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:40066086 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:40066086 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:88390523 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:88390523 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:97112454 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:97112454 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:46942720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:46942720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:31513947 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:31513947 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:31498617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:31498617 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:77888905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:77888905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:59939671 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:59939671 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50459176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50459176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74204051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74204051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74523819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74523819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:95909452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:95909452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:49650395 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:49650395 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74043309 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74043309 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17965140 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17965140 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34191158 A>T maps to ENST00000417195 *220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34191158 A>T maps to ENST00000417195 *220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71238240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71238240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:20896906 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:20896906 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:30447652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:30447652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:7743310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:7743310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:15444436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:15444436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:24468216 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:24468216 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:200882534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:200882534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169383665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169383665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179503847 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179503847 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:170981918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:170981918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16721474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16721474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247719775 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247719775 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247737827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247737827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12806517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12806517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12819515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12819515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57254434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57254434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:75044402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:75044402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55118377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55118377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185171770 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185171770 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233086346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233086346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16332317 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16332317 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34672497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34672497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31879818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31879818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31879848 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31879848 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31887529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31887529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31891578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31891578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:34572862 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:34572862 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31643443 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31643443 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31680472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31680472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:3305420 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:3305420 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31763077 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31763077 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:270052 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:270052 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37387168 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37387168 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:37458821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:37458821 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:47382495 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:47382495 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219221639 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219221639 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:26800282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:26800282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228475983 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228475983 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112736108 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112736108 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14746195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14746195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:118870227 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:118870227 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:81307587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:81307587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:81308392 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:81308392 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:81780680 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:81780680 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:8472624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:8472624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:98720422 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:98720422 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:99055653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:99055653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:71023589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:71023589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:71024620 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:71024620 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111312051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111312051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:37210300 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:37210300 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41904450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41904450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41203062 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41203062 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:11759244 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:11759244 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:11779696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:11779696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:53974387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:53974387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:53980875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:53980875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:99727530 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:99727530 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:99736993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:99736993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:121530725 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:121530725 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:121642647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:121642647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130182487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130182487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:157721106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:157721106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35705694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35705694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:40868734 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:40868734 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31734971 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31734971 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31736879 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31736879 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:25219017 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:25219017 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:23724319 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:23724319 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120797603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120797603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120797634 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120797634 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120841957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120841957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120884571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120884571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120887601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120887601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120935782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:120935782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:89939356 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:89939356 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27286202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27286202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77598670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77598670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:50145426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:50145426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35680957 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35680957 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:49913920 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:49913920 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:24451650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:24451650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:65124289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:65124289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13373747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13373747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13603863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13603863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13606627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13606627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:140943791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:140943791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2332196 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2332196 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2387057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2387057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2482750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2482750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2566634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2566634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2711897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2711897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2727480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2727480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:53778921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:53778921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181548539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181548539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181548569 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181548569 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181570136 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181570136 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181649626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181649626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181684347 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181684347 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181685135 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181685135 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181702955 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181702955 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181727058 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181727058 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181732421 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181732421 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181755038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:181755038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:49068470 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:49068470 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201021902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201021902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201041852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201041852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54254727 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54254727 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54616023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54616023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54644685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54644685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54715759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:54715759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:55038926 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:55038926 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:1950071 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:1950071 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:1963308 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:1963308 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:1983749 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:1983749 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:18569359 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:18569359 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:18795323 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:18795323 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:18807513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:18807513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:36976257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:36976257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:85030535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:85030535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:85703530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:85703530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:85740246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:85740246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:86061749 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:86061749 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:86063812 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:86063812 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62450148 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62450148 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62485032 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62485032 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62830055 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62830055 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27465160 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27465160 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:71423611 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:71423611 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:188280234 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:188280234 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:188280418 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:188280418 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:93063362 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:93063362 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:93090014 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:93090014 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44294081 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44294081 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:114468841 C>G maps to ENST00000511664 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:114468841 C>G maps to ENST00000511664 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:114682094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:114682094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:110733683 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:110733683 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:121691373 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:121691373 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12854738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12854738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:85628549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:85628549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:30955289 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:30955289 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:30980754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:30980754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64972338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64972338 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:110494644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:110494644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230927499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230927499 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:75784751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:75784751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2972089 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2972089 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2976628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2976628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:111289370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:111289370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:25315928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:25315928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:104963855 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:104963855 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142991516 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142991516 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:104879788 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:104879788 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:115489002 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:115489002 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:55012177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:55012177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10720692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10720692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:116091079 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:116091079 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:105489449 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:105489449 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:54573437 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:54573437 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:114202810 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:114202810 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14034454 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14034454 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:58287844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:58287844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:47777799 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:47777799 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31614411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31614411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92938260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92938260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128455529 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128455529 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42784190 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42784190 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179710511 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179710511 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:197504375 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:197504375 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:46086297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:46086297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:93646039 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:93646039 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:96282314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:96282314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:78073264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:78073264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63997026 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63997026 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:107096339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:107096339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:119966690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:119966690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:100605184 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:100605184 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85613890 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85613890 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85623916 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85623916 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:13792271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:13792271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:4251211 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:4251211 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47761464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47761464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34344968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34344968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34416173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34416173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34207332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:34207332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:4387870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:4387870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38721637 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38721637 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:56128689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:56128689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74476801 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74476801 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74512892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74512892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74520921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74520921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7551764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7551764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43865898 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43865898 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158227027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158227027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158298931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158298931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158259570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158259570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112534582 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112534582 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112644088 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:112644088 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:67592966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:67592966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35832178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35832178 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160801395 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160801395 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117311046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117311046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80118074 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80118074 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80165958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80165958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80166531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80166531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80193073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80193073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80299342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80299342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44751502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44751502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160650907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160650907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:6926529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:6926529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60783031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60783031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6591092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6591092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62007103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62007103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:119255888 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:119255888 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:14134054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:14134054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121805445 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121805445 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121822854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121822854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121836851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121836851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87013027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87013027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87042595 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87042595 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:100874164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:100874164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:115016177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:115016177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54410352 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54410352 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:193091532 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:193091532 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:24491639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:24491639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65006664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65006664 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65020305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65020305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65038539 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65038539 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65101830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65101830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65109523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:65109523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:21884545 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:21884545 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:22142658 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:22142658 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:82732877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:82732877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:82813116 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:82813116 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:83151460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:83151460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:83597570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:83597570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:83598682 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:83598682 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:59059274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:59059274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44815718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44815718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44846966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44846966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44850044 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44850044 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44852721 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44852721 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44884197 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44884197 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44889374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44889374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44938567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44938567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73195483 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73195483 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73485097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73485097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:25555615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:25555615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:60416914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:60416914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66424285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66424285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31316244 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31316244 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31316246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31316246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31317741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31317741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:63476885 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:63476885 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:61793358 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:61793358 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:26962179 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:26962179 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:202689435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:202689435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74001318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74001318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:123166238 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:123166238 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92403900 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92403900 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92423853 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92423853 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:20584822 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:20584822 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:21038863 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:21038863 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125871774 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125871774 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:15353680 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:15353680 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:72673313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:72673313 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:80758152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:80758152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51979988 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51979988 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45175828 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:45175828 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:42222340 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:42222340 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51723337 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51723337 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22310524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22310524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:34853143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:34853143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:34887078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:34887078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35047118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35047118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35062482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35062482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35064495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35064495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35141986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:35141986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:109805603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:109805603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:13042500 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:13042500 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134264752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134264752 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55856681 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55856681 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55890239 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55890239 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31910935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31910935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196874424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196874424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:117175517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:117175517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:57767588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:57767588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:132493215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:132493215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:98193849 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:98193849 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:61749597 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:61749597 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16648021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16648021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111781620 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111781620 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:443447 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:443447 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:447493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:447493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:136662860 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:136662860 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:239762381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:239762381 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:239936008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:239936008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104900456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104900456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104918394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104918394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:129476985 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:129476985 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:57464046 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:57464046 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:175252566 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:175252566 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46829543 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46829543 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66586476 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66586476 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86942071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86942071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86952761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86952761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:11898366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:11898366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:170441956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:170441956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:98244082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:98244082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10133379 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10133379 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:11056251 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:11056251 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14707556 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14707556 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70013123 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70013123 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70013159 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70013159 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:71037052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:71037052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141633910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141633910 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10217498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10217498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122763533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122763533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36508195 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36508195 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:72074247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:72074247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:139713233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:139713233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7301413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7301413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:36197459 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:36197459 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:619381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:619381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123384698 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123384698 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79058791 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79058791 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72226762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72226762 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:87670412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:87670412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:87674105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:87674105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:224563573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:224563573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:154763078 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:154763078 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54649192 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54649192 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40956050 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40956050 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34580071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34580071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:17463042 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:17463042 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41199119 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41199119 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41323557 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41323557 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41441373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41441373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:2967491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:2967491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:100114240 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:100114240 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99223661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99223661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99786982 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99786982 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99959982 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99959982 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99993506 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:99993506 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:145944602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:145944602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:146288186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:146288186 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:146805467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:146805467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:146864425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:146864425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147259198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147259198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147482452 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147482452 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147930397 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147930397 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147942360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:147942360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:39171284 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:39171284 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:76382500 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:76382500 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:76555865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:76555865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:124854405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:124854405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125083728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125083728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125285189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125285189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125367302 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125367302 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125498122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125498122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125516319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125516319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125611006 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125611006 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125611469 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125611469 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125611660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125611660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125624065 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125624065 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125627247 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125627247 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165559818 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165559818 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:55038404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:55038404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103427664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103427664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103453105 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103453105 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103470071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103470071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103492004 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:103492004 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:33153416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:33153416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75804745 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75804745 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75840941 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75840941 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75843927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75843927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75856112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75856112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71654422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71654422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121138170 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121138170 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121379502 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121379502 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101751636 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101751636 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101767100 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101767100 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101784855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101784855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32130959 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32130959 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32167842 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32167842 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105794589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105794589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70778422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70778422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70847822 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70847822 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70886532 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70886532 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55924147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55924147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56021647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56021647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56178020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56178020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56259083 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56259083 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139774751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139774751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139819869 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139819869 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139877740 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139877740 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139885027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139885027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86252219 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86252219 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86282458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86282458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86324324 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86324324 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109810735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109810735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:7476217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:7476217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:7491811 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:7491811 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48375877 G>A maps to ENST00000395281 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48375877 G>A maps to ENST00000395281 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48391619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48391619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189866205 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189866205 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110807604 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110807604 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110838701 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110838701 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:227912133 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:227912133 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:107479354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:107479354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:137704365 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:137704365 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189898751 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189898751 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189926205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189926205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189944596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189944596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:10084198 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:10084198 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:238243551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:238243551 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:238257320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:238257320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70935490 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70935490 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70949037 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70949037 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70965172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70965172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:3682637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:3682637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:460316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:460316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:15515464 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:15515464 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115617618 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115617618 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160304967 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160304967 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128995986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128995986 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:84200089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:84200089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74422030 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:74422030 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47605191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47605191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68976815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68976815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27946257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27946257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:42579416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:42579416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130021211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130021211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:129986522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:129986522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68397075 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68397075 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:57149360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:57149360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:131320628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:131320628 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:131875126 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:131875126 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:131894740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:131894740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:36711567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:36711567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9771457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9771457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211477064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211477064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211521385 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211521385 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211539831 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211539831 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:92625722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:92625722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:68552484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:68552484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29111657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29111657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:125554941 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:125554941 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207696916 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207696916 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207726001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207726001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207800117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207800117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197297504 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197297504 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:28731183 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:28731183 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:3860402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:3860402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:43907344 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:43907344 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43274274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43274274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49677085 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49677085 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49704448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49704448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5859835 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5859835 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:122720756 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:122720756 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36937561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36937561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:19315714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:19315714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:19328722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:19328722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:2876215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:2876215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3165097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3165097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:4757712 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:4757712 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34006577 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34006577 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34066734 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34066734 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34067957 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34067957 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34242966 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34242966 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34254401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34254401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34260575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34260575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34261231 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34261231 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34404787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34404787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34450512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34450512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34452427 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34452427 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34470530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:34470530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:113293388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:113293388 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:113326624 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:113326624 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389029 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389029 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389068 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389068 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389148 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:114389148 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166535162 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166535162 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23433448 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23433448 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23669237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23669237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23472164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23472164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23584118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:23584118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39784076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39784076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:138266021 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:138266021 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79463061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79463061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79596601 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79596601 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79634827 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79634827 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79812876 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79812876 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80097064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80097064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:68979337 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:68979337 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36390242 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36390242 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36396331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36396331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36476649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36476649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57578822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57578822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11012510 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11012510 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11098681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11098681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11181867 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11181867 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11223073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11223073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11346381 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11346381 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11586617 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11586617 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:99799464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:99799464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16932540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16932540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16970061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16970061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16970398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16970398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:55945053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:55945053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43168742 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43168742 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101515325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101515325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:111655647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:111655647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:107274414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:107274414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48994267 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48994267 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74902950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:74902950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:149101814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:149101814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:105921296 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:105921296 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22963964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22963964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143955641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143955641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143995866 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143995866 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51539283 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51539283 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51555470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51555470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51605090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51605090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219674534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219674534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:127945070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:127945070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41387380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41387380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41456994 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41456994 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41521166 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41521166 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41521196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41521196 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:96447795 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:96447795 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:42014978 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:42014978 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99261765 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99261765 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99277429 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99277429 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:100166294 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:100166294 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47394996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47394996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47403053 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47403053 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284598 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284598 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15640432 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15640432 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15764685 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15764685 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15726376 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15726376 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42917360 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42917360 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37690551 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37690551 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:39811615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:39811615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57969040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57969040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57969280 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57969280 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57970256 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:57970256 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58203355 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58203355 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58231320 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58231320 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58301327 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58301327 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58403281 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58403281 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58503089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58503089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58514270 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58514270 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58514841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58514841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58694435 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58694435 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58895868 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:58895868 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:72049784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:72049784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:85559580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:85559580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:6474680 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:6474680 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:6476346 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:6476346 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:16633459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:16633459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176893511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176893511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20178295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20178295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:117860646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:117860646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:117890660 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:117890660 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:49913909 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:49913909 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:49954299 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:49954299 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:50197687 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:50197687 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:50742045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:50742045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31230284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31230284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55038902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55038902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:36443352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:36443352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36759399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36759399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36767927 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36767927 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36768150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36768150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2064387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2064387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155006730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155006730 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52740375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52740375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52757000 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52757000 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61088906 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61088906 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50531140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50531140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:20979548 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:20979548 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108752961 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108752961 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176938992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176938992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176940669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176940669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:55086695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:55086695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:32492367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:32492367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:91040321 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:91040321 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:90028047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:90028047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:90028276 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:90028276 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49989676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49989676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:29956749 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:29956749 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:126605806 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:126605806 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197515798 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197515798 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197611787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197611787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:140285648 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:140285648 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:115153634 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:115153634 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:142162068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:142162068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66044685 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66044685 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89073701 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89073701 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179323188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179323188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56333545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56333545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:14453373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:14453373 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:14733683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:14733683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234297018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234297018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234356866 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234356866 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137170042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137170042 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137198675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137198675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137266579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137266579 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137330147 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137330147 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137374813 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137374813 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137406804 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:137406804 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:50133270 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:50133270 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55336999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55336999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12632722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12632722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:125432556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:125432556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:182847116 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:182847116 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:80677837 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:80677837 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:102028808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:102028808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:370973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:370973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189628868 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189628868 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122575374 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122575374 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:73334091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:73334091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:73347170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:73347170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:232042115 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:232042115 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40657943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40657943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:107859455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:107859455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11989877 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11989877 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:83203844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:83203844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:83601877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:83601877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:84642380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:84642380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:84726236 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:84726236 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85296880 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85296880 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:69698878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:69698878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:4175827 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:4175827 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:4260257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:4260257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:35367526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:35367526 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124389537 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124389537 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:31986448 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:31986448 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:32536045 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:32536045 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35991572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35991572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:1053645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:1053645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:1057310 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:1057310 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51839694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51839694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124418217 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124418217 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21631258 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21631258 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21723604 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21723604 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760503 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760503 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760640 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760640 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21781537 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21781537 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21826205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21826205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21858138 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21858138 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:76558087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:76558087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52384213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52384213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52394112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52394112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7704684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7704684 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196722070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196722070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196749217 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196749217 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196852570 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196852570 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196852574 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196852574 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196874830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196874830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196917861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196917861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38891041 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38891041 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38954418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38954418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38998254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38998254 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11511757 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11511757 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11550652 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11550652 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11647992 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11647992 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11684289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11684289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11725497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:11725497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34483301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34483301 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:132203428 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:132203428 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:25174050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:25174050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:66992565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:66992565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40152438 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40152438 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230231584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230231584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230298007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230298007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230305797 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230305797 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:225714116 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:225714116 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169126556 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169126556 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169135312 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169135312 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169141279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169141279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169141687 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169141687 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169157524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169157524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169172899 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169172899 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169402163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169402163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169402165 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169402165 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169504617 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169504617 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:111424282 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:111424282 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:111575870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:111575870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:340349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:340349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:53208122 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:53208122 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68023167 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68023167 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73353391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73353391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:115990124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:115990124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:116456142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:116456142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:116456151 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:116456151 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:116538574 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:116538574 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162875431 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162875431 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:153639632 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:153639632 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:153653488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:153653488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:154384371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:154384371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:154595514 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:154595514 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:154684298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:154684298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:109019204 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:109019204 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7869549 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7869549 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113850264 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113850264 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28574418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28574418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117376664 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117376664 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:41550753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:41550753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:41555290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:41555290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28910038 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28910038 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28968491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28968491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28986359 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28986359 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7556092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7556092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56433134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56433134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56444789 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56444789 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56462534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56462534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56495286 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56495286 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56765076 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:56765076 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:212240074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:212240074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73993912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73993912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30436418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30436418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:183948214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:183948214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167083059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167083059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:95457224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:95457224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:95616618 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:95616618 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:32586317 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:32586317 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44010775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44010775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44028652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44028652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:96237242 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:96237242 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108356314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108356314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108392775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108392775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:158522597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:158522597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48385767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48385767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184002973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184002973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95276837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95276837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172537828 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172537828 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:33722427 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:33722427 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57876460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57876460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74228006 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:74228006 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:22284809 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:22284809 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:245266398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:245266398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:44151497 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:44151497 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133014172 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133014172 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:38337592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:38337592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:38406920 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:38406920 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:62934443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:62934443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:140682476 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:140682476 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40231673 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40231673 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:45341246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:45341246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36505659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36505659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2403420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2403420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:117768098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:117768098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32687932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32687932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38245947 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38245947 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7476068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7476068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21186697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21186697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50610202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50610202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50653490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50653490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201981951 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201981951 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36901123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36901123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37307000 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37307000 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37355346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37355346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37382417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37382417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:107463301 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:107463301 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:107501117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:107501117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:100406458 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:100406458 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:42483789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:42483789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6898656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6898656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:43865870 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:43865870 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:132181433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:132181433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:131996592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:131996592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:131998972 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:131998972 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:132448039 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:132448039 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:132502646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:132502646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:132529575 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:132529575 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111601917 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111601917 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:111944831 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:111944831 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:120885440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:120885440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:89353713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:89353713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:89468558 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:89468558 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:222307502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:222307502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:222428327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:222428327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:96790660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:96790660 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134859776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134859776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134911722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134911722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:23101736 G>T maps to ENST00000374625 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:23101736 G>T maps to ENST00000374625 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:23240068 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:23240068 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184295274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184295274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:27373192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:27373192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:220196024 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:220196024 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:43500442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:43500442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56270119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56270119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56270340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56270340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:91372092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:91372092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:65279547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:65279547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:212483875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:212483875 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:212495152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:212495152 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:212589752 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:212589752 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:55746493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:55746493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:56469071 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:56469071 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:128015075 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:128015075 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:103528301 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:103528301 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:172341674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:172341674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:124624378 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:124624378 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54277988 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54277988 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152045321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152045321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152372716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152372716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:76929260 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:76929260 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216824096 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216824096 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217078645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217078645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217089141 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217089141 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217241435 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217241435 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158528137 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158528137 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158557339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158557339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158580984 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158580984 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:44010875 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:44010875 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:22797061 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:22797061 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128355041 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128355041 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:13940277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:13940277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:41606387 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:41606387 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:185798783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:185798783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5664988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5664988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29683135 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29683135 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38565338 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38565338 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72238863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72238863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:45645126 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:45645126 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133703377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133703377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133744191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133744191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133802753 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133802753 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133810841 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133810841 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133821515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133821515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133850079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:133850079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:65750170 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:65750170 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:66013920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:66013920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197029474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:197029474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46748467 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46748467 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169513502 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169513502 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:88427409 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:88427409 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:31840170 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:31840170 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:14607375 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:14607375 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:14709795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:14709795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153413764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153413764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47797088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47797088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:170686387 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:170686387 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139158023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139158023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139183307 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139183307 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139484989 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139484989 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:177164145 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:177164145 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19027262 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19027262 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:108099406 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:108099406 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:108105733 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:108105733 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:108261148 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:108261148 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:74178343 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:74178343 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:118968651 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:118968651 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:75746804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:75746804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:97631993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:97631993 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29240239 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29240239 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45489147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45489147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45542446 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45542446 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:119327526 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:119327526 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:10867349 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:10867349 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:91620616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:91620616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:68486334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:68486334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:62273284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:62273284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179019582 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179019582 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:46250567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:46250567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:97084623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:97084623 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110594570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110594570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:120895933 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:120895933 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:177226606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:177226606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:177251281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:177251281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:190250605 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:190250605 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:67666465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:67666465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:166063259 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:166063259 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:54791409 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:54791409 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:124798621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:124798621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33810804 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33810804 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:38751103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:38751103 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:13057813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:13057813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:13061981 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:13061981 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89828252 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89828252 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:98829543 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:98829543 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:99042188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:99042188 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:223511492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:223511492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:207636109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:207636109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150931213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150931213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150942865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150942865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:92569897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:92569897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127610514 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127610514 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127614199 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127614199 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127623236 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127623236 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127625044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127625044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127625532 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127625532 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127647127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127647127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127666390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127666390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127667056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127667056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127668324 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127668324 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127762075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127762075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:107276233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:107276233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:37424975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:37424975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:15770951 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:15770951 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:15802369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:15802369 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:71741088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:71741088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207132923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207132923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161480036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161480036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161482582 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161482582 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161643418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161643418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161647028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161647028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161563210 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161563210 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157773982 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157773982 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157790842 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157790842 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157558826 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157558826 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157559355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157559355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157567788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157567788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157485383 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157485383 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159776625 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159776625 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110327529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110327529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:125130989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:125130989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:108521753 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:108521753 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62356084 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:62356084 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:54476879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:54476879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:36975290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:36975290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14939189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14939189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:44388435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:44388435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:138193046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:138193046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102430525 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102430525 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102654894 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102654894 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102979027 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102979027 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:170867408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:170867408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:155531209 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:155531209 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:59904388 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:59904388 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:59936064 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:59936064 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:33964877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:33964877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241667227 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241667227 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:164466056 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:164466056 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:72743542 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:72743542 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21546992 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21546992 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:60972375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:60972375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128477409 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128477409 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128488456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128488456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128497046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128497046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:29004174 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:29004174 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:28601167 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:28601167 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:213032577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:213032577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33170754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33170754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33243668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33243668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240286661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240286661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240307734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240307734 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240308565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240308565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240333724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240333724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240334033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240334033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240421378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240421378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240439803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240439803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240555894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240555894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203225405 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203225405 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203226164 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203226164 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203270625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203270625 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159642549 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159642549 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159652895 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159652895 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172061756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172061756 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89407163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89407163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:71927857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:71927857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:94036134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:94036134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:86546402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:86546402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8196498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8196498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:90027282 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:90027282 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:71090456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:71090456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:114019589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:114019589 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:114299792 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:114299792 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:126143045 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:126143045 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14747129 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14747129 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14812569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14812569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14842200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14842200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14851809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14851809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:39453256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:39453256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13789643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13789643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13994463 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13994463 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37691896 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37691896 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:32761878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:32761878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:32818134 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:32818134 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49191197 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49191197 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49230940 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49230940 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49381387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49381387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49381661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:49381661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133505896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133505896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70499965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70499965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:39170244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:39170244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:39217453 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:39217453 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46010301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46010301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86662047 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86662047 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29541492 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29541492 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101156561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101156561 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101216082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101216082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101377070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101377070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:161302485 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:161302485 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:161302769 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:161302769 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:161317893 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:161317893 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:151535867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:151535867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47163105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47163105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:160721511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:160721511 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27182191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27182191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:151127946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:151127946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:46043280 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:46043280 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27254227 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27254227 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27597264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27597264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27598292 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:27598292 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26512779 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26512779 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26538674 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:26538674 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:30819811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:30819811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:30901551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:30901551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:49217132 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:49217132 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:898358 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:898358 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:88322888 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:88322888 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:88324839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:88324839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:49574348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:49574348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101599540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:101599540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:154801185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:154801185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:155069228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:155069228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:155143670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:155143670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230378906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230378906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:69813667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:69813667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11521276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11521276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:151700100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:151700100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:172824433 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:172824433 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:22747640 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:22747640 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:9885212 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:9885212 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153782422 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153782422 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:22729008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:22729008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155205823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155205823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:81539466 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:81539466 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89579664 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89579664 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89834037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89834037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74845919 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74845919 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74856029 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74856029 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74862467 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74862467 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76969650 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76969650 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76979887 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76979887 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55206144 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55206144 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23504790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23504790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:25010651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:25010651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61958340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61958340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31013562 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31013562 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31014724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31014724 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:88009054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:88009054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220108125 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220108125 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6609619 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6609619 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6639508 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6639508 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:42065783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:42065783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:42224355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:42224355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:54132519 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:54132519 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:3829223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:3829223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:92712517 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:92712517 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:39041340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:39041340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151230871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151230871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:175688064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:175688064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:175750001 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:175750001 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:58602366 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:58602366 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150632941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150632941 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150760218 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150760218 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150760835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150760835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29018055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29018055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62224194 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62224194 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39825864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39825864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57474927 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57474927 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:52418704 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:52418704 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235806051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235806051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93264438 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93264438 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:88677395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:88677395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101163820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101163820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167024493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167024493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167058134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167058134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167059340 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167059340 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42512404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42512404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:92408469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:92408469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:93419880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:93419880 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:34868635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:34868635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:176572896 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:176572896 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:46845898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:46845898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:129519478 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:129519478 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100365349 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100365349 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100388071 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100388071 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:131476637 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:131476637 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:131500253 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:131500253 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:154070675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:154070675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:25465274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:25465274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:25770299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:25770299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27721338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27721338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:57714562 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:57714562 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:90327057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:90327057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123464955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123464955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123475955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123475955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123489192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123489192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:47069561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:47069561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11736369 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11736369 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:10101600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:10101600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37432264 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37432264 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:152873379 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:152873379 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153174302 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153174302 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:122488700 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:122488700 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:105624094 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:105624094 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:105836836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:105836836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:87614384 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:87614384 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:87676221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:87676221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:87952560 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:87952560 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:94344128 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:94344128 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31204398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31204398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102180894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102180894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102247693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102247693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102250159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102250159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120461156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120461156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120591450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120591450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120648758 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120648758 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120685644 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120685644 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120690224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120690224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120827419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120827419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48922323 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48922323 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:66800024 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:66800024 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141521679 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141521679 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:34029638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:34029638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:34066172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:34066172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:34100731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:34100731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88386204 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88386204 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88386305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88386305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88582964 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88582964 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7333096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7333096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7340142 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7340142 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7340550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7340550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7782001 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:7782001 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126086471 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126086471 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126141603 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126141603 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126303191 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126303191 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126358581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126358581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126539892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:126539892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42429340 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42429340 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:16141978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:16141978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38127455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38127455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:27839072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:27839072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28064808 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28064808 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:52660975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:52660975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110282969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110282969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1055726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1055726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108672643 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108672643 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:106766302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:106766302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:108673498 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:108673498 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148734346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148734346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:144937398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:144937398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:145041017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:145041017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:144801811 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:144801811 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:9305651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:9305651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:105239239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:105239239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:122626319 T>A maps to ENST00000443194 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:122626319 T>A maps to ENST00000443194 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36108872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36108872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5254349 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5254349 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5284954 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5284954 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:153224763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:153224763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30689370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30689370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:45351988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:45351988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:45353534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:45353534 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:45472641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:45472641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55081103 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55081103 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42194943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42194943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:18466984 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:18466984 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:18747934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:18747934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:19035743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:19035743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:19035811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:19035811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156715007 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156715007 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41009273 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41009273 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41048300 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41048300 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41056059 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41056059 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41064815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41064815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41064820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41064820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41065356 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41065356 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:197208538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:197208538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:65162583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:65162583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93808321 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93808321 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:28457363 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:28457363 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56976828 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56976828 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:91740189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:91740189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:91843848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:91843848 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:81388207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:81388207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:210522131 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:210522131 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:222711641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:222711641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70820955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70820955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:119002425 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:119002425 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:26124323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:26124323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:27840162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:27840162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:221058126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:221058126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185833508 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185833508 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185933166 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185933166 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186105678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186105678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:43298040 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:43298040 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:173496090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:173496090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:173531367 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:173531367 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43057954 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43057954 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43058002 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43058002 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:177633022 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:177633022 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:86584512 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:86584512 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19030219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19030219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:27149694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:27149694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:27187377 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:27187377 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46607310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46607310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46654477 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46654477 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54428017 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54428017 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:100189542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:100189542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:18303328 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:18303328 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:100249982 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:100249982 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:100807965 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:100807965 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6453095 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6453095 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:72092983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:72092983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87538982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87538982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:25867910 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:25867910 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:25908538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:25908538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:96884613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:96884613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:96887613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:96887613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:97132180 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:97132180 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:97152061 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:97152061 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:97226002 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:97226002 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:43772522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:43772522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:43876830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:43876830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49335860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49335860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:118811494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:118811494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:119976455 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:119976455 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:122720842 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:122720842 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56565663 C>A maps to ENST00000428320 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56565663 C>A maps to ENST00000428320 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118525648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118525648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161496390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161496390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198358976 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198358976 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:135582720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:135582720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:113775601 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:113775601 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147929924 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147929924 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124249228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124249228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3142399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3142399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3182194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3182194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:123517225 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:123517225 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:71054034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:71054034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204820721 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204820721 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:78461199 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:78461199 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1068747 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:1068747 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94567913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94567913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:25679652 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:25679652 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:21202190 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:21202190 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:129226687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:129226687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:42232297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:42232297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:99491629 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:99491629 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:102809306 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:102809306 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:217543953 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:217543953 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53494813 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53494813 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:57939017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:57939017 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151156431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151156431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:118645242 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:118645242 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130407651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130407651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130419515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130419515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130543832 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:130543832 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18550287 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18550287 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18661367 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18661367 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:41137348 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:41137348 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159907435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159907435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50435966 G>T maps to ENST00000413698 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50435966 G>T maps to ENST00000413698 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50466153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50466153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50467525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:50467525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:37988522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:37988522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:158753576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:158753576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67794211 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67794211 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:52111472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:52111472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9945893 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9945893 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:102979292 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:102979292 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:103068669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:103068669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113809381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113809381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:29686465 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:29686465 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:190326989 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:190326989 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113875666 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113875666 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:27445834 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:27445834 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207075496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207075496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:6061222 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:6061222 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:3137210 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:3137210 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:166901277 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:166901277 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:166925952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:166925952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:110303874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:110303874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:111051642 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:111051642 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:242662728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:242662728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:41740048 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:41740048 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:30768966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:30768966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:142955672 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:142955672 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:143114190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:143114190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234078640 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234078640 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67264038 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67264038 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67266976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67266976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156815207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156815207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153743131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153743131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:95841373 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:95841373 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:154489288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:154489288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44425705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44425705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44425894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44425894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:98666226 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:98666226 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:237316808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:237316808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121491349 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:121491349 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:19729519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:19729519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:75923341 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:75923341 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156506758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156506758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156514800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156514800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:208281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:208281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:79607446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:79607446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:85954925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:85954925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55359059 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55359059 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:50679555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:50679555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74425024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74425024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:33001509 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:33001509 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2933172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2933172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145528565 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145528565 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145530814 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145530814 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68620720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68620720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68657188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68657188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68695100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:68695100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:52150062 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:52150062 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:52216072 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:52216072 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42458449 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42458449 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182323103 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182323103 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182323140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182323140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182339613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182339613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182388300 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182388300 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54805516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54805516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15561209 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15561209 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15614377 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15614377 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15646153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15646153 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15725837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:15725837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:37659580 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:37659580 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31404753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31404753 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31424695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31424695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:30494998 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:30494998 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31288415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31288415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31372908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31372908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:33233907 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:33233907 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45361783 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45361783 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45368616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45368616 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45380389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45380389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102220219 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102220219 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102235456 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102235456 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102367883 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102367883 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52811904 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52811904 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52812173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52812173 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52812235 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52812235 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7772359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7772359 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7614296 G>T maps to NM_001001851.2 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7614296 G>T maps to NM_001001851.2 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156667245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156667245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160920574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160920574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4647380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4647380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4649246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4649246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4825353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4825353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:5085253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:5085253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147008223 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147008223 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147053078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147053078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:15319082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:15319082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:27880660 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:27880660 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:28111290 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:28111290 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39778019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39778019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39778485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39778485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39803931 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39803931 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:123790020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:123790020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:156160482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:156160482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:48098275 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:48098275 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:73531264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:73531264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:17799373 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:17799373 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110768509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110768509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:211033649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:211033649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:211255889 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:211255889 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:211255891 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:211255891 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63246266 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63246266 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63403949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63403949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63483527 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63483527 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:19246012 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:19246012 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:19470315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:19470315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169780876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169780876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:170081053 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:170081053 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:170123278 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:170123278 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20851976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20851976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:21008454 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:21008454 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:21178411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:21178411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:21936298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:21936298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:155602268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:155602268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38824151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38824151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128773474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128773474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:39213083 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:39213083 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:39213178 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:39213178 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:88792681 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:88792681 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118956998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118956998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233783353 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233783353 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78771904 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78771904 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78844339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78844339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169810650 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:169810650 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:178389248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:178389248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73696832 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73696832 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73843773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73843773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73867232 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73867232 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196269659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196269659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196577339 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196577339 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:36645025 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:36645025 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:143838821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:143838821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:201369766 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:201369766 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:24180065 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:24180065 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:24180787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:24180787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215751501 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215751501 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:103441302 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:103441302 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:121972259 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:121972259 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122018106 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122018106 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6834585 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6834585 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6915871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6915871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6918305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6918305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55958975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55958975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55971176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55971176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142638225 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142638225 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142655126 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142655126 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:62442461 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:62442461 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:136554718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:136554718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:2811296 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:2811296 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26942570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26942570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:48353142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:48353142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:48376975 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:48376975 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:197422618 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:197422618 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:58939066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:58939066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46665837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46665837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:96999909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:96999909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154548358 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154548358 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:105516088 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:105516088 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34971161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34971161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24036444 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24036444 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24763056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24763056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24821923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24821923 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24825836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24825836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24833665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:24833665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:138540689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:138540689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:138611182 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:138611182 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:44213856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:44213856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:72289435 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:72289435 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:97269866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:97269866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:86522171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:86522171 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:86526708 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:86526708 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:34513787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:34513787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94039285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94039285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94041694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94041694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94120393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94120393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:59954860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:59954860 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:226320967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:226320967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100053575 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100053575 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100077234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100077234 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100136639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100136639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43458879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43458879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43550087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43550087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:45580262 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:45580262 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:1918341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:1918341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:20931703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:20931703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:16304321 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:16304321 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21013866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21013866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21039943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21039943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:91505769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:91505769 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:39735794 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:39735794 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:200974189 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:200974189 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:26179320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:26179320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57963209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57963209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:32337569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:32337569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:149803269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:149803269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:90190720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:90190720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55272156 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55272156 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55330068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55330068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55346434 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55346434 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55350800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55350800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:126367226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:126367226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157972568 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157972568 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158020153 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158020153 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:74326051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:74326051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44569920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44569920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:70445411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:70445411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:70469364 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:70469364 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:70514418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:70514418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51330042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51330042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51381281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51381281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51362900 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51362900 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51363383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51363383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:187177121 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:187177121 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:33628453 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:33628453 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241696257 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241696257 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241757995 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241757995 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152731941 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152731941 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53070044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53070044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38821220 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38821220 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39595187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39595187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39118341 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39118341 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53184973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53184973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39135358 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39135358 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52910865 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52910865 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52939551 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52939551 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52944079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52944079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52826762 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52826762 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53162367 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53162367 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53090316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53090316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53240157 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53240157 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53217598 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53217598 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52565867 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52565867 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39725916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39725916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39728291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39728291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31768256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31768256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31859777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31859777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39165436 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39165436 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35981351 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35981351 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:25917823 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:25917823 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:143779219 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:143779219 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130425505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130425505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130454808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130454808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6243169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6243169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:42143548 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:42143548 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:42157865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:42157865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:108843472 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:108843472 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55031437 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55031437 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201352394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201352394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55020233 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55020233 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6965193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6965193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6976127 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:6976127 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:7050580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:7050580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129687531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129687531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:21530185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:21530185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:112460574 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:112460574 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:209808835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:209808835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107692773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107692773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107738771 C>T maps to ENST00000414450 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107738771 C>T maps to ENST00000414450 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107746933 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107746933 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:113975665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:113975665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:33716294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:33716294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169622885 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169622885 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111428587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111428587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152659307 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152659307 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32741900 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:32741900 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66857251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66857251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:16513179 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:16513179 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:16531214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:16531214 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:16766929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:16766929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:88445409 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:88445409 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:36006903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:36006903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109010214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109010214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43221386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43221386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:66098939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:66098939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:48941120 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:48941120 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:104294215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:104294215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9542781 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9542781 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:40073087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:40073087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180217657 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180217657 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55106534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55106534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55087106 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55087106 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54823091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54823091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55176498 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55176498 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:31668723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:31668723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:128411948 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:128411948 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:128412221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:128412221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27950843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27950843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27982521 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27982521 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27990783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27990783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27995783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27995783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27999868 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27999868 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:28149191 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:28149191 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:28641460 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:28641460 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:185229487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:185229487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:185245250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:185245250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:90350366 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:90350366 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70389911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70389911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33881125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33881125 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165174909 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165174909 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165182695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165182695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150444651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150444651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:135186226 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:135186226 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:148244737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:148244737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:148349632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:148349632 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19299570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19299570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161007395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161007395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161055975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161055975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161087186 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161087186 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161087223 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161087223 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55590692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55590692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:82187621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:82187621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:62720405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:62720405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11849170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11849170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11852530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11852530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11942817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11942817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11955539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11955539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:197547398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:197547398 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:197557624 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:197557624 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40364537 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40364537 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40439900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40439900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40456860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40456860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40485948 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40485948 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40529146 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:40529146 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:25232315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:25232315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:140992510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:140992510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141027955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141027955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141055367 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141055367 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141182978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141182978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141474206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141474206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57581011 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57581011 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169985137 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:169985137 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:170053217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:170053217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46924222 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:46924222 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76377175 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76377175 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70611637 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70611637 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:54427947 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:54427947 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17907824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17907824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40137944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40137944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40557499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40557499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40557523 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40557523 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40634642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40634642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40988386 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40988386 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40988437 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:40988437 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:41415676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:41415676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:41423739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:41423739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70195664 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70195664 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70339239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70339239 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70385374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70385374 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70394755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70394755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70445925 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70445925 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70484346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70484346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:37133152 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:37133152 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:85638757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:85638757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:74505194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:74505194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:74562613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:74562613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:169548428 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:169548428 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:101608787 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:101608787 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:40651200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:40651200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80529372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80529372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:68686156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:68686156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:77008659 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:77008659 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115740891 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115740891 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115839788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115839788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115920130 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115920130 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:116018182 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:116018182 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:116163925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:116163925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33281294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33281294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33477980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33477980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33572318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:33572318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65311245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65311245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31549181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31549181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46484842 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46484842 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46497527 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:46497527 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144164467 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144164467 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31686680 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31686680 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:74922217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:74922217 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:219347114 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:219347114 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:219373329 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:219373329 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235927007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235927007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42445623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42445623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42448993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:42448993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:39918038 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:39918038 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:14738447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:14738447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:15450265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:15450265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:152488335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:152488335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:140968992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:140968992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:65673699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:65673699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77830554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77830554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77973088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77973088 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:78190955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:78190955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35791397 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:35791397 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:95719289 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:95719289 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95815971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95815971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95822776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95822776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95883069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95883069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75651570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75651570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21207552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21207552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21208109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21208109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67456128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67456128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67487408 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67487408 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:43350985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:43350985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:19380747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:19380747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30736620 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30736620 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:102482823 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:102482823 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:102493353 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:102493353 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:47912298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:47912298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:36107182 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:36107182 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:1812741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:1812741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16067909 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16067909 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16079647 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16079647 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:165150497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:165150497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8503530 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8503530 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:217234393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:217234393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:10397482 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:10397482 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:10414705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:10414705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:220815659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:220815659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:103878746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:103878746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:103923656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:103923656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57881752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57881752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57894021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57894021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:186946306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:186946306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:46383263 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:46383263 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:46487570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:46487570 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:66266325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:66266325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:162945152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:162945152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:36007192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:36007192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:103348941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:103348941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:70908767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:70908767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182946000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182946000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:100382456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:100382456 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13217349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13217349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:94230545 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:94230545 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:37638566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:37638566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:47311277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:47311277 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:47426534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:47426534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:47566401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:47566401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:63821380 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:63821380 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90434912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90434912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90503326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90503326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86176818 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86176818 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29542916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29542916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151101513 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151101513 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:40539395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:40539395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19257686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19257686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66293697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66293697 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:37395911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:37395911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15666611 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15666611 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:46777372 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:46777372 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:28135264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:28135264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89444228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:89444228 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74774217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74774217 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:158531729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:158531729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40422997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40422997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141727371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141727371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141740852 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141740852 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141755634 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141755634 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141785665 C>A maps to ENST00000475668 R2182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141785665 C>A maps to ENST00000475668 R2182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141796000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141796000 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:87199231 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:87199231 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74899321 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74899321 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:135027870 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:135027870 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:103569909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:103569909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38333728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38333728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:10422851 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:10422851 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37738132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37738132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14327907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14327907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14334350 G>T maps to ENST00000389126 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14334350 G>T maps to ENST00000389126 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47046341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47046341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:23812483 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:23812483 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56284416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56284416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:2527976 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:2527976 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:102565840 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:102565840 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:102573686 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:102573686 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55521757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55521757 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55524264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55524264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:102595615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:102595615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:33836780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:33836780 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:75431752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:75431752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108763513 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108763513 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108780723 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108780723 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124929361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124929361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:132695679 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:132695679 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:13175957 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:13175957 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43803463 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43803463 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43805595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43805595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:41888030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:41888030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:43834265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:43834265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:30513755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:30513755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60758521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60758521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:18154411 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:18154411 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179306783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179306783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64892872 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64892872 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43652015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43652015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60265157 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60265157 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60538718 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60538718 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60542993 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60542993 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60231725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60231725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59857103 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59857103 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59861085 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59861085 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60064812 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60064812 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80109362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80109362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:64956951 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:64956951 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:15998347 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:15998347 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:65744215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:65744215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:65821895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:65821895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56702012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56702012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121476050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121476050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:93576303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:93576303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:86575622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:86575622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56582510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56582510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:17199117 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:17199117 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:63444593 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:63444593 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30653419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30653419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237008152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237008152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:124632262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:124632262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8966619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8966619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8992981 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8992981 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9007031 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9007031 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9021494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9021494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:102045177 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:102045177 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47374198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47374198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:77752144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:77752144 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:77835588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:77835588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48599493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48599493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:15813704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:15813704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10233700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10233700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10263628 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10263628 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50812514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50812514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108112837 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108112837 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10399965 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10399965 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10405262 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10405262 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10411092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10411092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10428032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:10428032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23872386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23872386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23876118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23876118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:101257132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:101257132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:101259404 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:101259404 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44180796 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44180796 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16681405 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16681405 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16766405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:16766405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:109472790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:109472790 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:109550583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:109550583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:109817471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:109817471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:26273909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:26273909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:26304475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:26304475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57423916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57423916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31099942 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31099942 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31158922 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31158922 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:59430209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:59430209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8594952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:8594952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:109841714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:109841714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171034821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171034821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171230765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171230765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:72146614 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:72146614 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17311039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17311039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:95216614 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:95216614 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24389784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24389784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24402584 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24402584 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:69956991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:69956991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:40068720 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:40068720 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:40135957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:40135957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:41894717 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:41894717 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:41895015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:41895015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89867912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89867912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89903400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89903400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:174777663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:174777663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66847647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66847647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40685978 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40685978 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102051599 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:102051599 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:72434416 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:72434416 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48003847 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48003847 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50865065 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50865065 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:78270775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:78270775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:19394629 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:19394629 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20112281 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20112281 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:78362553 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:78362553 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:78574591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:78574591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:15467739 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:15467739 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:15506639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:15506639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204055852 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204055852 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:148754555 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:148754555 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16891785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16891785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16918082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16918082 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16923999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:16923999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120380025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120380025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158441556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158441556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158444821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158444821 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158449450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158449450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:97007237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:97007237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100403201 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100403201 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54912787 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54912787 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133503808 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133503808 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133554164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133554164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133713819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133713819 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133965641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133965641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134076314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134076314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134102020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134102020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134104279 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134104279 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134134334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134134334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134139336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134139336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134279984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:134279984 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44695639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44695639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124993063 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124993063 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21510764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21510764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21510990 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21510990 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:115751101 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:115751101 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:116015921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:116015921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:4768354 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:4768354 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:67376215 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:67376215 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:21101655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:21101655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152499459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152499459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:84035995 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:84035995 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:97338412 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:97338412 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:11192452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:11192452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:24810478 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:24810478 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:27183101 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:27183101 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:130987389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:130987389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27068290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27068290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:75551440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:75551440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20760789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20760789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20790937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:20790937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21114378 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21114378 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21176856 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21176856 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21251131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21251131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21594968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:21594968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45042400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45042400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45170740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45170740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45182079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:45182079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:70450809 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:70450809 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:70498485 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:70498485 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7224853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7224853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105331681 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105331681 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55420141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55420141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:30032942 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:30032942 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:30051569 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:30051569 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204956803 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204956803 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204982006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204982006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24846973 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24846973 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54687296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54687296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:61554414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:61554414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14088354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:14088354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13139657 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13139657 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104158448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104158448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:233784980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:233784980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:236154432 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:236154432 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:52495614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:52495614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:695709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:695709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156900018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156900018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:36975796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:36975796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29956605 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:29956605 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:124215812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:124215812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:124777111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:124777111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:124855398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:124855398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:125112598 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:125112598 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:125117249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:125117249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:63396263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:63396263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:119068555 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:119068555 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33463021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33463021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:173247324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:173247324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56316486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56316486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54301491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54301491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56410346 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56410346 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:5485024 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:5485024 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247592682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247592682 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247597810 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247597810 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56382064 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56382064 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56572977 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:56572977 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:101096816 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:101096816 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:69790378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:69790378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:144098929 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:144098929 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:892252 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:892252 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95086545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95086545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:203146939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:203146939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:117660408 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:117660408 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26096664 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26096664 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120462320 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120462320 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120523841 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120523841 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120549925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120549925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120559447 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120559447 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15300050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15300050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:46465298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:46465298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:155730719 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:155730719 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:155764330 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:155764330 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89125254 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89125254 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89190293 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89190293 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:101521259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:101521259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:34177012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:34177012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:34179759 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:34179759 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:132427136 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:132427136 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36340062 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36340062 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179526131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:179526131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153652923 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153652923 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:34739814 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:34739814 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:34884606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:34884606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:34885044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:34885044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:78446957 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:78446957 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:24329295 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:24329295 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:115391737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:115391737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:83835942 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:83835942 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84360908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84360908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84446981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84446981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84450738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84450738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84498527 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84498527 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84618405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84618405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84733508 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:84733508 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:76254328 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:76254328 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:105190459 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:105190459 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:5999553 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:5999553 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50149074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50149074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50208539 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50208539 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50551425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50551425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50723335 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50723335 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50850782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50850782 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50988007 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:50988007 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:51206506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:51206506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64390745 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64390745 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64453050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64453050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:78997373 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:78997373 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:79158857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:79158857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:79374330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:79374330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:79454624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:79454624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:59501305 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:59501305 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:93782098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:93782098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:40810294 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:40810294 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:18765635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:18765635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:5593449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:5593449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131315469 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131315469 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131550478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131550478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131550497 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131550497 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131682210 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131682210 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131692935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131692935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131701324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131701324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131720752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131720752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131722414 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131722414 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131724907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131724907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131737911 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131737911 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131808707 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131808707 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131852368 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131852368 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131864955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:131864955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132001230 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132001230 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132027856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132027856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132032551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132032551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132084354 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132084354 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132098039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132098039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132102249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132102249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132163484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132163484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:107867721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:107867721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:135083583 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:135083583 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:87332945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:87332945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:87563600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:87563600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88474544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88474544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88483800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88483800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88501989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88501989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88548701 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88548701 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88576292 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88576292 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88693348 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88693348 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88724462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:88724462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11798448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:11798448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:71740116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:71740116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73822213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73822213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:101092726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:101092726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:8472665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:8472665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24880094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24880094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:113432480 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:113432480 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192543283 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192543283 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:136083605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:136083605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228527604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228527604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:28074594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:28074594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186370382 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186370382 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:97614247 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:97614247 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:5923801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:5923801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:76019288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:76019288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:123525849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:123525849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167066406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167066406 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167407295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167407295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167463263 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167463263 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167489292 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167489292 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167529120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167529120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167631329 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167631329 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167641924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167641924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:183658273 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:183658273 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:78944459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:78944459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:79053527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:79053527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:13764408 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:13764408 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:114522028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:114522028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10312442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10312442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132302965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132302965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132305853 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132305853 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132305932 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132305932 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132410896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132410896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132470017 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132470017 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132691643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132691643 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132693338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132693338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132812752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132812752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132830483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:132830483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:133052829 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:133052829 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:133160012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:133160012 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:47779385 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:47779385 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:154439661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:154439661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159284541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:159284541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56030656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56030656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123848536 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123848536 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125391865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125391865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125511844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125511844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248099992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248099992 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248115451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248115451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248153563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248153563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248166526 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248166526 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248343188 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248343188 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248366332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248366332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248550834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248550834 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55432510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55432510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20387706 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20387706 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20248316 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20248316 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22310761 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22310761 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22328604 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22328604 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22335694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22335694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22340353 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22340353 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22350515 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22350515 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22351030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22351030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22363109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22363109 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22363111 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22363111 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22364388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22364388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22376531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:22376531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20611879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20611879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20212663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20212663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20214151 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20214151 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5409054 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5409054 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5410548 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5410548 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4665869 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4665869 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5142858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5142858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4509979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4509979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55594666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55594666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15052237 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15052237 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55872410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55872410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57934269 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57934269 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:31794585 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:31794585 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:31936914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:31936914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:24911690 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:24911690 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179197326 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179197326 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59361862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59361862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54603180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54603180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54606022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54606022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:16729504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:16729504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:149921118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:149921118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29583672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29583672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29625923 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29625923 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29630260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29630260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29649066 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:29649066 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41794747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:41794747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:107754581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:107754581 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38294393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38294393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:131553103 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:131553103 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:74000118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:74000118 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43541270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43541270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43558916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43558916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:101730196 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:101730196 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:163695256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:163695256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17555385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17555385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17680941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17680941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17690002 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17690002 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:55247766 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:55247766 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:71417202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:71417202 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:112686273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:112686273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35505538 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35505538 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56717782 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56717782 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:91352362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:91352362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39600866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39600866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:60995505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:60995505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176585188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176585188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176760738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176760738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176769154 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176769154 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176769182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176769182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176788720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176788720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:89469182 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:89469182 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:206050392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:206050392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:34635246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:34635246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161832920 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161832920 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161970053 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161970053 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161973490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161973490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162030743 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162030743 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162037322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162037322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162223763 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162223763 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162869167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162869167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162990915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:162990915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:75937502 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:75937502 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3938051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3938051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3938964 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3938964 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122432200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122432200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:226590108 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:226590108 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:44535803 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:44535803 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125648605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125648605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102526578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102526578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102583281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102583281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:127253788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:127253788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:127255362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:127255362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52662899 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52662899 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154926264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154926264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101070549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101070549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:55955421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:55955421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:56359671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:56359671 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:56360683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:56360683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:56416495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:56416495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140603049 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140603049 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140552403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140552403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82389930 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82389930 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82456009 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82456009 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:17871616 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:17871616 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:78784489 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:78784489 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:24580057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:24580057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:24580305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:24580305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:5563066 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:5563066 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:272908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:272908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:289655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:289655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:165842071 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:165842071 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178684814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178684814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178704946 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178704946 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178705136 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178705136 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178939677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:178939677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:183356118 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:183356118 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54943609 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54943609 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54967078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54967078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54969155 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54969155 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31862977 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:31862977 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:32037858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:32037858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:32252191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:32252191 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:72291876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:72291876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:72296671 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:72296671 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20705544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20705544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:14810520 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:14810520 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:14810621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:14810621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:66667270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:66667270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:144857517 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:144857517 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145002718 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145002718 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145021771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145021771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:58476382 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:58476382 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:59756473 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:59756473 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:628457 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:628457 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:629764 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:629764 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:95422263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:95422263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:136409614 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:136409614 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:136429779 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:136429779 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:54530058 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:54530058 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:54655046 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:54655046 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96761291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96761291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:332392 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:332392 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122869525 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122869525 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:39851086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:39851086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31995641 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31995641 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:73437066 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:73437066 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22578408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22578408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22767192 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22767192 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22770926 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22770926 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:8045937 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:8045937 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:239160464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:239160464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:152637930 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:152637930 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:77896572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:77896572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179526052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179526052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53693168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53693168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:54960387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:54960387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48522804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48522804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:3141600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:3141600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:97795190 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:97795190 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10479636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10479636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:114577197 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:114577197 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153310877 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153310877 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153312842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153312842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:71144472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:71144472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:100962659 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:100962659 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12718971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12718971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12803769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12803769 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58260785 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58260785 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58318055 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58318055 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58381037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58381037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:11022815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:11022815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:11045892 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:11045892 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:129764031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:129764031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:34501841 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:34501841 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:133549265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:133549265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120279973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120279973 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:18959946 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:18959946 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77469442 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77469442 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77578942 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77578942 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:21087997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:21087997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85718542 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:85718542 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:77661147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:77661147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:98357075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:98357075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204400624 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204400624 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:18701279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:18701279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:209182705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:209182705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99951100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99951100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77012024 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:77012024 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:47942154 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:47942154 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:81146041 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:81146041 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:81167418 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:81167418 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:81204693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:81204693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:110466366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:110466366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:110508993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:110508993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:110522854 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:110522854 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:51483870 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:51483870 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:51799149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:51799149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:79483846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:79483846 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43243375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43243375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125216746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125216746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125299718 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:125299718 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:20303490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:20303490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:20441962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:20441962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186876174 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186876174 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186934781 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186934781 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186948395 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186948395 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186948408 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186948408 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160813152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160813152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:44174297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:44174297 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40589232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:40589232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:9263138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:9263138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:9368093 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:9368093 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:95966750 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:95966750 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39790521 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39790521 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39797824 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39797824 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:155301123 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:155301123 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:155301141 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:155301141 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198838992 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198838992 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198841298 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198841298 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198953473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198953473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:17034008 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:17034008 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45897585 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45897585 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45897600 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45897600 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:67862070 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:67862070 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124159761 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124159761 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:16834757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:16834757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:30085800 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:30085800 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131954997 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131954997 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:132044884 C>A maps to ENST00000416266 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:132044884 C>A maps to ENST00000416266 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:65197268 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:65197268 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:43551824 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:43551824 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:68615474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:68615474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161162462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:161162462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:90210687 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:90210687 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:21143195 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:21143195 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:21143843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:21143843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100856046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100856046 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:114863487 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:114863487 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:146201827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:146201827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:145912810 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:145912810 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:20300193 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:20300193 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:20465877 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:20465877 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:126739036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:126739036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208233862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208233862 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208233870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208233870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208272428 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208272428 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208296758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:208296758 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:131832782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:131832782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:131850021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:131850021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:131864787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:131864787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:132192244 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:132192244 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:205818812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:205818812 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118231266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118231266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:127390195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:127390195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:42207681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:42207681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50902077 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50902077 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116171802 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116171802 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184083031 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184083031 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:53103124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:53103124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:72397653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:72397653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:77744998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:77744998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:105606628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:105606628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:75552100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:75552100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:38160148 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:38160148 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130862248 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130862248 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:19566126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:19566126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111225780 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111225780 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111226039 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:111226039 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167315135 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167315135 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120188338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120188338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:99284135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:99284135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:81789699 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:81789699 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:81953858 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:81953858 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49649310 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49649310 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203029681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:203029681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:27827252 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:27827252 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44840804 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:44840804 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27604917 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27604917 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:160530503 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:160530503 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:160552270 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:160552270 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:160704014 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:160704014 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:111162368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:111162368 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202407882 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202407882 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:37535752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:37535752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:37546645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:37546645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54974906 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54974906 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182850923 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:182850923 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:195250458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:195250458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:25441264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:25441264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:146006247 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:146006247 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:146137073 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:146137073 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:9547749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:9547749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94710939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94710939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:32123279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:32123279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:47084532 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:47084532 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19644517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19644517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12837072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12837072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:11548598 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:11548598 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:11201906 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:11201906 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:11462213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:11462213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:45124846 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:45124846 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:90124312 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:90124312 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:23509510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:23509510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47244250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47244250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47256469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47256469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47258695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47258695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47274839 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47274839 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47315660 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47315660 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68939375 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68939375 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:69136979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:69136979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:64184727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:64184727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57384648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57384648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57420439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57420439 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57430121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57430121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57456620 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57456620 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57477781 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57477781 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57500552 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57500552 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57507456 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57507456 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57507951 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57507951 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57509428 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57509428 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57512352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:57512352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:84668567 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:84668567 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:645926 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:645926 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:106800053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:106800053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23876365 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23876365 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24046661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24046661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24180632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24180632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:46315318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:46315318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:30324439 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:30324439 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:30346065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:30346065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:48743157 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:48743157 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76066547 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:76066547 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:35086168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:35086168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:48063639 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:48063639 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3667374 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3667374 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3692093 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:3692093 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:95946935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:95946935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13628906 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:13628906 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:57256023 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:57256023 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:57257095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:57257095 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:120021571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:120021571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:37265372 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:37265372 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:170656028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:170656028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:119234251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:119234251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142460643 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142460643 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228033622 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228033622 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150990686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150990686 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:18583459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:18583459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:227077836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:227077836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43375198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43375198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43244429 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43244429 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43594169 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43594169 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43266868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43266868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43330779 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43330779 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43770734 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43770734 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:109955771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:109955771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23751235 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23751235 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38146288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38146288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31106828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31106828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:97272118 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:97272118 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:98241506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:98241506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:11583991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:11583991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:11586666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:11586666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:27692303 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:27692303 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:97285518 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:97285518 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:48129563 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:48129563 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:114336949 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:114336949 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:27260457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:27260457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:214545863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:214545863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:214576366 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:214576366 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:114381266 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:114381266 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:114397252 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:114397252 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:112160484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:112160484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7065801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7065801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198608395 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198608395 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198665778 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198665778 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198718810 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198718810 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198721221 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:198721221 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:10513896 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:10513896 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8337794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8337794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8340501 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8340501 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8346977 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8346977 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8370813 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8370813 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8470874 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8470874 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8499917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8499917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8636909 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8636909 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8990541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8990541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8998116 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8998116 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:9021411 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:9021411 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:9023190 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:9023190 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:9542255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:9542255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44084189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44084189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:48161373 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:48161373 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:128327086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:128327086 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:128330149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:128330149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:128643578 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:128643578 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:157341635 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:157341635 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158039938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158039938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220162879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220162879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220168632 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220168632 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:15668394 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:15668394 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:71105970 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:71105970 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5207891 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5207891 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40727284 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40727284 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40743802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40743802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40766322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40766322 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40789861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40789861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40789874 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40789874 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40935010 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40935010 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40938717 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40938717 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:41371090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:41371090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29581987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29581987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29649657 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:29649657 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20458166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20458166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20512214 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20512214 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44136170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44136170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:110853126 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:110853126 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161042762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161042762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:52567336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:52567336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:58395909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:58395909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:51382318 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:51382318 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64526050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64526050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9310996 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9310996 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9315313 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9315313 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:163987675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:163987675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49081738 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49081738 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66180197 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:66180197 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:502649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:502649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:29759036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:29759036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:52544717 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:52544717 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:52552214 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:52552214 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:58120737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:58120737 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128877198 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128877198 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:205739261 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:205739261 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:66264293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:66264293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24738527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24738527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:110086364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:110086364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:4658142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:4658142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:68934972 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:68934972 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33442258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33442258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:41023424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:41023424 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12641796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12641796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:34795967 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:34795967 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:37137924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:37137924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85097199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85097199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85208152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85208152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85508574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85508574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85591931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:85591931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21925941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:21925941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:173729102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:173729102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:173898593 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:173898593 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:25216069 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:25216069 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80338836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80338836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80409193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:80409193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24572854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24572854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:79896440 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:79896440 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:127953115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:127953115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36120380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36120380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66407689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66407689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50098479 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50098479 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:161141659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:161141659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:29343589 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:29343589 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65042642 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65042642 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:4826752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:4826752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31976668 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31976668 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167627735 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:167627735 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110108527 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:110108527 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:36120752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:36120752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:112228885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:112228885 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79348449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79348449 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79348631 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79348631 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79349393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79349393 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79314642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79314642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79254877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79254877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120345519 A>G maps to NM_001159353.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120345519 A>G maps to NM_001159353.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65426169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65426169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103113384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103113384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103130996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103130996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103197707 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103197707 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103206997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103206997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103322549 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103322549 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103529818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103529818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:39310097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:39310097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:16532964 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:16532964 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107083231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107083231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107144272 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107144272 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:117243090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:117243090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:56481092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:56481092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:86012780 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:86012780 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240969647 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240969647 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241083437 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241083437 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241469817 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241469817 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63157067 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63157067 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63206850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63206850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49580093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:49580093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74475136 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74475136 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:30643395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:30643395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63671891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:63671891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:30527939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:30527939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:130934720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:130934720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:130935729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:130935729 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:130941021 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:130941021 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72809703 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72809703 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72961111 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72961111 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:104671574 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:104671574 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:104672497 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:104672497 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93106663 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93106663 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40495289 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40495289 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40570051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40570051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40573450 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40573450 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40693739 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:40693739 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87049588 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87049588 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87446937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87446937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87580981 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87580981 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87866141 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:87866141 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21025341 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21025341 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49735810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49735810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:105937174 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:105937174 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:141870376 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:141870376 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:141879390 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:141879390 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:59496931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:59496931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74152228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74152228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74155305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74155305 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:25376759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:25376759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:13949787 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:13949787 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:78350799 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:78350799 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44990078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44990078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:30777683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:30777683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:117290544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:117290544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:241514577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:241514577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:79043494 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:79043494 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:77526490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:77526490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:77599950 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:77599950 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:124744192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:124744192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77300626 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77300626 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10479343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10479343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48057386 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:48057386 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:68900726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:68900726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17972897 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17972897 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35867229 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35867229 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:26881282 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:26881282 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:26900542 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:26900542 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:166923931 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:166923931 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:3623150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:3623150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:39322844 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:39322844 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:39330331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:39330331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4189400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4189400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48559269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48559269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:38078421 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:38078421 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64005898 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64005898 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:60072316 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:60072316 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57231091 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57231091 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:67697403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:67697403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:218926020 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:218926020 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:93017654 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:93017654 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:93097003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:93097003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:36231897 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:36231897 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:36623901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:36623901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:36936756 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:36936756 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:45464773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:45464773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:116892647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:116892647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39019541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39019541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39034163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39034163 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237261753 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237261753 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237494023 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237494023 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237666807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237666807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237666912 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237666912 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237755022 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237755022 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237765498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237765498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237768604 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237768604 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237788800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237788800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237813401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237813401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237817539 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237817539 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237817803 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237817803 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237843945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237843945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237855569 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237855569 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237923275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237923275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33785350 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33785350 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33814585 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33814585 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33895183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:33895183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:34115368 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:34115368 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153362848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153362848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:134994597 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:134994597 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234247494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234247494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130467436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130467436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130535712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130535712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:169646433 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:169646433 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92767317 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:92767317 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:15918461 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:15918461 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:50876561 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:50876561 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:18436473 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:18436473 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:50906181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:50906181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28314416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28314416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39965808 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39965808 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:127781278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:127781278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:83552386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:83552386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102114137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102114137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:53972263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:53972263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62009928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62009928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25689549 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25689549 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:158867774 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:158867774 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:158921691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:158921691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:108066083 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:108066083 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38797613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38797613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38833314 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38833314 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166901478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166901478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166904359 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166904359 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166102051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166102051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166164219 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166164219 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166183296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166183296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:118042473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:118042473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165969304 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165969304 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62020583 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62020583 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62026917 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62026917 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62036873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62036873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38594238 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38594238 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:167330413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:167330413 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:167136846 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:167136846 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23226312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23226312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29983487 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29983487 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:43614195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:43614195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35201812 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35201812 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:1301286 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:1301286 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50319394 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50319394 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:243477948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:243477948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:243507424 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:243507424 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161326392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:161326392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71443714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71443714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71591371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71591371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:113873130 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:113873130 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:177902559 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:177902559 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145116810 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145116810 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39514285 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39514285 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:121657781 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:121657781 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25827591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25827591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169694834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169694834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169572649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169572649 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80456807 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:80456807 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84628728 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84628728 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84642093 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84642093 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84666378 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84666378 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:83035184 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:83035184 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156127926 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156127926 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9042872 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9042872 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9050638 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9050638 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9108454 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9108454 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9154865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9154865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9319563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9319563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9379918 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9379918 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9442457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9442457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9508767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9508767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115814541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115814541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151110647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151110647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48056735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48056735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:55878805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:55878805 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:75398824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:75398824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:17918688 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:17918688 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94913160 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94913160 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94956298 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94956298 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:95089888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:95089888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94938245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94938245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94940038 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:94940038 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61600226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61600226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61380052 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61380052 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61260371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61260371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61306601 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61306601 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61310994 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61310994 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:224856721 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:224856721 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:224865926 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:224865926 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109319695 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109319695 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:180036819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:180036819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42284728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42284728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42331107 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42331107 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42539701 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42539701 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:99870534 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:99870534 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65828207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65828207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52947434 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52947434 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41164413 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:41164413 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70198851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70198851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:174943587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:174943587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:155978093 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:155978093 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156186447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156186447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:23808854 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:23808854 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:14721323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:14721323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67133324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:67133324 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:108829992 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:108829992 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:25227205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:25227205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156776959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156776959 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:130509558 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:130509558 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:82331115 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:82331115 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:82363318 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:82363318 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:19817532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:19817532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:145433856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:145433856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:145446320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:145446320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:148168654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:148168654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51200302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51200302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:91721512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:91721512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41089451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41089451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3526620 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3526620 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16980266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16980266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39583496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39583496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72171841 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72171841 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72201796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72201796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38621027 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38621027 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:1915564 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:1915564 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164714303 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164714303 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164739219 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164739219 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164741602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164741602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164758936 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164758936 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164777670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164777670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160585492 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160585492 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160465811 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160465811 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160472992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:160472992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:103710779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:103710779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51384437 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51384437 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51393096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51393096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48544095 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48544095 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127466943 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127466943 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44665474 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44665474 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:34542574 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:34542574 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:122757707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:122757707 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:122765855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:122765855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:135369117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:135369117 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:135380324 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:135380324 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:135387755 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:135387755 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42789021 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42789021 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42939373 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:42939373 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43174252 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43174252 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43203079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43203079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43247081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43247081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:111458826 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:111458826 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:113466732 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:113466732 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25830722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25830722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25917151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25917151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25918610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25918610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25778296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:25778296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:100796090 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:100796090 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:20028888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:20028888 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228552049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228552049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35298614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35298614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35323248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35323248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15073179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15073179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:53597764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:53597764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:53600158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:53600158 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63057574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63057574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38350359 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:38350359 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160557544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160557544 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62931928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62931928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160645596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160645596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160663499 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160663499 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43267864 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43267864 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63138745 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63138745 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:138718385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:138718385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19612138 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19612138 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19665311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19665311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19705701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19705701 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:92905838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:92905838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:92915393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:92915393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:172749817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:172749817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37473667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37473667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:45973024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:45973024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42398991 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42398991 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58018522 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58018522 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107416862 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107416862 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103033313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103033313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:92352614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:92352614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:92355743 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:92355743 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153748851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153748851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:128351926 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:128351926 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85456036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85456036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85461988 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85461988 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85484002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85484002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45545371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45545371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45557692 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:45557692 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73121683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73121683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:170722941 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:170722941 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:170723709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:170723709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8073982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8073982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:32426970 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:32426970 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:118126098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:118126098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:133989529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:133989529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44983660 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44983660 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:99083719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:99083719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118292374 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118292374 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118320324 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118320324 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118326695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118326695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118421862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118421862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118453547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118453547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118462772 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:118462772 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:234075478 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:234075478 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150847147 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150847147 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:140051856 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:140051856 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50254781 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50254781 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54965465 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54965465 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:70824408 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:70824408 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:70913586 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:70913586 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47381383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47381383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57175482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57175482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:108089984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:108089984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:108145657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:108145657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:10753918 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:10753918 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:75880917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:75880917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76107307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76107307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27889955 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27889955 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220494259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220494259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220504499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220504499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:72263425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:72263425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74534959 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74534959 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51851019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51851019 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24918336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24918336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24919527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24919527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26700106 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26700106 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26730734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26730734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27429626 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27429626 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:108618232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:108618232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:48697131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:48697131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10971057 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:10971057 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:304296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:304296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:85266818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:85266818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110727867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:110727867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:1239457 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:1239457 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:1219795 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:1219795 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55732623 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55732623 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28544985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28544985 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:33324292 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:33324292 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70515900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70515900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70532529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70532529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70542193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:70542193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:479862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:479862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:143066412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:143066412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21468331 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21468331 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21472159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:21472159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20876216 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20876216 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20890329 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20890329 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20903533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:20903533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:74842444 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:74842444 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:92583284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:92583284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101606573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101606573 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:70650549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:70650549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101794271 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101794271 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20525543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20525543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20611814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20611814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:168112529 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:168112529 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:37439959 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:37439959 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:2115746 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:2115746 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:144449967 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:144449967 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:106889392 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:106889392 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:112350108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:112350108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72879433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72879433 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130911118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130911118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:21772555 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:21772555 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54575277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54575277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:88411651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:88411651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:246244803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:246244803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:246641977 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:246641977 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73447717 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73447717 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:84417450 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:84417450 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:84417716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:84417716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:1256034 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:1256034 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:25154870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:25154870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:25223784 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:25223784 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121650186 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121650186 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121748451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121748451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121774696 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:121774696 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:51571294 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:51571294 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1021416 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1021416 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1263280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1263280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27595404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27595404 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:130750306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:130750306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2303907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:2303907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22429846 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:22429846 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:108357046 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:108357046 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:7524327 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:7524327 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106565246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106565246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106602701 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106602701 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106602755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106602755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106630482 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106630482 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106675747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106675747 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106778188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106778188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106822575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106822575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106833539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:106833539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:107022997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:107022997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121341047 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121341047 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121427960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121427960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121459797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121459797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121460163 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121460163 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:157077942 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:157077942 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:24049025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:24049025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:24365347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:24365347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:24590908 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:24590908 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:16371720 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:16371720 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231113822 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231113822 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231177451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231177451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31318186 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31318186 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:214878956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:214878956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215068446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215068446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215126037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215126037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215145631 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215145631 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:118506360 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:118506360 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:22690311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:22690311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:49133865 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:49133865 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217915221 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:217915221 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52943348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52943348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52960587 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52960587 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52961148 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52961148 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:123946104 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:123946104 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:44336082 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:44336082 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:75125944 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:75125944 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:35763828 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:35763828 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:35793527 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:35793527 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228860427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228860427 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147486520 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147486520 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147491468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:147491468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:136372211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:136372211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:136476225 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:136476225 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234965827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234965827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:38543020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:38543020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38884945 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38884945 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158612496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158612496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158614263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158614263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158646169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158646169 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158653252 C>A maps to NM_003126.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158653252 C>A maps to NM_003126.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:131361169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:131361169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:42155794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:42155794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142740430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142740430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142745956 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142745956 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:76024713 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:76024713 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35987995 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35987995 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36024452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:36024452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64378087 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64378087 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64480760 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64480760 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9036363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9036363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9101813 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9101813 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74036609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74036609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141442036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141442036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:170663404 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:170663404 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:149529850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:149529850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48206500 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48206500 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48054817 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:48054817 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44317411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44317411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:86108084 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:86108084 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76725230 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:76725230 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:77094267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:77094267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:116830759 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:116830759 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:93011193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:93011193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:17368935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:17368935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104012344 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104012344 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104142700 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:104142700 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36439934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36439934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36573050 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:36573050 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:136141756 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:136141756 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:66785019 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:66785019 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:90676578 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:90676578 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74087156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74087156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:4331979 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:4331979 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:191931269 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:191931269 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47751590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47751590 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:172744767 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:172744767 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4076870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4076870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63970723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63970723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:43647819 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:43647819 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31948163 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:31948163 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:99164624 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:99164624 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:23826575 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:23826575 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5125674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5125674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:168996753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:168996753 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:99917236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:99917236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:99917353 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:99917353 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:81881488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:81881488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74485974 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74485974 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:16053066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:16053066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:31405896 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:31405896 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:31618116 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:31618116 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59562826 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59562826 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180962476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180962476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10786319 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:10786319 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:46307625 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:46307625 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:46359013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:46359013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70713549 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70713549 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:3913307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:3913307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4024738 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:4024738 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31584081 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:31584081 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39949294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39949294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:75490643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:75490643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:9769367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:9769367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:115486935 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:115486935 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:115527290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:115527290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:93606677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:93606677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12067512 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12067512 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12208621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12208621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:32999522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:32999522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152690362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152690362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152784417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152784417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:33407667 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:33407667 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48877122 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48877122 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:158438831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:158438831 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:210183267 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:210183267 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51133442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51133442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61300422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61300422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:97362111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:97362111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:97369109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:97369109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38681543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38681543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:123954853 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:123954853 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:10008338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:10008338 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:120758783 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:120758783 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23845380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23845380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23875234 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23875234 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23908142 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:23908142 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160043537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160043537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150469846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150469846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33467557 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:33467557 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19168215 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19168215 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:71609937 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:71609937 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:30688855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:30688855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74181383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:74181383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100025399 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:100025399 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28886892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28886892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100997386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100997386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:36351997 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:36351997 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:75989423 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:75989423 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:17385802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:17385802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:101667171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:101667171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:179320614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:179320614 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36611740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36611740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:107134096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:107134096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162273651 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162273651 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162275305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162275305 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:45144102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:45144102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85399304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85399304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85422390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85422390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85466388 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85466388 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85472134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:85472134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:19751550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:19751550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:115121005 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:115121005 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:139578827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:139578827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:52937330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:52937330 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:53303466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:53303466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:114901237 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:114901237 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:96180145 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:96180145 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:96180275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:96180275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149743599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149743599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:167794544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:167794544 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:44254320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:44254320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154516357 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154516357 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:115961126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:115961126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151748493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151748493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151752280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151752280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49854527 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49854527 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121035955 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121035955 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121035957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:121035957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48173302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48173302 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27208970 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27208970 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27220022 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:27220022 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20872974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20872974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:112039956 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:112039956 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56650684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56650684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56694844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56694844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:51727925 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:51727925 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:56680650 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:56680650 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:50803496 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:50803496 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36044220 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36044220 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:121992752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:121992752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:114294376 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:114294376 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141688760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141688760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:115624567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:115624567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:115725164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:115725164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:133472628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:133472628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31484938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:31484938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:218607387 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:218607387 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:135387899 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:135387899 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:30691731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:30691731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:92174404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:92174404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:92237560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:92237560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:89177586 C>A maps to NM_138960.3 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:89177586 C>A maps to NM_138960.3 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:2309022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:2309022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:43558981 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:43558981 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133925115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133925115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133985094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133985094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:122745369 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:122745369 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:3076321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:3076321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38240705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38240705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:24193857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:24193857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:24299804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:24299804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:52960438 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:52960438 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:71457472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:71457472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:11457253 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:11457253 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137748366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137748366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137996971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137996971 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:138110801 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:138110801 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:32617976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:32617976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156353249 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156353249 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39973719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39973719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:54216085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:54216085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:54219197 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:54219197 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:30024752 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:30024752 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:82317179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:82317179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60679593 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60679593 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:98129813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:98129813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35711510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35711510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62949835 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62949835 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62993235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62993235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:63032753 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:63032753 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:63128062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:63128062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154624010 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154624010 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:12924763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:12924763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30752938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30752938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:75445691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:75445691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:76115371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:76115371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165712567 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165712567 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:38237528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:38237528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68877496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68877496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:75618687 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:75618687 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:79614150 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:79614150 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:177020499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:177020499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192862883 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192862883 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44403888 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44403888 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44537324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44537324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44642419 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44642419 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98443746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98443746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129784959 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129784959 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129785506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129785506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86972002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86972002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:87024441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:87024441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48867321 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:48867321 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19243348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19243348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:87521701 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:87521701 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:135316182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:135316182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:112407238 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:112407238 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:39944433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:39944433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:8890541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:8890541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:166024031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:166024031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15426932 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15426932 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130724991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130724991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130734867 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130734867 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:190167607 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:190167607 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:129810365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:129810365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12785491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:12785491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:194330595 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:194330595 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:15494964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:15494964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:15519467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:15519467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20929044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20929044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133764276 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133764276 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133771049 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:133771049 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:112824743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:112824743 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:4297888 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:4297888 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:69101861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:69101861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51281355 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:51281355 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117979714 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117979714 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152235857 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152235857 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51396949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51396949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:7981039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:7981039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172229316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172229316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7460714 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:7460714 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:93600485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:93600485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:74957720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:74957720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201334855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:201334855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175049251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175049251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175068759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175068759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175087624 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175087624 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24741475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:24741475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175292345 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175292345 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175323661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175323661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175332650 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175332650 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175360253 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175360253 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175401856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175401856 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175454604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175454604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175647538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175647538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175650535 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175650535 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175668638 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175668638 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175684151 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175684151 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175685652 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175685652 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:218674515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:218674515 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:218695174 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:218695174 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:52978093 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:52978093 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:52978151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:52978151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:52993033 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:52993033 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:133362839 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:133362839 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21945286 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:21945286 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128807719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:128807719 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:113698026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:113698026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62514229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62514229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:144288741 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:144288741 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35689308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35689308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16204634 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16204634 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:188727702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:188727702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:188748485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:188748485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:20039206 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:20039206 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:10919356 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:10919356 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:239246849 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:239246849 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39626612 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:39626612 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:141033823 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:141033823 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:141359741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:141359741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123545304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123545304 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41117731 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41117731 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41159920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41159920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42283958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42283958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72674335 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72674335 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72704944 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72704944 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72774458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72774458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72774741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72774741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72947331 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:72947331 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:18631108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:18631108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4411067 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:4411067 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:54978619 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:54978619 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:119983251 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:119983251 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30071126 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30071126 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6472742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6472742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30115103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30115103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35738646 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:35738646 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55032308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55032308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248039155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248039155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:189022475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:189022475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:189025965 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:189025965 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:14378051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:14378051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:916272 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:916272 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:100278329 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:100278329 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72950137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72950137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72959356 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72959356 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72974024 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:72974024 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:38229206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:38229206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:73478070 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:73478070 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74039978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74039978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49691750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49691750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77391105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77391105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234851453 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234851453 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3483703 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3483703 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3483928 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3483928 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142611968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142611968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:98556868 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:98556868 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:98558799 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:98558799 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54697321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54697321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130356693 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130356693 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51601110 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51601110 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51623734 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51623734 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51682489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51682489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51882708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51882708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51892584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:51892584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:31787937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:31787937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50245112 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50245112 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143412204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143412204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:44927877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:44927877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128806760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:128806760 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100365093 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:100365093 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231067693 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231067693 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39159674 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39159674 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166797521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:166797521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156552366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156552366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:138872392 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:138872392 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:147824903 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:147824903 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:51774924 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:51774924 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117602775 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117602775 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124745860 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124745860 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:167753559 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:167753559 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:76329863 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:76329863 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46878868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46878868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179542668 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179542668 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179576157 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179576157 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179584651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179584651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179592125 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179592125 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179655574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179655574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:72233659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:72233659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57594366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57594366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35477799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35477799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35480575 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:35480575 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49391109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49391109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49399613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49399613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:158882788 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:158882788 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37916346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37916346 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37924708 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:37924708 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7905124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7905124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88911943 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:88911943 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71899570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71899570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:66520748 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:66520748 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:70968983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:70968983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:69113212 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:69113212 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154228082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154228082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:118239209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:118239209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10119481 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10119481 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5536214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5536214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:43351857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:43351857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42541759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42541759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:171681484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:171681484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5412544 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5412544 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:39505481 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:39505481 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234663456 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:234663456 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70073881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70073881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:36035778 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:36035778 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:36055820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:36055820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6460547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:6460547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:19746607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:19746607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:41757063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:41757063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:41796091 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:41796091 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20362074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20362074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17750386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17750386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17750469 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17750469 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35370196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35370196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35381255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:35381255 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54342712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54342712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54542314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54542314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54704569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54704569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54792900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:54792900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73832210 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73832210 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73839091 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73839091 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33475969 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33475969 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33501190 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:33501190 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176258746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176258746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73048252 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73048252 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41001557 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:41001557 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96090246 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96090246 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158922129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158922129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:97247847 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:97247847 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:43958419 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:43958419 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215808099 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215808099 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215955378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215955378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216390988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216390988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216400572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216400572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216405274 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216405274 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216420600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216420600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216420687 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216420687 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216570776 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216570776 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179419012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179419012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:20908309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:20908309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55559451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55559451 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:17135191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:17135191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:17135193 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:17135193 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:78181353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:78181353 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219346743 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219346743 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:53500467 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:53500467 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22016371 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22016371 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49373055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49373055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:6967480 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:6967480 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:11531028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:11531028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144852161 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144852161 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144871968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144871968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:190986193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:190986193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:75760866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:75760866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:106715266 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:106715266 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:106728957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:106728957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:106739694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:106739694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70796984 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:70796984 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:78005632 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:78005632 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:78005650 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:78005650 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6793015 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6793015 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:136661675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:136661675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108160137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108160137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108209070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108209070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108315498 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108315498 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:101185527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:101185527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:101189028 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:101189028 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:82849087 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:82849087 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43749659 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43749659 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:177642702 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:177642702 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:177648871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:177648871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:157188012 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:157188012 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:157188024 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:157188024 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:135618476 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:135618476 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156269057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:156269057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158829633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158829633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158935104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:158935104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:36956679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:36956679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:36970441 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:36970441 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:51449798 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:51449798 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:51455979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:51455979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:100182248 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:100182248 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:100568575 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:100568575 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62333624 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62333624 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62336369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:62336369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12302699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:12302699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122717272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122717272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184580511 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:184580511 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:25062170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:25062170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117692221 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117692221 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117714865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:117714865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:22158800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:22158800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:22167327 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:22167327 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98779258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98779258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98850944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98850944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:124007021 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:124007021 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:6103846 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:6103846 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:27218999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:27218999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74687329 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74687329 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:42415924 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:42415924 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70846958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70846958 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70885874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70885874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70961528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70961528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70964293 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:70964293 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:71036497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:71036497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:224760410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:224760410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:52234888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:52234888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20113303 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20113303 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20130106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:20130106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:118495317 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:118495317 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29164532 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29164532 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113139049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113139049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:74943648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:74943648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:78587209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:78587209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111985268 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111985268 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:54446480 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:54446480 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:54668683 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:54668683 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:33666481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:33666481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:68371620 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:68371620 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:84360442 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:84360442 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43743820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:43743820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44207954 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44207954 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38184142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38184142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38204961 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38204961 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:1953783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:1953783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:112390859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:112390859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15559177 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15559177 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:68638731 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:68638731 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:990988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:990988 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49362187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49362187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:40765317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:40765317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6014020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6014020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6023520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6023520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160157394 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160157394 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160176693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:160176693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:184187119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:184187119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:56254037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:56254037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10756711 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10756711 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14206560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14206560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:128896627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chrX:128896627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:21416969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:21416969 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180824635 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180824635 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142102102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142102102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142166801 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:142166801 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:21326913 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:21326913 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:74555422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:74555422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:44626580 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:44626580 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:135762840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:135762840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:112877994 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:112877994 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100388863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100388863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98349311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:98349311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:56179862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:56179862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:114018943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:114018943 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:114099619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:114099619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:151688151 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:151688151 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141053321 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141053321 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62521619 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62521619 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:45703576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:45703576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:45706376 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:45706376 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:89074627 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:89074627 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47575028 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47575028 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:129691049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:129691049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37205283 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37205283 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37346670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37346670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99999349 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99999349 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:99212639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:99212639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27158147 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27158147 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:145153935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:145153935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:145159003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:145159003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38064695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38064695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38084607 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:38084607 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:135517932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:135517932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:77761708 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:77761708 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:106365452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:106365452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:106659546 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:106659546 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:32397467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:32397467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:32419822 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:32419822 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:68272116 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:68272116 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:52626286 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:52626286 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:123847788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:123847788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:100637554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:100637554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:40695509 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:40695509 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:40723462 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:40723462 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:35862030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:35862030 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19789936 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19789936 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:64438323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:64438323 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:3458301 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:3458301 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:44511325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:44511325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:74585793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:74585793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:74597643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:74597643 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:56958409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:56958409 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43296107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43296107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:32336592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:32336592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:32344883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:32344883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64393474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64393474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21467208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21467208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21505101 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21505101 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21546695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21546695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21700476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21700476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21706526 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21706526 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:22270838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:22270838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72338180 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72338180 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58419052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58419052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:109727605 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:109727605 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22817462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22817462 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:95819057 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:95819057 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22642525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22642525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22693139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22693139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58042540 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58042540 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85342600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:85342600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:54573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:54573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58491794 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58491794 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116697588 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116697588 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:182025427 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:182025427 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47389453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47389453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:40784685 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:40784685 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124482573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:124482573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247202612 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247202612 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22362541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22362541 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:12015048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:12015048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:81582714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:81582714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:81751192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:81751192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:21492211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:21492211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:106352 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:106352 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:88709203 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:88709203 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57828335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:57828335 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52876621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52876621 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:23527639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:23527639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60638373 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60638373 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60638650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60638650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238050498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238050498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238053588 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238053588 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:49977220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:49977220 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:49983060 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:49983060 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:49983940 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:49983940 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:102181031 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:102181031 T>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58558263 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:58558263 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33953932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33953932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33954281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33954281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:116966865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:116966865 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:6560488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:6560488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:7222649 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:7222649 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:7296590 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:7296590 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:7402471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:7402471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:67514315 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:67514315 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:67197866 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:67197866 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:66996111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:66996111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:17453720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:17453720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:100560911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:100560911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:180291716 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:180291716 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:32334952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:32334952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:44072647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:44072647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:111847849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:111847849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:90746435 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:90746435 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:127934272 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:127934272 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:39610877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:39610877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:33863205 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:33863205 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:33865830 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:33865830 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:5268148 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:5268148 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:84355262 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:84355262 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:84367250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:84367250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:131972548 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:131972548 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:100652478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:100652478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:87288681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:87288681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:49289669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:49289669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:50207738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:50207738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:50223159 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:50223159 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:61407603 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:61407603 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:143501951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:143501951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:32832919 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:32832919 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:109859731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:109859731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:117131052 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:117131052 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:134133037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:134133037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:73646507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:73646507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:94536187 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:94536187 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:89341374 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:89341374 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:55483001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:55483001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:55515800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:55515800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:5961447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:5961447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:26416416 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:26416416 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:45708605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:45708605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:68753794 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:68753794 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:36072139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:36072139 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:47606010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:47606010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:32185033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:32185033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:24886989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:24886989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:86552239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:86552239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:156937638 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:156937638 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:46274804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:46274804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:77022300 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:77022300 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:66808257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:66808257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:57319494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:57319494 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:101017080 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:101017080 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:101326275 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:101326275 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:62605677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:62605677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:95229652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:95229652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176914827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176914827 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:177123381 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:177123381 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:119294712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:119294712 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:119988952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:119988952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:175941173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:175941173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:294090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:294090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:216191768 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:216191768 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:116931662 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:116931662 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:35776489 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:35776489 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:76851138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:76851138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:11064648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:11064648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:69908638 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:69908638 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:212861095 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:212861095 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:33420039 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:33420039 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:7859218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:7859218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:55800332 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:55800332 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:95804144 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:95804144 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:17515101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:17515101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:92494797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:92494797 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:78110940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:78110940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:78191797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:78191797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:99955149 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:99955149 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:105970795 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:105970795 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:73327076 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:73327076 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:49638526 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:49638526 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:13592277 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:13592277 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:244691457 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:244691457 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:244751739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:244751739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:178489647 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:178489647 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:34636607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:34636607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:44953754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:44953754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:63696520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:63696520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:8669567 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:8669567 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:71019976 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:71019976 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:41907765 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:41907765 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:54095181 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:54095181 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:97720971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:97720971 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:130161754 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:130161754 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:40848230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:40848230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120654796 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120654796 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120710435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120710435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13339480 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13339480 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:2386458 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:2386458 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:85702135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:85702135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:62681554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:62681554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:71428546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:71428546 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:12747240 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:12747240 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:71014528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:71014528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:115438690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:115438690 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:66480509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:66480509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:159103164 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:159103164 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:64010007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:64010007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:32768880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:32768880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:118705598 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:118705598 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:46218632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:46218632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:204602249 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:204602249 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:207510812 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:207510812 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:160541188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:160541188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:111342557 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:111342557 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:54409983 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:54409983 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:21961823 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:21961823 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:66948485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:66948485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:19550724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:19550724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:19690927 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:19690927 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:90599884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:90599884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:202695236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:202695236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:123167372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:123167372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:4850577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:4850577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:182528451 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:182528451 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:126497140 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:126497140 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:146765544 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:146765544 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:85121466 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:85121466 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:136551560 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:136551560 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:122208674 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:122208674 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:122211727 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:122211727 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:139660075 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:139660075 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:100044845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:100044845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:99386773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:99386773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:99673836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:99673836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:146864811 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:146864811 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:147022350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:147022350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:147924958 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:147924958 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:148018294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:148018294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:125294296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:125294296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:125300141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:125300141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:125624313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:125624313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:71570317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:71570317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:86469796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:86469796 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:86559759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:86559759 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:74770846 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:74770846 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:115610741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:115610741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:160260036 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:160260036 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:9979889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:9979889 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:36623950 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:36623950 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:49705487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:49705487 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:151904268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:151904268 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:3263486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:3263486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:3266829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:3266829 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:3488009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:3488009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:4232320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:4232320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:34138410 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:34138410 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113259902 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113259902 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113521638 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113521638 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:114355162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:114355162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:33127079 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:33127079 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:80225333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:80225333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:80400878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:80400878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:80602460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:80602460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:68537552 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:68537552 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:68803261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:68803261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:150778252 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:150778252 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:64118872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:64118872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:35993677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:35993677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:96457410 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:96457410 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:96556871 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:96556871 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:46619886 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:46619886 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:187129781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:187129781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:187129790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:187129790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:6263835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:6263835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:59797408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:59797408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:121994742 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:121994742 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:61645449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:61645449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:169342710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:169342710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:126380662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:126380662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:197566945 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:197566945 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:41572466 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:41572466 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:233077783 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:233077783 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:84641507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:84641507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:79572162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:79572162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:32475358 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:32475358 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:925064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:925064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:124362658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:124362658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:13845202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:13845202 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:13908678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:13908678 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:11737946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:11737946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:65749730 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:65749730 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:128799496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:128799496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:62958217 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:62958217 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:63056272 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:63056272 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:348136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:348136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:53171695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:53171695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:115649122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:115649122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:116534939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:116534939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:116598275 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:116598275 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:153584866 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:153584866 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:35013801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:35013801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:42055245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:42055245 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:32364442 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:32364442 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:95510392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:95510392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:15473878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:15473878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:83571878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:83571878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:12289330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:12289330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:44075090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:44075090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19926242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19926242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:44182878 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:44182878 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:42945325 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:42945325 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:65357335 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:65357335 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:37257365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:37257365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:45017994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:45017994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:31642238 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:31642238 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:100353380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:100353380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:44013450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:44013450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:129779735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:129779735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:131985270 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:131985270 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:77707188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:77707188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:97562320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:97562320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:29319782 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:29319782 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:66189734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:66189734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:134594255 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:134594255 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:51944028 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:51944028 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:212972178 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:212972178 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:47355861 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:47355861 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:128376328 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:128376328 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:93011523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:93011523 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:668505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:668505 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:28345093 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:28345093 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:133783354 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:133783354 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:65348782 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:65348782 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:6318522 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:6318522 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:46744884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:46744884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:154129463 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:154129463 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:14634606 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:14634606 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:58978994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:58978994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:58982053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:58982053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:170686413 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:170686413 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:184824718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:184824718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:93164824 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:93164824 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:29572364 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:29572364 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:29627121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:29627121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:91858280 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:91858280 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:68481335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:68481335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:62225641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:62225641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:10857272 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:10857272 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:114425108 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:114425108 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:177245132 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:177245132 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:166039445 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:166039445 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:5535076 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:5535076 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:92159620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:92159620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:48914626 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:48914626 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:9931159 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:9931159 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:15894403 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:15894403 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:161561511 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:161561511 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:114879227 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:114879227 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:95479778 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:95479778 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:192325106 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:192325106 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:176518579 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:176518579 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:152287977 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:152287977 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:240384083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:240384083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:172050676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:172050676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:79207525 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:79207525 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:190875127 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:190875127 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:12708487 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:12708487 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:49350208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:49350208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:162513652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:162513652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:96522188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:96522188 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:151166100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:151166100 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:47033838 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:47033838 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:160974617 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:160974617 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:27568917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:27568917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:27617965 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:27617965 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:49201170 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:49201170 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:49239302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:49239302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:88399584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:88399584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:33187430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:33187430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:4835377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:4835377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:172828872 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:172828872 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:42476462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:42476462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:233658628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:233658628 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:233695411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:233695411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:134239453 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:134239453 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:69466740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:69466740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:42224163 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:42224163 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:54129266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:54129266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:151023493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:151023493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:37341679 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:37341679 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:157448564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:157448564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:67644149 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:67644149 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:57390346 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:57390346 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:97267385 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:97267385 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:147410749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:147410749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:90146040 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:90146040 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:152915859 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:152915859 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:93239728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:93239728 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:94506328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:94506328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:101994061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:101994061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:120789913 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:120789913 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:9915211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:9915211 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:3030842 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:3030842 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:126652243 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:126652243 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:52858450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:52858450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:106635535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:106635535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:144995009 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:144995009 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:108953459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:108953459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:7876483 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:7876483 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:89600006 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:89600006 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:126075724 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:126075724 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:108077386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:108077386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:42841672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:42841672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:27782027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:27782027 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:75110617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:75110617 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:185897591 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:185897591 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:55348912 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:55348912 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:21073735 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:21073735 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:175437050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:175437050 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:25931793 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:25931793 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:97361977 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:97361977 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:148831829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:148831829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:113887260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:113887260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:220317347 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:220317347 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:78457720 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:78457720 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:78457722 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:78457722 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:103824962 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:103824962 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:135229174 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:135229174 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:110466854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:110466854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:95856797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:95856797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:154579502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:154579502 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:59984911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:59984911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:237249379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:237249379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:51885677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:51885677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:185320346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:185320346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:31435741 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:31435741 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:102351608 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:102351608 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:6066769 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:6066769 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:73484733 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:73484733 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:112385054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:112385054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:112462230 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:112462230 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:211002079 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:211002079 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:211183217 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:211183217 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19329953 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19329953 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19339729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19339729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19415947 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19415947 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19415970 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19415970 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:21937079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:21937079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:88739934 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:88739934 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:133260298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:133260298 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:44248585 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:44248585 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:24139800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:24139800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:128680013 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:128680013 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:86570976 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:86570976 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:34599116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:34599116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:94158441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:94158441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:117098432 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:117098432 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:137065103 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:137065103 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:86887477 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:86887477 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:187167554 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:187167554 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:241727321 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:241727321 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:52698624 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:52698624 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:130422824 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:130422824 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:42157228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:42157228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:21461808 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:21461808 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:107643341 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:107643341 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:209798710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:209798710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:225613904 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:225613904 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:16674494 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:16674494 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:36067000 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:36067000 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:41571178 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:41571178 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:109224163 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:109224163 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:27963560 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:27963560 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:33911647 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:33911647 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:148244096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:148244096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:160978348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:160978348 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:99380257 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:99380257 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:188277252 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:188277252 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:151370519 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:151370519 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:114447511 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:114447511 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:114447516 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:114447516 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:113642777 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:113642777 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:142574323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:142574323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:142818598 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:142818598 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:71317806 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:71317806 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:77397512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:77397512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:77748747 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:77748747 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:115584675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:115584675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:115624916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:115624916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:115774403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:115774403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:24686041 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:24686041 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:6653696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:6653696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:14643148 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:14643148 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:14898303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:14898303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:15260131 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:15260131 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:15586124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:15586124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:65593110 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:65593110 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:65903227 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:65903227 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:77651403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:77651403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:210356699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:210356699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42099008 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42099008 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:164481692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:164481692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:164490113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:164490113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:12978182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:12978182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:5967728 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:5967728 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:48065364 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:48065364 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:116617337 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:116617337 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:126713884 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:126713884 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:66709151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:66709151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:171758142 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:171758142 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:205548731 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:205548731 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:18387315 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:18387315 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:31467634 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:31467634 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:151954207 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:151954207 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:151954277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:151954277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:2537094 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:2537094 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:61379373 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:61379373 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:158809339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:158809339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:14930346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:14930346 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:78783680 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:78783680 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:56659759 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:56659759 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:121471614 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:121471614 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:63545807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:63545807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:63584428 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:63584428 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:29675566 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:29675566 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:176740929 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:176740929 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:23900919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:23900919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:109475651 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:109475651 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:171374427 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:171374427 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:171453213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:171453213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:171476128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:171476128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:47468104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:47468104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:3158692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:3158692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:40033689 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:40033689 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:2128320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:2128320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:88608839 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:88608839 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:101757043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:101757043 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:15550088 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:15550088 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:16901503 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:16901503 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:21806352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:21806352 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:112864034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:112864034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:106464571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:106464571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:133664352 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:133664352 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:134049055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:134049055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:21450354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:21450354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:72176037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:72176037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:178269256 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:178269256 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:21273129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:21273129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:21297130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:21297130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:5475342 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:5475342 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13126347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13126347 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:115638020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:115638020 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:71162833 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:71162833 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:17720800 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:17720800 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:99266174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:99266174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:63890605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:63890605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:69325681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:69325681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:34180748 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:34180748 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:25270202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:25270202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:76291941 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:76291941 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:51128405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:51128405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:51129342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:51129342 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:79912240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:79912240 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:107810786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:107810786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:32108176 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:32108176 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:162883925 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:162883925 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:24876170 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:24876170 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:138440413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:138440413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:186369985 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:186369985 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:123889998 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:123889998 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:167045700 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:167045700 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:167625259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:167625259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:102414781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:102414781 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:132307872 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:132307872 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:132641387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:132641387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:22364137 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:22364137 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:163213820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:163213820 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:117038615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:117038615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:169438230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:169438230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176434250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176434250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176490966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176490966 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176638023 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176638023 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:119086488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:119086488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:52263705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:52263705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:206467322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:206467322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:49982018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:49982018 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:154791281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:154791281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:56287655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:56287655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:57165961 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:57165961 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:67718019 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:67718019 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:290474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:290474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:165754526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:165754526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:178577211 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:178577211 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:178859749 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:178859749 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:72359230 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:72359230 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:144915662 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:144915662 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:58596656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:58596656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:58987087 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:58987087 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:66696462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:66696462 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:76707610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:76707610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:41793625 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:41793625 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:48531093 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:48531093 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:28265638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:28265638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:97721536 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:97721536 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:98073915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:98073915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:100979858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:100979858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:13045378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:13045378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:58261806 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:58261806 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:22155800 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:22155800 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:71925129 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:71925129 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:47715198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:47715198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:230047216 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:230047216 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:59714604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:59714604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:204394942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:204394942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:18621531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:18621531 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:71493764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:71493764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:15456852 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:15456852 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:51555127 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:51555127 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:20252337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:20252337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:186933390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:186933390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42300618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42300618 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:242425754 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:242425754 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:19318835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:19318835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:132093203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:132093203 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:155467585 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:155467585 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:94563369 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:94563369 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:84534534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:84534534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:84560744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:84560744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:24781394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:24781394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:65036031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:65036031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:39420323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:39420323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:49637506 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:49637506 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:89189557 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:89189557 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:160602069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:160602069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:202541851 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:202541851 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:94805469 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:94805469 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:52723580 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:52723580 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:110995679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:110995679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:45193090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:45193090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:47292841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:47292841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:69016104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:69016104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:69136602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:69136602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:57378095 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:57378095 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:57420034 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:57420034 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:3662919 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:3662919 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:16027301 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:16027301 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:79508828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:79508828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:43528318 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:43528318 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:43532010 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:43532010 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:43258351 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:43258351 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:24608168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:24608168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:9030871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:9030871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:9111978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:9111978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:61601132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:61601132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:71252815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:71252815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:41050219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:41050219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:29598338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:29598338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:74276687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:74276687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:52431994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:52431994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:57905338 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:57905338 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:103084148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:103084148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:63306059 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:63306059 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:79343870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:79343870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:155458215 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:155458215 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:161172394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:161172394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:103418070 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:103418070 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:39311569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:39311569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:73266542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:73266542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176075461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:176075461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:72913658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:72913658 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:63703076 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:63703076 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:63708842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:63708842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:119249291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:119249291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:87566279 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:87566279 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:31431631 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:31431631 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:78725311 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:78725311 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:11458424 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:11458424 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:94544781 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:94544781 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:200986 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:200986 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:213314602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:213314602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:78539372 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:78539372 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:14322776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:14322776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:157862451 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:157862451 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:1923359 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:1923359 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:72424603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:72424603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:33873390 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:33873390 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:153512505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:153512505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:5667040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:5667040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:27507173 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:27507173 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:159167095 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:159167095 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:166061775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:166061775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:174325125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:174325125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:99880132 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:99880132 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:7366637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:7366637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:155459512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:155459512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:156167260 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:156167260 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14661142 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14661142 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14719204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14719204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14725738 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14725738 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14909413 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:14909413 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:67101256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:67101256 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:223369153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:223369153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:87746488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:87746488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:25847042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:25847042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:119016492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:119016492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:3432472 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:3432472 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:95894780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:95894780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:92314870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:92314870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:35944889 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:35944889 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:103198159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:103198159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:108169173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:108169173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:1222064 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:1222064 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:28537489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:28537489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:46506026 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:46506026 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:142995426 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:142995426 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:143200486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:143200486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:143452138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:143452138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:71436601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:71436601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:45758653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:45758653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:109763105 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:109763105 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:246219639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:246219639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:90743801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:90743801 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:25154060 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:25154060 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:50892480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:50892480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:1354333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:1354333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:78221205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:78221205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:158347906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:158347906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:231067108 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:231067108 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:118660471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:118660471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:22675915 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:22675915 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:48361352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:48361352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:167878072 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:167878072 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:167944922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:167944922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:45691491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:45691491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:64539860 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:64539860 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:27998794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:27998794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:44232979 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:44232979 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:8861440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:8861440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:77452268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:77452268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:66774771 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:66774771 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:33897251 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:33897251 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:74531655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:74531655 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:87930198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:87930198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:4068551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:4068551 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:4081769 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:4081769 T>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:5417493 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr4:5417493 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:59553427 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:59553427 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:67443686 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:67443686 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:46360234 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:46360234 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:108914243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:108914243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:4246806 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:4246806 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:45251528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:45251528 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:27000401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:27000401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:223490121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:223490121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:152887761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:152887761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:75313642 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:75313642 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:6632285 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:6632285 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:7988405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:7988405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:47466057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr22:47466057 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:139565517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:139565517 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:114894245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:114894245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:70058635 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:70058635 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:114268357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:114268357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:134029751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:134029751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:128129112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:128129112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:138357494 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:138357494 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:63004465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:63004465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:63106233 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:63106233 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:98311206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:98311206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:75279747 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:75279747 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:103274778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:103274778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:132961135 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:132961135 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:44661615 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:44661615 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:48842294 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:48842294 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:158988728 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:158988728 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:15270341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:15270341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:44116411 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:44116411 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:201120815 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:201120815 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:154806624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:154806624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:74898582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:74898582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:175393053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:175393053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:31978875 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:31978875 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:59811231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:59811231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:59944689 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:59944689 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:113659661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:113659661 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:1380296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:1380296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:10937632 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:10937632 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:42365390 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:42365390 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:117664366 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:117664366 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:31363185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:31363185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:73915847 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:73915847 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:116599201 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:116599201 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:3446987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:3446987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:142622847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:142622847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:99622283 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:99622283 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:38515466 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:38515466 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:3336573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:3336573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:33036963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:33036963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:219600549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:219600549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:8066124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:8066124 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:99948488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:99948488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:43858262 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:43858262 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:41319449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:41319449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:126217048 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:126217048 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:215925408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:215925408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:216400366 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:216400366 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:216556551 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:216556551 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:11588725 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:11588725 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:144953944 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:144953944 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:108389572 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:108389572 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:48287508 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:48287508 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:37005829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:37005829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:58161527 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:58161527 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:107320238 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:107320238 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:36569852 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr20:36569852 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:37705839 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:37705839 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:2784471 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:2784471 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:78224300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:78224300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:128880531 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:128880531 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:217052547 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:217052547 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:217052549 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:217052549 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:130172338 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:130172338 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:11867981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:11867981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:135660210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:135660210 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:106365649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:106365649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:57286906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:57286906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:57286908 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:57286908 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:178764155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:178764155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:6960951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:6960951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:53396150 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:53396150 A>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:64174675 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:64174675 T>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:72755388 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:72755388 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:22847697 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:22847697 G>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:40796309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:40796309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:134392325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:134392325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:134424656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chrX:134424656 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:88604712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:88604712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:38032837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:38032837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:27486311 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:27486311 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:31344546 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:31344546 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:241813333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:241813333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:49955865 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:49955865 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:109444354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:109444354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:139852007 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:139852007 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:100042595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:100042595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:17438489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:17438489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:70031597 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:70031597 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:160114739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:160114739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr18:29246140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr18:29246140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:66298584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:66298584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:14738554 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:14738554 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:50582944 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:50582944 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:36911043 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:36911043 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:75115077 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:75115077 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:156899298 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:156899298 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:5753462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:5753462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:209036948 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:209036948 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:40314310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:40314310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:132084837 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:132084837 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:2757703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:2757703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:86063018 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:86063018 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:200722835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:200722835 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:46152342 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:46152342 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:179702493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:179702493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:176015962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:176015962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:88144990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:88144990 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:7804437 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:7804437 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr18:24532550 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr18:24532550 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:21393225 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:21393225 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:32778869 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:32778869 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:139882565 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:139882565 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:36730130 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:36730130 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:125673494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:125673494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:36665728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:36665728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:113420535 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:113420535 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:122941148 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:122941148 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:470560 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:470560 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:52788040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:52788040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:47283796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:47283796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:61113296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:61113296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:159174850 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:159174850 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:116538411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:116538411 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:100496608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:100496608 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:221876029 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:221876029 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:41292914 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:41292914 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:100015423 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:100015423 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:41572156 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:41572156 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:51869046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:51869046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:216680262 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:216680262 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:133602208 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:133602208 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:66085815 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:66085815 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:55187514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:55187514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:139180012 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:139180012 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:125103884 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:125103884 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:128491450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:128491450 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:79290856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:79290856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:79458083 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:79458083 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:44211932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:44211932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:12632856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:12632856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:132556371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:132556371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:89652624 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:89652624 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:235715361 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:235715361 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:50660833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:50660833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:94693217 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:94693217 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:10006437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:10006437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:140054473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:140054473 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:73142705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:73142705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:26236845 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:26236845 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:50358699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:50358699 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:105170208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:105170208 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:1399296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:1399296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:42457538 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:42457538 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:52821582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:52821582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:155893907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:155893907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:19491847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:19491847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:67338265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:67338265 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:43885761 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:43885761 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:10412589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:10412589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr13:70370861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr13:70370861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:33960657 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:33960657 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:145509751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:145509751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:197577739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:197577739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:33614459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:33614459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:14108532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:14108532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:2210439 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:2210439 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:66736989 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:66736989 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:217209808 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:217209808 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:136620148 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:136620148 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:8808247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:8808247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:8971890 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:8971890 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:9019960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:9019960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:1213091 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:1213091 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:49412492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:49412492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:171264121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:171264121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:21806532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:21806532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:112907047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:112907047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:120546765 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:120546765 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:115409787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:115409787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:154108532 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:154108532 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:102332438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:102332438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:123519488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:123519488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:74677434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:74677434 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:132642907 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:132642907 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:16059789 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:16059789 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:59420506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:59420506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr21:47217812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr21:47217812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr21:47217823 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr21:47217823 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:91238015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:91238015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:55913102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:55913102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:53852236 T>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:53852236 T>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:10467954 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:10467954 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:111664226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:111664226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:8789712 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:8789712 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:102056664 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:102056664 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:44536189 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:44536189 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:22104796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:22104796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:122273570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:122273570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:37531188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:37531188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:57461781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:57461781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:46314104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:46314104 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:61917508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:61917508 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:184026218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:184026218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:9209991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:9209991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:41515515 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:41515515 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:100143505 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:100143505 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:42972001 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:42972001 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:10131493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:10131493 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:11515989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:11515989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:240969389 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:240969389 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:63186285 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:63186285 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:106034545 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:106034545 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:30776224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:30776224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:17973708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:17973708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:78919632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:78919632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:184572585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:184572585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:237659763 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:237659763 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:4201509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:4201509 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:35653771 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:35653771 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:72611004 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:72611004 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:73740726 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:73740726 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:35314559 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:35314559 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:35314567 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:35314567 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:101372267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:101372267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr13:45970002 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr13:45970002 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:114492257 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:114492257 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:150715164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:150715164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:18266682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:18266682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:24909206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:24909206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:108609656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:108609656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:53438898 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:53438898 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:1258325 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:1258325 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:57020598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:57020598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:28994104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:28994104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:92981562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:92981562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:67932896 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:67932896 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:125483102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:125483102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:168250550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:168250550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:114837298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:114837298 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:23719086 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:23719086 A>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:20852689 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:20852689 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:70692617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:70692617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:153537911 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:153537911 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:188896001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:188896001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:186324933 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:186324933 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:65705394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr7:65705394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:42242257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:42242257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:54957786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:54957786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:101341848 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:101341848 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:31332301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:31332301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:31340013 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:31340013 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:143407866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:143407866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:122522530 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:122522530 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:38540556 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:38540556 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:17720636 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:17720636 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:38482218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:38482218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:38482227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:38482227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:57019365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:57019365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:816843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:816843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:53577368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:53577368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:37726371 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:37726371 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:53611627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:53611627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:30934456 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:30934456 T>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:30936717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:30936717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:57905545 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:57905545 C>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:46316285 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chrX:46316285 T>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:106241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:106241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr10:47082673 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr10:47082673 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:15544345 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:15544345 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr14:78183396 A>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr14:78183396 A>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr19:15166223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr19:15166223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr17:28512800 T>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr17:28512800 T>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:158225713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:158225713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:6701269 A>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:6701269 A>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:21613295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chrX:21613295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:70732671 C>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:70732671 C>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:125464492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:125464492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:34049154 A>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:34049154 A>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr20:44525547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr20:44525547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:107274470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:107274470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr22:32229786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr22:32229786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr7:86822726 T>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr7:86822726 T>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr7:21905997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr7:21905997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:176935090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:176935090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:132554024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:132554024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr18:10689469 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr18:10689469 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:46252256 G>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:46252256 G>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:94600894 A>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:94600894 A>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:96374753 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:96374753 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:27319768 A>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:27319768 A>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr19:51501190 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr19:51501190 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:160783376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:160783376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr18:32605520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr18:32605520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:29543027 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:29543027 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:220986561 A>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:220986561 A>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:78383758 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:78383758 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:107866880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr1:107866880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:52269097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:52269097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:51854744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:51854744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:68608068 T>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:68608068 T>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:89890840 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr12:89890840 G>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:23524610 G>A maps to NM_020227.2 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr5:23524610 G>A maps to NM_020227.2 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr13:48892642 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr13:48892642 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:87211865 T>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr2:87211865 T>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:117679206 A>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr6:117679206 A>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:10197502 G>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:10197502 G>C did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr17:71354413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr17:71354413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr13:24696579 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr13:24696579 C>T did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:66461837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr11:66461837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr7:150491186 C>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr7:150491186 C>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:85639797 T>G did not map to a codon.
Sequencing variant TCGA-17-Z035-01A-01W-0746-08 chr4:85639797 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:15121153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:15121153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr16:20451872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr16:20451872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:114691789 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:114691789 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:178548767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:178548767 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:58272420 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:58272420 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:148977890 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:148977890 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:50204486 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:50204486 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:131299574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:131299574 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:14578412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:14578412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:35240623 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:35240623 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:10342394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:10342394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr16:19641073 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr16:19641073 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:116660178 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:116660178 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:14756965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:14756965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:201020361 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:201020361 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:159159557 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:159159557 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:75601803 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:75601803 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:115485117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:115485117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:8633555 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:8633555 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:207946167 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:207946167 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:88520237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:88520237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr9:33265938 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr9:33265938 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:102108269 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:102108269 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:98999935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:98999935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:177677123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:177677123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:74680416 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:74680416 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:47602164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:47602164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:125557784 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:125557784 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:28859056 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:28859056 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:17197881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:17197881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:4797709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:4797709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:80600418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:80600418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:162619264 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:162619264 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr20:47835863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr20:47835863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:21642430 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:21642430 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:98015051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:98015051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:95614099 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:95614099 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:172584781 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:172584781 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:32610468 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:32610468 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr20:34776562 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr20:34776562 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:131197408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:131197408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:226027756 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:226027756 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:56492211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:56492211 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:102486430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:102486430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:103003024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:103003024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:164469427 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:164469427 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:13782586 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:13782586 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:48715417 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:48715417 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:48715437 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:48715437 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:49197173 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:49197173 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:162794635 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:162794635 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:117911747 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:117911747 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:5592719 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:5592719 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:28370036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:28370036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:28502158 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:28502158 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:29797815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:29797815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:29797817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:29797817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:25679283 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:25679283 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:201197473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:201197473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:110483919 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:110483919 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:44543312 G>A maps to NM_001100817.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:44543312 G>A maps to NM_001100817.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:63405822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:63405822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:79279737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr10:79279737 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:24179531 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:24179531 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:73491563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:73491563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:42825012 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:42825012 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:24564670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:24564670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr22:33953957 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr22:33953957 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:152551920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:152551920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:104308873 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:104308873 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:73567188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:73567188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:97820036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:97820036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:142030131 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:142030131 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:113993351 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:113993351 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:85396996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:85396996 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:66370299 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:66370299 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:66617168 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:66617168 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:10362896 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:10362896 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:34227373 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:34227373 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:193336772 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:193336772 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:23240003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:23240003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr9:138454840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr9:138454840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:176763930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:176763930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:206417843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:206417843 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:85670152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:85670152 C>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:22138724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:22138724 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:242319855 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:242319855 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:43197474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:43197474 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:202407850 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:202407850 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:68885362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:68885362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:209324458 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:209324458 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:38912824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:38912824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:103390039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:103390039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:149617364 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:149617364 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:64594588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:64594588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:33920122 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:33920122 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:3493809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr7:3493809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:101176112 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:101176112 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:155798688 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:155798688 G>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:43026867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:43026867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:63046987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:63046987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:51863349 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:51863349 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:186567768 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:186567768 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:220345387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:220345387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:36875957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr13:36875957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:104006713 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:104006713 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:32591530 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:32591530 A>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr9:114820655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr9:114820655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:85430903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:85430903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:114805043 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:114805043 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:138024669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:138024669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:126013470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:126013470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chrX:99839983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chrX:99839983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:32015797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr6:32015797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:43701470 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:43701470 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:223998126 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:223998126 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:188986438 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:188986438 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:179634723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:179634723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:23904904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:23904904 C>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:70505118 A>G maps to ENST00000514019 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:70505118 A>G maps to ENST00000514019 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:54847732 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:54847732 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:32452006 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:32452006 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:114570969 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:114570969 T>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:40454956 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:40454956 T>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:36724459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:36724459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:36724503 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:36724503 T>C did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:22235431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:22235431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:72523302 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr18:72523302 A>G did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:30934467 G>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:30934467 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:9242692 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:9242692 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:94544440 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:94544440 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:48209076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:48209076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:26598967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:26598967 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:35500733 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:35500733 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:35500744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:35500744 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:31478198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:31478198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:8414841 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:8414841 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:20635596 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:20635596 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:131972381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:131972381 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:70892715 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:70892715 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:41469811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:41469811 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:49962271 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:49962271 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:40745947 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:40745947 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:73799362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:73799362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:7948374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:7948374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:114269604 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:114269604 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:1752197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:1752197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:28914912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:28914912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:11084677 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:11084677 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr20:36953264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr20:36953264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:79999526 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:79999526 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:121598009 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:121598009 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:33137495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:33137495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:55678033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:55678033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:85058969 A>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:85058969 A>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:40193540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:40193540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:2488007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:2488007 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:64125809 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:64125809 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:72540723 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:72540723 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:48209266 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:48209266 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:105656564 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:105656564 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:28361234 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:28361234 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:125505070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:125505070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:48617340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:48617340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:15516330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:15516330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:103907535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:103907535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:76471674 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:76471674 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:11555939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:11555939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:169396402 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:169396402 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:51370722 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:51370722 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:116101371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:116101371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:350651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:350651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:137800544 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:137800544 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:108393089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:108393089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr20:33725651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr20:33725651 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:132032330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:132032330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:89499216 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:89499216 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:41607102 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:41607102 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:5617375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:5617375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr18:71797595 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr18:71797595 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:124993144 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:124993144 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:147019515 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:147019515 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:151393185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:151393185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:49354602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:49354602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:104122220 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:104122220 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:44191859 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:44191859 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:61994899 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:61994899 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:151228528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:151228528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:135454927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:135454927 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:123483366 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:123483366 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:88781046 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:88781046 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:52770441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:52770441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:5274641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:5274641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:236715504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:236715504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80678711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80678711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679077 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679077 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679204 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679204 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:39329016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:39329016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:56093777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:56093777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:52839958 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:52839958 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:19491863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:19491863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:113740621 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:113740621 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:196288589 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:196288589 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:196311382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:196311382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:23408692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:23408692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:27322628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:27322628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:114124456 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:114124456 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:51532814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:51532814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:53233173 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:53233173 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:154185632 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:154185632 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:161055879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:161055879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:35749726 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:35749726 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:210517879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:210517879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:16178005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:16178005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:123385113 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:123385113 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:11167533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:11167533 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:23885172 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:23885172 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr13:109328665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr13:109328665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:124216350 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:124216350 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:131258450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:131258450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:124266270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:124266270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:19552222 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:19552222 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:57136812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:57136812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:162535058 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:162535058 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:91715184 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:91715184 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:157684169 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:157684169 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:54953955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:54953955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:19375755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:19375755 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:20376940 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:20376940 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:2645950 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:2645950 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:130424393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:130424393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:155461270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:155461270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:4058921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:4058921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:152198382 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:152198382 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:18432627 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:18432627 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:61192521 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:61192521 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:85591894 A>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:85591894 A>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr13:34409731 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr13:34409731 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr15:33878411 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr15:33878411 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:166234058 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:166234058 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:243589923 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:243589923 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:4119227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:4119227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:9388827 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:9388827 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:94752628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:94752628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:68331092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:68331092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:47755851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:47755851 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:98633051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:98633051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:121551068 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:121551068 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:217915249 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:217915249 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:3349723 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:3349723 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:68424374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:68424374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:152464946 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:152464946 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:100537135 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:100537135 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:110353430 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:110353430 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:27229310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:27229310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:32559429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:32559429 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:156378411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:156378411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:153556148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chrX:153556148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:69077364 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:69077364 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:110099687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:110099687 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:98508109 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:98508109 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:5412279 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:5412279 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:168114341 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:168114341 T>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr22:41318270 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr22:41318270 T>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:43506603 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:43506603 T>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:217001956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:217001956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:44901230 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:44901230 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:59888 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:59888 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:63576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:63576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:18098016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:18098016 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:39440413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:39440413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr18:56268267 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr18:56268267 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:21902776 T>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:21902776 T>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr10:104616030 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr10:104616030 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:120112866 A>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:120112866 A>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr7:69379359 C>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr7:69379359 C>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:96035765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:96035765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr10:103308703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr10:103308703 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:170656133 T>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:170656133 T>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:97611200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:97611200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr22:24249493 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr22:24249493 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:117942159 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:117942159 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr11:83771197 A>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr11:83771197 A>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr7:142567793 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr7:142567793 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:212630680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:212630680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:5740441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr4:5740441 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:64456655 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:64456655 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:64456684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:64456684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:66196816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:66196816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:66196828 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:66196828 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:59890142 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:59890142 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:59890158 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:59890158 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:60082205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:60082205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:183901492 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:183901492 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr14:31571983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr14:31571983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:42819279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:42819279 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:186386598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:186386598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:147903696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:147903696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:117177814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:117177814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:154687079 T>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:154687079 T>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:188543053 T>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:188543053 T>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:40527391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:40527391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:33567132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:33567132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr7:20253884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr7:20253884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr16:15807870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr16:15807870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:167109098 A>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:167109098 A>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:119380032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr3:119380032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:57142115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:57142115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr17:12736408 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr17:12736408 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:76182982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:76182982 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:76182996 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:76182996 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:127448477 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:127448477 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:86901330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:86901330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:46953030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:46953030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:214223021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:214223021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:214223023 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:214223023 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:91047194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:91047194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:23718871 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:23718871 A>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:133945570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:133945570 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:133945592 C>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:133945592 C>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:133945596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr8:133945596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr11:113569956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr11:113569956 C>G did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:73194903 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr9:73194903 G>C did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:144732062 A>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr6:144732062 A>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:12568726 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr1:12568726 G>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:224783793 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr2:224783793 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:808701 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr5:808701 G>T did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr19:44662377 T>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr19:44662377 T>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr19:58046786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z038-01A-01W-0746-08 chr19:58046786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:215843832 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:215843832 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:24326254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:24326254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:26620543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:26620543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:105191445 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:105191445 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:95538225 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:95538225 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:104159887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:104159887 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:5750122 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:5750122 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:47059860 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:47059860 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:26824973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:26824973 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:46702018 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:46702018 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:15315612 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:15315612 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11026757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11026757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11037062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11037062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11046040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11046040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11064648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11064648 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11078573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:11078573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:66291183 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:66291183 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr22:18166099 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr22:18166099 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:96970634 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:96970634 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:32992008 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:32992008 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:48876634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:48876634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:34193619 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:34193619 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:9495456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:9495456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:33979851 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:33979851 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:207262996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:207262996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:37176143 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:37176143 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:2648864 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:2648864 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:67692709 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:67692709 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:32161959 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:32161959 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:15482764 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:15482764 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:33457533 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:33457533 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:21880571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:21880571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:1588716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:1588716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:196670604 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:196670604 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:10059656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:10059656 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:86898258 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:86898258 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:105832789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:105832789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:69279513 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:69279513 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:3194091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:3194091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:80686889 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:80686889 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:11397124 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:11397124 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:27945073 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:27945073 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:155226047 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:155226047 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:2064552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:2064552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:51749697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:51749697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:11805970 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:11805970 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:32860243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:32860243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:32860352 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:32860352 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:169140991 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:169140991 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:116622338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:116622338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:56736075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:56736075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:68840628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:68840628 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:68840708 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:68840708 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:231503296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:231503296 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:27302999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:27302999 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:57361949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:57361949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:97630084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:97630084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:156593330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:156593330 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:125083736 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:125083736 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:142469190 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:142469190 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:128486639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:128486639 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:190871389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:190871389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:12725069 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:12725069 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:132561627 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:132561627 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:41061184 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:41061184 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:29589091 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:29589091 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:49574420 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:49574420 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:173530779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:173530779 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:117823905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:117823905 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:96697673 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:96697673 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:94411993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:94411993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:9915984 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:9915984 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:145008943 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:145008943 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:30686797 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:30686797 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:32086434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:32086434 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:71708767 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:71708767 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:18818553 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:18818553 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:73985673 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:73985673 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:63901227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:63901227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:221054494 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:221054494 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:118958928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:118958928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:27134053 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:27134053 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:27668870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:27668870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:27669294 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:27669294 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:182339855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:182339855 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:31282441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:31282441 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:65337197 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:65337197 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:55962392 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:55962392 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:73494452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:73494452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:123267609 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:123267609 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:111583372 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:111583372 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:51327600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:51327600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:52797714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:52797714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:41672723 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:41672723 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:42910260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:42910260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:141709574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:141709574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:118003272 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:118003272 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:19431259 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:19431259 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:30748178 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:30748178 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:3835495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr20:3835495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:20212353 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:20212353 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:29520746 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:29520746 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr18:33838823 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr18:33838823 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:17083961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:17083961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:86437880 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:86437880 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:108205511 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:108205511 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr22:26242333 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr22:26242333 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:134268930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:134268930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:36381171 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:36381171 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:57074369 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:57074369 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:175812215 G>A maps to ENST00000509257 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:175812215 G>A maps to ENST00000509257 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:200017161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:200017161 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:32011081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:32011081 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:131355946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:131355946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:17625939 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:17625939 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr13:25883358 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr13:25883358 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:102312319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:102312319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:22352095 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:22352095 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:24846309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:24846309 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:55102945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:55102945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:102360819 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:102360819 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:98994204 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:98994204 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:33887131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:33887131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:145028444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:145028444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:95543798 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:95543798 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:22662356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:22662356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:65688657 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:65688657 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:198968507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:198968507 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:93131206 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:93131206 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:146085776 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:146085776 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:146085783 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:146085783 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:43357784 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:43357784 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:43359588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:43359588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:40986624 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:40986624 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:62005350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:62005350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:39726462 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr7:39726462 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:25326955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:25326955 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:79253387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:79253387 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:130967287 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:130967287 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:7137026 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:7137026 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:95712433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:95712433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:34145913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr15:34145913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:38991880 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:38991880 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:167163586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:167163586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:119718976 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:119718976 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:94960013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:94960013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr9:17786355 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr9:17786355 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr9:131777204 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr9:131777204 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:69651416 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:69651416 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:58016721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:58016721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:47182209 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:47182209 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:48690580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:48690580 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:101606533 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr5:101606533 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:96964846 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:96964846 T>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:1285285 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:1285285 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:22415580 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:22415580 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:16371302 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:16371302 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:16371304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:16371304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:172674646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:172674646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr9:131374229 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr9:131374229 A>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:104123885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:104123885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:4333893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:4333893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:56750368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:56750368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:61790606 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:61790606 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:64685107 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr14:64685107 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:63340236 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:63340236 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:61134448 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr17:61134448 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:12886260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr11:12886260 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:74320582 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:74320582 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:104463622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:104463622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:133428410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:133428410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:75970704 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:75970704 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:68930199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:68930199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:29736520 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr12:29736520 T>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr13:101264492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr13:101264492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:10972722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr21:10972722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:123957843 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:123957843 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:72942273 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:72942273 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:49714607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr19:49714607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:231048320 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:231048320 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:231048322 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:231048322 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:52501484 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr1:52501484 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:103297718 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr8:103297718 A>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:118975571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chrX:118975571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:49154843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr3:49154843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:177619694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:177619694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:58290994 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:58290994 A>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:78997972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:78997972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:168110725 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr2:168110725 T>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:38005924 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr6:38005924 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:99508142 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr10:99508142 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:3432779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr16:3432779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:59631 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr4:59631 C>G did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr22:20748986 G>C did not map to a codon.
Sequencing variant TCGA-17-Z040-01A-01W-0746-08 chr22:20748986 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87079175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87079175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87081221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87081221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:22085878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:22085878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:31591355 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:31591355 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:32126578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:32126578 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:80639603 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:80639603 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:236894716 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:236894716 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:127764646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:127764646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:127839101 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:127839101 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:1750445 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:1750445 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:19646678 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:19646678 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chrX:147891187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chrX:147891187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:86740840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:86740840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:19576289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:19576289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:56417021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:56417021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:104160330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:104160330 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:69420581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:69420581 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:99126092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:99126092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:68172247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:68172247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:49710692 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:49710692 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:7531738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:7531738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:35281301 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:35281301 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:90843944 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:90843944 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11021824 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11021824 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11025646 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11025646 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11030645 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11030645 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11057367 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:11057367 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:143569691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:143569691 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:94242990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:94242990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:33958670 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:33958670 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:31604933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:31604933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:47182779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:47182779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:64591359 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:64591359 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:81258989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:81258989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:58729755 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:58729755 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:24924602 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:24924602 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:13885424 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:13885424 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:24471205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:24471205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:220869866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:220869866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:1035021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:1035021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:63439151 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:63439151 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:157735351 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:157735351 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:149901548 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:149901548 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:40807150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:40807150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:34431504 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:34431504 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:2500188 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:2500188 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:159159588 G>T maps to NM_021189.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:159159588 G>T maps to NM_021189.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:30864402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:30864402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:30864409 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:30864409 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:20768861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:20768861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:85626622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:85626622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:46914332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:46914332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:207943591 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:207943591 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:60086854 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:60086854 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:60326594 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:60326594 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:45035080 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:45035080 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:243362554 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:243362554 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:110697643 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:110697643 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chrX:85166402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chrX:85166402 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:101015859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:101015859 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:37915265 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:37915265 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:11213183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:11213183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:95657819 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:95657819 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:88085688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:88085688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:147597042 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:147597042 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:76555320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:76555320 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:125282031 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:125282031 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:125517968 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:125517968 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:230783952 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:230783952 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:139641248 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:139641248 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:130292341 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:130292341 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:39123978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:39123978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:207793078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:207793078 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:167517203 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:167517203 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:2855760 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:2855760 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:3265258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:3265258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:4470319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:4470319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:113727788 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:113727788 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:16970474 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:16970474 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:101740610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:101740610 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:44874017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:44874017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:187129208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:187129208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:50282740 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:50282740 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:117187122 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:117187122 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:137472591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:137472591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:41590952 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:41590952 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:84732669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:84732669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:196611768 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:196611768 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:116510742 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:116510742 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:153647680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:153647680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:154426455 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:154426455 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:98015412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:98015412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:167068052 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:167068052 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:95270024 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:95270024 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:88882864 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:88882864 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:14788108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:14788108 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:132172514 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:132172514 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:220145571 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:220145571 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:133015234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:133015234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:133702328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:133702328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:133704599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:133704599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:94757158 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:94757158 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:64658385 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:64658385 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:66104629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:66104629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:139373747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:139373747 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:45489536 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:45489536 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:62305434 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:62305434 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:62623338 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:62623338 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:206153918 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:206153918 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:87494044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:87494044 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:58431197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:58431197 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:99091192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:99091192 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:92121512 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:92121512 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:159783446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:159783446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:65418457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:65418457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:32776798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:32776798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:17472549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:17472549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:47213286 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:47213286 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:16077195 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:16077195 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:89649804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:89649804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:89729399 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:89729399 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:54001459 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:54001459 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:131958234 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:131958234 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:70105739 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:70105739 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:93387794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:93387794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:67243964 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:67243964 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chrX:78426399 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chrX:78426399 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:40343682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:40343682 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:102498677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:102498677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:120479732 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:120479732 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:6982716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:6982716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:126353855 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:126353855 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:126690593 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:126690593 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:27871612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:27871612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:27874432 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:27874432 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:110280565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:110280565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:108634375 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:108634375 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:156476002 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:156476002 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:139484839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:139484839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:27100765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:27100765 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:66357092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:66357092 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:72100387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:72100387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:25730852 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:25730852 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:44683709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:44683709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:201197371 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:201197371 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:161052670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:161052670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:211017355 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:211017355 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:178419866 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:178419866 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:44702277 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:44702277 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:61361049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:61361049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:158025751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:158025751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:74476366 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:74476366 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:53312025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:53312025 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:49163967 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:49163967 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:16582331 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:16582331 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:55179556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:55179556 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:41420436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:41420436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:28004899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:28004899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:42288023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:42288023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:142238160 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:142238160 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:70161226 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:70161226 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:37134514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:37134514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:33568260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:33568260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:61710218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:61710218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:182925219 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:182925219 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:141796307 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:141796307 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:151937556 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:151937556 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:28430561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:28430561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:151363065 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:151363065 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:46067804 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:46067804 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:78368453 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:78368453 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:16891790 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:16891790 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:16908346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:16908346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:22698650 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:22698650 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:118979749 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:118979749 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:198248218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:198248218 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:21373602 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:21373602 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:69728983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:69728983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:25442009 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:25442009 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:153659433 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:153659433 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:34711108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:34711108 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:34899249 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:34899249 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:83666657 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:83666657 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:131847028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:131847028 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:167576353 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:167576353 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:132625532 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:132625532 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:69482168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:69482168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:117086458 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:117086458 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:24981904 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:24981904 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:32145082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:32145082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:726056 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:726056 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:176762883 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:176762883 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:69676757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:69676757 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:69692613 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:69692613 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:31731628 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:31731628 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:80015076 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:80015076 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:47344950 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:47344950 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:66916065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:66916065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:92954744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:92954744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:56448420 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:56448420 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:32063360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:32063360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:32099959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:32099959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:32288925 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:32288925 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:66736463 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:66736463 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:66736491 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:66736491 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:103780565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:103780565 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:41747938 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:41747938 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:22770890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:22770890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:100908563 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:100908563 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:98357049 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:98357049 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:131976591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:131976591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:39364103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:39364103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:46616084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:46616084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:160716776 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:160716776 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:146182943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:146182943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:57454088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:57454088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:57505053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:57505053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:6544044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:6544044 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:43285276 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:43285276 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:23758993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:23758993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:8215542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:8215542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:157834967 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:157834967 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:51379666 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr14:51379666 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:36611205 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:36611205 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:25586039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:25586039 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:54764337 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:54764337 A>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:59506014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:59506014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:94404806 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:94404806 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:77169178 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:77169178 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:213369004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:213369004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:158077662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:158077662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:38932942 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:38932942 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:237759119 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:237759119 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:47658154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:47658154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:38596258 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:38596258 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:169566525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:169566525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:83023518 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:83023518 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:17822436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:17822436 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:61647382 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:61647382 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:156087502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:156087502 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:52310442 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:52310442 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:138473751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr5:138473751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:42923282 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:42923282 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:43206848 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr18:43206848 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:75757372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:75757372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:143543280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:143543280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:21168506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:21168506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:33761418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:33761418 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:67397849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:67397849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:130913573 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:130913573 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:1133357 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:1133357 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:107956787 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:107956787 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:106464718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:106464718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:106769858 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:106769858 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:106897412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:106897412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:36723121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:36723121 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:53197331 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:53197331 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:191843735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:191843735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:53108419 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:53108419 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:67611189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:67611189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:13468243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:13468243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:36359091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:36359091 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:56685675 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:56685675 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:32526432 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr21:32526432 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:66644550 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:66644550 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:85345350 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr11:85345350 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:129807791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:129807791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:129891198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:129891198 C>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:129950303 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:129950303 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:23064825 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:23064825 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:175674184 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:175674184 T>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:42574442 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr20:42574442 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:59880190 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:59880190 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:209945393 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:209945393 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:123715105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:123715105 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:72857898 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:72857898 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:30072015 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:30072015 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:38111983 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr22:38111983 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:3424399 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr17:3424399 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:150176592 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:150176592 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:120433220 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:120433220 T>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:37889101 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:37889101 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:7927576 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:7927576 A>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:23339134 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr3:23339134 A>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:5412171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:5412171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:216465754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:216465754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:62734422 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:62734422 G>C did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:62312814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:62312814 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:54610543 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:54610543 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:27157982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr13:27157982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:84348749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:84348749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:78751159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr16:78751159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:123921949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:123921949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:68416 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:68416 C>T did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:53219830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:53219830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:88419730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:88419730 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:74273170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:74273170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:32478510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:32478510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:100253000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:100253000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:3653163 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:3653163 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:33661874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:33661874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:77369847 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:77369847 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:43860421 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:43860421 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:178559692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:178559692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:2895663 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:2895663 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:11807453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:11807453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:109663830 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:109663830 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:134222841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:134222841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:53534370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:53534370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:75531802 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:75531802 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:38530636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:38530636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:104162522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:104162522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:113747714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:113747714 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:54526588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:54526588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:99776725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:99776725 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:47059018 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:47059018 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:201474148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:201474148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:77412194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:77412194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:119722274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:119722274 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:119976577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:119976577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:212788266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:212788266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:112255263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:112255263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:10385772 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:10385772 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:3553325 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:3553325 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:74755624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:74755624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:11039061 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:11039061 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:11071479 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:11071479 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:57005319 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:57005319 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:99723645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:99723645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:60461804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:60461804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:32520691 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:32520691 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:36334115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:36334115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:17514463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:17514463 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:50373942 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:50373942 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:82783761 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:82783761 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:45704995 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:45704995 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:30804955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:30804955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:51770834 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:51770834 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:15444424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:15444424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:178489803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:178489803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:55108275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:55108275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:58899743 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:58899743 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:81586036 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:81586036 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:54034287 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:54034287 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:118845108 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:118845108 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:86335202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:86335202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:181721499 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:181721499 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:39996495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:39996495 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:201061307 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:201061307 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:71406161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:71406161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:209773488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:209773488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:116268243 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:116268243 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:43939214 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:43939214 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:92071602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:92071602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:92157943 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:92157943 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:180365948 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:180365948 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:31118127 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:31118127 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:59409337 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:59409337 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:33259581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:33259581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:73477351 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:73477351 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158323884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158323884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:35822886 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:35822886 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:160832282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:160832282 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:24492866 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:24492866 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:64982693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:64982693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:83821264 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:83821264 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:19473299 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:19473299 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:19916293 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:19916293 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:59167788 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:59167788 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:58557896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:58557896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:31287325 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:31287325 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:31299468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:31299468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:45202605 T>A maps to ENST00000396750 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:45202605 T>A maps to ENST00000396750 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:180064597 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:180064597 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:196706794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:196706794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:37758398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:37758398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:6702113 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:6702113 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:10161708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:10161708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:122864895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:122864895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:140123275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:140123275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:72234676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:72234676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:57996550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:57996550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:87670275 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:87670275 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:76311648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:76311648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:94056817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:94056817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:110853256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:110853256 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:107553846 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:107553846 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:10116926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:10116926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:129987583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:129987583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:207661794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:207661794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:1720554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:1720554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:28844190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:28844190 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:115263354 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:115263354 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:61949775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:61949775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:61987958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:61987958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:113841823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:113841823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:67680437 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:67680437 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:94704360 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:94704360 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:107263482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:107263482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:15658901 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:15658901 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:47853083 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:47853083 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:32459564 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:32459564 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:29891332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:29891332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:29978111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:29978111 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:186015675 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:186015675 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:186028966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:186028966 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:50118107 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:50118107 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:57684553 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:57684553 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:38159273 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:38159273 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:55621311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:55621311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:38980529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:38980529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:72310377 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:72310377 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98087394 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98087394 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:169150121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:169150121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:73255284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:73255284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:27157802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:27157802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:105404794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:105404794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:105440400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:105440400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:71740790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:71740790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:109524264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:109524264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:78475143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:78475143 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:44063259 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:44063259 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:38418156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:38418156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:37296264 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:37296264 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:11664640 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:11664640 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:134851441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:134851441 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184296302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184296302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:212248319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:212248319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:76964382 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:76964382 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:157068489 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:157068489 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:108464275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:108464275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:101354259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:101354259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:6224817 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:6224817 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:46742102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:46742102 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:57405246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:57405246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:47797529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:47797529 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:6235881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:6235881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:179731540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:179731540 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:176966184 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:176966184 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:62273772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:62273772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:68782207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:68782207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:166138687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:166138687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:45605176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:45605176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:112933261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:112933261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:127595073 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:127595073 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:15927939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:15927939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55385744 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55385744 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:161559646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:161559646 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:125082611 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:125082611 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:102520912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:102520912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:27939987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:27939987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:97052812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:97052812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:142469615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:142469615 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:29001514 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:29001514 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:180039730 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:180039730 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:147003434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:147003434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:26864017 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:26864017 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:131264181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:131264181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:43871198 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:43871198 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:39134527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:39134527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:27586123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:27586123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:51752878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:51752878 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:4881554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:4881554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:30670942 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:30670942 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:29706403 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:29706403 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:52996942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:52996942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:34945876 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:34945876 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:42468078 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:42468078 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:59599271 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:59599271 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:35226770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:35226770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:74490445 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:74490445 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:58480215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:58480215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:4867880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:4867880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155784288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155784288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:167024388 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:167024388 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:167059411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:167059411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:57693272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:57693272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:48919119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:48919119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:42620602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:42620602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:106558194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:106558194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:108647756 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:108647756 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:25078890 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:25078890 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:44880487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:44880487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:39881413 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:39881413 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:45353125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:45353125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:18914094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:18914094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:138724532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:138724532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:93806162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:93806162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:93839336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:93839336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91818723 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91818723 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91841052 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91841052 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:100134401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:100134401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:27100596 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:27100596 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:234761202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:234761202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:54674564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:54674564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:30501327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:30501327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:26868947 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:26868947 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:114384121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:114384121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:209880253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:209880253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:3215519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:3215519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:52878804 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:52878804 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:1070681 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:1070681 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:1616395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:1616395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:130410316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:130410316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:130419492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:130419492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:117120264 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:117120264 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:111674799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:111674799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:57168632 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:57168632 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:113596232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:113596232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:102636070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:102636070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:166904449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:166904449 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:75893524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:75893524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:31372360 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:31372360 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:102368049 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:102368049 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:231742645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:231742645 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:35208737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:35208737 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:123870983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:123870983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:211307358 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:211307358 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:169896509 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:169896509 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:170162876 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:170162876 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:36746756 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:36746756 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:15697933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:15697933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:123230411 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:123230411 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:100056398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:100056398 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:100133166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:100133166 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55290154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55290154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55268298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55268298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158021119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158021119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38698681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38698681 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:30322101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:30322101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:52992564 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:52992564 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:153132752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:153132752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:129571129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:129571129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:209803757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:209803757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:138417047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:138417047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:46704919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:46704919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:226108456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:226108456 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:205389525 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:205389525 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:66085594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:66085594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:39294475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:39294475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:48654612 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:48654612 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:54850070 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:54850070 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:14296361 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:14296361 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:133859479 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:133859479 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:25257419 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:25257419 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141291476 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141291476 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141806484 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141806484 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:169995242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:169995242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:7016369 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:7016369 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:101524122 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:101524122 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:77748823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:77748823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:75078140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:75078140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:160783796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:160783796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:39550143 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:39550143 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:95719285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:95719285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:102501756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:102501756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:16090861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:16090861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:164854387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:164854387 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:165110520 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:165110520 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:65551076 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:65551076 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:8953240 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:8953240 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:85422091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:85422091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:6390034 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:6390034 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:46794328 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:46794328 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:128865258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:128865258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:12246383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:12246383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:168271027 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:168271027 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:102586903 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:102586903 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:113237066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:113237066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:60234636 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:60234636 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:72754982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:72754982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:55752596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:55752596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:56704918 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:56704918 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:93575763 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:93575763 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:92700500 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:92700500 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236990305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236990305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:9016314 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:9016314 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:110021522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:110021522 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:30419044 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:30419044 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:109459158 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:109459158 T>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:26224650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:26224650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:2020394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:2020394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:89882098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:89882098 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:34160732 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:34160732 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:56010128 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:56010128 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:52722417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:52722417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:21115755 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:21115755 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:77170140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:77170140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236195566 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236195566 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:57093548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:57093548 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55493370 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55493370 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56485011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56485011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:24006668 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:24006668 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:52280192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:52280192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:105132414 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:105132414 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:18768731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:18768731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:49166836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:49166836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:102338036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:102338036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:228444663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:228444663 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:128692015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:128692015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:183659425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:183659425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247615289 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247615289 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247618033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247618033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247695822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247695822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:248138310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:248138310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:117089990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:117089990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:17563696 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:17563696 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:118982131 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:118982131 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:150839314 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chrX:150839314 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:100803130 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:100803130 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:30880086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:30880086 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:56138807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:56138807 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:5563036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:5563036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:59093400 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:59093400 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:136429773 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:136429773 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:173423609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:173423609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:31677995 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:31677995 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:58318093 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:58318093 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:110455412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:110455412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:160833971 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:160833971 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:8702922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:8702922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:67859274 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:67859274 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:132110504 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:132110504 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:161157863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:161157863 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:208212853 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:208212853 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:118200838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:118200838 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:38138607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:38138607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:42625873 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:42625873 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:147560953 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:147560953 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:10221354 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:10221354 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:76805950 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:76805950 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:45245682 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:45245682 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:23522334 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:23522334 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:64683063 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:64683063 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:3677719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:3677719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:23750794 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:23750794 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:48166808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:48166808 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:214656671 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:214656671 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:158308792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:158308792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:40748374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:40748374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:41409593 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:41409593 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:121657830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:121657830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:9349783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:9349783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:52426728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:52426728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:33433112 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:33433112 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:74451105 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:74451105 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:56936219 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:56936219 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:79386642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:79386642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:103270349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:103270349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:103270351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:103270351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:104664362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:104664362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:40695612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:40695612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:79174565 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:79174565 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:79174568 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:79174568 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:79638886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:79638886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:111318524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:111318524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:167241812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:167241812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:67732960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:67732960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:12121415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:12121415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:127820307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:127820307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:38993628 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:38993628 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:33927797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:33927797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:108929119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:108929119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:193922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:193922 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:35208753 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:35208753 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:122711921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:122711921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:61377398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:61377398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:61226774 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:61226774 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:7212788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:7212788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:85892391 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:85892391 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:72576470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:72576470 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:3675260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:3675260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:1917912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:1917912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:164786839 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:164786839 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:26883589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:26883589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:160460195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:160460195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:44682364 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:44682364 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:43314233 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:43314233 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:99379164 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:99379164 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:19496350 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:19496350 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:92352395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:92352395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:85467053 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:85467053 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:47397158 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:47397158 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:44513055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:44513055 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:190430408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:190430408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:205767263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:205767263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:75707653 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:75707653 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:75805239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:75805239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:55726004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:55726004 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:68325348 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:68325348 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:143236996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:143236996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:43880952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:43880952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:71569797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:71569797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:246078795 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:246078795 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:36521315 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:36521315 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:108431187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:108431187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:106562359 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:106562359 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:106865401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:106865401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:121495779 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:121495779 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:214727367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:214727367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:131374331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:131374331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:120003650 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:120003650 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:63970783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:63970783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:171520359 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:171520359 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:102691002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:102691002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:4508990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:4508990 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:31004828 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:31004828 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108871921 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108871921 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:4403777 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:4403777 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:75609965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:75609965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:12231935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:12231935 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:6631382 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:6631382 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38091855 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38091855 A>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:100228508 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:100228508 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:134128755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:134128755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184094267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184094267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98144564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98144564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98188362 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98188362 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:24664327 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:24664327 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:100287929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:100287929 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:101276133 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:101276133 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:101286898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:101286898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:150416336 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:150416336 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:175360363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:175360363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:218673557 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:218673557 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:47467857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:47467857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:10908931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:10908931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:10909713 C>A maps to ENST00000341326 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:10909713 C>A maps to ENST00000341326 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:10942867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:10942867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:72712818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:72712818 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:114513321 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:114513321 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:189026186 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:189026186 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:234854449 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:234854449 A>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:130356375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:130356375 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:51889329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:51889329 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:89338822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:89338822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:84373082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:84373082 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:70979843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:70979843 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:21974015 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:21974015 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:216595738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:216595738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:55567423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:55567423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:55642014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:55642014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:55642016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:55642016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:23093963 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:23093963 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:6853878 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:6853878 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:136637200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:136637200 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:77896159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:77896159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:77915815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:77915815 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:12302699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:12302699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:98828372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:98828372 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:74956074 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:74956074 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:68358621 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:68358621 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:43743610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:43743610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:228247950 C>A maps to ENST00000366753 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:228247950 C>A maps to ENST00000366753 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:30999159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:30999159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:108618695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:108618695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:17280989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:17280989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:142066055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:142066055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:145268431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:145268431 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:32403523 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:32403523 A>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247319841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:247319841 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:58574982 T>C maps to NM_001164527.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:58574982 T>C maps to NM_001164527.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:14827054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:14827054 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:53652729 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:53652729 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:21240856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:21240856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:38283112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:38283112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:52361468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:52361468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:53945336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:53945336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56833164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56833164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:58119989 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:58119989 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:112159471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:112159471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:20548543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:20548543 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:158630716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:158630716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:28337426 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:28337426 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:64617270 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:64617270 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:84588410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:84588410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:100182145 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:100182145 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:47681675 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:47681675 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:100349808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:100349808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:134260732 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:134260732 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:45924224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:45924224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:61978456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:61978456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:54520138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:54520138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:55407670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:55407670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:22239976 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:22239976 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:6502633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:6502633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:144194613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:144194613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:144315002 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:144315002 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:74882110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:74882110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:155308252 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:155308252 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176913185 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176913185 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176983778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176983778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:120065887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:120065887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:142176599 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:142176599 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:11026929 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:11026929 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:40757400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:40757400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:25031628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:25031628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:60559946 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:60559946 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:43294284 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:43294284 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:66108602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:66108602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:50369034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:50369034 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:50386198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:50386198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:104569444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:104569444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:66589944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:66589944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:76518155 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:76518155 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:47017313 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:47017313 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:75039298 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:75039298 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:175735326 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:175735326 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:40868074 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:40868074 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:27565489 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:27565489 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:140948492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:140948492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:181700417 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:181700417 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:181721125 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:181721125 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:47112288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:47112288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:70532886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:70532886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:39373777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:39373777 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:158146788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:158146788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:112065091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:112065091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:167489363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:167489363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:80108072 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:80108072 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:24511667 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:24511667 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:18020587 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:18020587 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:6196749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:6196749 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:170625360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:170625360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:49775324 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:49775324 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:71038390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:71038390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:27467840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:27467840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:99008317 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:99008317 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:146592418 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:146592418 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:230825681 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:230825681 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:94055426 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:94055426 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:139889947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:139889947 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:48380837 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:48380837 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:131436556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:131436556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:99771120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:99771120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:4646068 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:4646068 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:113276090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:113276090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:105865785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:105865785 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:50815346 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:50815346 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:41531897 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:41531897 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:41533252 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:41533252 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:85416099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:85416099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:98518734 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:98518734 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:55042174 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:55042174 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:110546730 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:110546730 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:56336146 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:56336146 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:223156533 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:223156533 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153996852 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153996852 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:38781991 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:38781991 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:38864051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:38864051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:38942451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:38942451 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:68025094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:68025094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:154183408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:154183408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:109056279 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:109056279 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:56327724 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:56327724 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:102508665 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:102508665 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:71766213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:71766213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:25718469 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:25718469 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:172538089 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:172538089 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:82512598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:82512598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:37156892 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:37156892 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:74439443 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:74439443 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:8875943 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:8875943 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:133833823 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:133833823 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:154137323 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:154137323 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:139152543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:139152543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:108104550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:108104550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:179727439 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:179727439 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:68500975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:68500975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:42695101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:42695101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:8766576 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:8766576 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:137821487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:137821487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:29002072 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:29002072 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:79385326 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:79385326 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:37708555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:37708555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153925386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153925386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:101073562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:101073562 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:26960379 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:26960379 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:88421092 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:88421092 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:69792675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:69792675 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:34648624 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:34648624 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:22777507 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:22777507 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153668564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:153668564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:85908426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:85908426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:144351443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:144351443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:121388032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:121388032 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:92738194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:92738194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:135455365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:135455365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:46830549 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:46830549 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:154145562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:154145562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:147400565 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:147400565 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:158281025 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:158281025 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:42895748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:42895748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:22569721 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:22569721 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:43436497 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:43436497 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:72641661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:72641661 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:81331855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:81331855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:42821772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:42821772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:129026474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:129026474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:70926999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:70926999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:155233309 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:155233309 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:143235748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:143235748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:31435379 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:31435379 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:45370107 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:45370107 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:124527713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:124527713 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:4774738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:4774738 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:156241787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:156241787 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:163241031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:163241031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:79306060 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:79306060 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:44273290 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:44273290 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:1374650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:1374650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:43496611 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:43496611 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:233498128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:233498128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:139697637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:139697637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:57962631 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:57962631 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:183210159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:183210159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:45757785 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:45757785 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:39660093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:39660093 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:117904336 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:117904336 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:54876602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:54876602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:129250508 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:129250508 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:21523682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:21523682 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:182853785 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:182853785 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:156729133 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:156729133 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:75117694 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:75117694 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:82409458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:82409458 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:77563482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:77563482 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:96431146 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:96431146 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:75022175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:75022175 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:6652917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:6652917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:151896835 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:151896835 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:186967963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:186967963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:48669320 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:48669320 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:15034989 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:15034989 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:31465118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:31465118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:138123435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:138123435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:36921755 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:36921755 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:15987465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:15987465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:30062325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:30062325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10303513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10303513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10309501 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10309501 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:27411200 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:27411200 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:27438707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:27438707 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:47489407 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:47489407 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:40204174 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:40204174 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:40104920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:40104920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:78510531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:78510531 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:36220079 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:36220079 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:6626380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:6626380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:161182312 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:161182312 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:47156935 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:47156935 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:50091947 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:50091947 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:7067770 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:7067770 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:50724387 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:50724387 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:50755670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:50755670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:17227980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:17227980 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:5585593 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:5585593 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:132124489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:132124489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:44501478 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:44501478 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:78413641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:78413641 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:201800351 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:201800351 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:117085900 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:117085900 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:32060265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:32060265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:17607144 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:17607144 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176708997 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176708997 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176766049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:176766049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:162720291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:162720291 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:139741315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:139741315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:150842788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:150842788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:59419009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:59419009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:65421541 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:65421541 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:144857561 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:144857561 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:144916438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:144916438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:145022583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:145022583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:45937960 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:45937960 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:143772020 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:143772020 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:230020503 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:230020503 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:36934386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:36934386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:51774037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:51774037 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:8745729 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:8745729 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:19460989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:19460989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:204236791 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:204236791 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:43986226 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:43986226 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:152936706 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:152936706 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:140358755 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:140358755 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:27808043 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:27808043 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:202509227 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:202509227 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:75238253 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:75238253 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:82597476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:82597476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:69015123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:69015123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:57512397 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:57512397 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:46069895 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:46069895 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:53798766 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:53798766 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:16037542 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:16037542 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43519578 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43519578 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43261590 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43261590 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:251787 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:251787 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:24615568 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:24615568 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:99042395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:99042395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:65847092 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:65847092 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:55708851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:55708851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:21619597 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:21619597 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:125791954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:125791954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:173662379 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:173662379 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:86633770 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:86633770 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:29938861 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:29938861 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:46272996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:46272996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:86491200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:86491200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:111701101 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:111701101 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:87410243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:87410243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:35827288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:35827288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:38959827 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:38959827 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:38959829 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:38959829 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:237837541 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:237837541 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:33905644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:33905644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:167208528 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:167208528 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:18516245 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:18516245 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:13868568 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:13868568 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:47873634 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:47873634 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:48051932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr15:48051932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:94770592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:94770592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:26618486 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:26618486 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:33073488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:33073488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:14303586 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:14303586 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7534280 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7534280 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:77645879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:77645879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:52002344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:52002344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:110925345 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:110925345 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:25820181 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:25820181 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:116563539 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:116563539 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:92407522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:92407522 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:17985240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:17985240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:55736429 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:55736429 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:12347543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:12347543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:108531573 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:108531573 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:152690333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:152690333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:222742738 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:222742738 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:61417771 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:61417771 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:121981886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:121981886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:11422123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:11422123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:98173109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:98173109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:103207530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:103207530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:154741185 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:154741185 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:175104953 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:175104953 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:20008690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:20008690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:20039270 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:20039270 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:103342915 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:103342915 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:30126067 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:30126067 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:14266585 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:14266585 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:72975680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:72975680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:98602680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:98602680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:3353477 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:3353477 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:43469377 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:43469377 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:179658061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:179658061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:3043521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:3043521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:156990437 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:156990437 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:42625699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:42625699 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:42641512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:42641512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:196098956 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:196098956 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:55563843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:55563843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:17203978 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr21:17203978 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:144811182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:144811182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:46020837 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:46020837 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:77907657 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr16:77907657 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:6771855 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:6771855 G>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:12567175 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:12567175 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:53000259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:53000259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:118482022 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:118482022 A>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:31628670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:31628670 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:44244334 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:44244334 T>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:81053439 G>T maps to ENST00000372347 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:81053439 G>T maps to ENST00000372347 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:7021064 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:7021064 T>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:129350195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chrX:129350195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:180679345 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:180679345 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:46722552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:46722552 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:22901868 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:22901868 T>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:130322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:130322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:48337902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:48337902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:20685854 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:20685854 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:31712383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:31712383 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:24324564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:24324564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:64466386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:64466386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:7788085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:7788085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:87897437 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:87897437 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:100387285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:100387285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:230839234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:230839234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:26672593 T>C maps to NM_001039775.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:26672593 T>C maps to NM_001039775.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:86198536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:86198536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:134225854 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:134225854 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:29498143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:29498143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:113348915 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:113348915 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:99145046 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:99145046 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:7506775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:7506775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:155939234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:155939234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:11402263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:11402263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:134257559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:134257559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:11059055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:11059055 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:33976828 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:33976828 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:15565151 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:15565151 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:40066980 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:40066980 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:15444525 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:15444525 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:247727018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:247727018 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:34684403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:34684403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:100450862 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:100450862 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:34664401 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:34664401 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:32290058 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:32290058 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:69502857 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:69502857 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:15623250 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:15623250 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:50145598 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:50145598 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:181570249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:181570249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:18691049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:18691049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:37026261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:37026261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:7060696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:7060696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:40947468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:40947468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:55602077 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:55602077 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:19467787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:19467787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:59159914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:59159914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:60033811 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:60033811 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:61689165 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:61689165 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:23587047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:23587047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:35139350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:35139350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:95277169 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:95277169 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:132646152 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:132646152 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:120166498 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:120166498 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:150674581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:150674581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:62286796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:62286796 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:21549925 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:21549925 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:125281836 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:125281836 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:103455194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:103455194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:93897338 A>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:93897338 A>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:1720812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:1720812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:2944596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:2944596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:3174521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:3174521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:10973862 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:10973862 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:39841182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:39841182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:58522160 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:58522160 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:50785464 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:50785464 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:169169464 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:169169464 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:123361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:123361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:137470405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:137470405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:107856439 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:107856439 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:107545716 A>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:107545716 A>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:4216647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:4216647 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:31718078 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:31718078 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:7720752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:7720752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:38709723 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:38709723 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:11660098 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:11660098 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:153794386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:153794386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:109050552 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:109050552 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:146792279 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:146792279 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:41550813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:41550813 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:36366917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:36366917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:50618207 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:50618207 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:96952259 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:96952259 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:69697153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:69697153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:122734375 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:122734375 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:118986195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:118986195 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:72127796 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:72127796 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:109155082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:109155082 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:117083326 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:117083326 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:187615816 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:187615816 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:68134104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:68134104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:240389387 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:240389387 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:109719085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:109719085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:151179576 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:151179576 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:27135344 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:27135344 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:52420478 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:52420478 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:47284968 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:47284968 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:45049582 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:45049582 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:176883151 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:176883151 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:93743572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:93743572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:94444106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:94444106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:37272794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:37272794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:66838661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:66838661 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:106810156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:106810156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:21727063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:21727063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:96367893 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:96367893 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:18624802 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:18624802 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:26044044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:26044044 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:130532627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:130532627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:18562706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:18562706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:102936671 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:102936671 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:15212218 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:15212218 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:142639417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:142639417 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:100103011 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:100103011 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:20720241 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:20720241 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:53311985 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:53311985 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:101013122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:101013122 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:8292271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:8292271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:63279187 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:63279187 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:104100479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:104100479 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:48660492 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:48660492 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:55178057 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:55178057 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:33910106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:33910106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:11945635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:11945635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:197554192 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:197554192 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:40486665 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:40486665 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:25488900 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:25488900 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:53787667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:53787667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:6500210 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:6500210 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:235865989 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:235865989 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:48019468 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:48019468 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:45923770 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:45923770 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:164528171 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:164528171 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:126705822 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:126705822 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:141782479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:141782479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:181003032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:181003032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:84764909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:84764909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr13:25826297 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr13:25826297 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:9025726 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:9025726 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:23901740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:23901740 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:26481990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:26481990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr13:102051509 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr13:102051509 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:15628979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:15628979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:115856266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:115856266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:52514813 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:52514813 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:99274505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:99274505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:55435297 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:55435297 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:15151294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:15151294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:155726452 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:155726452 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:69223110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:69223110 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:47531211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:47531211 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:84498412 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:84498412 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:5591950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:5591950 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:107856460 T>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:107856460 T>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:131743679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:131743679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:102342891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:102342891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:228482443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:228482443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:44713941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:44713941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:74079532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:74079532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:248166870 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:248166870 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:88346236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:88346236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:74834676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:74834676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:44543580 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:44543580 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:164811056 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:164811056 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140557438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140557438 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:33870573 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:33870573 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:85659374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:85659374 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:156877164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:156877164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:65404806 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:65404806 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:123022603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:123022603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:21116984 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:21116984 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:160605414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:160605414 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:151261134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:151261134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:23942907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:23942907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:6546364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:6546364 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:45218370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr22:45218370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:73678424 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:73678424 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:198677465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:198677465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:8319996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:8319996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:62217041 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:62217041 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:71315195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:71315195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:178809097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:178809097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:80390620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:80390620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:155477836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:155477836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:49573651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:49573651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:44989964 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:44989964 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:92765679 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:92765679 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:36689063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:36689063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:55489337 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:55489337 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:33785047 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:33785047 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:33938382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:33938382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:38921357 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:38921357 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:62045323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:62045323 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:52184398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:52184398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:169580627 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:169580627 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:44087756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:44087756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:94986176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:94986176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:94942513 G>C maps to ENST00000448305 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:94942513 G>C maps to ENST00000448305 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:155714675 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:155714675 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:82403854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:82403854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:148386235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:148386235 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:1538147 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:1538147 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:122822405 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:122822405 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:73698394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:73698394 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:60165236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:60165236 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:20037236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:20037236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:119013909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:119013909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:134373717 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:134373717 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:33170520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:33170520 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:20544377 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:20544377 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:121435834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:121435834 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:50667827 T>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:50667827 T>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:56236421 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:56236421 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:9113467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:9113467 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:5120438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:5120438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:4298380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:4298380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:12224772 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:12224772 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:114925185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:114925185 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:125900254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:125900254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:129749928 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:129749928 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:66360630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr18:66360630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:175355009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:175355009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:57157250 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:57157250 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:81511926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:81511926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:51744892 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:51744892 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:20764636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:20764636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:91233275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:91233275 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:190908594 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:190908594 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:10463082 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:10463082 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:23573885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:23573885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:138982694 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:138982694 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:5412325 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:5412325 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:34790918 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:34790918 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:33501225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:33501225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:35541058 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:35541058 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:145110311 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:145110311 A>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:42577576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:42577576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:6122593 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:6122593 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:141408495 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:141408495 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:108604278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:108604278 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:31604602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:31604602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:56378672 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:56378672 T>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:28145143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:28145143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:75200863 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:75200863 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:44530045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:44530045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:84519527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chrX:84519527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:116964536 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:116964536 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:3952949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:3952949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:7760747 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:7760747 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48626906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48626906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:66987233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:66987233 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:87168571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:87168571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:20668259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:20668259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:74759655 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:74759655 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:89020660 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:89020660 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:35497776 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:35497776 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:35562844 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:35562844 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:109691978 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:109691978 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:132294555 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:132294555 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:89391315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:89391315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:31591525 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:31591525 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:31594257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:31594257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:31674072 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:31674072 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:74035936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:74035936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:156930056 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:156930056 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:33624327 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:33624327 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:100692990 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:100692990 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:100821325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:100821325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:18905637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:18905637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:1569041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:1569041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:167839475 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:167839475 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:45724693 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:45724693 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7698195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7698195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:76415752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:76415752 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:244574781 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:244574781 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:148044219 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:148044219 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:4920328 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:4920328 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:58272816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:58272816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:43904535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:43904535 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:85677338 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:85677338 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:108276356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:108276356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:14797909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:14797909 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:69256237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:69256237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:150484661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:150484661 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:150505902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:150505902 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:47133426 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:47133426 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:36552769 G>T maps to NM_001177506.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:36552769 G>T maps to NM_001177506.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:201473887 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:201473887 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:183898398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:183898398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:83330525 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:83330525 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:114443807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:114443807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:21251055 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:21251055 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:195306014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:195306014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:30932243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:30932243 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:33442824 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:33442824 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141050075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141050075 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:119017762 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:119017762 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:130217954 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:130217954 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156924780 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156924780 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:35730773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:35730773 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:35750585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:35750585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:3680799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:3680799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:14994132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:14994132 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:14232201 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:14232201 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:119770558 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:119770558 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:119903901 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:119903901 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:120166156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:120166156 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:216209658 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:216209658 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:25981321 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:25981321 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:160059085 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:160059085 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138811003 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138811003 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:89993110 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:89993110 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:46755759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:46755759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:58024399 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:58024399 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:129146800 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:129146800 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:1986655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:1986655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:40494739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:40494739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:118424524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:118424524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:40037788 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:40037788 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:27085286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:27085286 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:44247717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:44247717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:244747148 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:244747148 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:247737315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:247737315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:75042379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:75042379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:87812706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:87812706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:184587596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:184587596 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:146617822 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:146617822 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:37122446 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:37122446 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:31735333 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:31735333 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:57373826 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:57373826 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:67425907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:67425907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:50198070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:50198070 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:65073499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:65073499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:140904433 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:140904433 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2659867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2659867 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2693606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2693606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:181478966 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:181478966 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:81624259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:81624259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:64876884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:64876884 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:134480367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:134480367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:35919881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:35919881 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:219892827 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:219892827 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:106130857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:106130857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:126132861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:126132861 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:96310884 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:96310884 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:52595981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:52595981 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6292069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6292069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:34416713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:34416713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:7633739 T>A maps to ENST00000432237 G1120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:7633739 T>A maps to ENST00000432237 G1120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:112054783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:112054783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135732304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135732304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:111296431 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:111296431 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:111319567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:111319567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:22654227 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:22654227 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44935370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44935370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:23523704 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:23523704 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:202698556 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:202698556 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:123165069 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:123165069 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:123165071 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:123165071 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:25473748 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:25473748 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:49438087 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:49438087 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:34055454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:34055454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:126633504 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:126633504 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:24665235 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:24665235 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:24722824 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:24722824 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:26804348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:26804348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143015397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143015397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143025407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143025407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154509474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154509474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154522348 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154522348 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:45871008 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:45871008 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:73731799 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:73731799 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:28499873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:28499873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:23848126 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:23848126 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:21549932 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:21549932 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:58392012 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:58392012 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:100207833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:100207833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:147384829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:147384829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:230805068 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:230805068 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:121238814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:121238814 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:121241026 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:121241026 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:101706289 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:101706289 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:86340468 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:86340468 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:109734974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:109734974 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:189851775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:189851775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:110864721 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:110864721 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107827691 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107827691 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107898792 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107898792 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107417576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107417576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107439491 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107439491 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:189917424 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:189917424 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:238265933 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:238265933 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:130311877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:130311877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:232665525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:232665525 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:27948193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:27948193 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:211481281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:211481281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:29135932 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:29135932 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:43907331 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:43907331 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:49701086 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:49701086 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:75898536 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:75898536 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:17201188 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:17201188 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:151135363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:151135363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:3253920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:3253920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34164198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34164198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:113277577 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:113277577 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:114110952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:114110952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:138094732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:138094732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:11117483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:11117483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:16656917 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:16656917 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:48996520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:48996520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:49034403 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:49034403 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:49039986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:49039986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:134304857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:134304857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:22990264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:22990264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74637205 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74637205 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:57769289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:57769289 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:49954208 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:49954208 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:91558306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:91558306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74592427 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74592427 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:49936628 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:49936628 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220288442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220288442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:24758609 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:24758609 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr22:19122550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr22:19122550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:154042240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:154042240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140909775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140909775 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:80668865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:80668865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:51089566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:51089566 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154003005 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154003005 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:108124803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:108124803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:83525858 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:83525858 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:13890974 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:13890974 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:13919511 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:13919511 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11711310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11711310 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11840565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11840565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:65831472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:65831472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:130988182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:130988182 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:25216654 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:25216654 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:67508427 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:67508427 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:83858406 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:83858406 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:73349478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:73349478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:105456682 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:105456682 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:32408848 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:32408848 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:46859822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:46859822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56166674 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56166674 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:23827926 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:23827926 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:110882010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:110882010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:129206056 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:129206056 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:36909932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:36909932 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:100380671 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:100380671 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:14732403 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:14732403 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:129883713 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:129883713 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:130008611 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:130008611 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:120569975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:120569975 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:185033793 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:185033793 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43507764 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43507764 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:51912598 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:51912598 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56276244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56276244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:102783021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:102783021 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:93113199 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:93113199 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:66013287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:66013287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154089945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154089945 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:184059276 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:184059276 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:139158017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:139158017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:139255342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:139255342 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:110594552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:110594552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:129092950 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:129092950 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:190195206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:190195206 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:119402039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:119402039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:14782484 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:14782484 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:14883643 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:14883643 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:92430617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:92430617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:15628493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:15628493 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:108387170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:108387170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:44388334 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:44388334 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138190400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138190400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:21549278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:21549278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:128477606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:128477606 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:28915154 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:28915154 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:216273238 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:216273238 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:79199935 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:79199935 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:79240281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:79240281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:85912601 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:85912601 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:180651294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:180651294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:101084359 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:101084359 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:151336642 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:151336642 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:161118880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:161118880 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:26825644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:26825644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:27725721 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:27725721 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:151818470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:151818470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:90012567 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:90012567 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:89652588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:89652588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:147231430 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:147231430 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:183942745 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:183942745 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:150757807 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:150757807 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:79820452 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:79820452 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:56374914 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:56374914 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:132439772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:132439772 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135498718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135498718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:13063366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:13063366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:125819142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:125819142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:122381509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:122381509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:122562113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:122562113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:88042845 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:88042845 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:141521684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:141521684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:135562527 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:135562527 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:108697121 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:108697121 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:105232264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:105232264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:19375752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:19375752 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:55039695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:55039695 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:48682733 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:48682733 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:18633738 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:18633738 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:242192362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:242192362 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:41009582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:41009582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:65427229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:65427229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:29694051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:29694051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:185934883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:185934883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:185985049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:185985049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:74654394 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:74654394 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr22:35659894 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr22:35659894 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:162898349 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:162898349 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:173525272 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:173525272 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:61627614 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:61627614 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:133632512 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:133632512 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:26139400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:26139400 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:209905756 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:209905756 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:119964339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:119964339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:65002403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:65002403 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:53751612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:53751612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135582045 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135582045 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:88732480 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:88732480 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:88732482 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:88732482 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:78450057 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:78450057 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:34715815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:34715815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:160431822 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:160431822 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42172024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42172024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:103040984 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:103040984 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:27457474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:27457474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:39785677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:39785677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:55164774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:55164774 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:120596227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:120596227 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156812171 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156812171 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:75914495 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:75914495 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156505056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156505056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156520174 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156520174 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:156679718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:156679718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:160914883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:160914883 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:147015700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:147015700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:123858374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:123858374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:124153094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:124153094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:124412632 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:124412632 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:7828322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:7828322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:119914578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:119914578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:49935288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:49935288 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:169812225 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:169812225 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:44284577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:44284577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:133488490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:133488490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:142649498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:142649498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:136595367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:136595367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141309654 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141309654 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:48676523 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:48676523 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:197402402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:197402402 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:42249449 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:42249449 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:46680842 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:46680842 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155893537 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155893537 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155893548 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155893548 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:84870493 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:84870493 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:24447404 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:24447404 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:70768558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:70768558 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:20949718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:20949718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:28980805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:28980805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:200968939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:200968939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:57969110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:57969110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:7829910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:7829910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:55247206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:55247206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158035476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158035476 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:51328989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:51328989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:39644468 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:39644468 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:52941472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:52941472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:53169121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:53169121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:52778619 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:52778619 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:52756496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:52756496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:31744617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:31744617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:31913883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:31913883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:134327419 C>A maps to ENST00000383222 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:134327419 C>A maps to ENST00000383222 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:153129756 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:153129756 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:153132394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:153132394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:153152422 A>G maps to ENST00000452593 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:153152422 A>G maps to ENST00000452593 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:6959304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:6959304 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:30756247 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:30756247 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:139649684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:139649684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:40094553 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:40094553 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:104310079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:104310079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:38493702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:38493702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:55106511 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:55106511 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:15554224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:15554224 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:70386464 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:70386464 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:197703312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:197703312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:165177460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:165177460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:161032567 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:161032567 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:34654891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:34654891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:62641410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:62641410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:62910272 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:62910272 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:104086287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:104086287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:141457752 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:141457752 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:142005042 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:142005042 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:170096347 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:170096347 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:68154220 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:68154220 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:67246942 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:67246942 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:120067581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:120067581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:70300558 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:70300558 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:40734091 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:40734091 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:160746709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:160746709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr22:21341876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr22:21341876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:140968494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:140968494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:140969696 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:140969696 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:77691640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:77691640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135304709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:135304709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:84118533 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:84118533 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138670619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138670619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138712043 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:138712043 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:94986024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:94986024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:90437506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:90437506 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:43851599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:43851599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:66739434 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:66739434 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107159114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:107159114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:75489857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:75489857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:154834806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:154834806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158813701 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158813701 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154020395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:154020395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:216809780 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:216809780 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:59939470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:59939470 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:15998437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:15998437 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:236973897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:236973897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:30046250 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:30046250 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:9009790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:9009790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:100694841 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:100694841 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:81102420 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:81102420 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:81102805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:81102805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:108216794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:108216794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:10304106 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:10304106 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:56552144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:56552144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:52524933 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:52524933 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:120107368 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:120107368 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:101795289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:101795289 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:100823377 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:100823377 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:46078969 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:46078969 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:90976559 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:90976559 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:133727415 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:133727415 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:134205091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:134205091 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:21384782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:21384782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:91855434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:91855434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:55974641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:55974641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:178262517 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:178262517 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:75583133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:75583133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:50052212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:50052212 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:50090787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:50090787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:52535439 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:52535439 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:63769468 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:63769468 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:5481285 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:5481285 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:247611664 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:247611664 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:56569598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:56569598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:43612973 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:43612973 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:31538075 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:31538075 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:155774778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:155774778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:101564847 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:101564847 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:132423270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:132423270 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:153659431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:153659431 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:153661418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:153661418 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:33514997 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:33514997 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:86203723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:86203723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:131682669 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:131682669 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:106464709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:106464709 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:16925763 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:16925763 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:62563751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:62563751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:101092098 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:101092098 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:228475732 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:228475732 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:67290528 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:67290528 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248247640 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248247640 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248366365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248366365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:22332697 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:22332697 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:29644165 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:29644165 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:74828488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:74828488 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:43547787 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:43547787 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:17548721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:17548721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:55116410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:55116410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:55248954 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:55248954 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:110345257 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:110345257 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:110407024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:110407024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:9519911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:9519911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:9524903 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:9524903 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:35457440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:35457440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:35492374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:35492374 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:35497253 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:35497253 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:226562153 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:226562153 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:150794056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:150794056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:150839354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:150839354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:91368384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:91368384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:55782594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:55782594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:41239533 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:41239533 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:165989858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:165989858 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:72291908 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:72291908 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:14695840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:14695840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:59258911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:59258911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:76587413 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:76587413 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:122829678 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:122829678 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:39878840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:39878840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:1971854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:1971854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:239165480 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:239165480 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:207241210 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:207241210 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:58349578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:58349578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:33799907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:33799907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:129773556 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:129773556 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:47675020 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:47675020 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:26890565 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:26890565 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:204428908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:204428908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:71404539 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:71404539 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:47924192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:47924192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110394615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110394615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110401412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110401412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110401417 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110401417 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110452895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110452895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155263995 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155263995 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:186902038 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:186902038 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:133700793 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:133700793 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:8364687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:8364687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:9389680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:9389680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179358545 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179358545 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:93150194 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:93150194 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:68618571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:68618571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:57750881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:57750881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:145794527 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:145794527 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44540121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44540121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:20125130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:20125130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:132186039 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:132186039 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:7621272 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:7621272 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:89895932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:89895932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:128605862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:128605862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:94935290 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:94935290 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:167341457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:167341457 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:6377504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:6377504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:6384118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:6384118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:63893653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:63893653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:110989586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:110989586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:23509748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:23509748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:44550031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:44550031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:69033344 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:69033344 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:82031529 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:82031529 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:36477058 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:36477058 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:2868653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:2868653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:43514446 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:43514446 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:43529238 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:43529238 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:43770535 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:43770535 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:71437492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:71437492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:117516789 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:117516789 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:209308340 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:209308340 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:70931902 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:70931902 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:7653464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:7653464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:71050356 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:71050356 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:71054683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:71054683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:52325703 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:52325703 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:52370044 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:52370044 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:46724318 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:46724318 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:20582193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:20582193 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:20582195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:20582195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:18474554 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:18474554 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:137774944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:137774944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:79348065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:79348065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:107047945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:107047945 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:116276565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:116276565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:130963581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:130963581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:40687115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:40687115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:87098402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:87098402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:87106726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:87106726 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:20978542 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:20978542 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:21511721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:21511721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:31521490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:31521490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:117653545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:117653545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:88991199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:88991199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:67200750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:67200750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:78829149 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:78829149 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:5967759 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:5967759 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:60076863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:60076863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:67753742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:67753742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237850876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237850876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:12679963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:12679963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:165972142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:165972142 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:29976410 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:29976410 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:108250765 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:108250765 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:84642088 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:84642088 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74898555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74898555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9197247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9197247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9318357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9318357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:61264719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:61264719 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:61328150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:61328150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:94917778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:94917778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:37431389 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:37431389 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:135144818 C>A maps to ENST00000372169 E2449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:135144818 C>A maps to ENST00000372169 E2449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:67098905 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:67098905 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:80406312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:80406312 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:145435379 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:145435379 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:146240473 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:146240473 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:52000315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:52000315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:52002318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:52002318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44665792 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44665792 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:43319025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:43319025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:42859182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:42859182 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:43117567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:43117567 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:92959790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:92959790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:37307113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:37307113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:92406528 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:92406528 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:85448916 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:85448916 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44987840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:44987840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74534678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:74534678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:70147644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:70147644 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:168212740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:168212740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6412230 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6412230 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:246165921 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:246165921 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:246396340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:246396340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:176048191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:176048191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:46191106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:46191106 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:121662114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:121662114 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:86215637 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:86215637 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:101624204 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:101624204 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:158288740 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:158288740 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:108380163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:108380163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:7650370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:7650370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:231135279 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:231135279 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:88776085 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:88776085 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:142120672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:142120672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:48865329 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:48865329 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:44041039 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:44041039 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220344490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220344490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:4434435 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:4434435 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:234967445 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:234967445 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158597322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158597322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158615407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:158615407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:131370562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:131370562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:40996177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:40996177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:206634212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:206634212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:119563140 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:119563140 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:76779422 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:76779422 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:36513091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:36513091 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:136191384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:136191384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:123176530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:123176530 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:38247334 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:38247334 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:191923365 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:191923365 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74473481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74473481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:31376380 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:31376380 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:147637558 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:147637558 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:25459508 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:25459508 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:70596166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:70596166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:70615400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:70615400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:152563651 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:152563651 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:62541032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:62541032 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:149730864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:149730864 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:159954387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:159954387 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:11078655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:11078655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:115120534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:115120534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:114841356 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:114841356 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:54885077 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:54885077 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:133046466 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:133046466 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:6716110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:6716110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:133478196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:133478196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:133497543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:133497543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:134145917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:134145917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:151820641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:151820641 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:137748571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:137748571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:84207864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:84207864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:98240076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:98240076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:2592718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:2592718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:38229027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:38229027 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:12254404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:12254404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:129822141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:129822141 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:122681244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:122681244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:159010619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:159010619 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:673479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:673479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:7258983 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:7258983 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:19716211 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:19716211 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:83444836 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:83444836 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:175536649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:175536649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:175654133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:175654133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:175669443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:175669443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:39750308 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:39750308 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:189448505 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:189448505 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:125575105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:125575105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:144365031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:144365031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:10973710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:10973710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:185655423 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:185655423 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:118889733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:118889733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:100274487 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:100274487 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:38213369 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:38213369 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:16319587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:16319587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:142605665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:142605665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:98591098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:98591098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:81554177 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:81554177 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156552731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:156552731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:15186803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:15186803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179516969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179516969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179517778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179517778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179585033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179585033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:52937163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:52937163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:56171787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:56171787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:43855155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:43855155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:86298076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:86298076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43367118 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43367118 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:162482254 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:162482254 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:54527318 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:54527318 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:176258422 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:176258422 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:229795145 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:229795145 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215844258 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215844258 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215853827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215853827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:216180236 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:216180236 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:11924524 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:11924524 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:144811416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:144811416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:108370260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:108370260 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:17272615 C>A maps to ENST00000421459 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:17272615 C>A maps to ENST00000421459 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:62241555 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:62241555 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:117689463 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:117689463 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:49951782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:49951782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:85551461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:85551461 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:100183299 G>T maps to ENST00000328526 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:100183299 G>T maps to ENST00000328526 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:128875918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:128875918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:128880502 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:128880502 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:128894413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:128894413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:58340695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:58340695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:197144307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:197144307 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:89049270 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:89049270 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:74598895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:74598895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:72926834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:72926834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:42713057 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:42713057 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:50803612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:50803612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:45985340 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:45985340 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:134482989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chrX:134482989 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:57018645 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:57018645 T>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:57085573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:57085573 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:57193858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:57193858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:53194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:53194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:58017709 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:58017709 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:58556786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:58556786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:7657230 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:7657230 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:7743158 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:7743158 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:67150238 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:67150238 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:107645538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:107645538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:67031695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:67031695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:87055957 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:87055957 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:20768099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:20768099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:21995516 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:21995516 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:94930188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:94930188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:204244894 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:204244894 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:100569717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:100569717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124813333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124813333 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:108014678 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:108014678 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:220396447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:220396447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:41904133 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:41904133 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:55076010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:55076010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:7474929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:7474929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:148675010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:148675010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:38519168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:38519168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:38961033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:38961033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:43771452 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:43771452 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:43837746 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:43837746 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:43856833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:43856833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:73171611 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:73171611 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:161165507 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:161165507 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:18718526 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:18718526 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:167863251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:167863251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:45753203 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:45753203 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:123066492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:123066492 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:100205474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:100205474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:89172333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:89172333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:88029499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:88029499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:100632915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:100632915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:86822821 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:86822821 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:100346510 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:100346510 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:129043136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:129043136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:96864313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:96864313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:151627080 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:151627080 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:134260951 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:134260951 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:105271083 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:105271083 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:58287357 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:58287357 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:104192379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:104192379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:38710526 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:38710526 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:63871951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:63871951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:3743510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:3743510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:85401880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:85401880 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:118081129 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:118081129 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:14751354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:14751354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:70026038 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:70026038 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:69351655 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:69351655 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:46135493 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:46135493 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:81921634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:81921634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:70037652 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:70037652 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:29727421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:29727421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:51238015 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:51238015 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:21252354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:21252354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:116703603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:116703603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:64219804 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:64219804 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:35207118 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:35207118 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:35240607 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:35240607 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:142587197 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:142587197 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:130217402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:130217402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:120298715 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:120298715 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:111929870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:111929870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:98513324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:98513324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:37986074 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:37986074 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:62415836 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:62415836 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:62124059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:62124059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:177000128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:177000128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:124358251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:124358251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:42480468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:42480468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:50223575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:50223575 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:117024782 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:117024782 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:90641847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:90641847 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:11047556 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:11047556 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:76012779 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:76012779 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:81272420 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:81272420 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:42127506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:42127506 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:34085792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:34085792 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:43279709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:43279709 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:92443020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:92443020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:59885754 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:59885754 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:55800990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:55800990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:108029179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:108029179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:115889610 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:115889610 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:118084662 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:118084662 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:88439688 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:88439688 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:112696853 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:112696853 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:31543251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:31543251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:73766132 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:73766132 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:45405787 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:45405787 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:7743517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:7743517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:50193197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:50193197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:170916554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:170916554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:31805230 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:31805230 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:14744887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:14744887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:159928774 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:159928774 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:123782544 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:123782544 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:165706820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:165706820 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:36298582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:36298582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:57378306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:57378306 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:67404649 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:67404649 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:67404670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:67404670 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:4666135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:4666135 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:86393097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:86393097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:9034600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:9034600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:35679159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:35679159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:140968155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:140968155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:2602665 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:2602665 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:2763120 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:2763120 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:181735775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:181735775 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:201034922 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:201034922 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:81591438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:81591438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:134576376 G>T maps to NM_033139.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:134576376 G>T maps to NM_033139.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:2963021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:2963021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:104905348 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:104905348 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:219895647 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:219895647 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106124754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106124754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106207384 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106207384 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106207633 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106207633 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:159214955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:159214955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:13100364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:13100364 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:191098558 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:191098558 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:69995040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:69995040 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:7549079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:7549079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:35836698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:35836698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:22142762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:22142762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:90546827 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:90546827 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:90584500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:90584500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:49031494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:49031494 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:196875872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:196875872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:196711236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:196711236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:49551812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:49551812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:50870543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:50870543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:7810089 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:7810089 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:61769555 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:61769555 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:21870329 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:21870329 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:72797303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:72797303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:86913140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:86913140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:72013471 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:72013471 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:140123683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:140123683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:140178165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:140178165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:57949036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:57949036 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:74418579 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:74418579 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:103354492 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:103354492 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:103381313 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:103381313 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:32149522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:32149522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:46907462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:46907462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:139791741 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:139791741 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:139838886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:139838886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:177694183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:177694183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:109790204 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:109790204 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:116967938 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:116967938 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189861229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189861229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:107938482 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:107938482 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189917014 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189917014 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189922255 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189922255 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:70981753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:70981753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:130021887 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:130021887 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:129938450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:129938450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:211542408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:211542408 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:8609221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:8609221 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:76259321 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:76259321 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:49696694 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:49696694 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:159683223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:159683223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:37322025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:37322025 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:3000298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:3000298 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:34089981 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:34089981 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:34192033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:34192033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:113332280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:113332280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:114291011 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:114291011 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:44751471 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:44751471 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:204732820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:204732820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:80085084 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:80085084 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:80390295 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:80390295 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124600569 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124600569 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:16006248 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:16006248 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:15733010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:15733010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:47433438 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:47433438 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:85416095 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:85416095 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:61490786 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:61490786 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:100676650 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:100676650 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:50451835 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:50451835 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:24353787 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:24353787 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:91550844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:91550844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:137150879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:137150879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:137271838 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:137271838 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:24435111 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:24435111 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189599309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:189599309 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:3978382 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:3978382 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124340176 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124340176 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124378868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:124378868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:21604051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:21604051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:21908330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:21908330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:11837391 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:11837391 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:186299930 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:186299930 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:132180074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:132180074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:84877940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:84877940 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:172277815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:172277815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:128823079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:128823079 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:111480997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:111480997 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:116447547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:116447547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:116534722 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:116534722 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:98012095 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:98012095 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:27154703 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:27154703 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:105441628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:105441628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:18576584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:18576584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:207564816 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:207564816 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:96242489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:96242489 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:108347819 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:108347819 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:108392861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:108392861 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:150480791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:150480791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:56149453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:56149453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:19962096 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:19962096 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:64574402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:64574402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:88857243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:88857243 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:8008798 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:8008798 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:111463759 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:111463759 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:5443993 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:5443993 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:66230963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:66230963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100410849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100410849 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:27396323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:27396323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:212569969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:212569969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:212578254 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:212578254 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:172315589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:172315589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:45607321 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:45607321 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:153372504 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:153372504 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:68194164 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:68194164 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:62273784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:62273784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:28075743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:28075743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:35074870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:35074870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:187525439 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:187525439 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:127697408 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:127697408 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:8191735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:8191735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:107356475 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:107356475 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:15928627 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:15928627 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:16582156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:16582156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:157738038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:157738038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:157653172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:157653172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:157508857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:157508857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:161680433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:161680433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:125351576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:125351576 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:155488679 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:155488679 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:128488843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:128488843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:28903677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:28903677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:240307581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:240307581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:171077372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:171077372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:171293160 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:171293160 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:216262660 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:216262660 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:41194333 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:41194333 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:114329696 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:114329696 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:13804511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:13804511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:49414762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:49414762 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:100174708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:100174708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:49191224 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:49191224 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:162306822 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:162306822 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:101369239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:101369239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:151130862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:151130862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:151130863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:151130863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:27271972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:27271972 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:27586349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:27586349 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:170224676 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:170224676 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:4872285 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:4872285 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:22707432 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:22707432 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:89664257 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:89664257 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:163004134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:163004134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:44198578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:44198578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:120580250 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:120580250 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:158378866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:158378866 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:55223617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:55223617 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:59610453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:59610453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:110390202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:110390202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:143922665 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:143922665 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:56374606 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:56374606 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:38056249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:38056249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:127660731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:127660731 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:167023837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:167023837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:167024136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:167024136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:50682327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:50682327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:11760984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:11760984 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:105775853 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:105775853 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:87676107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:87676107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:93511232 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:93511232 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:3029748 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:3029748 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:130763636 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:130763636 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:52671318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:52671318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:127447807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:127447807 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:144797821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:144797821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:134705080 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:134705080 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:236718362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:236718362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:93271857 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:93271857 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:43580967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:43580967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:65418948 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:65418948 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:29693106 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:29693106 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:186082978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:186082978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:42814284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:42814284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:35556768 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:35556768 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:100481591 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:100481591 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:26147692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:26147692 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:43837095 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:43837095 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:31722724 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:31722724 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:92503221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:92503221 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:71025329 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:71025329 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:88732020 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:88732020 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:25679916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:25679916 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:47114659 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:47114659 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:118648809 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:118648809 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:130415340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:130415340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:130626765 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:130626765 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:113783953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:113783953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:3143538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:3143538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:35876061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:35876061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:166896261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:166896261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:76744519 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:76744519 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:62550350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:62550350 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:15197262 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:15197262 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:15247159 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:15247159 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153721288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153721288 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153735137 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153735137 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:237253140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:237253140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:68661403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:68661403 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:56088338 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:56088338 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:31374127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:31374127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:4775015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:4775015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:105618436 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:105618436 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:147019346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:147019346 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:28031460 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:28031460 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:124113927 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:124113927 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:102823921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:102823921 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:113828921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:113828921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:196367927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:196367927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:67328627 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:67328627 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:24601347 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:24601347 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:8829042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:8829042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:55359272 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:55359272 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:70469365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:70469365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:166226721 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:166226721 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:51561693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:51561693 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:134997350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:134997350 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:135014888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:135014888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:39119844 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:39119844 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:52938286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:52938286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53008469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53008469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53237872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53237872 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53217099 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53217099 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:7002231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:7002231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:129637365 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:129637365 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:101016464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:101016464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:152748827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:152748827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:138413880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:138413880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:103869340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:103869340 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:48916014 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:48916014 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:48916069 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:48916069 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:124971873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:124971873 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:75626680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:75626680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:54779943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:54779943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:50589727 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:50589727 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:57022702 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:57022702 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:161043469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:161043469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:81893258 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:81893258 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:62679653 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:62679653 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:141091870 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:141091870 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:57579107 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:57579107 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:70573514 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:70573514 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:238683107 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:238683107 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:115560672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:115560672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:56879472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:56879472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:39838290 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:39838290 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:78116342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:78116342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:21201655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:21201655 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:161518107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:161518107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:135309416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:135309416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:42110567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:42110567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:165110741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:165110741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:165111021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:165111021 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:63667317 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:63667317 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:12951785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:12951785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:54531398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:54531398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:47315097 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:47315097 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:20929280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:20929280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:131908653 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:131908653 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:3298800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:3298800 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:8804426 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:8804426 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:39721908 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:39721908 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:150427726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:150427726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:150436249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:150436249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:2528161 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:2528161 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:220964775 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:220964775 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:220971111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:220971111 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:30432919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:30432919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:30435663 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:30435663 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:36921629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:36921629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:71591424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:71591424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:60229820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:60229820 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:59860172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:59860172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:121475862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:121475862 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:151256474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:151256474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30656662 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30656662 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30656683 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30656683 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30657795 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30657795 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30657949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30657949 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30658271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30658271 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30658299 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30658299 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30658336 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:30658336 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:45799068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:45799068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:42333761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:42333761 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:10400555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:10400555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:46900950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:46900950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:46763105 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:46763105 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:26239582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:26239582 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:171256677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:171256677 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:101797418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:101797418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:34140112 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:34140112 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:78604029 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:78604029 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:133531572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:133531572 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:133626452 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:133626452 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:115792180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:115792180 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:21076310 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:21076310 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:29884810 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:29884810 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:72204025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:72204025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:170384638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:170384638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:170482534 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:170482534 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:20869315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:20869315 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:70534576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:70534576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:29679454 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:29679454 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:204926960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:204926960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:151777825 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:151777825 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:14956768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:14956768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:117672272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:117672272 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:117728304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:117728304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:34204550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:34204550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:179534019 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:179534019 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153658398 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153658398 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:102625880 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:102625880 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:115364795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:115364795 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:84733392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:84733392 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:64458033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:64458033 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:79111533 C>T maps to ENST00000330071 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:79111533 C>T maps to ENST00000330071 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:87636067 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:87636067 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:88679008 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:88679008 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:183989103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:183989103 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:224424331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:224424331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:28171558 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:28171558 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:86848119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:86848119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:78437094 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:78437094 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:78437101 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:78437101 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:125391865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:125391865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248246879 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248246879 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248202546 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248202546 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248488058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:248488058 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:56246950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:56246950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:90926623 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:90926623 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:21696487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:21696487 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:26686710 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:26686710 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:72929411 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:72929411 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:3592996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:3592996 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:73611201 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:73611201 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:17570748 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:17570748 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:226576615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:226576615 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:55945096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:55945096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:56287655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:56287655 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:105199723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:105199723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:95388933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:95388933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:55144721 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:55144721 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:10952897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:10952897 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:102783370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:102783370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:61018485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:61018485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:100996908 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:100996908 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:73369756 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:73369756 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:18544316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:18544316 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:71439189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:71439189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:51503849 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:51503849 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:42373550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:42373550 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:46682036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:46682036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:160884884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:160884884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:26919279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:26919279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:26919281 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:26919281 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:9368226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:9368226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:171272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:171272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:23692140 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:23692140 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:17471479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:17471479 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:160229981 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:160229981 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:118364738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:118364738 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:118231513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:118231513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:19566123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:19566123 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:122334622 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:122334622 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:76805934 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:76805934 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:42681377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:42681377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:23510201 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:23510201 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:47317578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:47317578 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:46234815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:46234815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:48080600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:48080600 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:54628051 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:54628051 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:2868653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:2868653 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:152198463 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:152198463 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:104174491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:104174491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:43709714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:43709714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:43448230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:43448230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:43305344 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:43305344 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:15469917 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:15469917 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:23482478 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:23482478 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:71331180 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:71331180 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:8713368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:8713368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:8713384 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:8713384 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:29616185 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:29616185 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:121568036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:121568036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:52359498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:52359498 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:64522365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:64522365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9312480 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9312480 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9318488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9318488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9318629 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:9318629 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:37179584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:37179584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:135979810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:135979810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:57345793 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:57345793 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:79384249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:79384249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:79385438 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:79385438 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:108475247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:108475247 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:87201180 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:87201180 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:240934013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:240934013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:240986471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:240986471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:49580257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:49580257 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:21387587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:21387587 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:1066621 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:1066621 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:165386246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:165386246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:72427978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:72427978 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:237620165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:237620165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:237789115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:237789115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:134989100 C>A maps to NM_018666.2 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:134989100 C>A maps to NM_018666.2 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:73695768 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:73695768 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:200233471 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:200233471 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:38766851 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:38766851 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:166003579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:166003579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:118012061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:118012061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:167321927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:167321927 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:23223618 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:23223618 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:50207005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:50207005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:110383994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:110383994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:81952896 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:81952896 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:169586106 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:169586106 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:48060697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:48060697 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:48062528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr15:48062528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:55878824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:55878824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:94956262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:94956262 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:61387165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:61387165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100771626 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100771626 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:167512696 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:167512696 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:99929777 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:99929777 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:41122666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:41122666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:19115478 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:19115478 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:23778144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:23778144 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:14166789 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:14166789 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:201448230 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:201448230 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:171833468 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:171833468 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:264857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:264857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:52030926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:52030926 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:164757593 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:164757593 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:122755732 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:122755732 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:43212264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:43212264 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:25819479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:25819479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:35302386 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:35302386 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:172665975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:172665975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:6432009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:6432009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:40223819 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:40223819 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:9998723 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:9998723 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:58047907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:58047907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:18916963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:18916963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:32505860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:32505860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:55719038 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:55719038 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:168310185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:168310185 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:72914926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:72914926 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:2666801 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:2666801 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:47008998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:47008998 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:1161368 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:1161368 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:17937111 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:17937111 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106976620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:106976620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:107006864 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:107006864 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:231152695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:231152695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:31324237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:31324237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:118534034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:118534034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:32314549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:32314549 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:172607309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:172607309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:133711808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:133711808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:123945516 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:123945516 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:48901538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:48901538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:44329902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:44329902 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153065950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:153065950 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:158646152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:158646152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:65289516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:65289516 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:74057416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:74057416 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:57099549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:57099549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:85117781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:85117781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:52681439 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:52681439 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:53038482 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:53038482 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:53077586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:53077586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:90698125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:90698125 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:125946281 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:125946281 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:47227988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:47227988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:27013447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:27013447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:70962335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:70962335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:48559161 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:48559161 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:152523143 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:152523143 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:39818028 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr22:39818028 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53898715 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:53898715 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:33454957 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:33454957 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:19175750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:19175750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:96269794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:96269794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:100023808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:100023808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:99979834 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:99979834 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:85422341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:85422341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:168215839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:168215839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:92251488 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:92251488 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:132891704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:132891704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:49844577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:49844577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:65180332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:65180332 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:95539251 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:95539251 T>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:27109645 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:27109645 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:24729316 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr14:24729316 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:11419005 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:11419005 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:137918065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:137918065 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:138208636 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:138208636 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:138378418 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:138378418 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:155503251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:155503251 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:75315261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:75315261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:94972069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:94972069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:87494989 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:87494989 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:15556478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:15556478 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:117789103 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:117789103 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:19776020 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:19776020 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:175324463 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:175324463 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:175334908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:175334908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:218701074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:218701074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:189606906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:189606906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:18042836 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:18042836 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:72366181 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:72366181 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:186337168 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:186337168 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:10914280 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:10914280 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:14388652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr5:14388652 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100469126 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:100469126 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:72965925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr8:72965925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:180328338 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:180328338 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:38495129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:38495129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:38523249 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:38523249 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:179617806 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:179617806 C>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:49525115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:49525115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:5435355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:5435355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:135116244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr10:135116244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:100037448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:100037448 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:39772779 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:39772779 A>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:74393822 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr17:74393822 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:69885298 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:69885298 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:43543307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr21:43543307 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:41011139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:41011139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:48139213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:48139213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:17565898 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr11:17565898 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:6821907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:6821907 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:108226002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:108226002 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:177608714 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:177608714 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:98914216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:98914216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:6232407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:6232407 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:14943724 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:14943724 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:52158978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr13:52158978 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:177071447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:177071447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:170072268 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr6:170072268 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:116080655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:116080655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:167196624 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:167196624 T>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:137021781 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr9:137021781 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:241953804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:241953804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:44197437 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr20:44197437 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:184114660 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:184114660 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:78420705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:78420705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:168549545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:168549545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:31594944 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr2:31594944 G>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:128881442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chrX:128881442 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:64833019 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr12:64833019 T>G did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:180793778 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr1:180793778 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:60228024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr18:60228024 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:147106792 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:147106792 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:22171469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:22171469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:21605925 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr3:21605925 A>C did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:57188924 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr7:57188924 A>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:9583778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:9583778 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:53554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr4:53554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:3367175 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr16:3367175 G>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:38014229 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:38014229 C>T did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:53999378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z046-01A-01W-0746-08 chr19:53999378 C>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:16524960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:16524960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chrX:15567762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chrX:15567762 G>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:115535690 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:115535690 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr7:23738045 T>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr7:23738045 T>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr16:71405911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr16:71405911 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr16:71406148 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr16:71406148 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr15:40920454 C>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr15:40920454 C>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr16:57003171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr16:57003171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:43014383 A>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:43014383 A>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:14739505 A>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:14739505 A>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:225702677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:225702677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:97711606 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:97711606 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:2115853 T>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:2115853 T>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr12:52754605 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr12:52754605 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:40094515 C>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:40094515 C>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr8:22011778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr8:22011778 G>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:135516786 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:135516786 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr17:10310137 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr17:10310137 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr11:6865346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr11:6865346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:52838776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:52838776 C>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:163378391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:163378391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:186280750 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:186280750 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:27822933 G>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:27822933 G>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr14:69151671 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr14:69151671 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr17:2270745 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr17:2270745 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:116574279 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:116574279 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr5:101755462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr5:101755462 A>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:172643444 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:172643444 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:153085332 A>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:153085332 A>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:158647362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr1:158647362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:147636632 A>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:147636632 A>C did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr7:139529129 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr7:139529129 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:17729648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:17729648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr11:17519673 T>G did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr11:17519673 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:94497225 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:94497225 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:207429619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:207429619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:31126494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:31126494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:40755046 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:40755046 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:165649548 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:165649548 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr13:37539911 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr13:37539911 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:201485726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:201485726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:56766505 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:56766505 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:84459319 A>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:84459319 A>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:15437252 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:15437252 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:37387503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:37387503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:99410885 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:99410885 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:37122592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:37122592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:118222217 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:118222217 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:43025476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:43025476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:18621995 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:18621995 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:15522903 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:15522903 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:78921214 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:78921214 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:113668643 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:113668643 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:31256446 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:31256446 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:35029640 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:35029640 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:172491874 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:172491874 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:73491402 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:73491402 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:153475341 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:153475341 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:190864559 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:190864559 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:97156764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:97156764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:74034602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:74034602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:102442391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:102442391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:100378798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:100378798 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr10:87898879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr10:87898879 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:183823029 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr3:183823029 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr14:88789169 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr14:88789169 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr6:73765058 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr6:73765058 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:141385495 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:141385495 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr6:17849743 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr6:17849743 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:39637450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:39637450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:53085663 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:53085663 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr6:112441406 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr6:112441406 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:76970756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:76970756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:70346751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:70346751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:128864870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:128864870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:26219696 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:26219696 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:31141191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:31141191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:31141705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:31141705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:56249180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:56249180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:30486695 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr7:30486695 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:22570876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:22570876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:7075044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:7075044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr18:39629469 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr18:39629469 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:90220835 G>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:90220835 G>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:219136073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:219136073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:119237573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:119237573 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr9:98242638 A>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr9:98242638 A>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:6273047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:6273047 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr13:32360396 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr13:32360396 A>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:200246352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:200246352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:44665491 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:44665491 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:42397541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:42397541 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:20555375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:20555375 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:51664726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr8:51664726 A>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:140786782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:140786782 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:35771701 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:35771701 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:197008477 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:197008477 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:79281062 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:79281062 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:12903638 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:12903638 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:39995680 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:39995680 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr9:84202823 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr9:84202823 T>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:100296293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chrX:100296293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:122667010 A>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:122667010 A>C did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:70346666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr4:70346666 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr9:6504588 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr9:6504588 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:54544964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:54544964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:61036548 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr11:61036548 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:53983552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:53983552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:215876611 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:215876611 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:67250088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:67250088 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:87150775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:87150775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:44053464 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:44053464 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:133738438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:133738438 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220402062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220402062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:44070177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:44070177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:236907853 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:236907853 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:236918569 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:236918569 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:52309764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:52309764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:156899147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:156899147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:70926548 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:70926548 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:38884014 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:38884014 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:33630738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:33630738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:33658598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:33658598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:72504962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:72504962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:128862185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:128862185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:128956607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:128956607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:28212499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:28212499 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178553151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178553151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167789309 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167789309 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:31126495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:31126495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:33558870 G>A maps to ENST00000341637 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:33558870 G>A maps to ENST00000341637 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:100234861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:100234861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:100336860 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:100336860 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:148037046 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:148037046 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:100623986 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:100623986 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:100345605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:100345605 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26669331 C>T maps to NM_001039775.3 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26669331 C>T maps to NM_001039775.3 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:15511261 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:15511261 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:91570530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:91570530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:137776404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:137776404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:44289202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:44289202 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:134084975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:134084975 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:90333581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:90333581 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:117864725 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:117864725 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:117877092 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:117877092 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:69998550 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:69998550 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:242149688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:242149688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:201535509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:201535509 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:83360375 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:83360375 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:57042035 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:57042035 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:39441662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:39441662 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:50344447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:50344447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:32908665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:32908665 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:144460972 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:144460972 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:120312614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:120312614 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131704352 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131704352 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:135795421 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:135795421 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:966496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:966496 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:74977390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:74977390 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:98509010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:98509010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:123277109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:123277109 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:101037447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:101037447 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:176934441 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:176934441 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:3907699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:3907699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:160025568 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:160025568 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:17323048 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:17323048 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:160100180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:160100180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:130651121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:130651121 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:84497389 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:84497389 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36054242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36054242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:63534539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:63534539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:104225034 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:104225034 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:118770220 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:118770220 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:81303612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:81303612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:23637449 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:23637449 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:61722756 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:61722756 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:124092040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:124092040 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:93714666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:93714666 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:85933575 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:85933575 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:112642204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:112642204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:97102600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:97102600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:76644548 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:76644548 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:60506907 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:60506907 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:20243490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:20243490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:13797025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:13797025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:46097034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:46097034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:81283877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:81283877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:88151894 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:88151894 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:57347419 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:57347419 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:27905019 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:27905019 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:5360929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:5360929 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:136328713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:136328713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:121097720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:121097720 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:2716037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:2716037 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:2763116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:2763116 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:181753015 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:181753015 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:40075697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:40075697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:50417049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:50417049 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:54912970 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:54912970 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:85961789 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:85961789 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:7327237 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:7327237 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:114436159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:114436159 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:3773090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:3773090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96062476 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96062476 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:105464596 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:105464596 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:24878129 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:24878129 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:197521918 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:197521918 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:93648849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:93648849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:113176217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:113176217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:61592193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:61592193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:85626665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:85626665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:118694128 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:118694128 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:7647514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:7647514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:112647958 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:112647958 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:24536051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:24536051 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:64982487 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:64982487 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:19543962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:19543962 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:73544622 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:73544622 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:25572614 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:25572614 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:202671601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:202671601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:96780623 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:96780623 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:45029371 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:45029371 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:17956597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:17956597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:17629629 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:17629629 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:15789877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:15789877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:22328341 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:22328341 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:138248144 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:138248144 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:132470255 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:132470255 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:6204241 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:6204241 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:21876726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:21876726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:57468157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:57468157 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:78403677 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:78403677 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16279120 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16279120 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:26864102 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:26864102 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:87025406 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:87025406 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7794156 A>T maps to ENST00000381308 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7794156 A>T maps to ENST00000381308 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:56345146 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:56345146 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:6990252 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:6990252 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:103449613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:103449613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:75851658 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:75851658 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:101811913 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:101811913 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:32156631 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:32156631 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:32163952 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:32163952 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:94034568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:94034568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189839471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189839471 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189858938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189858938 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189868285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189868285 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:111155652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:111155652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:107908720 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:107908720 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:137624071 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:137624071 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:137715331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:137715331 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189906231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:189906231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:10078791 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:10078791 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:40768889 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:40768889 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:18897495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:18897495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:46103846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:46103846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17058163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17058163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:34219851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:34219851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:211512454 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:211512454 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:137597843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:137597843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:3790601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:3790601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:159683236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:159683236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:27026479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:27026479 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:19524522 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:19524522 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:19524526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:19524526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:4645078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:4645078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:67976571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:67976571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:23424812 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:23424812 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:77513802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:77513802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:67680534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:67680534 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:68381577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:68381577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:11411799 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:11411799 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:10789584 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:10789584 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:41497405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:41497405 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:46555745 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:46555745 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:47609955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:47609955 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:85415944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:85415944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:159663518 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:159663518 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:122000924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:122000924 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167936004 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167936004 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:155294922 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:155294922 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:36699754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:36699754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:53326036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:53326036 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:2113408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:2113408 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:134706994 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:134706994 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:186024522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:186024522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:50122860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:50122860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:46391376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:46391376 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:9694336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:9694336 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:95581821 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:95581821 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:84257184 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:84257184 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:3597382 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:3597382 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:124382206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:124382206 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:124382215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:124382215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:21628808 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:21628808 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:52417786 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:52417786 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20994268 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20994268 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:38810039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:38810039 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:69557041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:69557041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:132217927 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:132217927 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:15888597 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:15888597 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:44433895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:44433895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:50914978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:50914978 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11353907 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11353907 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73198506 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73198506 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:41458917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:41458917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:32395799 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:32395799 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30458314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30458314 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:41846944 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:41846944 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:82101927 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:82101927 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:95661839 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:95661839 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:71780342 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:71780342 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:137807428 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:137807428 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:77427879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:77427879 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:25766104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:25766104 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:131671647 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:131671647 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:21548106 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:21548106 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:57897588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:57897588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:3788293 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:3788293 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:19947323 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:19947323 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42941239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42941239 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:38435411 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:38435411 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:55242591 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:55242591 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:37296118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:37296118 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:101196562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:101196562 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:6903694 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:6903694 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:120594911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:120594911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:111970425 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:111970425 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:112018804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:112018804 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:134911680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:134911680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20871694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20871694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:101923657 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:101923657 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:66204802 C>A maps to ENST00000370616 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:66204802 C>A maps to ENST00000370616 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:40865548 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:40865548 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:161004597 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:161004597 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:197020110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:197020110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139153427 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139153427 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139153644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139153644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139160735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139160735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139380007 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139380007 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:30880255 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:30880255 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:30921743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:30921743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:62274288 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:62274288 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:10681855 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:10681855 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:24870974 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:24870974 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:131811790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:131811790 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:39887060 G>T maps to ENST00000377642 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:39887060 G>T maps to ENST00000377642 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:8997490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:8997490 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:207636106 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:207636106 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:92430650 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:92430650 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:150890112 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:150890112 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:48414407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:48414407 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:149762712 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:149762712 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:155510524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:155510524 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:54475765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:54475765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:32729473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:32729473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:192441805 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:192441805 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:137790835 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:137790835 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:102670639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:102670639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:167438507 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:167438507 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:116029878 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:116029878 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:60999887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:60999887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:71064869 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:71064869 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:114269750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:114269750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:127236212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:127236212 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:30255031 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:30255031 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:71686112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:71686112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:101258598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:101258598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:27128411 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:27128411 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:89910774 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:89910774 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:26570075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:26570075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:88893063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:88893063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:172735722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:172735722 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:173301592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:173301592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:48650073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:48650073 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:163209059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:163209059 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:134147090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:134147090 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:57861394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:57861394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39820164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39820164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:50295157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:50295157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:96691836 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:96691836 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:217804636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:217804636 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:154071695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:154071695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:9943860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:9943860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:14018650 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:14018650 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:66771141 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:66771141 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:66800231 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:66800231 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178418344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178418344 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:13241169 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:13241169 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:52622592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:52622592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:52847237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:52847237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:1056509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:1056509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:43015604 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:43015604 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:119923352 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:119923352 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30689090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30689090 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:18802026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:18802026 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:43506293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:43506293 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:89579483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:89579483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:193854684 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:193854684 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:75203329 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:75203329 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:32975645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:32975645 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:95223510 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:95223510 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:114383748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:114383748 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:118837612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:118837612 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:114010215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:114010215 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:38832535 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:38832535 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:82882067 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:82882067 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:79094222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:79094222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:79120917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:79120917 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:21237561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:21237561 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:65684079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:65684079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:99228798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:99228798 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:118623707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:118623707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:207041913 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:207041913 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:14159683 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:14159683 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39734908 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39734908 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:105242189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:105242189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:51952609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:51952609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:95432169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:95432169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:51896741 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:51896741 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:66583063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:66583063 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:50683297 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:50683297 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:52201519 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:52201519 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:52205907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:52205907 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:7604941 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:7604941 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:33661486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:33661486 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:35256008 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:35256008 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:65338901 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:65338901 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:211035070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:211035070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:154821431 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:154821431 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:36662627 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:36662627 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:18171809 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:18171809 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:202710909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:202710909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:34787462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:34787462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97000626 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97000626 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:94158301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:94158301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7671670 G>T maps to NM_001080429.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7671670 G>T maps to NM_001080429.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:138566077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:138566077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:43437679 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:43437679 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:20862467 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:20862467 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:20998339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:20998339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:72322559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:72322559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:91528213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:91528213 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:91533860 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:91533860 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:39733841 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:39733841 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:26152675 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:26152675 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55315501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55315501 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55377076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55377076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36349171 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36349171 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:6653359 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:6653359 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97575455 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97575455 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51358120 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51358120 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51361619 G>C maps to ENST00000444635 *181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51361619 G>C maps to ENST00000444635 *181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51361683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51361683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:241712233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:241712233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:134981685 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:134981685 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:66039578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:66039578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:29538222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:29538222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:10673394 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:10673394 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:39080836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:39080836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:52985175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:52985175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:31802567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:31802567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:129635764 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:129635764 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:55479452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:55479452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:95549824 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:95549824 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:71977205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:71977205 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:104310074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:104310074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55144341 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55144341 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55144404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55144404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55147064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55147064 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51890753 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51890753 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96478364 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96478364 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:165324696 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:165324696 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:148004822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:148004822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:81968877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:81968877 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:141079434 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:141079434 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:141272158 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:141272158 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:141459221 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:141459221 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:170115484 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:170115484 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:170148563 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:170148563 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:169574746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:169574746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:85446101 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:85446101 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26110046 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26110046 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:19418910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:19418910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:32677373 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:32677373 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:94109319 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:94109319 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:119735333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:119735333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:99016119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:99016119 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:182810431 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:182810431 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:100382481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:100382481 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:85485096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:85485096 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:47324157 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:47324157 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:37959827 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:37959827 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:41888846 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:41888846 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:126734328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:126734328 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:42866203 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:42866203 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:8702464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:8702464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:141754457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:141754457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:43277446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:43277446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:151970970 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:151970970 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:55517109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:55517109 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:33795388 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:33795388 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:29638177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:29638177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:29638300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:29638300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:108818389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:108818389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:30517090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:30517090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:1977311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:1977311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:68513741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:68513741 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:60165296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:60165296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:60182862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:60182862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:49723948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:49723948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:62367577 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:62367577 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:124641194 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:124641194 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100696651 G>A maps to NM_001040105.1 W4433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100696651 G>A maps to NM_001040105.1 W4433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:1253221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:1253221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:71346404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:71346404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:10428439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:10428439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:23887169 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:23887169 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:23893968 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:23893968 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:24384187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:24384187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:1926038 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:1926038 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:62871296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:62871296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:101727161 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:101727161 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:23361778 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:23361778 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:204009928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:204009928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:35731447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:35731447 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:120377669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:120377669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:41341829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:41341829 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:152554263 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:152554263 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:27065352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:27065352 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:73415159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:73415159 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:177580634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:177580634 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:52520713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:52520713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:124676275 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:124676275 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56313141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56313141 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55501765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55501765 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56372682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56372682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:48337819 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:48337819 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:69315191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:69315191 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:69329230 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:69329230 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:64436225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:64436225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:59522137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:59522137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:116429418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:116429418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:49414547 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:49414547 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:2290721 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:2290721 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:25895015 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:25895015 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:133053258 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:133053258 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:72011854 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:72011854 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:74677422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:74677422 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:53080953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:53080953 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:128414500 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:128414500 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:123900161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:123900161 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:6790217 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:6790217 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:29141261 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:29141261 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248138167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248138167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248166234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248166234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:55135315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:55135315 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:88299748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:88299748 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:179201242 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:179201242 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:63281368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:63281368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:25833575 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:25833575 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:49040083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:49040083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:57325798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:57325798 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:110416337 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:110416337 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:169633101 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:169633101 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:91352810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:91352810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:6748400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:6748400 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:55570537 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:55570537 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:55700795 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:55700795 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:53850946 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:53850946 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:20705450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:20705450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:144852365 T>A maps to NM_001198834.1 L2359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:144852365 T>A maps to NM_001198834.1 L2359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:21999818 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:21999818 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:41903761 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:41903761 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:8045882 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:8045882 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:28733890 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:28733890 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:77685128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:77685128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:160000239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:160000239 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:46570714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:46570714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:99997699 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:99997699 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:37138706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:37138706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:110402669 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:110402669 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131960334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131960334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:151149536 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:151149536 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:208841295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:208841295 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:118315204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:118315204 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:121186187 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:121186187 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:14983112 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:14983112 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:37792212 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:37792212 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:146236138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:146236138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:9588968 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:9588968 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:45117336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:45117336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:54394780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:54394780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:35081555 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:35081555 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:60671054 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:60671054 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43709731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43709731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43674439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43674439 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43262632 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43262632 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43765852 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43765852 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:32823997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:32823997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:98238998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:98238998 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:11590021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:11590021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:8449906 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:8449906 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:31468270 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:31468270 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:98116800 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:98116800 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:204302959 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:204302959 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:79292009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:79292009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:45480134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:45480134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:76416998 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:76416998 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:4833007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:4833007 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:24647745 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:24647745 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:74683182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:74683182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:192128253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:192128253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:100974592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:100974592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73007324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73007324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73029267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73029267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:62631939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:62631939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:151328053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:151328053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:74162443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:74162443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:72200012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:72200012 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:35835960 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:35835960 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26881586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26881586 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:78811857 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:78811857 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:90090183 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:90090183 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:123011231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:123011231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:93026647 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:93026647 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:93026718 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:93026718 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:116912126 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:116912126 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:159529242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:159529242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39007936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39007936 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39008785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39008785 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:237540585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:237540585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:33993115 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:33993115 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:34110891 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:34110891 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:50898330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:50898330 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:78142559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:78142559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:78146254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:78146254 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:38926898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:38926898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:166872011 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:166872011 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:118012168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:118012168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:57218036 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:57218036 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:18508066 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:18508066 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:169680597 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:169680597 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26142276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:26142276 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:4834195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:4834195 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:94776355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:94776355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:47103475 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:47103475 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:26941252 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:26941252 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:130509375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:130509375 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:19663435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:19663435 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:72891312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:72891312 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51647613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51647613 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16981865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16981865 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:2234291 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:2234291 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:48412940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:48412940 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:103701838 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:103701838 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:43262528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:43262528 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:22380854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:22380854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:119015218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:119015218 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:160677819 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:160677819 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:92379030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:92379030 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:5330275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:5330275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:140128066 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:140128066 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:75679362 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:75679362 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:1214209 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:1214209 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:45823726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:45823726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:20629279 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:20629279 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:139103435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:139103435 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:67298892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:67298892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:48466248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:48466248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:98774050 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:98774050 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:168127700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:168127700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:168179856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:168179856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:168310445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:168310445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:53407464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:53407464 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:45804818 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:45804818 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:156244513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:156244513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:70420342 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:70420342 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:169051475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:169051475 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:62233506 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:62233506 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:25219718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:25219718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:97101198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:97101198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:45360275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:45360275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:144337424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:144337424 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:99913243 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:99913243 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220338129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220338129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:51014415 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:51014415 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:153028922 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:153028922 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:55657300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:55657300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:54864844 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:54864844 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:13106961 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:13106961 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76024650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76024650 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:23637533 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:23637533 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:53045517 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:53045517 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:107423024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:107423024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:104125237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:104125237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:37369236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:37369236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:74072053 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:74072053 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:40460389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:40460389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:168812165 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:168812165 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:27098872 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:27098872 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:27099859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:27099859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:81837197 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:81837197 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:70515665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:70515665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39962930 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39962930 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:149877628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:149877628 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:10927690 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:10927690 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:64600695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:64600695 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:123969847 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:123969847 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:60581825 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:60581825 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:99706237 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:99706237 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:74181396 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:74181396 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:9677194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:9677194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:79282177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:79282177 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:79285951 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:79285951 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:114804257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:114804257 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:132891337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:132891337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:61083813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:61083813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:114045786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:114045786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:15211784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:15211784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:62265923 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:62265923 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:50810717 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:50810717 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:11441641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:11441641 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:11676676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:11676676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7998677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7998677 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:98165219 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:98165219 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:2591005 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:2591005 G>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:138858258 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:138858258 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:946031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:946031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:159031753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:159031753 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:74332844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:74332844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:68812309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:68812309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:68956205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:68956205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:12266693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:12266693 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:117567976 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:117567976 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:9538451 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:9538451 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55658245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:55658245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:175355119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:175355119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:175360324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:175360324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:218674925 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:218674925 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:113716074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:113716074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:68846294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:68846294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:103271308 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:103271308 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:10906885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:10906885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:72825667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:72825667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:30121678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:30121678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:155152075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:155152075 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:73424735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:73424735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:142625164 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:142625164 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:142626704 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:142626704 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100065312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100065312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:81606237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:81606237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:82275877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:82275877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:21703676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:21703676 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:117619205 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:117619205 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:135098866 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:135098866 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:151534744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:151534744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:77737559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:77737559 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36233705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36233705 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:86278706 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:86278706 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:42650893 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:42650893 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:114694389 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:114694389 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:100431673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:100431673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:43546919 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:43546919 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17738860 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17738860 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:33501225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:33501225 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:35769792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:35769792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:216497702 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:216497702 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:216538181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:216538181 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:78183487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:78183487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:145157244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:145157244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:116202105 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:116202105 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:42576998 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:42576998 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:158851290 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:158851290 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:153078308 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:153078308 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:100711663 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:100711663 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:62165361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:62165361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:70917683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:70917683 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:65242094 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:65242094 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:25056780 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:25056780 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:98846488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:98846488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:102676266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:102676266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:5269189 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:5269189 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:31611179 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:31611179 T>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:82576364 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:82576364 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:33263344 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:33263344 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:2408889 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chrX:2408889 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:42703209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:42703209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:60241245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:60241245 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:31610339 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:31610339 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:106646454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:106646454 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73442490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:73442490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:9517964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:9517964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:5012585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:5012585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:22257725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:22257725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:22838536 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:22838536 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:44751960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:44751960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:53462 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:53462 A>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:58511941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:58511941 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:52852622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:52852622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:179046185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:179046185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11608827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11608827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:5455441 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:5455441 A>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56757806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56757806 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:67501082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:67501082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:16244112 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:16244112 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:131329694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:131329694 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:67372710 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:67372710 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:77934886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:77934886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:114095521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:114095521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:4077127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:4077127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:119249579 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:119249579 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:124368609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:124368609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:193096427 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:193096427 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr21:42618022 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr21:42618022 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:60556364 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:60556364 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:26388562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:26388562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:81094672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:81094672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:74855702 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:74855702 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:8211098 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:8211098 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:146278339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:146278339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:140807789 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:140807789 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:181741120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:181741120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:201042895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:201042895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:27445612 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:27445612 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:76916079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:76916079 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:106209807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:106209807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:167400750 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:167400750 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:30365164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:30365164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:19481817 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:19481817 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:26959332 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:26959332 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:17897740 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:17897740 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:3293125 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:3293125 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:68374525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:68374525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:196965382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:196965382 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:49535452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:49535452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:175618126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:175618126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:125417631 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:125417631 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:23457010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:23457010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:103427477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:103427477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:101782502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:101782502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:7472367 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:7472367 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:74420333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:74420333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:28758705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:28758705 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:131404857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:131404857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:131415373 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:131415373 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:131442523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:131442523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:35500799 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:35500799 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:3351087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:3351087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:113697609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:113697609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:113988399 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:113988399 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:43007751 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:43007751 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:14976823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:14976823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:31566299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:31566299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chrX:50146950 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chrX:50146950 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:124329612 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:124329612 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:88580706 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:88580706 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:118574785 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:118574785 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:38790594 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:38790594 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:69597638 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:69597638 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:162877213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:162877213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:28736253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:28736253 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:221875742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:221875742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:95665181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:95665181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:93213294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:93213294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:43996244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:43996244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:120606214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:120606214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:65374202 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:65374202 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:1553965 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:1553965 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:6197384 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:6197384 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:93159769 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:93159769 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:86151412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:86151412 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:33035692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:33035692 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:159646793 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:159646793 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:79385777 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:79385777 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:13825084 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:13825084 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:155157867 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:155157867 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:130152915 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:130152915 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:89654557 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:89654557 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:19747509 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:19747509 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:93518807 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:93518807 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:9862655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:9862655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:42895786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:42895786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:156479777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:156479777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:37287707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:37287707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:37299193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:37299193 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:75221232 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:75221232 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:62482859 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:62482859 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:6253537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:6253537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:121579051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:121579051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:15267673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:15267673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:154568539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:154568539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:182395459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:182395459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:15647858 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:15647858 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:187519310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:187519310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:10622587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:10622587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:211092861 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:211092861 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:20731901 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:20731901 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:62044962 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:62044962 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:105508113 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:105508113 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:8930277 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:8930277 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:57961077 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:57961077 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:241732004 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:241732004 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:160952973 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:160952973 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:85985104 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:85985104 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:39844652 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:39844652 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:77789676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:77789676 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:87115369 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:87115369 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:46313002 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:46313002 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:102666048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:102666048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:132645330 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:132645330 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:48328078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:48328078 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:59940657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:59940657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:30656830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:30656830 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:15815538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:15815538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:10351893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:10351893 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:52556514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:52556514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:1926034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:1926034 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:101763101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:101763101 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:2986009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:2986009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:6626499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:6626499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:204981789 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:204981789 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:169718573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:169718573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:79589367 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:79589367 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:51254609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:51254609 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:3722156 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:3722156 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:58946615 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:58946615 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:31302177 C>A maps to ENST00000382310 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:31302177 C>A maps to ENST00000382310 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:9524884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:9524884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:9560730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:9560730 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:53859588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:53859588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:53859815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:53859815 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:54364789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:54364789 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:197738345 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:197738345 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:26910305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:26910305 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:161123294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:161123294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:57890151 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:57890151 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:77765664 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:77765664 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:81769546 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:81769546 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:22037368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:22037368 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:37518397 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:37518397 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:101984525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:101984525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:47296037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:47296037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:47342791 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:47342791 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:57158027 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:57158027 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:30100285 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:30100285 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:30133125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:30133125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:214171711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:214171711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:8748147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:8748147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:50384425 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:50384425 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:85800067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:85800067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:173787113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:173787113 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:155748914 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:155748914 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:7277510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:7277510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:7277512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:7277512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:74683195 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:74683195 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:192312098 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:192312098 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:166923853 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:166923853 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:34117696 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:34117696 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:127781275 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:127781275 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:80435146 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:80435146 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:84671681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:84671681 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:61569626 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:61569626 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:56352097 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:56352097 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:26730004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:26730004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:6441954 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:6441954 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:190444473 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:190444473 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75680261 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75680261 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75707843 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75707843 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:48703324 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:48703324 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:10858237 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:10858237 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:20618935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:20618935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:112057269 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:112057269 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:12162865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:12162865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:39240989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:39240989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:84999386 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:84999386 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:158597592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:158597592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:158622996 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:158622996 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:131361376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:131361376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:66460363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:66460363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:13140861 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:13140861 T>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:4076752 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:4076752 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:8435334 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:8435334 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:110598223 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:110598223 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:97362157 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:97362157 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:72289715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:72289715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:10419584 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:10419584 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:70741943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:70741943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:84300859 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:84300859 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:3028868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:3028868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:120471117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:120471117 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:15240863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:15240863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:43427705 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:43427705 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:83251422 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:83251422 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:74801867 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:74801867 T>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:32050186 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:32050186 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:17782830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:17782830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:42697232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:42697232 C>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:73000613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:73000613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:91121557 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:91121557 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:117638683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:117638683 C>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:179479522 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:179479522 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:48136267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:48136267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:54707112 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:54707112 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:216375038 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:216375038 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:216462836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:216462836 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:106761571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:106761571 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:42252585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:42252585 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:50512281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:50512281 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:98737720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:98737720 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:990830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:990830 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:990842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:990842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:30973741 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:30973741 G>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:21321219 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:21321219 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:38409662 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:38409662 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:79753038 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:79753038 A>C did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:52620308 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:52620308 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:21281750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:21281750 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:7629728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:7629728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:107589147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:107589147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:123342570 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:123342570 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:5146598 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:5146598 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:100673397 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:100673397 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:128956582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:128956582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:18636107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:18636107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:100197756 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:100197756 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119037158 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119037158 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:45891250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:45891250 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:38516384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:38516384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:41552961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:41552961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:114269408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:114269408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:62023495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:62023495 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:40824084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:40824084 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:116707678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:116707678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:58556403 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:58556403 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr21:27462250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr21:27462250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:141059289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:141059289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:24964410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:24964410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:176983743 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:176983743 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119500676 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119500676 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:69349360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:69349360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:215593378 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:215593378 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:171501461 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:171501461 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:160546764 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:160546764 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:15543334 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:15543334 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:29645163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:29645163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:40020229 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:40020229 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:95903362 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:95903362 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:34385476 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:34385476 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:44237425 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:44237425 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:75107165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:75107165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:55111081 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:55111081 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:123776383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:123776383 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:74073067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:74073067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:151936916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:151936916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:69552812 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:69552812 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:26842780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:26842780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:49957150 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:49957150 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:197594194 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:197594194 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:74497245 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:74497245 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:157804580 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:157804580 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:19502214 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:19502214 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:64981348 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:64981348 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:1588716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:1588716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:20649695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:20649695 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:214837203 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:214837203 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:40118273 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:40118273 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:125780988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:125780988 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:154508242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:154508242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:154508243 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:154508243 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:75830909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:75830909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:75840459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:75840459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:105819577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:105819577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:110817047 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:110817047 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:211480960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:211480960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:5868301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:5868301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:99661209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:99661209 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:4645810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:4645810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:206320421 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:206320421 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:35985703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:35985703 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:50595819 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:50595819 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:118572495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:118572495 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:124097857 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:124097857 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:6873989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:6873989 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:197704955 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:197704955 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:185997924 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:185997924 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:30624975 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:30624975 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:32591627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:32591627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:32614062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:32614062 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:116573228 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:116573228 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:116593991 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:116593991 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:74751022 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:74751022 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:28609406 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:28609406 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:183978894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:183978894 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:24078374 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:24078374 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:44067861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:44067861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:107514509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:107514509 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:28015991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:28015991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:120629663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:120629663 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:40216866 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:40216866 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:96130965 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:96130965 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:66013964 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:66013964 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:57419832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:57419832 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:190234279 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:190234279 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:98054986 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:98054986 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:161479886 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:161479886 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:95528452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:95528452 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:72710649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:72710649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:108377490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:108377490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:147084863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:147084863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:216285362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:216285362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:172070575 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:172070575 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:89391962 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:89391962 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:100617382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:100617382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:5831490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:5831490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:46042820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:46042820 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr21:34120696 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr21:34120696 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:81121308 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:81121308 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:48260233 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:48260233 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:155753966 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:155753966 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr21:30968954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr21:30968954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:47440722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:47440722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:41038741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:41038741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:41065624 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:41065624 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:191175534 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:191175534 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:27860999 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:27860999 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:186022871 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:186022871 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:87511801 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:87511801 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:183776412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:183776412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:53560896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:53560896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:148579522 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:148579522 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:27441333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:27441333 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:12957003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:12957003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:40332733 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:40332733 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:123128592 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:123128592 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:24834653 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:24834653 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:95508757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:95508757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:22463257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:22463257 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:17898351 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:17898351 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:39735195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:39735195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:50280166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:50280166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:52646310 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:52646310 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:153130023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:153130023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:129250579 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:129250579 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119576231 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119576231 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:55107415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:55107415 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:73535050 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:73535050 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:197701400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:197701400 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:78010310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:78010310 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:26211856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:26211856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:51640245 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:51640245 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:49021002 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:49021002 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:128083186 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:128083186 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:32720351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:32720351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:165110142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:165110142 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:82045203 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:82045203 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119744787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:119744787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:70347042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:70347042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:40572355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:40572355 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:141740023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:141740023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:198412992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:198412992 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:41956497 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:41956497 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:64958324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:64958324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:63526190 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:63526190 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:124626899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:124626899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:16703316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:16703316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:57110314 G>A maps to NM_001113203.1 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:57110314 G>A maps to NM_001113203.1 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:19735192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:19735192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:120611907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:120611907 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:34263366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:34263366 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:2940122 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:2940122 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:123697633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:123697633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:203467769 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:203467769 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:248099979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:248099979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:22333099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:22333099 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:125257137 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:125257137 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:21819150 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr18:21819150 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:226576293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:226576293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:91066149 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:91066149 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:74734044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:74734044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:31864646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:31864646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:35088991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:35088991 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:8789783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:8789783 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:75672861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:75672861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:57751608 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:57751608 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:72157611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:72157611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:20942824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:20942824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:50906151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:50906151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:75187430 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:75187430 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:79741440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:79741440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:16256608 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:16256608 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:71963052 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:71963052 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:40207433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:40207433 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:104356627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:104356627 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:94203550 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:94203550 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:57170208 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:57170208 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:53564526 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:53564526 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:53893505 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:53893505 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:42813663 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:42813663 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:16528717 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:16528717 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:108086463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:108086463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:56810039 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:56810039 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:79385626 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:79385626 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:117240576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:117240576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:72818765 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:72818765 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:104581159 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:104581159 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:73803248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:73803248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:4851174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:4851174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:60907031 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:60907031 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:151789562 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:151789562 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:26898442 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:26898442 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:237620085 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:237620085 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:34072641 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:34072641 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:153591322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:153591322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:39421423 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:39421423 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:102286655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:102286655 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:48058725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:48058725 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:94930930 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:94930930 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:26690554 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:26690554 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:1517677 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:1517677 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:159923713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:159923713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:87746811 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:87746811 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:44676786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:44676786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:122787416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:122787416 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:64366231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:64366231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:160551312 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:160551312 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:85461672 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:85461672 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:88218323 C>T maps to ENST00000429605 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:88218323 C>T maps to ENST00000429605 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:61510328 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:61510328 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:29285089 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:29285089 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:108608718 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:108608718 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:20905512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:20905512 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:105752421 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:105752421 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:67473512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:67473512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:17949973 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:17949973 T>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:21755845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:21755845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:88408089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:88408089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:231307843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:231307843 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:144337067 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:144337067 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:147550668 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:147550668 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:38063047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:38063047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:54694094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:54694094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:134137915 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:134137915 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:36483071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:36483071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:49055444 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:49055444 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:152560551 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:152560551 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:64487949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:64487949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:13561717 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:13561717 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:133475541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:133475541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:164394895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:164394895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:74876543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:74876543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:217724209 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:217724209 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:62514217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:62514217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:144245754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:144245754 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:209946491 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:209946491 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:118889790 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:118889790 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:67039425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:67039425 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:904344 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:904344 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:234915400 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:234915400 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:90794644 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr15:90794644 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:34790898 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:34790898 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:58469205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:58469205 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:234405288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:234405288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:144999405 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr6:144999405 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:77902398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:77902398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:150082471 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:150082471 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:65242471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:65242471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:119575445 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:119575445 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:52277840 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:52277840 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:241964605 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:241964605 A>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:27614071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:27614071 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:1754921 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:1754921 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:168098275 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:168098275 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:128902566 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chrX:128902566 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:183432944 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr3:183432944 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:68249316 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:68249316 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:64415064 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:64415064 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:74390002 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:74390002 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:91402868 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:91402868 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:57770708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:57770708 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:44101147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:44101147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:179079364 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:179079364 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:5242094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:5242094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:94413679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:94413679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr13:113530268 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr13:113530268 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:160146194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:160146194 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:119512370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:119512370 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:51707745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:51707745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:36946905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:36946905 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:15713414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:15713414 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:112648094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:112648094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:49074268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:49074268 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:40854579 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:40854579 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:41586213 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:41586213 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:55646092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:55646092 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:117544515 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:117544515 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:158261805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:158261805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:35836082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:35836082 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:37858756 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:37858756 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:8688823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:8688823 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:246785019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:246785019 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:189872732 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:189872732 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:54744208 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:54744208 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:113348813 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:113348813 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:19984845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:19984845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:27840807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:27840807 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:31191765 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:31191765 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr16:21145488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr16:21145488 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:38749012 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:38749012 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:102968011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:102968011 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:101659592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:101659592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:36324515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:36324515 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:37264317 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:37264317 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:76905586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:76905586 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:231155538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:231155538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:97329420 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:97329420 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:5958130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:5958130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:72755445 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:72755445 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:240308186 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:240308186 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:109275799 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:109275799 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:65161477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:65161477 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:112015786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:112015786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:161116208 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:161116208 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:26805870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:26805870 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:179751936 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:179751936 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:28493939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:28493939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:28501704 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:28501704 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr22:40355936 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr22:40355936 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:105231888 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:105231888 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:52219402 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:52219402 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:28388987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:28388987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:46607310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:46607310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:31795720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:31795720 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:3211514 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:3211514 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:118919111 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:118919111 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:148607185 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:148607185 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:320439 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:320439 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:57194465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:57194465 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:109742328 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:109742328 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:45205540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:45205540 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:45226427 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:45226427 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:36349538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:36349538 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:39636078 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:39636078 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:141665671 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:141665671 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:170103120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:170103120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:71151365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:71151365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:160786664 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:160786664 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:65550993 C>T maps to NM_145114.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:65550993 C>T maps to NM_145114.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:126755680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:126755680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:42872598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:42872598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:135170359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:135170359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:146575073 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:146575073 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:18145323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:18145323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr3:108174814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr3:108174814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr22:36717764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr22:36717764 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:171607600 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:171607600 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:62868053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:62868053 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:201757828 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:201757828 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:78553176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:78553176 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:31556973 G>C maps to NM_001145466.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:31556973 G>C maps to NM_001145466.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:3452465 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:3452465 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:7079460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:7079460 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:89177259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:89177259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:101604481 T>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:101604481 T>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:220421164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:220421164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:123810320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:123810320 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:72929384 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:72929384 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:133197813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:133197813 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:91368615 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:91368615 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:18972545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:18972545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:8792442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:8792442 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:55607202 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:55607202 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:81123006 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:81123006 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:18730267 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:18730267 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:131117306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:131117306 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:114380187 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:114380187 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:71066180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:71066180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:71286915 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:71286915 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:234238263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:234238263 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:122792965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:122792965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:135379935 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:135379935 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:37153893 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:37153893 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:56583109 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:56583109 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:51415274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:51415274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:158630969 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:158630969 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:48209401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chrX:48209401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:104127023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:104127023 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:70599997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:70599997 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr3:12199022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr3:12199022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:48877029 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:48877029 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:114832504 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:114832504 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:98173131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:98173131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:68919792 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:68919792 A>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:175360344 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:175360344 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:10941865 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:10941865 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:10942002 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr21:10942002 A>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:180625979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:180625979 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:110226570 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:110226570 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:135802577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:135802577 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:40104710 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:40104710 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:15267815 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:15267815 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:63973808 T>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:63973808 T>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr22:18570624 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr22:18570624 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:139609590 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:139609590 A>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:166574293 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:166574293 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:73688073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:73688073 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:1953699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:1953699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:9583962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:9583962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:53754778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:53754778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:12014536 C>G did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:12014536 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:7726669 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:7726669 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:89052423 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:89052423 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:100629973 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:100629973 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:179287793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:179287793 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:158390284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:158390284 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:87822557 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:87822557 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:207406943 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:207406943 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:207422343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:207422343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:77390015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:77390015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:7707122 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:7707122 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:76287505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:76287505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:87531453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:87531453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:106992378 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:106992378 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:106992416 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:106992416 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:106992891 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:106992891 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:137801299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:137801299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:58287208 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:58287208 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:202174128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:202174128 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:33122230 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:33122230 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:69298860 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:69298860 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:122617727 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:122617727 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:72047353 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:72047353 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:21242543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:21242543 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:68112270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:68112270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:32912451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:32912451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:28270258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:28270258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:177143600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:177143600 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:117062195 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:117062195 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:32095137 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:32095137 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:116931734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:116931734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:54070072 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:54070072 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:124235919 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:124235919 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:11047435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:11047435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:56534695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:56534695 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41903321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41903321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:136589175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:136589175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:81295629 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:81295629 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:12866161 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:12866161 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:79791870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:79791870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:100629330 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:100629330 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:118424186 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:118424186 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:60622662 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:60622662 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:30771820 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:30771820 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:30804956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:30804956 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:68270277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:68270277 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:18401979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:18401979 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:31670914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:31670914 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:73824702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:73824702 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:209045446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:209045446 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:207273325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:207273325 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:37167371 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:37167371 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:37210552 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:37210552 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:121642716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:121642716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:74073075 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:74073075 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:40936366 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:40936366 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:40967680 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:40967680 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:116190309 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:116190309 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:86358354 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:86358354 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:58234209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:58234209 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:231683214 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:231683214 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:18690998 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:18690998 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:115069178 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:115069178 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:122001153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:122001153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:93106985 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:93106985 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:219892810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:219892810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:96265868 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:96265868 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:43482490 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:43482490 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:14501928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:14501928 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:61747903 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:61747903 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:76550980 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:76550980 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:49031505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:49031505 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:182514851 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:182514851 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:136623309 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:136623309 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:113498263 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:113498263 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:43203812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:43203812 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:51871908 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:51871908 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:150661735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:150661735 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:87641371 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:87641371 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:135107145 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:135107145 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:3095688 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:3095688 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:125232468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:125232468 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:103477843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:103477843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:32156785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:32156785 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:139616915 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:139616915 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:130300390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:130300390 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:166325418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:166325418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:137600856 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:137600856 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:49814478 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:49814478 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:20021468 T>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:20021468 T>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:21281245 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:21281245 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:2819884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:2819884 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:113241179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:113241179 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:79422910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:79422910 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:80874539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:80874539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:35973919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:35973919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:35973921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:35973921 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:158287304 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:158287304 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:39843274 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:39843274 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:15976326 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:15976326 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:15739850 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:15739850 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:29957856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:29957856 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:154011445 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:154011445 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:329150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:329150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:518572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:518572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:21030851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:21030851 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:6740932 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:6740932 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:10897232 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:10897232 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:169143319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:169143319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:169477092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:169477092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:116593722 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:116593722 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:109027790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:109027790 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:56490115 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:56490115 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:56499808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:56499808 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:82122101 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:82122101 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:233346565 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:233346565 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:28408004 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:28408004 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:201983202 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:201983202 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:14785533 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:14785533 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:132149290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:132149290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:132491221 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:132491221 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:132491470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:132491470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:131211718 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:131211718 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:37599438 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:37599438 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:158536458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:158536458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:99202939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:99202939 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:66045133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:66045133 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:23017837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:23017837 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:16483363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:16483363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:139153365 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:139153365 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:10862003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:10862003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:62261014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:62261014 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:26152908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:26152908 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:49221412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:49221412 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:67666374 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:67666374 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:89807406 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:89807406 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:223511405 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:223511405 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:126336014 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:126336014 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:48725322 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:48725322 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:7762236 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:7762236 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17881714 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17881714 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:137778494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:137778494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:157665412 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:157665412 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:142517280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:142517280 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:89429926 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:89429926 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:89431802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:89431802 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:89651900 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:89651900 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:76996197 T>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:76996197 T>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:38997167 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:38997167 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr22:25019731 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr22:25019731 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:233712436 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:233712436 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150438154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150438154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150324692 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150324692 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:78601526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:78601526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17690483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17690483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:62223355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:62223355 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20322603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20322603 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:100388037 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:100388037 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:150407381 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:150407381 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123469787 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123469787 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:94031776 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:94031776 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:14769751 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:14769751 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:69750849 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:69750849 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:162775392 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:162775392 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:1066616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:1066616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:38414216 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:38414216 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:104440034 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:104440034 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:68645462 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:68645462 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:67685532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:67685532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:234079122 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:234079122 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:7749129 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:7749129 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:7763532 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:7763532 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:65351877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:65351877 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:75661933 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:75661933 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:96999878 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:96999878 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:59855295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:59855295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:138525055 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:138525055 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:55268358 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:55268358 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:56119935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:56119935 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:50732234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:50732234 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:22139092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:22139092 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:20361460 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:20361460 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:54779713 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:54779713 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:54721422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:54721422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:70490610 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:70490610 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr13:76416134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr13:76416134 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:81969249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:81969249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:100176141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:100176141 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:150158335 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:150158335 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:31540678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:31540678 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:46483021 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:46483021 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:140982900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:140982900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:45984983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:45984983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:100382435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:100382435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr22:42172316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr22:42172316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:46806698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:46806698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:12265427 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:12265427 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:151960228 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:151960228 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:2526848 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:2526848 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:113241552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:113241552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:28527426 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:28527426 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:26961266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:26961266 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:60230705 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:60230705 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:60201181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:60201181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:59939502 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:59939502 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:76349614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:76349614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:120800987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:120800987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:80181743 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:80181743 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:9008102 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:9008102 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:15835753 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:15835753 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:108117894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:108117894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:23888944 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:23888944 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:10316173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:10316173 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:211158388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:211158388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:72171957 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:72171957 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:89892359 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:89892359 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:78571476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:78571476 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:15519599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:15519599 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:54911261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:54911261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:160318990 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:160318990 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:20906899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:20906899 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:63830964 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:63830964 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:55502085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:55502085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:101089916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:101089916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:2638490 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:2638490 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:101564583 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:101564583 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:84625061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:84625061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:33468925 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:33468925 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:79117459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:79117459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:59512668 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:59512668 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:27272208 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:27272208 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:28200127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:28200127 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:123695445 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:123695445 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:22333344 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:22333344 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:73627749 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:73627749 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:103249225 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:103249225 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:61019474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:61019474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:162989861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:162989861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:136002932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:136002932 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:55590994 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:55590994 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:17804642 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:17804642 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:167412150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:167412150 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:167437736 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:167437736 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:183088788 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:183088788 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:31867885 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:31867885 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:20704680 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:20704680 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20384312 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20384312 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20386363 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20386363 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:57335143 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:57335143 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:179615881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:179615881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:60974817 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:60974817 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:85692751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:85692751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:131866698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:131866698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:152938003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:152938003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:118359683 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:118359683 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:68385444 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:68385444 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:113322224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:113322224 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:44428308 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:44428308 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:133536237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:133536237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:69028263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:69028263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:148604818 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:148604818 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:93650484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:93650484 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:36070695 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:36070695 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:128298213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:128298213 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:71066180 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:71066180 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:52348671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:52348671 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:1647407 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:1647407 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:174219784 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:174219784 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:125832719 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:125832719 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:36219966 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:36219966 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:211452488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:211452488 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:79384968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:79384968 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:103162698 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:103162698 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:100052448 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:100052448 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:72936599 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:72936599 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:41165854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:41165854 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:156450184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:156450184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:124766350 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:124766350 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:7023674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:7023674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:39070792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:39070792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:237868444 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:237868444 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:34157471 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:34157471 A>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:52106127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:52106127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:122634496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:122634496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:77880028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:77880028 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:100897619 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:100897619 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:45220930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:45220930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr22:18066167 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr22:18066167 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:45814154 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:45814154 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:118588440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:118588440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:18331601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:18331601 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:103237076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:103237076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:75677413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:75677413 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:76047961 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:76047961 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:344180 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:344180 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:74904191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:74904191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:108380098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:108380098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:231314714 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:231314714 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:32312664 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:32312664 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:16248701 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:16248701 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:55648878 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:55648878 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:45801958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:45801958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:52677125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:52677125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:77094627 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:77094627 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:22408190 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:22408190 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:36524423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:36524423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:17726561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:17726561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:191919189 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:191919189 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:36475469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:36475469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:74284678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:74284678 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:70498852 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:70498852 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:21830302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:21830302 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:79747161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:79747161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:156837112 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:156837112 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:100467465 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:100467465 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:92224103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:92224103 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:134034542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:134034542 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:138425294 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:138425294 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:166915511 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:166915511 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:38243573 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:38243573 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123756273 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123756273 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:83379883 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:83379883 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:83379889 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:83379889 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:35684985 C>T maps to ENST00000378309 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:35684985 C>T maps to ENST00000378309 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:186304763 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:186304763 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr13:20077496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr13:20077496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:10907071 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:10907071 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:112572735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:112572735 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:73014988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:73014988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:30105164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:30105164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:55035269 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:55035269 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:14507931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:14507931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:14507984 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:14507984 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:896994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:896994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:3458000 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:3458000 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:98491574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:98491574 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:2106266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:2106266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:31131474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:31131474 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:180322179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:180322179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:142967137 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:142967137 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:74396057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:74396057 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:43547015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:43547015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:129055078 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chrX:129055078 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:6843226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:6843226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:30949242 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:30949242 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:22848810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:22848810 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:130166194 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:130166194 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:145161474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:145161474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:135621130 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:135621130 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:77690783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:77690783 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:43078619 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:43078619 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:53015477 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:53015477 A>G did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:35260311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:35260311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:144733667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:144733667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:238053653 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:238053653 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr16:16180602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr16:16180602 C>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr6:56846444 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr6:56846444 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr21:40641665 A>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr21:40641665 A>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr20:60967946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr20:60967946 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:117303328 C>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:117303328 C>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr10:105793611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr10:105793611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr12:12980128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr12:12980128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr10:124376870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr10:124376870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr5:41070963 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr5:41070963 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr5:118862745 A>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr5:118862745 A>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:148011289 G>C did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:148011289 G>C did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr3:65922646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr3:65922646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr17:27447911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr17:27447911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr10:33619566 T>C did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr10:33619566 T>C did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr3:79136644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr3:79136644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr9:113241794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr9:113241794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr6:42036158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr6:42036158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:165788783 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:165788783 G>A did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr6:80722944 A>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr6:80722944 A>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr15:63866359 T>C did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr15:63866359 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:7714898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:7714898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:41105822 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:41105822 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67149888 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67149888 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67150314 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67150314 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67212183 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67212183 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:66986244 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:66986244 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67041592 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67041592 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:87195635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:87195635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:16170135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:16170135 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:183699461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:183699461 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:17448536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:17448536 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:15057490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:15057490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:44071685 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:44071685 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6156603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6156603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:89211618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:89211618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:66322867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:66322867 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:123301460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:123301460 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:100636506 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:100636506 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:43824149 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:43824149 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:73175337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:73175337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:73184999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:73184999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:7626455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:7626455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:7690714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:7690714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:123049913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:123049913 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:55190031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:55190031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:4744563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:4744563 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:75554983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:75554983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:125856619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:125856619 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:19555963 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:19555963 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114223919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114223919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114260526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114260526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:101563905 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:101563905 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5674856 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5674856 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:101413951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:101413951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20923977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20923977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:57004499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:57004499 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183617944 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183617944 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:21241817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:21241817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:141052923 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:141052923 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:49667673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:49667673 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:17914163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:17914163 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156916721 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156916721 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:66352973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:66352973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:66862969 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:66862969 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:66943741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:66943741 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:177142499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:177142499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:100978226 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:100978226 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:96761800 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:96761800 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:108143386 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:108143386 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:160025670 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:160025670 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:138828126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:138828126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:20066914 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:20066914 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:54714353 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:54714353 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:117278891 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:117278891 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28837214 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28837214 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:8110762 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:8110762 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:69599435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:69599435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:69599587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:69599587 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:41032396 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:41032396 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:11038702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:11038702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:165547234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:165547234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:32836670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:32836670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:31603372 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:31603372 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:56382729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:56382729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4598905 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4598905 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:93651863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:93651863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:81380595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:81380595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:91666347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:91666347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:12815838 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:12815838 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:228289027 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:228289027 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:109193886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:109193886 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:226784444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:226784444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:9510549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:9510549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:20270926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:20270926 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:3736318 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:3736318 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:200821013 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:200821013 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:88199143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:88199143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:81308172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:81308172 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:93928874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:93928874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:165711303 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:165711303 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:40909773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:40909773 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:57417948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:57417948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:53766746 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:53766746 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:54925359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:54925359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:54501418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:54501418 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:62751680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:62751680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:27455903 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:27455903 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:67691105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:67691105 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:78165349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:78165349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:105010543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:105010543 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:65793906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:65793906 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:31592620 T>C maps to ENST00000451887 L1L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:31592620 T>C maps to ENST00000451887 L1L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:93702066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:93702066 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:62533675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:62533675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:7521403 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:7521403 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:158147258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:158147258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:21760809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:21760809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:95174218 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:95174218 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:92247586 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:92247586 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:45024483 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:45024483 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:15789223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:15789223 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:104066633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:104066633 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:104098239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:104098239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:13069267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:13069267 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:88482763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:88482763 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138227116 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138227116 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:57005228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:57005228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:31912435 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:31912435 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:146756782 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:146756782 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:110002838 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:110002838 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:40350887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:40350887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:69202672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:69202672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:122217470 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:122217470 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:143029487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:143029487 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:143043574 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:143043574 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:36303813 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:36303813 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:87591485 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:87591485 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:26509804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:26509804 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:68544273 G>A maps to ENST00000409862 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:68544273 G>A maps to ENST00000409862 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:74385656 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:74385656 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:74414539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:74414539 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:3072390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:3072390 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:1367376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:1367376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:146826034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:146826034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:75842969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:75842969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:71655251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:71655251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:94034937 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:94034937 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139668132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139668132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139729135 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139729135 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139825090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139825090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:7476974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:7476974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107920670 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107920670 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107923870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107923870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107438492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107438492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107554107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:107554107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:238266377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:238266377 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:238267961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:238267961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:331640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:331640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36298706 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36298706 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:160304983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:160304983 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:130002837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:130002837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:68340383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:68340383 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:28747823 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:28747823 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:87541164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:87541164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:211452730 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:211452730 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:211542379 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:211542379 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:43884540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:43884540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:25599900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:25599900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:113316851 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:113316851 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:113599535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:113599535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:126714569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:126714569 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:11732208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:11732208 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:25042808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:25042808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150722681 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150722681 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:43167156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:43167156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:37652838 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:37652838 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:51504903 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:51504903 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100166318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100166318 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:16032982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:16032982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:15807348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:15807348 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:57489187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:57489187 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:160252957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:160252957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:31695780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:31695780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrY:15027208 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrY:15027208 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:55094235 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:55094235 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:70670244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:70670244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:44612370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:44612370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:6793704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:6793704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:29978325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:29978325 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:115079854 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:115079854 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:31687606 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:31687606 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:14741214 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:14741214 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:137407424 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:137407424 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:24114259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:24114259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:9676068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:9676068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:47879113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:47879113 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:154034035 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:154034035 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:95579388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:95579388 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:83544910 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:83544910 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:83878097 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:83878097 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:101201245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:101201245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:124391554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:124391554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:52383114 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:52383114 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:13820438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:13820438 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:38705825 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:38705825 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:11511386 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:11511386 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:46993385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:46993385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:28555402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:28555402 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169174290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169174290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169230219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169230219 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:25231991 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:25231991 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:116525851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:116525851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154264014 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154264014 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154379866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154379866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154679378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154679378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154684292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:154684292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:27163049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:27163049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:113850265 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:113850265 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:100505799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:100505799 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:117310153 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:117310153 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:41539139 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:41539139 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32409130 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32409130 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32462012 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32462012 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:71744061 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:71744061 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:71891326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:71891326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:207575337 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:207575337 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:137805898 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:137805898 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:121554256 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:121554256 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:43630299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:43630299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:40253981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:40253981 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:184043512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:184043512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:50642943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:50642943 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:45022099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:45022099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:107501342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:107501342 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:107514322 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:107514322 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:103986430 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:103986430 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:132176176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:132176176 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:39774446 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:39774446 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:44219321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:44219321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139323179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139323179 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:187073248 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:187073248 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:98982993 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:98982993 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:62147337 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:62147337 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:58620228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:58620228 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:126395313 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:126395313 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:73934198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:73934198 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:127622341 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:127622341 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:87380903 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:87380903 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:171326143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:171326143 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:40368248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:40368248 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:157559360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:157559360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:97368550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:97368550 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:108516632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:108516632 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:95773415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:95773415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:128487706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:128487706 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:240307062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:240307062 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:240307782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:240307782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:8205316 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:8205316 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:89747221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:89747221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:79207452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:79207452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:85924571 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:85924571 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:85987912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:85987912 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:132763526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:132763526 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:37427268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:37427268 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:35642098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:35642098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:161281136 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:161281136 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:161322970 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:161322970 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:27185049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:27185049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:46060226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:46060226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:161522610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:161522610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:88420726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:88420726 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:88432008 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:88432008 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:151700084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:151700084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:115342577 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:115342577 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:153784645 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:153784645 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:34128683 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:34128683 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:79117274 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:79117274 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:58009223 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:58009223 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:117824121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:117824121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:61958955 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:61958955 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:85912132 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:85912132 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150325646 G>A maps to ENST00000438845 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150325646 G>A maps to ENST00000438845 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:78560825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:78560825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:151266250 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:151266250 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:121411542 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:121411542 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:155823634 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:155823634 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:167024948 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:167024948 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:217671775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:217671775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:27219136 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:27219136 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:5554523 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:5554523 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:157368610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:157368610 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:157426094 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:157426094 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:176555944 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:176555944 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:6935529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:6935529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:123484120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:123484120 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:11777828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:11777828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:153026470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:153026470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:153029852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:153029852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:120745988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:120745988 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:48841879 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:48841879 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:48846309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:48846309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:7348397 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:7348397 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:52858929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:52858929 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108634871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108634871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:42628555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:42628555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:148712124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:148712124 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:119935143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:119935143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:45262919 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:45262919 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:240098311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:240098311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:18633382 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:18633382 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:93258613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:93258613 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:93260935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:93260935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:197194479 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:197194479 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:81388133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:81388133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:27833080 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:27833080 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:176316630 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:176316630 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:53398271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:53398271 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:221055724 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:221055724 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:185703786 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:185703786 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:185956691 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:185956691 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186031756 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186031756 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186075948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186075948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186107155 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186107155 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:55379009 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:55379009 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:43058090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:43058090 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:46629837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:46629837 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6458638 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6458638 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:26043823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:26043823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:114384029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:114384029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:97226335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:97226335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:43740491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:43740491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:99012155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:99012155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:122743768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:122743768 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:31733092 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:31733092 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:113856662 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:113856662 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:113815221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:113815221 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:147888966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:147888966 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:94229921 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:94229921 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:159023242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:159023242 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:99251357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:99251357 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47121289 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47121289 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47123147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47123147 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:130423224 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:130423224 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:103003545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:103003545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:113875718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:113875718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:67685421 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:67685421 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156812315 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156812315 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:19680969 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:19680969 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156501135 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156501135 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:54966911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:54966911 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:47189791 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:47189791 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:182400115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:182400115 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:52818543 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:52818543 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156638469 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156638469 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156641393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156641393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:26755442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:26755442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:147016420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:147016420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:123871860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:123871860 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:62732374 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:62732374 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:156241546 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:156241546 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:156254564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:156254564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:75601818 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:75601818 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:211034582 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:211034582 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:63447532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:63447532 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:215256827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:215256827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:138650231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:138650231 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:196448290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:196448290 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:36779957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:36779957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:24180207 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:24180207 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:2732828 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:2732828 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:137710731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:137710731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142659256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142659256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:75134000 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:75134000 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:43880660 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:43880660 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:24820936 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:24820936 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:94100780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:94100780 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:94120393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:94120393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108272596 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108272596 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:20862827 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:20862827 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:8887976 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:8887976 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:10402018 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:10402018 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:26152067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:26152067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:39513522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:39513522 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:39688439 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:39688439 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55246607 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55246607 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:36349506 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:36349506 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:74339044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:74339044 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:51378144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:51378144 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:139164240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:139164240 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:52863165 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:52863165 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:53084908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:53084908 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:52775313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:52775313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:31812498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:31812498 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:143642921 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:143642921 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:143797986 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:143797986 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:153132054 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:153132054 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:50735775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:50735775 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:6961803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:6961803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:107620993 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:107620993 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:209811357 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:209811357 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183103993 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183103993 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:133943332 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:133943332 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:21555561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:21555561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169697672 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169697672 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:22012901 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:22012901 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:93179091 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:93179091 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75614245 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75614245 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:76369501 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:76369501 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:76414307 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:76414307 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:160977327 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:160977327 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:82436236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:82436236 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:11945127 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:11945127 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:133859260 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:133859260 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:25257440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:25257440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:105578360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:105578360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:141264543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:141264543 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:141272181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:141272181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:141707757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:141707757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:52863791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:52863791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:34700056 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:34700056 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:35749979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:35749979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:75078652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:75078652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:75078676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:75078676 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:25098993 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:25098993 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:160797672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:160797672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:235878488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:235878488 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:77814925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:77814925 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:95824962 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:95824962 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:161523038 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:161523038 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:136977653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:136977653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:42109326 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:42109326 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:220808714 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:220808714 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:57882952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:57882952 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:149243566 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:149243566 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:151107729 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:151107729 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:70343154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:70343154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:131943164 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:131943164 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:42114034 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:42114034 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:116411789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:116411789 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141721626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141721626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141722254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141722254 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141736521 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141736521 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141765354 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141765354 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141780534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141780534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141796231 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:141796231 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:151927300 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:151927300 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:151935784 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:151935784 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6213340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6213340 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108780770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108780770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:67769327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:67769327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:67799762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:67799762 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:16981180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:16981180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:94223993 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:94223993 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:26976261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:26976261 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:139068979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:139068979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:95772095 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:95772095 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:60566023 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:60566023 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:59945729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:59945729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:49932444 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:49932444 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:21929594 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:21929594 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:149765119 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:149765119 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:237016013 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:237016013 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:100530152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:100530152 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:17573162 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:17573162 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:81102131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:81102131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:50720810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:50720810 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108135591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:108135591 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:10399211 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:10399211 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:23887134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:23887134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:10303000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:10303000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:16676283 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:16676283 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:26222471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:26222471 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:30248614 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:30248614 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:89896627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:89896627 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:174777510 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:174777510 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:90976612 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:90976612 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:22710637 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:22710637 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:136618740 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:136618740 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:133636530 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:133636530 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:21594651 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:21594651 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:47117782 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:47117782 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:29684519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:29684519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47587729 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47587729 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47587757 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47587757 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:52494096 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:52494096 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:125139491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:125139491 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:63768261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:63768261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:61881202 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:61881202 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56307667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56307667 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:101086938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:101086938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:169690891 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:169690891 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:32164911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:32164911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:89133284 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:89133284 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:69334987 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:69334987 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:33836494 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:33836494 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:170815045 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:170815045 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98254143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98254143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:39219274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:39219274 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:100926437 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:100926437 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:119536080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:119536080 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:115413941 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:115413941 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:131781565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:131781565 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156841652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156841652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156849986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156849986 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:61391344 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:61391344 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:71727611 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:71727611 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:3720234 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:3720234 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:101091692 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:101091692 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:167181950 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:167181950 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:183657892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:183657892 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:10313569 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:10313569 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248166396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248166396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4870504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4870504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:52863627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:52863627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:76769207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:76769207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:36887718 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:36887718 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:74000232 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:74000232 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:17666104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:17666104 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:28789053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:28789053 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:73721201 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:73721201 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:118973875 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:118973875 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:162475105 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:162475105 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:50124303 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:50124303 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:19026997 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:19026997 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:93008123 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:93008123 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:56136706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:56136706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:101983677 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:101983677 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:144921775 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:144921775 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:149283300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:149283300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:44108129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:44108129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:8054079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:8054079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:230459371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:230459371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:129208519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:129208519 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:11046336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:11046336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133849047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133849047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:43803523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:43803523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:68445893 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:68445893 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:17111269 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:17111269 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138407854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138407854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:46570799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:46570799 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:81224337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:81224337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:51920355 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:51920355 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:28785788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:28785788 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:40594422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:40594422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:204234328 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:204234328 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:131904419 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:131904419 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:131953195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:131953195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:68024189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:68024189 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:65158140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:65158140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:68620168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:68620168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:208206528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:208206528 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:28186657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:28186657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:84559287 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:84559287 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:18460625 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:18460625 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:124475595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:124475595 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:87322436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:87322436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:120170296 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:120170296 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:54786715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:54786715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:202527938 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:202527938 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55605664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55605664 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:54974130 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:54974130 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:104357273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:104357273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:9584683 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:9584683 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:82560084 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:82560084 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:47274815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:47274815 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:64084636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:64084636 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:46069962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:46069962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:177421032 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:177421032 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150325534 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150325534 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:4057171 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:4057171 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36483852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36483852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:86544452 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:86544452 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:73683963 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:73683963 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43674367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43674367 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43679694 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43679694 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43411391 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43411391 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43520149 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43520149 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43596021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43596021 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43772303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:43772303 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:109964361 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:109964361 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:11584134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:11584134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:136936176 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:136936176 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:44069225 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:44069225 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:40747035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:40747035 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:41400051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:41400051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:121701311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:121701311 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:158911719 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:158911719 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:107102801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:107102801 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:140110926 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:140110926 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:117869755 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:117869755 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:36231865 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:36231865 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:160251430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:160251430 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:79356751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:79356751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:94748693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:94748693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:127964805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:127964805 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114272415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114272415 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:36087572 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:36087572 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:103123312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:103123312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:73007868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:73007868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:130934835 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:130934835 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:104570881 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:104570881 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:87357171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:87357171 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:87373672 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:87373672 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:89322380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:89322380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:77617681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:77617681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:11376101 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:11376101 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:117735648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:117735648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:1756317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:1756317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:23959857 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:23959857 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:36688014 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:36688014 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:43913207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:43913207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:43623072 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:43623072 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:93088330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:93088330 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:237972128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:237972128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:18257352 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:18257352 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:130465975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:130465975 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:50903239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:50903239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:9871502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:9871502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:246921706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:246921706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:246930469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:246930469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:35524371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:35524371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:166210651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:166210651 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:166018979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:166018979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:23364419 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:23364419 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:9055141 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:9055141 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:243431052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:243431052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:9119015 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:9119015 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:35913391 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:35913391 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:42967042 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:42967042 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:99871451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:99871451 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:31979853 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:31979853 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:7218239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:7218239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:155756485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:155756485 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:155885563 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:155885563 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:105495413 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:105495413 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:157817614 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:157817614 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:157820704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:157820704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:72201904 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:72201904 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:44671696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:44671696 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:58016510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:58016510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:118165139 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:118165139 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:46601047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:46601047 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:18270102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:18270102 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75677069 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75677069 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:51856281 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:51856281 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:103281497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:103281497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:98924686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:98924686 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:20493252 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:20493252 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:20599872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:20599872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:168119600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:168119600 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:17923015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:17923015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156221312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:156221312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:127729524 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:127729524 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:96964863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:96964863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:25230253 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:25230253 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:51675247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:51675247 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:151630911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:151630911 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:106581863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:106581863 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:231065589 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:231065589 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:118629693 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:118629693 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:142795128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:142795128 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:52945841 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:52945841 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:133712476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:133712476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:16736611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:16736611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:123844192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:123844192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:147510740 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:147510740 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:167713292 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:167713292 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:104785764 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:104785764 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:119559864 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:119559864 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:52677068 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:52677068 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:77333341 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:77333341 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:110842097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:110842097 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:40485817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:40485817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:120002976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:120002976 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:43703546 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:43703546 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:108998392 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:108998392 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:33216371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:33216371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:75594528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:75594528 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:210334399 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:210334399 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:97362999 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:97362999 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:124013451 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:124013451 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:234594898 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:234594898 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:234603241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:234603241 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:141545553 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:141545553 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:107216181 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:107216181 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrY:6948719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrY:6948719 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:35271072 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:35271072 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:124181092 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:124181092 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:154514496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:154514496 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20842711 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20842711 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:10411887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:10411887 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:141692809 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:141692809 T>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:93518299 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:93518299 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:101910088 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:101910088 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:2321039 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:2321039 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:43577167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:43577167 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133913516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133913516 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:155451584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:155451584 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:43788444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:43788444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:70350726 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:70350726 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:171939284 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:171939284 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:35724965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:35724965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:81627321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:81627321 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:81628883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:81628883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:20009511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:20009511 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140021876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140021876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:69074206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:69074206 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:120201272 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:120201272 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:95639515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:95639515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:19653624 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:19653624 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:111782558 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:111782558 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:29904534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:29904534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:175328924 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:175328924 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:45315961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:45315961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:7578615 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:7578615 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:10952866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:10952866 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:42225852 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:42225852 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:30136067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:30136067 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:119983096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:119983096 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:154229448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:154229448 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:30072020 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:30072020 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:72729114 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:72729114 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:45052152 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:45052152 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:38165000 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:38165000 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:72984105 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:72984105 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:31334148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:31334148 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142625472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142625472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142627050 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142627050 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142574402 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142574402 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98519318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98519318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98592094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98592094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrY:6115595 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrY:6115595 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:75113263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:75113263 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:47233734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:47233734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179588905 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179588905 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179634770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179634770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179635561 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179635561 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179644664 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179644664 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:8122296 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:8122296 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:15601138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:15601138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:48091863 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:48091863 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75229545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75229545 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56174060 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56174060 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:43826564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:43826564 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:60128534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:60128534 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:156974173 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:156974173 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:10209373 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:10209373 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:42620052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:42620052 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:59337990 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:59337990 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:136540468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:136540468 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:128865646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:128865646 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:35988666 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:35988666 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:20362074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:20362074 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:176289880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:176289880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:35583602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:35583602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:167728667 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:167728667 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:127504741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:127504741 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:215812587 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:215812587 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216262181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216262181 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216462591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216462591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:179459934 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:179459934 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:99955266 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:99955266 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:117784190 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:117784190 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:144780217 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:144780217 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:106739618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:106739618 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:85808945 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:85808945 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:77859096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:77859096 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6832253 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6832253 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:35068146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:35068146 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:135053167 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:135053167 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:77902059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:77902059 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:100245423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:100245423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:58276166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:58276166 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:49842461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:49842461 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:85599293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:85599293 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:85626689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:85626689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:241946703 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:241946703 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:54603140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:54603140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:49373152 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:49373152 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:108634060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:108634060 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:167882312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:167882312 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:52895449 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:52895449 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:128876047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:128876047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28180976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28180976 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:17211909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:17211909 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:98355741 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:98355741 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:89061132 G>A maps to NM_207662.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:89061132 G>A maps to NM_207662.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:31784669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:31784669 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:72056597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:72056597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:116655727 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:116655727 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:111977723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:111977723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:21552320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:21552320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:12433301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:12433301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56925275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56925275 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:134425339 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chrX:134425339 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:115089258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:115089258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:50070669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:50070669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:187703648 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:187703648 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:48452201 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:48452201 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:101604269 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:101604269 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74040085 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74040085 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74040351 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74040351 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:131308931 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:131308931 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:33562527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:33562527 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:141336876 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:141336876 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:117121704 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:117121704 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:19644354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:19644354 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:73682529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:73682529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:38534157 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:38534157 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:54403504 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:54403504 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:139819922 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:139819922 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:125599823 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:125599823 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:6055195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:6055195 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:24035476 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:24035476 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:40829090 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:40829090 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:115323401 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:115323401 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:36093499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:36093499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:141049953 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:141049953 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:24981725 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:24981725 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:11204652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:11204652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:120317637 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:120317637 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57384798 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57384798 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:131130694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:131130694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:76387706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:76387706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:97487738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:97487738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:25284122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:25284122 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:3845874 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:3845874 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:152823560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:152823560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:60549719 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:60549719 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:15561294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:15561294 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:31624478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:31624478 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:41215513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:41215513 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:41215795 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:41215795 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:59924602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:59924602 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:32843937 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:32843937 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:98708797 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:98708797 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:76255237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:76255237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:97073554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:97073554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:103571417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:103571417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:31878732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:31878732 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:18377239 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:18377239 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:62318802 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:62318802 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:69437833 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:69437833 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:39306621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:39306621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:58235397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:58235397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:49933674 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:49933674 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:24432033 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:24432033 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:140881373 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:140881373 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:181707489 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:181707489 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:181727299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:181727299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:49070181 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:49070181 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:37333826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:37333826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:85985087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:85985087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27449564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27449564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:7339119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:7339119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:241528607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:241528607 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:15819327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:15819327 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:38845551 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:38845551 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:92940399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:92940399 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:60617835 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:60617835 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:169021340 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:169021340 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:160808160 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:160808160 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:35208287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:35208287 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:111437687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:111437687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:227348194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:227348194 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:24511368 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:24511368 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:21765011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:21765011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:21817275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:21817275 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:26906014 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:26906014 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:123313051 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:123313051 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:139866648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:139866648 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:47498391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:47498391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:31915898 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:31915898 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:133432931 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:133432931 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:203149568 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:203149568 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:8278089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:8278089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:17388324 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:17388324 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:1443077 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:1443077 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:147259107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:147259107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:125521218 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:125521218 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:101749482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:101749482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:86523668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:86523668 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:7420367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:7420367 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:189903940 T>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:189903940 T>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:47605385 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:47605385 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:84600393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:84600393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:83224595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:83224595 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:137567413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:137567413 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:5827138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:5827138 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:113564964 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:113564964 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:23804628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:23804628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:24939702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:24939702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:24940246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:24940246 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:79806304 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:79806304 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:11098919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:11098919 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:16721053 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:16721053 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:117422843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:117422843 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:43183857 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:43183857 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:36004194 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:36004194 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:76688410 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:76688410 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:155002517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:155002517 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57939922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57939922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:118163612 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:118163612 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:5388538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:5388538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:5366746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:5366746 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:32490439 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:32490439 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20996322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20996322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:13714463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:13714463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:132182718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:132182718 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:32895727 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:32895727 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:98097823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:98097823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:168670055 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:168670055 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:105436375 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:105436375 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:38884143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:38884143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:3979237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:3979237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:140535855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:140535855 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:140535858 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:140535858 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:184040319 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:184040319 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:80629027 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:80629027 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:40283763 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:40283763 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:89457154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:89457154 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:212488779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:212488779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:212576911 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:212576911 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:93091297 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:93091297 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:132937744 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:132937744 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:6146050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:6146050 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:57419894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:57419894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:82441608 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:82441608 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:134166361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:134166361 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:29222011 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:29222011 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:37598126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:37598126 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:150890259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:150890259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:127627159 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:127627159 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:37113381 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:37113381 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55400876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55400876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:161641443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:161641443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135279245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135279245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135288842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135288842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:110062636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:110062636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:180030130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:180030130 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:4794081 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:4794081 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:49430244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:49430244 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:183707281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:183707281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:52781417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:52781417 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:161281318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:161281318 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:26581763 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:26581763 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:191786028 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:191786028 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20326034 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20326034 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:94938598 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:94938598 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135455015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135455015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:47679961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:47679961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:154071695 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:154071695 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:108673704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:108673704 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:96386316 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:96386316 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:240037089 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:240037089 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:83808195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:83808195 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:43351280 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:43351280 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:93819045 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:93819045 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26092884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26092884 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26032348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26032348 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:27861116 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:27861116 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:53392564 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:53392564 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:49316832 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:49316832 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:70908114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:70908114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:70926177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:70926177 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:118922106 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:118922106 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:118649139 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:118649139 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:130415491 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:130415491 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:159897366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:159897366 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:159897801 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:159897801 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:111655216 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:111655216 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:76720782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:76720782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:62257134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:62257134 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:41272371 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:41272371 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:38409251 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:38409251 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:16445651 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:16445651 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:182390023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:182390023 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:31422392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:31422392 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:187495634 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:187495634 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:31372656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:31372656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:33626675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:33626675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:33646155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:33646155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:185276812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:185276812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:124211773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:124211773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:124211781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:124211781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:211032561 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:211032561 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:43887635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:43887635 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57176738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57176738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:72338889 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:72338889 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57943951 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57943951 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840294 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840294 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840320 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:55604779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:55604779 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:44584566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:44584566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:166235341 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:166235341 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:51381580 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:51381580 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:51358289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:51358289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:10560132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:10560132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9986177 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9986177 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:122155846 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:122155846 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:75900016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:75900016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:31986245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:31986245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:35979409 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:35979409 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:133928192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:133928192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:34157234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:34157234 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:152671339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:152671339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:40094606 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:40094606 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:75622447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:75622447 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:57016531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:57016531 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:76197467 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:76197467 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:161055030 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:161055030 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:44187654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:44187654 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:40137890 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:40137890 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:34706253 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:34706253 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:34706594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:34706594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:34706604 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:34706604 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:49021499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:49021499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135307073 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:135307073 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:63668363 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:63668363 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:138670046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:138670046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:6301849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:6301849 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:90397781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:90397781 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:109770689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:109770689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:104681518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:104681518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:30435711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:30435711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:30517087 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:30517087 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:139062764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:139062764 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:59837652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:59837652 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:60201481 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:60201481 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:16012543 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:16012543 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:56594069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:56594069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:9015561 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:9015561 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:23869689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:23869689 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:171238468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:171238468 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:128377907 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:128377907 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:72151993 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:72151993 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:101797102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:101797102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:35630282 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:35630282 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:141517531 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:141517531 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:97334422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:97334422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:21555895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:21555895 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:34261647 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:34261647 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:25760912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:25760912 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54318049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54318049 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:56552511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:56552511 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:139292403 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:139292403 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:203155830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:203155830 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:36340395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:36340395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108501728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108501728 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108502259 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108502259 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:107872763 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:107872763 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:88669650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:88669650 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:3800039 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:3800039 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:67899175 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:67899175 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:136081906 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:136081906 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:228476640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:228476640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:28234699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:28234699 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:74083013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:74083013 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:248185155 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:248185155 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:20483415 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:20483415 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:56125183 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:56125183 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:24905591 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:24905591 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:29631705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:29631705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:101721353 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:101721353 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:164776736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:164776736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:91237960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:91237960 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:20523217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:20523217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:31983776 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:31983776 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:61018518 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:61018518 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:98155199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:98155199 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:71829591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:71829591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:18942366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:18942366 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:99344387 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:99344387 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:18691351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:18691351 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:39537430 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:39537430 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:51612544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:51612544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:171377174 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:171377174 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:204236725 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:204236725 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:6527726 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:6527726 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:154901729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:154901729 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:50366040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:50366040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:89807999 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:89807999 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:30573622 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:30573622 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:104204992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:104204992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:37535560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:37535560 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:6349784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:6349784 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:23523295 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:23523295 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54403828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54403828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54409933 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54409933 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:43441113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:43441113 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:43571246 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:43571246 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:42959097 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:42959097 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:86333332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:86333332 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:98268676 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:98268676 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:198703581 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:198703581 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:198721323 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:198721323 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:8483987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:8483987 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:8485213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:8485213 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55708440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55708440 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:8248262 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:8248262 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:121681035 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:121681035 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:58389537 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:58389537 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9318870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9318870 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:122254245 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:122254245 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:178716031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:178716031 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:45223037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:45223037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:173898550 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:173898550 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:4844499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:4844499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57345785 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57345785 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:79312757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:79312757 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:46949395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:46949395 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:123983371 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:123983371 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:104922334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:104922334 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:96518747 C>G maps to ENST00000509481 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:96518747 C>G maps to ENST00000509481 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:21025306 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:21025306 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:20140897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:20140897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78351545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78351545 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:125402713 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:125402713 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:79174504 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:79174504 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:10449993 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:10449993 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:77245373 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:77245373 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:38178259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:38178259 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:57991941 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:57991941 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78795940 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78795940 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:67718518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:67718518 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:92983086 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:92983086 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:159533239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:159533239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:237893667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:237893667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:18322986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:18322986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:38622895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:38622895 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371293 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371325 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371478 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371478 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:105371488 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:99373968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:99373968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:36679974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:36679974 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:37153825 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:37153825 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:39431871 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:39431871 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:42003583 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:42003583 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:21468370 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:21468370 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:42330779 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:42330779 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:220501620 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:220501620 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:31495934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:31495934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27425642 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27425642 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27427301 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27427301 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:10974788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:10974788 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21168785 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21168785 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:71569855 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:71569855 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:24145419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:24145419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:121429255 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:121429255 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:121429284 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:121429284 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:109860651 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:109860651 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:16504990 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:16504990 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:16043915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:16043915 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:118512644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:118512644 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:24852921 T>C maps to ENST00000343003 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:24852921 T>C maps to ENST00000343003 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:99913631 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:99913631 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:35700909 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:35700909 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:35753610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:35753610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158650570 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158650570 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:65258406 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:65258406 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:45715490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:45715490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:74057171 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:74057171 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:120020486 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:120020486 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:8474272 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:8474272 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:169018200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:169018200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:74488245 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:74488245 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:25326188 T>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:25326188 T>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:70719901 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:70719901 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:48046972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:48046972 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:33535162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:33535162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:65180520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:65180520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:20859092 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:20859092 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:56634324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:56634324 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:56694832 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:56694832 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:92161365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:92161365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:128040990 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:128040990 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:83791444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:83791444 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:2552783 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:2552783 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:2616681 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:2616681 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:129842279 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:129842279 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:100287905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:100287905 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:44121582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:44121582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:37466383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:37466383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:29659633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:29659633 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:88568528 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:88568528 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:150443135 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:150443135 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:57067924 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:57067924 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55668916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55668916 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:63363239 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:63363239 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:10922098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:10922098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:115005673 T>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:115005673 T>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:57157047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:57157047 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:234878258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:234878258 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:109489187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:109489187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:94805684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:94805684 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:117620447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:117620447 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:117620739 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:117620739 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:46863391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:46863391 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:84355956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:84355956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:78178806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:78178806 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:49350847 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:49350847 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:7910792 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:7910792 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:108185407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:108185407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:6232232 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:6232232 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:48547494 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:48547494 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:73851419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:73851419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:117578278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:117578278 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:36550948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:36550948 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:37506781 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:37506781 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:68628760 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:68628760 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:108589998 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:108589998 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:108625801 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:108625801 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:52893797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:52893797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:31589624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:31589624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:111651440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:111651440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:82576284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:82576284 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:21330158 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:21330158 A>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:64139935 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chrX:64139935 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:100016857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:100016857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:158014180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:158014180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:44797418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:44797418 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:44513099 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:44513099 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:32332852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:32332852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:57200053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:57200053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:37646750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:37646750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:64885241 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:64885241 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:52439458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:52439458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:238048009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:238048009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:58189210 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:58189210 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:9010021 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:9010021 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:67111735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:67111735 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20698370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20698370 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:100498937 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:100498937 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:116449826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:116449826 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:35537981 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:35537981 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:132338448 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:132338448 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:31355550 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:31355550 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:179292325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:179292325 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:65492394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:65492394 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:39694771 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:39694771 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:100591630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:100591630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:64606722 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:64606722 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:150532069 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:150532069 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:25051071 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:25051071 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:25065110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:25065110 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:314504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:314504 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:86118219 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:86118219 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:101432910 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:101432910 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:77838393 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:77838393 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:43919174 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:43919174 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:71389485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:71389485 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:37438565 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:37438565 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:99188694 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:99188694 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:26619998 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:26619998 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:39441229 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:39441229 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:116701382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:116701382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:35189672 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:35189672 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:142152227 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:142152227 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:43473059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:43473059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:43481112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:43481112 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:153184185 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:153184185 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:23244702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:23244702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:104650501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:104650501 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:51974720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:51974720 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:1746856 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:1746856 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:63299656 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:63299656 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:11421659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:11421659 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193151775 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193151775 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193029557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193029557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:124239217 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:124239217 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:77266609 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:77266609 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:42553161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:42553161 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:29205840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:29205840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:26276833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:26276833 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:79747156 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:79747156 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:13578380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:13578380 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:31608423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:31608423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:140477777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:140477777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:50362547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:50362547 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:63445974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:63445974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:76250571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:76250571 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:93493070 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:93493070 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:66529036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:66529036 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:66529306 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:66529306 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:50582932 G>A maps to ENST00000358490 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:50582932 G>A maps to ENST00000358490 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:13645122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:13645122 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:30926044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:30926044 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:34667947 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:34667947 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:26802084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:26802084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:6702628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:6702628 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:207273063 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:207273063 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:99755237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:99755237 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:89900751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:89900751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:65142539 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:65142539 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:115101984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:115101984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:86062748 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:86062748 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:149602820 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:149602820 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:116550251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:116550251 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:96062590 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:96062590 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:119155517 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:119155517 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:74710342 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:74710342 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:32705158 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:32705158 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:112349237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:112349237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118706862 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118706862 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:32598106 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:32598106 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:72539160 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:72539160 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:72521801 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:72521801 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:80290637 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:80290637 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:33743838 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:33743838 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:54415867 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:54415867 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:21854704 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:21854704 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:25568653 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:25568653 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:13099676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:13099676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:65309886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:65309886 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:93543718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:93543718 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:203192824 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:203192824 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:45671205 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:45671205 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:57465059 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:57465059 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:143017686 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:143017686 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:40228699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:40228699 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:14720826 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:14720826 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:46104707 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:46104707 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:23456275 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:23456275 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:103468273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:103468273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:71655369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:71655369 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:55925681 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:55925681 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:139636059 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:139636059 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:139662034 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:139662034 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:116918421 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:116918421 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:189862421 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:189862421 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:120942800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:120942800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:148545909 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:148545909 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:166418654 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:166418654 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:68529215 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:68529215 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:3781080 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:3781080 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:36668828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:36668828 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:153924924 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:153924924 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:61950940 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:61950940 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:113702071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:113702071 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:18142439 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:18142439 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:70895435 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:70895435 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:41356334 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:41356334 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:99313706 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:99313706 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:104445039 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:104445039 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:50451588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:50451588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:155249393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:155249393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:38091900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:38091900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118582055 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118582055 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:74116035 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:74116035 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:132626018 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:132626018 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:66015138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:66015138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:59894898 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:59894898 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:56335226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:56335226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:14217602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:14217602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:42788618 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:42788618 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:182825598 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:182825598 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:96048544 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:96048544 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:69669514 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:69669514 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:32407900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:32407900 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:32867996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:32867996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:13692314 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:13692314 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:196851754 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:196851754 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:38862646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:38862646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:43660048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:43660048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:10883350 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:10883350 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98077981 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98077981 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:129209049 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:129209049 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:169463407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:169463407 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:74746518 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:74746518 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:158139123 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:158139123 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:43634543 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:43634543 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:28419822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:28419822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:19959660 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:19959660 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:38451299 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:38451299 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:63091845 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:63091845 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:63215245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:63215245 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:141566196 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:141566196 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:120809907 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:120809907 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:117658877 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:117658877 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:23764861 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:23764861 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:85595894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:85595894 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:10989797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:10989797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:79403426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:79403426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:120608146 C>T maps to NM_006209.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:120608146 C>T maps to NM_006209.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:40232108 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:40232108 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:38185540 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:38185540 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:56026385 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:56026385 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:34145282 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:34145282 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:20791948 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:20791948 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:138188157 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:138188157 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:44151736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:44151736 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:46876643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:46876643 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:61624443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:61624443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:47788931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:47788931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:184868577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:184868577 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:159048495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:159048495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:128370178 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:128370178 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:206141296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:206141296 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:187527385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:187527385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:92564776 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:92564776 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:92571013 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:92571013 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:48703112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:48703112 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:127697636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:127697636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:60133105 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:60133105 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:8201169 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:8201169 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:79391110 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:79391110 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:49244705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:49244705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:39169812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:39169812 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:27184267 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:27184267 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:114542874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:114542874 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:13005650 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:13005650 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:61996053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:61996053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:42467378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:42467378 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:59604641 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:59604641 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:150210747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:150210747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:6644756 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:6644756 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:104387343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:104387343 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:4862031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:4862031 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:93518746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:93518746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:22425796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:22425796 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:46956128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:46956128 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:28499816 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:28499816 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:28473415 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:28473415 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:48907936 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:48907936 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:46624892 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:46624892 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:197183251 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:197183251 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:28366457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:28366457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:100135224 C>G maps to NM_032425.4 S596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:100135224 C>G maps to NM_032425.4 S596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:176311025 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:176311025 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62489214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62489214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62489886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62489886 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62490393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62490393 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:19042288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:19042288 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:177034472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:177034472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:26862053 C>T maps to ENST00000398141 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:26862053 C>T maps to ENST00000398141 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:122929249 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:122929249 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:124273505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:124273505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:71025870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:71025870 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:95014218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:95014218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:163123985 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:163123985 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:133799691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:133799691 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:158750381 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:158750381 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:39734577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:39734577 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:154420689 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:154420689 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:155234895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:155234895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:155235948 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:155235948 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:75896502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:75896502 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:145533743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:145533743 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:42463097 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:42463097 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:6062057 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:6062057 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:134015693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:134015693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:170338717 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:170338717 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:215256646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:215256646 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:78649472 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:78649472 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:196288466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:196288466 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:55976527 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:55976527 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:26942341 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:26942341 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:26955621 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:26955621 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:42273036 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:42273036 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:55357477 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:55357477 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:118250648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:118250648 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:86527006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:86527006 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:113373721 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:113373721 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:16336962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:16336962 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:53185271 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:53185271 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:7050559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:7050559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:112535119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:112535119 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:113976820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:113976820 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:16692158 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:16692158 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:95552888 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:95552888 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:90354546 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:90354546 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:36114685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:36114685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:36116824 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:36116824 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:11908140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:11908140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:99358708 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:99358708 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:12353439 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:12353439 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:40717175 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:40717175 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63919946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63919946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:77708192 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:77708192 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:77754905 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:77754905 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:114092315 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:114092315 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:210557248 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:210557248 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63670485 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63670485 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:54527762 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:54527762 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:21887590 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:21887590 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:95022189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:95022189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:84117632 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:84117632 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:179227082 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:179227082 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:61263208 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:61263208 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:31729098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:31729098 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:121469060 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:121469060 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:151293233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:151293233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:30630649 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:30630649 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:7875226 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:7875226 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:100696585 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:100696585 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:77836125 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:77836125 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:48443286 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:48443286 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:10408059 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:10408059 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:36689586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:36689586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:76567042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:76567042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:31138309 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:31138309 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:101755759 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:101755759 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:101760200 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:101760200 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:78415494 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:78415494 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:15358802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:15358802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:16891136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:16891136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:183791507 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:183791507 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:119115382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:119115382 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:152553858 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:152553858 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:72076538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:72076538 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:129740165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:129740165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:55438891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:55438891 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:144101640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:144101640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:156752881 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:156752881 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:101584683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:101584683 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:34790056 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:34790056 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:6609859 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:6609859 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:102331118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:102331118 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:133041295 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:133041295 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:5775946 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:5775946 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:56756333 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:56756333 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:55703937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:55703937 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:74013231 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:74013231 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:20715230 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:20715230 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:20715240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:20715240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:103271214 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:103271214 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:77043671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:77043671 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:34606278 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:34606278 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:20813690 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:20813690 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:50117293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:50117293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:55996470 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:55996470 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:58571044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:58571044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:41582247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:41582247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:79697861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:79697861 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:47682266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:47682266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:47695784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:47695784 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:71401524 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:71401524 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:22168592 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:22168592 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:119337140 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:119337140 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:72163999 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:72163999 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:160222123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:160222123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:44157665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:44157665 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:75552588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:75552588 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:42599636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:42599636 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:147560227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:147560227 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:104205425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:104205425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:145969331 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:145969331 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:12856216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:12856216 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:69046288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:69046288 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:54394899 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:54394899 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:97278223 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:97278223 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:141828245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:141828245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:198666123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:198666123 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:8748015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:8748015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:128399843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:128399843 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:72175917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:72175917 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:61484554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:61484554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:174200660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:174200660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:36142051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:36142051 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:37175214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:37175214 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:85800037 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:85800037 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:160265099 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:160265099 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:173782450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:173782450 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:204312594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:204312594 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:48893941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:48893941 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:114271504 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:114271504 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:36177603 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:36177603 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:49073965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:49073965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:103234727 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:103234727 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:18234049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:18234049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:74658015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:74658015 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:73090310 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:73090310 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:86008568 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:86008568 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:153344675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:153344675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:72818968 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:72818968 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:21359667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:21359667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:124763561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:124763561 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:48080703 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:48080703 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:74657731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:74657731 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:33938729 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:33938729 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:134986564 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:134986564 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:246929455 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:246929455 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:38764739 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:38764739 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:38766608 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:38766608 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:166223930 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:166223930 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:100708473 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:100708473 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:83796829 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:83796829 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:102250123 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:102250123 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:110342588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:110342588 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:242275333 G>A maps to ENST00000457874 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:242275333 G>A maps to ENST00000457874 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:65473537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:65473537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:72619270 G>A maps to ENST00000419379 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:72619270 G>A maps to ENST00000419379 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:51218989 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:51218989 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:18256837 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:18256837 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:52146495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:52146495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:232539775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:232539775 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:232629162 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:232629162 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:110778226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:110778226 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:65944161 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:65944161 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:45978309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:45978309 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:104414116 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:104414116 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:190430059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:190430059 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:318890 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:318890 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:110716430 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:110716430 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:20668617 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:20668617 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:40402264 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:40402264 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98807613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98807613 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:20526710 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:20526710 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:46189573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:46189573 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:64799558 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:64799558 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:121441017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:121441017 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:231050638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:231050638 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:48522146 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:48522146 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:55655763 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:55655763 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:158587386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:158587386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:87846385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:87846385 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:35484040 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:35484040 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:48214052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:48214052 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:39542499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:39542499 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:53150575 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:53150575 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:60583996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:60583996 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:15643249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:15643249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:50803741 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:50803741 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:72058218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:72058218 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:38777870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:38777870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98310988 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98310988 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:93645474 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:93645474 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:42509967 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:42509967 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:57068278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:57068278 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:44006140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:44006140 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:71520474 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:71520474 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:114945572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:114945572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:6751306 G>C maps to ENST00000420690 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:6751306 G>C maps to ENST00000420690 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:72969944 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:72969944 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:16336867 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:16336867 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:2234037 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:2234037 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:180324016 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:180324016 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:166775972 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:166775972 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:89336657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:89336657 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:179590871 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:179590871 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:179602708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:179602708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:3042499 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:3042499 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:15508094 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:15508094 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:118235725 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:118235725 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:196129758 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:196129758 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:69886089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:69886089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:69978171 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:69978171 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:158974202 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:158974202 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:43958708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:43958708 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:215799251 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:215799251 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216246217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216246217 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216424443 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216424443 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:179458267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:179458267 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:144107321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:144107321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:11950895 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:11950895 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:52599142 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:52599142 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:106774617 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:106774617 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:2643054 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:2643054 A>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:123995027 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:123995027 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:9503274 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:9503274 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:167320080 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:167320080 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:66431603 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:66431603 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7684583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7684583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:17288608 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:17288608 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:56365270 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:56365270 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:21827145 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:21827145 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:217039983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:217039983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:67738585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:67738585 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:111697744 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chrX:111697744 T>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:68255909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:68255909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:147106545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:147106545 A>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:11895734 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:11895734 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:22153388 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:22153388 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:53302032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:53302032 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:38306475 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:38306475 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:58086988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:58086988 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:178391652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:178391652 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:124079701 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:124079701 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:38184451 G>C maps to ENST00000447434 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:38184451 G>C maps to ENST00000447434 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:21214639 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:21214639 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:113618190 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:113618190 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:3961242 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:3961242 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:105948646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:105948646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:169814771 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:169814771 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:20795031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:20795031 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:48172350 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:48172350 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:34184378 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:34184378 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:39607387 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:39607387 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:3655761 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:3655761 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:84685362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:84685362 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:7802596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:7802596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:46719709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:46719709 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:89525589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:89525589 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:100760680 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:100760680 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:101186037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:101186037 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr18:77108268 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr18:77108268 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:3652100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:3652100 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:97073229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:97073229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:5110234 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:5110234 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:244768912 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:244768912 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:247712617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:247712617 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:55151911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:55151911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:81309711 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:81309711 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:184598757 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:184598757 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:69552513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:69552513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:201035585 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:201035585 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:89408496 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:89408496 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:180381824 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:180381824 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:49089725 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:49089725 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:158325482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:158325482 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:193119588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:193119588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:31297610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:31297610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:90546758 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:90546758 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:50809538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:50809538 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:76522456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:76522456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:68409937 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:68409937 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:104065386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:104065386 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:243305789 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:243305789 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:184104736 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:184104736 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:30659759 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:30659759 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr18:72185679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr18:72185679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:57957088 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:57957088 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:34557720 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:34557720 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:146536713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:146536713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:107937872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:107937872 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr21:47420197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr21:47420197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:71004358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:71004358 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:54743622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:54743622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:43911319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:43911319 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:34102185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:34102185 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:64592820 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:64592820 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:16943247 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:16943247 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:49030520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:49030520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:16024898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:16024898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:5020941 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:5020941 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:61491151 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:61491151 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:32871856 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:32871856 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:111372265 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:111372265 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:154684363 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:154684363 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:46119640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:46119640 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:120844731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:120844731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:97200125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:97200125 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:55599011 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:55599011 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:236381768 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:236381768 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:14602249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:14602249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:68194136 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:68194136 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:62273880 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:62273880 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:14964410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:14964410 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:21548732 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:21548732 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:31081269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:31081269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:9873162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:9873162 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:110403513 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:110403513 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:37794642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:37794642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:104340212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:104340212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:130761107 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:130761107 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr22:46724899 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr22:46724899 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:14839228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:14839228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:119935112 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:119935112 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:45462138 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:45462138 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:93819388 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:93819388 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:120393540 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:120393540 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:102295896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:102295896 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:100189702 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:100189702 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:74756995 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:74756995 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:71053939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:71053939 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:65621994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:65621994 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:31415107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:31415107 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:31435087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:31435087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:226895756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:226895756 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:26571906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:26571906 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:26835344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:26835344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:134018273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:134018273 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:127641880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:127641880 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:29922202 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:29922202 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:6748982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:6748982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:6748984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:6748984 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:96997260 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:96997260 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:101868320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:101868320 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:200562987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:200562987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:11216332 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:11216332 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:38512141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:38512141 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:82302845 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:82302845 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:62897034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:62897034 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:141213881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:141213881 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:141987095 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:141987095 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:67878989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:67878989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:138687012 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:138687012 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr21:47697435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr21:47697435 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:52137265 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:52137265 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:52141772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:52141772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:105920678 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:105920678 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr22:26388489 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr22:26388489 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:52485901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:52485901 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50868620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50868620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:78570354 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:78570354 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:124979265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:124979265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:56520232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:56520232 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:153656051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:153656051 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:84733363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:84733363 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:50722946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:50722946 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:80271311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:80271311 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:135315280 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:135315280 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:102344131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:102344131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:95177380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:95177380 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:36909718 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:36909718 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:63283496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:63283496 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:138454760 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:138454760 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:6750987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:6750987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:73725831 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:73725831 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr13:113833486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr13:113833486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:1960743 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:1960743 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:106524805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:106524805 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:26913777 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:26913777 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:16872919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:16872919 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:23701144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:23701144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:20356966 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:20356966 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:65062202 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:65062202 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50916879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50916879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:49632086 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:49632086 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:22396909 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:22396909 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:69021932 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:69021932 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:55912625 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:55912625 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:141745225 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:141745225 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:131130572 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:131130572 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:198666180 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:198666180 A>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:57055436 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:57055436 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr13:49037786 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr13:49037786 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:73153195 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:73153195 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:117246483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:117246483 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:87565780 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:87565780 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:201974944 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:201974944 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:55609647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:55609647 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:237995995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:237995995 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:153513740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:153513740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:9077577 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:9077577 T>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr21:33064847 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr21:33064847 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr22:38051272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr22:38051272 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:100868895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:100868895 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:38654992 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:38654992 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:44682471 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:44682471 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:160677583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:160677583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:118165119 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:118165119 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:115575017 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chrX:115575017 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:23245178 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr14:23245178 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:186283979 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:186283979 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:206567071 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:206567071 G>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:84660606 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:84660606 A>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:113265604 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr9:113265604 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:15221573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:15221573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:152847441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:152847441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:60558416 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:60558416 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:98172800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:98172800 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:98180886 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:98180886 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:45125822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:45125822 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:175105909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:175105909 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:1488669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:1488669 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:55035157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:55035157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:85413555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:85413555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:30527079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:30527079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:179489061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:179489061 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:44191756 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:44191756 T>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:109536196 G>T maps to NM_003362.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:109536196 G>T maps to NM_003362.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:144613129 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr6:144613129 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:75622816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:75622816 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:38785352 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:38785352 C>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:35173542 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:35173542 C>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:54079854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:54079854 A>G did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:6781441 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:6781441 T>C did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:182027148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:182027148 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:146066581 G>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:146066581 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:35545495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:35545495 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:20557638 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:20557638 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:156945915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:156945915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:43769839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:43769839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:2886535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:2886535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:88035427 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:88035427 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:4834562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:4834562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:202614376 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:202614376 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:2578769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:2578769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:38462014 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:38462014 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:197889842 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:197889842 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:115310985 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:115310985 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:101185953 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:101185953 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:182554385 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:182554385 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:156626278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:156626278 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:37100679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:37100679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:34638337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:34638337 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:67699939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:67699939 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:3278643 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:3278643 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:184615049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:184615049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:31736762 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:31736762 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:201044784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:201044784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:3776833 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:3776833 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:31691049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:31691049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:64109380 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:64109380 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:112054896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:112054896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:72537632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:72537632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:46052469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:46052469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:20722525 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:20722525 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:14139346 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:14139346 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:64850829 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:64850829 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:113342072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:113342072 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:87878644 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:87878644 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:9768903 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:9768903 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:21272511 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:21272511 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:113000077 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:113000077 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:47811072 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:47811072 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:137407156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:137407156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:79571904 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:79571904 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:95773907 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:95773907 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:56716173 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:56716173 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:82512233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:82512233 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:38425322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:38425322 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:23693597 T>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:23693597 T>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:37311326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:37311326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:93221656 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:93221656 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:160969292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:160969292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:6244718 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:6244718 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:157739967 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:157739967 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:240334300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:240334300 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:151684458 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:151684458 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:236332068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:236332068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:90327116 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:90327116 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:28474016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:28474016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:94690698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:94690698 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:115335607 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:115335607 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:45474481 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:45474481 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:72647992 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:72647992 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:55147354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:55147354 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:33077668 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:33077668 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:185329578 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:185329578 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:7604928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:7604928 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:36746057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:36746057 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:18197273 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:18197273 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:55955714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:55955714 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:75137384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:75137384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:44116299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:44116299 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr13:45578633 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr13:45578633 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:233512304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:233512304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:44846492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:44846492 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:17598852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:17598852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:930363 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:930363 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:145503525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:145503525 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:95552913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:95552913 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:62449289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:62449289 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:141128081 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:141128081 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:120981463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:120981463 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:19444421 C>A maps to NM_001001671.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:19444421 C>A maps to NM_001001671.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:90387448 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:90387448 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:6377162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:6377162 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:33768703 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:33768703 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:89053604 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:89053604 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:92714459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:92714459 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:9026419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:9026419 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:42343672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:42343672 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr22:26351361 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr22:26351361 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:52488746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:52488746 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:101573813 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:101573813 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:152131963 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:152131963 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:95443147 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:95443147 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:79454267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:79454267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:108003181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:108003181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:22333202 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:22333202 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:17720790 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:17720790 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:108603414 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:108603414 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:19710228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:19710228 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:91066130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:91066130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:91368357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:91368357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:592722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:592722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:9784483 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:9784483 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:71401475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:71401475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:160798505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:160798505 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:81944443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:81944443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:242270857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:242270857 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:152936654 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:152936654 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:7619691 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:7619691 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:149214716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:149214716 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:63042241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:63042241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:63042443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:63042443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:45583889 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:45583889 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:142458266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:142458266 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:43765836 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:43765836 T>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:162197489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:162197489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:52336130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:52336130 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:220368626 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:220368626 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:76255149 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:76255149 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr13:48947673 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr13:48947673 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr13:25416151 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr13:25416151 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:31169604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:31169604 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:38760128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:38760128 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:67091481 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:67091481 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:103038547 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:103038547 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:170184813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:170184813 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:21036563 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:21036563 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:20886045 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:20886045 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:101815808 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:101815808 A>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:97127356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:97127356 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:97327493 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:97327493 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:64484968 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:64484968 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:120834021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:120834021 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr22:33254196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr22:33254196 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:85459188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:85459188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:125551293 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:125551293 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:65275094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr4:65275094 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:43766817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:43766817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:87024404 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:87024404 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:23012509 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:23012509 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr22:22313619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr22:22313619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr21:10952817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr21:10952817 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:5729731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:5729731 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:113196392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr11:113196392 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:84335562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:84335562 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:179443483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:179443483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:10132304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:10132304 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:234663897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:234663897 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:17743840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:17743840 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:35328634 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:35328634 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:35328650 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:35328650 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:35606025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:35606025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:216462888 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:216462888 A>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:62273443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:62273443 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:20145499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:20145499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:711857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr16:711857 T>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:31611207 T>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:31611207 T>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:128881770 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chrX:128881770 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:27837963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:27837963 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:78046604 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:78046604 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:87195566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:87195566 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:20666291 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:20666291 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:89042714 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:89042714 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:7249687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:7249687 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:20693867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:20693867 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:38518701 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:38518701 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:78365797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:78365797 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:7766702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:7766702 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:111892042 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:111892042 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:125824828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:125824828 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:18098416 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:18098416 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:29498223 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:29498223 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:38471611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:38471611 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:190557959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:190557959 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:98177029 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:98177029 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:55466376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:55466376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:5708896 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:5708896 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:101460685 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:101460685 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33385915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33385915 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33386200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33386200 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:36270987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:36270987 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:66937655 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:66937655 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:15306299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:15306299 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:176852241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:176852241 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:119977079 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:119977079 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:1387818 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:1387818 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:108178566 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:108178566 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:152806796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:152806796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:11049510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:11049510 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:69943497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:69943497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:17275181 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:17275181 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:111921923 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:111921923 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:56869440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:56869440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:15543556 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:15543556 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr13:31498736 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr13:31498736 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:49657620 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:49657620 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:46122594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:46122594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:41149894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:41149894 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:165711607 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:165711607 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:4087865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:4087865 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:120782290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:120782290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:44286855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:44286855 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:34118328 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:34118328 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:16649706 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:16649706 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:27384256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:27384256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:100859097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:100859097 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:21882691 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:21882691 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:44839280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:44839280 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:26886005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:26886005 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:122751834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:122751834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:31916806 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:31916806 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:196965398 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:196965398 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:50824220 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:50824220 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:110006083 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:110006083 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:120213791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:120213791 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:86898327 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:86898327 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:36204706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:36204706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:23847490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:23847490 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:103400525 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:103400525 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:103444119 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:103444119 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:86375840 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:86375840 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:109041100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:109041100 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:130001126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:130001126 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:28858963 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:28858963 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:34128333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:34128333 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:114389229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:114389229 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:126681257 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:126681257 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:49046760 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:49046760 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:99436637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:99436637 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:36759391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:36759391 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:162745782 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:162745782 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:70700791 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:70700791 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:223165063 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:223165063 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:83170839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:83170839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:169502910 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:169502910 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:37649266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:37649266 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:115200314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:115200314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:162862234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:162862234 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:44010826 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:44010826 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:71755422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:71755422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:108355452 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:108355452 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:34398209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:34398209 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:66361397 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:66361397 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:66439652 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:66439652 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:116595167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:116595167 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:74095668 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:74095668 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:62104157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:62104157 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:62148862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:62148862 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:10672703 C>T maps to NM_022068.2 G2663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:10672703 C>T maps to NM_022068.2 G2663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:118166706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:118166706 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:190130041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:190130041 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:89865684 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:89865684 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:89858440 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:89858440 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:126328352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:126328352 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:149754120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:149754120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:125022812 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:125022812 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:128489099 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:128489099 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:216230043 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:216230043 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:89409457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:89409457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:47645712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:47645712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:94343888 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:94343888 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:13715637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:13715637 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:88323693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:88323693 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:178414063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:178414063 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:32792490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:32792490 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:222716695 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:222716695 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:27100667 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:27100667 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:76476420 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:76476420 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:71127620 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:71127620 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:71220864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:71220864 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:201190882 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:201190882 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:102625952 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:102625952 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:103891986 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:103891986 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:1471175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:1471175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:22008781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:22008781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:15634140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:15634140 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:4774721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:4774721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:8553265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:8553265 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:211034005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:211034005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:36691047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:36691047 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:200584452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:200584452 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:10603001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:10603001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:52565916 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:52565916 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:39723453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:39723453 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:25919481 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:25919481 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:209807599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:209807599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:203741360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:203741360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:152760200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:152760200 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:169684971 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:169684971 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:48653191 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:48653191 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:54756859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:54756859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:26751740 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:26751740 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:129455735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:129455735 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:150444406 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:150444406 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:161071258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:161071258 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:141665728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:141665728 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:67401388 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:67401388 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:70482256 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:70482256 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:86043978 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:86043978 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:54840151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:54840151 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:54840153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:54840153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:19392584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:19392584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:31427527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:31427527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:65544177 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:65544177 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:141747581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:141747581 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:135011888 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:135011888 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:89054066 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:89054066 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:60269372 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:60269372 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:56670401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:56670401 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:237026968 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:237026968 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:23868309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:23868309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:36714237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:36714237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:76599713 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:76599713 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:76851456 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:76851456 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:158443759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:158443759 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:75563159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:75563159 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:152512311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:152512311 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:211843895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:211843895 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:70526019 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:70526019 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:63768435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:63768435 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:5415693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:5415693 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:55452713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:55452713 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:43700481 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:43700481 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:34243787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:34243787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:73013615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:73013615 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:5999206 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:5999206 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:229611357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:229611357 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:136081893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:136081893 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:228433465 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:228433465 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:220422839 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:220422839 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:58190778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:58190778 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:107709649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:107709649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:35547169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:35547169 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:142539656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:142539656 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:20704815 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:20704815 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:15082475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:15082475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:73453568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:73453568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:57358314 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:57358314 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:230468404 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:230468404 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:99511695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:99511695 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:106521445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:106521445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:1438690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:1438690 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:22140495 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:22140495 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:25156011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:25156011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:110456198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:110456198 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:110473979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:110473979 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:125281474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:125281474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:119336745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:119336745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:171330265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:171330265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:146309465 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:146309465 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:24755698 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:24755698 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:12835549 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:12835549 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:64160314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:64160314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:64160316 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:64160316 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:64160779 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:64160779 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:66526260 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:66526260 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:61857845 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:61857845 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:102065386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:102065386 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:132482835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:132482835 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:130884625 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:130884625 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:46935370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:46935370 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:70949591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:70949591 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:56886044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:56886044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:131911644 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:131911644 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:79338970 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:79338970 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:127977072 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:127977072 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:182569326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:182569326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:153345675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:153345675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:185060663 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:185060663 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:38949746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:38949746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:39439343 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:39439343 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:38904604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:38904604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:9054395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:9054395 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:101049253 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:101049253 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:223317598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:223317598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:249110992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:249110992 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:87185401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:87185401 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:72799281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:72799281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:52000280 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:52000280 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:75706513 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:75706513 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:1538423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:1538423 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:92406444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:92406444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:61503885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:61503885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:21392246 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:21392246 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:50492659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:50492659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:25220670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:25220670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:231050916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:231050916 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:99917153 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:99917153 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:12450837 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:12450837 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:14156817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:14156817 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:14282068 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:14282068 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:55648526 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:55648526 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:41078155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:41078155 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:152980220 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:152980220 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:7705738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:7705738 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:158504308 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:158504308 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:97363554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:97363554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:9994426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:9994426 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:100025154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:100025154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:9661032 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:9661032 T>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:9677596 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:9677596 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:85448068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:85448068 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:179565060 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:179565060 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:20848269 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:20848269 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:85553610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:85553610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:32497055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:32497055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:39973715 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:39973715 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:83784771 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:83784771 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:2592816 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:2592816 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:44403632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:44403632 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:98452828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:98452828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:19756128 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:19756128 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:195615191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:195615191 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:195615198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:195615198 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:55665259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:55665259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:175323781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:175323781 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:144444958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:144444958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:18062187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:18062187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:31368993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:31368993 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:49703714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:49703714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:179489859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:179489859 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:158910479 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:158910479 A>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:25600998 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:25600998 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:109926249 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:109926249 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:128914951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:128914951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:96181716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:96181716 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:48637209 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:48637209 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:17367578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:17367578 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:54554770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:54554770 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:98809609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:98809609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:241886442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:241886442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:111313115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:111313115 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:53302199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:53302199 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:74370900 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:74370900 T>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:31047979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:31047979 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:59676 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:59676 T>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:46388453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chrX:46388453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:102189357 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:102189357 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:56833711 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:56833711 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:108012290 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:108012290 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:135619408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:135619408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:5569035 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:5569035 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:156915124 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:156915124 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:84582187 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:84582187 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:1229332 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:1229332 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:131826477 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:131826477 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:1892943 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:1892943 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:100625457 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:100625457 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:41615755 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:41615755 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:114266955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:114266955 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:40832704 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:40832704 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:161021034 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:161021034 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:138870530 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:138870530 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:138901643 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:138901643 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:119509049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:119509049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:36959264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:36959264 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:5762568 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:5762568 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:32873347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:32873347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:50662747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:50662747 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:75036622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:75036622 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:31892647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:31892647 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:98865207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:98865207 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:127898249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:127898249 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:105495226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:105495226 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:35828521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:35828521 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:5455960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:5455960 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:43027620 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:43027620 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:58571119 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:58571119 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:4423913 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:4423913 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:40179895 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:40179895 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:111857700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:111857700 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:9793953 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:9793953 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:39171255 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:39171255 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:75855807 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:75855807 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:139767253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:139767253 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:86196531 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:86196531 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:197237471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:197237471 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:43657819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:43657819 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:34008577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:34008577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:34083347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:34083347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:34128801 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:34128801 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:80390010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:80390010 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:68040409 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:68040409 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:104184351 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:104184351 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:19984177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:19984177 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:41628046 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:41628046 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:16630280 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:16630280 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:24288991 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:24288991 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:135535214 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:135535214 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:169295015 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:169295015 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:69698991 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:69698991 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:124389678 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:124389678 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:124416424 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:124416424 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:196860136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:196860136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:441269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:441269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:28723486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:28723486 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:65637809 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:65637809 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:37366672 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:37366672 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:107535626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:107535626 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:107535639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:107535639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:89151552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:89151552 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:129822755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:129822755 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:5397852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:5397852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:43500989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:43500989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:89462128 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:89462128 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:50681410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:50681410 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:50738713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:50738713 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:54275341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:54275341 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:154189309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:154189309 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:129154261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:129154261 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:184863349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:184863349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:139160931 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:139160931 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:61014281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:61014281 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:94726846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:94726846 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:13061754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:13061754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:128481177 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:128481177 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:30698926 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:30698926 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:17491194 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:17491194 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:88419369 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:88419369 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:155265449 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:155265449 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:11400965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:11400965 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:110740362 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:110740362 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:76956618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:76956618 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:102432206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:102432206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:132833889 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:132833889 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:57609064 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:57609064 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:122387464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:122387464 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:66961680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:66961680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:73922621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:73922621 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:39884006 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:39884006 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:72645967 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:72645967 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:81391957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:81391957 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:75114864 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:75114864 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:22159915 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:22159915 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:20403818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:20403818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:53579261 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:53579261 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:148585656 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:148585656 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:21206512 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:21206512 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:68642524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:68642524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:155235707 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:155235707 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:77618888 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:77618888 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:50683243 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:50683243 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:3626532 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:3626532 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:120178473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:120178473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:137521474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:137521474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:39325205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:39325205 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:41620861 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:41620861 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:107613537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:107613537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:55177520 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:55177520 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:96315735 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:96315735 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:141298346 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:141298346 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:56401450 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:56401450 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:21217431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:21217431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:136709741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:136709741 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:179665194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:179665194 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:48473377 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:48473377 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:37375925 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:37375925 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:55532196 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:55532196 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:43812044 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:43812044 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:67768206 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:67768206 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:24705859 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:24705859 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:11851249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:11851249 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:28011507 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:28011507 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:49415502 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:49415502 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:52517878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:52517878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:40204372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:40204372 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:40115282 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:40115282 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:16890957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:16890957 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:152374946 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:152374946 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:63494650 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:63494650 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:95069330 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:95069330 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:69222963 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:69222963 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:163315659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:163315659 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:28228674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:28228674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:248247733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:248247733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:248247880 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:248247880 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:248722840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:248722840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:20388565 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:20388565 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:76765386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:76765386 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:59368251 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:59368251 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:21690110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:21690110 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:183096051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:183096051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:31917696 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:31917696 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:107533224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:107533224 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:55020234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:55020234 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:11111112 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:11111112 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:15403296 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:15403296 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:108698754 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:108698754 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:125267965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:125267965 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:159490909 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:159490909 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:59814330 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:59814330 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:171323013 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:171323013 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:242508960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:242508960 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:131947894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:131947894 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:146166891 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:146166891 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:118236534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:118236534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:24761475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:24761475 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:24762794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:24762794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:134393764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:134393764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:170465293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:170465293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:94708514 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:94708514 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:46891773 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:46891773 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:11461969 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:11461969 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:40767518 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:40767518 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:71477836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:71477836 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:9353998 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:9353998 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:174725884 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:174725884 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:117863083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:117863083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:48892089 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:48892089 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:21998951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:21998951 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:29617303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:29617303 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:55755676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:55755676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr21:43892896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr21:43892896 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:50861842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:50861842 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:123505040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:123505040 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:100704736 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:100704736 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:13868527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:13868527 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:1915231 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:1915231 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:164748394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:164748394 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:15064915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:15064915 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:107434476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:107434476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:57176817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:57176817 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:21349795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:21349795 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:45391529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:45391529 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:24145679 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr22:24145679 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:231281051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:231281051 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:217947892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:217947892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:158652983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:158652983 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:65233987 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:65233987 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:100481931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:100481931 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:104109794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:104109794 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:123202404 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:123202404 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:4418224 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:4418224 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:62550850 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:62550850 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:37984473 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:37984473 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:74178974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:74178974 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:141578386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:141578386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:102272640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:102272640 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:108472592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:108472592 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:42525344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:42525344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:52153327 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:52153327 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:68935631 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:68935631 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:175304752 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:175304752 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:21963233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:21963233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:123675581 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:123675581 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:211527676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:211527676 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr21:38480858 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr21:38480858 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:20760330 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:20760330 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179464276 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179464276 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179594783 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179594783 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179659594 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179659594 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:17763423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:17763423 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:215807693 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:215807693 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:216074374 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:216074374 T>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:153075270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:153075270 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:100352891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:100352891 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:58313308 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:58313308 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:85599264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:85599264 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:241953711 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:241953711 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:40532563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:40532563 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:152097110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chrX:152097110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:22907499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:22907499 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:53262331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:53262331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:12776439 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:12776439 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:66890999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:66890999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:66978696 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:66978696 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:87229397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:87229397 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:87082247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:87082247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:116233017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:116233017 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:109650547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:109650547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:80631423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:80631423 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:58516896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:58516896 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:20482259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:20482259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100244537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100244537 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:207407905 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:207407905 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:33534875 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:33534875 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:33624299 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:33624299 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:33631048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:33631048 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:5190276 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:5190276 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:73148811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:73148811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:45725876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:45725876 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:100062611 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:100062611 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:87531129 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:87531129 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:84516117 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:84516117 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:96890025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:96890025 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:134260352 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:134260352 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:134127461 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:134127461 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:74284071 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:74284071 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:50297750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:50297750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:102100279 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:102100279 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:113303475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:113303475 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:38543383 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:38543383 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:73941943 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:73941943 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:94022206 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:94022206 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:35051099 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:35051099 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:101510292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:101510292 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:169105644 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:169105644 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:75160470 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:75160470 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:33977936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:33977936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:99059234 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:99059234 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:150239450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:150239450 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:68730153 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:68730153 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:25228412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:25228412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:127230236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:127230236 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:47582590 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:47582590 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:24971425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:24971425 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:11314842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:11314842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:2986172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:2986172 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:77002948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:77002948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:131414294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:131414294 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:182559796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:182559796 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:193201894 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:193201894 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:42485991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:42485991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:52544576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:52544576 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:27137132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:27137132 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:59147705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:59147705 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:107389900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:107389900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:97960646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:97960646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:112999538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:112999538 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:113004181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:113004181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:31620939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:31620939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:50388477 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:50388477 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:9783175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:9783175 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:108011020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:108011020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:26407855 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:26407855 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:26377426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:26377426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:51768908 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:51768908 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:179398592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:179398592 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:73803394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:73803394 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:11887817 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:11887817 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:100434182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:100434182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:71099995 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:71099995 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:11768399 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:11768399 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:4073414 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:4073414 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:170156988 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:170156988 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:57340805 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:57340805 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:57422596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:57422596 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:35042599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:35042599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:111782844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:111782844 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:49711134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:49711134 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:181754358 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:181754358 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40069094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40069094 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:230933795 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:230933795 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:35910690 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:35910690 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:15164483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:15164483 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:142991494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:142991494 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:74572436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:74572436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:128755682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:128755682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:119943140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:119943140 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:119943142 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:119943142 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:111336723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:111336723 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:34326002 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:34326002 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43865561 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43865561 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:112564575 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:112564575 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:67562811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:67562811 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:118178143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:118178143 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:174224138 G>T maps to NM_031942.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:174224138 G>T maps to NM_031942.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:21752405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:21752405 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:63430021 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:63430021 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:85957601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:85957601 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:85964250 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:85964250 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:176002009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:176002009 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:134251824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:134251824 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:620434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:620434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:67833206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:67833206 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:11120822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:11120822 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:78061931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:78061931 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:8612374 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:8612374 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:73795246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:73795246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:150659363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:150659363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:147092681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:147092681 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:101797530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:101797530 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70850711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70850711 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70875810 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70875810 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:139774712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:139774712 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:107910359 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:107910359 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:61459267 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:61459267 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:68396115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:68396115 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:68430322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:68430322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:93851773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:93851773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:93897081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:93897081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:207825863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:207825863 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:207871033 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:207871033 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:3214612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:3214612 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:114449152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:114449152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:18126119 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:18126119 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:80646825 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:80646825 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:68936660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:68936660 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:113873231 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:113873231 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:76928454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:76928454 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:76928475 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:76928475 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:36156642 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:36156642 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:72278546 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:72278546 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:73418669 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:73418669 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:110653259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:110653259 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:110734385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:110734385 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:31255977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:31255977 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:49226182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:49226182 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:93781814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:93781814 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:153998547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:153998547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:435890 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:435890 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:122545972 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:122545972 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:96650001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:96650001 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:124325803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:124325803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:21760497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:21760497 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:20974537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:20974537 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:183608211 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:183608211 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:183608217 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:183608217 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:30017727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:30017727 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:105393277 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:105393277 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:29044370 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:29044370 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:95625226 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:95625226 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:25718934 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:25718934 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:150482301 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:150482301 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:55269311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:55269311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:186501347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:186501347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:101045057 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:101045057 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:185037978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:185037978 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:89448398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:89448398 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:27402089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:27402089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:44773933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:44773933 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:216741468 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:216741468 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:138613040 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:138613040 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:138619366 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:138619366 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:220045482 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:220045482 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:150403467 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:150403467 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:68788365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:68788365 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:92523016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:92523016 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:127704781 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:127704781 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:157488603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:157488603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:125072956 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:125072956 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:125078559 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:125078559 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:137717583 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:137717583 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:115969396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:115969396 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:128493722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:128493722 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:89756742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:89756742 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:151090005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:151090005 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:46980937 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:46980937 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:27185029 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:27185029 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:49173797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:49173797 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:61958347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:61958347 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:105623599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:105623599 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:119595215 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:119595215 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:30538311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:30538311 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:110260048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:110260048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:67353816 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:67353816 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:119925703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:119925703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:11136754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:11136754 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:45267411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:45267411 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:93184925 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:93184925 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:65392105 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:65392105 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:28463579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:28463579 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:91843573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:91843573 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:27861103 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:27861103 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186009048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186009048 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:174254162 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:174254162 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121434055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121434055 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121434284 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121434284 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:87511284 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:87511284 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:26043927 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:26043927 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:209880508 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:209880508 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:183823872 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:183823872 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:65684162 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:65684162 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:47121274 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:47121274 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:102842539 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:102842539 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:1527607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:1527607 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:2606809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:2606809 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:15648259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:15648259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:15689098 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:15689098 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:37567629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:37567629 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:30500398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:30500398 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:156608195 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:156608195 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:33633090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:33633090 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:120373153 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:120373153 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:215342472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:215342472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:78674558 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:78674558 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:178560319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:178560319 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70793935 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70793935 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:108357193 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:108357193 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:142643202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:142643202 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:123122322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:123122322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:118242278 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:118242278 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:93943840 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:93943840 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:138601459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:138601459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:118738948 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:118738948 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:91479121 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:91479121 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:200973842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:200973842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:55270400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:55270400 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:36353334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:36353334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:166231930 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:166231930 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:241712922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:241712922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:134981837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:134981837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:123014586 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:123014586 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:54866742 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:54866742 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:7038803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:7038803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:129592004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:129592004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:112435410 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:112435410 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:133942269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:133942269 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:133944215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:133944215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:154185287 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:154185287 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:68123279 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:68123279 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:53307310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:53307310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:54800031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:54800031 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:46884068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:46884068 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:70339176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:70339176 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:70502310 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:70502310 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:70542053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:70542053 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:119750653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:119750653 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:152173405 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:152173405 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:41613836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:41613836 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:151097854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:151097854 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:38333719 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:38333719 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:168344613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:168344613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:102709736 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:102709736 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:50553739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:50553739 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60160051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60160051 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60231852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60231852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:15967554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:15967554 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:65762710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:65762710 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:9003443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:9003443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:108147286 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:108147286 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:108220458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:108220458 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:52697644 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:52697644 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:23362045 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:23362045 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:19337982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:19337982 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:19359473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:19359473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:50197682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:50197682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:140110301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:140110301 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:10979713 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:10979713 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:56312863 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:56312863 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:56459661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:56459661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:101098848 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:101098848 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:10712192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:10712192 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:31537510 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:31537510 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:117657858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:117657858 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120463056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120463056 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120510148 C>A maps to NM_024408.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120510148 C>A maps to NM_024408.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:101582092 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:101582092 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:6007106 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:6007106 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:32463281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:32463281 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:154002313 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:154002313 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:10319680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:10319680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:48327668 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:48327668 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:158747482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:158747482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:46727135 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:46727135 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:76783667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:76783667 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:72929655 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:72929655 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:176681250 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:176681250 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:176809470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:176809470 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:142537153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:142537153 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:149312268 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:149312268 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:7361323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:7361323 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:153275172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:153275172 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:36931593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:36931593 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:98369360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:98369360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:99971200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:99971200 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:119336856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:119336856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:48603246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:48603246 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100855510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100855510 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:20534523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:20534523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:84622797 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:84622797 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:203014951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:203014951 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:81112223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:81112223 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:45117284 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:45117284 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:23522299 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:23522299 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:69009215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:69009215 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43430883 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43430883 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43520123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43520123 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43269786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:43269786 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:54115822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:54115822 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:17636165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:17636165 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:87691180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:87691180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:112145675 C>A maps to ENST00000394827 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:112145675 C>A maps to ENST00000394827 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:3001898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:3001898 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70963389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70963389 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:8465335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:8465335 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:157691526 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:157691526 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:158007134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:158007134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:158325540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:158325540 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:31405940 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:31405940 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:45377123 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:45377123 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:64514075 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:64514075 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:158946588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:158946588 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:107097158 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:107097158 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:72741391 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:72741391 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:133560606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:133560606 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:120461195 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:120461195 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:85774491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:85774491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:173913388 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:173913388 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:50096085 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:50096085 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:34400123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:34400123 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:192613591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:192613591 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:49582334 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:49582334 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:105105649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:105105649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:78357407 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:78357407 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:77542309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:77542309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:213277747 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:213277747 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:77377925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:77377925 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:108995803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:108995803 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:16635591 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:16635591 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:42392408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:42392408 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:18462168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:18462168 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:200193402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:200193402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:129886313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:129886313 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:62049883 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:62049883 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169702625 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169702625 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169580949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169580949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:26135288 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:26135288 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:55863580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:55863580 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:61259537 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:61259537 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:61562430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:61562430 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:61569860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:61569860 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100771537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100771537 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:70237105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:70237105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:25301258 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:25301258 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:52000277 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:52000277 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:72190355 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:72190355 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:170744600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:170744600 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:75708782 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:75708782 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:76047883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:76047883 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:20657791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:20657791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:40397380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:40397380 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:98773982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:98773982 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:20523953 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:20523953 A>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:70442640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:70442640 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:10258459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:10258459 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:231112872 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:231112872 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:142803865 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chrX:142803865 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:35773913 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:35773913 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:153005190 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:153005190 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:28004837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:28004837 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:134936485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:134936485 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:31571787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:31571787 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:31585495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:31585495 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:39959643 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:39959643 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:149879214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:149879214 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:29864218 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:29864218 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:152462489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:152462489 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:152464720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:152464720 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:152464723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:152464723 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr21:34015816 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr21:34015816 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:62536587 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:62536587 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:35830676 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:35830676 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:120772821 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:120772821 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:78295616 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:78295616 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:115117613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:115117613 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:59556189 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:59556189 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:160200622 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:160200622 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:62270814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:62270814 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:95230902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:95230902 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:92200518 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:92200518 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:72069519 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:72069519 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:39977152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:39977152 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:54219224 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:54219224 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:120476970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:120476970 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:66531692 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:66531692 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:83406885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:83406885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:68928291 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:68928291 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr21:42870033 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr21:42870033 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:43180566 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:43180566 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:175355467 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:175355467 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:113710387 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:113710387 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:144462958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:144462958 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186292814 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186292814 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr21:10969196 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr21:10969196 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:36520260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:36520260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:108572363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:108572363 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:73230718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:73230718 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:73442735 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:73442735 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:29173043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:29173043 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:88911102 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:88911102 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:70155316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:70155316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:190999999 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:190999999 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108116592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108116592 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108417742 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108417742 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:79862338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:79862338 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:42480174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:42480174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:66418016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:66418016 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:112382129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:112382129 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:40937207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:40937207 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:25633912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:25633912 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:32437852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:32437852 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:56364750 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:56364750 C>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:167051818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:167051818 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:56179481 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:56179481 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:77220564 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:77220564 A>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:44974514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:44974514 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:31809024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:31809024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:81070957 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:81070957 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:176477986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:176477986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:71743270 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:71743270 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:53754829 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:53754829 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:227813670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:227813670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:76063026 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:76063026 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:3984617 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:3984617 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:94476316 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:94476316 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:94476316 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:94476316 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:101571361 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:101571361 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:101571361 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:101571361 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:119024779 C>A maps to NM_001142505.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:119024779 C>A maps to NM_001142505.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:20548518 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:20548518 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:20548518 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:20548518 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:236849946 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:236849946 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:236849946 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:236849946 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:161166643 C>T maps to NM_005099.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:161166643 C>T maps to NM_005099.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:148695880 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:148695880 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:148695880 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:148695880 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:19642456 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:19642456 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:73828595 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:73828595 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:54230778 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:54230778 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr17:54230778 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr17:54230778 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:139914883 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:139914883 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:139914883 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:139914883 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:242151391 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:242151391 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:36598258 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:36598258 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:46244360 C>T maps to NM_152641.2 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:46244360 C>T maps to NM_152641.2 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:63845254 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:63845254 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:63400116 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:63400116 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr13:26129180 C>A maps to NM_016529.4 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr13:26129180 C>A maps to NM_016529.4 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr14:35255505 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr14:35255505 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:160284796 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:160284796 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:160284796 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:160284796 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:83932640 G>A maps to NM_001717.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:83932640 G>A maps to NM_001717.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:137505060 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:137505060 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:137505060 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:137505060 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:50315575 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:50315575 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:50315575 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:50315575 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:103783194 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:103783194 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:103783194 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:103783194 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:124661303 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:124661303 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:124661303 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:124661303 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr14:60575067 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr14:60575067 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:60575067 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:60575067 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:263635 C>T maps to NM_001013672.4 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr17:263635 C>T maps to NM_001013672.4 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:207200841 T>A maps to NM_023938.5 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:207200841 T>A maps to NM_023938.5 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:57349287 G>T maps to NM_000562.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:57349287 G>T maps to NM_000562.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr9:77598665 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr9:77598665 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr9:77598665 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr9:77598665 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:54109765 C>T maps to NM_020898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:54109765 C>T maps to NM_020898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:3041473 C>A maps to NM_001014437.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:3041473 C>A maps to NM_001014437.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:76828388 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:76828388 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:119926462 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:119926462 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr20:5902941 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr20:5902941 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:5902941 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:5902941 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr22:51018160 G>A maps to NM_005198.4 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr22:51018160 G>A maps to NM_005198.4 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:66613920 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:66613920 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr18:72234725 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr18:72234725 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:72234725 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:72234725 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr9:39085590 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr9:39085590 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:71657310 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:71657310 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr21:47544688 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr21:47544688 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:85838570 G>A maps to NM_001861.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:85838570 G>A maps to NM_001861.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:1254543 G>A maps to ENST00000434694 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:1254543 G>A maps to ENST00000434694 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:125673594 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:125673594 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:110465718 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:110465718 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:110465718 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:110465718 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:156850895 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:156850895 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:156850895 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:156850895 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:112958721 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:112958721 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:43167163 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:43167163 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr13:95114415 G>T maps to NM_001129889.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr13:95114415 G>T maps to NM_001129889.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:182674139 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:182674139 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:182674139 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:182674139 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:32174216 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:32174216 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:225672558 T>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:225672558 T>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:225672558 T>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:225672558 T>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:73138272 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:73138272 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:6088508 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:6088508 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:8045930 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:8045930 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:8045930 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:8045930 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr17:77079785 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr17:77079785 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:40433721 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:40433721 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:40433721 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:40433721 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:220154633 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:220154633 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:56114806 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:56114806 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:56114806 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:56114806 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:58629325 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:58629325 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:58629325 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:58629325 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:92088591 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:92088591 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:92088591 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:92088591 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:128679232 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:128679232 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:180053097 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:180053097 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr6:41564989 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr6:41564989 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:41564989 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:41564989 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:46060406 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:46060406 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:46060406 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:46060406 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:74501791 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:74501791 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:42526271 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:42526271 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:13768607 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:13768607 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:119748147 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:119748147 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:119748147 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:119748147 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:5593056 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:5593056 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:5593056 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:5593056 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:120299833 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:120299833 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:120299836 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:120299836 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:120299833 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:120299833 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:120299836 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:120299836 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr22:30533001 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr22:30533001 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr13:21219138 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr13:21219138 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr13:21219138 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr13:21219138 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:65687616 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:65687616 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:65687616 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:65687616 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:45931488 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:45931488 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:45931488 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:45931488 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:1516580 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:1516580 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:4741677 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:4741677 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:147019086 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:147019086 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:10600509 C>A maps to NM_203500.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:10600509 C>A maps to NM_203500.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:45212370 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:45212370 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:134322837 C>T maps to NM_178554.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:134322837 C>T maps to NM_178554.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:58860868 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:58860868 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:58860868 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:58860868 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:148343883 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:148343883 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:148343883 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:148343883 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:100172650 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:100172650 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:141946048 G>T maps to NM_018557.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:141946048 G>T maps to NM_018557.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr8:20110502 G>A maps to NM_021020.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr8:20110502 G>A maps to NM_021020.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr18:47801966 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr18:47801966 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:47801966 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:47801966 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:112418747 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:112418747 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:42866806 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:42866806 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:42866806 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:42866806 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:171399377 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr2:171399377 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:95103507 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:95103507 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:21804990 T>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:21804990 T>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:21804992 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:21804992 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:21805007 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:21805007 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:95387914 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:95387914 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:95387914 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:95387914 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:20949889 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:20949889 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:20949889 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:20949889 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:44916013 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:44916013 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:47120099 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:47120099 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:47120099 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:47120099 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:233897386 G>A maps to NM_005383.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:233897386 G>A maps to NM_005383.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:103970270 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:103970270 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:236154432 A>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:236154432 A>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:7060185 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:7060185 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:7060185 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:7060185 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:76243441 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:76243441 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chrX:152027453 G>T maps to NM_015922.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chrX:152027453 G>T maps to NM_015922.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:56468370 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:56468370 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:56468370 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:56468370 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:154031256 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:154031256 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:56875519 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:56875519 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:56875519 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:56875519 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:58170745 A>T maps to NM_001005469.1 L46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:58170745 A>T maps to NM_001005469.1 L46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:24910472 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:24910472 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:24910472 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:24910472 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:55662996 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:55662996 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:55662996 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:55662996 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:55996690 C>A maps to NM_001142763.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:55996690 C>A maps to NM_001142763.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:140741991 G>T maps to NM_018923.2 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:140741991 G>T maps to NM_018923.2 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:9343699 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:9343699 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:81970062 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr16:81970062 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:81970062 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:81970062 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:43907899 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:43907899 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:145789248 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:145789248 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:145789248 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:145789248 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:2129809 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:2129809 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:2129809 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:2129809 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:19571468 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr14:19571468 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr8:48845563 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr8:48845563 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:22290616 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr6:22290616 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr9:127167773 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr9:127167773 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr9:127167773 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr9:127167773 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:186643667 G>A maps to NM_000963.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:186643667 G>A maps to NM_000963.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:214538101 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:214538101 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:214538101 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:214538101 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:179538347 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr5:179538347 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:179538347 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr5:179538347 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:5105124 G>T maps to NM_021163.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr7:5105124 G>T maps to NM_021163.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr20:35660952 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr20:35660952 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:66833521 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:66833521 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:59341652 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:59341652 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:68895401 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:68895401 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:68895401 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:68895401 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:114309098 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:114309098 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:114309098 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:114309098 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:237608578 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr1:237608578 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:237608578 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:237608578 C>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:38753576 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr3:38753576 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:38753576 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:38753576 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:177929555 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:177929555 G>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:169580745 G>T maps to NM_003005.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr1:169580745 G>T maps to NM_003005.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr18:43247995 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr18:43247995 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:43247995 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:43247995 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:150770997 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr7:150770997 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:85279636 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr12:85279636 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:85279636 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr12:85279636 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:2775709 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr18:2775709 A>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:18878183 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:18878183 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:51032015 C>T maps to NM_032802.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:51032015 C>T maps to NM_032802.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:191839671 A>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr2:191839671 A>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:39145915 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr22:39145915 G>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:29997962 C>T maps to NM_016151.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr16:29997962 C>T maps to NM_016151.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:67406884 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr11:67406884 T>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:42510605 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:42510605 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr17:38991094 C>T maps to NM_001195386.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr17:38991094 C>T maps to NM_001195386.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:69101201 G>A maps to NM_007114.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr3:69101201 G>A maps to NM_007114.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:68688032 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr4:68688032 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:68688032 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr4:68688032 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr20:33608967 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr20:33608967 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:33608967 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr20:33608967 C>T did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:25652309 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr15:25652309 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:25652309 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr15:25652309 A>G did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:110007728 C>T maps to NM_033390.1 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr11:110007728 C>T maps to NM_033390.1 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:81153969 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr10:81153969 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:81153969 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr10:81153969 C>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:57868089 G>T maps to ENST00000391705 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:57868089 G>T maps to ENST00000391705 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:37582162 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:37582162 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:37582162 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:37582162 G>A did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:12693579 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01D-1040-01 chr19:12693579 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:12693579 T>C did not map to a codon.
Sequencing variant TCGA-35-3615-01A-01W-0928-08 chr19:12693579 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:121766285 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:121766285 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:20685434 G>T maps to NM_001163941.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:20685434 G>T maps to NM_001163941.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:20762553 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:20762553 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:17464435 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:17464435 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:39994247 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:39994247 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:179112278 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:179112278 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:35691600 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:35691600 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:185687189 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:185687189 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5568401 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5568401 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:158622311 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:158622311 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175899306 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175899306 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:7414679 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:7414679 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:32878078 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:32878078 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:8758238 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:8758238 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:106991258 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:106991258 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:5038111 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:5038111 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:97370990 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:97370990 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:38530512 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:38530512 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:54445525 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:54445525 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:54534411 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:54534411 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:37442661 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:37442661 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:197985971 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:197985971 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:35224744 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:35224744 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:23257168 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:23257168 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:100807893 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:100807893 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:27538410 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:27538410 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:194154400 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:194154400 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:42482020 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:42482020 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:130656408 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:130656408 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:40642417 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:40642417 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:136899807 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:136899807 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:1459520 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:1459520 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:26370528 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:26370528 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:118084606 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:118084606 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:122817535 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:122817535 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:101951913 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:101951913 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:34638361 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:34638361 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:45507064 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:45507064 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:16556391 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:16556391 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:179425863 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:179425863 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:75139259 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:75139259 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:207271380 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:207271380 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:175735629 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:175735629 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:74073209 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:74073209 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5963387 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5963387 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:150234454 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:150234454 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:61121320 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:61121320 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:49918471 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:49918471 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:2742880 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:2742880 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:54905660 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:54905660 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:18823252 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:18823252 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:7339642 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:7339642 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:66564738 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:66564738 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:57734231 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:57734231 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:169030906 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:169030906 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:158326284 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:158326284 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60776388 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60776388 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:137527078 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:137527078 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:73270111 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:73270111 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:26890072 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:26890072 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:40041691 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:40041691 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:47116946 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:47116946 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:21895651 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:21895651 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:67833422 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:67833422 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:62677089 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:62677089 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:120214156 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:120214156 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:49840387 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:49840387 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:95696399 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:95696399 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:11657312 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:11657312 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:56708900 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:56708900 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:147914687 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:147914687 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:46067469 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:46067469 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:101788261 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:101788261 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:7559678 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:7559678 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:47418254 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:47418254 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:148559605 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:148559605 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:69263297 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:69263297 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:211515048 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:211515048 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:137600570 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:137600570 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:75924632 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:75924632 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:84906836 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:84906836 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:1317309 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:1317309 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:1413471 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:1413471 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:34128332 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:34128332 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:23546736 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:23546736 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:16989183 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:16989183 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:17061813 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:17061813 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:15758455 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:15758455 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:169169231 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:169169231 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:100646423 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:100646423 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:14217621 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:14217621 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:182836206 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:182836206 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:84245834 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:84245834 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:170597952 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:170597952 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:75365237 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:75365237 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:52426818 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:52426818 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:7705164 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:7705164 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:196605667 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:196605667 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:340073 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:340073 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:57669875 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:57669875 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:4711544 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:4711544 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:172534391 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:172534391 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:99812279 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:99812279 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:101200604 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:101200604 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:14856930 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:14856930 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:139945863 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:139945863 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:101445741 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:101445741 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:5488976 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:5488976 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:89521834 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:89521834 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:64726974 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:64726974 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:5747074 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:5747074 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:66115211 C>T maps to ENST00000370616 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:66115211 C>T maps to ENST00000370616 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:17602965 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:17602965 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:14862909 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:14862909 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:48040229 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:48040229 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175162416 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175162416 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:192125778 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:192125778 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:123310985 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:123310985 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:128481050 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:128481050 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:216284111 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:216284111 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:49618893 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:49618893 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:49684358 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:49684358 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:32869203 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:32869203 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:46976210 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:46976210 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:161580442 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:161580442 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:898402 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:898402 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:48650963 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:48650963 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:72631408 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:72631408 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:75275350 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:75275350 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:117849208 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:117849208 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:42465799 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:42465799 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:150437874 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:150437874 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:102962445 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:102962445 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:120181413 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:120181413 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:105518573 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:105518573 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:121182854 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:121182854 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:26505810 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:26505810 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:5290651 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:5290651 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:100203100 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:100203100 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:88732417 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:88732417 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:113738816 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:113738816 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:57878923 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:57878923 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:3600677 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:3600677 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:156697501 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:156697501 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:31429544 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:31429544 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:46326734 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:46326734 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:156673183 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:156673183 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:33636532 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:33636532 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:120373134 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:120373134 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:29934480 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:29934480 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:101814922 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:101814922 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:55599402 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:55599402 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:86924397 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:86924397 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:241725410 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:241725410 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:135024343 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:135024343 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:21531774 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:21531774 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:136587151 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:136587151 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:40097766 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:40097766 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:73566348 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:73566348 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:100915220 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:100915220 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:99762233 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:99762233 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:85518341 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:85518341 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:235968000 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:235968000 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:166990842 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:166990842 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:45925463 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:45925463 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:3783107 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:3783107 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:54527774 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:54527774 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:85498522 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:85498522 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:43206959 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:43206959 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:50925984 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr22:50925984 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:6861262 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:6861262 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:118371888 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:118371888 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:132322634 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:132322634 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:132326124 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:132326124 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:5012418 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:5012418 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:10363028 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:10363028 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:19585127 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:19585127 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60559973 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60559973 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:31721238 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:31721238 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:93580227 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:93580227 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:149905931 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:149905931 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:30611549 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:30611549 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:236990114 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:236990114 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:10354321 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:10354321 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:18059688 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:18059688 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:109826822 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:109826822 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:171239524 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:171239524 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:76566993 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:76566993 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:95097716 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:95097716 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:31141568 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:31141568 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:31141969 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:31141969 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:183860347 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:183860347 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:170359225 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:170359225 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:21135336 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:21135336 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:101573415 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:101573415 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:117662800 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:117662800 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:115356705 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:115356705 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:206587502 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:206587502 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:184022093 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:184022093 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5923425 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5923425 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:123787696 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:123787696 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:183696311 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:183696311 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:248166595 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:248166595 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:56125431 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:56125431 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:17599783 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:17599783 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:12530096 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:12530096 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrY:5075523 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrY:5075523 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:30732465 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:30732465 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:56138034 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:56138034 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:55521645 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:55521645 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:101192997 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:101192997 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:144880586 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:144880586 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:650594 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:650594 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:15586206 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:15586206 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:76392385 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:76392385 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:8793451 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:8793451 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:32996338 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:32996338 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:18890378 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:18890378 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:242270865 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:242270865 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:134382665 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:134382665 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:99162871 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:99162871 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:38144679 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:38144679 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:131984547 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:131984547 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:35393584 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:35393584 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:104205213 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:104205213 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:151265707 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:151265707 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:53667196 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:53667196 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:113814506 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:113814506 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:40985779 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:40985779 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:99049972 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:99049972 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:71622350 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:71622350 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:18759571 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:18759571 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:40713283 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:40713283 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:40827638 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:40827638 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:5921392 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:5921392 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:64496313 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:64496313 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:18476639 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:18476639 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:48435355 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:48435355 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:161160109 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:161160109 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:6042001 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:6042001 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:87116261 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:87116261 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:87404379 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:87404379 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:38129165 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:38129165 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:34386049 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:34386049 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:19380081 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:19380081 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:219449447 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:219449447 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:43906397 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:43906397 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:39070590 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:39070590 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:153580196 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:153580196 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:38812603 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:38812603 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:242283021 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:242283021 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:67142837 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:67142837 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:130536143 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:130536143 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:41083198 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:41083198 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:57626862 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:57626862 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:39371247 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:39371247 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160589495 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160589495 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:44672630 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:44672630 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:25812051 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:25812051 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:103038557 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:103038557 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:45565055 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:45565055 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5327648 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:5327648 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:54929792 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:54929792 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:19610091 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:19610091 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:11151947 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:11151947 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:2740834 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:2740834 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:231033759 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:231033759 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:231118157 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:231118157 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:24979549 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:24979549 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:104151917 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:104151917 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:17737256 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:17737256 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:1203336 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:1203336 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:36824330 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:36824330 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:118838380 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:118838380 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:29776233 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:29776233 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:115417053 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:115417053 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:152826577 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:152826577 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:119944805 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:119944805 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:38700952 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:38700952 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:93464219 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:93464219 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:8051318 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:8051318 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:61489213 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:61489213 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:100029217 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:100029217 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:70411521 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:70411521 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:56704496 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:56704496 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:155571994 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:155571994 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:32044663 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:32044663 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:153548986 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:153548986 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:166910512 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:166910512 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:98180944 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:98180944 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:35698006 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:35698006 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:63000634 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:63000634 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:102191815 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:102191815 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:125946342 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:125946342 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:32959717 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:32959717 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:55832009 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:55832009 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:68810212 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:68810212 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:19775743 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr21:19775743 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:29709741 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:29709741 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:172226999 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:172226999 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:35747413 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:35747413 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:189012519 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:189012519 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:14390956 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:14390956 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:72987657 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:72987657 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:73168008 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:73168008 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:73442647 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:73442647 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:3200874 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:3200874 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:3261238 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:3261238 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:147830160 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:147830160 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:117634356 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:117634356 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:179629586 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:179629586 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:54941972 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:54941972 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:34929437 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:34929437 T>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:156967515 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:156967515 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:55598122 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:55598122 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:109510067 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:109510067 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:22021555 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:22021555 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:11531051 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:11531051 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:155169515 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:155169515 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:77896818 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:77896818 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:135638769 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chrX:135638769 T>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:100115120 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:100115120 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:70931059 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:70931059 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:38829523 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:38829523 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:203749309 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:203749309 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:167272640 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:167272640 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:33663429 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:33663429 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:43752612 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:43752612 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:68611505 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:68611505 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:939104 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:939104 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:32410782 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:32410782 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:61705819 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:61705819 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:180794175 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:180794175 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:7193048 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:7193048 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:38120332 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:38120332 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:81036850 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:81036850 A>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:81065186 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:81065186 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:9526279 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:9526279 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:53208177 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:53208177 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:12577467 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:12577467 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:238050183 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:238050183 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:238050590 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:238050590 C>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:53282162 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:53282162 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:21970285 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:21970285 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:21997650 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:21997650 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:73151152 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:73151152 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:76194210 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:76194210 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:108012460 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:108012460 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:147124192 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:147124192 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:131324609 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:131324609 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:20448549 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:20448549 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:81545901 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:81545901 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:37380702 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:37380702 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:24209636 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:24209636 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:33588684 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:33588684 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:109674306 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:109674306 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:247018988 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:247018988 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:8757006 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:8757006 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:41519585 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:41519585 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:114291044 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:114291044 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:69382303 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:69382303 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:99145079 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:99145079 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:2115421 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:2115421 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:141059476 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:141059476 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:120316255 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:120316255 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:177001423 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:177001423 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:160136562 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:160136562 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:160803474 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:160803474 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:156617578 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:156617578 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:59024538 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:59024538 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:56840663 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:56840663 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31601576 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31601576 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:116116510 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:116116510 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:108011249 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:108011249 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:109294973 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:109294973 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:31506821 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:31506821 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:99182743 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:99182743 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:36936444 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:36936444 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:899545 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:899545 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:11769249 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:11769249 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:34684273 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:34684273 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:20180557 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:20180557 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:112124763 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:112124763 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:57420288 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:57420288 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:46928610 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:46928610 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:93090351 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:93090351 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:105218593 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:105218593 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:223949389 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:223949389 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:19665986 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:19665986 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:2233815 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:2233815 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:86106345 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:86106345 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:46400067 C>A maps to NM_001123396.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:46400067 C>A maps to NM_001123396.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:67540335 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:67540335 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:72470859 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:72470859 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:60780727 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:60780727 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:83635986 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:83635986 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:61689272 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:61689272 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:205495789 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:205495789 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:179988993 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:179988993 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:49548165 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:49548165 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:6185921 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:6185921 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:101010244 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:101010244 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:57937650 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:57937650 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:3030015 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:3030015 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:55038468 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:55038468 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:103354272 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:103354272 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:103400226 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:103400226 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:86289113 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:86289113 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:61449931 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:61449931 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:3651774 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:3651774 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:334693 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:334693 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:211515044 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:211515044 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:49665555 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:49665555 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:113347756 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:113347756 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:113871273 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:113871273 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:10992501 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:10992501 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:11346808 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:11346808 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:70256085 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:70256085 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:16957316 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:16957316 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:17157610 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:17157610 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:202934680 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:202934680 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:145690321 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:145690321 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:50828403 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:50828403 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:135371581 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:135371581 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:99260304 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:99260304 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:6652472 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:6652472 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:14216295 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:14216295 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:137269861 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:137269861 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:137294216 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:137294216 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:127555504 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:127555504 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:83676299 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:83676299 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:25498450 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:25498450 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:45671612 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:45671612 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:348399 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:348399 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:80584307 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:80584307 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:158141018 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:158141018 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:236646541 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:236646541 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:3985436 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:3985436 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:60469122 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:60469122 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:34761598 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:34761598 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:131276034 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:131276034 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:111956697 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:111956697 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:134920201 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:134920201 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142565986 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142565986 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:204103600 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:204103600 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:40194578 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:40194578 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:40860859 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:40860859 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:148511234 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:148511234 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:161004745 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:161004745 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:175933971 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:175933971 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:2695658 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:2695658 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:40702714 T>G maps to NM_001083124.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:40702714 T>G maps to NM_001083124.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:10140744 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:10140744 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92535111 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92535111 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:117612320 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:117612320 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:63987584 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:63987584 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:28963909 A>T maps to NM_001159920.1 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:28963909 A>T maps to NM_001159920.1 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:240458237 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:240458237 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:71021607 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:71021607 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:35642125 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:35642125 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:171702583 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:171702583 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:173269650 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:173269650 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:22696346 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:22696346 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:22729630 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:22729630 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:44190500 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:44190500 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:42985522 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:42985522 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:55198791 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:55198791 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129467430 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129467430 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:9935018 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:9935018 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:34008231 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:34008231 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:110231398 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:110231398 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:52219650 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:52219650 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:153223099 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:153223099 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:13524874 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:13524874 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:242170420 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:242170420 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:65411951 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:65411951 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:91844774 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:91844774 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:26202876 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:26202876 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:129025700 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:129025700 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:118510676 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:118510676 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:8304266 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:8304266 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:21187545 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:21187545 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:27679285 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:27679285 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:65621152 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:65621152 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:2155356 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:2155356 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:35861271 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:35861271 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:128041178 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:128041178 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:100948471 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:100948471 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:155100177 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:155100177 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:7162968 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:7162968 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:31336211 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:31336211 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:31384812 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:31384812 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:52823628 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:52823628 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:7759585 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:7759585 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:156638226 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:156638226 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:26628207 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:26628207 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:139800005 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:139800005 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:78580127 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:78580127 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:78580147 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:78580147 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:40312563 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:40312563 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:138670417 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:138670417 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:72339141 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:72339141 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:34263189 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:34263189 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:66040630 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:66040630 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:29534513 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:29534513 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:154179043 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:154179043 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:145562003 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:145562003 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:36057808 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:36057808 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:97377554 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:97377554 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:96278780 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:96278780 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:161016266 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:161016266 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:141441478 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:141441478 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:53716631 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:53716631 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:70446170 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:70446170 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:157182278 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:157182278 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:33246319 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:33246319 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:24998133 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:24998133 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:160708663 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:160708663 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:54839688 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:54839688 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:172945217 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:172945217 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:172945221 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:172945221 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:217148263 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:217148263 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:119732243 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:119732243 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:74701872 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:74701872 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:182934004 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:182934004 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:37617809 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:37617809 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:126738206 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:126738206 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:88767695 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:88767695 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:21458131 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:21458131 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:128116782 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:128116782 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:141778562 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:141778562 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:130927492 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:130927492 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:74709402 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:74709402 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:49435673 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:49435673 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:55519724 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:55519724 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:123641455 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:123641455 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:17875915 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:17875915 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:121467627 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:121467627 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:100699564 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:100699564 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:67524892 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:67524892 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:10404158 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:10404158 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:211179549 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:211179549 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:76886413 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:76886413 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:78392347 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:78392347 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:134022832 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:134022832 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:134038952 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:134038952 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:160321646 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:160321646 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:198225495 G>C maps to ENST00000367383 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:198225495 G>C maps to ENST00000367383 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:20939723 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:20939723 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:55512300 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:55512300 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:34243743 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:34243743 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:44560478 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:44560478 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:139934535 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:139934535 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:5948761 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:5948761 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:206617765 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:206617765 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:135322899 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:135322899 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:13384855 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:13384855 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:24911442 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:24911442 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:26690203 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:26690203 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:241079773 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:241079773 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:41739716 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:41739716 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:23794375 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:23794375 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:103306518 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:103306518 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:35492423 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:35492423 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:176809252 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:176809252 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:119097408 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:119097408 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:79851512 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:79851512 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:205983603 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:205983603 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:12499564 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:12499564 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:91715192 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:91715192 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:55780261 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:55780261 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:47942151 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:47942151 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:81208552 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:81208552 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:81254000 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:81254000 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:59814625 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:59814625 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:65197347 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:65197347 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31827563 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31827563 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:121258459 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:121258459 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:29233234 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:29233234 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:37536601 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:37536601 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:242105747 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:242105747 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:6513616 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:6513616 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:110983530 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:110983530 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:12854686 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:12854686 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:82611190 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:82611190 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:23522320 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:23522320 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:47245841 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:47245841 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:69031066 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:69031066 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:57146031 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:57146031 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:61788816 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:61788816 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:48733566 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:48733566 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:48790257 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:48790257 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:35089561 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:35089561 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142458579 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142458579 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:11574360 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:11574360 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:44072369 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:44072369 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:8380267 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:8380267 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:220164679 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:220164679 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:158913506 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:158913506 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:49141463 G>A maps to ENST00000452739 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:49141463 G>A maps to ENST00000452739 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:173891778 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:173891778 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:25215854 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:25215854 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:53608972 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:53608972 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:129543514 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:129543514 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:25725548 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:25725548 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:105261101 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:105261101 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:88998119 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:88998119 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:2000733 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:2000733 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:110757322 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:110757322 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:32356797 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:32356797 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:33936759 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:33936759 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:237893688 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:237893688 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:18108621 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:18108621 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:50869523 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:50869523 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:147261641 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:147261641 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:123524361 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:123524361 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:50292798 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:50292798 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:71398283 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:71398283 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:30856244 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:30856244 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:169660890 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:169660890 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:156130170 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:156130170 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:95090209 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:95090209 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:9506103 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:9506103 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:148431678 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:148431678 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:52152224 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:52152224 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:164786791 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:164786791 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:100464249 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:100464249 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:43224152 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:43224152 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:70263486 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:70263486 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:74542252 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:74542252 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:51865390 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:51865390 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:110717278 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:110717278 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:55731750 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:55731750 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:170214165 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:170214165 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:23608612 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:23608612 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:70633340 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:70633340 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:57847885 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:57847885 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:17877753 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:17877753 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:51314703 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:51314703 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:1263059 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:1263059 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:106924245 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:106924245 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:101206246 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:101206246 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:147499564 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:147499564 T>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:55903663 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:55903663 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:149520960 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:149520960 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:57099812 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:57099812 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:17432488 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:17432488 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:80567437 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:80567437 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:75490672 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:75490672 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:33592510 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:33592510 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:72315329 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:72315329 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:114841346 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:114841346 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:139717339 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:139717339 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:151825793 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:151825793 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:98180605 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:98180605 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:50155471 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:50155471 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:20067528 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:20067528 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:103271242 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:103271242 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129569308 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129569308 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:86806455 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:86806455 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:153565757 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:153565757 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77703168 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77703168 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77710630 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77710630 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:69095237 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:69095237 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:68935728 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:68935728 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:117979477 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:117979477 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:128696196 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:128696196 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:55035197 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:55035197 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:230650609 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:230650609 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142625438 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142625438 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:47251539 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:47251539 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:80747669 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:80747669 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:22862759 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:22862759 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:52977859 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:52977859 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:166579968 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:166579968 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:41877534 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:41877534 A>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:96222644 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:96222644 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:61034796 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:61034796 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:6130969 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:6130969 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:128528311 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:128528311 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:167319801 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:167319801 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:113082163 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:113082163 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:228769534 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:228769534 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:37506957 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:37506957 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:993806 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:993806 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:108618772 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:108618772 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:31558932 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:31558932 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:30379479 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:30379479 C>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:42705454 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:42705454 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:64139198 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chrX:64139198 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:87447927 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:87447927 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:35847068 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:35847068 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:140482164 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:140482164 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:44732551 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:44732551 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:44803894 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:44803894 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:28295325 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:28295325 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:44579019 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:44579019 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:57876261 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:57876261 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:53901369 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:53901369 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:2333456 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:2333456 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:87133793 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:87133793 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:20698331 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:20698331 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:220075878 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:220075878 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:30557510 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:30557510 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44051682 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44051682 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:15059921 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:15059921 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:32419180 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:32419180 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:100252960 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:100252960 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:114670906 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:114670906 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:39607167 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:39607167 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:24298539 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:24298539 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:24253337 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:24253337 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33616206 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33616206 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33662248 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33662248 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:64640392 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:64640392 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:7784383 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:7784383 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:70904842 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:70904842 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:100350315 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:100350315 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:84519730 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:84519730 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:109377494 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:109377494 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:19611160 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:19611160 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:105252422 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:105252422 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:110924303 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:110924303 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:233320855 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:233320855 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:104118310 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:104118310 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:104119995 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:104119995 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:54526373 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:54526373 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:48773312 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:48773312 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:68794562 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:68794562 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:118454749 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:118454749 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:155922384 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:155922384 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:157527236 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:157527236 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176915037 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176915037 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:138433785 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:138433785 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:11021202 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:11021202 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:11039102 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:11039102 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:91182016 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:91182016 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:156628185 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:156628185 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:32429128 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:32429128 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:59934403 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:59934403 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:56383180 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:56383180 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:33137736 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:33137736 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:90161342 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:90161342 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:13666738 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:13666738 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:58485591 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:58485591 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:172425549 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:172425549 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:247737763 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:247737763 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:33642868 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:33642868 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:99443401 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:99443401 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:31536013 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:31536013 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:43453734 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:43453734 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:30619351 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:30619351 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:2623650 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:2623650 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:40536006 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:40536006 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:86388023 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:86388023 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:181547025 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:181547025 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:181728080 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:181728080 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:81626470 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:81626470 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:81689936 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:81689936 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:71411556 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:71411556 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:92970682 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:92970682 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:126142148 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:126142148 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:191076002 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:191076002 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:537875 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:537875 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:38710798 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:38710798 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158301138 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158301138 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158262800 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158262800 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:72519861 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:72519861 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:117057430 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:117057430 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:54429226 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:54429226 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:137626511 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:137626511 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:19571615 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:19571615 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:123173542 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:123173542 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:92300682 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:92300682 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:47498795 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:47498795 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:11317165 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:11317165 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:25467082 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:25467082 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:29130297 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:29130297 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:203150441 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:203150441 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:12254357 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:12254357 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102816166 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102816166 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184075391 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184075391 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:122849348 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:122849348 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:99008486 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:99008486 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:3097912 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:3097912 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:33139708 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:33139708 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:48268098 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:48268098 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:86361915 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:86361915 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:48376559 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:48376559 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:107455051 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:107455051 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:70935578 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:70935578 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:115553894 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:115553894 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:211503845 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:211503845 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:75926375 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:75926375 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:45882289 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:45882289 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:1424438 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:1424438 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:113259405 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:113259405 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:100079044 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:100079044 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:111732801 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:111732801 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:150769477 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:150769477 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:49052587 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:49052587 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:134292299 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:134292299 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:84574101 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:84574101 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:127960837 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:127960837 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:14913771 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:14913771 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:100172837 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:100172837 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:16004733 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:16004733 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:15769234 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:15769234 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:109294150 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:109294150 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:113612639 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:113612639 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:62499731 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:62499731 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:32161131 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:32161131 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:117166002 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:117166002 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:54936094 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:54936094 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:125453020 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:125453020 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:118500869 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:118500869 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:124401327 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:124401327 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:13716889 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:13716889 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:196859375 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:196859375 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:442068 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:442068 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:162862232 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:162862232 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:154595524 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:154595524 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:32264285 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:32264285 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102506080 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102506080 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:183994569 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:183994569 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:140705883 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:140705883 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:67841070 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:67841070 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:43831284 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:43831284 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:89088815 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:89088815 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:678551 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:678551 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:111469521 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:111469521 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:120850797 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:120850797 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:89499321 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:89499321 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:212426881 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:212426881 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:212587265 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:212587265 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:102822464 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:102822464 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:138619566 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:138619566 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17641780 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17641780 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:71200704 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:71200704 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:137323850 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:137323850 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:61013992 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:61013992 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:91701553 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:91701553 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:93396890 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:93396890 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:163066581 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:163066581 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:168461780 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:168461780 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:85925241 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:85925241 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:32768131 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:32768131 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:132763550 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:132763550 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:39153449 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:39153449 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:39170372 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:39170372 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:161281318 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:161281318 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:46976422 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:46976422 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:88420674 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:88420674 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:73759374 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:73759374 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:34131383 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:34131383 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:141905161 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:141905161 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:121712730 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:121712730 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17688706 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17688706 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:180666448 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:180666448 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:38040518 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:38040518 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:93299760 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:93299760 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:99769705 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:99769705 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:57697326 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:57697326 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:109441225 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:109441225 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:146350534 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:146350534 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:146755936 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:146755936 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:119666043 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:119666043 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:110282236 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:110282236 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:27483257 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:27483257 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:144918643 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:144918643 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:52220137 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:52220137 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:37255773 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:37255773 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:58150681 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:58150681 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:29858229 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:29858229 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:29897092 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:29897092 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:186134327 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:186134327 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:115166448 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:115166448 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:94225416 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:94225416 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:129221461 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:129221461 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:117209029 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:117209029 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:166906008 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:166906008 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:100961439 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:100961439 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:212151609 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:212151609 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:61790031 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:61790031 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:30522495 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:30522495 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:660065 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:660065 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:155566052 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:155566052 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7753313 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7753313 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:142649418 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:142649418 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:3761438 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:3761438 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:108285523 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:108285523 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:104639594 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:104639594 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:39693260 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:39693260 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55267557 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55267557 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55272082 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55272082 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55278100 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55278100 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:51322673 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:51322673 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:186440337 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:186440337 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:38907346 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:38907346 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:53201034 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:53201034 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55019473 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55019473 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:183097700 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:183097700 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:182858521 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:182858521 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:98817773 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:98817773 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:152671720 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:152671720 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:136569739 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:136569739 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:21807647 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:21807647 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:76970961 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:76970961 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:71947173 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:71947173 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:124988604 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:124988604 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:75622510 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:75622510 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55176498 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55176498 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:197687368 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:197687368 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:160963893 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:160963893 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:82437442 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:82437442 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:110790749 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:110790749 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:141201813 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:141201813 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:235865983 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:235865983 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:21208256 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:21208256 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:20031770 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:20031770 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:119739908 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:119739908 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:85422359 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:85422359 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:43855443 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:43855443 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:21971303 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:21971303 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:43280022 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:43280022 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:50582320 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:50582320 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:4355069 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:4355069 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:17891797 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:17891797 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:34958193 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:34958193 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:60150530 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:60150530 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:16026395 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:16026395 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:22006335 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:22006335 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:32235039 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:32235039 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:7869241 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:7869241 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:23861993 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:23861993 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:18030043 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:18030043 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:27438884 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:27438884 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:26501000 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:26501000 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:76867144 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:76867144 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:24401720 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:24401720 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:48719695 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:48719695 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:119036143 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:119036143 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:84014587 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:84014587 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:178274977 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:178274977 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:20691365 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:20691365 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:45168671 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:45168671 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:31827406 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:31827406 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:236148584 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:236148584 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:25493690 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:25493690 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:56436477 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:56436477 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:96116773 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:96116773 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:117693639 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:117693639 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:106861808 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:106861808 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:32328284 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:32328284 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:44467134 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:44467134 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:706869 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:706869 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:50964748 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:50964748 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:154412082 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:154412082 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:107361804 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:107361804 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:16730682 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:16730682 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:163235406 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:163235406 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:78975501 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:78975501 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176760627 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176760627 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:206036919 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:206036919 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:53852847 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:53852847 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:58206675 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:58206675 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:65384016 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:65384016 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:136476907 C>T maps to ENST00000446774 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:136476907 C>T maps to ENST00000446774 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:21999803 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:21999803 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:64104533 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:64104533 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:22115062 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:22115062 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:96416954 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:96416954 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:229890307 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:229890307 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:9782021 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:9782021 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:110448510 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:110448510 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:110527553 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:110527553 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:51918981 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:51918981 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:125221150 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:125221150 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:9388750 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:9388750 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:131949185 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:131949185 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:131951755 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:131951755 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:40826061 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:40826061 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:31827874 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:31827874 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:133225371 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:133225371 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:38158288 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:38158288 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:16279186 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr22:16279186 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:45883656 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:45883656 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:182825953 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:182825953 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:75214371 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:75214371 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:104357256 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:104357256 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:12941573 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:12941573 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44556017 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44556017 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:68942698 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:68942698 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:57398012 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:57398012 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:120112111 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:120112111 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:24202571 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:24202571 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:53218868 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:53218868 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:30103586 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:30103586 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:12837534 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:12837534 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:30664443 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:30664443 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:150867322 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:150867322 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:58318637 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:58318637 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:40991042 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:40991042 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:57058541 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:57058541 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:77212828 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:77212828 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:131116682 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:131116682 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:47448252 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:47448252 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:70954366 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:70954366 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:62153636 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:62153636 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55716649 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:55716649 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:45381861 G>A maps to NM_002856.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:45381861 G>A maps to NM_002856.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:21593273 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:21593273 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:9309676 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:9309676 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:163991560 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:163991560 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:140125515 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:140125515 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:178834025 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:178834025 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:114261161 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:114261161 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:211468955 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:211468955 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:79385628 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:79385628 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:74664671 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:74664671 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:3275462 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:3275462 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:192127742 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:192127742 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:240978225 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:240978225 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:182615839 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:182615839 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:130890815 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:130890815 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:130897368 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:130897368 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:87113622 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:87113622 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:7154835 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:7154835 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:30331752 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:30331752 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:104323347 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:104323347 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:123699398 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:123699398 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:41827924 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:41827924 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:24020264 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:24020264 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:67199987 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:67199987 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:78882416 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:78882416 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:77445588 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:77445588 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:12939664 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:12939664 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:26687996 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:26687996 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:166866436 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:166866436 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:165984654 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:165984654 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:169694838 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:169694838 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:61325700 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:61325700 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:120923758 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:120923758 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:41083071 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:41083071 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:164760713 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:164760713 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:130168427 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:130168427 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:150663555 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:150663555 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:46758519 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:46758519 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:27891685 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:27891685 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:40392220 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:40392220 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:40402049 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:40402049 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:20868013 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:20868013 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:101834599 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:101834599 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:98799638 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:98799638 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:84375116 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:84375116 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:47014564 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:47014564 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:86227868 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:86227868 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:231159055 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:231159055 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:22657675 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:22657675 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:35807184 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:35807184 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:44170913 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:44170913 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:32263951 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:32263951 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158646200 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158646200 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:30712110 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:30712110 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:104054002 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:104054002 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:104064446 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:104064446 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:4425352 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:4425352 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:39967128 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:39967128 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:115420833 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:115420833 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:152763125 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:152763125 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:202565789 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:202565789 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:57407194 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:57407194 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:159913268 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:159913268 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33457240 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33457240 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:106092441 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:106092441 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:80879531 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:80879531 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:168278153 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:168278153 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:79283611 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:79283611 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:139575331 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:139575331 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:67243185 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:67243185 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102881177 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102881177 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:20848648 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:20848648 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:2411434 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:2411434 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:169621663 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:169621663 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:19776067 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:19776067 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:175306574 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:175306574 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:38643788 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:38643788 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:43739759 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:43739759 A>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:103249311 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:103249311 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:20049552 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:20049552 A>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:10916336 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:10916336 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:141321323 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:141321323 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:51475752 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:51475752 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:33593688 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:33593688 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:15928529 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:15928529 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:94865720 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:94865720 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:179504758 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:179504758 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:179542824 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:179542824 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:179553066 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:179553066 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:157049760 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:157049760 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:35991413 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:35991413 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:132618566 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:132618566 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:132620195 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:132620195 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:58343472 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:58343472 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:157213147 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:157213147 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:17279222 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:17279222 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:79842250 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:79842250 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:46712817 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:46712817 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:38766500 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:38766500 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184584876 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184584876 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:158718995 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:158718995 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:134203379 G>A maps to ENST00000377863 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:134203379 G>A maps to ENST00000377863 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:56015034 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:56015034 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:142089539 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:142089539 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:100383767 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:100383767 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:47572318 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:47572318 T>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:31783127 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:31783127 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:72004449 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:72004449 T>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:58379889 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:58379889 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:68257557 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:68257557 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:147131423 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:147131423 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:136650008 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chrX:136650008 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:99097795 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:99097795 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:36963699 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:36963699 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:36963802 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:36963802 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:53431 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:53431 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:53282056 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:53282056 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:53238116 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:53238116 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:7637117 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:7637117 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:44269926 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:44269926 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:22025691 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:22025691 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:44102185 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:44102185 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:116335075 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:116335075 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:148637839 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:148637839 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:109691917 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:109691917 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:44071939 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:44071939 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:23564590 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:23564590 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:55058376 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:55058376 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:55081987 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:55081987 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:70830446 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:70830446 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:20482617 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:20482617 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:20448753 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:20448753 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:81568734 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:81568734 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:236912738 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:236912738 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:39618663 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:39618663 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:33661863 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:33661863 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:178551969 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:178551969 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:70901767 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:70901767 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:100316543 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:100316543 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:241813511 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:241813511 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:86261449 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:86261449 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:116153920 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:116153920 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:110951169 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:110951169 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:43905664 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:43905664 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:38574615 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:38574615 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:108315708 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:108315708 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:14797483 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:14797483 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:99166796 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:99166796 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26621310 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26621310 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26646139 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26646139 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:90340610 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:90340610 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:29386559 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:29386559 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:39358302 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:39358302 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:36541706 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:36541706 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:23874609 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:23874609 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:27327843 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:27327843 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:153804120 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:153804120 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:62337214 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:62337214 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:57867566 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:57867566 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:156908398 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:156908398 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7523278 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7523278 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:58825771 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:58825771 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:160395108 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:160395108 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:51064136 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:51064136 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:3022001 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:3022001 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:97498561 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:97498561 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:62550768 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:62550768 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:197053651 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:197053651 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:119903519 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:119903519 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:1387843 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:1387843 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:175939288 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:175939288 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:77264813 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:77264813 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:57743866 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:57743866 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:41745579 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:41745579 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:11039158 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:11039158 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:215610600 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:215610600 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:60679830 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:60679830 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:96703585 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:96703585 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:65494498 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:65494498 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:60273119 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:60273119 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:61869229 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:61869229 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:22051704 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:22051704 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:16775670 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:16775670 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30104164 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30104164 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:36953269 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:36953269 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:140487387 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:140487387 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:41201262 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:41201262 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:79948344 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:79948344 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:26465745 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:26465745 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:96972520 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:96972520 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:103783346 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:103783346 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:103783389 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:103783389 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:244756637 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:244756637 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:210016685 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:210016685 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:179478582 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:179478582 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:20071685 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:20071685 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:17951075 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:17951075 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:45947089 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:45947089 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:33642124 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:33642124 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:44931340 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:44931340 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:105959691 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:105959691 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:99891039 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:99891039 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:111849174 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:111849174 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:43490698 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:43490698 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:41160553 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:41160553 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:74073170 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:74073170 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:36294172 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:36294172 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:71298474 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:71298474 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:127902227 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:127902227 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:49987875 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:49987875 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:27884610 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:27884610 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:7799432 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:7799432 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:97718384 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:97718384 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:116190610 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:116190610 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:27561470 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:27561470 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:35676227 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:35676227 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:65130149 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:65130149 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:13418717 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:13418717 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18439998 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18439998 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18440045 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18440045 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18795553 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18795553 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:86028483 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:86028483 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:14990163 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:14990163 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:71275272 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:71275272 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:49899951 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:49899951 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:64950569 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:64950569 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:75741387 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:75741387 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:111303474 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:111303474 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:25302540 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:25302540 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:104904887 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:104904887 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:70205762 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:70205762 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:66541771 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:66541771 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:92926564 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:92926564 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:179742555 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:179742555 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:77265624 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:77265624 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:180377195 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:180377195 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:191078965 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:191078965 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:30446050 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:30446050 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160810928 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160810928 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:72538992 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:72538992 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160518220 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160518220 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:49852427 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:49852427 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:193219877 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:193219877 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:174231808 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:174231808 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:21842475 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:21842475 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:26902526 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:26902526 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:37686772 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:37686772 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:40041401 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:40041401 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:14869929 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:14869929 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:15809915 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:15809915 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:214791840 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:214791840 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:214830197 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:214830197 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:49448833 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:49448833 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:40116532 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:40116532 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:53319681 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:53319681 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:23768978 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:23768978 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:34180419 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:34180419 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:113513458 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:113513458 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:45491439 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:45491439 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:9791174 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:9791174 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:87660174 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:87660174 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:74535811 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:74535811 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:2787143 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:2787143 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:2967298 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:2967298 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:125521464 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:125521464 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:103388867 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:103388867 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:103400538 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:103400538 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:75811565 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:75811565 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:101817684 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:101817684 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:55988988 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:55988988 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:177666128 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:177666128 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:86430756 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:86430756 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:7420253 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:7420253 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:111134846 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:111134846 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107826235 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107826235 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107412956 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107412956 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107437625 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:107437625 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:189927868 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:189927868 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:3665247 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:3665247 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:31294239 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:31294239 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:47462119 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:47462119 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:129908680 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:129908680 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:148905795 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:148905795 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:197192286 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:197192286 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:28609915 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:28609915 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:159684362 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:159684362 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:122724858 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:122724858 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:113267696 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:113267696 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:113563125 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:113563125 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:71110522 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:71110522 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:122950202 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:122950202 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:80085025 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:80085025 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:88029177 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:88029177 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:55948815 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:55948815 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:101871018 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:101871018 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:22960688 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:22960688 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:135352537 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:135352537 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:15806583 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:15806583 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:15659138 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:15659138 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:121929323 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:121929323 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:136517328 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:136517328 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:172314296 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:172314296 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:167944258 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:167944258 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160195229 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:160195229 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:17426837 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:17426837 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110714688 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110714688 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110714691 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110714691 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:108811238 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:108811238 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:47859007 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:47859007 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:113607473 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:113607473 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:16135459 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:16135459 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:220288597 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:220288597 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:69397578 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:69397578 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:185882894 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:185882894 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:125451530 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:125451530 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:125452995 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:125452995 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:83243647 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:83243647 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:78351538 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:78351538 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:124311114 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:124311114 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6587783 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6587783 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:31389051 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:31389051 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:169188645 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:169188645 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:169494413 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:169494413 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:169507095 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:169507095 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:109023310 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:109023310 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:42064700 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:42064700 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:32418943 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:32418943 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:5790420 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:5790420 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:30452729 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:30452729 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:102486119 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:102486119 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:172586208 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:172586208 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:44001324 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:44001324 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:71762365 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:71762365 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:139134499 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:139134499 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:42959152 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:42959152 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:38463129 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:38463129 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:37367024 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:37367024 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:23764885 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:23764885 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:50663022 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:50663022 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:37284090 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:37284090 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:111441532 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:111441532 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:120608212 C>A maps to NM_006209.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:120608212 C>A maps to NM_006209.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:132498023 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:132498023 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:111598059 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:111598059 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:111956427 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:111956427 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:16451704 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:16451704 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:89457407 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:89457407 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:66230704 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:66230704 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:97329756 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:97329756 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:142566518 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:142566518 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:220170737 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:220170737 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:37866522 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:37866522 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:212568780 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:212568780 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:56207604 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:56207604 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:54277783 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:54277783 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:158591575 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:158591575 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:22837359 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:22837359 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:133767754 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:133767754 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:133833681 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:133833681 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:88422680 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:88422680 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:70052580 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:70052580 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:175906004 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:175906004 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:14765733 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:14765733 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:14816765 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:14816765 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:131840262 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:131840262 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15262763 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15262763 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15838252 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15838252 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:15410342 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:15410342 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:24977272 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:24977272 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:49203989 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:49203989 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:89882413 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:89882413 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:10067892 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:10067892 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:99042121 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:99042121 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:126401101 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:126401101 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:13679440 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:13679440 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:137778214 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:137778214 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:157659956 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:157659956 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:53385809 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:53385809 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:38275299 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:38275299 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:97054036 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:97054036 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:67270783 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:67270783 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:72441307 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:72441307 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:33014682 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:33014682 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:153592548 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:153592548 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:65415484 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:65415484 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:114268855 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:114268855 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:52271878 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:52271878 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:39431936 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:39431936 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:13838384 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:13838384 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:48603933 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:48603933 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:32808578 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:32808578 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:17489064 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:17489064 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:151060785 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:151060785 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:161118888 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:161118888 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:161576337 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:161576337 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:26534747 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:26534747 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:30875485 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:30875485 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:88419943 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:88419943 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:24123492 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:24123492 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:92078043 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:92078043 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:89599177 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:89599177 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:163005715 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:163005715 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:120576408 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:120576408 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:74863114 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:74863114 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:158372286 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:158372286 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:118028882 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:118028882 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:55223965 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:55223965 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:38880862 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:38880862 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:25397889 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:25397889 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:20797638 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:20797638 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:134147209 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:134147209 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:121736177 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:121736177 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:175564773 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:175564773 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:131958440 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:131958440 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:175324841 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:175324841 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:90159563 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:90159563 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:141535482 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:141535482 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:146669705 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:146669705 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:7456888 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:7456888 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:52701244 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:52701244 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:228333807 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:228333807 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:135299731 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:135299731 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:30662550 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:30662550 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:155255849 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:155255849 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:37306242 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:37306242 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:43503438 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:43503438 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:66712590 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:66712590 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:124792768 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:124792768 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:28451170 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:28451170 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30006373 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30006373 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:14924070 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:14924070 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:12136196 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:12136196 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:29974691 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:29974691 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:185986058 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:185986058 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:162900350 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:162900350 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:43058122 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:43058122 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:54675050 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:54675050 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:30500294 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:30500294 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:119988062 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:119988062 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:148843382 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:148843382 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:87680718 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:87680718 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:88041056 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:88041056 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:220284292 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:220284292 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:148582473 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:148582473 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:21209226 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:21209226 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:47119022 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:47119022 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:160431832 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:160431832 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:111656055 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:111656055 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:190363738 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:190363738 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:3117725 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:3117725 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:27375237 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:27375237 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:15257143 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:15257143 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:156813924 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:156813924 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7172530 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7172530 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:75871614 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:75871614 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:123142544 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:123142544 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:44171363 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:44171363 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:68643858 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:68643858 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:26806742 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:26806742 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:39927834 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:39927834 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:124048911 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:124048911 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:88792822 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:88792822 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:2798315 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:2798315 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:138647048 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:138647048 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:138648680 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:138648680 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:36455031 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:36455031 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:48887436 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:48887436 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:35907737 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:35907737 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:22602916 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:22602916 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:27640205 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:27640205 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:175777569 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:175777569 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:16362298 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:16362298 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:16488513 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:16488513 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:51900309 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:51900309 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:132051342 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:132051342 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:170001193 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:170001193 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:20805122 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:20805122 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51517962 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51517962 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51581197 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51581197 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:39594726 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:39594726 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:52886346 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:52886346 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32410538 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32410538 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:153135153 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:153135153 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:50713737 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:50713737 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:71553379 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:71553379 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:6985218 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:6985218 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:129712465 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:129712465 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:21343291 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:21343291 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:119562497 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:119562497 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:152770266 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:152770266 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:53313871 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:53313871 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:189688704 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:189688704 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:71953250 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:71953250 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:104309480 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:104309480 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:54848103 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:54848103 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:55176396 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:55176396 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:55176410 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:55176410 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:45715941 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:45715941 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:160968678 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:160968678 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:62679440 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:62679440 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:47260212 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:47260212 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:42368192 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:42368192 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:133932304 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:133932304 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:113616015 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:113616015 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141092220 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141092220 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141201814 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141201814 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141597484 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141597484 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141708031 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141708031 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:30362755 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:30362755 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:70650451 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:70650451 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:101564891 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:101564891 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:33335853 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:33335853 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:6626770 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:6626770 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:1997255 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:1997255 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:12043408 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:12043408 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7975483 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7975483 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:27686698 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:27686698 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:165110854 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:165110854 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:186980258 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:186980258 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:70895629 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:70895629 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:49959613 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:49959613 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:90424500 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:90424500 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:41888677 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:41888677 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:88767739 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:88767739 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:15468018 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:15468018 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141760102 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141760102 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:12230985 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:12230985 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:50926012 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:50926012 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:14345625 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:14345625 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:2043489 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:2043489 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:49446329 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:49446329 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:238443346 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:238443346 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:154859664 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:154859664 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:102824817 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:102824817 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:102662334 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:102662334 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158812245 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158812245 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158814024 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158814024 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:79177440 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:79177440 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:41958784 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:41958784 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:24726948 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:24726948 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:181019023 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:181019023 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:17905785 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:17905785 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:56020789 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:56020789 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:60563024 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:60563024 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:47656862 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:47656862 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:31713139 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:31713139 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:149907873 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:149907873 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9002339 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9002339 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9011577 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9011577 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9020884 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9020884 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:42343677 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:42343677 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:10408447 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:10408447 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:10545706 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:10545706 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:10366580 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:10366580 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:36696852 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:36696852 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:34883763 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:34883763 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:109845820 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:109845820 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:2057021 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:2057021 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:140264215 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:140264215 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:46083384 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:46083384 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:19905953 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:19905953 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:78593379 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:78593379 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:47049008 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:47049008 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:120383061 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:120383061 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:23931359 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:23931359 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:118976095 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:118976095 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:10979833 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:10979833 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:55983407 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:55983407 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:72646675 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:72646675 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:27069037 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:27069037 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:68215479 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:68215479 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:101571488 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:101571488 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:33370039 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:33370039 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:153665940 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:153665940 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:34873878 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:34873878 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:102594879 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:102594879 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:200080523 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:200080523 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:107872761 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:107872761 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:104179086 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:104179086 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2094510 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2094510 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:132016414 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:132016414 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:17332934 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:17332934 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:37331777 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:37331777 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:37358353 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:37358353 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:224468738 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:224468738 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15107483 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15107483 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:241760926 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:241760926 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:247695884 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:247695884 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:248138751 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:248138751 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:4660920 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:4660920 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56125160 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56125160 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:38883861 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:38883861 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:26750669 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:26750669 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:3807019 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:3807019 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:110395576 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:110395576 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:35513732 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:35513732 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:39591138 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:39591138 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:34739443 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:34739443 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:51483055 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:51483055 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140734677 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140734677 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:82508556 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:82508556 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:17445901 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:17445901 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:165806384 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:165806384 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:31793198 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:31793198 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:149311800 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:149311800 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:149312188 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:149312188 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:149312213 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:149312213 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:20381071 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:20381071 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:98041614 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:98041614 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:129782740 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:129782740 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:34505613 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:34505613 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:21084034 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:21084034 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:98383298 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:98383298 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:8808352 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:8808352 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:186862033 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:186862033 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:59814582 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:59814582 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:132109544 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:132109544 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:43992450 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:43992450 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:72188043 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:72188043 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:139306773 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:139306773 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:102944534 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:102944534 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7621678 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7621678 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:133256530 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:133256530 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:106889961 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:106889961 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:77765709 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:77765709 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:30097257 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:30097257 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:19571454 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:19571454 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:16287150 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:16287150 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:18748514 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:18748514 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:76805630 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:76805630 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:159638395 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:159638395 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:135720270 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:135720270 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:40542716 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:40542716 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:70980284 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:70980284 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:108138464 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:108138464 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:68950643 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:68950643 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:68967938 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:68967938 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:151262370 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:151262370 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:106768847 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:106768847 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:30194636 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:30194636 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:47200386 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:47200386 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:54040697 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:54040697 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:20529773 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:20529773 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:4705046 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:4705046 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:95953255 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:95953255 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:150980987 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:150980987 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:43576601 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:43576601 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:56174053 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:56174053 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:71437517 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:71437517 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:112890949 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:112890949 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:70925735 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:70925735 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:198723643 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:198723643 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:8341036 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:8341036 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:55702948 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:55702948 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:40709433 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:40709433 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:41076721 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:41076721 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:29644212 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:29644212 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:29647148 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:29647148 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:52287311 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:52287311 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:25273030 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:25273030 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:57913382 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:57913382 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:58022098 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:58022098 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:16222842 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:16222842 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:76253372 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:76253372 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:36018447 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:36018447 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:114385122 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:114385122 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:145610501 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:145610501 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:127950788 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:127950788 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:120337199 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:120337199 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:103215882 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:103215882 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:61145519 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:61145519 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:192613654 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:192613654 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:72921105 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:72921105 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:130898861 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:130898861 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:21044114 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:21044114 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:87106021 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:87106021 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:87866204 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:87866204 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:31406915 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:31406915 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:18406459 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:18406459 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:11448621 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:11448621 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:123699362 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:123699362 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:49120495 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:49120495 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:45212666 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:45212666 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:237619788 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:237619788 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:84815205 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:84815205 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:44372571 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:44372571 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:15882881 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:15882881 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:26691684 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:26691684 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38833766 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38833766 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:118015704 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:118015704 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38591729 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38591729 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:144874008 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:144874008 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:45916151 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:45916151 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:50304946 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:50304946 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:18516490 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:18516490 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:134032791 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:134032791 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:13971032 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:13971032 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:52474719 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:52474719 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:48052236 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:48052236 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:13380834 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:13380834 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:95057022 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:95057022 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:135158815 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:135158815 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:85894335 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:85894335 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51207297 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51207297 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:37974574 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:37974574 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:146248481 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:146248481 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:110918223 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:110918223 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:60098907 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:60098907 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:92374423 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:92374423 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:131114892 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:131114892 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:176824678 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:176824678 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18270150 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:18270150 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:125727505 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:125727505 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:57176803 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:57176803 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:10861573 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:10861573 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:368909 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:368909 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:20874723 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:20874723 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:20542994 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:20542994 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:168175100 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:168175100 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:12427195 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:12427195 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:84417472 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:84417472 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:121587220 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:121587220 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:51569656 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:51569656 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:108447927 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:108447927 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:53804597 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:53804597 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:142605294 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:142605294 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:35712823 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:35712823 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:220312668 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:220312668 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:44862613 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:44862613 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:136602830 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:136602830 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:167658830 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:167658830 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:51018679 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:51018679 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158607814 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158607814 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158644007 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158644007 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158646208 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158646208 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:6668411 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:6668411 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:206610200 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:206610200 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:85129903 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:85129903 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:44257711 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:44257711 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:104060049 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:104060049 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:104081785 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:104081785 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:152980524 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:152980524 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:74074992 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:74074992 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:25444046 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:25444046 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:27005003 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:27005003 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:29801631 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:29801631 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:58440720 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:58440720 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:64465094 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:64465094 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:38313334 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:38313334 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:13373496 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:13373496 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:153649129 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:153649129 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:38117270 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:38117270 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:28883889 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:28883889 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:36288038 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:36288038 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:106083811 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chrX:106083811 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:36611761 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:36611761 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2026980 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2026980 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:114841431 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:114841431 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:1627465 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:1627465 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:167791288 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:167791288 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:36553830 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:36553830 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:26902950 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:26902950 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:133947997 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:133947997 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:11445870 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:11445870 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32554687 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32554687 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:76115332 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:76115332 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:75968407 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:75968407 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:75969252 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:75969252 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:42525509 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:42525509 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:100324933 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:100324933 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:19653214 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:19653214 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:29664946 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:29664946 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:117827203 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:117827203 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:12267130 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:12267130 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:6667507 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:6667507 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:201334197 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:201334197 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:1491805 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:1491805 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:202275713 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:202275713 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:138268771 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:138268771 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:4622219 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:4622219 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:189064957 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:189064957 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:100465726 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:100465726 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:116631303 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:116631303 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:142572924 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:142572924 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:135787663 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:135787663 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2105534 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:2105534 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:120496857 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:120496857 T>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:98288649 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:98288649 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:166747253 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:166747253 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:179571691 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:179571691 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:37907198 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:37907198 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154229504 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154229504 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:39771667 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:39771667 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:69870881 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:69870881 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:69513258 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:69513258 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:176295774 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:176295774 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:35579916 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:35579916 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216262564 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216262564 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216538492 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216538492 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:57642901 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:57642901 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:171673539 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:171673539 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:6825422 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:6825422 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:101200326 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:101200326 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:82832690 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:82832690 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:86996336 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:86996336 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:134114736 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:134114736 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:122748447 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:122748447 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:60906351 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:60906351 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:117715127 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:117715127 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:61058827 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:61058827 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:27151878 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:27151878 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:177046588 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:177046588 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:10076964 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:10076964 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:109525410 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:109525410 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:109553410 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:109553410 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:124138433 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:124138433 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:37438087 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:37438087 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141419103 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141419103 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:968344 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:968344 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:40932641 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:40932641 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:32413443 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:32413443 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:168510483 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:168510483 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:31628751 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:31628751 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:111648230 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:111648230 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:217057339 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:217057339 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:21324712 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:21324712 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:138713708 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:138713708 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:88957849 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:88957849 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:144332656 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:144332656 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:57929096 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:57929096 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:32354565 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:32354565 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:53657126 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:53657126 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:28214173 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:28214173 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:44762276 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:44762276 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:56969661 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:56969661 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30537539 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30537539 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:37314697 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:37314697 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:29438579 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:29438579 A>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:21214690 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:21214690 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:136103031 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:136103031 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:12780811 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:12780811 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:48564092 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:48564092 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:39468319 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:39468319 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:73175254 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:73175254 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:74315042 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:74315042 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:78819668 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:78819668 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:129270250 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:129270250 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:129271010 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:129271010 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:38431291 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:38431291 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:38500864 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:38500864 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:25391657 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:25391657 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:41542219 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:41542219 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:114161741 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:114161741 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:36655978 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:36655978 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:23886819 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:23886819 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:11312992 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:11312992 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:17982962 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:17982962 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:176913171 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:176913171 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:23985259 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:23985259 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:150720843 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:150720843 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:50226742 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:50226742 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:76856099 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:76856099 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:32197660 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:32197660 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:31603922 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:31603922 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:33407244 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:33407244 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:64875036 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:64875036 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:45686403 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:45686403 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:95918723 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:95918723 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:209049627 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:209049627 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:125971689 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:125971689 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:48533865 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:48533865 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:181706656 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:181706656 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:44281963 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:44281963 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:2951988 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:2951988 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:34416496 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:34416496 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:167417724 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:167417724 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:111435177 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:111435177 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:21755992 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:21755992 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:26905970 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:26905970 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:15343481 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:15343481 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:27016276 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:27016276 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:150908235 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:150908235 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:70851854 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:70851854 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:107421878 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:107421878 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:189929403 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:189929403 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:109046013 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:109046013 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:131388393 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:131388393 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:125602100 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:125602100 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:8613720 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:8613720 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:197333009 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:197333009 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:46851259 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:46851259 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:68026233 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:68026233 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:77470450 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:77470450 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:11411627 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:11411627 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:25043049 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:25043049 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:49005504 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:49005504 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:49034415 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:49034415 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:99445236 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:99445236 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:48981445 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:48981445 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:85415593 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:85415593 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:43131429 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:43131429 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:31349615 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:31349615 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:24178869 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:24178869 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:69397411 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:69397411 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:35071469 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:35071469 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:31747956 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:31747956 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:52394177 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:52394177 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:234652077 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:234652077 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:98092367 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:98092367 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:57678864 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:57678864 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:82554001 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:82554001 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:42949676 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:42949676 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:8008846 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:8008846 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:39116584 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:39116584 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:184039950 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:184039950 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:131247614 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:131247614 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:56270501 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:56270501 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:158580835 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:158580835 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:45630118 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:45630118 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:133849756 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:133849756 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:187195501 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:187195501 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:46871628 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:46871628 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:8161028 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:8161028 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:102518755 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:102518755 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:102670653 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:102670653 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:69631241 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:69631241 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:152323007 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:152323007 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153594892 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153594892 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:171227131 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:171227131 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:47754083 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:47754083 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:109270707 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:109270707 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:94039628 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:94039628 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:14797459 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:14797459 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:37732489 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:37732489 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:12738517 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:12738517 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:48551738 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:48551738 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:4306111 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:4306111 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:31066562 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:31066562 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:151393208 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:151393208 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:151819144 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:151819144 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:26569895 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:26569895 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:130027143 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:130027143 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:134181164 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:134181164 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:175603948 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:175603948 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:132795751 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:132795751 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:67432222 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:67432222 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:37282893 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:37282893 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:110210924 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:110210924 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:106849534 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:106849534 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:7894771 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:7894771 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:36110834 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:36110834 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:41058130 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:41058130 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:43283496 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:43283496 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:124716732 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:124716732 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:65411881 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:65411881 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:120347142 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:120347142 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:81355130 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:81355130 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:21099837 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:21099837 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:160469621 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:160469621 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr22:17577831 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr22:17577831 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:102625946 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:102625946 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:6061545 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:6061545 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:35871066 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:35871066 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:62288602 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:62288602 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:38356973 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:38356973 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:77690190 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:77690190 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:31425591 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:31425591 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:31435088 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:31435088 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:30529242 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:30529242 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:133966533 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:133966533 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:124281950 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:124281950 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:63416779 T>C maps to ENST00000453406 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:63416779 T>C maps to ENST00000453406 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:169780999 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:169780999 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:21918602 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:21918602 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:53241141 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:53241141 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:136555067 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:136555067 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:19569060 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:19569060 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:47157459 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:47157459 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:8793131 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:8793131 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:94120394 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:94120394 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:118687291 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:118687291 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:175220264 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:175220264 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:55278619 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:55278619 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:31210438 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:31210438 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:25958137 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:25958137 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:55179299 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:55179299 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:100906996 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:100906996 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:24784870 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:24784870 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:166987219 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:166987219 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:119749987 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:119749987 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:84125474 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:84125474 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:74899329 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:74899329 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:43207956 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:43207956 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:39706100 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:39706100 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:151891052 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:151891052 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:154889843 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:154889843 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:154009496 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:154009496 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:71530116 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:71530116 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:60233378 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:60233378 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:60105492 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:60105492 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:76345886 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:76345886 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:151358402 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:151358402 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:15892588 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:15892588 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:33584584 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:33584584 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:10322187 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:10322187 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:2678400 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:2678400 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:109847329 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:109847329 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:40103676 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:40103676 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:40133634 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:40133634 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:22696659 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:22696659 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:75562936 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:75562936 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:84024275 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:84024275 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:14125573 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:14125573 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:15295950 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:15295950 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:179544698 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:179544698 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:106374913 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:106374913 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:101093395 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:101093395 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:148730984 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:148730984 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:23792709 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:23792709 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:9524979 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:9524979 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:176585642 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:176585642 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:162990379 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:162990379 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:150828401 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:150828401 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74733843 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74733843 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:144875860 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:144875860 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:18944493 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:18944493 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:17111599 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:17111599 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:18276919 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:18276919 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:130435221 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:130435221 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:102051012 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:102051012 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:146307685 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:146307685 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153700005 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:153700005 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:24906285 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:24906285 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:27845693 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:27845693 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:23509926 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:23509926 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:227075894 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:227075894 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:8484411 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:8484411 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:136403120 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:136403120 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:17699714 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:17699714 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:45222662 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:45222662 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:170679246 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:170679246 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:33134047 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:33134047 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:47034361 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:47034361 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:17065625 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:17065625 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:34409539 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:34409539 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:106977023 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:106977023 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:240978226 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:240978226 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:152315444 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:152315444 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:78681814 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:78681814 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:45997241 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:45997241 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:165377565 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:165377565 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237817547 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237817547 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237880482 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237880482 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:3377959 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:3377959 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:151345020 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:151345020 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:9202062 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:9202062 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:118767555 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:118767555 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:61562435 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:61562435 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:81318867 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:81318867 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:104495587 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:104495587 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:51628840 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:51628840 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:164733967 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:164733967 T>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:44672621 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:44672621 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:62931251 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:62931251 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:63066368 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:63066368 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:62948378 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:62948378 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:95822309 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:95822309 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:196599805 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:196599805 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:190430007 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:190430007 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:125731286 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:125731286 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:42334954 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:42334954 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr22:32445884 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr22:32445884 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:21359076 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:21359076 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:168201216 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:168201216 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:130930281 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:130930281 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:186284531 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:186284531 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:179312162 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:179312162 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:106802788 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:106802788 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:24048664 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:24048664 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:35670142 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:35670142 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:23612329 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:23612329 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:48218133 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:48218133 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:53155417 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:53155417 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:70599987 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:70599987 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:115455571 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:115455571 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:70677996 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:70677996 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:142880398 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:142880398 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:100997604 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:100997604 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:107133843 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:107133843 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:114841541 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:114841541 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:59633783 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:59633783 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:124181820 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:124181820 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:115973035 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:115973035 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:104474739 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:104474739 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:36784513 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:36784513 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:114014387 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:114014387 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:56827312 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:56827312 A>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:75435732 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:75435732 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:45101854 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:45101854 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:10971749 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:10971749 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:30114995 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:30114995 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:248039831 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:248039831 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:20767059 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:20767059 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:99890829 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:99890829 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:234676636 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:234676636 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:35396702 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:35396702 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:17522926 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:17522926 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:23101908 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:23101908 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:155119027 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:155119027 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:29136534 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:29136534 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:31596901 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:31596901 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:166960201 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:166960201 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:1197228 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:1197228 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:70471018 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:70471018 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:293307 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:293307 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:9583989 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:9583989 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:53207839 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:53207839 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:46315354 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chrX:46315354 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:136268724 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:136268724 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:45508773 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:45508773 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr15:43637889 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr15:43637889 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:6331845 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:6331845 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:99071360 A>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:99071360 A>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:31625729 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:31625729 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:110477257 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:110477257 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr14:67826328 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr14:67826328 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:40953973 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:40953973 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:37450920 G>A maps to ENST00000373405 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:37450920 G>A maps to ENST00000373405 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr16:55883472 T>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr16:55883472 T>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:6184514 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:6184514 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:11889223 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:11889223 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:131404817 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:131404817 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr10:16932280 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr10:16932280 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:186303110 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:186303110 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr5:169138887 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr5:169138887 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr21:37541592 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr21:37541592 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:102291788 A>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:102291788 A>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr8:124975488 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr8:124975488 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr15:91421973 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr15:91421973 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr4:47034147 C>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr4:47034147 C>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:100977279 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:100977279 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:46177477 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:46177477 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:24467286 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:24467286 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:108635108 T>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:108635108 T>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:42155732 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:42155732 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:33095785 A>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr6:33095785 A>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr7:150656628 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr7:150656628 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr13:42265334 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr13:42265334 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:44145081 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:44145081 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:39661140 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:39661140 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:38905655 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:38905655 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:37886186 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:37886186 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:12649170 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:12649170 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr20:33320356 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr20:33320356 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:888049 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:888049 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:208225579 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:208225579 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr4:2083497 A>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr4:2083497 A>G did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr7:106768781 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr7:106768781 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:123595862 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:123595862 T>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:65427375 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:65427375 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:49737089 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:49737089 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:137328231 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:137328231 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:11258799 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:11258799 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:104093056 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:104093056 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:40489766 A>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:40489766 A>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:101014038 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr9:101014038 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr2:171906238 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr2:171906238 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:52889346 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:52889346 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:100496451 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr12:100496451 G>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:111986758 G>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:111986758 G>C did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:9730016 A>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr19:9730016 A>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:249151918 C>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:249151918 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:35616199 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:35616199 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:89382383 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:89382383 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:147127386 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:147127386 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:236900394 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:236900394 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:161162112 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:161162112 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:43941375 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:43941375 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr9:140074621 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr9:140074621 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:41566186 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:41566186 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:1554720 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:1554720 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:50238753 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:50238753 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:3471344 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:3471344 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:28531272 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:28531272 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:79979211 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:79979211 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:95923354 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:95923354 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:81009985 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:81009985 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:80363182 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:80363182 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:14801514 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:14801514 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:133095456 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:133095456 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:34214748 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:34214748 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr9:95875264 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr9:95875264 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:538070 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:538070 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:69983505 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:69983505 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:227213905 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:227213905 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:205496073 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:205496073 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:120313852 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:120313852 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:62212352 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:62212352 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:6990126 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:6990126 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:87670099 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:87670099 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:58614701 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:58614701 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:109895626 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:109895626 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:43018252 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:43018252 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:6477475 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:6477475 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:140960301 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:140960301 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:76547780 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:76547780 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:63976309 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:63976309 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:25897472 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr8:25897472 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:13624395 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:13624395 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:29621066 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:29621066 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:74443821 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:74443821 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:212615500 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:212615500 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:39762834 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:39762834 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:103498714 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:103498714 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:138194933 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:138194933 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:45811775 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:45811775 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:50284762 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:50284762 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:93160133 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:93160133 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:150980966 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:150980966 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:127866420 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:127866420 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:37457330 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:37457330 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:48421079 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:48421079 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:63979042 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:63979042 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:114292160 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:114292160 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:48622483 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:48622483 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:53990589 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:53990589 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:100551616 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:100551616 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:120823750 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:120823750 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr9:19078075 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr9:19078075 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:5255512 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:5255512 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:185958556 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:185958556 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:147830969 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:147830969 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:1616432 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:1616432 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:61909119 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:61909119 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:31429342 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:31429342 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:52851978 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:52851978 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:18200617 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:18200617 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:202731751 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:202731751 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:19455990 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:19455990 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:55378196 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:55378196 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr10:135010457 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr10:135010457 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:201351491 A>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:201351491 A>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:129794507 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:129794507 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:141459869 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:141459869 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:44145099 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:44145099 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:47610985 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:47610985 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:47648331 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:47648331 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:30133362 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:30133362 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:119742038 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:119742038 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:49441647 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:49441647 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:168353015 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:168353015 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr18:48327641 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr18:48327641 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:32270863 A>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:32270863 A>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:9730588 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:9730588 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:36678578 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:36678578 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:672622 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:672622 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:57436771 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:57436771 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:32260122 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:32260122 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:55421371 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:55421371 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179226636 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179226636 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:226549293 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:226549293 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:44532417 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:44532417 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:20704889 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:20704889 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:26448203 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:26448203 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:15477693 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:15477693 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr10:118354422 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr10:118354422 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:43222003 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:43222003 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:61952520 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:61952520 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:99027448 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:99027448 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:192778177 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:192778177 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:151168338 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:151168338 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:30528161 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:30528161 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:25439215 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:25439215 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:49993862 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:49993862 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:179025937 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:179025937 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:9817535 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:9817535 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:76797375 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:76797375 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:166221825 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:166221825 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:243430922 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:243430922 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:8220096 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:8220096 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:18234029 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:18234029 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:48385896 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:48385896 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:1064119 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:1064119 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:116580052 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:116580052 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:3209406 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:3209406 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:21446806 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:21446806 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:33680276 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:33680276 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:33690839 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:33690839 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:34207293 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:34207293 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:3759336 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:3759336 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:52684374 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:52684374 A>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:41244289 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:41244289 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:70678258 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:70678258 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:150460017 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:150460017 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:101395653 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:101395653 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:66547834 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:66547834 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:4294443 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:4294443 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:101294713 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:101294713 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:10909656 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:10909656 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:33632262 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:33632262 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179617815 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179617815 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179639635 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179639635 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:8119396 A>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:8119396 A>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:34934960 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:34934960 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:216138892 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:216138892 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:30216228 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:30216228 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:62164182 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:62164182 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:85609062 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:85609062 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:177071545 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:177071545 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:76747210 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:76747210 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:123019495 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:123019495 C>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:64814468 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr12:64814468 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:11870041 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:11870041 G>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:62364769 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:62364769 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:56981156 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:56981156 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:180307909 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:180307909 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:58301465 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:58301465 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:47747305 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chrX:47747305 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:67018059 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:67018059 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:48204198 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:48204198 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:101604055 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:101604055 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:20556391 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:20556391 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:39525482 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:39525482 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:156936221 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:156936221 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:77369844 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:77369844 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:88027133 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:88027133 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:58128352 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:58128352 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:233323243 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:233323243 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:41522309 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:41522309 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:431687 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:431687 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:21255221 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:21255221 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:156928982 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:156928982 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:2876490 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:2876490 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:197091437 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:197091437 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:3910965 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:3910965 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:64664163 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:64664163 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:194182841 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:194182841 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:55329661 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:55329661 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:79389318 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:79389318 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:31601478 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:31601478 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:31601482 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:31601482 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:11412770 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:11412770 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:34922316 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:34922316 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76158105 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76158105 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:48882867 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:48882867 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:72952105 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:72952105 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:179426077 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:179426077 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:112018546 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:112018546 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:156264459 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:156264459 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:33679250 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:33679250 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:57347347 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:57347347 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:39308253 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:39308253 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:39331765 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:39331765 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:50212394 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:50212394 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:86180891 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:86180891 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:53821130 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:53821130 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:181690809 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:181690809 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:44274205 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:44274205 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:86125710 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:86125710 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:34344821 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:34344821 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:30313081 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:30313081 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:60893344 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:60893344 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:174223871 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:174223871 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:61749321 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:61749321 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:843996 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:843996 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:74447648 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:74447648 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:87674069 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:87674069 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:147259225 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:147259225 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:23456225 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:23456225 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:121243688 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:121243688 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:139706688 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:139706688 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:139819812 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:139819812 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:139833358 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:139833358 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:111083125 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:111083125 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:107438144 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:107438144 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:137713783 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:137713783 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:3691244 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:3691244 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:1247189 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:1247189 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:151904629 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:151904629 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:34011857 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:34011857 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:34209243 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:34209243 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:148929562 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:148929562 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:23472292 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:23472292 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:1207165 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:1207165 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:10794643 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:10794643 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:1780046 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:1780046 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:25044045 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:25044045 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:59787176 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:59787176 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:86070991 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:86070991 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:122075667 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:122075667 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:50977050 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:50977050 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:50994219 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:50994219 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:110644576 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:110644576 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:117168529 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:117168529 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:1626371 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:1626371 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:53930524 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:53930524 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:52426819 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:52426819 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:13829601 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:13829601 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:100851497 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:100851497 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:172007680 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:172007680 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:169509998 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:169509998 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:441748 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:441748 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr21:37584191 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr21:37584191 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57671825 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57671825 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:1273344 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:1273344 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:71817451 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:71817451 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:236572481 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:236572481 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:28386770 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:28386770 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:117657217 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:117657217 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:119307832 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:119307832 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:185038298 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:185038298 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:134514682 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:134514682 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:128046548 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:128046548 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:95677301 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:95677301 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:5564435 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:5564435 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:143421908 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:143421908 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:45718429 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:45718429 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:10672736 G>C maps to NM_022068.2 V2652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:10672736 G>C maps to NM_022068.2 V2652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:153674681 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:153674681 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:13729761 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:13729761 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:242418424 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:242418424 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:48818507 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:48818507 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:48905427 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:48905427 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:157767629 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:157767629 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:42927176 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:42927176 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:79103288 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:79103288 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:4312057 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:4312057 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:52781060 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:52781060 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:33311195 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:33311195 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:100973873 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:100973873 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:22729379 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:22729379 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:926183 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:926183 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:14622548 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:14622548 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:4855201 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:4855201 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:220364541 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:220364541 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:50231850 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:50231850 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:28808314 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:28808314 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:25840181 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:25840181 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:13095309 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:13095309 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:86468103 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:86468103 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:19136548 C>T maps to NM_005315.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:19136548 C>T maps to NM_005315.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:130774812 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:130774812 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:19380735 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:19380735 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:84353494 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:84353494 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:65479882 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:65479882 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:89414139 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:89414139 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:149857804 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:149857804 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:120302033 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:120302033 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:21083526 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:21083526 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:82923772 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:82923772 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:79094106 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:79094106 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:130411722 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:130411722 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:130419502 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:130419502 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:81578229 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:81578229 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:55210620 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:55210620 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:15200003 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:15200003 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:15212427 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:15212427 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:396951 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:396951 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:54780335 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:54780335 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:7679143 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:7679143 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:227920041 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:227920041 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:124436268 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:124436268 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:150646172 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:150646172 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:99441776 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:99441776 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:422055 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:422055 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:55980530 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:55980530 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:142659145 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:142659145 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:34242122 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:34242122 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:33374667 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:33374667 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:55341915 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:55341915 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:55354425 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:55354425 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:86869413 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:86869413 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:122152479 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:122152479 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:53202334 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:53202334 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr21:31914168 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr21:31914168 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:107600785 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:107600785 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:48624241 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:48624241 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:141609388 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:141609388 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:70505514 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:70505514 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:40618847 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:40618847 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:102108992 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:102108992 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:43822176 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:43822176 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:43351998 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:43351998 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:94882709 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:94882709 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:31465926 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:31465926 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:132329612 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:132329612 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:55539368 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:55539368 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:60159969 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:60159969 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:816878 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:816878 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:56670938 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:56670938 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:1096272 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:1096272 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:10223650 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:10223650 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:23897917 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:23897917 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:192272961 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:192272961 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936241 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936241 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936389 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936389 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:16056803 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:16056803 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:45269001 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:45269001 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:70502464 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:70502464 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:52535775 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:52535775 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:69375416 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:69375416 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:39988775 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:39988775 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:156841341 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:156841341 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:27621145 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:27621145 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:13361195 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:13361195 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:102332503 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:102332503 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:123556614 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:123556614 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:143747362 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:143747362 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:179260132 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:179260132 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:26739540 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:26739540 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:94510857 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:94510857 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:146076982 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:146076982 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:111964311 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:111964311 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:40564326 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:40564326 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:150839502 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:150839502 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:82456081 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:82456081 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr21:47831065 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr21:47831065 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:195969347 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:195969347 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:105204593 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:105204593 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:107551225 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:107551225 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:31908631 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:31908631 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:179597585 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:179597585 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:77026760 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:77026760 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:111539233 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:111539233 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:51655913 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:51655913 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:51934391 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:51934391 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:59812352 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:59812352 A>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:23691649 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:23691649 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:20944819 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:20944819 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:145609338 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:145609338 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:38160134 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:38160134 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:58733924 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:58733924 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:9594954 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:9594954 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:57145326 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:57145326 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:64142762 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:64142762 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:6527019 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:6527019 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:3530235 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chrX:3530235 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:3692377 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:3692377 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:93593250 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:93593250 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:142459543 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:142459543 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:43687514 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:43687514 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:209309304 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:209309304 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:49196153 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:49196153 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:8518456 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:8518456 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:8633140 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:8633140 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:157361512 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:157361512 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:157691349 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:157691349 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:136433175 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:136433175 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:4861955 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:4861955 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:85774497 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:85774497 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:173830168 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:173830168 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:22349538 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:22349538 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:49223989 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:49223989 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:150073580 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:150073580 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:17747099 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:17747099 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:9801289 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:9801289 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:117248781 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:117248781 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:121287107 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:121287107 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:3388074 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:3388074 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:72921307 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:72921307 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:240978133 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:240978133 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:31529238 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:31529238 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:79638901 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:79638901 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:114309075 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:114309075 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:237756989 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:237756989 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:237802537 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:237802537 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:130466427 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:130466427 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:50832574 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:50832574 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:68377237 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:68377237 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:155228816 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:155228816 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:38967097 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:38967097 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:123509034 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:123509034 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:38639473 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:38639473 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:43605995 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:43605995 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:71427593 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:71427593 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:83774605 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:83774605 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:67155076 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:67155076 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:113303642 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:113303642 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:1695554 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:1695554 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:100774745 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:100774745 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:64337060 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:64337060 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:38355520 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:38355520 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:116569708 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:116569708 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:28548545 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:28548545 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:130912942 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:130912942 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:246093296 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:246093296 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:231367882 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:231367882 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:52938324 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:52938324 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:167658519 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:167658519 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:53049135 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:53049135 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:53076714 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:53076714 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:191841513 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:191841513 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:27099176 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:27099176 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:46294925 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:46294925 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:113212225 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:113212225 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:105139623 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:105139623 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:96152711 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:96152711 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:90489426 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:90489426 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:11513937 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:11513937 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:72699321 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:72699321 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:37470785 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:37470785 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:2408683 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:2408683 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:47384333 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:47384333 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:154155628 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:154155628 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:211534209 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:211534209 A>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:67062331 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:67062331 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:142625964 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:142625964 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:122680630 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:122680630 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:76183197 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:76183197 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:103354652 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:103354652 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:70066084 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:70066084 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:35954588 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:35954588 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:41504778 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:41504778 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:73780791 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:73780791 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:216052522 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:216052522 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:216219955 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:216219955 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:55547284 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:55547284 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:30226771 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:30226771 T>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:177650633 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:177650633 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:12348414 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:12348414 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:52991146 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:52991146 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:184648227 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:184648227 G>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:177098355 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:177098355 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:1126222 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:1126222 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:1171007 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:1171007 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:241943423 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:241943423 T>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:28145342 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:28145342 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:17228666 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:17228666 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:89061322 G>T maps to NM_207662.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:89061322 G>T maps to NM_207662.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57932862 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57932862 A>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:21606299 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:21606299 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:116968504 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:116968504 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:87150766 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:87150766 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:100617783 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:100617783 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:116211625 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:116211625 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:43213399 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:43213399 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:31351224 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:31351224 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:185709702 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:185709702 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:3517753 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:3517753 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:87957939 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:87957939 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:91651732 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:91651732 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:105243413 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:105243413 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:27542016 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:27542016 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:25033722 C>A maps to NM_139058.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:25033722 C>A maps to NM_139058.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:26153117 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:26153117 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:70255993 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:70255993 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr21:11047543 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr21:11047543 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:17276075 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:17276075 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:112998029 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:112998029 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:112999310 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:112999310 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:113003078 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:113003078 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:32145137 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:32145137 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:78235011 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:78235011 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:114436063 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:114436063 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:36633432 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:36633432 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:74710142 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:74710142 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr18:64236021 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr18:64236021 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:138291784 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:138291784 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr15:57815641 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr15:57815641 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr21:36088930 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr21:36088930 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:17342498 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:17342498 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:103453302 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:103453302 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:70881787 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:70881787 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:109780971 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:109780971 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:227920541 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:227920541 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:18895272 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:18895272 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr18:47808910 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr18:47808910 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:202931530 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:202931530 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:20160569 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:20160569 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:47845539 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:47845539 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:5366833 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:5366833 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:38158601 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:38158601 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:56212686 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:56212686 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:111462375 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:111462375 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:98012717 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:98012717 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:76855300 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:76855300 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:20402458 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:20402458 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:141570352 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:141570352 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:56487512 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:56487512 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:13949471 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:13949471 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:139209936 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:139209936 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:45489972 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:45489972 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:16111174 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:16111174 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:42939842 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:42939842 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:64010858 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:64010858 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:64011204 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:64011204 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:89953590 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:89953590 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:144644329 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:144644329 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:73985932 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:73985932 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:42841692 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:42841692 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:48018981 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:48018981 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:38348711 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:38348711 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:182391939 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:182391939 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:11304854 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:11304854 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:32740257 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:32740257 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:32741852 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:32741852 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:136558027 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:136558027 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:103868123 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:103868123 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:11224163 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:11224163 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:141200286 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:141200286 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:70502362 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:70502362 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:70502404 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:70502404 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:24518650 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:24518650 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:143845995 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:143845995 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:65373666 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:65373666 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:113738166 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:113738166 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:151101512 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:151101512 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:42849058 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:42849058 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:158538124 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:158538124 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:131147948 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:131147948 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:66205804 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:66205804 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:36453339 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:36453339 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:76349620 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:76349620 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:100512724 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:100512724 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:10442348 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:10442348 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:15542279 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:15542279 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:21124653 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:21124653 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:110941953 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:110941953 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:34791595 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:34791595 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:52306293 A>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:52306293 A>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:51206466 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:51206466 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:132306922 A>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:132306922 A>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:102584788 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:102584788 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:79862845 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:79862845 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:107551138 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:107551138 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:10687492 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:10687492 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:118512944 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:118512944 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:605794 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:605794 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:209141396 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:209141396 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:3206125 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:3206125 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:8862201 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:8862201 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:67862367 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:67862367 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr16:90130187 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr16:90130187 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:64089012 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:64089012 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:61728164 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:61728164 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:4905221 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:4905221 A>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:22175613 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:22175613 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:150036956 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:150036956 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:38997203 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:38997203 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:153509701 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:153509701 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:50246602 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:50246602 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:113871875 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:113871875 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:9054012 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:9054012 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:14166722 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:14166722 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:15297857 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:15297857 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:51645441 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:51645441 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:4865547 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:4865547 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:176821245 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:176821245 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:84455674 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:84455674 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr16:18826740 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr16:18826740 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:183484895 T>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:183484895 T>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:153633646 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:153633646 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:51465788 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:51465788 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:158331086 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:158331086 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:53498109 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:53498109 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:95364315 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:95364315 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:41008235 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:41008235 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:153047751 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:153047751 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:52674308 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:52674308 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:86067631 C>A maps to ENST00000393803 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:86067631 C>A maps to ENST00000393803 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:57495988 T>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:57495988 T>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:87910054 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:87910054 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:108872194 A>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:108872194 A>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730603 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730603 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730635 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730635 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:75876618 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:75876618 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:17747624 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:17747624 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:100451280 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:100451280 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:109352125 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chrX:109352125 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:74808403 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:74808403 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:189582012 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:189582012 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:38237471 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:38237471 G>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:49845952 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:49845952 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr15:54793191 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr15:54793191 T>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:35605997 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:35605997 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:113700168 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:113700168 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:144769929 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:144769929 C>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:33239328 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:33239328 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:52234722 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:52234722 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:41322588 T>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:41322588 T>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:41347290 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:41347290 C>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:848867 C>G did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:848867 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:52603575 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:52603575 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:7714772 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:7714772 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:215823922 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:215823922 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:215928674 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:215928674 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:67113956 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:67113956 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:67028171 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:67028171 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:100493988 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:100493988 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:34184114 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:34184114 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:226376846 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:226376846 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:55065188 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:55065188 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20482755 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20482755 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20552209 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20552209 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20563830 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20563830 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:158656062 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:158656062 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:33751700 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:33751700 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:77325412 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:77325412 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:28213286 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:28213286 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:130276059 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:130276059 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:145617133 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:145617133 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:147744372 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:147744372 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:87531186 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:87531186 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:100347087 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:100347087 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:109667836 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:109667836 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:34998785 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:34998785 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:21329870 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:21329870 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:77987426 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:77987426 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:96912749 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:96912749 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:5246487 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:5246487 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:101434373 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:101434373 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:3730687 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:3730687 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:113353770 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:113353770 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:85674297 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:85674297 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:85694888 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:85694888 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:111214510 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:111214510 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:53817784 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:53817784 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:115231371 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:115231371 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:38516427 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:38516427 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:108306100 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:108306100 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:41615423 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:41615423 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:62444366 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:62444366 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:54526382 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:54526382 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:111553079 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:111553079 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:5961103 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:5961103 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:101462131 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:101462131 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:33932608 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:33932608 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83330736 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83330736 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83358122 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83358122 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31542228 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31542228 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:29409378 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:29409378 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:68740585 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:68740585 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:116693691 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:116693691 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:28509360 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:28509360 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:64208330 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:64208330 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:105601046 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:105601046 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:36212456 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:36212456 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130218844 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130218844 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:1807964 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:1807964 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:1876529 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:1876529 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:157510712 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:157510712 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:28229770 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:28229770 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:69489927 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:69489927 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:2947468 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:2947468 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:94413653 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:94413653 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:176983743 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:176983743 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:24095154 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:24095154 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:32085190 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:32085190 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:64667916 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:64667916 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:47517713 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:47517713 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:47517785 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:47517785 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:25266921 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:25266921 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:25283720 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:25283720 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:28890515 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:28890515 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:3853732 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:3853732 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:10443667 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:10443667 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:36051703 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:36051703 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:42588328 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:42588328 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:111957618 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:111957618 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153170405 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153170405 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:11058126 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:11058126 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:143599406 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:143599406 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:70037888 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:70037888 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:33186082 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:33186082 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:23606328 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:23606328 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:51696809 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:51696809 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:102239003 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:102239003 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:220232156 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:220232156 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:32944775 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:32944775 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:32948001 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:32948001 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:50356034 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:50356034 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:37704276 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:37704276 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180375419 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180375419 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180377624 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180377624 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:56381771 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:56381771 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:63519961 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:63519961 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:45928101 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:45928101 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:112720874 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:112720874 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:64609387 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:64609387 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:40630863 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:40630863 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:19567084 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:19567084 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:179504204 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:179504204 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:92694936 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:92694936 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247737284 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247737284 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:28203093 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:28203093 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:178482180 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:178482180 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:9498889 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:9498889 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:31763458 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:31763458 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:264794 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:264794 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:88825283 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:88825283 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:63631144 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:63631144 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:63631843 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:63631843 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:151914509 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:151914509 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:151939298 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:151939298 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:49987883 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:49987883 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77599773 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77599773 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:20774597 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:20774597 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140941273 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140941273 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:181765708 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:181765708 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:48694964 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:48694964 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:54660585 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:54660585 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:1949780 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:1949780 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:115049565 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:115049565 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:86063990 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:86063990 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:62498518 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:62498518 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:16590161 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:16590161 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:3779743 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:3779743 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:104937573 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:104937573 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:219890889 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:219890889 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:30765377 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:30765377 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:77283254 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:77283254 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:93687512 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:93687512 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126114801 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126114801 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126132878 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126132878 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:96292019 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:96292019 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:96292527 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:96292527 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:78070928 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:78070928 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:85396023 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:85396023 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:13799213 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:13799213 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31116302 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31116302 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:17073465 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:17073465 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:7521406 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:7521406 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:71058740 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:71058740 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:121822329 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:121822329 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:149962323 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:149962323 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:149983521 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:149983521 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:100856433 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:100856433 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:91980575 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:91980575 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:68720471 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:68720471 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:85957634 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:85957634 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:90613560 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:90613560 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:46058410 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:46058410 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:22336148 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:22336148 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:104095861 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:104095861 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:49061305 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:49061305 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:56997134 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:56997134 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:196876503 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:196876503 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:49527196 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:49527196 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:37775235 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:37775235 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126449364 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126449364 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:146747960 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:146747960 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:6194356 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:6194356 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:61978289 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:61978289 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7358599 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7358599 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:46784047 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:46784047 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:143028570 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:143028570 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:154508364 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:154508364 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:77564705 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:77564705 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:81743229 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:81743229 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:57994333 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:57994333 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:87670048 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:87670048 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:26513789 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:26513789 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:205031161 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:205031161 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:100208003 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:100208003 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:147674912 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:147674912 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:147844492 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:147844492 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:125504772 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:125504772 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7836273 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7836273 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:110223215 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:110223215 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:189868285 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:189868285 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:137694687 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:137694687 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130361589 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130361589 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:160261321 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:160261321 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:128993974 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:128993974 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83222808 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83222808 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:211473344 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:211473344 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:125558510 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:125558510 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:197325896 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:197325896 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:27007954 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:27007954 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:37334595 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:37334595 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:2824065 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:2824065 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3062957 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3062957 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:113308007 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:113308007 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:113585691 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:113585691 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:113694867 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:113694867 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:58220093 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:58220093 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:138148111 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:138148111 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:117385854 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:117385854 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:36004213 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:36004213 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:45023391 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:45023391 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:54653292 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:54653292 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:94835796 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:94835796 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41454957 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41454957 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:99260405 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:99260405 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:5016864 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:5016864 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:87514490 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:87514490 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:53321477 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:53321477 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31696948 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31696948 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:103907538 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:103907538 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:134680836 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:134680836 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:55034873 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:55034873 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:118636161 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:118636161 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:29845622 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:29845622 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:29891334 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:29891334 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:126202794 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:126202794 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137266529 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137266529 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:55317862 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:55317862 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:12110963 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:12110963 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:394828 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:394828 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:402354 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:402354 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:13072129 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:13072129 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:83500977 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:83500977 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:124328258 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:124328258 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:21789179 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:21789179 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:13770852 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:13770852 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:38816345 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:38816345 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:11543761 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:11543761 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72278171 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72278171 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:31383028 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:31383028 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:31389237 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:31389237 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:117783110 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:117783110 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:53259951 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:53259951 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:67344838 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:67344838 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:162864961 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:162864961 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:4688943 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:4688943 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100510264 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100510264 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:7559413 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:7559413 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:56354520 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:56354520 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:56473995 T>C maps to ENST00000361203 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:56473995 T>C maps to ENST00000361203 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:25656747 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:25656747 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:113533228 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:113533228 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7133797 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7133797 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:102505913 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:102505913 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:95439664 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:95439664 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:131757178 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:131757178 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:50244092 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:50244092 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:48385705 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:48385705 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:184688540 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:184688540 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:83360488 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:83360488 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:78477256 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:78477256 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:2409323 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:2409323 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:42509827 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:42509827 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:42510127 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:42510127 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:77075477 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:77075477 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:677486 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:677486 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:132179896 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:132179896 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:131179130 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:131179130 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:5406686 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:5406686 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:5410546 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:5410546 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:22921713 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:22921713 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56206431 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56206431 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128046467 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128046467 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:103498742 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:103498742 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:45700900 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:45700900 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:14709583 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:14709583 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:153407639 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:153407639 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:170657230 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:170657230 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:17641503 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:17641503 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:286092 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:286092 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:91549443 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:91549443 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:34960894 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:34960894 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:67575278 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:67575278 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:94727408 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:94727408 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:124206449 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:124206449 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:172628723 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:172628723 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:147790183 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:147790183 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:175160385 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:175160385 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:125023114 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:125023114 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:123748591 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:123748591 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:69631259 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:69631259 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:45603704 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:45603704 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:78398798 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:78398798 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128471052 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128471052 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:240306874 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:240306874 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46367795 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46367795 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:52187181 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:52187181 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:49448327 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:49448327 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:48516977 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:48516977 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83447707 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:83447707 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:49189749 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:49189749 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:53878267 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:53878267 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:43871403 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:43871403 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:144346365 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:144346365 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:46252267 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:46252267 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:160837924 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:160837924 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:161522615 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:161522615 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:171675253 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:171675253 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:151704839 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:151704839 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:62402221 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:62402221 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:101016048 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:101016048 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:11616066 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:11616066 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:99816179 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:99816179 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:237075175 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:237075175 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:34117881 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:34117881 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:34131590 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:34131590 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:44186231 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:44186231 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:52996761 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:52996761 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153667260 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153667260 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:61995505 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:61995505 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:9765241 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:9765241 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:50289055 C>A maps to ENST00000446079 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:50289055 C>A maps to ENST00000446079 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:231406909 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:231406909 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:157332583 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:157332583 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119887270 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119887270 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:8589162 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:8589162 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:123468919 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:123468919 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:122319873 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:122319873 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:87379583 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:87379583 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:66962662 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:66962662 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:27503585 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:27503585 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:197629200 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:197629200 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:1060340 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:1060340 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:60774020 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:60774020 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:42145852 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:42145852 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:108631641 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:108631641 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:108635390 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:108635390 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:108691260 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:108691260 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:115345512 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:115345512 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:5593310 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:5593310 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:135363116 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:135363116 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:18868970 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:18868970 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:769534 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:769534 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31778438 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31778438 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31605940 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31605940 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31605944 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:31605944 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:197298148 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:197298148 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:26087763 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:26087763 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46815634 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46815634 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:12120111 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:12120111 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:71010258 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:71010258 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:38308735 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:38308735 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:186113528 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:186113528 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:80374025 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:80374025 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:80377160 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:80377160 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:46671082 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:46671082 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:100503532 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:100503532 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:63233572 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:63233572 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:186384028 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:186384028 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:148802057 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:148802057 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31777645 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31777645 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:16343785 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:16343785 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:87726232 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:87726232 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:8306034 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:8306034 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:53588985 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:53588985 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:94985115 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:94985115 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:160497130 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:160497130 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130410903 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130410903 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130415608 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:130415608 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:3131950 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:3131950 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:3134156 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:3134156 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:82586001 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:82586001 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:100948515 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:100948515 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:99149824 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:99149824 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:118864649 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:118864649 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:52386270 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:52386270 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:187520884 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:187520884 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:31368560 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:31368560 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:31391488 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:31391488 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:9558927 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:9558927 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70521648 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70521648 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:161056430 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:161056430 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:64982041 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:64982041 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:124432079 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:124432079 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:42729869 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:42729869 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:75434840 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:75434840 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:215256726 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:215256726 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:78649086 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:78649086 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:37455506 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:37455506 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:55977013 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:55977013 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:142651476 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:142651476 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:62407073 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:62407073 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:75139405 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:75139405 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:35628065 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:35628065 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:57180083 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:57180083 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:100082583 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:100082583 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:28119594 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:28119594 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:57943920 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:57943920 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:57970479 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:57970479 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55237900 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55237900 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:55593516 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:55593516 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51532472 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51532472 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:9752257 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:9752257 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:45741485 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:45741485 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:47980042 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:47980042 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:31869470 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:31869470 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:130454535 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:130454535 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:112493803 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:112493803 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:211301169 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:211301169 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:64751151 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:64751151 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:46704865 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:46704865 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:93172725 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:93172725 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:202272256 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:202272256 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:202276589 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:202276589 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:206765217 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:206765217 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:27521132 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:27521132 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:148009940 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:148009940 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:160966590 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:160966590 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:161087438 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:161087438 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:82188305 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:82188305 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:62641574 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:62641574 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:141093412 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:141093412 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:141122212 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:141122212 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:141625408 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:141625408 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170145682 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170145682 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170145684 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170145684 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:32530063 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:32530063 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:47639343 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:47639343 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:46486724 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:46486724 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:34263664 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:34263664 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:45875807 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:45875807 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:39782810 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:39782810 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:148798491 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:148798491 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:30269672 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:30269672 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:140992887 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:140992887 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:77708174 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:77708174 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:109155850 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:109155850 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:21208457 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:21208457 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:67521010 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:67521010 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:156296261 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:156296261 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50695497 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50695497 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:32677325 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:32677325 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:165110577 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:165110577 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:165118893 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:165118893 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:119750072 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:119750072 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:119750106 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:119750106 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:82043598 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:82043598 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:138699972 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:138699972 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:90432662 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:90432662 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151073937 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151073937 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70357886 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70357886 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:126771051 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:126771051 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:21624230 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:21624230 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:99342814 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:99342814 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:86383404 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:86383404 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:74934234 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:74934234 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:103572715 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:103572715 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:18389667 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:18389667 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:151926958 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:151926958 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:4965296 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:4965296 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:53485074 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:53485074 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:132329826 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:132329826 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:158812271 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:158812271 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:77227335 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:77227335 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:174537857 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:174537857 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:124936921 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:124936921 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:26960132 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:26960132 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:47710184 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:47710184 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:149903975 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:149903975 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:187454825 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:187454825 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11254509 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11254509 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:30655386 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:30655386 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:42331600 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:42331600 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:15813989 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:15813989 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10248472 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10248472 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10400283 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10400283 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10433464 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10433464 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10543833 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:10543833 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23869717 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23869717 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23871844 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23871844 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23874801 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23874801 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23885188 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23885188 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:31047861 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:31047861 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128327352 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128327352 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128339424 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128339424 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:24424319 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:24424319 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:89891408 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:89891408 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:15628946 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:15628946 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:35615016 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:35615016 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:16892055 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:16892055 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:16915725 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:16915725 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55417618 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55417618 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:152553804 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:152553804 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:84035364 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:84035364 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:52676017 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:52676017 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:45000902 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:45000902 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:41235168 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:41235168 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:25477487 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:25477487 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:51226455 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:51226455 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:119068535 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:119068535 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:65029546 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:65029546 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:57111107 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:57111107 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56300795 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56300795 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56312886 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56312886 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247597297 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247597297 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:144101616 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:144101616 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:117669991 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:117669991 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:117701683 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:117701683 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26116060 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26116060 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100129157 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100129157 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:89155031 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:89155031 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:52449071 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:52449071 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:115411742 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:115411742 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:50722987 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:50722987 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:64428679 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:64428679 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:152027481 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:152027481 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:152031054 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:152031054 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:123718997 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:123718997 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:104866273 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:104866273 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:9086205 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:9086205 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:73789826 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:73789826 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:69103103 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:69103103 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:153965593 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:153965593 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:3726348 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:3726348 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:62564933 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:62564933 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:13762483 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:13762483 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:13786120 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:13786120 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:102462381 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:102462381 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:193333428 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:193333428 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:67290643 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:67290643 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248113155 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248113155 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248308448 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248308448 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248437126 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248437126 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:55682123 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:55682123 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:143701027 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:143701027 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:59345601 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:59345601 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:36885930 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:36885930 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:112542646 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:112542646 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:35492400 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:35492400 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:73727283 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:73727283 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:39597741 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:39597741 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:161990304 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:161990304 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:31815481 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:31815481 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:55973879 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:55973879 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:24605307 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:24605307 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:183032946 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:183032946 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:20705773 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:20705773 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:145016138 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:145016138 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:149283344 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:149283344 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:54953671 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:54953671 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:19367580 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:19367580 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:24513068 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:24513068 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:31983823 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:31983823 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:4117421 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:4117421 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:179533490 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:179533490 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:54985180 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:54985180 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:118370258 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:118370258 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:58342233 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:58342233 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:54022107 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:54022107 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:79650326 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:79650326 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:151214575 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:151214575 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:22144954 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:22144954 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:25121377 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:25121377 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:47927530 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:47927530 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:48581018 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:48581018 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:40586454 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:40586454 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:161160269 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:161160269 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:100855982 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:100855982 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:74315133 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:74315133 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:82357046 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:82357046 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:118199463 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:118199463 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:121230883 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:121230883 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94935711 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94935711 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:75552086 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:75552086 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:14983107 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:14983107 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:120180335 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:120180335 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94903325 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94903325 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:94732254 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:94732254 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:121828724 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:121828724 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:23521076 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:23521076 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:44586879 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:44586879 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:62198148 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:62198148 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:57512832 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:57512832 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:50191342 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:50191342 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:48083499 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:48083499 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:3702356 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:3702356 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:153520575 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:153520575 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:18067491 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:18067491 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:45130866 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:45130866 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:113949863 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:113949863 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:227077909 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:227077909 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:43690701 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:43690701 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:43771680 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:43771680 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:40477035 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:40477035 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:107334816 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:107334816 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:1143717 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:1143717 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11579306 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11579306 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:71328161 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:71328161 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:71418562 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:71418562 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:27310767 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:27310767 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:157984995 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:157984995 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:71078132 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:71078132 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:29581713 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:29581713 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:121597075 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:121597075 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:220384374 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:220384374 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:2866677 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:2866677 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:79317850 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:79317850 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:135958975 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:135958975 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:125617996 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:125617996 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:79386432 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:79386432 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:107080567 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:107080567 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:117249832 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:117249832 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:153365018 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:153365018 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:163172523 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:163172523 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:240969436 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:240969436 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:130897399 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:130897399 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:104930761 C>T maps to ENST00000424048 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:104930761 C>T maps to ENST00000424048 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:49743301 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:49743301 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:105937715 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:105937715 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:106016113 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:106016113 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:18457300 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:18457300 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:6269922 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:6269922 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:1090673 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:1090673 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:117609598 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:117609598 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:48063794 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:48063794 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:48091367 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:48091367 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153631967 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153631967 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:99054344 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:99054344 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:78865275 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:78865275 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:43897649 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:43897649 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:33163924 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:33163924 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:237936817 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:237936817 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:33876545 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:33876545 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:76696786 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:76696786 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:25652561 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:25652561 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:29983543 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:29983543 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:102283706 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:102283706 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:81968960 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:81968960 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:53925856 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:53925856 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50644658 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50644658 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:83739927 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:83739927 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:122634240 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:122634240 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:61160145 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:61160145 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:167183194 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:167183194 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:29898876 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:29898876 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31946169 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31946169 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31946178 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31946178 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:148441802 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:148441802 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:52149018 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:52149018 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:52129429 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:52129429 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51959012 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51959012 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:115317019 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:115317019 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:1915472 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:1915472 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31931986 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:31931986 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:160593821 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:160593821 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:48524892 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:48524892 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:122755761 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:122755761 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:122811997 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:122811997 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26800699 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26800699 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:135376425 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:135376425 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43253069 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43253069 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43262193 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43262193 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:73693481 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:73693481 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:20008257 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:20008257 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:46945967 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:46945967 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:64368151 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:64368151 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:92352808 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:92352808 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:9892341 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:9892341 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:47173647 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:47173647 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:33168966 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:33168966 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:95330288 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:95330288 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70148689 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:70148689 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:40366495 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:40366495 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:70633329 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:70633329 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:173505130 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:173505130 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:48472152 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:48472152 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:21350124 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:21350124 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:128633830 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:128633830 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:156243244 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:156243244 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128845341 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128845341 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:86257156 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:86257156 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:101625091 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:101625091 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:179319663 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:179319663 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:108339056 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:108339056 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:106907367 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:106907367 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:23737535 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:23737535 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:231067563 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:231067563 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:118642150 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:118642150 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:35792572 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:35792572 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44170793 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44170793 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44171544 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44171544 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:158639648 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:158639648 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:4253000 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:4253000 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:109192720 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:109192720 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:149502692 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:149502692 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153063478 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:153063478 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:52677008 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:52677008 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:52682351 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:52682351 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:100151992 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:100151992 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:99786202 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:99786202 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:5448580 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:5448580 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:5458479 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:5458479 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:39546836 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:39546836 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:75659656 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:75659656 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109002888 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109002888 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:49100181 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:49100181 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:39955696 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:39955696 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:32909544 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:32909544 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:33405289 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:33405289 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:35900313 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:35900313 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:7488056 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:7488056 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100532939 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:100532939 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:53895652 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:53895652 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:102244012 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:102244012 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:13610570 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:13610570 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:176750981 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:176750981 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:89977672 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:89977672 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:104376486 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:104376486 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:104471793 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:104471793 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:27197663 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:27197663 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:69843920 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:69843920 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:69898598 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:69898598 A>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:50696814 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:50696814 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41847698 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41847698 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:218609195 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:218609195 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:43545160 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:43545160 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:3074227 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:3074227 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:11441715 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:11441715 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:171853281 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:171853281 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:19488926 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:19488926 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:19489006 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:19489006 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:76130844 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:76130844 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:44403632 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:44403632 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:125899958 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:125899958 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:100863562 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:100863562 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:57916971 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:57916971 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:45430009 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:45430009 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:22881834 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:22881834 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:24815922 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:24815922 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:144397841 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:144397841 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:42680225 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:42680225 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:186332405 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:186332405 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:123686072 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:123686072 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:72969023 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:72969023 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:67061783 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:67061783 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:72973717 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:72973717 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77397488 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77397488 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:234879161 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:234879161 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:46650796 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:46650796 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:113211338 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:113211338 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:15186851 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:15186851 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:219618721 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:219618721 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179442277 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179442277 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179588927 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179588927 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72246280 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72246280 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:112402208 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:112402208 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:8103113 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:8103113 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:49398566 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:49398566 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:9337147 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:9337147 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:70148412 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:70148412 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:19713871 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:19713871 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:43541421 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:43541421 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:35403092 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:35403092 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:54528647 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:54528647 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:115067171 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:115067171 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:118986660 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:118986660 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:36159570 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:36159570 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126207125 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:126207125 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:17542672 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:17542672 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:216219959 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:216219959 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:216462804 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:216462804 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:234433232 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:234433232 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:50838793 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:50838793 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:5034003 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:5034003 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:144750882 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:144750882 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:8433437 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:8433437 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53770943 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53770943 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:54614753 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:54614753 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:98822874 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:98822874 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:98844897 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:98844897 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:102612942 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:102612942 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:224619520 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:224619520 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:85560337 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:85560337 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:122399783 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:122399783 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:228735028 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:228735028 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:1962706 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:1962706 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:175446017 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:175446017 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:96025822 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:96025822 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:54280244 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chrX:54280244 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:34986529 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:34986529 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:31567507 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:31567507 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:21335369 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:21335369 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:112860955 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:112860955 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:46550121 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:46550121 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:144590138 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:144590138 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:57064965 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:57064965 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58096300 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58096300 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140482051 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140482051 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:6976860 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:6976860 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:44679239 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:44679239 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53313839 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53313839 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58962929 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58962929 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53625893 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53625893 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:56606661 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:56606661 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:7083875 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:7083875 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:64972 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:64972 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:81733893 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:81733893 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:57781732 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:57781732 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:238045983 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:238045983 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:70299364 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:70299364 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:215917191 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:215917191 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:215917193 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:215917193 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:66914176 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:66914176 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:66915346 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:66915346 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:20687652 G>T maps to NM_001163941.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:20687652 G>T maps to NM_001163941.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:44052003 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:44052003 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:44100900 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:44100900 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:148521774 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:148521774 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:148622134 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:148622134 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:148602689 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:148602689 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:123301508 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:123301508 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:33616188 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:33616188 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:64521876 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:64521876 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:167794134 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:167794134 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:7820627 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:7820627 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:70904852 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:70904852 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:67361001 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:67361001 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:26627596 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:26627596 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:74307936 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:74307936 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:58124495 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:58124495 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:87572017 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:87572017 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:183960560 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:183960560 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:121773308 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:121773308 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:41547718 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:41547718 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:201531517 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:201531517 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:24442597 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:24442597 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:118451820 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:118451820 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:69040393 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:69040393 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:6895013 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:6895013 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:145763249 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:145763249 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:131704277 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:131704277 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:18964191 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:18964191 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:23257481 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:23257481 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:131138089 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:131138089 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:197053578 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:197053578 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:197107878 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:197107878 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:108121359 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:108121359 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:160048043 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:160048043 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:84449248 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:84449248 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:77105354 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:77105354 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:79164928 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:79164928 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:104225420 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:104225420 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:31597267 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:31597267 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:133166284 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:133166284 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:55739809 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:55739809 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:83931667 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:83931667 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:92470180 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:92470180 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:105692650 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:105692650 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:40588693 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:40588693 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:579482 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:579482 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:26468860 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:26468860 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:111426969 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:111426969 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:134259297 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:134259297 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:88377039 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:88377039 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45502542 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45502542 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:244715606 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:244715606 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:172431311 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:172431311 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:38274836 C>T maps to ENST00000446260 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:38274836 C>T maps to ENST00000446260 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:31763432 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:31763432 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:56675798 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:56675798 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32789920 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32789920 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:165714963 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:165714963 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:120906169 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:120906169 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:140145687 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:140145687 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:181620469 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:181620469 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:201081550 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:201081550 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:54109898 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:54109898 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:114434363 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:114434363 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:2968425 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:2968425 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:111319903 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:111319903 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:42931752 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:42931752 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:191107175 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:191107175 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:111330843 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:111330843 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:539913 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:539913 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:64108861 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:64108861 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:28701852 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:28701852 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:2499514 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:2499514 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158152105 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158152105 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:72537712 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:72537712 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:208061567 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:208061567 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:21951454 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:21951454 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:19520712 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:19520712 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:61689280 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:61689280 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:21968266 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:21968266 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:4715959 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:4715959 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:214816821 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:214816821 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:243303203 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:243303203 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:180006233 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:180006233 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:432948 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:432948 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:29440107 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:29440107 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:42552777 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:42552777 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:233409471 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:233409471 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:49840440 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:49840440 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:71038539 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:71038539 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:141316925 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:141316925 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:7302052 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:7302052 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:62289154 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:62289154 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:87674044 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:87674044 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:1320245 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:1320245 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:75796348 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:75796348 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139606188 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139606188 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139788141 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139788141 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139819828 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139819828 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139838812 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:139838812 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:189859623 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:189859623 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:111077258 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:111077258 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:227914765 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:227914765 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:107449607 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:107449607 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:107462815 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:107462815 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:46737284 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:46737284 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:166408577 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:166408577 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:197237508 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:197237508 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:30702209 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:30702209 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:209027789 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:209027789 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:3224542 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:3224542 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:113301566 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:113301566 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:113402883 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:113402883 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:11110884 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:11110884 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:49032992 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:49032992 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:15658843 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:15658843 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:20135730 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:20135730 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:27945087 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:27945087 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:58514584 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:58514584 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:42818822 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:42818822 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:34126443 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:34126443 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:115079436 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:115079436 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140957953 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140957953 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:47985607 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:47985607 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:408655 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:408655 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:124385350 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:124385350 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:196722013 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:196722013 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11568094 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11568094 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11827024 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11827024 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:49742617 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:49742617 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:50757268 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:50757268 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:131848959 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:131848959 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:66252767 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:66252767 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:154379835 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:154379835 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:64055010 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:64055010 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:93812178 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:93812178 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:45404927 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:45404927 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:348663 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:348663 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:57670499 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:57670499 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:158500251 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:158500251 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:2402420 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:2402420 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:41567352 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:41567352 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:73482907 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:73482907 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:11664686 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:11664686 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:132516358 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:132516358 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:89478162 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:89478162 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:134968360 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:134968360 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:722596 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:722596 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:37866775 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:37866775 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56495851 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56495851 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:44804523 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:44804523 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:53682785 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:53682785 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:72229717 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:72229717 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:133833816 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:133833816 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:68055730 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:68055730 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:46281163 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:46281163 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:116784346 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:116784346 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:58621919 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:58621919 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25023945 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25023945 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:87494870 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:87494870 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:89857780 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:89857780 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:35078406 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:35078406 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:161600995 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:161600995 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:157670160 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:157670160 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:128487050 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:128487050 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:153437456 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:153437456 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:47772418 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:47772418 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:45976289 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:45976289 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:153927853 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:153927853 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:26806026 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:26806026 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:26558192 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:26558192 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:30683289 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:30683289 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:179729391 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:179729391 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:100564721 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:100564721 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45096788 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45096788 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:95034835 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:95034835 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:52712787 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:52712787 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:89975946 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:89975946 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:104476241 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:104476241 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:28427529 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:28427529 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:71021126 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:71021126 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:33095794 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:33095794 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:29857396 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:29857396 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:23637568 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:23637568 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:27169273 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:27169273 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:175111325 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:175111325 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:70884564 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:70884564 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:113738707 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:113738707 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:39734552 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:39734552 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:27357722 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:27357722 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:1539272 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:1539272 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:2611709 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:2611709 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:54966342 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:54966342 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:50687312 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:50687312 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56078797 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56078797 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:7763015 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:7763015 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:160851655 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:160851655 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:4715183 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:4715183 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:124378373 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:124378373 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:40312457 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:40312457 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:88693645 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:88693645 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:73494185 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:73494185 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:245530706 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:245530706 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:57957544 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:57957544 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:33367931 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:33367931 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:51327104 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:51327104 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:135020312 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:135020312 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:32410762 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:32410762 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:63414823 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:63414823 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:48963043 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:48963043 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:129478612 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:129478612 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:133901989 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:133901989 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:152659200 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:152659200 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:136562310 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:136562310 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:109086204 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:109086204 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:51443032 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:51443032 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:71834076 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:71834076 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:156104872 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:156104872 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:81892934 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:81892934 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:197553670 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:197553670 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:59276601 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:59276601 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:70385468 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:70385468 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:56910872 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:56910872 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:133425897 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:133425897 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:20110254 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:20110254 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:67920407 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:67920407 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:16177731 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:16177731 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:119752154 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:119752154 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:162940736 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:162940736 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:103349992 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:103349992 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:113714872 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:113714872 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:35813678 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:35813678 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:37184256 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:37184256 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:141767215 C>T maps to ENST00000475668 V1665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:141767215 C>T maps to ENST00000475668 V1665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:141795596 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:141795596 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56845341 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56845341 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56846751 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56846751 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:37057966 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:37057966 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:20354791 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:20354791 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:89086776 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:89086776 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158817414 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158817414 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:108813938 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:108813938 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:68777375 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:68777375 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:56022591 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:56022591 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:24418935 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:24418935 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:60230466 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:60230466 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:11853946 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:11853946 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:86575298 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:86575298 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:149907353 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:149907353 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:92714401 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:92714401 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9038376 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9038376 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:100674547 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:100674547 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:15838970 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:15838970 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:10248472 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:10248472 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:10267633 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:10267633 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:23898979 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:23898979 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44179886 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44179886 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:26454990 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:26454990 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:95123701 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:95123701 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:102051498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:102051498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:134047105 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:134047105 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:124886832 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:124886832 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:179334849 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:179334849 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:152528872 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:152528872 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:37052707 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:37052707 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1037836 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1037836 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:57077250 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:57077250 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:56422945 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:56422945 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:183273669 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:183273669 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:101093779 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:101093779 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:26093498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:26093498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:15281391 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:15281391 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:120430580 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:120430580 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:110901028 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:110901028 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32774652 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32774652 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32786322 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32786322 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:119501541 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:119501541 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:119501543 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:119501543 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:119501602 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:119501602 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:6632140 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:6632140 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:107950603 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:107950603 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:154076747 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:154076747 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:57970676 C>G maps to NM_001004459.1 *326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:57970676 C>G maps to NM_001004459.1 *326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:3323760 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:3323760 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:55339545 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:55339545 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:59282372 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:59282372 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:142749354 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:142749354 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:148709898 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:148709898 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:29607732 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:29607732 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:1584319 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:1584319 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:101725228 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:101725228 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:43289719 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:43289719 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:169612312 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:169612312 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:60995493 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:60995493 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176525309 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176525309 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176640026 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176640026 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:101121522 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:101121522 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140574583 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140574583 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:101304185 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:101304185 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:65385071 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:65385071 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:71495556 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:71495556 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:165829540 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:165829540 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:178528570 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:178528570 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:144859667 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:144859667 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:120548230 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:120548230 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:95380832 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:95380832 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:48537620 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:48537620 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:71904452 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:71904452 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:18446953 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:18446953 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:88996905 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:88996905 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:110424444 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:110424444 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:32977150 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:32977150 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:42376057 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:42376057 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179350530 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179350530 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:161137585 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:161137585 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:126749081 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:126749081 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:72170248 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:72170248 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:44280252 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:44280252 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:121238683 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:121238683 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:30106348 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:30106348 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:39503653 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:39503653 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:27841065 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:27841065 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:306221 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:306221 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:11035530 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:11035530 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:133543822 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:133543822 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:68989738 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:68989738 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:23848658 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:23848658 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:141539039 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:141539039 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:43430514 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:43430514 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:127177084 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:127177084 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24612994 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24612994 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24614408 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24614408 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:209302471 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:209302471 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:129845793 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:129845793 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:52348475 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:52348475 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:52348483 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:52348483 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:51404379 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:51404379 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:76251969 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:76251969 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:205069465 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:205069465 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:24573095 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:24573095 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:114260998 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:114260998 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:65042498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:65042498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:125622058 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:125622058 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:79348927 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:79348927 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:103132489 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:103132489 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:16475218 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:16475218 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:192321431 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:192321431 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:156347048 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:156347048 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:104664379 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:104664379 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:104897498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:104897498 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:105001673 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:105001673 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:25442860 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:25442860 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:58037547 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:58037547 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:53645030 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:53645030 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:53721884 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:53721884 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:17622339 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:17622339 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:5977704 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:5977704 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:108996155 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:108996155 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237632498 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237632498 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237729814 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237729814 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:21990401 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:21990401 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:1542236 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:1542236 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25652523 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25652523 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:238896696 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:238896696 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:18485243 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:18485243 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:81951976 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:81951976 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:115813657 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:115813657 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:223386706 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:223386706 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:13599136 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:13599136 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:129294482 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:129294482 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25918684 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25918684 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25849905 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:25849905 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:36686153 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:36686153 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:38317701 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:38317701 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:62372845 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:62372845 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:18280240 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:18280240 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:27905081 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:27905081 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:24902455 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:24902455 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1244962 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1244962 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:20864454 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:20864454 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:168175276 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:168175276 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:84453479 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:84453479 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:168999392 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:168999392 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:68397358 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:68397358 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:51617104 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:51617104 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:51705211 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:51705211 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108337085 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108337085 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108536259 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108536259 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:106974109 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:106974109 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:123977507 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:123977507 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:220331867 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:220331867 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158584985 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158584985 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158590358 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158590358 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158646145 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158646145 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:48218103 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:48218103 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:22354361 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:22354361 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:8474493 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:8474493 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:48547322 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:48547322 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:104377021 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:104377021 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:63601171 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:63601171 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:10978948 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:10978948 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:152060430 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:152060430 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:35088591 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:35088591 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:179558030 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:179558030 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:35443641 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:35443641 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:92195260 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:92195260 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:2411779 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:2411779 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:43735951 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:43735951 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:169648422 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:169648422 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:121342173 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:121342173 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:32639369 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr21:32639369 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:98156847 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:98156847 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:120471071 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:120471071 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:5733833 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:5733833 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:38995326 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:38995326 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:72699375 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:72699375 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:18729129 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:18729129 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:69097123 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:69097123 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:152226391 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:152226391 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:6439582 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:6439582 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:6440155 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:6440155 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:32011939 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:32011939 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:17772602 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:17772602 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:144344682 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:144344682 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:35689924 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:35689924 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:186315206 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:186315206 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:36871224 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:36871224 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:142510006 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:142510006 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:101342794 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:101342794 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:31330098 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:31330098 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:31354657 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:31354657 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:99718971 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:99718971 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:122519157 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:122519157 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:231114777 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:231114777 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179665048 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179665048 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:19486548 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:19486548 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:234656718 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:234656718 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:36035764 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:36035764 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:17763417 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:17763417 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:97243176 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:97243176 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:215953151 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:215953151 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:216496779 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:216496779 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:78167022 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:78167022 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:133308654 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:133308654 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:36982035 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:36982035 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:100245445 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:100245445 A>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:100835928 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:100835928 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:42454055 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:42454055 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:65253305 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chrX:65253305 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:54544206 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:54544206 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:71175942 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:71175942 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:85701172 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:85701172 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:76759071 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:76759071 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:113092244 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:113092244 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:68628100 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:68628100 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:31571265 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:31571265 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:216995761 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:216995761 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:27412645 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:27412645 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:100369425 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:100369425 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:100374022 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:100374022 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:138749475 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:138749475 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:52947417 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:52947417 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:195936392 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:195936392 T>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:195937442 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:195937442 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:29643084 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:29643084 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:3169031 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:3169031 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:16465128 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:16465128 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:67050476 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:67050476 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:230841616 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:230841616 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:134216573 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:134216573 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:18095690 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:18095690 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:66106278 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:66106278 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:109193599 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:109193599 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:223958276 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:223958276 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr14:92136363 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr14:92136363 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:159856535 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:159856535 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:21883027 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:21883027 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:36518177 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:36518177 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:175819714 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:175819714 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr16:70524367 T>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr16:70524367 T>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr21:46888720 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr21:46888720 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495699 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495699 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495733 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495733 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495744 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495744 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:52774168 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:52774168 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:38964139 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:38964139 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:169188493 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:169188493 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:131846943 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:131846943 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:144662612 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:144662612 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:52370324 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:52370324 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:93956747 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:93956747 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:56204295 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:56204295 C>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:60224686 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:60224686 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:23023499 A>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:23023499 A>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:33044746 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:33044746 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:35651727 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:35651727 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:176733291 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:176733291 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:26199742 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:26199742 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:185984587 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:185984587 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:55201910 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:55201910 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:133967358 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:133967358 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:38682391 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:38682391 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr14:50732256 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr14:50732256 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21402352 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21402352 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21404247 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21404247 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21404596 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21404596 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21407148 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21407148 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21407215 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr18:21407215 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:22148733 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:22148733 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:206768964 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:206768964 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:8015849 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:8015849 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:10433105 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:10433105 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:62848686 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:62848686 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:183538141 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:183538141 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:21555881 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:21555881 T>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:25147326 T>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:25147326 T>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr16:2147795 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr16:2147795 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:242109134 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:242109134 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:18834027 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:18834027 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:220165617 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:220165617 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:121616943 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:121616943 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:205739406 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:205739406 C>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:31448719 T>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:31448719 T>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr3:113335107 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr3:113335107 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:2451272 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:2451272 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:51362325 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:51362325 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr12:44403373 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr12:44403373 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr3:49869281 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr3:49869281 G>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:3457868 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:3457868 A>C did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:59338369 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:59338369 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:73832406 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:73832406 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:161132037 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:161132037 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr21:17246918 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr21:17246918 G>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:190334205 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:190334205 A>G did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:135524673 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:135524673 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:100594469 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:100594469 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:195041319 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:195041319 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:32421065 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:32421065 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:33549176 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:33549176 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:5240116 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:5240116 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:5232732 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:5232732 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:5240116 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:5240116 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:100588973 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:100588973 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:100588973 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:100588973 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:78353333 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:78353333 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:131879977 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:131879977 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:247053417 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:247053417 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:247053417 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:247053417 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:62287632 G>A maps to NM_001620.1 G4752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:62287632 G>A maps to NM_001620.1 G4752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:222867494 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:222867494 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:222860901 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:222860901 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:222867494 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:222867494 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:19201120 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:19201120 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:233271580 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:233271580 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:178834572 C>G maps to NM_004673.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:178834572 C>G maps to NM_004673.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:133317909 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:133317909 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:133317911 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:133317911 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:4202203 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:4202203 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:71811580 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:71811580 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:29398754 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:29398754 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:145763264 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:145763264 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:145763264 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:145763264 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:111955319 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:111955319 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:62926367 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:62926367 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:62926367 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:62926367 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:232091518 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:232091518 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:232091518 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:232091518 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:2936568 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:2936568 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:2936568 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:2936568 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:62490735 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:62490735 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:77268334 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:77268334 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:77268334 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:77268334 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:26114360 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:26114360 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:26114360 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:26114360 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:26155828 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:26155828 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:142253859 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:142253859 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:142253859 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:142253859 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:364509 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:364509 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:39932096 G>A maps to NM_001123385.1 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:39932096 G>A maps to NM_001123385.1 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:23631619 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:23631619 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:42127650 C>T maps to NM_207406.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:42127650 C>T maps to NM_207406.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:112993282 C>A maps to ENST00000273395 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:112993282 C>A maps to ENST00000273395 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:31625602 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:31625602 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:31625602 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:31625602 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:137504236 C>T maps to NM_006696.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:137504236 C>T maps to NM_006696.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:124050532 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:124050532 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:124050532 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:124050532 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:93755060 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:93755060 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:93755060 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:93755060 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:40505761 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:40505761 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:40505761 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:40505761 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:115884852 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:115884852 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:8136413 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:8136413 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr18:30672693 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr18:30672693 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:34684498 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:34684498 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:45947471 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:45947471 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr21:43327742 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr21:43327742 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:97554920 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:97554920 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:181719571 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:181719571 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:64873681 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:64873681 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:64873681 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:64873681 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:93108924 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:93108924 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:122002990 C>A maps to NM_001178065.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:122002990 C>A maps to NM_001178065.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:26524435 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:26524435 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:26524435 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:26524435 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:52821602 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:52821602 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr18:66564796 T>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr18:66564796 T>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:77266307 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:77266307 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:77266307 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:77266307 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:40948053 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:40948053 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:55563912 A>G maps to ENST00000436346 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:55563912 A>G maps to ENST00000436346 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:22078832 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:22078832 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:22078832 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:22078832 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:42225164 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:42225164 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr9:123920081 G>T maps to NM_007018.4 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr9:123920081 G>T maps to NM_007018.4 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:117265521 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:117265521 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:117265521 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:117265521 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:117232482 G>A maps to NM_000492.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:117232482 G>A maps to NM_000492.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:87026101 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:87026101 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:87026101 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:87026101 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:22214191 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:22214191 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:22214191 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:22214191 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:1445201 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:1445201 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:121222150 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:121222150 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:121222150 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:121222150 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:105791908 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:105791908 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:70745665 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:70745665 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:70894705 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:70894705 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:70894705 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:70894705 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:139642845 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:139642845 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:139642845 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:139642845 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:139737683 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:139737683 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:130285780 C>A maps to NM_001102608.1 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:130285780 C>A maps to NM_001102608.1 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:70964919 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:70964919 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:70964919 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:70964919 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160269079 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160269079 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:14095187 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:14095187 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:36759765 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:36759765 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:36759765 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:36759765 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:4154887 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:4154887 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:4154887 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:4154887 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:28534646 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:28534646 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:28534646 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:28534646 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:30693084 G>A maps to ENST00000348438 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:30693084 G>A maps to ENST00000348438 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:4645153 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:4645153 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:4645153 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:4645153 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:67662412 G>T maps to NM_006565.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:67662412 G>T maps to NM_006565.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:67663407 C>T maps to NM_006565.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:67663407 C>T maps to NM_006565.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:1782764 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:1782764 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:43152464 G>A maps to ENST00000354495 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:43152464 G>A maps to ENST00000354495 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:111779889 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:111779889 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:111779889 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:111779889 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:36089895 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:36089895 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:36089895 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:36089895 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:57536491 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:57536491 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:58514810 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:58514810 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:95112520 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:95112520 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:95112520 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:95112520 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:20873932 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:20873932 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:20873932 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:20873932 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:68962533 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:68962533 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:68962533 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:68962533 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:127526744 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:127526744 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:127526744 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:127526744 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:32717135 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:32717135 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:32717135 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:32717135 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:7681837 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:7681837 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:220246018 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:220246018 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:113858241 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:113858241 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:113858241 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:113858241 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr18:32446129 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr18:32446129 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr18:32446129 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr18:32446129 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:25656672 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:25656672 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:19247268 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:19247268 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:19247268 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:19247268 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:12294677 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:12294677 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:12294677 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:12294677 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr22:44028080 C>T maps to NM_022785.3 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr22:44028080 C>T maps to NM_022785.3 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:52334358 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:52334358 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:42396828 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:42396828 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:111434799 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:111434799 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:111434799 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:111434799 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:132514757 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:132514757 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:132514757 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:132514757 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:60195589 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:60195589 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:60195589 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:60195589 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:57319094 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:57319094 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:57319094 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:57319094 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:128936078 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:128936078 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:128936078 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:128936078 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:128357113 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:128357113 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:128357113 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:128357113 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:127653768 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:127653768 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:76205681 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:76205681 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:125324199 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:125324199 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:27209237 C>T maps to ENST00000394906 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:27209237 C>T maps to ENST00000394906 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:159644718 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:159644718 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:71847262 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:71847262 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:78430041 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:78430041 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:28385431 T>A maps to NM_017412.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:28385431 T>A maps to NM_017412.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:46312155 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:46312155 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:46312155 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:46312155 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:89894938 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:89894938 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:89894938 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:89894938 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:49360847 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:49360847 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:109113749 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:109113749 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:53374113 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:53374113 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:53374113 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:53374113 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:141900396 T>C maps to NM_001039547.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:141900396 T>C maps to NM_001039547.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:86399773 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr9:86399773 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr9:86399773 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr9:86399773 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:50742266 C>A maps to NM_005311.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:50742266 C>A maps to NM_005311.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:87484053 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:87484053 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:88123667 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:88123667 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:87484053 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:87484053 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:88123667 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:88123667 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:94316698 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:94316698 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:94316698 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:94316698 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:88258685 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:88258685 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:88258685 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:88258685 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:45945663 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:45945663 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:65483611 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:65483611 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:65483611 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:65483611 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:28544752 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:28544752 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:43033146 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:43033146 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:100123169 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:100123169 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:100807621 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:100807621 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:122752544 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:122752544 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:114141815 T>A maps to NM_000868.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:114141815 T>A maps to NM_000868.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:53562501 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:53562501 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:53562501 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:53562501 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:160062027 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:160062027 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160062027 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160062027 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:35871033 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:35871033 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:60002318 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:60002318 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:60002318 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:60002318 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:121547858 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:121547858 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:121547858 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:121547858 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:75989203 G>T maps to NM_006633.2 V1310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:75989203 G>T maps to NM_006633.2 V1310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:44180314 T>C maps to NM_016123.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:44180314 T>C maps to NM_016123.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:182395439 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:182395439 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:182395439 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:182395439 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:15599967 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:15599967 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:15599967 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:15599967 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:31392354 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:31392354 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:24538100 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:24538100 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:24538100 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:24538100 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:39921346 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:39921346 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:39921346 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:39921346 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:63246644 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:63246644 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:63246644 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:63246644 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:29918493 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:29918493 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:201369695 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:201369695 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:29035077 C>A maps to NM_015254.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:29035077 C>A maps to NM_015254.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:47288895 C>T maps to NM_182902.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:47288895 C>T maps to NM_182902.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:9995127 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:9995127 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:32127721 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:32127721 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr21:32127721 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr21:32127721 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:55014925 G>T maps to NM_002288.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:55014925 G>T maps to NM_002288.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:101020169 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:101020169 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:101020169 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:101020169 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:36250715 G>T maps to NM_174902.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:36250715 G>T maps to NM_174902.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:53298302 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:53298302 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:53298302 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:53298302 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:18393831 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:18393831 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:62641147 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:62641147 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:99418684 G>T maps to NM_001037317.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:99418684 G>T maps to NM_001037317.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:133827982 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:133827982 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:133827982 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:133827982 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:40136264 G>T maps to NM_020929.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:40136264 G>T maps to NM_020929.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:6625305 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:6625305 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:75650120 G>T maps to NM_020932.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:75650120 G>T maps to NM_020932.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:10791900 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:10791900 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:10791900 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:10791900 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:27687192 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:27687192 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:99019467 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:99019467 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:99019467 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:99019467 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:156444815 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:156444815 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:156444815 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:156444815 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:24416898 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:24416898 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:42934968 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:42934968 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:42934968 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:42934968 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:9089294 G>T maps to NM_024690.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:9089294 G>T maps to NM_024690.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:45795183 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:45795183 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:45795183 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:45795183 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:10357298 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:10357298 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:10357298 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:10357298 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:23857978 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:23857978 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:101910742 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:101910742 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:101910742 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:101910742 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:16908279 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:16908279 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:115898298 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:115898298 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:115898298 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:115898298 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:130881249 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:130881249 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:5420970 T>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:5420970 T>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:64389988 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:64389988 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:64419492 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:64419492 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:64419492 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:64419492 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:13427850 C>A maps to NM_024923.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:13427850 C>A maps to NM_024923.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:28228718 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:28228718 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:123463131 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr12:123463131 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:128415863 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:128415863 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:143748276 C>A maps to NM_012365.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:143748276 C>A maps to NM_012365.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:6942198 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:6942198 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:6942198 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:6942198 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:48510589 C>A maps to NM_001005512.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:48510589 C>A maps to NM_001005512.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:55540901 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:55540901 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:55761411 C>G maps to NM_003697.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:55761411 C>G maps to NM_003697.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:158517961 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:158517961 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:158517961 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:158517961 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:179226620 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:179226620 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:149919054 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:149919054 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:41850323 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:41850323 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:41850323 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:41850323 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:17563740 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:17563740 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:17563740 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:17563740 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:17664701 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:17664701 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:17664701 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:17664701 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:56720126 C>T maps to NM_001127460.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:56720126 C>T maps to NM_001127460.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:69696179 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:69696179 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:55839045 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:55839045 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:58299496 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:58299496 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:142606647 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:142606647 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:165846422 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:165846422 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:165846422 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:165846422 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:70177369 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:70177369 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:70177369 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:70177369 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:45935822 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:45935822 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:64088953 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:64088953 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:71813131 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:71813131 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:71813131 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:71813131 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:106524541 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:106524541 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:106524541 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:106524541 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:65153784 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:65153784 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:153040090 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:153040090 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:24722655 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:24722655 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:106821052 A>T maps to NM_018082.5 K394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:106821052 A>T maps to NM_018082.5 K394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:22314476 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:22314476 A>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:75573146 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:75573146 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:75573159 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:75573159 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:75573192 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:75573192 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:75573146 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:75573146 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:75573159 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:75573159 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:75573192 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:75573192 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:11312011 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:11312011 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:11312011 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:11312011 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:148575783 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:148575783 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:43237390 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:43237390 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:11562976 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:11562976 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:11562976 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:11562976 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:220159873 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:220159873 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:40730952 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:40730952 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:40735576 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:40735576 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:40730952 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:40730952 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:40735576 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:40735576 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:29633587 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:29633587 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:32665070 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr20:32665070 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:88228553 T>A maps to NM_020320.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:88228553 T>A maps to NM_020320.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:86672762 A>T maps to NM_002890.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:86672762 A>T maps to NM_002890.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:82354941 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:82354941 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:82354941 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:82354941 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:95353811 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:95353811 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:95353811 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:95353811 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:192321384 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:192321384 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:192321384 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:192321384 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:25701815 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:25701815 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:88012856 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:88012856 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:49258688 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:49258688 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:79174739 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:79174739 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:79174739 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:79174739 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:40498767 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:40498767 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:178999424 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:178999424 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:237843958 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:237843958 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:34028577 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:34028577 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:34034667 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:34034667 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:33927741 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:33927741 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:33945029 C>A maps to NM_001036.3 A1418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:33945029 C>A maps to NM_001036.3 A1418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:34028577 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:34028577 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr9:91617196 C>A maps to NM_005226.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr9:91617196 C>A maps to NM_005226.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:134988394 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:134988394 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:134988394 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:134988394 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:84362714 G>T maps to NM_001012980.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:84362714 G>T maps to NM_001012980.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:9917583 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:9917583 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:9917583 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:9917583 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:27507370 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:27507370 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:165969466 G>T maps to NM_006922.3 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:165969466 G>T maps to NM_006922.3 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:123508904 G>T maps to NM_018400.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:123508904 G>T maps to NM_018400.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:12185279 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:12185279 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:12185279 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:12185279 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:110303921 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:110303921 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:110303921 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:110303921 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:94964179 G>T maps to NM_173850.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:94964179 G>T maps to NM_173850.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr22:26769421 C>T maps to NM_021115.4 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr22:26769421 C>T maps to NM_021115.4 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:42088918 T>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:42088918 T>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:232596627 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:232596627 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:232596627 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:232596627 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:27023020 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:27023020 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:27023020 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:27023020 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160582250 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160582250 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:160458827 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:160458827 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160458827 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:160458827 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:100787145 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:100787145 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:119026198 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr10:119026198 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:119026198 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr10:119026198 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:42287589 C>A maps to NM_006749.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:42287589 C>A maps to NM_006749.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:150656992 G>T maps to NM_001145017.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:150656992 G>T maps to NM_001145017.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:1201698 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:1201698 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:20657997 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:20657997 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:20657997 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:20657997 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:67290780 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr16:67290780 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:101834577 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr5:101834577 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:101834577 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr5:101834577 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:96954406 G>A maps to NM_014014.3 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:96954406 G>A maps to NM_014014.3 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:25213282 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:25213282 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:16036455 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:16036455 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:16036455 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:16036455 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:142803634 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:142803634 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:142803634 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:142803634 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:45801725 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr2:45801725 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:45801725 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:45801725 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:48818790 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:48818790 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:74473360 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:74473360 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:74473360 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:74473360 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:152534963 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:152534963 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:152685918 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr6:152685918 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:152534963 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:152534963 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:152685918 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:152685918 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:60575247 G>A maps to NM_003185.3 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr20:60575247 G>A maps to NM_003185.3 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:111732247 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr3:111732247 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:111732247 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr3:111732247 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:72987317 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:72987317 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:72987317 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:72987317 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:179562934 C>A maps to ENST00000444136 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:179562934 C>A maps to ENST00000444136 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:20854172 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr14:20854172 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:374029 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:374029 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:151847169 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:151847169 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:70344663 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr15:70344663 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:70344663 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr15:70344663 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:166960624 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:166960624 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:126137132 C>A maps to NM_052907.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr12:126137132 C>A maps to NM_052907.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:5776095 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:5776095 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:36236381 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:36236381 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:20927980 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr14:20927980 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:23058163 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:23058163 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:23058163 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:23058163 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:32052274 C>A maps to ENST00000375244 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:32052274 C>A maps to ENST00000375244 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:68844364 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:68844364 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:10909784 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:10909784 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:10944860 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:10944860 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:11014887 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr21:11014887 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:165961193 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:165961193 T>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:19864787 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr22:19864787 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:156013768 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:156013768 C>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:73712392 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr11:73712392 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:73712392 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr11:73712392 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:70355071 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr4:70355071 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:70355071 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr4:70355071 C>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:20352501 C>G maps to ENST00000424589 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr16:20352501 C>G maps to ENST00000424589 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:18974436 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:18974436 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:216380819 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr1:216380819 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:216380819 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr1:216380819 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:47099946 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:47099946 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:47099946 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chrX:47099946 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:49350591 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr17:49350591 A>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:49357466 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr17:49357466 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:100169004 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr8:100169004 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:100169004 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:100169004 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:53016599 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr13:53016599 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:98797774 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr2:98797774 G>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:71130352 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:71130352 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:71130352 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:71130352 T>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:46619112 T>C maps to ENST00000242848 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr13:46619112 T>C maps to ENST00000242848 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:138739781 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:138739781 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:74598832 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chrX:74598832 G>C did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:77618185 G>T maps to NM_024721.4 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr8:77618185 G>T maps to NM_024721.4 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:28056963 C>T maps to NM_003447.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr6:28056963 C>T maps to NM_003447.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:22817159 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:22817159 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:22817159 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:22817159 A>G did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:37880894 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:37880894 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:36963640 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr19:36963640 C>A did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:55980500 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01D-1553-08 chr7:55980500 G>T did not map to a codon.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:52794387 T>C maps to NM_001010851.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:52794387 T>C maps to NM_001010851.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:149153029 G>A maps to ENST00000440594 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr7:149153029 G>A maps to ENST00000440594 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:57176422 C>A maps to NM_001005850.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2655-01A-01W-0928-08 chr19:57176422 C>A maps to NM_001005850.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:58862707 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:58862707 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:58862707 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:58862707 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:7760603 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:7760603 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:7760603 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:7760603 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:151474961 G>A maps to NM_207365.3 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:151474961 G>A maps to NM_207365.3 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:170987528 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:170987528 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:170987528 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:170987528 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:67151276 C>A maps to NM_080282.3 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:67151276 C>A maps to NM_080282.3 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:48316261 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:48316261 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:48619719 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:48619719 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:94474442 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:94474442 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:94544771 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:94544771 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:94474442 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:94474442 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:94544771 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:94544771 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:67090734 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:67090734 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:66920777 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:66920777 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:66920777 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:66920777 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:67028512 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:67028512 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:67028512 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:67028512 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:87174431 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:87174431 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:87081268 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:87081268 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43404064 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43404064 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:43404064 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:43404064 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:48141344 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:48141344 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:17470035 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:17470035 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:17470035 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:17470035 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:119028818 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:119028818 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:119028818 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:119028818 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:100498948 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:100498948 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:109577157 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:109577157 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:109577157 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:109577157 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132361035 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132361035 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:132361035 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:132361035 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:128598410 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:128598410 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:128598410 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:128598410 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:32366496 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:32366496 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:32366496 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:32366496 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:6309911 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:6309911 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:55059536 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:55059536 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:80655618 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:80655618 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:229568982 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:229568982 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:229568982 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:229568982 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:127708130 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:127708130 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:127708130 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:127708130 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:156934215 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:156934215 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:156934215 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:156934215 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:24187792 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:24187792 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:33631089 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:33631089 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:33649114 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:33649114 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:33631089 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:33631089 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:33649114 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:33649114 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:72509868 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:72509868 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:5319166 C>A maps to NM_139056.2 C1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:5319166 C>A maps to NM_139056.2 C1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:77353733 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:77353733 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:77359657 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:77359657 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:77353733 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:77353733 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:77359657 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:77359657 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:64769559 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:64769559 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:64520745 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:64520745 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:64524826 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:64524826 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:64641632 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:64641632 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:64524826 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:64524826 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:64598960 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:64598960 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:84611263 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:84611263 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:84611263 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:84611263 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:46640629 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:46640629 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:7521027 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:7521027 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:7767038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:7767038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:7521027 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:7521027 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:7767038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:7767038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:123038502 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:123038502 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:123038502 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:123038502 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:131797655 G>T maps to NM_001115.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:131797655 G>T maps to NM_001115.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:2895841 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:2895841 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:1866486 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:1866486 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:1866486 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:1866486 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:114107680 C>T maps to NM_138430.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:114107680 C>T maps to NM_138430.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:3769829 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:3769829 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:148686894 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:148686894 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:147967381 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:147967381 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:147743878 G>T maps to NM_002025.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:147743878 G>T maps to NM_002025.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:147967381 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:147967381 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:132270356 G>A maps to NM_014423.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:132270356 G>A maps to NM_014423.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:86838536 C>A maps to NM_152336.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:86838536 C>A maps to NM_152336.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:50311969 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:50311969 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:178388447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:178388447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:178388447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:178388447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:105421814 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:105421814 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:105421814 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:105421814 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77929268 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77929268 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:77949063 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:77949063 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:77949063 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:77949063 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:58302787 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:58302787 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:58302787 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:58302787 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125872468 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125872468 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125877629 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125877629 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:125872400 C>G maps to ENST00000273450 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:125872400 C>G maps to ENST00000273450 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:38516621 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:38516621 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:38516621 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:38516621 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:14798451 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:14798451 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:14798451 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:14798451 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:70002983 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:70002983 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:101430706 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:101430706 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:45810525 C>T maps to NM_001142679.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:45810525 C>T maps to NM_001142679.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:46112113 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:46112113 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:169105620 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:169105620 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:169105620 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:169105620 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:124706028 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:124706028 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:124706028 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:124706028 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:150955498 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:150955498 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:150955498 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:150955498 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:36553070 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:36553070 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:36553070 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:36553070 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71792425 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71792425 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71792425 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71792425 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:72047360 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:72047360 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:72047360 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:72047360 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:36369655 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:36369655 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:21227119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:21227119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:21227119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:21227119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:21239498 G>T maps to NM_000384.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:21239498 G>T maps to NM_000384.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:33019874 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:33019874 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:50344588 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:50344588 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:50344588 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:50344588 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:153750761 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:153750761 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:11187672 G>T maps to NM_013427.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:11187672 G>T maps to NM_013427.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156909828 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156909828 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:27059287 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:27059287 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:27059287 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:27059287 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:101801656 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:101801656 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:138014741 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:138014741 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:138014741 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:138014741 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:98514434 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:98514434 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:98514434 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:98514434 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:17916792 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:17916792 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:17916792 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:17916792 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:122968761 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:122968761 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:123065570 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:123065570 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:122968761 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:122968761 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:123065570 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:123065570 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:131193185 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:131193185 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:177136683 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:177136683 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197060987 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197060987 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197102470 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197102470 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197060987 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197060987 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197102470 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197102470 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:150720746 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:150720746 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:152814179 G>A maps to NM_001001344.2 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:152814179 G>A maps to NM_001001344.2 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:111957943 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:111957943 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:63553907 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:63553907 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:63553907 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:63553907 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:79169608 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:79169608 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:11049485 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:11049485 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:143603576 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:143603576 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:38493912 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:38493912 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:160182033 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:160182033 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:73009199 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:73009199 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:73009199 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:73009199 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:33545220 G>A maps to NM_198428.2 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:33545220 G>A maps to NM_198428.2 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:59024872 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:59024872 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:18209220 G>T maps to NM_153346.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:18209220 G>T maps to NM_153346.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:78373282 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:78373282 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:78373282 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:78373282 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:60562749 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:60562749 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:60562749 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:60562749 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:55803156 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:55803156 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:59961503 T>A maps to NM_004330.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:59961503 T>A maps to NM_004330.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:13605955 A>G maps to NM_148894.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:13605955 A>G maps to NM_148894.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:31620694 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:31620694 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:31620694 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:31620694 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:65916017 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:65916017 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:28464260 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:28464260 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:1466780 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:1466780 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:79936969 T>C maps to NM_153252.4 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:79936969 T>C maps to NM_153252.4 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:112198677 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:112198677 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:124923181 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:124923181 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:56393538 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:56393538 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:56393538 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:56393538 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:77806778 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:77806778 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:77806778 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:77806778 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:108276127 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:108276127 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:108276127 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:108276127 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:61539457 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:61539457 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:112717327 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:112717327 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:97073310 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:97073310 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:97073310 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:97073310 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:93653196 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:93653196 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:81223071 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:81223071 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:76452118 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:76452118 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:74192093 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:74192093 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:74192093 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:74192093 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:76452379 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:76452379 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:76452379 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:76452379 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67178684 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67178684 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:67178684 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:67178684 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:49408054 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:49408054 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:22986095 C>A maps to NM_000491.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:22986095 C>A maps to NM_000491.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:77040265 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:77040265 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:34033347 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:34033347 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:34033347 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:34033347 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75097783 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75097783 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:75042609 T>A maps to NM_001002912.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:75042609 T>A maps to NM_001002912.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:75097612 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:75097612 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:178490159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:178490159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:178489730 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:178489730 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:60491230 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:60491230 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:60491230 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:60491230 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:31873971 C>T maps to NM_033197.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:31873971 C>T maps to NM_033197.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:45598868 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:45598868 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:73768379 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:73768379 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:73768379 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:73768379 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:54558012 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:54558012 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:63349300 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:63349300 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:99897072 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:99897072 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:58856152 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:58856152 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:58856152 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:58856152 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:113486362 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:113486362 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:113486362 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:113486362 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:81307880 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:81307880 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:71200713 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:71200713 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:71200713 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:71200713 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:5527279 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:5527279 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:123725387 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:123725387 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:37211202 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:37211202 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:37211202 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:37211202 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:165714861 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:165714861 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:165714863 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:165714863 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:88150896 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:88150896 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:40955833 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:40955833 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:120737690 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:120737690 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:120737690 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:120737690 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:120911453 A>T maps to NM_024913.4 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:120911453 A>T maps to NM_024913.4 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:35045841 C>A maps to NM_203299.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:35045841 C>A maps to NM_203299.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:86570402 C>A maps to NM_032307.3 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:86570402 C>A maps to NM_032307.3 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:4635422 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:4635422 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:4635422 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:4635422 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:27556698 C>T maps to NM_018325.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:27556698 C>T maps to NM_018325.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:114467663 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:114467663 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:114467663 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:114467663 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:49731209 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:49731209 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:121088331 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:121088331 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:121099131 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:121099131 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:121088331 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:121088331 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:13445185 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:13445185 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:13445185 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:13445185 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:2711002 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:2711002 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:2706205 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:2706205 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:2711002 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:2711002 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:53815793 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:53815793 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:53815793 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:53815793 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:181740583 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:181740583 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:181740583 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:181740583 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:49069088 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:49069088 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:49069088 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:49069088 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:81799835 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:81799835 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:81799835 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:81799835 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:1995276 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:1995276 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:1995276 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:1995276 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:152727145 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:152727145 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:152727145 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:152727145 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:36976308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:36976308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71411469 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71411469 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71411469 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71411469 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:134653159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:134653159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:134653159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:134653159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:105209689 G>T maps to NM_015916.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:105209689 G>T maps to NM_015916.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:200709128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:200709128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:200709128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:200709128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:85625789 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:85625789 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:30966563 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:30966563 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:75737779 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:75737779 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:75737779 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:75737779 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:2957067 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:2957067 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:116260374 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:116260374 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:116260374 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:116260374 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:26524382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:26524382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:26524382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:26524382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:219903372 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:219903372 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:219903372 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:219903372 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:185593277 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:185593277 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:185593277 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:185593277 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:128445745 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:128445745 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:119061007 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:119061007 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:119061645 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:119061645 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:119061007 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:119061007 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:77322499 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:77322499 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:119957761 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:119957761 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46521468 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46521468 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:112335749 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:112335749 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:74440083 A>T maps to NM_133493.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:74440083 A>T maps to NM_133493.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158299063 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158299063 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158261700 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158261700 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158323729 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158323729 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158323729 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158323729 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:35836515 C>A maps to NM_001771.3 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:35836515 C>A maps to NM_001771.3 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160811266 C>A maps to NM_001166663.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160811266 C>A maps to NM_001166663.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:5465462 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:5465462 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:80006915 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:80006915 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:118213393 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:118213393 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:157803125 T>A maps to NM_005894.2 K299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:157803125 T>A maps to NM_005894.2 K299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:45215951 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:45215951 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:103416641 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:103416641 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:103416641 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:103416641 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:44841624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:44841624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:44841624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:44841624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:60469903 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:60469903 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:39456810 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:39456810 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:42225228 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:42225228 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:15789158 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:15789158 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:15789158 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:15789158 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:122736482 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:122736482 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:49048049 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:49048049 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:49048049 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:49048049 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117281623 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117281623 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117281623 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117281623 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:88535087 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:88535087 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:180080330 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:180080330 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:180080330 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:180080330 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:14722768 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:14722768 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:14722768 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:14722768 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:55860291 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:55860291 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:55860291 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:55860291 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67007028 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67007028 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:196871740 C>A maps to NM_006684.2 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:196871740 C>A maps to NM_006684.2 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196946875 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196946875 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:196946875 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:196946875 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196709592 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196709592 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:50835835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:50835835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:50835835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:50835835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:6173019 G>A maps to NM_015557.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:6173019 G>A maps to NM_015557.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:111770279 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:111770279 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:111770279 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:111770279 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23767593 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23767593 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:130940540 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:130940540 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:43890470 C>T maps to ENST00000413657 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:43890470 C>T maps to ENST00000413657 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:11896215 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:11896215 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:1499235 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:1499235 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:40228576 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:40228576 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:98241752 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:98241752 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71047031 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71047031 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71047031 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71047031 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141645061 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141645061 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141645061 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141645061 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:35763070 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:35763070 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:35764964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:35764964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:35763070 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:35763070 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:35764964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:35764964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:140265581 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:140265581 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:140265583 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:140265583 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:140265581 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:140265581 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:88249006 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:88249006 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87641336 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87641336 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:87641336 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:87641336 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:87645121 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:87645121 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:21508494 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:21508494 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:154732032 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:154732032 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:154732032 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:154732032 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:58610308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:58610308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:58610308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:58610308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:135048034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:135048034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:135048034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:135048034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:41419238 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:41419238 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:41419238 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:41419238 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:205030381 C>A maps to NM_005076.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:205030381 C>A maps to NM_005076.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:74315626 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:74315626 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:1415641 A>C maps to NM_014461.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:1415641 A>C maps to NM_014461.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:76587151 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:76587151 A>T did not map to a codon.
Alternatively spliced codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:51111276 C>A maps to ENST00000395542 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:51111276 C>A maps to ENST00000395542 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:107188898 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:107188898 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23453752 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23453752 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:23453752 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:23453752 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:71582219 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:71582219 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:121322172 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:121322172 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:121322172 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:121322172 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101806778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101806778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101824746 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101824746 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:101806778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:101806778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:101817382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:101817382 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:32149649 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:32149649 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:46914554 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:46914554 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:70866476 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:70866476 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:94048917 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:94048917 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:94046982 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:94046982 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:94048917 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:94048917 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139629312 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139629312 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139643071 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139643071 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139643071 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139643071 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:189849688 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:189849688 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:189872627 G>A maps to NM_000090.3 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:189872627 G>A maps to NM_000090.3 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:111132682 G>T maps to NM_001846.2 G902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:111132682 G>T maps to NM_001846.2 G902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:137655626 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:137655626 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:137715348 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:137715348 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:137715348 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:137715348 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47541288 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47541288 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:48629038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:48629038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:48629038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:48629038 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:321619 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:321619 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:321619 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:321619 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:130288722 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:130288722 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:36145449 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:36145449 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:36145449 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:36145449 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:46737328 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:46737328 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:46737328 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:46737328 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:148596349 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:148596349 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:83215960 G>A maps to ENST00000261723 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:83215960 G>A maps to ENST00000261723 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:93898080 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:93898080 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:93898080 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:93898080 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:166326062 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:166326062 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:166326062 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:166326062 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:36715859 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:36715859 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:36715859 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:36715859 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:211515046 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:211515046 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:211515046 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:211515046 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197411193 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197411193 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197411193 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197411193 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:49808565 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:49808565 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:49808565 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:49808565 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:33171287 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:33171287 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45893462 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45893462 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:19263714 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:19263714 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61973646 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61973646 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:2976186 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:2976186 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:2967786 C>A maps to NM_033225.5 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:2967786 C>A maps to NM_033225.5 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:34190860 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:34190860 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:34238408 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:34238408 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:34037411 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:34037411 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:34190860 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:34190860 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:34238408 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:34238408 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:113313972 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:113313972 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:113313972 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:113313972 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:113668509 T>A maps to NM_198123.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:113668509 T>A maps to NM_198123.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:148925235 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:148925235 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:148925235 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:148925235 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:24940199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:24940199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:24940199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:24940199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:33120403 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:33120403 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:33120403 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:33120403 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:79422960 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:79422960 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:80772074 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:80772074 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:79422960 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:79422960 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:80772074 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:80772074 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:68936737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:68936737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:68936737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:68936737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:10981744 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:10981744 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:16716560 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:16716560 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:16982287 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:16982287 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:16982287 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:16982287 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:55948537 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:55948537 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:107904742 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:107904742 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:101840602 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:101840602 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:101840602 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:101840602 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:61121426 C>G maps to NM_001161454.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:61121426 C>G maps to NM_001161454.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:143958385 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:143958385 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:143959054 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:143959054 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:41350371 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:41350371 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:135373487 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:135373487 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:99445078 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:99445078 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:99445078 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:99445078 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:99311279 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:99311279 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:99311279 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:99311279 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:85404013 C>A maps to NM_053281.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:85404013 C>A maps to NM_053281.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:85559988 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:85559988 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:122075633 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:122075633 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:122000927 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:122000927 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:122075633 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:122075633 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:136508755 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:136508755 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:50942429 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:50942429 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:155250574 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:155250574 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:155298497 G>T maps to NM_017639.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:155298497 G>T maps to NM_017639.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:36410404 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:36410404 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:41207057 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:41207057 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44605693 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44605693 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44605695 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44605695 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:44605693 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:44605693 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:44605695 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:44605695 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90020840 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90020840 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90028404 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90028404 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:49977032 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:49977032 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:49977032 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:49977032 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:29977159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:29977159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:29977159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:29977159 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:126347 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:126347 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:126347 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:126347 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:126433705 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:126433705 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:126433705 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:126433705 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:33054338 G>A maps to NM_001077242.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:33054338 G>A maps to NM_001077242.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:117228832 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:117228832 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:14797229 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:14797229 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:14216489 C>A maps to NM_004080.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:14216489 C>A maps to NM_004080.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:14797229 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:14797229 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:186015364 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:186015364 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:186015364 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:186015364 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:137096787 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:137096787 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:50146626 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:50146626 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:50146626 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:50146626 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:37647545 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:37647545 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:37647545 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:37647545 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:60555001 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:60555001 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:51100219 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:51100219 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:44680135 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:44680135 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:53927079 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:53927079 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:53927079 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:53927079 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:124325763 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:124325763 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:124325763 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:124325763 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:21599210 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:21599210 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:21599210 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:21599210 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21008587 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21008587 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:11783612 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:11783612 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:11840934 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:11840934 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:11783612 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:11783612 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:73669579 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:73669579 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132196552 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132196552 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:28528036 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:28528036 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:101643711 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:101643711 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:101643711 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:101643711 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:225661641 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:225661641 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:63048785 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:63048785 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:63048785 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:63048785 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:304774 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:304774 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:304774 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:304774 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:65109070 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:65109070 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:116283453 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:116283453 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:116283453 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:116283453 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54135250 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54135250 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54135265 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54135265 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:54135265 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:54135265 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:134006446 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:134006446 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:111674255 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:111674255 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:111674255 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:111674255 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:100486547 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:100486547 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:100486547 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:100486547 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:28654569 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:28654569 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:28654613 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:28654613 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117387250 C>A maps to NM_020693.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117387250 C>A maps to NM_020693.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:28934273 C>A maps to NM_001942.2 Y705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:28934273 C>A maps to NM_001942.2 Y705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:29040748 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:29040748 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:29040748 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:29040748 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:32446245 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:32446245 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:25606863 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:25606863 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:25606863 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:25606863 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122288914 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122288914 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:122288914 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:122288914 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:58956148 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:58956148 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:58956148 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:58956148 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:183882761 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:183882761 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:102476787 G>T maps to NM_001376.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:102476787 G>T maps to NM_001376.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71730501 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71730501 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71817455 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71817455 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71730501 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71730501 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71753316 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71753316 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71817455 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:71817455 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:158139079 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:158139079 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:21548181 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:21548181 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:21548181 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:21548181 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:172491840 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:172491840 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:172491840 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:172491840 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:65824891 G>A maps to ENST00000450752 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:65824891 G>A maps to ENST00000450752 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:148427646 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:148427646 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:148427646 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:148427646 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:22291724 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:22291724 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:22237037 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:22237037 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:22291724 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:22291724 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:82532978 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:82532978 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:140672247 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:140672247 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:53400187 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:53400187 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:53400187 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:53400187 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:103988648 A>T maps to NM_152310.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:103988648 A>T maps to NM_152310.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:2891214 G>T maps to NM_032048.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:2891214 G>T maps to NM_032048.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:225699551 C>A maps to ENST00000284563 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:225699551 C>A maps to ENST00000284563 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:132147333 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:132147333 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:132194287 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:132194287 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:132147333 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:132147333 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:132194287 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:132194287 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:150601401 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:150601401 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:40456137 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:40456137 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:110348496 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:110348496 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:5630368 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:5630368 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:5630368 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:5630368 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:29323865 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:29323865 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:222307443 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:222307443 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:222307443 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:222307443 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22928015 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22928015 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:27379874 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:27379874 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:27379874 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:27379874 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:56270729 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:56270729 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:96121723 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:96121723 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:96121723 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:96121723 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:39947640 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:39947640 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:39947640 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:39947640 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:23713520 T>C maps to NM_033266.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:23713520 T>C maps to NM_033266.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:152265374 C>A maps to NM_001122741.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:152265374 C>A maps to NM_001122741.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:5730916 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:5730916 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:93029338 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:93029338 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:93029338 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:93029338 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:94594604 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:94594604 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:94594604 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:94594604 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:74099686 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:74099686 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:113798161 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:113798161 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:176832264 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:176832264 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:169551805 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:169551805 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:169551805 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:169551805 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:154157068 G>A maps to NM_000132.3 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:154157068 G>A maps to NM_000132.3 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:88422657 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:88422657 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:88422657 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:88422657 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:96320838 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:96320838 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139161031 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139161031 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139189683 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139189683 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139207466 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139207466 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139189683 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139189683 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139207466 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139207466 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139209900 G>A maps to NM_015912.3 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:139209900 G>A maps to NM_015912.3 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:61023710 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:61023710 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:61083902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:61083902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:61083902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:61083902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:6240319 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:6240319 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:62083840 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:62083840 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:187608314 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:187608314 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:187608314 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:187608314 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:29255790 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:29255790 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43613766 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43613766 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43613766 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43613766 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:68055692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:68055692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:68055692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:68055692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:68241717 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:68241717 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:113266600 C>T maps to NM_001004440.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:113266600 C>T maps to NM_001004440.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:113266600 C>T maps to NM_001004440.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:113266600 C>T maps to NM_001004440.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:190250720 C>A maps to NM_199051.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:190250720 C>A maps to NM_199051.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:67675061 C>T maps to NM_173526.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:67675061 C>T maps to NM_173526.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:131822937 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:131822937 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:40702835 C>T maps to NM_001083124.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:40702835 C>T maps to NM_001083124.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:40702835 C>T maps to NM_001083124.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:40702835 C>T maps to NM_001083124.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:33876671 G>T maps to NM_178468.4 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:33876671 G>T maps to NM_178468.4 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:85139043 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:85139043 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:64373465 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:64373465 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:92531038 A>T maps to ENST00000298047 L1620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:92531038 A>T maps to ENST00000298047 L1620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:64888834 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:64888834 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:127671920 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:127671920 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:127671920 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:127671920 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:161680652 G>A maps to NM_001184866.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:161680652 G>A maps to NM_001184866.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:125109469 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:125109469 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:125113597 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:125113597 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:125109469 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:125109469 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:125113597 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:125113597 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:142506698 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:142506698 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:28602307 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:28602307 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:240306300 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:240306300 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:240306300 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:240306300 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:89413710 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:89413710 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:89424599 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:89424599 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:71929837 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:71929837 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:71929837 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:71929837 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:86602481 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:86602481 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:114257954 A>T maps to NM_012184.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:114257954 A>T maps to NM_012184.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:168463474 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:168463474 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:69360559 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:69360559 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:69360559 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:69360559 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:131227987 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:131227987 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:131227987 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:131227987 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:49444597 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:49444597 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:12516993 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:12516993 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:12516993 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:12516993 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:48592644 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:48592644 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:48592644 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:48592644 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:49210403 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:49210403 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:120130653 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:120130653 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:162954854 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:162954854 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47556895 C>T maps to ENST00000397748 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47556895 C>T maps to ENST00000397748 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61901976 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61901976 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:61901976 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:61901976 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117711950 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117711950 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117711950 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117711950 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:39130754 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:39130754 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:39130754 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:39130754 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:112020598 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:112020598 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:112020598 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:112020598 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:17451134 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:17451134 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:17451134 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:17451134 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:101370372 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:101370372 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:46334590 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:46334590 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:46334590 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:46334590 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:151533049 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:151533049 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:47427875 G>T maps to NM_000812.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:47427875 G>T maps to NM_000812.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:151131076 G>A maps to NM_004961.3 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:151131076 G>A maps to NM_004961.3 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:27453677 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:27453677 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:89895077 G>A maps to NM_002042.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:89895077 G>A maps to NM_002042.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:49369850 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:49369850 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:49369850 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:49369850 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:882786 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:882786 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:31135330 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:31135330 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:31135330 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:31135330 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:173803856 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:173803856 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:173803856 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:173803856 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:130101922 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:130101922 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:72618402 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:72618402 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:72618402 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:72618402 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:76990495 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:76990495 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61995315 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61995315 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:59610486 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:59610486 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:59610486 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:59610486 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:14591628 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:14591628 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46181125 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46181125 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:46181125 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:46181125 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:6589150 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:6589150 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:6589150 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:6589150 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:39046705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:39046705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:39046705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:39046705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:9756593 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:9756593 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:9756593 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:9756593 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:131958333 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:131958333 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:220366107 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:220366107 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:220366107 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:220366107 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:30520220 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:30520220 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:30520220 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:30520220 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:94047717 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:94047717 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:157426763 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:157426763 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:34890733 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:34890733 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:34890733 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:34890733 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:135429795 C>T maps to NM_153834.3 Q1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:135429795 C>T maps to NM_153834.3 Q1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:105518392 G>T maps to NM_013345.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:105518392 G>T maps to NM_013345.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:124386576 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:124386576 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:124386576 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:124386576 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:133174583 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:133174583 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:133174583 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:133174583 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:11736150 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:11736150 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:105804493 C>A maps to NM_000829.3 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:105804493 C>A maps to NM_000829.3 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:93511468 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:93511468 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:94690277 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:94690277 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:93511468 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:93511468 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:94690277 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:94690277 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:101878313 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:101878313 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:101878313 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:101878313 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:37338047 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:37338047 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:37338047 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:37338047 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:3006136 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:3006136 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:3006136 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:3006136 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:121190063 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:121190063 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:86415734 C>T maps to NM_000840.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:86415734 C>T maps to NM_000840.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:88386666 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:88386666 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:88386666 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:88386666 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:126173068 G>A maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:126173068 G>A maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:52663829 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:52663829 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:52858888 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:52858888 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110200049 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110200049 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110257933 C>A maps to ENST00000369813 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110257933 C>A maps to ENST00000369813 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:89975865 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:89975865 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:108627168 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:108627168 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:106888444 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:106888444 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:108652428 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:108652428 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:65425805 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:65425805 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:25075913 G>T maps to NM_033423.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:25075913 G>T maps to NM_033423.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:42996758 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:42996758 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:122626342 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:122626342 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:122626342 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:122626342 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:45396926 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:45396926 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:141005721 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:141005721 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:141005721 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:141005721 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:48196166 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:48196166 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156721085 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156721085 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:6995464 C>A maps to NM_001135565.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:6995464 C>A maps to NM_001135565.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:145245885 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:145245885 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:138727306 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:138727306 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:138727306 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:138727306 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:65409396 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:65409396 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:65409396 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:65409396 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:26093223 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:26093223 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:91794384 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:91794384 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:91794384 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:91794384 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:91794570 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:91794570 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:42738368 C>A maps to NM_020707.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:42738368 C>A maps to NM_020707.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:75221301 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:75221301 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:75221301 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:75221301 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:26124160 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:26124160 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:26124160 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:26124160 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:149858221 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:149858221 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:149858221 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:149858221 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:234762654 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:234762654 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:38139632 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:38139632 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:38139632 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:38139632 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:148777446 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:148777446 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:186107157 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:186107157 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:186114768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:186114768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:186083063 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:186083063 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:186114768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:186114768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:76456308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:76456308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:76456308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:76456308 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:76472699 C>A maps to NM_004133.4 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:76472699 C>A maps to NM_004133.4 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26240185 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26240185 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:26240185 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:26240185 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:83543935 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:83543935 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:83543935 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:83543935 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:46805161 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:46805161 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:54403671 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:54403671 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18316469 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18316469 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18316469 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18316469 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:84240261 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:84240261 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:6452733 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:6452733 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:6452733 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:6452733 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:209878478 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:209878478 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118439003 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118439003 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118460770 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118460770 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:118439003 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:118439003 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:31712416 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:31712416 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:114082455 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:114082455 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:70908692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:70908692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71103062 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71103062 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71220571 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:71220571 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:70908692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:70908692 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71103062 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71103062 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71220571 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:71220571 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:220315368 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:220315368 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:45651050 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:45651050 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50327584 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50327584 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:159998597 T>A maps to ENST00000483754 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:159998597 T>A maps to ENST00000483754 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:45932542 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:45932542 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:45932542 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:45932542 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:68696884 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:68696884 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:151164626 C>A maps to NM_178822.4 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:151164626 C>A maps to NM_178822.4 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18745666 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18745666 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18745666 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18745666 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160063199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160063199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160063199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160063199 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:111673502 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:111673502 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:111673502 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:111673502 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:14153293 G>T maps to NM_004843.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:14153293 G>T maps to NM_004843.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:3131893 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:3131893 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:3131893 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:3131893 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:79673607 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:79673607 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:79673607 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:79673607 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:57850767 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:57850767 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:15243084 G>T maps to NM_001031853.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:15243084 G>T maps to NM_001031853.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:1519027 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:1519027 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:59962346 G>A maps to NM_020748.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:59962346 G>A maps to NM_020748.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:128632152 G>T maps to NM_015693.3 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:128632152 G>T maps to NM_015693.3 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:30837233 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:30837233 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:19830881 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:19830881 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:75918957 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:75918957 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:75918957 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:75918957 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156507149 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156507149 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:156507149 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:156507149 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:396690 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:396690 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77948568 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77948568 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:31422033 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:31422033 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:31422033 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:31422033 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:31383686 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:31383686 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:31383686 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:31383686 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:3939949 G>T maps to NM_170678.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:3939949 G>T maps to NM_170678.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:45366889 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:45366889 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:73724341 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:73724341 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:124538551 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:124538551 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:124538551 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:124538551 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:52818396 C>T maps to NM_002215.2 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:52818396 C>T maps to NM_002215.2 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:7773793 C>A maps to NM_002216.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:7773793 C>A maps to NM_002216.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:24426443 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:24426443 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:24426443 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:24426443 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:5126874 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:5126874 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:147019031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:147019031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:147019031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:147019031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:15513093 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:15513093 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:15513093 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:15513093 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24041134 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24041134 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:24041134 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:24041134 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:124053025 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:124053025 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:124053025 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:124053025 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:62738854 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:62738854 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:62738854 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:62738854 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:73479951 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:73479951 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:73479951 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:73479951 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:17793206 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:17793206 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:17793206 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:17793206 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150648496 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150648496 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:150648496 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:150648496 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:49937034 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:49937034 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:63468327 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:63468327 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:118960760 C>T maps to NM_181840.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:118960760 C>T maps to NM_181840.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:133152308 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:133152308 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:133152308 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:133152308 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:73696654 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:73696654 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:73696654 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:73696654 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:215777453 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:215777453 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:215759873 G>C maps to NM_016121.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:215759873 G>C maps to NM_016121.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:215777453 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:215777453 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:86718114 C>T maps to NM_001146688.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:86718114 C>T maps to NM_001146688.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:202735990 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:202735990 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:202735990 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:202735990 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:142651691 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:142651691 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:142651691 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:142651691 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:2820098 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:2820098 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:15729468 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:15729468 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43889028 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43889028 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43891435 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43891435 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43889028 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43889028 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43891435 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43891435 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43909129 T>C maps to NM_015284.2 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43909129 T>C maps to NM_015284.2 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:27765432 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:27765432 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:27765432 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:27765432 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:55356792 G>A maps to NM_001098815.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:55356792 G>A maps to NM_001098815.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:75555263 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:75555263 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:57193735 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:57193735 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:57193735 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:57193735 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:72293677 G>T maps to NM_014431.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:72293677 G>T maps to NM_014431.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:34415150 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:34415150 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94101055 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94101055 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94101055 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94101055 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:59942666 T>A maps to NM_020854.3 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:59942666 T>A maps to NM_020854.3 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:36854256 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:36854256 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:29048492 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:29048492 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:29048492 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:29048492 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:72338733 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:72338733 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:241658641 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:241658641 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:241658641 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:241658641 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:29810855 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:29810855 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:29810855 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:29810855 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55377733 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55377733 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55377733 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55377733 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:126306856 G>A maps to NM_032531.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:126306856 G>A maps to NM_032531.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:130417830 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:130417830 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:73636957 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:73636957 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:73636957 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:73636957 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51327019 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51327019 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:51327019 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:51327019 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:135011790 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:135011790 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:186440180 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:186440180 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:186440180 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:186440180 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:52910578 A>G maps to NM_000424.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:52910578 A>G maps to NM_000424.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:71249014 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:71249014 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:71249014 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:71249014 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:130378623 G>T maps to NM_032438.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:130378623 G>T maps to NM_032438.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55020356 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55020356 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:6976125 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:6976125 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:6976125 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:6976125 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:129511366 A>T maps to NM_000426.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:129511366 A>T maps to NM_000426.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:112494031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:112494031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:112494031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:112494031 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:107745082 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:107745082 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:107745082 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:107745082 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:133962640 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:133962640 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:119580318 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:119580318 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:119580318 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:119580318 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:36993348 G>T maps to NM_004139.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:36993348 G>T maps to NM_004139.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:152552358 T>G maps to NM_032563.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:152552358 T>G maps to NM_032563.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:152552406 G>T maps to NM_032563.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:152552406 G>T maps to NM_032563.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:152681628 C>T maps to NM_178356.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:152681628 C>T maps to NM_178356.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:75150746 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:75150746 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:36018904 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:36018904 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:66042550 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:66042550 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:66042550 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:66042550 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:76970702 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:76970702 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:25013900 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:25013900 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:25014017 G>A maps to NM_018176.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:25014017 G>A maps to NM_018176.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:22005800 C>A maps to NM_139278.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:22005800 C>A maps to NM_139278.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:49520184 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:49520184 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:111874562 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:111874562 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:111874562 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:111874562 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197890481 C>A maps to NM_020204.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:197890481 C>A maps to NM_020204.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:108861584 G>A maps to NM_001098268.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:108861584 G>A maps to NM_001098268.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54848656 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54848656 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55147919 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55147919 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55146211 C>A maps to ENST00000427581 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55146211 C>A maps to ENST00000427581 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55147919 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55147919 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54746495 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54746495 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54743049 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54743049 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:54746495 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:54746495 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55174613 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55174613 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55175158 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55175158 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55175158 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:55175158 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156106668 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156106668 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:129453364 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:129453364 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:148016365 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:148016365 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:121402392 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:121402392 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:121402392 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:121402392 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:160998096 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:160998096 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:160998096 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:160998096 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:81967921 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:81967921 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:2922222 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:2922222 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:2922222 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:2922222 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:170010811 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:170010811 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:53747619 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:53747619 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:71185459 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:71185459 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:48474404 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:48474404 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:85438656 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:85438656 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:74648614 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:74648614 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:80530119 C>A maps to NM_178839.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:80530119 C>A maps to NM_178839.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:77745830 G>A maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:77745830 G>A maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:115805318 C>A maps to NM_002338.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:115805318 C>A maps to NM_002338.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:33174088 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:33174088 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:33442568 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:33442568 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:33442568 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:33442568 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:74972697 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:74972697 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:74972697 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:74972697 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43966017 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43966017 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43966017 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43966017 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:39945450 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:39945450 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:39945450 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:39945450 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:151896835 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:151896835 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:140983001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:140983001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:140983001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:140983001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:140809942 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:140809942 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:109117173 G>C maps to NM_002372.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:109117173 G>C maps to NM_002372.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:242162036 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:242162036 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:242162036 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:242162036 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:165110490 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:165110490 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:220752847 G>A maps to NM_018650.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:220752847 G>A maps to NM_018650.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:45769741 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:45769741 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:186938943 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:186938943 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:186938943 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:186938943 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:43922339 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:43922339 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:47801654 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:47801654 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:1581087 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:1581087 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:47315115 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:47315115 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:37561571 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:37561571 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:156438559 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:156438559 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:3298785 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:3298785 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:126666978 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:126666978 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:126666978 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:126666978 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:42862464 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:42862464 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:42112001 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:42112001 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:99970128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:99970128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:99970128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:99970128 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141734529 G>T maps to ENST00000475668 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141734529 G>T maps to ENST00000475668 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141740037 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141740037 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141765176 C>A maps to ENST00000475668 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:141765176 C>A maps to ENST00000475668 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:74899481 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:74899481 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:74899481 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:74899481 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:43232886 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:43232886 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:43232886 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:43232886 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:38664294 G>A maps to NM_021242.4 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:38664294 G>A maps to NM_021242.4 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:7634817 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:7634817 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:7634817 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:7634817 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:122617835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:122617835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:122617835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:122617835 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:89198858 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:89198858 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:89198858 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:89198858 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158811813 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158811813 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158811813 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158811813 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:174537961 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:174537961 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:174537961 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:174537961 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:13125096 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:13125096 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:16978979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:16978979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:17076221 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:17076221 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:16978979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:16978979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18159296 G>A maps to NM_054031.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18159296 G>A maps to NM_054031.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:60274424 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:60274424 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:60274424 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:60274424 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:72754931 A>T maps to NM_005098.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:72754931 A>T maps to NM_005098.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:47690446 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:47690446 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:121457873 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:121457873 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:121457873 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:121457873 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:151277327 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:151277327 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:9712910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:9712910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:9712910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:9712910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:11193403 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:11193403 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:236988760 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:236988760 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:236988760 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:236988760 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:30072407 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:30072407 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:9038272 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:9038272 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:9038272 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:9038272 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:9047920 G>T maps to NM_024690.2 S11237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:9047920 G>T maps to NM_024690.2 S11237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:100680894 A>C maps to NM_001040105.1 T2066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:100680894 A>C maps to NM_001040105.1 T2066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:42811571 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:42811571 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:42811571 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:42811571 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:42771257 C>T maps to NM_002463.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:42771257 C>T maps to NM_002463.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:102020705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:102020705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:102020705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:102020705 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:203137865 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:203137865 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:77837726 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:77837726 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:48441132 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:48441132 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:48441132 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:48441132 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:15847437 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:15847437 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:10420001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:10420001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:10446622 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:10446622 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:10448801 G>A maps to NM_017534.5 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:10448801 G>A maps to NM_017534.5 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:23853534 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:23853534 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:23853534 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:23853534 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:26422330 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:26422330 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:26422330 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:26422330 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:31105501 C>A maps to NM_015194.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:31105501 C>A maps to NM_015194.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:47373437 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:47373437 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:47373437 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:47373437 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:24388532 G>A maps to ENST00000330966 H1282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:24388532 G>A maps to ENST00000330966 H1282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:76736088 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:76736088 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:101797006 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:101797006 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:73868895 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:73868895 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:15701450 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:15701450 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:15417225 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:15417225 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:15701450 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:15701450 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:16894129 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:16894129 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:16901286 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:16901286 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3193455 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3193455 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:41309910 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:41309910 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:41318321 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:41318321 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:41309910 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:41309910 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:41318321 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:41318321 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:21486633 G>T maps to NM_201537.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:21486633 G>T maps to NM_201537.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119059180 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119059180 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:119059180 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:119059180 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:119158233 C>A maps to NM_004784.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:119158233 C>A maps to NM_004784.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:10979454 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:10979454 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:10979454 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:10979454 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:152512819 G>A maps to NM_001164507.1 H2114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:152512819 G>A maps to NM_001164507.1 H2114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:72400909 C>A maps to NM_173808.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:72400909 C>A maps to NM_173808.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52797445 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52797445 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:52797445 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:52797445 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:127089783 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:127089783 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:20982130 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:20982130 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:20982130 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:20982130 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156644958 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156644958 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:70423368 G>T maps to NM_153181.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:70423368 G>T maps to NM_153181.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:41060586 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:41060586 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:41060586 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:41060586 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:233791951 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:233791951 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:63831078 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:63831078 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:63831078 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:63831078 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:61874101 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:61874101 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:40175883 C>T maps to ENST00000316082 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:40175883 C>T maps to ENST00000316082 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:172662180 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:172662180 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:85417017 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:85417017 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:85417017 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:85417017 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:32477680 G>T maps to NM_021209.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:32477680 G>T maps to NM_021209.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:144097390 G>A maps to ENST00000467773 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:144097390 G>A maps to ENST00000467773 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:156747083 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:156747083 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:162039934 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:162039934 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:89106818 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:89106818 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44573286 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44573286 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:44573286 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:44573286 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:92929644 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:92929644 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:200116835 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:200116835 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:200116835 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:200116835 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:127306143 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:127306143 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:24145767 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:24145767 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:24145767 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:24145767 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:64409969 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:64409969 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:78993115 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:78993115 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:78748475 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:78748475 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:78748475 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:78748475 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:78993115 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:78993115 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:6611753 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:6611753 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:131240962 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:131240962 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:107973207 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:107973207 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:107973207 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:107973207 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156834307 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156834307 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156786036 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156786036 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:87636430 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:87636430 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:163298634 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:163298634 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:229602601 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:229602601 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:229622034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:229622034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:229622034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:229622034 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:135310153 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:135310153 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:135310153 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:135310153 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:183989184 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:183989184 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:183989184 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:183989184 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:56878327 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:56878327 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:56878327 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:56878327 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:3697904 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:3697904 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:3697904 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:3697904 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:62569273 G>A maps to NM_006362.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:62569273 G>A maps to NM_006362.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24877033 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24877033 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:24877033 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:24877033 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:228523917 C>A maps to NM_001098623.1 S5495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:228523917 C>A maps to NM_001098623.1 S5495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:128722832 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:128722832 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:128722832 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:128722832 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:183664645 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:183664645 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:50943219 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:50943219 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:50943219 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:50943219 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44735843 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:44735843 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:127566287 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:127566287 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:47754189 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:47754189 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:47754189 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:47754189 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:58034386 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:58034386 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:58034386 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:58034386 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:247695357 C>T maps to NM_198074.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:247695357 C>T maps to NM_198074.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248099994 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248099994 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248099832 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248099832 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248099994 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248099994 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248247801 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248247801 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248366270 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248366270 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248366270 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248366270 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248487613 A>T maps to NM_001004691.1 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248487613 A>T maps to NM_001004691.1 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248551409 G>T maps to NM_001005471.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:248551409 G>T maps to NM_001005471.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:20528424 C>T maps to NM_001004717.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:20528424 C>T maps to NM_001004717.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:22383506 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:22383506 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:4661634 C>G maps to NM_001004751.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:4661634 C>G maps to NM_001004751.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:55563648 C>T maps to NM_001004735.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:55563648 C>T maps to NM_001004735.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55762105 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55762105 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:55762105 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:55762105 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:98188533 C>G maps to NM_001004736.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:98188533 C>G maps to NM_001004736.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:56000764 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:56000764 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:56000764 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:56000764 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158687392 G>T maps to ENST00000368146 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158687392 G>T maps to ENST00000368146 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:124413478 G>T maps to NM_001005195.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:124413478 G>T maps to NM_001005195.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:56510306 T>C maps to NM_001005284.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:56510306 T>C maps to NM_001005284.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:24910523 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:24910523 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:24910523 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:24910523 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:77749226 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:77749226 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:77749226 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:77749226 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21747485 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21747485 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:21737979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:21737979 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:26690190 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:26690190 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:26696879 C>A maps to NM_194248.2 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:26696879 C>A maps to NM_194248.2 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:23240418 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:23240418 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:23240418 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:23240418 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:79804554 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:79804554 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:20706082 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:20706082 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:20706082 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:20706082 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:66001696 G>A maps to NM_018026.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:66001696 G>A maps to NM_018026.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:17596638 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:17596638 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:17596638 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:17596638 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:55247099 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:55247099 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:77085291 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:77085291 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:77085291 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:77085291 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:44585217 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:44585217 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:154775015 C>A maps to NM_007349.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:154775015 C>A maps to NM_007349.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47329245 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47329245 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47350782 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:47350782 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:47329245 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:47329245 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:91237943 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:91237943 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:91456339 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:91456339 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:91237943 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:91237943 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:91456339 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:91456339 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:55996850 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:55996850 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:56138764 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:56138764 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:56138764 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:56138764 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140255191 G>T maps to NM_018903.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140255191 G>T maps to NM_018903.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140181996 C>T maps to NM_018906.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140181996 C>T maps to NM_018906.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140504016 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140504016 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140504016 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140504016 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140559207 G>A maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140559207 G>A maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140712338 G>T maps to NM_018912.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140712338 G>T maps to NM_018912.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140783352 A>T maps to NM_018921.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:140783352 A>T maps to NM_018921.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:82387820 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:82387820 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:82453744 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:82453744 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:82387820 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:82387820 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:17868210 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:17868210 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:55512124 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:55512124 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:55512124 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:55512124 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:72307580 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:72307580 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:14793553 T>C maps to ENST00000455098 C340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:14793553 T>C maps to ENST00000455098 C340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:18330264 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:18330264 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:144854299 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:144854299 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:95425129 A>T maps to NM_006204.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:95425129 A>T maps to NM_006204.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:44119000 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:44119000 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:44119000 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:44119000 G>T did not map to a codon.
Alternatively spliced codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:55124842 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:55124842 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:55124842 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:55124842 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122829930 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122829930 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:70179941 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:70179941 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:31908856 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:31908856 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:31908856 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:31908856 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:153068739 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:153068739 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:41587844 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:41587844 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:64335370 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:64335370 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:64335370 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:64335370 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:8047244 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:8047244 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:8047244 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:8047244 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:7870083 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:7870083 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:7870083 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:7870083 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:152682169 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:152682169 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:152601092 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:152601092 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:152682169 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:152682169 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:77895334 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:77895334 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:179529713 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:179529713 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:179529713 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:179529713 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:6261766 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:6261766 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:75415337 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:75415337 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:22051347 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:22051347 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:11022087 G>T maps to ENST00000303905 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:11022087 G>T maps to ENST00000303905 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:11068426 A>T maps to ENST00000303905 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:11068426 A>T maps to ENST00000303905 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:45975092 C>A maps to ENST00000257821 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:45975092 C>A maps to ENST00000257821 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:120266092 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:120266092 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:120266092 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:120266092 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:41750471 C>A maps to NM_003924.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:41750471 C>A maps to NM_003924.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:44426602 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:44426602 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:44426602 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:44426602 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:204416816 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:204416816 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:36935737 C>T maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:36935737 C>T maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:65467726 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:65467726 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:47925685 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:47925685 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:47925685 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:47925685 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2162318 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2162318 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:51934347 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:51934347 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:51934347 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:51934347 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:123039186 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:123039186 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:125267644 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:125267644 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:125267644 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:125267644 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:159518086 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:159518086 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:159518086 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:159518086 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:20416396 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:20416396 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:20416396 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:20416396 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:160826640 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:160826640 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28815740 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28815740 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28821732 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28821732 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:28821732 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:28821732 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:28855887 C>T maps to NM_153021.4 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:28855887 C>T maps to NM_153021.4 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:8352141 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:8352141 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:8352141 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:8352141 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:219492944 A>T maps to ENST00000432688 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:219492944 A>T maps to ENST00000432688 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:41510643 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:41510643 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:41510643 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:41510643 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:145007614 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:145007614 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:145049200 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:145049200 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:131935719 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:131935719 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:132066683 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:132066683 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:131935719 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:131935719 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:132066683 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:132066683 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:43937476 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:43937476 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:43937476 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:43937476 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:131844131 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:131844131 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:131866250 G>A maps to NM_020911.1 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:131866250 G>A maps to NM_020911.1 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:129279566 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:129279566 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118225390 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118225390 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:121209248 C>A maps to ENST00000393672 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:121209248 C>A maps to ENST00000393672 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:97679 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:97679 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:38154928 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:38154928 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:38154928 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:38154928 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:124511119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:124511119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:124511119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:124511119 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:19573003 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:19573003 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:18824740 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:18824740 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:18824740 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:18824740 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:27799116 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:27799116 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:81108690 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:81108690 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43126518 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43126518 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43126518 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:43126518 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:22048980 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:22048980 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:202400954 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:202400954 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:45895688 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:45895688 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:146086737 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:146086737 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:146086737 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:146086737 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94731787 C>T maps to NM_058237.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94731787 C>T maps to NM_058237.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46888250 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46888250 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:47087208 C>T maps to NM_005972.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:47087208 C>T maps to NM_005972.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:43279668 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:43279668 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:43279668 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:43279668 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:121737749 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:121737749 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:121737749 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:121737749 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:23522647 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:23522647 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:23522647 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:23522647 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:24196564 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:24196564 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:24046866 C>A maps to NM_002738.6 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:24046866 C>A maps to NM_002738.6 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:24196564 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:24196564 A>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:30095615 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:30095615 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:48744517 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:48744517 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:48744517 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:48744517 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:120354907 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:120354907 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54625416 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:54625416 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:109241224 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:109241224 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:120022157 G>T maps to NM_016644.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:120022157 G>T maps to NM_016644.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:33786547 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:33786547 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:33786547 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:33786547 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:79468995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:79468995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:79468995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:79468995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43421980 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43421980 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43430512 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43430512 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43528752 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43528752 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43601537 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43601537 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43421980 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43421980 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43430512 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43430512 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43528752 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43528752 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43601384 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43601384 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43601537 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:43601537 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:35761598 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:35761598 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:11594436 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:11594436 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:125149045 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:125149045 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:125149045 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:125149045 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:46944738 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:46944738 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18754823 C>A maps to NM_032781.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:18754823 C>A maps to NM_032781.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:198723576 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:198723576 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:198723576 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:198723576 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:8376745 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:8376745 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:8484042 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:8484042 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:8376745 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:8376745 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:8484042 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:8484042 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:62248419 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:62248419 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:61728161 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:61728161 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:62248419 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:62248419 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:157341533 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:157341533 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:40790289 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:40790289 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:52252001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:52252001 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:52370246 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:52370246 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:57661934 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:57661934 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:72176541 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:72176541 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:154490315 G>T maps to NM_171998.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:154490315 G>T maps to NM_171998.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:110086365 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:110086365 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:110086365 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:110086365 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:34813771 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:34813771 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:34813771 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:34813771 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:2935768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:2935768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:2935768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:2935768 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:50368056 G>A maps to NM_170714.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:50368056 G>A maps to NM_170714.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:56940110 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:56940110 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:43942876 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:43942876 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:43942876 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:43942876 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:68192623 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:68192623 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:68192623 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:68192623 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:79254917 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:79254917 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:34404942 A>T maps to NM_002915.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:34404942 A>T maps to NM_002915.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:74657792 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:74657792 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:74657792 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:74657792 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:107078751 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:107078751 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:107078751 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:107078751 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:19304656 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:19304656 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:19304656 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:19304656 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:100479468 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:100479468 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:183853842 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:183853842 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:183853842 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:183853842 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:73165951 A>T maps to NM_001080479.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:73165951 A>T maps to NM_001080479.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:192312065 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:192312065 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:192312065 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:192312065 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156346891 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:156346891 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:22868121 C>T maps to NM_001160036.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:22868121 C>T maps to NM_001160036.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:124007938 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:124007938 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:124007938 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:124007938 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:105026851 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:105026851 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:105026851 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:105026851 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:93125369 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:93125369 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:93125369 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:93125369 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:96508993 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:96508993 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:96508993 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:96508993 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:40695490 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:40695490 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:40695490 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:40695490 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67681404 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67681404 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:21424253 C>A maps to NM_002934.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:21424253 C>A maps to NM_002934.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:25356049 G>A maps to ENST00000381927 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:25356049 G>A maps to ENST00000381927 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:5760559 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:5760559 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:78667282 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:78667282 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:18619671 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:18619671 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125691122 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125691122 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:10469885 G>T maps to NM_178857.5 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:10469885 G>T maps to NM_178857.5 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:21813233 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:21813233 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:8281100 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:8281100 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:58009172 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:58009172 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:78854318 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:78854318 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:99130130 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:99130130 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:11935947 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:11935947 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43623572 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43623572 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62294125 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62294125 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62305088 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62305088 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46000122 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46000122 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:159494025 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:159494025 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:159494025 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:159494025 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:165389056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:165389056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:165389056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:165389056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237604834 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237604834 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237893717 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237893717 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237604834 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237604834 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237729942 G>A maps to NM_001035.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237729942 G>A maps to NM_001035.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237893717 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237893717 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237955445 G>T maps to NM_001035.2 T4535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:237955445 G>T maps to NM_001035.2 T4535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:33765777 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:33765777 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:33765777 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:33765777 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:134992774 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:134992774 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:134992774 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:134992774 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:119505958 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:119505958 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:55236949 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:55236949 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:55236949 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:55236949 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:128757523 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:128757523 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:84349255 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:84349255 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:84349255 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:84349255 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:9985306 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:9985306 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:224463261 C>A maps to NM_003469.4 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:224463261 C>A maps to NM_003469.4 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:166025351 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:166025351 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:166025351 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:166025351 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:123524583 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:123524583 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:62018709 C>G maps to NM_000334.4 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:62018709 C>G maps to NM_000334.4 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:139301895 G>A maps to NM_001039707.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:139301895 G>A maps to NM_001039707.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:113836438 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:113836438 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:113836438 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:113836438 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:30865962 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:30865962 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:30865962 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:30865962 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:5053368 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:5053368 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119745613 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119745613 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:151340635 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:151340635 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:169698624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:169698624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:169698624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:169698624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50220472 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50220472 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:9108440 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:9108440 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:9108440 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:9108440 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122642417 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122642417 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122629254 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:122629254 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:122642417 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:122642417 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94750230 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94750230 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94750230 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94750230 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94914952 G>T maps to NM_001080451.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94914952 G>T maps to NM_001080451.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94845954 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94845954 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94845954 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:94845954 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:61328497 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:61328497 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:61328497 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:61328497 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179981606 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179981606 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:29897070 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:29897070 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:26761402 C>A maps to NM_021115.4 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:26761402 C>A maps to NM_021115.4 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:7214427 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:7214427 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:7214427 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:7214427 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:67154723 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:67154723 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:67154723 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:67154723 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:42213456 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:42213456 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:42213456 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:42213456 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:67679619 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:67679619 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:67679619 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:67679619 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:51143399 G>T maps to NM_001080420.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:51143399 G>T maps to NM_001080420.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:72873745 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:72873745 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:72873745 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:72873745 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:51914384 G>A maps to NM_033130.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:51914384 G>A maps to NM_033130.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:52031217 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:52031217 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51957681 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51957681 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:164737624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:164737624 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:57232318 G>A maps to NM_001100595.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:57232318 G>A maps to NM_001100595.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26779700 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26779700 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:26779577 G>A maps to NM_003930.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:26779577 G>A maps to NM_003930.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160589778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160589778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160589778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160589778 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160708986 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160708986 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160708986 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:160708986 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:70263455 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:70263455 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:70263455 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:70263455 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:103701509 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:103701509 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:6597648 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:6597648 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:121634398 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:121634398 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:121634398 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:121634398 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:25849498 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:25849498 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:25769243 C>A maps to NM_005495.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:25769243 C>A maps to NM_005495.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:36686205 C>A maps to NM_004172.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:36686205 C>A maps to NM_004172.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:38316549 G>T maps to NM_004256.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:38316549 G>T maps to NM_004256.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:38350686 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:38350686 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:38350686 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:38350686 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:3324005 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:3324005 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:3324005 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:3324005 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:131671761 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:131671761 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:131671761 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:131671761 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:131705590 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:131705590 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:46638782 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:46638782 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:92355524 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:92355524 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:92407147 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:92407147 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:92407147 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:92407147 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:27481081 C>T maps to NM_003459.4 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:27481081 C>T maps to NM_003459.4 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:44223447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:44223447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:44223447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:44223447 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:118598723 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:118598723 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:118598723 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:118598723 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:58036698 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:58036698 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:79250739 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:79250739 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75708483 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75708483 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:75708483 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:75708483 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:8385340 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:8385340 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:8385340 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:8385340 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:33954455 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:33954455 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:72166738 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:72166738 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:72300256 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:72300256 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:26714268 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:26714268 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:32647633 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:32647633 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:101576499 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:101576499 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:10967662 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:10967662 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:10967662 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:10967662 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:330507 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:330507 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:85266250 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:85266250 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:1213973 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:1213973 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:1213591 C>A maps to NM_001003841.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:1213591 C>A maps to NM_001003841.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:20639586 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:20639586 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87235402 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87235402 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:17396447 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:17396447 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:17396447 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:17396447 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:70513149 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:70513149 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:70513149 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:70513149 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:173502735 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:173502735 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:173502735 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:173502735 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:103090057 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:103090057 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:48431737 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:48431737 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:21450291 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:21450291 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:20886041 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:20886041 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:20886041 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:20886041 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:70667569 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:70667569 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:70706594 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:70706594 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:70667569 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:70667569 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:70706594 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:70706594 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:98824673 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:98824673 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:168151503 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:168151503 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:2191191 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:2191191 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:2191191 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:2191191 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:45802672 T>A maps to NM_148674.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:45802672 T>A maps to NM_148674.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:33052932 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:33052932 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:214504120 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:214504120 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:214504120 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:214504120 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:246673570 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:246673570 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:10273751 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:10273751 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:127339009 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:127339009 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:96970435 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:96970435 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:96970435 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:96970435 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:46190771 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:46190771 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:46190771 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:46190771 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:137483857 C>A maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:137483857 C>A maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:231162201 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:231162201 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:231162201 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:231162201 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:118693336 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:118693336 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:140336458 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:140336458 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:140336458 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:140336458 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:24697587 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:24697587 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:24697587 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:24697587 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:99913516 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:99913516 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:99913516 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:99913516 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:35793322 G>T maps to NM_024867.3 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:35793322 G>T maps to NM_024867.3 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:89934656 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:89934656 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:136476388 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:136476388 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:153005015 C>A maps to NM_003125.2 C65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:153005015 C>A maps to NM_003125.2 C65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55655750 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55655750 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:55655750 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:55655750 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158589183 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158589183 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158612857 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158612857 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158637963 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158637963 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158589183 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158589183 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158612857 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158612857 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158637963 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:158637963 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:45826565 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:45826565 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:64480810 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:64480810 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:64480810 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:64480810 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:130059931 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:130059931 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:130060320 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:130060320 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:130059931 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:130059931 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:53045887 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:53045887 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:53045887 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:53045887 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:53124598 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:53124598 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:55021551 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:55021551 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:68436839 T>A maps to NM_012108.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:68436839 T>A maps to NM_012108.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:37814805 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:37814805 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:37814805 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:37814805 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:192011544 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:192011544 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:192011544 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:192011544 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:134040417 G>T maps to NM_173575.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:134040417 G>T maps to NM_173575.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61790732 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:61790732 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:61790732 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:61790732 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:4422553 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:4422553 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:4422553 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:4422553 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:121076185 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:121076185 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:149877219 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:149877219 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46347197 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:46347197 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:152763329 G>T maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:152763329 G>T maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:64678610 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:64678610 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:64678610 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:64678610 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45277522 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45277522 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55685663 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55685663 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:7324197 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:7324197 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:85459315 T>A maps to NM_001162953.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:85459315 T>A maps to NM_001162953.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:47685901 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:47685901 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:102197167 C>T maps to NM_152334.2 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:102197167 C>T maps to NM_152334.2 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:6639556 C>A maps to NM_138697.3 Y813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:6639556 C>A maps to NM_138697.3 Y813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:75901814 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:75901814 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:75901814 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr13:75901814 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:85446331 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:85446331 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:85446331 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:85446331 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:168208126 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:168208126 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3600657 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3600657 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:101396373 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:101396373 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:101396373 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:101396373 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:52927070 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:52927070 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:114918423 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:114918423 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:114918423 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:114918423 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:44255644 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:44255644 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:46657598 G>T maps to NM_001010870.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:46657598 G>T maps to NM_001010870.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:97872931 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:97872931 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:20854508 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:20854508 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43921871 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:43921871 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:107224573 G>A maps to NM_031273.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:107224573 G>A maps to NM_031273.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:50697056 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:50697056 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:50697056 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:50697056 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:115580561 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:115580561 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:115580561 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:115580561 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:43733546 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:43733546 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:43733546 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:43733546 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:133479602 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:133479602 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:30715821 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:30715821 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:30715821 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:30715821 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:92174228 C>A maps to NM_003243.4 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:92174228 C>A maps to NM_003243.4 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:105924802 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:105924802 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:105924802 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:105924802 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:133923801 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:133923801 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:133923801 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:133923801 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:134125712 C>A maps to NM_003235.4 Y2540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:134125712 C>A maps to NM_003235.4 Y2540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:32589755 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:32589755 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:32554697 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:32554697 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:32589755 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:32589755 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:56811917 C>A maps to NM_003920.3 E1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:56811917 C>A maps to NM_003920.3 E1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:82322995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:82322995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:82308672 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:82308672 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:82322995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:82322995 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:166981295 A>T maps to ENST00000507499 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:166981295 A>T maps to ENST00000507499 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:75403107 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:75403107 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:2605066 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:2605066 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:2517339 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:2517339 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:2605066 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:2605066 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:19485649 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:19485649 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:19485649 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:19485649 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:76113394 C>A maps to NM_007267.6 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:76113394 C>A maps to NM_007267.6 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:133098489 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:133098489 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:133098489 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:133098489 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52867622 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52867622 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:52867622 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:52867622 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:19232320 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:19232320 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:87494879 C>A maps to NM_153354.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:87494879 C>A maps to NM_153354.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:150500823 C>T maps to NM_018487.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:150500823 C>T maps to NM_018487.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:15433592 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:15433592 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:100275842 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:100275842 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:100275842 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:100275842 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:44122030 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:44122030 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:44122030 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:44122030 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77722811 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77722811 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:77722811 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:77722811 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:133723276 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:133723276 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:133723276 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:133723276 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117800086 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117800086 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117800086 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:117800086 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:37499652 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:37499652 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:37499652 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr22:37499652 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:117826977 A>C maps to NM_002160.2 Y1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:117826977 A>C maps to NM_002160.2 Y1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:12157230 G>T maps to NM_001243.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:12157230 G>T maps to NM_001243.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:7462317 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:7462317 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:99852724 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:99852724 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:99852724 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:99852724 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:1947507 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:1947507 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:175046489 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:175046489 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:175046489 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:175046489 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:72199498 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:72199498 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:72199498 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:72199498 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:32017466 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:32017466 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:235277264 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:235277264 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:235277264 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:235277264 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21945516 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21945516 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:43720076 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:43720076 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:144344383 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:144344383 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:144344383 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:144344383 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:10971751 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:10971751 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:10971751 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:10971751 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2223444 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2223444 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:45478947 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:45478947 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:45478947 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:45478947 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:45522608 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:45522608 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:189068504 C>A maps to NM_178556.3 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:189068504 C>A maps to NM_178556.3 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:908071 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:908071 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:908071 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:908071 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:100274268 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:100274268 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:100274268 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:100274268 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:72965975 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:72965975 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:72965975 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:72965975 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:101359858 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:101359858 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:101359858 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:101359858 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:45784219 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:45784219 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:45784219 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr21:45784219 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:73531918 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:73531918 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:73478166 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:73478166 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:73531918 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:73531918 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:2433485 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:2433485 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:77362999 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:77362999 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141955556 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141955556 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:81562915 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:81562915 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:81562915 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:81562915 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67859196 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:67859196 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:67859196 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:67859196 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:15225902 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:15225902 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:15225902 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:15225902 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:124751500 C>G maps to NM_001139442.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:124751500 C>G maps to NM_001139442.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:30458920 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:30458920 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:30458920 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:30458920 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:179457056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:179457056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179457056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179457056 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179567140 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179567140 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179592522 C>T maps to NM_133378.4 K5350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:179592522 C>T maps to NM_133378.4 K5350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:54942230 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:54942230 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:72245629 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:72245629 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:72245629 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:72245629 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:8061245 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:8061245 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:15546645 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:15546645 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:48069579 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:48069579 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:48069581 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:48069581 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:48069579 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:48069579 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:48069581 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:48069581 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:11791946 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:11791946 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:11791946 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:11791946 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:52486660 G>A maps to NM_015913.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:52486660 G>A maps to NM_015913.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:37901756 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:37901756 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:37901756 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:37901756 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:76168365 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:76168365 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:33467034 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:33467034 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:33467034 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:33467034 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:19432176 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:19432176 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:39515800 C>A maps to NM_003359.3 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr4:39515800 C>A maps to NM_003359.3 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:234669910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:234669910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:234669910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:234669910 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:70070509 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:70070509 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:70071071 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:70071071 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:36066765 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:36066765 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:36066765 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:36066765 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:41861076 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:41861076 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:41861076 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:41861076 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-44-2656-01A-02W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:91483496 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:91483496 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:91483496 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr15:91483496 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:33513589 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:33513589 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:33513589 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr17:33513589 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:73051160 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:73051160 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:167711254 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:167711254 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:167717625 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:167717625 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:167717625 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:167717625 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216221757 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216221757 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216595084 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216595084 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:216051128 C>T maps to ENST00000366943 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:216051128 C>T maps to ENST00000366943 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:216595084 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:216595084 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23116930 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23116930 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:23116930 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:23116930 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:75290090 C>T maps to NM_152586.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:75290090 C>T maps to NM_152586.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:6975137 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:6975137 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:6975137 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:6975137 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:41043660 C>T maps to NM_001039590.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:41043660 C>T maps to NM_001039590.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:6837125 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:6837125 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71160339 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:71160339 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77907504 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:77907504 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:77907504 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr14:77907504 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:100883149 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:100883149 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:69356723 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:69356723 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:184587420 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:184587420 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:184632746 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:184632746 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:184587420 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:184587420 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:184632746 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:184632746 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:17830659 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:17830659 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:17830659 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:17830659 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:124007381 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:124007381 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:28824469 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:28824469 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:88220278 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:88220278 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:88220278 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr10:88220278 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:71142006 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:71142006 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:71142006 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr7:71142006 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110432717 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110432717 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110454586 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110454586 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:110446485 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:110446485 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:113084797 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:113084797 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:113084797 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:113084797 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:67340410 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:67340410 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:1937165 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:1937165 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:29924314 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:29924314 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:68628637 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:68628637 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:68628637 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:68628637 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:990232 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:990232 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:990232 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:990232 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:96062328 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:96062328 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:96062328 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr9:96062328 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228248007 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228248007 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:31605845 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:31605845 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:31605845 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:31605845 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:21369902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:21369902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:21369902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:21369902 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:48431644 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:48431644 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:75987969 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:75987969 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:22817989 A>G maps to NM_014870.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:22817989 A>G maps to NM_014870.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:64139944 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chrX:64139944 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:64139002 A>T maps to NM_018684.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:64139002 A>T maps to NM_018684.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:64139944 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chrX:64139944 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:819582 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:819582 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:77690475 C>A maps to NM_024721.4 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:77690475 C>A maps to NM_024721.4 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:147130651 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:147130651 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:40438794 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:40438794 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:40438794 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr8:40438794 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:35577245 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:35577245 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:35847280 G>T maps to NM_005095.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:35847280 G>T maps to NM_005095.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:43143572 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:43143572 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:43143572 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:43143572 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:6977815 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:6977815 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:74672731 C>G maps to NM_007345.3 Y1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr18:74672731 C>G maps to NM_007345.3 Y1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:44891466 T>A maps to NM_152354.3 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:44891466 T>A maps to NM_152354.3 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:28971703 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:28971703 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:28971703 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr6:28971703 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:176468252 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:176468252 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:176471259 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:176471259 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:176468252 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:176468252 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:178506335 A>T maps to NM_014594.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr5:178506335 A>T maps to NM_014594.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:37733342 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:37733342 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:54767847 G>C maps to NM_001130967.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr12:54767847 G>C maps to NM_001130967.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:58427737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:58427737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:58427737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:58427737 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:31047964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:31047964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:31047964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:31047964 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:53983466 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr19:53983466 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:60636947 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:60636947 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21217023 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21217023 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:21217023 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr16:21217023 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:76054721 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:76054721 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:238051763 C>A maps to NM_021186.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr1:238051763 C>A maps to NM_021186.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:102187729 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:102187729 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:102187729 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr3:102187729 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:136262084 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr2:136262084 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:44505619 C>T maps to NM_080752.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr20:44505619 C>T maps to NM_080752.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:113621819 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:113621819 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:113621819 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02W-0928-08 chr11:113621819 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87179930 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87179930 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87046856 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87046856 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:48201620 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:48201620 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:43702587 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:43702587 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:953255 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:953255 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:109696581 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:109696581 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:81503197 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:81503197 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:114697475 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:114697475 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2938176 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2938176 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:136319480 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:136319480 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:28210695 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:28210695 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:84659817 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:84659817 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:41216076 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:41216076 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:123071496 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:123071496 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:76330359 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:76330359 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:161575120 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:161575120 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:41456965 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:41456965 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:84515880 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:84515880 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:117104100 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:117104100 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:3750169 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:3750169 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:113277790 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:113277790 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:25379026 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:25379026 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:114153430 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:114153430 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:241421493 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:241421493 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:16664554 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:16664554 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:37415024 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:37415024 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:99640693 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:99640693 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:46119969 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:46119969 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:39477645 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:39477645 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:47192878 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:47192878 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:73071332 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:73071332 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:97215627 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:97215627 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:109225653 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:109225653 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:69489778 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:69489778 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:2999162 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:2999162 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:2936545 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:2936545 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:95221789 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:95221789 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:138880816 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:138880816 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:160156217 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:160156217 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:77276690 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:77276690 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:11038685 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:11038685 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:11098887 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:11098887 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:15574390 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:15574390 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:15527333 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:15527333 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1466161 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1466161 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:180416005 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:180416005 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:112743791 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:112743791 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:46942987 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:46942987 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:89724599 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:89724599 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:8738321 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:8738321 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:61430121 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:61430121 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:20270908 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:20270908 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:88825279 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:88825279 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:48955705 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:48955705 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:113092699 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:113092699 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:5969070 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:5969070 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:5977784 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:5977784 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:43495261 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:43495261 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:151865940 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:151865940 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:69434010 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:69434010 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:13563580 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:13563580 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:181741179 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:181741179 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:76834939 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:76834939 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:104936890 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:104936890 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:55028255 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:55028255 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:92047503 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:92047503 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:105439129 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:105439129 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:57122237 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:57122237 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:42931454 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:42931454 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:92979090 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:92979090 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:128454627 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:128454627 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:74560505 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:74560505 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:7556499 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:7556499 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:66492490 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:66492490 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158300978 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158300978 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:35822410 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:35822410 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137527305 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137527305 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137527307 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137527307 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73437175 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73437175 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73537412 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73537412 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:196757588 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:196757588 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:196621178 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:196621178 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:6181340 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:6181340 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:6215655 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:6215655 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:175618558 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:175618558 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:233393556 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:233393556 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:233406068 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:233406068 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:86954870 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:86954870 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:87012770 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:87012770 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:28500079 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:28500079 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:150645697 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:150645697 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:40297659 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:40297659 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:101814852 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:101814852 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:70778227 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:70778227 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:94035083 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:94035083 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:109841670 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:109841670 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:109895671 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:109895671 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:107414540 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:107414540 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:238266451 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:238266451 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:130284511 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:130284511 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:48619814 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:48619814 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:166325425 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:166325425 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:57147135 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:57147135 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:207804186 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:207804186 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:145619309 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:145619309 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:2777424 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:2777424 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:45892360 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:45892360 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:25617280 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:25617280 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:208994631 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:208994631 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:34968211 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:34968211 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:34257916 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:34257916 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:113331979 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:113331979 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:113565051 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:113565051 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:23805991 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:23805991 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:11018033 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:11018033 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:44873998 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:44873998 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:105882610 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:105882610 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:36156455 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:36156455 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:94834512 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:94834512 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:15790984 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:15790984 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:24808751 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:24808751 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:20000192 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:20000192 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:242707040 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:242707040 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:59111925 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:59111925 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:74597014 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:74597014 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:50544308 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:50544308 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:30037809 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:30037809 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:124033898 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:124033898 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:3786363 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:3786363 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:50133508 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:50133508 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:41585641 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:41585641 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140961982 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140961982 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:69669110 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:69669110 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:72281139 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:72281139 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:132218565 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:132218565 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:117789044 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:117789044 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:117789046 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:117789046 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:169507394 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:169507394 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:49647601 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:49647601 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:80631313 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:80631313 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:132058424 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:132058424 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:132511900 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:132511900 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:132514726 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:132514726 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:464619 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:464619 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:154185180 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:154185180 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:139210034 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:139210034 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:175530805 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:175530805 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:88994212 G>A maps to NM_001099338.1 Q795Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:88994212 G>A maps to NM_001099338.1 Q795Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:116779693 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:116779693 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:101540842 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:101540842 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190250666 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190250666 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190250668 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190250668 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:67573937 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:67573937 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:38202513 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:38202513 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:124206199 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:124206199 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:85133737 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:85133737 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:149762689 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:149762689 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:137777067 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:137777067 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:157773940 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:157773940 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:157659723 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:157659723 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:155533847 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:155533847 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:2908414 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:2908414 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:32698392 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:32698392 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:17445613 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:17445613 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:170236508 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:170236508 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:166611280 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:166611280 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:62400866 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:62400866 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:9872869 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:9872869 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:8115675 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:8115675 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:58007451 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:58007451 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:179758402 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:179758402 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:117823849 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:117823849 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:147380050 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:147380050 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:141896153 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:141896153 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:133360731 C>G maps to NM_001172557.1 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:133360731 C>G maps to NM_001172557.1 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:132440206 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:132440206 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:46993515 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:46993515 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:57713394 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:57713394 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:28493647 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:28493647 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:146708272 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:146708272 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:27499794 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:27499794 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:5246738 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:5246738 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:32796289 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:32796289 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:18868767 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:18868767 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:63931063 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:63931063 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186031737 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186031737 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186114527 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186114527 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:173531140 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:173531140 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:76452092 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:76452092 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:41800370 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:41800370 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:27203114 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:27203114 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:176981544 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:176981544 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:43918608 G>A maps to ENST00000372426 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:43918608 G>A maps to ENST00000372426 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:82912443 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:82912443 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:91144499 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:91144499 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:25672688 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:25672688 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:3111825 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:3111825 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:154420480 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:154420480 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:31382903 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:31382903 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:33633508 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:33633508 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:17952392 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:17952392 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:6062334 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:6062334 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:147040493 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:147040493 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:124175392 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:124175392 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:75681565 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:75681565 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:178977919 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:178977919 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:55964819 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:55964819 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:142659358 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:142659358 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:73491814 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:73491814 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:29433986 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:29433986 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:1379597 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:1379597 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:36868180 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:36868180 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:132062005 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:132062005 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:69595301 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:69595301 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:57957496 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:57957496 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:170015762 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:170015762 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55350858 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55350858 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:27951195 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:27951195 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:202887570 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:202887570 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:86869089 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:86869089 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:241750152 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:241750152 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:186450505 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:186450505 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:39635008 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:39635008 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:31802578 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:31802578 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:153133042 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:153133042 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:107615892 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:107615892 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:209790689 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:209790689 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:107746544 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:107746544 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:128996091 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:128996091 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:104309227 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:104309227 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:104309439 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:104309439 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55087689 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55087689 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:54779995 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:54779995 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:97373406 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:97373406 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:8606961 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:8606961 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:76197471 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:76197471 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:39976176 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:39976176 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:56344997 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:56344997 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:151271096 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:151271096 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:105502824 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:105502824 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:141806457 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:141806457 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:99824904 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:99824904 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:133687822 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:133687822 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:70339160 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:70339160 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:85554308 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:85554308 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:41805131 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:41805131 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:160766163 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:160766163 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:20193791 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:20193791 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:140969659 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:140969659 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:77096935 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:77096935 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:71206732 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:71206732 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:217148179 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:217148179 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:220773121 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:220773121 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:119182512 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:119182512 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:138667478 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:138667478 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:127327869 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:127327869 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:94288818 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:94288818 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:70356682 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:70356682 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:679845 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:679845 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:222827454 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:222827454 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:19405787 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:19405787 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2526821 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2526821 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2527911 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2527911 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2319564 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:2319564 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:43804519 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:43804519 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:154007671 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:154007671 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:99804580 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:99804580 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:825404 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:825404 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:21929855 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:21929855 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:30066710 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:30066710 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1081157 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1081157 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:113537922 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:113537922 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:3261948 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:3261948 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:10355865 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:10355865 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:23857757 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:23857757 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:2678412 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:2678412 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:3102656 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:3102656 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:101735253 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:101735253 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:101763617 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:101763617 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:20071617 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:20071617 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:20122720 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:20122720 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:16901209 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:16901209 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:16916735 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:16916735 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:113140760 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:113140760 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:19360466 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:19360466 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:6631847 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:6631847 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:21488912 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:21488912 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:52726883 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:52726883 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:3434548 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:3434548 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:25443013 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:25443013 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:63777273 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:63777273 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:65028880 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:65028880 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:56491019 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:56491019 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:43181348 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:43181348 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:162270280 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:162270280 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:36322518 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:36322518 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:115373867 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:115373867 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:64453463 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:64453463 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:156844566 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:156844566 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:1837634 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:1837634 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:163298730 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:163298730 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:37351501 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:37351501 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:102337495 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:102337495 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:113357091 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:113357091 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:228491119 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:228491119 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:6865341 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:6865341 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248128614 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248128614 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248167234 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248167234 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:20344287 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:20344287 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:99963020 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:99963020 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:53422594 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:53422594 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140242794 G>A maps to ENST00000502505 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140242794 G>A maps to ENST00000502505 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140569344 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140569344 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:73440389 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:73440389 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:77373477 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:77373477 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:74066804 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:74066804 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:133806860 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:133806860 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:49950835 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:49950835 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:209169067 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:209169067 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:130831396 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:130831396 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:94352910 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:94352910 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:20301964 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:20301964 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:42434106 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:42434106 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:9433935 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:9433935 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219498292 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219498292 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:18846520 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:18846520 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:153043157 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:153043157 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:129277470 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:129277470 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:102938948 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:102938948 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:118368483 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:118368483 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:118187471 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:118187471 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:118236065 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:118236065 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:46686068 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:46686068 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:113299992 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:113299992 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:37464840 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:37464840 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:6374147 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:6374147 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:47262611 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:47262611 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:720140 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:720140 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:179314916 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:179314916 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:45221290 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:45221290 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:43571243 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:43571243 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:15486098 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:15486098 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:32825921 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:32825921 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:1145168 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:1145168 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:48140892 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:48140892 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:112168698 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:112168698 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:18763664 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:18763664 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:191178922 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:191178922 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:154933309 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:154933309 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:73315132 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:73315132 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:13634813 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:13634813 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:2935738 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:2935738 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:48881623 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:48881623 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:20565056 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:20565056 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:79312478 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:79312478 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:73029176 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:73029176 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:8190393 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:8190393 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:77090121 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:77090121 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:68896914 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:68896914 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:12945974 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:12945974 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:49517960 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:49517960 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:237660143 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:237660143 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:169646138 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:169646138 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:50875922 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:50875922 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:26723348 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:26723348 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:128921883 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:128921883 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:128924678 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:128924678 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:84349253 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:84349253 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:82034491 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:82034491 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:10354219 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:10354219 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:92087514 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:92087514 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:30735256 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:30735256 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:51215138 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:51215138 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:145153920 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:145153920 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:49183145 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:49183145 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:57627208 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:57627208 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:159923508 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:159923508 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:44668972 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:44668972 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:25925890 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:25925890 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:15075094 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:15075094 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:95849089 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:95849089 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:44983612 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:44983612 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:110741161 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:110741161 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:1244503 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:1244503 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:170198018 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:170198018 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:23282099 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:23282099 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:21172117 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:21172117 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:133667689 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:133667689 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:168213054 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:168213054 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:57835616 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:57835616 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:17961447 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:17961447 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:70444599 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:70444599 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:10683035 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:10683035 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:231112826 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:231112826 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:139322435 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:139322435 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:55648418 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:55648418 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158609520 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158609520 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158617522 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158617522 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158622502 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158622502 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:153046924 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:153046924 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:109246299 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:109246299 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:130058380 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:130058380 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:103988315 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:103988315 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:36587621 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:36587621 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:136139832 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:136139832 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:146722717 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:146722717 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:121100490 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:121100490 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:24584178 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:24584178 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:10956294 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:10956294 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:152638169 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:152638169 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:79701797 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:79701797 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:97369239 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:97369239 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:120801180 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:120801180 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:38301989 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:38301989 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:121060362 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:121060362 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44948423 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44948423 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:2380895 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:2380895 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:169625210 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:169625210 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:155500339 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:155500339 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:167020815 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:167020815 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:63017384 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:63017384 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:75355149 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:75355149 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:32955919 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:32955919 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:86969985 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:86969985 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:9304926 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:9304926 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:94808048 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:94808048 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:12251007 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:12251007 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:74801677 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:74801677 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:175105920 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:175105920 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:47317602 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:47317602 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:10998175 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:10998175 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:23556206 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:23556206 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:30136039 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:30136039 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:155156177 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:155156177 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:45028941 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:45028941 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:189025799 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:189025799 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:45786601 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:45786601 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:142622548 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:142622548 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:98497180 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:98497180 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:120450649 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:120450649 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:71533699 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:71533699 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:94876365 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:94876365 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:5446698 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:5446698 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:70361644 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:70361644 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:43505660 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:43505660 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:40999724 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:40999724 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:17181065 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:17181065 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:61697760 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:61697760 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:120169846 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:120169846 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:155127651 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chrX:155127651 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:108311135 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:108311135 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:101185530 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:101185530 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:177632899 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:177632899 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:86996059 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:86996059 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:133065703 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:133065703 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:38937850 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:38937850 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:97342633 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:97342633 C>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:43638418 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:43638418 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:142054270 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:142054270 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:17202950 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:17202950 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:135756689 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:135756689 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:31650034 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:31650034 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:28116622 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:28116622 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:44570091 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:44570091 G>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:49525159 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:49525159 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44761744 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44761744 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:20829049 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:20829049 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:9407935 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:9407935 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:58015903 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:58015903 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:135965469 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:135965469 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:7743542 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:7743542 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:9007508 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:9007508 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:94586507 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:94586507 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:94586507 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:94586507 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:87165935 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:87165935 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:87165935 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:87165935 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:17469909 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:17469909 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:17469909 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:17469909 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:40012396 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:40012396 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:40012396 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:40012396 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:74762795 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:74762795 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:183906243 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:183906243 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:183906243 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:183906243 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:43711094 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:43711094 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:43711094 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:43711094 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:76200677 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:76200677 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:76209521 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:76209521 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:76209521 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:76209521 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:124813282 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:124813282 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:124813282 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:124813282 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:80626557 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:80626557 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:80626557 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:80626557 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:90699438 G>T maps to NM_001141945.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:90699438 G>T maps to NM_001141945.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:74146761 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:74146761 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:74146761 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:74146761 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:207395587 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:207395587 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:207408165 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:207408165 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:207395587 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:207395587 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:28296389 G>T maps to NM_007038.3 C925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:28296389 G>T maps to NM_007038.3 C925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:45699927 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:45699927 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:45699927 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:45699927 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:24800385 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:24800385 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:24800385 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:24800385 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:100140121 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:100140121 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:76153868 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:76153868 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:76153868 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:76153868 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:112033146 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:112033146 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:161560381 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:161560381 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:241808572 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:241808572 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:247071180 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:247071180 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:42872544 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:42872544 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:4875555 C>A maps to NM_001040177.1 C74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:4875555 C>A maps to NM_001040177.1 C74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:74276148 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:74276148 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:74276148 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:74276148 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:61894040 T>A maps to NM_020987.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:61894040 T>A maps to NM_020987.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:37453891 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:37453891 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:37482151 C>A maps to ENST00000374660 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:37482151 C>A maps to ENST00000374660 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:431933 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:431933 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:431933 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:431933 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:69372563 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:69372563 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:80929818 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:80929818 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:36589247 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:36589247 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:26800863 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:26800863 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:26800863 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:26800863 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:115336940 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:115336940 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:115336940 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:115336940 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:127231265 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:127231265 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:11196360 C>T maps to NM_013427.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:11196360 C>T maps to NM_013427.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:177142480 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:177142480 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:177142480 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:177142480 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:1561077 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:1561077 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:161762215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:161762215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:161762215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:161762215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:25263594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:25263594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:25263594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:25263594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:10420008 G>A maps to NM_001001331.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:10420008 G>A maps to NM_001001331.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:70231403 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:70231403 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:70231403 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:70231403 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:28381958 T>C maps to NM_022461.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:28381958 T>C maps to NM_022461.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:11029762 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:11029762 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:79419954 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:79419954 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:143623593 G>T maps to NM_001702.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:143623593 G>T maps to NM_001702.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:69728484 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:69728484 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:165548020 A>T maps to NM_000055.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:165548020 A>T maps to NM_000055.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:61719196 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:61719196 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:61719196 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:61719196 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:53793869 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:53793869 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:203378404 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:203378404 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:203242409 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:203242409 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:151016364 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:151016364 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:28521251 C>T maps to NM_004899.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:28521251 C>T maps to NM_004899.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:118101764 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:118101764 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:118101764 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:118101764 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:61543748 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:61543748 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:6804696 G>A maps to NM_153685.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:6804696 G>A maps to NM_153685.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:97052114 T>C maps to ENST00000342887 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:97052114 T>C maps to ENST00000342887 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:60933824 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:60933824 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:95884078 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:95884078 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:95884078 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:95884078 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:16365523 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:16365523 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:77044100 C>A maps to ENST00000392445 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:77044100 C>A maps to ENST00000392445 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:75107254 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:75107254 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:31651553 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:31651553 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:45929039 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:45929039 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:73768560 C>T maps to ENST00000334126 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:73768560 C>T maps to ENST00000334126 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:71200714 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:71200714 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:71200714 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:71200714 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:71021699 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:71021699 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:146617640 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:146617640 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:146617640 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:146617640 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:41916969 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:41916969 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:32323401 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:32323401 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:32323401 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:32323401 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:6840802 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:6840802 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:120906590 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:120906590 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:120906590 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:120906590 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:140997284 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:140997284 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:140997284 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:140997284 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:54333360 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:54333360 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:1974559 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:1974559 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:44266269 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:44266269 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:110814216 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:110814216 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:110814216 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:110814216 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:223934686 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:223934686 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:223934686 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:223934686 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:160164915 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:160164915 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:160164915 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:160164915 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:38847194 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:38847194 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:38847194 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:38847194 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:169927725 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:169927725 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:23658869 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:23658869 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:31611608 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:31611608 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31693475 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31693475 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:28444212 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:28444212 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:111336972 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:111336972 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:111336972 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:111336972 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:6292832 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:6292832 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:6292832 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:6292832 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:69986637 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:69986637 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:17072819 C>G maps to NM_014406.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:17072819 C>G maps to NM_014406.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:20915819 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:20915819 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:25568697 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:25568697 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:25583176 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:25583176 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:25583176 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:25583176 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:31318141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:31318141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:31318141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:31318141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:26903677 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:26903677 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:26903677 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:26903677 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:49836270 G>T maps to NM_001007540.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:49836270 G>T maps to NM_001007540.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:49836270 G>T maps to NM_001007540.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:49836270 G>T maps to NM_001007540.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:115149075 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:115149075 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:17630515 C>G maps to NM_033070.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:17630515 C>G maps to NM_033070.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:25459319 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:25459319 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:196683122 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:196683122 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:196697462 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:196697462 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:196683122 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:196683122 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:10137384 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:10137384 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:10226001 G>T maps to NM_016511.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:10226001 G>T maps to NM_016511.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:7890256 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:7890256 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:129681938 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:129681938 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:129681938 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:129681938 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:36228162 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:36228162 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:7293796 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:7293796 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:7293796 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:7293796 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:41365317 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:41365317 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:41365317 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:41365317 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:100095349 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:100095349 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:100208112 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:100208112 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:100095349 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:100095349 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:100208112 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:100208112 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:103444751 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:103444751 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:103444751 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:103444751 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:101817202 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:101817202 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:55926526 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:55926526 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:139734262 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:139734262 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:48387875 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:48387875 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:48387875 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:48387875 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:76101881 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:76101881 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:19023782 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:19023782 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:54735964 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:54735964 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:148563202 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:148563202 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:148563202 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:148563202 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:101808486 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:101808486 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:101808486 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:101808486 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:69656387 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:69656387 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:5838672 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:5838672 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:33175606 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:33175606 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:33175606 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:33175606 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:34006353 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:34006353 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:34006353 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:34006353 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:113299138 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:113299138 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:113299267 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:113299267 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:113392720 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:113392720 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:113299267 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:113299267 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:113392720 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:113392720 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:77488803 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:77488803 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:77488803 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:77488803 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:67726504 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:67726504 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:11732419 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:11732419 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:11732419 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:11732419 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:16638216 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:16638216 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:112999275 G>T maps to NM_018704.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:112999275 G>T maps to NM_018704.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:35974045 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:35974045 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:35937817 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:35937817 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:35937817 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:35937817 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:35974045 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:35974045 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:41450537 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:41450537 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:106118505 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:106118505 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:73422415 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:73422415 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:73422415 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:73422415 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:6661904 G>A maps to NM_003737.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:6661904 G>A maps to NM_003737.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:61077161 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:61077161 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:61886918 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:61886918 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:91057320 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:91057320 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:91057320 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:91057320 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:50121560 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:50121560 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:54572987 T>C maps to NM_019030.2 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:54572987 T>C maps to NM_019030.2 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:60490350 C>A maps to NM_001042517.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:60490350 C>A maps to NM_001042517.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:80672103 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:80672103 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:80672103 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:80672103 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:83195416 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:83195416 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:52361819 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:52361819 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:13820644 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:13820644 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:13820644 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:13820644 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:13839711 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:13839711 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:11513659 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:11513659 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:11784401 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:11784401 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:25220536 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:25220536 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:25220536 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:25220536 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:98012145 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:98012145 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:97547758 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:97547758 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:98012145 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:98012145 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:27150119 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:27150119 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:56510623 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:56510623 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:56510623 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:56510623 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:32391881 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:32391881 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:32391881 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:32391881 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:20482889 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:20482889 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:20482889 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:20482889 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:25702280 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:25702280 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:25898596 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:25898596 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:25702280 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:25702280 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:25898596 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:25898596 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:184001500 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:184001500 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:109547216 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:109547216 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42940927 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42940927 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42940927 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42940927 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:34395011 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:34395011 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:34395011 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:34395011 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:8008773 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:8008773 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:8008773 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:8008773 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37264643 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37264643 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:37264643 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:37264643 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:107514601 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:107514601 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:107514601 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:107514601 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:79383280 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:79383280 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:14884565 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:14884565 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:111469536 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:111469536 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:111469536 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:111469536 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:111975824 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:111975824 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:111975824 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:111975824 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:32582489 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:32582489 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:32582489 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:32582489 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:143096425 C>A maps to NM_005232.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:143096425 C>A maps to NM_005232.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:66467291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:66467291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:66467291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:66467291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:29509475 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:29509475 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:236385170 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:236385170 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:216741280 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:216741280 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:216741280 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:216741280 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:553805 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:553805 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:553805 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:553805 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:6267177 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:6267177 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:6267177 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:6267177 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:197026085 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:197026085 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:82443459 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:82443459 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:82443459 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:82443459 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:51855349 G>A maps to NM_145019.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:51855349 G>A maps to NM_145019.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:139145139 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:139145139 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:139323318 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:139323318 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:139145139 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:139145139 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:61023982 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:61023982 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:61023982 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:61023982 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:187618831 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:187618831 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:16743449 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:16743449 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:3849963 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:3849963 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:177242619 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:177242619 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:177242619 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:177242619 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:67573488 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:67573488 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:67573488 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:67573488 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:25024530 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:25024530 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:124786510 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:124786510 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:33810354 C>A maps to ENST00000395190 G350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:33810354 C>A maps to ENST00000395190 G350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:14883647 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:14883647 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:14883647 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:14883647 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:29485708 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:29485708 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:150923124 G>A maps to NM_001447.2 I2521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:150923124 G>A maps to NM_001447.2 I2521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:150948411 G>T maps to NM_001447.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:150948411 G>T maps to NM_001447.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:92531656 G>T maps to ENST00000298047 V1826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:92531656 G>T maps to ENST00000298047 V1826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:117604776 T>A maps to NM_033624.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:117604776 T>A maps to NM_033624.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:40368028 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:40368028 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:157653172 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:157653172 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:67272055 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:67272055 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:67272055 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:67272055 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:110037963 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:110037963 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:128486497 C>A maps to NM_001458.4 R1370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:128486497 C>A maps to NM_001458.4 R1370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:128487757 G>A maps to NM_001458.4 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:128487757 G>A maps to NM_001458.4 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:171227173 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:171227173 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:171227173 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:171227173 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:13782540 G>A maps to NM_018027.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:13782540 G>A maps to NM_018027.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:37739991 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:37739991 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:37739991 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:37739991 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:5644852 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:5644852 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:54145841 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:54145841 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:54145866 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:54145866 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:54145841 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:54145841 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:54145866 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:54145866 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:46312310 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:46312310 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:46312310 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:46312310 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:153792355 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:153792355 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:153792355 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:153792355 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:230391231 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:230391231 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:16252590 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:16252590 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:16252590 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:16252590 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:11607723 C>G maps to NM_002052.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:11607723 C>G maps to NM_002052.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:56065273 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:56065273 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:89732313 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:89732313 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:89732313 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:89732313 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:120614021 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:120614021 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:33971759 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:33971759 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:33971759 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:33971759 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42988647 G>T maps to NM_002055.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42988647 G>T maps to NM_002055.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42989120 G>C maps to NM_002055.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42989120 G>C maps to NM_002055.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:6592235 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:6592235 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:6592235 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:6592235 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:92729161 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:92729161 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:92729161 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:92729161 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:9757859 G>T maps to NM_004246.1 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:9757859 G>T maps to NM_004246.1 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:19808291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:19808291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:19808291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:19808291 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:28838062 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:28838062 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:217784539 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:217784539 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:100387663 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:100387663 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:27333070 A>G maps to NM_005288.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:27333070 A>G maps to NM_005288.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:19883303 G>T maps to NM_016235.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:19883303 G>T maps to NM_016235.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:158281394 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:158281394 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:158281394 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:158281394 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:37346221 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:37346221 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:37346221 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:37346221 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:104432902 G>T maps to NM_133445.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:104432902 G>T maps to NM_133445.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:52659103 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:52659103 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:52659103 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:52659103 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:52702269 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:52702269 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:52702269 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:52702269 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:108627058 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:108627058 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:108627058 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:108627058 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:108708206 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:108708206 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:108638598 G>T maps to ENST00000218006 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:108638598 G>T maps to ENST00000218006 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:25100901 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:25100901 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:41033052 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:41033052 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:41033052 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:41033052 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:97218681 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:97218681 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:97218681 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:97218681 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:27578093 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:27578093 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:26189411 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:26189411 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:40720299 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:40720299 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:40720299 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:40720299 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:43052639 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:43052639 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:43052639 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:43052639 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:42761159 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:42761159 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:46690584 C>A maps to NM_024016.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:46690584 C>A maps to NM_024016.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:88236550 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:88236550 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:118850559 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:118850559 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:148839600 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:148839600 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:148839600 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:148839600 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:118434155 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:118434155 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:118436036 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:118436036 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:118436036 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:118436036 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:22181570 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:22181570 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:53608002 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:53608002 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:50326123 C>A maps to ENST00000336089 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:50326123 C>A maps to ENST00000336089 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:118624530 G>T maps to NM_152538.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:118624530 G>T maps to NM_152538.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:67833707 G>T maps to NM_001559.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:67833707 G>T maps to NM_001559.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:52102075 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:52102075 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:52102075 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:52102075 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:104511932 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:104511932 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:104511932 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:104511932 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:67648488 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:67648488 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:67648488 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:67648488 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:207072917 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:207072917 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:207072917 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:207072917 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:1475003 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:1475003 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:123105064 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:123105064 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:128441221 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:128441221 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:52201562 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:52201562 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:52201562 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:52201562 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:54797397 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:54797397 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:54797397 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:54797397 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:30492757 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:30492757 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:45367166 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:45367166 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:45367166 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:45367166 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:7763077 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:7763077 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:156638259 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:156638259 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:156673056 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:156673056 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:156638259 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:156638259 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:156673056 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:156673056 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:6058393 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:6058393 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:6058393 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:6058393 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:146991679 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:146991679 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:146991679 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:146991679 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:20153367 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:20153367 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:20153367 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:20153367 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:111146879 G>T maps to NM_004974.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:111146879 G>T maps to NM_004974.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:40327893 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:40327893 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:78850106 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:78850106 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:55979648 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:55979648 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:96996019 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:96996019 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:123095594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:123095594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:57190446 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:57190446 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:57190446 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:57190446 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:59895372 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:59895372 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:113388976 G>A maps to NM_001009899.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:113388976 G>A maps to NM_001009899.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:16336949 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:16336949 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:16336949 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:16336949 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:34319234 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:34319234 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:57963761 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:57963761 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:57963761 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:57963761 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:169947177 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:169947177 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:169947177 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:169947177 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:70549965 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:70549965 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:70549965 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:70549965 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:38954298 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:38954298 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:38950231 G>A maps to NM_181535.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:38950231 G>A maps to NM_181535.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:53186468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:53186468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:53186468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:53186468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:31859736 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:31859736 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:31859736 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:31859736 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:31691606 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:31691606 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:35978603 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:35978603 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:35978603 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:35978603 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:143746580 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:143746580 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:143746580 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:143746580 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:129674482 C>T maps to NM_000426.3 R1566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:129674482 C>T maps to NM_000426.3 R1566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:112450019 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:112450019 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:133914176 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:133914176 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:133914176 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:133914176 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:133932443 G>T maps to ENST00000355048 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:133932443 G>T maps to ENST00000355048 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:128990540 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:128990540 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:128990540 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:128990540 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:169697831 G>T maps to NM_005565.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:169697831 G>T maps to NM_005565.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:33744910 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:33744910 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:1824880 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:1824880 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:1824880 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:1824880 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:38496378 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:38496378 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:38496378 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:38496378 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:28150756 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:28150756 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:28150756 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:28150756 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:101110441 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:101110441 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:57013088 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:57013088 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:57013088 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:57013088 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:2444344 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:2444344 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:129458113 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:129458113 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:42368204 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:42368204 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:42368204 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:42368204 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:141253039 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:141253039 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:170050427 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:170050427 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:170050427 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:170050427 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:44204556 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:44204556 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:133673736 G>T maps to ENST00000250173 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:133673736 G>T maps to ENST00000250173 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:101606439 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:101606439 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:101606439 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:101606439 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42114709 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42114709 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42114709 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42114709 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:179200765 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:179200765 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:179200765 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:179200765 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:67923354 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:67923354 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:67923354 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:67923354 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:1810344 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:1810344 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:70892218 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:70892218 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:70892218 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:70892218 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:13246126 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:13246126 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:13246126 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:13246126 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:116420147 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:116420147 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:116420147 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:116420147 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:131912667 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:131912667 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:141760196 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:141760196 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:141760196 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:141760196 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:16510705 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:16510705 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:16510705 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:16510705 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:37777134 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:37777134 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:37777134 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:37777134 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:12623215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:12623215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:12623215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:12623215 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:5906855 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:5906855 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:5906855 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:5906855 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:151935751 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:151935751 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:33839966 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:33839966 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:47656892 G>T maps to NM_000251.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:47656892 G>T maps to NM_000251.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:9724973 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:9724973 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:9002092 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:9002092 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:9008064 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:9008064 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:9002092 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:9002092 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:9008064 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:9008064 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:1213655 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:1213655 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:1219586 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:1219586 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:1262068 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:1262068 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:1213655 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:1213655 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:50954515 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:50954515 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:50954515 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:50954515 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:10204781 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:10204781 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:10204781 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:10204781 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:10350964 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:10350964 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:10312945 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:10312945 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:171458580 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:171458580 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:171458580 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:171458580 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:2065665 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:2065665 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:41897472 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:41897472 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:89891341 G>T maps to NM_005467.3 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:89891341 G>T maps to NM_005467.3 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:78147594 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:78147594 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:78147594 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:78147594 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:34139978 G>T maps to NM_024662.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:34139978 G>T maps to NM_024662.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:15523531 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:15523531 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:15523531 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:15523531 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:133636513 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:133636513 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:133636513 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:133636513 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:41304232 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:41304232 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:124914759 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:124914759 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:124914759 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:124914759 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:84034540 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:84034540 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:20699659 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:20699659 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:20699659 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:20699659 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:45170057 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:45170057 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:73566112 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:73566112 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:73566112 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:73566112 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:29528378 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:29528378 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:29528378 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:29528378 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:29657517 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:29657517 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:77170071 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:77170071 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:77170071 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:77170071 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:3452609 G>T maps to ENST00000269778 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:3452609 G>T maps to ENST00000269778 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:25450615 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:25450615 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:25450615 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:25450615 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:63777918 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:63777918 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:173993444 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:173993444 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:7061106 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:7061106 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:7061106 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:7061106 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:56539898 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:56539898 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:56544903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:56544903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:56539898 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:56539898 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:56544903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:56544903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:132636233 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:132636233 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:14989244 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:14989244 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:140327858 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:140327858 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:115258836 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:115258836 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:115258838 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:115258838 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:115258836 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:115258836 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:115258838 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:115258838 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:84118481 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:84118481 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:84118481 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:84118481 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:50318333 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:50318333 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:50318333 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:50318333 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:176686967 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:176686967 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:176686967 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:176686967 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:212912852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:212912852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:212912852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:212912852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:59514476 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:59514476 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:135258391 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:135258391 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:135258391 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:135258391 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:133044326 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:133044326 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:133044326 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:133044326 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:123663868 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:123663868 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:123663868 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:123663868 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:9967990 C>T maps to NM_058164.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:9967990 C>T maps to NM_058164.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:193332873 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:193332873 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:193332873 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:193332873 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:54147207 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:54147207 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:154411266 C>A maps to NM_001145279.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:154411266 C>A maps to NM_001145279.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:48597082 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:48597082 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:247835560 G>C maps to NM_001005487.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:247835560 G>C maps to NM_001005487.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:248343332 G>T maps to NM_001004688.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:248343332 G>T maps to NM_001004688.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:5364169 C>G maps to NM_001005567.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:5364169 C>G maps to NM_001005567.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:5799228 A>T maps to NM_001001922.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:5799228 A>T maps to NM_001001922.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:21109283 G>T maps to NM_001001968.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:21109283 G>T maps to NM_001001968.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:57798413 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:57798413 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:57798413 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:57798413 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:148716451 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:148716451 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:148716451 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:148716451 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:31287086 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:31287086 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:29650692 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:29650692 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:49455830 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:49455830 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:49455830 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:49455830 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:176661179 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:176661179 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:176661179 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:176661179 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:128725282 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:128725282 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:128725282 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:128725282 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:134111244 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:134111244 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:134111244 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:134111244 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:55719476 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:55719476 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:55719476 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:55719476 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:82868475 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:82868475 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:93031352 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:93031352 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:93031352 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:93031352 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:71498683 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:71498683 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:71498683 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:71498683 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:31917663 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:31917663 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31829889 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31829889 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31917663 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:31917663 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:232602682 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:232602682 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:39851297 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:39851297 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:39851297 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:39851297 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:131703055 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:131703055 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:131703055 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:131703055 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:21174933 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:21174933 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:73428299 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:73428299 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:73428299 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:73428299 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:130839646 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:130839646 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:130839646 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:130839646 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:110442129 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:110442129 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:110455866 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:110455866 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:51701096 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:51701096 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:51701096 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:51701096 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:9319710 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:9319710 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:9319710 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:9319710 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:19418827 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:19418827 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:19418827 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:19418827 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:6530441 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:6530441 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:12012856 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:12012856 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:20534469 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:20534469 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:20534469 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:20534469 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:82355574 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:82355574 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:82355574 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:82355574 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:152158594 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:152158594 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:44276627 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:44276627 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:133256254 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:133256254 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:133256254 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:133256254 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:39125674 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:39125674 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:39125674 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:39125674 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:54976614 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:54976614 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:54976614 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:54976614 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:146070810 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:146070810 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:146070810 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:146070810 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:70981462 G>T maps to NM_024504.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:70981462 G>T maps to NM_024504.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:47267408 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:47267408 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:47267408 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:47267408 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:186269416 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:186269416 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:186269416 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:186269416 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:35070162 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:35070162 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:35070162 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:35070162 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:36422594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:36422594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:36422594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:36422594 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43699020 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43699020 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:43699020 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:43699020 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43687549 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43687549 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:43687549 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:43687549 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43421816 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43421816 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43771691 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:43771691 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:130886278 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:130886278 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:117517064 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:117517064 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:3007518 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:3007518 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:3007518 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:3007518 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:198703338 C>G maps to ENST00000271610 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:198703338 C>G maps to ENST00000271610 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:8470946 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:8470946 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:8470946 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:8470946 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:15668623 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:15668623 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:15668623 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:15668623 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:40748658 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:40748658 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:40748658 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:40748658 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:112101051 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:112101051 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:112101051 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:112101051 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:157154710 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:157154710 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:157154710 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:157154710 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:52320976 G>T maps to NM_144651.4 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:52320976 G>T maps to NM_144651.4 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:52339181 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:52339181 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:9301591 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:9301591 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:9301591 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:9301591 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:74275084 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:74275084 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:32995144 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:32995144 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:32995144 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:32995144 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:220373992 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:220373992 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:220427548 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:220427548 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:220373992 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:220373992 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:220427548 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:220427548 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:20017689 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:20017689 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:131945235 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:131945235 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:136031196 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:136031196 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:36265656 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:36265656 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:21925963 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:21925963 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:21925963 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:21925963 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:3266365 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:3266365 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:3266365 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:3266365 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:105010525 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:105010525 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:105010525 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:105010525 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:78688789 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:78688789 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:94493468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:94493468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:94493468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:94493468 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:33244072 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:33244072 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:33244072 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:33244072 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:43906470 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:43906470 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:45998402 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:45998402 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:45998402 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:45998402 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:237711905 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:237711905 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:237711905 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:237711905 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:134988769 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chrX:134988769 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:134988769 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chrX:134988769 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:39847517 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:39847517 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:76869038 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:76869038 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:18457730 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:18457730 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:50900254 C>A maps to ENST00000337034 R881R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:50900254 C>A maps to ENST00000337034 R881R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:51980624 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:51980624 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:51980624 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:51980624 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:25689862 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:25689862 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:25689862 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:25689862 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:38835558 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:38835558 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:38835558 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:38835558 A>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:151139935 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:151139935 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:151139935 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:151139935 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:102249074 G>C maps to NM_015490.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:102249074 G>C maps to NM_015490.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:12185253 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:12185253 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:12185253 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:12185253 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:91940958 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:91940958 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:13894607 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:13894607 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:13894607 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:13894607 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:151338092 C>A maps to ENST00000435071 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:151338092 C>A maps to ENST00000435071 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:169578721 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:169578721 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:169578721 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:169578721 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:84669986 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:84669986 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:4556233 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:4556233 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:95088803 G>T maps to ENST00000393080 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:95088803 G>T maps to ENST00000393080 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:42531705 G>T maps to NM_015559.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:42531705 G>T maps to NM_015559.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:26709618 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:26709618 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:26709618 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:26709618 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37951986 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37951986 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:99862416 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:99862416 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:99862416 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:99862416 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:42088918 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr20:42088918 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:50462232 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:50462232 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:50462232 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:50462232 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:51956035 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:51956035 T>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:65413582 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:65413582 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:27022920 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:27022920 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:27022920 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:27022920 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:36152974 G>T maps to NM_005983.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:36152974 G>T maps to NM_005983.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:44664186 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:44664186 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:22360228 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:22360228 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:100787049 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:100787049 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:100787049 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:100787049 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:63066946 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:63066946 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:63066946 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:63066946 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:64360096 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:64360096 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:92350328 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:92350328 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:92350328 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:92350328 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:150719856 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:150719856 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:46596959 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:46596959 C>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:44502666 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:44502666 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42340308 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:42340308 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42340308 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:42340308 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:220497825 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:220497825 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:44466748 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:44466748 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:44466748 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:44466748 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:170218852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:170218852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:170218852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:170218852 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:133692424 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:133692424 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:98819968 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:98819968 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:168093467 C>A maps to NM_003062.2 A1521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:168093467 C>A maps to NM_003062.2 A1521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:168201304 C>A maps to NM_003062.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr5:168201304 C>A maps to NM_003062.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:18844353 C>A maps to ENST00000389467 L2900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:18844353 C>A maps to ENST00000389467 L2900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:139283128 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:139283128 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:51363184 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:51363184 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:51363184 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:51363184 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:36743131 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr13:36743131 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:36743131 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr13:36743131 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:97131922 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:97131922 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:214162029 G>T maps to NM_024532.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:214162029 G>T maps to NM_024532.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:172643081 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:172643081 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:172643081 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:172643081 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:97327312 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:97327312 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:89920848 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:89920848 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:158605903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:158605903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:158632332 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:158632332 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:158605903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:158605903 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:158624559 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:158624559 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:9034825 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:9034825 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:9034825 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:9034825 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:44385983 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:44385983 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:28099796 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:28099796 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:912907 G>A maps to ENST00000456758 W955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:912907 G>A maps to ENST00000456758 W955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:31590552 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:31590552 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:152532560 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:152532560 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:152532560 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:152532560 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:84214844 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:84214844 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:84214844 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:84214844 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:32633200 G>T maps to NM_153809.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:32633200 G>T maps to NM_153809.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:152058155 G>A maps to NM_001008536.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:152058155 G>A maps to NM_001008536.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:20837788 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr14:20837788 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:20837788 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr14:20837788 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:43552760 G>A maps to NM_201631.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:43552760 G>A maps to NM_201631.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:134042064 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:134042064 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:11466207 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:11466207 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:137852370 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:137852370 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:137852370 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:137852370 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:54191518 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:54191518 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:98155946 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:98155946 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:120476353 C>T maps to NM_138554.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:120476353 C>T maps to NM_138554.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:76135130 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:76135130 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:12270058 T>C maps to NM_018374.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:12270058 T>C maps to NM_018374.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:67263046 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:67263046 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:12777052 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:12777052 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:205053310 G>A maps to NM_203376.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:205053310 G>A maps to NM_203376.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:29659657 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr12:29659657 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:29659657 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr12:29659657 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:6664857 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:6664857 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:9413361 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:9413361 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:55656722 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:55656722 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:42697208 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr20:42697208 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:7578555 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:7578555 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:68853446 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:68853446 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:10934859 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:10934859 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:10934859 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:10934859 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:10936147 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:10936147 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:36896654 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:36896654 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:110099685 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:110099685 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:110099685 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:110099685 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:77419569 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:77419569 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:77419569 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:77419569 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:234862446 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:234862446 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:38501405 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr21:38501405 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:38501405 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:38501405 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:179590783 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:179590783 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:179542346 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:179542346 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:179590783 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:179590783 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37890141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37890141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37928068 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:37928068 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:37890141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:37890141 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:37928068 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:37928068 T>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:12708115 G>T maps to NM_000550.2 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:12708115 G>T maps to NM_000550.2 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:88924635 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:88924635 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:88924635 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:88924635 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:138980094 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:138980094 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:59338445 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:59338445 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:13271810 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr10:13271810 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:234557063 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:234557063 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:234557063 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:234557063 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:234557072 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:234557072 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:70148192 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:70148192 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:70148192 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:70148192 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:176301208 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr5:176301208 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:96106147 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:96106147 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:96106147 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:96106147 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:21991532 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:21991532 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:21991532 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:21991532 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:126208252 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:126208252 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:126223025 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:126223025 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:126224958 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr3:126224958 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:126208252 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:126208252 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:126223025 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:126223025 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:126224958 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:126224958 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:17554814 G>T maps to NM_153676.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:17554814 G>T maps to NM_153676.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:216051311 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:216051311 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:216051311 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:216051311 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:30415862 T>C maps to NM_006447.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr21:30415862 T>C maps to NM_006447.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:161130697 C>T maps to NM_012475.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:161130697 C>T maps to NM_012475.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:144724344 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr6:144724344 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:144724344 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr6:144724344 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:77918708 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:77918708 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:77918708 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:77918708 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:177648849 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr4:177648849 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:177648849 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr4:177648849 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:87018100 C>A maps to NM_016206.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr3:87018100 C>A maps to NM_016206.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:2651656 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:2651656 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:118942725 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:118942725 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:12460229 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr1:12460229 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:12460229 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr1:12460229 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:134109793 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr11:134109793 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:134109793 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr11:134109793 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:42209751 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr22:42209751 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:9538669 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr17:9538669 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:9538669 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr17:9538669 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:29165339 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:29165339 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:29165339 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:29165339 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:74650851 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr2:74650851 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:74650851 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr2:74650851 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:137021719 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr9:137021719 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:137021719 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:137021719 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:158679865 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:158679865 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:158679865 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:158679865 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:36594885 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:36594885 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:54353140 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:54353140 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:54446657 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:54446657 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:54353140 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:54353140 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:54446657 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:54446657 A>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:10892673 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr8:10892673 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:10755797 C>A maps to NM_173683.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:10755797 C>A maps to NM_173683.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:10892673 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr8:10892673 C>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:152373297 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:152373297 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:37126596 G>T maps to NM_032226.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr9:37126596 G>T maps to NM_032226.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:30134176 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr22:30134176 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:74536210 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:74536210 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:74624442 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr18:74624442 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:74536210 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr18:74536210 A>G did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:64383030 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr10:64383030 C>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:49559248 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr16:49559248 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:49559248 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr16:49559248 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:52538782 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:52538782 T>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:37967371 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:37967371 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:64821521 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr15:64821521 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:64821521 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr15:64821521 G>T did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:56954087 G>T maps to ENST00000342634 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:56954087 G>T maps to ENST00000342634 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:64004154 C>G maps to NM_178558.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:64004154 C>G maps to NM_178558.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:57184253 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr19:57184253 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:100866096 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr7:100866096 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:100866096 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01W-0928-08 chr7:100866096 G>C did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:58556365 G>A did not map to a codon.
Sequencing variant TCGA-44-2659-01A-01D-0969-08 chr19:58556365 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:220396413 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:220396413 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr20:31604684 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr20:31604684 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:33417745 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:33417745 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:112324261 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:112324261 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:149937660 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:149937660 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:61859155 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:61859155 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:107814595 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:107814595 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:36563090 C>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:36563090 C>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:17085880 A>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:17085880 A>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr20:23667850 G>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr20:23667850 G>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:47280986 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:47280986 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr17:20160707 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr17:20160707 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:95499162 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:95499162 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:7914845 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:7914845 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:617608 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:617608 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:17892641 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:17892641 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:70512579 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:70512579 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:88820606 T>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:88820606 T>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:24781650 A>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:24781650 A>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr5:176859360 C>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr5:176859360 C>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:153225647 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chrX:153225647 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:37670626 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:37670626 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:55020299 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:55020299 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:226109507 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:226109507 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:70066628 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:70066628 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr8:17818029 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr8:17818029 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:151212391 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:151212391 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:242451593 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:242451593 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:56088990 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:56088990 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:9302261 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:9302261 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:136004742 G>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:136004742 G>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:153588242 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:153588242 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:9121642 C>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:9121642 C>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:234536894 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:234536894 T>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:53455477 C>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:53455477 C>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:375609 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:375609 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:159052439 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:159052439 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:139802433 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:139802433 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr21:45838465 C>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr21:45838465 C>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:43221465 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr6:43221465 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:39150707 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:39150707 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:139974383 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:139974383 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr17:76794433 G>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr17:76794433 G>C did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:43162978 G>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:43162978 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:66873504 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:66873504 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:66873504 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:66873504 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:87037291 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:87037291 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:87037291 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:87037291 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:21964925 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:21964925 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:21964925 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:21964925 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:21965114 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:21965114 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:44078696 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:44078696 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:44078696 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:44078696 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:35580232 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:35580232 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:20492312 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:20492312 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:5567248 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:5567248 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:64747520 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:64747520 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:64747520 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:64747520 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:49168126 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:49168126 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:49168126 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:49168126 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:111878415 C>T maps to NM_016824.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:111878415 C>T maps to NM_016824.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:236716110 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:236716110 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:88200259 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:88200259 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:88200259 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:88200259 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:5135858 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:5135858 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr18:56245979 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr18:56245979 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:4777188 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:4777188 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:4777188 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:4777188 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:36429516 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:36429516 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:36429516 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:36429516 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:114438395 G>T maps to NM_006594.2 S592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:114438395 G>T maps to NM_006594.2 S592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:34904741 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:34904741 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:34904832 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:34904832 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:34904832 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:34904832 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:156928749 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:156928749 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:156928749 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:156928749 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:97516811 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:97516811 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:97516811 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:97516811 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:155452249 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:155452249 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:155452249 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:155452249 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:97486050 G>A maps to NM_183356.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:97486050 G>A maps to NM_183356.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:7045359 C>G maps to NM_001940.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:7045359 C>G maps to NM_001940.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:160063811 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:160063811 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:110781291 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:110781291 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:63898772 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:63898772 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:70250922 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:70250922 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:70250922 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:70250922 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:11047566 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:11047566 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:75263783 G>A maps to NM_001170714.1 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:75263783 G>A maps to NM_001170714.1 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:27720907 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:27720907 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:96044876 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:96044876 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:96044876 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:96044876 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:41267811 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:41267811 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:116124769 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:116124769 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:56381762 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:56381762 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:56381762 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:56381762 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:76224357 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:76224357 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:76224357 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:76224357 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:111385768 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:111385768 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:64697601 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:64697601 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:19641031 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:19641031 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:19641031 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:19641031 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:53686333 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:53686333 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:23698079 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:23698079 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:23698079 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:23698079 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:60499417 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:60499417 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:60499417 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:60499417 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:31874062 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:31874062 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:46122351 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:46122351 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:46122351 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:46122351 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr22:32548010 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr22:32548010 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:40193012 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:40193012 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:42971543 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:42971543 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:140870386 C>G maps to ENST00000277549 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:140870386 C>G maps to ENST00000277549 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:49075760 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:49075760 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:49075760 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:49075760 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:49086775 T>A maps to NM_005183.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:49086775 T>A maps to NM_005183.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:65027116 G>T maps to NM_014405.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:65027116 G>T maps to NM_014405.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:40852232 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:40852232 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:40852232 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:40852232 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:89435210 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:89435210 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:89435210 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:89435210 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:28443846 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:28443846 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:66358452 C>T maps to NM_018219.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:66358452 C>T maps to NM_018219.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:2480921 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:2480921 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:2480921 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:2480921 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:78081870 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:78081870 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:78081870 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:78081870 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:35201737 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:35201737 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:33743967 G>C maps to NM_203331.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:33743967 G>C maps to NM_203331.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:14507288 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:14507288 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:14507288 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:14507288 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:66430156 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:66430156 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:89695225 C>A maps to NM_004365.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:89695225 C>A maps to NM_004365.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:184076690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:184076690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:184076690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:184076690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:73245493 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:73245493 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:73245493 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:73245493 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:58580599 C>T maps to NM_016284.3 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:58580599 C>T maps to NM_016284.3 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:17298311 G>T maps to NM_017738.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:17298311 G>T maps to NM_017738.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:7851747 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:7851747 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:7851747 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:7851747 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:71193339 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:71193339 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:71193339 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:71193339 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:33138502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:33138502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:33138502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:33138502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:70859805 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:70859805 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:70859805 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:70859805 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:111077485 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:111077485 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:74806912 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:74806912 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:228109738 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:228109738 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:228109738 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:228109738 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:48610495 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:48610495 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:48610495 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:48610495 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:148596501 T>C maps to NM_001870.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:148596501 T>C maps to NM_001870.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:173383197 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:173383197 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:173383197 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:173383197 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:211542707 A>G maps to NM_001122633.1 *1507W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:211542707 A>G maps to NM_001122633.1 *1507W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:153945571 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:153945571 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:153945571 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:153945571 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:76254546 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:76254546 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:76254546 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:76254546 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:2876053 A>G maps to NM_033225.5 H2658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:2876053 A>G maps to NM_033225.5 H2658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:58223087 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:58223087 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:58223087 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:58223087 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:83126619 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:83126619 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:83126619 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:83126619 T>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:99447119 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:99447119 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:99447119 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:99447119 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:87516280 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:87516280 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:87516280 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:87516280 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:32678509 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:32678509 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:110555765 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:110555765 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:24756941 C>A maps to NM_001127453.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:24756941 C>A maps to NM_001127453.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:24112543 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:24112543 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:125470822 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:125470822 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:125470822 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:125470822 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:57651093 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:57651093 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:57651093 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:57651093 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:95598045 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:95598045 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr14:95598045 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr14:95598045 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:38790665 G>T maps to ENST00000327475 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:38790665 G>T maps to ENST00000327475 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:33026679 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:33026679 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:183593846 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:183593846 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:132184796 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:132184796 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:132184963 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:132184963 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:132184796 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:132184796 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:56217357 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:56217357 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:40140657 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:40140657 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:40140657 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:40140657 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:58196437 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:58196437 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:103360901 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:103360901 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:103360901 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:103360901 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:29046858 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:29046858 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:17581486 C>T maps to NM_006870.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:17581486 C>T maps to NM_006870.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:95705560 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:95705560 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:80577334 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:80577334 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:71838545 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:71838545 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:65824428 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:65824428 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:65824428 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:65824428 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:36324256 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:36324256 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:36324256 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:36324256 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:52329943 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:52329943 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:52329943 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:52329943 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:7480516 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:7480516 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:7480516 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:7480516 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:18583424 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:18583424 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:73462318 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:73462318 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:53156717 G>A maps to ENST00000370918 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:53156717 G>A maps to ENST00000370918 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:225699606 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:225699606 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:685776 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:685776 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:132190303 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:132190303 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:46587747 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:46587747 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:46587747 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:46587747 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:34766488 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:34766488 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:7918278 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:7918278 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:93131466 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:93131466 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:93131466 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:93131466 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:93159384 G>A maps to NM_005665.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:93159384 G>A maps to NM_005665.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:56768496 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:56768496 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:56768496 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:56768496 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:133682420 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:133682420 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:133682420 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:133682420 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:25743888 G>T maps to NM_152704.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:25743888 G>T maps to NM_152704.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:114401678 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:114401678 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:114401678 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:114401678 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:8376827 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:8376827 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:13058113 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:13058113 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:13058113 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:13058113 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:101146615 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:101146615 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:41927056 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:41927056 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:72696066 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:72696066 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:4553269 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:4553269 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:17122442 C>A maps to NM_144997.5 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:17122442 C>A maps to NM_144997.5 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:128489737 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:128489737 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:52249101 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:52249101 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:52249101 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:52249101 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:61899269 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:61899269 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:61899269 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:61899269 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:180671581 C>T maps to NM_005087.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:180671581 C>T maps to NM_005087.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:50593173 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:50593173 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:30661019 G>A maps to NM_002047.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:30661019 G>A maps to NM_002047.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:153782583 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:153782583 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:153782583 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:153782583 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:72634140 G>T maps to ENST00000504199 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:72634140 G>T maps to ENST00000504199 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:154299373 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:154299373 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:154299690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:154299690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:154299706 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:154299706 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:154299690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:154299690 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:154299706 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:154299706 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:75763965 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:75763965 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:75763965 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:75763965 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:33581686 A>G maps to NM_018025.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:33581686 A>G maps to NM_018025.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:142623348 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:142623348 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:99947430 C>G maps to NM_004951.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:99947430 C>G maps to NM_004951.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:35502532 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:35502532 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:65476146 T>A maps to NM_138737.3 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:65476146 T>A maps to NM_138737.3 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:28369409 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:28369409 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:32916704 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:32916704 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:29896815 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:29896815 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:11302246 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:11302246 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:43917150 G>A maps to NM_001190880.1 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:43917150 G>A maps to NM_001190880.1 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:6658506 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:6658506 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:6658506 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:6658506 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:46733776 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:46733776 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:46733776 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:46733776 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:18735941 C>T maps to NM_173588.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:18735941 C>T maps to NM_173588.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:5995218 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:5995218 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:5995218 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:5995218 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:12029063 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:12029063 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:105242215 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:105242215 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:60005150 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:60005150 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:60005150 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:60005150 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:123143206 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:123143206 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:123143206 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:123143206 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:13217011 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:13217011 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:13217011 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:13217011 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:31374751 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:31374751 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:31374751 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:31374751 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:160922534 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:160922534 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:160922534 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:160922534 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:128263324 C>A maps to NM_017969.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:128263324 C>A maps to NM_017969.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:6051523 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:6051523 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:6051523 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:6051523 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:124237113 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:124237113 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:124237113 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:124237113 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:137713558 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:137713558 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:137713558 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:137713558 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:43893318 C>T maps to NM_015284.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:43893318 C>T maps to NM_015284.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:128695986 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:128695986 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:97279370 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:97279370 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:97279370 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:97279370 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:43497627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:43497627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr18:43497627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr18:43497627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:1920441 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:1920441 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:44893619 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:44893619 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:137518699 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:137518699 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:137518699 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:137518699 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:91514508 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:91514508 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:91514508 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:91514508 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:145697660 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:145697660 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:136963998 G>T maps to NM_017415.2 C526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:136963998 G>T maps to NM_017415.2 C526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:187149393 T>A maps to NM_000892.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:187149393 T>A maps to NM_000892.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:39022847 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:39022847 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:39022847 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:39022847 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:39634122 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:39634122 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:112437027 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:112437027 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:112437027 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:112437027 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:183192587 A>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:183192587 A>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:225592094 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:225592094 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:225592094 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:225592094 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:17963470 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:17963470 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:17963470 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:17963470 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:75602967 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:75602967 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:105406165 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:105406165 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:105406165 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:105406165 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:73559279 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:73559279 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:96350699 G>A maps to NM_005575.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:96350699 G>A maps to NM_005575.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:56344682 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:56344682 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:57567683 C>T maps to NM_002332.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:57567683 C>T maps to NM_002332.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:86039159 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:86039159 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:41105475 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:41105475 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:41105497 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:41105497 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:41105475 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:41105475 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:12773979 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:12773979 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:210569126 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:210569126 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:210569126 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:210569126 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:185169073 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:185169073 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:70351936 C>G maps to ENST00000333646 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:70351936 C>G maps to ENST00000333646 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:70352265 C>A maps to ENST00000333646 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:70352265 C>A maps to ENST00000333646 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:222832864 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:222832864 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:222832864 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:222832864 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:37059087 C>T maps to NM_000249.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:37059087 C>T maps to NM_000249.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:152064994 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:152064994 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:152064994 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:152064994 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:154836502 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:154836502 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:49575978 C>T maps to NM_014484.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:49575978 C>T maps to NM_014484.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:108754117 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:108754117 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:108754117 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:108754117 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:4348886 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:4348886 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:49723443 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:49723443 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:55489448 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:55489448 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:55489448 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:55489448 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:70165186 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:70165186 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:70165186 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:70165186 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:77760048 C>G maps to NM_015057.4 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:77760048 C>G maps to NM_015057.4 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:2071592 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:2071592 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:88635798 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:88635798 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:16921338 A>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:16921338 A>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:198248313 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:198248313 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:34284399 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:34284399 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:34284399 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:34284399 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:26449575 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:26449575 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:26449575 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:26449575 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:175812221 C>T maps to ENST00000451293 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:175812221 C>T maps to ENST00000451293 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:26110160 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:26110160 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:26110160 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:26110160 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:27250702 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:27250702 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:131719194 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:131719194 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:131719194 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:131719194 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:57618592 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:57618592 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:123870874 G>T maps to NM_001163278.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:123870874 G>T maps to NM_001163278.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:78383450 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:78383450 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:78383450 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:78383450 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:247920841 G>T maps to NM_012353.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:247920841 G>T maps to NM_012353.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:248167014 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:248167014 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:248167014 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:248167014 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:59131925 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:59131925 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:17555009 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:17555009 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:17555009 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:17555009 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:169630395 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:169630395 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:169630395 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:169630395 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:25064709 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:25064709 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:25064709 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:25064709 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:50074341 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:50074341 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:50074341 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:50074341 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:82763877 C>T maps to NM_033026.5 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:82763877 C>T maps to NM_033026.5 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:62896763 C>T maps to NM_018257.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:62896763 C>T maps to NM_018257.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:20602575 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:20602575 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:70190451 C>T maps to NM_017990.3 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:70190451 C>T maps to NM_017990.3 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:15098195 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:15098195 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:15098226 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:15098226 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:15098195 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:15098195 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:15098226 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:15098226 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:204435748 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:204435748 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:51929717 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:51929717 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:51889441 G>A maps to NM_138694.3 I1722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:51889441 G>A maps to NM_138694.3 I1722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:51929717 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:51929717 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:64029860 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:64029860 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:64029860 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr11:64029860 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:100853758 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:100853758 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:100853758 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:100853758 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:103044263 C>T maps to NM_000533.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:103044263 C>T maps to NM_000533.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:126751200 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:126751200 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:131866496 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:131866496 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:131866496 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:131866496 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:190738168 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:190738168 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:74880721 C>T maps to NM_016218.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:74880721 C>T maps to NM_016218.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:124503574 G>A maps to NM_015450.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:124503574 G>A maps to NM_015450.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:13743177 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:13743177 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:90124211 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:90124211 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:227083039 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:227083039 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:49196207 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:49196207 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:49196207 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:49196207 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:198721686 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:198721686 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:198721686 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:198721686 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:128321380 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:128321380 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:128321380 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:128321380 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:163836961 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:163836961 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:70133582 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:70133582 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:70133582 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:70133582 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:51667887 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:51667887 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:51667887 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:51667887 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:20475970 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr20:20475970 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:20475970 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr20:20475970 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:178802458 A>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:178802458 A>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:25542960 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:25542960 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:127961292 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:127961292 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:127961292 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:127961292 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:36122005 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:36122005 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:36122005 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:36122005 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:55560137 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:55560137 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:55560241 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:55560241 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:55560137 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:55560137 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:113190976 G>A maps to NM_005054.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:113190976 G>A maps to NM_005054.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:152273025 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:152273025 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:152273025 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:152273025 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:6269943 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:6269943 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:78988149 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:78988149 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:78988149 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:78988149 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:115024747 G>C maps to NM_001163790.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr9:115024747 G>C maps to NM_001163790.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:68897293 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:68897293 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:68897293 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:68897293 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:123003362 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:123003362 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:123003362 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:123003362 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:107069279 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:107069279 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:107069279 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:107069279 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:37077122 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:37077122 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:237550553 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:237550553 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:237806521 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:237806521 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:237550553 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:237550553 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:34040855 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:34040855 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:34145244 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:34145244 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:75305186 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:75305186 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:75305186 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:75305186 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:144874323 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:144874323 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:120221963 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:120221963 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:169562792 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:169562792 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:169562792 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:169562792 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:37422507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:37422507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:37422507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:37422507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:29883922 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:29883922 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:145379541 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:145379541 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:145379541 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr5:145379541 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:407753 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:407753 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:1074628 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:1074628 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:121634003 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:121634003 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:121634003 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:121634003 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:25850951 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:25850951 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:73274131 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:73274131 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:32428078 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:32428078 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:32428078 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:32428078 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:44222316 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:44222316 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:44222520 G>C maps to NM_178148.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:44222520 G>C maps to NM_178148.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:67486179 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:67486179 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:67486257 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:67486257 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:165755216 G>T maps to ENST00000409662 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:165755216 G>T maps to ENST00000409662 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:55725966 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:55725966 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:55725966 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:55725966 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:33351507 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:33351507 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:33351507 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:33351507 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:48573360 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr18:48573360 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr18:48575670 C>G maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr18:48575670 C>G maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:127569507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:127569507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:127569507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:127569507 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:231109627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:231109627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:231109627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:231109627 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:24825709 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr13:24825709 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:24825709 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr13:24825709 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:100482701 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:100482701 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:182760646 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:182760646 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:77094489 G>C maps to NM_152996.2 *306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr1:77094489 G>C maps to NM_152996.2 *306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:96858054 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:96858054 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:4473514 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:4473514 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:4473514 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:4473514 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:73115038 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:73115038 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:73115038 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:73115038 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:130444612 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr9:130444612 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:70596266 G>A maps to NM_014465.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr4:70596266 G>A maps to NM_014465.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:123973012 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:123973012 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:123973012 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:123973012 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:120843826 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:120843826 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:120843826 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:120843826 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:27825559 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:27825559 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:27825559 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:27825559 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:114837285 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:114837285 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:114837285 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:114837285 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:115981281 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr10:115981281 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:115981281 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr10:115981281 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:56650711 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:56650711 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:56650711 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr17:56650711 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:51718529 C>T maps to NM_015926.4 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:51718529 C>T maps to NM_015926.4 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:51504576 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr12:51504576 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:51504576 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr12:51504576 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:70443901 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:70443901 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:27052157 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:27052157 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:9332796 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr11:9332796 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr22:37469467 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr22:37469467 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:45406210 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:45406210 T>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:45483286 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr21:45483286 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:45483286 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr21:45483286 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:45668078 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:45668078 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:45668078 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:45668078 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:98478961 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:98478961 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:98497312 G>A maps to ENST00000359863 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:98497312 G>A maps to ENST00000359863 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:15903642 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:15903642 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:99696502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:99696502 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:89338840 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:89338840 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr14:89338840 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr14:89338840 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:179476038 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:179476038 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:156981716 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:156981716 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:156981716 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:156981716 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:186343594 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr4:186343594 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:150385793 G>C maps to NM_024518.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:150385793 G>C maps to NM_024518.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:33491318 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:33491318 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:35425503 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:35425503 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:158991235 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr2:158991235 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:158991235 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr2:158991235 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:144875738 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr6:144875738 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:145103244 C>G maps to NM_007124.2 L2940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr6:145103244 C>G maps to NM_007124.2 L2940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:62304382 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr15:62304382 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:62304382 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr15:62304382 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:40926568 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr17:40926568 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:224619512 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:224619512 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:117566948 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:117566948 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:167293689 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr3:167293689 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:167293689 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:167293689 A>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:37443277 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr5:37443277 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:709169 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:709169 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:71593290 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:71593290 G>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:183515957 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr3:183515957 G>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:100345113 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:100345113 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:100345113 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr7:100345113 T>C did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:11857552 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:11857552 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:11857552 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:11857552 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:144332686 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr8:144332686 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:106813278 G>A maps to NM_012082.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr8:106813278 G>A maps to NM_012082.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:68222053 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr14:68222053 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr14:68222053 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr14:68222053 C>T did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:44604933 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr19:44604933 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:44604933 G>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr19:44604933 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-44-2662-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:31073108 C>T maps to ENST00000417110 F99F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-2662-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:31073108 C>T maps to ENST00000417110 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:134424856 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chrX:134424856 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:134424856 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chrX:134424856 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:71913921 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr16:71913921 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:71913921 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01W-0928-08 chr16:71913921 C>A did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:30329308 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr7:30329308 A>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:45504492 C>G did not map to a codon.
Sequencing variant TCGA-44-2662-01A-01D-0969-08 chr1:45504492 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:247055225 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:247055225 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:247055225 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:247055225 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:5724264 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:5724264 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:17313467 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:17313467 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:45260842 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:45260842 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:1432843 C>A maps to ENST00000382179 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:1432843 C>A maps to ENST00000382179 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:124459088 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:124459088 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:40034803 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:40034803 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:13443615 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:13443615 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:202131374 G>T maps to NM_001080125.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:202131374 G>T maps to NM_001080125.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:85597492 T>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:85597492 T>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr5:54415560 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr5:54415560 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:97492445 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:97492445 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:97492445 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:97492445 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:125671705 C>T maps to NM_130773.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:125671705 C>T maps to NM_130773.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:19554349 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:19554349 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr20:56094442 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr20:56094442 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:16716880 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:16716880 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:41449149 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:41449149 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr7:101559645 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr7:101559645 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:156819758 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:156819758 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr5:156819758 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr5:156819758 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:162740300 A>G maps to NM_006182.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:162740300 A>G maps to NM_006182.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chrX:134707802 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chrX:134707802 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:134707802 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:134707802 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:51376490 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:51376490 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr8:105463394 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr8:105463394 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr20:35399618 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr20:35399618 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:89744278 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:89744278 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:80583585 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:80583585 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr19:46117996 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr19:46117996 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:46117996 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:46117996 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr20:34782047 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr20:34782047 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr20:34782047 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr20:34782047 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr9:133572860 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr9:133572860 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:46748536 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:46748536 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:57207597 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:57207597 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:57207597 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:57207597 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:78410017 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:78410017 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:37835016 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:37835016 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:57712044 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:57712044 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr5:89923107 C>A maps to NM_032119.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr5:89923107 C>A maps to NM_032119.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr6:28474301 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr6:28474301 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr6:28474301 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr6:28474301 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:236745919 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:236745919 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr9:100693563 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr9:100693563 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr9:100693563 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr9:100693563 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:173327621 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:173327621 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:4759027 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:4759027 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:4759027 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:4759027 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:65482335 C>G maps to NM_182710.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:65482335 C>G maps to NM_182710.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:155904165 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:155904165 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:155904165 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:155904165 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:10525537 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:10525537 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:77746184 C>T maps to NM_001134745.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:77746184 C>T maps to NM_001134745.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:65813600 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:65813600 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:49928031 G>A maps to NM_002447.2 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:49928031 G>A maps to NM_002447.2 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:63579261 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:63579261 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:3241385 C>T maps to NM_015419.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:3241385 C>T maps to NM_015419.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr22:36697141 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr22:36697141 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr4:140265338 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr4:140265338 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:201763487 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:201763487 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr6:41046801 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr6:41046801 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr19:51874994 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr19:51874994 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:51874994 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr19:51874994 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:43180274 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:43180274 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:79555942 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:79555942 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:200012848 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:200012848 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr8:32621514 G>A maps to NM_013956.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr8:32621514 G>A maps to NM_013956.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:176711018 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:176711018 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:93803375 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:93803375 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:53861490 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:53861490 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr15:44038799 C>T maps to NM_005313.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr15:44038799 C>T maps to NM_005313.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:126747836 G>A maps to NM_032242.3 E1557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:126747836 G>A maps to NM_032242.3 E1557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:106770125 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:106770125 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:67166720 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:67166720 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:24135317 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:24135317 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr13:113815355 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr13:113815355 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr13:113815355 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr13:113815355 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:54126862 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:54126862 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:220166478 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:220166478 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:220166478 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:220166478 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr14:68331942 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr14:68331942 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:46740075 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:46740075 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr17:48560140 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr17:48560140 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr8:108970254 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr8:108970254 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:70597632 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:70597632 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:228567057 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:228567057 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:46584900 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chrX:46584900 T>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr15:97328095 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr15:97328095 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:206592802 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:206592802 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr14:81862604 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr14:81862604 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:30205958 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:30205958 G>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:108998414 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr2:108998414 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr10:29821396 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr10:29821396 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:29819538 G>A maps to NM_021738.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:29819538 G>A maps to NM_021738.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:29821396 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:29821396 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:114910684 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr10:114910684 A>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr4:166963382 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr4:166963382 C>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:50156780 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:50156780 T>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:68941375 G>A maps to NM_024562.1 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:68941375 G>A maps to NM_024562.1 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:10618752 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:10618752 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:12164681 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:12164681 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:201341151 T>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:201341151 T>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:201341151 T>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:201341151 T>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:65726509 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr11:65726509 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr22:50662902 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr22:50662902 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr22:50662902 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr22:50662902 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:993763 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:993763 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:993763 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr12:993763 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr17:48432010 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr17:48432010 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:48432010 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr17:48432010 A>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:203787860 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:203787860 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:203787860 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr1:203787860 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:2881770 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr16:2881770 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:48297912 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:48297912 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:48297912 G>A did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01W-0928-08 chr3:48297912 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:244601123 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:244601123 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:244601123 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:244601123 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chrX:2933386 G>A maps to NM_001011719.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chrX:2933386 G>A maps to NM_001011719.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:72883820 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:72883820 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:72883820 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:72883820 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:4634554 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:4634554 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:4634554 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:4634554 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr14:45706935 T>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr14:45706935 T>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:32583776 C>T maps to NM_002982.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:32583776 C>T maps to NM_002982.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr11:44640275 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr11:44640275 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:44640275 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:44640275 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:196964797 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:196964797 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:196964797 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:196964797 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr13:110827140 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr13:110827140 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr13:110827140 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr13:110827140 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr15:79231356 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr15:79231356 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:53378868 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:53378868 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr9:131016922 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr9:131016922 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr2:225729556 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr2:225729556 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr2:225729556 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr2:225729556 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:109056429 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:109056429 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:109056429 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:109056429 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:36379377 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:36379377 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr15:76551754 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr15:76551754 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr15:76551754 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr15:76551754 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr18:74980500 T>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr18:74980500 T>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr15:51634287 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr15:51634287 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:33370048 A>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:33370048 A>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:155093437 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:155093437 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:155093437 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:155093437 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:123101338 A>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:123101338 A>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr19:7675542 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr19:7675542 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr19:7675542 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr19:7675542 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:39633998 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:39633998 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:52646151 C>T maps to ENST00000257935 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:52646151 C>T maps to ENST00000257935 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:117977498 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:117977498 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr20:44642445 T>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr20:44642445 T>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr20:44642445 T>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr20:44642445 T>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr10:26315293 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr10:26315293 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr10:26315293 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr10:26315293 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr8:41839344 A>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr8:41839344 A>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr8:41839344 A>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr8:41839344 A>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:59667794 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:59667794 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr11:34129963 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr11:34129963 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:34129963 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:34129963 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:124882554 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:124882554 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:124882554 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:124882554 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:228505983 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:228505983 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:2453031 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:2453031 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:2453038 T>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr1:2453038 T>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr6:32130748 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr6:32130748 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr5:23509858 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr5:23509858 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr16:31151519 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr16:31151519 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:184020691 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:184020691 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr10:89624150 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr10:89624150 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr20:2987929 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr20:2987929 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:114358569 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:114358569 C>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr11:65429396 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr11:65429396 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:65429396 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr11:65429396 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr21:45104303 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr21:45104303 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr15:34117766 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr15:34117766 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:92734749 G>A maps to NM_017654.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr7:92734749 G>A maps to NM_017654.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:38645178 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:38645178 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:47162161 G>A maps to NM_014159.6 R1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:47162161 G>A maps to NM_014159.6 R1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:52955589 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:52955589 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:52955589 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:52955589 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr10:70246838 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr10:70246838 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr10:98819297 G>C maps to ENST00000371057 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr10:98819297 G>C maps to ENST00000371057 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:44048437 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr7:44048437 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr20:13539764 T>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr20:13539764 T>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:72314370 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr12:72314370 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:235596494 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:235596494 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:235605077 A>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:235605077 A>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:67242205 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr1:67242205 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr4:156829005 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr4:156829005 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr4:156829005 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr4:156829005 T>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr14:20859304 A>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr14:20859304 A>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr9:82335291 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr9:82335291 G>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:29725031 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr12:29725031 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:53014370 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:53014370 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:53014370 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:53014370 G>C did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr2:29093170 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr2:29093170 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr2:29093170 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr2:29093170 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:39179934 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr3:39179934 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:39179934 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr3:39179934 G>A did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr2:181925549 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr2:181925549 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr2:181925549 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr2:181925549 C>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr8:35542276 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr8:35542276 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:57474564 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr17:57474564 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:57474564 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr17:57474564 A>G did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr19:38294291 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01D-1489-08 chr19:38294291 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr19:38294291 C>T did not map to a codon.
Sequencing variant TCGA-44-2666-01A-01W-0928-08 chr19:38294291 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:8976534 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:8976534 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:8976534 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:8976534 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:107558536 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:107558536 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:107558536 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:107558536 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:66913417 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:66913417 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:66913417 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:66913417 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:67020349 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:67020349 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:67023741 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:67023741 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:67020349 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:67020349 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:48218286 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:48218286 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:48218286 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:48218286 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:43706024 G>T maps to NM_004915.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:43706024 G>T maps to NM_004915.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:34356868 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:34356868 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:34356868 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:34356868 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:35641899 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:35641899 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:35641899 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:35641899 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:89169202 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:89169202 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:89169202 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:89169202 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:114170208 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:114170208 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:114170208 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:114170208 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:20422711 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:20422711 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:20429360 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:20429360 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:20448780 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:20448780 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:20429360 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:20429360 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:53906141 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:53906141 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:158637226 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:158637226 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:156991272 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:156991272 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:156991272 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:156991272 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:207454281 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:207454281 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:207457277 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:207457277 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:207454281 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:207454281 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:207457277 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:207457277 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:33662190 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:33662190 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:33662190 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:33662190 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:77323147 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:77323147 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:77318092 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:77318092 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:77323147 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:77323147 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:128990177 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:128990177 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:161165311 C>A maps to NM_005099.4 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:161165311 C>A maps to NM_005099.4 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:7698358 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:7698358 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:24791240 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:24791240 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:24791240 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:24791240 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:31121310 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:31121310 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:31121310 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:31121310 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:100232648 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:100232648 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:100232648 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:100232648 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:119306728 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:119306728 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:119306728 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:119306728 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:159377795 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:159377795 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:147967676 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:147967676 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:49119142 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:49119142 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:159032629 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:159032629 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:4829865 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:4829865 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:4829865 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:4829865 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:109366317 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:109366317 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:109366317 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:109366317 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:101984538 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:101984538 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:101984538 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:101984538 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:6901775 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:6901775 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:202215956 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:202215956 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:202215956 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:202215956 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:190593279 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:190593279 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:190593279 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:190593279 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:73950894 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:73950894 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:73950894 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:73950894 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:27355418 A>G maps to NM_014915.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:27355418 A>G maps to NM_014915.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:45782067 G>A maps to NM_001142679.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:45782067 G>A maps to NM_001142679.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:242135097 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:242135097 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:201480922 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:201480922 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:201485713 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:201485713 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:201485713 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:201485713 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:139942167 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:139942167 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:39428330 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:39428330 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:39428330 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:39428330 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:30927490 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:30927490 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:30927490 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:30927490 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:69034444 A>G maps to NM_001007231.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:69034444 A>G maps to NM_001007231.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:96795775 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:96795775 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:96799594 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:96799594 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:96795775 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:96795775 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:176913181 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:176913181 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:176913181 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:176913181 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:119625742 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:119625742 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:120053825 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:120053825 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:120053825 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:120053825 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:96756653 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:96756653 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:138879494 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:138879494 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:138825774 T>C maps to NM_173694.4 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:138825774 T>C maps to NM_173694.4 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:138879494 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:138879494 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:25264878 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:25264878 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:25264878 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:25264878 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:160099832 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:160099832 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:160099832 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:160099832 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:198509590 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:198509590 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:198509590 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:198509590 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:54727360 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:54727360 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:54727360 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:54727360 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:26413588 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:26413588 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:26413588 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:26413588 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:154319214 C>T maps to NM_020452.3 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:154319214 C>T maps to NM_020452.3 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:116919708 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:116919708 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:3470666 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:3470666 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:3470666 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:3470666 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:29207151 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:29207151 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:27076967 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:27076967 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:27076967 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:27076967 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:112089380 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:112089380 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:45253100 G>A maps to NM_153274.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:45253100 G>A maps to NM_153274.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:51717761 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:51717761 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:55803103 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:55803103 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:43325941 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:43325941 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:43325941 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:43325941 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:15536145 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:15536145 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:15536145 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:15536145 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:74369632 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:74369632 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:31619550 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:31619550 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:26390121 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:26390121 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:26390121 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:26390121 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:111414781 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:111414781 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:124458144 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:124458144 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:124458144 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:124458144 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:127429314 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:127429314 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33620594 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33620594 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33620606 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33620606 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:33620594 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:33620594 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:124661075 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:124661075 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:61551639 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:61551639 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:45675251 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:45675251 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:76524981 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:76524981 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:76524981 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:76524981 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:95884112 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:95884112 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:95884112 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:95884112 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:65032210 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:65032210 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:65032210 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:65032210 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:93015489 G>T maps to NM_153040.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:93015489 G>T maps to NM_153040.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:90128937 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:90128937 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:34185353 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:34185353 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:34185353 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:34185353 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:30903417 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:30903417 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:30903417 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:30903417 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:30505667 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:30505667 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:172437622 C>A maps to NM_139240.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:172437622 C>A maps to NM_139240.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:57252988 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:57252988 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:57252988 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:57252988 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:75139092 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:75139092 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:162353097 G>A maps to NM_001135240.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:162353097 G>A maps to NM_001135240.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:172538331 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:172538331 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:24964570 C>A maps to NM_020531.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:24964570 C>A maps to NM_020531.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:46097382 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:46097382 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:63349191 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:63349191 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:63349191 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:63349191 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:196241803 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:196241803 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:87812519 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:87812519 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:71020208 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:71020208 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:71020208 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:71020208 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:31740878 G>A maps to NM_025258.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:31740878 G>A maps to NM_025258.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:157731873 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:157731873 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:23740597 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:23740597 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:108524468 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:108524468 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:108524468 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:108524468 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:12864023 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:12864023 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:86559771 G>A maps to NM_032307.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:86559771 G>A maps to NM_032307.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:86142078 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:86142078 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:81600958 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:81600958 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:18630001 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:18630001 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:18630001 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:18630001 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:35909944 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:35909944 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:35909944 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:35909944 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:2237130 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:2237130 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:104825537 A>G maps to NM_001225.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:104825537 A>G maps to NM_001225.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:55012085 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:55012085 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:180381800 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:180381800 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:180381800 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:180381800 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:132290384 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:132290384 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:34417480 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:34417480 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:34417480 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:34417480 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158325683 T>C maps to NM_030893.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158325683 T>C maps to NM_030893.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:112648180 C>A maps to NM_138806.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:112648180 C>A maps to NM_138806.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:19721653 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:19721653 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:19721653 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:19721653 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:59166450 C>A maps to NM_031891.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:59166450 C>A maps to NM_031891.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:60428092 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:60428092 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:109812141 G>A maps to NM_001408.2 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:109812141 G>A maps to NM_001408.2 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:196964819 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:196964819 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:196964819 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:196964819 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:110670478 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:110670478 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:57731243 A>G maps to NM_032866.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:57731243 A>G maps to NM_032866.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:54997024 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:54997024 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:50833718 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:50833718 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:93545280 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:93545280 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:93545280 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:93545280 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:21895651 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:21895651 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:53330937 A>T maps to ENST00000219084 R1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:53330937 A>T maps to ENST00000219084 R1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:23767570 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:23767570 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:23767570 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:23767570 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:69196823 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:69196823 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:113518384 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:113518384 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:113518384 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:113518384 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:10194218 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:10194218 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:150644623 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:150644623 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:150644623 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:150644623 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:123384682 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:123384682 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:123384697 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:123384697 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:123384697 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:123384697 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:72179780 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:72179780 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:72179780 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:72179780 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:6262723 T>A maps to NM_001037329.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:6262723 T>A maps to NM_001037329.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:154732032 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:154732032 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:154732032 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:154732032 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:41318286 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:41318286 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:41318286 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:41318286 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:1367363 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:1367363 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:146741087 G>T maps to NM_014141.5 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:146741087 G>T maps to NM_014141.5 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:125232522 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:125232522 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:103462562 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:103462562 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:103462562 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:103462562 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:33145297 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:33145297 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:33145297 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:33145297 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:105832879 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:105832879 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:105832879 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:105832879 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:46914425 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:46914425 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:139767711 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:139767711 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:139767711 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:139767711 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:109784438 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:109784438 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:109861853 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:109861853 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:10096342 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:10096342 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:238234153 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:238234153 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:238234153 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:238234153 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:24543138 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:24543138 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:24543138 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:24543138 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:207644535 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:207644535 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:207644535 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:207644535 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:43907385 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:43907385 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:43907385 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:43907385 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:5868514 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:5868514 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:5868514 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:5868514 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:149453162 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:149453162 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:149453162 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:149453162 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:113358491 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:113358491 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:113358491 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:113358491 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33118193 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33118193 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33129609 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:33129609 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:11159644 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:11159644 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:11159644 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:11159644 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:88027473 C>T maps to NM_001814.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:88027473 C>T maps to NM_001814.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:44868745 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:44868745 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:44868745 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:44868745 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:202933871 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:202933871 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:27945229 T>A maps to ENST00000435845 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:27945229 T>A maps to ENST00000435845 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:242682044 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:242682044 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:39846147 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:39846147 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:85415502 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:85415502 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:109281145 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:109281145 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:109281145 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:109281145 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:50560623 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:50560623 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:50560623 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:50560623 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:176939770 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:176939770 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:6479182 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:6479182 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:137257502 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:137257502 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:137308319 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:137308319 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:137341036 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:137341036 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:137257502 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:137257502 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:137308319 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:137308319 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:2209644 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:2209644 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:436350 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:436350 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:436350 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:436350 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:38933510 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:38933510 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:32381101 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:32381101 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:50885023 C>T maps to NM_032110.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:50885023 C>T maps to NM_032110.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:196659325 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:196659325 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:196659325 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:196659325 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:196859145 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:196859145 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:11532616 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:11532616 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:72297288 G>A maps to NM_023036.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:72297288 G>A maps to NM_023036.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:157208653 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:157208653 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:157208653 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:157208653 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:31383625 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:31383625 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:94344788 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:94344788 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:169506136 C>A maps to NM_004946.2 S1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:169506136 C>A maps to NM_004946.2 S1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:68021438 G>T maps to NM_022355.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:68021438 G>T maps to NM_022355.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:154684207 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:154684207 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:28604458 A>G maps to NM_001941.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:28604458 A>G maps to NM_001941.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:117303985 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:117303985 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:117303985 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:117303985 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:205116681 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:205116681 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:205117242 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:205117242 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:205116681 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:205116681 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:205117242 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:205117242 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:350735 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:350735 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:82122229 G>T maps to ENST00000372198 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:82122229 G>T maps to ENST00000372198 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:44001176 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:44001176 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:71762080 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:71762080 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:233347415 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:233347415 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:127981080 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:127981080 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:127981080 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:127981080 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:42931057 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:42931057 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:42931057 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:42931057 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:55232938 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:55232938 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:55232938 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:55232938 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:37374157 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:37374157 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:37374157 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:37374157 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:186502524 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:186502524 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:186502524 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:186502524 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:132196788 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:132196788 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:132203405 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:132203405 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:132203405 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:132203405 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:97367039 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:97367039 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:220145626 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:220145626 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:110300683 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:110300683 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:110300683 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:110300683 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:37864638 G>A maps to NM_004448.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:37864638 G>A maps to NM_004448.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:236384243 G>A maps to NM_019891.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:236384243 G>A maps to NM_019891.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:74019326 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:74019326 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:74019326 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:74019326 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:58555485 C>A maps to ENST00000474531 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:58555485 C>A maps to ENST00000474531 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:225266017 G>T maps to NM_001122779.1 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:225266017 G>T maps to NM_001122779.1 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:17664236 T>C maps to ENST00000335393 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:17664236 T>C maps to ENST00000335393 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:62080892 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:62080892 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:62080892 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:62080892 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:179782939 C>A maps to NM_173509.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:179782939 C>A maps to NM_173509.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:29674804 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:29674804 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:10677739 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:10677739 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:10677739 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:10677739 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:129083780 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:129083780 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:177250579 G>T maps to NM_021165.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:177250579 G>T maps to NM_021165.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:28060853 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:28060853 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:54805780 C>A maps to NM_001010872.1 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:54805780 C>A maps to NM_001010872.1 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:92495400 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:92495400 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:92573951 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:92573951 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:92495400 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:92495400 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:92573951 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:92573951 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:126367707 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:126367707 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:126367707 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:126367707 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:150889896 A>T maps to NM_033085.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:150889896 A>T maps to NM_033085.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:111749877 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:111749877 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:124985646 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:124985646 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:125078957 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:125078957 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:124985646 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:124985646 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:102375359 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:102375359 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:102375359 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:102375359 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:34324148 C>A maps to NM_025135.2 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:34324148 C>A maps to NM_025135.2 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:152286757 C>A maps to NM_002016.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:152286757 C>A maps to NM_002016.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:240370499 C>A maps to ENST00000406993 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:240370499 C>A maps to ENST00000406993 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:146675290 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:146675290 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:146675290 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:146675290 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:159635922 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:159635922 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:80544150 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:80544150 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:114284742 G>T maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:114284742 G>T maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:30433404 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:30433404 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:32776199 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:32776199 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:32776199 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:32776199 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:183702970 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:183702970 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:183723562 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:183723562 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:162431520 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:162431520 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:1960911 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:1960911 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:13067597 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:13067597 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:88420460 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:88420460 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:88420460 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:88420460 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:166605224 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:166605224 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:174219403 C>T maps to NM_017423.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:174219403 C>T maps to NM_017423.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:57976596 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:57976596 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:57976596 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:57976596 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:58006691 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:58006691 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:58006691 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:58006691 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:42990861 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:42990861 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:137593428 C>A maps to NM_001496.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:137593428 C>A maps to NM_001496.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:55223727 G>A maps to NM_207410.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:55223727 G>A maps to NM_207410.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:40344424 C>T maps to NM_032484.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:40344424 C>T maps to NM_032484.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:42629108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:42629108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:42629108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:42629108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:59611610 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:59611610 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:59611610 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:59611610 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:183933015 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:183933015 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:183933015 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:183933015 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:11825091 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:11825091 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:11747116 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:11747116 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:11825091 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:11825091 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:121447979 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:121447979 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:121447979 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:121447979 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:94482464 G>T maps to NM_005708.3 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:94482464 G>T maps to NM_005708.3 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:135438315 C>A maps to NM_153834.3 R2307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:135438315 C>A maps to NM_153834.3 R2307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:142759324 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:142759324 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:27333528 G>A maps to NM_005288.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:27333528 G>A maps to NM_005288.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:110086510 C>A maps to NM_031936.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:110086510 C>A maps to NM_031936.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:101972151 G>A maps to NM_138437.5 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:101972151 G>A maps to NM_138437.5 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:87596612 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:87596612 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:94436451 G>T maps to NM_001510.2 G695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:94436451 G>T maps to NM_001510.2 G695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:121212200 A>T maps to NM_005308.2 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:121212200 A>T maps to NM_005308.2 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:27551676 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:27551676 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:27551676 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:27551676 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:103267764 G>A maps to NM_001002916.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:103267764 G>A maps to NM_001002916.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:43698345 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:43698345 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:43698345 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:43698345 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:55039687 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:55039687 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:44656796 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:44656796 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:73945267 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:73945267 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:73945267 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:73945267 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:40998816 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:40998816 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:65147078 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:65147078 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:65147078 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:65147078 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:63991320 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:63991320 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:28482071 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:28482071 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:193854165 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:193854165 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:40098204 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:40098204 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:40098204 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:40098204 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:97200927 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:97200927 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:97200927 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:97200927 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:149785266 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:149785266 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:148759886 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:148759886 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:148759886 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:148759886 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:186141072 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:186141072 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:8533571 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:8533571 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:27182746 C>T maps to NM_019102.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:27182746 C>T maps to NM_019102.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:26860725 T>A maps to NM_022081.4 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:26860725 T>A maps to NM_022081.4 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:18318260 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:18318260 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:18318260 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:18318260 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:6462265 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:6462265 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:114010103 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:114010103 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:114010103 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:114010103 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:70841869 G>T maps to NM_032821.2 P4992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:70841869 G>T maps to NM_032821.2 P4992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:52874027 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:52874027 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:78453902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:78453902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:78453902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:78453902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:34617535 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr21:34617535 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:65622020 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:65622020 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:65622020 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:65622020 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:47075345 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:47075345 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:47075345 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:47075345 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:217543050 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:217543050 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:133806091 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:133806091 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:113832209 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:113832209 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:113832209 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:113832209 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:113832363 C>T maps to NM_032556.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:113832363 C>T maps to NM_032556.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23842144 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23842144 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:23842144 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:23842144 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:55164776 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:55164776 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:55164776 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:55164776 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:35876455 C>G maps to NM_002185.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:35876455 C>G maps to NM_002185.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:91034541 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:91034541 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:91034541 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:91034541 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:75923417 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:75923417 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:75950244 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:75950244 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:75923417 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:75923417 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:396877 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:396877 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:128588453 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:128588453 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:52370858 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:52370858 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:52370858 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:52370858 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:54803185 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:54803185 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:54803185 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:54803185 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31424229 C>A maps to ENST00000444228 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31424229 C>A maps to ENST00000444228 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31429490 C>A maps to ENST00000444228 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31429490 C>A maps to ENST00000444228 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31372607 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31372607 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31391185 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:31391185 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31372607 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31372607 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31384648 G>T maps to NM_000887.3 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31384648 G>T maps to NM_000887.3 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31391185 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:31391185 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:7768846 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:7768846 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:7768846 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:7768846 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:26596615 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:26596615 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:105613764 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:105613764 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:6083524 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:6083524 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:6083524 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:6083524 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:124160958 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:124160958 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:123863304 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:123863304 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:124160958 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:124160958 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:170371488 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:170371488 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:170371488 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:170371488 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:78651260 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:78651260 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:78651260 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:78651260 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:73867319 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:73867319 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110984409 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110984409 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:53244105 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:53244105 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:62757661 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:62757661 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:62757661 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:62757661 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:197410139 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:197410139 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:197410139 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:197410139 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:27715389 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:27715389 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:27782857 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:27782857 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:27715389 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:27715389 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:27782857 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:27782857 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:118227916 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:118227916 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:118227916 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:118227916 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:70775266 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:70775266 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:70775266 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:70775266 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:94160827 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:94160827 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:1368990 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:1368990 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:43497730 G>C maps to NM_020964.2 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:43497730 G>C maps to NM_020964.2 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:28091007 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:28091007 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:28091007 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:28091007 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:55597385 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:55597385 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:45729977 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:45729977 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:149419946 G>T maps to NM_032534.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:149419946 G>T maps to NM_032534.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:91842367 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:91842367 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:53041738 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:53041738 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:53041738 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:53041738 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:56086090 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:56086090 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:56086090 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:56086090 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:98831348 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:98831348 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:98831348 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:98831348 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:73634512 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:73634512 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:30755862 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:30755862 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:138556231 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:138556231 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:138556231 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:138556231 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:16899833 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:16899833 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:51453260 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:51453260 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:39299283 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:39299283 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:25030069 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:25030069 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:73530110 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:73530110 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:73530110 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:73530110 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:62801786 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:62801786 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:19818480 C>G maps to NM_000237.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:19818480 C>G maps to NM_000237.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:99772755 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:99772755 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:151412272 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:151412272 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:140995623 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:140995623 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:141130548 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:141130548 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:141641671 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:141641671 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:140995623 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:140995623 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:141130548 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:141130548 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:46943000 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:46943000 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:90179863 C>T maps to NM_032270.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:90179863 C>T maps to NM_032270.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:40689415 A>C maps to NM_198578.3 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:40689415 A>C maps to NM_198578.3 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:31555159 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:31555159 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:31555159 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:31555159 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:75052555 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:75052555 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:6626682 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:6626682 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:6626682 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:6626682 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:219383917 A>T maps to NM_138794.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:219383917 A>T maps to NM_138794.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:14066277 C>T maps to ENST00000310348 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:14066277 C>T maps to ENST00000310348 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:164853828 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:164853828 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:217123968 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:217123968 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:217123968 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:217123968 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:29455776 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:29455776 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:18254531 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:18254531 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:31194491 G>T maps to NM_002379.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:31194491 G>T maps to NM_002379.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:65544437 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:65544437 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:183013261 T>A maps to NM_015078.2 K501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:183013261 T>A maps to NM_015078.2 K501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:127324075 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:127324075 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:17616233 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:17616233 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:66215345 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:66215345 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:42095477 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:42095477 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:8814707 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:8814707 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:141796108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:141796108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:141796108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:141796108 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:74902071 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:74902071 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:74902071 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:74902071 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:43206827 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:43206827 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:43276957 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:43276957 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:43276957 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:43276957 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118339473 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118339473 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118339473 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118339473 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:89131070 T>A maps to NM_005941.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:89131070 T>A maps to NM_005941.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:20244254 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:20244254 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:20244254 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:20244254 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118105959 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118105959 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118105959 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118105959 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:60154046 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:60154046 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:60165317 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:60165317 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:60154046 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:60154046 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:60165317 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:60165317 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:60102397 C>G maps to NM_139249.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:60102397 C>G maps to NM_139249.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:56569849 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:56569849 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:56569849 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:56569849 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:237057969 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:237057969 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:9024496 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:9024496 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:9075970 T>G maps to NM_024690.2 P3825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:9075970 T>G maps to NM_024690.2 P3825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:113538016 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:113538016 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:10204268 C>T maps to NM_003802.2 *1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:10204268 C>T maps to NM_003802.2 *1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:10428360 C>A maps to NM_017534.5 G1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:10428360 C>A maps to NM_017534.5 G1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:23853902 C>T maps to NM_002471.3 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:23853902 C>T maps to NM_002471.3 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:10303525 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:10303525 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:18034879 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:18034879 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:192254993 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:192254993 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:192254993 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:192254993 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:26455129 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:26455129 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:26455129 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:26455129 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:24433661 C>T maps to ENST00000330966 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:24433661 C>T maps to ENST00000330966 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:62844831 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:62844831 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:62844831 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:62844831 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:15372539 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:15372539 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:16894211 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:16894211 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:54892997 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:54892997 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:52660549 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:52660549 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:45269705 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:45269705 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:52507528 C>G maps to NM_007361.3 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:52507528 C>G maps to NM_007361.3 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:55508759 C>T maps to NM_017852.3 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:55508759 C>T maps to NM_017852.3 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:150698540 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:150698540 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:15277960 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:15277960 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:15277960 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:15277960 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:32184740 G>T maps to NM_004557.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:32184740 G>T maps to NM_004557.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:101607207 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:101607207 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:101607207 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:101607207 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:6008349 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:6008349 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:115372217 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:115372217 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:115372217 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:115372217 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:176709316 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:176709316 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:176709316 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:176709316 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:6602490 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:6602490 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:6602490 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:6602490 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:87285620 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:87285620 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:228480971 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:228480971 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:228480971 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:228480971 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:228511035 G>T maps to NM_001098623.1 V5127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:228511035 G>T maps to NM_001098623.1 V5127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:28141440 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:28141440 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:28141440 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:28141440 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:102296450 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:102296450 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:102296450 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:102296450 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:193360447 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:193360447 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:132306150 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:132306150 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:132306150 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:132306150 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158548786 G>A maps to NM_001004477.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158548786 G>A maps to NM_001004477.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:125511887 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:125511887 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:248138330 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:248138330 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:248138388 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:248138388 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:22368979 C>A maps to NM_001004719.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:22368979 C>A maps to NM_001004719.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:56042956 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:56042956 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:56042956 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:56042956 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:142749604 C>G maps to NM_001001667.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:142749604 C>G maps to NM_001001667.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:31871585 T>A maps to NM_017784.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:31871585 T>A maps to NM_017784.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:92082482 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:92082482 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:176681211 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:176681211 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:206041389 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:206041389 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:205978256 A>T maps to ENST00000406610 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:205978256 A>T maps to ENST00000406610 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:134071162 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:134071162 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:55849884 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:55849884 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:55943195 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:55943195 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:55943195 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:55943195 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:140346518 G>A maps to NM_018899.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:140346518 G>A maps to NM_018899.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:66638193 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:66638193 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:183095611 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:183095611 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:20792689 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:20792689 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:20792689 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:20792689 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:144852594 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:144852594 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:144881363 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:144881363 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:144881363 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:144881363 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:95380616 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:95380616 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:95380616 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:95380616 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:15134400 G>A maps to NM_006205.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:15134400 G>A maps to NM_006205.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:136359273 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:136359273 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:55139950 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:55139950 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:149503794 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:149503794 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:149503794 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:149503794 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:179525415 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:179525415 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:179525415 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:179525415 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:137187735 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:137187735 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:137187735 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:137187735 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:48501053 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:48501053 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:48501053 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:48501053 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:45992987 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:45992987 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118520662 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118520662 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118520662 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118520662 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:21119258 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:21119258 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:21119258 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:21119258 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:21174933 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:21174933 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:204428918 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:204428918 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:3185759 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:3185759 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:3185759 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:3185759 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110396315 C>T maps to ENST00000426474 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110396315 C>T maps to ENST00000426474 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110439381 A>G maps to ENST00000426474 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110439381 A>G maps to ENST00000426474 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110477364 G>T maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:110477364 G>T maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:44441504 G>T maps to NM_004571.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr21:44441504 G>T maps to NM_004571.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:42364435 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:42364435 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:42364435 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:42364435 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:145027962 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:145027962 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:131935281 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:131935281 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:131935727 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:131935727 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:131948494 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:131948494 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:132110058 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:132110058 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:131935727 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:131935727 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:131948494 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:131948494 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:131960580 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:131960580 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:132110058 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:132110058 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:30165627 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:30165627 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:131844508 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:131844508 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:131844508 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:131844508 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:140399957 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:140399957 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:42196451 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:42196451 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:57887209 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:57887209 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:57887209 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:57887209 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:6380401 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:6380401 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:6380401 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:6380401 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:90128789 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:90128789 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:90128789 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:90128789 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:81122391 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:81122391 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:23509440 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:23509440 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:23509440 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:23509440 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:47350885 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:47350885 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:82096114 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:82096114 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:50188236 G>A maps to NM_001536.3 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:50188236 G>A maps to NM_001536.3 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23397428 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23397428 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:23397428 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:23397428 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:45128367 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:45128367 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:150998277 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:150998277 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:14632616 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:14632616 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:14632616 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:14632616 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:141874392 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:141874392 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:141712745 G>A maps to NM_005607.4 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:141712745 G>A maps to NM_005607.4 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:141874392 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:141874392 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:87725094 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:87725094 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:214705937 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:214705937 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:214705937 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:214705937 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:2987923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:2987923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:2987923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:2987923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:198668801 C>T maps to ENST00000271610 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:198668801 C>T maps to ENST00000271610 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:8076446 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:8076446 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:8076446 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr18:8076446 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:157413546 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:157413546 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:71066566 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:71066566 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:71066566 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:71066566 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:121608167 T>C maps to NM_002851.2 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:121608167 T>C maps to NM_002851.2 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:105102888 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:105102888 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:37735070 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:37735070 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:27826731 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:27826731 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:27826731 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:27826731 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:135907896 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:135907896 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:135907896 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:135907896 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:85774708 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:85774708 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:85774708 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:85774708 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:25502581 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:25502581 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:25502583 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:25502583 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:114792859 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:114792859 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:114792859 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:114792859 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:26218336 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:26218336 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:26220751 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:26220751 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:26218336 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:26218336 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:26220751 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:26220751 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23378501 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:23378501 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:36218098 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:36218098 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:103294528 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:103294528 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:103294528 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:103294528 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:175958395 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:175958395 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:175958395 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:175958395 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:56390226 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:56390226 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:73026493 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:73026493 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:73026493 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:73026493 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:87352377 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:87352377 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:87352379 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:87352379 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:87352377 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:87352377 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:87352379 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:87352379 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:25399640 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr13:25399640 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:1090648 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:1090648 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:1090648 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:1090648 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:11484040 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:11484040 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:11484040 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:11484040 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:10450329 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:10450329 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:94537932 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:94537932 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:96883 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:96883 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:96883 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:96883 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:89629282 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:89629282 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:89629282 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:89629282 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:114310968 G>A maps to NM_018364.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:114310968 G>A maps to NM_018364.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:77409520 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:77409520 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:74659878 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:74659878 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:237608842 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:237608842 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:237608842 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:237608842 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:33905336 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:33905336 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:18257308 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:18257308 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:18257308 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:18257308 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:21992889 G>A maps to NM_005407.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:21992889 G>A maps to NM_005407.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:136561578 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:136561578 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:83626447 G>A maps to NM_001037582.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:83626447 G>A maps to NM_001037582.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:52082890 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:52082890 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:52082890 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:52082890 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:75523492 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:75523492 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:75523492 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:75523492 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:90760867 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:90760867 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:90760867 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:90760867 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:151111848 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:151111848 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:151111848 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:151111848 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:61324832 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:61324832 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:61471397 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr18:61471397 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:64863747 G>A maps to NM_014755.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:64863747 G>A maps to NM_014755.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:179982216 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:179982216 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:179982216 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:179982216 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:179989358 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:179989358 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:26707997 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:26707997 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:42977157 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:42977157 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:42977157 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:42977157 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:49183050 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:49183050 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:49183050 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:49183050 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:52031153 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:52031153 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:16962103 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:16962103 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:232626585 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:232626585 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:232626585 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:232626585 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:164777157 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:164777157 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:164727305 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:164727305 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:164777157 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:164777157 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:48381848 C>G maps to NM_020846.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:48381848 C>G maps to NM_020846.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:160721245 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:160721245 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:160721245 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:160721245 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:44673595 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:44673595 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:44673595 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:44673595 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:99358624 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:99358624 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:64330023 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:64330023 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:19634835 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:19634835 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:19634835 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:19634835 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:92900438 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr14:92900438 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:85486829 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:85486829 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:85486829 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:85486829 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:45557990 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:45557990 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:44503189 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:44503189 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:105255029 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:105255029 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:108123470 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:108123470 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:75683464 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:75683464 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:162799418 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:162799418 A>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:72319399 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:72319399 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:72166000 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:72166000 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:72166000 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:72166000 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:72319399 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:72319399 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:32482261 T>A maps to NM_000343.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:32482261 T>A maps to NM_000343.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:32631036 G>T maps to NM_014227.2 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:32631036 G>T maps to NM_014227.2 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:85279238 A>T maps to NM_182767.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:85279238 A>T maps to NM_182767.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:20649682 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:20649682 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:20649684 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:20649684 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:20623177 G>T maps to NM_004211.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:20623177 G>T maps to NM_004211.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:20649682 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:20649682 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:20649684 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:20649684 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:170204286 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:170204286 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:144903923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:144903923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:144903923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:144903923 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:11107153 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:11107153 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:11107354 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:11107354 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:11107159 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:11107159 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:95197501 G>T maps to NM_001128429.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:95197501 G>T maps to NM_001128429.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:71227950 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:71227950 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:71227950 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:71227950 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:73447440 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:73447440 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:96953334 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:96953334 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:96953334 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:96953334 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:7594074 G>T maps to NM_152551.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:7594074 G>T maps to NM_152551.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:25207168 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:25207168 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:50709902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:50709902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:50709902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:50709902 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:106675466 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:106675466 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:107012487 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr10:107012487 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:107012487 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr10:107012487 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:31324154 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:31324154 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:118609282 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:118609282 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:151042995 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:151042995 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:151042995 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:151042995 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:172835525 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr3:172835525 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:172835525 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:172835525 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:35753907 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:35753907 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:35753907 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr5:35753907 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158596836 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:158596836 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158583602 G>T maps to NM_003126.2 C2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158583602 G>T maps to NM_003126.2 C2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158596836 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:158596836 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:38031334 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:38031334 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:38031334 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:38031334 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:60740593 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:60740593 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:60740593 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:60740593 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:68442865 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:68442865 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:48523794 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr13:48523794 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:109313387 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:109313387 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:85648857 A>G maps to NM_032184.1 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:85648857 A>G maps to NM_032184.1 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:110019409 C>A maps to NM_001040709.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:110019409 C>A maps to NM_001040709.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:202571228 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:202571228 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:202571228 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:202571228 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:7439166 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:7439166 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:7439166 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:7439166 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:122634998 G>A maps to NM_016945.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:122634998 G>A maps to NM_016945.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:26585921 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:26585921 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:114841478 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:114841478 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:114841478 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:114841478 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:95539154 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:95539154 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:50796435 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:50796435 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:50796435 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:50796435 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:132351138 T>C maps to NM_016521.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:132351138 T>C maps to NM_016521.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:115624233 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:115624233 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:43801862 C>T maps to ENST00000330266 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:43801862 C>T maps to ENST00000330266 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:70358348 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr15:70358348 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:126139091 A>T maps to NM_052907.2 K1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr12:126139091 A>T maps to NM_052907.2 K1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:19231471 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:19231471 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:133723297 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:133723297 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:133723297 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:133723297 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:112870472 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:112870472 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:29725269 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:29725269 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:201333392 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:201333392 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:201333392 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:201333392 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:175037032 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:175037032 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:175037032 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:175037032 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:45406197 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:45406197 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:45406197 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:45406197 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:72416410 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr12:72416410 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:1457679 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:1457679 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:118005389 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:118005389 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:118005389 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:118005389 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:108568148 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr3:108568148 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:165891176 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:165891176 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:165891176 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:165891176 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:14419783 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:14419783 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:72951882 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:72951882 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:31767327 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:31767327 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrY:9305907 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrY:9305907 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:46863433 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr17:46863433 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:46863433 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr17:46863433 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:179584083 T>C maps to NM_133378.4 S6767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:179584083 T>C maps to NM_133378.4 S6767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:15519577 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr8:15519577 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118263360 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:118263360 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118263360 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:118263360 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:39511521 T>C maps to NM_003359.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:39511521 T>C maps to NM_003359.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:69520039 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:69520039 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:69520039 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:69520039 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:34801975 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:34801975 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:150289599 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:150289599 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:96091524 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr4:96091524 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:96091524 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr4:96091524 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:18967551 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:18967551 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:113674067 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:113674067 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:113674067 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:113674067 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:144745116 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:144745116 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:144745116 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:144745116 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:31748465 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr6:31748465 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:31748465 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr6:31748465 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:100709120 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:100709120 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:98844804 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr2:98844804 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:98844804 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:98844804 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:27734857 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:27734857 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:27734857 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:27734857 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:64065847 T>C maps to NM_080666.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr14:64065847 T>C maps to NM_080666.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:44163206 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr20:44163206 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:44163206 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:44163206 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:5256876 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr7:5256876 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:5256876 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr7:5256876 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:134203505 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr8:134203505 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:32421405 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:32421405 A>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:168106862 G>A maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr2:168106862 G>A maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:28128625 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:28128625 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:28128625 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr16:28128625 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:17235281 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr16:17235281 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:37305737 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr9:37305737 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:37305737 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr9:37305737 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:19197517 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr11:19197517 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:19197517 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr11:19197517 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:101166870 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chrX:101166870 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:101166870 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chrX:101166870 C>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:35480536 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr1:35480536 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:35480536 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr1:35480536 T>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:43123435 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr5:43123435 T>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:22193726 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:22193726 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:44932363 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:44932363 T>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:25667110 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr20:25667110 G>C did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:37726792 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:37726792 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:37726792 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:37726792 G>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:30936619 C>A maps to NM_014717.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:30936619 C>A maps to NM_014717.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:9450099 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:9450099 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:9450099 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:9450099 G>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:12432050 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:12432050 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:23941485 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr19:23941485 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:23941485 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr19:23941485 C>G did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:24087462 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr22:24087462 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:24087462 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01W-0928-08 chr22:24087462 C>A did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:66824544 A>T did not map to a codon.
Sequencing variant TCGA-44-2668-01A-01D-0969-08 chr15:66824544 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:31438888 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:31438888 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:131322422 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:131322422 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:20481059 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:20481059 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:64519033 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:64519033 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:154561023 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:154561023 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:131922163 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:131922163 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:148458797 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:148458797 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:129008531 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:129008531 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:21241853 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:21241853 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:45422550 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:45422550 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:100957990 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:100957990 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:3918721 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:3918721 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:10429875 A>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:10429875 A>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:70070755 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:70070755 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:31611663 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:31611663 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:45314629 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:45314629 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:97102360 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:97102360 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:16611552 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:16611552 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:247719675 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:247719675 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:33367454 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:33367454 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:86158166 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:86158166 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:49079353 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:49079353 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:18828083 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:18828083 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:49089787 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:49089787 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:98204344 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:98204344 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:98204357 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:98204357 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:883319 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:883319 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:113509756 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:113509756 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:19167844 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:19167844 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:87623925 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:87623925 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:2813305 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:2813305 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:36379923 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:36379923 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:140954415 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:140954415 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:60566763 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:60566763 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:35154199 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:35154199 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr14:74125779 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr14:74125779 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:117677467 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:117677467 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:144661905 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:144661905 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:8017360 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:8017360 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:29650080 T>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:29650080 T>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:225707423 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:225707423 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:103499632 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:103499632 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:40405803 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:40405803 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:142505601 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:142505601 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:49381585 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:49381585 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:120115856 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:120115856 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:78428752 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:78428752 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:180680629 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:180680629 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:151124165 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:151124165 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:171699062 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:171699062 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:33283426 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:33283426 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:9846410 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:9846410 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:53010218 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:53010218 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:233655924 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:233655924 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:129442038 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:129442038 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:56226451 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:56226451 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:102661775 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr8:102661775 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:153029840 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:153029840 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:153217162 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:153217162 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:31116931 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:31116931 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:70331243 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:70331243 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:30789837 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:30789837 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:24537989 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:24537989 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:10626469 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:10626469 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:154512348 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:154512348 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:113697694 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:113697694 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:39761013 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:39761013 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:200950286 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:200950286 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:57971451 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:57971451 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47298930 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47298930 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:55290179 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:55290179 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:183382555 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:183382555 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:137034112 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:137034112 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:33777748 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:33777748 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:48643128 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:48643128 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:141607651 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:141607651 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:70460371 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:70460371 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:119522514 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:119522514 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47969957 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47969957 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:150903266 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:150903266 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:116417341 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:116417341 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:131113968 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:131113968 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:123699211 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:123699211 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:216811892 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:216811892 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:16900006 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:16900006 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:5494952 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:5494952 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:29957767 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:29957767 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:124604097 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:124604097 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:182763625 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:182763625 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:32724938 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:32724938 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:73862485 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:73862485 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:88679302 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:88679302 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:101623635 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:101623635 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:228491840 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:228491840 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:248166399 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:248166399 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:21730538 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:21730538 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:121605549 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:121605549 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr14:23776926 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr14:23776926 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:50185487 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:50185487 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:91675526 C>T maps to ENST00000356934 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:91675526 C>T maps to ENST00000356934 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:105201504 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:105201504 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:45935328 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:45935328 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:65374343 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:65374343 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:14689792 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr12:14689792 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:89868263 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:89868263 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:24722747 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:24722747 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:42599883 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:42599883 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:52870578 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:52870578 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:43773662 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:43773662 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:11446295 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:11446295 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:174190065 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:174190065 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:155129368 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:155129368 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:10132206 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:10132206 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:103557404 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:103557404 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:85576436 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:85576436 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr9:37770039 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr9:37770039 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:163042676 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:163042676 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:25712419 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:25712419 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:46770873 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:46770873 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:79067492 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:79067492 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:18622484 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:18622484 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:67865079 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr18:67865079 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:237804322 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:237804322 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47456232 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr3:47456232 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:50059942 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr13:50059942 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:70572903 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:70572903 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:7212851 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:7212851 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:42195206 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:42195206 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:100838104 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:100838104 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:216894 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:216894 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:27480929 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:27480929 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:156248852 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:156248852 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:21213380 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr22:21213380 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:17931278 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:17931278 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:16077503 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:16077503 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:231108310 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:231108310 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:88773996 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr6:88773996 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:136328348 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr5:136328348 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:153043798 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:153043798 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:182763892 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:182763892 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:28030134 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:28030134 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:17738947 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr10:17738947 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr9:130427643 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr9:130427643 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:35798037 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:35798037 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:60584235 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:60584235 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:142919079 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:142919079 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:9661093 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:9661093 A>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:79282898 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:79282898 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:76129660 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:76129660 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:20020901 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:20020901 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:69100154 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr4:69100154 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:1947512 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr11:1947512 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:24306970 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:24306970 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:23556278 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr7:23556278 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:31342955 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr15:31342955 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:50250811 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr19:50250811 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:19410971 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:19410971 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr21:43560621 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr21:43560621 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:8994540 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr16:8994540 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:30207440 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr17:30207440 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:224759079 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:224759079 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:224759126 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr2:224759126 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:85559915 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr1:85559915 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:50704830 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chr20:50704830 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:152610043 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1265-08 chrX:152610043 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:58858350 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:58858350 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:67078903 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:67078903 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:35691746 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:35691746 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:20481155 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:20481155 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:100267993 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:100267993 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:26648834 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:26648834 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:109358789 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:109358789 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:125651381 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:125651381 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:854794 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:854794 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:40895199 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:40895199 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:74977165 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:74977165 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:123658330 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:123658330 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:50223225 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:50223225 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:33246357 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:33246357 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:70763331 A>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:70763331 A>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:4627460 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:4627460 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:39597115 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:39597115 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:154172904 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:154172904 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:118870018 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:118870018 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:71020088 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:71020088 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:23729108 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:23729108 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:2742743 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:2742743 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:40030821 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:40030821 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:104916167 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:104916167 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:116311164 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:116311164 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:119103453 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:119103453 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:68630151 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:68630151 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:74519646 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:74519646 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:43020760 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:43020760 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:85957425 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:85957425 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:18643178 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:18643178 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:131356184 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:131356184 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:136623024 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:136623024 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:78927971 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:78927971 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:16362883 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:16362883 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:66611141 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:66611141 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:6260416 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:6260416 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:99786761 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:99786761 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:61459169 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:61459169 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:3673509 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:3673509 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:9570742 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:9570742 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:148894323 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:148894323 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:113871360 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:113871360 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:111776001 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:111776001 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:15769377 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:15769377 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:47860160 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:47860160 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:31630895 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:31630895 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:30630529 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:30630529 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:21730310 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:21730310 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:21757384 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:21757384 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:21856356 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:21856356 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:11547822 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:11547822 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:83818498 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:83818498 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:38709527 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:38709527 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:105440464 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:105440464 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:113878571 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:113878571 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:71797970 A>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:71797970 A>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:137799536 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:137799536 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:131665610 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:131665610 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:36505617 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:36505617 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:212530204 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:212530204 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:14765300 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:14765300 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:48760509 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:48760509 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:102553678 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:102553678 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:137801921 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:137801921 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:170847397 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:170847397 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:176524500 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:176524500 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:2968861 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:2968861 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:47033583 A>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:47033583 A>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:31147697 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:31147697 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:58007947 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:58007947 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:135498731 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:135498731 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:89319064 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:89319064 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:48678430 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:48678430 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:32975725 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:32975725 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:72088611 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:72088611 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:152185494 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:152185494 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:5687274 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:5687274 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:65002477 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:65002477 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:94973044 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:94973044 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:1639815 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:1639815 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:160485335 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:160485335 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:166944552 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:166944552 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:242648851 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:242648851 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:156811138 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:156811138 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:68695251 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:68695251 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:196397125 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:196397125 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:44133716 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:44133716 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:29410975 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:29410975 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:43496395 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:43496395 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:57958834 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:57958834 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:86888698 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:86888698 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:153706524 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:153706524 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:118124391 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:118124391 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:59274343 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:59274343 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:31555781 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:31555781 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:6616094 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:6616094 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:1779328 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:1779328 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:30432970 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:30432970 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:11177385 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:11177385 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:10429910 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:10429910 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:36678572 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:36678572 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:46393832 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:46393832 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:124820232 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:124820232 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:204921286 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:204921286 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:21118657 A>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:21118657 A>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:49172580 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:49172580 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:153416512 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:153416512 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:179257092 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:179257092 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:169432646 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:169432646 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:223085763 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:223085763 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr21:47350836 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr21:47350836 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:66723565 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:66723565 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:45937765 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:45937765 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:61017380 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:61017380 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:75412833 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:75412833 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:11013899 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:11013899 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:60505964 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:60505964 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:153037581 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:153037581 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:94691011 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:94691011 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:118305594 T>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:118305594 T>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:38352656 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:38352656 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:76254706 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:76254706 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:37531188 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:37531188 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:16528646 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:16528646 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:220162895 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:220162895 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:220166238 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:220166238 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:49223940 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:49223940 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:79254063 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:79254063 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:17167140 A>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:17167140 A>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:18264984 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:18264984 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:108041850 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:108041850 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:53461399 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:53461399 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17345263 T>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17345263 T>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17345333 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17345333 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:1902394 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:1902394 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:129294125 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:129294125 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:118604230 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:118604230 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:84046577 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:84046577 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:149578956 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:149578956 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:44475795 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:44475795 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:98816907 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr10:98816907 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:130912970 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:130912970 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:36903769 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:36903769 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:65268585 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:65268585 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:133524651 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:133524651 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:130068702 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:130068702 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:99134595 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:99134595 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:758935 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:758935 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:141490126 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:141490126 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:13307826 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:13307826 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:101650222 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:101650222 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:156390072 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:156390072 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:84200403 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:84200403 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:83795501 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:83795501 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:114154210 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:114154210 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:20926712 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:20926712 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:68708417 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:68708417 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:83358900 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:83358900 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr21:11013060 A>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr21:11013060 A>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:96259674 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:96259674 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:67860330 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:67860330 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:47101794 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:47101794 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:101760204 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:101760204 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:9954221 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:9954221 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:42569342 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:42569342 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:6126199 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:6126199 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:48932787 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chrX:48932787 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:62606909 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:62606909 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:78389318 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:78389318 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:21346034 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:21346034 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:72832635 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:72832635 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:29644804 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:29644804 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:44806321 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:44806321 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:57930985 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:57930985 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:32354596 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:32354596 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:60643147 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:60643147 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:7382935 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:7382935 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:44268085 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:44268085 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:41105676 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:41105676 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:215866255 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:215866255 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:67028184 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:67028184 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:150912626 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:150912626 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:89043005 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:89043005 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:51370656 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:51370656 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:19231744 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:19231744 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:915335 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:915335 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:109697787 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:109697787 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100488526 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100488526 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23538844 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23538844 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6354913 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6354913 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:229567953 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:229567953 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:236891067 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:236891067 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123332559 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123332559 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8654283 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8654283 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:33588545 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:33588545 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:43826369 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:43826369 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:28306778 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:28306778 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:64606733 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:64606733 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7784629 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7784629 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:49530772 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:49530772 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:148048660 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:148048660 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:148054887 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:148054887 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:109663948 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:109663948 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159038198 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159038198 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159038508 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159038508 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:4719352 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:4719352 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:134222223 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:134222223 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:5242097 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:5242097 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:43908275 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:43908275 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:3718822 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:3718822 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:3729200 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:3729200 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:4536631 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:4536631 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56246000 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56246000 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:112542753 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:112542753 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:91948851 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:91948851 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:73979400 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:73979400 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:37442597 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:37442597 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:101462379 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:101462379 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:22279206 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:22279206 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:45761614 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:45761614 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:36661406 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:36661406 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16345294 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16345294 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:57570219 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:57570219 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156914256 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156914256 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:42396276 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:42396276 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:56771094 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:56771094 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:131704284 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:131704284 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:964826 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:964826 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:66517444 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:66517444 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:3661636 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:3661636 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94420887 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94420887 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:30202158 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:30202158 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:176926735 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:176926735 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:177002011 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:177002011 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:119943388 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:119943388 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:117067579 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:117067579 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:294530 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:294530 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:51099081 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:51099081 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:47493054 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:47493054 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:25264401 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:25264401 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:193156788 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:193156788 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:193183720 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:193183720 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160129080 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160129080 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160156346 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160156346 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:81606106 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:81606106 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:153664269 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:153664269 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:138413314 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:138413314 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:26151106 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:26151106 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:26402170 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:26402170 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:26411230 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:26411230 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:76931694 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:76931694 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:347697 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:347697 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:829515 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:829515 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:381796 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:381796 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:29205773 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:29205773 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:11047589 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:11047589 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:32194076 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:32194076 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:70065637 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:70065637 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:72877185 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:72877185 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23606095 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23606095 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23615087 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23615087 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:152771606 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:152771606 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:15509127 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:15509127 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113002509 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113002509 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:31601491 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:31601491 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:220246038 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:220246038 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:136916668 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:136916668 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15378420 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15378420 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:26448918 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:26448918 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:104557872 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:104557872 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:31510739 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:31510739 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:50193050 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:50193050 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154177944 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154177944 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154185162 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154185162 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:35743537 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:35743537 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:20033429 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:20033429 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:46097578 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:46097578 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:34166534 G>A maps to NM_019596.5 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:34166534 G>A maps to NM_019596.5 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:10295278 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:10295278 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27361198 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27361198 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:99413734 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:99413734 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:165693635 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:165693635 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:3754342 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:3754342 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:36294269 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:36294269 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:148312285 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:148312285 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:66418140 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:66418140 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:96044360 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:96044360 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:135602756 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:135602756 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:49730926 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:49730926 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:24455566 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:24455566 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:60965852 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:60965852 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:13363932 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:13363932 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:2613865 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:2613865 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:53535533 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:53535533 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201016618 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201016618 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:1943325 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:1943325 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:24268292 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:24268292 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:24366359 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:24366359 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:71571316 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:71571316 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:12857204 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:12857204 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2951945 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2951945 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2963812 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2963812 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:2239582 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:2239582 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:131605145 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:131605145 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:93646522 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:93646522 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:80129780 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:80129780 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:119866453 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:119866453 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:118688557 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:118688557 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158298023 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158298023 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72527720 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72527720 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:208072591 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:208072591 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:118210392 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:118210392 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:111304156 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:111304156 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:103416312 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:103416312 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:21884017 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:21884017 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:19721646 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:19721646 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:68853410 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:68853410 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:59157723 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:59157723 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:60470148 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:60470148 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31322877 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31322877 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31323515 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31323515 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:105661086 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:105661086 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:110947903 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:110947903 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:21968275 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:21968275 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:43015916 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:43015916 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:3293292 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:3293292 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:117233038 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:117233038 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:34059739 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:34059739 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:66976709 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:66976709 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:4409848 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:4409848 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:4429351 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:4429351 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:7806545 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:7806545 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:203194101 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:203194101 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:23116468 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:23116468 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:141524615 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:141524615 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:42581162 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:42581162 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:233399823 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:233399823 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16272225 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16272225 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143020554 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143020554 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:8286765 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:8286765 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:8289545 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:8289545 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:140281578 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:140281578 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:81735259 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:81735259 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23847784 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23847784 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:57994667 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:57994667 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:26515041 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:26515041 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:41423089 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:41423089 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:205042740 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:205042740 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:147815071 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:147815071 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:39178101 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:39178101 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:103427839 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:103427839 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33145570 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33145570 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:75840485 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:75840485 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:121344351 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:121344351 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:101749382 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:101749382 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:70733618 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:70733618 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:139631816 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:139631816 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:139825016 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:139825016 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111098171 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111098171 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:107407979 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:107407979 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:130363953 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:130363953 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:48615840 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:48615840 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:71011649 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:71011649 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:61460891 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:61460891 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:128982865 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:128982865 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:47708552 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:47708552 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:129933123 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:129933123 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:129938670 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:129938670 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:129945838 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:129945838 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:148575194 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:148575194 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:166325876 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:166325876 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:818127 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:818127 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:101829444 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:101829444 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:49703162 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:49703162 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159684158 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159684158 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:99696155 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:99696155 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:151133460 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:151133460 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:186257005 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:186257005 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:149437174 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:149437174 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:2813043 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:2813043 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:113277871 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:113277871 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:113648978 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:113648978 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:113702293 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:113702293 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:114448863 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:114448863 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:23433495 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:23433495 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:44740818 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:44740818 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:61511983 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:61511983 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143960607 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143960607 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99367912 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99367912 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15793115 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15793115 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15996945 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15996945 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:47496892 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:47496892 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:48973505 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:48973505 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:48973507 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:48973507 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:59002473 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:59002473 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:50848395 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:50848395 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:36367659 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:36367659 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:91572090 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:91572090 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:31251011 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:31251011 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:118572259 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:118572259 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:140221568 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:140221568 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:111741194 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:111741194 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:31613378 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:31613378 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:117165336 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:117165336 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:19035860 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:19035860 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:14722151 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:14722151 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:185882675 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:185882675 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:185997779 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:185997779 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:37597997 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:37597997 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:80672000 T>G maps to ENST00000422005 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:80672000 T>G maps to ENST00000422005 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:73348273 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:73348273 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:83170831 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:83170831 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:1581254 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:1581254 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:101195107 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:101195107 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:124323330 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:124323330 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:13708039 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:13708039 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:196661268 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:196661268 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:38820605 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:38820605 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11696993 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11696993 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:34485240 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:34485240 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72297055 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72297055 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220146343 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220146343 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:32873784 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:32873784 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:31386208 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:31386208 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:111584998 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:111584998 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:25101316 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:25101316 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:67344966 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:67344966 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:116101361 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:116101361 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:116526063 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:116526063 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27164672 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27164672 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:122290645 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:122290645 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:45453241 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:45453241 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:32612315 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:32612315 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:2279718 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:2279718 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:158500386 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:158500386 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:4234871 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:4234871 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:236631366 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:236631366 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:62129280 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:62129280 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:233546152 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:233546152 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:140638039 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:140638039 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2412252 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2412252 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:23705078 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:23705078 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:129208742 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:129208742 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:37354439 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:37354439 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:73450801 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:73450801 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:10995163 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:10995163 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110346577 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110346577 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132561929 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132561929 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:120835995 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:120835995 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:89390901 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:89390901 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:134644611 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:134644611 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:134920578 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:134920578 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100403407 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100403407 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16503254 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16503254 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:91396093 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:91396093 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:23721426 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:23721426 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:54275326 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:54275326 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:76929101 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:76929101 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:133622472 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:133622472 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:37785050 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:37785050 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:66094393 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:66094393 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:40865464 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:40865464 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:113801934 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:113801934 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:133941867 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:133941867 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:130948286 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:130948286 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143056561 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143056561 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:139207382 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:139207382 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:74095253 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:74095253 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:222923199 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:222923199 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:29234249 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:29234249 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:62104170 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:62104170 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:10671786 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:10671786 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:114465537 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:114465537 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:150970272 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:150970272 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:114507818 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:114507818 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:40415782 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:40415782 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124818615 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124818615 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:10140681 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:10140681 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:35424178 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:35424178 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29450255 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29450255 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:92353726 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:92353726 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127710261 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127710261 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:15927929 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:15927929 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:15927935 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:15927935 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100184161 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100184161 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124545498 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124545498 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:230861766 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:230861766 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:16578649 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:16578649 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:117448435 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:117448435 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159272630 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159272630 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161483835 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161483835 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157740180 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157740180 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157550265 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157550265 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72862392 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72862392 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125023084 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125023084 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125078854 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125078854 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125079975 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125079975 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125103927 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:125103927 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:95535445 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:95535445 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:191861763 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:191861763 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:102670778 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:102670778 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:49260109 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:49260109 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:84605673 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:84605673 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240308464 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240308464 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:12704382 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:12704382 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43869023 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43869023 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:39169562 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:39169562 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:101061686 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:101061686 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:161292701 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:161292701 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27126227 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27126227 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:1960948 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:1960948 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27571835 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27571835 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27571837 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27571837 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27586118 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:27586118 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:90012097 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:90012097 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:153756063 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:153756063 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:16263880 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:16263880 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:173232935 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:173232935 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:173301166 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:173301166 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:34906818 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:34906818 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:89525728 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:89525728 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:44228499 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:44228499 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57311944 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57311944 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:58009513 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:58009513 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:154306887 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:154306887 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:74063021 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:74063021 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:55266542 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:55266542 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100280513 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:100280513 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:150416335 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:150416335 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:14593829 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:14593829 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:35894691 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:35894691 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57865861 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57865861 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:151229709 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:151229709 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:56867226 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:56867226 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:129442080 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:129442080 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:183913488 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:183913488 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:183920058 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:183920058 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:182354737 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:182354737 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:93286036 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:93286036 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:96689825 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:96689825 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:32180071 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:32180071 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:50497977 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:50497977 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27861951 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27861951 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72429968 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72429968 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113604631 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113604631 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:94145722 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:94145722 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:37324536 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:37324536 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:104335452 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:104335452 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:14558766 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:14558766 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:3038966 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:3038966 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33990498 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33990498 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:7348423 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:7348423 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:52662466 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:52662466 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120461470 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120461470 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:18361253 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:18361253 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:1046859 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:1046859 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:108628407 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:108628407 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:108652140 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:108652140 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140075531 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140075531 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:156459759 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:156459759 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:5290995 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:5290995 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156713852 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156713852 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:37247991 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:37247991 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:45469632 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:45469632 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:65423423 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:65423423 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120365226 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120365226 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:222715344 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:222715344 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:29897160 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:29897160 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:185704280 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:185704280 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:55406797 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:55406797 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21679517 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21679517 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:83277875 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:83277875 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8520517 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8520517 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:12874439 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:12874439 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:29140053 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:29140053 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:30997685 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:30997685 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:56553582 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:56553582 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:148842430 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:148842430 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:87726240 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:87726240 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:88039840 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:88039840 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10445565 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10445565 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94567238 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94567238 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:21367389 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:21367389 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:118428530 T>A maps to NM_020153.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:118428530 T>A maps to NM_020153.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47104010 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47104010 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45957087 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45957087 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159901752 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159901752 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:42146321 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:42146321 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:50436079 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:50436079 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:9948314 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:9948314 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:27456475 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:27456475 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:14162619 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:14162619 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:70328050 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:70328050 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111367724 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111367724 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:242644013 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:242644013 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:134594440 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:134594440 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:233995471 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:233995471 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:15212479 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:15212479 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:15260690 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:15260690 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:9450369 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:9450369 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:30802260 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:30802260 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:173344279 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:173344279 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:173349785 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:173349785 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:15714545 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:15714545 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:31421712 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:31421712 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:31277254 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:31277254 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:78622738 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:78622738 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:4706741 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:4706741 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:6066530 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:6066530 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:139827468 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:139827468 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:124282085 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:124282085 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:39285744 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:39285744 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:2591809 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:2591809 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:2683344 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:2683344 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:2683346 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:2683346 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:62069893 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:62069893 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137766188 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137766188 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142638577 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142638577 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142659376 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142659376 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:48639867 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:48639867 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:84872830 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:84872830 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:44159802 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:44159802 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:101828830 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:101828830 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94113050 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94113050 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:43497818 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:43497818 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:69521722 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:69521722 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:30254776 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:30254776 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:899185 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:899185 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:70681380 C>A maps to NM_020866.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:70681380 C>A maps to NM_020866.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:183382991 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:183382991 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51329776 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51329776 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:48722703 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:48722703 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:139164246 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:139164246 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53232850 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53232850 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53217605 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53217605 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53342822 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53342822 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:118020256 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:118020256 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:6886277 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:6886277 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:129250533 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:129250533 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:112463542 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:112463542 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107708404 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107708404 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:183096317 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:183096317 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:860864 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:860864 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:21549521 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:21549521 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:36983645 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:36983645 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:136555731 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:136555731 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:136565893 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:136565893 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:11210878 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:11210878 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2566917 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2566917 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:180241152 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:180241152 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55175135 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55175135 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:226475277 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:226475277 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:96478145 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:96478145 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:36117772 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:36117772 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:165218610 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:165218610 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:28155855 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:28155855 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:148193784 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:148193784 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:56329886 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:56329886 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141092138 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141092138 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141110677 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141110677 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141128180 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141128180 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141143662 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141143662 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141441362 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141441362 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141458259 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141458259 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141459544 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:141459544 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:53747623 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:53747623 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:169572826 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:169572826 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:70226091 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:70226091 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:238657972 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:238657972 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:135614760 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:135614760 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:160697205 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:160697205 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160793745 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160793745 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:235879977 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:235879977 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:47317026 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:47317026 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:140809598 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:140809598 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:12774457 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:12774457 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:103673138 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:103673138 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:52339290 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:52339290 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:44077079 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:44077079 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:119739335 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:119739335 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:152174030 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:152174030 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:183056750 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:183056750 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:113719440 G>T maps to ENST00000423251 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:113719440 G>T maps to ENST00000423251 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:49959209 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:49959209 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:49959211 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:49959211 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:2405748 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:2405748 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:8802173 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:8802173 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:40428900 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:40428900 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:141750753 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:141750753 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:99252886 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:99252886 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:24449105 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:24449105 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:36220023 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:36220023 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:73013711 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:73013711 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:220936223 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:220936223 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:60476072 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:60476072 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:49936281 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:49936281 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:4864419 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:4864419 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:25826202 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:25826202 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7886658 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7886658 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9011133 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9011133 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9056072 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9056072 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:102076360 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:102076360 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:203144910 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:203144910 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:15838947 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:15838947 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:10435342 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:10435342 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23869812 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23869812 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23873427 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23873427 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23874762 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23874762 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:33575200 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:33575200 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:36737395 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:36737395 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:3273176 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:3273176 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:26434346 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:26434346 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:12649218 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:12649218 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:203055094 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:203055094 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:5081740 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:5081740 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:101747880 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:101747880 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:23360134 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:23360134 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:16892442 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:16892442 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:54930671 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:54930671 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:183888672 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:183888672 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:71185831 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:71185831 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:46256792 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:46256792 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:21318563 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:21318563 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:56132985 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:56132985 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:24701537 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:24701537 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:140347451 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:140347451 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:42782977 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:42782977 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:204978639 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:204978639 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:36387225 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:36387225 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:33311227 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:33311227 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:99208108 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:99208108 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:57085288 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:57085288 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:57100528 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:57100528 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7982962 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7982962 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7984714 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7984714 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54304409 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54304409 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55501842 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55501842 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:144101630 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:144101630 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:144101932 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:144101932 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:16364153 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:16364153 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:150699245 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:150699245 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:132422938 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:132422938 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:32781024 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:32781024 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:127263079 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:127263079 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:200008739 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:200008739 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:200018041 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:200018041 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107875138 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107875138 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:6604196 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:6604196 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:107979472 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:107979472 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:102886480 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:102886480 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:135263686 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:135263686 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:73227578 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:73227578 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:102337629 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:102337629 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:729320 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:729320 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:8790616 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:8790616 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:28200121 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:28200121 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:123538826 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:123538826 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:183664578 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:183664578 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:137815334 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:137815334 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:153496322 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:153496322 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:88414740 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:88414740 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:47754377 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:47754377 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248005253 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248005253 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143973631 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143973631 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247751603 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247751603 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248247087 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248247087 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248247668 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248247668 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248437218 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248437218 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248437229 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248437229 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158670442 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158670442 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:56058583 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:56058583 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:24870630 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:24870630 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:52248145 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:52248145 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:21692967 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:21692967 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72921498 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:72921498 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29630544 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29630544 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:17668369 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:17668369 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:150842673 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:150842673 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:21689832 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:21689832 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:223160153 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:223160153 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:55588210 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:55588210 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:105165711 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:105165711 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:20786565 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:20786565 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:66384212 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:66384212 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:149283304 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:149283304 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:660498 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:660498 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:232603770 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:232603770 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:55087414 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:55087414 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:149514256 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:149514256 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:32077525 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:32077525 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:41900597 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:41900597 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:179597700 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:179597700 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:8159985 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:8159985 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:3844949 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:3844949 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13336345 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13336345 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:21098844 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:21098844 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:65114813 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:65114813 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160000082 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160000082 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:629047 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:629047 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:630779 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:630779 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:106524484 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:106524484 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:8753153 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:8753153 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57993226 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57993226 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:3660867 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:3660867 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:47925179 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:47925179 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137257249 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137257249 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110455413 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110455413 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:51768587 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:51768587 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:44449837 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:44449837 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:8696896 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:8696896 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:145006526 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:145006526 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:19459504 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:19459504 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:131948925 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:131948925 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:131960363 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:131960363 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:68613864 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:68613864 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:161160295 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:161160295 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:145820678 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:145820678 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:118359465 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:118359465 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:7870223 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:7870223 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:44279922 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:44279922 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:7605227 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:7605227 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:124464129 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:124464129 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287206 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287206 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287210 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287210 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:48222711 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:48222711 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:52728930 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:52728930 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:9570086 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:9570086 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:73047216 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:73047216 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:11421702 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:11421702 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74538530 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74538530 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:105776622 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:105776622 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:68999896 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:68999896 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:716752 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:716752 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:24196596 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:24196596 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:46203899 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:46203899 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54410212 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54410212 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57257127 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57257127 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57279140 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57279140 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:170699233 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:170699233 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142460066 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142460066 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:43699634 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:43699634 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:43439523 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:43439523 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99048223 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99048223 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:47448249 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:47448249 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:198671479 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:198671479 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:198677228 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:198677228 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55702801 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55702801 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:112138745 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:112138745 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158908059 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158908059 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:220440456 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:220440456 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120413141 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120413141 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:55948930 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:55948930 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:102717144 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:102717144 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:85441839 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:85441839 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:170640790 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:170640790 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:109393757 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:109393757 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:21925962 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:21925962 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:21936222 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:21936222 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:80382876 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:80382876 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56940073 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56940073 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:46190825 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:46190825 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79312428 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79312428 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79386539 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79386539 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:103389852 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:103389852 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43602030 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43602030 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43612206 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43612206 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43615703 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:43615703 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:73136208 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:73136208 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:3418534 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:3418534 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:182572553 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:182572553 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:241161966 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:241161966 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:25718664 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:25718664 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:95099120 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:95099120 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33512609 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33512609 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:42875632 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:42875632 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:87398408 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:87398408 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:49739875 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:49739875 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:141868975 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:141868975 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6270127 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6270127 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:2513615 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:2513615 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:77366529 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:77366529 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:18690945 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:18690945 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:8707066 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:8707066 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:2001034 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:2001034 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:146017335 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:146017335 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:19376722 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:19376722 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:36421220 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:36421220 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:237993769 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:237993769 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:15882898 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:15882898 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:128924736 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:128924736 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:83552683 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:83552683 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:147260904 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:147260904 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:18275191 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:18275191 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:139304458 G>A maps to ENST00000446833 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:139304458 G>A maps to ENST00000446833 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:3860953 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:3860953 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:97529541 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:97529541 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:101060666 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:101060666 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:26127768 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:26127768 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:61328207 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:61328207 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:57374174 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:57374174 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:167159973 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:167159973 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:150934742 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:150934742 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:7262273 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:7262273 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:120907274 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:120907274 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:130509558 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:130509558 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51192282 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51192282 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:96339248 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:96339248 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:77631271 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:77631271 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:3683827 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:3683827 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:52133029 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:52133029 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159921657 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159921657 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127507507 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127507507 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:25813573 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:25813573 T>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:25826617 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:25826617 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:62749557 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:62749557 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:43269811 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:43269811 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:63137512 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:63137512 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:9630247 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:9630247 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156169566 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156169566 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:92401548 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:92401548 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:118147719 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:118147719 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47782380 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47782380 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:44986051 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:44986051 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:234458699 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:234458699 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:50253107 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:50253107 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33170036 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33170036 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:125731601 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:125731601 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:18004476 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:18004476 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:10976659 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:10976659 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:1235799 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:1235799 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:28530082 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:28530082 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:87226885 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:87226885 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:70148668 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:70148668 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:40657533 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:40657533 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:143297756 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:143297756 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:74914560 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:74914560 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:70706673 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:70706673 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:168189788 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:168189788 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:84455651 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:84455651 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:98639926 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:98639926 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:51449213 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:51449213 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:1093719 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:1093719 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:1205028 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:1205028 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:108377781 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:108377781 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:108439365 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:108439365 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:108458950 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:108458950 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:204085495 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:204085495 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:231041484 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:231041484 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:215145614 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:215145614 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:144337436 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:144337436 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:172834903 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:172834903 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:52926769 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:52926769 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123844161 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123844161 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:48825193 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:48825193 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:46276761 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:46276761 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:28993605 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:28993605 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158626345 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158626345 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158651163 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158651163 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158651176 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158651176 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:54826186 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:54826186 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:78023321 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:78023321 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:64519951 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:64519951 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:48047040 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:48047040 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74563514 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74563514 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:52536290 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:52536290 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:104118664 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:104118664 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:191926403 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:191926403 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:89854322 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:89854322 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:219553626 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:219553626 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35102250 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35102250 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:125920214 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:125920214 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:9281761 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:9281761 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:896191 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:896191 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21851947 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21851947 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21851981 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21851981 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:136220841 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:136220841 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:75537846 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:75537846 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:12192690 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:12192690 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:12200100 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:12200100 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:32909927 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:32909927 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:152599125 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:152599125 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:119979119 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:119979119 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66812320 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66812320 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:38693628 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:38693628 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:1729231 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:1729231 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:29989364 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:29989364 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:150464059 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:150464059 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:17448046 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:17448046 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:17747671 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:17747671 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:79277766 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:79277766 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:59485395 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:59485395 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:114832472 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:114832472 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:114837132 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:114837132 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:115987608 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:115987608 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53452351 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53452351 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:71219179 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:71219179 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:36766846 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr20:36766846 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:133906336 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:133906336 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:155504665 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:155504665 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:43777280 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:43777280 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:76853735 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:76853735 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35699958 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35699958 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:83791715 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:83791715 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:75369808 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:75369808 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:76113295 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:76113295 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:98452786 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:98452786 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:32956989 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:32956989 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:38972820 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:38972820 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:44117944 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:44117944 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:31266349 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:31266349 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:52194301 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:52194301 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:19653278 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:19653278 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:19666983 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:19666983 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29736289 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29736289 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29736291 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29736291 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29786025 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29786025 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29786292 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:29786292 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:6442131 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:6442131 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:6530969 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:6530969 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:150422393 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:150422393 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201328680 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201328680 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175096309 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175096309 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175334925 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175334925 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175363181 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175363181 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:35718092 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:35718092 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:35743296 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:35743296 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:72366134 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:72366134 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10969920 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10969920 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10971225 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10971225 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10971845 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10971845 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:209936108 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:209936108 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:72667429 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:72667429 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248027962 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:248027962 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:4622415 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:4622415 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:31357177 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:31357177 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:45860559 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:45860559 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142574820 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142574820 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:98545837 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:98545837 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:141954778 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:141954778 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54695492 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54695492 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143365768 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143365768 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:85413374 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:85413374 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:71519257 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:71519257 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:75082642 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:75082642 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:40091398 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:40091398 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:51760289 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:51760289 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:76243077 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:76243077 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:113277758 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:113277758 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179418212 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179418212 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2698688 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:2698688 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:19748720 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:19748720 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:48088372 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:48088372 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:36876546 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:36876546 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154524036 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154524036 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:109921600 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:109921600 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:156971380 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:156971380 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:156991051 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:156991051 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:42626592 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:42626592 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19432993 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19432993 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19470604 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19470604 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:103293804 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:103293804 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:93673491 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:93673491 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:171682507 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:171682507 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13275670 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13275670 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132405809 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132405809 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:33477306 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:33477306 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161009948 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161009948 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:17552584 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:17552584 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:62696500 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:62696500 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:85836452 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:85836452 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:5039030 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:5039030 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:144843386 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:144843386 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160388709 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:160388709 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:101197150 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:101197150 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:17277925 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:17277925 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:2650282 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:2650282 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:100352769 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:100352769 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54554658 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:54554658 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:85742231 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:85742231 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:20178354 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:20178354 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113127923 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113127923 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:74908368 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:74908368 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:74951952 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:74951952 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:36582439 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:36582439 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:190316656 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:190316656 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33655337 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33655337 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:10098191 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:10098191 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:168510385 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:168510385 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:2688515 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:2688515 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:2729346 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:2729346 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:10755410 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:10755410 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:17291966 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:17291966 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:183435414 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:183435414 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:27400899 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:27400899 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:64138863 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:64138863 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:111624966 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:111624966 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:28489433 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:28489433 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:27159201 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:27159201 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:77745556 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:77745556 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:75182481 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:75182481 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:152087478 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:152087478 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11882102 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11882102 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3169231 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3169231 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:44599278 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:44599278 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:74606826 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:74606826 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:145979532 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:145979532 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:38385624 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:38385624 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:49525137 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:49525137 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:57194288 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:57194288 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:22836000 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:22836000 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:22836711 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:22836711 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:31041610 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:31041610 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9449201 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9449201 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:22290995 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chrX:22290995 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:22379328 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:22379328 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:35260641 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:35260641 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:58016875 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:58016875 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57184253 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57184253 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:102181119 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:102181119 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:58564631 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:58564631 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:3917898 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:3917898 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:35344012 A>G maps to NM_012138.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:35344012 A>G maps to NM_012138.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:160198310 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:160198310 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr6:160198310 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr6:160198310 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:47261646 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:47261646 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr11:47261646 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr11:47261646 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:100336159 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:100336159 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:84465792 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:84465792 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr8:124748162 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr8:124748162 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:99109349 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:99109349 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:6423993 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:6423993 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:90672638 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:90672638 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr5:90672638 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr5:90672638 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:47583958 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:47583958 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr4:47583958 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr4:47583958 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr21:11085851 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr21:11085851 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:65905888 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:65905888 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:65905888 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:65905888 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chrX:79988922 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chrX:79988922 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:93100405 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:93100405 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:93100405 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:93100405 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:70525901 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:70525901 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:3671780 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:3671780 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:3671780 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:3671780 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr19:43858550 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr19:43858550 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr19:43858550 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr19:43858550 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr15:93552600 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr15:93552600 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr7:146471510 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr7:146471510 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr7:146829774 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr7:146829774 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:189856362 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:189856362 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:84902347 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:84902347 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr16:84902347 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr16:84902347 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr15:91178244 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr15:91178244 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr8:95795752 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr8:95795752 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:43933204 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:43933204 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:139993206 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:139993206 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:29438709 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:29438709 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:47606266 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:47606266 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:95512209 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:95512209 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr8:12040442 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr8:12040442 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:97933220 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:97933220 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:4488387 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:4488387 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr6:76063271 C>T maps to NM_015687.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr6:76063271 C>T maps to NM_015687.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr5:180041240 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr5:180041240 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr4:48636352 A>C maps to NM_015030.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr4:48636352 A>C maps to NM_015030.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:9850346 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:9850346 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:220103788 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:220103788 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chrX:122488684 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chrX:122488684 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:33524367 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:33524367 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr20:33524367 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr20:33524367 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:100533891 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:100533891 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:100533891 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:100533891 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:59986925 T>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:59986925 T>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:59986929 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:59986929 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:3661311 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:3661311 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr16:75675406 A>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr16:75675406 A>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:7014140 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:7014140 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr16:29816618 T>C maps to NM_007317.1 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr16:29816618 T>C maps to NM_007317.1 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:45738428 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:45738428 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:39675116 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:39675116 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:39675116 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:39675116 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr21:46012383 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr21:46012383 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr8:29963390 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr8:29963390 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:148176240 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:148176240 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr4:140641169 C>G maps to ENST00000509479 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr4:140641169 C>G maps to ENST00000509479 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:137018655 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:137018655 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:51043784 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:51043784 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr22:51043784 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr22:51043784 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chrX:119739547 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chrX:119739547 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:68715237 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:68715237 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:38183459 A>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:38183459 A>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:155162638 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:155162638 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:211179574 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:211179574 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr18:70416304 A>G maps to NM_153181.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr18:70416304 A>G maps to NM_153181.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:117726155 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:117726155 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:117726155 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:117726155 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:160719 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:160719 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:199997047 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:199997047 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:199997047 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:199997047 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:50847149 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:50847149 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:50847149 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:50847149 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:134008131 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:134008131 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:82147632 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:82147632 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr15:91523759 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr15:91523759 T>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:129788649 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:129788649 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr11:129788649 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr11:129788649 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:3701350 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:3701350 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:49133544 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:49133544 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr3:49133544 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr3:49133544 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:32125101 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:32125101 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr11:32125101 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr11:32125101 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:78936640 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:78936640 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:78936640 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:78936640 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:62319169 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:62319169 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr20:62319169 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr20:62319169 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr5:171765852 C>T maps to NM_001017995.2 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr5:171765852 C>T maps to NM_001017995.2 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:25812020 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:25812020 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr6:25812020 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr6:25812020 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:24902180 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:24902180 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:110740026 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:110740026 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:110740026 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:110740026 C>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:39237899 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:39237899 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:39237899 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:39237899 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:54895768 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:54895768 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:54895768 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:54895768 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:115527499 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:115527499 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:115527499 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr1:115527499 T>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:61488707 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:61488707 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:179457913 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:179457913 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:234463015 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:234463015 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:122724256 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr12:122724256 A>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:58362213 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr2:58362213 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:58362213 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr2:58362213 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:42209911 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:42209911 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr22:42209911 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr22:42209911 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:40948620 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:40948620 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:40948620 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr17:40948620 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:69199019 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:69199019 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:14658741 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr9:14658741 C>G did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr14:68215370 T>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr14:68215370 T>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr14:68215370 T>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1105-08 chr14:68215370 T>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr19:44732556 G>C did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr19:44732556 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:48634508 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:48634508 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:48550738 A>T maps to NM_152701.3 T4528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:48550738 A>T maps to NM_152701.3 T4528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:183667662 C>A maps to NM_005688.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:183667662 C>A maps to NM_005688.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:17464658 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:17464658 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:17464658 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:17464658 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:61561184 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:61561184 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:61564147 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:61564147 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:61561184 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:61561184 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:61564147 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:61564147 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:20480762 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:20480762 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20480762 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20480762 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:39502997 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:39502997 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:39502997 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:39502997 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:39581360 C>A maps to NM_014237.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:39581360 C>A maps to NM_014237.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:156991473 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:156991473 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:156991473 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:156991473 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:73188855 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:73188855 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:84659801 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:84659801 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:84659801 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:84659801 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:167779890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:167779890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:167779890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:167779890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:131833727 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:131833727 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:132002962 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:132002962 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:132052590 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:132052590 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:131833727 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:131833727 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:132052590 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:132052590 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:67364386 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:67364386 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:203134619 C>T maps to NM_001048230.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:203134619 C>T maps to NM_001048230.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:76358801 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:76358801 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:76358801 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:76358801 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:100353472 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:100353472 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:100353472 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:100353472 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:434429 G>A maps to NM_020731.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:434429 G>A maps to NM_020731.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:186335057 G>C maps to ENST00000273784 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:186335057 G>C maps to ENST00000273784 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:4771897 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:4771897 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:4771897 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:4771897 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:134254140 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:134254140 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:134254140 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:134254140 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:5040684 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:5040684 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:104190578 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:104190578 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:104190578 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:104190578 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:34175367 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:34175367 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:34175367 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:34175367 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:202483878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:202483878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:202483878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:202483878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:11188890 C>T maps to NM_054028.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:11188890 C>T maps to NM_054028.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:41584918 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:41584918 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:41581078 C>A maps to ENST00000415018 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:41581078 C>A maps to ENST00000415018 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:41584918 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:41584918 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:113803111 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:113803111 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:114158798 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:114158798 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:113803111 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:113803111 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:114158798 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:114158798 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:33096660 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:33096660 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:21209790 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:21209790 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:21209790 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:21209790 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:36589258 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:36589258 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:2111838 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:2111838 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:2111838 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:2111838 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:63579602 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:63579602 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:63579602 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:63579602 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:58465265 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:58465265 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:24975637 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:24975637 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:24975637 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:24975637 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:11162552 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:11162552 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:155931857 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:155931857 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:155931857 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:155931857 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:63845389 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:63845389 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:63845389 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:63845389 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:123007013 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:123007013 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:197058975 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:197058975 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:197058975 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:197058975 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:176983874 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:176983874 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:176983874 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:176983874 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:1403795 G>C maps to NM_001039211.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:1403795 G>C maps to NM_001039211.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:161790981 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:161790981 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:161790981 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:161790981 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:107393161 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:107393161 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:113488978 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:113488978 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:42482015 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:42482015 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:42482015 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:42482015 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:36051553 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:36051553 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:36051553 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:36051553 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:176049250 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:176049250 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:176049250 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:176049250 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:50351525 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:50351525 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:71604060 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:71604060 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:71604060 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:71604060 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr21:11026655 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr21:11026655 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:1396021 G>T maps to NM_003933.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:1396021 G>T maps to NM_003933.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:76740021 C>G maps to NM_024685.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:76740021 C>G maps to NM_024685.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:127511920 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:127511920 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:70818541 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:70818541 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:70818541 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:70818541 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:69098253 C>A maps to NM_014482.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:69098253 C>A maps to NM_014482.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:43289198 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:43289198 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:43297724 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:43297724 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:43289198 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:43289198 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:43297724 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:43297724 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:137486820 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:137486820 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:137486820 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:137486820 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56400644 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56400644 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56400644 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56400644 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:11908753 G>A maps to NM_153256.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:11908753 G>A maps to NM_153256.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:62432975 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:62432975 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:40114570 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:40114570 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:112646246 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:112646246 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:112646246 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:112646246 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:81371379 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:81371379 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:76488666 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:76488666 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:76488666 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:76488666 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:23468205 G>A maps to NM_021944.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:23468205 G>A maps to NM_021944.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:29230999 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:29230999 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:50665945 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:50665945 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:50665945 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:50665945 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:51769158 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:51769158 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:51769162 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:51769162 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:51769158 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:51769158 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:51769162 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:51769162 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:75055218 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:75055218 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:75055218 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:75055218 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:34684197 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:34684197 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:34684197 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:34684197 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:61576188 C>T maps to NM_017896.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:61576188 C>T maps to NM_017896.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:18370988 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:18370988 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:18370988 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:18370988 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3234370 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3234370 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3803010 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3803010 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3803010 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3803010 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:75916056 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:75916056 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:74847849 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:74847849 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:119452195 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:119452195 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:119452195 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:119452195 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:14813427 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:14813427 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:88202661 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:88202661 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:88202661 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:88202661 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:81307685 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:81307685 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:40948088 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:40948088 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:120911526 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:120911526 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:120911526 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:120911526 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:112462460 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:112462460 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:27891294 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:27891294 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:27891294 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:27891294 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:49708883 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:49708883 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:49708883 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:49708883 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:49142168 G>T maps to NM_001217.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:49142168 G>T maps to NM_001217.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:13386556 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:13386556 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:13386556 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:13386556 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:181740384 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:181740384 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:1259499 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:1259499 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:1950020 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:1950020 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:1950020 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:1950020 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:18824998 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:18824998 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:18824998 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:18824998 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54445372 C>T maps to NM_031896.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54445372 C>T maps to NM_031896.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:174969256 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:174969256 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:174969256 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:174969256 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:44293939 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:44293939 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:138713800 C>A maps to ENST00000409386 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:138713800 C>A maps to ENST00000409386 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:2955024 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:2955024 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:2955024 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:2955024 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:202068562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:202068562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:202068562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:202068562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:121972964 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:121972964 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:121972964 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:121972964 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:89408537 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:89408537 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:89408537 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:89408537 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:57762246 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:57762246 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:57762246 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:57762246 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:77265971 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:77265971 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:77265971 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:77265971 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:126138878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:126138878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:126138878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:126138878 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:64001939 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:64001939 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:191075676 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:191075676 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:191075676 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:191075676 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:7639047 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:7639047 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:7639047 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:7639047 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:7811982 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:7811982 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:7811982 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:7811982 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:157805487 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:157805487 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:157805487 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:157805487 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3781364 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3781364 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3781364 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3781364 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:24487743 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:24487743 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:24487743 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:24487743 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:60449072 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:60449072 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:50801306 A>G maps to NM_004196.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:50801306 A>G maps to NM_004196.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:80879269 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:80879269 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:80879269 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:80879269 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:6709106 C>A maps to ENST00000309577 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:6709106 C>A maps to ENST00000309577 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:40042044 C>T maps to NM_032221.3 E2350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:40042044 C>T maps to NM_032221.3 E2350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:21863423 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:21863423 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:21863423 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:21863423 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:16652922 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:16652922 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:16652922 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:16652922 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71571551 C>A maps to NM_001166395.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71571551 C>A maps to NM_001166395.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:24532186 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:24532186 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:87012867 C>A maps to ENST00000263723 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:87012867 C>A maps to ENST00000263723 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:143036570 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:143036570 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:143036570 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:143036570 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:141643857 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:141643857 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:7303677 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:7303677 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:7303677 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:7303677 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:3554623 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:3554623 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:3554623 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:3554623 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:22208544 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:22208544 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:99008272 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:99008272 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:99008272 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:99008272 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:87738643 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:87738643 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:87738643 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:87738643 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:205030312 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:205030312 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:146741275 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:146741275 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:147914551 C>G maps to NM_014141.5 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:147914551 C>G maps to NM_014141.5 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:125204318 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:125204318 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:125204318 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:125204318 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:75848103 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:75848103 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:75848103 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:75848103 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:110839400 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:110839400 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:111130347 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:111130347 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:107865153 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:107865153 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:130289562 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:130289562 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:48614642 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:48614642 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:47643837 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:47643837 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:47643837 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:47643837 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:4390917 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:4390917 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:4390917 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:4390917 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:31439549 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:31439549 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:31439549 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:31439549 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:207822919 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:207822919 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:207822919 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:207822919 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:125516683 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:125516683 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:125516683 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:125516683 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:76254476 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:76254476 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:76254476 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:76254476 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:1424514 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:1424514 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:1424514 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:1424514 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:2965484 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:2965484 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:4645892 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:4645892 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:4645892 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:4645892 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113267392 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113267392 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113568850 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:113568850 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:113421166 G>T maps to NM_198123.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:113421166 G>T maps to NM_198123.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:113657363 C>T maps to NM_198123.1 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:113657363 C>T maps to NM_198123.1 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:67748708 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:67748708 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:11565243 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:11565243 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:11565243 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:11565243 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:3563834 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:3563834 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:70275342 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:70275342 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:17171352 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:17171352 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:17171352 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:17171352 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:48997005 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:48997005 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:51504463 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:51504463 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:51504463 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:51504463 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:99329067 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:99329067 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:99329067 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:99329067 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:16025584 G>T maps to NM_021187.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:16025584 G>T maps to NM_021187.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:1418489 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:1418489 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:1418489 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:1418489 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:50451743 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:50451743 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:50451743 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:50451743 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:50923678 C>A maps to NM_005215.3 S897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:50923678 C>A maps to NM_005215.3 S897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:31327079 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:31327079 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:31327079 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:31327079 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:34621451 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:34621451 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:34621451 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:34621451 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:110576255 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:110576255 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:110576255 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:110576255 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:70722000 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:70722000 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:70722005 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:70722005 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:44611442 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:44611442 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:44611442 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:44611442 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:32487950 G>A maps to NM_014314.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:32487950 G>A maps to NM_014314.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:50016256 G>T maps to NM_001037498.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:50016256 G>T maps to NM_001037498.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:9680699 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:9680699 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:24541641 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:24541641 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:38159208 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:38159208 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:38159208 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:38159208 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:84245608 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:84245608 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:84245925 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:84245925 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:84245608 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:84245608 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:84245925 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:84245925 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:32563219 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:32563219 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:32563219 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:32563219 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:35993174 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:35993174 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:35993174 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:35993174 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:13820608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:13820608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:196718075 G>T maps to NM_018897.2 T2924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:196718075 G>T maps to NM_018897.2 T2924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:56151455 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:56151455 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:56151455 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:56151455 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:117819890 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:117819890 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:169230286 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:169230286 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:169267704 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:169267704 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169230286 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169230286 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169267704 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169267704 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169483862 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169483862 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:51197941 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:51197941 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:63008221 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:63008221 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:63008221 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:63008221 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54135450 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54135450 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54135450 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54135450 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:7563931 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:7563931 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:7563931 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:7563931 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:7585489 G>T maps to NM_004415.2 T2665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:7585489 G>T maps to NM_004415.2 T2665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:58949494 A>T maps to NM_015177.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:58949494 A>T maps to NM_015177.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:112262322 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:112262322 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:40316981 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:40316981 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:40316981 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:40316981 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:4700241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:4700241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:4700241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:4700241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:71778360 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:71778360 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:71778360 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:71778360 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:137796601 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:137796601 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:131666255 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:131666255 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:131666255 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:131666255 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:8016094 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:8016094 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:47500597 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:47500597 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:73457080 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:73457080 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:33744406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:33744406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:33744406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:33744406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:101183241 T>G maps to ENST00000397927 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:101183241 T>G maps to ENST00000397927 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:77707126 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:77707126 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:77707126 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:77707126 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:97477751 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:97477751 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:89391034 G>T maps to NM_005233.5 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:89391034 G>T maps to NM_005233.5 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56270369 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56270369 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56274636 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56274636 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56270369 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56270369 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56274636 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56274636 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:212529879 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:212529879 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:5682822 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:5682822 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:5803929 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:5803929 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:44151590 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:44151590 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:44151590 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:44151590 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:64567627 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:64567627 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:76029423 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:76029423 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:140138566 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:140138566 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:140138566 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:140138566 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:222919869 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:222919869 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:222919869 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:222919869 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:29867329 C>A maps to ENST00000269209 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:29867329 C>A maps to ENST00000269209 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:24976549 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:24976549 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:131822772 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:131822772 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:10107450 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:10107450 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3128051 T>A maps to NM_021826.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3128051 T>A maps to NM_021826.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:48420060 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:48420060 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:161187953 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:161187953 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:161187953 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:161187953 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:157556385 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:157556385 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:157556385 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:157556385 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:124988045 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:124988045 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:125115353 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:125115353 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:124988045 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:124988045 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:125115353 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:125115353 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:69588312 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:69588312 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:135291287 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:135291287 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:135291287 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:135291287 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:97052765 C>T maps to NM_020482.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:97052765 C>T maps to NM_020482.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:153588256 G>C maps to NM_001110556.1 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:153588256 G>C maps to NM_001110556.1 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:29001853 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:29001853 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:29007852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:29007852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:29001853 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:29001853 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:29007852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:29007852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:29068986 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:29068986 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:43320573 C>A maps to NM_005892.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:43320573 C>A maps to NM_005892.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:171155083 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:171155083 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:171155083 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:171155083 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:203225392 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:203225392 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:86600889 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:86600889 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:86600889 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:86600889 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169533119 C>G maps to NM_012188.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169533119 C>G maps to NM_012188.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:44974150 A>T maps to NM_032135.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:44974150 A>T maps to NM_032135.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:44976030 C>A maps to NM_032135.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:44976030 C>A maps to NM_032135.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71318652 C>A maps to NM_018348.5 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71318652 C>A maps to NM_018348.5 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:37427631 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:37427631 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:37427631 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:37427631 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:180630643 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:180630643 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:180630643 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:180630643 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:29578523 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:29578523 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:46334748 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:46334748 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:46334748 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:46334748 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:27160145 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:27160145 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:161569395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:161569395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:161569395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:161569395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:51759510 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:51759510 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:51759510 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:51759510 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:72618102 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:72618102 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:158409366 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:158409366 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:117884614 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:117884614 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:117884614 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:117884614 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:27910596 C>A maps to NM_001085454.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:27910596 C>A maps to NM_001085454.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:110418598 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:110418598 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:110418598 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:110418598 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:33038874 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:33038874 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:33038874 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:33038874 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:6606507 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:6606507 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:6606507 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:6606507 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:102968377 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:102968377 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:102976890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:102976890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:102968377 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:102968377 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:102976890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:102976890 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:20328493 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:20328493 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20328493 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20328493 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:23306032 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:23306032 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:23306032 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:23306032 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:142758527 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:142758527 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:142758527 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:142758527 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:113623283 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:113623283 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:113604126 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:113604126 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:122616902 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:122616902 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:122616902 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:122616902 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:94343883 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:94343883 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:94343883 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:94343883 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:7456996 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:7456996 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:27558946 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:27558946 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:27558946 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:27558946 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:19078159 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:19078159 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:19078159 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:19078159 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:5247762 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:5247762 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:5247762 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:5247762 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:64067495 T>A maps to ENST00000261887 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:64067495 T>A maps to ENST00000261887 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:143081589 G>A maps to NM_006734.3 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:143081589 G>A maps to NM_006734.3 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:31128545 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:31128545 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:31128545 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:31128545 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:162909665 C>T maps to NM_001142556.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:162909665 C>T maps to NM_001142556.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:173491285 A>T maps to NM_015980.3 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:173491285 A>T maps to NM_015980.3 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:38795455 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:38795455 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:18301446 G>C maps to NM_181507.1 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:18301446 G>C maps to NM_181507.1 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:18303487 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:18303487 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:99129186 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:99129186 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:99129186 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:99129186 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:21976734 C>G maps to NM_005144.4 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:21976734 C>G maps to NM_005144.4 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:114405689 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:114405689 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:114405689 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:114405689 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:231988652 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:231988652 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:113865531 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:113865531 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:94563223 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:94563223 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:94563223 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:94563223 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:102964543 T>A maps to NM_016232.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:102964543 T>A maps to NM_016232.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:27454549 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:27454549 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:27454549 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:27454549 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:68645483 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:68645483 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:68645483 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:68645483 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:166926993 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:166926993 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:166926993 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:166926993 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:19800280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:19800280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:19800280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:19800280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:33067497 A>T maps to ENST00000262650 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:33067497 A>T maps to ENST00000262650 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:52211397 G>T maps to NM_181501.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:52211397 G>T maps to NM_181501.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:15730142 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:15730142 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:31421643 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:31421643 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:31421643 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:31421643 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:187529426 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:187529426 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:187529426 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:187529426 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:7750964 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:7750964 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:7750964 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:7750964 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:54776265 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:54776265 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:54776265 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:54776265 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:7659033 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:7659033 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:48835305 C>T maps to NM_021999.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:48835305 C>T maps to NM_021999.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:64982746 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:64982746 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:64982746 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:64982746 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:124052942 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:124052942 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:17794267 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:17794267 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:17794267 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:17794267 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:215368530 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:215368530 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:154821444 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:154821444 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:138647116 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:138647116 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:36694373 G>T maps to NM_001031836.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:36694373 G>T maps to NM_001031836.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:55961742 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:55961742 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:30317503 G>A maps to NM_020848.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:30317503 G>A maps to NM_020848.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:241726851 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:241726851 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:39761734 C>A maps to ENST00000395670 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:39761734 C>A maps to ENST00000395670 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55272293 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55272293 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55272293 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55272293 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55325107 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55325107 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55325107 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55325107 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:51462293 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:51462293 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:51462293 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:51462293 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:39594295 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:39594295 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:39594295 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:39594295 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:52884747 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:52884747 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:52884747 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:52884747 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:39346674 A>G maps to NM_001190460.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:39346674 A>G maps to NM_001190460.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:39346674 A>G maps to NM_001190460.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:39346674 A>G maps to NM_001190460.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:201356818 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:201356818 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:129649484 C>G maps to NM_000426.3 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:129649484 C>G maps to NM_000426.3 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:206781730 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:206781730 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:206781730 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:206781730 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:48639210 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:48639210 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55107392 G>C maps to NM_006863.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55107392 G>C maps to NM_006863.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54779754 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54779754 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54779754 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54779754 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:96443236 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:96443236 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:96443236 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:96443236 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:8251750 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:8251750 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:97816092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:97816092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:97816092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:97816092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:160961337 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:160961337 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:161005989 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:161005989 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:161056024 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:161056024 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:160961337 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:160961337 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:161005989 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:161005989 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:161056024 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:161056024 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:1477511 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:1477511 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:1477511 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:1477511 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:141283978 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:141283978 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:141571476 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:141571476 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:141283978 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:141283978 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:57603411 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:57603411 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:57603411 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:57603411 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:68190899 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:68190899 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:68190899 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:68190899 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:70225868 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:70225868 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:70225868 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:70225868 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:40761585 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:40761585 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:68857482 G>T maps to NM_178011.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:68857482 G>T maps to NM_178011.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:71821339 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:71821339 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:71821339 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:71821339 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:143866995 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:143866995 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:143866995 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:143866995 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:39790501 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:39790501 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:141293068 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:141293068 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:141293068 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:141293068 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:21204042 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:21204042 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:136935099 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:136935099 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:42111876 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:42111876 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:186944313 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:186944313 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:18255562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:18255562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:18255562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:18255562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:3778977 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:3778977 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:3778977 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:3778977 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:138650237 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:138650237 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:138650237 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:138650237 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:54529084 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:54529084 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:54529084 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:54529084 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:85431432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:85431432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:85431432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:85431432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:6377619 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:6377619 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:6377619 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:6377619 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:94245196 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:94245196 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:86267845 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:86267845 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:86267845 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:86267845 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:150834276 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:150834276 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:150834276 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:150834276 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:131937142 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:131937142 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:40428572 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:40428572 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:89209241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:89209241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:89339217 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:89339217 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:89339217 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:89339217 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:102668251 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:102668251 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:102668255 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:102668255 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:102668251 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:102668251 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:102668255 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:102668255 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:5011854 G>A maps to NM_021801.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:5011854 G>A maps to NM_021801.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:44639525 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:44639525 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:44639525 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:44639525 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:198398650 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:198398650 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:198398650 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:198398650 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:39876767 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:39876767 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:39876767 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:39876767 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:62929425 C>T maps to ENST00000393630 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:62929425 C>T maps to ENST00000393630 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:224831530 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:224831530 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:224831530 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:224831530 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:179310383 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:179310383 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:179310383 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:179310383 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:72754874 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:72754874 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:72754874 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:72754874 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:31727787 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:31727787 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:31727787 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:31727787 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:174152131 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:174152131 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:56667827 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:56667827 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:56667827 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:56667827 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:7900288 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:7900288 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:7900288 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:7900288 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:30066846 G>C maps to NM_001033602.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:30066846 G>C maps to NM_001033602.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:8962053 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:8962053 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:9010878 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:9010878 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:9024555 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:9024555 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:8962053 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:8962053 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9010878 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9010878 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9024555 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9024555 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9071875 A>G maps to NM_024690.2 P5190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9071875 A>G maps to NM_024690.2 P5190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:113459433 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:113459433 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:48441612 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:48441612 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:48441612 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:48441612 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:10408677 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:10408677 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:10408677 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:10408677 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:10550788 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:10550788 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:10550788 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:10550788 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:10299837 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:10299837 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:10299837 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:10299837 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:128341984 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:128341984 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:128341984 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:128341984 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:12626138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:12626138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:12626138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:12626138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:164049998 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:164049998 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:164049998 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:164049998 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:78392029 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:78392029 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:78392029 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:78392029 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:15696790 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:15696790 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:204009249 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:204009249 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:204009249 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:204009249 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:183889669 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:183889669 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:33337074 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:33337074 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:33337074 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:33337074 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:207003265 C>A maps to ENST00000455934 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:207003265 C>A maps to ENST00000455934 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:152581899 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:152581899 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:152581899 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:152581899 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr22:29886352 G>A maps to NM_021076.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr22:29886352 G>A maps to NM_021076.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:20969044 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:20969044 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:20969044 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:20969044 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:45170909 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:45170909 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:45170909 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:45170909 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:204950909 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:204950909 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:204950909 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:204950909 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:204951176 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:204951176 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:50090454 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:50090454 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:50090454 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:50090454 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:104155596 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:104155596 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:63768829 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:63768829 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:63768829 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:63768829 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:7318562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:7318562 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:101093866 T>A maps to NM_001011717.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:101093866 T>A maps to NM_001011717.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:117723829 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:117723829 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:24329280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:24329280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:24329280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:24329280 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:115355601 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:115355601 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:115423468 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:115423468 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:115355601 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:115355601 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:24134756 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:24134756 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:24146307 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:24146307 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:24134756 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:24134756 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:24146307 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:24146307 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:131720381 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:131720381 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:131720381 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:131720381 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:101615452 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:101615452 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:101615452 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:101615452 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:28230274 C>A maps to NM_000275.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:28230274 C>A maps to NM_000275.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:71062454 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:71062454 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:183600671 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:183600671 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:9791930 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:9791930 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:9791930 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:9791930 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:161954548 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:161954548 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:107288800 C>T maps to NM_001001919.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:107288800 C>T maps to NM_001001919.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:247695851 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:247695851 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:247695851 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:247695851 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:29012091 C>A maps to NM_030903.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:29012091 C>A maps to NM_030903.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56232385 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:56232385 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56232385 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:56232385 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:20344410 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:20344410 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:20344410 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:20344410 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:56344906 G>T maps to NM_001004741.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:56344906 G>T maps to NM_001004741.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:124294272 C>A maps to NM_001005196.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:124294272 C>A maps to NM_001005196.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:56128507 C>A maps to NM_001005205.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:56128507 C>A maps to NM_001005205.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:21742138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:21742138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:21742138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:21742138 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:111970271 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:111970271 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:111970271 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:111970271 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:3583112 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:3583112 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:72946374 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:72946374 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:72946374 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:72946374 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:163149062 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:163149062 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:163149062 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:163149062 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3891139 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:3891139 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3891139 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3891139 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:69672371 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:69672371 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:69672371 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:69672371 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:206418004 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:206418004 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:206418004 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:206418004 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:145058148 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:145058148 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:145058148 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:145058148 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:150780276 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:150780276 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:150780276 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:150780276 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:21687762 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:21687762 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:21689022 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:21689022 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:21687762 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:21687762 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:21689022 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:21689022 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:102540934 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:102540934 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:102540934 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:102540934 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:91238473 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:91238473 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140810273 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:140810273 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140810273 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140810273 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140812209 G>T maps to NM_003735.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140812209 G>T maps to NM_003735.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140731095 G>A maps to NM_018922.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140731095 G>A maps to NM_018922.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140799010 G>T maps to NM_018927.2 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140799010 G>T maps to NM_018927.2 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:78686488 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:78686488 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:66631077 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:66631077 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:165802040 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:165802040 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:165895689 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:165895689 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:165956876 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:165956876 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:165802040 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:165802040 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:165895689 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:165895689 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:165956876 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:165956876 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:66833363 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:66833363 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:66833363 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:66833363 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:144919117 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:144919117 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:144919117 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:144919117 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:79618747 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:79618747 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:79618747 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:79618747 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:60978994 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:60978994 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:230468555 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:230468555 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:230468555 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:230468555 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:153303329 C>A maps to NM_020393.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:153303329 C>A maps to NM_020393.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:64114123 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:64114123 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:64114123 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:64114123 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:26881651 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:26881651 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:26881651 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:26881651 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:18544313 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:18544313 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:39535092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:39535092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:39535092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:39535092 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:8790036 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:8790036 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:8790036 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:8790036 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:130834575 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:130834575 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:130834575 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:130834575 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:20416374 C>A maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:20416374 C>A maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:8709900 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:8709900 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:8709900 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:8709900 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:8862494 G>C maps to NM_015192.2 *1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:8862494 G>C maps to NM_015192.2 *1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:40582479 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:40582479 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:9360851 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:9360851 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:9459461 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:9459461 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:9360851 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:9360851 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:9459461 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:9459461 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:131936514 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:131936514 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:131951655 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:131951655 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:131936514 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:131936514 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:131951655 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:131951655 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:43921509 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:43921509 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:150129459 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:150129459 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:150129459 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:150129459 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:68621099 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:68621099 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:12024851 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:12024851 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:12024851 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:12024851 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:72159706 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:72159706 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:39645225 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:39645225 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:39645225 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:39645225 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:130878105 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:130878105 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:56989595 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:56989595 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:56989595 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:56989595 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:202406860 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:202406860 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:202406860 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:202406860 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:202406947 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:202406947 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:42862737 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:42862737 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:170020753 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:170020753 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:170020753 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:170020753 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:48744304 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:48744304 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:48744304 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:48744304 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:48775079 C>A maps to NM_006904.6 E1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:48775079 C>A maps to NM_006904.6 E1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43380657 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43380657 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43380657 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43380657 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43429741 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43429741 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43433927 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43433927 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43433927 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43433927 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43453869 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43453869 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43770536 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:43770536 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43770536 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:43770536 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:11595454 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:11595454 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:11595454 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:11595454 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:125145834 G>T maps to NM_000962.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:125145834 G>T maps to NM_000962.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:77266395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:77266395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:77266395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:77266395 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:198700602 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:198700602 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:198711620 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:198711620 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:198711620 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:198711620 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:157997860 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:157997860 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:220161452 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:220161452 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:220161452 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:220161452 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:29618567 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:29618567 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:29618567 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:29618567 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:9333632 A>T maps to NM_002864.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:9333632 A>T maps to NM_002864.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:220330961 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:220330961 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:8932030 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:8932030 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:8932030 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:8932030 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:9513020 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:9513020 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:9513020 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:9513020 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:135982744 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:135982744 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:170725661 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:170725661 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:113553692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:113553692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:113553692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:113553692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:79896613 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:79896613 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:79896613 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:79896613 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:145603197 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:145603197 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:145603197 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:145603197 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:36120653 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:36120653 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:36120653 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:36120653 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:50102345 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:50102345 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:50102345 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:50102345 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:139181187 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:139181187 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:139181187 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:139181187 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:103159715 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:103159715 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:103160053 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:103160053 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:103557492 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:103557492 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:103159715 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:103159715 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:103557492 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:103557492 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:43612221 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:43612221 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:43612221 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:43612221 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:175957579 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:175957579 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:175957579 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:175957579 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:41178141 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:41178141 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:93300536 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:93300536 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:93300540 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:93300540 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:93300536 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:93300536 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:93300540 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:93300540 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:167143364 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:167143364 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:78576460 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:78576460 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:103237347 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:103237347 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:114319739 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:114319739 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:114319739 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:114319739 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:12939861 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:12939861 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:12939861 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:12939861 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:60072160 C>A maps to NM_021136.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:60072160 C>A maps to NM_021136.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:67733310 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:67733310 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:25291041 G>A maps to NM_001031680.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:25291041 G>A maps to NM_001031680.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:33937085 C>A maps to NM_016568.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:33937085 C>A maps to NM_016568.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:165380404 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:165380404 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:165380404 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:165380404 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:38942546 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:38942546 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:38942546 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:38942546 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:34103124 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:34103124 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:169650995 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:169650995 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:169650995 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:169650995 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:100598692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:100598692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:100598692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:100598692 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:166258948 A>T maps to NM_006745.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:166258948 A>T maps to NM_006745.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:158787129 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:158787129 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:158991563 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:158991563 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:158787129 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:158787129 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:38755297 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:38755297 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:166866191 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:166866191 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr22:43658695 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr22:43658695 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr22:43658695 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr22:43658695 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:35212535 A>G maps to ENST00000394681 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:35212535 A>G maps to ENST00000394681 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:4150217 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:4150217 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:4247585 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:4247585 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:4150217 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:4150217 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:4247585 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:4247585 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:192711132 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:192711132 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:192711132 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:192711132 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:74707190 C>T maps to NM_003612.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:74707190 C>T maps to NM_003612.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:185341816 A>T maps to ENST00000427465 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:185341816 A>T maps to ENST00000427465 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:55865857 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:55865857 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:242283468 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:242283468 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:242283468 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:242283468 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:94909641 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:94909641 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:94909641 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:94909641 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:95029669 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:95029669 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:95029669 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:95029669 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:94931008 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:94931008 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:94931008 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:94931008 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:61570671 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:61570671 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:61570671 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:61570671 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:167164354 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:167164354 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:167164354 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:167164354 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:84255728 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:84255728 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:84255728 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:84255728 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:146247375 T>A maps to ENST00000367503 I1095I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:146247375 T>A maps to ENST00000367503 I1095I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:117058368 T>A maps to NM_001040455.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:117058368 T>A maps to NM_001040455.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:164748366 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:164748366 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:46247979 G>A maps to NM_003726.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:46247979 G>A maps to NM_003726.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:160604514 G>T maps to NM_003037.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:160604514 G>T maps to NM_003037.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:1074608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:1074608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:1074608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:1074608 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:43217059 C>T maps to NM_007163.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:43217059 C>T maps to NM_007163.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:25918583 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:25918583 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:19674053 C>A maps to NM_020689.3 Y492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:19674053 C>A maps to NM_020689.3 Y492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:78197142 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:78197142 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:78197142 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:78197142 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:27478153 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:27478153 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:27478153 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:27478153 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:75681628 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:75681628 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:51844609 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:51844609 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:18918280 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:18918280 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:18918280 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:18918280 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:110716457 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:110716457 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:110716457 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:110716457 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:170216487 C>A maps to NM_020949.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:170216487 C>A maps to NM_020949.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:70527750 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:70527750 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:70527750 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:70527750 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:103095196 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:103095196 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:21205247 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:21205247 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:33687260 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:33687260 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:2698037 A>T maps to NM_015295.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:2698037 A>T maps to NM_015295.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:70444583 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr14:70444583 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:70444583 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:70444583 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:25154727 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:25154727 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:25154727 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:25154727 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:51449383 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:51449383 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:51664531 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:51664531 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:51449383 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:51449383 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:51664531 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:51664531 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:106865416 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:106865416 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:106865416 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:106865416 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:231102057 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:231102057 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:231102057 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:231102057 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:118539079 G>A maps to NM_206996.2 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:118539079 G>A maps to NM_206996.2 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:91025680 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:91025680 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:91025680 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:91025680 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:55910532 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:55910532 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:55910532 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:55910532 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:234975852 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:234975852 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:234975852 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:234975852 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:158612492 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:158612492 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:158612492 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:158612492 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:74041189 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:74041189 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:2818262 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:2818262 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:116774263 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:116774263 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:116774263 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:116774263 T>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:52550805 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:52550805 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:52550805 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:52550805 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:104044203 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:104044203 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:104044203 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:104044203 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:47751648 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:47751648 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:74515887 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr8:74515887 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:74515887 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:74515887 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:74481406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:74481406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:74481406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:74481406 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:4509120 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:4509120 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:4509120 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:4509120 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:67571121 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:67571121 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:67571121 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:67571121 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:70592732 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:70592732 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:4025531 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:4025531 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:4025531 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:4025531 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:7437130 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:7437130 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:7437130 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:7437130 A>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:132938807 G>T maps to NM_001033080.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:132938807 G>T maps to NM_001033080.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:26756480 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:26756480 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:26756480 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:26756480 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:170873781 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:170873781 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:170873781 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:170873781 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:50696860 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:50696860 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:50696860 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:50696860 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:133418346 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:133418346 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:133418346 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:133418346 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:89177107 G>T maps to NM_138960.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:89177107 G>T maps to NM_138960.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:2380909 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:2380909 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:2380909 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:2380909 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:169632586 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:169632586 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:169632586 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:169632586 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:2796237 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:2796237 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:2796237 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:2796237 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20748249 T>A maps to ENST00000431224 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20748249 T>A maps to ENST00000431224 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:70353099 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr15:70353099 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:70353099 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:70353099 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:60598086 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:60598086 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:60598086 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:60598086 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:2597906 G>A maps to NM_080751.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:2597906 G>A maps to NM_080751.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:44770555 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:44770555 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:44770555 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:44770555 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55832246 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:55832246 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55832246 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55832246 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:15425241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:15425241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:15425241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:15425241 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:130762208 G>T maps to NM_052913.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:130762208 G>T maps to NM_052913.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:25817873 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:25817873 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:25817873 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:25817873 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:29924384 A>G maps to NM_016127.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:29924384 A>G maps to NM_016127.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:4292587 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:4292587 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:154774605 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:154774605 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:29757257 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:29757257 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:29757257 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:29757257 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:93586769 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:93586769 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:93586769 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:93586769 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:175067546 C>G maps to NM_022093.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:175067546 C>G maps to NM_022093.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:175328960 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:175328960 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:175328960 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:175328960 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:25674335 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr3:25674335 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:25674335 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:25674335 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:42695473 G>T maps to ENST00000348077 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:42695473 G>T maps to ENST00000348077 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:6330810 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:6330810 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr21:10934905 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr21:10934905 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr21:10952842 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr21:10952842 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr21:10934905 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr21:10934905 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr21:10952842 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr21:10952842 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:230672374 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:230672374 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:230672374 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:230672374 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:54953207 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chrX:54953207 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:54953207 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:54953207 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:73478055 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:73478055 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:73478055 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:73478055 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:77376767 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr9:77376767 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:77376767 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:77376767 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:116430677 C>T maps to NM_014112.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:116430677 C>T maps to NM_014112.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:116631412 C>A maps to NM_014112.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:116631412 C>A maps to NM_014112.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:135782333 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:135782333 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:2337895 C>A maps to NM_139022.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:2337895 C>A maps to NM_139022.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:43250287 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr6:43250287 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:75113580 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:75113580 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:75113580 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:75113580 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:55253538 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:55253538 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:33037798 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:33037798 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:30474941 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:30474941 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:30474941 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:30474941 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:179572216 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:179572216 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:179572216 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:179572216 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:151534971 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:151534971 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:151534971 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:151534971 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:37927786 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:37927786 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:37927786 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:37927786 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:10238754 A>T maps to NM_001105562.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:10238754 A>T maps to NM_001105562.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:5415528 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:5415528 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:5415528 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:5415528 A>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:234628347 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:234628347 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:234628347 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:234628347 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:176306802 C>T maps to NM_133369.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:176306802 C>T maps to NM_133369.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:96256817 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:96256817 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:96256817 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:96256817 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:18968169 G>C maps to ENST00000418384 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:18968169 G>C maps to ENST00000418384 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:17552572 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:17552572 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:17552572 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:17552572 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:215802112 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:215802112 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:215802112 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:215802112 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:113699990 A>T maps to NM_020886.2 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:113699990 A>T maps to NM_020886.2 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:48238558 C>A maps to NM_001017535.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:48238558 C>A maps to NM_001017535.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:37000952 C>T maps to NM_053276.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:37000952 C>T maps to NM_053276.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:79959802 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:79959802 T>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:122720195 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr12:122720195 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:122720195 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:122720195 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:22166854 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:22166854 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:22166854 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:22166854 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:49842569 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:49842569 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:88220146 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr10:88220146 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:88220146 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:88220146 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:27216298 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr13:27216298 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:20137488 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr2:20137488 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:20137488 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:20137488 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:241901852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr1:241901852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:241901852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:241901852 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:37379351 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr5:37379351 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:37379351 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:37379351 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:1640948 A>T maps to NM_001163809.1 S1932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:1640948 A>T maps to NM_001163809.1 S1932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:66425981 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr17:66425981 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:5270432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr7:5270432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:5270432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:5270432 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:32439104 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr11:32439104 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:32439104 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:32439104 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:21349292 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:21349292 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:21349292 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:21349292 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:17228385 G>A maps to NM_022166.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:17228385 G>A maps to NM_022166.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:56195374 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr20:56195374 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:4314882 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr4:4314882 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:4314882 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:4314882 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:82615027 T>A maps to NM_024699.2 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:82615027 T>A maps to NM_024699.2 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:5290716 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr18:5290716 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:5290716 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:5290716 C>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:58579297 C>A maps to NM_007134.1 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:58579297 C>A maps to NM_007134.1 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:22193449 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:22193449 C>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71482342 C>A maps to NM_145911.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71482342 C>A maps to NM_145911.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:22235504 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:22235504 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:22235504 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:22235504 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53311269 C>A maps to NM_006969.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53311269 C>A maps to NM_006969.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54072434 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:54072434 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54072434 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54072434 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53611536 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53611536 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53611536 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53611536 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53352243 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53352243 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53352243 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53352243 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:47927584 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chrX:47927584 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53686316 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr19:53686316 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53686316 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:53686316 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:22939190 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:22939190 G>C did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:21212977 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:21212977 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:21212980 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1458-08 chr16:21212980 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:21212977 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:21212977 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:21212980 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:21212980 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:89052430 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:89052430 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:108881532 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:108881532 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:33892006 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:33892006 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:18639426 A>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:18639426 A>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:129062858 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:129062858 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:67450316 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:67450316 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:121790214 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:121790214 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:101460594 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:101460594 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:49020263 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:49020263 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:55373901 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:55373901 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:77798636 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:77798636 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:54122048 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:54122048 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:87927232 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:87927232 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:181480758 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:181480758 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:120494850 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:120494850 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:21884503 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:21884503 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:68544213 G>A maps to ENST00000409862 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:68544213 G>A maps to ENST00000409862 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:103461671 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:103461671 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:101817735 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:101817735 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr22:27024418 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr22:27024418 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:113662261 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:113662261 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:58218484 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:58218484 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:101848475 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:101848475 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:38302548 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:38302548 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:19035125 A>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:19035125 A>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:126214666 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:126214666 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:955734 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:955734 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:22055046 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:22055046 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:426847 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:426847 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:99537825 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:99537825 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:184034674 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:184034674 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:37618332 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:37618332 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:24332299 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:24332299 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:159667900 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:159667900 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:4796546 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:4796546 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:77930529 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:77930529 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:26793341 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:26793341 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:49230969 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chrX:49230969 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:146480780 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:146480780 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:106698600 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:106698600 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:113850096 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:113850096 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:18174822 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:18174822 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:132015184 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:132015184 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:237317256 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:237317256 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:121547296 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:121547296 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:156645053 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:156645053 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr14:55862764 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr14:55862764 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:154505954 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:154505954 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:47289495 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:47289495 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:53169461 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:53169461 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:133954713 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:133954713 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:203739873 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:203739873 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:90436046 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:90436046 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:148252092 C>A maps to ENST00000369202 E4550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:148252092 C>A maps to ENST00000369202 E4550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:56320530 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:56320530 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:141128894 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:141128894 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:160636418 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:160636418 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:207605622 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:207605622 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:141755585 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:141755585 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:151902404 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:151902404 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:28002154 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:28002154 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:41332896 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:41332896 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:9726653 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:9726653 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:1019506 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:1019506 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:113547342 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:113547342 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:8587233 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:8587233 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:128394513 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:128394513 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:71169640 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:71169640 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:70526002 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:70526002 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:50765749 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:50765749 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66188927 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66188927 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66189744 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66189744 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:45668306 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:45668306 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:28141318 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:28141318 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:137967663 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:137967663 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:4190720 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:4190720 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:25075699 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:25075699 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:31824236 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:31824236 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:98994232 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:98994232 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:207108748 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:207108748 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:18544291 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:18544291 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:96064079 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:96064079 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118187665 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118187665 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:42226872 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:42226872 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:101163566 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:101163566 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:23831054 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:23831054 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:8248183 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:8248183 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:135894334 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:135894334 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:135894336 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:135894336 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:79384587 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:79384587 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:100079154 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:100079154 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:3319835 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:3319835 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:74150239 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:74150239 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:94537937 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:94537937 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:41823207 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:41823207 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:4148250 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:4148250 C>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:108970254 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:108970254 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr21:15918654 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr21:15918654 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:4269769 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:4269769 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:75677081 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:75677081 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:21471662 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:21471662 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:186570600 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:186570600 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:23728511 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:23728511 T>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:136221647 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:136221647 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:79693430 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:79693430 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:102264627 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:102264627 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:10954185 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:10954185 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:121989628 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:121989628 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:133935511 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:133935511 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:71457585 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:71457585 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:35699901 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:35699901 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr20:30729762 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr20:30729762 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:226037572 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:226037572 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:68788684 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:68788684 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr21:42839624 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr21:42839624 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr21:10909556 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr21:10909556 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:202277706 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:202277706 T>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:108565882 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr3:108565882 C>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:14398884 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:14398884 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:170806647 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:170806647 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:170933890 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:170933890 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:170851090 A>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:170851090 A>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:17729677 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:17729677 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:144808666 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:144808666 T>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:44803987 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:44803987 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:64415023 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:64415023 A>G did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:64983 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:64983 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:53913177 G>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:53913177 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr7:99702384 T>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr7:99702384 T>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:112726993 A>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:112726993 A>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr6:70909298 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr6:70909298 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:117071494 T>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:117071494 T>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:48383460 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:48383460 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:17181838 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:17181838 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:47279868 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:47279868 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:31838888 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:31838888 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:40701594 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:40701594 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:52724466 G>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:52724466 G>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr6:29896313 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr6:29896313 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:60326034 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:60326034 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr16:70996127 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr16:70996127 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:54793312 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:54793312 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:148253043 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:148253043 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:1481213 A>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:1481213 A>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:116444228 T>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:116444228 T>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:97666317 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:97666317 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr4:2252431 G>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr4:2252431 G>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr20:33587959 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr20:33587959 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:30078943 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:30078943 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr8:63502384 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr8:63502384 A>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr20:2633825 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr20:2633825 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:62569569 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:62569569 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr2:231927200 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr2:231927200 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:15669680 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:15669680 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:116356198 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:116356198 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:161326721 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:161326721 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chrX:118543988 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chrX:118543988 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:31042477 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:31042477 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:75685033 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:75685033 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chrX:70147952 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chrX:70147952 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:484612 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:484612 C>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:4458777 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:4458777 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr14:102964629 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr14:102964629 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:17752380 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:17752380 A>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:9724870 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:9724870 G>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr2:71660179 G>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr2:71660179 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:48450009 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:48450009 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:133600326 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:133600326 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:179102282 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:179102282 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:112171663 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:112171663 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:40040560 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:40040560 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:156991374 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:156991374 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:24167590 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:24167590 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:100328035 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:100328035 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:32138469 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:32138469 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:129037009 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:129037009 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:233244188 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:233244188 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:85677279 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:85677279 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:9195481 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:9195481 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:10468328 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:10468328 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:39421507 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:39421507 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:143973858 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:143973858 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:94667210 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:94667210 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:131140159 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:131140159 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:119943076 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:119943076 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:113503391 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:113503391 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:63973677 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:63973677 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:118948625 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:118948625 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:27148754 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:27148754 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:49701678 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:49701678 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:31498600 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:31498600 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:90416528 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:90416528 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:91655536 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:91655536 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:36983240 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:36983240 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:17385022 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:17385022 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:10582561 A>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:10582561 A>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr21:33839915 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr21:33839915 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:26677472 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:26677472 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:14744779 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:14744779 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:164435360 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:164435360 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:121526350 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:121526350 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:33371025 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:33371025 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:74587868 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:74587868 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48547202 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48547202 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:181745145 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:181745145 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201046042 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201046042 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:159161611 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:159161611 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:111311504 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:111311504 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:80108021 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:80108021 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:12252327 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:12252327 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:85128006 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:85128006 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:140178314 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:140178314 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:224922424 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:224922424 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:1036327 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:1036327 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:165548647 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:165548647 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:177669301 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:177669301 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:110866263 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:110866263 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:189931038 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:189931038 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:70963244 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:70963244 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:70965021 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:70965021 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:818274 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:818274 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:125521757 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:125521757 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:87021085 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:87021085 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:4645246 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:4645246 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:65649362 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:65649362 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:143959112 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:143959112 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:100756760 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:100756760 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:72040241 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:72040241 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:39088996 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:39088996 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:433613 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:433613 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:435816 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:435816 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:21858036 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:21858036 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:196786792 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:196786792 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:11604288 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:11604288 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:34490298 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:34490298 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:38030776 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:38030776 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:98082546 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:98082546 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:225750604 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:225750604 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:109050949 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:109050949 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:74063549 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:74063549 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54135177 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54135177 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr21:38385960 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr21:38385960 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:95499010 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:95499010 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:71839991 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:71839991 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:34400480 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:34400480 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:89462266 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:89462266 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:212252600 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:212252600 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:103510578 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:103510578 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:27284568 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:27284568 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97750066 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97750066 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:80454731 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:80454731 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:17813426 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:17813426 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:45606512 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:45606512 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:16632426 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:16632426 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:137777774 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:137777774 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:4488426 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:4488426 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:153885949 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:153885949 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:28623360 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:28623360 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:240421100 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:240421100 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:171168729 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:171168729 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:171178145 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:171178145 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:230385081 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:230385081 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:9829012 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:9829012 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:35885151 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:35885151 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:134241510 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:134241510 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:88667596 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:88667596 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:135441382 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:135441382 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:168055035 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:168055035 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:26087557 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:26087557 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:22217021 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:22217021 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:147900612 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:147900612 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:25671725 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:25671725 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:159976498 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:159976498 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:21205029 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:21205029 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:47121253 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:47121253 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:35875775 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:35875775 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:121579119 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:121579119 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:15212193 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:15212193 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:85951880 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:85951880 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:26775076 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:26775076 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:96047272 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:96047272 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:78674616 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:78674616 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:113740629 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:113740629 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:122013804 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:122013804 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:27783032 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:27783032 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:57189424 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:57189424 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:59895929 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:59895929 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:166160190 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:166160190 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:241723854 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:241723854 A>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:52642149 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:52642149 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54867920 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54867920 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:129581983 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:129581983 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:21531759 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:21531759 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:145493568 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:145493568 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48631010 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48631010 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54722345 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54722345 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:129458381 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:129458381 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:105511461 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:105511461 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:141747244 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:141747244 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:62850792 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:62850792 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:54965334 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:54965334 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:63666047 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:63666047 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:57905976 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:57905976 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:29457358 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:29457358 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:43929508 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:43929508 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:131914029 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:131914029 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:100030794 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:100030794 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:49575313 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:49575313 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:8997329 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:8997329 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:113547437 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:113547437 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:77718791 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:77718791 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:10318356 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:10318356 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:171358187 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:171358187 A>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97009752 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97009752 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:119176667 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:119176667 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:140213784 A>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:140213784 A>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:51874939 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:51874939 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:183247838 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:183247838 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:5987963 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:5987963 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:200080539 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:200080539 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:79176062 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:79176062 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:88420119 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:88420119 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:88679110 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:88679110 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:48887593 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:48887593 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:62730175 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:62730175 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:13160732 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:13160732 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:248263646 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:248263646 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:9214003 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:9214003 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:26696257 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:26696257 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:43272817 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:43272817 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:19027126 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:19027126 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:55583184 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:55583184 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:55583305 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:55583305 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:56360539 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:56360539 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:144854707 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:144854707 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:144951922 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:144951922 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:22452026 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:22452026 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:8051854 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:8051854 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:145581137 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:145581137 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:145581145 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:145581145 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:51882470 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:51882470 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:119347541 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:119347541 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48565121 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48565121 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:42293322 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:42293322 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:161133948 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:161133948 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:133218751 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:133218751 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:99282741 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:99282741 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:149833180 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:149833180 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:186279109 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:186279109 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54394833 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54394833 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:15701954 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:15701954 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:24738689 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:24738689 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:68878250 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:68878250 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:26217417 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:26217417 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:91503340 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:91503340 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:182638722 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:182638722 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:66099661 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:66099661 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:182550585 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:182550585 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:88991072 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:88991072 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:237813143 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:237813143 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:55237028 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:55237028 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:167289283 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:167289283 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:18485672 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:18485672 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:138463543 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:138463543 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:38621436 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:38621436 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:38633375 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:38633375 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:1908672 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr20:1908672 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:164757633 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:164757633 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:32391101 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:32391101 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:27423285 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:27423285 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:10976919 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:10976919 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:96953508 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:96953508 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:96969088 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:96969088 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:101629772 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:101629772 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:158588980 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:158588980 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:158639070 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:158639070 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:48218013 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chrX:48218013 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:4091485 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:4091485 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:33529880 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:33529880 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:52943026 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:52943026 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:50786533 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:50786533 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:100225339 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:100225339 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:76851734 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:76851734 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:76853505 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:76853505 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:69095266 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:69095266 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201337404 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201337404 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:218669162 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:218669162 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:71510525 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:71510525 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:57168626 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:57168626 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:230787156 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:230787156 G>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:231047117 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:231047117 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:91161816 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:91161816 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:118257351 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:118257351 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr21:43504411 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr21:43504411 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:118949442 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:118949442 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:36556620 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:36556620 C>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:41264942 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:41264942 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:41264944 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:41264944 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:41310380 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:41310380 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:100364483 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:100364483 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:79751467 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:79751467 T>G did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:44681833 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:44681833 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:74546607 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:74546607 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:57703222 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:57703222 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:22843796 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr22:22843796 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:4810688 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:4810688 G>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:52937408 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:52937408 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:20133958 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:20133958 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:461511 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:461511 T>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:149174591 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:149174591 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:67524258 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:67524258 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:48234087 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:48234087 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:51371122 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:51371122 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:17405448 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:17405448 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:35454938 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:35454938 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:35600209 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:35600209 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:74040030 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:74040030 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:131323941 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:131323941 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:20486820 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:20486820 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42857162 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42857162 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42857178 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42857178 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:100234942 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:100234942 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:178358512 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:178358512 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:178378691 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:178378691 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:26672509 G>C maps to NM_001039775.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:26672509 G>C maps to NM_001039775.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:114204090 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:114204090 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:37414966 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:37414966 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:6030186 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:6030186 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:32987511 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:32987511 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:32917862 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:32917862 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:143973949 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:143973949 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:47538622 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:47538622 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:29205559 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:29205559 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr21:11047680 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr21:11047680 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:127826483 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:127826483 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:28618574 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:28618574 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:59821654 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:59821654 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:71392866 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:71392866 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:115529411 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:115529411 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:115531901 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:115531901 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:61253252 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:61253252 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:16620131 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:16620131 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:31891746 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:31891746 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:54025127 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:54025127 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:2595484 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:2595484 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:181706895 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:181706895 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:201062976 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:201062976 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:81599131 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:81599131 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:188243641 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:188243641 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:186392060 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:186392060 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:103433265 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:103433265 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:24537381 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:24537381 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:65006767 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:65006767 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:19483748 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:19483748 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:73442340 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:73442340 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:85972826 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:85972826 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:90355767 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:90355767 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:37443588 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:37443588 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:214821311 G>A maps to ENST00000391896 L1L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:214821311 G>A maps to ENST00000391896 L1L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:146728244 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:146728244 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:40127914 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:40127914 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:111781581 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:111781581 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:23767156 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:23767156 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:143043902 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:143043902 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:10153243 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:10153243 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:16351245 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:16351245 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:33140769 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:33140769 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:139648852 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:139648852 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:125526715 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:125526715 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:6465512 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:6465512 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:28763752 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:28763752 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:75925020 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:75925020 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:113266335 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:113266335 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:122060139 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:122060139 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:80136944 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:80136944 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:16957227 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:16957227 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:85416251 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:85416251 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:45409970 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:45409970 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:45410013 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:45410013 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:50705277 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:50705277 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:110573946 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:110573946 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:140269610 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:140269610 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:32509364 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:32509364 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:118479668 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:118479668 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:11827328 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:11827328 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:131011104 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:131011104 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:128821639 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:128821639 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:116520101 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:116520101 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:117309749 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:117309749 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:56342389 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:56342389 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:107215862 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:107215862 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:38370346 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:38370346 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:18561234 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:18561234 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:53133855 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:53133855 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:131191340 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:131191340 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:110300519 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:110300519 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:37605552 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:37605552 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:242030407 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:242030407 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:56756338 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:56756338 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:94700596 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:94700596 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:169493192 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:169493192 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:74773856 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:74773856 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:29268296 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:29268296 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:68788089 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:68788089 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:116836660 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:116836660 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:59064463 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:59064463 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:10135897 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:10135897 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:99100407 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:99100407 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:150890935 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:150890935 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:127648632 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:127648632 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55385835 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55385835 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:108295115 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:108295115 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:45590602 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:45590602 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:240306224 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:240306224 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:52192461 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:52192461 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:12701487 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:12701487 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:117711111 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:117711111 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:47163247 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:47163247 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:81410974 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:81410974 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:121741986 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:121741986 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:151229878 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:151229878 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:57478683 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:57478683 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:235715384 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:235715384 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:167745633 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:167745633 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:47684904 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:47684904 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:240656260 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:240656260 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:102503140 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:102503140 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:104375590 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:104375590 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:27544601 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:27544601 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:15613320 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:15613320 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:140073644 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:140073644 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:240066538 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:240066538 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:41057329 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:41057329 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:65221063 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:65221063 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:46620395 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:46620395 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:110628938 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:110628938 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:29973174 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:29973174 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:67685538 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:67685538 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:6061914 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:6061914 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:6063696 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:6063696 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:134463831 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:134463831 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:2641190 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:2641190 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:145534008 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:145534008 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:70522110 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:70522110 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:156641180 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:156641180 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:156650041 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:156650041 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:103441356 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:103441356 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:64673507 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:64673507 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:100126311 C>G maps to ENST00000375206 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:100126311 C>G maps to ENST00000375206 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55283151 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55283151 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55344333 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55344333 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:10584682 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:10584682 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:39502935 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:39502935 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54875800 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54875800 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:36103485 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:36103485 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:65633890 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:65633890 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:133881944 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:133881944 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:141083483 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:141083483 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:141083489 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:141083489 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:44152129 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:44152129 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:166962173 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:166962173 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:151896251 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:151896251 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:49642910 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:49642910 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:20197025 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:20197025 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:37626301 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:37626301 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:15652241 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:15652241 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:44639749 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:44639749 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:30517120 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:30517120 T>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:71616171 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:71616171 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:92714570 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:92714570 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:30823047 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:30823047 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:47368494 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:47368494 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:10431949 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:10431949 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:111349010 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:111349010 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:34881201 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:34881201 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:62836348 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:62836348 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:89902007 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:89902007 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:78334268 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:78334268 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:54901470 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:54901470 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:54912533 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:54912533 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:16011522 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:16011522 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:56063336 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:56063336 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:20969028 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:20969028 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:37016101 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:37016101 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:85414743 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:85414743 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:129347660 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:129347660 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:102594967 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:102594967 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:87482439 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:87482439 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:102270472 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:102270472 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:16729470 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:16729470 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:29583860 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:29583860 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:150931004 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:150931004 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:138454469 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:138454469 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:40565944 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:40565944 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:14695268 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:14695268 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:239164623 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:239164623 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:21068879 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:21068879 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:151274489 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:151274489 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:204410550 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:204410550 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:47913440 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:47913440 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:45897767 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:45897767 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:45566944 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:45566944 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:132169703 C>A maps to NM_181775.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:132169703 C>A maps to NM_181775.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:57044797 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:57044797 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:23826014 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:23826014 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:45197946 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:45197946 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:43227992 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:43227992 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:43674427 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:43674427 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:43523264 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:43523264 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:11579719 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:11579719 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:11579721 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:11579721 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:473829 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:473829 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:141753494 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:141753494 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:8317960 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:8317960 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:8341991 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:8341991 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:121623625 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:121623625 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:121674319 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:121674319 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:21621371 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:21621371 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:122290734 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:122290734 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:63306890 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:63306890 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:33745578 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:33745578 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:95351676 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:95351676 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:73656958 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:73656958 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:112214481 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:112214481 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:323669 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:323669 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:163042126 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:163042126 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:156351335 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:156351335 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:63510425 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:63510425 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:68912329 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:68912329 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:219457013 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:219457013 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:62063944 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:62063944 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:71410747 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:71410747 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:95034406 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:95034406 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:100774962 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:100774962 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:81317783 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:81317783 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:51648280 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:51648280 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:160460755 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:160460755 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:62763344 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:62763344 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:75862324 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:75862324 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42334988 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42334988 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42340240 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:42340240 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:110719234 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:110719234 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:133667638 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:133667638 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:108536223 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:108536223 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:106961055 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:106961055 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:16505960 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:16505960 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:214878865 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:214878865 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:100483441 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:100483441 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:22439495 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:22439495 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:52537138 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:52537138 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:87912578 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:87912578 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:1220720 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:1220720 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:8494589 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:8494589 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr21:46229075 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr21:46229075 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:136202823 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:136202823 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:223465688 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:223465688 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:13316796 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:13316796 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:74868103 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:74868103 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:27172592 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:27172592 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:53457303 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:53457303 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:15657906 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chrX:15657906 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:68919561 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:68919561 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:103307410 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:103307410 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:4410992 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:4410992 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:73461255 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:73461255 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:2433234 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:2433234 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:16320922 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:16320922 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:98602081 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:98602081 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:179534522 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:179534522 A>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:96648273 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:96648273 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:121157680 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:121157680 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:96141059 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:96141059 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:17517184 C>A maps to NM_153676.3 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:17517184 C>A maps to NM_153676.3 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54561904 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54561904 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:39245752 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:39245752 G>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:68374754 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:68374754 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:72822795 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:72822795 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:115818719 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:115818719 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:73490696 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:73490696 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:58145374 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:58145374 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:38184275 C>A maps to ENST00000447434 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:38184275 C>A maps to ENST00000447434 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:99074070 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:99074070 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:126655063 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:126655063 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr18:12351267 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr18:12351267 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:243715922 T>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:243715922 T>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:40505766 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:40505766 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:127422790 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:127422790 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:113052527 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:113052527 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr4:98947148 A>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr4:98947148 A>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr6:157720782 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr6:157720782 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:30887808 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:30887808 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:227261542 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:227261542 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr19:45017030 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr19:45017030 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr6:49448881 A>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr6:49448881 A>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr6:33141058 G>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr6:33141058 G>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr17:48272903 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr17:48272903 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:76259096 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:76259096 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:68076813 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:68076813 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr11:61632615 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr11:61632615 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr11:92616572 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr11:92616572 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:27772797 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:27772797 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:42467008 T>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:42467008 T>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:185959708 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:185959708 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr3:183772488 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr3:183772488 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:196438229 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:196438229 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:169961457 T>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:169961457 T>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:128393965 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:128393965 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:101756572 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:101756572 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:133210610 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:133210610 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr14:19566141 G>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr14:19566141 G>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr7:141537977 T>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr7:141537977 T>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:130912689 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:130912689 C>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:92765877 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:92765877 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:50026061 A>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:50026061 A>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr16:69293881 T>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr16:69293881 T>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:91560281 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:91560281 G>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr9:116085061 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr9:116085061 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr19:58234547 G>C did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr19:58234547 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:101567313 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:101567313 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:8428373 A>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:8428373 A>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:39521222 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:39521222 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:72511832 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:72511832 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:25062620 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:25062620 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:50311959 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:50311959 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:74270224 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:74270224 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:29445294 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:29445294 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:115231165 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:115231165 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:10524121 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:10524121 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:90582651 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:90582651 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:117876024 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:117876024 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:26621015 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:26621015 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:156906915 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:156906915 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203683461 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203683461 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:76777710 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:76777710 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:72954201 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:72954201 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:36965505 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:36965505 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:36965523 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:36965523 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:36965628 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:36965628 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:165703319 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:165703319 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:17531651 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:17531651 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:52827127 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:52827127 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:55570735 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:55570735 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:95897174 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:95897174 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:156870086 A>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:156870086 A>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:157801570 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:157801570 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:176016318 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:176016318 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:122818553 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:122818553 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:65472655 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:65472655 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:6260720 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:6260720 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:41374626 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:41374626 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:71654283 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:71654283 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139631545 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139631545 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139631567 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139631567 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139767678 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139767678 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:189926229 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:189926229 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:128976549 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:128976549 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:68937729 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:68937729 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:1403674 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:1403674 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:156786240 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:156786240 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:100679042 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:100679042 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:70700749 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:70700749 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:137150611 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:137150611 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:50122614 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:50122614 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:42354308 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:42354308 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:74746117 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:74746117 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:50594940 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:50594940 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:100515011 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:100515011 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:95457217 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:95457217 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:55249252 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:55249252 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:37376052 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:37376052 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:47612193 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:47612193 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:76523761 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:76523761 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:22824372 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:22824372 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:156593298 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:156593298 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:58459074 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:58459074 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr13:99042199 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr13:99042199 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:52781595 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:52781595 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:46060683 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:46060683 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:155252756 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:155252756 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:10874218 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:10874218 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:120593035 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:120593035 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:75272324 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:75272324 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:74508688 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:74508688 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:46839841 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:46839841 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:105859447 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:105859447 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:42563733 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:42563733 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:52671383 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:52671383 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:144765119 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:144765119 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:42162320 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:42162320 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:18630138 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:18630138 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:135582375 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:135582375 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:21216619 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:21216619 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:54799728 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:54799728 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:15697458 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:15697458 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:31424350 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:31424350 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:6150538 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:6150538 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:36792968 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:36792968 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:24809200 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:24809200 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:94171023 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:94171023 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:72339150 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:72339150 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:55604557 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:55604557 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:241714080 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:241714080 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:38922970 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:38922970 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:38937431 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:38937431 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:52980699 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:52980699 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:53169137 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:53169137 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:6264069 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:6264069 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107732055 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107732055 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152648490 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152648490 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:93182688 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:93182688 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:141299314 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:141299314 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:77975063 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:77975063 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:49632509 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:49632509 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:3781676 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:3781676 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:168802633 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:168802633 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:20354920 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:20354920 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:48603139 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:48603139 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:46900947 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:46900947 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:128317361 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:128317361 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:29683810 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:29683810 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:204955153 C>T maps to ENST00000367172 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:204955153 C>T maps to ENST00000367172 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:69627735 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:69627735 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:61873770 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:61873770 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:162326616 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:162326616 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:69752193 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:69752193 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107800773 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107800773 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107824774 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107824774 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:37328574 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:37328574 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:131243981 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:131243981 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:125274081 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:125274081 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248138757 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248138757 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248166364 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248166364 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:123777121 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:123777121 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:29648169 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:29648169 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:176671713 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:176671713 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:145074915 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:145074915 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:110397738 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:110397738 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:95995656 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:95995656 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:96025354 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:96025354 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:131936440 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:131936440 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:131949242 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:131949242 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:208206913 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:208206913 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:190708891 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:190708891 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:42840505 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:42840505 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:5283388 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:5283388 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:131130808 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:131130808 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:158109654 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:158109654 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:29637338 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:29637338 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:44142453 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:44142453 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:153957265 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:153957265 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:117866437 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:117866437 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:134505585 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:134505585 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:103275852 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:103275852 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:18234432 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:18234432 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:117248122 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:117248122 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:192312051 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:192312051 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:34094348 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:34094348 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:234247305 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:234247305 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:91949686 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:91949686 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:97533412 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:97533412 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:55902058 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:55902058 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:61323313 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:61323313 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:61459587 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:61459587 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:134638605 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:134638605 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:19559942 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:19559942 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:43314470 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr18:43314470 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:4840121 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:4840121 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107303518 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:107303518 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:118598586 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:118598586 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:168199734 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:168199734 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:168947572 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:168947572 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:51664732 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:51664732 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:118596735 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:118596735 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:123848934 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:123848934 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:89621028 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:89621028 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:52686386 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:52686386 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:75491011 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:75491011 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:67402446 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:67402446 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:155170406 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:155170406 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr13:100206730 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr13:100206730 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:74958005 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:74958005 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:218677203 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:218677203 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:132571439 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:132571439 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:209936615 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:209936615 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:112579050 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:112579050 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:55035062 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:55035062 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:189068533 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:189068533 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:141955209 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:141955209 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:179638871 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:179638871 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:162482390 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:162482390 T>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:96090608 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:96090608 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:184544100 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:184544100 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:71036409 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:71036409 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:137004979 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:137004979 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203816896 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203816896 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:52627914 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:52627914 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:147106604 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:147106604 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:47919948 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chrX:47919948 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:56703951 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:56703951 A>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr9:94087833 C>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr9:94087833 C>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr17:42945542 A>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr17:42945542 A>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:88425637 A>G did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:88425637 A>G did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:186082198 C>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:186082198 C>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr5:52218563 G>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr5:52218563 G>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:160605498 T>C did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:160605498 T>C did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr19:42853598 A>G did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr19:42853598 A>G did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:160879403 C>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:160879403 C>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr17:40986735 T>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr17:40986735 T>A did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:158946427 A>C did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:158946427 A>C did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:156337523 G>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:156337523 G>T did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr9:2088666 T>C did not map to a codon.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr9:2088666 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:87151341 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:87151341 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:116203985 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:116203985 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:20648648 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:20648648 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:20488571 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:20488571 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:69347513 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:69347513 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:43641345 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:43641345 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:156849542 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:156849542 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:39694575 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:39694575 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:39131922 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:39131922 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:77325492 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:77325492 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:18574456 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:18574456 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:7626141 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:7626141 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:41471996 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:41471996 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:125831611 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:125831611 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:50306918 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:50306918 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:45941138 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:45941138 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:202572577 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:202572577 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:190575912 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:190575912 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:56637708 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:56637708 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:33997939 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:33997939 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:51237241 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:51237241 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:21256134 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:21256134 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:145763253 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:145763253 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:11187822 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:11187822 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:57870447 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:57870447 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:73071021 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:73071021 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:66347873 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:66347873 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:23759432 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:23759432 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:124381249 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:124381249 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:108142313 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:108142313 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:138820032 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:138820032 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:138865475 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:138865475 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:11029637 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:11029637 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:11029706 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:11029706 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:69945060 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:69945060 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:112051769 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:112051769 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:36182220 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:36182220 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:100608114 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:100608114 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:26393508 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:26393508 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:180377608 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:180377608 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:105900795 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:105900795 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:128153568 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:128153568 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:36910695 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:36910695 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:170955899 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:170955899 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:16695691 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:16695691 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:32554929 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:32554929 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:111091357 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:111091357 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:32267549 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:32267549 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:32339548 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:32339548 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:42989268 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:42989268 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:40979768 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:40979768 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:77681844 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:77681844 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:49710785 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:49710785 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:50149795 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:50149795 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:9018901 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:9018901 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:18807778 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:18807778 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:54106545 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:54106545 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:188216769 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:188216769 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:32697246 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:32697246 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:86108851 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:86108851 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:34324711 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:34324711 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:30365802 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:30365802 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:83158976 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:83158976 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:66948063 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:66948063 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:62545584 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:62545584 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:151681890 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:151681890 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:214782025 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:214782025 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:87795866 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:87795866 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:14163325 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:14163325 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:418223 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:418223 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:78923766 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:78923766 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:170627966 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:170627966 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:76573584 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:76573584 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:7839673 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:7839673 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:103467329 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:103467329 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:94044450 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:94044450 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:61956759 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:61956759 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:139788153 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:139788153 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:227979202 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:227979202 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:107464299 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:107464299 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:137716414 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:137716414 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:47532526 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:47532526 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:211441260 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:211441260 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:125557402 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:125557402 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739132 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739132 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739135 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739135 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:159684153 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:159684153 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:4646134 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:4646134 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:33987215 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:33987215 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:23731256 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:23731256 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:11397037 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:11397037 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:16932532 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:16932532 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:44876390 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:44876390 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:74654221 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:74654221 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:86047524 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:86047524 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:27945290 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:27945290 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:72256077 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:72256077 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:85416111 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:85416111 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:106142119 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:106142119 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:44096268 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:44096268 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:50929286 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:50929286 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:91539799 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:91539799 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:19352252 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:19352252 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:32232952 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:32232952 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:137406756 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:137406756 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:80668676 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:80668676 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:54074086 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:54074086 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:32456305 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:32456305 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:124322984 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:124322984 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:52406110 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:52406110 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:152915426 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:152915426 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:62120252 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:62120252 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:38435116 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:38435116 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:176070282 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:176070282 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:134959961 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:134959961 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:16552854 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:16552854 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:45873523 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:45873523 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:76967020 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:76967020 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:216741277 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:216741277 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:44219262 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:44219262 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:2815989 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:2815989 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54160572 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54160572 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:134156561 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:134156561 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:24331744 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:24331744 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:152864382 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:152864382 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:131825722 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:131825722 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:10081089 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:10081089 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:29423294 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:29423294 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:45937980 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:45937980 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:127599407 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:127599407 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:147784395 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:147784395 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:157659521 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:157659521 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:35941664 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:35941664 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:58135960 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:58135960 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:28636348 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:28636348 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:8201259 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:8201259 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:41533764 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:41533764 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:13838314 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:13838314 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:52182274 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:52182274 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:32706106 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:32706106 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:121187647 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:121187647 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:151138889 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:151138889 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:898292 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:898292 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:172735944 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:172735944 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:30661853 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:30661853 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:22729404 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:22729404 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:44228634 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:44228634 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:85781594 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:85781594 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:8095228 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:8095228 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:14548165 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:14548165 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:37690446 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:37690446 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:11758307 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:11758307 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:66786618 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:66786618 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:66911598 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:66911598 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:33539720 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:33539720 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:36394174 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:36394174 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:236729098 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:236729098 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:66718994 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:66718994 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:65411934 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:65411934 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:28493666 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:28493666 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:81336684 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:81336684 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:43002070 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:43002070 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:97203235 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:97203235 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:55381281 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:55381281 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:122287012 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:122287012 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:71220651 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:71220651 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:47109376 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:47109376 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:201197370 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:201197370 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:114250133 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:114250133 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:9456434 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:9456434 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:52836634 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:52836634 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54815107 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:54815107 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:24535029 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:24535029 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:39740414 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:39740414 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:78846405 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:78846405 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:44285049 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:44285049 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:138677117 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:138677117 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:6734916 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:6734916 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:123239239 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:123239239 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:233512326 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:233512326 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:52886333 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:52886333 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:52827435 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:52827435 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:53166447 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:53166447 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:129480207 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:129480207 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:112465909 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:112465909 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:80198965 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:80198965 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:75147631 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:75147631 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:135288386 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:135288386 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:73559405 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:73559405 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:209603725 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:209603725 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:100903580 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:100903580 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:118148117 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:118148117 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:82407742 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:82407742 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:151835257 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:151835257 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:30354888 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:30354888 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:47333428 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:47333428 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:139748410 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:139748410 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:21207678 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:21207678 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:119748249 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:119748249 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:100369157 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:100369157 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:94945071 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:94945071 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:207630018 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:207630018 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:172195572 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:172195572 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:103353272 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:103353272 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:129914361 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:129914361 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:132645260 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:132645260 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:64956848 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:64956848 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:56704906 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:56704906 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:48459601 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:48459601 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:23861700 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:23861700 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:30421683 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:30421683 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:26166185 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:26166185 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:128346153 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:128346153 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:69882108 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:69882108 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:153197424 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:153197424 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:89892317 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:89892317 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:201749426 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:201749426 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:78534246 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:78534246 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:47038685 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:47038685 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:47038944 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:47038944 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:148594231 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:148594231 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:134274542 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:134274542 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:119115341 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:119115341 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:56477415 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:56477415 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:79910770 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:79910770 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:27064783 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:27064783 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:89106501 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:89106501 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:36340097 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:36340097 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:333741 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:333741 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:50724418 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:50724418 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:56867361 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:56867361 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:102332778 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:102332778 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:113355322 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:113355322 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:228463740 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:228463740 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:133046997 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:133046997 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:124028303 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:124028303 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:78437092 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:78437092 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:67290384 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:67290384 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:52850703 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:52850703 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:24854887 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:24854887 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:39592063 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:39592063 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:176661495 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:176661495 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:91714744 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:91714744 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:78794639 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:78794639 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:290246 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:290246 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:178862858 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:178862858 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:54249935 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:54249935 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:48186586 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:48186586 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:45175688 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:45175688 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:129753159 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:129753159 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:60642600 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:60642600 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:71532397 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:71532397 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:32955524 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:32955524 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:44159542 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:44159542 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:96014517 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:96014517 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:132066591 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:132066591 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:160222273 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:160222273 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:46658394 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:46658394 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:124503322 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:124503322 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:64872630 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:64872630 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:90731336 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:90731336 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:71328206 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:71328206 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:15668393 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:15668393 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:40280424 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:40280424 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:36598044 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:36598044 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:80409318 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:80409318 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:53580823 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:53580823 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:49076037 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:49076037 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:73657630 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:73657630 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:33517250 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:33517250 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:10473895 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:10473895 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:24018422 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:24018422 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:50001380 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:50001380 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:114354249 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:114354249 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67696065 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67696065 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67872933 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67872933 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:71644081 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:71644081 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:41143757 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:41143757 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:38946064 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:38946064 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:237660130 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:237660130 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:237753865 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:237753865 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:33927046 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:33927046 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:34034706 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:34034706 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:15885048 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:15885048 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:30865902 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:30865902 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:13846175 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:13846175 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:7290438 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:7290438 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:19701922 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:19701922 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:591556 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:591556 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:601719 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:601719 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:72196610 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:72196610 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:78293812 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:78293812 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:127446009 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:127446009 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:15063935 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:15063935 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:15075015 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:15075015 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:8200107 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:8200107 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:33951519 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:33951519 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:48708299 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:48708299 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:10971109 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:10971109 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:70149960 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:70149960 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:46521948 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:46521948 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:98816043 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:98816043 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:20540983 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:20540983 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:6415868 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:6415868 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:1690319 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:1690319 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:48791096 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:48791096 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:54839185 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:54839185 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:11119776 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:11119776 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:38019190 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:38019190 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:100485188 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:100485188 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:53077596 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:53077596 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:104054242 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:104054242 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:171517129 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:171517129 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:91809767 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:91809767 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:12112160 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:12112160 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:44004244 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:44004244 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:37893283 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:37893283 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:27857753 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:27857753 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:13514863 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:13514863 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:18539620 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:18539620 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:2315718 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:2315718 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:133980004 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:133980004 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:169642064 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:169642064 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:156351544 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:156351544 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:166910705 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:166910705 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:19041390 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:19041390 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:68829042 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:68829042 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:23058173 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:23058173 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:22995578 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:22995578 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:1147550 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:1147550 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:144380158 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:144380158 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:186305609 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:186305609 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:135567002 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:135567002 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:45834002 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:45834002 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:3458178 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:3458178 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:142626248 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:142626248 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:66482835 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:66482835 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:93688767 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:93688767 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:128941188 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:128941188 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:19699310 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:19699310 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:91482942 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:91482942 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:216011315 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:216011315 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:55600099 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:55600099 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:58268047 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:58268047 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:5035772 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:5035772 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:41003922 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:41003922 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:101185497 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:101185497 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:95668487 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:95668487 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:58276143 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:58276143 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:61032545 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:61032545 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:110428446 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:110428446 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:9544956 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:9544956 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:33256834 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:33256834 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:49044994 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:49044994 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:68352470 C>A maps to ENST00000295122 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:68352470 C>A maps to ENST00000295122 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:38420635 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:38420635 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:128894694 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:128894694 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:56185427 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:56185427 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:6646146 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:6646146 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:135622976 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:135622976 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:106431304 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:106431304 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:70472409 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chrX:70472409 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:38108038 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:38108038 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:52937104 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:52937104 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:8932669 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:8932669 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:56734247 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:56734247 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:33648814 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:33648814 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:113277448 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:113277448 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:108315639 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:108315639 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:186318033 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:186318033 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:150201623 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:150201623 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:77424936 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:77424936 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:7521144 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:7521144 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:160136903 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:160136903 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:13338053 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:13338053 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:107234619 A>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:107234619 A>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:18192068 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:18192068 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:93633703 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:93633703 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr15:91341409 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr15:91341409 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:136913604 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:136913604 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:121441898 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:121441898 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:42255126 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:42255126 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:44396193 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:44396193 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:51728439 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:51728439 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr16:61747951 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr16:61747951 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:48691252 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:48691252 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:40951284 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:40951284 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:48391709 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:48391709 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:107418312 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:107418312 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:34209261 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:34209261 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:117368344 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:117368344 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:143997372 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:143997372 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:110574029 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:110574029 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:49233758 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:49233758 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:224363385 A>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:224363385 A>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:7680720 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:7680720 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:230377687 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:230377687 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:174870116 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:174870116 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:37311410 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:37311410 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:14757903 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:14757903 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:111412350 A>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:111412350 A>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:92511224 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:92511224 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:62104091 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:62104091 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:171240424 A>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:171240424 A>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:47745921 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:47745921 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:151819908 T>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:151819908 T>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:130094644 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:130094644 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:131285141 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:131285141 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:114142017 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:114142017 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:23353086 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:23353086 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:113540174 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:113540174 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:102785262 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:102785262 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:187531390 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:187531390 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr21:46314874 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr21:46314874 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr15:40708483 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr15:40708483 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:1360234 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:1360234 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:119576566 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:119576566 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:211336643 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:211336643 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:49621341 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:49621341 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:148252279 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:148252279 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:113638686 A>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:113638686 A>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:76376846 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:76376846 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:6581030 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:6581030 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr18:19438632 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr18:19438632 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:43806054 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:43806054 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:21797238 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:21797238 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:233791669 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:233791669 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:176707498 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:176707498 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:248166533 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:248166533 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:195954396 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:195954396 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:2568869 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:2568869 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:110366527 A>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:110366527 A>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:27609005 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:27609005 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:102349971 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:102349971 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:42863217 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:42863217 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:135810137 A>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:135810137 A>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:128483730 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:128483730 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:114403974 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:114403974 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:23374694 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:23374694 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:106310708 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:106310708 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:156024936 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:156024936 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:46326838 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr12:46326838 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr22:40797719 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr22:40797719 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:9912669 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chrX:9912669 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:38633180 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:38633180 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:159839548 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:159839548 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr13:37439591 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr13:37439591 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:156247842 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:156247842 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:52917979 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:52917979 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:158631226 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:158631226 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:130064018 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:130064018 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:8483328 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:8483328 T>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:125477857 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:125477857 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:201926394 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:201926394 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:57888873 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:57888873 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:68844282 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:68844282 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:189013144 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:189013144 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:77502857 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:77502857 G>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:19486802 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:19486802 T>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr15:41188334 T>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr15:41188334 T>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:118491196 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:118491196 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:100013511 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:100013511 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:26497025 C>A maps to ENST00000270812 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:26497025 C>A maps to ENST00000270812 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:58231613 C>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:58231613 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:89414525 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:89414525 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:80640894 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:80640894 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:236900341 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:236900341 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:158390389 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:158390389 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:207406687 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:207406687 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:84488856 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:84488856 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:148680814 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:148680814 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:116056567 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:116056567 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:129265422 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:129265422 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:4771899 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:4771899 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:58247559 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:58247559 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:125928448 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:125928448 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:7950421 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:7950421 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:114176841 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:114176841 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:39479946 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:39479946 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:33386846 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:33386846 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:47430232 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:47430232 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:1547050 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:1547050 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:52511912 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:52511912 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:11039318 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:11039318 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:11039320 A>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:11039320 A>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:152988532 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:152988532 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:41917063 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:41917063 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:112046187 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:112046187 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:129155220 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:129155220 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:17492543 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:17492543 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:22037118 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:22037118 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:134363846 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:134363846 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:220232076 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:220232076 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:30804918 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:30804918 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:247719801 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:247719801 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:20168822 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:20168822 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:63540451 A>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:63540451 A>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:37209864 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:37209864 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:7831886 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:7831886 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:170156935 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:170156935 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:120907142 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:120907142 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:2613702 C>T maps to ENST00000399634 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:2613702 C>T maps to ENST00000399634 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:54483021 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:54483021 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:17556693 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:17556693 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:42691594 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:42691594 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:40951476 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:40951476 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:77247223 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:77247223 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:180334033 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:180334033 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:180334035 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:180334035 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:71058781 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:71058781 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:28538911 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:28538911 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:214825321 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:214825321 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:89705316 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:89705316 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:40052342 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:40052342 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:361384 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:361384 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:383541 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:383541 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:19638183 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:19638183 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:30659769 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:30659769 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:140282156 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:140282156 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:40840011 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:40840011 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:7850812 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:7850812 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:103412356 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:103412356 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:121383261 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:121383261 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:107437602 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:107437602 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:137642616 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:137642616 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:4466395 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:4466395 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:131300383 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:131300383 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:113350061 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:113350061 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:113657233 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:113657233 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:114389116 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:114389116 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:74654300 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:74654300 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:143998688 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:143998688 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:85559527 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:85559527 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:85559529 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:85559529 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24586757 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24586757 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:17805112 T>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:17805112 T>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:155312271 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:155312271 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:14996079 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:14996079 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:31256669 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:31256669 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:42644788 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:42644788 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24113978 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24113978 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:233195494 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:233195494 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:83673917 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:83673917 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:124359396 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:124359396 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:183605155 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:183605155 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:169129280 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:169129280 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:169423009 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:169423009 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:154587603 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:154587603 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:44120232 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:44120232 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:183860959 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:183860959 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:100345067 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:100345067 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:48119240 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:48119240 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:66467234 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:66467234 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:22928026 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:22928026 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:239025449 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:239025449 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:55172503 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:55172503 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:107823181 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:107823181 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:89858870 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:89858870 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:163075856 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:163075856 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:40337036 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:40337036 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:127671644 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:127671644 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:37441717 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:37441717 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:38292019 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:38292019 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:135279253 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:135279253 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:106002684 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:106002684 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:13782495 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:13782495 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:46305704 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:46305704 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:46390488 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:46390488 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:170222177 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:170222177 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:104019668 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:104019668 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:94362394 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:94362394 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:55091858 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:55091858 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:75275088 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:75275088 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:59610072 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:59610072 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:35045634 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:35045634 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:86399529 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:86399529 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:134243834 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:134243834 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:74365169 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:74365169 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:88650565 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:88650565 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:102074078 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:102074078 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:37319109 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:37319109 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:134696093 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:134696093 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:41033001 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:41033001 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:96313837 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:96313837 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:210797061 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:210797061 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:221055719 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:221055719 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:27150308 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:27150308 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:46606821 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:46606821 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:46606838 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:46606838 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:148770680 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:148770680 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:94267792 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:94267792 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:23509546 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:23509546 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:1475017 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:1475017 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:143324295 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:143324295 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:34818809 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:34818809 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:138531203 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:138531203 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:104624006 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:104624006 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:48686769 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:48686769 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:39577328 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:39577328 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:107710340 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:107710340 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:107707064 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:107707064 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:129076970 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:129076970 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:18451591 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:18451591 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:55144404 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:55144404 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:156104511 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:156104511 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:140992520 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:140992520 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:242162357 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:242162357 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:75317067 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:75317067 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:20060443 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:20060443 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:47690548 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:47690548 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:66796015 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:66796015 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:108719562 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:108719562 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:60767807 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:60767807 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:100674616 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:100674616 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:1372986 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:1372986 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:171260753 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:171260753 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:47463533 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:47463533 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:171607973 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:171607973 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:95069720 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:95069720 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:160326672 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:160326672 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:161180317 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:161180317 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:101568462 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:101568462 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:31656884 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:31656884 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:56421915 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:56421915 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:15177201 T>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:15177201 T>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:96109747 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:96109747 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:157182171 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:157182171 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:107866075 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:107866075 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:176709696 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:176709696 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:5603346 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:5603346 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:102337308 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:102337308 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:123556009 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:123556009 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:78399347 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:78399347 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:161976069 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:161976069 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:248247580 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:248247580 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:22332645 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:22332645 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:58275597 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:58275597 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:38271300 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:38271300 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:32059876 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:32059876 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:163735808 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:163735808 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:55104033 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:55104033 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:39669326 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:39669326 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:91715179 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:91715179 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:99605774 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:99605774 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:165806328 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:165806328 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:111672952 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:111672952 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:6371811 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:6371811 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:22210424 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:22210424 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:25144755 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:25144755 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:102054420 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:102054420 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:131948880 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:131948880 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:48463484 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:48463484 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:57877297 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:57877297 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:146070556 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:146070556 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:64693485 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:64693485 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:228004869 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:228004869 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:139218196 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:139218196 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:43698996 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:43698996 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:23738318 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:23738318 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:87622341 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:87622341 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:45527337 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr21:45527337 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:135809940 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:135809940 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:22197544 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:22197544 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:16871022 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:16871022 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:103181057 A>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:103181057 A>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:9804302 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:9804302 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:79314095 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:79314095 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:103322554 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:103322554 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:103417121 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:103417121 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:18457368 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:18457368 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:38176771 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:38176771 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:113334280 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:113334280 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:20185603 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:20185603 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:38942302 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:38942302 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:237753865 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:237753865 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:237982322 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:237982322 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:33765370 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:33765370 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:200137489 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:200137489 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:17771519 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:17771519 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:169559338 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:169559338 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:22019916 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:22019916 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:9859206 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:9859206 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:1538103 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:1538103 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:35313758 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:35313758 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:172693925 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:172693925 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:23425711 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:23425711 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:103038574 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:103038574 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:55729082 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:55729082 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:40388006 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:40388006 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:103125491 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:103125491 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:61297621 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:61297621 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:144903882 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:144903882 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:45741300 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:45741300 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:90650498 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:90650498 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:41008663 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:41008663 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:94794916 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:94794916 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:149512182 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:149512182 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:48054601 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:48054601 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:52673658 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:52673658 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:23751822 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:23751822 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:147588363 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:147588363 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:10898396 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:10898396 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:152577925 T>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:152577925 T>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:150463278 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:150463278 A>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:19168187 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:19168187 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:38046204 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:38046204 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:114823173 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:114823173 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:49844709 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:49844709 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:27212621 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:27212621 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:51737634 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:51737634 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:114294583 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:114294583 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:122840876 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:122840876 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:153539065 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:153539065 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:138197056 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:138197056 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:60028841 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:60028841 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:122078405 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:122078405 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:38320679 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr13:38320679 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:54471044 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chrX:54471044 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:39505957 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:39505957 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:128890557 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:128890557 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:216348556 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:216348556 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:144758659 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:144758659 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:70816777 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:70816777 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:91549583 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:91549583 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:64193150 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:64193150 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:50482552 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:50482552 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:85715977 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:85715977 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:36581183 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:36581183 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:54339909 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:54339909 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:21335383 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:21335383 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:138713294 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:138713294 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:144331921 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:144331921 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:57193646 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:57193646 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:30934360 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:30934360 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:53450 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:53450 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:76063013 A>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:76063013 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:8991100 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:8991100 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:67080516 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:67080516 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:66872910 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:66872910 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:87150194 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:87150194 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:48733379 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:48733379 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:100566522 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:100566522 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:179102294 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:179102294 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:20492069 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:20492069 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:81536857 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:81536857 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:114691786 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:114691786 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8651426 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8651426 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:136290613 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:136290613 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154560581 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154560581 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:76131435 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:76131435 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:244600238 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:244600238 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247079427 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247079427 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:77876658 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:77876658 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:86273624 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:86273624 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:31309833 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:31309833 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:46439358 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:46439358 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:2740398 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:2740398 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:41554115 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:41554115 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:82917010 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:82917010 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:117864799 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:117864799 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:100205876 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:100205876 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:26465280 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:26465280 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:124701205 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:124701205 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:99065267 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:99065267 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:21265356 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:21265356 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:94668649 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:94668649 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:73077011 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:73077011 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:10491256 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:10491256 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:76856369 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:76856369 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:35814568 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:35814568 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:76777596 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:76777596 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:70049173 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:70049173 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:60689652 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:60689652 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51717785 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51717785 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:133784502 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:133784502 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:36938789 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:36938789 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:65936498 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:65936498 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:40590348 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:40590348 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:8950883 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:8950883 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:40846367 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:40846367 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:19586382 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:19586382 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:162825237 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:162825237 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:11015006 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:11015006 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:35240677 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:35240677 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:47581787 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:47581787 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:26672835 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:26672835 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:106688296 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:106688296 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:63667033 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:63667033 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:165706745 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:165706745 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:35754983 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:35754983 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:4074638 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:4074638 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:1037472 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:1037472 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:53777181 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:53777181 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:24372570 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:24372570 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:159163166 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:159163166 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:93055916 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:93055916 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:75587727 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:75587727 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:88958491 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:88958491 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:34325504 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:34325504 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:40831556 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:40831556 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:56125661 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:56125661 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:74502553 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:74502553 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:118222509 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:118222509 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:19506440 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:19506440 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:24535742 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:24535742 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:24493046 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:24493046 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:21854748 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:21854748 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:19473206 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:19473206 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:105662543 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:105662543 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:1635607 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:1635607 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67274735 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67274735 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:14862180 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:14862180 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:21860375 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:21860375 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:136623133 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:136623133 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:10174904 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:10174904 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11657615 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11657615 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:140151269 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:140151269 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:103474109 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:103474109 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:48388309 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:48388309 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:227946779 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:227946779 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:47422708 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:47422708 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:48608498 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:48608498 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:8608443 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:8608443 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:49668343 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:49668343 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:37329054 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:37329054 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:3063022 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:3063022 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:34092194 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:34092194 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:113323146 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:113323146 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:138147833 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:138147833 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:17026056 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:17026056 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:119694493 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:119694493 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:101877295 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:101877295 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:105768192 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:105768192 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:74630853 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:74630853 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:85969468 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:85969468 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:16633472 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:16633472 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:31312425 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:31312425 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:155236878 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:155236878 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:91546751 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:91546751 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:41196623 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:41196623 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:41196753 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:41196753 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:134147114 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:134147114 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:70694185 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:70694185 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:29992945 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:29992945 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:9164866 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:9164866 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:42772546 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:42772546 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:80668655 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:80668655 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:69717028 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:69717028 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:21621704 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:21621704 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:21011876 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:21011876 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13830678 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13830678 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13769342 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13769342 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:196915751 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:196915751 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:38723881 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:38723881 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:38828216 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:38828216 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:31387845 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:31387845 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:154598681 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:154598681 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:31795829 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:31795829 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:28710700 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:28710700 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:41496028 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:41496028 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:32373973 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:32373973 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:68109433 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:68109433 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:348323 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:348323 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:152915421 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:152915421 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:20490381 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:20490381 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:172500074 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:172500074 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38426957 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38426957 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38464231 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38464231 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:55266313 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:55266313 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:140646768 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:140646768 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:141570641 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:141570641 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:233422772 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:233422772 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:8927928 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:8927928 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:120596123 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:120596123 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:131996332 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:131996332 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:25203650 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:25203650 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:16461351 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:16461351 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:220152159 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:220152159 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:51860176 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:51860176 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:56488990 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:56488990 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:14027868 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:14027868 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:148544505 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:148544505 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:88427596 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:88427596 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:53122760 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:53122760 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:91389342 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:91389342 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:91701600 C>A maps to NM_207491.2 Y673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:91701600 C>A maps to NM_207491.2 Y673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:17606054 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:17606054 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:163029271 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:163029271 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:127641187 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:127641187 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:15500767 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:15500767 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:16578685 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:16578685 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:157772116 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:157772116 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161682098 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161682098 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:124982198 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:124982198 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:125076834 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:125076834 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:128480744 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:128480744 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:240637373 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:240637373 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:47753977 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:47753977 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:89424366 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:89424366 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:118159 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:118159 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:69225534 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:69225534 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:197483437 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:197483437 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:29541911 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:29541911 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:69787323 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:69787323 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:8100176 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:8100176 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:175649604 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:175649604 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:102153963 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:102153963 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:100559805 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:100559805 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:46117354 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:46117354 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:123468505 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:123468505 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:7456634 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:7456634 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:27480912 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:27480912 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:105259272 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:105259272 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:119929519 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:119929519 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39883480 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39883480 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39883484 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39883484 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:5254361 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:5254361 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:30672123 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:30672123 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:50685207 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:50685207 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:197208502 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:197208502 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:92825040 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:92825040 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:89326273 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:89326273 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:123342999 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:123342999 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:75216182 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:75216182 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:149783927 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:149783927 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:148786163 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:148786163 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:148786165 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:148786165 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:43852732 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:43852732 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:33172419 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:33172419 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:114010326 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:114010326 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:114141130 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:114141130 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:148564240 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:148564240 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30712022 G>A maps to ENST00000376377 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30712022 G>A maps to ENST00000376377 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:1621552 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:1621552 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:117142549 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:117142549 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:159710927 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:159710927 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:114250205 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:114250205 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62414464 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62414464 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:59972625 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:59972625 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:91019794 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:91019794 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:50689500 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:50689500 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:173362652 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:173362652 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:160853357 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:160853357 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:160920526 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:160920526 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:160920802 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:160920802 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:6083538 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:6083538 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:112329756 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:112329756 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:211192664 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:211192664 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:40312478 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:40312478 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:233807330 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:233807330 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67013642 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67013642 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:66999630 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:66999630 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:58988697 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:58988697 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:2606842 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:2606842 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:94121823 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:94121823 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:36853999 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:36853999 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:16486937 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:16486937 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:57963979 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:57963979 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:202880883 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:202880883 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:18775280 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:18775280 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:136969566 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:136969566 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:53201957 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:53201957 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:134362142 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:134362142 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:153137515 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:153137515 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:209790948 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:209790948 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:154179118 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:154179118 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:156695346 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:156695346 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38506579 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38506579 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:54804217 G>T maps to ENST00000391745 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:54804217 G>T maps to ENST00000391745 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:83891404 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:83891404 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:90488428 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:90488428 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:28130362 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:28130362 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:197547130 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:197547130 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:141441413 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:141441413 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:238643908 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:238643908 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:24936088 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:24936088 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:235887232 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:235887232 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:235887273 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:235887273 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:39917737 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:39917737 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:148794992 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:148794992 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:151896286 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:151896286 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:151283260 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:151283260 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:184428504 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:184428504 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:43343869 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:43343869 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:156281610 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:156281610 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:220777582 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:220777582 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:47690549 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:47690549 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:90494669 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:90494669 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:150932192 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:150932192 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:3294342 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:3294342 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:3299058 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:3299058 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:88767709 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:88767709 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:141754726 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:141754726 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:47040509 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:47040509 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:49438781 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:49438781 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:220928189 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:220928189 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161275779 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161275779 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:149908141 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:149908141 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8994388 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8994388 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:42813964 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:42813964 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:10227214 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:10227214 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:23886039 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:23886039 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:2685514 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:2685514 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:2040075 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:2040075 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:22652834 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:22652834 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:21129658 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:21129658 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:72241784 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:72241784 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:25470474 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:25470474 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247593143 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247593143 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:56477760 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:56477760 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:169256499 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:169256499 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:117701879 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:117701879 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:26084399 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:26084399 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:26116033 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:26116033 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:79535907 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:79535907 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:64428201 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:64428201 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:79454564 G>T maps to ENST00000330071 G876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:79454564 G>T maps to ENST00000330071 G876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:6620480 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:6620480 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:229593882 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:229593882 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:13363376 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:13363376 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62572865 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62572865 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:101092984 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:101092984 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:57619577 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:57619577 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:98113279 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:98113279 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:248112029 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:248112029 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:22383457 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:22383457 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:48920323 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:48920323 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:21737814 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:21737814 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:29597297 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:29597297 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:17699491 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:17699491 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:49453916 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:49453916 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150769947 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150769947 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:91369117 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:91369117 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:142542290 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:142542290 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:31918500 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:31918500 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:149301323 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:149301323 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:19375861 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:19375861 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:95578762 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:95578762 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:56757263 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:56757263 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:6258250 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:6258250 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:21096391 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:21096391 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:18691059 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:18691059 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:28315194 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:28315194 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:110498868 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:110498868 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:8720983 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:8720983 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:64033750 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:64033750 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:204217932 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:204217932 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:143042 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:143042 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:49030875 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:49030875 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:131859696 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:131859696 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154897564 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154897564 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:86255229 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:86255229 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:113322138 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:113322138 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:131975930 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:131975930 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:31133065 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:31133065 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:56976844 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:56976844 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:242109377 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:242109377 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:23521303 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:23521303 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11552356 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11552356 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:48710724 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:48710724 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:12837809 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:12837809 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:73653715 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:73653715 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:43519185 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:43519185 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:43520061 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:43520061 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:38153668 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:38153668 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:20356403 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:20356403 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:87683876 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:87683876 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:18754991 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:18754991 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:8483986 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:8483986 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:55709992 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:55709992 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:8085887 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr18:8085887 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:112138327 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:112138327 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:52336294 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:52336294 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:9316941 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:9316941 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:153954986 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:153954986 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:125832754 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:125832754 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:17707008 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:17707008 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:17282876 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:17282876 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:36059963 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:36059963 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:79384694 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:79384694 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:103270651 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:103270651 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11526553 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:11526553 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:116270672 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:116270672 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:241094092 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:241094092 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:63507851 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:63507851 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:12940504 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:12940504 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:45515071 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:45515071 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:237886376 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:237886376 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:33928775 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:33928775 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:20786211 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:20786211 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:129812123 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:129812123 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:38750952 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:38750952 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:62045264 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:62045264 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:177906304 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:177906304 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:101814918 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:101814918 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:153958134 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:153958134 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:41086394 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:41086394 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:100457736 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:100457736 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:45195113 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:45195113 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:119012997 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:119012997 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:35287029 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:35287029 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:104412573 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:104412573 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:56630711 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:56630711 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:19470343 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:19470343 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:3208895 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:3208895 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:72319138 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:72319138 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51864384 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51864384 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:110734897 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:110734897 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:44482673 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:44482673 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:47940831 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:47940831 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:72764253 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:72764253 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:61299284 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:61299284 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:45795280 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:45795280 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:214478427 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:214478427 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:127498047 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:127498047 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:82720635 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:82720635 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:106976591 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:106976591 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:24697411 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:24697411 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:172766663 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:172766663 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:35498243 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:35498243 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:48218287 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:48218287 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:48218827 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:48218827 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:8715637 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:8715637 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:52550344 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:52550344 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:123200292 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:123200292 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:58456601 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:58456601 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:66811070 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:66811070 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:61291200 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:61291200 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:39811495 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:39811495 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:97362150 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:97362150 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:120843890 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:120843890 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:139657364 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:139657364 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:139657367 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:139657367 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:54934577 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:54934577 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:43805812 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:43805812 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:164392982 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:164392982 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:126068668 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:126068668 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:5763372 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:5763372 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:19737656 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:19737656 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:40711594 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr22:40711594 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:144364956 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:144364956 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:20024536 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:20024536 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:10998440 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr21:10998440 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:17204259 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:17204259 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:118532289 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:118532289 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:41168761 G>A maps to ENST00000373108 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:41168761 G>A maps to ENST00000373108 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:18631142 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:18631142 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:64887113 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:64887113 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:28876884 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:28876884 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:38225609 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:38225609 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:3417123 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:3417123 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:110232362 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:110232362 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:15187036 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:15187036 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:100008237 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr13:100008237 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:42290099 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:42290099 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:59339009 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:59339009 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:128935269 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:128935269 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:234675588 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:234675588 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:69512759 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:69512759 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:70155481 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:70155481 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:34827439 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:34827439 A>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:17720620 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:17720620 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:17758069 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:17758069 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:17777333 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:17777333 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:74513437 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:74513437 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:126201092 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:126201092 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:216405188 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:216405188 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:216500899 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:216500899 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30889122 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30889122 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:46025594 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:46025594 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:36943671 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:36943671 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150572048 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:150572048 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:133015074 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:133015074 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:51451365 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:51451365 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:122723068 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:122723068 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:38805347 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:38805347 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:122396789 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:122396789 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:44417429 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:44417429 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:6012864 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:6012864 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:168511124 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:168511124 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:17294296 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:17294296 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:100383909 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:100383909 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:111624719 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:111624719 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:99214672 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:99214672 A>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:50713849 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:50713849 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:50776544 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:50776544 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:57646223 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:57646223 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:140483036 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:140483036 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:47862054 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:47862054 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:24288562 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:24288562 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:129362945 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chrX:129362945 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:25667059 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:25667059 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:57883007 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:57883007 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:47886334 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:47886334 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:238051536 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:238051536 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:66978849 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:66978849 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:169830480 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:169830480 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:148586545 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:148586545 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:76190402 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:76190402 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:155028997 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:155028997 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:79080465 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:79080465 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:131964279 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:131964279 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:50307913 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:50307913 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:77984489 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:77984489 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:96890212 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:96890212 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:137801496 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:137801496 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:125850119 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:125850119 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41513274 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41513274 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41522545 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41522545 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:43133198 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:43133198 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:99898149 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:99898149 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:26353815 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:26353815 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:101368502 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:101368502 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:36109389 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:36109389 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:24885533 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:24885533 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:145759398 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:145759398 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:58830858 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:58830858 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:27554137 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:27554137 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:26839047 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:26839047 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:119737473 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:119737473 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:119943141 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:119943141 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:96779352 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:96779352 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:216200871 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:216200871 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:138882099 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:138882099 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:25276227 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:25276227 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:194180296 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:194180296 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:160105514 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:160105514 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:50244026 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:50244026 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:61867932 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:61867932 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:7861998 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:7861998 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:137475930 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:137475930 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:886954 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:886954 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55814999 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55814999 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:15713579 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:15713579 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:107937683 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:107937683 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:81289165 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:81289165 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:32905797 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:32905797 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:45502608 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:45502608 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:200876862 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:200876862 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:18365243 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:18365243 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:31683108 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:31683108 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:742591 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:742591 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:50598512 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:50598512 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:98762099 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:98762099 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:41172183 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:41172183 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:32293212 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:32293212 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:127804196 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:127804196 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:39073160 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:39073160 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:39073604 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:39073604 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:181759780 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:181759780 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:1262142 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:1262142 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:7331417 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:7331417 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:71406161 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:71406161 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:3040125 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:3040125 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:26597676 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:26597676 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:86120477 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:86120477 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:78081780 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:78081780 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:158325066 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:158325066 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:207941318 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:207941318 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:89245760 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:89245760 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:62544402 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:62544402 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:117265969 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:117265969 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:13068239 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:13068239 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:55893435 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:55893435 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:49548726 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:49548726 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:6194766 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:6194766 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:443199 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:443199 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:109937384 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:109937384 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:87672172 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:87672172 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:87673462 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:87673462 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:100095307 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:100095307 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:99690517 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:99690517 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:125547728 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:125547728 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:51111473 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:51111473 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:103428161 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:103428161 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:139767983 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:139767983 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:86488362 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:86488362 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:86590522 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:86590522 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:71012453 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:71012453 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:14488033 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:14488033 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:83989539 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:83989539 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:19079216 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:19079216 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:129986301 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:129986301 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:83221440 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:83221440 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:27576292 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:27576292 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:61988469 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:61988469 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:2799908 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:2799908 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:113678691 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:113678691 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:23545529 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:23545529 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:80782800 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:80782800 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:80782802 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:80782802 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:80831171 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:80831171 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:41442195 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:41442195 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:99283003 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:99283003 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:37695372 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:37695372 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:124329405 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:124329405 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:39381741 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:39381741 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:14996038 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:14996038 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:23669724 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:23669724 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:169157527 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:169157527 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:31630900 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:31630900 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:14741225 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:14741225 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:55340689 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:55340689 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:55349178 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:55349178 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:24577852 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:24577852 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:96603404 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:96603404 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:108124791 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:108124791 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:7111627 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:7111627 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:101193397 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:101193397 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:170597273 C>A maps to ENST00000406743 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:170597273 C>A maps to ENST00000406743 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:124339027 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:124339027 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:32509376 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:32509376 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:13735210 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:13735210 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:40152591 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:40152591 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:220247995 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:220247995 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:129179650 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:129179650 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:169145633 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:169145633 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:51274917 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:51274917 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:25220530 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:25220530 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:65799564 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:65799564 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:29038922 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:29038922 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:56496635 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:56496635 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:348319 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:348319 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:172533349 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:172533349 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:52374284 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:52374284 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:42953217 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:42953217 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:37917400 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:37917400 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:23297537 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:23297537 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:132537777 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:132537777 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:120831671 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:120831671 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:134968457 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:134968457 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:184293536 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:184293536 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:15777427 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:15777427 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:56482200 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:56482200 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:76552820 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:76552820 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:29695513 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:29695513 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:57684696 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:57684696 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:45633569 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:45633569 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:184764062 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:184764062 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:150391734 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:150391734 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:150396373 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:150396373 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:116779689 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:116779689 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:28086025 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:28086025 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:37093350 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:37093350 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:161641115 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:161641115 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:161565512 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:161565512 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:157567642 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:157567642 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:14949223 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:14949223 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:33014219 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:33014219 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:28891567 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:28891567 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:147062921 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:147062921 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:65510870 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:65510870 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:46967349 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:46967349 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:46995297 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:46995297 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:161578769 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:161578769 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:27586106 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:27586106 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:88884551 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:88884551 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:155265414 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:155265414 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:11292686 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:11292686 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:173873451 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:173873451 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:9822885 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:9822885 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:8111627 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:8111627 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:42465876 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:42465876 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:151228576 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:151228576 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:129428904 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:129428904 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:36229166 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:36229166 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:47678423 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:47678423 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:46856258 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:46856258 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:142689053 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:142689053 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:46931702 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:46931702 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:153174097 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:153174097 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:94316705 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:94316705 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:34007947 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:34007947 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:48949790 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:48949790 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:90001555 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:90001555 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:145038114 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:145038114 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:35775623 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:35775623 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:5573266 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:5573266 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:41049339 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:41049339 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:41054946 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:41054946 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:28441802 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:28441802 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:33369368 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:33369368 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:71136583 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:71136583 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:32628031 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:32628031 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:186143520 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:186143520 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:176973883 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:176973883 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:209879977 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:209879977 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:113854040 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:113854040 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:147862720 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:147862720 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:129231103 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:129231103 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:23391221 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:23391221 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:62228507 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:62228507 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:15198782 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:15198782 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:155094328 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:155094328 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:156813051 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:156813051 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:156814473 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:156814473 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:28654035 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:28654035 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:61780111 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:61780111 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:30843421 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:30843421 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:74961493 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:74961493 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:31427737 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:31427737 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:52854231 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:52854231 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:7614395 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:7614395 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:156645114 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:156645114 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:155893914 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:155893914 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:63416747 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:63416747 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:196205251 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:196205251 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:18213690 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:18213690 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:7046739 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:7046739 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:85106427 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:85106427 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:43447438 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:43447438 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:44872271 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:44872271 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57975156 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57975156 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55348940 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55348940 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55377918 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55377918 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:38905688 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:38905688 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:53223984 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:53223984 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:153138763 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:153138763 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:130407512 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:130407512 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:6997909 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:6997909 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:107745143 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:107745143 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:133911831 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:133911831 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:37074821 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:37074821 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:36975116 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:36975116 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:226128566 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:226128566 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:65609843 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:65609843 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:18394646 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:18394646 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:202276366 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:202276366 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:124976225 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:124976225 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:126161930 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:126161930 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:5711730 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:5711730 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57573928 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57573928 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:70385234 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:70385234 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:135635327 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:135635327 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:160711127 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:160711127 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:14474028 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:14474028 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:47310709 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:47310709 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:151899633 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:151899633 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:27830893 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:27830893 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:140993019 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:140993019 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:65344699 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:65344699 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:6588586 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:6588586 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:138724575 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:138724575 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:47664608 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:47664608 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:47311066 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:47311066 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:86208987 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:86208987 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:29557501 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:29557501 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:6378630 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:6378630 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:151879741 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:151879741 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:21913675 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:21913675 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:102595372 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:102595372 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:60561424 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:60561424 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:56667402 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:56667402 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:17512182 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:17512182 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:100692508 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:100692508 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:42338472 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:42338472 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10214670 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10214670 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10405997 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10405997 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10303543 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10303543 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:76877214 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:76877214 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:144657543 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:144657543 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:106509344 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:106509344 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:54926116 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:54926116 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:21499134 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:21499134 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:178262518 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:178262518 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:70450861 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:70450861 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:236187255 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:236187255 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:173322895 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:173322895 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55485749 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55485749 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:162335085 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:162335085 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:35802001 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:35802001 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:32463064 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:32463064 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:37358075 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:37358075 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:25914356 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:25914356 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:113403518 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:113403518 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:136082502 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:136082502 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:198313 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:198313 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:123838772 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:123838772 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:50953833 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:50953833 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:50964733 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:50964733 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:161967509 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:161967509 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55578926 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55578926 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:6815837 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:6815837 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:123814677 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:123814677 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55927900 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55927900 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:59367844 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:59367844 A>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:57270898 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:57270898 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:7716477 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:7716477 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:17555381 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:17555381 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:39589041 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:39589041 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:30732250 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:30732250 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:144873861 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:144873861 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:149294397 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:149294397 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:57329083 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:57329083 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:57358363 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:57358363 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:169824770 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:169824770 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:47694795 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:47694795 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:138477996 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:138477996 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:99956739 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:99956739 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:3646196 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:3646196 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:22163626 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:22163626 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:102059576 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:102059576 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:8352141 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:8352141 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:242540232 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:242540232 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:131950928 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:131950928 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:161173109 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:161173109 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:131817986 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:131817986 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:131870228 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:131870228 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:129290328 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:129290328 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:118315064 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:118315064 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:140354832 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:140354832 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:95045524 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:95045524 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:81762870 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:81762870 T>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:6325018 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:6325018 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:32123763 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:32123763 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:19644152 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:19644152 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:90142070 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:90142070 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:23509788 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:23509788 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:47258889 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:47258889 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:68982125 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:68982125 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:69039670 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:69039670 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:23393093 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:23393093 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:16002288 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:16002288 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:43348409 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:43348409 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:43520298 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:43520298 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:43570569 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:43570569 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:1107880 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:1107880 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:18750444 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:18750444 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:8389502 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:8389502 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:20478657 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:20478657 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:64525992 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:64525992 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:113804842 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:113804842 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:173882135 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:173882135 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:85615294 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:85615294 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:80382848 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:80382848 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:29938769 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:29938769 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:79385696 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:79385696 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:103137240 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:103137240 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:8715956 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:8715956 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:33348333 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:33348333 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:323725 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:323725 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:163042540 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:163042540 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:25620790 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:25620790 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:42878236 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:42878236 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:13949727 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:13949727 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:77614095 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:77614095 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:10461537 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:10461537 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:60789855 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:60789855 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:1440273 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:1440273 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:152129478 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:152129478 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:152129522 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:152129522 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:67754007 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:67754007 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:39052105 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:39052105 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237713805 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237713805 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:34048485 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:34048485 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:128926952 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:128926952 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:166856102 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:166856102 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:62018119 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:62018119 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:29966030 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:29966030 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:55912166 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:55912166 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:61562468 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:61562468 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:26702164 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:26702164 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:23821264 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:23821264 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:134618432 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:134618432 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:41088240 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:41088240 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:132160213 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:132160213 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:117057127 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:117057127 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:52034326 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:52034326 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:1457826 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:1457826 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:1615853 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:1615853 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:6606241 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:6606241 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:43319050 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:43319050 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:63078463 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:63078463 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:160664592 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:160664592 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:92900348 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:92900348 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:8428027 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:8428027 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:74535260 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:74535260 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:121726755 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:121726755 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:96949249 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:96949249 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:50711508 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:50711508 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:108366901 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:108366901 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:121340567 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:121340567 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:121448145 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:121448145 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:231193448 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:231193448 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:22678011 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:22678011 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:147594418 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:147594418 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:139326392 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:139326392 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:65241819 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:65241819 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:133524672 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:133524672 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:2210385 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:2210385 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:44284488 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:44284488 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:104099534 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:104099534 A>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:46331178 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:46331178 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:46365748 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:46365748 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:48065432 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:48065432 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:10958966 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:10958966 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:70613119 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:70613119 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:47685324 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:47685324 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:28889958 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:28889958 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:59485333 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:59485333 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:96152718 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:96152718 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:195785606 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:195785606 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:133973080 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:133973080 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:56816455 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:56816455 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:19375399 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:19375399 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:226041530 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:226041530 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:205053466 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:205053466 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:68810100 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:68810100 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:175324530 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:175324530 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:47453484 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:47453484 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:60031373 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:60031373 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:80954839 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:80954839 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:10909547 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:10909547 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:10971815 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:10971815 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:202249025 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:202249025 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:72969364 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:72969364 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:5798751 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:5798751 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:5877949 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:5877949 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:85413593 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:85413593 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:91060069 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:91060069 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179490202 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179490202 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179535936 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179535936 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179595956 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179595956 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:44193197 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:44193197 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:133712230 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:133712230 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:156974682 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:156974682 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:170933696 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:170933696 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:136533786 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:136533786 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:234663864 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:234663864 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:234621631 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:234621631 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:30415996 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr21:30415996 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:61697884 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:61697884 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:155169494 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:155169494 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:108116041 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:108116041 A>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:77901514 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:77901514 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:52990247 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr13:52990247 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:65242610 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chrX:65242610 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:124012204 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:124012204 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:85729686 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:85729686 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:9497414 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:9497414 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:38172083 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:38172083 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:6021526 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:6021526 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:27418996 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:27418996 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:44469354 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:44469354 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:64414706 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:64414706 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:74364977 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:74364977 G>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:95818311 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:95818311 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:2823001 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:2823001 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:40523249 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:40523249 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:23941407 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:23941407 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:7645405 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:7645405 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:153006226 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:153006226 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:148616888 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:148616888 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:20557511 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:20557511 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:156957807 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:156957807 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:24181280 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:24181280 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:131812890 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:131812890 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:147919117 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:147919117 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr14:96954782 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr14:96954782 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:112054470 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:112054470 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:114290995 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:114290995 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:4751200 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:4751200 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:193272692 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:193272692 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:42482024 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:42482024 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:31619605 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:31619605 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:33589603 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:33589603 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:50212177 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:50212177 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:86386659 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:86386659 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:1950118 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:1950118 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:44144255 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:44144255 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:19683281 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:19683281 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:57546616 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:57546616 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:26581648 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:26581648 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:64117012 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:64117012 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:158301089 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:158301089 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:8692340 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:8692340 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:140265315 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:140265315 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:99931799 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:99931799 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:75848104 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:75848104 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:61938805 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:61938805 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:77155037 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:77155037 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:3046572 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:3046572 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:64081462 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:64081462 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:85949914 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:85949914 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:16646787 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:16646787 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:104439294 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:104439294 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:169348573 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:169348573 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:12791236 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:12791236 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:68012575 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:68012575 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:63976136 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:63976136 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:207583006 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:207583006 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:65359396 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:65359396 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:101386441 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:101386441 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:56492211 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:56492211 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:191861712 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:191861712 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:48512056 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:48512056 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:46976149 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:46976149 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:89979016 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:89979016 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:907491 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:907491 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:156533575 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:156533575 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:153214720 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:153214720 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:50534447 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:50534447 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:3449366 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:3449366 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:26240190 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:26240190 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:314372 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:314372 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:23381815 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:23381815 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:31482157 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:31482157 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:17954484 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:17954484 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:142650764 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:142650764 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:53518837 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:53518837 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:136957873 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:136957873 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:54870254 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:54870254 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:25143445 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:25143445 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:169677663 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:169677663 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:148008505 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:148008505 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:133623534 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:133623534 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:15480555 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:15480555 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr22:42190312 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr22:42190312 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:32157105 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:32157105 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:28349810 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:28349810 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:108746501 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:108746501 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:59863193 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:59863193 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:1091578 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:1091578 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:81101443 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:81101443 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:16699742 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:16699742 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:16890852 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:16890852 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:16891941 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:16891941 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:56463812 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:56463812 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:139232195 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr5:139232195 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:51056659 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:51056659 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:106396370 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:106396370 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:174946517 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:174946517 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:127255615 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:127255615 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:93038128 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:93038128 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:144881003 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:144881003 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:15198523 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:15198523 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:33984174 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:33984174 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:33794404 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:33794404 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:8626923 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:8626923 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:96081829 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:96081829 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:131949242 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:131949242 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:103044227 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:103044227 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:103045418 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:103045418 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr14:19571462 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr14:19571462 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:52871233 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:52871233 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:31161492 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:31161492 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:237177 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:237177 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:27289031 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:27289031 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr9:96859540 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr9:96859540 T>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:112915394 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:112915394 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:48153034 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:48153034 C>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:65427295 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:65427295 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:144463541 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:144463541 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:109779252 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:109779252 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr14:81953968 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr14:81953968 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:167508123 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:167508123 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:70599478 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:70599478 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:95838115 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:95838115 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:88210863 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:88210863 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:75901824 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:75901824 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:107022017 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:107022017 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:134925507 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:134925507 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:152770831 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:152770831 A>G did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:133473594 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr3:133473594 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:103216788 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:103216788 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:93621997 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr10:93621997 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710458 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710458 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710674 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710674 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710972 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710972 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113711028 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113711028 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113711153 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113711153 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715183 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715183 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715248 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715248 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715289 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715289 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715969 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715969 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113717795 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113717795 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113718055 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113718055 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113722336 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113722336 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113728669 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113728669 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113728732 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113728732 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113728835 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113728835 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113729531 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113729531 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113729840 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113729840 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:72338006 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:72338006 A>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:108303376 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:108303376 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:128879332 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chrX:128879332 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr13:21374919 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr13:21374919 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:138768511 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:138768511 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:57176831 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:57176831 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:21211213 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr16:21211213 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:20685241 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:20685241 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:22048278 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:22048278 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:47329298 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:47329298 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:76199394 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:76199394 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:7125018 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:7125018 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:40062973 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:40062973 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:43846308 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:43846308 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:88015983 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:88015983 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:32150195 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:32150195 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:159042885 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:159042885 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:40746076 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:40746076 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:74280742 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:74280742 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:112220791 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:112220791 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:41552590 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:41552590 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:99119406 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:99119406 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:142292637 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:142292637 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:18021630 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:18021630 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:106534677 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:106534677 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:98957387 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:98957387 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:35785938 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:35785938 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:3920810 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:3920810 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:161735995 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:161735995 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:193159246 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:193159246 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:141595802 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:141595802 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:58196974 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:58196974 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:32801144 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:32801144 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:48260220 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:48260220 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:33644701 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:33644701 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:136588434 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:136588434 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:12864191 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:12864191 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:3119648 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:3119648 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:137500374 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:137500374 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:137504141 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:137504141 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:15717003 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:15717003 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:111368193 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:111368193 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:62439410 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:62439410 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:45928089 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:45928089 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:60574883 A>G maps to ENST00000404681 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:60574883 A>G maps to ENST00000404681 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:54892155 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:54892155 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:45601974 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:45601974 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:26998290 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:26998290 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:75929267 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:75929267 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:57839898 T>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:57839898 T>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:184618733 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:184618733 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:48544821 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:48544821 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:181763973 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:181763973 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:181763982 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:181763982 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:201042470 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:201042470 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:185593714 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:185593714 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:179702563 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:179702563 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:120510307 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:120510307 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:7635026 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:7635026 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:158262685 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:158262685 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:100933492 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:100933492 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:176016286 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:176016286 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:50824673 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:50824673 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:113346492 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:113346492 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:6166854 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:6166854 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:203154230 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:203154230 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:1507246 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:1507246 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:86313299 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:86313299 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:107431040 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:107431040 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:61454066 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:61454066 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:68535135 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:68535135 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:172379250 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:172379250 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:100756626 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:100756626 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:100696223 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:100696223 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:154001097 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:154001097 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:182847132 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:182847132 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:1617976 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:1617976 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:118507007 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:118507007 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:124420113 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:124420113 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:52396947 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:52396947 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:38917468 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:38917468 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:31369093 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:31369093 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:98092433 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:98092433 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:311896 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:311896 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:99462606 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:99462606 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:2222271 C>G maps to ENST00000221482 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:2222271 C>G maps to ENST00000221482 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:101487057 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:101487057 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:146804534 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:146804534 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:118183673 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:118183673 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:45403018 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:45403018 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:44107531 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:44107531 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:82431295 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:82431295 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:82523148 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:82523148 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:55218935 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:55218935 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:110914578 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:110914578 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:27587540 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:27587540 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:2403185 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:2403185 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:107506564 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:107506564 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:120580407 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:120580407 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:103499567 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:103499567 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:138178913 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:138178913 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:57618939 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:57618939 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:130294102 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:130294102 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:71238216 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:71238216 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:67578374 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:67578374 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:41043609 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:41043609 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:124989636 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:124989636 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:155491524 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:155491524 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:65652290 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:65652290 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:27210260 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:27210260 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:14306197 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:14306197 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:33180499 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:33180499 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:240306963 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:240306963 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:71927838 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:71927838 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:71927868 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:71927868 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:13782363 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:13782363 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:49191146 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:49191146 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:31058695 T>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:31058695 T>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:161575991 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:161575991 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:4881568 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:4881568 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:89598914 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:89598914 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:56868558 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:56868558 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:150620740 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:150620740 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:155754958 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:155754958 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:156566152 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:156566152 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:34101350 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:34101350 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:65440960 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:65440960 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:153221007 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:153221007 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:63953891 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:63953891 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:72649044 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:72649044 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:29974803 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:29974803 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:29974844 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:29974844 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:173473738 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:173473738 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:46607301 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:46607301 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:72107646 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:72107646 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:21231576 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:21231576 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:155232526 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:155232526 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:108957817 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:108957817 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:20189998 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:20189998 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:149954191 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:149954191 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:63246420 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:63246420 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:137760120 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:137760120 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:94110087 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:94110087 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:20992648 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:20992648 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:103663207 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:103663207 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:51325132 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:51325132 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:38935926 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:38935926 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:124988801 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:124988801 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:176764568 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:176764568 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:141609090 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:141609090 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:160755638 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:160755638 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:103672873 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:103672873 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:19416228 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:19416228 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:1816174 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:1816174 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:90397930 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:90397930 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:876966 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:876966 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:38320659 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:38320659 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:67442270 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:67442270 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:37732123 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:37732123 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:37732148 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:37732148 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:14937714 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:14937714 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:21862071 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:21862071 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:151206707 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:151206707 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:95598700 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:95598700 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:17163500 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:17163500 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:66844581 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:66844581 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:5075344 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:5075344 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:140402884 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:140402884 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:178272774 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:178272774 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:3462610 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:3462610 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:103822510 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:103822510 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:23012193 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:23012193 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:43666707 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:43666707 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:206562453 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:206562453 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:50318355 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:50318355 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:106460500 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:106460500 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:6890840 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:6890840 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:69482632 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:69482632 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:21819436 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:21819436 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:26695303 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:26695303 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:29644223 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:29644223 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:28841073 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:28841073 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:34408533 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:34408533 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:122274115 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:122274115 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:134111322 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:134111322 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:55755363 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:55755363 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:54250186 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:54250186 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:44037279 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:44037279 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:42932420 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:42932420 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:16220082 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:16220082 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:28310286 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:28310286 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:6441253 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:6441253 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:51609086 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:51609086 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:131481806 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:131481806 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:201289378 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:201289378 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:7889709 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:7889709 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:65063280 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:65063280 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:70222739 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:70222739 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:7586646 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:7586646 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:68414351 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:68414351 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:84234491 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:84234491 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:40486422 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:40486422 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:136912955 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:136912955 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:45375437 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:45375437 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:51401739 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:51401739 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:10817972 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:10817972 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:178753527 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:178753527 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:33149484 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:33149484 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:65043728 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:65043728 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:35899011 G>T maps to NM_203418.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:35899011 G>T maps to NM_203418.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:18406125 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:18406125 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:31588712 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:31588712 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:35826747 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:35826747 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:35833323 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:35833323 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:20174429 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:20174429 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:67741267 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:67741267 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:67760095 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:67760095 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:15858200 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:15858200 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:65824203 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:65824203 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:4363689 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:4363689 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:72116923 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:72116923 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:92911585 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:92911585 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:45560622 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:45560622 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:140128233 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:140128233 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:234458685 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:234458685 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:220504184 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:220504184 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:70617195 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:70617195 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:21762042 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:21762042 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:90743276 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:90743276 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:78197249 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:78197249 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:16208589 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:16208589 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:22700123 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:22700123 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:12454313 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:12454313 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:158612434 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:158612434 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:131346540 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:131346540 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:64437357 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:64437357 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:149495085 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:149495085 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:104157461 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:104157461 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:99784021 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:99784021 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:4112436 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:4112436 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:63971612 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:63971612 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:48822501 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:48822501 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:37152176 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:37152176 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:125475491 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:125475491 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:104332782 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:104332782 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:138347762 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:138347762 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:13011063 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:13011063 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:158499458 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:158499458 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:77394947 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chrX:77394947 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:13306610 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:13306610 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:72987587 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:72987587 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:2024477 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:2024477 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:106729379 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:106729379 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:151742813 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:151742813 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:20850611 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:20850611 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:169640511 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:169640511 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:63045833 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:63045833 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:40717279 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:40717279 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:102272952 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:102272952 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:43810004 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:43810004 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:201386166 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:201386166 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:43771444 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:43771444 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:44006894 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr20:44006894 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:211546059 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:211546059 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:57134137 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:57134137 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:230667267 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:230667267 A>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:81448668 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:81448668 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:39153854 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:39153854 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:117634430 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:117634430 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:179585067 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:179585067 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:22862930 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:22862930 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:3048412 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:3048412 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:9337425 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:9337425 A>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:19421527 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:19421527 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:18963775 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:18963775 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:35066894 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:35066894 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:12333221 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:12333221 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:86732843 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:86732843 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:190313060 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:190313060 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:184240641 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:184240641 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:168549443 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:168549443 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:54344401 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:54344401 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:100386736 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:100386736 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:73437566 A>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:73437566 A>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:6953445 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:6953445 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:58301566 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:58301566 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:78041913 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:78041913 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:7743286 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:7743286 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:67283903 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:67283903 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:44065836 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:44065836 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:100568828 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:100568828 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:134131326 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:134131326 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:61566522 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:61566522 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:132086441 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:132086441 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:20565073 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:20565073 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:69354645 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:69354645 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:39089467 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:39089467 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:33637670 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:33637670 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:33662169 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:33662169 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:5200459 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:5200459 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:128956598 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:128956598 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:28302122 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:28302122 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:7804848 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:7804848 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:112106585 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:112106585 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:31539548 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:31539548 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:6054706 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:6054706 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:77763164 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:77763164 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:5041213 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:5041213 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:5248375 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:5248375 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:105268884 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:105268884 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49967300 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49967300 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:125831600 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:125831600 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:112222999 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:112222999 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:8438540 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:8438540 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:14798274 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:14798274 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:69390953 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:69390953 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:33110133 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:33110133 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:37453987 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:37453987 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:82917012 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:82917012 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:75156235 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:75156235 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:49662076 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:49662076 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:120329010 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:120329010 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:28151319 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:28151319 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:150801767 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:150801767 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:100978895 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:100978895 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:62430584 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:62430584 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:197055853 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:197055853 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:124373908 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:124373908 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160105557 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160105557 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:28893744 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:28893744 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:32969822 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:32969822 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:161142000 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:161142000 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:171492686 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:171492686 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:22494502 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:22494502 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:16744380 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:16744380 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:111750181 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:111750181 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55670877 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55670877 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:31652243 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:31652243 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:121966791 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:121966791 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:165713991 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:165713991 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:165714098 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:165714098 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:88125317 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:88125317 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:170160107 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:170160107 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:120906572 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:120906572 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:89897596 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:89897596 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:103213256 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:103213256 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:77692295 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:77692295 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:227153531 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:227153531 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:140968191 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:140968191 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:40059638 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:40059638 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:62450995 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:62450995 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:209779579 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:209779579 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:48733992 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:48733992 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:130898050 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:130898050 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:118753762 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:118753762 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:2499028 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:2499028 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:74512934 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:74512934 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:135741114 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:135741114 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:24498414 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:24498414 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:44869575 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:44869575 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:48680561 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:48680561 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:50854759 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:50854759 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:51019829 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:51019829 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:45671150 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:45671150 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:46806336 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:46806336 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:40225730 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:40225730 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:155233696 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:155233696 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:98996630 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:98996630 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:146997224 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:146997224 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:125671578 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:125671578 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:101759434 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:101759434 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:70847568 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:70847568 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:139790735 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:139790735 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:48619721 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:48619721 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:61459368 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:61459368 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160287170 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160287170 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:67970271 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:67970271 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:6840276 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:6840276 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131095741 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131095741 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:4466426 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:4466426 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:69279725 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:69279725 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:209010451 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:209010451 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:113599545 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:113599545 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:11412267 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:11412267 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:35338532 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:35338532 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:101842075 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:101842075 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:135368947 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:135368947 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:47466781 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:47466781 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:72249455 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:72249455 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:176887425 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:176887425 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:49226400 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:49226400 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:6794242 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:6794242 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65998351 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65998351 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:41590874 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:41590874 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:61526554 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:61526554 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:88580761 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:88580761 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:124350392 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:124350392 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:49742638 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:49742638 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:10916668 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:10916668 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:68026106 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:68026106 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:116497263 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:116497263 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:116497480 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:116497480 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:116535445 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:116535445 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:154519679 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:154519679 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:154684565 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:154684565 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:63977671 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:63977671 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:32902280 A>G maps to ENST00000392250 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:32902280 A>G maps to ENST00000392250 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:95657481 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:95657481 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:4708159 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:4708159 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:108373220 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:108373220 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:233347706 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:233347706 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:62340228 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:62340228 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:38352150 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:38352150 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:50661107 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:50661107 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:107535728 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:107535728 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:6937693 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:6937693 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:132054697 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:132054697 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:133802479 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:133802479 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:159197435 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:159197435 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:14816192 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:14816192 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:68194543 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:68194543 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131825931 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131825931 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:92344054 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:92344054 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:48744716 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:48744716 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:48776234 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:48776234 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:73490963 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:73490963 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:141019877 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:141019877 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:60091725 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:60091725 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:97063748 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:97063748 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:240307798 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:240307798 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:121187546 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:121187546 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:2278756 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:2278756 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:39170375 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:39170375 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:47408630 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:47408630 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:898373 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:898373 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:6646576 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:6646576 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:8105945 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:8105945 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:61995315 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:61995315 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:42187808 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:42187808 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:54948824 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:54948824 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:50232089 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:50232089 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:31066120 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:31066120 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:104449571 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:104449571 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:130777850 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:130777850 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:52700879 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:52700879 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:110212023 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:110212023 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:189452678 G>A maps to ENST00000451191 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:189452678 G>A maps to ENST00000451191 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:121356145 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:121356145 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:92848878 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:92848878 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:81374492 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:81374492 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:149858489 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:149858489 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:119988121 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:119988121 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:92502208 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:92502208 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:118926189 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:118926189 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:82922531 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:82922531 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:94267434 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:94267434 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65681000 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65681000 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:102811578 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:102811578 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:23401269 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:23401269 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:160469383 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:160469383 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:133799726 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:133799726 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:113539431 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:113539431 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:55201861 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:55201861 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:10787706 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:10787706 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:10787725 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:10787725 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:234072309 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:234072309 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:47296907 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:47296907 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:88654246 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:88654246 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:36693934 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:36693934 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:55968292 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:55968292 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:35940566 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:35940566 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:44681231 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:44681231 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:72347061 G>A maps to ENST00000389917 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:72347061 G>A maps to ENST00000389917 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:169993777 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:169993777 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55287048 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55287048 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55270414 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55270414 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51381195 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51381195 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51506891 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51506891 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:52941573 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:52941573 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:130399808 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:130399808 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:129511226 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:129511226 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:183091403 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:183091403 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:133914125 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:133914125 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:37005422 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:37005422 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:54474853 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:54474853 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:226075391 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:226075391 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:156763045 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:156763045 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:197881489 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:197881489 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55112041 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55112041 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55146785 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55146785 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:54721147 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:54721147 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:42912282 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:42912282 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:16704096 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:16704096 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:141291574 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:141291574 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:12353088 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:12353088 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:196388615 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:196388615 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:56954604 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:56954604 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:41799231 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:41799231 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:24750621 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:24750621 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:160732241 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:160732241 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:44301983 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:44301983 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:89815302 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:89815302 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:29599234 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:29599234 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:67520946 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:67520946 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:55518563 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:55518563 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:12975595 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:12975595 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:47695344 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:47695344 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:94050455 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:94050455 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:42854213 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:42854213 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:158543760 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:158543760 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:141784295 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:141784295 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:21903707 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:21903707 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:118370255 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:118370255 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:108719518 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:108719518 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:71516726 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:71516726 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:70162610 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:70162610 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:10433110 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:10433110 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:10450697 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:10450697 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:46899710 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:46899710 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:45291052 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:45291052 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:19934751 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:19934751 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:16911787 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:16911787 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:158456861 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:158456861 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:37268329 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:37268329 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:15761017 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:15761017 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:101574100 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:101574100 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:236189474 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:236189474 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:63777332 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:63777332 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:50664047 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:50664047 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:7065313 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:7065313 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:15183393 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:15183393 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:36326472 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:36326472 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:115412812 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:115412812 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:107799646 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:107799646 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:11802030 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:11802030 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:22382451 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:22382451 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:21690097 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:21690097 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:51532175 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:51532175 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:91715111 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:91715111 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:56140240 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:56140240 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:31847680 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:31847680 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:153277376 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:153277376 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:26890332 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:26890332 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:71605889 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:71605889 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:47921702 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:47921702 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:2141949 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:2141949 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:4720172 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:4720172 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:161837 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:161837 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:131866446 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:131866446 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:41974914 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:41974914 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:84614518 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:84614518 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:42603793 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:42603793 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:36839472 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:36839472 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:244849996 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:244849996 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:23524367 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:23524367 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:219689206 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:219689206 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:116052668 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:116052668 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:43349540 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:43349540 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:43529211 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:43529211 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:43601550 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:43601550 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:96863801 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:96863801 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:96863807 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:96863807 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:96863838 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:96863838 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:44019069 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:44019069 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:15747808 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:15747808 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:40710729 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:40710729 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:29606248 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:29606248 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:227773517 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:227773517 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:123915010 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:123915010 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:105105905 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:105105905 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:43384671 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:43384671 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:179440334 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:179440334 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:2017006 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:2017006 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:77671593 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:77671593 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:113303158 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:113303158 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:237813133 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:237813133 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:34093135 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:34093135 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:12679891 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:12679891 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:38648367 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:38648367 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:55065244 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:55065244 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:35208300 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:35208300 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:169680613 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:169680613 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:42385434 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:42385434 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:61166611 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:61166611 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:52146748 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:52146748 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51650593 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:51650593 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:75668238 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:75668238 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:232564323 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:232564323 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:19520788 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:19520788 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:5339967 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:5339967 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:42340293 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:42340293 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:14489071 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:14489071 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:70146910 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:70146910 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:98655032 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:98655032 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:62543648 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:62543648 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:84417476 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:84417476 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:70520729 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:70520729 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:108366911 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:108366911 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:153122649 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:153122649 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158585227 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158585227 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158648052 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158648052 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:85113322 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:85113322 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:74076332 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:74076332 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:68472006 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:68472006 T>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:172755224 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:172755224 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:75505484 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:75505484 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:152470532 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:152470532 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:33403144 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:33403144 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:155829721 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:155829721 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:32635603 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:32635603 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:186271935 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:186271935 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:139636136 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:139636136 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:145850157 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:145850157 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:149743608 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:149743608 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:79354470 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:79354470 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:72050103 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:72050103 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:32638251 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:32638251 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:43777324 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:43777324 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:56824589 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:56824589 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:39973855 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:39973855 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:84205675 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:84205675 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:5766177 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:5766177 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:150501817 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:150501817 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:57466490 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:57466490 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:124983921 C>T maps to ENST00000340456 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:124983921 C>T maps to ENST00000340456 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:12994776 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:12994776 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:175334107 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:175334107 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:47440552 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:47440552 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:53037909 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:53037909 T>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:6978184 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:6978184 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:10998231 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:10998231 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:10998276 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:10998276 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:185637311 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:185637311 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:27147572 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:27147572 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:57138478 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:57138478 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49671384 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49671384 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:12693927 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:12693927 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:30423694 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:30423694 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:219411561 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:219411561 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:100479870 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:100479870 A>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:12401966 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:12401966 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:122729394 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:122729394 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:177067374 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:177067374 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:151079073 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:151079073 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:168098536 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:168098536 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:74649885 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:74649885 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:136650014 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chrX:136650014 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:44798858 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:44798858 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:12246305 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:12246305 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:58455222 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:58455222 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:52978556 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:52978556 A>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:116770606 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:116770606 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:139913624 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:139913624 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:48234394 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:48234394 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:15588556 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:15588556 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:55080314 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:55080314 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:23722140 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:23722140 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:87765390 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:87765390 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:5262962 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:5262962 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:7520842 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:7520842 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:31103010 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:31103010 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:26614360 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:26614360 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:88011123 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:88011123 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:58127797 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:58127797 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:76342118 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:76342118 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:35046480 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:35046480 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:27354612 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:27354612 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:58827596 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:58827596 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:183599586 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:183599586 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:119625829 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:119625829 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:113465093 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:113465093 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:119512633 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:119512633 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:28915206 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:28915206 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:87151877 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:87151877 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:72861463 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:72861463 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:59969156 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:59969156 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:50363896 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:50363896 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:61250007 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:61250007 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:32789858 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:32789858 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:106694216 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:106694216 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:100445757 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:100445757 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:98947358 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:98947358 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:43496519 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:43496519 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:41199815 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:41199815 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:99404267 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:99404267 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:135698509 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:135698509 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:181549919 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:181549919 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:181706899 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:181706899 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:54496080 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:54496080 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:159163170 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:159163170 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:97763951 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:97763951 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:33422322 C>T maps to ENST00000427840 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:33422322 C>T maps to ENST00000427840 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:92923774 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:92923774 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:92923776 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:92923776 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:44621827 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:44621827 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:227333180 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:227333180 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:49558526 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:49558526 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:184104733 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:184104733 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:45811587 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:45811587 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:37858743 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:37858743 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:10131476 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:10131476 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:17528370 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:17528370 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:87655888 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:87655888 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:103461609 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:103461609 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:189864149 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:189864149 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:107863701 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:107863701 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47410246 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47410246 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:8608932 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:8608932 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:75941786 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:75941786 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:18888324 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:18888324 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:113318175 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:113318175 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:38776356 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:38776356 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:58198102 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:58198102 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:105763848 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:105763848 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:204116892 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:204116892 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:6227204 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:6227204 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:85969819 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:85969819 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:36763248 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:36763248 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:169157542 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:169157542 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:197514994 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:197514994 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:31577443 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:31577443 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:50119278 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:50119278 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:2139044 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:2139044 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47976018 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47976018 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:85164152 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:85164152 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:53932381 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:53932381 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:20986390 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:20986390 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:21033452 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:21033452 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:13758858 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:13758858 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:28559566 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:28559566 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:117731273 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:117731273 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:100502237 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:100502237 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:205156525 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:205156525 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:25708065 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:25708065 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:183995648 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:183995648 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:65835888 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:65835888 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:34809731 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:34809731 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:216692773 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:216692773 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:72182086 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:72182086 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:66205156 G>T maps to ENST00000370616 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:66205156 G>T maps to ENST00000370616 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:40870093 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:40870093 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:96305468 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:96305468 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:184792914 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:184792914 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:58639296 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:58639296 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:129098498 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:129098498 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:130874424 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:130874424 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:16096891 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:16096891 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:159272685 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:159272685 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:192125689 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:192125689 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:30709767 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:30709767 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:28644582 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:28644582 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:216290040 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:216290040 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:65418231 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:65418231 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:120130551 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:120130551 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:133512318 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:133512318 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:101258832 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:101258832 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:68453149 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:68453149 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:22729489 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:22729489 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:102423877 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:102423877 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:141889375 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:141889375 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:134243608 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:134243608 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:57719909 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:57719909 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:90059091 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:90059091 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:35500297 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:35500297 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:113604333 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:113604333 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:11779006 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:11779006 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:153026392 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:153026392 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:31045553 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:31045553 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:37271640 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:37271640 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:176860074 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:176860074 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:146480428 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:146480428 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:146492697 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:146492697 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:45261935 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:45261935 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:83599509 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:83599509 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:83730177 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:83730177 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:124792372 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:124792372 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:63922839 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:63922839 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:210536146 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:210536146 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:38796171 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:38796171 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:87511242 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:87511242 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:114384040 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:114384040 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:3211445 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:3211445 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:33331083 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:33331083 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:61600875 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:61600875 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:215179257 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:215179257 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:178977913 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:178977913 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:118219337 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:118219337 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:55346498 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:55346498 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:55377958 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:55377958 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:52843230 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:52843230 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153707055 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153707055 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:129608942 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:129608942 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:129670339 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:129670339 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:75626492 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:75626492 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:81282951 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:81282951 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:85279509 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:85279509 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:25232030 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:25232030 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:141607579 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:141607579 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:74969271 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:74969271 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:140966847 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:140966847 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:65347058 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:65347058 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:6622833 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:6622833 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:31434327 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:31434327 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47695088 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47695088 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:55517815 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:55517815 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:14932586 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:14932586 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:113231996 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:113231996 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:43818176 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:43818176 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:60264642 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:60264642 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:59945597 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:59945597 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:76365198 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:76365198 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:42780166 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:42780166 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:23888305 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:23888305 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:16758367 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:16758367 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:69925954 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:69925954 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:1843158 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:1843158 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:175436123 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:175436123 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:140349770 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:140349770 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:236195639 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:236195639 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:144101903 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:144101903 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:176691850 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:176691850 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:18766474 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:18766474 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:132306185 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:132306185 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:248246873 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:248246873 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:16312619 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:16312619 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:8794925 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:8794925 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:73719803 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:73719803 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:125647265 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:125647265 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47333748 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47333748 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47769208 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:47769208 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:233393708 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:233393708 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:31876718 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:31876718 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:32209622 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:32209622 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:144995026 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:144995026 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:44152095 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:44152095 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153068803 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153068803 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:73651680 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:73651680 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:77381506 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:77381506 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:46522722 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:46522722 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:151204853 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:151204853 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:142836472 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:142836472 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:110482516 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:110482516 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:51924903 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:51924903 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:42445713 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:42445713 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:171329424 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:171329424 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:145789248 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:145789248 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:129291865 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:129291865 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:24755688 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:24755688 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:7670473 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:7670473 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:43124215 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:43124215 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:60749297 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:60749297 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:50025527 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:50025527 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:43373361 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:43373361 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:43519857 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:43519857 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:24615483 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:24615483 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:44084919 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:44084919 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:157691297 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:157691297 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:13371598 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:13371598 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:13697163 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:13697163 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:114397649 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:114397649 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:106362105 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:106362105 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:79349079 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:79349079 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:103183336 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:103183336 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153208945 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153208945 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:204128776 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:204128776 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:100058762 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:100058762 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:183871589 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:183871589 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:176795122 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:176795122 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:63905140 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:63905140 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:117662288 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:117662288 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:38078415 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:38078415 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:100731826 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:100731826 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:87436667 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:87436667 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:32363407 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:32363407 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:237608852 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:237608852 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:152005431 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:152005431 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:55251379 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:55251379 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:38740128 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:38740128 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:177937138 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:177937138 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:13866815 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:13866815 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:94912993 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:94912993 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:100775013 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:100775013 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:67154803 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:67154803 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:232539168 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:232539168 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:38600810 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:38600810 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:160709249 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:160709249 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:220496609 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:220496609 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:85266261 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:85266261 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:87235359 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:87235359 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:40392218 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:40392218 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:27596059 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:27596059 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:101596493 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:101596493 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:140357950 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:140357950 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158604186 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158604186 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:54877225 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:54877225 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:112200077 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:112200077 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153047495 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:153047495 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:104063255 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:104063255 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:99779702 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:99779702 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:6998018 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:6998018 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:151747032 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:151747032 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:35443103 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:35443103 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:155579288 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:155579288 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:135388543 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:135388543 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:2297666 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:2297666 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:32825491 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:32825491 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:15405877 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:15405877 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:108472448 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:108472448 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:43432451 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:43432451 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:133763934 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:133763934 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:103599231 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:103599231 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:138202504 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:138202504 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:138202511 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:138202511 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:201382395 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:201382395 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:189581916 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:189581916 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:186287492 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:186287492 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:186294835 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:186294835 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:10935033 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:10935033 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:10969056 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:10969056 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:73458089 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:73458089 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:77353535 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:77353535 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:3424414 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:3424414 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:47222241 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:47222241 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:26624398 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:26624398 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:215939930 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:215939930 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:216500925 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:216500925 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:216538205 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:216538205 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:6836606 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:6836606 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:100821843 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:100821843 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:122720129 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:122720129 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:177094608 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:177094608 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:108634005 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:108634005 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:32437897 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:32437897 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:32437933 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:32437933 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:31572746 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:31572746 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:167992308 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:167992308 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:74649738 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:74649738 A>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:195937654 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:195937654 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:58572930 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:58572930 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6964543 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6964543 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6964545 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6964545 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:53339 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:53339 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:47919782 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chrX:47919782 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:51352627 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:51352627 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:6894946 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:6894946 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:76920007 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:76920007 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:48884520 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:48884520 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:62104036 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:62104036 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:21765049 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:21765049 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:37439252 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:37439252 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr19:4408872 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr19:4408872 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:21609393 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:21609393 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:205033385 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:205033385 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:30199182 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:30199182 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:61188097 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:61188097 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:125639676 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:125639676 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:58158085 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:58158085 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:85559926 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:85559926 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:91572375 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:91572375 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:118626010 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:118626010 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:118627112 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:118627112 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:29044411 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:29044411 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:82122909 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:82122909 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:38462951 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:38462951 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:73609247 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:73609247 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:1825998 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:1825998 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:37607163 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:37607163 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:58166917 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:58166917 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:29450291 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:29450291 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:18158294 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:18158294 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:172050826 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:172050826 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:89756922 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:89756922 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:110390376 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:110390376 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:102074243 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:102074243 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:16170262 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chrX:16170262 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:177015178 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:177015178 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:70693746 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:70693746 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:33058368 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:33058368 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:153737606 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:153737606 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:207945747 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:207945747 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:50942749 A>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:50942749 A>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:50942752 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:50942752 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:197554193 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:197554193 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:105544284 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:105544284 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:24120341 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:24120341 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:78119039 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:78119039 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:118057456 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:118057456 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:50694206 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:50694206 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:29845194 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:29845194 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:31047984 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:31047984 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:76924895 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:76924895 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:129754130 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:129754130 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:18770678 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:18770678 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:61441058 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:61441058 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:9801160 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:9801160 T>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:159284479 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:159284479 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:21702889 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:21702889 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:107709542 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:107709542 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr13:67477612 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr13:67477612 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:20801572 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:20801572 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:28817388 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:28817388 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:120763617 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:120763617 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:30092276 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:30092276 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:131951057 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:131951057 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:47274792 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:47274792 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:27218939 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:27218939 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr9:98278892 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr9:98278892 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:51697440 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:51697440 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr13:48916721 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr13:48916721 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:50153044 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:50153044 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:172395340 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:172395340 C>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:122632682 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:122632682 G>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr15:49126845 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr15:49126845 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr15:75673831 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr15:75673831 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:1460760 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:1460760 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:44317243 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:44317243 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:155167780 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:155167780 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr9:120471037 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr9:120471037 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:24675465 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:24675465 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:7962845 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr20:7962845 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr13:113143800 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr13:113143800 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:19524564 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:19524564 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:128865501 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:128865501 T>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:6970050 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr12:6970050 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:119575488 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:119575488 T>C did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr4:85701218 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr4:85701218 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:158679643 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:158679643 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:57457724 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:57457724 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:85015441 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:85015441 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:57194440 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:57194440 A>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:136269161 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr2:136269161 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:107558163 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:107558163 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:48231746 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:48231746 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:16276104 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:16276104 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:89034841 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:89034841 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:6306639 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:6306639 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:80667541 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:80667541 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131325009 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131325009 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:20552290 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:20552290 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:42847338 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:42847338 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:178567147 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:178567147 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:148059834 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:148059834 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:33478635 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:33478635 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:134250070 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:134250070 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:58254090 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:58254090 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:50304034 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:50304034 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:73716670 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:73716670 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:242149086 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:242149086 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:150967857 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:150967857 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:77590183 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:77590183 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:128851279 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:128851279 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:176845615 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:176845615 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:116943325 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:116943325 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:11038590 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:11038590 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:143570683 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:143570683 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:127826708 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:127826708 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:30034595 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:30034595 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:93683972 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:93683972 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:73317629 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:73317629 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:45697049 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:45697049 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:76452300 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:76452300 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:30447611 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:30447611 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:143704329 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:143704329 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:81309661 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:81309661 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:181765800 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:181765800 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:81667563 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:81667563 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:93108490 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:93108490 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:230895162 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:230895162 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:25272361 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:25272361 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:185599617 T>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:185599617 T>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:20769828 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:20769828 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:128757592 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:128757592 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:64121091 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:64121091 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr18:34854500 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr18:34854500 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:203194755 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:203194755 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:19226635 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:19226635 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:146817992 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:146817992 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:125204547 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:125204547 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:46888134 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:46888134 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:110827788 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:110827788 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:131895292 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:131895292 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:17257774 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:17257774 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:1413051 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:1413051 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:480447 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:480447 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:80808956 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:80808956 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:36405995 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:36405995 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:17168812 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:17168812 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:22989933 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:22989933 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:85950220 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:85950220 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:50120968 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:50120968 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:72133038 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:72133038 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:40257260 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:40257260 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:131847609 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:131847609 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:63976121 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:63976121 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr18:28605663 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr18:28605663 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:62126147 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:62126147 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:32611263 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:32611263 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:43829565 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:43829565 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:66286338 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:66286338 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:23702438 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:23702438 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:44012090 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:44012090 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:242052697 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:242052697 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:45607269 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:45607269 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:14816187 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:14816187 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:35077149 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:35077149 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:127670325 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:127670325 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:55396960 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:55396960 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:137772784 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:137772784 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:171252227 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:171252227 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:171944779 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:171944779 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:114299554 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:114299554 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:42719626 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:42719626 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:183942604 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:183942604 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:58477936 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:58477936 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:1034567 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:1034567 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:108635383 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:108635383 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:36113675 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:36113675 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:149785258 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:149785258 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:71055340 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:71055340 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:29974549 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:29974549 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:113860140 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:113860140 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:112115599 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:112115599 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:47123147 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:47123147 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:113832688 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:113832688 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:113887243 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:113887243 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17927619 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17927619 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:7132155 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:7132155 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:95871886 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:95871886 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:201844233 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:201844233 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:2629457 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:2629457 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:35478329 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:35478329 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:15646153 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:15646153 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:93482916 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:93482916 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:147024597 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:147024597 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:119915821 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:119915821 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:211276959 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:211276959 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:196311174 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:196311174 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:123130527 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:123130527 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:4910913 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:4910913 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:207988369 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:207988369 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:52913031 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:52913031 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:45970556 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:45970556 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:75596527 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:75596527 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:75116909 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:75116909 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:23190902 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:23190902 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:133811994 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:133811994 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:122669056 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:122669056 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:40653252 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:40653252 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:56911833 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:56911833 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:127325429 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:127325429 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:205549684 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:205549684 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:222814759 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:222814759 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:10393020 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:10393020 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:53471923 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:53471923 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:223559262 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:223559262 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:62937046 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:62937046 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:100212861 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:100212861 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:7489139 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:7489139 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:36462435 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:36462435 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:9005052 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:9005052 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:42751928 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:42751928 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:70164317 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:70164317 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:101720990 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:101720990 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:152548753 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:152548753 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:27157392 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:27157392 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:39618385 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:39618385 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:39618391 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr13:39618391 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:51288550 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:51288550 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:56363730 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:56363730 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:110962358 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:110962358 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:115364709 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:115364709 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:115375459 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:115375459 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:50148972 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:50148972 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:2996309 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:2996309 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131528654 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131528654 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:139746678 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:139746678 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:65387781 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:65387781 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:66620998 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:66620998 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:156873561 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:156873561 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:27238323 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:27238323 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:28761083 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:28761083 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:118354441 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:118354441 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:44116038 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:44116038 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:122334599 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:122334599 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:13514259 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:13514259 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:121674300 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:121674300 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:121674321 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:121674321 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:113795814 T>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:113795814 T>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:206702583 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:206702583 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:103294512 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:103294512 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:240933902 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:240933902 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:63149681 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:63149681 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:90026276 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:90026276 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:30343133 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr21:30343133 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:79639079 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:79639079 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:39015858 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:39015858 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:237982265 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:237982265 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:31152311 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:31152311 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:23382994 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:23382994 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:48023096 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:48023096 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr18:61390733 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr18:61390733 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:57381745 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:57381745 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52115766 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52115766 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:164772951 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:164772951 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:25811562 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:25811562 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:169437325 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:169437325 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:38315684 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:38315684 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:4841287 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:4841287 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:68411718 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:68411718 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:33951505 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:33951505 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:33984696 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:33984696 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:85286002 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:85286002 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:55731793 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:55731793 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:61296510 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:61296510 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:88773956 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:88773956 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:142596609 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:142596609 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:153028923 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:153028923 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:158605957 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:158605957 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:134916564 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:134916564 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:39772213 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:39772213 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:160006849 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:160006849 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:9661111 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:9661111 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:145838956 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:145838956 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:114925164 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:114925164 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:167791598 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:167791598 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:56700197 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:56700197 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:92200204 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:92200204 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:24727668 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:24727668 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:133923493 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:133923493 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:149205326 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:149205326 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:159032141 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:159032141 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:15426912 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:15426912 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:195591097 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:195591097 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:1957413 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:1957413 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:42214378 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:42214378 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:228584917 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:228584917 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:5700212 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:5700212 T>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:900691 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:900691 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:73255625 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr9:73255625 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:234878659 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:234878659 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:110238348 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:110238348 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:98519232 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:98519232 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:39172085 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:39172085 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:59337807 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:59337807 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:234630444 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:234630444 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17760419 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17760419 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:96106042 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:96106042 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:118969115 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chrX:118969115 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:17527436 A>T maps to NM_153676.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:17527436 A>T maps to NM_153676.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:61036386 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:61036386 G>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:177037183 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:177037183 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:113081308 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:113081308 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:108618654 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:108618654 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:57194440 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:57194440 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52905227 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52905227 A>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:29440883 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:29440883 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:238050586 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:238050586 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:58862751 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:58862751 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:75555019 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:75555019 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:25390385 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:25390385 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:94230269 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:94230269 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:100803873 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:100803873 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:138914390 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:138914390 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:42229867 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:42229867 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:55435712 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:55435712 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr22:24432662 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr22:24432662 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:3680248 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:3680248 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:60890290 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:60890290 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:176017070 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:176017070 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:104030305 A>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:104030305 A>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr16:58608502 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr16:58608502 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:7546880 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:7546880 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:130363891 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:130363891 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:69326414 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:69326414 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:29132220 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:29132220 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:154002556 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:154002556 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:153996366 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:153996366 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:216741462 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:216741462 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:69704264 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:69704264 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:6244203 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:6244203 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:62273638 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:62273638 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:161514359 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:161514359 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:54475464 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chrX:54475464 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:173232911 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:173232911 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:150267104 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:150267104 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:29018308 A>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:29018308 A>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:133365527 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:133365527 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr20:33516602 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr20:33516602 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:65146227 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:65146227 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:118649137 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:118649137 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:123120413 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:123120413 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:45220277 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:45220277 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr16:3016122 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr16:3016122 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:14222946 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:14222946 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:143866988 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:143866988 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:135076373 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:135076373 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:71516985 C>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:71516985 C>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:195492322 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:195492322 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr16:67208857 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr16:67208857 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:95751906 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:95751906 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:111941472 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:111941472 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:59811222 T>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:59811222 T>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:100859164 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:100859164 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:53104270 T>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:53104270 T>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:131894080 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:131894080 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:129812530 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:129812530 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:173951742 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:173951742 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:32122292 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:32122292 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:40695521 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:40695521 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:55200864 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:55200864 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:9044392 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:9044392 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:70318953 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:70318953 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:52033879 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:52033879 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:107677362 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:107677362 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:54929502 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:54929502 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:35753663 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:35753663 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:35806410 A>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:35806410 A>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:155979225 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:155979225 G>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:38652175 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:38652175 T>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:116430699 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:116430699 C>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:154218862 A>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:154218862 A>C did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:100014547 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:100014547 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:52626270 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:52626270 C>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:64889 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr4:64889 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr22:29449562 C>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr22:29449562 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:215834911 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:215834911 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:139910730 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:139910730 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:139910732 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:139910732 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:15058801 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:15058801 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:135630344 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:135630344 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:131324306 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:131324306 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:20432543 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:20432543 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:9642185 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:9642185 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:100003328 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:100003328 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:1866753 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:1866753 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:60879669 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:60879669 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:132278646 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:132278646 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:202580592 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:202580592 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:854800 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:854800 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:41555496 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:41555496 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:92021769 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:92021769 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:70779418 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:70779418 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:37414855 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:37414855 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:22233020 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:22233020 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:46119943 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:46119943 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:62333383 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:62333383 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:97214933 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:97214933 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:110878301 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:110878301 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:53955999 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:53955999 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:119976488 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:119976488 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:1391654 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:1391654 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:134365891 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:134365891 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:35224151 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:35224151 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:40114521 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:40114521 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:15973808 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:15973808 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:128911005 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:128911005 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:97562852 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:97562852 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:49726661 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:49726661 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:54913186 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:54913186 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:44323679 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:44323679 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:110492072 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:110492072 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:32667457 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:32667457 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:180377396 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:180377396 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:30435596 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:30435596 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:74521812 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:74521812 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:100928174 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:100928174 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:21884030 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:21884030 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:26890440 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:26890440 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:26915701 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:26915701 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:22305037 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:22305037 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:50857452 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:50857452 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:98195661 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:98195661 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:433340 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:433340 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:39073771 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:39073771 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:125192267 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:125192267 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:33137349 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:33137349 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:111084623 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:111084623 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:10087869 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:10087869 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:10089180 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:10089180 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:47409798 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:47409798 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:238267599 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:238267599 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:70963286 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:70963286 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:71004336 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:71004336 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:232672166 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:232672166 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:47628358 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:47628358 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:17122242 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:17122242 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:49802967 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:49802967 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:68535155 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:68535155 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:17110398 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:17110398 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:48993664 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:48993664 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:58160900 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:58160900 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:96746004 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:96746004 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:37836341 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:37836341 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:104442726 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:104442726 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:59982766 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:59982766 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:55625227 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:55625227 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:55625236 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:55625236 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:13777521 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:13777521 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:58190432 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:58190432 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:28574630 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:28574630 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:28909824 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:28909824 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:38350496 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:38350496 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:11664794 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:11664794 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:53133887 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:53133887 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:132194316 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:132194316 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:120851007 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:120851007 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:110294456 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:110294456 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:118816779 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:118816779 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:49103523 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:49103523 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:37111053 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:37111053 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:14922044 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:14922044 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:128486553 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:128486553 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:1394884 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:1394884 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:47408635 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:47408635 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:16261281 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:16261281 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:30514417 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:30514417 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:133353212 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:133353212 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:46096394 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:46096394 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:94690313 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:94690313 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:81668976 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:81668976 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:127447932 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:127447932 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:134705392 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:134705392 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr15:50535204 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr15:50535204 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:41018430 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:41018430 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:96317848 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:96317848 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:81374215 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:81374215 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:234762680 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:234762680 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:176314385 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:176314385 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:186120575 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:186120575 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:54395705 G>A maps to ENST00000371376 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:54395705 G>A maps to ENST00000371376 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:25699520 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:25699520 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:75893131 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:75893131 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:182400122 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:182400122 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:15572983 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:15572983 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:86683859 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:86683859 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:94148873 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:94148873 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:21426239 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:21426239 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:71977219 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:71977219 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:104308762 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:104308762 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:82062283 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:82062283 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:47297246 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:47297246 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:42357299 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:42357299 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr15:71151849 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr15:71151849 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:2255961 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:2255961 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:21205694 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:21205694 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:186968218 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:186968218 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:141718968 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:141718968 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:1498776 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:1498776 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:104681551 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:104681551 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:13112009 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:13112009 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:60163968 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:60163968 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:72755869 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:72755869 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:64892568 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:64892568 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:11855490 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:11855490 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:77798751 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:77798751 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:109614133 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr13:109614133 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:171240386 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:171240386 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:113076195 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:113076195 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:50197603 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:50197603 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:91940422 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:91940422 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:20699648 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:20699648 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:204937914 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:204937914 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:33290742 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:33290742 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:48038209 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:48038209 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:247592822 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:247592822 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:183221612 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:183221612 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:50966396 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:50966396 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:20443609 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:20443609 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:56125084 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:56125084 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:72937962 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:72937962 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:41861666 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:41861666 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:73967116 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:73967116 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:91368332 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:91368332 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:55913108 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:55913108 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:165863928 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:165863928 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:95373001 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:95373001 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:15082575 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:15082575 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:98469291 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:98469291 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:131913286 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:131913286 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:22029477 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:22029477 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:22396940 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:22396940 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:94708572 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:94708572 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:11421099 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:11421099 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:11461836 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:11461836 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:43433883 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:43433883 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:139108574 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:139108574 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:36128439 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:36128439 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:35948122 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr22:35948122 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:206702434 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:206702434 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:127957591 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:127957591 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:238730508 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:238730508 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:108474544 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:108474544 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:11527251 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:11527251 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:7411713 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:7411713 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:86993214 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:86993214 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:30776392 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:30776392 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:77089845 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:77089845 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:153963201 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:153963201 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:83419406 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:83419406 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:78882741 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr17:78882741 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:179008120 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:179008120 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:237837377 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:237837377 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:153591307 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:153591307 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:38835165 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:38835165 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:52201251 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:52201251 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:4285244 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:4285244 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:102248505 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:102248505 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:9054449 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr5:9054449 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:38610526 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr19:38610526 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:92959803 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:92959803 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:66376822 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:66376822 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:48319026 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chrX:48319026 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:306086 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:306086 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:20599866 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:20599866 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:18880639 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:18880639 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:231134798 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:231134798 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:131347214 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr9:131347214 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:149522262 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr7:149522262 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:53045575 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr8:53045575 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:44257942 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:44257942 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:152991937 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:152991937 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:4508865 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:4508865 A>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:180953987 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:180953987 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:64449309 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:64449309 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:64678626 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:64678626 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:85453959 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:85453959 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:115114055 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr12:115114055 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:61485230 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:61485230 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:35443916 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr6:35443916 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr15:70344874 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr15:70344874 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:166916352 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:166916352 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:166929310 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:166929310 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:2596748 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr20:2596748 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:192818282 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:192818282 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:68964460 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:68964460 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:117799991 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:117799991 T>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:111796026 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr3:111796026 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:12250932 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:12250932 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:1946371 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:1946371 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:10959673 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:10959673 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:193029171 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:193029171 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:45826050 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr21:45826050 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:2115704 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:2115704 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:179526476 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:179526476 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:190905589 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:190905589 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:94734 G>T maps to ENST00000447903 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr10:94734 G>T maps to ENST00000447903 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:141489736 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:141489736 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:216172522 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:216172522 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:216495183 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:216495183 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:11952184 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr11:11952184 A>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:9009018 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr16:9009018 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:38478256 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr1:38478256 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:128526402 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr2:128526402 T>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:68260748 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr14:68260748 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:22932075 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr18:22932075 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:106367 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1265-08 chr4:106367 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:9246017 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:9246017 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:94463320 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:94463320 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:22065791 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:22065791 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:24350140 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:24350140 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:247068973 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:247068973 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:11200128 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:11200128 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:131703932 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:131703932 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:56869591 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:56869591 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:26448791 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:26448791 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:88388252 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:88388252 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:97147476 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:97147476 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:100795529 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:100795529 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:16770304 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:16770304 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:150252214 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:150252214 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:118981184 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:118981184 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:14731388 A>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:14731388 A>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:54122023 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:54122023 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:140811944 T>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:140811944 T>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:71275627 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:71275627 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:12857276 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:12857276 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:49080855 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:49080855 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:101481445 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:101481445 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:203151800 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:203151800 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:11884618 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:11884618 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:40225185 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:40225185 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:238255340 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:238255340 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:9754615 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:9754615 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:211542010 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:211542010 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:207857310 A>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:207857310 A>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:35464664 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:35464664 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:86983742 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:86983742 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:19297484 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:19297484 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:67986589 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:67986589 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:41471681 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:41471681 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:32480357 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:32480357 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:38840136 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:38840136 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:169144339 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:169144339 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:29038931 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:29038931 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:4711720 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:4711720 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr22:31844263 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr22:31844263 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:27303225 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:27303225 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:6897701 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:6897701 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:197008682 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:197008682 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:57419201 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:57419201 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:179019567 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:179019567 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:18087560 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:18087560 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:38294175 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:38294175 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:161483863 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:161483863 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:157771088 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:157771088 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:171244686 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:171244686 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:48608698 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:48608698 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:50497762 T>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:50497762 T>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:117116851 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:117116851 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:37285272 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:37285272 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:27481856 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:27481856 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:7866242 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:7866242 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:96351892 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:96351892 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:28483141 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:28483141 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:191125987 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:191125987 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:27799466 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:27799466 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:43295812 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:43295812 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:27457425 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:27457425 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:27375203 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:27375203 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:31429991 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:31429991 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:61619849 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:61619849 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:36767168 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:36767168 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:2595022 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:2595022 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:86451767 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:86451767 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:57969841 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:57969841 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:70549688 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:70549688 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:153129174 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chrX:153129174 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:62903630 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:62903630 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:42373449 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:42373449 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:57577349 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:57577349 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:112403902 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:112403902 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:677314 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:677314 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:60310114 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:60310114 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:70713248 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:70713248 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:10366822 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:10366822 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:59517105 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:59517105 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:19360472 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:19360472 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:71060465 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:71060465 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:140327575 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:140327575 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:88423449 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:88423449 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:3593335 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:3593335 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:31143861 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:31143861 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:31923434 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:31923434 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:633677 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:633677 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:209214630 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:209214630 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:102059658 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:102059658 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:8755425 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:8755425 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:23526334 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:23526334 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:68989551 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:68989551 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:62193360 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:62193360 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:113819449 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:113819449 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:60668843 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:60668843 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:56980775 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:56980775 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:79385598 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:79385598 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:8416142 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:8416142 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:85578149 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:85578149 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:116353679 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:116353679 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:74150275 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:74150275 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:117647337 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:117647337 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:6257675 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:6257675 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:90089716 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:90089716 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:95033255 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:95033255 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:82369141 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:82369141 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:47911799 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:47911799 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:100772641 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:100772641 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:103228794 A>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:103228794 A>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:108123662 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr9:108123662 G>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:183485279 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:183485279 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:10279846 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:10279846 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:31762321 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:31762321 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:51617373 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:51617373 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:36520470 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:36520470 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:108489711 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:108489711 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr22:37603877 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr22:37603877 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:70600056 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:70600056 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:67926679 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:67926679 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:56738329 C>A maps to ENST00000453538 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:56738329 C>A maps to ENST00000453538 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:122213511 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:122213511 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:5759014 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:5759014 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:30363617 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:30363617 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:142612256 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:142612256 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:64113049 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:64113049 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:67356694 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:67356694 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:69973682 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:69973682 G>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:53578975 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:53578975 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:32369300 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:32369300 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:38404077 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:38404077 A>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:247473791 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:247473791 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:67080279 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:67080279 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:150532709 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:150532709 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:237028795 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:237028795 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:4744748 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:4744748 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:3730409 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:3730409 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:85695253 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:85695253 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:4098994 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:4098994 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:37423000 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:37423000 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:175939622 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:175939622 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:161829920 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:161829920 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:194181230 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:194181230 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:43666067 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:43666067 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:153663859 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:153663859 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:42524129 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:42524129 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:32801176 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:32801176 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:97922810 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:97922810 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:23616073 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:23616073 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:50559427 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:50559427 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:67698893 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:67698893 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:10614102 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:10614102 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:58472677 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:58472677 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:88828512 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:88828512 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:71024671 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:71024671 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:47698470 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:47698470 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:130473487 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:130473487 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:117396044 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:117396044 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:15727766 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:15727766 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:49071486 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:49071486 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:40527402 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:40527402 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:48737601 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:48737601 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:94162432 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:94162432 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:78071217 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:78071217 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:64119537 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:64119537 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:7042891 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:7042891 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10256278 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10256278 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258473 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258473 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:47501525 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:47501525 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:21884217 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:21884217 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:68842774 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:68842774 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:68842790 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:68842790 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:59072163 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:59072163 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:58545293 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:58545293 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:56851591 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:56851591 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:101719203 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:101719203 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:143020512 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:143020512 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:8286792 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:8286792 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:147259537 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:147259537 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:147336164 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:147336164 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:101784551 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:101784551 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:48376794 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:48376794 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:77155191 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:77155191 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:211507148 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:211507148 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:80620476 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:80620476 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:69423433 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:69423433 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70326278 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70326278 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:204131519 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:204131519 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:41450828 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:41450828 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:234375660 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:234375660 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:35071388 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:35071388 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:31241240 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:31241240 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:72310155 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:72310155 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:114428954 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:114428954 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:130982719 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:130982719 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:31384939 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:31384939 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:56467846 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:56467846 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:45396621 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:45396621 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:77438637 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:77438637 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:142564138 G>T maps to ENST00000436299 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:142564138 G>T maps to ENST00000436299 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:71424796 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:71424796 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:12264088 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:12264088 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:187192967 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:187192967 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:156592454 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:156592454 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:17602745 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:17602745 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:9000149 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:9000149 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:1015985 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:1015985 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:72754618 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:72754618 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:30698669 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:30698669 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:161521110 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:161521110 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:26582000 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:26582000 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:41399490 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:41399490 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:121708680 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:121708680 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:14622527 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:14622527 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:1722148 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:1722148 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:54558955 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:54558955 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:131029841 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:131029841 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:157425217 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:157425217 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:158262732 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:158262732 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:42621101 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:42621101 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:79650968 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:79650968 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:71154656 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:71154656 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:138722048 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:138722048 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:68549336 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:68549336 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:27668596 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:27668596 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:136710635 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:136710635 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:156811126 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:156811126 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:37725289 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:37725289 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:54777844 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:54777844 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:10600237 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:10600237 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:123164148 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:123164148 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:118713524 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:118713524 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:72322630 C>T maps to ENST00000440684 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:72322630 C>T maps to ENST00000440684 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:241722553 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:241722553 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:161071265 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:161071265 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:99771137 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:99771137 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:50122228 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:50122228 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:62854864 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:62854864 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48821877 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48821877 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:39838414 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:39838414 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:12044435 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:12044435 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:85770259 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:85770259 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:136603752 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:136603752 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:94836783 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:94836783 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70356610 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70356610 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:116418534 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:116418534 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:88024936 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:88024936 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:141796115 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:141796115 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:106204995 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:106204995 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:132641741 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:132641741 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:100701351 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:100701351 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48605671 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48605671 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:23851778 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:23851778 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:40223925 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:40223925 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:134262578 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:134262578 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:104160335 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:104160335 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:160340481 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:160340481 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:96117823 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:96117823 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:35802707 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:35802707 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:115357596 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:115357596 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:84733418 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:84733418 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:97614377 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:97614377 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70764404 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:70764404 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:21747770 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:21747770 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:65998229 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:65998229 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:108581102 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:108581102 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:178684941 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:178684941 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:153317565 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:153317565 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:144093266 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:144093266 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:44409661 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:44409661 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:204434553 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:204434553 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:151219505 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:151219505 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:108698477 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:108698477 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:8755103 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:8755103 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:81934171 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:81934171 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:131955374 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:131955374 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:36604904 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:36604904 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:79767753 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:79767753 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:75573218 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:75573218 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:122278334 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:122278334 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:53217355 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:53217355 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:22290655 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:22290655 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:68386105 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:68386105 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:71830446 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:71830446 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:142460609 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:142460609 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:43266868 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:43266868 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:220167273 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:220167273 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:61169699 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:61169699 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:108103033 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:108103033 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:133266993 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:133266993 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:37194168 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:37194168 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:79348845 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:79348845 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:114320782 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:114320782 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:11512647 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:11512647 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:124763443 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:124763443 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:45748445 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:45748445 A>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:134986616 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:134986616 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:108218810 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:108218810 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:169696745 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:169696745 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:156130170 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:156130170 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:19707501 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:19707501 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:61322851 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:61322851 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:85894691 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:85894691 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:104495566 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:104495566 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:57626876 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:57626876 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:45241992 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:45241992 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:62763435 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:62763435 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:39438030 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:39438030 G>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:32428305 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:32428305 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:176825293 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:176825293 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:234444773 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:234444773 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:19470019 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:19470019 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:70512628 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:70512628 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:133692485 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:133692485 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:41482041 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:41482041 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:108377864 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:108377864 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:121454123 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:121454123 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:65264597 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:65264597 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:74583258 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:74583258 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:57638882 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:57638882 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:5400149 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:5400149 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:64476633 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr14:64476633 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:155829700 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:155829700 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:71168867 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:71168867 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:114724536 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:114724536 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:151747047 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:151747047 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:65175489 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:65175489 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:121039327 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:121039327 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:2193057 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:2193057 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:98145793 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:98145793 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:30732861 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:30732861 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:72469058 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:72469058 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:12198221 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:12198221 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:31338467 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr15:31338467 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:3090607 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:3090607 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:24906632 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:24906632 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:30228699 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:30228699 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:154456585 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:154456585 A>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:114298100 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:114298100 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:124012958 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:124012958 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:17232176 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:17232176 A>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:72029455 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:72029455 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:178349609 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:178349609 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:40532545 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:40532545 T>C did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:152087506 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chrX:152087506 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:53545 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:53545 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:3366834 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:3366834 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:102157312 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:102157312 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:58119664 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:58119664 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:74763002 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:74763002 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:35578618 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:35578618 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:73434534 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:73434534 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:64629839 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:64629839 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:145617074 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:145617074 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:134225912 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:134225912 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:73830527 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:73830527 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:49714866 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:49714866 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:80872723 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:80872723 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:190532354 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:190532354 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:29220227 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:29220227 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:7051005 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:7051005 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:25953268 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:25953268 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:73038613 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:73038613 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:138432325 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:138432325 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:121436824 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:121436824 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:143570553 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:143570553 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:160295732 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:160295732 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:154186502 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:154186502 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:20208832 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:20208832 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:86249328 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:86249328 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:54961852 T>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:54961852 T>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:42702567 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:42702567 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:11537168 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:11537168 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:42304856 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:42304856 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:56130641 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:56130641 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:85128006 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:85128006 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:69189673 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:69189673 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:10168363 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:10168363 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:33156668 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:33156668 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:139609104 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:139609104 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:160309906 T>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:160309906 T>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:61988386 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:61988386 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:4494828 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:4494828 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:47604044 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:47604044 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:16970127 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:16970127 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:48976494 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:48976494 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:50121058 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:50121058 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:46400700 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:46400700 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:38105498 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:38105498 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:11622638 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:11622638 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:220239498 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:220239498 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:169098199 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:169098199 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:57507801 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:57507801 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:31857193 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:31857193 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:40326491 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:40326491 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:32610066 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:32610066 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:10637348 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:10637348 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:14884714 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:14884714 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:727019 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:727019 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:23713903 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:23713903 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:236383991 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:236383991 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:76551318 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:76551318 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:11159765 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:11159765 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:154213133 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:154213133 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:220045341 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:220045341 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:71212579 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:71212579 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:74137555 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:74137555 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:136563883 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:136563883 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr13:114504826 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr13:114504826 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:224344890 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:224344890 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:101146006 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:101146006 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr13:29008405 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr13:29008405 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:89409240 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:89409240 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:71026709 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:71026709 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:153774133 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:153774133 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:19533015 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:19533015 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:58008065 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:58008065 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:74018088 T>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:74018088 T>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:73234573 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:73234573 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:9739613 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:9739613 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:102977070 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:102977070 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:235715288 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:235715288 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:27499801 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:27499801 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:89570952 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:89570952 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:27776411 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:27776411 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:38139453 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:38139453 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:148763813 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:148763813 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:186120954 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:186120954 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:24147138 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:24147138 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:36070499 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:36070499 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:133632323 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:133632323 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:52906106 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:52906106 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:65684456 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:65684456 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:81598992 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:81598992 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:27456082 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:27456082 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:131100478 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:131100478 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:62613950 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:62613950 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:105302370 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:105302370 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:67677187 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:67677187 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:156509594 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:156509594 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:161053000 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:161053000 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:160850572 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:160850572 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:160919819 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:160919819 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:24426669 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:24426669 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:8926549 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:8926549 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:200946272 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:200946272 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:158057528 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:158057528 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:44588044 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:44588044 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:52943754 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:52943754 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:53091362 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:53091362 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:153136029 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chrX:153136029 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:37005155 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:37005155 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:22142392 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:22142392 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:63989861 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:63989861 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:197723036 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:197723036 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:148344543 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:148344543 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:82452645 C>A maps to ENST00000370717 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:82452645 C>A maps to ENST00000370717 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:165533123 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:165533123 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:40758865 C>A maps to ENST00000446130 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:40758865 C>A maps to ENST00000446130 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:29600039 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:29600039 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:65369179 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:65369179 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:156283321 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:156283321 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:44074063 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:44074063 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:37604235 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:37604235 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:42865203 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:42865203 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:13188755 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:13188755 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:41907164 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:41907164 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:75874222 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:75874222 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:55693287 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:55693287 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr22:30412732 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr22:30412732 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:15854359 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:15854359 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:2685514 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:2685514 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:47581622 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:47581622 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:1983030 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:1983030 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:89892583 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:89892583 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:50868716 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:50868716 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:149922367 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:149922367 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:56148462 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:56148462 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:25477490 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:25477490 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:11907522 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:11907522 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:142662063 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:142662063 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:157182141 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:157182141 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:115383399 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:115383399 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:33475496 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:33475496 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:47869352 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:47869352 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:131765444 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:131765444 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr13:25899063 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr13:25899063 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:224499624 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:224499624 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:55714359 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:55714359 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:76844910 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:76844910 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:40564314 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr15:40564314 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:140571983 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:140571983 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:47819895 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:47819895 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:66701193 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:66701193 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:8049655 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:8049655 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr22:25155739 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr22:25155739 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:139312568 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr9:139312568 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:43487383 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:43487383 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:149842429 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:149842429 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:102483828 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:102483828 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:54975734 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:54975734 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:145979812 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:145979812 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:37635681 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:37635681 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:43689345 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:43689345 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:97311853 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:97311853 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:198648987 G>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:198648987 G>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:58380879 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:58380879 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:21940092 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:21940092 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:130782163 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:130782163 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:178110796 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:178110796 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:74442311 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:74442311 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:46191071 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:46191071 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:211452512 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:211452512 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:87404355 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:87404355 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:4847875 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:4847875 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:91365830 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:91365830 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:219457145 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:219457145 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:187086386 G>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:187086386 G>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:62018076 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:62018076 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:167304317 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:167304317 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:55078437 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:55078437 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:5053342 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:5053342 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:31896499 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:31896499 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:61654574 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr18:61654574 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:85892325 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:85892325 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:67155795 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:67155795 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:145158165 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:145158165 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:45233168 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:45233168 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:46270466 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:46270466 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:47285605 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:47285605 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:220028046 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:220028046 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:39432848 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:39432848 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:19218620 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:19218620 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:21469800 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:21469800 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:23244554 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:23244554 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:168149355 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:168149355 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:106983136 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:106983136 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:44048437 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:44048437 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:18655730 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:18655730 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:64238718 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:64238718 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:28148859 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:28148859 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:115489049 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:115489049 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:64655239 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:64655239 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:68661651 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:68661651 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:7032156 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr4:7032156 C>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:98170293 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:98170293 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr22:35728922 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr22:35728922 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:6636051 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:6636051 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:100074810 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:100074810 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:2132359 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:2132359 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:38573590 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr21:38573590 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:179478706 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:179478706 A>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:64083741 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:64083741 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:77921873 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:77921873 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:49362860 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr17:49362860 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:57019083 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:57019083 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:2843641 G>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:2843641 G>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:46715496 T>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:46715496 T>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:58315681 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:58315681 T>C did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:88218725 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:88218725 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:43638416 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:43638416 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:9598348 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:9598348 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:65471465 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:65471465 A>G did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:78466671 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:78466671 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:64823781 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:64823781 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:64827498 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr12:64827498 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:52961077 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:52961077 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:58096255 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:58096255 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:44797364 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:44797364 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:52817558 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:52817558 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:62597379 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:62597379 G>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:53952612 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:53952612 G>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:143079310 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr7:143079310 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:154557556 T>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:154557556 T>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:91645619 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:91645619 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr8:41615541 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr8:41615541 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr8:124693322 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr8:124693322 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:142601849 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:142601849 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:101186553 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:101186553 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:98015075 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:98015075 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr20:35748285 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr20:35748285 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:23959916 A>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:23959916 A>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:149984388 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:149984388 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr10:73562619 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr10:73562619 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:47085944 A>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:47085944 A>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:87018939 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:87018939 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:162745671 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:162745671 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:124395019 T>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:124395019 T>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:52416634 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:52416634 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr10:69565331 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr10:69565331 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:15523083 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:15523083 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:242625330 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:242625330 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:31854545 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:31854545 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:158554105 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:158554105 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:112945182 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:112945182 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:108912142 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:108912142 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:151820359 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:151820359 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:34648626 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:34648626 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:34884092 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:34884092 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:133403251 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:133403251 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:40361898 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:40361898 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:10130879 G>A maps to ENST00000472167 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:10130879 G>A maps to ENST00000472167 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:26093485 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:26093485 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:97200673 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:97200673 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:6461676 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:6461676 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:107885930 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:107885930 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:26980641 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:26980641 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:55210666 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:55210666 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:173335846 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:173335846 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:31277538 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:31277538 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:55106065 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:55106065 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:96322230 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:96322230 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:46562967 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:46562967 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:136680944 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:136680944 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:63670266 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:63670266 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:40859156 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:40859156 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:179322450 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:179322450 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:93545225 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:93545225 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:65316162 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:65316162 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr21:42821302 A>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr21:42821302 A>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:57435120 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:57435120 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:170827250 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:170827250 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr14:20824398 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr14:20824398 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:101864968 T>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:101864968 T>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:118506082 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:118506082 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:40582688 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:40582688 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:6535037 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:6535037 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:153037539 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:153037539 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:72398734 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:72398734 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:119373487 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:119373487 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:111230772 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:111230772 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:27809526 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr12:27809526 T>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:55606986 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:55606986 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:11546861 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:11546861 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:198711191 A>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:198711191 A>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr20:40877234 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr20:40877234 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:136393625 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:136393625 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr14:36190837 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr14:36190837 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr17:78516090 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr17:78516090 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr10:99139220 G>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr10:99139220 G>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:38959912 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:38959912 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:45783136 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr15:45783136 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr18:12495983 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr18:12495983 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:136219498 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:136219498 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr14:64375839 A>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr14:64375839 A>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:70613125 T>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chrX:70613125 T>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:179558221 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:179558221 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr21:19647370 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr21:19647370 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr17:40762274 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr17:40762274 C>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:140080272 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:140080272 C>G did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:140080353 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:140080353 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:19989280 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:19989280 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:30029634 G>C did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:30029634 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:94577262 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:94577262 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:913926 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:913926 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:150749495 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:150749495 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:8401270 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:8401270 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:131303596 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:131303596 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:24304565 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:24304565 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:5236987 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:5236987 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:100636862 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:100636862 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:43945744 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:43945744 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:7724742 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:7724742 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:74360838 T>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:74360838 T>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:74360841 T>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:74360841 T>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:77825489 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:77825489 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:110825740 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:110825740 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:41580610 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:41580610 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:113748338 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:113748338 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:114203803 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:114203803 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:37438413 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:37438413 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:68740195 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:68740195 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:129899654 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:129899654 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:11353979 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:11353979 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:155932074 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:155932074 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:28151618 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:28151618 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:15262538 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:15262538 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:176934458 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:176934458 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:1390997 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:1390997 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:113459421 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:113459421 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:42474742 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:42474742 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:77218046 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:77218046 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:76918760 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:76918760 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:142266757 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:142266757 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:13494492 A>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:13494492 A>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:51685315 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:51685315 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:128153146 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:128153146 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:76246860 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:76246860 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:113086924 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:113086924 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:7178037 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:7178037 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:200880410 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:200880410 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:179425798 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:179425798 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:99890777 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:99890777 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:184604009 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:184604009 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:123782506 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:123782506 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:32789897 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:32789897 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:112420621 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:112420621 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:27296926 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:27296926 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:201022789 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:201022789 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:86063644 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:86063644 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:39225519 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:39225519 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:25307168 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:25307168 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:28459594 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:28459594 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:28605356 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:28605356 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:59399927 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:59399927 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:49839066 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:49839066 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:101443478 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:101443478 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:102123091 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:102123091 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:120288114 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:120288114 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:11867150 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:11867150 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:16375116 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:16375116 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:37858375 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:37858375 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:106171457 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:106171457 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:14706001 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:14706001 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:71046423 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:71046423 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:154522220 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:154522220 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:73800963 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:73800963 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:23846632 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:23846632 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:121292900 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:121292900 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:70642593 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:70642593 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:70856881 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:70856881 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:94026966 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:94026966 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:139647220 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:139647220 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:109765820 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:109765820 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:189918794 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:189918794 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:130300778 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:130300778 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:25601129 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:25601129 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:37322238 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:37322238 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:61973978 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:61973978 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:113392715 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:113392715 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:39796254 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:39796254 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:80390274 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:80390274 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:22933912 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:22933912 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:143998971 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:143998971 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:41594576 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:41594576 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:135371747 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:135371747 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:99445921 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:99445921 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:76677203 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:76677203 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:61077644 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:61077644 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:50596839 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:50596839 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:135470215 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:135470215 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:134130845 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:134130845 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:140219375 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:140219375 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:12640462 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:12640462 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40259996 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40259996 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:102028756 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:102028756 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:32662523 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:32662523 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:38743850 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:38743850 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:32954754 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:32954754 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:28971275 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:28971275 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:7577112 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:7577112 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:172583208 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:172583208 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:71778901 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:71778901 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:132967936 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:132967936 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65766888 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65766888 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:2408974 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:2408974 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:79411948 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:79411948 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:39993606 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:39993606 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:4858675 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:4858675 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:75174212 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:75174212 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:97311585 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:97311585 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:94120926 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:94120926 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:94128936 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:94128936 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:39755276 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:39755276 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:133802456 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:133802456 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40880976 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40880976 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:197021820 C>A maps to NM_001994.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:197021820 C>A maps to NM_001994.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:169495042 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:169495042 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:14563709 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:14563709 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:74096660 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:74096660 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:86151179 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:86151179 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:150421724 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:150421724 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:47919936 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:47919936 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:144810987 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:144810987 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:157716564 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:157716564 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:125113292 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:125113292 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:240305889 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:240305889 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:89404907 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:89404907 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:12724792 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:12724792 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:162376130 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:162376130 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:7495462 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:7495462 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:35612269 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:35612269 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:46994724 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:46994724 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:161116180 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:161116180 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:49208487 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:49208487 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:153784619 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:153784619 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:163215991 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:163215991 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:109113597 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:109113597 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:179757680 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:179757680 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:73235424 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:73235424 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:85909789 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:85909789 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:30683543 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:30683543 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:30695575 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:30695575 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:30746965 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:30746965 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:23309544 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:23309544 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:154056104 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:154056104 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:19087028 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:19087028 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:130761681 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:130761681 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:15610156 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:15610156 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:154247615 C>G maps to ENST00000453365 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:154247615 C>G maps to ENST00000453365 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:32793076 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:32793076 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:31237198 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:31237198 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:70100899 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:70100899 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:84164679 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:84164679 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:145537623 C>G maps to ENST00000415363 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:145537623 C>G maps to ENST00000415363 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:122753014 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:122753014 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:53652066 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:53652066 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:201184624 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:201184624 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:113738763 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:113738763 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:143129921 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:143129921 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:15714555 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:15714555 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:54780207 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:54780207 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:163279772 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:163279772 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:78846168 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:78846168 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:34539177 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:34539177 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:94101016 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:94101016 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:91469258 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:91469258 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:57963492 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:57963492 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:57963760 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:57963760 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:158064210 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:158064210 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:10532186 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:10532186 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:186459268 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:186459268 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:39032578 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:39032578 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:129722555 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:129722555 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:66067030 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:66067030 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:54756307 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:54756307 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:82434717 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:82434717 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:62935759 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:62935759 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6994299 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6994299 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6994303 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6994303 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:134165305 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:134165305 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:44399671 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:44399671 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:85623500 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:85623500 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:42448234 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:42448234 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:49022352 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:49022352 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:12019130 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:12019130 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:137041541 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:137041541 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:71201083 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:71201083 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:49959218 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:49959218 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:60032986 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:60032986 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:2544760 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:2544760 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:205567042 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:205567042 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:131083887 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:131083887 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:2526336 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:2526336 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:102825033 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:102825033 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:34094988 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:34094988 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:90844464 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:90844464 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:108829687 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:108829687 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:124962074 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:124962074 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:54665900 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:54665900 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:36921527 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:36921527 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:105654525 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:105654525 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:24403517 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:24403517 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:80083233 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:80083233 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:81102524 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:81102524 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:47375930 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:47375930 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:101753131 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:101753131 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:16890826 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:16890826 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:67379311 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:67379311 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:21319314 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:21319314 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:89224423 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:89224423 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:139934346 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:139934346 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:72897518 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:72897518 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:52260369 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:52260369 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:52260372 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:52260372 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:50692737 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:50692737 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:51056825 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:51056825 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:135042215 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:135042215 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:113344788 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:113344788 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:228494927 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:228494927 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:29364386 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:29364386 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:77060266 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:77060266 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:55664897 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:55664897 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:20705092 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:20705092 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:34969209 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:34969209 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:8049892 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:8049892 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:22108475 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:22108475 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:44048079 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:44048079 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:49951178 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:49951178 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:25115648 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:25115648 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:102051228 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:102051228 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:45267447 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:45267447 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:208276661 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:208276661 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:72410096 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:72410096 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:22037689 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:22037689 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:104251282 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:104251282 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:9550018 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr18:9550018 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:120928108 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:120928108 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:57173138 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:57173138 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:3692199 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:3692199 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:150325220 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:150325220 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:170699587 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:170699587 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:150990708 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:150990708 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:43418920 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:43418920 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32808689 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32808689 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40729713 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40729713 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40985621 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:40985621 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:99040743 G>C maps to ENST00000398089 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:99040743 G>C maps to ENST00000398089 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:98218541 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:98218541 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:97299164 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:97299164 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:209307218 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:209307218 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:43106762 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:43106762 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:214656220 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:214656220 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:214705598 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:214705598 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:8713573 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:8713573 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:36236213 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:36236213 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:91505102 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:91505102 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65423105 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65423105 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:43615229 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:43615229 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:186508237 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:186508237 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:54799998 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:54799998 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:77366445 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:77366445 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:117715577 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:117715577 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:120635307 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:120635307 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:56986127 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:56986127 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:54705038 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:54705038 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:108913184 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:108913184 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:136595420 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:136595420 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:123513396 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:123513396 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:169839331 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:169839331 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:39536548 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:39536548 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:83098448 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:83098448 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:83277717 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:83277717 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:43150528 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:43150528 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:29891087 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:29891087 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:7423922 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:7423922 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:67147548 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:67147548 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:72614366 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:72614366 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:116747571 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:116747571 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:232564315 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:232564315 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:1459267 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:1459267 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:164781357 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:164781357 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:1074625 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:1074625 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65149532 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65149532 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:25676291 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:25676291 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92917547 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92917547 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:205765990 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:205765990 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:125741506 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:125741506 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:75862185 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:75862185 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:46495107 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:46495107 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:56567458 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:56567458 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:56568418 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:56568418 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65619185 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:65619185 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:121457172 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:121457172 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:140786481 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:140786481 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:46276899 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:46276899 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:147475377 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:147475377 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:136448299 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:136448299 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:158612571 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:158612571 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:30734164 T>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:30734164 T>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:48056799 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:48056799 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:48818748 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:48818748 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:131306160 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:131306160 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:64676052 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:64676052 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:79702649 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:79702649 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:107216201 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:107216201 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:149758368 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:149758368 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:156832597 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:156832597 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:179660080 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:179660080 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:138033624 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:138033624 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:165788946 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:165788946 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:24646221 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:24646221 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:201104700 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:201104700 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:12994288 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:12994288 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:5360156 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:5360156 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32017395 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32017395 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:2226668 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:2226668 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:230643780 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:230643780 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:77435401 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:77435401 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:98609987 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:98609987 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:100074836 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:100074836 A>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:100074840 A>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:100074840 A>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:166758114 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:166758114 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:166769263 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:166769263 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:3154048 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:3154048 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:43669152 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:43669152 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:44194194 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:44194194 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:132404471 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:132404471 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:17531181 C>A maps to NM_153676.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:17531181 C>A maps to NM_153676.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:179482018 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:179482018 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:78166923 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:78166923 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:120177780 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:120177780 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6964801 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6964801 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:100821809 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:100821809 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:62214245 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:62214245 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6232096 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:6232096 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:48932785 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:48932785 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:48932787 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:48932787 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:137007851 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:137007851 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:1009849 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:1009849 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:61721288 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:61721288 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:27412449 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:27412449 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:46585481 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:46585481 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:129665848 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:129665848 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:44802453 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:44802453 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:125029738 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:125029738 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:152137912 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chrX:152137912 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:54079845 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:54079845 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:22817241 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:22817241 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:2827750 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:2827750 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:146806771 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:146806771 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:22941943 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:22941943 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:60638402 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:60638402 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:21210256 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:21210256 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:79093922 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:79093922 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:139913596 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:139913596 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:80638478 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:80638478 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:23751336 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:23751336 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:20494252 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:20494252 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:236889199 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:236889199 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:156916249 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:156916249 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:64569326 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:64569326 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:7707763 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:7707763 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:112033161 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:112033161 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:19568162 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:19568162 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:183616704 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:183616704 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:68113758 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:68113758 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:148980853 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:148980853 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73125235 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73125235 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:7047628 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:7047628 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:25962124 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:25962124 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99055822 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99055822 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67514998 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67514998 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67515000 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67515000 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:42487454 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:42487454 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:42551162 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:42551162 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:143624734 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:143624734 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:23631819 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:23631819 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:41291036 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:41291036 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50169462 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50169462 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:28521116 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:28521116 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:36178345 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:36178345 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:26409613 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:26409613 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:8946916 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:8946916 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:8734957 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:8734957 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:13620997 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:13620997 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:40832425 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:40832425 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:17385047 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:17385047 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:207314680 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:207314680 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:99796914 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:99796914 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:69621317 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:69621317 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:98660088 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:98660088 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:2716100 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:2716100 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:174979301 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:174979301 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:32224561 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:32224561 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:91776105 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:91776105 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:28605346 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:28605346 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:28605388 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:28605388 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:69458795 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:69458795 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:35818999 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:35818999 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:73476905 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:73476905 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158153636 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158153636 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:160805877 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:160805877 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:207925404 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:207925404 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:21883445 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:21883445 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:123233755 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:123233755 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:22333548 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:22333548 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:22310364 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:22310364 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:40111897 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:40111897 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:42581253 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:42581253 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:65399020 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:65399020 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:120241293 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:120241293 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:19167662 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:19167662 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:31344242 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:31344242 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:46039396 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:46039396 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:103444490 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:103444490 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:32167810 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:32167810 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:117027437 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:117027437 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:189855102 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:189855102 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:110855803 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:110855803 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:227925019 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:227925019 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:107782952 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:107782952 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:83977993 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:83977993 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99687058 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99687058 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99687070 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99687070 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:1414368 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:1414368 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:34003032 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:34003032 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:113347804 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:113347804 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:68979296 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:68979296 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:41383725 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:41383725 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:109281447 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:109281447 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:20178575 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:20178575 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:20180948 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:20180948 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:61627971 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:61627971 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:55056113 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:55056113 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:37656899 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:37656899 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140907992 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140907992 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:170598010 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:170598010 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:196865657 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:196865657 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:132220425 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:132220425 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:98078337 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:98078337 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:98058678 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:98058678 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:146785352 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:146785352 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:103182781 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:103182781 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:207575367 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:207575367 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:22268435 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:22268435 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:44198655 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:44198655 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:109215616 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:109215616 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:8016480 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:8016480 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:18632881 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:18632881 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:4859787 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:4859787 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:43872694 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:43872694 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:25205983 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:25205983 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:112029653 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:112029653 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:15338930 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:15338930 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:212484048 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:212484048 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:212543996 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:212543996 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:138179622 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:138179622 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:57698505 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:57698505 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:130705589 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:130705589 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:71238226 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:71238226 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30825110 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30825110 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30825161 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30825161 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:10691236 G>C maps to NM_022068.2 L2332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:10691236 G>C maps to NM_022068.2 L2332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:58639319 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:58639319 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:114514648 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:114514648 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:67666104 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:67666104 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:78313284 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:78313284 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:22646210 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:22646210 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:161595803 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67263490 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67263490 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:240306326 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:240306326 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:240497280 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:240497280 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:101061496 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:101061496 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:97711636 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:97711636 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99799775 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99799775 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:5808295 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:5808295 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:179751150 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:179751150 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:42153125 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:42153125 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:4861377 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:4861377 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:45095926 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:45095926 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:45097002 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:45097002 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:67490428 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:67490428 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:27215437 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:27215437 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:47492797 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:47492797 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:228336332 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:228336332 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:127451416 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:127451416 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140073515 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140073515 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:197194258 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:197194258 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:69683002 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:69683002 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:119964262 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:119964262 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:31728952 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:31728952 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:163138093 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:163138093 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:46543911 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:46543911 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140041718 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140041718 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:41373175 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:41373175 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:197616624 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:197616624 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:46308569 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:46308569 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:124393475 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:124393475 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:78872247 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:78872247 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:73332390 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:73332390 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:136638122 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:136638122 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:6483286 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:6483286 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:28976369 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:28976369 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:200968472 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:200968472 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:26174625 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:26174625 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:23164581 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:23164581 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:45978612 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:45978612 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:31914242 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:31914242 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:25976034 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:25976034 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:206769278 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:206769278 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:55147117 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:55147117 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:27528218 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:27528218 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:58834724 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:58834724 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:921432 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:921432 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:141773490 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:141773490 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:53792511 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:53792511 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:46745978 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:46745978 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:77130815 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:77130815 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:136923206 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:136923206 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:66190516 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:66190516 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:37187187 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:37187187 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:49415781 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:49415781 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:151040065 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:151040065 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:39881217 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:39881217 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:34958969 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:34958969 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:68667949 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:68667949 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:60073746 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:60073746 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:108117734 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:108117734 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:10558036 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:10558036 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:10361077 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:10361077 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:89896312 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:89896312 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:101760019 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:101760019 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:100426739 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:100426739 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:124884915 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:124884915 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:35312902 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:35312902 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:149915211 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:149915211 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:119114863 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:119114863 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:27152623 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:27152623 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:27203853 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:27203853 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:52701618 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:52701618 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:42681379 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:42681379 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:57047849 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:57047849 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:52260341 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:52260341 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:229600710 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:229600710 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248636562 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248636562 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:74015300 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:74015300 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:78981147 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:78981147 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:91675612 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:91675612 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:71476482 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:71476482 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:31855499 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:31855499 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:102783591 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:102783591 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:27248872 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:27248872 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:139744638 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:139744638 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21068844 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21068844 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:44435121 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:44435121 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:81157237 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:81157237 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:51656000 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:51656000 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:131481907 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:131481907 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:38538945 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:38538945 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:204199510 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:204199510 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:153699710 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:153699710 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:72162828 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:72162828 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:89862395 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:89862395 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:81678086 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:81678086 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:11201048 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:11201048 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:57159639 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:57159639 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:24185904 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:24185904 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:170002470 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:170002470 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:2103680 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:2103680 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:142460268 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:142460268 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:109964557 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:109964557 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:1651935 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:1651935 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:176729836 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:176729836 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:56374310 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:56374310 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:33445680 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:33445680 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67805823 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:67805823 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:22206803 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:22206803 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:65270552 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:65270552 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:47006899 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:47006899 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:155145279 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:155145279 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:43613961 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:43613961 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:19945586 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:19945586 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:154633587 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:154633587 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:8704204 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:8704204 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:67781558 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:67781558 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:38995291 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:38995291 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50899496 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50899496 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:76878414 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:76878414 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:26982863 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:26982863 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:30795743 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:30795743 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:82000000 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:82000000 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:169563045 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:169563045 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:90760892 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:90760892 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:57382080 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:57382080 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:36568999 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:36568999 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:70237121 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:70237121 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:81373912 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:81373912 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:23808901 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:23808901 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:111884866 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:111884866 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:49148056 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:49148056 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:116719724 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:116719724 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:72190690 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:72190690 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73274488 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73274488 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:48326353 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:48326353 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:40401951 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:40401951 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:57310943 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:57310943 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:25230376 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:25230376 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:51621570 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:51621570 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:24048626 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:24048626 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:94994631 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:94994631 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158588931 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158588931 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:100484870 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:100484870 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:63964631 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:63964631 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:146722496 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:146722496 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:149877634 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:149877634 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:29770825 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:29770825 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:158509830 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:158509830 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:159464544 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:159464544 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:142880451 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:142880451 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:59620403 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:59620403 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:179660105 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:179660105 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:218607276 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:218607276 T>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:39998789 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:39998789 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:35717583 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:35717583 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:8077423 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:8077423 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:945388 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:945388 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:212538536 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:212538536 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:44102977 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:44102977 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:83379944 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:83379944 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:83424668 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:83424668 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:42267746 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:42267746 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:119945542 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:119945542 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:195608804 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:195608804 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:9623967 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:9623967 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:12880439 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:12880439 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:33623978 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:33623978 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:81499328 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:81499328 A>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:81610779 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:81610779 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:115600087 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:115600087 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:116601141 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:116601141 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:94842558 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:94842558 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179458654 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179458654 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:99890506 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:99890506 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21921997 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21921997 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:19499630 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:19499630 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:24911155 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:24911155 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:118828127 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:118828127 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:118828746 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:118828746 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:75286572 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:75286572 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:108160382 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:108160382 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:38766410 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:38766410 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:50512442 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:50512442 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:48933521 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chrX:48933521 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:113079154 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:113079154 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:37379348 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:37379348 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:38434498 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:38434498 T>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:69971204 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:69971204 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:41318562 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:41318562 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:132339026 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:132339026 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:147130531 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:147130531 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:38260676 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:38260676 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:180309775 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:180309775 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:37918745 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:37918745 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:40954613 G>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:40954613 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:215891754 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:215891754 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:107568728 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:107568728 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:66991913 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:66991913 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:169780347 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:169780347 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:87179478 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:87179478 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:20739387 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:20739387 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:48753228 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:48753228 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183643308 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183643308 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:74762461 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:74762461 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:150915803 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:150915803 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35470205 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35470205 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35640136 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35640136 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:150745901 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:150745901 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:111850587 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:111850587 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:20488864 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:20488864 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:123334017 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:123334017 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:127798491 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:127798491 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:5239459 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:5239459 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:178548491 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:178548491 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:130288908 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:130288908 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:49166401 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:49166401 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:26099622 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:26099622 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:50311825 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:50311825 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:177636206 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:177636206 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:247067393 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:247067393 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:86265155 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:86265155 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:134252802 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:134252802 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:40739742 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:40739742 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:45891206 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:45891206 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:38500824 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:38500824 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:14797238 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:14797238 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:241447119 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:241447119 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:70820142 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:70820142 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:97505935 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:97505935 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:27355481 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:27355481 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:150204267 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:150204267 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:90341011 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:90341011 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124715075 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124715075 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:47747049 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:47747049 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:83360725 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:83360725 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:90451661 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:90451661 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36369706 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36369706 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:116701406 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:116701406 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:25228442 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:25228442 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121304837 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121304837 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:156914692 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:156914692 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:9437400 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:9437400 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:97493845 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:97493845 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26079284 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26079284 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161761754 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161761754 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161761758 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161761758 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:108142173 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:108142173 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:138823099 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:138823099 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:25268490 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:25268490 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160109658 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160109658 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:119509177 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:119509177 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:77108074 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:77108074 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:35742775 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:35742775 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:46114408 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:46114408 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:102946244 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:102946244 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:160285636 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:160285636 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:18187563 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:18187563 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:14743568 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:14743568 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:88651854 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:88651854 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:92442958 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:92442958 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:26446233 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:26446233 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:180374388 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:180374388 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105902161 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105902161 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:120070915 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:120070915 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:64877943 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:64877943 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:97150344 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:97150344 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:90782802 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:90782802 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:49411617 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:49411617 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:20932308 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:20932308 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51770794 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51770794 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:55277462 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:55277462 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:55049656 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:55049656 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:10594214 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:10594214 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:46000517 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:46000517 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32545831 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32545831 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26998205 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26998205 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26654588 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26654588 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:37121710 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:37121710 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:6865847 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:6865847 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:48080876 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:48080876 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:120906224 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:120906224 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:39289126 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:39289126 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:98680525 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:98680525 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:131590994 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:131590994 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35674510 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35674510 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:48542604 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:48542604 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:13341144 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:13341144 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:181714437 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:181714437 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:1254480 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:1254480 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:201035347 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:201035347 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:201035349 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:201035349 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:54921935 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:54921935 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:37341032 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:37341032 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:85985157 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:85985157 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:86028222 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:86028222 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:159163607 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:159163607 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:27446665 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:27446665 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:48733682 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:48733682 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:15819543 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:15819543 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:116243726 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:116243726 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38849273 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38849273 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:105400709 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:105400709 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:77807723 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:77807723 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:70515060 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:70515060 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179736064 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179736064 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:197539092 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:197539092 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:123265707 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:123265707 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:132287350 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:132287350 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:86126095 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:86126095 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:26483222 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:26483222 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:158261820 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:158261820 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160808219 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160808219 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51729551 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51729551 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35610825 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35610825 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:149962105 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:149962105 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:38450768 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:38450768 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:24593654 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:24593654 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:21882818 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:21882818 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:21884072 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:21884072 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:95185947 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:95185947 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:19520745 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:19520745 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:85957608 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:85957608 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:31981730 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:31981730 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:18606353 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:18606353 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:36653339 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:36653339 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125875588 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125875588 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125893184 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125893184 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:56874614 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:56874614 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:637596 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:637596 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55883455 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55883455 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:50828524 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:50828524 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6169753 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6169753 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:133428173 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:133428173 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:85149331 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:85149331 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:136623180 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:136623180 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:184072521 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:184072521 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:184075728 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:184075728 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:10223794 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:10223794 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:6261278 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:6261278 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:87672125 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:87672125 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:56709034 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:56709034 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:3080534 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:3080534 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:125281817 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:125281817 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:7838528 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:7838528 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:33148721 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:33148721 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:121239647 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:121239647 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:121290840 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:121290840 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:46900493 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:46900493 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:70850658 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:70850658 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:70850812 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:70850812 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:109817892 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:109817892 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:109862481 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:109862481 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:117064008 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:117064008 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:47548966 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:47548966 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:70976488 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:70976488 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:40777504 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:40777504 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:238004452 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:238004452 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:4408219 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:4408219 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:148601652 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:148601652 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:131963140 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:131963140 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:125514290 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:125514290 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207644886 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207644886 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:197396575 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:197396575 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:36703900 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:36703900 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49676980 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49676980 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:2830850 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:2830850 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:77252845 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:77252845 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:11199479 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:11199479 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:41462927 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:41462927 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:17032233 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:17032233 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44866825 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44866825 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:143997188 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:143997188 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:94836213 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:94836213 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:127961197 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:127961197 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:135347239 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:135347239 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:42027478 G>T maps to ENST00000439847 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:42027478 G>T maps to ENST00000439847 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:48982373 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:48982373 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:24761386 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:24761386 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242684448 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242684448 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:39381763 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:39381763 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:72147231 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:72147231 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:155671643 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:155671643 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:16638883 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:16638883 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:150121492 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:150121492 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:176941685 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:176941685 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:169194353 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:169194353 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:37632677 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:37632677 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:32407589 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:32407589 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:13891030 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:13891030 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:196866376 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:196866376 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:72310523 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:72310523 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:132185918 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:132185918 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:58178973 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:58178973 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:116226354 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:116226354 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:154560997 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:154560997 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:109028004 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:109028004 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:109031579 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:109031579 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:134010506 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:134010506 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:100509721 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:100509721 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:28597986 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:28597986 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:28923406 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:28923406 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183888086 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183888086 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:38858939 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:38858939 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:40320989 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:40320989 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:71817489 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:71817489 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:108380823 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:108380823 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:141549563 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:141549563 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:32690092 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:32690092 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:32694024 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:32694024 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:73459479 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:73459479 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:80626290 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:80626290 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:60063569 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:60063569 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:79474728 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:79474728 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:42522254 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:42522254 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:132171080 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:132171080 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132466567 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132466567 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132504519 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132504519 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:131186822 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:131186822 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:14013917 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:14013917 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:128426045 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:128426045 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:100582493 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:100582493 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:148524145 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:148524145 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:197031843 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:197031843 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:169541585 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:169541585 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:113771982 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:113771982 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:46874018 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:46874018 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:153414210 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:153414210 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:175533517 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:175533517 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:51829549 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:51829549 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:116779574 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:116779574 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:87491269 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:87491269 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35076142 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35076142 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242422953 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242422953 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48777562 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48777562 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48805629 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48805629 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:8174021 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:8174021 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:157667405 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:157667405 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124982244 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124982244 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:125023000 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:125023000 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:155531076 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:155531076 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:135290814 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:135290814 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:78388984 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:78388984 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:84603694 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:84603694 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:128488819 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:128488819 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:240306309 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:240306309 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:50047381 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:50047381 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:216240283 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:216240283 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89424575 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89424575 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:14770549 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:14770549 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:4306046 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:4306046 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:39169918 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:39169918 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:27136488 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:27136488 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:151562842 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:151562842 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:173269919 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:173269919 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:130149690 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:130149690 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:9939765 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:9939765 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:22737878 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:22737878 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:74764460 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:74764460 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:92944028 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:92944028 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:74041685 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:74041685 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:33447220 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:33447220 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:61994883 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:61994883 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:47041651 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:47041651 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:90604175 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:90604175 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:175649872 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:175649872 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:129383909 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:129383909 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:129467748 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:129467748 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:110295521 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:110295521 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:4867585 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:4867585 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:1624687 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:1624687 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:127651395 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:127651395 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:28837892 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:28837892 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:101157290 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:101157290 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:176883174 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:176883174 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:72443245 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:72443245 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:123489024 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:123489024 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:153175028 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:153175028 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:101878808 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:101878808 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:37346219 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:37346219 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:9927800 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:9927800 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:47440837 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:47440837 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:110215788 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:110215788 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:106617424 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:106617424 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121363833 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121363833 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:28538287 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:28538287 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:191175544 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:191175544 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:27806821 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:27806821 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:185703872 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:185703872 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:55360210 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:55360210 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:1749018 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:1749018 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:121439027 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:121439027 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:19049117 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:19049117 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30533479 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30533479 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46805972 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46805972 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:99007593 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:99007593 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:70896518 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:70896518 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183819225 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183819225 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:52876493 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:52876493 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:27688469 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:27688469 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:185434084 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:185434084 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:102644668 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:102644668 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:28677496 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:28677496 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:166905812 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:166905812 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:76712737 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:76712737 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:120606672 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:120606672 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41337297 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41337297 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:143007290 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:143007290 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121583433 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121583433 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:15260635 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:15260635 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:7143118 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:7143118 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:44424292 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:44424292 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:98655368 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:98655368 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:158980620 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:158980620 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:156535996 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:156535996 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55360215 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55360215 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:128430779 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:128430779 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:68661431 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:68661431 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:54798071 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:54798071 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:56088202 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:56088202 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:185276524 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:185276524 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:15374314 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:15374314 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:42814931 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:42814931 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39766348 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39766348 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:20113960 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:20113960 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:20167363 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:20167363 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:127646500 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:127646500 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:156139562 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:156139562 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:88658538 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:88658538 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:36763179 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:36763179 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:42142256 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:42142256 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:138628267 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:138628267 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:72324036 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:72324036 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:113775341 A>G maps to ENST00000483766 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:113775341 A>G maps to ENST00000483766 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:100013132 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:100013132 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:36870432 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:36870432 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:16352494 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:16352494 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:10421943 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:10421943 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:39696649 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:39696649 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:45228014 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:45228014 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26177090 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:26177090 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42985753 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42985753 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:47371645 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:47371645 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:70681209 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:70681209 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:166238893 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:166238893 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:23180293 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:23180293 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51329004 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51329004 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:117037483 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:117037483 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39122620 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39122620 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:52865405 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:52865405 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:52778741 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:52778741 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:46117900 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:46117900 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:71293996 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:71293996 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:32185343 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:32185343 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39405901 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39405901 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39411548 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:39411548 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:35979448 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:35979448 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:118198720 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:118198720 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:153138664 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:153138664 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:6046655 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:6046655 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:48962263 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:48962263 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:6947102 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:6947102 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:107643404 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:107643404 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:149982846 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:149982846 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:25967532 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:25967532 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:27393063 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:27393063 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:206775924 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:206775924 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:54804019 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:54804019 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:54850418 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:54850418 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:90982122 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:90982122 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:39983386 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:39983386 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:56332365 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:56332365 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:57589572 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:57589572 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:44116767 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:44116767 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:24524409 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:24524409 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:134175164 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:134175164 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:100618082 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:100618082 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:31774498 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:31774498 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41804844 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41804844 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:24759747 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:24759747 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:25099004 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:25099004 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:39696957 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:39696957 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:166987040 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:166987040 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:78755014 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:78755014 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:210565125 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:210565125 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:102490091 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:102490091 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:186943418 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:186943418 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:186947727 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:186947727 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:12969279 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:12969279 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:46487485 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:46487485 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:138686913 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:138686913 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:35804340 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:35804340 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:150877615 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:150877615 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:60039225 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:60039225 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:42180488 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:42180488 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:228220377 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:228220377 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:158541419 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:158541419 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:18362207 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:18362207 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:36873656 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:36873656 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:154862056 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:154862056 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:102667955 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:102667955 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:1342157 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:1342157 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:41345320 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:41345320 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:62364066 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:62364066 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113459599 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113459599 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:102020716 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:102020716 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:77713244 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:77713244 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:10415870 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:10415870 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23897947 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23897947 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:211163027 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:211163027 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:109562284 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:109562284 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:109817502 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:109817502 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52645877 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52645877 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:76872196 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:76872196 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:113442764 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:113442764 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:71209591 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:71209591 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101720125 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101720125 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101728338 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101728338 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:18258445 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:18258445 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:90983303 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:90983303 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:120382992 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:120382992 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:133721193 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:133721193 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:16055347 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:16055347 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:2606290 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:2606290 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:206988866 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:206988866 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:20959472 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:20959472 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:69646615 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:69646615 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:47583599 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:47583599 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:42084836 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:42084836 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:99205190 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:99205190 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:125144451 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:125144451 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:56539943 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:56539943 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:55453135 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:55453135 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:183253711 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:183253711 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:183273935 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:183273935 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:43667368 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:43667368 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6585874 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6585874 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:32164901 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:32164901 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:120430209 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:120430209 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89073111 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89073111 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36342065 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36342065 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:2937707 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:2937707 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:105179111 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:105179111 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:33510590 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:33510590 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:64435165 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:64435165 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:40778313 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:40778313 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:107866741 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:107866741 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:110255538 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:110255538 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:154033351 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:154033351 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:8791440 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:8791440 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:113440631 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:113440631 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:9800994 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:9800994 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:15103716 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:15103716 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161967493 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161967493 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:132305961 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:132305961 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248437203 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248437203 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:3140892 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:3140892 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:31795837 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:31795837 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23237423 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23237423 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:90690527 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:90690527 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:103260259 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:103260259 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:35457396 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:35457396 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125647477 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125647477 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:164790682 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:164790682 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:100915131 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:100915131 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101179907 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101179907 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:134076052 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:134076052 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82784422 G>A maps to NM_033026.5 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82784422 G>A maps to NM_033026.5 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:62905030 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:62905030 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:233225745 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:233225745 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105166350 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105166350 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165752901 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165752901 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165843906 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165843906 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:183070892 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:183070892 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:18324362 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:18324362 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:144879612 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:144879612 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:44171127 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:44171127 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7343348 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7343348 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:54985241 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:54985241 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45739150 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45739150 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:99191973 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:99191973 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:97892003 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:97892003 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:144032927 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:144032927 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:34457328 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:34457328 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:18942355 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:18942355 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207105950 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207105950 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:49951239 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:49951239 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:51524788 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:51524788 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:145463987 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:145463987 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:75671309 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:75671309 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:64022321 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:64022321 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:131948923 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:131948923 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:37226092 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:37226092 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:126731064 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:126731064 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:208252543 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:208252543 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:118187610 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:118187610 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:118307004 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:118307004 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:43010710 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:43010710 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:113304528 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:113304528 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:38145683 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:38145683 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:42681223 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:42681223 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:63195544 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:63195544 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:145726035 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:145726035 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:37529103 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:37529103 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:75239054 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:75239054 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:94712933 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:94712933 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:94731151 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:94731151 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:23518136 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:23518136 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:2082424 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:2082424 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:30103537 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:30103537 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:53564514 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:53564514 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:53667406 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:53667406 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:1563584 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:1563584 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240984464 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240984464 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:86518645 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:86518645 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:35777331 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:35777331 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:32810062 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:32810062 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:74338072 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:74338072 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:1099548 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:1099548 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:8376507 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:8376507 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:8492836 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:8492836 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:44087745 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:44087745 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:31453015 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:31453015 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:52233513 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:52233513 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:119768421 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:119768421 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128483659 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128483659 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:24737853 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:24737853 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:51208451 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:51208451 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:33433247 T>A maps to ENST00000339934 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:33433247 T>A maps to ENST00000339934 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:20616360 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:20616360 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:21940105 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:21940105 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:173787053 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:173787053 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:173891526 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:173891526 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:80513385 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:80513385 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:49027258 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:49027258 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:24574666 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:24574666 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:17284959 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:17284959 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23353841 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23353841 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:8505711 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:8505711 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32590328 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32590328 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:117245728 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:117245728 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:3424627 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:3424627 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:63890756 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:63890756 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228873486 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228873486 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:87376965 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:87376965 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:31504658 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:31504658 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:30302725 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:30302725 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:30329598 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:30329598 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:123695687 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:123695687 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:117710494 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:117710494 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:23960102 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:23960102 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:93306379 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:93306379 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:15157043 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:15157043 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:127440469 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:127440469 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:158261869 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:158261869 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41769311 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41769311 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:127831682 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:127831682 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:165397867 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:165397867 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38950988 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38950988 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38995020 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38995020 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237880686 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237880686 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237895503 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237895503 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:34129231 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:34129231 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:18458360 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:18458360 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:200137424 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:200137424 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:50893412 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:50893412 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:50149470 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:50149470 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:165970488 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:165970488 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:167142777 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:167142777 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:29966032 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:29966032 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:175260534 T>G maps to NM_001193528.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:175260534 T>G maps to NM_001193528.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:71344889 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:71344889 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121657896 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121657896 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:84666198 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:84666198 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:9238004 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:9238004 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48022550 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48022550 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48053315 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48053315 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:61564840 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:61564840 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30749095 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30749095 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:65819836 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:65819836 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:67148110 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:67148110 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:52070939 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:52070939 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:2834172 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:2834172 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:235949507 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:235949507 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:17789337 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:17789337 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:49182855 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:49182855 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52130373 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52130373 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:100901484 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:100901484 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:164792545 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:164792545 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46289056 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46289056 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:122763293 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:122763293 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:25830927 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:25830927 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:104419778 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:104419778 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:85486874 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:85486874 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:46633330 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:46633330 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:18270152 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:18270152 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:40402517 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:40402517 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:67291057 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:67291057 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:20569082 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:20569082 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:168100407 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:168100407 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:56574663 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:56574663 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:38787751 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:38787751 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:2195826 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:2195826 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:214497961 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:214497961 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:19192283 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:19192283 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:203830708 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:203830708 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:12220440 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:12220440 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:75949595 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:75949595 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:179310483 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:179310483 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:108366794 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:108366794 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:106675474 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:106675474 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:106982827 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:106982827 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:231313917 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:231313917 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:231090526 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:231090526 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:118539143 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:118539143 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:118629687 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:118629687 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:144337133 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:144337133 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:217824368 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:217824368 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:16200954 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:16200954 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:66458680 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:66458680 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:142747501 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:142747501 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:4247929 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:4247929 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:629272 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:629272 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:182794428 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:182794428 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:116769838 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:116769838 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:90706913 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:90706913 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:38008228 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:38008228 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:43600676 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:43600676 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:104269086 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:104269086 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:70517293 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:70517293 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:70539926 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:70539926 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:108881547 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:108881547 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:48048525 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:48048525 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27009700 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27009700 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27010555 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27010555 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113194165 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113194165 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:25555337 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:25555337 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152738280 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152738280 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152826240 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152826240 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:158482916 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:158482916 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:45268091 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:45268091 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:45275814 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:45275814 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:23845293 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:23845293 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:100533867 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chrX:100533867 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30688846 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30688846 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:67172996 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:67172996 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:96259973 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:96259973 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:15641498 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:15641498 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:186276172 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:186276172 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42713853 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42713853 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:45776992 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:45776992 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:85446330 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:85446330 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:85448391 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:85448391 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:115117296 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:115117296 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:160201219 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:160201219 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:124179681 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:124179681 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:24667123 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:24667123 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:100235933 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:100235933 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20846469 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20846469 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20852925 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20852925 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:69391532 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:69391532 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:55206205 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:55206205 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:114288090 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:114288090 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:218614441 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:218614441 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:133920387 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:133920387 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169620155 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169620155 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169635042 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169635042 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:32519380 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:32519380 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:29993906 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:29993906 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:167020285 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:167020285 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35725779 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:35725779 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:27143247 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:27143247 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:114152628 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:114152628 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:38234611 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:38234611 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:87492314 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:87492314 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:94822190 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:94822190 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:133723079 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:133723079 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:42503974 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:42503974 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68708347 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68708347 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68935548 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68935548 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:2415869 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:2415869 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:66381173 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:66381173 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:108922167 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:108922167 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:108959153 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:108959153 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:128641088 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:128641088 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:10934882 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:10934882 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:10973800 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:10973800 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42232416 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42232416 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:12858384 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:12858384 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:57168626 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:57168626 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:72951938 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:72951938 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:72987486 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:72987486 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:77378083 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:77378083 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:234846212 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:234846212 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:142575276 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:142575276 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:81448771 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:81448771 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:33002841 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:33002841 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:40746841 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:40746841 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:43572444 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:43572444 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:219618203 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:219618203 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:76175477 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:76175477 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46846927 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46846927 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179500673 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179500673 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179646078 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179646078 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179665038 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:179665038 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:54941001 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:54941001 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:132233831 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:132233831 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:66548533 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:66548533 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:162558375 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:162558375 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:34936046 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:34936046 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68547936 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68547936 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:43829721 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:43829721 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:83733740 A>T maps to NM_198920.1 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:83733740 A>T maps to NM_198920.1 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:62444112 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:62444112 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:96599462 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:96599462 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:176306196 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:176306196 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:76802966 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:76802966 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:70818813 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:70818813 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:6853852 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:6853852 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:108299853 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:108299853 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:76981982 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:76981982 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:98809274 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:98809274 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:1175306 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:1175306 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:2770638 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:2770638 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:108618684 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:108618684 A>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:32456224 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:32456224 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:32456226 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:32456226 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:31587158 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:31587158 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183493576 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:183493576 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:56185195 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:56185195 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:46539288 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:46539288 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:89063214 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:89063214 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:44986846 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:44986846 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:145161403 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:145161403 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:99129943 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:99129943 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:40438809 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:40438809 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:35862116 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:35862116 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:53577382 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:53577382 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:58723433 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:58723433 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44100228 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44100228 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:37966925 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:37966925 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52870073 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52870073 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:53987241 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:53987241 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:126670461 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:126670461 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:123304905 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:123304905 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:87758042 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:87758042 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:33616274 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:33616274 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:79080755 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:79080755 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:7772947 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:7772947 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:50346145 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:50346145 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:86702070 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:86702070 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:47689011 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:47689011 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:202494591 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:202494591 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:115231537 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:115231537 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:37423047 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:37423047 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:45803118 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:45803118 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:141049414 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:141049414 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:4624419 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:4624419 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:57303523 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:57303523 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:30186593 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:30186593 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:42492393 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:42492393 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:77294262 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:77294262 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:62449067 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:62449067 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:31598895 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:31598895 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:39922713 T>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:39922713 T>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:18195539 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:18195539 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:127810922 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:127810922 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:10332280 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:10332280 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:4430431 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:4430431 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:9497021 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:9497021 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:60991177 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:60991177 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:159928839 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:159928839 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:165715037 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:165715037 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:66407015 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:66407015 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:105217832 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:105217832 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:104905936 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:104905936 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:132290414 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:132290414 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:45115286 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:45115286 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:7521433 A>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:7521433 A>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:167401002 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:167401002 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:121774256 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:121774256 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:21883648 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:21883648 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:11356043 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:11356043 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:11356046 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:11356046 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:21873364 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:21873364 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:73765501 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:73765501 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:184069700 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:184069700 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:16377112 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:16377112 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:72183647 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:72183647 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:109748432 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:109748432 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:189859094 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:189859094 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:40779955 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:40779955 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:3673773 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:3673773 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:83215281 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:83215281 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:3216496 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:3216496 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:114449163 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:114449163 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:46610098 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:46610098 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:136670154 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:136670154 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:114138408 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:114138408 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:176941688 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:176941688 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:9229217 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:9229217 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:31605416 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:31605416 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:61542111 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:61542111 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:38994241 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:38994241 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:11513657 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:11513657 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:25463079 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:25463079 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:292495 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:292495 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:23829550 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:23829550 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:31836123 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:31836123 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:80626253 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:80626253 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:225685403 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:225685403 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:89457077 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:89457077 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:212590041 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:212590041 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:598814 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:598814 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:66044828 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:66044828 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:109158961 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:109158961 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:16572033 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:16572033 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:139180332 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:139180332 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:89653368 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:89653368 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:9000950 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:9000950 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:172633532 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:172633532 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:157665023 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:157665023 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:6093085 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:6093085 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:241661364 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:241661364 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:76072431 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:76072431 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:159677742 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:159677742 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:12720226 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:12720226 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:5643056 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:5643056 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:162459299 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:162459299 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:61897565 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:61897565 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:42713674 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:42713674 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:36147683 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:36147683 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:23296801 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:23296801 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:11767046 T>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:11767046 T>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:14558744 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:14558744 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:103267689 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:103267689 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:18631327 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:18631327 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:50534353 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:50534353 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:93779134 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:93779134 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:28375287 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:28375287 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:120369566 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:120369566 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:29798226 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:29798226 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:114405680 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:114405680 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:67199350 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:67199350 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:153053615 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:153053615 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140028039 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140028039 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140028052 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140028052 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:14157461 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:14157461 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:62614074 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:62614074 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:42806413 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:42806413 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:202743890 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:202743890 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:142640342 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:142640342 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:19571334 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:19571334 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:24564365 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:24564365 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:86474029 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:86474029 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:45213044 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:45213044 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55271925 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55271925 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55272201 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55272201 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55344302 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55344302 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:211306025 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:211306025 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55087672 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55087672 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55098622 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:55098622 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:209603909 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:209603909 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:62845510 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:62845510 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:172945143 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:172945143 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:21215388 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:21215388 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:165111266 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:165111266 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:21886562 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:21886562 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:85498260 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:85498260 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:69230317 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:69230317 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:29533254 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:29533254 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:67391952 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:67391952 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:56231470 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:56231470 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:123651077 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:123651077 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:149807596 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:149807596 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:10315586 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:10315586 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:48004055 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:48004055 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:201754308 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:201754308 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:21808026 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:21808026 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:54922000 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:54922000 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:115773825 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:115773825 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:52777560 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:52777560 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:70531927 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:70531927 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:204956703 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:204956703 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:57047553 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr16:57047553 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:36342117 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:36342117 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:32775107 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:32775107 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:34790028 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:34790028 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:119526028 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:119526028 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:40137519 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:40137519 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:105648806 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:105648806 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:5920598 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:5920598 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248684906 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248684906 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248437124 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248437124 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:26684913 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:26684913 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:32060397 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:32060397 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:176809425 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:176809425 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:119094808 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:119094808 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:91237718 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:91237718 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:136268712 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:136268712 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:54019924 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:54019924 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:22880510 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:22880510 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:161139673 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:161139673 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:114874644 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:114874644 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:153033676 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:153033676 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:38125373 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:38125373 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:40206970 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:40206970 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:12853777 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:12853777 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:64795521 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:64795521 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:57257220 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:57257220 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:214705802 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:214705802 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:121616194 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:121616194 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:121699091 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:121699091 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:1642592 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:1642592 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:37177492 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:37177492 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:125014319 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:125014319 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:125620514 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:125620514 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:79254111 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:79254111 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:117245821 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:117245821 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:177574709 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:177574709 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:178989678 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:178989678 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:237504963 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:237504963 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:237881856 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:237881856 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:38764847 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:38764847 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:81954032 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:81954032 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:122642416 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:122642416 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:122658189 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:122658189 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:105277790 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:105277790 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:61600169 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:61600169 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:13965762 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:13965762 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:67105423 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:67105423 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:57627455 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:57627455 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:65417574 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:65417574 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:164725666 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:164725666 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:109888319 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:109888319 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:88883274 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr14:88883274 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:149481820 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:149481820 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:48209377 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:48209377 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:104063303 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:104063303 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:4103358 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:4103358 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:171583833 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:171583833 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:132793370 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:132793370 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:79747419 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:79747419 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:124008070 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:124008070 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:153648607 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:153648607 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:52928795 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:52928795 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:105924049 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:105924049 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:122760346 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:122760346 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:165737880 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:165737880 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:36236378 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:36236378 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:60027180 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:60027180 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:38567725 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:38567725 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:186324978 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:186324978 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:31340192 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:31340192 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:110226534 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:110226534 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:190905531 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:190905531 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:161133555 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:161133555 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:27256621 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:27256621 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:117566678 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chrX:117566678 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:167850490 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:167850490 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:44624593 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:44624593 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57862999 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57862999 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57908327 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57908327 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:58067431 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:58067431 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:53986963 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:53986963 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:53158724 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:53158724 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9872752 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9872752 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:102187790 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:102187790 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:69752303 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:69752303 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:219131552 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:219131552 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:17419206 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:17419206 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:22063976 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:22063976 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:73152107 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:73152107 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:128620261 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:128620261 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:50472894 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:50472894 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:114173111 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:114173111 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:25038262 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:25038262 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:148683829 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:148683829 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:178634734 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:178634734 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:18717986 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:18717986 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr22:26044462 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr22:26044462 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:68740837 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:68740837 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:28229386 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:28229386 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:32096444 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:32096444 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:11039152 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:11039152 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:58979977 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:58979977 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:133129360 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:133129360 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:51689740 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:51689740 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:43807107 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:43807107 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:59969351 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:59969351 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:11899336 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:11899336 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:115897054 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:115897054 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:46958351 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:46958351 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:27064256 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:27064256 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:49061599 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:49061599 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:57085302 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:57085302 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:24773550 A>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:24773550 A>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:18432607 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:18432607 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:117405358 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:117405358 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:27465045 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:27465045 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:64956053 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:64956053 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:75672619 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:75672619 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:76866366 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:76866366 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:106125540 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:106125540 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:135732340 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:135732340 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:35222563 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:35222563 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:123860618 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:123860618 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:196871771 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:196871771 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:61754118 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:61754118 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:178044502 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:178044502 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:100211994 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:100211994 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:137696928 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:137696928 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:818256 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:818256 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:19362598 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:19362598 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:143958419 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:143958419 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:48978302 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:48978302 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:43111479 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:43111479 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:103907481 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:103907481 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:30859338 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:30859338 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:15753330 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:15753330 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:95572320 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:95572320 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:83501839 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:83501839 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:10277234 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:10277234 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:169472740 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:169472740 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:97956165 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:97956165 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:97956169 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:97956169 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:19259357 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:19259357 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:120598615 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:120598615 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:55717936 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:55717936 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:150384881 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:150384881 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:123260218 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:123260218 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:14846097 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:14846097 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:75600695 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:75600695 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:47033925 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:47033925 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:171704380 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:171704380 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:72633961 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:72633961 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007204 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007204 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007389 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007389 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:23498168 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:23498168 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:26534969 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:26534969 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:66786311 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:66786311 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:42429213 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:42429213 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:156631661 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:156631661 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:794180 T>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:794180 T>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:25726196 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:25726196 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:228646247 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:228646247 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:150672760 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:150672760 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:41142767 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:41142767 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:201823861 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:201823861 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:52825980 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:52825980 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:35228976 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:35228976 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:44589741 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:44589741 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:44935890 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:44935890 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:114204751 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:114204751 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:22623921 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:22623921 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:59894731 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:59894731 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:166243063 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:166243063 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:197890805 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:197890805 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:15516291 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr21:15516291 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:24525000 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:24525000 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:33411915 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:33411915 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:31646822 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:31646822 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:47297311 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:47297311 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:47298227 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:47298227 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:156437571 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:156437571 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:12241744 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:12241744 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:57735984 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:57735984 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:102036189 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:102036189 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:15817980 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:15817980 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:112512596 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:112512596 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:70375011 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:70375011 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:69487949 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:69487949 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:66631477 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:66631477 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:55152189 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:55152189 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:15222100 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:15222100 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:7076632 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:7076632 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:106523676 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:106523676 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131815180 T>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131815180 T>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131195563 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131195563 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:76239577 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:76239577 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:27834471 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:27834471 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:44836193 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:44836193 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr13:20356444 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr13:20356444 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:139110714 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:139110714 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:150078891 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:150078891 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:7281083 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:7281083 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:24644860 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:24644860 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:73654332 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:73654332 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:22863719 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:22863719 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:92655180 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:92655180 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:100736362 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:100736362 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:52476352 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:52476352 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:249111094 A>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:249111094 A>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:105361457 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:105361457 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:44673849 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:44673849 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:118588405 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:118588405 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:115572320 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chrX:115572320 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:170218741 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:170218741 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:20523993 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:20523993 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:47009097 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:47009097 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:115566940 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:115566940 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:53774038 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:53774038 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:118616658 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:118616658 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:66476297 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:66476297 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:45983039 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:45983039 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:136341945 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:136341945 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:96858013 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:96858013 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:23872017 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:23872017 T>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:31571784 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:31571784 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:45777123 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:45777123 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:57384138 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:57384138 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:79354496 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:79354496 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:157158723 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:157158723 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:196051380 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:196051380 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:6976726 C>T maps to NM_001159287.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:6976726 C>T maps to NM_001159287.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:41248669 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:41248669 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:189018139 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:189018139 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:2136399 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:2136399 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58140934 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58140934 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:166789416 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:166789416 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:103300568 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:103300568 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:17327160 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:17327160 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:58422684 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:58422684 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:101705806 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:101705806 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:144780271 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:144780271 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:38785319 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:38785319 T>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:114057715 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:114057715 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:72024570 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:72024570 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:72036493 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:72036493 G>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:72041446 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:72041446 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:58352373 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:58352373 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:75185434 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:75185434 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:22171833 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:22171833 C>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:25666081 G>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:25666081 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:57222635 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:57222635 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:67188649 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:67188649 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:67113933 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:67113933 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:87144539 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:87144539 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:20685267 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:20685267 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:44073244 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:44073244 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:43743642 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:43743642 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:31343091 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:31343091 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:185709940 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:185709940 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:207460939 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:207460939 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:24177920 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:24177920 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:33662201 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:33662201 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:43771375 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:43771375 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:43833271 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:43833271 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:64538064 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:64538064 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:84706569 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:84706569 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:154569799 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:154569799 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:7691001 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:7691001 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:100266282 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:100266282 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:100063721 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:100063721 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:100063989 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:100063989 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:67051129 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:67051129 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88055520 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88055520 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:74320872 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:74320872 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:5032331 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:5032331 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:202211449 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:202211449 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:38476052 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:38476052 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:104166312 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:104166312 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:114176838 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:114176838 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:114264348 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:114264348 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:241465582 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:241465582 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:21244946 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:21244946 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:29725804 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:29725804 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:71783620 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:71783620 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:51242139 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:51242139 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:36362084 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:36362084 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:47424594 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:47424594 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:72412830 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:72412830 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:16531233 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:16531233 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:123007008 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:123007008 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:131088538 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:131088538 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:119382511 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:119382511 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:107394964 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:107394964 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:108175669 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:108175669 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:138908998 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:138908998 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:160147224 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:160147224 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:138441294 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:138441294 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:1796655 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:1796655 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:47218866 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:47218866 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:11029542 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:11029542 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:11047543 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:11047543 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:134319793 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:134319793 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:171561167 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:171561167 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:107258737 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:107258737 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61870668 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61870668 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:13616837 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:13616837 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31606701 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31606701 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31627073 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31627073 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31631304 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31631304 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:15733497 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:15733497 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:92604821 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:92604821 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4430313 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4430313 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:90420855 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:90420855 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:34647064 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:34647064 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:74729911 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:74729911 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:77804296 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:77804296 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:51887256 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:51887256 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:30462165 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:30462165 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:179380263 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:179380263 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31811578 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:31811578 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:14709756 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:14709756 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:81308885 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:81308885 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:121629329 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:121629329 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:90499593 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:90499593 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:181708262 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:181708262 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:181725311 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:181725311 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:55043402 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:55043402 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:1965437 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:1965437 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:152717373 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:152717373 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:93073150 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:93073150 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:106139681 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:106139681 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:93705086 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:93705086 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:56420623 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:56420623 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:7653623 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:7653623 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:149983441 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:149983441 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:100858741 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:100858741 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:227216980 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:227216980 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:19471344 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:19471344 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:85956518 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:85956518 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:205498422 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:205498422 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:214836864 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:214836864 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:47483655 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:47483655 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:432379 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:432379 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:175673515 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:175673515 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61980991 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61980991 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:86894259 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:86894259 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:67133122 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:67133122 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:143017679 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:143017679 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:143028774 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:143028774 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:8689617 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:8689617 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:73731814 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:73731814 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:19226983 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:19226983 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:87674124 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:87674124 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:21488971 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:21488971 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:58582512 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:58582512 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:58582514 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:58582514 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7837874 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7837874 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:51327224 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:51327224 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:32138490 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:32138490 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:70637770 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:70637770 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:189866376 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:189866376 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:137690124 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:137690124 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:137707844 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:137707844 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:70952249 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:70952249 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:130021882 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:130021882 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:211456740 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:211456740 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:125506687 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:125506687 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:125506698 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:125506698 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:43907387 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:43907387 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:20022307 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:20022307 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:209010406 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:209010406 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:4645933 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:4645933 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:113657526 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:113657526 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:16716319 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:16716319 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119672690 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119672690 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:49032732 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:49032732 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:58071769 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:58071769 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:58514088 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:58514088 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:106118684 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:106118684 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:172314678 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:172314678 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:154995562 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:154995562 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:61090630 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:61090630 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:50537933 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:50537933 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:6794162 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:6794162 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:137206750 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:137206750 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:12628245 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:12628245 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:189599657 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:189599657 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:223164131 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:223164131 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:83502075 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:83502075 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:124380925 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:124380925 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:32380885 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:32380885 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:76430065 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:76430065 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:11666935 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:11666935 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:162903856 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:162903856 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:154519639 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:154519639 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:98011765 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:98011765 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:117310238 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:117310238 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:167082843 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:167082843 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7132213 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7132213 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:103060299 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:103060299 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4705717 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4705717 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:71778162 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:71778162 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:108392918 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:108392918 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:150484748 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:150484748 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:109527342 C>A maps to ENST00000376651 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:109527342 C>A maps to ENST00000376651 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:68840766 C>T maps to ENST00000338901 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:68840766 C>T maps to ENST00000338901 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:69249396 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:69249396 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:49637177 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:49637177 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:75475980 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:75475980 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:37052856 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:37052856 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:60198429 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:60198429 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:103499354 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:103499354 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:22826402 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:22826402 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:549143 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:549143 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:47841457 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:47841457 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:63413234 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:63413234 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:184853654 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:184853654 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29245178 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29245178 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:62147390 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:62147390 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:51826488 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:51826488 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:120867383 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:120867383 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119394644 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119394644 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119425232 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:119425232 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:124792207 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:124792207 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:89858563 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:89858563 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:92613737 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:92613737 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:137774506 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:137774506 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:55233635 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:55233635 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:36988304 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:36988304 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:72715149 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:72715149 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:128638220 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:128638220 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:114019593 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:114019593 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:114329804 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:114329804 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:12728792 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:12728792 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:49381375 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:49381375 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4870356 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4870356 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:114537744 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:114537744 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:9829867 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:9829867 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:75263754 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:75263754 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:76938780 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:76938780 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:31014580 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:31014580 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:42187791 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:42187791 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:104396880 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:104396880 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:48978894 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:48978894 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:129519553 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:129519553 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:19049005 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:19049005 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:139243083 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:139243083 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:122551196 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:122551196 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:146747739 A>G maps to NM_001114329.1 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:146747739 A>G maps to NM_001114329.1 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:88582936 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:88582936 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:126079231 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:126079231 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:106697536 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:106697536 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:105280883 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:105280883 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:108935784 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:108935784 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:172778895 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:172778895 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:153221631 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:153221631 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:73617589 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:73617589 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:18868753 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:18868753 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:236714073 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:236714073 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:113865396 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:113865396 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:3148484 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:3148484 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:118923182 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:118923182 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:23401103 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:23401103 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:46664362 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:46664362 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:201195306 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:201195306 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:118624649 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:118624649 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:113591173 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:113591173 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:27441329 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:27441329 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:68646162 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:68646162 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:70330148 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:70330148 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:3146488 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:3146488 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:10788124 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:10788124 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:242662322 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:242662322 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:156514158 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:156514158 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:145530221 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:145530221 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:7780575 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:7780575 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:54780277 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:54780277 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:35107549 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:35107549 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:68172470 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:68172470 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:73751905 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:73751905 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:138678012 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:138678012 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142640995 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142640995 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142641366 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142641366 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142651544 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142651544 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:70171519 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:70171519 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:15692614 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:15692614 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:2605384 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:2605384 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:94087402 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:94087402 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:233514642 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:233514642 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:111585237 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:111585237 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:245704254 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:245704254 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:45216368 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:45216368 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:145695057 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:145695057 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:55255109 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:55255109 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:51363277 G>A maps to NM_001648.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:51363277 G>A maps to NM_001648.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:186461475 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:186461475 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:66042115 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:66042115 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:149420811 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:149420811 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:39019652 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:39019652 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:52882020 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:52882020 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:143790927 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:143790927 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:112462800 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:112462800 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:104309457 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:104309457 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:54780517 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:54780517 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:161006350 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:161006350 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:99764491 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:99764491 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:99766360 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:99766360 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141264281 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141264281 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141819596 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141819596 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:100624027 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:100624027 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:120054528 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:120054528 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:34718338 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:34718338 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:33622195 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:33622195 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:151283213 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:151283213 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:75004995 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:75004995 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:55479570 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:55479570 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:119728883 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:119728883 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:151112333 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:151112333 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:3297274 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:3297274 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88755828 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88755828 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:119612645 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:119612645 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:228217346 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:228217346 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:141721962 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:141721962 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:74690190 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:74690190 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:108690319 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:108690319 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:179311817 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:179311817 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:86588111 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:86588111 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:9726683 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:9726683 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:11175570 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:11175570 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:10398135 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:10398135 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:36708025 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:36708025 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:18039721 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:18039721 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109847222 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109847222 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:12639333 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:12639333 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:95079597 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:95079597 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:35864686 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:35864686 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:115751123 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:115751123 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:84028084 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:84028084 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:45004561 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:45004561 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:29661881 G>T maps to NM_001042492.2 E1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:29661881 G>T maps to NM_001042492.2 E1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:52505698 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:52505698 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:25462854 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:25462854 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:5436131 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:5436131 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:142409828 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:142409828 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:72897571 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:72897571 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:11907499 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:11907499 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:5603343 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:5603343 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:88484050 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:88484050 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:102337820 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:102337820 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:28231963 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:28231963 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248100034 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248100034 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248246929 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248246929 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248247834 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248247834 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4968386 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4968386 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:38254968 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:38254968 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:241079553 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:241079553 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:111962358 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:111962358 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:17725352 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:17725352 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:161990321 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:161990321 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:44515035 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:44515035 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:55755537 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:55755537 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:56138391 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:56138391 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:165844812 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:165844812 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:178863361 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:178863361 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:153070737 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:153070737 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:3171995 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:3171995 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:74065895 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:74065895 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:55626226 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:55626226 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:130846219 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:130846219 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:110416733 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:110416733 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:51882193 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:51882193 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:51934485 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:51934485 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:133784950 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:133784950 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:45568459 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:45568459 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:131955525 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:131955525 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:126725053 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:126725053 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:131831113 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:131831113 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:153043161 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:153043161 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:94676280 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:94676280 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:25387718 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:25387718 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:132020884 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:132020884 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:42621605 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:42621605 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:122273573 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:122273573 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:57267740 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:57267740 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:27786527 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:27786527 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:40207000 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:40207000 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:82069962 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:82069962 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:24614205 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:24614205 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:209271876 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:209271876 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:3001865 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:3001865 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:55708894 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:55708894 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:52336051 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:52336051 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:32307883 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:32307883 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:9310441 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:9310441 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:122291120 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:122291120 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:33442285 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:33442285 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:80007765 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:80007765 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:107154837 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:107154837 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:182638800 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:182638800 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:73026454 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:73026454 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:652939 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:652939 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:37009250 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:37009250 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:35860907 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:35860907 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:2016832 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:2016832 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:60076922 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:60076922 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:32365871 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:32365871 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:38959804 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:38959804 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237608537 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237608537 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237801625 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237801625 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237886366 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237886366 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237965073 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237965073 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:5654317 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:5654317 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:169650503 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:169650503 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:78218471 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:78218471 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:38763676 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:38763676 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:71427814 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:71427814 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:169578722 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:169578722 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:150329497 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:150329497 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:61256070 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:61256070 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:70599216 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:70599216 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:45565285 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:45565285 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:156784799 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:156784799 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:46357451 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:46357451 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:52033264 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:52033264 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:1905547 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:1905547 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:73094095 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:73094095 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:160576921 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:160576921 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:220032796 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:220032796 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:69909043 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:69909043 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:75862346 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:75862346 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:42338832 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:42338832 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:48690613 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:48690613 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:115568915 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:115568915 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:110734897 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:110734897 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:1233113 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:1233113 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:103317506 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:103317506 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:21015270 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:21015270 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:112358131 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:112358131 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:88390403 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:88390403 T>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:139281867 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:139281867 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:139291570 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:139291570 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:953384 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:953384 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:2309171 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:2309171 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:45360326 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:45360326 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:16010815 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:16010815 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:118571032 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:118571032 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:118574204 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:118574204 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:140358174 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:140358174 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:54855126 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:54855126 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:87839150 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:87839150 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:149497137 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:149497137 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:48049141 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:48049141 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:86071713 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:86071713 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:116612081 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:116612081 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:123195226 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:123195226 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:57501924 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:57501924 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:120002951 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:120002951 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:53089388 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:53089388 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:48382478 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:48382478 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:888326 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:888326 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109332486 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109332486 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152698105 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152698105 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:77395108 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:77395108 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:763636 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:763636 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:160053089 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:160053089 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:6636363 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:6636363 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:28885907 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:28885907 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:101648715 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:101648715 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:85448332 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:85448332 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:50807829 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:50807829 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:48896621 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:48896621 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:122767956 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chrX:122767956 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:164394954 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:164394954 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:171910422 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:171910422 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:64883356 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:64883356 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:12271646 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:12271646 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:44693351 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:44693351 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:105995419 C>T maps to NM_025268.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:105995419 C>T maps to NM_025268.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:50059526 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:50059526 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:15430191 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:15430191 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:20927675 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:20927675 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:74905350 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:74905350 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:175087662 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:175087662 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:175113400 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:175113400 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:175355111 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:175355111 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:39658161 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:39658161 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:1488334 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:1488334 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:20056581 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:20056581 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:10969172 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:10969172 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:36871020 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:36871020 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:72987747 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:72987747 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:101359572 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:101359572 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:234891604 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:234891604 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:16332320 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:16332320 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:52037992 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:52037992 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:99579207 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:99579207 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:43220673 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:43220673 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:43569685 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:43569685 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:43829505 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:43829505 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:69693378 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:69693378 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:35386116 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:35386116 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:216262524 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:216262524 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:6131272 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:6131272 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:128466953 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:128466953 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:54398576 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:54398576 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:33642040 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:33642040 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:68659929 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:68659929 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:167086433 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:167086433 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:47587513 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:47587513 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:100016709 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:100016709 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131513631 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131513631 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:178336848 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:178336848 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:123963749 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:123963749 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:27435610 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:27435610 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:53989741 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:53989741 A>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:47881207 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:47881207 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:58564793 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:58564793 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:119029105 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:119029105 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:179078697 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:179078697 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:74302840 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:74302840 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:177651797 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:177651797 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:71876358 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:71876358 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:109530599 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:109530599 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:233323488 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:233323488 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:25232932 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:25232932 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:130217633 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:130217633 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:231115027 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:231115027 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:77036950 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:77036950 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:373126 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:373126 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:49457184 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:49457184 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:14756019 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:14756019 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56113409 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56113409 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:36946755 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:36946755 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:64722332 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:64722332 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:115080670 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:115080670 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:19683077 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:19683077 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:110595214 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:110595214 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:549768 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:549768 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:25573411 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:25573411 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:109813784 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:109813784 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:55905511 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:55905511 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:202005028 T>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:202005028 T>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:4429632 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:4429632 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:10996114 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:10996114 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:16351450 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:16351450 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:95669098 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:95669098 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:95669104 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:95669104 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:57770951 A>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:57770951 A>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:11657810 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:11657810 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:228118391 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:228118391 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:61178660 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:61178660 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:149439148 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:149439148 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:41386277 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:41386277 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:15626190 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:15626190 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:57927158 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:57927158 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:66624420 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:66624420 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:113850265 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:113850265 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:150482561 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:150482561 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45316676 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45316676 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:78111885 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:78111885 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:32793193 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:32793193 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:44355864 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:44355864 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:144359755 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:144359755 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:128409338 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:128409338 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:35514099 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:35514099 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:105623618 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:105623618 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:156629497 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:156629497 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:140056865 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:140056865 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:70992713 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:70992713 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:118959905 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:118959905 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:38791442 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:38791442 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:84229972 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:84229972 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:33173333 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:33173333 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:114010114 A>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:114010114 A>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:206942089 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:206942089 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:22023125 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr18:22023125 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:31424390 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:31424390 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:31383682 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:31383682 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:27872595 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:27872595 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:48822969 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:48822969 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:75555536 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:75555536 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:72350228 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:72350228 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:36353330 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:36353330 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:60922089 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:60922089 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:39895003 T>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:39895003 T>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:53877927 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:53877927 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:57906272 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:57906272 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:94245196 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:94245196 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:38187772 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:38187772 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:66795917 A>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:66795917 A>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:128138083 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:128138083 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:109771049 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:109771049 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:37754407 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:37754407 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:220978319 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:220978319 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:64951694 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:64951694 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:52767656 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:52767656 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:44799500 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:44799500 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:117092988 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:117092988 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:149915751 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:149915751 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56716281 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56716281 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:289023 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:289023 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:31864462 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:31864462 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:20396260 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:20396260 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:129764221 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:129764221 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:21174273 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:21174273 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:48369960 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:48369960 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:12475336 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:12475336 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:95942162 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:95942162 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:123583050 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:123583050 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:131128901 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:131128901 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:198718470 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:198718470 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:220427109 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:220427109 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:667164 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:667164 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:12632256 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:12632256 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:21939639 C>T maps to ENST00000374757 *328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:21939639 C>T maps to ENST00000374757 *328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:127957969 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:127957969 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:36217887 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:36217887 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:32124823 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:32124823 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:50031653 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:50031653 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:192316416 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:192316416 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:722070 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:722070 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45098081 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45098081 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2305518 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2305518 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:136215118 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:136215118 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:99118235 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:99118235 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr8:93017286 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr8:93017286 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:128783910 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:128783910 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:20404069 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:20404069 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:108222726 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:108222726 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:19413044 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:19413044 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr8:42323223 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr8:42323223 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:130854057 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:130854057 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:57176842 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:57176842 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:32477991 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:32477991 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:44468415 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:44468415 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:144465860 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:144465860 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:45779256 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:45779256 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:121425784 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:121425784 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:218023962 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:218023962 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:123900635 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:123900635 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:13074348 A>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:13074348 A>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:33271854 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:33271854 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:38029287 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:38029287 T>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:57535854 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:57535854 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56824638 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56824638 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:84235267 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:84235267 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:76133752 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:76133752 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:75602436 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:75602436 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:93579831 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:93579831 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr8:9618931 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr8:9618931 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:40313077 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:40313077 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:115615416 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:115615416 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:99740099 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:99740099 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:179528852 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:179528852 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:5033834 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:5033834 T>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:2840555 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr20:2840555 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:65449033 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:65449033 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:43543454 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:43543454 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:152087651 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chrX:152087651 C>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:40578105 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:40578105 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:53989741 A>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:53989741 A>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:22585717 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr19:22585717 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:17424162 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:17424162 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:150912603 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:150912603 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:24304640 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:24304640 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:135084110 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:135084110 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:46605015 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:46605015 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:140386619 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:140386619 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:167787544 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:167787544 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:60878865 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:60878865 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:236706381 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:236706381 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:135732736 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:135732736 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:243715972 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:243715972 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:46717054 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:46717054 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:41577166 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:41577166 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:41580989 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:41580989 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:125599741 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:125599741 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:69957774 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:69957774 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:150484920 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:150484920 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:16345160 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:16345160 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:24966124 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:24966124 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:111862126 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:111862126 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:26411446 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:26411446 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:91182019 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:91182019 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:26276134 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:26276134 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:88635752 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:88635752 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:32843930 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:32843930 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:50916363 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:50916363 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:57075768 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:57075768 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:20055037 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:20055037 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:45598841 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:45598841 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:27439533 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:27439533 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:119452371 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:119452371 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:41149251 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:41149251 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:41149694 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:41149694 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:54095508 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:54095508 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:127899808 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:127899808 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:69728222 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:69728222 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:181763956 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:181763956 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:40015445 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:40015445 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:201028482 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:201028482 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:201046030 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:201046030 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:132290516 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:132290516 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:26483501 C>A maps to NM_000730.2 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:26483501 C>A maps to NM_000730.2 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:24578482 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:24578482 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:46056305 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:46056305 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:34852956 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:34852956 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:49551669 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:49551669 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:50835617 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:50835617 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:6707376 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:6707376 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:101719237 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:101719237 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:2777839 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:2777839 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:39178103 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:39178103 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:103461466 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:103461466 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:33134817 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:33134817 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:139629071 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:139629071 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:86515892 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:86515892 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:107898750 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:107898750 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:137655450 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:137655450 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:61451245 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:61451245 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:99824143 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:99824143 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:47708480 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:47708480 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:166405845 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:166405845 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:207753825 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:207753825 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:2808799 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:2808799 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:34067829 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:34067829 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:113304708 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:113304708 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:18143612 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:18143612 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:23472255 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:23472255 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:67662541 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:67662541 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:68040210 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:68040210 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:11565012 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:11565012 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:25043077 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:25043077 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:16949759 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:16949759 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:41704913 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:41704913 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:19334867 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:19334867 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:14722127 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:14722127 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:185882584 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:185882584 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:329192 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:329192 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:108124876 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:108124876 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:84732062 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:84732062 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:79589106 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:79589106 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:38858601 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:38858601 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:11687957 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:11687957 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:28648807 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:28648807 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:28923327 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:28923327 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:35002629 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:35002629 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:131675984 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:131675984 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:184009096 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:184009096 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:93979433 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:93979433 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:7916659 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:7916659 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:176832945 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:176832945 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:126131432 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:126131432 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:139380237 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:139380237 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:99023776 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:99023776 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:58639259 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:58639259 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:152861340 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:152861340 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:119428016 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:119428016 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:8761670 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:8761670 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:242402907 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:242402907 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:15614061 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:15614061 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:161514426 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:161514426 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:124985581 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:124985581 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:102454320 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:102454320 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:33014720 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:33014720 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:47033587 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:47033587 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:120594833 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:120594833 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:61958368 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:61958368 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:31014553 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:31014553 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:685384 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:685384 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:80038828 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:80038828 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:121448016 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:121448016 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:126883291 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:126883291 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:130774858 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:130774858 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:120461421 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:120461421 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:25078743 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:25078743 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:236761365 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:236761365 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:99118160 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:99118160 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:14913620 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:14913620 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:45956753 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:45956753 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:41364282 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:41364282 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:61781302 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:61781302 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:47485262 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:47485262 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:20734430 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:20734430 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:123170559 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:123170559 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:123239555 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:123239555 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:94156388 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:94156388 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:55286983 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:55286983 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:45403186 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:45403186 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:183211746 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:183211746 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:10601764 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:10601764 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:52756580 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:52756580 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:6237959 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:6237959 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:55025936 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:55025936 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:135177951 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:135177951 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:155670426 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:155670426 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:141298683 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:141298683 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:70486898 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:70486898 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:33477736 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:33477736 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:160766225 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:160766225 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:15412193 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:15412193 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:54840889 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:54840889 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:10808943 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:10808943 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:16067902 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:16067902 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:165110150 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:165110150 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:6312588 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:6312588 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:151085855 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:151085855 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:141778533 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:141778533 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:18389288 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:18389288 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:23312765 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:23312765 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:49575102 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:49575102 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:132637010 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:132637010 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:47641403 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:47641403 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:121534984 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:121534984 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:30630608 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:30630608 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:8982131 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:8982131 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:45016328 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:45016328 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:26414286 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:26414286 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:62850200 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:62850200 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:160325561 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:160325561 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:56235291 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:56235291 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:73013538 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:73013538 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:6623301 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:6623301 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:110305451 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:110305451 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:101572263 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:101572263 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:123695765 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:123695765 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:193376631 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:193376631 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:4945668 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:4945668 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:21689934 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:21689934 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:26781332 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:26781332 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:53849892 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:53849892 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:47801774 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:47801774 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:66829339 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:66829339 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:120527805 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:120527805 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:148702533 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:148702533 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:97023606 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:97023606 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:41831703 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:41831703 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:45939055 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:45939055 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:49754900 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:49754900 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:77672264 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:77672264 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:2161930 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:2161930 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:81929381 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:81929381 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:150123251 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:150123251 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:161134170 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:161134170 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:142430565 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:142430565 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:118368528 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:118368528 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:24722501 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chrX:24722501 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:1089823 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:1089823 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:103904695 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:103904695 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:23521387 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:23521387 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:48719902 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:48719902 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:139218114 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:139218114 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:43690436 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:43690436 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:141900636 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:141900636 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:157370935 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:157370935 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:157414360 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:157414360 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:64521686 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:64521686 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:163836391 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:163836391 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:10124142 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:10124142 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:79347938 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:79347938 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:49604606 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:49604606 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:11933937 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:11933937 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:38949396 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:38949396 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:76425092 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:76425092 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:75303139 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:75303139 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:158541399 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:158541399 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:61228314 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:61228314 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:30972898 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:30972898 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:4290667 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:4290667 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:154458885 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:154458885 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:159802603 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:159802603 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:44675107 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:44675107 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:33334899 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:33334899 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:143513922 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:143513922 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:20864472 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:20864472 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:20890307 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:20890307 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:168176668 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:168176668 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:139286581 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:139286581 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:121649383 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:121649383 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:186168394 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:186168394 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:214727153 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:214727153 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:48902500 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:48902500 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:35753907 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:35753907 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:153065949 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:153065949 T>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:141443634 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:141443634 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:28003935 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:28003935 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:124115627 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:124115627 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:149882371 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:149882371 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:100983074 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:100983074 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:26905972 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:26905972 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:92163594 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:92163594 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:43560259 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:43560259 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:2411388 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:2411388 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:43568859 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:43568859 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:102849704 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:102849704 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:19647665 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:19647665 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:51706884 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:51706884 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:32029539 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:32029539 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:10942856 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:10942856 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:27074992 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:27074992 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:104414405 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:104414405 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:142612745 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:142612745 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:179586534 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:179586534 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:157018263 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:157018263 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:69886166 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:69886166 A>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:112385911 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:112385911 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:68649099 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:68649099 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:16470620 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:16470620 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:149172600 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:149172600 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:35260576 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:35260576 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:53983090 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:53983090 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:52580475 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:52580475 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:52603892 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:52603892 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:7568443 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:7568443 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:7714986 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:7714986 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:7760513 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:7760513 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:9225138 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:9225138 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:69783968 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:69783968 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:70299343 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:70299343 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:48450283 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:48450283 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:67249888 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:67249888 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:169791993 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:169791993 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:183646659 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:183646659 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:183904544 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:183904544 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:119029458 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:119029458 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220397567 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220397567 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:156760100 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:156760100 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6309594 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6309594 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6312304 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6312304 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:8807768 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:8807768 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136302802 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136302802 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136303559 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136303559 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:130342835 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:130342835 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161165914 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161165914 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:64547230 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:64547230 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:7698565 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:7698565 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:50326808 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:50326808 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:131848480 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:131848480 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150839455 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150839455 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:241812329 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:241812329 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:135679256 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:135679256 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:91687421 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:91687421 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:5041539 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:5041539 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:49967042 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:49967042 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:183960547 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:183960547 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6374137 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6374137 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:29474155 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:29474155 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:61958061 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:61958061 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:70758025 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:70758025 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:10035064 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:10035064 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:71779542 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:71779542 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36363245 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36363245 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161192527 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161192527 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45448325 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45448325 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:32989593 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:32989593 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:68184191 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:68184191 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:24880744 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:24880744 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:155919985 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:155919985 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7005367 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7005367 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150718260 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150718260 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:47592944 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:47592944 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:25276046 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:25276046 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:160143829 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:160143829 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:52520616 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:52520616 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:70064118 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:70064118 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:32893163 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:32893163 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:50170838 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:50170838 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:128150157 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:128150157 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:90397865 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:90397865 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:15661763 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:15661763 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:200867605 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:200867605 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:179437806 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:179437806 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:179504154 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:179504154 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:112020455 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:112020455 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:75065730 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:75065730 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:24727704 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:24727704 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:226784684 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:226784684 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:33974318 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:33974318 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:32808251 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:32808251 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:26647035 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:26647035 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6693169 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6693169 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:133647066 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:133647066 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:37209439 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:37209439 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:43475160 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:43475160 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:157744438 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:157744438 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:120629985 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:120629985 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:139722845 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:139722845 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:86158014 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:86158014 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:67288471 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:67288471 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:140972744 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:140972744 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:181620651 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:181620651 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:40054081 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:40054081 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:81978994 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:81978994 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:24358023 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:24358023 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:27457198 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:27457198 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:7342260 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:7342260 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:93107033 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:93107033 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:44283141 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:44283141 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:75699616 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:75699616 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:19683366 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:19683366 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:104972100 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:104972100 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:104972244 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:104972244 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:55756197 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:55756197 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:92905436 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:92905436 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:94818599 C>A maps to ENST00000393113 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:94818599 C>A maps to ENST00000393113 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:130897701 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:130897701 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6292046 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6292046 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:32647249 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:32647249 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:42016393 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:42016393 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:158227186 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:158227186 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:41925909 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:41925909 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51729396 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51729396 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51729640 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51729640 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:80108052 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:80108052 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:80108332 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:80108332 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:80300262 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:80300262 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:10502117 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:10502117 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:59170141 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:59170141 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:59170496 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:59170496 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:105624630 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:105624630 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:72667055 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:72667055 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43025289 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43025289 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:46760392 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:46760392 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:123935821 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:123935821 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:56823317 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:56823317 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:117265562 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:117265562 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:49535473 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:49535473 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:49547627 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:49547627 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:50863103 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:50863103 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:50870608 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:50870608 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:111772459 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:111772459 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:233404410 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:233404410 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:113522303 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:113522303 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:16356606 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:16356606 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45495828 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45495828 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:140280937 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:140280937 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:24975647 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:24975647 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:99008470 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:99008470 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:103484466 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:103484466 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:121170562 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:121170562 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:70852727 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:70852727 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61959358 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61959358 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:130025213 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:130025213 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148614502 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148614502 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50209379 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50209379 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:149439188 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:149439188 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:110466875 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:110466875 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:61987903 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:61987903 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:34011844 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:34011844 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:113363373 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:113363373 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:113599264 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:113599264 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:113694657 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:113694657 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:114448880 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:114448880 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:70261869 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:70261869 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:16942580 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:16942580 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:143958346 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:143958346 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:41382364 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:41382364 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:41382586 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:41382586 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:16006295 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:16006295 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:59830538 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:59830538 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57476810 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57476810 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57491768 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57491768 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:137888932 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:137888932 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:50976857 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:50976857 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:74592168 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:74592168 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:108564338 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:108564338 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:94527507 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:94527507 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:135537744 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:135537744 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:29978118 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:29978118 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:207924 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:207924 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6479630 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:6479630 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:140287402 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:140287402 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:20074602 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:20074602 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56331167 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56331167 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56332804 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56332804 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:42644815 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:42644815 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:182841639 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:182841639 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61525742 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61525742 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:21775527 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:21775527 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7720822 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7720822 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:11684315 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:11684315 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:183619846 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:183619846 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131010349 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131010349 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:169477110 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:169477110 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:32945950 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:32945950 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:98206096 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:98206096 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:41647901 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:41647901 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:5787749 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:5787749 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:82126744 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:82126744 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:95668812 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:95668812 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:103029633 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:103029633 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:71730293 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:71730293 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:207530851 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:207530851 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:67917733 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:67917733 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:139564531 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:139564531 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:8008859 T>C maps to ENST00000449102 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:8008859 T>C maps to ENST00000449102 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:37172864 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:37172864 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:48523148 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:48523148 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:120575280 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:120575280 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:131979422 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:131979422 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:131992504 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:131992504 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:25203620 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:25203620 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:97167405 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:97167405 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:22924751 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:22924751 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:124624445 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:124624445 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:128426157 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:128426157 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:148525826 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:148525826 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:6251014 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:6251014 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:197026403 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:197026403 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:17653138 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:17653138 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:17664399 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:17664399 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:71232105 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:71232105 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:139163422 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:139163422 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:53122864 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:53122864 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:62080942 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:62080942 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:126490340 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:126490340 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:166039454 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:166039454 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:166135183 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:166135183 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:94764224 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:94764224 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:45636392 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:45636392 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:112942951 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:112942951 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:127653967 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:127653967 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:15928726 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:15928726 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:27696991 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:27696991 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:157737015 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:157737015 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:125318509 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:125318509 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128483989 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128483989 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:29001840 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:29001840 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:28599147 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:28599147 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:240306505 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:240306505 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:171178096 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:171178096 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:79396826 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:79396826 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:86152982 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:86152982 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:69299393 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:69299393 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4310331 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4310331 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:162306893 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:162306893 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:43870197 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:43870197 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:111983198 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:111983198 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:89974337 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:89974337 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:861352 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:861352 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:155307077 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:155307077 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:31167693 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:31167693 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:130127661 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:130127661 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:89734989 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:89734989 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:63929992 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:63929992 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:59608577 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:59608577 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:110418687 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:110418687 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:6554665 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:6554665 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:158073820 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:158073820 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:16290586 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:16290586 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:72953618 A>G maps to NM_018652.4 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:72953618 A>G maps to NM_018652.4 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:121433901 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:121433901 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:155726713 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:155726713 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:217793068 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:217793068 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:98250824 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:98250824 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:46095189 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:46095189 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:28473410 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:28473410 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:9984825 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:9984825 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:27492361 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:27492361 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:89984594 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:89984594 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:19380640 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:19380640 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23419680 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23419680 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:19056229 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:19056229 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:48678439 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:48678439 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:65486249 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:65486249 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:28380866 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:28380866 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:35673873 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:35673873 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:74016441 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:74016441 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:149399186 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:149399186 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148757979 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148757979 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:100453570 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:100453570 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:99129330 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:99129330 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:119987868 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:119987868 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:22176465 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:22176465 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:123508269 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:123508269 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:71149584 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:71149584 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:159019452 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:159019452 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:308076 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:308076 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:27700259 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:27700259 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:185407474 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:185407474 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:45956765 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:45956765 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:130423166 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:130423166 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:117146106 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:117146106 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:27372039 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:27372039 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:155231223 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:155231223 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:206893115 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:206893115 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156813134 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156813134 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:123142939 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:123142939 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:145532958 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:145532958 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42461731 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42461731 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:52357000 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:52357000 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:15702826 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:15702826 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:30495319 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:30495319 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:31383913 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:31383913 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:54817239 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:54817239 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:7658912 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:7658912 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:7684116 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:7684116 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:96992328 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:96992328 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:24444072 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:24444072 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:5089870 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:5089870 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:62734218 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:62734218 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:4920839 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:4920839 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:120387727 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:120387727 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:211032485 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:211032485 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:211034921 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:211034921 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:63316264 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:63316264 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:88737033 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:88737033 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:62077989 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:62077989 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:110984376 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:110984376 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:136594391 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:136594391 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:24810605 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:24810605 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:34319135 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:34319135 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:86473944 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:86473944 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:45205738 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:45205738 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:57962873 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:57962873 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:32306959 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:32306959 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55346705 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55346705 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:53344261 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:53344261 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:38953535 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:38953535 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39521338 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39521338 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:52843197 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:52843197 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:53162447 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:53162447 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:32253915 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:32253915 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31720932 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31720932 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:129775234 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:129775234 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:21620172 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:21620172 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:32745435 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:32745435 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:25189361 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:25189361 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:109086190 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:109086190 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:66102766 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:66102766 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:93180255 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:93180255 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:75626631 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:75626631 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55142772 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55142772 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:28150751 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:28150751 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:73552067 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:73552067 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:141055643 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:141055643 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:46896300 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:46896300 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:68204295 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:68204295 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:72083576 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:72083576 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62850635 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62850635 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:54426011 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:54426011 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:70446032 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:70446032 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:70482021 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:70482021 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:40714813 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:40714813 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:77748804 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:77748804 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:39802770 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:39802770 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:39845829 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:39845829 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:145161147 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:145161147 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:56401713 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:56401713 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:21208480 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:21208480 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:185136012 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:185136012 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:42110920 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:42110920 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:217142254 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:217142254 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:94111069 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:94111069 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:3844799 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:3844799 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:113740613 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:113740613 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:138701680 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:138701680 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:42154565 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:42154565 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:2367655 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:2367655 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:141797478 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:141797478 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:33768770 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:33768770 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:89053646 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:89053646 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:89128994 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:89128994 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:102487839 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:102487839 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:31712965 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:31712965 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203144311 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203144311 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23872546 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23872546 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23883195 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23883195 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:3277949 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:3277949 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:30418703 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:30418703 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:123458923 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:123458923 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:16902612 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:16902612 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:26343830 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:26343830 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:45004144 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:45004144 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:171034897 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:171034897 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:12655669 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:12655669 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:34163374 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:34163374 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:201687957 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:201687957 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:19854167 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:19854167 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:134022724 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:134022724 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:46279622 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:46279622 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:170400444 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:170400444 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:73594950 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:73594950 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:50139610 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:50139610 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:51211094 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:51211094 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:5947503 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:5947503 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55450171 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55450171 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:117658101 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:117658101 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:33502705 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:33502705 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:79176038 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:79176038 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:11802407 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:11802407 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131730713 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131730713 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131752576 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131752576 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:102335169 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:102335169 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:105659990 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:105659990 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:159284476 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:159284476 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248202597 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248202597 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:56258856 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:56258856 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:56043108 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:56043108 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:36909672 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:36909672 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:195955803 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:195955803 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:21728153 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:21728153 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:79803678 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:79803678 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105814719 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105814719 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:9547087 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:9547087 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:223158476 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:223158476 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:82387849 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:82387849 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:66821340 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:66821340 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:144866005 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:144866005 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:54347828 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:54347828 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:239161492 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:239161492 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:33904000 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:33904000 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:77895425 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:77895425 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:77896444 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:77896444 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:58330468 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:58330468 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:120277741 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:120277741 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:71403942 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:71403942 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:47930109 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:47930109 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:110420266 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:110420266 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:110456826 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:110456826 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:39800784 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:39800784 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:81929596 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:81929596 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:145016544 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:145016544 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:132109566 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:132109566 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:132110250 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:132110250 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:182098 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:182098 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:131912381 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:131912381 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156209461 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156209461 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:108151151 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:108151151 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:84570663 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:84570663 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:62532640 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:62532640 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:19571450 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:19571450 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:111249802 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:111249802 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:149210211 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:149210211 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203024847 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203024847 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:41120574 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:41120574 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:37531464 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:37531464 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:37536303 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:37536303 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:182827154 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:182827154 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:146236145 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:146236145 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:12919416 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:12919416 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:47317279 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:47317279 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:169999074 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:169999074 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:53564494 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:53564494 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23391638 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:23391638 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:18781223 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:18781223 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43514113 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43514113 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43233647 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43233647 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43679259 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43679259 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43679999 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43679999 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43448241 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43448241 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43527490 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43527490 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43571215 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43571215 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43576773 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43576773 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:239090 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:239090 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:97217099 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:97217099 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:99063828 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:99063828 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:136939583 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:136939583 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220161135 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220161135 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:40944657 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:40944657 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:41514385 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:41514385 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:1537989 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:1537989 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42030613 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42030613 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:73315918 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:73315918 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:140107368 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:140107368 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:52555128 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:52555128 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:220363695 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:220363695 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:37163552 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:37163552 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:129961450 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:129961450 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:48143135 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:48143135 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:48953815 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:48953815 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:145617080 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:145617080 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:139172009 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:139172009 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65054747 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65054747 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:125639639 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:125639639 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79348675 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79348675 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79384329 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79384329 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45525532 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45525532 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:103131031 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:103131031 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:103180962 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:103180962 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:204135283 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:204135283 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:7734386 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:7734386 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:117237065 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:117237065 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:35751583 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:35751583 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:192153422 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:192153422 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:163044416 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:163044416 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156348336 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156348336 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:228871771 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:228871771 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:38954986 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:38954986 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:40695527 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:40695527 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:5339746 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:5339746 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:87100601 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:87100601 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:44027420 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:44027420 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:63496831 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:63496831 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:124749647 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:124749647 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77257238 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77257238 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:38136075 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:38136075 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:17973043 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:17973043 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:26899665 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:26899665 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:91338347 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:91338347 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:17616120 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:17616120 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:77402169 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:77402169 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:60097106 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:60097106 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:60097112 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:60097112 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:45405799 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:45405799 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:237663961 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:237663961 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:237806597 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:237806597 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:33893788 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:33893788 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:100572835 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:100572835 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:127730874 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:127730874 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62023010 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62023010 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62043669 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62043669 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:12198006 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:12198006 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:91940983 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:91940983 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:48051991 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:48051991 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:48245271 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:48245271 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51648274 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51648274 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:164781163 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:164781163 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:164781178 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:164781178 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:159923982 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:159923982 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:127446020 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:127446020 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100452391 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100452391 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:66265121 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:66265121 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61595778 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61595778 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:63143247 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:63143247 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:92364248 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:92364248 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:118174169 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:118174169 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:42077831 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:42077831 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:21467866 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:21467866 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:19451486 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:19451486 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:21392215 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:21392215 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156221155 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:156221155 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:101825087 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:101825087 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:25154279 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:25154279 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:53514556 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:53514556 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:16502098 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:16502098 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:118550605 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:118550605 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:140358268 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:140358268 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:144337403 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:144337403 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:3397778 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:3397778 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:228855919 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:228855919 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:1161518 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:1161518 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:2351682 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:2351682 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:158623283 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:158623283 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:66455620 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:66455620 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:36031072 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:36031072 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112196946 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112196946 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112197200 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112197200 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74066575 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74066575 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:109196146 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:109196146 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:57095661 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:57095661 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:48117317 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:48117317 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:53126712 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:53126712 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:191922630 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:191922630 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:180945564 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:180945564 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:21829177 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:21829177 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:113241855 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:113241855 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:29819445 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:29819445 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:12200173 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:12200173 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:34072115 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:34072115 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:66811387 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:66811387 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55686394 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55686394 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:39777673 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:39777673 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:23835999 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:23835999 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:60551210 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:60551210 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:141673489 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:141673489 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:75923287 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:75923287 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:19750870 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:19750870 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61490632 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:61490632 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:102906563 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:102906563 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:48173477 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:48173477 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:93516542 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:93516542 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:133473248 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:133473248 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:30733164 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:30733164 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:2290211 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:2290211 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:134034416 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:134034416 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:3075831 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:3075831 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:71534923 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:71534923 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:32526813 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:32526813 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:32582355 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:32582355 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:153556104 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:153556104 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:35721816 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:35721816 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:105368457 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:105368457 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:76130347 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:76130347 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:87492411 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:87492411 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:39944433 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:39944433 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:19765050 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:19765050 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:94767132 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:94767132 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:29669430 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:29669430 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:74819585 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:74819585 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:1944163 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:1944163 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:76083230 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:76083230 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:39706142 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:39706142 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:6328534 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:6328534 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:72355437 G>A maps to ENST00000266669 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:72355437 G>A maps to ENST00000266669 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:239256182 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:239256182 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:72956871 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:72956871 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:57128704 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:57128704 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:117655222 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:117655222 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:46747956 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:46747956 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:135651232 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:135651232 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:116599194 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:116599194 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:73513545 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:73513545 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128801487 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128801487 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:166781000 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:166781000 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:76368393 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:76368393 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:179528469 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:179528469 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:29175324 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:29175324 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:73050605 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:73050605 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:96106511 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:96106511 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:167717802 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:167717802 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:43958549 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:43958549 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:215847398 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:215847398 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:9010304 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:9010304 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:177608326 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:177608326 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:49842472 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:49842472 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36549664 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36549664 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36580043 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36580043 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:241958615 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:241958615 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:709128 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:709128 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:68619174 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:68619174 A>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:128886335 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:128886335 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:217040383 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:217040383 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100383576 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100383576 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:136651238 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chrX:136651238 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:45858632 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:45858632 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:44495948 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:44495948 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:44590955 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:44590955 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:64159205 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:64159205 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:57193627 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:57193627 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:56903217 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:56903217 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:16465142 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:16465142 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:247207045 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:247207045 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:22379269 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:22379269 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:53741860 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:53741860 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38159927 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38159927 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:88956637 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:88956637 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:53059091 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:53059091 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:21106279 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:21106279 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:58563741 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:58563741 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:187694631 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:187694631 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:126184954 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:126184954 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:52610567 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:52610567 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:67079295 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:67079295 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:27059960 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:27059960 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:31415819 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:31415819 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:23723543 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:23723543 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:66328258 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:66328258 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:147967584 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:147967584 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:49962278 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:49962278 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:134089480 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:134089480 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:124358259 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:124358259 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:234184258 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:234184258 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:375780 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:375780 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:72861509 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:72861509 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:107517293 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:107517293 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:152772495 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:152772495 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:28613819 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:28613819 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:112999541 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:112999541 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:65871801 C>A maps to ENST00000321892 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:65871801 C>A maps to ENST00000321892 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:36185670 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:36185670 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:100608446 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:100608446 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:26368292 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:26368292 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:179401536 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:179401536 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:49311448 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:49311448 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:86570613 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:86570613 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:139733630 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:139733630 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:53753863 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:53753863 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:109404660 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:109404660 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:118701564 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:118701564 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:24537861 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:24537861 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:64984588 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:64984588 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:61823462 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:61823462 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:130550675 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:130550675 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:135099198 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:135099198 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:1320227 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:1320227 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:103379283 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:103379283 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:101749457 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:101749457 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:105796198 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:105796198 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:48267629 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:48267629 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:109817710 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:109817710 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:131274257 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:131274257 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:29126304 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:29126304 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:207644500 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:207644500 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:137570274 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:137570274 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:153924990 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:153924990 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:11564972 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:11564972 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:19948083 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:19948083 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:47859244 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:47859244 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:31577709 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:31577709 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:24529722 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:24529722 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:78296602 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:78296602 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:25470840 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:25470840 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:19956745 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:19956745 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:44108241 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:44108241 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:38407343 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:38407343 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:184041943 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:184041943 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:97471789 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:97471789 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:97200279 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:97200279 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:20808083 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:20808083 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:5823879 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:5823879 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:204103942 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:204103942 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:55170120 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:55170120 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:177166082 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:177166082 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:121004157 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:121004157 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:67573546 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:67573546 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:119402012 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:119402012 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:240372088 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:240372088 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:80544349 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:80544349 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:12708256 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:12708256 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:75276140 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:75276140 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:931814 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:931814 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:233613813 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:233613813 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:131020242 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:131020242 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:87406911 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:87406911 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:1051910 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:1051910 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:1051912 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:1051912 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:41142767 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:41142767 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:52112120 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:52112120 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:113742393 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:113742393 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:75806659 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:75806659 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:5114046 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:5114046 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:139827166 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:139827166 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:163302485 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:163302485 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:122017877 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:122017877 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:55961729 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:55961729 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:39880264 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:39880264 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:75146137 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:75146137 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:104309039 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:104309039 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:126301958 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:126301958 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:135186093 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:135186093 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:82188524 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:82188524 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:52863785 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:52863785 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:31540517 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:31540517 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:144184466 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:144184466 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:160661759 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:160661759 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:39481554 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:39481554 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:66427829 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:66427829 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:151078490 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:151078490 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:12284133 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:12284133 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:67450196 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:67450196 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:102449743 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:102449743 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:124922137 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:124922137 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:41888163 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:41888163 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:35753919 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:35753919 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:35753978 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:35753978 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:56703775 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:56703775 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:149764894 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:149764894 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:113524460 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:113524460 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:74191728 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:74191728 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:124858953 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:124858953 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:84028310 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:84028310 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:95062038 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:95062038 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:117696772 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:117696772 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:44572924 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:44572924 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:35809648 C>A maps to ENST00000447210 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:35809648 C>A maps to ENST00000447210 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:119528802 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:119528802 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:92923503 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:92923503 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:32505178 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:32505178 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:156836591 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:156836591 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:102332726 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:102332726 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:128699670 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:128699670 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:131260862 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:131260862 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:32000216 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:32000216 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:3167241 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:3167241 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:37829166 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:37829166 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:110482820 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:110482820 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:160843552 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:160843552 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:8702950 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:8702950 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:171395614 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:171395614 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:140389625 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:140389625 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:43197321 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:43197321 T>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:19573049 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:19573049 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:39246902 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:39246902 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:48755716 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:48755716 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:22294586 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:22294586 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:93615609 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:93615609 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:805445 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:805445 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:48140833 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:48140833 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:40714293 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr20:40714293 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:31437373 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:31437373 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:65332052 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:65332052 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:5925558 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:5925558 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:21944579 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:21944579 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:150037117 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:150037117 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr13:27845857 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr13:27845857 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:5096851 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:5096851 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:79385642 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:79385642 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:152298356 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:152298356 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:104780824 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:104780824 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:10450233 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:10450233 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:116948720 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:116948720 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:38948942 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:38948942 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:237804118 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:237804118 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:84815280 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:84815280 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:18260482 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:18260482 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:118012058 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:118012058 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:74711045 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:74711045 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr22:19709132 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr22:19709132 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:31902012 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:31902012 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:8218655 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:8218655 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:85286009 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:85286009 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:173506243 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:173506243 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr18:46447668 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr18:46447668 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:15433730 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:15433730 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:25156044 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:25156044 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:85031735 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:85031735 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:35774178 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:35774178 A>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:134478337 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:134478337 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:57638590 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:57638590 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:64854127 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:64854127 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:1552866 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:1552866 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:69402420 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:69402420 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:153557720 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:153557720 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:167022081 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:167022081 A>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:60694646 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:60694646 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:45430011 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:45430011 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:68929004 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:68929004 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:5413638 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:5413638 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:74742536 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:74742536 T>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:132401464 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:132401464 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:75134866 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:75134866 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:121154924 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:121154924 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:78187616 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:78187616 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:9002395 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:9002395 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:135638788 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chrX:135638788 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:79245724 C>A maps to ENST00000402655 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:79245724 C>A maps to ENST00000402655 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:7684770 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:7684770 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:87447927 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:87447927 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:144772427 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:144772427 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:76069709 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:76069709 C>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr15:58936032 T>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr15:58936032 T>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:121303938 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:121303938 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr11:74988620 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr11:74988620 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr12:110777243 C>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr12:110777243 C>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr14:54416745 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr14:54416745 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr18:21109023 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr18:21109023 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr11:104872964 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr11:104872964 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr8:113649248 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr8:113649248 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr5:160758166 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr5:160758166 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr1:118429401 T>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr1:118429401 T>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:113604570 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:113604570 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:113604606 G>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:113604606 G>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr9:138657087 T>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr9:138657087 T>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr12:121618277 C>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr12:121618277 C>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr12:50026768 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr12:50026768 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr19:43596048 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr19:43596048 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr15:45470301 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr15:45470301 G>A did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:164733102 C>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr3:164733102 C>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr2:27481580 T>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr2:27481580 T>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr6:33170015 A>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr6:33170015 A>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr15:42519861 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr15:42519861 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr9:135273508 T>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr9:135273508 T>G did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr1:71546570 A>C did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr1:71546570 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:69759298 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:69759298 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:30553781 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:30553781 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:128627981 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:128627981 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:27494123 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:27494123 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:236889366 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:236889366 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:128018912 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:128018912 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:156932614 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:156932614 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:33881125 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:33881125 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:73433034 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:73433034 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:7804862 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:7804862 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:12366892 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:12366892 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:134135470 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:134135470 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:19611102 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:19611102 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:21239523 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:21239523 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:17907140 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:17907140 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:156909258 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:156909258 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:85991318 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:85991318 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:119512456 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:119512456 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:15561294 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:15561294 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:26238533 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:26238533 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:61150905 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:61150905 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:270178 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:270178 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr21:33974133 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr21:33974133 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:40972773 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:40972773 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:89901015 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:89901015 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:1919406 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:1919406 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:3786540 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:3786540 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:39529819 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:39529819 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:110606339 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:110606339 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:114611780 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:114611780 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:80290603 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:80290603 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:91973558 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:91973558 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:49536577 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:49536577 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:440564 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:440564 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:8693514 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:8693514 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:205033608 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:205033608 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:40771463 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:40771463 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:4408222 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:4408222 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:36714406 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:36714406 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:94072871 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:94072871 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:113668586 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:113668586 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:114448760 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:114448760 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:23476618 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:23476618 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:150778145 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:150778145 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:49867079 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:49867079 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:110576266 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:110576266 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:118582346 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:118582346 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:21826985 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:21826985 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:11671587 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:11671587 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:225669890 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:225669890 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:32464843 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:32464843 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:19115987 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:19115987 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:72234400 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:72234400 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:28362226 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:28362226 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:119327193 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:119327193 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:187518811 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:187518811 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:157490733 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:157490733 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:32764281 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:32764281 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:97058418 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:97058418 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:128486277 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:128486277 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:14775757 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:14775757 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:40031845 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:40031845 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:7499359 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:7499359 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:46976152 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:46976152 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:89732273 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:89732273 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:47284865 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:47284865 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:117121731 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:117121731 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:94138121 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:94138121 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:120707585 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:120707585 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:178416416 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:178416416 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:23416970 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:23416970 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:75094919 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:75094919 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:75109222 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:75109222 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:3137589 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:3137589 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:35857027 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:35857027 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:54795925 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:54795925 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:146971196 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:146971196 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:196394953 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:196394953 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:70293473 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:70293473 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:10675568 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:10675568 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:52708939 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:52708939 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:129250337 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:129250337 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:133920845 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:133920845 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:203741096 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:203741096 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:38504032 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:38504032 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:62894656 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:62894656 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:39983248 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:39983248 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:197598393 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:197598393 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:141232927 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:141232927 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:42342005 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:42342005 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:42445486 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:42445486 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:90382915 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:90382915 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:119609205 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:119609205 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:141776012 C>A maps to ENST00000475668 A1763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:141776012 C>A maps to ENST00000475668 A1763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:102464127 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:102464127 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:102592295 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:102592295 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:100843665 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:100843665 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59857104 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59857104 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59857725 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59857725 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:68480730 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:68480730 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:9017160 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:9017160 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10404365 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10404365 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10354051 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10354051 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:2044060 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:2044060 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:6618788 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:6618788 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:133636388 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:133636388 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:24914229 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:24914229 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:24965174 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:24965174 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:198166965 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:198166965 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:77170316 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:77170316 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:236189161 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:236189161 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:124676362 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:124676362 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:84733759 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:84733759 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:107691474 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:107691474 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:11800122 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:11800122 A>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:110287815 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:110287815 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:13381345 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:13381345 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:106396567 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:106396567 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:46032228 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:46032228 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248167048 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248167048 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248167295 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248167295 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248247363 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248247363 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:148733440 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:148733440 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:117087492 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:117087492 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:127251538 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:127251538 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:31815436 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:31815436 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:58240667 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:58240667 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:136472231 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:136472231 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:20376592 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:20376592 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:99358840 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:99358840 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:25158305 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:25158305 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:68028657 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:68028657 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:43927885 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:43927885 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:131831114 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:131831114 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:35388098 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:35388098 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:49642921 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:49642921 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:27746977 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:27746977 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:37518146 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:37518146 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:23509861 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:23509861 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:82125714 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:82125714 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:36302976 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:36302976 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43371899 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43371899 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43709569 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43709569 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43680498 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43680498 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43430890 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43430890 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43576562 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43576562 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:71439907 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:71439907 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:209357909 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:209357909 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:88945230 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:88945230 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:71314017 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:71314017 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229422168 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229422168 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:76260132 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:76260132 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:109378659 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:109378659 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:20581442 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:20581442 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:35690698 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:35690698 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:65042710 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:65042710 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:145742188 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:145742188 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:204136992 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:204136992 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:101018191 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:101018191 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:72977045 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:72977045 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:41165846 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:41165846 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:12883565 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:12883565 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:156024927 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:156024927 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:23401637 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:23401637 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:237519261 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:237519261 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:5668040 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:5668040 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:200246580 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:200246580 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:166164293 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:166164293 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:50649441 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:50649441 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:101046457 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:101046457 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:67161181 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:67161181 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:51207300 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:51207300 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:72861977 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:72861977 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:164755822 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:164755822 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:159921433 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:159921433 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:122755725 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:122755725 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:107350481 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:107350481 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:1208833 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:1208833 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:55725743 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:55725743 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:67300258 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:67300258 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:217311908 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:217311908 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:49831548 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:49831548 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:130748485 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:130748485 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:121444860 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:121444860 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:32265566 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:32265566 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:158605858 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:158605858 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:9069841 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:9069841 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:109192759 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:109192759 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:149508615 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:149508615 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:48209005 G>A maps to NM_175711.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chrX:48209005 G>A maps to NM_175711.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:74472399 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:74472399 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:48523483 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:48523483 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:9749780 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:9749780 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:120809130 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:120809130 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229737880 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229737880 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:47188354 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:47188354 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:114841491 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:114841491 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:35085942 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:35085942 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:50810800 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:50810800 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:56725547 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:56725547 T>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:5734020 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:5734020 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:138860696 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:138860696 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:119941226 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:119941226 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:16855908 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:16855908 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:144345201 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:144345201 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr21:10916318 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr21:10916318 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:55035145 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:55035145 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248023899 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248023899 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:3432083 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:3432083 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:94848165 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:94848165 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:20774141 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:20774141 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:179640062 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:179640062 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:22836196 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:22836196 A>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:132394423 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:132394423 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:156990504 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:156990504 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:128918637 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:128918637 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:150385935 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:150385935 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:79968253 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:79968253 T>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:113145172 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:113145172 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:113145229 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:113145229 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:241958593 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:241958593 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:124154753 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:124154753 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:69959120 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:69959120 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:37941030 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:37941030 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:74671787 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:74671787 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:58231623 T>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:58231623 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:20488787 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:20488787 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:20440909 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:20440909 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr21:28213506 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr21:28213506 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:86702095 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:86702095 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:109359905 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:109359905 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:98508935 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:98508935 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:57605534 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:57605534 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:119422198 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:119422198 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:81636980 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:81636980 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:122078588 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:122078588 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr17:3776586 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr17:3776586 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:30313324 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:30313324 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:101451279 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:101451279 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:32393595 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:32393595 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chrX:107935876 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chrX:107935876 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:207885931 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:207885931 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:88779858 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:88779858 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:49018756 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:49018756 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:49937359 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:49937359 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:169948266 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:169948266 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:223156418 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:223156418 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr18:32428227 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr18:32428227 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:4705941 T>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:4705941 T>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:96945095 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:96945095 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:1137745 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:1137745 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:51853660 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:51853660 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:126518132 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:126518132 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:29268166 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:29268166 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:46261062 A>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:46261062 A>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:166135208 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:166135208 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:92539509 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:92539509 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:186120680 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:186120680 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:3122942 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:3122942 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:207073600 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:207073600 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:62350082 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:62350082 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:143033590 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:143033590 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr21:31913899 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr21:31913899 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:152538321 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:152538321 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:140995667 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:140995667 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:17835734 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:17835734 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:64892161 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:64892161 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:92714458 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:92714458 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:26432335 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:26432335 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:76596540 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:76596540 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:21250863 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:21250863 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr9:14313357 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr9:14313357 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:161206191 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:161206191 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:96059767 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:96059767 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:156845738 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:156845738 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:3714303 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:3714303 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:55996724 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:55996724 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:98369671 A>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:98369671 A>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:151204698 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:151204698 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:12012838 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:12012838 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:131912378 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:131912378 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:173454449 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:173454449 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:76251903 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:76251903 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr9:110086379 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr9:110086379 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:107082962 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:107082962 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:237906791 C>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:237906791 C>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:77089479 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:77089479 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:49309001 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:49309001 A>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:13899777 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:13899777 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:48056280 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr15:48056280 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:234041512 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:234041512 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:50257420 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:50257420 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:85255319 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:85255319 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr5:135510365 A>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr5:135510365 A>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr8:101195562 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr8:101195562 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:68456586 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:68456586 T>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chrX:79279692 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chrX:79279692 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:192922311 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:192922311 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:698733 T>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:698733 T>G did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:175048873 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:175048873 G>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr13:20004701 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr13:20004701 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:189064866 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:189064866 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr14:81449234 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr14:81449234 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:132237133 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:132237133 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:167709481 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:167709481 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr17:1634325 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr17:1634325 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:2882200 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr16:2882200 G>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:48370488 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:48370488 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:7637388 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:7637388 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:16218858 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:16218858 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:211075038 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:211075038 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:6312374 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:6312374 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:156936184 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:156936184 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:39694616 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:39694616 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:154557538 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:154557538 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:41471853 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:41471853 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:110475115 T>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:110475115 T>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:49763466 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:49763466 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:74865121 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:74865121 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:80844827 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:80844827 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:100978476 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:100978476 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:197087150 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:197087150 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:32087507 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:32087507 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:36963984 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:36963984 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:100793491 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:100793491 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:20168566 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:20168566 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:118983111 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:118983111 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:138669575 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:138669575 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:2952837 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:2952837 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:191087847 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:191087847 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:56130676 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:56130676 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:61689340 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:61689340 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:98195825 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:98195825 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:29090114 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:29090114 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:36227768 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:36227768 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:146471292 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:146471292 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:124783391 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:124783391 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:121344987 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:121344987 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:107829750 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:107829750 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:28848735 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:28848735 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:17185533 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:17185533 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:126694532 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:126694532 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:96580486 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:96580486 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:14996071 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:14996071 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:31256446 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:31256446 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:95593178 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:95593178 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:80668729 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:80668729 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:404853 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:404853 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:34982179 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:34982179 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:74228041 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:74228041 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:52319146 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:52319146 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:186501394 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:186501394 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:220219802 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:220219802 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:128050426 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:128050426 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:50682335 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:50682335 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:137844354 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:137844354 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:5617333 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:5617333 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr13:113777248 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr13:113777248 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:62104201 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:62104201 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:48808597 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:48808597 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:15935165 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:15935165 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:40408235 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:40408235 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:80684578 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:80684578 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:42647569 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:42647569 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:118849598 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:118849598 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:39127935 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:39127935 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:29555636 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:29555636 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr13:114549480 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr13:114549480 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:56065216 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:56065216 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:58008212 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:58008212 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:58477978 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:58477978 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:19808924 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:19808924 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:37691660 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:37691660 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:106558190 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:106558190 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:93836042 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:93836042 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:89575329 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:89575329 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:8822243 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:8822243 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:121582508 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:121582508 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:128637411 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:128637411 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:201840000 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:201840000 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:16298129 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:16298129 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:88658827 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:88658827 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:44160366 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:44160366 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:34787445 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:34787445 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:241731961 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:241731961 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:123075811 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:123075811 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:156763119 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:156763119 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:16757913 T>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:16757913 T>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:100174870 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:100174870 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:4539945 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:4539945 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:150184391 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:150184391 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:41105542 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:41105542 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:112439856 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:112439856 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:37588168 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:37588168 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:38184128 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:38184128 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:12065638 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:12065638 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:128858592 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:128858592 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:21940817 T>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:21940817 T>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:60285517 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:60285517 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:11293423 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:11293423 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:45797266 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:45797266 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:50779925 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:50779925 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:23893885 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:23893885 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:36684276 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:36684276 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:192251908 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:192251908 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:164069621 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:164069621 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:71297983 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:71297983 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr13:101944498 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr13:101944498 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:207003175 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:207003175 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:26092480 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:26092480 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:170833446 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:170833446 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:33481380 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:33481380 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:104179376 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:104179376 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:132016123 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:132016123 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:71733473 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:71733473 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:224514211 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:224514211 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:113448305 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:113448305 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:76019383 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:76019383 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:9792518 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:9792518 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:161987082 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:161987082 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:195955564 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:195955564 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:17552486 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:17552486 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:39589081 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:39589081 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:108603304 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:108603304 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:122278480 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:122278480 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:41831546 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:41831546 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:8159805 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr17:8159805 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:33258273 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:33258273 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:38444637 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:38444637 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:98388267 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:98388267 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:2140652 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:2140652 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:102054960 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:102054960 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:121265488 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:121265488 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:105750482 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:105750482 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55967894 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55967894 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:15656799 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:15656799 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:119547749 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:119547749 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:9318499 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:9318499 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:107141162 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:107141162 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:67681739 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:67681739 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:6267417 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:6267417 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:237886327 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:237886327 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:32972180 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:32972180 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:161326721 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:161326721 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:3991344 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:3991344 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:81961415 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:81961415 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55863503 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55863503 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:40863456 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:40863456 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:75682258 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:75682258 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:39371627 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:39371627 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:100795394 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:100795394 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:98984429 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:98984429 G>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:32650212 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:32650212 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:160142554 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:160142554 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:147450053 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:147450053 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:54712058 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:54712058 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18655692 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18655692 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:74472409 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:74472409 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:48389327 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:48389327 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:114875009 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:114875009 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:162091730 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:162091730 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:67815337 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:67815337 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:35721932 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:35721932 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:226044793 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:226044793 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:2413565 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:2413565 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:12183325 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:12183325 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:68839522 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:68839522 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:3544383 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:3544383 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:36896600 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:36896600 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:55032828 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:55032828 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:100389586 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:100389586 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:99759042 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:99759042 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:103274014 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:103274014 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18579656 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18579656 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:24906618 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr22:24906618 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:216019062 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:216019062 C>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:47098927 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:47098927 G>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:6058416 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:6058416 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:6219952 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:6219952 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:113146014 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:113146014 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:68611414 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:68611414 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:128885595 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chrX:128885595 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:43484438 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:43484438 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:174062862 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:174062862 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:44988649 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:44988649 A>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:146115298 G>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:146115298 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:229665905 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:229665905 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:48117615 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:48117615 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:16161980 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:16161980 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:48744862 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:48744862 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:22068532 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:22068532 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:183907285 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:183907285 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:35508205 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:35508205 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:40025124 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:40025124 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20487290 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20487290 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20548793 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20548793 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:39564275 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:39564275 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:87563912 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:87563912 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:33615819 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:33615819 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:5191937 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:5191937 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:178585637 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:178585637 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:84558707 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:84558707 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:7724811 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:7724811 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:100207957 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:100207957 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:148048192 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:148048192 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:76201120 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:76201120 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:135611745 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:135611745 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:8757732 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:8757732 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:49962336 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:49962336 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:3726202 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:3726202 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:114153504 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:114153504 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:27388875 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:27388875 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:101437437 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:101437437 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:101490493 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:101490493 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:69272010 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:69272010 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:43218185 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:43218185 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:156909772 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:156909772 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:98513760 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:98513760 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:25023070 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:25023070 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:197055910 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:197055910 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:47565846 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:47565846 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:19766305 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:19766305 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:42474761 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:42474761 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:28915422 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:28915422 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:117059778 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:117059778 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:33644461 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:33644461 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:120070332 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:120070332 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:169391573 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:169391573 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:179437861 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:179437861 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:67222848 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:67222848 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:49066291 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:49066291 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:152711654 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:152711654 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:86063642 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:86063642 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:93116328 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:93116328 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:40535802 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:40535802 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:57106565 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:57106565 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:180377425 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:180377425 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:180381557 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:180381557 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:63685393 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:63685393 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:64125968 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:64125968 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158227308 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158227308 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158263215 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158263215 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:107766174 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:107766174 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:227259819 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:227259819 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:25319821 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:25319821 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:19473882 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:19473882 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:25572822 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:25572822 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:85972244 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:85972244 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:202698741 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:202698741 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:49030412 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:49030412 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:117262839 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:117262839 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:55867044 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:55867044 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:55909016 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:55909016 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:23768666 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:23768666 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:70013159 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:70013159 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:72145611 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:72145611 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:22213923 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:22213923 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:21613221 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:21613221 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:205035455 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:205035455 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:103345530 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:103345530 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:33136569 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:33136569 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:101809892 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:101809892 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:61939446 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:61939446 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:139609067 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:139609067 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:139712299 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:139712299 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:117015254 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:117015254 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:107923987 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:107923987 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:238271886 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:238271886 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:1249402 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:1249402 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:69646788 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:69646788 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:17183686 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:17183686 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:166535182 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:166535182 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:126715737 C>T maps to NM_022802.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:126715737 C>T maps to NM_022802.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:106459798 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:106459798 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:134304900 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:134304900 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:23930092 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:23930092 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:22929909 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:22929909 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:57480494 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:57480494 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:87525864 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:87525864 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:85786975 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:85786975 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:15735455 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:15735455 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:35981582 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:35981582 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:169188880 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:169188880 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:154004925 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:154004925 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:31196968 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:31196968 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:21031295 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:21031295 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:13769805 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:13769805 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:38939604 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:38939604 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:139257631 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:139257631 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:63005185 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:63005185 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:441463 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:441463 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:28667797 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:28667797 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:80019861 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:80019861 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:93246589 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:93246589 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:44198615 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:44198615 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:49699007 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:49699007 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:66439760 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:66439760 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:184297424 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:184297424 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:27645381 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:27645381 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:13950826 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:13950826 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:133782347 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:133782347 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:154128267 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:154128267 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:120240642 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:120240642 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:51048259 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:51048259 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:170639494 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:170639494 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:137289286 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:137289286 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:37029628 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:37029628 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:163066354 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:163066354 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:150891305 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:150891305 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:8156281 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:8156281 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:117593772 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:117593772 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:207143406 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:207143406 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:157718562 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:157718562 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:110327793 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:110327793 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:91435197 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:91435197 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:125351415 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:125351415 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179342048 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179342048 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:128564200 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:128564200 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:147106585 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:147106585 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:216263920 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:216263920 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:216296709 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:216296709 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:114258218 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:114258218 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:69265514 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:69265514 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:12627816 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:12627816 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:162459210 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:162459210 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:97753562 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:97753562 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:9820437 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:9820437 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:53364799 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:53364799 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:48416262 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:48416262 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:153667323 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:153667323 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:5815928 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:5815928 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:61996175 G>A maps to ENST00000452158 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:61996175 G>A maps to ENST00000452158 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:61959200 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:61959200 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102962476 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102962476 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:129429155 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:129429155 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:150761732 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:150761732 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:121400811 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:121400811 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:53074126 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:53074126 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:105482974 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:105482974 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48847291 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48847291 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:110201417 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:110201417 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:145039782 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:145039782 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48674126 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:48674126 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:18801962 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:18801962 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:28473612 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:28473612 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:43042473 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:43042473 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:87512039 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:87512039 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:70897888 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:70897888 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:159998645 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:159998645 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:90969508 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:90969508 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:30486511 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:30486511 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:3942007 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:3942007 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:124438334 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:124438334 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:154504245 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:154504245 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:118242270 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:118242270 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:86869644 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:86869644 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:52778629 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:52778629 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:32253886 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:32253886 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:6971839 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:6971839 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:83852071 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:83852071 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr13:76409482 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr13:76409482 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:145746222 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:145746222 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:115805415 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:115805415 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:144178808 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:144178808 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:143857446 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:143857446 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:117013721 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:117013721 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:21207628 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:21207628 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:220791514 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:220791514 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:198570097 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:198570097 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:112421167 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:112421167 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:13214900 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:13214900 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:6338123 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:6338123 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:47504195 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:47504195 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:90437794 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:90437794 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:84102594 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:84102594 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:70341754 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:70341754 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:50334759 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:50334759 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:3304797 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:3304797 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:141767224 C>T maps to ENST00000475668 R1668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:141767224 C>T maps to ENST00000475668 R1668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:12264341 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:12264341 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:49432982 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:49432982 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:45965896 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:45965896 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:58073751 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:58073751 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:108788661 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:108788661 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:154014796 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:154014796 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:48350200 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:48350200 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:60231889 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:60231889 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:72754741 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:72754741 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:55464679 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:55464679 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:63444663 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:63444663 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:108127309 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:108127309 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:89868066 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:89868066 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:134038591 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:134038591 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:24951087 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:24951087 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:55424267 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:55424267 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:21490119 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:21490119 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:8248379 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:8248379 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:130748791 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:130748791 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:233839289 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:233839289 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102632352 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102632352 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:54327133 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:54327133 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:96108913 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:96108913 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:26095987 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:26095987 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:61389756 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:61389756 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102338041 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102338041 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4904110 T>A maps to NM_001004759.1 *355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4904110 T>A maps to NM_001004759.1 *355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158670504 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158670504 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158747471 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:158747471 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:55249302 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:55249302 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:79866976 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:79866976 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:165843643 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:165843643 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:15103630 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:15103630 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:31725708 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:31725708 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:230472731 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:230472731 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:71007063 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:71007063 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:71804079 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:71804079 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:502490 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:502490 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:629204 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:629204 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:25145502 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:25145502 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:110420475 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:110420475 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:59812288 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:59812288 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:81903951 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:81903951 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:18836324 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:18836324 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:118225440 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:118225440 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:42196224 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:42196224 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:42218897 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:42218897 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:87311145 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:87311145 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:42599862 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:42599862 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:42599871 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:42599871 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:147562009 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:147562009 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:104220590 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:104220590 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:121828810 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:121828810 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:48710728 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:48710728 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:102040199 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:102040199 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:50180438 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:50180438 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:43359625 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:43359625 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:151234800 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:151234800 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:79002382 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:79002382 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:33433504 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:33433504 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:170626622 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:170626622 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:131351357 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:131351357 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:173659690 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:173659690 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:86509393 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:86509393 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:240966100 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:240966100 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:53458021 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:53458021 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:87105987 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:87105987 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:87110369 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:87110369 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:1073533 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:1073533 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:79639114 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:79639114 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:20181003 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:20181003 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:39009696 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:39009696 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:39063771 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:39063771 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:5645429 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:5645429 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:38835223 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:38835223 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:30862946 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:30862946 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:84647692 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:84647692 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:84649436 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:84649436 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:101176100 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:101176100 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:80552634 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:80552634 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:121640967 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:121640967 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:62985019 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:62985019 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:6457632 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:6457632 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:128694756 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:128694756 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:32417360 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:32417360 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:108071979 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:108071979 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:101581336 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:101581336 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:44468470 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:44468470 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:135080745 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:135080745 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:143223077 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:143223077 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:21028139 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:21028139 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:168222599 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:168222599 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:168690705 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:168690705 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:17934791 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:17934791 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:35793528 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:35793528 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:13074324 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:13074324 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:18655718 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:18655718 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:56218481 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:56218481 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:105029065 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:105029065 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:191859967 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:191859967 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:53078334 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:53078334 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:155850854 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:155850854 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:70617377 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:70617377 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:99707699 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:99707699 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:77393165 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:77393165 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:111719425 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:111719425 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:2569490 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:2569490 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:79281067 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:79281067 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102529696 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:102529696 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:61491434 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:61491434 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:50796254 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:50796254 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:133481011 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:133481011 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:44935023 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:44935023 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:11860795 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:11860795 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:41367708 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:41367708 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:150501865 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:150501865 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:46156845 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:46156845 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:40717289 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:40717289 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:10916333 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:10916333 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:71506885 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:71506885 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:108549695 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:108549695 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:100367686 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:100367686 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179393172 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179393172 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:151537168 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:151537168 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:669192 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:669192 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:154524206 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:154524206 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:109537158 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:109537158 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:216462805 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:216462805 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:18640663 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:18640663 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:129059188 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:129059188 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:100245875 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:100245875 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:177100787 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:177100787 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:113118860 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:113118860 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:21367490 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:21367490 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:33252383 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:33252383 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:100013587 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:100013587 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:6628215 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:6628215 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:188923925 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:188923925 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:79735979 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:79735979 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:147114294 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:147114294 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:267422 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:267422 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:7024066 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:7024066 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:72347732 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr18:72347732 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:134483290 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chrX:134483290 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:37427557 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:37427557 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:38282692 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:38282692 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:47892432 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:47892432 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:86173254 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:86173254 T>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:58551770 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:58551770 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:113644416 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:113644416 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:20744512 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:20744512 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:156847707 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:156847707 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:26669459 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:26669459 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:36160538 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:36160538 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr12:46290733 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr12:46290733 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:176998714 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:176998714 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:31606666 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:31606666 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:31626777 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:31626777 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:222902904 A>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:222902904 A>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:93928833 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:93928833 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:48649199 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:48649199 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:24372629 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:24372629 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:62095864 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:62095864 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:74493583 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:74493583 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:93548000 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:93548000 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:233396384 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:233396384 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:205039501 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:205039501 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:211533036 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:211533036 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:11082708 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:11082708 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:16990446 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:16990446 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:219647312 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:219647312 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:6505556 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:6505556 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:75511353 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:75511353 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:183597151 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:183597151 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:53226850 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:53226850 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:65688002 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:65688002 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:48626581 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:48626581 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:93973489 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:93973489 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:76553796 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:76553796 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:93202297 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:93202297 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:197029964 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:197029964 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr13:113773363 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr13:113773363 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:139155456 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:139155456 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:2695632 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:2695632 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:163040046 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:163040046 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:180053084 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr5:180053084 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr9:128025910 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr9:128025910 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:235715663 A>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:235715663 A>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chrX:132437408 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chrX:132437408 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:81336754 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:81336754 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:75183379 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:75183379 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:31424070 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:31424070 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:35107552 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:35107552 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:39845340 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:39845340 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:160011166 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:160011166 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:176812422 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:176812422 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:51900367 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:51900367 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:55593343 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:55593343 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:41687892 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:41687892 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:60230097 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:60230097 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:17168855 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:17168855 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:88722720 A>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:88722720 A>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:31139284 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:31139284 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:2999610 A>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:2999610 A>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:47165746 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:47165746 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:169279382 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:169279382 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:248167197 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:248167197 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:124180713 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:124180713 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:55860657 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:55860657 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:88313274 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:88313274 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:31793812 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:31793812 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:145015766 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:145015766 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr12:130851566 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr12:130851566 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:2209683 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:2209683 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:70118638 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr11:70118638 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr14:94642346 A>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr14:94642346 A>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:75761024 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:75761024 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr9:8376556 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr9:8376556 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:41420128 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:41420128 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr22:37196916 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr22:37196916 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:104987762 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:104987762 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:48556914 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:48556914 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:102265085 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:102265085 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr18:61564604 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr18:61564604 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:30992257 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:30992257 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:144445674 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:144445674 G>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:70130402 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:70130402 T>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chrX:48053791 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chrX:48053791 G>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:99786260 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:99786260 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:34004180 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:34004180 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:26622429 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:26622429 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:74819609 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:74819609 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:72975819 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:72975819 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:50870771 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:50870771 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:142627054 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:142627054 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:5064780 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:5064780 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:100204992 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr8:100204992 T>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:85654501 A>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:85654501 A>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:40936666 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr17:40936666 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:17221515 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:17221515 C>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:145162636 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:145162636 C>A did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:71546732 G>T did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:71546732 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:7382945 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:7382945 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:48335272 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:48335272 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:66880040 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:66880040 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:58491030 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:58491030 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:20565058 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:20565058 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:127797286 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:127797286 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:7789656 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:7789656 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:31124844 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:31124844 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:70890465 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:70890465 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:89172684 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:89172684 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:74364806 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:74364806 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:247051676 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:247051676 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:29450337 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:29450337 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:112022946 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:112022946 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:112592043 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:112592043 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:114274073 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:114274073 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:99188503 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:99188503 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:101295474 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:101295474 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:201459945 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:201459945 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:72055682 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:72055682 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:154295601 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:154295601 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:72491964 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:72491964 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:6499430 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:6499430 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:4623802 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:4623802 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:76956351 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:76956351 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:101312108 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:101312108 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:119737476 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:119737476 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:64676737 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:64676737 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:28842279 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:28842279 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:11039407 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:11039407 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:112991862 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:112991862 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:36959353 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:36959353 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:108011057 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:108011057 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:100612590 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:100612590 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:16745807 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:16745807 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:122817132 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:122817132 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:10332292 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:10332292 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:39611494 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:39611494 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:31480628 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:31480628 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:65888216 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:65888216 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:65897426 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:65897426 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:30672587 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:30672587 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:231376720 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:231376720 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:169762917 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:169762917 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:226186816 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:226186816 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:111889255 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:111889255 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:3735195 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:3735195 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:20040901 C>T maps to ENST00000450019 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:20040901 C>T maps to ENST00000450019 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:2753495 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:2753495 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:165715845 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:165715845 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:118822286 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:118822286 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:40965092 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:40965092 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:53820829 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:53820829 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:54913030 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:54913030 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:62501902 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:62501902 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:27454795 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:27454795 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:71275514 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:71275514 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:44281961 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:44281961 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:44302697 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:44302697 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:241533295 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:241533295 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:116280739 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:116280739 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:92054294 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:92054294 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:58287830 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:58287830 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:32779856 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:32779856 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:124428132 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:124428132 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:32690053 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:32690053 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:73476033 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:73476033 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:112666766 C>T maps to NM_138806.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:112666766 C>T maps to NM_138806.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7483065 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7483065 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:137664243 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:137664243 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:21883274 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:21883274 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:21883648 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:21883648 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:68557893 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:68557893 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:17680557 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:17680557 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:34854502 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:34854502 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:182412283 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:182412283 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55860279 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55860279 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:196918574 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:196918574 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:196644996 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:196644996 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:50828427 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:50828427 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:93485295 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:93485295 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:203194164 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:203194164 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:233405027 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:233405027 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:24524214 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:24524214 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:86900453 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:86900453 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143038935 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143038935 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:58619200 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:58619200 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:74414569 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:74414569 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:74414950 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:74414950 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:2924926 G>T maps to NM_175607.1 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:2924926 G>T maps to NM_175607.1 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:146817985 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:146817985 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:76350440 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:76350440 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:125521465 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:125521465 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103352679 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103352679 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103462545 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103462545 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:121208879 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:121208879 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:121267642 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:121267642 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:61929205 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:61929205 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:139642887 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:139642887 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:109738528 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:109738528 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:48369667 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:48369667 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:227912326 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:227912326 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:107437735 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:107437735 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:189928078 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:189928078 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:54737199 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:54737199 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:148559786 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:148559786 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:15063616 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:15063616 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:115282539 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:115282539 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:113421122 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:113421122 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:138253738 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:138253738 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:96609916 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:96609916 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:96612441 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:96612441 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:99375531 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:99375531 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:72014708 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:72014708 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:85969799 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:85969799 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:61493399 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:61493399 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:6652652 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:6652652 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:36379737 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:36379737 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:52752826 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:52752826 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:200628332 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:200628332 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:49977078 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:49977078 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:11851638 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:11851638 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:73347792 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:73347792 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:79576495 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:79576495 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:124328212 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:124328212 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:21901405 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:21901405 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:196618998 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:196618998 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:11700910 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:11700910 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:65864447 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:65864447 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:58196463 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:58196463 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:220250826 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:220250826 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:154598647 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:154598647 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:28612109 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:28612109 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:56482757 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:56482757 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:183994877 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:183994877 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:150482264 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:150482264 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:65824186 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:65824186 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:62327386 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:62327386 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:43926591 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:43926591 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:14758241 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:14758241 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:77709477 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:77709477 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:139944559 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:139944559 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:132551300 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:132551300 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:46611572 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:46611572 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:111938751 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:111938751 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:111970111 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:111970111 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:27378491 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:27378491 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:103486935 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:103486935 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:7917923 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:7917923 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:187209001 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:187209001 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:14563113 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:14563113 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:139278124 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:139278124 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:150920057 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:150920057 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:127692896 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:127692896 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:99353207 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:99353207 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:72858839 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:72858839 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:125023003 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:125023003 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:4800591 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:4800591 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:100207831 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:100207831 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:183699727 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:183699727 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:83438668 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:83438668 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:151170657 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:151170657 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:27124257 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:27124257 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:89899795 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:89899795 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:134212619 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:134212619 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:151234536 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:151234536 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:141385920 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:141385920 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:44719087 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:44719087 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:133357343 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:133357343 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:94197777 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:94197777 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:122537109 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:122537109 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:72978384 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:72978384 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:145040799 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:145040799 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:26507174 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:26507174 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:140073470 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:140073470 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:41055816 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:41055816 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:97177370 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:97177370 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:26156533 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:26156533 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:149398966 G>A maps to NM_001024599.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:149398966 G>A maps to NM_001024599.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:30137840 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:30137840 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:186022934 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:186022934 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:21978773 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:21978773 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:87530231 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:87530231 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:97226844 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:97226844 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:148770667 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:148770667 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:20005367 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:20005367 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:160485619 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:160485619 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:114239720 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:114239720 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:166925880 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:166925880 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:35463073 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:35463073 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:47196405 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:47196405 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:15559256 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:15559256 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:15760928 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:15760928 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:4821202 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:4821202 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:33641318 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:33641318 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:185269293 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:185269293 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:133182527 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:133182527 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:36721887 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:36721887 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:2757371 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:2757371 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:73467939 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:73467939 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:27751300 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:27751300 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:94120072 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:94120072 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:94120083 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:94120083 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:100090444 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:100090444 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:44645612 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:44645612 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:200569250 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:200569250 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:39720007 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:39720007 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:6882247 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:6882247 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:31206806 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:31206806 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:16513544 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:16513544 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:48654414 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:48654414 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:90526197 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:90526197 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:148193696 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:148193696 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:81893014 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:81893014 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:81969102 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:81969102 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:82416655 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:82416655 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62845510 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62845510 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:141232701 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:141232701 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:169985443 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:169985443 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:53728280 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:53728280 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:33488322 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:33488322 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:160735891 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:160735891 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:160765918 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:160765918 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:2041802 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:2041802 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:75654346 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:75654346 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:164854262 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:164854262 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:164854264 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:164854264 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:138696967 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:138696967 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:138724719 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:138724719 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:37622483 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:37622483 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:15008411 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:15008411 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:135075045 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:135075045 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:140624699 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:140624699 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:168281293 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:168281293 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:24124380 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:24124380 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:90848857 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:90848857 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:174537898 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:174537898 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:68668124 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:68668124 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:60233780 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:60233780 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:11854622 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:11854622 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9019981 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9019981 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:81112084 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:81112084 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:10348285 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:10348285 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:23851834 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:23851834 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:23884824 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:23884824 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:171034880 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:171034880 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:171243918 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:171243918 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:57109567 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:57109567 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:57110842 T>A maps to NM_001113203.1 K1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:57110842 T>A maps to NM_001113203.1 K1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:101795333 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:101795333 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:78400192 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:78400192 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:90982840 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:90982840 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:120384921 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:120384921 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:17814135 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:17814135 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:124824808 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:124824808 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:27256239 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:27256239 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:33307151 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:33307151 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:125144411 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:125144411 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:63831126 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:63831126 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:57076011 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:57076011 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:56363305 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:56363305 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:18543047 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:18543047 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:26116038 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:26116038 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:150703474 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:150703474 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:69320712 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:69320712 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:24329251 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:24329251 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:33475482 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:33475482 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:18766473 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:18766473 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:229593872 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:229593872 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:102339861 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:102339861 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:102343727 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:102343727 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248166969 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248166969 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248167152 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248167152 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248167322 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248167322 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:55433582 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:55433582 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:22332767 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:22332767 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:22333130 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:22333130 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:158736500 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:158736500 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:123625329 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:123625329 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:88318755 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:88318755 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:46729467 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:46729467 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:38293720 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:38293720 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:17566289 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:17566289 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:226570957 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:226570957 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:165989970 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:165989970 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:95389009 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:95389009 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:55155068 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:55155068 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:48525020 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:48525020 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:34435388 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:34435388 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:98412420 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:98412420 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:111554083 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:111554083 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:14578649 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:14578649 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:125268012 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:125268012 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:33021741 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:33021741 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:42050581 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:42050581 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:131948374 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:131948374 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:132110107 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:132110107 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:118880303 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:118880303 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:131815417 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:131815417 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:131866995 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:131866995 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:44154837 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:44154837 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:38153085 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:38153085 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:38158808 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:38158808 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:19566168 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:19566168 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:149216723 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:149216723 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:26151301 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:26151301 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:146086383 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:146086383 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:69104796 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:69104796 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:32116987 C>G maps to ENST00000375149 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:32116987 C>G maps to ENST00000375149 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:142459540 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:142459540 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:228004906 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:228004906 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43352056 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43352056 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43523269 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43523269 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43576959 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43576959 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:45293035 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:45293035 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:43126748 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:43126748 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:43128365 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:43128365 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:87689139 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:87689139 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:8319767 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:8319767 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:55711934 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:55711934 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:128411250 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:128411250 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:5215196 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:5215196 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:121568129 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:121568129 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:87847048 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:87847048 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:114391842 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:114391842 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:170305250 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:170305250 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:35695053 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:35695053 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:79928560 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:79928560 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:66411618 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:66411618 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:129537745 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:129537745 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:17736576 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:17736576 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:136276069 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:136276069 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:72932394 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:72932394 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:119293137 C>A maps to NM_001099685.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:119293137 C>A maps to NM_001099685.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:5304602 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:5304602 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:158595821 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:158595821 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:25399699 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:25399699 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:115060048 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:115060048 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:68912604 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:68912604 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:47120966 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:47120966 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:93306042 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:93306042 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:93026710 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:93026710 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:45399573 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:45399573 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:39002870 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:39002870 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237896932 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237896932 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237941961 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237941961 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:33873610 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:33873610 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:6695619 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:6695619 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:51171013 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:51171013 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:18338425 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:18338425 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:43625261 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:43625261 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:100728057 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:100728057 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:57218026 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:57218026 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:25823604 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:25823604 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:81965716 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:81965716 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:77926986 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:77926986 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:9475767 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:9475767 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:7247934 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:7247934 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:37946948 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:37946948 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:45571858 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:45571858 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:440979 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:440979 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:52033925 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:52033925 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:164760752 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:164760752 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:56920204 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:56920204 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:122787428 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:122787428 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:26821003 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:26821003 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:35395907 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:35395907 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:107427256 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:107427256 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:103015134 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:103015134 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92307684 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92307684 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92352515 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92352515 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:47778716 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:47778716 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:75708812 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:75708812 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:139745218 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:139745218 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:85266823 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:85266823 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55703371 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55703371 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:1414768 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:1414768 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:40882384 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:40882384 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:6414413 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:6414413 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:121726746 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:121726746 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:78189633 T>G maps to ENST00000416259 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:78189633 T>G maps to ENST00000416259 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:231222755 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:231222755 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:48860918 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:48860918 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:89612989 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:89612989 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:55910468 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:55910468 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:158622475 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:158622475 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:123215181 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chrX:123215181 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:27470172 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:27470172 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:113312458 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:113312458 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:152466646 T>C maps to NM_033071.2 T8269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:152466646 T>C maps to NM_033071.2 T8269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:152774699 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:152774699 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:115117547 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:115117547 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:151748188 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:151748188 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:115857785 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:115857785 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:100231029 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:100231029 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:79378215 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:79378215 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:166964395 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:166964395 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:167021824 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:167021824 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:165788761 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:165788761 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:193059058 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:193059058 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:133100011 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:133100011 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:19232526 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:19232526 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:15433926 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:15433926 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:12779899 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:12779899 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:26652400 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:26652400 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:68688289 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:68688289 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:68929045 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:68929045 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:68934314 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:68934314 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:74929263 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:74929263 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:185655539 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:185655539 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:123892287 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:123892287 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248023843 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248023843 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:31362531 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:31362531 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:234891681 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:234891681 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:65721000 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:65721000 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:43086817 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:43086817 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:179578924 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:179578924 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:176396452 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:176396452 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:35579941 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:35579941 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:215987021 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:215987021 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:49336074 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:49336074 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:50785681 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:50785681 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:108322133 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:108322133 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:17277909 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:17277909 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:118944472 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:118944472 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:53007715 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:53007715 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:53007717 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:53007717 A>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:38810738 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:38810738 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:9536124 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:9536124 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:134896259 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:134896259 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:5239103 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:5239103 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:68627437 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:68627437 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:184210853 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:184210853 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:168550550 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:168550550 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:101371320 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:101371320 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:52930698 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:52930698 T>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:38119970 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:38119970 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:178339730 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:178339730 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:62595354 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:62595354 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:56621090 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:56621090 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:57829817 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:57829817 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:113631403 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:113631403 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:76730736 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:76730736 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:108921346 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:108921346 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:114176509 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:114176509 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:26655185 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:26655185 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:5139594 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:5139594 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:46113730 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:46113730 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr4:169102829 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr4:169102829 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr15:83334361 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr15:83334361 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:157014171 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:157014171 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:23980261 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:23980261 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:96761534 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:96761534 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr13:25268511 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr13:25268511 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:62384435 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:62384435 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:70840466 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:70840466 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:22058778 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:22058778 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:40234680 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:40234680 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:227153455 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:227153455 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:52821404 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:52821404 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:55543030 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:55543030 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:21883327 A>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:21883327 A>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:1588772 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:1588772 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:50856835 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:50856835 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr4:104027347 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr4:104027347 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr22:29130365 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr22:29130365 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:154520396 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:154520396 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:33145987 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:33145987 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:139815073 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:139815073 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:36939358 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:36939358 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:467013 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:467013 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:70904686 T>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:70904686 T>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:74604909 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:74604909 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:72285902 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:72285902 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:117748866 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:117748866 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr4:110834392 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr4:110834392 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:150599668 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:150599668 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:220152724 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:220152724 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:137793207 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:137793207 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:30708891 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:30708891 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:240555728 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:240555728 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:171077205 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:171077205 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:89756866 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:89756866 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr9:37744347 T>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr9:37744347 T>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:33588818 A>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:33588818 A>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:90004585 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:90004585 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:73132391 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:73132391 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:20398079 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:20398079 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:113803629 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:113803629 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:160849074 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:160849074 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:185270340 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:185270340 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:170371505 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:170371505 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:200959254 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:200959254 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:173702817 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:173702817 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:39036033 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:39036033 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr22:33673268 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr22:33673268 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:920073 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:920073 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:46884070 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:46884070 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:25426818 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:25426818 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:18420682 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:18420682 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:235964449 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:235964449 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:148794783 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:148794783 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:136693818 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:136693818 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:151078142 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:151078142 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:104722394 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:104722394 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:30433003 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:30433003 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:55729384 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:55729384 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:830998 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:830998 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr15:31217957 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr15:31217957 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr9:88593301 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr9:88593301 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr13:52684571 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr13:52684571 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:43700083 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:43700083 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:56500025 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:56500025 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:53852868 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:53852868 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:51938341 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:51938341 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr21:48063422 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr21:48063422 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:57255797 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:57255797 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:1647135 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:1647135 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:238735993 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:238735993 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:103234381 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:103234381 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:100027143 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:100027143 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:134987659 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chrX:134987659 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:51200825 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:51200825 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:65235691 T>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:65235691 T>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:133529916 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:133529916 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:53079327 A>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:53079327 A>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:89791165 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:89791165 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:98138708 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:98138708 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:19474981 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:19474981 T>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr9:108522399 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr9:108522399 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:14498823 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:14498823 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:126319847 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr6:126319847 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr22:46742502 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr22:46742502 A>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:115600148 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:115600148 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:161127115 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:161127115 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:72868504 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:72868504 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:43163000 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:43163000 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:100014671 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:100014671 C>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:825387 G>C did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr5:825387 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:67267473 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:67267473 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:15610304 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:15610304 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:241812309 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:241812309 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:109978149 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:109978149 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:43919642 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:43919642 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:94027745 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:94027745 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:68114001 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:68114001 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:117061314 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:117061314 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:117607384 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:117607384 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:11026810 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:11026810 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr22:23596222 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr22:23596222 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:72539323 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:72539323 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:105921672 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:105921672 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:10332046 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:10332046 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100792079 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100792079 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:170961577 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:170961577 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:114470264 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:114470264 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:126126011 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:126126011 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:7527022 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:7527022 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:112080562 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:112080562 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:95161146 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:95161146 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:48688272 T>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:48688272 T>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:179938069 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:179938069 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:93523985 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:93523985 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:93524175 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:93524175 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:40764547 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:40764547 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:10193907 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:10193907 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:10559968 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:10559968 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:17088093 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:17088093 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:232656575 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:232656575 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:145625939 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:145625939 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:75977456 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:75977456 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:17164685 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:17164685 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:49046709 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:49046709 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:96731835 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:96731835 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:140956962 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:140956962 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:13911488 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:13911488 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:83868249 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:83868249 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:162851635 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:162851635 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:154645369 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:154645369 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:33871962 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:33871962 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:73462546 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:73462546 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:89157102 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:89157102 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:50283748 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:50283748 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:50284789 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:50284789 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:120489791 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:120489791 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:48192439 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:48192439 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:18868871 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:18868871 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:91781918 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:91781918 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:118466669 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:118466669 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:41142826 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:41142826 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:20141465 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:20141465 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:81180151 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:81180151 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:53162393 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:53162393 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:143685381 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:143685381 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:145529277 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:145529277 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:47614324 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:47614324 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:41798041 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:41798041 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:160676434 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:160676434 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:20083018 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:20083018 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:881765 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:881765 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:21968118 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:21968118 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:2318993 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:2318993 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:120795765 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:120795765 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:113449572 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:113449572 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:192250497 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:192250497 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr16:48580306 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr16:48580306 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:201776953 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:201776953 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:240921676 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:240921676 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:21120556 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:21120556 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:204923895 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:204923895 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr16:50666371 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr16:50666371 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:79910828 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:79910828 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:63995006 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:63995006 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr13:113832458 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr13:113832458 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:101983871 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:101983871 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:207105951 T>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:207105951 T>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:138423379 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:138423379 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:8792351 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:8792351 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:146307603 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:146307603 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:42218902 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:42218902 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:149216732 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr5:149216732 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:182852546 G>T maps to ENST00000280295 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:182852546 G>T maps to ENST00000280295 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:40562948 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:40562948 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:22292895 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:22292895 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr16:31099151 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr16:31099151 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:54124088 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:54124088 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr18:8406202 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr18:8406202 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:125765717 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:125765717 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:117862743 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:117862743 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr13:50108474 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr13:50108474 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:103180585 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:103180585 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:103180625 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:103180625 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:8866362 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:8866362 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:200173448 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:200173448 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:4281608 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:4281608 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:39536293 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:39536293 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:1712155 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:1712155 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:11099961 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:11099961 C>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:106918642 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:106918642 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:231106061 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:231106061 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:36014604 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:36014604 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:74639578 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:74639578 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:70883599 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:70883599 A>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:50803684 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:50803684 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:134128746 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:134128746 T>G did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:189013106 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:189013106 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:15189719 T>G maps to NM_001168340.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:15189719 T>G maps to NM_001168340.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:103722778 T>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:103722778 T>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:25599467 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:25599467 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:118244461 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:118244461 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:47102207 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:47102207 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:5050361 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:5050361 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:158935385 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:158935385 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:65259691 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chrX:65259691 T>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:61050423 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:61050423 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:61050429 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:61050429 A>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100819907 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100819907 G>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:106062 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr4:106062 A>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:88847430 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:88847430 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:56833780 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:56833780 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:69825539 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:69825539 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:100569435 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:100569435 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:236658920 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:236658920 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:74535732 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:74535732 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:165648624 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:165648624 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:38067483 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:38067483 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:82625916 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:82625916 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:102542293 T>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:102542293 T>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:110809088 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:110809088 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:42794270 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:42794270 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr7:76924257 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr7:76924257 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:19543932 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:19543932 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:196963407 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:196963407 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:76259379 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:76259379 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:43898644 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:43898644 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:17061798 T>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:17061798 T>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:176938673 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:176938673 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:327358 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:327358 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chrX:32328176 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chrX:32328176 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:11604643 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:11604643 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:131001627 T>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:131001627 T>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:169186587 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:169186587 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:18003601 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:18003601 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:5735280 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:5735280 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:107700309 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:107700309 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:157771617 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:157771617 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:104337733 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:104337733 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:88420872 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:88420872 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:128025820 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:128025820 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:241569287 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:241569287 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:87379853 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:87379853 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:66725429 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:66725429 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:117866259 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:117866259 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:95432293 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:95432293 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:237300823 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:237300823 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:33063787 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:33063787 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:93428754 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:93428754 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:178543324 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:178543324 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:100085102 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:100085102 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:72338223 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:72338223 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:88106382 A>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:88106382 A>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:82409476 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:82409476 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:95715245 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:95715245 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:16067561 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:16067561 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:58152339 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:58152339 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:109768516 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:109768516 G>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:54377752 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:54377752 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:65987364 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:65987364 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:165829628 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:165829628 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:44045952 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:44045952 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:161127336 A>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:161127336 A>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:145724259 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:145724259 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:133542190 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:133542190 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:24614413 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:24614413 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:44019084 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:44019084 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:35898978 G>A maps to NM_203418.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:35898978 G>A maps to NM_203418.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:8704739 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:8704739 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:56510447 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:56510447 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:45093924 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:45093924 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:237801624 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:237801624 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:51171516 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:51171516 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr7:83032094 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr7:83032094 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:109315584 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:109315584 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:45490820 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:45490820 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:138287575 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:138287575 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:31926914 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr6:31926914 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:106907570 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:106907570 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:44170691 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:44170691 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:45801903 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:45801903 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:33578965 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:33578965 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:27673816 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:27673816 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:61490555 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:61490555 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:126448608 G>T maps to NM_025195.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:126448608 G>T maps to NM_025195.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:117620453 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:117620453 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:75204481 T>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:75204481 T>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:138994419 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:138994419 A>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:103298088 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:103298088 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:30414891 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:30414891 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:113724894 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:113724894 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:76794671 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:76794671 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:159832246 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:159832246 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:68129275 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr14:68129275 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:167046053 T>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr3:167046053 T>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:825469 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:825469 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:244214607 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:244214607 G>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:27805812 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:27805812 A>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:52383447 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:52383447 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:20668465 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:20668465 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:101591909 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:101591909 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:109661793 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:109661793 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:109661798 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:109661798 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:58514713 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:58514713 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:141006084 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:141006084 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:20483114 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:20483114 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:39537480 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:39537480 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:24334068 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:24334068 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:50325832 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:50325832 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:131916432 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:131916432 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:148068786 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:148068786 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:74301970 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:74301970 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:100329900 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:100329900 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:113748529 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:113748529 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:10026384 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:10026384 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:90347443 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:90347443 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:70035164 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:70035164 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:26848971 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:26848971 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:139943780 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:139943780 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:84258821 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:84258821 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:35781138 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:35781138 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:220085369 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:220085369 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:1811739 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:1811739 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:143562549 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:143562549 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:70071410 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:70071410 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:13494469 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:13494469 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:137499602 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:137499602 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:100613164 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:100613164 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:111794876 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:111794876 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:170955625 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:170955625 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:220038063 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:220038063 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:14762971 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:14762971 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:4125452 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:4125452 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:98690245 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:98690245 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:227171592 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:227171592 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:54604169 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:54604169 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:64876836 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:64876836 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:15096261 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:15096261 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:241533900 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:241533900 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:44148765 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:44148765 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:30886542 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:30886542 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:35910450 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:35910450 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:104937551 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:104937551 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:68629786 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:68629786 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:130898002 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:130898002 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158300955 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158300955 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:62006910 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:62006910 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:58571517 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:58571517 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:63547582 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:63547582 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:21974559 A>T maps to NM_058197.4 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:21974559 A>T maps to NM_058197.4 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:49030439 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:49030439 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:418043 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:418043 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:66643753 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:66643753 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:179993992 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:179993992 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:41374667 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:41374667 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:205033989 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:205033989 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:74385597 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:74385597 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:76501224 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:76501224 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:55027025 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:55027025 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:86355337 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:86355337 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:107802268 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:107802268 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:10084180 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:10084180 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:10096467 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:10096467 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:48613228 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:48613228 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:47840019 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:47840019 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:125528293 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:125528293 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:125558607 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:125558607 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:37328988 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:37328988 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:37331521 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:37331521 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:2944824 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:2944824 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:34049140 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:34049140 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113349998 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113349998 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113358305 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113358305 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:114031235 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:114031235 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:47603998 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:47603998 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:166451758 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:166451758 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:39763375 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:39763375 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:66332544 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:66332544 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:48993684 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:48993684 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:57537870 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:57537870 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:43107425 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:43107425 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:112312475 G>T maps to ENST00000513585 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:112312475 G>T maps to ENST00000513585 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:162725423 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:162725423 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:35984499 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:35984499 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:31566359 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:31566359 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:46400076 C>T maps to ENST00000421244 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:46400076 C>T maps to ENST00000421244 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:79933672 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:79933672 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:30639185 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:30639185 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:83525468 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:83525468 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:72308103 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:72308103 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:116573172 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:116573172 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:65779976 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:65779976 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:63977658 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:63977658 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:36324451 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:36324451 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:13642111 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:13642111 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:38458549 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:38458549 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:21307471 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:21307471 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:14883381 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:14883381 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:139945643 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:139945643 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:16455881 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:16455881 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:133622638 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:133622638 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:139158305 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:139158305 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:15820910 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:15820910 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:101540807 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:101540807 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:48713084 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:48713084 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:8165956 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:8165956 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:97349767 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:97349767 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:157650723 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:157650723 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:45603517 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:45603517 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:109284550 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:109284550 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:41552695 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:41552695 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:85862722 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:85862722 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:131234554 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:131234554 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:48564826 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:48564826 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:161324498 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:161324498 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:26582018 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:26582018 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:101011502 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:101011502 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:74865728 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:74865728 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:5827101 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:5827101 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:74055139 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:74055139 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:85779913 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:85779913 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:61958592 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:61958592 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:42629273 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:42629273 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:121726544 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:121726544 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:663351 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:663351 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:2875478 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:2875478 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:56531910 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:56531910 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:57596964 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:57596964 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:13715646 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:13715646 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:52658788 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:52658788 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:18361081 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:18361081 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:43519178 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:43519178 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:222695918 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:222695918 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:222715288 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:222715288 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:31248134 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:31248134 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29691170 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29691170 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29798400 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29798400 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:30149585 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:30149585 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:186395690 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:186395690 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:53573633 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:53573633 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:95036846 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:95036846 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:39776554 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:39776554 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:113786739 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:113786739 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:76735069 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:76735069 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:100965003 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:100965003 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:62504495 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:62504495 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:57842986 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:57842986 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:121551246 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:121551246 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:15199811 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:15199811 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:48152892 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:48152892 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:182395539 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:182395539 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:31282233 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:31282233 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:54818474 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:54818474 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:128250757 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:128250757 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:64953314 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:64953314 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:30814494 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:30814494 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:5022096 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:5022096 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:21926133 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:21926133 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:39278872 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:39278872 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:118960838 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:118960838 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:196274534 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:196274534 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:142638293 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:142638293 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:142659255 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:142659255 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:24582370 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:24582370 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:43493632 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:43493632 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:241656826 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:241656826 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:39994097 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:39994097 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:39994151 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:39994151 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:51380291 G>T maps to NM_001002231.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:51380291 G>T maps to NM_001002231.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:52843690 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:52843690 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:52774789 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:52774789 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:50768899 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:50768899 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:55018974 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:55018974 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:55021834 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:55021834 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:209788494 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:209788494 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:55467812 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:55467812 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:18485687 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:18485687 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:54966525 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:54966525 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:202245329 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:202245329 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:18138697 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:18138697 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:150444674 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:150444674 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:62445435 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:62445435 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:62449492 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:62449492 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:151271105 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:151271105 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:141055258 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:141055258 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:141571401 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:141571401 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:170065918 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:170065918 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:14474230 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:14474230 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:65365286 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:65365286 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:78754591 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:78754591 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:51715151 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:51715151 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:131163289 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:131163289 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:2535736 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:2535736 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29638998 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29638998 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:28436393 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:28436393 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:60741784 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:60741784 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:224831448 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:224831448 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:64891943 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:64891943 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:154293884 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:154293884 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:38283016 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:38283016 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:153043512 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:153043512 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:81102499 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:81102499 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:10316082 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:10316082 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:16674948 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:16674948 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:109644701 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:109644701 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:26270185 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:26270185 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:48596396 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:48596396 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:50865188 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:50865188 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:78147602 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:78147602 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:8381357 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:8381357 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:21191532 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:21191532 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:29576238 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:29576238 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:132635964 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:132635964 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:47535634 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:47535634 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:32463032 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:32463032 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:32471998 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:32471998 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:51206287 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:51206287 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:6605241 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:6605241 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:107866765 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:107866765 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:32319278 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:32319278 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:135282249 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:135282249 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:134026317 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:134026317 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:113433281 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:113433281 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:228402842 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:228402842 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:71064273 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:71064273 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:167625732 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:167625732 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:167675389 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:167675389 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:78443640 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:78443640 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:53602883 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:53602883 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123900307 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123900307 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:125376973 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:125376973 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248185235 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248185235 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248308285 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248308285 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123810292 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123810292 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:52851471 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:52851471 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:26725159 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:26725159 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29583891 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29583891 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:43284833 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:43284833 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:176811629 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:176811629 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:14700283 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:14700283 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:91138017 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:91138017 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:24572134 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:24572134 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:17823760 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:17823760 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:3641684 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:3641684 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:3645874 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:3645874 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:47906319 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:47906319 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:68045030 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:68045030 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:126751209 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:126751209 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:208218404 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:208218404 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:131879025 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:131879025 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:131883441 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:131883441 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:84634173 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:84634173 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:22314226 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:22314226 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:76794228 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:76794228 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:131885445 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:131885445 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:110977583 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:110977583 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:23517955 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:23517955 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:45122523 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr22:45122523 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:227068276 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:227068276 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:43348629 G>C maps to ENST00000449000 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:43348629 G>C maps to ENST00000449000 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:43688813 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:43688813 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:43411019 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:43411019 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:86348590 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:86348590 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:45307783 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:45307783 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:96827132 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:96827132 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8449899 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8449899 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8504468 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8504468 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:55718416 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:55718416 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:158325360 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:158325360 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:220161603 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:220161603 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:15704326 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:15704326 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:8955463 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:8955463 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:79945046 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:79945046 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:103322529 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:103322529 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:15262004 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:15262004 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:74662598 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:74662598 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:101084366 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:101084366 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:73029226 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:73029226 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:31526096 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:31526096 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:24626902 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:24626902 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:55609263 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:55609263 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:48073435 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:48073435 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:43902866 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:43902866 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:62298988 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:62298988 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:159566334 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:159566334 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:38942577 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:38942577 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:174292239 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:174292239 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:71920719 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:71920719 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:25689565 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:25689565 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:29976369 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:29976369 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:71346524 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:71346524 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:108218734 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:108218734 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:9066420 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:9066420 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:61310634 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:61310634 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:52962180 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:52962180 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:82348574 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:82348574 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:1908405 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:1908405 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:27022788 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:27022788 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:122757398 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:122757398 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:119026617 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:119026617 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:140055462 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:140055462 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:18242090 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:18242090 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:47381378 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:47381378 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:75680202 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:75680202 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:24888358 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:24888358 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:26700145 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:26700145 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:48701565 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:48701565 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:333522 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:333522 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:156223236 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:156223236 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:121780445 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:121780445 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:51362326 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:51362326 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:51449155 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:51449155 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:1079467 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:1079467 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:144337346 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:144337346 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:3343341 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:3343341 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:44046812 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:44046812 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:55914086 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:55914086 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158653090 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158653090 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:131339594 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:131339594 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:17373573 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:17373573 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:68471960 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:68471960 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:171544701 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:171544701 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:892323 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:892323 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:202572282 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:202572282 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:85435009 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:85435009 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:33458623 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:33458623 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:100961604 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:100961604 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:27190514 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:27190514 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:50805560 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:50805560 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:2320490 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:2320490 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:71953116 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:71953116 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:32496831 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:32496831 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:66551130 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:66551130 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:72469764 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:72469764 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:19687405 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:19687405 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:103216340 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:103216340 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29709751 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29709751 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:66350136 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:66350136 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:175049197 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:175049197 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:5354590 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:5354590 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:189604441 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:189604441 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:10933748 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:10933748 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:30121597 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:30121597 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:30128164 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:30128164 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:165962700 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:165962700 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:72935107 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:72935107 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:111078376 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chrX:111078376 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:45783988 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:45783988 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:51873148 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:51873148 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:180320032 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:180320032 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:99759097 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:99759097 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:1119233 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:1119233 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179499397 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179499397 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179590389 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179590389 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:37927821 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:37927821 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:83733788 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:83733788 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:118244408 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:118244408 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:59337165 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:59337165 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:70148398 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:70148398 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:73780778 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:73780778 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:215933286 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:215933286 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:179501816 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:179501816 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:5038422 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:5038422 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:8988571 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:8988571 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:82779472 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:82779472 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:51455666 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:51455666 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:17830642 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:17830642 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:6121228 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:6121228 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:110424490 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:110424490 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:120965377 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:120965377 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:168114687 G>A maps to ENST00000420519 E577E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:168114687 G>A maps to ENST00000420519 E577E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:82499254 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:82499254 A>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:21328899 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:21328899 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:100345751 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:100345751 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:27180148 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:27180148 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:68222596 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:68222596 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:68222598 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:68222598 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:57193642 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:57193642 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:58551709 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:58551709 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:58563760 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:58563760 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:111726072 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:111726072 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:69391002 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:69391002 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:197098264 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:197098264 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr10:28970557 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr10:28970557 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:45316499 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:45316499 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:36946782 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:36946782 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:191093238 C>A maps to NM_178335.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:191093238 C>A maps to NM_178335.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:22358220 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:22358220 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr8:121345020 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr8:121345020 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:70856621 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:70856621 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:242680507 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:242680507 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:68087629 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:68087629 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:66013941 C>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:66013941 C>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:40701621 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:40701621 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:54497729 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:54497729 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:78444301 C>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:78444301 C>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:29527450 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:29527450 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:27840096 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:27840096 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:30006823 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:30006823 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:153055160 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:153055160 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:78790370 C>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:78790370 C>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:37151073 G>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:37151073 G>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:24750658 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:24750658 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr14:23862749 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr14:23862749 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:54312782 A>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:54312782 A>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:242066932 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:242066932 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:103042909 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:103042909 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:54626961 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:54626961 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:46873305 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:46873305 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:8317971 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:8317971 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:220344181 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:220344181 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:125791621 T>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:125791621 T>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:34287491 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:34287491 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:35864948 A>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:35864948 A>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:39871151 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:39871151 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:68331710 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:68331710 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:170715645 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:170715645 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:18850989 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:18850989 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:158637882 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:158637882 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:16773013 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:16773013 A>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:89177043 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chrX:89177043 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:54219235 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:54219235 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:66639556 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:66639556 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:84231651 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:84231651 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr21:10907110 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr21:10907110 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:50875387 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:50875387 A>G did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:42600255 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:42600255 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:78578501 T>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:78578501 T>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr12:72013256 G>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr12:72013256 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr9:19424529 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr9:19424529 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:43833625 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:43833625 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:77951939 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:77951939 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:43340416 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:43340416 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:25238281 A>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:25238281 A>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:31669839 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:31669839 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:80253407 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:80253407 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:32491706 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:32491706 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:85944357 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:85944357 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:122775839 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:122775839 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:1894853 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:1894853 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:35237962 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:35237962 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:23955357 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:23955357 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:2753491 A>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:2753491 A>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:86245698 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:86245698 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:54872834 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:54872834 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:26528938 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:26528938 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:208605367 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:208605367 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:3783698 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:3783698 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:175992421 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:175992421 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:147964315 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:147964315 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:89662089 A>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:89662089 A>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:27012047 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:27012047 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:66021845 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:66021845 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:153909236 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:153909236 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:75364925 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:75364925 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chrX:32328140 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chrX:32328140 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:41521783 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:41521783 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:134514402 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:134514402 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:97361645 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:97361645 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chrX:49113187 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chrX:49113187 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:180630549 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:180630549 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:220102884 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:220102884 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:1718767 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:1718767 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:90125038 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:90125038 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:35512775 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:35512775 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:27856236 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:27856236 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:52657544 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:52657544 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:13542207 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:13542207 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:42188977 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:42188977 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:42189015 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:42189015 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:81335568 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:81335568 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:210761217 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:210761217 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:27238156 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:27238156 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:70989185 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:70989185 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr13:21181798 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr13:21181798 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:155094562 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:155094562 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:44580977 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:44580977 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:169812503 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:169812503 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:142659397 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:142659397 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:22697148 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:22697148 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:160286029 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:160286029 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:60910195 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:60910195 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:101115175 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:101115175 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:151388762 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:151388762 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:220805673 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:220805673 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:47315145 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:47315145 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:24683409 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:24683409 A>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:141785658 C>A maps to ENST00000475668 Y2179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:141785658 C>A maps to ENST00000475668 Y2179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:110006723 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:110006723 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:29638805 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:29638805 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:132649114 A>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:132649114 A>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:31537160 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:31537160 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:175811463 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:175811463 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:175813813 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:175813813 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:4745280 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:4745280 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:55405808 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:55405808 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:23236653 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:23236653 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:72296590 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:72296590 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:149311639 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:149311639 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:28817595 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:28817595 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:27239437 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:27239437 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:67584450 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:67584450 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:18865974 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:18865974 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:108150994 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr7:108150994 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:1091772 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:1091772 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:60756654 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:60756654 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:57372257 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:57372257 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:48831586 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:48831586 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:43702475 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:43702475 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:31479804 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:31479804 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr9:125836553 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr9:125836553 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:2000750 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:2000750 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:38948367 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:38948367 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:95085494 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr14:95085494 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:7214658 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:7214658 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:43310931 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:43310931 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:172725073 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:172725073 T>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:601211 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:601211 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205535 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205535 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205541 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205541 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205664 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205664 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205983 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34205983 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34206122 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34206122 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207241 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207241 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207278 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207278 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207283 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207283 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207379 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207379 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:85115981 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:85115981 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:44268624 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:44268624 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:44988379 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:44988379 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:234536883 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:234536883 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:114823225 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:114823225 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:122063983 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:122063983 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:57069778 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:57069778 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:175049278 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr1:175049278 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:144696687 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:144696687 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:41865674 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:41865674 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr9:35366900 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr9:35366900 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:48272936 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr12:48272936 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:53889527 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr15:53889527 T>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167855883 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167855883 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167882277 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167882277 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:101378533 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:101378533 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:149778066 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:149778066 G>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:56896633 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:56896633 G>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:16465784 G>C did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:16465784 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:7629966 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:7629966 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:107589501 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:107589501 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:67111488 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:67111488 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:67024004 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:67024004 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:87035566 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:87035566 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:20738226 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:20738226 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:17416025 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:17416025 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:17434920 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:17434920 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:148625995 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:148625995 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:44069546 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:44069546 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:20635555 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:20635555 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100244136 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100244136 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:127843971 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:127843971 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:207474735 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:207474735 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:33576136 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:33576136 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:18504970 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:18504970 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:18718408 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:18718408 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:70922832 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:70922832 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:73047866 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:73047866 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:7811567 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:7811567 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:147967550 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:147967550 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:148059310 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:148059310 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:236617780 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:236617780 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:47681983 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:47681983 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:19813324 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:19813324 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:86284144 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:86284144 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:91725995 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:91725995 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:134215685 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:134215685 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:19612376 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:19612376 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:58247298 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:58247298 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:125854371 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:125854371 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:43920660 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:43920660 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:29606780 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:29606780 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:233272499 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:233272499 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:41557873 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:41557873 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:41573152 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:41573152 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:61932653 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:61932653 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:26555919 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:26555919 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101381202 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101381202 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101413968 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101413968 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:22283566 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:22283566 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:69304501 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:69304501 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:80828640 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:80828640 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:80992828 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:80992828 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:36572085 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:36572085 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:36616054 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:36616054 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:29386538 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:29386538 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:7818600 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:7818600 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:47648707 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:47648707 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:69002620 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:69002620 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:11200337 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:11200337 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:11352822 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:11352822 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:57870481 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:57870481 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135760185 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135760185 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:58772653 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:58772653 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:235383559 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:235383559 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:66534451 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:66534451 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:31476281 A>G maps to NM_024742.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:31476281 A>G maps to NM_024742.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:69500010 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:69500010 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77021378 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77021378 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:14609577 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:14609577 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:96755864 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:96755864 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:193032637 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:193032637 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:36041669 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:36041669 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:36054496 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:36054496 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:73036052 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:73036052 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67476967 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67476967 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:50190201 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:50190201 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:74754000 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:74754000 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:41744608 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:41744608 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:828483 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:828483 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:11039276 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:11039276 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:1388883 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:1388883 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156622017 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156622017 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:51689809 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:51689809 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:169338844 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:169338844 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:92457918 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:92457918 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:124097608 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:124097608 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26463789 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26463789 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:105920733 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:105920733 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:76260926 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:76260926 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:21680172 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:21680172 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:111973158 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:111973158 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:45712151 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:45712151 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156386677 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156386677 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:35517645 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:35517645 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:8212796 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:8212796 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:6686929 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:6686929 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:118866928 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:118866928 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:56655657 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:56655657 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71202001 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71202001 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:165712898 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:165712898 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:40909774 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:40909774 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:31746991 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:31746991 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:120704475 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:120704475 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:108524399 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:108524399 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:10557712 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:10557712 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:135762990 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:135762990 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:86392879 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:86392879 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:24492065 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:24492065 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:181691073 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:181691073 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:81641405 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:81641405 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:71743591 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:71743591 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:12595109 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:12595109 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64977409 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64977409 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:37899159 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:37899159 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:104937537 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:104937537 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:96076322 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:96076322 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:23682514 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:23682514 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:78055327 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:78055327 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:45115295 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:45115295 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:74528289 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:74528289 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:837419 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:837419 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118209948 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118209948 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:103425912 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:103425912 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:193121442 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:193121442 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:174232426 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:174232426 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:21884288 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:21884288 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:21975499 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:21975499 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:63530200 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:63530200 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:40132364 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:40132364 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:58145274 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:58145274 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:50845234 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:50845234 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:80719048 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:80719048 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:122734823 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:122734823 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:56890588 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:56890588 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:49044713 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:49044713 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:196716451 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:196716451 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:109919661 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:109919661 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:136623090 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:136623090 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:34354913 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:34354913 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:10133118 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:10133118 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:9809459 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:9809459 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:140281581 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:140281581 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:88249383 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:88249383 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87673938 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87673938 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:21534380 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:21534380 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:135129641 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:135129641 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:17235808 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:17235808 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:74351764 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:74351764 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:147092896 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:147092896 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:103428151 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:103428151 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70646641 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70646641 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70672648 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70672648 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:94056486 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:94056486 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:56141529 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:56141529 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:139767335 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:139767335 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:139815023 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:139815023 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:109783707 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:109783707 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:189927655 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:189927655 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:10090435 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:10090435 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:238269724 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:238269724 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70961819 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70961819 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:139077136 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:139077136 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130289968 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130289968 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130295013 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130295013 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:128987846 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:128987846 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:128987862 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:128987862 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:148601395 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:148601395 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:57155138 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:57155138 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:68522273 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:68522273 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:50208457 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:50208457 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:197398517 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:197398517 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:91168875 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:91168875 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97605330 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97605330 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97608236 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97608236 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:3216591 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:3216591 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:34123756 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:34123756 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:113812516 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:113812516 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70802106 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70802106 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71110626 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71110626 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:99800107 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:99800107 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:70261827 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:70261827 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:16870769 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:16870769 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:225346807 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:225346807 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:101821688 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:101821688 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:107275090 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:107275090 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:70326314 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:70326314 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104426969 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104426969 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:168013997 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:168013997 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:74597688 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:74597688 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:110544904 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:110544904 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:108562508 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:108562508 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:118579412 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:118579412 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:47849973 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:47849973 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:74104593 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:74104593 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:29896312 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:29896312 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:29956329 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:29956329 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:6475668 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:6475668 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:32289841 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:32289841 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:117165375 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:117165375 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:19118829 C>T maps to ENST00000383058 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:19118829 C>T maps to ENST00000383058 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:14378341 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:14378341 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:137148182 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:137148182 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:50146597 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:50146597 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:37619998 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:37619998 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7660235 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7660235 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7679507 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7679507 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:38830021 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:38830021 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:183620957 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:183620957 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:25472445 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:25472445 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:129216870 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:129216870 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:169477106 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:169477106 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:429659 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:429659 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:37620567 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:37620567 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:162902170 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:162902170 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:41560955 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:41560955 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:57665746 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:57665746 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:66768031 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:66768031 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67228930 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67228930 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:77423599 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:77423599 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:83433050 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:83433050 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:148457191 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:148457191 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:74229018 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:74229018 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:38406127 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:38406127 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:24082538 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:24082538 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:28426163 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:28426163 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7476124 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7476124 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:184049679 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:184049679 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:6928342 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:6928342 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:66213738 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:66213738 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:66213744 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:66213744 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97184996 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97184996 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97311617 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:97311617 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:22923972 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:22923972 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:23219578 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:23219578 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:1599148 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:1599148 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103483795 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103483795 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:75246682 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:75246682 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:216741515 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:216741515 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:56525879 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:56525879 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:56532701 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:56532701 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:100598997 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:100598997 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:133749296 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:133749296 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:73052880 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:73052880 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:148512460 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:148512460 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:138613140 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:138613140 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:57419872 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:57419872 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:14765938 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:14765938 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:54184101 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:54184101 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:220045541 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:220045541 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:175526170 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:175526170 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:74411033 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:74411033 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:74095432 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:74095432 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:74096685 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:74096685 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:187627595 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:187627595 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:68194259 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:68194259 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:89118102 G>C maps to ENST00000330762 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:89118102 G>C maps to ENST00000330762 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:129091373 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:129091373 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:95504851 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:95504851 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87517342 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87517342 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33876449 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33876449 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:8761845 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:8761845 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:48787276 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:48787276 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:127611614 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:127611614 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:107684000 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:107684000 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:135272754 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:135272754 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52957176 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52957176 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:159274014 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:159274014 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:124985585 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:124985585 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:125081774 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:125081774 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:95797929 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:95797929 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135279218 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135279218 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135290606 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135290606 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:72712104 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:72712104 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240555699 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240555699 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:171079893 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:171079893 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:147090234 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:147090234 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:49204670 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:49204670 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:22563799 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:22563799 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:116734 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:116734 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:71037318 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:71037318 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118849642 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118849642 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:79199930 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:79199930 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:131264786 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:131264786 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29541779 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29541779 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29542554 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29542554 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:161300030 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:161300030 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:161324017 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:161324017 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:161115926 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:161115926 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:46099398 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:46099398 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:89908037 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:89908037 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:4854523 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:4854523 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:16261185 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:16261185 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:9822900 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:9822900 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:163003724 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:163003724 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:163003757 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:163003757 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:55309738 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:55309738 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52999204 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52999204 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:75160018 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:75160018 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33451080 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33451080 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:61995702 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:61995702 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:46184981 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:46184981 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:33059850 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:33059850 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:151208694 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:151208694 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:14550573 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:14550573 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:58605977 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:58605977 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:19745300 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:19745300 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:57485472 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:57485472 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:54569522 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:54569522 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:155741066 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:155741066 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:46095228 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:46095228 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:13825685 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:13825685 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:142711494 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:142711494 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123469824 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123469824 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:113638695 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:113638695 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:126172988 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:126172988 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:122640886 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:122640886 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:42156291 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:42156291 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:18633404 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:18633404 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:18869044 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:18869044 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:45475599 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:45475599 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124794530 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124794530 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:65409516 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:65409516 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:28441570 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:28441570 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:81339448 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:81339448 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26217621 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26217621 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26033860 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26033860 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:71075621 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:71075621 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:71142151 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:71142151 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:186099267 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:186099267 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:138722048 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:138722048 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:8530149 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:8530149 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:177016885 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:177016885 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:115216465 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:115216465 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:55776855 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:55776855 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:107882458 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:107882458 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:185541030 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:185541030 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:206972372 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:206972372 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:39760494 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:39760494 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:111034907 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:111034907 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:30012021 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:30012021 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:30012181 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:30012181 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:153736715 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:153736715 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:75969933 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:75969933 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:182344793 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:182344793 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:182396569 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:182396569 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:15649533 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:15649533 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:31409058 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:31409058 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:7697523 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:7697523 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:78618354 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:78618354 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:49245224 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:49245224 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:6145238 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:6145238 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:21918521 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:21918521 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:78674827 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:78674827 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:70794138 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:70794138 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:113699508 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:113699508 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:44133827 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:44133827 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:5047744 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:5047744 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55980505 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55980505 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:142658286 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:142658286 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:26942338 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:26942338 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:35628257 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:35628257 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:13228954 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:13228954 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:36888959 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:36888959 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:8926243 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:8926243 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:17777457 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:17777457 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:16493398 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:16493398 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:21039939 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:21039939 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72348944 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72348944 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:91489015 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:91489015 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:10464033 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:10464033 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:241750107 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:241750107 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:123097812 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:123097812 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:123098361 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:123098361 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:53040843 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:53040843 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:117992963 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:117992963 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:112462131 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:112462131 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:136561715 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:136561715 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:36248606 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:36248606 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:135288489 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:135288489 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:104309699 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:104309699 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:55142759 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:55142759 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:75111698 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:75111698 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:148346593 G>A maps to ENST00000369202 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:148346593 G>A maps to ENST00000369202 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:48290699 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:48290699 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:161005971 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:161005971 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:82432321 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:82432321 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:82452675 A>T maps to ENST00000370717 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:82452675 A>T maps to ENST00000370717 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:82452991 G>T maps to ENST00000370715 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:82452991 G>T maps to ENST00000370715 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62845601 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62845601 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62933995 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62933995 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:141115806 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:141115806 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:170012962 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:170012962 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:99825119 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:99825119 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:1905562 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:1905562 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:160765909 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:160765909 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:99908989 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:99908989 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:166985561 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:166985561 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:151870312 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:151870312 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:102456514 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:102456514 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:22143122 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:22143122 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:165111489 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:165111489 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:63656438 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:63656438 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:20110007 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:20110007 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:70944903 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:70944903 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:70946037 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:70946037 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:151073657 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:151073657 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:131903927 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:131903927 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:42840850 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:42840850 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:21463280 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:21463280 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:141726896 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:141726896 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:141756617 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:141756617 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100843631 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100843631 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:94203629 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:94203629 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:60269414 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:60269414 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:120785153 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:120785153 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:30658233 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:30658233 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237016234 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237016234 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:9018067 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:9018067 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:9038470 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:9038470 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:195475696 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:195475696 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10398480 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10398480 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10428483 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10428483 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10435250 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10435250 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10537273 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10537273 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10363240 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10363240 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10315660 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10315660 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:211163124 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:211163124 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:111358180 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:111358180 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30409593 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30409593 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:46746758 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:46746758 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:2675454 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:2675454 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:109475687 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:109475687 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:26157128 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:26157128 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:8601353 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:8601353 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:45014657 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:45014657 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:26462570 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:26462570 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:171264476 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:171264476 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:76542704 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:76542704 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:95132880 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:95132880 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62831116 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62831116 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:89885664 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:89885664 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64820930 C>T maps to ENST00000340252 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64820930 C>T maps to ENST00000340252 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:101833785 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:101833785 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:19905764 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:19905764 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20119100 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20119100 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:16892786 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:16892786 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:124922573 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:124922573 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:152417258 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:152417258 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:152544926 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:152544926 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:75580003 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:75580003 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20959506 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20959506 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:182542405 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:182542405 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:30057101 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:30057101 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:33332520 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:33332520 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:104519782 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:104519782 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:77732877 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:77732877 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:236195667 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:236195667 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:52534917 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:52534917 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:173525372 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:173525372 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:173525444 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:173525444 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:5810836 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:5810836 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:3614851 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:3614851 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:56467477 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:56467477 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:56477779 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:56477779 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:56477781 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:56477781 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:140327639 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:140327639 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:132418734 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:132418734 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:200116597 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:200116597 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:115357722 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:115357722 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:84118651 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:84118651 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:50850442 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:50850442 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64427722 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64427722 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:79176096 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:79176096 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:18745414 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:18745414 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:107963808 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:107963808 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:101091630 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:101091630 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247979039 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247979039 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:143657038 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:143657038 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124413575 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124413575 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:88331734 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:88331734 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:161220163 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:161220163 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72923429 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72923429 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72938165 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72938165 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:40034455 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:40034455 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:9524993 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:9524993 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:112687383 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:112687383 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:77960843 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:77960843 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:162989944 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:162989944 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:226580054 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:226580054 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:728711 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:728711 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:56140311 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:56140311 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:117099084 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:117099084 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:165756860 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:165756860 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:31918556 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:31918556 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:66723039 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:66723039 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:66838394 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:66838394 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:157731920 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:157731920 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55125097 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55125097 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30533721 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30533721 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:31983858 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:31983858 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4849327 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4849327 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:46098391 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:46098391 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118495566 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118495566 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:77567232 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:77567232 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:21188757 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:21188757 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:59821946 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:59821946 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:1444789 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:1444789 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:110412647 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:110412647 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:51920328 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:51920328 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:119337150 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:119337150 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:20469902 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:20469902 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:242271245 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:242271245 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:132109715 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:132109715 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:151107478 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:151107478 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:150123303 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:150123303 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:161152033 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:161152033 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:131872071 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:131872071 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:8906832 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:8906832 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:28186862 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:28186862 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:108150871 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:108150871 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:52130542 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:52130542 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:16279359 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:16279359 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:167341086 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:167341086 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:18768098 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:18768098 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:81732893 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:81732893 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:27835727 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:27835727 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:42792874 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:42792874 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:4960771 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:4960771 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:27607029 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:27607029 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:150538009 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:150538009 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145972653 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145972653 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:146086563 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:146086563 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:135768222 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:135768222 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:63888613 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:63888613 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94703802 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94703802 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94731172 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94731172 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:129785509 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:129785509 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:70978416 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:70978416 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:43246292 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:43246292 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:68939591 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:68939591 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:24135065 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:24135065 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:169952989 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:169952989 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:54011287 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:54011287 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:23397455 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:23397455 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:150310578 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:150310578 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:150321806 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:150321806 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:4056898 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:4056898 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:1559517 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:1559517 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:1564751 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:1564751 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:170689118 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:170689118 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:119229563 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:119229563 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:119237554 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:119237554 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:113951607 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:113951607 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43233589 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43233589 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43527564 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43527564 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:109968973 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:109968973 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:35778272 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:35778272 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:65346485 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:65346485 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:11579698 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:11579698 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:88970867 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:88970867 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:70949640 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:70949640 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:70949986 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:70949986 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:8331773 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:8331773 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:8143586 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:8143586 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:15652343 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:15652343 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:20491353 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:20491353 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:119545238 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:119545238 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:49138141 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:49138141 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:180166390 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:180166390 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:13370331 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:13370331 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:69504353 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:69504353 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:68888880 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:68888880 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:4839129 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:4839129 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:22184599 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:22184599 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:86676246 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:86676246 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:114784222 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:114784222 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:18471026 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:18471026 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:73569703 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:73569703 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:103128620 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:103128620 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:73658541 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:73658541 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:79349906 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:79349906 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:79384318 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:79384318 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:103194050 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:103194050 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:103236887 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:103236887 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:103290887 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:103290887 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:1825946 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:1825946 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:117252431 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:117252431 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:73002749 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:73002749 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:241083295 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:241083295 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104831623 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104831623 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:40500651 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:40500651 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:49737834 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:49737834 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:11484050 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:11484050 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:35436136 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:35436136 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:17617166 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:17617166 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:16823920 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:16823920 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:92998336 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:92998336 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:38993388 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:38993388 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237801598 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237801598 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237919539 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237919539 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237972196 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237972196 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:33926712 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:33926712 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:5654556 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:5654556 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:134988090 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:134988090 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:51176096 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:51176096 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:62021053 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:62021053 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:23203592 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:23203592 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:97614557 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:97614557 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:169702804 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:169702804 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:83606524 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:83606524 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:84694729 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:84694729 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:83029607 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:83029607 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:9190651 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:9190651 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:55914084 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:55914084 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:2949009 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:2949009 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:173876435 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:173876435 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:120919214 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:120919214 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:52895758 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:52895758 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:145157928 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:145157928 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77692083 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77692083 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52031088 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52031088 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52033241 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52033241 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:1630064 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:1630064 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:164705046 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:164705046 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:48490380 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:48490380 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:44665330 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:44665330 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:121641882 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:121641882 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:22387292 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:22387292 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:100795394 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:100795394 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107350695 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107350695 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107352928 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107352928 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:92401486 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:92401486 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:50521114 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:50521114 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:76107318 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:76107318 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:72338392 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:72338392 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101603666 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101603666 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1232285 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1232285 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:45817563 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:45817563 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:173470158 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:173470158 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:103124754 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:103124754 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135076886 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:135076886 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:168201448 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:168201448 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:2088461 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:2088461 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:47721881 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:47721881 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:55831070 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:55831070 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156244368 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156244368 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156244566 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156244566 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:128849254 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:128849254 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:21755550 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:21755550 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:88408079 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:88408079 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:90647672 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:90647672 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:51449064 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:51449064 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:51571097 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:51571097 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:138586173 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:138586173 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:108431236 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:108431236 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:231065714 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:231065714 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:231267731 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:231267731 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:118530449 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:118530449 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:118535300 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:118535300 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:88411270 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:88411270 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:35700933 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:35700933 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:228973498 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:228973498 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:89922514 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:89922514 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4390991 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4390991 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:153066231 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:153066231 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:158584191 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:158584191 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:158589209 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:158589209 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:66476573 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:66476573 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:45619951 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:45619951 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:36014671 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:36014671 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149489632 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149489632 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149494477 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149494477 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:53045794 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:53045794 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:98512692 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:98512692 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:100231284 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:100231284 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:52555802 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:52555802 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:74473107 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:74473107 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:125898292 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:125898292 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70596416 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70596416 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:29756822 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:29756822 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:46331046 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:46331046 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:152454386 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:152454386 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:33560368 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:33560368 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:77388806 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:77388806 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34493269 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34493269 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34797365 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34797365 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:45141245 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:45141245 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:59477533 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:59477533 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62698260 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62698260 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145858033 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145858033 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:52896443 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:52896443 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:156829999 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:156829999 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:156838701 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:156838701 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:49860456 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:49860456 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:133473543 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:133473543 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:133487022 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:133487022 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:133487078 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:133487078 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:2411685 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:2411685 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:133881925 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:133881925 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:43798776 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:43798776 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:138414562 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:138414562 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166916356 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166916356 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166946697 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166946697 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:63044381 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:63044381 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:102190127 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:102190127 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30743011 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30743011 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:60695345 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:60695345 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:108522819 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:108522819 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:69111238 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:69111238 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:68995517 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:68995517 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:19755918 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:19755918 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:173010503 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:173010503 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:31544649 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:31544649 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:1860814 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:1860814 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:1957394 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:1957394 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175048461 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175048461 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:217724357 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:217724357 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12825811 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12825811 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175331735 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175331735 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:72355293 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:72355293 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103295795 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103295795 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:20066853 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:20066853 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:10942856 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:10942856 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118529777 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118529777 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:54978735 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:54978735 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6487010 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6487010 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:30115164 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:30115164 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:189026097 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:189026097 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:14487459 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:14487459 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:230654583 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:230654583 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:72946446 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:72946446 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:72951077 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:72951077 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:72964794 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:72964794 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:98574466 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:98574466 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:65721243 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:65721243 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:51873135 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:51873135 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:82267186 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:82267186 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:44941314 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:44941314 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:39149411 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:39149411 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:166755186 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:166755186 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:32858899 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:32858899 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:147824672 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:147824672 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:89310241 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:89310241 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:9839506 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:9839506 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179459374 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179459374 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179495492 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179495492 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179517753 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179517753 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179526458 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179526458 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179659380 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179659380 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:22842197 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:22842197 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:132390743 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:132390743 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:43833515 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:43833515 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:74743667 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:74743667 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156012437 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156012437 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:18610240 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:18610240 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:96489553 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:96489553 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:234663728 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:234663728 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70152663 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70152663 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:17738479 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:17738479 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:215808089 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:215808089 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:22078141 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:22078141 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:31760737 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:31760737 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:108315511 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:108315511 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156269022 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:156269022 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:62223232 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:62223232 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:184586831 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:184586831 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:97319405 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:97319405 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:61050435 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:61050435 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:119628303 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:119628303 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:170059368 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:170059368 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:37379353 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:37379353 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:228210322 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:228210322 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:108620677 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:108620677 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:69922199 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:69922199 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:31558964 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:31558964 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:168106953 C>T maps to NM_152381.5 Q3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:168106953 C>T maps to NM_152381.5 Q3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:128887106 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:128887106 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:180832784 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:180832784 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:216983578 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:216983578 A>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:67731847 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:67731847 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:135743310 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:135743310 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:101383712 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:101383712 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:111624846 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chrX:111624846 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12273957 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12273957 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123596629 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123596629 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:32953381 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:32953381 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:37155482 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:37155482 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247486581 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247486581 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:71625960 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:71625960 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247202107 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247202107 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12088821 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12088821 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:88956800 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:88956800 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:21216718 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:21216718 A>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr20:61914089 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr20:61914089 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr16:24931300 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr16:24931300 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr21:35275765 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr21:35275765 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:123177475 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:123177475 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr18:13113743 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr18:13113743 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:42808229 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:42808229 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:95598833 A>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:95598833 A>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:69712170 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:69712170 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr2:71753487 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr2:71753487 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:99897995 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:99897995 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:26792929 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:26792929 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr7:151817827 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr7:151817827 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:77770861 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:77770861 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:23844698 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:23844698 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:102235754 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:102235754 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:100070196 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:100070196 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:69549129 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:69549129 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:153136431 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:153136431 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:39918266 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:39918266 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:65568194 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:65568194 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr16:3294398 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr16:3294398 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:29635518 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:29635518 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:11781890 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:11781890 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:77644855 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:77644855 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr2:15693631 A>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr2:15693631 A>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:28235619 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:28235619 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:43536897 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:43536897 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:31983819 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:31983819 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr2:87096021 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr2:87096021 T>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr7:156468319 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr7:156468319 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:128350744 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:128350744 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:80406172 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:80406172 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:41382536 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:41382536 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:111870257 C>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:111870257 C>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr12:20885797 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr12:20885797 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:7324081 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:7324081 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr4:27024673 A>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr4:27024673 A>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:70602338 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chrX:70602338 T>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr4:26640460 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr4:26640460 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:170881380 A>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:170881380 A>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr11:86782701 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr11:86782701 C>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr19:59059581 A>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr19:59059581 A>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr4:189067840 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr4:189067840 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:77502690 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:77502690 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr11:113233251 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr11:113233251 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:25584471 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:25584471 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr8:146112217 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr8:146112217 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:229661916 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:229661916 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:20685482 C>A maps to NM_001163941.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:20685482 C>A maps to NM_001163941.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:16272551 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:16272551 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:89034795 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:89034795 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:132363795 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:132363795 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:80643485 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:80643485 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:8407535 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:8407535 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:185678693 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:185678693 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:20559638 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:20559638 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:43833653 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:43833653 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:100182111 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:100182111 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:150814308 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:150814308 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr21:45400792 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr21:45400792 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:32877967 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:32877967 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:29940383 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:29940383 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:203831606 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:203831606 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:139884597 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:139884597 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:69382300 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:69382300 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:37486073 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:37486073 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:99223144 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:99223144 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:115335992 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:115335992 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:36271638 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:36271638 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:101090425 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:101090425 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:96796067 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:96796067 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:138914274 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:138914274 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:70048966 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:70048966 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:45250563 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:45250563 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:22069309 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:22069309 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:26450235 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:26450235 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:111425441 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:111425441 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:105385644 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:105385644 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:45723070 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:45723070 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:179354543 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:179354543 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:57185665 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:57185665 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:226187054 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:226187054 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:31814863 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:31814863 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:219219143 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:219219143 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:6713375 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:6713375 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:98633810 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:98633810 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:47822945 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:47822945 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:34654527 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:34654527 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:42994879 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:42994879 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:88154184 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:88154184 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:121427048 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:121427048 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:24445546 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:24445546 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:140962970 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:140962970 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:149636275 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:149636275 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:44144289 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:44144289 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:92887605 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:92887605 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:191100669 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:191100669 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:32854467 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:32854467 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:58564275 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:58564275 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:31302201 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:31302201 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:89760647 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:89760647 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:182403758 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:182403758 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:132470355 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:132470355 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:146756887 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:146756887 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:23767250 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:23767250 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:42563854 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:42563854 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:143044080 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:143044080 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:14693908 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:14693908 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:150906870 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:150906870 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:87673969 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:87673969 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:74383777 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:74383777 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:7843310 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:7843310 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:86241248 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:86241248 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:46114329 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:46114329 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:24543220 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:24543220 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:207644470 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:207644470 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:21279134 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:21279134 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:34238129 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:34238129 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:10790095 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:10790095 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:16871066 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:16871066 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:43172630 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:43172630 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:139040410 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:139040410 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:156721743 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:156721743 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:74631498 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:74631498 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:41595021 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:41595021 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:15990077 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:15990077 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:187120253 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:187120253 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:86068108 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:86068108 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:121930550 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:121930550 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:176884407 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:176884407 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:30863108 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:30863108 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:15742604 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:15742604 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:140273859 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:140273859 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:115079947 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:115079947 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:182811841 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:182811841 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:468733 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:468733 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:21913128 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:21913128 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:21062955 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:21062955 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:13885093 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:13885093 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:196726418 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:196726418 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:225684101 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:225684101 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:111379141 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:111379141 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:62940873 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:62940873 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:62953175 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:62953175 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:172525486 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:172525486 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:93244826 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:93244826 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:36354250 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:36354250 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:159601865 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:159601865 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:29664519 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:29664519 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:94695454 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:94695454 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:44193352 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:44193352 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:139209927 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:139209927 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:101519957 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:101519957 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:161560920 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:161560920 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:161561520 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:161561520 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:137804498 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:137804498 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:34205326 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:34205326 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:142504896 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:142504896 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:79340085 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:79340085 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:32731404 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:32731404 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:32759379 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:32759379 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:26569921 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:26569921 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:151805009 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:151805009 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:154310951 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:154310951 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:85781215 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:85781215 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:145139235 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:145139235 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:156568896 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:156568896 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:47059696 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:47059696 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:105774479 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:105774479 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:86493753 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:86493753 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:18380311 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:18380311 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:1043053 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:1043053 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:19035609 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:19035609 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:28361720 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:28361720 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:76459717 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:76459717 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:21986718 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:21986718 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:37533834 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:37533834 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:1475072 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:1475072 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:15730040 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:15730040 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:33648292 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:33648292 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:30829461 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:30829461 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:6843573 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:6843573 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1346744 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1346744 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:119205482 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:119205482 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:153706570 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:153706570 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:112438874 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:112438874 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:130914412 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:130914412 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:75606584 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:75606584 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:90988178 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:90988178 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr21:15579127 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr21:15579127 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:76379463 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:76379463 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:62933852 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:62933852 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:70489096 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:70489096 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:40653202 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:40653202 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:151900848 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:151900848 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:140969708 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:140969708 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:10397494 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:10397494 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:94983272 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:94983272 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:168845573 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:168845573 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:42866751 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:42866751 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:66775016 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:66775016 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:8800680 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:8800680 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:74774474 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:74774474 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:42049866 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:42049866 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:38328973 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:38328973 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:11884314 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:11884314 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:95783792 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:95783792 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:831142 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:831142 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:121457667 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:121457667 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:98718982 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:98718982 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:55470453 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:55470453 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:149761154 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:149761154 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:9018261 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:9018261 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:102053372 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:102053372 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:47360788 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:47360788 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:15810936 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:15810936 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10204767 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10204767 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:108102325 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:108102325 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:108127305 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:108127305 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:52521133 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:52521133 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:17322658 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:17322658 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:48634329 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:48634329 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:164049971 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:164049971 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:204037331 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:204037331 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:21098859 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:21098859 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:63769575 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:63769575 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:101086848 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:101086848 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:101089901 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:101089901 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:43174707 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:43174707 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:150703922 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:150703922 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:100098830 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:100098830 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:32600292 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:32600292 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:80163885 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:80163885 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:69135549 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:69135549 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:56868623 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:56868623 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:6897836 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:6897836 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248512050 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248512050 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248487929 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248487929 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248084245 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248084245 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:48346344 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:48346344 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:146080514 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:146080514 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:169837280 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:169837280 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:176740037 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:176740037 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:205978322 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:205978322 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:161807727 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:161807727 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:12530275 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:12530275 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:150770095 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:150770095 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:52637790 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:52637790 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:105194133 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:105194133 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:165956897 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:165956897 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:71438867 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:71438867 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:142836737 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:142836737 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:9453405 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:9453405 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:131951828 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:131951828 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:131960495 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:131960495 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:118228670 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:118228670 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:49651313 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:49651313 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:212534192 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:212534192 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:69026601 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:69026601 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:15993843 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:15993843 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:18430337 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:18430337 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:151239876 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:151239876 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:62259224 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:62259224 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:105142791 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:105142791 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:21602742 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:21602742 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:28050349 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:28050349 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:40438442 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:40438442 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:17736442 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:17736442 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:21998132 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:21998132 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:240975484 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:240975484 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:87113547 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:87113547 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:179405137 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:179405137 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:39322857 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:39322857 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:9917628 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:9917628 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:166929793 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:166929793 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:167089785 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:167089785 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:50053097 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:50053097 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:102249431 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:102249431 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:9226924 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:9226924 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:9337942 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:9337942 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:185347652 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:185347652 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:37949322 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:37949322 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:19165155 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:19165155 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:10738342 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:10738342 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:101588817 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:101588817 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:112343558 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr10:112343558 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:98639626 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:98639626 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:69303945 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:69303945 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:82720654 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:82720654 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:7668758 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:7668758 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:45345183 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:45345183 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:157073588 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:157073588 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:34207423 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:34207423 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:142605118 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:142605118 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:158584868 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:158584868 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:158632749 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:158632749 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:66466353 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:66466353 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:104106244 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:104106244 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:123197113 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:123197113 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:23702577 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:23702577 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:147581743 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:147581743 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:70515707 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:70515707 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:223402410 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:223402410 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:37935963 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:37935963 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:34171065 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:34171065 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:100548083 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:100548083 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:33456225 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:33456225 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:100239147 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:100239147 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:43514222 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:43514222 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:184090234 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:184090234 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:77705861 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:77705861 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:94808002 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:94808002 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:144380112 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:144380112 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:186324471 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:186324471 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:202252387 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:202252387 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:57952107 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:57952107 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:122665629 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:122665629 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:59339147 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:59339147 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:20911075 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:20911075 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:129042030 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:129042030 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:133311788 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:133311788 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:77919629 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:77919629 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:64147477 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:64147477 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:116091331 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:116091331 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:190316466 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:190316466 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1956799 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1956799 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:31637537 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:31637537 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:128881795 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:128881795 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:216982415 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:216982415 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:32903845 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:32903845 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:167077581 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:167077581 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:57440691 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:57440691 T>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:44946862 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:44946862 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:32340104 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:32340104 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:52856838 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:52856838 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:53207860 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:53207860 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:9406090 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:9406090 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:53077547 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:53077547 C>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:134428211 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chrX:134428211 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:38161103 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:38161103 A>G did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37383496 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37383496 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:30395538 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:30395538 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:3969895 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:3969895 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:67148713 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:67148713 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:67014529 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:67014529 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20482660 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20482660 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20488797 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20488797 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:156940419 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:156940419 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:100739503 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:100739503 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:43840390 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:43840390 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:247020946 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:247020946 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:247068776 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:247068776 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:101433896 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:101433896 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:159557665 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:159557665 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:115336423 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:115336423 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:98985922 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:98985922 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:17942256 G>C maps to NM_004315.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:17942256 G>C maps to NM_004315.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:52502842 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:52502842 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:101315739 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:101315739 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:197097544 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:197097544 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:96791901 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:96791901 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:160026024 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:160026024 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:47517443 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:47517443 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:33066409 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:33066409 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:11026836 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:11026836 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:79951397 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:79951397 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:26506761 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:26506761 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:56382392 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:56382392 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr13:31498410 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr13:31498410 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:57185675 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:57185675 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:75065246 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:75065246 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:47581631 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:47581631 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:20030989 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:20030989 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:23961585 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:23961585 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:200824645 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:200824645 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:8675686 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:8675686 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:99771262 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:99771262 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:112125070 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:112125070 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:27558364 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:27558364 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:91090509 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:91090509 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:104878092 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:104878092 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:92058148 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:92058148 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:14029550 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:14029550 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:13040234 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:13040234 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:111290730 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:111290730 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:30308273 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:30308273 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:24498500 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:24498500 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:73490368 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:73490368 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:31294039 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:31294039 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:117267236 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:117267236 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117243041 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117243041 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:6190213 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:6190213 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:29394315 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:29394315 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:87029467 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:87029467 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:6981958 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:6981958 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:65472567 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:65472567 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:21579528 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:21579528 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:21627174 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:21627174 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:147183019 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:147183019 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:103444195 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:103444195 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:109971270 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:109971270 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:48613017 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:48613017 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:15520395 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:15520395 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160260100 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160260100 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:166389021 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:166389021 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:211539586 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:211539586 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:10868272 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:10868272 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:4851842 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:4851842 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:113650902 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:113650902 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:64592497 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:64592497 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:10982046 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:10982046 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:15772299 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:15772299 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117386041 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117386041 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117450773 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117450773 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:187118466 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:187118466 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:58522100 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:58522100 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160210207 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160210207 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:49986945 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:49986945 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:19345882 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:19345882 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:14797365 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:14797365 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:108124802 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:108124802 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:101198327 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:101198327 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:21721151 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:21721151 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:13788777 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:13788777 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:225635386 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:225635386 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:117814712 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:117814712 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:56472095 A>G maps to ENST00000361203 L2233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:56472095 A>G maps to ENST00000361203 L2233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:32374319 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:32374319 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:34398475 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:34398475 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:79392808 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:79392808 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:93955243 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:93955243 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:44818452 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:44818452 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:23713879 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:23713879 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:76965258 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:76965258 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:109148823 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:109148823 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:61083989 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:61083989 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:177466248 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:177466248 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:2691507 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:2691507 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:124789602 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:124789602 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:170387291 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:170387291 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:176520556 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:176520556 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:41056062 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:41056062 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:101304341 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:101304341 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:26575228 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:26575228 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:163212866 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:163212866 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:30544350 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:30544350 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:92755672 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:92755672 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:17690181 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:17690181 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:143921844 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:143921844 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:155815397 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:155815397 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:132670041 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:132670041 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:144297009 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:144297009 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:134896240 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:134896240 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:105795002 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:105795002 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:27802647 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:27802647 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:145037951 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:145037951 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:5592780 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:5592780 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:31248722 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:31248722 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:27237755 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:27237755 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:53751552 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:53751552 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:160493976 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:160493976 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:113674892 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:113674892 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:57876275 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:57876275 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:31382400 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:31382400 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:139794027 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:139794027 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:111145815 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:111145815 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:40317400 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:40317400 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:15694589 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:15694589 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:43900848 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:43900848 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:27689012 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:27689012 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:20981355 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:20981355 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:8888000 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:8888000 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:116858524 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:116858524 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:44846492 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:44846492 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:20992835 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:20992835 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:200961369 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:200961369 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:39537531 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:39537531 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:152799831 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:152799831 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:111903844 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:111903844 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:27522981 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:27522981 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:185232350 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:185232350 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:97400112 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:97400112 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:114357171 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:114357171 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:170113561 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:170113561 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:86027600 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:86027600 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:37580132 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:37580132 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:141785589 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:141785589 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:141802531 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:141802531 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:127459198 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:127459198 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:50591725 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:50591725 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:59860248 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:59860248 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:60075570 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:60075570 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:10555978 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:10555978 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:45300360 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:45300360 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr13:109562325 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr13:109562325 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:40204345 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:40204345 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:55276716 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:55276716 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr13:35619055 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr13:35619055 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:134050951 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:134050951 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:21317949 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:21317949 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:56139268 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:56139268 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:134871380 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:134871380 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:129751923 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:129751923 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:56481878 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:56481878 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:50883581 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:50883581 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:9124455 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:9124455 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:101093982 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:101093982 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:17571337 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:17571337 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:193333442 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:193333442 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:107331443 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:107331443 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:55540863 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:55540863 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:179209007 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:179209007 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:21696547 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:21696547 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:176762846 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:176762846 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:205978326 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:205978326 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:51480444 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:51480444 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:91238181 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:91238181 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:91714860 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:91714860 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:33877527 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:33877527 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:183291391 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:183291391 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:66723461 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:66723461 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:31847443 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:31847443 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:179537809 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:179537809 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:58318044 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:58318044 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:51887574 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:51887574 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:201288900 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:201288900 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:131935308 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:131935308 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:132109723 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:132109723 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:89189556 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:89189556 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:113522065 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:113522065 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526600 G>A maps to NM_020227.2 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526600 G>A maps to NM_020227.2 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:186269109 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:186269109 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:43348898 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:43348898 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:15506707 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:15506707 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:5276844 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:5276844 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:134454755 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:134454755 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:79384872 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:79384872 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:103252319 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:103252319 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:192129573 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:192129573 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:87128070 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:87128070 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:31429688 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:31429688 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:151331327 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:151331327 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:49743571 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:49743571 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:53639302 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:53639302 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:38178330 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:38178330 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:15166735 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:15166735 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:60069843 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:60069843 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:237789138 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:237789138 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:123524447 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:123524447 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:82034526 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:82034526 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:84694656 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:84694656 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:9197540 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:9197540 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:19388525 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:19388525 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:35652957 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:35652957 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:2831139 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:2831139 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:148388673 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:148388673 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:7534881 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:7534881 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:127514404 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:127514404 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:78210990 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:78210990 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:170736220 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:170736220 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:118598572 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:118598572 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:162719629 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:162719629 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:17988750 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:17988750 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:170214356 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:170214356 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:170214498 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:170214498 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:21353666 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:21353666 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:20555631 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:20555631 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:130910819 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:130910819 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:96950907 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:96950907 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:64795118 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:64795118 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:108438959 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:108438959 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:140358295 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:140358295 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:53049130 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:53049130 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:5399975 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:5399975 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:134927624 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:134927624 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:105912806 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:105912806 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:2384035 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:2384035 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:82337954 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:82337954 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:167022108 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:167022108 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:167022110 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:167022110 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:105361894 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:105361894 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:68953168 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:68953168 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:74905376 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:74905376 T>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:175360616 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:175360616 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:23556188 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:23556188 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:77457060 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:77457060 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:231081093 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:231081093 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:74398655 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:74398655 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:43367403 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:43367403 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:103289439 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:103289439 A>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:176301186 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:176301186 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:108247310 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:108247310 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:38937756 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:38937756 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:54610348 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:54610348 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:73279757 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:73279757 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:203748850 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:203748850 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:167217935 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:167217935 C>G did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:36582093 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:36582093 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:37726963 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:37726963 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:134873386 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:134873386 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:167759982 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:167759982 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:167760501 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:167760501 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:111628589 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:111628589 G>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:88690963 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:88690963 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:129665898 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:129665898 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:158066743 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:158066743 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:136650987 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chrX:136650987 C>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:44803064 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:44803064 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:30583417 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:30583417 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:238050258 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:238050258 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12786059 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12786059 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:67269928 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:67269928 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:67099178 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:67099178 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:67099180 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:67099180 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:169850173 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:169850173 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:101596119 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:101596119 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:44101692 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:44101692 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:179089219 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:179089219 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:8029632 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:8029632 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:148577967 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:148577967 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:132294811 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:132294811 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:131296195 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:131296195 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:156899238 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:156899238 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:156921691 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:156921691 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:3655362 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:3655362 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24793470 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24793470 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24795477 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24795477 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:131949231 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:131949231 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:100197672 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:100197672 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:147891456 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:147891456 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:148035034 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:148035034 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:148044221 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:148044221 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:100368630 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:100368630 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:12363880 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:12363880 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:178355745 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:178355745 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:50311713 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:50311713 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:101425463 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:101425463 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:183967124 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:183967124 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:45869879 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:45869879 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:202483859 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:202483859 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:203789673 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:203789673 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:115238065 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:115238065 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:110824120 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:110824120 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:114171084 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:114171084 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:36713441 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:36713441 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:26825314 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:26825314 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:21224590 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:21224590 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:21256486 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:21256486 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:106534697 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:106534697 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:135772673 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:135772673 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:62875750 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:62875750 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:1748941 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:1748941 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:197094377 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:197094377 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176903199 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176903199 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:106682089 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:106682089 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47574792 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47574792 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:152813494 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:152813494 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:54714475 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:54714475 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:79173735 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:79173735 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:168726545 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:168726545 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:11049567 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:11049567 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:33543419 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:33543419 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129189787 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129189787 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:152770673 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:152770673 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:102003867 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:102003867 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:40610525 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:40610525 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:79971551 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:79971551 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:105564767 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:105564767 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:93486821 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:93486821 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:97137341 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:97137341 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:93043543 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:93043543 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:57252887 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:57252887 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:186359732 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:186359732 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:20052234 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:20052234 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:32550129 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:32550129 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:45601986 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:45601986 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:40959515 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:40959515 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:33370970 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:33370970 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:201013704 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:201013704 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:201052195 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:201052195 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:50418418 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:50418418 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:54445017 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:54445017 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:159166864 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:159166864 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:71419409 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:71419409 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:46925869 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:46925869 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:35904632 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:35904632 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:56163776 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:56163776 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:219874055 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:219874055 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:92861894 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:92861894 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:119960658 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:119960658 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:4397889 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:4397889 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:4397891 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:4397891 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:49110286 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:49110286 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:67531510 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:67531510 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:208062249 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:208062249 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:121822290 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:121822290 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:54468502 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:54468502 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:205497109 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:205497109 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:123206134 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:123206134 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:28538931 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:28538931 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:49054526 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:49054526 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:66969709 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:66969709 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:49539371 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:49539371 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:6214699 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:6214699 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:447414 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:447414 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:85119851 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:85119851 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:85158836 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:85158836 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:848000 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:848000 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:26817903 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:26817903 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:16356211 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:16356211 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:6978641 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:6978641 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:139219201 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:139219201 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:57759572 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:57759572 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47945101 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47945101 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:150907119 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:150907119 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:246823459 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:246823459 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:34552644 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:34552644 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:39154375 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:39154375 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:230820987 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:230820987 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:103387027 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:103387027 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:33143701 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:33143701 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:75839970 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:75839970 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:121295835 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:121295835 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:61957094 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:61957094 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:139629008 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:139629008 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:109862704 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:109862704 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:189915944 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:189915944 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:71012514 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:71012514 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:61459169 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:61459169 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:120960560 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:120960560 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:175305867 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:175305867 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:28610175 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:28610175 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:46846823 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:46846823 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:4494768 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:4494768 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:113236881 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:113236881 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:23546594 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:23546594 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:41473263 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:41473263 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:112958686 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:112958686 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:117359695 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:117359695 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:18933873 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:18933873 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:115593933 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:115593933 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:84627834 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:84627834 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:84650149 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:84650149 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:39381531 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:39381531 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:39381543 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:39381543 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:176894890 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:176894890 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:36521631 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:36521631 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:91550778 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:91550778 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:108547736 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:108547736 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:169182260 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:169182260 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:179319921 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:179319921 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:42793810 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:42793810 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:137294432 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:137294432 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:96171605 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:96171605 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:154001255 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:154001255 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:83501918 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:83501918 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:83502394 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:83502394 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:79555725 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:79555725 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:170594558 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:170594558 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:33229437 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:33229437 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88583075 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88583075 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:21789478 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:21789478 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:21051298 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:21051298 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:11583980 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:11583980 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:11672315 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:11672315 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:183605254 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:183605254 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:98084189 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:98084189 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:128817118 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:128817118 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:169454778 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:169454778 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:111484738 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:111484738 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:111517024 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:111517024 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:68036947 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:68036947 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:64045439 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:64045439 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:28981002 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:28981002 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:23847582 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:23847582 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:45446641 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:45446641 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:10631773 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:10631773 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:5395217 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:5395217 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:43503779 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:43503779 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:23219269 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:23219269 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:160970371 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:160970371 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:138619417 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:138619417 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:177473997 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:177473997 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:222922751 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:222922751 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:176951057 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:176951057 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:176951067 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:176951067 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153674078 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153674078 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:38294238 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:38294238 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:87368895 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:87368895 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:17865960 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:17865960 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:125033681 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:125033681 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:108171399 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:108171399 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:125351419 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:125351419 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:152287710 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:152287710 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153590547 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153590547 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:240307116 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:240307116 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:240374281 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:240374281 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:240635818 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:240635818 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:89395460 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:89395460 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:42776662 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:42776662 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:74671564 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:74671564 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:79367866 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:79367866 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:14788866 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:14788866 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:69521295 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:69521295 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:3527168 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:3527168 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153906436 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153906436 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153941733 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153941733 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46252685 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46252685 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46312364 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46312364 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:161113499 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:161113499 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:26569887 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:26569887 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:242716405 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:242716405 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:31189190 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:31189190 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:174238924 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:174238924 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:99799010 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:99799010 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61994661 C>A maps to ENST00000441409 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61994661 C>A maps to ENST00000441409 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61959188 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61959188 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:6532949 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:6532949 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:175604183 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:175604183 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:175688071 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:175688071 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:57485265 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:57485265 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:54567836 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:54567836 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:68610585 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:68610585 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:20327418 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:20327418 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:47645718 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:47645718 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:95335702 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:95335702 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:131621616 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:131621616 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:8589098 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:8589098 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:89979398 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:89979398 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:94376752 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:94376752 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:108619475 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:108619475 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:21712496 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:21712496 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:154247797 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:154247797 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:45461866 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:45461866 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:71007005 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:71007005 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:186106579 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:186106579 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:186135819 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:186135819 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:43755398 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:43755398 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:43772330 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:43772330 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88231547 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88231547 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:15755505 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:15755505 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:113865274 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:113865274 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:53561452 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:53561452 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:148586552 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:148586552 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:112108009 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:112108009 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:1616134 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:1616134 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:26999579 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:26999579 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:102813512 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:102813512 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:118623376 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:118623376 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:130415405 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:130415405 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:18554340 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:18554340 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:41165449 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:41165449 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:137479412 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:137479412 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:68642442 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:68642442 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:55206563 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:55206563 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:27372177 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:27372177 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:42451882 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:42451882 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31422252 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31422252 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:187511633 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:187511633 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31367142 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31367142 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:9547107 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:9547107 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:46321679 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:46321679 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:7759490 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:7759490 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:27084630 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:27084630 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:163393399 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:163393399 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:27315391 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:27315391 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:24582438 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:24582438 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:15694629 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:15694629 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:42465422 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:42465422 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:96976536 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:96976536 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:96997506 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:96997506 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:5454624 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:5454624 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:24810882 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:24810882 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:109715045 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:109715045 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:1916777 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:1916777 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:116859805 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:116859805 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:241726812 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:241726812 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:39709676 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:39709676 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:42985739 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:42985739 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:49213240 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:49213240 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:51534201 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:51534201 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:123054447 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:123054447 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:39597225 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:39597225 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:52980815 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:52980815 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:52790833 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:52790833 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:31869430 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:31869430 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153133424 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153133424 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:129479460 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:129479460 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:129513742 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:129513742 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:107600005 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:107600005 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:25175865 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:25175865 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:139650835 G>A maps to ENST00000392896 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:139650835 G>A maps to ENST00000392896 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:103869024 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:103869024 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:88451569 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:88451569 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:18391106 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:18391106 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:18391138 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:18391138 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:76427583 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:76427583 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:96329350 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:96329350 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:153233505 C>A maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:153233505 C>A maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:78011508 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:78011508 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:81968032 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:81968032 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:62445258 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:62445258 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:114357601 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:114357601 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:141660832 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:141660832 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:165532687 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:165532687 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:40748354 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:40748354 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:138210659 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:138210659 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:32530015 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:32530015 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:33518426 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:33518426 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:24759896 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:24759896 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:160765943 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:160765943 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:1309086 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:1309086 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:1309147 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:1309147 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:1309160 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:1309160 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:141292016 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:141292016 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:91450479 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:91450479 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:156296834 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:156296834 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:16177773 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:16177773 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:3781688 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:3781688 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:112389745 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:112389745 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:48874495 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:48874495 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:150883128 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:150883128 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:70352930 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:70352930 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:42095529 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:42095529 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:42172323 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:42172323 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:141767033 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:141767033 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:31477803 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:31477803 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:36875766 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:36875766 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:134030760 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:134030760 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:154019430 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:154019430 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:41958261 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:41958261 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:167745275 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:167745275 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:99811099 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:99811099 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:35514621 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:35514621 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:60160344 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:60160344 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:60482704 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:60482704 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:64949254 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:64949254 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:149906026 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:149906026 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:100692275 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:100692275 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:45798699 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:45798699 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:3247988 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:3247988 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:47356832 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:47356832 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:153027240 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:153027240 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:108214564 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:108214564 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:10541070 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:10541070 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:10300382 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:10300382 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:8595472 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:8595472 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:76545768 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:76545768 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:78582309 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:78582309 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:16891108 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:16891108 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:113076758 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:113076758 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:71185974 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:71185974 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:130852931 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:130852931 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:77732668 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:77732668 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:124676333 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:124676333 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:63768165 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:63768165 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:56499321 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:56499321 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:33468621 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:33468621 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:117693685 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:117693685 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:117698477 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:117698477 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:26114666 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:26114666 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:44561204 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:44561204 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:45608959 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:45608959 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:100955645 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:100955645 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:115405558 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:115405558 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:102335189 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:102335189 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:113446822 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:113446822 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:128696343 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:128696343 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153490693 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:153490693 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:248185160 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:248185160 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:4936939 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:4936939 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:48919246 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:48919246 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:201822280 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:201822280 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:31724990 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:31724990 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:45886169 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:45886169 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:20234013 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:20234013 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:29630601 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:29630601 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:111966125 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:111966125 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:39590758 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:39590758 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:150773213 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:150773213 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:52621346 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:52621346 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:154920449 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:154920449 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:58240774 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:58240774 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:140574556 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:140574556 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:47754256 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:47754256 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:142545904 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:142545904 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:72293419 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:72293419 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:144886092 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:144886092 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:39876087 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:39876087 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:31725551 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:31725551 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:54978578 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:54978578 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:45309682 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:45309682 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:71877520 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:71877520 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:47622697 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:47622697 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:67569147 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:67569147 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:111539908 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:111539908 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:51640783 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:51640783 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:44430033 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:44430033 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:26917216 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:26917216 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:9402201 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:9402201 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:105396483 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:105396483 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:126741728 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:126741728 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:102938969 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:102938969 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:140441711 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:140441711 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:44118468 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:44118468 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:86260758 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:86260758 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:128610416 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:128610416 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:38144089 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:38144089 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:43152320 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:43152320 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:122280679 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:122280679 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:23814312 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:23814312 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:37536416 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:37536416 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:146257540 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:146257540 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:68984684 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:68984684 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:36459084 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:36459084 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:2870848 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:2870848 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:43530355 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:43530355 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:12724671 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:12724671 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:11583941 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:11583941 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:474084 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:474084 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:220172159 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:220172159 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:40828067 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:40828067 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:40979482 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:40979482 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:40981014 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:40981014 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:52233590 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:52233590 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:28919867 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:28919867 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:109389242 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:109389242 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:15567096 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:15567096 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:74459027 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:74459027 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:74477408 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:74477408 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:47039449 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:47039449 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:114384064 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:114384064 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:36122147 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:36122147 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:36080720 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:36080720 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:79312760 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:79312760 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:79254364 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:79254364 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:103322542 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:103322542 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:151198982 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:151198982 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:40500614 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:40500614 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:31436062 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:31436062 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:141868674 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:141868674 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:74151252 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:74151252 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:47121001 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:47121001 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:32336008 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:32336008 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237494121 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237494121 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237969681 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237969681 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:9980857 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:9980857 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:75309109 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:75309109 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:61977749 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:61977749 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:50052624 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:50052624 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:56822758 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:56822758 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:158532358 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:158532358 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43129650 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43129650 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:152056102 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:152056102 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:164716196 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:164716196 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:48412964 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:48412964 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:44672000 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:44672000 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:129285334 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:129285334 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:119017449 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:119017449 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:65245589 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:65245589 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:65245591 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:65245591 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:70259758 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:70259758 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:18064009 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:18064009 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:128351809 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:128351809 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:42037186 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:42037186 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:103189242 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:103189242 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:75805204 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:75805204 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:72332027 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:72332027 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:24919142 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:24919142 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:17994460 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:17994460 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:55733606 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:55733606 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:170214369 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:170214369 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:173571085 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:173571085 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:168212819 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:168212819 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:144903892 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:144903892 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:1168597 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:1168597 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:101630055 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:101630055 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:118555087 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:118555087 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:140358426 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:140358426 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:158627110 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:158627110 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:85115657 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:85115657 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:52682697 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:52682697 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:57640562 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:57640562 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:40474932 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:40474932 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:99171846 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:99171846 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:37152240 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:37152240 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:25288227 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:25288227 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:46341917 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:46341917 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:9629203 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:9629203 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:71606282 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:71606282 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:50381711 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:50381711 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:107115859 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:107115859 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:74859149 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:74859149 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:114724518 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:114724518 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:114724521 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:114724521 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:56665209 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:56665209 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:32513556 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:32513556 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:38851200 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:38851200 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:74300877 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:74300877 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:136384216 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:136384216 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:101769791 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:101769791 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:103216430 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:103216430 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:31543732 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:31543732 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:9584130 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:9584130 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:201337150 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:201337150 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:1439922 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:1439922 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:10914576 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:10914576 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:10920045 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:10920045 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:10922028 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:10922028 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:27522075 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:27522075 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:72987514 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:72987514 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:45821481 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:45821481 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:53114341 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:53114341 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:39171650 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:39171650 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:43565473 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:43565473 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:179587298 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:179587298 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:54947400 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:54947400 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:4204759 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:4204759 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:59068420 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:59068420 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:156962928 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:156962928 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:70070451 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:70070451 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:70078207 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:70078207 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:70152425 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:70152425 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:109539647 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:109539647 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:61455908 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:61455908 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:144117058 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:144117058 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129040221 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129040221 A>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129055586 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:129055586 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:136650886 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:136650886 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12422932 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12422932 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:22132700 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:22132700 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:6131342 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:6131342 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:42336237 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr22:42336237 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:71130630 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:71130630 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:131397358 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:131397358 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32413739 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32413739 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32449978 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32449978 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:78312490 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:78312490 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:6682572 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:6682572 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:67738452 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chrX:67738452 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:28489193 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:28489193 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:44968471 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:44968471 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:57193641 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:57193641 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:23844855 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:23844855 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:61561180 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:61561180 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:96747029 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:96747029 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:127806590 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:127806590 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:87757863 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:87757863 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:39634693 A>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:39634693 A>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:113803029 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:113803029 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:124706046 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:124706046 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:36275302 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:36275302 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:131067069 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:131067069 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:62577895 G>T maps to NM_020164.4 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:62577895 G>T maps to NM_020164.4 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:24095139 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:24095139 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:129173293 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:129173293 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:61870002 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:61870002 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:93494647 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:93494647 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:185196382 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:185196382 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:118984729 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:118984729 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:88126327 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:88126327 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr9:35826172 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr9:35826172 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr16:57733885 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr16:57733885 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:93649734 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:93649734 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:7521406 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:7521406 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:7808150 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:7808150 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:208072189 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:208072189 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:26818192 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:26818192 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:10163198 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:10163198 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:41418891 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:41418891 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:71654409 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:71654409 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:10089212 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:10089212 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:17056291 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:17056291 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:67680436 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:67680436 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:83141484 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:83141484 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr22:37707483 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr22:37707483 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:50589598 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:50589598 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:140285335 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:140285335 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:958904 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:958904 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:101731665 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:101731665 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:55211206 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:55211206 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:41292950 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:41292950 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:45789716 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:45789716 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:99076820 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:99076820 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:121941977 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:121941977 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:79391328 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:79391328 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:178413778 G>T maps to ENST00000319065 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:178413778 G>T maps to ENST00000319065 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:38122731 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:38122731 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:240016553 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:240016553 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:100185490 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:100185490 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:1516169 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:1516169 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:56091220 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:56091220 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:26942073 T>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:26942073 T>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:52892438 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:52892438 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:52884196 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:52884196 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:50528560 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:50528560 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:55086090 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:55086090 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:54845126 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:54845126 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:102113257 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:102113257 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:2041674 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:2041674 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:57884171 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:57884171 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:151855940 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:151855940 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:52606268 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:52606268 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:78415685 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:78415685 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:204063924 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:204063924 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:126211681 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:126211681 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:132635786 T>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:132635786 T>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:64444525 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:64444525 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:22333110 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:22333110 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:110459620 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chrX:110459620 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:6743820 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:6743820 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:53854969 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:53854969 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr21:47768889 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr21:47768889 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:48501131 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:48501131 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:61016133 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:61016133 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:99936375 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:99936375 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:169733 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:169733 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:37535587 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:37535587 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:242105744 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr2:242105744 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:170695592 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:170695592 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:43571184 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:43571184 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:5220962 T>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:5220962 T>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:40735282 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:40735282 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:176145159 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:176145159 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:75525732 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:75525732 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:52003091 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:52003091 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:51628847 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:51628847 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr9:19520812 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr9:19520812 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:69158480 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:69158480 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:1244700 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:1244700 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:57500437 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:57500437 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:61483717 A>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:61483717 A>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:78295882 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:78295882 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:57568004 T>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:57568004 T>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:81660569 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:81660569 A>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:42511774 T>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr15:42511774 T>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr14:76198574 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr14:76198574 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:66582687 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr7:66582687 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:13271570 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:13271570 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:96137370 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:96137370 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:54385183 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:54385183 C>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:57649754 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:57649754 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:178503622 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:178503622 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:58551959 G>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:58551959 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:1065434 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:1065434 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:15511219 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:15511219 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:117119127 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:117119127 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:36501774 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:36501774 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:56647785 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:56647785 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:4751200 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:4751200 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:1743364 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:1743364 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:111405299 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:111405299 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:62187995 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:62187995 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:111795867 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:111795867 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:61842263 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:61842263 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:68720498 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:68720498 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:16383337 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:16383337 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:157218692 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:157218692 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:23846420 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:23846420 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:54655946 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:54655946 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:117002470 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:117002470 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:173337417 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:173337417 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69265509 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69265509 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69326434 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69326434 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69326649 G>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69326649 G>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:207883642 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:207883642 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:113933799 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:113933799 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr10:12159612 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr10:12159612 A>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:11790292 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:11790292 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:31454179 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:31454179 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:116539923 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:116539923 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:73994267 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:73994267 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:6897649 A>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:6897649 A>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:6503505 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:6503505 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:43058157 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:43058157 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:308103 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:308103 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr3:53892852 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr3:53892852 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:39778033 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:39778033 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:27781387 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:27781387 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr18:43450466 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr18:43450466 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:57969809 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:57969809 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:43212924 C>A maps to ENST00000236040 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:43212924 C>A maps to ENST00000236040 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:36245234 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:36245234 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:59284030 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:59284030 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:99006570 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:99006570 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:50515156 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:50515156 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:154020019 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:154020019 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:46754928 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:46754928 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:27447787 A>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:27447787 A>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr10:95211782 G>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr10:95211782 G>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:103528247 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:103528247 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:228505468 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:228505468 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:123538838 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:123538838 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:31284163 G>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:31284163 G>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:79804955 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:79804955 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:127251540 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:127251540 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:233344194 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:233344194 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:34938158 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:34938158 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:15141605 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:15141605 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:81214697 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:81214697 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:51938410 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:51938410 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:103041667 A>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:103041667 A>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:70964593 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr8:70964593 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr21:43226298 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr21:43226298 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:27356606 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:27356606 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:113942395 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:113942395 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:170610448 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:170610448 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:170610454 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:170610454 T>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:103138395 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:103138395 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr18:13760036 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr18:13760036 C>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:123499813 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:123499813 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:127520579 T>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:127520579 T>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:61598913 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:61598913 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:79682632 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:79682632 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:176820661 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr5:176820661 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:56628833 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:56628833 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:28833868 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:28833868 A>G did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:48046210 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:48046210 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:52682433 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chrX:52682433 C>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:6820592 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:6820592 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:55475290 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:55475290 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69756738 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr12:69756738 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:37130956 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr19:37130956 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr18:22669582 T>C did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr18:22669582 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:69759376 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:69759376 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:67257449 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:67257449 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:67014037 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:67014037 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:67014037 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:67014037 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:48118010 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:48118010 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:48174498 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:48174498 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:48118010 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:48118010 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:48174498 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:48174498 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:16138551 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:16138551 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:16138551 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:16138551 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:48741534 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:48741534 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:48741534 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:48741534 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:17448583 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:17448583 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:17464964 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:17464964 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:17448583 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:17448583 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:17464964 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:17464964 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:21998515 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:21998515 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:31348429 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:31348429 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:31348429 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:31348429 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:55070115 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:55070115 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:11685763 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:11685763 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:132036132 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:132036132 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:20636756 C>A maps to NM_052956.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:20636756 C>A maps to NM_052956.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20494625 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20494625 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:79478179 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:79478179 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:39142376 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:39142376 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:39142376 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:39142376 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:33577294 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:33577294 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:77401714 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:77401714 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:77401714 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:77401714 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:43770515 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:43770515 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:43770515 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:43770515 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:43856733 C>T maps to ENST00000389420 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:43856733 C>T maps to ENST00000389420 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:45717378 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:45717378 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:45742955 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:45742955 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:45717378 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:45717378 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:45742955 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:45742955 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:7690925 G>T maps to NM_020546.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:7690925 G>T maps to NM_020546.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:111878332 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:111878332 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:111878332 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:111878332 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:141296227 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:141296227 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:109667831 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:109667831 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:109667831 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:109667831 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:143458134 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:143458134 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:77876758 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:77876758 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:77876758 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:77876758 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:96881726 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:96881726 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:5239001 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:5239001 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:5239001 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:5239001 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:243788253 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:243788253 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:58256302 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:58256302 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:63885122 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:63885122 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:63885122 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:63885122 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:233271578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:233271578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:233271578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:233271578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:46718331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:46718331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:46718331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:46718331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:115220841 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:115220841 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:115220841 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:115220841 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:38534171 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:38534171 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:38534171 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:38534171 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:77257781 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:77257781 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:101765535 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:101765535 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:101765535 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:101765535 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:62444266 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:62444266 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:61874083 T>C maps to NM_020987.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:61874083 T>C maps to NM_020987.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:62444266 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:62444266 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:15762736 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:15762736 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:4747326 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:4747326 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:26621323 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:26621323 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:26621323 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:26621323 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:101295491 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:101295491 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:101295491 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:101295491 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:22283596 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:22283596 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:22283596 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:22283596 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:165118749 T>A maps to NM_012403.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:165118749 T>A maps to NM_012403.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:69304604 A>G maps to NM_032208.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:69304604 A>G maps to NM_032208.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:77425191 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:77425191 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:63579581 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:63579581 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:32988050 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:32988050 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:35155026 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:35155026 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:86915607 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:86915607 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:43481384 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:43481384 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:17961111 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:17961111 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:41477011 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:41477011 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:41477011 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:41477011 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:35729466 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:35729466 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:35729466 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:35729466 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:94413885 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:94413885 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:94413885 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:94413885 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:176845596 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:176845596 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:176903497 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:176903497 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:176845596 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:176845596 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:176903497 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:176903497 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:26032685 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:26032685 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:117067547 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:117067547 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117067547 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117067547 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:3917686 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:3917686 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:3917686 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:3917686 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:11382131 A>G maps to NM_006395.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:11382131 A>G maps to NM_006395.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:108188040 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:108188040 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:160140883 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:160140883 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:119512495 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:119512495 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:35693046 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:35693046 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:35693046 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:35693046 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:28378138 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:28378138 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:42598305 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:42598305 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr21:42598305 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr21:42598305 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:33392627 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:33392627 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:52645563 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:52645563 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:30253650 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:30253650 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:30253650 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:30253650 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:32712887 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:32712887 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:32712887 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:32712887 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:26267806 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:26267806 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:26267842 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:26267842 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:26267806 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:26267806 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:26267842 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:26267842 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:15375582 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:15375582 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:15375582 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:15375582 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:167906268 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:167906268 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:32372643 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:32372643 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:32372643 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:32372643 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:104557951 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:104557951 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:104557951 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:104557951 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:105951928 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:105951928 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:105951928 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:105951928 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:62430633 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:62430633 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:62430633 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:62430633 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:122827171 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:122827171 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:27078801 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:27078801 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:27081462 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:27081462 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:27081512 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:27081512 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:27078801 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:27078801 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:40040705 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:40040705 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:40041817 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:40041817 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:40040705 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:40040705 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:74825597 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:74825597 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:74825597 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:74825597 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:81428996 G>A maps to ENST00000458088 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:81428996 G>A maps to ENST00000458088 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:90144434 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:90144434 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:80367166 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:80367166 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:80367166 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:80367166 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42239189 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42239189 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42239189 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42239189 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:30554588 C>A maps to NM_001105528.1 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:30554588 C>A maps to NM_001105528.1 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:36250455 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:36250455 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:44235831 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:44235831 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:44235831 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:44235831 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:119914665 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:119914665 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:119914665 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:119914665 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:179416881 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:179416881 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:57185333 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:57185333 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:57185333 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:57185333 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:233086547 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:233086547 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:60987501 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:60987501 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:31661395 G>T maps to NM_182658.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:31661395 G>T maps to NM_182658.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:258067 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:258067 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:258067 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:258067 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:73825445 C>T maps to ENST00000334126 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:73825445 C>T maps to ENST00000334126 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:197674126 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:197674126 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:197674126 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:197674126 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:6686480 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:6686480 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:159928876 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:159928876 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:159928876 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:159928876 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:97597754 C>T maps to NM_198468.2 W1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:97597754 C>T maps to NM_198468.2 W1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:48086244 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:48086244 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:57411794 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:57411794 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:57411794 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:57411794 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:4625265 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:4625265 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:49711133 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:49711133 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:24487905 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:24487905 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:13445408 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:13445408 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:2602684 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:2602684 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:2675527 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:2675527 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:2602684 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:2602684 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:2714752 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:2714752 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:40052574 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:40052574 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:3785872 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:3785872 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:230903520 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:230903520 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:230927573 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:230927573 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:35910342 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:35910342 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:43927758 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:43927758 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:74311182 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:74311182 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:74311182 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:74311182 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:97779093 T>C maps to NM_001159747.1 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:97779093 T>C maps to NM_001159747.1 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:92887756 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:92887756 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:92887875 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:92887875 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:92887756 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:92887756 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:106125437 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:106125437 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:106130882 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:106130882 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:106130882 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:106130882 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:49912884 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:49912884 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:27614178 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:27614178 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:27614178 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:27614178 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:120510565 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:120510565 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:120510565 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:120510565 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:42299484 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:42299484 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:42299484 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:42299484 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:33281435 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:33281435 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:33281435 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:33281435 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:74466545 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:74466545 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:71060026 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:71060026 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:71060026 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:71060026 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:72540856 C>T maps to NM_006678.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:72540856 C>T maps to NM_006678.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:35218482 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:35218482 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:35222803 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:35222803 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:157811522 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:157811522 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:157811522 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:157811522 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:193205521 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:193205521 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:21760455 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:21760455 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:21882748 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:21882748 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:21882748 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:21882748 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:64239489 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:64239489 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:64239489 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:64239489 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:66426326 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:66426326 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:66426326 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:66426326 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:26890137 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:26890137 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:26903714 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:26903714 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:1586706 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:1586706 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:123184937 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:123184937 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:123184937 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:123184937 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:92300892 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:92300892 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:92300892 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:92300892 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:80638574 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:80638574 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:80638574 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:80638574 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:123920101 A>C maps to NM_007018.4 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:123920101 A>C maps to NM_007018.4 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:95263187 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:95263187 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:95263226 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:95263226 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:95263187 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:95263187 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:47115946 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:47115946 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196744096 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196744096 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196749109 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196749109 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:196744096 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:196744096 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:196749109 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:196749109 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:117242934 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:117242934 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117242934 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117242934 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:40125886 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:40125886 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:53308300 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:53308300 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:150932244 C>A maps to NM_019015.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:150932244 C>A maps to NM_019015.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:46776328 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:46776328 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:170601383 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:170601383 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:11879713 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:11879713 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:140277664 C>T maps to NM_022131.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:140277664 C>T maps to NM_022131.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:108686655 C>T maps to NM_001142344.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:108686655 C>T maps to NM_001142344.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:108710199 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:108710199 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:87682960 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:87682960 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:58580243 G>C maps to NM_016284.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:58580243 G>C maps to NM_016284.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:41419199 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:41419199 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:41419199 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:41419199 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:74334436 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:74334436 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:74334436 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:74334436 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:1427541 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:1427541 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:1427541 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:1427541 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:33133821 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:33133821 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:33133821 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:33133821 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:61944619 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:61944619 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:55923899 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:55923899 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:55923899 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:55923899 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:7563785 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:7563785 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:7561459 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:7561459 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:189872535 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:189872535 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:110827814 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:110827814 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227964452 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227964452 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227973845 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227973845 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:227964452 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:227964452 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:227973845 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:227973845 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:10114433 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:10114433 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:10114433 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:10114433 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:101473133 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:101473133 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:101473133 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:101473133 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:46658489 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:46658489 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:46658489 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:46658489 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:83224461 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:83224461 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:125622259 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:125622259 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:207867884 G>A maps to NM_175710.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:207867884 G>A maps to NM_175710.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207751638 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207751638 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:197297544 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:197297544 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:197297544 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:197297544 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:45891800 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:45891800 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:45891800 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:45891800 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:37319521 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:37319521 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:2857689 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:2857689 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:3165797 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:3165797 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:2857689 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:2857689 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:113842039 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:113842039 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:113651000 A>G maps to NM_198123.1 Y1150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:113651000 A>G maps to NM_198123.1 Y1150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:113842039 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:113842039 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:80875161 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:80875161 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:68535191 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:68535191 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:68535191 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:68535191 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:206319093 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:206319093 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:57571563 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:57571563 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117424260 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117424260 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117424273 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:117424273 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:16960850 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:16960850 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:17152664 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:17152664 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:16960850 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:16960850 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:76927398 A>T maps to NM_002416.1 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:76927398 A>T maps to NM_002416.1 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:105891405 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:105891405 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:37697074 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:37697074 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:37697074 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:37697074 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:58515012 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:58515012 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:58515012 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:58515012 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:58550226 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:58550226 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42824437 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42824437 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42824437 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42824437 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:176887282 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:176887282 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:50547601 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:50547601 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:169383280 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:169383280 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:169348278 A>T maps to NM_001012967.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:169348278 A>T maps to NM_001012967.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:31577452 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:31577452 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:68949536 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:68949536 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:14231479 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:14231479 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:14231479 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:14231479 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:14661112 G>A maps to NM_004080.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:14661112 G>A maps to NM_004080.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:137407411 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:137407411 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:137198577 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:137198577 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:137407411 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:137407411 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:47884642 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:47884642 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:95572634 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:95572634 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:107844968 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:107844968 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:107845747 T>A maps to NM_014421.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:107845747 T>A maps to NM_014421.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:12943773 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:12943773 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:12943773 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:12943773 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:124344981 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:124344981 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:31341837 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:31341837 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:31341837 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:31341837 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:52428845 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:52428845 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:38976552 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:38976552 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:38976552 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:38976552 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:186299100 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:186299100 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:186299100 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:186299100 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:118971089 C>A maps to NM_001382.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:118971089 C>A maps to NM_001382.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:26485501 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:26485501 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:26485501 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:26485501 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:113858286 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:113858286 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:113858286 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:113858286 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:28577023 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:28577023 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:28577023 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:28577023 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:28577029 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:28577029 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:41683911 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:41683911 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr21:41683911 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr21:41683911 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:28923370 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:28923370 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:28923370 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:28923370 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:88533353 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:88533353 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:88533353 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:88533353 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:56504640 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:56504640 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:56504640 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:56504640 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:15637914 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:15637914 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:15637914 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:15637914 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107214305 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107214305 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:107214305 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:107214305 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:207530512 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:207530512 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:207530512 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:207530512 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:108396541 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:108396541 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:158140211 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:158140211 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:25708041 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:25708041 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:25708041 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:25708041 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:233346355 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:233346355 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:127651820 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:127651820 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:236647670 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:236647670 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:83550108 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:83550108 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:83550108 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:83550108 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:41948216 C>T maps to NM_001956.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:41948216 C>T maps to NM_001956.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:49647612 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:49647612 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:49647612 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:49647612 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:1295873 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:1295873 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:82533697 C>A maps to NM_024580.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:82533697 C>A maps to NM_024580.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:38463171 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:38463171 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:110914569 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:110914569 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:40301767 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:40301767 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:117658740 C>A maps to ENST00000411422 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:117658740 C>A maps to ENST00000411422 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:29630394 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:29630394 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:42530317 A>G maps to NM_019063.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:42530317 A>G maps to NM_019063.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:7031661 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:7031661 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:7031661 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:7031661 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:139946242 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:139946242 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:27760633 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:27760633 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:46587569 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:46587569 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:97439073 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:97439073 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:97439073 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:97439073 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:103501800 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:103501800 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:103501800 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:103501800 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:13971018 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:13971018 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:67220362 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:67220362 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:118830507 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:118830507 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:133849980 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:133849980 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:66063321 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:66063321 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:65443543 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:65443543 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:66063321 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:66063321 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:82370794 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:82370794 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:82371584 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:82371584 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:82370794 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:82370794 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:82371584 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:82371584 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:175919293 G>A maps to NM_014613.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:175919293 G>A maps to NM_014613.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:143554554 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:143554554 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:139155395 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:139155395 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:139380235 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:139380235 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:139155395 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:139155395 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:139380235 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:139380235 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:84390092 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:84390092 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:222922782 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:222922782 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:222922782 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:222922782 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:45490110 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:45490110 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:45490110 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:45490110 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:51892505 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:51892505 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:51892505 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:51892505 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:16740921 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:16740921 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:16740921 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:16740921 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:190424084 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:190424084 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:35079413 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:35079413 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:35079413 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:35079413 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:163055369 A>T maps to NM_004460.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:163055369 A>T maps to NM_004460.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:29486612 C>T maps to NM_018099.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:29486612 C>T maps to NM_018099.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:45958896 G>A maps to ENST00000402984 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:45958896 G>A maps to ENST00000402984 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:48723049 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:48723049 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:48723049 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:48723049 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:5956066 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:5956066 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:5956066 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:5956066 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:55386657 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:55386657 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:35941683 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:35941683 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:35941683 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:35941683 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:1006102 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:1006102 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:99552026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:99552026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:99552026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:99552026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:1352997 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:1352997 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:1352997 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:1352997 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:45603641 T>A maps to NM_002013.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:45603641 T>A maps to NM_002013.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:84607512 C>T maps to NM_001001670.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:84607512 C>T maps to NM_001001670.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:49227539 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:49227539 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:46376129 A>T maps to NM_004497.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:46376129 A>T maps to NM_004497.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:4794032 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:4794032 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:118851197 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:118851197 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:79360269 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:79360269 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:79455557 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:79455557 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:79360269 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:79360269 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:79455557 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:79455557 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:37724226 T>C maps to NM_014907.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:37724226 T>C maps to NM_014907.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:32776614 A>T maps to NM_023037.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:32776614 A>T maps to NM_023037.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:52779454 G>A maps to NM_013409.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:52779454 G>A maps to NM_013409.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:52781497 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:52781497 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:111982922 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:111982922 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:153944167 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:153944167 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:153944167 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:153944167 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:151123795 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:151123795 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:26570060 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:26570060 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:26570060 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:26570060 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:166621626 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:166621626 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:151704859 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:151704859 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:151704859 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:151704859 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:76954629 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:76954629 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:76954629 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:76954629 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:61995376 G>T maps to NM_000515.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:61995376 G>T maps to NM_000515.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:100284450 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:100284450 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:100284450 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:100284450 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:110429604 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:110429604 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:110429604 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:110429604 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:134147820 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:134147820 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:134182049 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:134182049 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:134147820 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:134147820 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:6588506 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:6588506 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:6588506 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:6588506 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:121732830 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:121732830 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:92754744 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:92754744 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:92754744 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:92754744 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:14627185 C>T maps to NM_002063.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:14627185 C>T maps to NM_002063.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:220366835 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:220366835 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:220366835 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:220366835 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:93555535 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:93555535 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:93555535 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:93555535 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:44713077 T>C maps to NM_138335.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:44713077 T>C maps to NM_138335.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:167023847 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:167023847 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973288 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973288 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973301 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973301 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973376 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:48973376 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973288 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973288 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973301 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973301 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973376 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973376 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973450 C>T maps to NM_015698.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:48973450 C>T maps to NM_015698.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:95273307 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:95273307 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:95273307 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:95273307 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:37900485 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:37900485 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:105795525 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:105795525 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:30959583 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:30959583 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:121093433 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:121093433 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:88780374 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:88780374 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:126249296 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:126249296 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:126249296 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:126249296 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:144966153 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:144966153 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:144966153 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:144966153 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:60774368 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:60774368 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:156631669 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:156631669 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:156631669 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:156631669 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:21728644 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:21728644 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:31944657 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:31944657 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:31944657 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:31944657 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:15609520 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:15609520 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:122626239 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:122626239 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:122626239 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:122626239 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42855860 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42855860 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:37302746 G>A maps to NM_019024.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:37302746 G>A maps to NM_019024.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:58134603 C>T maps to NM_022070.4 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:58134603 C>T maps to NM_022070.4 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:41005767 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:41005767 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:41005767 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:41005767 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:139488508 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:139488508 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:139488508 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:139488508 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:43490383 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:43490383 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:197194218 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:197194218 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:197194472 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:197194472 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:197194218 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:197194218 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:197194472 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:197194472 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:100128992 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:100128992 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:100535060 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:100535060 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:19348892 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:19348892 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:19348892 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:19348892 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:27782452 G>T maps to NM_021066.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:27782452 G>T maps to NM_021066.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:143080971 G>C maps to NM_006734.3 Y2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:143080971 G>C maps to NM_006734.3 Y2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:71075715 C>T maps to NM_033496.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:71075715 C>T maps to NM_033496.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:71075715 C>T maps to NM_033496.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:71075715 C>T maps to NM_033496.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:71010246 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:71010246 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:71010246 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:71010246 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:29961701 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:29961701 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:148759926 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:148759926 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:185815074 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:185815074 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:43297158 T>C maps to NM_002130.6 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:43297158 T>C maps to NM_002130.6 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:245018902 C>T maps to NM_031844.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:245018902 C>T maps to NM_031844.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:46657363 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:46657363 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:54404854 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:54404854 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:54404854 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:54404854 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:176988914 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:176988914 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:176988914 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:176988914 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:175413099 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:175413099 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:175413099 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:175413099 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:63326317 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:63326317 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:114383791 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:114383791 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:122930823 C>T maps to NM_006597.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:122930823 C>T maps to NM_006597.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:198353667 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:198353667 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:198353667 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:198353667 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:31714482 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:31714482 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:31714482 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:31714482 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:53657805 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:53657805 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:220319069 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:220319069 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:79129580 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:79129580 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:201184302 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:201184302 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:201184302 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:201184302 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:151174592 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:151174592 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:28677274 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:28677274 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:28677274 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:28677274 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:27456537 C>G maps to NM_181079.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:27456537 C>G maps to NM_181079.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:79673005 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:79673005 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:79673005 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:79673005 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:121712503 C>A maps to ENST00000344209 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:121712503 C>A maps to ENST00000344209 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:76728443 G>A maps to NM_001563.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:76728443 G>A maps to NM_001563.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:100951485 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:100951485 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:111371524 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:111371524 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:111371524 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:111371524 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:99193583 C>T maps to NM_001134224.1 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:99193583 C>T maps to NM_001134224.1 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:142950154 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:142950154 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:2170330 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:2170330 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:2170330 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:2170330 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:106614449 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:106614449 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:201827571 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:201827571 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:201827571 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:201827571 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:153281729 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:153281729 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156668849 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156668849 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156670881 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156670881 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:156670881 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:156670881 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:147016512 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:147016512 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:147016512 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:147016512 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:64976850 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:64976850 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:42814790 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:42814790 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:39919202 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:39919202 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:39919202 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:39919202 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:62747331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:62747331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:62747331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:62747331 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:170336018 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:170336018 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:111146591 C>T maps to NM_004974.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:111146591 C>T maps to NM_004974.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:75444632 C>A maps to NM_139137.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:75444632 C>A maps to NM_139137.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:210970654 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:210970654 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:19384040 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:19384040 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:19432277 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:19432277 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:19384040 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:19384040 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196205219 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196205219 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196342233 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:196342233 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:36763472 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:36763472 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:136657254 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:136657254 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:136657254 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:136657254 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:24601416 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:24601416 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:57181272 G>T maps to NM_020722.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:57181272 G>T maps to NM_020722.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:118687203 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:118687203 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158063316 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158063316 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:158063316 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:158063316 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:70549747 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:70549747 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:53516292 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:53516292 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:9994732 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:9994732 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:241719036 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:241719036 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:241719036 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:241719036 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:160285712 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:160285712 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:91865873 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:91865873 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:91865873 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:91865873 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:53009026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:53009026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:53009026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:53009026 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:143712288 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:143712288 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:130404859 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:130404859 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:42143557 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:42143557 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:6972998 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:6972998 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:6982655 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:6982655 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:6972998 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:6972998 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:112461244 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:112461244 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107669708 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107669708 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:107669708 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:107669708 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:152595432 C>G maps to NM_178431.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:152595432 C>G maps to NM_178431.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:76970712 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:76970712 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:25967593 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:25967593 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:25967593 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:25967593 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:113906216 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:113906216 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:48620930 G>A maps to NM_000234.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:48620930 G>A maps to NM_000234.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:74567681 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:74567681 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20833035 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20833035 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:20833035 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:20833035 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:23155746 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:23155746 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:78010953 C>A maps to NM_005296.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:78010953 C>A maps to NM_005296.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:151765773 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:151765773 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:151765773 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:151765773 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:66432180 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:66432180 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:113638832 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:113638832 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:113638832 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:113638832 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:170097414 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:170097414 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:25471358 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:25471358 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:25471358 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:25471358 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:54427875 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:54427875 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:54427875 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:54427875 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1905418 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1905418 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:1905418 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:1905418 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:140984474 G>T maps to NM_177456.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:140984474 G>T maps to NM_177456.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:140984474 G>T maps to NM_177456.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:140984474 G>T maps to NM_177456.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:35803259 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:35803259 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:35803259 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:35803259 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:12013829 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:12013829 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:53881316 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:53881316 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:185135163 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:185135163 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:185135163 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:185135163 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:43366555 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:43366555 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:39090802 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:39090802 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:39090802 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:39090802 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:160619565 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:160619565 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:31194231 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:31194231 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:31194231 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:31194231 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:47799765 C>A maps to ENST00000424334 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:47799765 C>A maps to ENST00000424334 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:29528417 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:29528417 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:37565296 G>C maps to NM_004774.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:37565296 G>C maps to NM_004774.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:43852784 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:43852784 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:43852784 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:43852784 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:28135224 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:28135224 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:21655747 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:21655747 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:21655747 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:21655747 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:48703797 G>A maps to NM_016626.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:48703797 G>A maps to NM_016626.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:40433392 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:40433392 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:40433392 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:40433392 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:140587103 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:140587103 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:140587103 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:140587103 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:41281317 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:41281317 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:129907465 C>A maps to NM_002417.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:129907465 C>A maps to NM_002417.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:56289821 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:56289821 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:56289821 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:56289821 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:37053622 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:37053622 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:151891349 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:151891349 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118366732 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118366732 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:118366732 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:118366732 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:146567083 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:146567083 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:146572342 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:146572342 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:146567083 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:146567083 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:154878335 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:154878335 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:174537946 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:174537946 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:174537946 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:174537946 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:131216894 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:131216894 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:60068592 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:60068592 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:72754873 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:72754873 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:72754873 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:72754873 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:149919610 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:149919610 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:100510935 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:100510935 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1158281 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1158281 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1215493 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1215493 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1262070 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:1262070 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:47361034 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:47361034 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:47361034 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:47361034 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:81112270 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:81112270 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:81112270 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:81112270 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:10369628 C>T maps to NM_017533.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:10369628 C>T maps to NM_017533.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:23862273 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:23862273 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:23882918 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:23882918 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:23892938 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:23892938 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:23882918 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:23882918 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:23892938 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:23892938 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:2678622 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:2678622 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:2678622 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:2678622 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:16680325 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:16680325 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:109550578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:109550578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:109550578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:109550578 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:95216595 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:95216595 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:95216595 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:95216595 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:175294005 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:175294005 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:175294005 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:175294005 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:782380 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:782380 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:36202191 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:36202191 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:36202191 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:36202191 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:16894103 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:16894103 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:16894139 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:16894139 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:16910378 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:16910378 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:21801676 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:21801676 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:36029490 G>A maps to NM_001014839.1 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:36029490 G>A maps to NM_001014839.1 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:54914810 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:54914810 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:54914810 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:54914810 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:115856585 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:115856585 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:116030109 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:116030109 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:152467403 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:152467403 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:152467403 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:152467403 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:72163598 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:72163598 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:27244068 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:27244068 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:27244068 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:27244068 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:130889526 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:130889526 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:70532263 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:70532263 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:103866542 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:103866542 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:103866542 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:103866542 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:45681259 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:45681259 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:73884609 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:73884609 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:119501524 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:119501524 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:79434537 G>T maps to NM_004796.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:79434537 G>T maps to NM_004796.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:86177026 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:86177026 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:88423448 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:88423448 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:88575953 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:88575953 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:88423448 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:88423448 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:88575953 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:88575953 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:34323721 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:34323721 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:73743881 G>A maps to NM_001005743.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:73743881 G>A maps to NM_001005743.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:135258379 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:135258379 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:118015365 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:118015365 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:101092341 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:101092341 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:101092341 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:101092341 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:28141199 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:28141199 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:28235641 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:28235641 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:28141199 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:28141199 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:28235641 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:28235641 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:128694646 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:128694646 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:128694646 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:128694646 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:123631059 G>C maps to NM_001163278.1 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:123631059 G>C maps to NM_001163278.1 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:50946223 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:50946223 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:50946223 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:50946223 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:44687384 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:44687384 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:44687384 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:44687384 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:7961051 G>A maps to NM_001003745.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:7961051 G>A maps to NM_001003745.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:248247332 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:248247332 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:248247332 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:248247332 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55418304 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55418304 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:4674112 G>T maps to NM_152430.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:4674112 G>T maps to NM_152430.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:158735614 G>A maps to NM_001005185.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:158735614 G>A maps to NM_001005185.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:14991870 G>C maps to NM_030901.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:14991870 G>C maps to NM_030901.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:21739596 C>T maps to ENST00000286149 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:21739596 C>T maps to ENST00000286149 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:72926821 G>A maps to NM_178160.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:72926821 G>A maps to NM_178160.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:31862302 A>G maps to ENST00000382902 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:31862302 A>G maps to ENST00000382902 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:740337 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:740337 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:6742736 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:6742736 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:6742736 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:6742736 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:176675664 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:176675664 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:119124829 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:119124829 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:119124829 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:119124829 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:89475535 C>G maps to NM_001015880.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:89475535 C>G maps to NM_001015880.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:50056009 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:50056009 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:5442101 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:5442101 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:5605983 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:5605983 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:5442101 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:5442101 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:5605983 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:5605983 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:56360206 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:56360206 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:56360206 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:56360206 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:58241007 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:58241007 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:58241007 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:58241007 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:141236764 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:141236764 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:100200281 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:100200281 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:14810569 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:14810569 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:14810569 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:14810569 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:66723194 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:66723194 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:66838407 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:66838407 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:66723194 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:66723194 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:66838407 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:66838407 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:17491505 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:17491505 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:20410589 C>T maps to NM_174924.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:20410589 C>T maps to NM_174924.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:70166027 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:70166027 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:70166027 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:70166027 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:33252925 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:33252925 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:33252925 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:33252925 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:1960689 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:1960689 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:41961505 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:41961505 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:41585227 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:41585227 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:45935203 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:45935203 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:3176837 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:3176837 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:28253578 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:28253578 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:28253578 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:28253578 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:58318160 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:58318160 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:34438822 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:34438822 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:45970630 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:45970630 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:45309532 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:45309532 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:43803720 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:43803720 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:43803720 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:43803720 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:44047575 A>T maps to NM_015937.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:44047575 A>T maps to NM_015937.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:18577622 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:18577622 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:18577622 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:18577622 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:106524640 C>T maps to NM_002649.2 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:106524640 C>T maps to NM_002649.2 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:46527514 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:46527514 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:46527514 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:46527514 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:8784283 G>A maps to NM_001142633.1 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:8784283 G>A maps to NM_001142633.1 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:6371462 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:6371462 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:6371462 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:6371462 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:51586694 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:51586694 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:51940968 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:51940968 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:51586694 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:51586694 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:31532871 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:31532871 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42363551 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42363551 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:42363551 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:42363551 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:42434277 G>A maps to ENST00000397272 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:42434277 G>A maps to ENST00000397272 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:9343490 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:9343490 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:9343490 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:9343490 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:219487616 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:219487616 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:39791268 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:39791268 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:39791268 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:39791268 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:17056429 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:17056429 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:17056429 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:17056429 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:41510482 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:41510482 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:105397020 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:105397020 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:68045395 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:68045395 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:114877596 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:114877596 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:126726844 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:126726844 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:131908476 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:131908476 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:118380530 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:118380530 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:118380530 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:118380530 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:118203901 A>G maps to NM_001011709.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:118203901 A>G maps to NM_001011709.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:55895112 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:55895112 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:55895112 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:55895112 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:2177887 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:2177887 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:86274399 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:86274399 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:86274399 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:86274399 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:7415054 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:7415054 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:7415054 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:7415054 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:79773359 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:79773359 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:79773359 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:79773359 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:75608735 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:75608735 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:167370603 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:167370603 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:120175881 G>A maps to NM_014352.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:120175881 G>A maps to NM_014352.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:82763574 G>T maps to NM_000307.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:82763574 G>T maps to NM_000307.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:81747127 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:81747127 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:81747127 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:81747127 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:202338694 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:202338694 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:202465791 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:202465791 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:202338694 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:202338694 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:202465791 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:202465791 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:104251167 G>A maps to NM_015316.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:104251167 G>A maps to NM_015316.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:182826021 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:182826021 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:182826021 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:182826021 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:30655031 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:30655031 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:30655031 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:30655031 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:23522756 C>T maps to NM_020227.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:23522756 C>T maps to NM_020227.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:186279074 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:186279074 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:54385942 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:54385942 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:54042111 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:54042111 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:54042111 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:54042111 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:148559745 T>C maps to NM_138364.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:148559745 T>C maps to NM_138364.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:20414613 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:20414613 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:20414613 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:20414613 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:4705019 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:4705019 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:18905887 C>T maps to NM_016335.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:18905887 C>T maps to NM_016335.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:62626447 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:62626447 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:1581070 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:1581070 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:1581070 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:1581070 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:12817284 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:12817284 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:43352208 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:43352208 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:239174 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:239174 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:151237257 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:151237257 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:151237257 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:151237257 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:71627021 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:71627021 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:21011690 G>T maps to NM_001010915.3 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:21011690 G>T maps to NM_001010915.3 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:62278398 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:62278398 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:157930975 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:157930975 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:71139814 C>A maps to NM_002849.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:71139814 C>A maps to NM_002849.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:52359849 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:52359849 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:51390573 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:51390573 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:18311290 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:18311290 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:18311290 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:18311290 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:135920706 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:135920706 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:135920706 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:135920706 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:125782612 A>T maps to NM_012197.3 K557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:125782612 A>T maps to NM_012197.3 K557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:76251860 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:76251860 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:76251860 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:76251860 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:17695401 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:17695401 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:17695401 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:17695401 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:134505752 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:134505752 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:134505752 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:134505752 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:173879406 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:173879406 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:173879406 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:173879406 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:130883566 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:130883566 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:179529265 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:179529265 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:79324411 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:79324411 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:79324411 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:79324411 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:33783409 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:33783409 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:33783409 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:33783409 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:15593399 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:15593399 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:50137832 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:50137832 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:43940360 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:43940360 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:103160031 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:103160031 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:8424338 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:8424338 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:85578242 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:85578242 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:85578242 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:85578242 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:117244220 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:117244220 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:117248729 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:117248729 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:117244220 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:117244220 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:86007124 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:86007124 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:163043249 G>C maps to NM_001102445.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:163043249 G>C maps to NM_001102445.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:72985273 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:72985273 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:72985273 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:72985273 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:241161912 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:241161912 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:241161912 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:241161912 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:22872179 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:22872179 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:22872179 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:22872179 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:30538359 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:30538359 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:73026417 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:73026417 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:104987815 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:104987815 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:87377098 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:87377098 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:87377098 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:87377098 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:104324448 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:104324448 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:104324448 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:104324448 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:30776106 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:30776106 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:55745711 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrX:55745711 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:55745711 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:55745711 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:16794724 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:16794724 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:16794724 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:16794724 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:45991668 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:45991668 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:45991668 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:45991668 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:107035615 G>A maps to NM_032730.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:107035615 G>A maps to NM_032730.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:32376217 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:32376217 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:32376217 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:32376217 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:33937436 C>A maps to NM_016568.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:33937436 C>A maps to NM_016568.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:38931275 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:38931275 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:237868660 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:237868660 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:237802405 G>A maps to NM_001035.2 G2340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:237802405 G>A maps to NM_001035.2 G2340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:237868660 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:237868660 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33873859 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33873859 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33873870 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33873870 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:34111907 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:34111907 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:33873859 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:33873859 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:33955874 G>A maps to NM_001036.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:33955874 G>A maps to NM_001036.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:153363076 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:153363076 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:153363076 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:153363076 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:18267161 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:18267161 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:18267161 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:18267161 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:18253000 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:18253000 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:68312237 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:68312237 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:200213972 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:200213972 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:31103134 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:31103134 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:31103134 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:31103134 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:25670108 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:25670108 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:25670108 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:25670108 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:41564599 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:41564599 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:41564599 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:41564599 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:38743163 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:38743163 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:38755305 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:38755305 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:166900187 A>T maps to NM_001165963.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:166900187 A>T maps to NM_001165963.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:166900187 A>T maps to NM_001165963.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:166900187 A>T maps to NM_001165963.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:123516160 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:123516160 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:123516160 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:123516160 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:62020999 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:62020999 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:76895163 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:76895163 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:4277429 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:4277429 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:4277429 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:4277429 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:71394317 G>T maps to NM_001144952.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:71394317 G>T maps to NM_001144952.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:169563082 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:169563082 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:169563082 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:169563082 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:61600476 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:61600476 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:61600476 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr18:61600476 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:28607140 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:28607140 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:28607140 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:28607140 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:46316237 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:46316237 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:46316237 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:46316237 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:81372775 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:81372775 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:49160176 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:49160176 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:146246015 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:146246015 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:146246015 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:146246015 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:56347974 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:56347974 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:56347974 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:56347974 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:65417992 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:65417992 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:65417992 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:65417992 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:164733518 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:164733518 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:2234680 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:2234680 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:70244995 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:70244995 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:70244995 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:70244995 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:25918619 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:25918619 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:131722481 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:131722481 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:92911712 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:92911712 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:92911712 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:92911712 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107323603 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107323603 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107330834 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:107330834 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:103017306 A>T maps to ENST00000354356 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:103017306 A>T maps to ENST00000354356 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:16682239 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:16682239 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:46601278 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:46601278 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:46601533 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:46601533 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:46601278 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:46601278 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:205631991 C>G maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:205631991 C>G maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:72319074 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:72319074 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:72420933 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:72420933 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:72319074 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:72319074 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:72420933 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:72420933 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:74451872 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:74451872 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:74451872 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:74451872 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:24895480 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:24895480 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:24895480 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:24895480 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:307847 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:307847 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:11059649 T>A maps to NM_003042.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:11059649 T>A maps to NM_003042.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:59224502 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:59224502 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:59224502 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:59224502 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:146461415 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:146461415 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:47632110 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:47632110 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:55808846 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:55808846 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:55808846 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:55808846 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:130932730 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:130932730 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:246093032 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:246093032 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:127732149 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:127732149 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:127732149 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:127732149 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:25200113 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:25200113 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:2309410 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:2309410 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:603046 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:603046 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:231193364 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:231193364 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:16727320 C>T maps to NM_198546.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:16727320 C>T maps to NM_198546.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:99913227 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:99913227 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:75123481 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:75123481 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:136314882 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:136314882 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:14156955 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:14156955 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55648589 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55648589 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55653325 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55653325 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:55648589 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:55648589 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:55653325 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:55653325 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158592677 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158592677 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:158592677 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:158592677 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:94794785 C>G maps to NM_006415.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr9:94794785 C>G maps to NM_006415.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:104942527 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:104942527 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:104942527 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:104942527 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:54707729 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:54707729 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:54707729 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:54707729 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:57105906 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:57105906 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:57105906 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:57105906 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:23016251 G>T maps to NM_001052.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:23016251 G>T maps to NM_001052.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:53028763 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:53028763 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:134478231 C>A maps to NM_173344.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:134478231 C>A maps to NM_173344.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:86090335 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:86090335 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:86090335 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:86090335 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:68437018 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:68437018 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:47761389 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:47761389 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:47761389 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:47761389 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:36467533 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:36467533 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:36467533 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:36467533 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:74281317 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:74281317 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:48896838 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:48896838 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:48896838 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:48896838 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:74476121 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:74476121 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:74476121 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:74476121 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:37076791 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:37076791 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:37076791 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:37076791 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:70515569 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:70515569 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:70515569 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:70515569 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:48033871 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:48033871 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:48033871 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:48033871 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:31573432 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:31573432 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:31573432 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:31573432 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:44982433 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:44982433 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:149883571 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:149883571 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:75469693 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:75469693 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:75469693 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:75469693 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:16773136 C>T maps to NM_032796.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:16773136 C>T maps to NM_032796.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:160031763 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:160031763 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:10959721 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:10959721 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:13567749 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:13567749 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:167796235 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:167796235 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:35108430 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:35108430 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:154516364 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:154516364 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:3120263 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:3120263 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:3120263 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:3120263 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:53449280 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:53449280 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:20871391 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:20871391 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:69391329 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:69391329 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:69391329 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:69391329 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:1258781 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:1258781 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:246719865 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:246719865 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:115624255 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:115624255 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:115624255 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:115624255 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:105890201 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:105890201 A>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:2375093 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:2375093 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:2375093 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:2375093 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:43778908 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:43778908 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:43778908 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:43778908 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:76452075 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:76452075 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:11509421 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:11509421 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:156381702 C>G maps to NM_138379.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:156381702 C>G maps to NM_138379.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:168165947 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:168165947 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:168165947 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:168165947 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:60690039 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:60690039 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:105361662 C>T maps to NM_030788.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:105361662 C>T maps to NM_030788.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:165788876 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:165788876 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:165788876 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:165788876 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:48358150 C>T maps to NM_001143842.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:48358150 C>T maps to NM_001143842.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:129694056 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:129694056 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:130184284 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:130184284 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:129694056 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:129694056 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:130184284 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:130184284 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:148554838 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:148554838 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:148554838 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:148554838 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:48741763 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:48741763 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:48741763 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:48741763 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:15470621 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:15470621 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:119155825 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:119155825 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:57917064 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:57917064 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:57917064 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:57917064 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:4294545 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:4294545 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:68699136 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:68699136 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:117789095 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:117789095 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:117789095 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:117789095 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:83424681 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:83424681 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:83424681 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:83424681 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:170858354 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:170858354 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:175097582 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:175097582 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:186327833 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:186327833 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:186327833 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:186327833 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:10969904 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr21:10969904 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr21:10969904 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr21:10969904 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:17204078 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:17204078 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:17204078 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:17204078 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:72955930 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:72955930 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:72955930 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:72955930 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:230679753 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:230679753 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:230679753 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:230679753 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:100470536 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:100470536 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:49719371 G>T maps to NM_005480.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr12:49719371 G>T maps to NM_005480.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:49684471 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:49684471 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:99689319 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:99689319 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:9305869 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:9305869 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:9305869 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:9305869 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:6115580 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chrY:6115580 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:6115580 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrY:6115580 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:91077031 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr14:91077031 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:89323697 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:89323697 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:117618732 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:117618732 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:117618732 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:117618732 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:80741162 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:80741162 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:80741162 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:80741162 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:43465871 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr22:43465871 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:167754836 A>T maps to NM_031949.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:167754836 A>T maps to NM_031949.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179574230 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179574230 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179592238 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179592238 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179660022 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179660022 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179664701 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:179664701 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:179574230 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:179574230 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:179592238 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:179592238 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:179660022 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:179660022 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:40818441 C>T maps to NM_016437.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:40818441 C>T maps to NM_016437.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:113223608 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr13:113223608 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:10463006 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:10463006 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:10463006 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:10463006 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:103718492 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:103718492 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:103718492 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:103718492 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:170911872 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:170911872 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42286811 G>A maps to NM_014233.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:42286811 G>A maps to NM_014233.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:54528703 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:54528703 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:54528703 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:54528703 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:158922351 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:158922351 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:158922351 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:158922351 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:33891680 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:33891680 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:216219936 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:216219936 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:216348529 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:216348529 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:216501000 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:216501000 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:216348529 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:216348529 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:216501000 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:216501000 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:58285629 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:58285629 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:58285629 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:58285629 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:61597819 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:61597819 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:76817976 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:76817976 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:76817976 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:76817976 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:41025488 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:41025488 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:41064756 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chrX:41064756 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:57015899 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:57015899 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:57015899 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr20:57015899 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:31748351 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:31748351 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:153078345 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:153078345 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:153078345 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr6:153078345 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:134095248 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:134095248 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:134095248 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr11:134095248 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:38836630 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:38836630 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:38948929 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:38948929 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:54610348 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:54610348 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:98823025 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:98823025 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:98823025 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:98823025 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:6166948 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:6166948 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:71176998 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:71176998 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:71176998 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:71176998 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:110428387 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:110428387 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:110428387 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr5:110428387 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:167240286 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:167240286 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:167240286 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:167240286 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:228788696 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:228788696 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:228788696 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr2:228788696 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:68352353 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:68352353 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:90278899 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:90278899 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:90278899 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr15:90278899 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:141416081 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:141416081 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:141416081 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr7:141416081 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:134232796 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:134232796 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:134232796 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr8:134232796 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:68620704 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:68620704 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:68620704 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:68620704 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:21823961 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:21823961 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:17353366 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:17353366 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:17353366 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:17353366 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:183474580 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:183474580 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:44624660 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:44624660 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:44624660 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr4:44624660 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:27437998 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr10:27437998 T>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:22837736 C>A maps to NM_014870.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:22837736 C>A maps to NM_014870.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:52981762 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:52981762 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:52981762 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:52981762 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:67441685 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:67441685 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:67441685 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr16:67441685 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:115819007 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:115819007 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:147108712 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:147108712 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:147108712 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:147108712 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:50380530 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:50380530 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:50380530 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr3:50380530 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:9530646 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:9530646 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:21792501 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:21792501 G>C did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:12540929 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:12540929 A>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:38089280 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:38089280 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:38089280 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr19:38089280 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:86123354 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:86123354 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:238048629 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:238048629 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:238048629 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr1:238048629 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38028494 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38028494 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38028500 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38028500 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38028503 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38028503 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:38028500 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:38028500 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:38031515 C>T maps to NM_199321.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:38031515 C>T maps to NM_199321.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:38031553 C>T maps to NM_199321.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01W-0928-08 chr17:38031553 C>T maps to NM_199321.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:113644494 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:113644494 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:58858215 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:58858215 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:66899348 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:66899348 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:95696787 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:95696787 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:95696787 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:95696787 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:31438824 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:31438824 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:48543287 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:48543287 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:48543287 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:48543287 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:81648823 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:81648823 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:24249671 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:24249671 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:77356176 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:77356176 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:43777291 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:43777291 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:43777291 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:43777291 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:116059241 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:116059241 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:50307596 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:50307596 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:50307596 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:50307596 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:31868347 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:31868347 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:112048029 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:112048029 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:101462074 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:101462074 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:101462074 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:101462074 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:235359311 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:235359311 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:235359311 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:235359311 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:7081932 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:7081932 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:216214387 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:216214387 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:51096751 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:51096751 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:113505179 A>C maps to NM_001690.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:113505179 A>C maps to NM_001690.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:52549429 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:52549429 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:52549429 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:52549429 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:45003661 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:45003661 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:45003661 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:45003661 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr21:11085600 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr21:11085600 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr21:11039044 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr21:11039044 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:56999682 C>T maps to NM_013449.3 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:56999682 C>T maps to NM_013449.3 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:13579270 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:13579270 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:45472740 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:45472740 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:91691110 G>T maps to NM_001102368.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:91691110 G>T maps to NM_001102368.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:76449107 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:76449107 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:76449107 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:76449107 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:11013906 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:11013906 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:34684220 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:34684220 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:24950656 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:24950656 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr21:33830051 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr21:33830051 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr21:33830051 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr21:33830051 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:6707344 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:6707344 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:37170014 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:37170014 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:37170014 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:37170014 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:39612309 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:39612309 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:39612309 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:39612309 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:38385738 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:38385738 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:13365803 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:13365803 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:13365803 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:13365803 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:65014201 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:65014201 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:17551850 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:17551850 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:17551850 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:17551850 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:41535064 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:41535064 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:49314744 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:49314744 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:219869207 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:219869207 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:77246897 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:77246897 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:3678009 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:3678009 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:64092697 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:64092697 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:64092697 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:64092697 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:4262229 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:4262229 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:149792007 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:149792007 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:104061955 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:104061955 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:104061955 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:104061955 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:49048413 G>A maps to NM_001194998.1 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:49048413 G>A maps to NM_001194998.1 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:57731824 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:57731824 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:9940470 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:9940470 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:11884530 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:11884530 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:11884530 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:11884530 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:11062909 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:11062909 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:74443828 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:74443828 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:122849278 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:122849278 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:201719418 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:201719418 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:62412102 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:62412102 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:47840724 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:47840724 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:47840724 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:47840724 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:103491968 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:103491968 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:103491968 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:103491968 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:76104109 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:76104109 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:148552243 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:148552243 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:148552243 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:148552243 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:211518855 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:211518855 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:211518855 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:211518855 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:125639699 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:125639699 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:47712882 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:47712882 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:44806942 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:44806942 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:44806942 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:44806942 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:99434066 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:99434066 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:15732949 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:15732949 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:45429902 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:45429902 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:45429902 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:45429902 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:53326881 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:53326881 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:53326881 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:53326881 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:69715195 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:69715195 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:69715195 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:69715195 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:10244835 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:10244835 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:10244835 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:10244835 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:7577930 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:7577930 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:25766149 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:25766149 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:131646711 G>A maps to ENST00000355311 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:131646711 G>A maps to ENST00000355311 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:56102262 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:56102262 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:71497369 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:71497369 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:71497369 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:71497369 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:212589970 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:212589970 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:212589970 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:212589970 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:15091226 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:15091226 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:15091226 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:15091226 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:89801886 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:89801886 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:89801886 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:89801886 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:147820884 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:147820884 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:157718499 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:157718499 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:157718499 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:157718499 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:91438583 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:91438583 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:186358966 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:186358966 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:186358966 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:186358966 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:102670570 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:102670570 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:102670570 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:102670570 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:153485165 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:153485165 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:216236617 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:216236617 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:216236617 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:216236617 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:50316080 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:50316080 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:170224460 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:170224460 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:170224460 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:170224460 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:151818707 C>T maps to NM_022087.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:151818707 C>T maps to NM_022087.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:155143223 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:155143223 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr21:34889465 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr21:34889465 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:101012210 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:101012210 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:89734358 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:89734358 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:89734358 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:89734358 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:42064792 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:42064792 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:231406869 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:231406869 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:231406869 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:231406869 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:93518679 C>T maps to NM_004466.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:93518679 C>T maps to NM_004466.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:95327091 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:95327091 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:57689911 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:57689911 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:66961497 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:66961497 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:37284393 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:37284393 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:96322516 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:96322516 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:96322516 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:96322516 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:65147068 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:65147068 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:65147068 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:65147068 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:94452137 C>G maps to NM_002729.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:94452137 C>G maps to NM_002729.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:26044316 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:26044316 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:71048494 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:71048494 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:118960267 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:118960267 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:132388062 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:132388062 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:135585184 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:135585184 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:23885761 C>T maps to NM_002167.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:23885761 C>T maps to NM_002167.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:104961307 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:104961307 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:22768235 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:22768235 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:49064512 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:49064512 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:95877660 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:95877660 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:46182454 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:46182454 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:75914497 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr5:75914497 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:75914497 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:75914497 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:149944428 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:149944428 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:6150574 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:6150574 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:196303206 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:196303206 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:196303206 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:196303206 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:71949405 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:71949405 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:138552663 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:138552663 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:52647342 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:52647342 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:52647342 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:52647342 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:63418910 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:63418910 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:6999366 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:6999366 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr18:21513989 A>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr18:21513989 A>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:21513989 A>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:21513989 A>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:32745898 A>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:32745898 A>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:46732928 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:46732928 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:18487466 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:18487466 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:35989305 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:35989305 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:54800124 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:54800124 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:54800124 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:54800124 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:96906021 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:96906021 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:82061873 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:82061873 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:82061873 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:82061873 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:100179735 G>T maps to NM_002319.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:100179735 G>T maps to NM_002319.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:74621378 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:74621378 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:74621378 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:74621378 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:56862930 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:56862930 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:56862930 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:56862930 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:20112536 G>A maps to NM_021020.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:20112536 G>A maps to NM_021020.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:117944870 A>C maps to NM_006699.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:117944870 A>C maps to NM_006699.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:20202889 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:20202889 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:112766149 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:112766149 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:112766149 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:112766149 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:151921088 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:151921088 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:55531018 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr16:55531018 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:108776233 G>A maps to NM_014429.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:108776233 G>A maps to NM_014429.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:31332410 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:31332410 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:31332410 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:31332410 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:41955402 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:41955402 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:47709955 G>C maps to NM_000251.1 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:47709955 G>C maps to NM_000251.1 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:105916553 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:105916553 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:11273753 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:11273753 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:11273753 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:11273753 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:135515665 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:135515665 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:135515665 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:135515665 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:10260908 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:10260908 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:10450589 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:10450589 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:10362502 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:10362502 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:10362502 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:10362502 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:36717703 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:36717703 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:36717703 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:36717703 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:27424662 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:27424662 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:26462559 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:26462559 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:52571635 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:52571635 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:128366434 G>A maps to ENST00000389524 Q932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:128366434 G>A maps to ENST00000389524 Q932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:24426111 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:24426111 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:24426160 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:24426160 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:24426160 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:24426160 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:152496707 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:152496707 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:204948556 C>A maps to ENST00000367172 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:204948556 C>A maps to ENST00000367172 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:47892632 T>G maps to NM_152995.4 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:47892632 T>G maps to NM_152995.4 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:129317692 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:129317692 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:129317701 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:129317701 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:129317692 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:129317692 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:129317701 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:129317701 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:2937232 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:2937232 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:18937478 C>T maps to NM_182543.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:18937478 C>T maps to NM_182543.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:113444409 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:113444409 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:183664319 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:183664319 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:183664319 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:183664319 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:50959810 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:50959810 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:247694782 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:247694782 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:247694782 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:247694782 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:55889776 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:55889776 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:55889776 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:55889776 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:30660799 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:30660799 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:3938097 G>A maps to NM_020367.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:3938097 G>A maps to NM_020367.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:657855 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:657855 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:66239988 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:66239988 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:10459251 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:10459251 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:15408261 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chrX:15408261 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:15408261 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:15408261 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:59812274 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:59812274 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:8678178 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:8678178 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:8678178 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:8678178 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:54826138 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:54826138 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:203030092 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:203030092 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:203030092 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:203030092 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:47305394 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:47305394 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:10395958 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:10395958 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:10395958 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:10395958 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:150998174 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:150998174 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:150998174 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:150998174 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:40944252 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:40944252 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:178310649 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:178310649 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:204126308 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:204126308 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:204126308 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:204126308 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:25338250 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:25338250 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:25338250 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:25338250 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:34288861 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:34288861 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:35827583 C>G maps to NM_002951.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:35827583 C>G maps to NM_002951.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:237843723 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:237843723 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:33822771 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:33822771 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:33822771 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr15:33822771 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:33321431 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:33321431 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:134990426 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:134990426 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:55753420 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:55753420 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:53740093 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr4:53740093 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:102249671 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:102249671 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:156128695 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:156128695 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:122629996 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:122629996 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:56598326 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:56598326 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr18:61231204 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr18:61231204 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:61231204 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:61231204 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:61327901 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr18:61327901 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:29908967 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:29908967 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:26694877 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:26694877 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:26694877 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:26694877 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:25263005 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:25263005 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:20016679 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:20016679 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:20016679 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:20016679 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:88218186 G>A maps to NM_006416.4 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:88218186 G>A maps to NM_006416.4 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:31833120 C>T maps to NM_025257.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:31833120 C>T maps to NM_025257.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:85266386 T>A maps to NM_182767.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:85266386 T>A maps to NM_182767.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:55728141 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr16:55728141 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:101631627 G>A maps to NM_180991.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:101631627 G>A maps to NM_180991.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:88328773 G>T maps to NM_015567.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr13:88328773 G>T maps to NM_015567.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:70352018 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:70352018 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:70352230 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:70352230 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:108521456 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr10:108521456 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:108521456 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr10:108521456 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:231033727 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:231033727 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:231033727 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:231033727 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:123599914 G>A maps to NM_001174046.1 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:123599914 G>A maps to NM_001174046.1 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:158632847 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr1:158632847 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:35470093 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr14:35470093 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:35470093 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr14:35470093 T>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:57496711 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr12:57496711 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:57496711 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:57496711 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:146657785 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr5:146657785 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:47228394 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:47228394 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:30310288 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr17:30310288 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:85431863 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:85431863 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:85431863 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:85431863 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:37985772 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:37985772 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:120818423 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:120818423 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:120818423 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:120818423 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:32797630 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr6:32797630 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:54617691 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:54617691 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:100225836 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:100225836 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:100225836 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:100225836 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:72058388 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr12:72058388 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:52972445 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr13:52972445 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:33255453 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr22:33255453 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:94808054 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr8:94808054 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:68934241 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr4:68934241 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:99854064 C>G maps to NM_022144.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chrX:99854064 C>G maps to NM_022144.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:100100547 C>A maps to NM_014820.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:100100547 C>A maps to NM_014820.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:32829544 G>C maps to NM_052841.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr1:32829544 G>C maps to NM_052841.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:90800273 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:90800273 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:30459126 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:30459126 C>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:30458832 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:30458832 C>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:179643947 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:179643947 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:179643947 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:179643947 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:157000037 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:157000037 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:17728416 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:17728416 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:113672135 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:113672135 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:11941941 C>T maps to ENST00000399455 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:11941941 C>T maps to ENST00000399455 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:50731406 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr15:50731406 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:144811455 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr6:144811455 G>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:54545618 G>A maps to NM_198481.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:54545618 G>A maps to NM_198481.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:123332371 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr7:123332371 T>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:128482332 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:128482332 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:128482332 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:128482332 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:20182142 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:20182142 T>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:190334004 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:190334004 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:30989874 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr8:30989874 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:58380427 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr11:58380427 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:58380427 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr11:58380427 A>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:18297555 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:18297555 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:18297555 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr20:18297555 G>C did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:64293188 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:64293188 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:22154331 G>T maps to NM_007153.3 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:22154331 G>T maps to NM_007153.3 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:44541962 G>A maps to ENST00000436261 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr3:44541962 G>A maps to ENST00000436261 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:44541962 G>A maps to ENST00000436261 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr3:44541962 G>A maps to ENST00000436261 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:62596352 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr20:62596352 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:30934317 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:30934317 C>T did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:36967452 G>A maps to NM_001145343.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:36967452 G>A maps to NM_001145343.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:99171065 C>T maps to NM_001083956.1 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr7:99171065 C>T maps to NM_001083956.1 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:22375755 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr19:22375755 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:22375755 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr19:22375755 G>A did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:24087098 G>A maps to NM_021916.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr22:24087098 G>A maps to NM_021916.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:185800482 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01D-1040-01 chr2:185800482 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:185800482 A>G did not map to a codon.
Sequencing variant TCGA-55-1594-01A-01W-0928-08 chr2:185800482 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:70310247 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:70310247 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:94574114 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:94574114 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:119024705 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:119024705 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:89178684 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:89178684 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:43635169 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:43635169 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:33549520 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:33549520 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:167805450 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:167805450 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:100237012 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:100237012 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:148049133 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:148049133 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:161575172 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:161575172 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:109663844 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:109663844 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:4829789 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:4829789 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:101425675 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:101425675 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:56448085 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:56448085 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:115231559 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:115231559 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:37454154 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:37454154 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:69972346 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:69972346 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:69420602 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:69420602 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:49712512 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:49712512 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:121289730 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:121289730 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57870899 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57870899 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:5220494 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:5220494 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:138884316 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:138884316 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:42492797 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:42492797 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:137505152 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:137505152 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:78084270 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:78084270 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:60466672 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:60466672 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:31695644 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:31695644 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:256467 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:256467 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:118867242 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:118867242 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:184614952 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:184614952 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:175763946 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:175763946 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:127901386 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:127901386 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:69688736 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:69688736 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:86115951 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:86115951 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:49093384 T>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:49093384 T>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:28458531 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:28458531 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158299036 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158299036 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:111325759 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:111325759 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:38450863 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:38450863 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:26915711 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:26915711 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:105615274 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:105615274 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:48275402 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:48275402 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:18895216 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:18895216 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:47628278 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:47628278 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr13:46632575 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr13:46632575 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:211504639 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:211504639 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:1331405 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:1331405 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48339454 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48339454 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:27021628 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:27021628 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:27012291 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:27012291 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:34189983 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:34189983 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:113987937 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:113987937 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:114111195 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:114111195 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:10772810 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:10772810 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:35994204 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:35994204 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:96732013 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:96732013 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41630814 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41630814 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:115143584 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:115143584 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:102027868 A>G maps to NM_001362.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:102027868 A>G maps to NM_001362.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:32663082 C>A maps to ENST00000357033 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:32663082 C>A maps to ENST00000357033 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:70191946 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:70191946 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:11572652 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:11572652 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:89703135 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:89703135 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:186502304 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:186502304 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:129203062 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:129203062 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:62375660 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:62375660 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:6896609 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:6896609 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:120605866 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:120605866 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:16496037 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:16496037 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:34136177 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:34136177 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:23721646 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:23721646 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:103497225 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:103497225 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:5798976 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:5798976 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:75919098 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:75919098 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:154182322 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:154182322 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:16477955 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:16477955 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:139155444 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:139155444 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:118968428 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:118968428 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:152857874 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:152857874 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:10070483 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:10070483 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:172629174 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:172629174 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr13:28919715 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr13:28919715 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:147022065 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:147022065 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:89423996 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:89423996 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:37443832 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:37443832 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:17443595 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:17443595 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:29541929 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:29541929 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:151336625 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:151336625 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:24629835 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:24629835 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:42483488 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:42483488 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:94159683 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:94159683 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:141526433 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:141526433 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:34029666 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:34029666 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:6903611 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:6903611 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:144928020 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:144928020 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:144928052 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:144928052 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:26477076 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:26477076 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153228905 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153228905 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:48682233 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:48682233 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:31585352 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:31585352 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:92848848 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:92848848 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:138758726 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:138758726 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135583114 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135583114 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:183772868 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:183772868 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:148585625 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:148585625 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:25679178 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:25679178 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:65622571 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:65622571 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:55195673 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:55195673 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:99182411 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:99182411 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:143226508 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:143226508 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:234104230 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:234104230 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:145539489 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:145539489 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:54776266 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:54776266 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:19432273 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:19432273 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:6814606 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:6814606 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:55956359 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:55956359 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:24762123 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:24762123 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:51329825 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:51329825 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:51362774 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:51362774 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:52882426 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:52882426 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:31913932 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:31913932 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:31913954 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:31913954 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:109004632 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:109004632 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:54818979 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:54818979 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:42367974 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:42367974 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:54418222 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:54418222 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:9094324 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:9094324 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:166973412 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:166973412 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:140953472 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:140953472 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:43366550 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:43366550 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:100395867 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:100395867 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:37187563 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:37187563 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:2535557 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:2535557 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:18306705 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:18306705 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:10177546 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:10177546 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:149901258 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:149901258 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:15826686 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:15826686 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:54905484 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:54905484 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr18:70525973 T>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr18:70525973 T>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:17742401 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:17742401 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:29954821 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:29954821 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:5947524 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:5947524 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:5947526 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:5947526 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:54318305 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:54318305 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:56223992 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:56223992 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:179533784 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:179533784 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:101092438 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:101092438 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:13786083 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:13786083 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:74078613 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:74078613 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:47775775 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:47775775 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:122064964 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:122064964 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:21698669 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:21698669 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:21739771 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:21739771 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:9520342 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:9520342 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:9520344 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:9520344 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:20787794 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:20787794 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:58286622 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:58286622 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57984952 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57984952 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:161159490 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:161159490 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153693897 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:153693897 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:118320962 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:118320962 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:122280328 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:122280328 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:149206540 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:149206540 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:18800570 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:18800570 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:146077810 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:146077810 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:11083046 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:11083046 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:23524411 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:23524411 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:53223858 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:53223858 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:30664595 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:30664595 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:43773656 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:43773656 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:63996662 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:63996662 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:54122077 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:54122077 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:43107026 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:43107026 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:157414048 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:157414048 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:123954504 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:123954504 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:4662121 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:4662121 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:34829926 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:34829926 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:5977957 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:5977957 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:2861282 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:2861282 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:21938084 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:21938084 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:178433250 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:178433250 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:211485976 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:211485976 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:107047991 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:107047991 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:30331738 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:30331738 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:78680290 T>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:78680290 T>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:178999665 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:178999665 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:33955694 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:33955694 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:26715560 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:26715560 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:52002488 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:52002488 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:160580534 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:160580534 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:95820626 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:95820626 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:70643678 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:70643678 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:68338172 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:68338172 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:67358474 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:67358474 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:45758932 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:45758932 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:28835104 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:28835104 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:51664797 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:51664797 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:101630016 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:101630016 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:108432551 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:108432551 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:106959943 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:106959943 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158589177 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158589177 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158639463 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158639463 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:43146744 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:43146744 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:119552204 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:119552204 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:149489613 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:149489613 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:37373189 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:37373189 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr13:99116092 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr13:99116092 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:48848486 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:48848486 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48879048 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48879048 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:37259211 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:37259211 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:72988683 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:72988683 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:132565421 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:132565421 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:248027963 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:248027963 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:31234407 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:31234407 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:71533739 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:71533739 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:43570417 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:43570417 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:68490008 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:68490008 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:68531065 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:68531065 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:20359461 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:20359461 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:35398838 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:35398838 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:45682977 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr22:45682977 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:216260242 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:216260242 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:77237617 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:77237617 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135631209 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:135631209 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:65252653 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:65252653 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:98851063 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:98851063 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr18:54348648 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr18:54348648 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:168513089 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:168513089 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:167992325 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:167992325 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:129350203 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:129350203 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:46332838 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chrX:46332838 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:21477666 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:21477666 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:56854162 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:56854162 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:58117828 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:58117828 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:101590382 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:101590382 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:101590382 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:101590382 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:30557816 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:30557816 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:30557816 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:30557816 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:8022096 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:8022096 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:35583092 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:35583092 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:207452764 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:207452764 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:207452764 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:207452764 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:73156845 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:73156845 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:73186679 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:73186679 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:73156845 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:73156845 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:15511731 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:15511731 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr19:15511731 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr19:15511731 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:91642044 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:91642044 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:29751964 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:29751964 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:21900146 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:21900146 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:21900146 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:21900146 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:77257805 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:77257805 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:77257805 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:77257805 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:70740272 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:70740272 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:37481827 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:37481827 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:29409388 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:29409388 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:10471498 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:10471498 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:10471498 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:10471498 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:112162745 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:112162745 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:112162745 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:112162745 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:21266344 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:21266344 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:68139537 T>A maps to NM_006421.3 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:68139537 T>A maps to NM_006421.3 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:155935546 G>A maps to NM_001162383.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:155935546 G>A maps to NM_001162383.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:157495269 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:157495269 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:157495269 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:157495269 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:177190045 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:177190045 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:177190045 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:177190045 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:101186925 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:101186925 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:176853724 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:176853724 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:176853724 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:176853724 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:112255591 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:112255591 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:343555 C>T maps to NM_003502.3 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:343555 C>T maps to NM_003502.3 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:168725371 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:168725371 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr21:11038766 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr21:11038766 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:11038766 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:11038766 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:180326300 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:180326300 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:56393544 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:56393544 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:56393544 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:56393544 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:68031300 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:68031300 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:4563766 C>A maps to ENST00000359075 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:4563766 C>A maps to ENST00000359075 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:67702009 C>T maps to ENST00000291011 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:67702009 C>T maps to ENST00000291011 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:71233217 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:71233217 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:40955389 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:40955389 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:40955389 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:40955389 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:40899890 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:40899890 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:40899890 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:40899890 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:116185835 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:116185835 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:116185835 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:116185835 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:86253805 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:86253805 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:86253805 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:86253805 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:181705620 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:181705620 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:181719608 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:181719608 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:181705620 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:181705620 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:181719608 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:181719608 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:48667691 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:48667691 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:174978974 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:174978974 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:174978974 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:174978974 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:116275697 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:116275697 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:116275697 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:116275697 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:121973003 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:121973003 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:121973003 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:121973003 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr21:44479545 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr21:44479545 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:89408624 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:89408624 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:89408624 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:89408624 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:67531444 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:67531444 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:67531444 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:67531444 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:83173835 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:83173835 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:21065232 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:21065232 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:17680397 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:17680397 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:17680397 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:17680397 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:214821290 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:214821290 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:93563197 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:93563197 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:93563200 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:93563200 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:93563197 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:93563197 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:93563200 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:93563200 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:86898147 C>T maps to NM_006536.5 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:86898147 C>T maps to NM_006536.5 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:74447153 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:74447153 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:140122319 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:140122319 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:140122319 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:140122319 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:6990179 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:6990179 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:54896977 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:54896977 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:95392588 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:95392588 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:2944463 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:2944463 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:103544260 G>T maps to NM_080629.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:103544260 G>T maps to NM_080629.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:139611251 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:139611251 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:86196116 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:86196116 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:137688343 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:137688343 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:137688343 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:137688343 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:47708332 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:47708332 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:47708332 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:47708332 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:211455112 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:211455112 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:34208794 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:34208794 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:34285451 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:34285451 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:34285451 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:34285451 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:113694627 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:113694627 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:113246673 A>G maps to NM_198123.1 L3554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:113246673 A>G maps to NM_198123.1 L3554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:113254005 T>A maps to NM_198123.1 K3471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:113254005 T>A maps to NM_198123.1 K3471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:113694627 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:113694627 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:148457366 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:148457366 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:148457366 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:148457366 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:18933234 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:18933234 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:69458866 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:69458866 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:69458866 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:69458866 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:37708204 G>T maps to NM_013385.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:37708204 G>T maps to NM_013385.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:39869181 G>C maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:39869181 G>C maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:59113520 C>A maps to NM_016651.5 S727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:59113520 C>A maps to NM_016651.5 S727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr12:100657685 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr12:100657685 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:100657685 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:100657685 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:137282529 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:137282529 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:137282529 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:137282529 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr13:60667930 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr13:60667930 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr13:60737652 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr13:60737652 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:11790354 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:11790354 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:11790354 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:11790354 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:169483832 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:169483832 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:169483832 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:169483832 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:63099327 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:63099327 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr13:99575504 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr13:99575504 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr13:99575504 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr13:99575504 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:116226095 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:116226095 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:97700640 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:97700640 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:97700640 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:97700640 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:183995660 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:183995660 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:183995660 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:183995660 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:45011970 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:45011970 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:45011970 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:45011970 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:77079715 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:77079715 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:120633840 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:120633840 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:120633840 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:120633840 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:66201912 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:66201912 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:13950827 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:13950827 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:592613 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:592613 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:592613 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:592613 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:208489110 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:208489110 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:208489110 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:208489110 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:130341169 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:130341169 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:130341169 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:130341169 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:177166285 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:177166285 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:82574914 G>T maps to NM_001008226.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:82574914 G>T maps to NM_001008226.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:10135024 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:10135024 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:10135024 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:10135024 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:163099770 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:163099770 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:163099770 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:163099770 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:92526039 G>A maps to ENST00000298047 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:92526039 G>A maps to ENST00000298047 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:8160758 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:8160758 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:40363393 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:40363393 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:115965312 A>G maps to ENST00000446284 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:115965312 A>G maps to ENST00000446284 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:240308562 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:240308562 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:240308562 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:240308562 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr13:49752747 C>A maps to NM_001079673.1 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr13:49752747 C>A maps to NM_001079673.1 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:80529849 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:80529849 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:71026062 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:71026062 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:71026062 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:71026062 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:17450470 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:17450470 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:17450470 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:17450470 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:161277950 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:161277950 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chrX:151337132 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chrX:151337132 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:81387877 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:81387877 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:95265332 T>C maps to NM_181702.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:95265332 T>C maps to NM_181702.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:51643269 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:51643269 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:51643269 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:51643269 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:39040613 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:39040613 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:39040613 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:39040613 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:155615702 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:155615702 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:155615702 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:155615702 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:100368683 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:100368683 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:100368683 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:100368683 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:37298808 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:37298808 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:63961970 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:63961970 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:63961970 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:63961970 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:71008169 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:71008169 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:71008169 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:71008169 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:32557550 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:32557550 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:186105682 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:186105682 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:95012033 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:95012033 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:94973151 G>A maps to ENST00000375660 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:94973151 G>A maps to ENST00000375660 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:68549133 T>A maps to NM_000619.2 *167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:68549133 T>A maps to NM_000619.2 *167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:3118154 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:3118154 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:3118154 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:3118154 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:309363 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:309363 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:73847964 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:73847964 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:19563559 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:19563559 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:19563559 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:19563559 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:126067959 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:126067959 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:126067959 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:126067959 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:15729638 C>T maps to NM_014647.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:15729638 C>T maps to NM_014647.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:128706347 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:128706347 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:115407878 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:115407878 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:28991502 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:28991502 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:241676331 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:241676331 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:39545944 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:39545944 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:39545944 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:39545944 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:55328121 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:55328121 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr19:55328121 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr19:55328121 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:30349753 G>T maps to NM_020805.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:30349753 G>T maps to NM_020805.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:32573643 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:32573643 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:32573643 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:32573643 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:54872442 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:54872442 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr19:54872442 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr19:54872442 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:101019516 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:101019516 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:18434299 A>G maps to NM_017448.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:18434299 A>G maps to NM_017448.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:90526230 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:90526230 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:70225833 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:70225833 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:70488885 C>A maps to NM_020794.2 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:70488885 C>A maps to NM_020794.2 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:41799787 G>A maps to NM_002344.5 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:41799787 G>A maps to NM_002344.5 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:6612753 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:6612753 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:6612753 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:6612753 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:71267477 C>A maps to NM_033141.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:71267477 C>A maps to NM_033141.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:187003539 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:187003539 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:187003539 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:187003539 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:43537082 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:43537082 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:43537082 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:43537082 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:2526501 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:2526501 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:75881898 C>T maps to NM_014763.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:75881898 C>T maps to NM_014763.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:17573569 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:17573569 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:10439777 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:10439777 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:10297636 C>A maps to NM_002472.2 E1699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:10297636 C>A maps to NM_002472.2 E1699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:123375979 T>C maps to NM_053025.3 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:123375979 T>C maps to NM_053025.3 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:47406709 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:47406709 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:47406709 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:47406709 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:78582296 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:78582296 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:71036820 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:71036820 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:71036820 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:71036820 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr12:124832633 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr12:124832633 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:123190665 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:123190665 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:123190665 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:123190665 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:25459483 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:25459483 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:7065230 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:7065230 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:7065230 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:7065230 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:115394054 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:115394054 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:115394054 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:115394054 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:33543157 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:33543157 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:33543157 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:33543157 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:44770477 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:44770477 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:18766492 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:18766492 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:18766492 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:18766492 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:156785952 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:156785952 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:156785952 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:156785952 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:110287766 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:110287766 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:110287766 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:110287766 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:203468031 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:203468031 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:24905868 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:24905868 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:66009152 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:66009152 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:66009152 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:66009152 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:112625306 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:112625306 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:55721651 C>A maps to NM_001142763.1 G962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:55721651 C>A maps to NM_001142763.1 G962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:47775558 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr21:47775558 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:71444880 T>C maps to NM_014982.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:71444880 T>C maps to NM_014982.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:17434236 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:17434236 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:72293700 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:72293700 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:144951960 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:144951960 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:647476 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:647476 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:96416741 C>G maps to NM_005392.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:96416741 C>G maps to NM_005392.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:51917745 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:51917745 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:155261780 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:155261780 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:155261780 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:155261780 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:242253059 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:242253059 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:242253059 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:242253059 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:131870003 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:131870003 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:131887643 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:131887643 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:131870003 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:131870003 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:131887643 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:131887643 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:118236529 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:118236529 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:118236529 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:118236529 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:121187352 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:121187352 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:121187352 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:121187352 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:35590989 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:35590989 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:35590989 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:35590989 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:127923294 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:127923294 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:74527239 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:74527239 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:74527239 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:74527239 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:23524574 C>A maps to NM_020227.2 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:23524574 C>A maps to NM_020227.2 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:150301010 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:150301010 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:74340919 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:74340919 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:162251579 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:162251579 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:214556632 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:214556632 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:214556632 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:214556632 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:198703599 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:198703599 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:198703599 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:198703599 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:15704358 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:15704358 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:40980916 G>T maps to ENST00000373198 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:40980916 G>T maps to ENST00000373198 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:27822644 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:27822644 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:27822644 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:27822644 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chrX:69504377 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chrX:69504377 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chrX:69504377 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chrX:69504377 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:99363412 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:99363412 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:63312066 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:63312066 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:178412213 G>T maps to ENST00000263528 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:178412213 G>T maps to ENST00000263528 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:173915512 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:173915512 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:103129145 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:103129145 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:79349385 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:79349385 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:103629459 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:103629459 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:72945022 C>G maps to NM_004296.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:72945022 C>G maps to NM_004296.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:33493528 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr19:33493528 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:7122776 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:7122776 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:39928597 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:39928597 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:19378287 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:19378287 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:19378287 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:19378287 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:77445836 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr11:77445836 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:77445836 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:77445836 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:108913208 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:108913208 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:108913208 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:108913208 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:237923195 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:237923195 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:237870245 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:237870245 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:237880667 G>A maps to NM_001035.2 L3498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:237880667 G>A maps to NM_001035.2 L3498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:237923195 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:237923195 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:33825664 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:33825664 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:166010961 C>T maps to NM_006922.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:166010961 C>T maps to NM_006922.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:18523046 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:18523046 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:83634562 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:83634562 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:83634562 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:83634562 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:9136542 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:9136542 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:9136542 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:9136542 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:101080532 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:101080532 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:101085251 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:101085251 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:101080532 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:101080532 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:101085251 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:101085251 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:75489175 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:75489175 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:61262140 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr18:61262140 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:7326243 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:7326243 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:7326243 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:7326243 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:99851648 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:99851648 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:14094972 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:14094972 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:46257355 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:46257355 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:46257355 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:46257355 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:48527320 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:48527320 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:48527320 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:48527320 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:113464873 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:113464873 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:48426859 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:48426859 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:8023639 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:8023639 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:21317748 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:21317748 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:121648047 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:121648047 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:108430969 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr10:108430969 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:108430969 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr10:108430969 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:97328457 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:97328457 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:97328457 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:97328457 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:44171586 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:44171586 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:12506571 C>A maps to NM_001128626.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr18:12506571 C>A maps to NM_001128626.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:141693947 G>A maps to NM_030964.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr5:141693947 G>A maps to NM_030964.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:6634006 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr5:6634006 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:41246782 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr22:41246782 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:41246782 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:41246782 T>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:74089280 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:74089280 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:48897165 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:48897165 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:48897165 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:48897165 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:120764164 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:120764164 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:70539459 C>A maps to NM_001128206.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:70539459 C>A maps to NM_001128206.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:93629548 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:93629548 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:93629548 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:93629548 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:28887554 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:28887554 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:17349629 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:17349629 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:17349629 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:17349629 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:162279766 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:162279766 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:85422433 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr6:85422433 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:15211779 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:15211779 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:27210458 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:27210458 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:72039384 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:72039384 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:72039384 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:72039384 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:11633038 G>T maps to ENST00000423059 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:11633038 G>T maps to ENST00000423059 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:137988828 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:137988828 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:27052284 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:27052284 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:27052284 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:27052284 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:81625716 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:81625716 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:148555130 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:148555130 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:148555130 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:148555130 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:195613813 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:195613813 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:195613813 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:195613813 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:123957834 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr6:123957834 A>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:73012638 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr12:73012638 C>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:57134502 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:57134502 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:142503716 A>T maps to ENST00000476941 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:142503716 A>T maps to ENST00000476941 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:99759061 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:99759061 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:99759061 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:99759061 A>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:138851547 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr7:138851547 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:138851547 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr7:138851547 G>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:76186178 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr14:76186178 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:76186178 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr14:76186178 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:179600340 T>A maps to NM_133378.4 T3700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:179600340 T>A maps to NM_133378.4 T3700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:43398253 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr15:43398253 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:26620936 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:26620936 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:35384223 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr9:35384223 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:35384223 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr9:35384223 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:35605994 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:35605994 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:35605994 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:35605994 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:76832157 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:76832157 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:106782444 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:106782444 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:106782444 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:106782444 T>C did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:177604974 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr4:177604974 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:177604974 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr4:177604974 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:12406758 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr1:12406758 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:12406758 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:12406758 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:2846783 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr20:2846783 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:22151409 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr16:22151409 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:22151409 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr16:22151409 G>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:124012558 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr11:124012558 C>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:190328383 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr2:190328383 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:190328383 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr2:190328383 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:46345932 C>A maps to NM_058238.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr22:46345932 C>A maps to NM_058238.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:5983833 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:5983833 G>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:142103585 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr3:142103585 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:142103585 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr3:142103585 C>T did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:42713351 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr15:42713351 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:40554748 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr8:40554748 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:40554748 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr8:40554748 T>A did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:151259951 G>A maps to NM_020832.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr1:151259951 G>A maps to NM_020832.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:57829575 C>T maps to NM_178457.1 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr20:57829575 C>T maps to NM_178457.1 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:34842535 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01D-1040-01 chr17:34842535 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:34842535 A>G did not map to a codon.
Sequencing variant TCGA-55-1596-01A-01W-0928-08 chr17:34842535 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:67256426 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:67256426 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:67290773 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:67290773 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:66992187 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:66992187 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:67024557 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:67024557 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:169792047 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:169792047 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:48138974 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:48138974 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:25349326 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:25349326 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:148620447 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:148620447 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:109634705 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:109634705 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:32364843 C>A maps to ENST00000430493 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:32364843 C>A maps to ENST00000430493 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:15612928 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:15612928 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:48538811 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:48538811 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:100253028 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:100253028 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:66330218 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:66330218 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:39199958 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:39199958 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:52312931 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:52312931 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:123317393 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:123317393 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:5182040 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:5182040 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:100649099 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:100649099 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:1009255 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:1009255 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:31124337 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:31124337 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:100205963 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:100205963 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:40762370 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:40762370 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:74363524 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:74363524 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:135611405 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:135611405 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:45710007 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:45710007 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:86262210 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:86262210 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:114195866 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:114195866 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:90582809 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:90582809 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:33090555 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:33090555 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:198011904 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:198011904 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:71808350 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:71808350 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:2114304 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:2114304 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:21246299 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:21246299 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:30930916 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:30930916 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:156914131 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:156914131 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:120300645 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:120300645 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:120338033 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:120338033 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:73067667 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:73067667 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:106510663 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:106510663 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135761523 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135761523 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:58795063 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:58795063 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:176934191 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:176934191 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:119770301 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:119770301 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:42479736 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:42479736 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:7557846 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:7557846 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:130711882 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:130711882 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:154313262 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:154313262 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:33407238 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:33407238 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:101409279 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:101409279 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:55748406 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:55748406 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:50211242 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:50211242 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:79939719 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:79939719 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:180375506 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:180375506 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56397413 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56397413 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56404910 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56404910 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:80997133 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:80997133 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:91626632 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:91626632 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:105453292 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:105453292 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:4804507 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:4804507 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:79205612 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:79205612 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:13387585 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:13387585 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:30873089 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:30873089 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:58473088 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:58473088 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:31893984 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:31893984 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:219225396 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:219225396 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:6682075 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:6682075 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:119428746 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:119428746 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:49313793 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:49313793 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:110620077 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:110620077 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:31804939 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:31804939 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:127898646 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:127898646 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:89906719 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:89906719 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:67405781 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:67405781 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:50008331 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:50008331 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:63632873 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:63632873 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:40066629 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:40066629 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:201031710 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:201031710 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:81599140 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:81599140 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:62484954 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:62484954 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:46930407 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:46930407 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:134645465 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:134645465 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:44294022 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:44294022 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:30878878 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:30878878 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:2963802 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:2963802 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:65788444 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:65788444 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:88968121 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:88968121 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:123109 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:123109 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:92970665 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:92970665 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:159854432 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:159854432 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:159854440 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:159854440 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:32675500 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:32675500 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:227300366 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:227300366 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:59203553 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:59203553 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:123184881 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:123184881 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:22303731 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:22303731 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:135942365 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:135942365 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:14720082 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:14720082 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:196711225 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:196711225 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:61765328 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:61765328 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:432620 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:432620 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:11012195 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:11012195 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:130943117 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:130943117 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:72070120 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:72070120 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:87670432 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:87670432 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:1369105 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:1369105 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:39171151 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:39171151 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:76573766 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:76573766 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:7851701 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:7851701 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:103355922 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:103355922 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:139749822 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:139749822 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:189854877 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:189854877 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:228124818 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:228124818 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:227919207 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:227919207 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:107865898 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:107865898 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:137582639 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:137582639 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:137713814 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:137713814 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:48611168 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:48611168 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:48613253 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:48613253 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:61453101 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:61453101 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:160295243 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:160295243 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:3824523 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:3824523 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:30701758 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:30701758 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:33992710 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:33992710 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:134947844 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:134947844 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:80816719 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:80816719 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:111745145 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:111745145 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:143957011 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:143957011 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:39394496 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:39394496 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:85415294 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:85415294 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:114454828 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:114454828 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:176940557 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:176940557 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:197716132 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:197716132 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:54552475 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:54552475 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:37623551 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:37623551 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:410292 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:410292 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:118463825 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:118463825 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52356436 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52356436 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:13866450 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:13866450 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:34493420 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:34493420 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:169507114 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:169507114 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:71747372 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:71747372 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:44178303 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:44178303 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:44168458 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:44168458 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:133022970 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:133022970 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:36909918 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:36909918 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:37262329 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:37262329 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:21927300 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:21927300 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:96533433 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:96533433 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:158529908 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:158529908 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:157104091 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:157104091 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:101340073 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:101340073 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:92100300 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:92100300 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:13659810 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:13659810 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:30941290 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:30941290 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:161514810 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:161514810 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:157666158 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:157666158 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:32764272 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:32764272 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:34323859 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:34323859 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:30065926 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:30065926 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:28883125 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:28883125 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:49175392 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:49175392 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:49227737 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:49227737 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:69236876 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:69236876 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:12712627 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:12712627 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:27193063 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:27193063 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:151818122 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:151818122 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:89895195 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:89895195 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:155157890 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:155157890 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:52998848 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:52998848 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:40345090 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:40345090 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:92101266 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:92101266 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:67646458 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:67646458 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:176923437 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:176923437 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:50674010 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:50674010 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:11780632 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:11780632 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:30910010 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:30910010 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:106697917 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:106697917 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:25077017 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:25077017 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:103267409 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:103267409 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:7886990 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:7886990 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:240016657 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:240016657 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:18868728 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:18868728 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:18975280 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:18975280 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:242195579 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:242195579 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:91817068 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:91817068 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:62207963 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:62207963 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:76472781 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:76472781 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:183770809 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:183770809 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:23507941 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:23507941 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:160514938 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:160514938 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:160517306 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:160517306 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:1539272 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:1539272 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:173334178 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:173334178 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:7605409 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:7605409 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:96991492 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:96991492 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:211032708 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:211032708 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142651189 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142651189 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:75143477 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:75143477 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:3747509 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:3747509 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:42263652 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:42263652 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:123095681 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:123095681 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:1890436 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:1890436 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:17954133 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:17954133 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:169951076 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:169951076 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:55263327 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:55263327 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:88900186 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:88900186 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:38906519 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:38906519 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:31744691 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:31744691 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:56126530 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:56126530 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:130381143 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:130381143 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:129649344 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:129649344 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:40093181 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:40093181 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:48935955 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:48935955 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:55144825 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:55144825 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:55176016 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:55176016 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:41684565 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:41684565 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:58724323 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:58724323 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:197717395 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:197717395 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:55584840 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:55584840 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:151835257 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:151835257 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:141128880 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:141128880 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:122677641 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:122677641 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:130247910 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:130247910 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:143846266 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:143846266 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:53694646 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:53694646 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:96034179 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:96034179 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:21215322 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:21215322 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:91228300 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:91228300 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:39090637 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:39090637 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135309403 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135309403 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:165110176 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:165110176 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:63666004 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:63666004 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:186947724 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:186947724 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:82039922 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:82039922 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:100390743 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:100390743 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:99694901 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:99694901 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:47342908 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:47342908 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:60112779 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:60112779 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:37386704 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:37386704 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:36657153 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:36657153 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:326347 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:326347 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:151846284 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:151846284 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:60753981 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:60753981 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:60059638 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:60059638 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:31727101 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:31727101 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:68509920 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:68509920 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56581268 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56581268 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:8962040 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:8962040 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:1217677 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:1217677 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:171508024 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:171508024 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:47511001 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:47511001 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:95147443 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:95147443 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:40251628 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:40251628 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:1920771 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:1920771 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:20073024 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:20073024 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:102884713 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:102884713 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:113103637 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:113103637 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:134080412 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:134080412 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:140108924 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:140108924 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:27173291 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:27173291 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52778361 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52778361 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:37057470 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:37057470 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:124979277 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:124979277 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:63768741 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:63768741 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:50666381 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:50666381 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:72897944 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:72897944 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:34818231 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:34818231 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:98254089 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:98254089 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:119534134 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:119534134 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:15065575 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:15065575 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:59512714 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:59512714 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:106466390 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:106466390 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:101623602 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:101623602 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:101623605 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:101623605 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:102343879 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:102343879 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:47656734 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:47656734 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:131258433 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:131258433 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:78431321 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:78431321 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:50960565 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:50960565 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:145108314 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:145108314 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:16059804 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:16059804 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:248487891 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:248487891 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:45886172 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:45886172 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:105847240 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:105847240 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:17567296 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:17567296 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:9524838 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:9524838 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:176585880 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:176585880 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:44587909 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:44587909 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:154745872 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:154745872 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:91368898 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:91368898 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:56077207 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:56077207 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:53422642 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:53422642 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:140430990 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:140430990 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:78506308 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:78506308 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:5522386 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:5522386 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:10577402 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:10577402 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:144865992 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:144865992 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:54362071 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:54362071 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:102783877 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:102783877 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:92148182 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:92148182 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:58318078 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:58318078 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:27277023 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:27277023 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:22828881 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:22828881 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:36936676 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:36936676 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:110445489 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:110445489 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:72502877 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:72502877 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:131477030 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:131477030 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:8665848 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:8665848 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:9346312 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:9346312 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:18837255 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:18837255 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:30804816 G>A maps to NM_172236.1 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:30804816 G>A maps to NM_172236.1 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:50906595 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:50906595 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:43148005 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:43148005 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:7539110 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:7539110 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:37536600 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:37536600 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:131909770 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:131909770 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:63861874 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:63861874 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:68999911 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:68999911 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:82010962 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:82010962 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:95952517 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:95952517 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142460448 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142460448 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:31146443 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:31146443 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:43269862 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:43269862 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:11562988 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:11562988 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:62164886 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:62164886 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:44064615 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:44064615 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:163985667 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:163985667 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:139108614 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:139108614 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:113799035 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:113799035 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:26332621 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:26332621 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:27815670 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:27815670 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:178745996 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:178745996 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:130828524 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:130828524 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:79307565 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:79307565 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:38901749 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:38901749 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:155148466 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:155148466 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:50102317 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:50102317 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:79312276 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:79312276 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:103629558 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:103629558 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:100974797 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:100974797 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:104924505 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:104924505 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:31582943 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:31582943 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:33402944 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:33402944 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:92654488 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:92654488 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:14303290 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:14303290 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:42393897 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:42393897 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:93023208 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:93023208 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:237759006 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:237759006 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:237788943 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:237788943 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:237789138 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:237789138 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:119593183 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:119593183 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:48202959 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:48202959 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:50897847 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:50897847 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:5053349 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:5053349 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:145116002 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:145116002 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:40009470 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:40009470 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:9197191 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:9197191 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:7212872 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:7212872 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:42196679 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:42196679 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:4400304 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:4400304 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:56913448 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:56913448 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:1064427 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:1064427 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:43204879 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:43204879 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:38359682 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:38359682 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:79682775 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:79682775 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:107338565 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:107338565 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:205892840 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:205892840 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:150723185 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:150723185 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:45814191 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:45814191 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135112152 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:135112152 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:48573353 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:48573353 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:61910809 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:61910809 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:106864510 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:106864510 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:17907544 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:17907544 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:183511691 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:183511691 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:88396403 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:88396403 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:10286766 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:10286766 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:69279457 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:69279457 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:35055518 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:35055518 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:106917108 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:106917108 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:215145529 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:215145529 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:118509151 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:118509151 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:95011108 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:95011108 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:220337564 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:220337564 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:158650593 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:158650593 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:30715721 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:30715721 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:74086286 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:74086286 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:191864281 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:191864281 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:169020025 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:169020025 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:31012356 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:31012356 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:109340939 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:109340939 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:84650980 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:84650980 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:67548789 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:67548789 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:45066616 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:45066616 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:91795752 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:91795752 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:66811413 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:66811413 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:132939367 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:132939367 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:68665363 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:68665363 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:55895505 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:55895505 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:168208420 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:168208420 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:59543429 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:59543429 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:35090141 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:35090141 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:179631495 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:179631495 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:51497884 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:51497884 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:114287390 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:114287390 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:105900903 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:105900903 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:89177842 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:89177842 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:24731212 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:24731212 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:11468416 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:11468416 T>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:32508144 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:32508144 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:54208012 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:54208012 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:4684168 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:4684168 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:44402649 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:44402649 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:15599957 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:15599957 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:138487820 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:138487820 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:94807497 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:94807497 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:94822190 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:94822190 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:7259313 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:7259313 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:93609409 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:93609409 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:144380138 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:144380138 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:10998063 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:10998063 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:89537733 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:89537733 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:67086986 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:67086986 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:38237538 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:38237538 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:141952033 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:141952033 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:91233276 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:91233276 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:50487646 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:50487646 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:19739927 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:19739927 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:88961177 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:88961177 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:69535512 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:69535512 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:69974126 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:69974126 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:35954242 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:35954242 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:96469794 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:96469794 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:216497085 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:216497085 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:179437870 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:179437870 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:113675813 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:113675813 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:6155199 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:6155199 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:149262283 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:149262283 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:171678732 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:171678732 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:6854202 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:6854202 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:177632877 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:177632877 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:46696802 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:46696802 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:53024756 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:53024756 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:65253192 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chrX:65253192 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:54610641 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:54610641 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:116008549 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:116008549 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:123994267 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:123994267 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:124016119 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:124016119 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:177081354 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:177081354 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:128471124 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:128471124 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:31594986 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:31594986 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:17280953 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:17280953 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:56366919 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:56366919 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:56367337 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:56367337 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:42024311 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr22:42024311 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:145182343 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:145182343 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:178488945 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:178488945 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:74376136 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:74376136 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:57987891 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:57987891 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:71894646 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:71894646 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:49977047 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:49977047 A>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr7:87785186 A>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr7:87785186 A>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:33630757 T>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:33630757 T>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr9:18639426 A>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr9:18639426 A>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr11:433470 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr11:433470 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr22:36588020 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr22:36588020 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr17:79952825 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr17:79952825 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr3:9775767 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr3:9775767 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr14:76121072 A>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr14:76121072 A>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr19:55678042 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr19:55678042 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:115457382 A>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:115457382 A>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:21882648 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:21882648 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chrX:49777818 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chrX:49777818 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr2:98263949 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr2:98263949 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:157548365 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:157548365 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:28903739 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:28903739 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:49761194 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:49761194 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr9:37692530 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr9:37692530 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr2:165351171 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr2:165351171 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:77625933 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr13:77625933 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr6:11233443 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr6:11233443 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:12219774 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:12219774 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr11:3143533 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr11:3143533 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr2:60998827 T>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr2:60998827 T>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr20:34528977 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr20:34528977 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:145477636 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:145477636 T>C did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:145477897 T>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:145477897 T>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr14:51372343 A>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr14:51372343 A>G did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:26134940 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:26134940 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr14:20926894 A>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr14:20926894 A>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr22:42339543 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr22:42339543 C>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:122667992 C>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:122667992 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:20768140 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:20768140 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:108004504 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:108004504 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:156945995 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:156945995 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:33891750 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:33891750 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:109663808 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:109663808 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:134260377 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:134260377 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:5041581 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:5041581 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:4535115 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:4535115 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:113278022 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:113278022 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:21894433 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:21894433 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:43194972 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:43194972 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:175795766 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:175795766 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:123466488 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:123466488 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:66391359 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:66391359 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:9543306 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:9543306 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:79970045 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:79970045 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:11340998 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:11340998 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:25947249 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:25947249 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:69944888 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:69944888 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chrX:129146857 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chrX:129146857 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:36954583 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:36954583 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:33135101 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:33135101 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:10342364 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:10342364 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:76549113 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:76549113 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:1012017 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:1012017 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:178489784 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:178489784 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:31879579 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:31879579 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:35662334 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:35662334 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:188223674 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:188223674 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:117144249 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:117144249 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:45870745 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:45870745 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:147092603 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:147092603 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:147182904 T>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:147182904 T>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:61936922 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:61936922 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:227917161 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:227917161 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:74422038 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:74422038 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:9768984 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:9768984 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:113293366 T>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:113293366 T>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:31639142 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:31639142 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:18162328 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:18162328 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:242707056 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:242707056 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:24586394 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:24586394 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:234346822 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:234346822 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:83183753 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:83183753 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:78351743 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:78351743 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:7644065 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:7644065 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:116594009 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:116594009 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:62341371 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:62341371 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:117768113 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:117768113 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:124792851 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:124792851 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:36818169 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:36818169 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr13:32836647 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr13:32836647 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr13:114531470 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr13:114531470 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:128200649 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:128200649 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:42695244 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:42695244 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:52425554 T>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:52425554 T>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:176883339 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:176883339 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:87373088 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:87373088 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1859416 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1859416 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:19015589 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:19015589 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:93237942 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:93237942 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:1073449 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:1073449 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:156504262 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:156504262 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:54967803 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:54967803 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:133949405 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:133949405 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:124397189 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:124397189 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:63447530 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:63447530 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chrY:21869673 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chrY:21869673 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:53238052 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:53238052 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:152552129 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:152552129 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:51883635 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:51883635 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:90975660 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:90975660 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:165183134 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:165183134 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:141777754 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:141777754 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:139995663 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:139995663 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:65374991 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:65374991 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:150877530 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:150877530 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:876966 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:876966 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:36665312 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:36665312 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:131149248 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:131149248 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:60766029 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:60766029 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:149906064 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:149906064 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:47368226 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:47368226 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:15854311 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:15854311 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:10348077 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:10348077 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:10356407 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:10356407 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:45297467 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:45297467 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:75397402 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:75397402 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:62836508 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:62836508 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:50197856 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:50197856 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:124904423 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:124904423 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:60394782 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:60394782 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:204966229 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:204966229 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:25477473 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:25477473 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:33463010 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:33463010 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:144101845 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:144101845 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:119535876 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:119535876 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:206562129 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:206562129 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:52562149 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:52562149 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:74658809 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:74658809 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:248138230 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:248138230 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:248738097 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:248738097 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:289562 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:289562 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:149499157 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:149499157 C>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:74056735 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:74056735 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:67262525 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:67262525 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:20304749 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:20304749 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:57750973 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:57750973 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:102950942 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:102950942 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:44285156 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:44285156 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:621051 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:621051 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:131995709 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:131995709 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:18910501 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr22:18910501 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:18870970 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:18870970 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:43679939 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:43679939 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:97299454 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:97299454 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:89653754 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:89653754 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:32377458 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:32377458 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:40827789 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:40827789 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:50395104 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:50395104 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:56975177 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:56975177 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:192778167 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:192778167 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:104672480 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:104672480 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:87113884 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:87113884 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr18:67688069 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr18:67688069 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:33765563 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:33765563 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:38802665 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:38802665 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:84658271 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:84658271 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:84727059 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:84727059 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr18:61310641 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr18:61310641 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:46248172 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:46248172 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:31931906 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:31931906 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:98993344 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:98993344 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:7640004 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:7640004 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:101199498 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:101199498 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:35644671 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:35644671 A>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:147209108 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:147209108 T>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:54712254 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:54712254 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:26215627 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:26215627 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:113197463 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:113197463 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:132873814 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:132873814 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:71604095 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:71604095 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chrX:79281086 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chrX:79281086 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:85536592 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:85536592 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:115963714 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:115963714 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:65188544 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr4:65188544 T>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:105896809 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:105896809 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:27259482 A>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:27259482 A>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:12777034 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:12777034 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:5352095 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:5352095 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:113723791 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:113723791 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1275252 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1275252 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:123698896 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:123698896 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:14336587 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:14336587 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:28854137 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:28854137 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:54527195 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:54527195 A>G did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:145649183 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:145649183 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:70800743 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:70800743 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:31599910 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:31599910 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:44797363 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:44797363 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr13:20412015 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr13:20412015 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:45985448 A>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:45985448 A>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:247264931 A>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:247264931 A>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:22375771 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:22375771 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:53989805 C>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:53989805 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:67170942 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:67170942 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:51297982 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:51297982 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:89187115 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:89187115 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20563422 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20563422 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:31144469 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:31144469 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:100009804 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:100009804 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:96954771 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:96954771 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:109392082 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:109392082 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:202153269 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:202153269 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:99121138 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:99121138 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:66268932 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:66268932 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:29185092 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:29185092 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:81460020 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:81460020 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:141595788 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:141595788 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:124236999 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:124236999 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:116919734 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:116919734 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:69703536 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:69703536 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:26265504 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:26265504 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:100608441 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:100608441 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:21806752 T>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:21806752 T>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:112703825 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:112703825 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:90778936 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:90778936 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:76121176 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:76121176 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:5680447 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:5680447 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100033233 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100033233 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:121098167 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:121098167 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:34304499 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:34304499 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:33259311 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:33259311 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:7812413 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:7812413 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:193205261 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:193205261 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:24535748 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:24535748 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:18631439 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:18631439 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:18018127 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:18018127 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:34061188 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:34061188 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:55860015 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:55860015 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:196712774 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:196712774 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:106632706 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:106632706 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:154507139 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:154507139 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:189854904 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:189854904 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:111091026 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:111091026 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:93851739 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:93851739 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:50200542 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:50200542 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:36933886 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:36933886 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:156731412 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:156731412 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:47278435 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:47278435 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:37638883 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:37638883 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20952918 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20952918 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:66260110 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:66260110 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:45397817 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:45397817 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:236646635 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:236646635 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:184034357 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:184034357 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:79392850 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:79392850 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:25304913 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:25304913 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:111519621 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:111519621 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:72129124 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:72129124 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:245005600 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:245005600 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:16578743 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:16578743 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:180057163 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:180057163 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:153399388 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:153399388 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:4306073 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:4306073 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:30253373 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:30253373 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:120574968 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:120574968 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:57913796 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:57913796 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:110390305 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:110390305 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:30521019 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:30521019 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:132670080 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:132670080 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:4936693 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:4936693 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:158262696 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:158262696 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:66961854 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:66961854 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:42621289 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:42621289 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:19377143 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:19377143 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:50557761 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:50557761 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:66708983 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:66708983 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:31322452 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:31322452 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:31322829 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:31322829 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:148757346 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:148757346 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:83347178 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:83347178 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:3148842 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:3148842 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:2640289 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:2640289 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:27679583 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:27679583 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:160517359 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:160517359 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:217528845 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:217528845 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:111662724 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr9:111662724 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:32671963 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:32671963 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:66611257 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:66611257 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:67210546 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:67210546 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:39745559 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:39745559 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:55278477 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:55278477 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:74339024 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:74339024 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:88116720 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:88116720 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:51480789 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:51480789 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:129724952 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:129724952 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:170081728 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:170081728 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:53761994 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:53761994 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:137017053 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:137017053 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:12982037 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:12982037 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:43232304 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:43232304 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:154859989 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:154859989 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:2321446 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:2321446 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:149905236 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:149905236 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:15854355 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:15854355 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:10295386 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:10295386 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:40694953 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:40694953 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:71036905 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:71036905 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:58538632 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:58538632 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:55421241 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:55421241 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:65088484 G>T maps to ENST00000506539 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:65088484 G>T maps to ENST00000506539 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:57077561 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:57077561 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:162124162 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:162124162 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:69314572 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:69314572 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:16890130 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:16890130 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:16918384 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:16918384 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:31837373 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:31837373 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrY:5441979 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrY:5441979 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:141331051 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:141331051 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140579306 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140579306 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:144923630 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:144923630 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:77380590 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:77380590 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:73468214 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:73468214 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:9779004 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:9779004 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:28290700 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:28290700 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:41475571 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:41475571 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:131960543 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:131960543 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100855517 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100855517 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:46656197 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:46656197 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:102522192 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:102522192 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:52716117 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:52716117 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:35591049 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:35591049 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:11339599 T>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:11339599 T>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:45980162 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:45980162 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:35068403 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:35068403 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:3701382 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:3701382 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:11579583 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:11579583 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:21998022 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:21998022 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:153206850 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:153206850 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:8674605 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:8674605 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:227731885 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:227731885 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:177569837 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:177569837 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:28241028 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:28241028 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:79800493 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:79800493 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:50845325 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:50845325 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:50898677 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:50898677 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:27764623 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:27764623 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:38833771 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:38833771 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:165969337 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:165969337 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:52168195 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:52168195 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:115813917 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:115813917 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:70590034 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:70590034 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:85890376 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:85890376 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:113285206 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:113285206 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:4180713 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:4180713 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:103698435 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:103698435 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:20621244 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:20621244 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:23249262 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:23249262 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:111901273 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:111901273 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:168189532 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:168189532 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:98654647 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:98654647 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:16720904 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:16720904 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:70520843 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:70520843 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:25207211 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:25207211 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:186515026 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:186515026 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:108536276 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:108536276 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:55657541 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:55657541 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:78036661 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:78036661 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:53076721 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:53076721 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:99917186 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:99917186 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:149880914 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:149880914 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:152665454 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:152665454 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:120805533 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:120805533 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:100531187 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chrX:100531187 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:41704007 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:41704007 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:151861594 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:151861594 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:126128835 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:126128835 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:42820541 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:42820541 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:700596 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:700596 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:68929019 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:68929019 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:24820839 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:24820839 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:154155388 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:154155388 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:20138063 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr13:20138063 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:30080125 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:30080125 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:13220549 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:13220549 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:122803409 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:122803409 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:179632673 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:179632673 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:69106386 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:69106386 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:49845789 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:49845789 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:234622614 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:234622614 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:45689225 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:45689225 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:41170819 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:41170819 G>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:40925993 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:40925993 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr21:40768887 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr21:40768887 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:174097223 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:174097223 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:72036430 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:72036430 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:80862990 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:80862990 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:44619617 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:44619617 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:22257814 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:22257814 A>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:14830167 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:14830167 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:148873684 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:148873684 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:52937148 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:52937148 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:52876543 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:52876543 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100861384 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100861384 A>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:58120023 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:58120023 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:7435291 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:7435291 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:9265180 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:9265180 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:9265180 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:9265180 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:70298757 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:70298757 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:67187503 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:67187503 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:67187503 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:67187503 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:169830484 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:169830484 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:169836337 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:169836337 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:169830484 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:169830484 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:169836337 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:169836337 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:87041060 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:87041060 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:43406297 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:43406297 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48218374 G>T maps to NM_032583.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48218374 G>T maps to NM_032583.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48149222 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48149222 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48167811 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48167811 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48172003 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48172003 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48149222 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48149222 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48167811 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48167811 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48172003 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:48172003 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:16110578 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:16110578 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:16110578 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:16110578 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:111710642 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:111710642 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:111710642 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:111710642 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:204260251 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:204260251 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:204260251 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:204260251 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:211085420 C>G maps to NM_001608.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:211085420 C>G maps to NM_001608.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:6309965 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:6309965 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:61561657 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:61561657 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:140979119 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:140979119 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:140979119 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:140979119 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20490055 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20490055 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20490055 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20490055 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:229568342 G>T maps to NM_001100.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:229568342 G>T maps to NM_001100.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:148657173 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:148657173 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:148657173 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:148657173 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:33549668 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:33549668 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:33549668 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:33549668 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:72520010 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:72520010 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:5189935 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:5189935 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:43925995 C>A maps to ENST00000389420 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:43925995 C>A maps to ENST00000389420 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:28296584 G>A maps to NM_007038.3 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:28296584 G>A maps to NM_007038.3 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:79080790 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:79080790 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:123008910 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:123008910 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:123021834 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:123021834 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:123021896 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:123021896 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:123021896 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:123021896 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:33562426 C>T maps to ENST00000373441 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:33562426 C>T maps to ENST00000373441 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:70904797 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:70904797 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:70904797 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:70904797 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:119300943 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:119300943 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:119300943 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:119300943 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:244574490 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:244574490 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:244600113 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:244600113 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:244600113 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:244600113 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:74369007 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:74369007 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:230846666 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:230846666 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:230846666 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:230846666 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:109669073 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:109669073 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:109669073 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:109669073 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:35035423 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:35035423 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:35035423 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:35035423 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:129053372 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:129053372 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:129053372 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:129053372 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:32878561 G>A maps to NM_000687.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:32878561 G>A maps to NM_000687.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:159035666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:159035666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:159042974 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:159042974 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:159035666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:159035666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:159042974 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:159042974 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:45706342 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:45706342 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:4712779 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:4712779 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:77784056 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:77784056 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:33205040 G>T maps to NM_004274.4 E1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:33205040 G>T maps to NM_004274.4 E1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:134261813 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:134261813 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:134261813 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:134261813 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:137792424 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:137792424 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:125836786 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:125836786 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:112235925 G>T maps to NM_000690.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:112235925 G>T maps to NM_000690.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:30081107 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:30081107 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:38710503 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:38710503 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:43921136 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:43921136 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:202483914 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:202483914 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:202483914 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:202483914 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:101771328 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:101771328 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:101771328 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:101771328 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:37433904 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:37433904 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:37451814 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:37451814 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:37433904 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:37433904 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:37451814 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:37451814 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:94014518 A>T maps to NM_032290.3 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:94014518 A>T maps to NM_032290.3 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:21261201 T>A maps to NM_145865.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:21261201 T>A maps to NM_145865.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:22257905 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:22257905 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:34009642 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:34009642 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:144314075 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:144314075 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:144525525 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:144525525 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:144314075 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:144314075 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:144525525 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:144525525 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131785809 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131785809 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:35730928 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:35730928 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:17920779 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:17920779 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:17920779 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:17920779 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:177142260 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:177142260 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:177142260 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:177142260 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:113479730 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:113479730 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:113479730 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:113479730 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:28906165 C>A maps to NM_173201.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:28906165 C>A maps to NM_173201.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:10428301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:10428301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:10428301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:10428301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:40647248 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:40647248 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:40647248 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:40647248 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:124241307 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:124241307 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:124241307 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:124241307 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:44441770 G>A maps to NM_004047.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:44441770 G>A maps to NM_004047.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:67487284 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:67487284 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:42571134 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:42571134 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:42571134 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:42571134 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:111922959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:111922959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:111922959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:111922959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:57743782 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:57743782 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:11026640 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:11026640 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:11049683 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:11049683 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:11026640 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:11026640 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:11049683 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:11049683 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:69703642 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:69703642 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:69703642 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:69703642 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:160294972 C>A maps to NM_013450.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:160294972 C>A maps to NM_013450.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56536209 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56536209 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:56536209 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:56536209 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:156618447 C>G maps to NM_021948.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:156618447 C>G maps to NM_021948.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:7862863 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:7862863 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:887359 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:887359 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:105695088 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:105695088 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:36337045 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:36337045 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:36337045 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:36337045 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:108042980 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:108042980 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:3634694 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:3634694 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:100617440 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:100617440 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:100617440 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:100617440 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:93268814 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:93268814 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:93268814 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:93268814 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:82871003 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:82871003 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:82871003 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:82871003 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:95934126 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:95934126 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:95934126 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:95934126 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:24922546 C>A maps to NM_018958.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:24922546 C>A maps to NM_018958.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:90138747 G>T maps to NM_152259.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:90138747 G>T maps to NM_152259.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:119914653 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:119914653 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:119914653 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:119914653 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12815805 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12815805 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:12815805 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:12815805 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:226176061 T>G maps to NM_152608.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:226176061 T>G maps to NM_152608.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:151020973 C>A maps to NM_017860.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:151020973 C>A maps to NM_017860.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:56728433 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:56728433 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:43338920 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:43338920 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:63401727 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:63401727 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:63401727 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:63401727 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:47552815 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:47552815 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:71098639 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:71098639 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:71098639 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:71098639 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:56212810 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:56212810 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:88138332 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:88138332 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:88138332 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:88138332 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:31736733 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:31736733 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:31736733 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:31736733 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:42971887 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:42971887 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:42971887 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:42971887 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:6862914 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:6862914 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:6862914 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:6862914 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:120687057 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:120687057 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:120687057 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:120687057 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:39341478 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:39341478 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:39341478 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:39341478 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:15678674 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:15678674 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:15678674 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:15678674 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:140901161 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:140901161 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:140972590 G>T maps to ENST00000277549 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:140972590 G>T maps to ENST00000277549 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:181724328 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:181724328 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:181724328 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:181724328 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:1969333 C>G maps to NM_172364.4 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:1969333 C>G maps to NM_172364.4 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:86062182 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:86062182 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:86062182 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:86062182 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:134552465 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:134552465 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:30955325 C>A maps to ENST00000295055 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:30955325 C>A maps to ENST00000295055 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:75685420 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:75685420 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:25261484 G>T maps to NM_018272.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:25261484 G>T maps to NM_018272.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:74311200 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:74311200 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:58314661 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:58314661 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:58314661 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:58314661 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:109432343 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:109432343 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:109432343 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:109432343 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:74572175 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:74572175 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:180351860 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:180351860 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:86098510 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:86098510 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:86098510 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:86098510 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:91755745 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:91755745 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:91755745 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:91755745 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:74516859 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:74516859 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:74516859 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:74516859 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:7559188 T>C maps to ENST00000416109 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:7559188 T>C maps to ENST00000416109 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158152204 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158152204 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:167404822 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:167404822 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:72469523 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:72469523 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:72477849 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:72477849 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:137665110 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:137665110 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:227219082 T>G maps to ENST00000366766 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:227219082 T>G maps to ENST00000366766 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:64606194 A>G maps to NM_017525.2 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:64606194 A>G maps to NM_017525.2 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:73330514 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:73330514 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:73330514 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:73330514 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:58567502 G>T maps to NM_177980.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:58567502 G>T maps to NM_177980.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:63492140 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:63492140 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:63492140 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:63492140 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:63511298 G>C maps to NM_004361.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:63511298 G>C maps to NM_004361.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:61851500 C>A maps to NM_001796.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:61851500 C>A maps to NM_001796.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:26915966 G>A maps to NM_016279.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:26915966 G>A maps to NM_016279.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:205499521 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:205499521 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:205499521 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:205499521 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:46050867 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:46050867 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:46050867 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:46050867 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:34854815 G>C maps to NM_020180.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:34854815 G>C maps to NM_020180.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:46765041 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:46765041 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:46765041 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:46765041 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:104070210 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:104070210 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:104070210 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:104070210 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:134278165 T>C maps to NM_025180.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:134278165 T>C maps to NM_025180.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:55905754 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:55905754 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:50873173 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:50873173 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:50873173 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:50873173 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:6181092 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:6181092 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:184104631 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:184104631 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:233406158 G>A maps to NM_005199.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:233406158 G>A maps to NM_005199.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:139219032 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:139219032 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:139219032 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:139219032 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:8665070 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:8665070 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:8665070 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:8665070 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:154509357 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:154509357 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:25166707 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:25166707 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:65472592 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:65472592 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:140167651 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:140167651 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:57937711 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:57937711 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:57996581 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:57996581 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:57937711 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:57937711 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:57996581 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:57996581 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:87641333 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:87641333 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:87641333 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:87641333 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:135078626 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:135078626 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:135078626 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:135078626 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:99941252 G>T maps to NM_014361.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:99941252 G>T maps to NM_014361.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:99945011 T>C maps to NM_014361.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:99945011 T>C maps to NM_014361.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:76587725 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:76587725 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:76587725 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:76587725 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:125530308 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:125530308 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:125281943 G>T maps to NM_130773.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:125281943 G>T maps to NM_130773.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:125530308 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:125530308 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:103364181 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:103364181 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:103467971 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:103467971 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:103467971 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:103467971 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:33153628 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:33153628 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:75801182 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:75801182 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:75801182 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:75801182 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:75899097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:75899097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:71703962 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:71703962 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:71703962 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:71703962 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:121220514 G>A maps to NM_021110.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:121220514 G>A maps to NM_021110.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:101829429 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:101829429 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:101822337 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:101822337 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:101829429 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:101829429 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:105813756 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:105813756 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:105813756 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:105813756 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:139609342 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:139609342 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:189859296 G>T maps to NM_000090.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:189859296 G>T maps to NM_000090.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:189929365 G>T maps to NM_000393.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:189929365 G>T maps to NM_000393.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:47532850 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:47532850 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:238256572 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:238256572 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:238256572 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:238256572 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:319981 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:319981 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:319981 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:319981 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:47685847 G>A maps to NM_006587.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:47685847 G>A maps to NM_006587.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:129914846 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:129914846 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:211467185 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:211467185 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:211467185 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:211467185 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:125528161 C>A maps to NM_198148.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:125528161 C>A maps to NM_198148.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:8608444 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:8608444 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:8608819 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:8608819 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:8608444 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:8608444 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:43910947 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:43910947 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153925959 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153925959 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:153925959 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:153925959 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:2808658 G>T maps to NM_033225.5 S3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:2808658 G>T maps to NM_033225.5 S3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:34291145 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:34291145 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113253922 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113253922 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:113253922 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:113253922 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:113988230 C>A maps to NM_198123.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:113988230 C>A maps to NM_198123.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:126694435 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:126694435 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:126694435 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:126694435 T>A did not map to a codon.
Alternatively spliced codon TCGA-64-1676-01A-01W-0928-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-64-1676-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:11111230 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:11111230 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:11111230 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:11111230 C>A did not map to a codon.
Alternatively spliced codon TCGA-64-1676-01A-01W-0928-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-64-1676-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:72374758 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:72374758 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:219676936 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:219676936 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:219676936 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:219676936 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:41707396 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:41707396 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:99310927 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:99310927 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:15636083 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:15636083 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:15636083 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:15636083 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:158286960 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:158286960 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:27841105 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:27841105 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:27841105 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:27841105 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:39375243 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:39375243 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:39375243 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:39375243 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:72420454 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:72420454 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:44098022 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:44098022 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:88885854 G>T maps to NM_152418.3 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:88885854 G>T maps to NM_152418.3 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:31287204 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:31287204 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:14976895 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:14976895 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:15983174 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:15983174 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:23018527 C>T maps to NM_182699.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:23018527 C>T maps to NM_182699.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:169348524 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:169348524 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:169348524 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:169348524 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:66063762 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:66063762 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:66063762 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:66063762 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:186038372 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:186038372 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:137172360 G>A maps to NM_004717.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:137172360 G>A maps to NM_004717.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:137172360 G>A maps to NM_004717.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:137172360 G>A maps to NM_004717.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:50163553 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:50163553 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:50146202 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:50146202 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:50163553 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:50163553 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:12150039 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:12150039 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:12150039 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:12150039 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:140905599 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:140905599 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:140905599 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:140905599 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:61537544 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:61537544 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:355908 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:355908 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:355908 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:355908 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:11985954 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:11985954 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:11985954 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:11985954 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:41222806 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:41222806 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:124337429 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:124337429 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:124337429 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:124337429 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:1056128 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:1056128 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:1056128 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:1056128 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:124364245 G>A maps to NM_207437.3 R2726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:124364245 G>A maps to NM_207437.3 R2726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:21747562 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:21747562 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20986463 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20986463 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20994323 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20994323 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:21122842 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:21122842 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20986463 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20986463 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20994323 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20994323 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:21122842 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:21122842 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:13752424 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:13752424 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:13752424 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:13752424 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:38758174 A>G maps to ENST00000327475 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:38758174 A>G maps to ENST00000327475 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:11511683 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:11511683 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:11511683 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:11511683 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:34506559 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:34506559 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:72310217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:72310217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:72310217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:72310217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:74095796 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:74095796 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:31383151 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:31383151 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:31383151 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:31383151 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:169507294 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:169507294 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:169507294 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:169507294 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:63084480 C>G maps to ENST00000371140 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:63084480 C>G maps to ENST00000371140 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:99520150 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:99520150 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:99520150 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:99520150 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:21768282 C>G maps to NM_003974.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:21768282 C>G maps to NM_003974.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:65790064 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:65790064 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:105404917 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:105404917 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:105404917 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:105404917 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:29043955 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:29043955 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:56472156 G>A maps to ENST00000361203 N2212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:56472156 G>A maps to ENST00000361203 N2212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:56437105 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:56437105 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:56472156 G>A maps to ENST00000361203 N2212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:56472156 G>A maps to ENST00000361203 N2212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:113515245 C>A maps to NM_004416.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:113515245 C>A maps to NM_004416.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:103128357 C>T maps to NM_001080463.1 L3502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:103128357 C>T maps to NM_001080463.1 L3502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:80583595 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:80583595 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:80583595 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:80583595 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:71795055 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:71795055 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:71795291 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:71795291 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:71795055 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:71795055 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:71795291 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:71795291 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:207528120 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:207528120 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:131761568 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:131761568 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:131761568 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:131761568 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:69157603 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:69157603 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:69157603 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:69157603 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:63999395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:63999395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:38352577 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:38352577 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:36381062 C>T maps to NM_012199.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:36381062 C>T maps to NM_012199.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:141557552 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:141557552 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:141557552 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:141557552 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:37382024 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:37382024 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:37382024 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:37382024 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:14866329 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:14866329 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:14866329 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:14866329 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:71495424 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:71495424 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:71495424 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:71495424 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:120631580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:120631580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:120631580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:120631580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:112003751 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:112003751 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:47604030 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:47604030 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:89462153 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:89462153 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:222298794 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:222298794 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:222298794 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:222298794 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:66242817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:66242817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:66242817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:66242817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:23234355 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:23234355 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:23234355 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:23234355 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:142566455 G>T maps to NM_004445.3 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:142566455 G>T maps to NM_004445.3 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:1519477 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:1519477 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:47355624 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:47355624 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:47355624 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:47355624 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:217241627 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:217241627 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:158531730 C>G maps to NM_020728.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:158531730 C>G maps to NM_020728.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:157062423 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:157062423 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:157062423 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:157062423 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:73052879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:73052879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:73052879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:73052879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:154128035 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:154128035 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:61580913 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:61580913 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:109159082 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:109159082 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:109159082 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:109159082 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:25744473 C>A maps to NM_152704.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:25744473 C>A maps to NM_152704.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:225265636 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:225265636 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:89772322 G>A maps to NM_014883.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:89772322 G>A maps to NM_014883.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:187077231 G>T maps to ENST00000356371 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:187077231 G>T maps to ENST00000356371 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:84406123 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:84406123 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:103420218 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:103420218 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:62260994 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:62260994 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:62260994 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:62260994 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:58619931 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:58619931 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:58619931 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:58619931 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:190068274 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:190068274 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:190068274 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:190068274 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:119407281 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:119407281 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:134151626 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:134151626 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:242402802 G>T maps to NM_014808.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:242402802 G>T maps to NM_014808.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:92620172 G>A maps to ENST00000298047 G4315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:92620172 G>A maps to ENST00000298047 G4315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:127597671 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:127597671 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:127597671 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:127597671 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:37093316 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:37093316 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:123527228 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:123527228 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:161561212 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:161561212 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:157737418 C>T maps to ENST00000469986 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:157737418 C>T maps to ENST00000469986 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:157737418 C>T maps to ENST00000469986 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:157737418 C>T maps to ENST00000469986 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:157551200 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:157551200 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:157551200 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:157551200 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:125109516 C>T maps to NM_001039112.2 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:125109516 C>T maps to NM_001039112.2 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:7324972 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:7324972 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:7324972 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:7324972 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:102378992 T>G maps to NM_175929.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:102378992 T>G maps to NM_175929.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:84605323 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:84605323 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:128496778 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:128496778 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:128496778 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:128496778 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:28636254 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:28636254 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:28636254 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:28636254 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:240519038 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:240519038 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:240519038 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:240519038 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:50045836 C>G maps to NM_175736.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:50045836 C>G maps to NM_175736.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:171240300 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:171240300 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:171240300 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:171240300 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:94009625 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:94009625 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:89429915 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:89429915 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:89429915 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:89429915 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:168458119 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:168458119 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:48584627 A>T maps to NM_015030.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:48584627 A>T maps to NM_015030.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:127238848 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:127238848 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:29523646 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:29523646 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:29523646 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:29523646 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:46252654 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:46252654 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:46252654 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:46252654 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:161118899 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:161118899 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:161118899 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:161118899 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:88419820 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:88419820 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:88419820 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:88419820 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:11454395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:11454395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:11454395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:11454395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:89523825 G>A maps to NM_002053.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:89523825 G>A maps to NM_002053.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:34128536 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:34128536 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:34128536 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:34128536 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:120586187 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:120586187 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:120586187 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:120586187 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:172163025 G>T maps to NM_198407.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:172163025 G>T maps to NM_198407.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:78512062 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:78512062 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:90604138 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:90604138 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:90604138 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:90604138 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:151228659 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:151228659 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:58604549 T>C maps to NM_145016.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:58604549 T>C maps to NM_145016.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:58605832 G>T maps to NM_145016.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:58605832 G>T maps to NM_145016.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:52417529 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:52417529 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:52417529 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:52417529 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:30520232 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:30520232 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:30520232 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:30520232 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:167025199 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:167025199 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:46979704 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:46979704 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:46979704 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:46979704 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:135443807 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:135443807 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:135428121 G>T maps to NM_153834.3 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:135428121 G>T maps to NM_153834.3 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:135443807 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:135443807 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:22426108 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:22426108 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:22426108 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:22426108 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:100378722 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:100378722 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:100378722 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:100378722 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:131487639 G>T maps to NM_207364.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:131487639 G>T maps to NM_207364.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:124386509 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:124386509 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:124386509 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:124386509 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:94134233 G>C maps to NM_016540.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:94134233 G>C maps to NM_016540.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:117128060 G>C maps to NM_148963.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:117128060 G>C maps to NM_148963.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:165430217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:165430217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:165430217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:165430217 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:37901262 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:37901262 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:10103949 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:10103949 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:10103949 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:10103949 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:94377137 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:94377137 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:94377137 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:94377137 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:42526522 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:42526522 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:42526522 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:42526522 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:72842194 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:72842194 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:72842194 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:72842194 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:66957417 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:66957417 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:146480399 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:146480399 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:146480399 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:146480399 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:34029650 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:34029650 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:34029650 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:34029650 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:38122752 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:38122752 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:38122752 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:38122752 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:52700874 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:52700874 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:52700874 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:52700874 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:59944242 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:59944242 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:42162344 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:42162344 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:42162344 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:42162344 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:145020715 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:145020715 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:5336910 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:5336910 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:5336910 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:5336910 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:121363562 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:121363562 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:121363562 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:121363562 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:18868899 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:18868899 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:18868899 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:18868899 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:43436450 A>G maps to NM_015052.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:43436450 A>G maps to NM_015052.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:124692484 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:124692484 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:81359162 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:81359162 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:81372117 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:81372117 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:185959563 G>A maps to NM_031935.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:185959563 G>A maps to NM_031935.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:162910959 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:162910959 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:178080659 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:178080659 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:178080659 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:178080659 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:46700181 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:46700181 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:14248434 G>T maps to NM_006041.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:14248434 G>T maps to NM_006041.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:119987820 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:119987820 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:119987820 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:119987820 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:22155851 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:22155851 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:113816545 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:113816545 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:94596007 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:94596007 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:94596007 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:94596007 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:129231390 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:129231390 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:129231390 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:129231390 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:23358628 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:23358628 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:23387441 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:23387441 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:111663616 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:111663616 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:18172010 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:18172010 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:18172012 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:18172012 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:81585041 G>T maps to NM_172217.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:81585041 G>T maps to NM_172217.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:166926195 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:166926195 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:43922292 C>T maps to NM_175882.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:43922292 C>T maps to NM_175882.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:234090907 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:234090907 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:59947352 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:59947352 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:209968831 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:209968831 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:209968831 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:209968831 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:76629328 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:76629328 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:42457269 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:42457269 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:42457269 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:42457269 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:52285377 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:52285377 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:52285377 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:52285377 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182392195 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182392195 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:54812727 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:54812727 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:15590597 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:15590597 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:15688753 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:15688753 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:15590597 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:15590597 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:15688753 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:15688753 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:31309151 G>T maps to NM_001145808.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:31309151 G>T maps to NM_001145808.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:31388255 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:31388255 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:31388255 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:31388255 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:7614177 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:7614177 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:226822506 C>A maps to NM_002221.3 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:226822506 C>A maps to NM_002221.3 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:24427343 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:24427343 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:24427343 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:24427343 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:59970756 A>T maps to ENST00000356057 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:59970756 A>T maps to ENST00000356057 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:156232097 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:156232097 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:156232097 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:156232097 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110774787 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110774787 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:110754217 G>T maps to NM_004978.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:110754217 G>T maps to NM_004978.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:96040850 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:96040850 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:96040850 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:96040850 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:88792842 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:88792842 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:88792842 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:88792842 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:64064882 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:64064882 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:64064882 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:64064882 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:78799165 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:78799165 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:78799165 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:78799165 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:62076555 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:62076555 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:62044882 G>C maps to NM_172107.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:62044882 G>C maps to NM_172107.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:62076555 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:62076555 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:196300262 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:196300262 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:196300262 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:196300262 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:77727719 G>A maps to NM_023930.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:77727719 G>A maps to NM_023930.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:44176685 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:44176685 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:44176685 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:44176685 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:7013673 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:7013673 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:142650886 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:142650886 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:142650886 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:142650886 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:24598485 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:24598485 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:24598485 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:24598485 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:22659605 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:22659605 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:22659605 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:22659605 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:241706458 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:241706458 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:51901353 G>T maps to NM_032559.4 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:51901353 G>T maps to NM_032559.4 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:55247735 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:55247735 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:55247735 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:55247735 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:70413070 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:70413070 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:70413070 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:70413070 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:152733825 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:152733825 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:152733825 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:152733825 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:91830044 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:91830044 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:39079199 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:39079199 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:39079199 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:39079199 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:53167221 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:53167221 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:53167221 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:53167221 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:52710626 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:52710626 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:52710626 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:52710626 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:46021720 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:46021720 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31768325 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31768325 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:31768325 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:31768325 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:31768508 C>T maps to NM_181599.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:31768508 C>T maps to NM_181599.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:153137994 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:153137994 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:153137994 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:153137994 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:7012195 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:7012195 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:7012195 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:7012195 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:107667261 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:107667261 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:107667261 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:107667261 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:152759840 C>T maps to NM_178353.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:152759840 C>T maps to NM_178353.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:169689811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:169689811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:169689811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:169689811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:11213192 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:11213192 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:109010078 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:109010078 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:66083706 G>A maps to NM_002303.5 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:66083706 G>A maps to NM_002303.5 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:27395082 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:27395082 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:27395082 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:27395082 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:202245409 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:202245409 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:202245409 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:202245409 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:48958533 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:48958533 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:28150836 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:28150836 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:90534390 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:90534390 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:49497770 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:49497770 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:33886332 G>A maps to NM_005574.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:33886332 G>A maps to NM_005574.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:76407430 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:76407430 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:141031878 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:141031878 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:141526926 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:141526926 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:141526926 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:141526926 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:170112575 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:170112575 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:170112575 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:170112575 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:99798553 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:99798553 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:99798553 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:99798553 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:76377112 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:76377112 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:62859211 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:62859211 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:62859211 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:62859211 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:70611391 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:70611391 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:70621301 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:70621301 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:70611391 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:70611391 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:70304075 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:70304075 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:86041979 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:86041979 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:47636178 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:47636178 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:21349426 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:21349426 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:30254904 C>T maps to NM_002365.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:30254904 C>T maps to NM_002365.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:140984395 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:140984395 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:140969329 G>T maps to NM_138702.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:140969329 G>T maps to NM_138702.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:140984395 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:140984395 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:78130848 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:78130848 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:78130848 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:78130848 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:12491435 G>A maps to NM_018050.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:12491435 G>A maps to NM_018050.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:43364127 G>A maps to ENST00000344686 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:43364127 G>A maps to ENST00000344686 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:48248366 G>T maps to NM_002747.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:48248366 G>T maps to NM_002747.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:165111393 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:165111393 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:164466874 G>T maps to ENST00000514618 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:164466874 G>T maps to ENST00000514618 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:165111393 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:165111393 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:119727849 C>A maps to NM_006770.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:119727849 C>A maps to NM_006770.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:82034993 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:82034993 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:82034993 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:82034993 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:136626439 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:136626439 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:136626439 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:136626439 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:47913308 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:47913308 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:151134111 C>T maps to NM_053002.4 Q2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:151134111 C>T maps to NM_053002.4 Q2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:134814867 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:134814867 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:134814867 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:134814867 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:71067425 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:71067425 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:126776494 C>T maps to NM_032446.2 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:126776494 C>T maps to NM_032446.2 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:112778848 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:112778848 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:112778848 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:112778848 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:19288710 G>T maps to NM_001198695.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:19288710 G>T maps to NM_001198695.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:119216678 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:119216678 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:135077582 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:135077582 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:1560314 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:1560314 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:18463433 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:18463433 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:18463433 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:18463433 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:20365600 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:20365600 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:20365600 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:20365600 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:238434452 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:238434452 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:238434452 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:238434452 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:146576325 G>T maps to NM_172250.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:146576325 G>T maps to NM_172250.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:89131198 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:89131198 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158811788 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158811788 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:100843432 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:100843432 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:100843432 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:100843432 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:60230079 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:60230079 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:60230079 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:60230079 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:60064674 G>T maps to NM_148975.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:60064674 G>T maps to NM_148975.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56670941 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56670941 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:98657188 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:98657188 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:63569782 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:63569782 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:63569782 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:63569782 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:11180067 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:11180067 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:11180067 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:11180067 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:237054770 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:237054770 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:29881602 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:29881602 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:29881602 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:29881602 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:8962035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:8962035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:9009173 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:9009173 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:9009175 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:9009175 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:9080346 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:9080346 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:8962035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:8962035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:9009173 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:9009173 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:9009175 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:9009175 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:3248431 G>T maps to NM_015419.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:3248431 G>T maps to NM_015419.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:77739295 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:77739295 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:241070374 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:241070374 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:81101339 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:81101339 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:108218455 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:108218455 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:10430421 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:10430421 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:10430421 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:10430421 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:10356666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:10356666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:10356666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:10356666 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23862515 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23862515 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23867879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23867879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23862515 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23862515 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23866763 C>A maps to NM_002471.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23866763 C>A maps to NM_002471.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23867879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23867879 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23884104 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23884104 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23884104 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:23884104 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:45299252 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:45299252 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:45299252 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:45299252 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:16674170 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:16674170 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:18054406 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:18054406 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:18054406 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:18054406 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:26163959 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:26163959 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:26163959 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:26163959 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:109844479 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:109844479 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:47361912 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:47361912 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:76623720 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:76623720 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:76623720 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:76623720 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:76909504 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:76909504 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:76909504 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:76909504 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:128331737 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:128331737 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:1915752 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:1915752 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:80246770 G>T maps to NM_032693.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:80246770 G>T maps to NM_032693.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:89880731 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:89880731 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:89880731 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:89880731 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:78515587 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:78515587 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:35756430 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:35756430 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:35756430 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:35756430 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:112832188 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:112832188 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:22849674 G>T maps to NM_004540.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:22849674 G>T maps to NM_004540.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:158494629 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:158494629 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:134292651 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:134292651 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:149918783 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:149918783 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:149918783 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:149918783 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:67379274 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:67379274 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:46133981 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:46133981 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:46133981 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:46133981 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:236192919 C>A maps to NM_002508.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:236192919 C>A maps to NM_002508.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:43666911 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:43666911 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:50744733 C>A maps to NM_022162.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:50744733 C>A maps to NM_022162.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:155774755 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:155774755 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:157183026 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:157183026 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:50645574 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:50645574 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:51149828 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:51149828 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:51149828 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:51149828 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:88679405 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:88679405 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:2289454 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:2289454 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:2289454 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:2289454 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:135286353 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:135286353 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:135286353 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:135286353 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:153995617 C>T maps to NM_207308.2 Q1426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:153995617 C>T maps to NM_207308.2 Q1426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:134051079 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:134051079 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:722617 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:722617 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:28141302 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:28141302 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:28141302 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:28141302 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:102359239 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:102359239 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:55735297 G>A maps to NM_001005491.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:55735297 G>A maps to NM_001005491.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123900208 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123900208 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123900208 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123900208 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123900721 C>A maps to ENST00000375021 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123900721 C>A maps to ENST00000375021 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:107332059 G>T maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:107332059 G>T maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:247835509 C>A maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:247835509 C>A maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:114090286 G>T maps to ENST00000374428 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:114090286 G>T maps to ENST00000374428 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248138835 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248138835 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:248138835 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:248138835 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248569194 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248569194 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123811223 C>T maps to NM_001001965.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123811223 C>T maps to NM_001001965.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:56380870 T>A maps to NM_001004740.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:56380870 T>A maps to NM_001004740.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:21108971 A>G maps to NM_001001968.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:21108971 A>G maps to NM_001001968.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123777158 C>T maps to NM_001005197.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:123777158 C>T maps to NM_001005197.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:56511221 G>T maps to NM_001005284.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:56511221 G>T maps to NM_001005284.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77761565 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77761565 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:77761565 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:77761565 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:101725026 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:101725026 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:163378325 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:163378325 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:163378325 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:163378325 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:81905542 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:81905542 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:77051811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:77051811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:77051811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:77051811 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:28866673 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:28866673 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:28866673 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:28866673 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:176679323 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:176679323 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:176679323 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:176679323 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:176738882 C>T maps to NM_020318.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:176738882 C>T maps to NM_020318.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:51592697 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:51592697 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:51592697 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:51592697 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:161969830 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:161969830 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:161969830 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:161969830 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:125617384 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:125617384 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:125617384 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:125617384 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:223158468 G>C maps to NM_013942.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:223158468 G>C maps to NM_013942.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:223158468 G>C maps to NM_013942.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:223158468 G>C maps to NM_013942.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:134076219 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:134076219 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:134076219 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:134076219 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrY:5441302 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrY:5441302 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrY:5441302 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrY:5441302 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrY:5449875 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrY:5449875 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:99658491 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:99658491 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:141234085 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:141234085 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:31144039 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:31144039 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:31144039 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:31144039 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:142537296 G>T maps to NM_013363.3 Y376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:142537296 G>T maps to NM_013363.3 Y376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:78804691 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:78804691 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:72289563 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:72289563 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:72291897 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:72291897 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:72289563 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:72289563 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:72291897 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:72291897 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:20704817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:20704817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:20704817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:20704817 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:66827247 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:66827247 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:66827247 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:66827247 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20410408 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:20410408 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20410408 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:20410408 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:57333218 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:57333218 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:57333218 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:57333218 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:239165692 C>A maps to NM_022817.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:239165692 C>A maps to NM_022817.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:48573119 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:48573119 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:48573119 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:48573119 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153283301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153283301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:153283301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:153283301 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:26881656 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:26881656 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:33225839 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:33225839 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:33225839 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:33225839 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:106513258 G>T maps to NM_002649.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:106513258 G>T maps to NM_002649.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:3644325 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:3644325 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:81167389 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:81167389 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:81167389 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:81167389 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:89289989 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:89289989 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:89289989 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:89289989 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:201263012 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:201263012 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:9457443 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:9457443 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:9457443 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:9457443 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:105398568 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:105398568 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131948893 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131948893 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:131953180 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:131953180 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:48447093 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:48447093 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:48447093 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:48447093 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:50714403 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:50714403 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:82355609 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:82355609 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:82355609 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:82355609 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:7607845 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:7607845 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:133245352 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:133245352 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:133245352 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:133245352 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:121215822 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:121215822 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:121215822 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:121215822 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:39125440 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:39125440 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:39125440 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:39125440 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:76809247 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:76809247 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:76809247 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:76809247 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:54974308 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:54974308 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182827131 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182827131 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182852497 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182852497 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182852499 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:182852499 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182827131 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182827131 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182852497 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182852497 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182852499 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:182852499 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:47087823 G>A maps to NM_005972.4 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:47087823 G>A maps to NM_005972.4 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:19644420 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:19644420 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:19644420 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:19644420 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12954376 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12954376 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:70980359 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:70980359 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:23521359 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:23521359 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:84651020 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:84651020 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:48712010 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:48712010 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:48712010 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:48712010 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:82090664 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:82090664 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:82090797 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:82090797 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:82090797 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:82090797 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:5294628 G>T maps to NM_144773.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:5294628 G>T maps to NM_144773.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:16008395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:16008395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:16008395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:16008395 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:57252181 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:57252181 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:57252181 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:57252181 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:43421780 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:43421780 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:43421780 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:43421780 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:43448773 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:43448773 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:43261692 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:43261692 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:43261692 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:43261692 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:54161614 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:54161614 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:43571959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:43571959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:43571959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:43571959 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:71331317 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:71331317 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:71331317 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:71331317 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:125140304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:125140304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:125140304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:125140304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:141712916 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:141712916 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:87701590 T>G maps to NM_080685.2 S1981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:87701590 T>G maps to NM_080685.2 S1981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:18753999 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:18753999 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:70951641 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:70951641 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:8451871 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:8451871 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:8748030 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:8748030 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:8748124 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:8748124 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:8451871 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:8451871 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:8748030 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:8748030 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:8748124 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:8748124 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:157691110 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:157691110 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:15677651 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:15677651 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:71094882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:71094882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:71094882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:71094882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:29708206 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:29708206 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:42966066 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:42966066 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:42966085 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:42966085 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:42966066 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:42966066 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:61674204 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:61674204 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:28916236 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:28916236 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:28916236 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:28916236 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:17699754 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:17699754 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:17699754 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:17699754 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:95412525 C>T maps to NM_012415.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:95412525 C>T maps to NM_012415.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:155203433 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:155203433 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:74441942 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:74441942 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:74441942 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:74441942 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:110108580 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:110108580 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:36112502 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:36112502 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:36112502 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:36112502 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:79349035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:79349035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:79350264 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:79350264 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:79349035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:79349035 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:79350264 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:79350264 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:103136907 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:103136907 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:103393678 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:103393678 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:103136907 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:103136907 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:103393678 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:103393678 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:30060818 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:30060818 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:30060818 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:30060818 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:24040540 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:24040540 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:24040540 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:24040540 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:87157743 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:87157743 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:87157743 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:87157743 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:116303912 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:116303912 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:163042539 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:163042539 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:163042539 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:163042539 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:74475749 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:74475749 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:49397506 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:49397506 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:40705941 C>T maps to NM_012421.3 S1856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:40705941 C>T maps to NM_012421.3 S1856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:44030161 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:44030161 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:4845846 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:4845846 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:4845846 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:4845846 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:119207085 C>T maps to NM_032015.3 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:119207085 C>T maps to NM_032015.3 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:24617144 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:24617144 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:24617144 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:24617144 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:30780746 G>T maps to ENST00000452273 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:30780746 G>T maps to ENST00000452273 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:30780746 G>T maps to ENST00000452273 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:30780746 G>T maps to ENST00000452273 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:56510625 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:56510625 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:56510625 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:56510625 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:34393058 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:34393058 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:26885234 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:26885234 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:26885234 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:26885234 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:166864429 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:166864429 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:17595601 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:17595601 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:108995489 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:108995489 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:108995489 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:108995489 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:948096 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:948096 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:187416441 C>T maps to NM_001004312.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:187416441 C>T maps to NM_001004312.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:71629435 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:71629435 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:71629435 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:71629435 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:93004038 G>T maps to NM_175634.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:93004038 G>T maps to NM_175634.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:36259466 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr21:36259466 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:32340071 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:32340071 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:39027321 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:39027321 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:237659694 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:237659694 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:237659694 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:237659694 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:237817570 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:237817570 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:101704716 C>A maps to NM_001400.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:101704716 C>A maps to NM_001400.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:134992516 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:134992516 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:134992516 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:134992516 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:128707375 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:128707375 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:128707375 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:128707375 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:50900218 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:50900218 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:50900218 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:50900218 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:127734178 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:127734178 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:127734178 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:127734178 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:25691246 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:25691246 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:25691246 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:25691246 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:62025513 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:62025513 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:50140754 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:50140754 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:50140754 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:50140754 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:50192496 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:50192496 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:243652562 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:243652562 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:39556194 A>C maps to NM_006364.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:39556194 A>C maps to NM_006364.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:13912363 T>A maps to NM_025229.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:13912363 T>A maps to NM_025229.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:84658676 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:84658676 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:84658676 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:84658676 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:122631816 G>T maps to NM_001031702.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:122631816 G>T maps to NM_001031702.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:26135658 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:26135658 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:26135658 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:26135658 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:26688318 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:26688318 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:26702123 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:26702123 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:26688318 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:26688318 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:26702123 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr22:26702123 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:7285493 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:7285493 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:7285493 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:7285493 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:46338937 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:46338937 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:156184830 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:156184830 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:14181531 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:14181531 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:14181531 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:14181531 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:67101546 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:67101546 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:67101546 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:67101546 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:156784832 G>T maps to NM_001161441.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:156784832 G>T maps to NM_001161441.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:130509324 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:130509324 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:38092060 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:38092060 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:38633873 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:38633873 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:87752867 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:87752867 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56906416 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56906416 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:56901118 G>A maps to NM_000339.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:56901118 G>A maps to NM_000339.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:56906416 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:56906416 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:122809424 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:122809424 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:122809424 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:122809424 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:6604532 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:6604532 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:113456701 G>A maps to NM_003051.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:113456701 G>A maps to NM_003051.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62951042 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62951042 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:62951042 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:62951042 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:160828310 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:160828310 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:160828310 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:160828310 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:62751942 G>A maps to NM_004790.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:62751942 G>A maps to NM_004790.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62767038 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62767038 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:62767038 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:62767038 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:19698031 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:19698031 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:19698031 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:19698031 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:16064784 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:16064784 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:9097502 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:9097502 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:9118379 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:9118379 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:10027562 C>A maps to NM_001001290.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:10027562 C>A maps to NM_001001290.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:118174009 C>A maps to NM_173851.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:118174009 C>A maps to NM_173851.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:31033207 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:31033207 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:118596609 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:118596609 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:118596609 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:118596609 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:18276307 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:18276307 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:18276307 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:18276307 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75707527 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75707527 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75707606 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75707606 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:76107210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:76107210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:75672393 C>A maps to NM_152697.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:75672393 C>A maps to NM_152697.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:75707606 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:75707606 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:76107210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:76107210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:19445752 G>T maps to ENST00000395585 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:19445752 G>T maps to ENST00000395585 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:162661083 G>T maps to NM_001178015.1 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:162661083 G>T maps to NM_001178015.1 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110741194 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110741194 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:1235533 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:1235533 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:11061858 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:11061858 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:11061858 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:11061858 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:55729050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:55729050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:55729050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:55729050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:48504416 G>T maps to ENST00000417961 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:48504416 G>T maps to ENST00000417961 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:143236651 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:143236651 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:143236651 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:143236651 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:143346103 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:143346103 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:143346440 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:143346440 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21454050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21454050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:21454050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:21454050 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:21355422 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:21355422 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21196580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21196580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:21196580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:21196580 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:168096926 C>A maps to NM_003062.2 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:168096926 C>A maps to NM_003062.2 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:18897027 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:18897027 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:18907283 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:18907283 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:18897027 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:18897027 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:18907283 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:18907283 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:70497060 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:70497060 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:70497060 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:70497060 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:130913492 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:130913492 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:84375097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:84375097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:84375097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:84375097 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:130784043 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:130784043 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:12371770 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:12371770 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:12371770 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:12371770 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:108337331 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:108337331 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:108337331 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:108337331 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:106960960 A>G maps to NM_014978.1 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr10:106960960 A>G maps to NM_014978.1 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:231326264 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:231326264 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:231326264 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:231326264 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:34207414 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:34207414 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:52938448 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:52938448 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:52938448 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:52938448 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158582417 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158582417 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158587490 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158587490 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158604243 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158604243 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158610001 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158610001 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158612177 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158612177 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158655227 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158655227 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158587490 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158587490 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158604243 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158604243 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158612177 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158612177 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158644392 A>T maps to NM_003126.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:158644392 A>T maps to NM_003126.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:54848482 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:54848482 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:54848482 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:54848482 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:65218909 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:65218909 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:65249326 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:65249326 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:65249326 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:65249326 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:54707992 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:54707992 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:48117034 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:48117034 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:76775596 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:76775596 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:22486882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:22486882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:22486882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:22486882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:99796384 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:99796384 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:99796384 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:99796384 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:56748661 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:56748661 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:56748661 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:56748661 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:23709580 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:23709580 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:43624014 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:43624014 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:120977786 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:120977786 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:120977786 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:120977786 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:44235792 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:44235792 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:31587960 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:31587960 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:31587960 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:31587960 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:113166888 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:113166888 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:113166888 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:113166888 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:29819727 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:29819727 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:58475034 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:58475034 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:58475034 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:58475034 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:152716828 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:152716828 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:152716828 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:152716828 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:66812116 C>A maps to NM_001177880.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:66812116 C>A maps to NM_001177880.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:111730734 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:111730734 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:111730734 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:111730734 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:162091766 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:162091766 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:162091766 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:162091766 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:143141255 C>G maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:143141255 C>G maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:71604707 T>A maps to NM_000353.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:71604707 T>A maps to NM_000353.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:47188273 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr22:47188273 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:44555226 G>A maps to NM_145653.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:44555226 G>A maps to NM_145653.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:53018254 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:53018254 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:53018254 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:53018254 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:53303412 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:53303412 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:104441929 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:104441929 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:104441929 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr14:104441929 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:65175440 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:65175440 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:120976488 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:120976488 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:120976488 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:120976488 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:10729816 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:10729816 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:10729816 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:10729816 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:71220967 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:71220967 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:50697067 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:50697067 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:50697067 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:50697067 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:141762547 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:141762547 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:141762547 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:141762547 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:93516786 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:93516786 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:93519433 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:93519433 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:93519433 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:93519433 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:54618758 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:54618758 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:44934882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:44934882 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:43559172 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:43559172 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:169648570 G>A maps to NM_003247.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:169648570 G>A maps to NM_003247.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:122755272 G>A maps to NM_001081550.1 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:122755272 G>A maps to NM_001081550.1 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:11418943 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:11418943 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:11630032 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:11630032 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:11418943 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:11418943 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:11630032 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:11630032 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:43779578 G>T maps to NM_005424.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:43779578 G>T maps to NM_005424.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:153692093 T>C maps to NM_145720.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:153692093 T>C maps to NM_145720.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:54214561 C>A maps to NM_014464.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:54214561 C>A maps to NM_014464.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:166910469 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:166910469 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:166935712 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:166935712 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:63088514 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:63088514 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:63088514 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:63088514 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:149051182 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:149051182 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:149051182 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:149051182 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:75387408 G>A maps to NM_138691.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:75387408 G>A maps to NM_138691.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:79614582 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:79614582 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:79614582 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:79614582 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:129694236 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:129694236 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:129694236 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:129694236 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:32955915 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:32955915 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:32962069 G>T maps to NM_207313.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:32962069 G>T maps to NM_207313.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:42824405 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:42824405 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:42824405 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr19:42824405 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:83417292 C>T maps to NM_001080506.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:83417292 C>T maps to NM_001080506.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:15601531 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:15601531 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:15601531 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:15601531 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:63189052 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:63189052 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:108510255 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:108510255 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:56669048 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:56669048 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:56669048 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:56669048 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:74876521 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:74876521 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:68725196 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:68725196 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:68725196 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:68725196 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:68725498 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:68725498 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:113566248 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:113566248 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:113566248 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr11:113566248 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:117797465 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:117797465 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:117797465 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:117797465 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12186306 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12186306 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:12186306 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:12186306 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:74902191 C>T maps to NM_001112808.2 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:74902191 C>T maps to NM_001112808.2 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:47479070 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:47479070 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:47479070 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:47479070 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:72366518 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:72366518 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:72366518 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:72366518 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:144320477 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:144320477 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:144320477 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:144320477 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:6639070 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:6639070 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:186306080 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:186306080 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:186306080 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:186306080 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:1306415 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:1306415 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:20137796 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:20137796 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:20137796 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:20137796 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:67190464 C>A maps to NM_003789.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:67190464 C>A maps to NM_003789.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:123688195 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:123688195 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:42166915 G>T maps to NM_001042646.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:42166915 G>T maps to NM_001042646.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248031024 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248031024 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248031401 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248031401 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:248028077 G>A maps to NM_015431.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:248028077 G>A maps to NM_015431.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:75028154 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:75028154 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:75028154 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:75028154 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:38237445 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr13:38237445 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77423090 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77423090 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:77378051 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:77378051 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:77423090 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:77423090 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:234847525 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:234847525 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrY:9306515 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrY:9306515 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrY:9306515 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrY:9306515 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:33042737 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:33042737 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:179593547 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:179593547 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:179602663 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:179602663 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:179669444 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:179669444 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:179593547 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:179593547 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:179602663 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:179602663 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:179669444 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:179669444 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:19747920 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:19747920 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:41856232 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:41856232 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:166577954 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:166577954 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:166577954 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:166577954 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:36048934 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:36048934 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:36048934 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr5:36048934 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:115586822 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:115586822 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:115586822 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:115586822 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:162469655 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:162469655 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:35381260 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:35381260 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:35381260 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr9:35381260 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:54586107 C>A maps to ENST00000260323 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:54586107 C>A maps to ENST00000260323 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:158991221 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:158991221 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:158991221 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:158991221 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:216419856 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:216419856 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:216257908 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:216257908 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:216419856 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:216419856 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:76815803 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:76815803 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:76815803 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:76815803 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:50759273 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:50759273 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:50759273 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:50759273 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:145051672 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:145051672 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:145051672 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:145051672 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:70814952 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:70814952 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:42251818 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:42251818 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:56059121 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:56059121 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:56059121 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:56059121 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:133072128 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:133072128 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:133072128 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr6:133072128 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:100352756 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:100352756 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:100352756 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:100352756 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:62304304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr15:62304304 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12382036 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:12382036 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:12382036 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr1:12382036 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:85600422 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:85600422 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:85658523 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:85658523 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:39184081 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr4:39184081 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:241907973 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:241907973 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:124105753 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:124105753 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:124105753 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:124105753 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:228771915 A>T maps to NM_178821.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:228771915 A>T maps to NM_178821.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:141413963 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:141413963 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:141413963 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:141413963 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:66418072 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:66418072 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:66418072 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr17:66418072 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:49374185 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:49374185 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:44851323 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:44851323 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:31567665 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:31567665 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:2692690 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:2692690 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:2692793 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chrX:2692793 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:2692690 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:2692690 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:2692793 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chrX:2692793 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:168074610 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:168074610 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:168074610 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:168074610 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:56362210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:56362210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:56365613 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:56365613 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:56362210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:56362210 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:56365613 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr8:56365613 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:216974248 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:216974248 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:58345405 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:58345405 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:58345405 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr12:58345405 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:142090047 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:142090047 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:142090047 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:142090047 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:166960175 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:166960175 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:145274896 C>A maps to NM_014795.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:145274896 C>A maps to NM_014795.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:68251268 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:68251268 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:68268647 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:68268647 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:2880224 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:2880224 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:44801257 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:44801257 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:44801257 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:44801257 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:219510760 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:219510760 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:219510760 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr2:219510760 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:45131768 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:45131768 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:45131768 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:45131768 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:49559352 C>A maps to NM_015069.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr16:49559352 C>A maps to NM_015069.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:22671868 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:22671868 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:22671868 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr18:22671868 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:31038694 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:31038694 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:64023482 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:64023482 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:149151030 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:149151030 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:88965692 G>T maps to NM_181646.2 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:88965692 G>T maps to NM_181646.2 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:57765943 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:57765943 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:57765943 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr20:57765943 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:50121454 C>A maps to NM_007009.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr7:50121454 C>A maps to NM_007009.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:58552021 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:58552021 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:126180701 C>A maps to NM_025112.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01W-0928-08 chr3:126180701 C>A maps to NM_025112.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:125612686 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:125612686 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:25003790 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:25003790 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:207482244 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:207482244 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:119582872 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:119582872 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:20061975 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:20061975 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:55321183 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:55321183 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:142170967 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:142170967 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:11039021 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:11039021 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:21785749 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:21785749 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:72532425 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:72532425 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:112605117 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:112605117 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:26799060 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:26799060 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:165713013 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:165713013 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:181731862 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:181731862 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:181732713 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:181732713 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:81978993 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:81978993 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:1984342 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:1984342 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:62503732 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:62503732 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:45067233 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:45067233 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:64235608 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:64235608 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:50864020 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:50864020 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:180012115 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:180012115 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:37760058 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:37760058 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:21897117 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:21897117 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:11016138 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:11016138 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:87018984 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:87018984 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:72185925 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:72185925 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:179996440 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:179996440 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:115553787 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:115553787 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:36790876 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:36790876 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:28857803 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:28857803 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:33998576 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:33998576 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:67963802 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:67963802 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:96602807 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:96602807 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:154991263 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:154991263 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:49226374 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:49226374 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:85163540 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:85163540 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:21584805 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:21584805 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:10283904 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:10283904 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:169144556 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:169144556 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:169496914 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:169496914 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:66254835 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:66254835 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:25610107 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:25610107 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:245250110 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:245250110 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:142568266 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:142568266 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:56478752 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:56478752 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:45725887 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:45725887 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:201927763 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:201927763 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:89660172 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:89660172 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:119438434 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:119438434 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:157667219 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:157667219 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:157668078 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:157668078 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:38285344 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:38285344 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:28919691 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:28919691 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:33304555 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:33304555 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:50044916 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:50044916 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:93998698 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:93998698 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:49196410 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:49196410 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:113937324 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:113937324 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:79351416 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:79351416 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:116360491 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:116360491 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:133491924 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:133491924 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:24181063 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:24181063 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:9873090 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:9873090 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:9885217 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:9885217 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:158402287 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:158402287 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:69573155 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:69573155 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:30540137 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:30540137 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:78509305 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:78509305 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:1749261 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:1749261 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:157367458 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:157367458 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:25839894 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:25839894 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:19063616 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:19063616 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:48190973 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:48190973 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:18989087 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:18989087 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:92821694 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:92821694 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:69721027 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:69721027 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:38348601 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:38348601 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:237272692 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:237272692 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:62073705 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:62073705 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:109740086 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:109740086 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:11983605 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:11983605 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:55270350 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:55270350 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:55270493 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:55270493 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:81242137 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:81242137 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:48368460 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:48368460 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:67384093 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:67384093 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:33505281 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:33505281 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:148798512 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:148798512 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:135301891 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:135301891 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:168867382 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:168867382 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:40422654 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:40422654 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:165620344 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:165620344 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:21914513 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:21914513 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:97256324 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:97256324 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:237023293 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:237023293 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:9010588 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:9010588 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:102071208 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:102071208 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:30387878 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:30387878 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:78570343 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:78570343 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:16890760 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:16890760 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:24810239 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:24810239 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:70518412 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:70518412 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:162326689 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:162326689 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:163295789 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:163295789 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:102332420 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:102332420 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:51093143 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:51093143 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:226550781 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:226550781 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:142546378 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:142546378 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:10565640 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:10565640 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:186423408 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:186423408 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:119327818 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:119327818 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:145799491 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:145799491 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:18768132 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:18768132 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:81762874 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:81762874 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:64699105 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:64699105 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:105733565 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:105733565 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:49398422 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:49398422 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:53822250 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:53822250 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:43687652 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:43687652 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:30804535 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:30804535 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:141774264 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:141774264 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:87847069 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:87847069 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:163043992 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:163043992 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:95091085 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:95091085 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:21811147 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:21811147 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:39459304 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:39459304 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:237954724 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:237954724 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:153362788 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:153362788 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:47468561 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:47468561 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:166019345 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:166019345 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:84644550 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:84644550 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:95033272 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:95033272 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:61562417 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:61562417 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:135173780 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:135173780 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:49118044 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:49118044 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:49118081 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:49118081 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:25778015 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:25778015 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:35919284 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:35919284 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:32422495 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:32422495 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:57850451 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:57850451 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:2200650 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:2200650 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:39325478 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:39325478 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:231117273 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:231117273 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:49075773 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:49075773 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:44344042 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:44344042 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:100473151 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:100473151 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:52676930 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:52676930 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:53092579 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:53092579 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:39540913 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:39540913 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:68660767 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:68660767 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:160051027 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:160051027 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:20871614 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:20871614 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:36760910 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:36760910 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:123754942 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:123754942 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:42683241 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:42683241 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:113711319 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:113711319 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:10942693 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:10942693 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:209949128 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:209949128 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:73012627 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:73012627 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:58177111 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:58177111 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:138818497 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:138818497 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:63985408 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:63985408 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:57958546 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:57958546 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:103341704 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:103341704 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:215853473 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:215853473 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:106761627 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:106761627 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:241959541 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:241959541 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:43650735 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:43650735 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:37506990 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:37506990 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:68358605 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:68358605 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:128890408 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chrX:128890408 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:27408099 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:27408099 T>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:187370371 A>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:187370371 A>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:99212146 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:99212146 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:28331627 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:28331627 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:44621873 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:44621873 A>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:44621982 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr3:44621982 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:64159245 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:64159245 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:58085146 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:58085146 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:44101180 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:44101180 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:30548665 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:30548665 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:238050908 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:238050908 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:48375246 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:48375246 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:66992244 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:66992244 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:43416589 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:43416589 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:17438418 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:17438418 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:119028921 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:119028921 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:132295781 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:132295781 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:89391293 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:89391293 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:7240032 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:7240032 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:31352470 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:31352470 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:147121846 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:147121846 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:35085393 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:35085393 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:131897085 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:131897085 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:111891988 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:111891988 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:100203766 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:100203766 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:151646935 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:151646935 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:85958712 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:85958712 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:870751 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:870751 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:82924483 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:82924483 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:82924489 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:82924489 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:197873554 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:197873554 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:5722050 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:5722050 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:5963403 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:5963403 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:79503473 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:79503473 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:83328190 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:83328190 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:99042112 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:99042112 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:57045640 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:57045640 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:21256096 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:21256096 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:45409801 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:45409801 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:33386937 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:33386937 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:36069944 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:36069944 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:141051888 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:141051888 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:157192627 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:157192627 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:62595151 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:62595151 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:176927477 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:176927477 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:14610119 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:14610119 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160099235 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160099235 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:10428273 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:10428273 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:10625925 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:10625925 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:172410841 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:172410841 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:76875837 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:76875837 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:11049710 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:11049710 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:112046196 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:112046196 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:56857167 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:56857167 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:32661278 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:32661278 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:43279798 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:43279798 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:108042928 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:108042928 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:4626137 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:4626137 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:81371127 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:81371127 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:58471399 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:58471399 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:81427721 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:81427721 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:77798619 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:77798619 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:73139583 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:73139583 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:24470881 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:24470881 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:172425688 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:172425688 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:179452360 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:179452360 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:182873577 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:182873577 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:14731397 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:14731397 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:76489222 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:76489222 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:71024015 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:71024015 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:184585240 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:184585240 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:42971660 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:42971660 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:181700228 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:181700228 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:201054193 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:201054193 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:14991402 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:14991402 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:134626055 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:134626055 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:149624786 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:149624786 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:44148592 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:44148592 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:35910650 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:35910650 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:104869517 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:104869517 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:52602211 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:52602211 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:1326278 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:1326278 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:43866218 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:43866218 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:158301086 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:158301086 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:158146918 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:158146918 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:103508272 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:103508272 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:59195150 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:59195150 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:49547414 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:49547414 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:50824161 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:50824161 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:50828666 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:50828666 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:53260430 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:53260430 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:403584 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:403584 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:29252187 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:29252187 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:26805862 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:26805862 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:98243986 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:98243986 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:11096920 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:11096920 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:92814730 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:92814730 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:42902105 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:42902105 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:125262189 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:125262189 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:51111051 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:51111051 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:103354559 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:103354559 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:70850884 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:70850884 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:94029478 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:94029478 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:139869405 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:139869405 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:189872576 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:189872576 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:47422365 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:47422365 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:49676822 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:49676822 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:84911137 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:84911137 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:70804988 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:70804988 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:18168204 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:18168204 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:19209934 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:19209934 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:24937901 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:24937901 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:57571071 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:57571071 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:16709789 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:16709789 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:74636354 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:74636354 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:52743854 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:52743854 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:176942555 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:176942555 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:169195280 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:169195280 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:140268663 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:140268663 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:120977677 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:120977677 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:234371402 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:234371402 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:95557025 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:95557025 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:4431040 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:4431040 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:21730601 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:21730601 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:11522854 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:11522854 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:220150678 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:220150678 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:31383384 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:31383384 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:169135326 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:169135326 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:169141244 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:169141244 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:64045725 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:64045725 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:205117250 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:205117250 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:44704037 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:44704037 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:95657412 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:95657412 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:71871069 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:71871069 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:137821251 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:137821251 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:172525463 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:172525463 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:141458777 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:141458777 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:103988351 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:103988351 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:101196668 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:101196668 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:97518658 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:97518658 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:66439285 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:66439285 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:110293497 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:110293497 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:56270715 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:56270715 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:128028815 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:128028815 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:103484057 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:103484057 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:75248538 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:75248538 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:76964495 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:76964495 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:216896518 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:216896518 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:56536321 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:56536321 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:133580491 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:133580491 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:133580504 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:133580504 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160971011 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160971011 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160971019 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:160971019 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:31845871 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:31845871 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:81042092 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:81042092 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:139380051 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:139380051 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:61011255 C>T maps to ENST00000435852 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:61011255 C>T maps to ENST00000435852 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:79585912 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:79585912 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:10671621 C>A maps to NM_022068.2 G2721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:10671621 C>A maps to NM_022068.2 G2721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:8762959 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:8762959 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:89849559 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:89849559 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:45669019 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:45669019 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:45669038 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:45669038 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:150885054 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:150885054 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:48796169 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:48796169 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:48796174 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:48796174 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:48888461 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:48888461 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:8153083 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:8153083 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:48049350 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:48049350 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:157771595 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:157771595 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:54476617 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:54476617 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:191861946 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:191861946 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:69588305 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:69588305 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:240333665 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:240333665 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:153415438 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:153415438 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:50059434 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:50059434 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:12724905 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:12724905 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:27184359 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:27184359 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:151128010 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:151128010 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:27453300 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:27453300 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:170221313 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:170221313 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:30880410 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:30880410 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:120592986 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:120592986 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:69204684 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:69204684 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:33110297 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:33110297 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:183942625 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:183942625 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:54581129 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:54581129 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:133357506 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:133357506 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:132458604 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:132458604 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:110903038 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:110903038 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:110903040 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:110903040 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:47646938 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:47646938 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:100374909 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:100374909 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:123489044 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:123489044 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:18988569 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:18988569 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:197172027 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:197172027 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:65415099 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:65415099 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:33052718 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:33052718 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:185987597 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:185987597 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:83349088 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:83349088 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:113860093 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:113860093 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:79126231 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:79126231 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:42275733 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:42275733 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:29972871 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:29972871 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:104651666 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:104651666 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:35874745 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:35874745 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:82588522 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:82588522 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:100949731 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:100949731 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:61908955 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:61908955 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:61917508 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:61917508 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:61781379 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:61781379 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:75970539 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:75970539 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:53267521 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:53267521 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:66638683 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:66638683 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:68650678 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:68650678 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:31276829 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:31276829 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:45351646 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:45351646 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:52815944 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:52815944 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:41231437 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:41231437 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:26810546 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:26810546 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:150644630 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:150644630 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:178968383 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:178968383 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:142650726 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:142650726 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:136657431 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:136657431 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:24902241 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:24902241 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:96972163 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:96972163 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:47281407 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:47281407 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:55367480 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:55367480 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:53071364 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:53071364 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:52882036 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:52882036 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:39726320 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:39726320 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:31798333 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:31798333 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:54870272 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:54870272 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:17964568 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:17964568 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:83859511 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:83859511 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:16753562 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:16753562 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:141115770 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:141115770 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:141143629 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:141143629 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:71302061 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:71302061 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:238656996 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:238656996 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:85434222 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:85434222 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:65425415 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:65425415 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:71496324 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:71496324 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:87432485 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:87432485 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:87432487 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:87432487 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:165109716 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:165109716 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:119699849 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:119699849 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:40573737 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:40573737 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:126705571 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:126705571 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:126705575 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:126705575 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:99960520 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:99960520 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:140171820 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:140171820 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:168363033 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:168363033 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:90874610 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:90874610 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:174987488 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:174987488 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:59831812 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:59831812 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:124631831 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:124631831 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:9020870 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:9020870 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:1213223 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:1213223 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:10257932 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:10257932 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:10293752 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:10293752 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:1998829 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:1998829 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:16891122 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:16891122 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:204915423 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:204915423 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:23938920 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:23938920 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:23938923 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:23938923 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:25791363 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:25791363 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:51875331 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:51875331 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:65029213 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:65029213 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:56421923 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:56421923 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:56515550 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:56515550 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70518383 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:70518383 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:84498237 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:84498237 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:1438956 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:1438956 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:59512610 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:59512610 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:87636370 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:87636370 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:88703426 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:88703426 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:51075775 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:51075775 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:153995571 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:153995571 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:13383234 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:13383234 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:101096607 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:101096607 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:101097667 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:101097667 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:228482373 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:228482373 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:28141593 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:28141593 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:103573181 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:103573181 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:167525021 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:167525021 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:50943446 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:50943446 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:161969778 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:161969778 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:88331836 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:88331836 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:17566162 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:17566162 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:23647872 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:23647872 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:8030914 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:8030914 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:233152643 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:233152643 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:24597372 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:24597372 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:55146465 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:55146465 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:55156787 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:55156787 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:156879772 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:156879772 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:57329064 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:57329064 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:57334860 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:57334860 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:230503933 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:230503933 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:33383456 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:33383456 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:20466215 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:20466215 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:133220649 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:133220649 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:149212099 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:149212099 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:149212134 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:149212134 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:203028291 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:203028291 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:203028293 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:203028293 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:69012131 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:69012131 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:40767544 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:40767544 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:141537560 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:141537560 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:43343386 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:43343386 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:43412010 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:43412010 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:43573686 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:43573686 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:11577458 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:11577458 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:157370933 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:157370933 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:15593241 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:15593241 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:5219927 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:5219927 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:121597311 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:121597311 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:1684239 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:1684239 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:42969753 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:42969753 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:40438718 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:40438718 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:79385914 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:79385914 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:86018417 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:86018417 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:163042539 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:163042539 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:63157134 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:63157134 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:42870365 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:42870365 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:41107606 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:41107606 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:7403149 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:7403149 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:29617319 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:29617319 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:21811443 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:21811443 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:47120254 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:47120254 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:150414318 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:150414318 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:153963170 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:153963170 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:10264824 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:10264824 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:99125813 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:99125813 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:237868509 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:237868509 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:148855766 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:148855766 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:200246412 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:200246412 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:75144321 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:75144321 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:38649573 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:38649573 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:52106876 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:52106876 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:102258632 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:102258632 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:151341800 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:151341800 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:61308032 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr18:61308032 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:100777183 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:100777183 C>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr22:30738934 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr22:30738934 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:70590032 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:70590032 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:23821248 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:23821248 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:105495599 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:105495599 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:51192440 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:51192440 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:47285846 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:47285846 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:92908402 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:92908402 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:8073954 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:8073954 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:190444531 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:190444531 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:101555651 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:101555651 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:23244610 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:23244610 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:21174355 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:21174355 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:22012523 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chrX:22012523 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:33076710 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:33076710 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:46195115 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:46195115 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:51351044 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr8:51351044 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:107023016 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:107023016 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:123593616 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:123593616 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:35793459 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:35793459 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:17364935 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:17364935 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:104030831 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:104030831 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:90695183 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr10:90695183 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:197008459 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:197008459 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:23821149 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:23821149 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:81799334 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:81799334 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:9471807 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:9471807 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:37421500 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:37421500 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:899725 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:899725 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:39964521 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:39964521 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:75621168 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr5:75621168 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:763682 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:763682 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:763699 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:763699 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:212981035 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:212981035 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:17226518 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:17226518 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:114839735 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:114839735 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:24667093 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:24667093 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:24667144 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:24667144 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:100245650 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr9:100245650 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:65165788 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:65165788 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:65165793 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:65165793 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:20836574 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:20836574 T>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:20859699 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:20859699 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:70346773 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr15:70346773 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:112415413 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:112415413 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:51716376 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:51716376 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:217724296 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:217724296 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:175335313 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:175335313 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:10951203 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr21:10951203 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:189020355 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:189020355 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:189022465 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:189022465 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:16331602 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr17:16331602 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:30475101 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:30475101 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:57598478 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:57598478 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:62356483 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:62356483 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:99970406 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr13:99970406 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:93685531 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr14:93685531 T>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:70071184 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr4:70071184 A>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:215812452 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:215812452 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:234459966 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:234459966 T>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:149285748 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr6:149285748 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:75694666 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr11:75694666 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:241886561 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:241886561 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:241886580 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:241886580 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:65471666 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr12:65471666 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:28124183 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:28124183 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:101378601 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:101378601 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:145181857 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:145181857 G>C did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:57293513 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:57293513 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:35817107 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr1:35817107 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:45865285 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr20:45865285 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:3188962 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr16:3188962 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:57193644 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr7:57193644 G>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:52977389 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:52977389 C>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:56925504 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:56925504 A>G did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:23941664 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr19:23941664 G>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:101833751 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr3:101833751 C>A did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:187694417 A>T did not map to a codon.
Sequencing variant TCGA-64-1678-01A-01W-0928-08 chr2:187694417 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:112174906 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:112174906 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:4771896 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:4771896 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:17920959 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:17920959 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:40226044 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:40226044 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chrX:100604832 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chrX:100604832 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chrX:100604832 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chrX:100604832 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:123311051 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:123311051 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr19:8122904 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr19:8122904 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr14:50796932 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr14:50796932 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr14:50796932 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr14:50796932 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr10:11047330 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr10:11047330 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr10:11047330 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr10:11047330 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:46799938 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:46799938 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr11:46799938 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr11:46799938 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:107013190 G>A maps to NM_006348.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:107013190 G>A maps to NM_006348.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:207870818 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:207870818 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:207870818 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:207870818 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr20:29977125 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr20:29977125 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr20:29977125 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr20:29977125 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:196664037 T>A maps to NM_018897.2 L3445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:196664037 T>A maps to NM_018897.2 L3445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr6:31938642 C>A maps to ENST00000418489 *213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr6:31938642 C>A maps to ENST00000418489 *213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr10:99201065 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr10:99201065 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:175533628 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:175533628 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:175533628 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:175533628 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr9:35563754 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr9:35563754 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr3:68802077 G>C maps to NM_182522.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr3:68802077 G>C maps to NM_182522.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:190250664 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:190250664 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:190250664 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:190250664 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:154311862 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:154311862 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:154311862 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:154311862 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:59603164 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:59603164 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr16:9858027 C>A maps to NM_000833.3 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr16:9858027 C>A maps to NM_000833.3 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr19:19043861 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr19:19043861 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:19043861 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:19043861 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:75888772 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:75888772 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:173352614 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:173352614 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr16:31429894 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr16:31429894 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:187541827 A>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:187541827 A>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:52858761 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:52858761 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr18:6311631 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr18:6311631 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr18:6311631 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr18:6311631 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr6:129691178 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr6:129691178 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr6:129691178 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr6:129691178 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr21:40778293 G>T maps to NM_152505.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr21:40778293 G>T maps to NM_152505.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:148004974 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:148004974 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:100174662 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:100174662 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:100174662 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:100174662 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:53699329 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:53699329 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:53699329 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:53699329 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr15:91449665 C>G maps to NM_006122.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr15:91449665 C>G maps to NM_006122.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr17:12032654 A>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr17:12032654 A>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr17:12032654 A>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr17:12032654 A>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:102712759 T>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:102712759 T>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:76922836 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:76922836 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr11:76922836 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr11:76922836 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr14:74947112 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr14:74947112 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:223066080 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:223066080 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:223066080 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr2:223066080 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:66620319 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:66620319 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:48454627 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr3:48454627 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:22102608 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:22102608 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:81732819 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:81732819 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:43290581 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:43290581 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:198677396 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:198677396 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:198677396 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:198677396 A>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr14:103187589 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr14:103187589 G>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:176012984 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:176012984 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr17:78328040 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr17:78328040 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:178989682 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr5:178989682 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:178989682 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:178989682 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:128699520 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:128699520 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr3:127785934 C>T maps to ENST00000464451 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr3:127785934 C>T maps to ENST00000464451 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr18:61304925 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr18:61304925 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr18:61304925 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr18:61304925 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:135377050 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:135377050 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:135377050 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:135377050 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr10:108427575 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr10:108427575 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr10:108427575 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr10:108427575 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:121447980 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr11:121447980 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr11:121447980 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr11:121447980 C>A did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:231077420 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr2:231077420 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr8:53071616 G>A maps to NM_014682.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr8:53071616 G>A maps to NM_014682.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr4:26921324 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr4:26921324 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:70570722 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr8:70570722 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr8:70570722 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr8:70570722 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:166845369 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr1:166845369 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:166845369 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:166845369 T>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:100229864 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr7:100229864 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:100229864 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:100229864 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:19491595 T>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr1:19491595 T>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr12:101674815 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr12:101674815 C>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:118533287 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr12:118533287 C>G did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr15:53901834 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr15:53901834 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr15:53901834 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr15:53901834 G>T did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:167850948 C>T maps to NM_001161661.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr5:167850948 C>T maps to NM_001161661.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:100348588 A>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr7:100348588 A>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr19:9764562 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02D-0969-08 chr19:9764562 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:9764562 G>C did not map to a codon.
Sequencing variant TCGA-64-1680-01A-02W-0928-08 chr19:9764562 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:107558517 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:107558517 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:107579731 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:107579731 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:48764866 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:48764866 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:109670453 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:109670453 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:42857161 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:42857161 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:39089664 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:39089664 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:134250188 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:134250188 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:56184096 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:56184096 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:112058574 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:112058574 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:2740045 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:2740045 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:150956938 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:150956938 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:1806306 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:1806306 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr15:35830443 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr15:35830443 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:118949055 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:118949055 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:32224806 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:32224806 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:41895838 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:41895838 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:26458824 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:26458824 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:26458853 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:26458853 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:4614449 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:4614449 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:4614452 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:4614452 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:100054362 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:100054362 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:65014294 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:65014294 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:2979356 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:2979356 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:72470584 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:72470584 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:2641501 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:2641501 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr21:19638461 G>T maps to ENST00000400131 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr21:19638461 G>T maps to ENST00000400131 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:150909382 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:150909382 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:2944499 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:2944499 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:146829325 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:146829325 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:101812255 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:101812255 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:137714941 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:137714941 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:48337584 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:48337584 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:2963988 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:2963988 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:43171395 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:43171395 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:231902812 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:231902812 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:46282849 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:46282849 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:11660045 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:11660045 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:11778241 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:11778241 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:11790296 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:11790296 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:169144557 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:169144557 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:1939176 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:1939176 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr13:96242386 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr13:96242386 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:56763094 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:56763094 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:97090933 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:97090933 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:15935214 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:15935214 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:6690609 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:6690609 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:34324203 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:34324203 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:240307599 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:240307599 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr13:49688902 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr13:49688902 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:48577874 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:48577874 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:61901031 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:61901031 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:46060731 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:46060731 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:42467897 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:42467897 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:6589352 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:6589352 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:1726637 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:1726637 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:66935840 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:66935840 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:58144703 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:58144703 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:27114804 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:27114804 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:70902437 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:70902437 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:39735153 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:39735153 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:39735176 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:39735176 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:47297272 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:47297272 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:48148418 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:48148418 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:65305229 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:65305229 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:211033266 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:211033266 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:62604457 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:62604457 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:19459784 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:19459784 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:42984762 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:42984762 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:153138239 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:153138239 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:66088686 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:66088686 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:104048593 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:104048593 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:33623341 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:33623341 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:16021754 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:16021754 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:151870259 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:151870259 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:141291937 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:141291937 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:48252325 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:48252325 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:89086994 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:89086994 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:102586889 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:102586889 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:49723936 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:49723936 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr15:59497720 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr15:59497720 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:45005520 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:45005520 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:23377871 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:23377871 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:784382 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:784382 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:16893036 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:16893036 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:160327798 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:160327798 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:32474463 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:32474463 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:57108604 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:57108604 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:206590585 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:206590585 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:134039405 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:134039405 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:101623731 C>T maps to NM_022053.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:101623731 C>T maps to NM_022053.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:143826151 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:143826151 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:248099552 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:248099552 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:72921564 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:72921564 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:165808768 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:165808768 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:20384291 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:20384291 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:76397304 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:76397304 A>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:51947111 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:51947111 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:41475688 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:41475688 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:179360447 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:179360447 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:145824248 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:145824248 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:50902843 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:50902843 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:19563566 T>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:19563566 T>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr22:16279395 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr22:16279395 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:9584851 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:9584851 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:57081864 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:57081864 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:114367828 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:114367828 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:61192321 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:61192321 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:9312860 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:9312860 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:102699136 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:102699136 G>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:99338056 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:99338056 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:130815579 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:130815579 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:64496328 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:64496328 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr13:79951663 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr13:79951663 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:111710562 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:111710562 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:123524257 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:123524257 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:83740218 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:83740218 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:9122702 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:9122702 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:63064674 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:63064674 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:8073846 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:8073846 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:18270169 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:18270169 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:51869096 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:51869096 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:24874061 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:24874061 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:18902112 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:18902112 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:46196198 T>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:46196198 T>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:4863260 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:4863260 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:35753894 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:35753894 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:220336763 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:220336763 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:1164079 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:1164079 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:158593064 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:158593064 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:38247378 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:38247378 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:96852685 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:96852685 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:191934398 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:191934398 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:7706879 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:7706879 A>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:39943971 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:39943971 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:33592258 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:33592258 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:55686194 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:55686194 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:85428604 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:85428604 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:114832517 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:114832517 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:106715496 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:106715496 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:34648383 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chrX:34648383 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:77376567 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:77376567 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:20764632 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:20764632 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:30525159 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:30525159 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:109520642 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:109520642 C>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:36943408 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:36943408 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:67288262 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:67288262 A>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:67301468 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:67301468 T>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:99525532 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:99525532 T>C did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:37203793 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:37203793 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:53499 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr4:53499 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:53156032 C>G did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:53156032 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:52580455 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:52580455 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:7102110 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:7102110 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:67145071 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:67145071 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:66986907 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:66986907 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:87160536 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:87160536 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:76709874 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:76709874 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:223785893 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:223785893 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:20481151 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:20481151 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:236889099 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:236889099 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33616224 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33616224 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:178579269 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:178579269 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:73154386 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:73154386 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:7690789 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:7690789 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:7857149 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:7857149 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:132235413 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:132235413 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:125833591 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:125833591 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:46719711 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:46719711 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:61965481 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:61965481 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:4126557 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:4126557 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:37506810 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:37506810 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:26682070 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:26682070 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:27354852 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:27354852 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:68111059 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:68111059 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:12728634 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:12728634 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:3685428 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:3685428 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:77020176 G>A maps to ENST00000513494 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:77020176 G>A maps to ENST00000513494 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:5693044 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:5693044 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:65557513 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:65557513 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:119487963 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:119487963 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:119976614 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:119976614 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53925480 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53925480 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:112267529 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:112267529 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:119504769 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:119504769 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:111997055 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:111997055 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:138424420 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:138424420 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:117704161 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:117704161 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:63938020 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:63938020 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:72912697 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:72912697 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:81303678 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:81303678 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:91303718 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:91303718 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:50354563 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:50354563 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:26508569 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:26508569 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:72539528 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:72539528 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:105901939 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:105901939 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:33573607 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:33573607 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:40629889 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:40629889 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:49407821 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:49407821 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:20953624 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:20953624 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:67591381 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:67591381 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:32804072 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:32804072 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:138668509 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:138668509 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:170671525 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:170671525 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:37211526 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:37211526 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:99729023 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:99729023 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:100815323 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:100815323 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:131050815 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:131050815 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:13363948 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:13363948 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:140938206 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:140938206 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:2714817 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:2714817 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:201046957 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:201046957 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:81595046 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:81595046 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:1994338 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:1994338 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:2017306 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:2017306 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:18550970 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:18550970 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43927664 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43927664 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:116166560 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:116166560 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:219875445 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:219875445 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:119926743 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:119926743 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:30303975 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:30303975 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:74490335 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:74490335 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158301237 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158301237 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:135738411 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:135738411 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:24487753 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:24487753 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:24509644 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:24509644 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:95188635 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:95188635 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:26881756 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:26881756 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:135946251 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:135946251 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:67006075 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:67006075 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:57007457 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:57007457 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:146724411 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:146724411 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:29539445 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:29539445 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:136623212 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:136623212 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:87029473 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:87029473 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:10124338 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:10124338 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:8291014 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:8291014 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:29344476 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:29344476 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:62366899 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:62366899 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:58582518 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:58582518 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:146471306 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:146471306 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:39178480 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:39178480 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:103491352 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:103491352 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:75848159 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:75848159 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:75865852 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:75865852 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:46912665 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:46912665 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:70859701 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:70859701 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:139833735 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:139833735 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:117063929 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:117063929 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:137697098 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:137697098 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:3690909 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:3690909 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:3690924 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:3690924 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:232656415 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:232656415 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:69018106 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:69018106 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:129946599 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:129946599 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:131253971 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:131253971 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:49815802 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:49815802 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:27018632 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:27018632 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:27021631 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:27021631 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53567072 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53567072 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:113249653 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:113249653 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:113668325 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:113668325 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:11732244 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:11732244 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:70267697 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:70267697 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:36118071 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:36118071 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:72204889 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:72204889 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:72278760 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:72278760 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:90255685 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:90255685 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:24592340 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:24592340 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:24205409 C>T maps to ENST00000378450 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:24205409 C>T maps to ENST00000378450 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:31237149 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:31237149 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:176940636 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:176940636 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:84732497 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:84732497 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:196673302 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:196673302 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:196892822 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:196892822 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:11713434 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:11713434 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:2288442 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:2288442 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:58186558 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:58186558 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:98087044 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:98087044 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:169097692 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:169097692 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:169139278 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:169139278 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:25266491 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:25266491 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:168683704 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:168683704 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:44036926 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:44036926 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:96241927 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:96241927 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:131757297 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:131757297 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:22285172 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:22285172 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:40265982 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:40265982 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:120816387 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:120816387 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:99808423 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:99808423 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:80629066 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:80629066 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:134884996 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:134884996 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:14028026 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:14028026 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:76552794 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:76552794 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:5567106 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:5567106 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:29664191 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:29664191 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:133827161 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:133827161 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:74134643 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:74134643 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:190130038 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:190130038 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:40702628 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:40702628 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:172629328 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:172629328 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:13669493 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:13669493 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:127607680 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:127607680 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:207143334 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:207143334 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:137804533 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:137804533 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:157488209 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:157488209 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:108436278 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:108436278 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:91432678 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:91432678 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:123274542 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:123274542 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:155530682 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:155530682 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:58138444 C>A maps to ENST00000357272 V2126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:58138444 C>A maps to ENST00000357272 V2126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:28891597 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:28891597 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:49444422 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:49444422 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:39127992 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:39127992 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:29589470 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:29589470 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:161302526 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:161302526 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:27182298 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:27182298 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:88431763 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:88431763 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:31135281 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:31135281 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:31165242 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:31165242 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:132688276 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:132688276 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:11348536 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:11348536 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:69646915 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:69646915 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:31015321 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:31015321 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:42467360 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:42467360 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:134239992 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:134239992 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:131289840 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:131289840 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:5545812 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:5545812 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:134898646 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:134898646 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:100387998 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:100387998 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:119905416 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:119905416 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:8584421 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:8584421 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:87407289 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:87407289 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:176859225 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:176859225 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:86415508 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:86415508 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:42145923 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:42145923 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:228334710 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:228334710 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:7875950 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:7875950 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:17170920 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:17170920 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:13523005 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:13523005 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:236735618 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:236735618 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:69716514 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:69716514 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:81346722 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:81346722 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:31237186 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:31237186 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:43299124 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:43299124 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:148868528 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:148868528 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:100773233 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:100773233 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:192988530 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:192988530 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:87726278 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:87726278 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:8305881 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:8305881 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70841399 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70841399 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70954438 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70954438 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158970060 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158970060 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:27676796 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:27676796 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:27676839 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:27676839 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:17578875 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr22:17578875 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:27356124 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:27356124 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:35871070 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:35871070 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:76731782 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:76731782 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:62263128 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:62263128 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:105208069 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:105208069 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:234072262 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:234072262 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:121541343 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:121541343 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:128627637 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:128627637 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:9466808 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:9466808 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:250282 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:250282 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:15599981 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:15599981 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:7759472 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:7759472 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:7786302 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:7786302 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:5126556 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:5126556 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:2255199 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:2255199 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:124412580 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:124412580 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:78846231 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:78846231 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:53240963 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:53240963 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:46284907 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:46284907 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:55367374 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:55367374 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:123246319 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:123246319 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:36846580 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:36846580 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:55251994 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:55251994 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:126305135 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:126305135 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:10192637 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:10192637 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:30322056 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:30322056 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:52841366 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:52841366 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53169436 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53169436 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:129250248 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:129250248 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:129467999 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:129467999 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:154173578 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:154173578 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:88469825 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:88469825 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:75149561 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:75149561 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206772646 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206772646 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:156549003 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:156549003 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:76378696 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:76378696 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:42360349 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:42360349 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:71151288 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:71151288 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:84193480 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:84193480 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:52869342 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:52869342 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:37151105 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:37151105 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:40634189 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:40634189 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:24750853 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:24750853 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:160735740 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:160735740 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:143851158 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:143851158 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:235902285 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:235902285 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:166962084 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:166962084 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:65438896 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:65438896 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:19416297 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:19416297 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:20043600 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:20043600 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:44055854 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:44055854 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:45775013 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:45775013 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:3789351 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:3789351 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:31191568 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:31191568 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:13825667 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:13825667 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:100368792 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:100368792 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:136627681 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:136627681 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:47670204 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:47670204 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:90362923 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:90362923 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:47912596 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:47912596 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:74936289 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:74936289 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:42003573 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:42003573 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:118350863 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:118350863 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:102819652 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:102819652 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:56358132 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:56358132 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:56667479 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:56667479 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:121457857 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:121457857 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:47653335 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:47653335 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:47653337 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:47653337 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:32235274 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:32235274 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:10399522 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:10399522 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:10533278 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:10533278 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:101257077 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:101257077 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:34862280 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:34862280 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:17317261 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:17317261 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:66850377 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:66850377 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:35730043 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:35730043 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:16891475 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:16891475 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:56122020 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:56122020 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:52520663 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:52520663 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:3600407 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:3600407 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:120459357 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:120459357 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:98254540 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:98254540 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:25264848 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:25264848 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:108496158 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:108496158 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:52277629 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:52277629 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:206605166 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:206605166 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:206630447 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:206630447 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:50170835 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:50170835 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:78709801 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:78709801 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:80271348 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:80271348 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:1426547 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:1426547 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:131742867 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:131742867 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:25881940 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:25881940 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:53602928 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:53602928 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:248684930 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:248684930 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:94505494 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:94505494 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:20231576 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:20231576 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:32058190 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:32058190 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:29649407 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:29649407 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:111966361 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:111966361 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:17418822 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:17418822 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:25026371 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:25026371 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:55581534 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:55581534 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:138450016 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:138450016 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140189247 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140189247 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140762381 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140762381 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:93031309 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:93031309 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:78803462 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:78803462 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:28800749 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:28800749 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:75761494 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:75761494 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:39535062 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:39535062 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:9775846 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:9775846 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:8738819 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:8738819 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:130847291 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:130847291 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:22163411 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:22163411 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:47920223 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:47920223 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:110445571 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:110445571 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:14578613 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:14578613 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:30784195 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:30784195 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:28821699 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:28821699 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:8678237 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:8678237 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:38810930 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:38810930 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:132110030 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:132110030 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:93149726 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:93149726 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:68038672 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:68038672 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:20335729 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:20335729 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:131815198 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:131815198 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:118305810 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:118305810 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:106851157 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:106851157 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:38158074 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:38158074 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:149221757 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:149221757 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:149854523 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:149854523 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:80189567 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:80189567 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:63858435 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:63858435 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:37543235 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:37543235 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:113814249 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:113814249 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43371806 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43371806 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43688765 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43688765 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43579898 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43579898 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:186645535 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:186645535 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:209271754 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:209271754 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:136912612 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:136912612 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:40713579 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:40713579 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:44132698 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:44132698 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:64514682 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:64514682 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158906989 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158906989 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:220341142 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:220341142 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:133560113 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:133560113 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:20392910 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:20392910 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:99300402 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:99300402 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206757706 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206757706 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:125645411 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:125645411 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:79385665 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:79385665 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103180616 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103180616 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103215938 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103215938 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:43606964 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:43606964 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:117241715 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:117241715 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:163122533 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:163122533 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:105235885 C>A maps to ENST00000339750 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:105235885 C>A maps to ENST00000339750 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:87364731 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:87364731 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:38170067 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:38170067 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:92645476 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:92645476 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:166999851 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:166999851 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:38973577 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:38973577 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237538100 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237538100 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237895334 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237895334 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237896898 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237896898 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237965250 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:237965250 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:91995895 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:91995895 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:44971346 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:44971346 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:61231115 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:61231115 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:167159884 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:167159884 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:52977625 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:52977625 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:154473805 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:154473805 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:96324251 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:96324251 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:1615853 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:1615853 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:160589728 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:160589728 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:6943340 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:6943340 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:100812015 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:100812015 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103051718 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103051718 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:44200466 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:44200466 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:46623500 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:46623500 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33947229 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33947229 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:85264530 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:85264530 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:48461679 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:48461679 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:98778736 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:98778736 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:168123463 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:168123463 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:71232762 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:71232762 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:1079147 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:1079147 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:108339033 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:108339033 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:108437227 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:108437227 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:106849634 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:106849634 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:123594980 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:123594980 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:172641953 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:172641953 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:97328106 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:97328106 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:35727670 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:35727670 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:220326811 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:220326811 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:147475356 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:147475356 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:55904855 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:55904855 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:38614713 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:38614713 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:55648557 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:55648557 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:55648706 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:55648706 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:85130303 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:85130303 T>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:57642448 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:57642448 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:108863847 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:108863847 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:115417045 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:115417045 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:58476867 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:58476867 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:152646445 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:152646445 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:64445805 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:64445805 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:64897465 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:64897465 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:23907164 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:23907164 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:105145019 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:105145019 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27856404 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27856404 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:74173962 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:74173962 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:74178587 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:74178587 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:132944641 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:132944641 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:104460727 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:104460727 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:69830218 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:69830218 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:120470781 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:120470781 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:142983427 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:142983427 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:68928492 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:68928492 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:111769684 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:111769684 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:101315135 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:101315135 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:144380093 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:144380093 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:1439920 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:1439920 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:1488655 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:1488655 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:10920239 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:10920239 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:10951464 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr21:10951464 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:209955543 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:209955543 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:41254488 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:41254488 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:72973730 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:72973730 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:30475160 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:30475160 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:179595580 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:179595580 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:179622669 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:179622669 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:138954049 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:138954049 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43308166 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43308166 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:99327985 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:99327985 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:70346227 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:70346227 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:33501392 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:33501392 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:17552621 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:17552621 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:53492172 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:53492172 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:75302897 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:75302897 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:41026658 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:41026658 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:160385713 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:160385713 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:82779289 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:82779289 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:8433433 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:8433433 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:38948570 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:38948570 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:37438124 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:37438124 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:54687884 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:54687884 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:31628753 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:31628753 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:61718000 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:61718000 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:143549608 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:143549608 A>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:31650304 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:31650304 A>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:72991276 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:72991276 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:147108671 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:147108671 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:101153021 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chrX:101153021 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:44511177 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:44511177 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:38127071 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:38127071 T>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58039058 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58039058 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:64952 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:64952 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58015997 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58015997 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:23545575 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:23545575 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:100865742 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:100865742 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:58863971 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:58863971 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:53715372 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:53715372 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:125571020 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:125571020 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:35766394 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:35766394 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:73953425 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:73953425 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:229568662 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:229568662 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:158655924 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:158655924 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:58974558 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:58974558 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:28307117 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:28307117 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:64547235 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:64547235 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136403361 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136403361 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:150528079 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:150528079 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:45701614 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:45701614 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:25057632 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:25057632 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:31540021 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:31540021 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:55051145 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:55051145 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:43918970 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:43918970 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:38501085 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:38501085 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:33134326 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:33134326 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:33134591 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:33134591 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:15754942 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:15754942 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:99338178 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:99338178 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:242135416 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:242135416 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:72071389 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:72071389 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:127229109 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:127229109 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:94650361 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:94650361 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:130217092 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:130217092 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:130220674 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:130220674 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:73949703 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:73949703 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:150720739 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:150720739 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:113536076 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:113536076 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:160105598 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:160105598 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:42474125 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:42474125 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:113508565 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:113508565 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:1801890 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:1801890 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:50217733 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:50217733 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:35703129 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:35703129 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41727212 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41727212 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:71603758 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:71603758 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:11098761 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:11098761 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:17276109 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:17276109 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:160182488 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:160182488 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:70070560 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:70070560 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:7845349 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:7845349 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:43292795 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:43292795 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:112991177 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:112991177 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:1478276 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:1478276 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:112646277 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:112646277 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:81289077 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:81289077 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:179339106 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:179339106 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:61431162 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:61431162 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:74855387 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:74855387 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:191064419 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:191064419 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:32322971 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:32322971 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:97609800 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:97609800 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:120782253 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:120782253 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:1248520 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:1248520 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:71275310 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:71275310 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:209781344 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:209781344 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:30888280 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:30888280 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:41646363 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:41646363 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:116243739 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:116243739 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:116260443 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:116260443 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:106118382 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:106118382 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:106207443 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:106207443 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:139101212 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:139101212 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:73461435 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:73461435 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:28943319 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:28943319 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72537609 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72537609 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:15850293 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:15850293 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:14508146 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:14508146 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:21883957 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:21883957 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:31299469 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:31299469 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:15789206 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:15789206 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:22307457 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:22307457 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48696236 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48696236 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:196695582 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:196695582 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:151509827 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:151509827 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:29440518 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:29440518 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:136622966 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:136622966 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:190026243 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:190026243 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:57728797 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:57728797 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:88296902 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:88296902 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:87673917 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:87673917 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:74414932 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:74414932 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:32151633 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:32151633 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:70890521 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:70890521 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:86453387 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:86453387 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:189863349 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:189863349 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:107936238 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:107936238 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:10114440 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:10114440 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:47409474 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:47409474 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48613763 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48613763 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:61458577 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:61458577 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:47605308 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:47605308 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:207885806 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:207885806 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131864125 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131864125 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113326308 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113326308 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113420531 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113420531 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113599511 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113599511 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113694948 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113694948 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:18162537 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:18162537 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:44873733 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:44873733 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:36156445 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:36156445 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:127944668 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:127944668 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41533416 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41533416 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:27945362 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:27945362 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:124329461 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:124329461 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:151161093 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:151161093 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:154996468 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:154996468 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:112298537 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:112298537 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49986684 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49986684 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:29960640 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:29960640 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:140269426 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:140269426 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:182836043 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:182836043 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:122575271 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:122575271 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:12943186 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:12943186 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:32361411 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:32361411 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:124349059 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:124349059 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:21789515 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:21789515 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:13871951 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:13871951 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:196741504 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:196741504 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:38885648 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:38885648 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:31375283 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:31375283 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:162894789 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:162894789 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:154679204 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:154679204 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:113866428 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:113866428 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:28989225 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:28989225 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:71828074 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:71828074 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:158524200 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:158524200 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39307033 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39307033 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:148427916 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:148427916 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:48522897 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:48522897 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:37989791 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:37989791 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:38227035 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:38227035 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:16504738 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:16504738 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:29521238 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:29521238 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:13698189 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:13698189 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:133783667 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:133783667 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:57419577 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:57419577 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:22999695 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:22999695 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:143056553 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:143056553 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:175528534 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:175528534 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:17813265 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:17813265 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:110581196 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:110581196 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:190203444 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:190203444 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:90770501 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:90770501 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:33339138 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:33339138 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:175160362 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:175160362 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48423105 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48423105 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:17881117 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:17881117 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:125094782 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:125094782 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:36979441 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:36979441 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:102454431 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:102454431 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:38285345 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:38285345 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:27939643 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:27939643 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:29012522 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:29012522 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:161116421 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:161116421 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:26806017 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:26806017 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:26806068 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:26806068 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:46066550 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:46066550 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:46066620 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:46066620 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:89891535 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:89891535 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:153792045 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:153792045 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:179744138 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:179744138 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:179762988 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:179762988 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:55196407 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:55196407 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:61994972 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:61994972 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:233613548 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:233613548 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:42088079 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:42088079 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:52420446 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:52420446 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:135441385 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:135441385 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10133427 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10133427 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10135891 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10135891 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:14555335 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:14555335 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:7722033 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:7722033 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:95235081 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:95235081 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:110201538 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:110201538 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:134696096 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:134696096 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52220211 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52220211 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:30662600 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:30662600 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36394903 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36394903 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:18869078 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:18869078 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:58133008 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:58133008 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:74014055 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:74014055 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:26197027 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:26197027 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:32557548 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:32557548 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:30142534 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:30142534 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:186383747 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:186383747 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:26147609 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:26147609 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:114405343 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:114405343 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:99007587 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:99007587 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:3726709 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:3726709 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:88041053 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:88041053 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:183773238 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:183773238 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3142433 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3142433 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:220320718 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:220320718 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:52878366 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:52878366 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:308135 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:308135 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:160445783 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:160445783 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:6054678 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:6054678 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:6104028 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:6104028 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:154401664 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:154401664 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:15260438 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:15260438 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:36005242 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:36005242 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:75858097 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:75858097 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:52344448 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:52344448 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:52361933 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:52361933 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:182347391 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:182347391 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:15573177 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:15573177 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:15648217 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:15648217 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:31383875 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:31383875 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:156676047 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:156676047 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:156679581 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:156679581 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:27084701 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:27084701 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:676865 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:676865 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:170344725 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:170344725 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:211035491 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:211035491 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:163257104 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:163257104 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:78646870 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:78646870 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:73905173 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:73905173 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:138648832 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:138648832 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:138676807 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:138676807 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:36767089 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:36767089 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:38878548 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:38878548 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:43900754 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:43900754 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:55356105 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:55356105 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:138530883 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:138530883 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:86568313 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:86568313 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:200530079 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:200530079 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55250051 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55250051 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55263627 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55263627 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:30267097 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:30267097 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:173703474 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:173703474 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:51466448 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:51466448 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:139164785 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:139164785 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:54867559 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:54867559 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:112462796 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:112462796 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107695925 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107695925 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:133911723 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:133911723 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:133945243 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:133945243 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:37000012 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:37000012 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:25143890 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:25143890 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:109010214 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:109010214 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:202163597 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:202163597 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:35787258 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:35787258 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:113909035 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:113909035 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55179042 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55179042 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:161016349 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:161016349 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:62849023 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:62849023 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:99358713 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:99358713 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:141128886 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:141128886 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:65350183 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:65350183 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:77814821 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:77814821 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:21207906 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:21207906 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:65375702 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:65375702 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39090820 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39090820 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:47913669 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:47913669 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:128419836 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:128419836 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:164853965 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:164853965 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:119748237 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:119748237 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:162944523 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:162944523 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:113741977 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:113741977 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:48875660 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:48875660 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:90403779 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:90403779 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:150881606 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:150881606 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:151095976 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:151095976 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:116410112 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:116410112 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:126770990 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:126770990 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:42839593 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:42839593 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:15666316 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:15666316 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:60525245 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:60525245 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:103572980 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:103572980 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:50926232 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:50926232 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:122489828 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:122489828 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:151944918 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:151944918 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:21815397 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:21815397 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:10359665 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:10359665 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:23887107 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:23887107 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:23900212 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:23900212 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:123332911 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:123332911 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:123454406 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:123454406 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:26482244 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:26482244 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:171249020 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:171249020 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72768466 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72768466 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72769860 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72769860 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:15601748 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:15601748 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:90976831 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:90976831 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:113130862 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:113130862 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:132988810 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:132988810 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:80122302 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:80122302 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:207007394 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:207007394 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:45171159 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:45171159 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:47579380 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:47579380 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:63768391 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:63768391 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:63776050 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:63776050 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:63777404 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:63777404 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:56482106 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:56482106 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:56499155 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:56499155 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:150704419 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:150704419 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:69347861 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:69347861 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:5987881 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:5987881 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107822186 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107822186 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:13384656 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:13384656 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:101576828 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:101576828 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:228486427 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:228486427 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:123870796 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:123870796 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:50943165 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:50943165 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:74678127 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:74678127 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72939258 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72939258 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:48780397 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:48780397 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:1585495 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:1585495 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:40027304 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:40027304 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:6742545 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:6742545 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:119097406 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:119097406 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:156215136 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:156215136 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:47361418 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:47361418 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:82474545 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:82474545 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:289550 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:289550 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:65421300 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:65421300 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:44108132 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:44108132 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:55144485 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:55144485 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:149513409 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:149513409 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:39875862 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:39875862 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:107566696 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:107566696 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:69507685 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:69507685 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:209134258 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:209134258 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:99950971 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:99950971 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:42046328 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:42046328 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:12017831 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:12017831 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:12018010 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:12018010 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:131859726 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:131859726 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:160239747 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:160239747 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:82763298 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:82763298 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:18845334 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:18845334 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:22029253 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:22029253 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:94725264 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:94725264 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:12836279 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:12836279 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:23522332 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:23522332 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:170009802 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:170009802 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:62659948 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:62659948 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:139192787 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:139192787 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:113958725 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:113958725 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:42891134 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:42891134 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:209355332 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:209355332 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:6878941 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:6878941 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:214705500 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:214705500 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:61989205 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:61989205 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:52233534 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:52233534 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:36598062 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:36598062 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:238820076 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:238820076 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:79310346 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:79310346 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:33116223 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:33116223 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:79312558 A>G maps to ENST00000454188 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:79312558 A>G maps to ENST00000454188 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:103294492 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:103294492 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:8415472 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:8415472 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:107075930 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:107075930 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3314172 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3314172 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:240933325 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:240933325 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:240969400 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:240969400 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49583331 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49583331 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:38960460 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:38960460 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:84567142 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:84567142 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:87013160 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:87013160 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:49735705 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:49735705 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:42720423 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:42720423 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:55534201 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:55534201 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:157993811 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:157993811 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:67753759 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:67753759 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:12142638 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:12142638 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:165406477 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:165406477 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:34040549 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:34040549 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:34078208 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:34078208 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:100598390 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:100598390 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:165986886 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:165986886 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:4272882 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:4272882 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:83634566 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:83634566 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:77949618 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:77949618 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:150917339 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:150917339 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:67137560 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:67137560 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:67154973 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:67154973 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:130540832 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:130540832 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:19192409 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:19192409 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:84287068 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:84287068 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:49118129 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:49118129 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:601705 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:601705 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:232649545 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:232649545 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:78337493 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:78337493 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:34546859 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:34546859 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:129293586 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:129293586 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:160863757 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:160863757 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:103017971 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:103017971 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:170732586 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:170732586 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:47780408 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:47780408 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:58055929 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:58055929 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:27439620 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:27439620 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:27475314 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:27475314 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:24888570 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:24888570 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:10971121 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:10971121 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:55690562 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:55690562 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:87226560 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:87226560 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72764448 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:72764448 A>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:168310185 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:168310185 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:71562164 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:71562164 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:51569589 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:51569589 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:1168873 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:1168873 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:142605089 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:142605089 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:123848704 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:123848704 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:35697767 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:35697767 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:89598804 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:89598804 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:55904872 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:55904872 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:55653319 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:55653319 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:52685547 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:52685547 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:99761439 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:99761439 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:31420028 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:31420028 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:53077254 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:53077254 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:84668319 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:84668319 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136203043 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136203043 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:113166497 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:113166497 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:115489022 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:115489022 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:58440417 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:58440417 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:109618665 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:109618665 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:160042489 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:160042489 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:54885560 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:54885560 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:152057340 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:152057340 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:31007169 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:31007169 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:151742668 C>A maps to ENST00000321531 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:151742668 C>A maps to ENST00000321531 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:48170597 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:48170597 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:195791400 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:195791400 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:133975183 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:133975183 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:157164843 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:157164843 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:11582807 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:11582807 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:11632860 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:11632860 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:32575213 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:32575213 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:156347576 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:156347576 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:54219274 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:54219274 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:114956440 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:114956440 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:112407809 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:112407809 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:108510526 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:108510526 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:54506564 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:54506564 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:44103976 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:44103976 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:19698981 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:19698981 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:37494372 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:37494372 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:103216365 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chrX:103216365 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:117844311 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:117844311 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:152214115 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:152214115 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:152235870 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:152235870 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:7997839 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:7997839 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:175086034 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:175086034 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:10916316 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:10916316 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:10934018 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:10934018 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:88926507 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:88926507 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:72969097 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:72969097 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:31332587 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:31332587 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:73442746 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:73442746 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:2426086 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:2426086 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:2432799 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:2432799 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:77358876 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:77358876 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:142627355 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:142627355 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:71833785 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:71833785 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:113205803 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:113205803 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:15226077 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:15226077 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:9869037 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:9869037 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:110655095 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:110655095 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:59339291 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:59339291 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:150267902 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:150267902 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:43557470 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:43557470 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:54340973 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:54340973 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:17370569 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:17370569 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:5037177 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:5037177 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:177632918 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:177632918 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:86996308 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:86996308 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:98823752 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:98823752 T>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:98844592 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:98844592 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:241913067 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:241913067 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:228736385 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:228736385 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:67299228 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:67299228 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:96061653 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:96061653 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:116960853 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:116960853 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:108626744 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:108626744 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:44624424 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:44624424 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:167086369 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:167086369 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131513848 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131513848 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:32385790 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:32385790 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:64291821 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:64291821 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:44620970 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:44620970 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:22272256 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:22272256 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:57869298 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:57869298 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:37727053 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:37727053 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:64917 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:64917 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52627351 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52627351 T>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:53155988 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:53155988 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:136023098 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:136023098 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:113618859 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:113618859 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:48141375 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:48141375 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:17449828 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:17449828 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:236917489 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:236917489 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:64625113 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:64625113 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:31144583 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:31144583 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:45708423 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:45708423 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:202207027 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:202207027 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:37481977 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:37481977 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:4750842 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:4750842 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:988745 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:988745 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:33387139 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:33387139 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:49791329 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:49791329 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:135769995 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:135769995 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:131092097 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:131092097 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:160151423 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:160151423 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:50224144 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:50224144 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:11047557 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:11047557 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:31674670 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:31674670 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:55758736 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:55758736 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:16419688 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:16419688 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:31606252 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:31606252 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:40044036 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:40044036 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:112686105 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:112686105 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:24471190 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:24471190 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:5086822 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:5086822 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:64946613 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:64946613 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:169661206 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:169661206 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:41160502 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:41160502 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:10557717 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:10557717 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:65051403 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:65051403 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:14990284 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:14990284 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:12833123 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:12833123 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:77768251 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:77768251 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:131599854 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:131599854 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:92977953 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:92977953 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:179737077 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:179737077 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:16649781 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:16649781 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:34540016 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:34540016 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:32646624 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:32646624 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:74512923 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:74512923 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:7656239 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:7656239 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:65006036 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:65006036 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:90613294 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:90613294 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:93545296 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:93545296 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:6206116 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:6206116 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:40046052 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:40046052 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:78403367 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:78403367 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:45823046 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:45823046 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:7883346 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:7883346 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:150906831 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:150906831 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:57994859 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:57994859 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:58583886 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:58583886 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:58587803 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:58587803 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:1427493 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:1427493 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:32149103 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:32149103 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139606213 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139606213 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:137570116 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:137570116 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:1401546 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:1401546 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:113293307 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:113293307 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:113841834 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:113841834 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:70810749 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:70810749 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:68139117 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:68139117 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:11110842 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:11110842 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:55950844 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:55950844 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:111729169 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:111729169 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:107274912 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:107274912 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:107288833 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:107288833 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:52774237 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:52774237 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:41704337 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:41704337 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:19999910 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:19999910 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:85906178 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:85906178 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:55042132 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:55042132 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:137082165 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:137082165 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:83641286 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:83641286 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:53930611 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:53930611 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:225702468 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:225702468 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:25216686 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:25216686 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:26484677 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:26484677 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:113866430 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:113866430 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:100509831 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:100509831 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:131755502 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:131755502 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:233349014 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:233349014 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:233349416 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:233349416 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:55218932 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:55218932 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:852862 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:852862 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:62378223 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:62378223 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:66439606 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:66439606 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:220160405 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:220160405 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:15091330 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:15091330 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:187197549 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:187197549 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:58877059 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:58877059 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139255337 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139255337 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:175533727 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:175533727 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:127671130 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:127671130 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:125076537 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:125076537 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:125115559 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:125115559 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:34092355 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:34092355 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:58128604 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:58128604 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:71050258 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:71050258 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:49189812 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:49189812 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:121187597 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:121187597 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:46976476 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:46976476 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:151128484 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:151128484 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:155157907 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:155157907 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:11642799 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:11642799 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:34907103 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:34907103 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:163208788 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:163208788 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:74860277 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:74860277 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:131022331 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:131022331 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:13825625 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:13825625 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:37324540 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:37324540 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:126173980 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:126173980 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:27802612 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:27802612 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:106697188 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:106697188 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:115345759 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:115345759 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:43704682 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:43704682 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:55039654 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:55039654 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:48675904 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:48675904 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:236721499 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:236721499 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:61621800 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:61621800 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:100242379 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:100242379 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:54395613 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:54395613 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:21531424 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:21531424 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:79107407 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:79107407 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:18704824 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:18704824 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:50439074 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:50439074 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:23845092 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:23845092 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:132015312 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:132015312 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:143044604 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:143044604 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:75896572 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:75896572 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:15720605 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:15720605 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:15726160 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:15726160 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:124578064 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:124578064 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:24524163 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:24524163 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:124413394 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:124413394 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44585851 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44585851 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44595781 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44595781 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:88693896 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:88693896 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:154687512 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:154687512 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:36666330 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:36666330 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:24039512 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:24039512 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:94046467 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:94046467 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:233489466 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:233489466 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:200562771 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:200562771 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:39760731 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:39760731 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55272306 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55272306 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:117053386 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:117053386 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:53039307 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:53039307 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:52963550 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:52963550 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:56128172 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:56128172 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:55025702 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:55025702 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:6886896 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:6886896 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:6974860 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:6974860 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:139639593 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:139639593 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:136587265 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:136587265 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:109010104 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:109010104 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:54969075 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:54969075 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:54784408 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:54784408 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:97814281 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:97814281 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:165182757 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:165182757 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:42373400 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:42373400 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:86001050 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:86001050 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:141215320 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:141215320 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:26751036 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:26751036 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:45911921 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:45911921 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:31549950 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:31549950 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:166974261 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:166974261 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:110849132 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:110849132 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:21201828 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:21201828 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:67995594 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:67995594 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:53876178 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:53876178 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:128083201 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:128083201 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:84124571 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:84124571 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:138671988 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:138671988 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:70342770 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:70342770 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:134889619 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:134889619 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:36607499 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:36607499 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:151970754 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:151970754 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:168297698 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:168297698 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:102745500 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:102745500 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:132325097 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:132325097 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:108723614 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:108723614 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:151420687 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:151420687 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:4455405 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:4455405 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:67488645 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:67488645 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:42343992 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:42343992 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:10359944 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:10359944 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:211167109 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:211167109 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:44179349 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:44179349 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:123359068 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:123359068 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:76919627 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:76919627 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:174974332 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:174974332 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:20066490 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:20066490 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:16892595 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:16892595 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:16893412 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:16893412 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:22907043 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:22907043 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:97025860 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:97025860 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:124870471 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:124870471 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:2577893 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:2577893 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:134254108 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:134254108 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:21191532 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:21191532 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:33338635 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:33338635 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55445796 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55445796 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:15177482 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:15177482 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:101581278 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:101581278 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:34145374 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:34145374 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:153654150 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:153654150 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:164246970 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:164246970 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:127302509 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:127302509 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:51254603 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:51254603 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:106477526 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:106477526 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:167673640 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:167673640 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:248138772 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:248138772 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:20295561 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:20295561 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:21897447 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:21897447 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:179192943 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:179192943 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:21730667 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:21730667 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:79805064 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:79805064 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:28835439 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:28835439 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:55569343 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:55569343 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:142545886 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:142545886 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:66619833 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:66619833 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:144867763 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:144867763 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:66637186 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:66637186 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:76704699 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:76704699 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:114571928 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:114571928 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:76395661 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:76395661 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:11046417 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:11046417 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:11046528 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:11046528 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:111564657 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:111564657 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:48556421 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:48556421 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:46679935 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:46679935 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:8737867 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:8737867 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:18892213 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:18892213 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:153692732 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:153692732 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:72398842 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:72398842 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:38160178 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:38160178 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:43152284 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:43152284 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:130867957 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:130867957 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:11117980 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:11117980 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:84610340 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:84610340 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:84610355 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:84610355 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:3573107 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:3573107 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:150980992 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:150980992 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:43420706 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:43420706 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:17636082 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:17636082 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:8713807 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:8713807 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:113784370 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:113784370 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:72739392 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:72739392 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:73441888 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:73441888 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:150342442 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:150342442 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:170679967 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:170679967 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:38340711 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:38340711 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:178389558 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:178389558 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:155145562 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:155145562 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:183873864 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:183873864 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:86008011 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:86008011 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:72984965 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:72984965 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:241518926 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:241518926 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:151181737 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:151181737 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:18399716 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:18399716 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:77651357 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:77651357 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:118889010 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:118889010 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:75376886 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:75376886 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:51968606 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:51968606 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:123005088 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:123005088 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:46539428 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:46539428 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:67727028 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:67727028 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:38934510 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:38934510 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:39009664 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:39009664 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:84815187 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:84815187 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:44353025 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:44353025 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:200173429 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:200173429 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:50893613 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:50893613 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:38784123 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:38784123 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:38651478 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:38651478 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:169581704 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:169581704 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:61310850 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:61310850 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51218869 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51218869 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:3672473 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:3672473 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51629330 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51629330 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:232581227 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:232581227 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:45235685 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:45235685 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:45188621 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:45188621 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:45191993 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:45191993 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:49937170 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:49937170 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:92911696 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:92911696 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:165765141 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:165765141 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:3218176 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:3218176 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:302381 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:302381 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:21450277 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:21450277 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:183503063 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:183503063 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:96971125 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:96971125 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:101620666 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:101620666 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:101648075 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:101648075 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:34931471 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:34931471 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:106971024 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:106971024 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:16506035 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:16506035 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:88411811 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:88411811 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:55648309 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:55648309 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:131346860 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:131346860 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:18655965 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:18655965 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:38024247 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:38024247 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:121037522 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:121037522 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:138333644 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:138333644 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:46345341 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:46345341 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44561663 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:44561663 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:122760215 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chrX:122760215 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:155465669 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:155465669 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:12270858 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:12270858 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55831570 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55831570 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:9332873 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:9332873 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:74874737 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:74874737 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:1860844 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:1860844 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:47409268 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:47409268 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:144398309 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:144398309 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:10959689 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:10959689 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:42226304 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:42226304 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:141415594 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:141415594 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:30156315 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:30156315 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:57139867 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:57139867 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:234872048 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:234872048 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:234894522 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:234894522 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:142572552 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:142572552 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:81448841 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:81448841 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:85413326 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:85413326 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:49582592 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:49582592 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:22867134 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:22867134 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:56180770 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:56180770 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:43982357 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:43982357 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:5530857 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:5530857 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:43959290 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:43959290 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:215807653 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:215807653 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:215963747 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:215963747 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:216074274 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:216074274 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:216256729 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:216256729 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:216424527 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:216424527 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:70732761 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:70732761 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:64211149 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:64211149 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:54567133 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:54567133 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:67299560 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:67299560 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:54363728 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:54363728 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:1639550 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:1639550 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:32418004 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:32418004 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:168098537 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:168098537 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:10756537 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:10756537 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:736744 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:736744 T>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:72921029 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:72921029 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:145158892 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:145158892 T>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:64126487 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:64126487 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:43143483 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:43143483 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:6977861 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:6977861 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:22902162 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:22902162 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:7714824 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:7714824 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:9027628 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:9027628 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:94510089 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:94510089 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:67109546 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:67109546 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87179965 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87179965 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87229543 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87229543 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:17474561 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:17474561 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:8010868 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:8010868 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:109644721 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:109644721 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:32365682 C>A maps to ENST00000430493 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:32365682 C>A maps to ENST00000430493 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:185697592 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:185697592 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20548546 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20548546 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20556415 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20556415 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42847080 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42847080 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87737439 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87737439 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:24255026 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:24255026 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:64747169 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:64747169 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145617268 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145617268 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:167791451 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:167791451 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:7698240 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:7698240 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:131826546 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:131826546 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:909686 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:909686 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:100200543 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:100200543 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:203097871 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:203097871 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:119304956 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:119304956 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:159398779 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:159398779 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:148679016 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:148679016 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:236706322 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:236706322 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:957542 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:957542 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:970602 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:970602 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247059105 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247059105 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:45707077 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:45707077 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:96858455 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:96858455 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:96945029 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:96945029 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:134221590 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:134221590 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:137792390 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:137792390 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:125828743 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:125828743 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:125929165 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:125929165 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:104297233 G>A maps to NM_001008218.1 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:104297233 G>A maps to NM_001008218.1 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:113264194 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:113264194 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:33113554 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:33113554 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:17438405 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:17438405 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:99093375 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:99093375 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:21227104 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:21227104 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:21246574 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:21246574 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:33387158 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:33387158 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:47588816 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:47588816 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:107209282 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:107209282 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:144245131 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:144245131 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:98995162 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:98995162 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:1828333 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:1828333 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156911550 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156911550 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:100228625 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:100228625 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:2999125 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:2999125 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:1743364 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:1743364 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:12856384 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:12856384 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:176983813 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:176983813 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:124333436 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:124333436 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:10657465 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:10657465 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:194169423 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:194169423 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54063611 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54063611 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:154315512 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:154315512 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:11047423 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:11047423 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:69759243 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:69759243 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:35234171 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:35234171 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:75263989 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:75263989 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:52601741 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:52601741 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:127806095 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:127806095 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:97983466 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:97983466 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:13583841 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:13583841 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:149871605 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:149871605 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41276129 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41276129 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:15360011 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:15360011 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32843760 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32843760 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:580361 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:580361 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:111431837 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:111431837 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:124712587 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:124712587 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118137884 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118137884 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:108256707 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:108256707 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:40675009 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:40675009 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43332456 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43332456 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7329270 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7329270 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:73139539 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:73139539 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:244643148 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:244643148 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:169388189 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:169388189 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:170940797 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:170940797 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75036734 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75036734 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:150256784 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:150256784 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:34611600 G>A maps to ENST00000373973 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:34611600 G>A maps to ENST00000373973 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:45557283 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:45557283 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74842035 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74842035 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:113486349 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:113486349 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:81309140 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:81309140 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123753594 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123753594 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:118805030 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:118805030 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:36291344 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:36291344 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:6864439 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:6864439 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:120906182 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:120906182 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:69730551 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:69730551 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:111826616 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:111826616 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:86158161 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:86158161 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:49956899 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:49956899 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:24459704 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:24459704 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:65120488 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:65120488 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181702189 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181702189 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181725948 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181725948 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181754677 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181754677 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181754966 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181754966 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:49070746 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:49070746 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:27448141 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:27448141 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54115108 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54115108 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:12870689 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:12870689 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:20810238 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:20810238 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:30953539 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:30953539 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:110494366 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:110494366 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:75706544 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:75706544 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:2237335 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:2237335 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:70509541 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:70509541 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:219874830 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:219874830 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:159107533 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:159107533 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32669670 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32669670 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:61829893 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:61829893 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:32739562 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:32739562 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:130899607 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:130899607 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:64119554 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:64119554 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:32684723 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:32684723 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:34432799 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:34432799 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:33255013 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:33255013 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158323884 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158323884 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35835871 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35835871 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:47592010 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:47592010 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41931463 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41931463 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:80276203 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:80276203 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:80276205 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:80276205 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:111368457 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:111368457 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:14499642 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:14499642 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100963613 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100963613 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100964458 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100964458 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:227228030 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:227228030 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:65032454 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:65032454 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:21883080 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:21883080 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:19473825 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:19473825 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:59206436 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:59206436 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44841906 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44841906 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:73462101 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:73462101 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:25589628 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:25589628 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:31302430 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:31302430 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:63529814 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:63529814 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:61688055 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:61688055 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31958554 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31958554 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31982966 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31982966 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:85556554 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:85556554 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:42128179 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:42128179 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:22310859 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:22310859 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196919930 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196919930 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196874476 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196874476 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49547452 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49547452 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49558645 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49558645 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:50854443 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:50854443 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7814692 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7814692 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:203153669 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:203153669 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:85158493 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:85158493 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:184104584 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:184104584 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:16284216 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:16284216 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:10042373 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:10042373 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:10162867 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:10162867 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:16356930 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:16356930 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:201719309 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:201719309 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:22208374 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:22208374 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:32491134 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:32491134 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:21534582 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:21534582 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:41123264 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:41123264 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:146471329 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:146471329 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:148112448 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:148112448 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:51204047 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:51204047 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103352681 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103352681 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103385722 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103385722 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103471711 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103471711 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:75839976 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:75839976 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:71655286 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:71655286 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:177676031 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:177676031 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:86621921 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:86621921 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:111156435 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:111156435 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:107840538 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:107840538 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:137703107 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:137703107 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:238244727 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:238244727 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:47625770 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:47625770 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:4458074 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:4458074 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:130024347 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:130024347 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:148562567 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:148562567 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:28711867 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:28711867 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:101829323 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:101829323 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:211452603 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:211452603 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:8607645 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:8607645 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:148926984 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:148926984 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197298195 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197298195 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197398516 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197398516 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197407897 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197407897 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:27021342 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:27021342 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:208986725 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:208986725 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75180339 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75180339 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:19297445 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:19297445 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:34190094 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:34190094 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:113392564 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:113392564 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:80211141 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:80211141 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:150771611 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:150771611 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:117375212 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:117375212 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:55962527 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:55962527 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:49019259 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:49019259 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:25163540 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:25163540 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:74631743 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:74631743 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41455133 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41455133 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:187131578 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:187131578 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42815922 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42815922 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74594430 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74594430 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:95131208 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:95131208 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:110574340 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:110574340 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:169214842 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:169214842 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:169232421 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:169232421 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:18236635 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:18236635 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:186015085 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:186015085 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:30638277 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:30638277 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:154017576 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:154017576 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41599345 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41599345 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:231885539 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:231885539 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:101194826 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:101194826 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:96639049 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:96639049 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:42354261 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:42354261 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:21934679 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:21934679 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:196834868 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:196834868 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:11795288 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:11795288 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220147653 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220147653 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:157151370 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:157151370 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:169101514 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:169101514 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:50824125 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:50824125 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:83828545 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:83828545 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:63991537 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:63991537 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:64040972 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:64040972 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:134010259 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:134010259 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113495972 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113495972 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:76857661 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:76857661 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102999622 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102999622 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:4711845 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:4711845 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:137813579 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:137813579 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:158267168 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:158267168 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67916256 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67916256 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:57897408 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:57897408 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:93278248 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:93278248 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:28320373 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:28320373 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:43995766 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:43995766 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:44198749 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:44198749 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:63999712 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:63999712 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:38425036 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:38425036 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:183860204 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:183860204 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:36922270 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:36922270 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:36895147 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:36895147 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:37256146 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:37256146 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:107514307 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:107514307 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:79470927 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:79470927 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:2885190 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:2885190 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:27761886 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:27761886 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:5396035 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:5396035 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:134514571 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:134514571 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:184293613 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:184293613 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100320870 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100320870 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:220153628 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:220153628 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:96117577 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:96117577 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:102820042 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:102820042 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:158534155 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:158534155 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:14028501 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:14028501 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:56765815 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:56765815 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:57699359 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:57699359 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:160969629 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:160969629 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:6167909 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:6167909 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:113771779 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:113771779 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:153390741 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:153390741 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:184767186 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:184767186 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220045024 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220045024 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:139153623 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:139153623 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:79797564 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:79797564 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:102719029 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:102719029 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:45512868 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:45512868 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:30891976 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:30891976 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:126395117 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:126395117 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92523467 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92523467 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:127674797 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:127674797 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:8154867 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:8154867 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:102580102 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:102580102 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:15928642 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:15928642 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100184156 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100184156 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:159271986 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:159271986 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161641129 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161641129 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:157665414 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:157665414 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:157485460 G>A maps to NM_001195388.1 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:157485460 G>A maps to NM_001195388.1 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:125131752 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:125131752 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:6096635 C>T maps to NM_017671.4 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:6096635 C>T maps to NM_017671.4 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:91428190 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:91428190 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:84603709 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:84603709 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:84603713 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:84603713 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27208023 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27208023 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:171162368 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:171162368 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89420632 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89420632 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:114256806 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:114256806 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:118849965 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:118849965 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:79238710 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:79238710 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:14797767 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:14797767 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:85958078 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:85958078 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:48559203 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:48559203 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:47557347 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:47557347 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35611932 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35611932 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:169761156 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:169761156 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:26825653 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:26825653 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:151809025 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:151809025 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:171685941 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:171685941 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:230378979 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:230378979 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:173301564 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:173301564 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62394442 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62394442 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62396217 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62396217 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62400849 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62400849 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62406811 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62406811 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:69586322 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:69586322 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:117849234 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:117849234 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:42465500 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:42465500 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:75816873 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:75816873 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:58605903 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:58605903 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:19751490 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:19751490 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:57474421 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:57474421 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:102164038 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:102164038 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:1412443 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:1412443 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:101180608 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:101180608 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145139556 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145139556 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42501870 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42501870 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:99768130 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:99768130 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:133174566 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:133174566 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35510013 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35510013 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:104448836 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:104448836 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:14552835 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:14552835 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:3030839 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:3030839 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:126409873 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:126409873 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:126542586 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:126542586 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:14772322 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:14772322 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:127447908 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:127447908 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:82940519 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:82940519 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:172779026 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:172779026 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:17186187 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:17186187 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:156479246 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:156479246 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:83832670 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:83832670 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242174778 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242174778 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:236736264 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:236736264 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:73967197 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:73967197 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:40998294 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:40998294 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:31576757 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:31576757 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:43447136 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:43447136 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:43546662 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:43546662 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:43581631 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:43581631 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:124792115 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:124792115 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:28482076 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:28482076 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:26183981 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:26183981 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:35789385 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:35789385 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:60312695 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:60312695 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:176964474 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:176964474 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:100481635 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:100481635 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:104326485 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:104326485 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:3149686 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:3149686 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:129233202 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:129233202 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:185541101 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:185541101 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:130410271 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:130410271 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:41173180 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:41173180 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:117859031 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:117859031 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:102626298 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:102626298 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3118192 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3118192 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3132012 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3132012 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:35856992 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:35856992 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:166896489 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:166896489 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:128034703 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:128034703 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:62545356 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:62545356 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:62582972 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:62582972 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:38409346 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:38409346 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:19700504 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:19700504 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30805116 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30805116 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30827805 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30827805 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:123092744 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:123092744 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:16341034 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:16341034 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:15639333 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:15639333 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:15720658 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:15720658 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:37831761 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:37831761 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:31391193 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:31391193 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:156649789 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:156649789 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:4816885 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:4816885 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:15430446 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:15430446 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:155893778 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:155893778 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49944163 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49944163 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:63483471 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:63483471 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:163369191 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:163369191 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:19479501 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:19479501 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:128708969 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:128708969 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:88693666 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:88693666 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:88792836 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:88792836 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215368182 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215368182 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:38818063 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:38818063 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:78846231 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:78846231 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:62044943 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:62044943 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:18112228 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:18112228 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:138642912 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:138642912 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196448399 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196448399 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:25315781 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:25315781 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:142650744 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:142650744 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26951225 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26951225 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:27692862 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:27692862 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:42335149 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:42335149 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:44172087 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:44172087 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34740365 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34740365 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:94044104 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:94044104 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:108279369 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:108279369 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180886938 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180886938 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:200523544 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:200523544 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:200971530 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:200971530 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:36350338 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:36350338 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:70275705 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:70275705 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:70413322 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:70413322 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:183368108 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:183368108 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:97561553 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:97561553 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51330129 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51330129 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51381923 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51381923 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:47978649 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:47978649 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52884522 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52884522 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52845257 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52845257 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52966144 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52966144 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39726651 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39726651 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:119211071 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:119211071 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:41612353 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:41612353 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54866780 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54866780 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54867645 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54867645 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:107600842 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:107600842 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:154182998 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:154182998 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:68123045 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:68123045 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:152637024 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:152637024 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:139652453 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:139652453 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:16587476 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:16587476 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:16590282 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:16590282 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:226108846 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:226108846 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:156763571 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:156763571 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:66042632 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:66042632 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:66088697 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:66088697 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:104308573 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:104308573 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:104309187 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:104309187 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75596371 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75596371 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:48639151 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:48639151 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55085189 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55085189 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55176160 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55176160 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54761078 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54761078 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:90985061 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:90985061 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:90427214 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:90427214 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:2934503 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:2934503 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:133827995 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:133827995 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:57569181 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:57569181 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:85438630 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:85438630 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:74575279 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:74575279 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:65314866 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:65314866 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:143867130 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:143867130 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:4283674 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:4283674 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:54978392 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:54978392 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:10589894 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:10589894 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11735034 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11735034 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:166973339 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:166973339 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:141290630 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:141290630 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:79082683 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:79082683 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:75656606 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:75656606 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:21206477 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:21206477 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:39108377 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:39108377 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:50929562 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:50929562 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:47963398 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:47963398 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:220791647 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:220791647 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:220799535 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:220799535 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:66437818 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:66437818 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:3778602 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:3778602 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:31188732 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:31188732 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:31189604 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:31189604 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:31194162 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:31194162 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:98943173 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:98943173 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:47801935 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:47801935 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:129152873 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:129152873 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:54529126 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:54529126 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:70944874 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:70944874 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:113740610 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:113740610 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:138689784 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:138689784 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:52134159 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:52134159 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:150881587 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:150881587 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:60023739 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:60023739 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:37187206 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:37187206 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62434554 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62434554 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:170677818 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:170677818 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:165623638 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:165623638 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:19378024 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:19378024 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:47025964 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:47025964 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:151039694 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:151039694 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:168315511 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:168315511 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40720377 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40720377 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:2535800 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:2535800 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:89068352 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:89068352 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:89339259 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:89339259 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102449729 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102449729 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41888474 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:41888474 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:202558753 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:202558753 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:44084200 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:44084200 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:104160912 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:104160912 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:60296946 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:60296946 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:86575886 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:86575886 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:9719629 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:9719629 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237001685 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237001685 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:125601805 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:125601805 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:30072525 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:30072525 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:9007663 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:9007663 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1221952 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1221952 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:23885115 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:23885115 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:16902484 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:16902484 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:26388539 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:26388539 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:52568024 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:52568024 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:2056736 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:2056736 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:41800536 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:41800536 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:153197675 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:153197675 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89903161 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89903161 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:120790053 C>A maps to NM_199461.2 Y247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:120790053 C>A maps to NM_199461.2 Y247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:78334046 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:78334046 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:15506614 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:15506614 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:16892335 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:16892335 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:16893051 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:16893051 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54893128 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54893128 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54914392 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:54914392 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:15968779 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:15968779 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:21499167 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:21499167 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:119174650 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:119174650 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:124922029 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:124922029 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:67379817 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:67379817 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:32258670 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:32258670 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:5495189 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:5495189 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:37064562 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:37064562 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:124676568 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:124676568 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:63769230 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:63769230 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:7063577 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:7063577 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55485244 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55485244 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247582053 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247582053 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56477782 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56477782 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:175815677 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:175815677 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26108313 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26108313 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:34888347 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:34888347 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:108502607 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:108502607 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:129317715 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:129317715 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:84625160 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:84625160 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:6599857 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:6599857 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:132204850 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:132204850 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156849271 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156849271 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:88726825 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:88726825 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:33202917 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:33202917 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:163297193 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:163297193 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:41331554 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:41331554 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113444524 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113444524 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:228494902 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:228494902 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:228520488 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:228520488 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:71067917 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:71067917 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:123516701 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:123516701 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:123663705 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:123663705 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:167182306 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:167182306 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:132812796 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:132812796 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:47779327 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:47779327 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158435339 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158435339 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6913786 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6913786 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248247620 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248247620 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248247738 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248247738 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:22332971 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:22332971 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:5020210 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:5020210 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103808890 C>A maps to NM_181747.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103808890 C>A maps to NM_181747.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:77745656 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:77745656 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:21742116 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:21742116 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:31796142 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:31796142 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:29614985 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:29614985 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:29648073 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:29648073 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:133197532 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:133197532 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57114201 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57114201 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:56504552 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:56504552 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:110366330 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:110366330 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:35456396 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:35456396 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:3899209 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:3899209 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:14676032 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:14676032 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:20815116 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:20815116 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:102566401 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:102566401 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:102587470 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:102587470 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:127251561 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:127251561 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:55581557 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:55581557 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:233344476 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:233344476 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:71513865 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:71513865 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:41239496 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:41239496 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:85679574 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:85679574 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:55138807 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:55138807 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:10929170 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:10929170 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:54975427 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:54975427 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:6261506 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:6261506 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:197712779 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:197712779 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:71692470 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:71692470 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:131703595 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:131703595 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:131703917 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:131703917 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:35094436 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:35094436 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:17167338 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:17167338 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:39609246 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:39609246 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:50356546 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:50356546 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:110401422 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:110401422 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:110482702 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:110482702 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:125255341 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:125255341 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:59814631 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:59814631 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:28789740 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:28789740 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:28789842 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:28789842 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:8698549 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:8698549 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:18848044 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:18848044 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:40876169 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:40876169 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:19506724 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:19506724 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:131935266 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:131935266 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:43927792 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:43927792 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:4839199 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:4839199 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:126749030 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:126749030 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:131844473 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:131844473 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:131872126 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:131872126 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118355852 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118355852 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118364828 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118364828 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118307691 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:118307691 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:53543268 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:53543268 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:134388751 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:134388751 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:124480938 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:124480938 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:16279391 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:16279391 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:16287186 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:16287186 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23797581 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23797581 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:40211187 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:40211187 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:9562079 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:9562079 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:23509101 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:23509101 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:145199613 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:145199613 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:105771495 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:105771495 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:69017250 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:69017250 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:57398084 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:57398084 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:57158188 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:57158188 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:48790465 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:48790465 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:142457419 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:142457419 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:18793369 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:18793369 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43522743 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43522743 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43576588 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43576588 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67942624 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67942624 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:23751176 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:23751176 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:65340937 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:65340937 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:54149742 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:54149742 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:805467 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:805467 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11574629 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11574629 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:27701853 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:27701853 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8501070 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8501070 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:5286033 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:5286033 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:40757306 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:40757306 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:121597091 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:121597091 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:1648338 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:1648338 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:74286986 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:74286986 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180155357 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180155357 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:13378358 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:13378358 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:72741406 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:72741406 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:8940733 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:8940733 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:131931246 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:131931246 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:33446640 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:33446640 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:121050903 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:121050903 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:170626797 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:170626797 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:36270161 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:36270161 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:69036587 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:69036587 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:178380795 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:178380795 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:178410823 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:178410823 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:74235396 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:74235396 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79348452 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79348452 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79350260 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79350260 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79384866 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79384866 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79385741 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:79385741 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103130445 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103130445 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103244703 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103244703 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:100019052 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:100019052 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:163137969 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:163137969 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:73029215 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:73029215 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:241099827 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:241099827 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:49583234 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:49583234 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:90023381 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:90023381 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:25599283 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:25599283 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:119249254 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:119249254 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:104581200 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:104581200 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:104973125 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:104973125 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:43385797 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:43385797 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:21047355 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:21047355 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:31429560 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:31429560 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:151785400 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:151785400 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:37359395 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:37359395 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:35833127 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:35833127 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:78516008 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:78516008 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:38078699 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:38078699 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:38095353 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:38095353 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100738822 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100738822 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:187416828 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:187416828 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87370922 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:87370922 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:155294113 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:155294113 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237551514 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237551514 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237608547 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237608547 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237796775 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:237796775 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:153347109 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:153347109 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:39869130 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:39869130 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:71923600 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:71923600 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:136595405 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:136595405 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:27824141 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:27824141 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:174312229 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:174312229 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:54826832 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:54826832 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:83606314 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:83606314 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:9042986 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:9042986 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:115818121 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:115818121 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:48022783 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:48022783 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7473578 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7473578 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:110350699 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:110350699 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:61259756 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:61259756 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:61323406 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:61323406 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:64064293 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:64064293 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:36946140 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:36946140 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:67755903 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:67755903 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:223317209 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:223317209 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:64968032 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:64968032 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:145383584 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:145383584 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:46655348 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:46655348 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:52002671 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:52002671 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:164727002 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:164727002 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:2234311 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:2234311 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:103718109 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:103718109 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26821352 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26821352 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:135366289 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:135366289 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:22364937 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:22364937 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:64366240 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:64366240 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:38316313 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:38316313 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:172691216 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:172691216 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:18070678 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:18070678 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:6433461 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:6433461 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:107414695 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:107414695 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:95290213 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:95290213 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42340168 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:42340168 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74479238 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74479238 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:24895463 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:24895463 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:24909446 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:24909446 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:149576273 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:149576273 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:44467345 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:44467345 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40366862 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40366862 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:111988939 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:111988939 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:480127 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:480127 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21349862 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21349862 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21355638 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21355638 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21391851 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21391851 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21175771 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:21175771 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:106858612 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:106858612 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:17913205 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:17913205 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:183518881 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:183518881 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:70419096 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:70419096 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:84324565 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:84324565 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:51569692 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:51569692 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:86277093 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:86277093 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108434726 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108434726 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108438987 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108438987 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:231313917 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:231313917 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:215274849 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:215274849 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26912270 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26912270 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4863264 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4863264 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:172641961 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:172641961 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3352050 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3352050 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:44328106 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:44328106 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220332169 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220332169 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220332279 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220332279 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220341529 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220341529 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220341567 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:220341567 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:89611204 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:89611204 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:167833910 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:167833910 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55652818 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55652818 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158585250 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158585250 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158626559 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158626559 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158651106 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158651106 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158653035 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158653035 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:13053193 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:13053193 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:30740170 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:30740170 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:62174614 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:62174614 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:182785397 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:182785397 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:134488272 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:134488272 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:90697796 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:90697796 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40354325 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40354325 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:23871747 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:23871747 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:219556839 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:219556839 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180933676 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180933676 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27010459 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27010459 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27023850 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27023850 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27025108 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:27025108 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:113275160 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:113275160 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:115400158 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:115400158 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:85648916 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:85648916 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:152560624 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:152560624 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:39760178 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:39760178 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:33532744 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:33532744 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:38008380 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:38008380 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:37299038 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:37299038 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:28886706 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:28886706 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:9673184 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:9673184 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:179558152 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:179558152 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:104492514 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:104492514 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:70450474 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:70450474 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:50681881 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:50681881 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43766725 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43766725 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43771155 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43771155 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:133475875 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:133475875 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:36776545 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:36776545 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:43560423 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:43560423 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:43585555 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:43585555 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:134024419 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:134024419 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:134108321 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:134108321 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:11632779 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:11632779 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:70443654 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:70443654 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:32537391 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:32537391 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:155485820 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:155485820 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:156381791 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:156381791 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:84202839 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:84202839 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:82269040 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:82269040 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:82323189 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:82323189 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:166999244 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:166999244 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:63017351 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:63017351 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:98414013 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:98414013 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:5754306 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:5754306 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:39944444 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:39944444 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:98940249 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:98940249 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:68934588 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:68934588 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:19685425 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:19685425 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:29757038 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:29757038 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:24234411 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:24234411 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:6442364 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:6442364 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:170811559 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:170811559 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57069467 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57069467 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201382135 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201382135 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:74957689 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:74957689 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:175293684 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:175293684 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:175332790 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:175332790 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:189607032 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:189607032 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:188707187 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:188707187 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:20039550 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:20039550 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:20066929 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:20066929 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:20067794 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:20067794 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:141285682 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:141285682 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:73012610 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:73012610 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:40313475 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:40313475 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:72975656 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:72975656 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:50925277 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:50925277 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:234872067 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:234872067 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:142569427 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:142569427 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:231081094 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:231081094 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40095151 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40095151 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62503054 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62503054 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179443487 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179443487 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179447385 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179447385 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:72218554 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:72218554 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:151512776 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:151512776 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:19738423 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:19738423 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:19748334 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:19748334 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:154238929 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:154238929 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:154524002 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:154524002 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:109959374 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:109959374 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:118243414 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:118243414 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:43252976 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:43252976 T>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:103291193 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:103291193 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:103306084 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:103306084 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:103354693 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:103354693 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:136505763 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:136505763 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:70460812 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:70460812 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:70346328 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:70346328 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:69964460 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:69964460 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:35954246 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:35954246 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:126201070 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:126201070 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215812409 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215812409 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:216222098 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:216222098 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:113705087 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:113705087 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:61558392 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:61558392 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:72872700 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:72872700 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:144757051 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:144757051 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:106729028 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:106729028 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:78011437 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:78011437 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:101197880 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:101197880 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:82850753 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:82850753 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:219294217 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:219294217 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:100454877 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:100454877 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40925711 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:40925711 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:6140833 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:6140833 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:71036222 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:71036222 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:10079202 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:10079202 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:241964542 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:241964542 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:27618559 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:27618559 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:2770672 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:2770672 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:78859466 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:78859466 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:87448010 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:87448010 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:31591560 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:31591560 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:58347493 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:58347493 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:38454546 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:38454546 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:17228601 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:17228601 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:46577533 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:46577533 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:52923945 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:52923945 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:111624590 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:111624590 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:99214593 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:99214593 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:31791231 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:31791231 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:72004553 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:72004553 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:115811583 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:115811583 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:36900714 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:36900714 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:57649713 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:57649713 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:40438799 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:40438799 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6962864 C>G maps to NM_013250.2 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6962864 C>G maps to NM_013250.2 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:31906243 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:31906243 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:58962952 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:58962952 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:43127491 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:43127491 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:49559189 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:49559189 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:22018889 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:22018889 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:22836108 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:22836108 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:99218977 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:99218977 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:44751718 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:44751718 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:44751906 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:44751906 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:27825866 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:27825866 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:38282413 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:38282413 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:41006195 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:41006195 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:84525620 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chrX:84525620 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:185731270 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:185731270 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:88956838 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:88956838 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:57829835 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:57829835 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:21215802 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:21215802 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:187702301 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:187702301 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:113639462 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:113639462 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4005735 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4005735 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:67250678 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:67250678 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:22005184 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:22005184 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:185687961 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:185687961 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:130284766 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:130284766 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:67364148 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:67364148 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:32879406 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:32879406 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:134256449 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:134256449 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:5687070 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:5687070 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:31625101 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:31625101 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:119625792 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:119625792 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr18:31322838 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr18:31322838 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:160147223 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:160147223 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:111990052 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:111990052 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:79170677 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:79170677 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:31661131 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:31661131 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:51695956 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:51695956 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:83689300 T>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:83689300 T>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:103793009 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:103793009 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:61252759 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:61252759 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:162344975 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:162344975 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:5975251 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:5975251 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:97616243 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:97616243 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:97563391 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:97563391 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:201021666 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:201021666 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:81978873 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:81978873 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:42646598 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:42646598 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:43927465 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:43927465 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:47774980 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:47774980 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:78086864 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:78086864 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:62545252 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:62545252 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:233405016 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:233405016 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:94053592 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:94053592 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:139819893 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:139819893 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:78635981 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:78635981 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr14:24592134 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr14:24592134 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:13845136 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:13845136 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:2223211 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:2223211 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:71828050 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:71828050 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:71840446 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:71840446 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:95274411 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:95274411 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:62341286 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:62341286 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:6903763 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:6903763 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:111463881 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:111463881 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:223512024 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:223512024 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:92614092 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:92614092 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:108516643 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:108516643 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:89407463 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:89407463 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:22696332 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:22696332 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:127224377 C>A maps to NM_024523.5 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:127224377 C>A maps to NM_024523.5 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:44197619 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:44197619 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:158060161 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:158060161 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:68173404 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:68173404 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:37899320 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:37899320 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:183776384 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:183776384 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:113742406 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:113742406 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:77632278 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:77632278 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:15726163 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:15726163 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:24518415 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:24518415 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:241722602 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:241722602 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:200950033 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:200950033 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:55179542 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:55179542 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:141250137 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:141250137 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:44184466 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:44184466 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr21:47626549 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr21:47626549 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:160793672 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:160793672 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:39696653 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:39696653 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:119739853 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:119739853 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:3779354 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:3779354 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:119181236 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:119181236 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:130137703 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:130137703 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:15455718 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:15455718 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:141805561 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:141805561 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:131099381 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:131099381 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:100841369 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:100841369 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:50957495 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:50957495 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:10219146 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:10219146 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr22:36697183 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr22:36697183 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:128384546 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:128384546 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:76442202 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:76442202 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:54925692 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:54925692 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:150706193 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:150706193 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:135074051 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:135074051 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:62570879 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:62570879 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:228556722 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:228556722 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr13:53615999 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr13:53615999 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:102540915 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:102540915 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:15083106 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:15083106 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:230459044 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:230459044 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:129773460 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:129773460 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:56150944 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:56150944 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:102503116 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:102503116 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:113253576 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:113253576 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:11035375 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:11035375 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:11182902 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:11182902 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:23523008 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:23523008 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:55974513 T>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:55974513 T>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:231925940 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:231925940 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:178359130 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:178359130 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:86509378 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:86509378 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:35436175 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:35436175 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:108995491 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:108995491 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:92998998 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:92998998 G>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:243504502 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:243504502 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:51647484 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:51647484 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:25812049 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:25812049 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:33702523 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:33702523 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:59182334 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:59182334 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:39222531 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:39222531 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:158626336 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:158626336 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:48206416 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:48206416 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:139655521 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:139655521 T>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:50696490 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:50696490 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr13:95228540 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr13:95228540 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:63076137 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:63076137 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:67263061 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:67263061 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:108521629 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:108521629 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:179833903 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:179833903 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:202254674 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:202254674 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248027992 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248027992 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:165961174 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:165961174 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:231334737 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:231334737 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr13:38319967 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr13:38319967 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:132240476 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:132240476 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:19699331 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:19699331 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:35608087 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:35608087 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:216246403 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:216246403 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:82789278 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:82789278 G>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:82876057 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:82876057 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:219299216 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:219299216 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:38048332 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:38048332 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:65253199 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chrX:65253199 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:85604999 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:85604999 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:90272188 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:90272188 T>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:72024813 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:72024813 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:32333150 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:32333150 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:58004130 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:58004130 A>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:22817320 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:22817320 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:53544 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:53544 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:67300881 T>C maps to ENST00000392677 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:67300881 T>C maps to ENST00000392677 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:1051731 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:1051731 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:48261884 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:48261884 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:48261884 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:48261884 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:40029886 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:40029886 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:33614565 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:33614565 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:33614565 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:33614565 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:5146225 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:5146225 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:5146225 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:5146225 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:25046043 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:25046043 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:25046043 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:25046043 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:186338326 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:186338326 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:49964049 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:49964049 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:5129738 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:5129738 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:233244767 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:233244767 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:115231456 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:115231456 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:115231456 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:115231456 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:25384856 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:25384856 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:25384856 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:25384856 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr13:111535916 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr13:111535916 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:67952113 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:67952113 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:15836819 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:15836819 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:15836819 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:15836819 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:242162767 G>A maps to ENST00000402430 W883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:242162767 G>A maps to ENST00000402430 W883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:47133422 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:47133422 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:47133422 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:47133422 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:2127037 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:2127037 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:21227026 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:21227026 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:64208359 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:64208359 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:64208359 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:64208359 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:153750761 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:153750761 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:17960913 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:17960913 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:17960913 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:17960913 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:109274603 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:109274603 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:109274603 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:109274603 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:73950275 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:73950275 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:73950275 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:73950275 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:1743384 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:1743384 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:3385071 C>T maps to NM_000049.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:3385071 C>T maps to NM_000049.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:176998756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:176998756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:176998756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:176998756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:10382278 G>A maps to NM_001001331.2 N1009N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:10382278 G>A maps to NM_001001331.2 N1009N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:35692911 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:35692911 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:153171454 C>A maps to NM_000054.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:153171454 C>A maps to NM_000054.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr21:11049523 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr21:11049523 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:32520795 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:32520795 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr20:36159050 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr20:36159050 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:36159050 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:36159050 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:32841722 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:32841722 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:79942332 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:79942332 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:50916416 C>A maps to NM_182554.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:50916416 C>A maps to NM_182554.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:61559842 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:61559842 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:57960334 A>G maps to NM_018168.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:57960334 A>G maps to NM_018168.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:34648809 T>C maps to ENST00000438749 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:34648809 T>C maps to ENST00000438749 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr18:52258616 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr18:52258616 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:14003570 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:14003570 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr20:35507614 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr20:35507614 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:20051411 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:20051411 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:20051421 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:20051421 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:74834435 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:74834435 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:74834435 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:74834435 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:175763779 C>A maps to ENST00000443967 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:175763779 C>A maps to ENST00000443967 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:36200220 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:36200220 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:36200220 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:36200220 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:41158734 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:41158734 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:41158734 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:41158734 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:110620367 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:110620367 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:110620367 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:110620367 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:127911206 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:127911206 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:127911206 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:127911206 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:40934406 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:40934406 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:40934406 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:40934406 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:24432037 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:24432037 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:24432037 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:24432037 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:2716321 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:2716321 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:2716321 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:2716321 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:181480553 G>A maps to ENST00000357570 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:181480553 G>A maps to ENST00000357570 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:76992922 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:76992922 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:76992922 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:76992922 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:110496261 A>G maps to NM_014289.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:110496261 A>G maps to NM_014289.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:104874187 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:104874187 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:104874187 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:104874187 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:197550940 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:197550940 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:149938919 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:149938919 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:149938919 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:149938919 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:73270727 C>A maps to ENST00000398860 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:73270727 C>A maps to ENST00000398860 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:58587464 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:58587464 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:58145229 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:58145229 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:58145229 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:58145229 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:88472796 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:88472796 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:196696127 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:196696127 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:196696127 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:196696127 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:50828374 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:50828374 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:419495 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:419495 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:419495 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:419495 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:42565701 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:42565701 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:11073249 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:11073249 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:10280533 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:10280533 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:87755666 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:87755666 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:87755666 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:87755666 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:1427296 C>A maps to NM_014461.2 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:1427296 C>A maps to NM_014461.2 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr13:46060599 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr13:46060599 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:56029201 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:56029201 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:56029201 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:56029201 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:19087068 G>T maps to NM_016138.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:19087068 G>T maps to NM_016138.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:211473090 A>G maps to NM_001122633.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:211473090 A>G maps to NM_001122633.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:151904571 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:151904571 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:151904571 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:151904571 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:149456664 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:149456664 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:34312506 G>A maps to ENST00000373381 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:34312506 G>A maps to ENST00000373381 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:113648993 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:113648993 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:113648993 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:113648993 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:114186032 G>A maps to NM_198123.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:114186032 G>A maps to NM_198123.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:111786209 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:111786209 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:149101917 C>A maps to NM_001013845.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:149101917 C>A maps to NM_001013845.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:115593060 A>G maps to NM_001017978.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:115593060 A>G maps to NM_001017978.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:27997128 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:27997128 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:27997128 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:27997128 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:55039269 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:55039269 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:19033421 C>T maps to NM_019070.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:19033421 C>T maps to NM_019070.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:49989651 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:49989651 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:49989651 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:49989651 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:65998420 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:65998420 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:65998420 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:65998420 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:154007623 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:154007623 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:69718461 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:69718461 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:69718461 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:69718461 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:22451960 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:22451960 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:183586871 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:183586871 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:134017472 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:134017472 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:117340756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:117340756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:117340756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:117340756 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:45401233 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:45401233 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:345692 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:345692 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:103182881 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:103182881 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:103182881 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:103182881 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:83433307 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:83433307 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:52355188 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:52355188 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:52380597 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:52380597 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:52355188 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:52355188 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:42937718 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:42937718 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:42937718 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:42937718 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:79357453 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:79357453 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:79357453 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:79357453 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:101200596 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:101200596 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:101200596 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:101200596 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:6901605 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:6901605 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:14884603 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:14884603 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:132147129 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:132147129 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:132147129 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:132147129 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr18:5437892 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr18:5437892 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:111643268 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:111643268 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:111643268 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:111643268 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:89259777 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:89259777 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:89259777 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:89259777 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:220174370 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:220174370 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:220174370 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:220174370 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:60188173 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:60188173 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:60188173 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:60188173 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:64726779 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:64726779 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr13:113797967 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr13:113797967 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:154130514 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:154130514 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:154158392 G>T maps to NM_000132.3 I1224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:154158392 G>T maps to NM_000132.3 I1224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:51425401 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:51425401 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:51425401 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:51425401 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:153382024 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:153382024 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:201927871 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:201927871 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:17643133 G>T maps to ENST00000335393 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:17643133 G>T maps to ENST00000335393 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:71190772 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:71190772 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:71190772 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:71190772 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:29245209 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:29245209 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:92531938 C>G maps to ENST00000298047 Y1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:92531938 C>G maps to ENST00000298047 Y1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:92623915 C>A maps to ENST00000298047 S4469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:92623915 C>A maps to ENST00000298047 S4469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:55880640 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:55880640 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:55880640 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:55880640 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:161518541 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:161518541 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:161518541 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:161518541 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:111749506 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:111749506 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:4479489 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:4479489 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:128496847 C>A maps to NM_001458.4 I2478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:128496847 C>A maps to NM_001458.4 I2478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:109271180 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:109271180 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:109271180 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:109271180 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:89424357 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:89424357 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:12693115 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:12693115 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:12693115 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:12693115 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:17472628 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:17472628 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:17472628 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:17472628 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:132685655 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:132685655 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:153825532 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:153825532 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:153825532 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:153825532 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:72623708 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:72623708 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:72623708 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:72623708 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:69645581 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:69645581 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:69645581 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:69645581 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:175649853 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:175649853 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:175649853 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:175649853 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:74365053 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr15:74365053 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:167728077 T>C maps to NM_014498.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:167728077 T>C maps to NM_014498.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:28808412 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:28808412 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:20331131 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:20331131 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:20331131 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:20331131 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:135475653 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:135475653 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:135475653 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:135475653 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:134886238 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:134886238 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:150345445 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:150345445 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:150345445 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:150345445 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:89920949 G>T maps to NM_032119.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:89920949 G>T maps to NM_032119.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:19871804 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:19871804 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:19871804 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:19871804 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:123468866 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:123468866 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:23421767 T>C maps to NM_017815.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:23421767 T>C maps to NM_017815.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:236749501 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:236749501 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:124731953 G>A maps to NM_020733.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:124731953 G>A maps to NM_020733.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:28424342 T>C maps to NM_004667.4 T2988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr15:28424342 T>C maps to NM_004667.4 T2988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:75185674 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:75185674 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:139299278 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:139299278 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:91061831 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:91061831 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:91061831 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:91061831 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:130416318 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:130416318 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:130416318 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:130416318 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:219920174 G>A maps to NM_002181.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:219920174 G>A maps to NM_002181.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:57168352 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:57168352 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:57168352 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:57168352 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:35856919 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:35856919 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:48726110 G>A maps to ENST00000395509 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:48726110 G>A maps to ENST00000395509 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:48149605 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:48149605 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:37514987 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:37514987 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:37514987 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:37514987 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:31409286 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:31409286 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:20167605 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:20167605 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:142655386 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:142655386 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:142655386 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:142655386 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:43907003 T>C maps to NM_015284.2 G1589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:43907003 T>C maps to NM_015284.2 G1589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:75548818 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:75548818 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:1900275 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:1900275 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:1900275 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:1900275 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:91474692 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:91474692 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:86880893 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:86880893 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:9148020 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:9148020 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:29495022 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:29495022 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:29495022 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:29495022 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:39671964 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:39671964 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:39671964 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:39671964 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:53189526 G>T maps to ENST00000309505 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:53189526 G>T maps to ENST00000309505 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:52827567 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:52827567 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:52710519 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:52710519 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:52710519 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:52710519 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:52754853 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:52754853 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:52761048 C>T maps to NM_002283.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:52761048 C>T maps to NM_002283.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr18:6973045 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr18:6973045 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr18:6973045 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr18:6973045 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:112476951 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:112476951 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:112476951 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:112476951 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:21788433 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:21788433 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:21788433 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:21788433 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:36057607 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:36057607 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:36057607 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:36057607 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:205388588 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:205388588 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:205388588 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:205388588 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:104309109 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:104309109 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:104309109 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:104309109 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:55143265 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:55143265 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:54778427 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:54778427 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:148016410 G>A maps to ENST00000310701 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:148016410 G>A maps to ENST00000310701 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:148016410 G>A maps to ENST00000310701 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:148016410 G>A maps to ENST00000310701 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:7092726 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:7092726 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:7092726 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:7092726 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:33614512 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:33614512 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:33614512 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:33614512 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:151899873 A>G maps to NM_005367.5 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:151899873 A>G maps to NM_005367.5 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:65673842 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:65673842 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:91269677 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:91269677 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:91269677 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:91269677 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:128358882 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:128358882 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:128358882 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:128358882 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:119185141 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:119185141 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:119185141 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:119185141 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:47670271 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:47670271 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:47670271 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:47670271 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:204513587 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:204513587 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:204513587 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:204513587 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:38192395 G>A maps to NM_014815.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:38192395 G>A maps to NM_014815.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:129904903 T>A maps to NM_002417.4 K1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:129904903 T>A maps to NM_002417.4 K1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:14915126 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:14915126 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:41954990 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:41954990 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:41898570 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:41898570 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:131205315 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:131205315 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:131205315 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:131205315 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:56673679 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:56673679 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:56673679 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:56673679 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:9739688 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:9739688 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:63574870 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:63574870 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:63574870 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:63574870 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:125577891 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:125577891 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:125577891 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:125577891 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:1081892 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:1081892 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:140265264 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:140265264 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:140265264 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:140265264 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:48017994 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:48017994 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:113102362 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:113102362 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:113102362 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:113102362 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:6626864 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:6626864 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:6626864 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:6626864 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:123197913 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:123197913 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:123197913 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:123197913 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:152467393 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:152467393 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:152467393 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:152467393 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:72740662 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:72740662 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:72740662 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:72740662 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:74716537 G>A maps to NM_006656.5 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:74716537 G>A maps to NM_006656.5 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:29679224 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:29679224 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:204954990 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:204954990 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:57104586 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr16:57104586 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:57104586 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr16:57104586 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:152138399 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:152138399 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:65715740 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:65715740 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:65715740 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:65715740 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:105132285 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:105132285 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:105189910 T>C maps to NM_198465.2 Y1369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:105189910 T>C maps to NM_198465.2 Y1369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:80130074 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:80130074 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:80130076 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:80130076 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:80130074 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:80130074 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:80130076 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:80130076 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:152027211 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:152027211 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:152027211 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:152027211 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:123719173 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr10:123719173 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:123719173 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:123719173 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:101572216 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:101572216 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:101572216 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:101572216 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:101096790 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:101096790 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:101096790 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:101096790 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:50946022 G>A maps to NM_018245.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:50946022 G>A maps to NM_018245.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:248167033 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:248167033 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:248167033 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:248167033 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:248263678 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:248263678 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:248757057 G>T maps to NM_001004693.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:248757057 G>T maps to NM_001004693.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:51412418 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:51412418 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:51412418 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:51412418 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:55433034 G>C maps to NM_001004704.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:55433034 G>C maps to NM_001004704.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:5173254 G>A maps to NM_012375.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:5173254 G>A maps to NM_012375.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:55562906 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:55562906 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:125313779 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:125313779 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:226580691 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:226580691 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:226580691 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:226580691 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:134111443 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:134111443 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:78506291 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:78506291 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:78506291 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:78506291 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:54794316 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:54794316 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:73437349 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:73437349 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:4116323 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:4116323 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:4116323 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:4116323 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:179525379 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:179525379 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:179525379 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:179525379 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:133559477 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:133559477 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr18:44426478 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr18:44426478 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:45568238 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:45568238 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:150129497 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:150129497 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:17488188 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:17488188 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:153691505 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:153691505 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:20940345 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:20940345 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:20940345 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:20940345 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:84606464 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:84606464 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:133256575 T>C maps to ENST00000455752 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:133256575 T>C maps to ENST00000455752 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:7656625 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:7656625 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:7656625 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:7656625 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:28169912 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:28169912 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:86544395 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:86544395 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:86544395 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:86544395 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:43519797 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:43519797 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:43519797 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:43519797 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:55716907 G>T maps to NM_002842.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:55716907 G>T maps to NM_002842.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:157931354 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:157931354 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr20:40739174 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr20:40739174 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:40739174 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr20:40739174 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:220345427 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:220345427 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:220345427 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:220345427 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:16232694 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:16232694 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:42461329 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:42461329 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:6441398 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:6441398 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:6441398 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:6441398 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:141259373 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:141259373 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:183853735 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:183853735 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:73178272 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:73178272 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:49463562 C>A maps to NM_144593.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:49463562 C>A maps to NM_144593.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:21167997 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr14:21167997 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:33406782 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:33406782 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:38145110 T>C maps to NM_001034853.1 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:38145110 T>C maps to NM_001034853.1 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:34385330 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:34385330 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:34385330 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:34385330 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:54705254 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:54705254 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:237890502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:237890502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:237890502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:237890502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:134994942 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:134994942 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:134994942 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:134994942 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:130505349 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:130505349 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:130505349 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:130505349 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:38830356 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:38830356 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:151140045 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:151140045 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:92065385 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:92065385 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:92065385 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:92065385 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:118763132 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:118763132 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr13:44971452 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr13:44971452 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr13:44971452 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr13:44971452 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:123875096 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:123875096 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:123875096 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:123875096 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:132250563 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:132250563 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:155885570 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:155885570 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:155885570 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:155885570 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:2834798 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:2834798 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:2834798 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:2834798 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:72117373 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:72117373 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:1053369 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:1053369 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:63078457 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:63078457 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:63078457 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:63078457 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:63149533 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr11:63149533 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:63149533 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr11:63149533 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:37198874 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr14:37198874 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:98989170 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:98989170 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:98989170 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:98989170 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:153750883 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:153750883 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:153750883 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:153750883 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:130169335 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:130169335 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:118598586 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:118598586 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:150844518 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:150844518 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:47172033 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:47172033 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:47172033 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:47172033 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:18250885 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:18250885 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:19618557 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:19618557 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:108604525 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:108604525 G>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:168098447 G>T maps to NM_003062.2 G1294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr5:168098447 G>T maps to NM_003062.2 G1294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:153012822 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:153012822 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:153012822 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:153012822 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:158613036 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:158613036 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:158618525 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:158618525 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:158613036 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:158613036 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:158618525 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:158618525 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:126011615 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:126011615 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:126011615 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:126011615 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:45806915 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:45806915 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:45806915 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:45806915 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:99912015 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:99912015 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:136141123 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:136141123 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:146730869 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:146730869 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:134929865 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:134929865 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:37095163 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:37095163 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:108994679 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:108994679 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:108994679 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:108994679 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:47432470 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:47432470 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:120773108 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:120773108 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:120773108 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:120773108 T>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:50811153 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:50811153 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:122747706 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:122747706 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:29915163 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr22:29915163 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:29915163 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr22:29915163 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr21:32559433 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr21:32559433 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr21:32559433 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr21:32559433 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:153555596 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:153555596 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:153555596 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:153555596 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:38831003 C>A maps to NM_006068.3 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:38831003 C>A maps to NM_006068.3 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:94984964 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr12:94984964 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:15662939 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:15662939 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:15670615 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:15670615 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:94776059 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr8:94776059 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:94776059 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr8:94776059 A>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:47436556 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:47436556 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:6329036 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:6329036 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:6329036 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:6329036 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:48112480 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:48112480 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:69111368 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:69111368 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:69111368 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:69111368 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr21:43826502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr21:43826502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr21:43826502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr21:43826502 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:83763710 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:83763710 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:10093696 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:10093696 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:10093696 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:10093696 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:138977895 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:138977895 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:138977895 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:138977895 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:156012100 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:156012100 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:19437396 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr1:19437396 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:19437396 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr1:19437396 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:69520984 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:69520984 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:69520984 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:69520984 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:73813012 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:73813012 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:5036452 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr17:5036452 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:6825305 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr19:6825305 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:6825305 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:6825305 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:80584988 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:80584988 A>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:122380652 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr12:122380652 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:37701030 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr5:37701030 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:7592604 C>T maps to NM_018081.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr17:7592604 C>T maps to NM_018081.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:2712566 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chrX:2712566 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:2712566 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chrX:2712566 G>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:168096519 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr2:168096519 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:168096519 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:168096519 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:168110397 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr2:168110397 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:100461538 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr9:100461538 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:100461538 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr9:100461538 C>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:43523797 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr6:43523797 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:43523797 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr6:43523797 T>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:2274774 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr4:2274774 C>A did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:21465632 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:21465632 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:21552222 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:21552222 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:21552222 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:21552222 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:31165981 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr10:31165981 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:57199979 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr7:57199979 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:57199979 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr7:57199979 A>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:44751847 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01D-0969-08 chr3:44751847 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:44751847 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr3:44751847 C>G did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:60068 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr4:60068 G>T did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:23938433 T>C did not map to a codon.
Sequencing variant TCGA-67-3770-01A-01W-0928-08 chr19:23938433 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:7760772 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:7760772 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:7760772 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:7760772 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:215840443 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:215840443 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:215840443 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:215840443 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:48443530 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:48443530 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:94505587 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:94505587 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:94544949 C>A maps to NM_000350.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:94544949 C>A maps to NM_000350.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:67290917 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:67290917 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:20721100 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:20721100 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:16235219 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:16235219 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:95696733 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:95696733 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:183696483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:183696483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:183696483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:183696483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:17482024 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:17482024 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:17482024 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:17482024 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:89034360 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:89034360 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:58279172 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:58279172 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:7994682 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:7994682 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:211085208 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:211085208 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:76216216 A>T maps to ENST00000370834 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:76216216 A>T maps to ENST00000370834 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:31341135 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:31341135 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220397706 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220397706 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:220397706 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:220397706 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:135602963 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:135602963 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:32408672 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:32408672 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:32408672 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:32408672 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:41916030 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:41916030 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:78500310 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:78500310 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20488173 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20488173 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:20442242 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:20442242 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20442242 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20442242 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:33462854 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:33462854 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:100244459 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:100244459 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:100244459 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:100244459 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236912413 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236912413 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236918344 C>T maps to NM_001103.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236918344 C>T maps to NM_001103.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:114697527 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:114697527 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:114697527 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:114697527 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:24359023 G>T maps to ENST00000380789 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:24359023 G>T maps to ENST00000380789 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72520069 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72520069 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72520069 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72520069 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:5242151 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:5242151 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:100695331 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:100695331 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:100695331 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:100695331 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:43824098 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:43824098 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:43824098 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:43824098 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:84442201 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:84442201 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:84442201 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:84442201 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:41215892 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:41215892 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:41215892 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:41215892 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:123016353 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:123016353 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:123015088 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:123015088 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:111879158 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:111879158 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:111879158 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:111879158 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:100240137 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:100240137 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:100240137 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:100240137 C>A did not map to a codon.
Alternatively spliced codon TCGA-67-3771-01A-01W-0928-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-67-3771-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:96780505 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:96780505 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:26043306 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:26043306 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:88047193 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:88047193 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:148054826 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:148054826 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:148054826 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:148054826 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:64780560 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:64780560 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:50311636 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:50311636 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:177636518 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:177636518 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247076762 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247076762 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:135811301 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:135811301 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:105408230 G>A maps to NM_138420.2 D4519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:105408230 G>A maps to NM_138420.2 D4519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:105416867 C>G maps to NM_138420.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:105416867 C>G maps to NM_138420.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:62294196 C>A maps to NM_001620.1 G2564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:62294196 C>A maps to NM_001620.1 G2564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:186333642 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:186333642 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:186333642 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:186333642 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:143654304 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:143654304 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:143654304 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:143654304 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:159032613 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:159032613 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:42871180 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:42871180 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:4747356 T>C maps to NM_006422.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:4747356 T>C maps to NM_006422.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:101425403 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:101425403 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:101425403 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:101425403 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:3726107 G>A maps to ENST00000403787 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:3726107 G>A maps to ENST00000403787 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:233244132 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:233244132 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:202206970 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:202206970 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:202206970 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:202206970 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:202633662 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:202633662 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:202606350 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:202606350 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:202633662 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:202633662 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:46534225 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:46534225 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:46534225 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:46534225 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:38424384 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:38424384 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:38424384 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:38424384 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:71398273 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:71398273 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:71398273 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:71398273 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:104120404 G>T maps to NM_020978.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:104120404 G>T maps to NM_020978.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:41572402 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:41572402 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:41572402 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:41572402 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:41581036 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:41581036 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:114209647 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:114209647 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:114282129 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:114282129 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:114209647 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:114209647 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:241439488 C>A maps to ENST00000401804 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:241439488 C>A maps to ENST00000401804 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:73979739 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:73979739 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:73962874 A>C maps to NM_032217.3 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:73962874 A>C maps to NM_032217.3 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:37434053 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:37434053 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:55396241 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:55396241 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:6055287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:6055287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:6055287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:6055287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:165118605 G>A maps to NM_012403.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:165118605 G>A maps to NM_012403.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:90346961 G>A maps to NM_001150.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:90346961 G>A maps to NM_001150.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:69350006 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:69350006 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:69297878 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:69297878 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:201470222 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:201470222 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:29745134 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:29745134 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29745134 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29745134 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:83332600 C>A maps to NM_004644.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:83332600 C>A maps to NM_004644.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:99053213 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:99053213 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:99096993 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:99096993 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:99042287 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:99042287 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:99053213 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:99053213 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:29368185 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:29368185 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:29368185 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:29368185 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:49716254 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:49716254 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:49716254 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:49716254 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:36369785 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:36369785 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36369785 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36369785 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:129996685 G>A maps to NM_001642.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:129996685 G>A maps to NM_001642.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:116693505 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:116693505 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:21227065 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:21227065 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:21227065 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:21227065 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:21234951 T>C maps to NM_000384.2 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:21234951 T>C maps to NM_000384.2 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:116701674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:116701674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:72410006 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:72410006 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:72410006 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:72410006 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:36160520 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:36160520 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:141059052 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:141059052 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:153793572 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:153793572 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:32103261 C>A maps to NM_018287.5 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:32103261 C>A maps to NM_018287.5 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:42407923 G>T maps to NM_199002.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:42407923 G>T maps to NM_199002.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:28270327 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:28270327 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:232142979 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:232142979 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:35785900 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:35785900 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:35785900 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:35785900 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:69497548 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:69497548 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:78251368 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:78251368 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:76955970 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:76955970 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:104650267 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:104650267 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:104632994 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:104632994 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131087180 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131087180 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131146528 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:131146528 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:237149791 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:237149791 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:237149791 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:237149791 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:54014608 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:54014608 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:30218209 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:30218209 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:30218209 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:30218209 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:101109583 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:101109583 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:62559543 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:62559543 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:62559543 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:62559543 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:176833753 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:176833753 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:176833753 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:176833753 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:119567806 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:119567806 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:119567806 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:119567806 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:11372932 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:11372932 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:51038740 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:51038740 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:25925893 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:25925893 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:25925893 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:25925893 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:160076379 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:160076379 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113470539 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113470539 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113490623 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113490623 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:113470539 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:113470539 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:182555028 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:182555028 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:25276002 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:25276002 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:25276002 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:25276002 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160147169 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160147169 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160147169 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160147169 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:141632746 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:141632746 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:141632746 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:141632746 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:90003832 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:90003832 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:67487340 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:67487340 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:55368337 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:55368337 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:142169887 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:142169887 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:142279311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:142279311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:142169887 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:142169887 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:142279311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:142279311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:8113427 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:8113427 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57744081 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57744081 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:11021104 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:11021104 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:11021104 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:11021104 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:11038954 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:11038954 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:11058082 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:11058082 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143569925 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143569925 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:69640529 A>G maps to NM_001704.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:69640529 A>G maps to NM_001704.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:171492733 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:171492733 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:160284417 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:160284417 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:52674699 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:52674699 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:59465989 G>A maps to ENST00000340746 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:59465989 G>A maps to ENST00000340746 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:58786578 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:58786578 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:49458379 C>T maps to NM_198799.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:49458379 C>T maps to NM_198799.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:187447837 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:187447837 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:187447837 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:187447837 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:23596784 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:23596784 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:23596784 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:23596784 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:61730374 C>G maps to NM_001139443.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:61730374 C>G maps to NM_001139443.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:127816806 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:127816806 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:102196378 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:102196378 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61870964 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61870964 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:91294956 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:91294956 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:96035849 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:96035849 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:96035849 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:96035849 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:16437680 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:16437680 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:31620701 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:31620701 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:31620701 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:31620701 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:36932540 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:36932540 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:36932540 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:36932540 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:154299927 G>C maps to ENST00000399042 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:154299927 G>C maps to ENST00000399042 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105678535 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105678535 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:40582650 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:40582650 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:79965837 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:79965837 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:32834256 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:32834256 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:582442 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:582442 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:103310675 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:103310675 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:103310675 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:103310675 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:111395636 C>T maps to NM_004336.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:111395636 C>T maps to NM_004336.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:63441107 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:63441107 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:77818330 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:77818330 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:77818330 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:77818330 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:78084269 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:78084269 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72541682 G>T maps to NM_152710.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72541682 G>T maps to NM_152710.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:128191330 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:128191330 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118084764 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118084764 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:82796962 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:82796962 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:76123846 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:76123846 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:65892077 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:65892077 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:65892077 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:65892077 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:89777625 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:89777625 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:55677956 C>T maps to ENST00000301249 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:55677956 C>T maps to ENST00000301249 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:179503095 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:179503095 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:184535641 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:184535641 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:184535641 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:184535641 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:228363177 A>G maps to NM_001010867.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:228363177 A>G maps to NM_001010867.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:32682976 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:32682976 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:32682976 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:32682976 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:30610284 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:30610284 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61151439 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61151439 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:61151439 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:61151439 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:31676932 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:31676932 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:31676932 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:31676932 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:24964767 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:24964767 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:55052204 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:55052204 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:31901507 G>A maps to ENST00000437789 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:31901507 G>A maps to ENST00000437789 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220039038 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220039038 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:210969065 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:210969065 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:228497783 C>A maps to NM_020161.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:228497783 C>A maps to NM_020161.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:184801038 G>C maps to NM_001025266.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:184801038 G>C maps to NM_001025266.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:207262801 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:207262801 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:8467052 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:8467052 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:8467052 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:8467052 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:71096818 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:71096818 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:56208993 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:56208993 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:56208993 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:56208993 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41181412 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41181412 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41181412 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41181412 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:97621181 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:97621181 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:6634023 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:6634023 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:6634023 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:6634023 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:57372550 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:57372550 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:57372550 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:57372550 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:57411381 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:57411381 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:144124452 C>A maps to NM_173687.2 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:144124452 C>A maps to NM_173687.2 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:86249392 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:86249392 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:86244665 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:86244665 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:86249392 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:86249392 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:15790763 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:15790763 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:15790763 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:15790763 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:9011798 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:9011798 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:9011798 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:9011798 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:13368153 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:13368153 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:13443768 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:13443768 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:13368153 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:13368153 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:13443768 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:13443768 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:181480711 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:181480711 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:181719671 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:181719671 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:181753013 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:181753013 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:181480711 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:181480711 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:181719671 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:181719671 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:181753013 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:181753013 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:81667326 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:81667326 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:18807794 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:18807794 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:18816494 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:18816494 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:159161975 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:159161975 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:71416735 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:71416735 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:71416735 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:71416735 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:179134106 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:179134106 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:40895065 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:40895065 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:40895065 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:40895065 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:96089901 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:96089901 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:10702814 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:10702814 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:65793535 G>C maps to NM_053054.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:65793535 G>C maps to NM_053054.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:119170449 G>T maps to NM_005188.2 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:119170449 G>T maps to NM_005188.2 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14029040 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14029040 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:70515319 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:70515319 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:70515319 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:70515319 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:23662183 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:23662183 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:23662183 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:23662183 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179730379 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179730379 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179730379 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179730379 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:11542025 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:11542025 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:159889168 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:159889168 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:159889168 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:159889168 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:8644549 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:8644549 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:191074838 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:191074838 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123308004 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123308004 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:123308004 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:123308004 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:132290039 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:132290039 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:118764240 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:118764240 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:118764240 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:118764240 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:34341011 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:34341011 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:34341011 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:34341011 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:99997441 C>T maps to NM_005190.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:99997441 C>T maps to NM_005190.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:35814957 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:35814957 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:73476789 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:73476789 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:74446007 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:74446007 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:74446007 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:74446007 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158225197 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158225197 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158299526 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158299526 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:74003563 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:74003563 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:74003563 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:74003563 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:51728893 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:51728893 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51728291 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51728291 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51728893 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51728893 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:35243287 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:35243287 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:35243287 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:35243287 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:121828257 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:121828257 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:149999766 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:149999766 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:100961682 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:100961682 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:100983734 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:100983734 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:3783726 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:3783726 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:536053 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:536053 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:227381663 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:227381663 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:151028081 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:151028081 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:24511389 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:24511389 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:65025617 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:65025617 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:65025617 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:65025617 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:22580667 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:22580667 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:73375216 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:73375216 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:73375216 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:73375216 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:25585687 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:25585687 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:60485724 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:60485724 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:31313630 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:31313630 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:31313630 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:31313630 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:105653115 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:105653115 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:105653115 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:105653115 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:68531323 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:68531323 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:68531323 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:68531323 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:4892411 G>T maps to ENST00000328908 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:4892411 G>T maps to ENST00000328908 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:15802844 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:15802844 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:34833912 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:34833912 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:34833912 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:34833912 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:117241625 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:117241625 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:196946691 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:196946691 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4429820 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4429820 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:4429820 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:4429820 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:6692638 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:6692638 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:6212446 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:6212446 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:29120917 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:29120917 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29120917 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29120917 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:111860530 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:111860530 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:203191502 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:203191502 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:67833135 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:67833135 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:404848 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:404848 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:42585953 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:42585953 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:120150569 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:120150569 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113518369 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113518369 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:53036484 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:53036484 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:46784136 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:46784136 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:46784136 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:46784136 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:86909730 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:86909730 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:16359839 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:16359839 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:31538944 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:31538944 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:14710888 C>G maps to ENST00000417570 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:14710888 C>G maps to ENST00000417570 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:68547177 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:68547177 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:68547177 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:68547177 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:10529634 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:10529634 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:3570052 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:3570052 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:100515472 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:100515472 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:100523169 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:100523169 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:100523169 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:100523169 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:10288574 G>A maps to NM_138809.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:10288574 G>A maps to NM_138809.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:23846327 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:23846327 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:72244401 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:72244401 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:154735743 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:154735743 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:97493651 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:97493651 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:54652317 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:54652317 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40959980 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40959980 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40959980 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40959980 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:125671586 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:125671586 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:125405303 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:125405303 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:125671586 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:125671586 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:7837917 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:7837917 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:103427579 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:103427579 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:139763841 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:139763841 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:139763841 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:139763841 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:86578264 T>C maps to NM_152890.5 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:86578264 T>C maps to NM_152890.5 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:7399920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:7399920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:7399920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:7399920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:189859245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:189859245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:189870874 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:189870874 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189859245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189859245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189870874 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189870874 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:110821964 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:110821964 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:110839026 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:110839026 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:110821964 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:110821964 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189912898 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189912898 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189943873 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:189943873 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:128984246 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:128984246 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:128984246 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:128984246 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57490420 G>C maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57490420 G>C maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:47605759 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:47605759 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:109055931 T>C maps to ENST00000420959 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:109055931 T>C maps to ENST00000420959 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:30232607 G>C maps to NM_032609.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:30232607 G>C maps to NM_032609.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:166325217 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:166325217 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:175305789 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:175305789 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:211465464 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:211465464 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:211542777 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:211542777 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:2775091 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:2775091 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:125506267 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:125506267 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:126129406 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:126129406 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4170210 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4170210 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:4170210 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:4170210 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:43911513 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:43911513 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:122735461 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:122735461 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:122735461 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:122735461 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:107395161 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:107395161 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:107395161 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:107395161 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149449638 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149449638 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149433913 C>A maps to NM_005211.3 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149433913 C>A maps to NM_005211.3 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149449638 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149449638 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:3267177 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:3267177 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:34052086 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:34052086 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:34052086 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:34052086 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:34082430 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:34082430 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:114185957 G>A maps to NM_198123.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:114185957 G>A maps to NM_198123.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:23729626 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:23729626 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:23729626 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:23729626 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:19998838 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:19998838 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:80772261 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:80772261 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:80772261 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:80772261 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:36407878 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:36407878 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:11082808 G>T maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:11082808 G>T maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150779123 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150779123 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:16911875 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:16911875 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:101502846 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:101502846 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:101916811 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:101916811 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:101671404 C>T maps to ENST00000360264 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:101671404 C>T maps to ENST00000360264 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:101916811 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:101916811 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:49052638 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:49052638 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:44873292 G>C maps to NM_001178134.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:44873292 G>C maps to NM_001178134.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:36007663 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:36007663 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:36007663 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:36007663 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:143955875 T>A maps to ENST00000377675 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:143955875 T>A maps to ENST00000377675 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:143995832 A>G maps to NM_000498.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:143995832 A>G maps to NM_000498.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:104596781 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:104596781 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:75014928 C>G maps to NM_000499.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:75014928 C>G maps to NM_000499.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:94836199 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:94836199 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:94836199 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:94836199 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:41601044 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:41601044 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:41601044 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:41601044 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:41700359 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:41700359 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:41700359 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:41700359 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:99313317 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:99313317 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99313317 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99313317 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:65680383 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:65680383 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:59821813 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:59821813 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:59002448 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:59002448 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:72131071 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:72131071 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:24586027 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:24586027 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:24586027 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:24586027 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:125298589 C>A maps to NM_001013628.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:125298589 C>A maps to NM_001013628.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:69550292 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:69550292 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:27997644 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:27997644 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:27997644 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:27997644 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160209913 G>C maps to NM_015726.3 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160209913 G>C maps to NM_015726.3 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:155161977 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:155161977 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:36699914 C>G maps to NM_004734.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:36699914 C>G maps to NM_004734.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14976829 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14976829 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:17420414 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:17420414 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61080924 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61080924 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:61080924 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:61080924 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:101111161 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:101111161 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:101111161 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:101111161 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:162735900 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:162735900 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:108709330 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:108709330 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:108709330 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:108709330 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:118579309 G>A maps to NM_006773.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:118579309 G>A maps to NM_006773.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:15736940 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:15736940 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:134118605 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:134118605 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:134118605 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:134118605 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:70670188 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:70670188 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:200617381 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:200617381 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:169196689 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:169196689 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:49986628 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:49986628 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:29966126 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:29966126 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:29966126 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:29966126 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:170381 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:170381 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:170381 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:170381 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:197704816 G>A maps to NM_001195216.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:197704816 G>A maps to NM_001195216.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:197704816 G>A maps to NM_001195216.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:197704816 G>A maps to NM_001195216.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:142190927 G>T maps to NM_014957.2 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:142190927 G>T maps to NM_014957.2 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:31577437 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:31577437 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:32217451 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:32217451 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:32217451 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:32217451 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:32217560 G>A maps to NM_001136029.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:32217560 G>A maps to NM_001136029.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:10529147 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:10529147 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:75507351 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:75507351 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:75507351 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:75507351 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:185982978 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:185982978 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:186024799 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:186024799 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:2209549 G>A maps to NM_145177.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:2209549 G>A maps to NM_145177.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:72140088 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:72140088 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:72140088 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:72140088 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:182856178 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:182856178 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:140956993 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:140956993 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:140956993 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:140956993 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:51069066 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:51069066 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:83673924 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:83673924 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:83691416 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:83691416 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:83673924 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:83673924 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:83691416 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:83691416 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:85164561 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:85164561 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:1626284 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:1626284 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:1626284 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:1626284 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:32827847 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:32827847 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:78296956 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:78296956 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:78296956 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:78296956 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:78340325 G>A maps to NM_013391.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:78340325 G>A maps to NM_013391.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:70179498 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:70179498 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:21640204 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:21640204 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:21783935 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:21783935 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:21640204 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:21640204 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:21783935 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:21783935 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:57487971 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:57487971 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:57487971 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:57487971 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:7661801 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:7661801 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:7661801 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:7661801 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20959735 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20959735 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:13753671 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:13753671 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:13753671 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:13753671 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:38790860 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:38790860 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:38790860 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:38790860 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:11584253 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:11584253 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:11584253 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:11584253 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:34506883 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:34506883 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:4496845 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:4496845 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:73680450 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:73680450 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:183608468 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:183608468 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:183608468 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:183608468 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:6591339 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:6591339 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:6591339 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:6591339 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:172308017 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:172308017 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:94337612 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:94337612 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:50825098 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:50825098 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:51275047 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:51275047 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:51392311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:51392311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:286582 G>C maps to NM_203447.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:286582 G>C maps to NM_203447.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:53205190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:53205190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:53205190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:53205190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:68024509 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:68024509 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:116548968 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:116548968 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:154672476 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:154672476 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:65799771 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:65799771 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:113286151 A>T maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:113286151 A>T maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:28574372 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:28574372 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:28574372 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:28574372 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:41506073 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:41506073 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:28993525 C>A maps to NM_001134453.1 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:28993525 C>A maps to NM_001134453.1 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:35381108 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:35381108 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:32405318 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:32405318 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:25678411 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:25678411 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:76111921 T>C maps to NM_020892.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:76111921 T>C maps to NM_020892.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:45430222 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:45430222 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:45397882 C>G maps to NM_014080.4 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:45397882 C>G maps to NM_014080.4 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:44703734 G>A maps to NM_022076.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:44703734 G>A maps to NM_022076.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:312007 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:312007 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:7133926 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:7133926 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:7133926 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:7133926 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:46784876 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:46784876 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:103106398 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:103106398 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:37700254 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:37700254 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:71883180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:71883180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:71883180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:71883180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:158158029 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:158158029 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:43630024 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:43630024 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:65824386 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:65824386 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:128060644 C>T maps to NM_021937.3 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:128060644 C>T maps to NM_021937.3 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:36194190 A>G maps to NM_030636.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:36194190 A>G maps to NM_030636.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:44177978 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:44177978 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:55259305 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:55259305 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:55259305 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:55259305 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:32687872 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:32687872 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:39114612 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:39114612 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53400127 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53400127 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:23693560 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:23693560 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:23693560 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:23693560 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:23762244 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:23762244 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:37382166 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:37382166 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:37382166 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:37382166 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:67236948 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:67236948 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62372923 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62372923 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:77076938 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:77076938 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:43843787 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:43843787 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:120581374 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:120581374 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132539637 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132539637 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132561056 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132561056 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132561162 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132561162 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132498235 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132498235 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132539637 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132539637 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132561056 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132561056 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132561162 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:132561162 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:149402777 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:149402777 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:149402777 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:149402777 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110299528 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110299528 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:37871870 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:37871870 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:29514671 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:29514671 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236415487 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236415487 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:124624472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:124624472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:124624472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:124624472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64081700 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64081700 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64081700 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64081700 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:76553565 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:76553565 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:76553565 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:76553565 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:159611592 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:159611592 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:159611592 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:159611592 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:40194758 C>T maps to NM_005239.4 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:40194758 C>T maps to NM_005239.4 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:11991991 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:11991991 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:11128684 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:11128684 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:72128920 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:72128920 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:65443452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:65443452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:65443452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:65443452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:169528469 C>T maps to ENST00000367796 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:169528469 C>T maps to ENST00000367796 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:14563799 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:14563799 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14563218 G>C maps to NM_031453.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14563218 G>C maps to NM_031453.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14563799 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:14563799 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:57658048 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:57658048 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:45731123 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:45731123 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:208489132 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:208489132 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:184863019 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:184863019 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:143056143 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:143056143 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:177163716 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:177163716 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:177163716 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:177163716 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:107973307 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:107973307 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:187611699 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:187611699 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:84384864 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:84384864 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:45523812 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:45523812 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45523812 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45523812 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:29527255 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:29527255 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:86185687 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:86185687 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:86185687 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:86185687 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:51826389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:51826389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:46280388 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:46280388 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:46279924 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:46279924 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:20879648 G>A maps to NM_207334.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:20879648 G>A maps to NM_207334.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:24332336 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:24332336 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:177242591 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:177242591 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:87516624 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:87516624 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:54735506 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:54735506 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45624669 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45624669 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45624671 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:45624671 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:163029264 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:163029264 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:98996182 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:98996182 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:98996182 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:98996182 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:3127277 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:3127277 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:3127277 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:3127277 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150774530 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150774530 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150921750 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150921750 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150921750 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150921750 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150924903 C>A maps to NM_001447.2 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150924903 C>A maps to NM_001447.2 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:48766915 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:48766915 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:48766915 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:48766915 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:48830056 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:48830056 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:127727872 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:127727872 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:8151237 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:8151237 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:8176732 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:8176732 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:8151237 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:8151237 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:8176732 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:8176732 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:107560014 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:107560014 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:161519644 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:161519644 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:161519644 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:161519644 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:137778452 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:137778452 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:137778452 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:137778452 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157719509 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157719509 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:157719509 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:157719509 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157551287 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157551287 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:157551287 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:157551287 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:157551322 G>T maps to NM_031282.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:157551322 G>T maps to NM_031282.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:114879139 C>A maps to NM_020177.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:114879139 C>A maps to NM_020177.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:97368992 C>T maps to NM_001113382.1 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:97368992 C>T maps to NM_001113382.1 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:108290707 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:108290707 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:95528484 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:95528484 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:176518124 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:176518124 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:76029652 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:76029652 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:24276674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:24276674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:24276674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:24276674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:28971082 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:28971082 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:180043887 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:180043887 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:171240670 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:171240670 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:147106528 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:147106528 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:147106528 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:147106528 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:171830225 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:171830225 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:171830225 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:171830225 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:172025376 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:172025376 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:39448548 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:39448548 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:39435726 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:39435726 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:39448548 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:39448548 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:13702485 T>A maps to NM_018027.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:13702485 T>A maps to NM_018027.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:83451384 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:83451384 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:83451384 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:83451384 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:30253354 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:30253354 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:30253354 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:30253354 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:31089992 C>T maps to NM_031894.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:31089992 C>T maps to NM_031894.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:61897137 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:61897137 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:61897137 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:61897137 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:66200211 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:66200211 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:66200211 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:66200211 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:17446054 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:17446054 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:17446054 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:17446054 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:161115881 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:161115881 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:161521030 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:161521030 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:49611951 C>T maps to NM_002044.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:49611951 C>T maps to NM_002044.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:153796537 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:153796537 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:153796537 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:153796537 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:154996775 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:154996775 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:155102560 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:155102560 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:16249872 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:16249872 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:16249872 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:16249872 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:128111649 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:128111649 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:128111649 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:128111649 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:114542676 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:114542676 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:114542676 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:114542676 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:8111425 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:8111425 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:8111425 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:8111425 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:153825473 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:153825473 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:155209348 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:155209348 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:89652831 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:89652831 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:89727871 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:89727871 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:89727871 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:89727871 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:48428802 C>T maps to NM_004962.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:48428802 C>T maps to NM_004962.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:137593711 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:137593711 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:33438058 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:33438058 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:33442457 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:33442457 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:33438058 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:33438058 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:33442457 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:33442457 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40344577 C>T maps to NM_032484.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40344577 C>T maps to NM_032484.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31011703 C>T maps to NM_000823.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31011703 C>T maps to NM_000823.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:175598516 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:175598516 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:110290712 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:110290712 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88820282 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88820282 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150760645 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150760645 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150760645 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150760645 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:1930450 A>T maps to NM_001500.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:1930450 A>T maps to NM_001500.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:3118847 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:3118847 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:127651447 C>A maps to NM_002077.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:127651447 C>A maps to NM_002077.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:100561197 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:100561197 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:100561197 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:100561197 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:133358785 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:133358785 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20331154 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:20331154 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:217784227 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:217784227 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:217784227 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:217784227 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:42478466 C>T maps to NM_001002909.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:42478466 C>T maps to NM_001002909.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:135431522 C>T maps to NM_153834.3 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:135431522 C>T maps to NM_153834.3 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:26533739 C>T maps to NM_001145168.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:26533739 C>T maps to NM_001145168.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:47684540 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:47684540 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:131439263 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:131439263 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:131439263 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:131439263 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:27720713 C>T maps to NM_005281.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:27720713 C>T maps to NM_005281.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:105859434 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:105859434 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:46094343 C>A maps to NM_005282.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:46094343 C>A maps to NM_005282.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:80010093 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:80010093 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:54456043 G>A maps to NM_001008397.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:54456043 G>A maps to NM_001008397.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:123481048 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:123481048 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:123481048 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:123481048 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:102649187 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:102649187 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:105577155 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:105577155 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:87407334 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:87407334 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:87468805 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:87468805 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:102372430 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:102372430 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:9862549 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:9862549 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:121203351 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:121203351 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:126746809 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:126746809 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:110211844 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:110211844 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:110213869 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:110213869 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110211844 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110211844 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110213869 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:110213869 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:30436704 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:30436704 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:30436704 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:30436704 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:74131335 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:74131335 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:73024326 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:73024326 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:127447981 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:127447981 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:127447981 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:127447981 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:144826724 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:144826724 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:54326504 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:54326504 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:7915093 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:7915093 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:121363642 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:121363642 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:121363642 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:121363642 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:18631289 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:18631289 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:18633707 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:18633707 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:37299427 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:37299427 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:37299427 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:37299427 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:58147968 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:58147968 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41005625 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41005625 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:43548526 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:43548526 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:197118638 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:197118638 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:197118638 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:197118638 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:197157202 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:197157202 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:96334088 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:96334088 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:92818459 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:92818459 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:91794632 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:91794632 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:46815569 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:46815569 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:25726877 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:25726877 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:25726877 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:25726877 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:33053969 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:33053969 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:29864643 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:29864643 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:29864643 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:29864643 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:185815084 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:185815084 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:185953208 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:185953208 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:185815084 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:185815084 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:186156838 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:186156838 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:26545529 A>G maps to NM_006353.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:26545529 A>G maps to NM_006353.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:83277658 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:83277658 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:83277658 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:83277658 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:38796435 C>A maps to NM_138394.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:38796435 C>A maps to NM_138394.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18327657 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18327657 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18327657 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18327657 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:63235915 C>A maps to NM_054108.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:63235915 C>A maps to NM_054108.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:22040785 G>T maps to NM_021624.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:22040785 G>T maps to NM_021624.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:114598467 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:114598467 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:29142080 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:29142080 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29142080 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29142080 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:119958292 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:119958292 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:45050351 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:45050351 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:161495728 C>A maps to NM_002155.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:161495728 C>A maps to NM_002155.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:656539 C>A maps to NM_148959.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:656539 C>A maps to NM_148959.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:71004270 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:71004270 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:95015833 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:95015833 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:315103 G>T maps to ENST00000328221 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:315103 G>T maps to ENST00000328221 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:27672724 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:27672724 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:42232376 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:42232376 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:47121243 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:47121243 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:47119760 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:47119760 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:47121243 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:47121243 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:201195333 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:201195333 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:51825270 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:51825270 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51825270 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51825270 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:130409887 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:130409887 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:130420063 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:130420063 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:130409887 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:130409887 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:130420063 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:130420063 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18736220 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18736220 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18735747 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18735747 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18736220 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:18736220 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:42176905 G>T maps to NM_001556.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:42176905 G>T maps to NM_001556.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:213878498 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:213878498 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:213878498 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:213878498 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113765397 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113765397 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113765397 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113765397 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:102642487 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:102642487 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:29973188 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:29973188 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:29973188 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:29973188 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:190326974 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:190326974 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:190326974 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:190326974 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:207039432 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:207039432 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:24469443 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:24469443 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:239082404 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:239082404 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:111035083 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:111035083 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:111161595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:111161595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:111035083 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:111035083 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:111161595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:111161595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:242662727 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:242662727 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156816690 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156816690 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:128629674 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:128629674 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:52177874 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:52177874 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:52374761 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:52374761 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:30509281 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:30509281 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:30507391 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:30507391 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:73738594 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:73738594 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:156638417 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:156638417 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:156638417 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:156638417 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160924389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160924389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160924389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160924389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:26553191 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:26553191 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:33644513 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:33644513 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:6050536 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:6050536 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:6050536 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:6050536 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:64943191 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:64943191 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:64943191 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:64943191 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:62713409 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:62713409 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:211256396 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:211256396 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:49950938 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:49950938 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:49950938 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:49950938 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:169810915 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:169810915 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:155711161 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:155711161 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:128786275 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:128786275 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:118960609 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:118960609 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118960609 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118960609 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:233802285 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:233802285 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:78651441 C>G maps to NM_001161352.1 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:78651441 C>G maps to NM_001161352.1 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:44271914 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:44271914 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:34302539 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:34302539 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:36454966 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:36454966 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:36454984 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:36454984 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:122012564 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:122012564 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105344717 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105344717 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:24566721 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:24566721 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:24566721 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:24566721 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:43855627 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:43855627 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:58988569 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:58988569 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:55355132 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:55355132 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:55355132 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:55355132 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:84859424 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:84859424 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:84859424 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:84859424 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72289612 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72289612 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72289612 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:72289612 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:138595879 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:138595879 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:20929235 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:20929235 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:20929299 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:20929299 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:20770338 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:20770338 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:20929235 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:20929235 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:20929299 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:20929299 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:29018230 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:29018230 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:16359916 C>T maps to NM_024704.4 Q910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:16359916 C>T maps to NM_024704.4 Q910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:16362811 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:16362811 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:16408001 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:16408001 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:10436462 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:10436462 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:10436462 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:10436462 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:45205401 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:45205401 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:45218723 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:45218723 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55327926 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55327926 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:44587910 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:44587910 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:205307613 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:205307613 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205307613 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205307613 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:70281697 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:70281697 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:70469137 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:70469137 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:86772824 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:86772824 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:241731982 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:241731982 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:241755135 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:241755135 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:241731982 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:241731982 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:241755135 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:241755135 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:39092741 C>A maps to NM_015515.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:39092741 C>A maps to NM_015515.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:39595231 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:39595231 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:53010125 G>A maps to NM_175068.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:53010125 G>A maps to NM_175068.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53088587 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53088587 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:53088587 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:53088587 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:117964809 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:117964809 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:7043160 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:7043160 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:129588415 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:129588415 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:112506689 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:112506689 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:112469633 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:112469633 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:55467799 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:55467799 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:20233066 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:20233066 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:149997674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:149997674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:152538336 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:152538336 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88446770 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88446770 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88447079 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88447079 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:88446770 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:88446770 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:88447079 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:88447079 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:132209843 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:132209843 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:132209843 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:132209843 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:109086349 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:109086349 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:109086349 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:109086349 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:18387102 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:18387102 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:93179113 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:93179113 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:126783308 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:126783308 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:226465685 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:226465685 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:28150736 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:28150736 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:27950731 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:27950731 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:28150736 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:28150736 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:91005362 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:91005362 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:5692222 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:5692222 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:5692222 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:5692222 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:160959095 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:160959095 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:211923465 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:211923465 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:82188848 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:82188848 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:82188848 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:82188848 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:62542728 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:62542728 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:62542728 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:62542728 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:99764810 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:99764810 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:99380292 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:99380292 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:151520207 A>C maps to NM_006726.3 P1999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:151520207 A>C maps to NM_006726.3 P1999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:42355848 T>A maps to NM_152447.3 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:42355848 T>A maps to NM_152447.3 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4539721 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4539721 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:141250380 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:141250380 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:141264318 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:141264318 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:170002220 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:170002220 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:170002220 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:170002220 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:46895179 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:46895179 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:194080146 G>T maps to NM_001135057.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:194080146 G>T maps to NM_001135057.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:7231810 G>T maps to NM_001105581.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:7231810 G>T maps to NM_001105581.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:122674673 C>G maps to ENST00000289014 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:122674673 C>G maps to ENST00000289014 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:122674673 C>G maps to ENST00000289014 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:122674673 C>G maps to ENST00000289014 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:70501955 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:70501955 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:238664709 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:238664709 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:238664709 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:238664709 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:37100213 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:37100213 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:85638752 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:85638752 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:235964165 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:235964165 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:39752942 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:39752942 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:39752942 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:39752942 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:13983118 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:13983118 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:13983118 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:13983118 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:166960579 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:166960579 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:166960579 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:166960579 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:140995103 C>A maps to NM_005462.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:140995103 C>A maps to NM_005462.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:141293130 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:141293130 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:117948084 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:117948084 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:12028688 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:12028688 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:210588469 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:210588469 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:210588469 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:210588469 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:206904866 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:206904866 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:31434627 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:31434627 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:31434627 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:31434627 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:165110188 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:165110188 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:12958372 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:12958372 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:82040624 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:82040624 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:54527719 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:54527719 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:20153081 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:20153081 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:112406906 T>C maps to NM_001085377.1 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:112406906 T>C maps to NM_001085377.1 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:113719263 C>T maps to NM_001112732.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:113719263 C>T maps to NM_001112732.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:127324019 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:127324019 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:127324019 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:127324019 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:37620157 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:37620157 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:37620157 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:37620157 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:83938468 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:83938468 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:6378449 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:6378449 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:118552289 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:118552289 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:3294474 G>C maps to NM_000243.2 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:3294474 G>C maps to NM_000243.2 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:46766761 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:46766761 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:46766761 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:46766761 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:60501733 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:60501733 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:89449994 C>A maps to NM_005928.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:89449994 C>A maps to NM_005928.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:39884737 G>T maps to NM_001098270.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:39884737 G>T maps to NM_001098270.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:43232315 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:43232315 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:43232315 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:43232315 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:222837526 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:222837526 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:56847964 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:56847964 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:129903115 T>A maps to NM_002417.4 K2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:129903115 T>A maps to NM_002417.4 K2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:151935712 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:151935712 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:151970711 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:151970711 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:152006996 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:152006996 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:36865409 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:36865409 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:36871816 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:36871816 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:36865409 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:36865409 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:36871816 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:36871816 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:110003026 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:110003026 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:2535349 C>T maps to NM_033467.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:2535349 C>T maps to NM_033467.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:154864836 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:154864836 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:89339532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:89339532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:89339532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:89339532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:102565920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:102565920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:55525622 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:55525622 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158811924 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158811924 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158812889 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158812889 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:27358835 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:27358835 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:27358835 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:27358835 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:39880458 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:39880458 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108776167 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108776167 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108746545 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108746545 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108776167 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108776167 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108778672 C>T maps to NM_014429.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108778672 C>T maps to NM_014429.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:43805991 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:43805991 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:17039273 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:17039273 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:94219071 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:94219071 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:66204421 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:66204421 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:125084969 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:125084969 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:125084969 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:125084969 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:10649325 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:10649325 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:47739383 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:47739383 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:47739383 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:47739383 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:56692050 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:56692050 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:56692050 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:56692050 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:56701980 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:56701980 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:93576078 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:93576078 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:151256054 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:151256054 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:151256054 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:151256054 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:68478240 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:68478240 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:30387726 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:30387726 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:11297962 C>A maps to NM_004958.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:11297962 C>A maps to NM_004958.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236975956 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236975956 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236975956 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236975956 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9024309 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9024309 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9072072 C>A maps to NM_024690.2 E5125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9072072 C>A maps to NM_024690.2 E5125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:195488598 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:195488598 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1155220 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1155220 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1024786 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1024786 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1033116 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1033116 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:1033116 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:1033116 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:4442215 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:4442215 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:4442215 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:4442215 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:42331554 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:42331554 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:42344532 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:42344532 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:102060587 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:102060587 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:102060587 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:102060587 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50945489 C>A maps to NM_004533.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50945489 C>A maps to NM_004533.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:47364313 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:47364313 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:47364313 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:47364313 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:77695683 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:77695683 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:77695683 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:77695683 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:77780734 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:77780734 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50785110 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50785110 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108112807 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108112807 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108117748 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108117748 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108175758 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108175758 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:10417528 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:10417528 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:23854990 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:23854990 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:23855952 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:23855952 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:211155674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:211155674 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:46763483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:46763483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:46763483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:46763483 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:109859231 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:109859231 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:192280721 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:192280721 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:171225957 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:171225957 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:171225957 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:171225957 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:95139808 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:95139808 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:2027038 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:2027038 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:2027038 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:2027038 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:41834583 C>T maps to NM_006766.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:41834583 C>T maps to NM_006766.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:30257705 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:30257705 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:41892885 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:41892885 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:41929420 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:41929420 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:41929420 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:41929420 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:19998523 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:19998523 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40685602 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40685602 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:101747913 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:101747913 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:101747913 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:101747913 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:46083318 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:46083318 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:47038417 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:47038417 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:36046754 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:36046754 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:16902745 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:16902745 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:134093888 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:134093888 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:172351223 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:172351223 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:183850995 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:183850995 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:183850995 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:183850995 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75563576 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75563576 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75566382 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75566382 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:119114644 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:119114644 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:115898491 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:115898491 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:115769465 A>T maps to NM_022569.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:115769465 A>T maps to NM_022569.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:1391228 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:1391228 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152432197 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152432197 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:152432197 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:152432197 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:11185640 T>A maps to NM_006403.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:11185640 T>A maps to NM_006403.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:72740528 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:72740528 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52797323 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52797323 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:52797323 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:52797323 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:45004704 A>T maps to NM_001145107.1 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:45004704 A>T maps to NM_001145107.1 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:29559580 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:29559580 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:13201251 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:13201251 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:101571649 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:101571649 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:129762496 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:129762496 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:129762496 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:129762496 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:33313607 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:33313607 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236195688 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236195688 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236195688 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:236195688 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:25493373 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:25493373 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:25493373 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:25493373 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31655570 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31655570 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:124676441 G>T maps to NM_001040214.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:124676441 G>T maps to NM_001040214.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:57062311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:57062311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57062311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:57062311 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:56382249 G>A maps to NM_134444.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:56382249 G>A maps to NM_134444.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:56544114 G>C maps to NM_153447.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:56544114 G>C maps to NM_153447.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56465807 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56465807 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:56465807 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:56465807 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:101097042 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:101097042 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132631994 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132631994 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:14958618 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:14958618 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:14989988 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:14989988 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:18542751 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:18542751 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:16364119 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:16364119 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:117660522 T>A maps to ENST00000338101 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:117660522 T>A maps to ENST00000338101 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:26094706 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:26094706 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150697443 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150697443 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:100118018 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:100118018 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:100118018 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:100118018 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:108064652 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:108064652 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:108064652 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:108064652 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:132431945 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:132431945 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:34791014 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:34791014 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:34791014 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:34791014 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:78447416 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:78447416 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:100934573 G>A maps to ENST00000392986 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:100934573 G>A maps to ENST00000392986 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:108502646 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:108502646 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:108502646 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:108502646 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:92929579 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:92929579 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:115391513 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:115391513 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:107820955 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:107820955 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:107850078 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:107850078 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:107850078 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:107850078 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:107878290 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:107878290 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:1433841 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:1433841 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:212955341 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:212955341 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:59515721 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:59515721 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:18765287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:18765287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:18765287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:18765287 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:9124657 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:9124657 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:87342554 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:87342554 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:87342554 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:87342554 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:88522571 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:88522571 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:88522571 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:88522571 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:2290723 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:2290723 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:34263447 C>G maps to NM_006703.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:34263447 C>G maps to NM_006703.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:37364145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:37364145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:37364145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:37364145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:3774422 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:3774422 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:3789740 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:3789740 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:224491580 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:224491580 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:91150684 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:91150684 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:113400362 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:113400362 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:126091384 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:126091384 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:138439694 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:138439694 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:138439694 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:138439694 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:133037060 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:133037060 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:123556155 G>A maps to NM_001163278.1 D1479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:123556155 G>A maps to NM_001163278.1 D1479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:13753125 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:13753125 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:50943155 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:50943155 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:193364865 A>G maps to NM_130837.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:193364865 A>G maps to NM_130837.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:57995948 C>T maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:57995948 C>T maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247695645 G>T maps to NM_198074.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:247695645 G>T maps to NM_198074.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:248636501 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:248636501 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:180581965 C>A maps to NM_206880.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:180581965 C>A maps to NM_206880.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:48266602 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:48266602 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:48266602 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:48266602 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:6024417 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:6024417 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:55681455 G>A maps to NM_001001960.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:55681455 G>A maps to NM_001001960.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:55889782 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:55889782 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:125286263 G>C maps to NM_022776.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:125286263 G>C maps to NM_022776.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:21747289 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:21747289 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179209050 G>A maps to ENST00000392505 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179209050 G>A maps to ENST00000392505 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179209050 G>A maps to ENST00000392505 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179209050 G>A maps to ENST00000392505 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:76786601 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:76786601 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:7718156 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:7718156 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41739744 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41739744 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41801114 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:41801114 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:65983532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:65983532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:65983532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:65983532 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:65988745 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:65988745 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:17592142 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:17592142 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:17592142 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:17592142 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:55102689 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:55102689 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:55102689 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:55102689 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:124482850 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:124482850 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:124482850 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:124482850 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:108576015 C>A maps to NM_005443.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:108576015 C>A maps to NM_005443.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:206058069 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:206058069 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:139756469 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:139756469 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:50055591 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:50055591 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:44583833 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:44583833 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:80015033 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:80015033 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:80015033 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:80015033 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:102506213 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:102506213 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:127254019 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:127254019 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:91237673 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:91237673 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:55892843 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:55892843 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:55570512 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:55570512 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:55626692 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:55626692 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:55892843 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:55892843 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:56288109 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:56288109 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:56360533 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:56360533 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:140174545 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:140174545 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:140174545 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:140174545 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:17794928 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:17794928 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:1483626 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:1483626 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:195975229 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:195975229 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:195975240 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:195975240 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:165895712 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:165895712 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:165895712 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:165895712 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31867782 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31867782 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31793151 A>T maps to NM_001191057.1 L659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31793151 A>T maps to NM_001191057.1 L659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31867769 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31867769 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31867782 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:31867782 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:20705005 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:20705005 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:20705005 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:20705005 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:20774218 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:20774218 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:144922675 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:144922675 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149286808 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149286808 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149286808 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149286808 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:95399998 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:95399998 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:95399998 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:95399998 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:66631464 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:66631464 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:39870873 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:39870873 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:102780322 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:102780322 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:57330169 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:57330169 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57330169 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:57330169 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:64321775 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:64321775 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:7342954 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:7342954 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:7342954 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:7342954 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:139682725 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:139682725 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:139682725 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:139682725 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:249208011 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:249208011 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:97847499 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:97847499 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:153303169 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:153303169 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:153303169 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:153303169 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:76415831 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:76415831 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:58318416 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:58318416 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:58318416 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:58318416 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:27234113 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:27234113 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:79672699 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:79672699 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:18942677 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:18942677 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:18942677 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:18942677 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:18970785 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:18970785 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:60384515 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:60384515 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:151266849 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:151266849 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:151266849 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:151266849 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:230020566 C>G maps to NM_017933.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:230020566 C>G maps to NM_017933.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:18499546 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:18499546 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:18499546 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:18499546 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123485802 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123485802 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:94330993 A>G maps to NM_152431.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:94330993 A>G maps to NM_152431.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:47882628 C>A maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:47882628 C>A maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:102052900 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:102052900 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:102052900 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:102052900 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:110412244 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:110412244 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:110412244 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:110412244 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:110487546 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:110487546 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:48578087 G>A maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:48578087 G>A maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:42363778 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:42363778 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:42363778 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:42363778 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:8689500 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:8689500 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:81944010 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:81944010 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:132110012 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:132110012 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:131949261 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:131949261 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:132110012 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:132110012 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:57751637 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:57751637 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:126749362 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:126749362 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205811918 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205811918 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:82356863 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:82356863 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50367696 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50367696 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50367696 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50367696 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50369650 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50369650 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118220676 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118220676 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118314891 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:118314891 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:108151193 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:108151193 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:121192173 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:121192173 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:121192173 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:121192173 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:53103546 C>T maps to NM_182595.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:53103546 C>T maps to NM_182595.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:46668969 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:46668969 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:46656016 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:46656016 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:99142458 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:99142458 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:122263422 T>A maps to NM_001030059.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:122263422 T>A maps to NM_001030059.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149214841 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149214841 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149214841 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149214841 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:12475258 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:12475258 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:57261426 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:57261426 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:81688595 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:81688595 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:89189311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:89189311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:89189311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:89189311 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:46003649 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:46003649 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:242102980 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:242102980 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:111608383 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:111608383 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:146086143 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:146086143 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:48758545 A>C maps to NM_005710.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:48758545 A>C maps to NM_005710.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:23518119 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:23518119 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:23524370 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:23524370 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:203455882 C>T maps to NM_201348.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:203455882 C>T maps to NM_201348.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57146355 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57146355 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:57146355 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:57146355 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:186275423 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:186275423 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:186275423 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:186275423 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:219693169 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:219693169 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:48802801 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:48802801 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:54032265 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:54032265 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:3686259 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:3686259 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:36297251 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:36297251 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36297251 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36297251 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:62648233 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:62648233 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:49691389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:49691389 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:152200846 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:152200846 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:73581798 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:73581798 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113955198 C>T maps to NM_012455.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113955198 C>T maps to NM_012455.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:43530536 G>A maps to ENST00000306308 H2H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:43530536 G>A maps to ENST00000306308 H2H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:43371806 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:43371806 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:43371806 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:43371806 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:43757684 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:43757684 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:87081588 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:87081588 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:14632471 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:14632471 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:36909032 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:36909032 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:61909385 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:61909385 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:151237633 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:151237633 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:54161582 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:54161582 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50360332 C>T maps to NM_017432.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:50360332 C>T maps to NM_017432.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:120712935 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:120712935 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:2985551 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:2985551 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:3003288 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:3003288 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:3003288 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:3003288 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:70928574 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:70928574 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:198648230 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:198648230 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:198673789 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:198673789 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:198697464 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:198697464 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:8483971 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:8483971 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:8143826 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:8143826 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:8143826 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:8143826 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220164232 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220164232 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:220162887 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:220162887 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:40746990 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:40746990 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:41306452 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:41306452 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:121676606 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:121676606 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:31425211 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:31425211 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:52370003 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:52370003 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:52370003 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:52370003 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64518938 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64518938 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:100152097 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:100152097 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:100152097 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:100152097 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:9308882 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:9308882 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:9356283 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:9356283 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:17492486 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:17492486 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:74303405 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:74303405 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:113798631 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:113798631 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:113798631 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:113798631 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:9859393 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:9859393 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40280323 C>A maps to NM_201434.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:40280323 C>A maps to NM_201434.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:73390820 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:73390820 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:73390820 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:73390820 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:37637245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:37637245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:37637245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:37637245 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:17699798 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:17699798 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:17699798 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:17699798 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:39736215 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:39736215 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:37182832 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:37182832 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:99273624 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:99273624 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:48144027 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:48144027 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:178426711 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:178426711 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205072910 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:205072910 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:29910491 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:29910491 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:50116014 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:50116014 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:50116014 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:50116014 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:32125146 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:32125146 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:57346019 T>A maps to NM_003708.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:57346019 T>A maps to NM_003708.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:34256918 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:34256918 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:34251572 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:34251572 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:79349305 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:79349305 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:79349305 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:79349305 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:8425881 G>A maps to NM_012102.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:8425881 G>A maps to NM_012102.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108475437 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108475437 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108475437 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:108475437 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:175957453 G>A maps to NM_022457.5 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:175957453 G>A maps to NM_022457.5 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:14077444 C>T maps to NM_002918.4 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:14077444 C>T maps to NM_002918.4 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:117244399 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:117244399 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:117244399 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:117244399 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:86007640 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:86007640 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:192546044 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:192546044 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:54791615 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:54791615 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:100994030 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:100994030 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:100994030 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:100994030 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:240964830 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:240964830 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:240964830 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:240964830 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:63164443 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:63164443 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:63749763 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:63749763 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:63749763 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:63749763 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:72960001 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:72960001 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:104780469 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:104780469 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:104780469 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:104780469 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:3083293 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:3083293 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:87122236 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:87122236 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:87865817 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:87865817 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:20978604 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:20978604 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:158634915 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:158634915 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:141832201 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:141832201 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:101282246 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:101282246 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:90034660 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:90034660 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:10461586 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:10461586 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:77300553 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:77300553 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:77300564 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:77300564 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:77300553 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:77300553 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:77300564 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:77300564 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:68915452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:68915452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:68915452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:68915452 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:210867289 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:210867289 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:210867289 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:210867289 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:89627940 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:89627940 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:93307457 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:93307457 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:43902829 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:43902829 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:43902829 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:43902829 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:116949478 C>T maps to NM_001010892.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:116949478 C>T maps to NM_001010892.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:187088746 T>C maps to NM_022147.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:187088746 T>C maps to NM_022147.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:237838200 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:237838200 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:237893667 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:237893667 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:237995984 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:237995984 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:33992037 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:33992037 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:33992037 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:33992037 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:34137358 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:34137358 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:33292343 C>G maps to NM_022753.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:33292343 C>G maps to NM_022753.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:55226863 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:55226863 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:55226863 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:55226863 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:15870685 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:15870685 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:15870685 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:15870685 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128773896 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128773896 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:50902689 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:50902689 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123801938 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123801938 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123821055 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:123821055 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:123821055 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:123821055 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:77134779 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:77134779 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:159104816 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:159104816 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:38812612 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:38812612 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:52100153 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:52100153 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:55072767 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:55072767 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:76912083 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:76912083 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:20403999 G>A maps to NM_001006946.1 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:20403999 G>A maps to NM_001006946.1 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:251413 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:251413 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:3378056 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:3378056 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:71410751 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:71410751 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:71410751 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:71410751 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:18485256 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:18485256 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:12985299 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:12985299 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:13845696 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:13845696 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:13845696 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:13845696 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:83640675 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:83640675 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:80387869 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:80387869 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:80546043 A>G maps to NM_006379.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:80546043 A>G maps to NM_006379.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:84657208 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:84657208 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:90764743 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:90764743 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4552426 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:4552426 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:48022877 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:48022877 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:94770685 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:94770685 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:94770685 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:94770685 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:61305165 G>A maps to NM_002974.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:61305165 G>A maps to NM_002974.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:61465988 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:61465988 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:61465988 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:61465988 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179982197 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179982197 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179982197 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179982197 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:9482392 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:9482392 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:38442653 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:38442653 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:31969016 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:31969016 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:19141920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:19141920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:19141920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:19141920 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:26939457 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:26939457 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:65008894 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:65008894 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:65008894 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:65008894 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:162368640 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:162368640 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:156776987 G>A maps to NM_001161441.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:156776987 G>A maps to NM_001161441.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:2822197 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:2822197 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:2822197 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:2822197 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:152043450 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:152043450 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:152043450 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:152043450 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:171800731 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:171800731 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:110048968 C>G maps to NM_001099289.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:110048968 C>G maps to NM_001099289.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:157820535 G>T maps to NM_003030.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:157820535 G>T maps to NM_003030.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:601546 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:601546 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:52002323 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:52002323 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:52147284 C>A maps to NM_001098612.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:52147284 C>A maps to NM_001098612.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:51656191 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:51656191 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51656191 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51656191 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51626624 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:51626624 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:16963977 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:16963977 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39389218 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39389218 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160458762 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160458762 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160458762 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160458762 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160460825 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:160460825 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:103710521 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:103710521 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:45239295 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:45239295 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:6606403 G>T maps to NM_177550.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:6606403 G>T maps to NM_177550.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:43311194 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:43311194 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:43311194 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:43311194 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:111527986 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:111527986 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:111527986 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:111527986 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:25850939 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:25850939 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:46957673 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:46957673 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:228552716 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:228552716 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:228552716 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:228552716 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113414855 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113414855 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113414855 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113414855 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:116609103 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:116609103 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:172648202 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:172648202 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:48897107 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:48897107 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:37344342 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:37344342 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:8088460 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:8088460 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:27481774 G>T maps to NM_003459.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:27481774 G>T maps to NM_003459.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150701582 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150701582 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150701582 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150701582 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150715146 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:150715146 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:105198866 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:105198866 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:105198866 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:105198866 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57252749 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57252749 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:19463714 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:19463714 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:42337005 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:42337005 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:42335713 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:42335713 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:42337005 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:42337005 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:27444609 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:27444609 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:26708123 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:26708123 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:108624894 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:108624894 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:108624894 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:108624894 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:45807299 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:45807299 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:45807299 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:45807299 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:1421803 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:1421803 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:14518661 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:14518661 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:14485105 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:14485105 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:14518661 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:14518661 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:170214600 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:170214600 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:170214600 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:170214600 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:103148764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:103148764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:103148764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:103148764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61296209 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61296209 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:107578451 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:107578451 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:107578451 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:107578451 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:88406165 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:88406165 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:48604256 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:48604256 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:127341073 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:127341073 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:127341073 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:127341073 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31732845 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31732845 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:31732845 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:31732845 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:51415460 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:51415460 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:51415460 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:51415460 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:26411972 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:26411972 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:101601063 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:101601063 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:101601063 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:101601063 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:2314870 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:2314870 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:158342654 G>T maps to NM_016224.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:158342654 G>T maps to NM_016224.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:108339276 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:108339276 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:108339276 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:108339276 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:108412114 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:108412114 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:108427612 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:108427612 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:50628182 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:50628182 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:204086866 G>T maps to ENST00000367203 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:204086866 G>T maps to ENST00000367203 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:231112595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:231112595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:231112595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:231112595 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:231176056 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:231176056 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:46002952 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:46002952 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:46002976 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:46002976 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:46002952 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:46002952 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:31324728 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:31324728 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64938713 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64938713 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64938713 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:64938713 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:9416303 G>C maps to NM_025106.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:9416303 G>C maps to NM_025106.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:158607700 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:158607700 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158607700 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:158607700 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:45801710 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:45801710 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:26885906 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:26885906 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:26885906 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:26885906 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:149475832 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:149475832 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:85115650 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:85115650 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:48209101 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:48209101 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:48209101 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:48209101 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:52686347 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:52686347 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:52686347 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:52686347 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:130058638 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:130058638 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:44386405 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:44386405 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:44386405 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:44386405 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:8718303 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:8718303 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:8718303 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:8718303 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:130656765 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:130656765 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:130656765 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:130656765 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:104049140 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:104049140 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:104131610 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:104131610 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:136087830 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:136087830 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152988768 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152988768 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:37815438 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:37815438 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:37815438 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:37815438 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:44077046 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:44077046 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:81879213 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:81879213 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:81879213 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:81879213 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:4483787 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:4483787 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:132785290 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:132785290 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:46293861 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:46293861 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:46293861 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:46293861 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:891532 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:891532 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:891532 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:891532 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:48046758 G>T maps to ENST00000453071 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:48046758 G>T maps to ENST00000453071 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:48046758 G>T maps to ENST00000453071 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:48046758 G>T maps to ENST00000453071 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:39950276 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:39950276 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:109311916 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:109311916 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:46968903 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:46968903 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:62550716 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:62550716 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:37953525 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:37953525 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:37953525 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:37953525 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:7056720 A>C maps to NM_152293.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:7056720 A>C maps to NM_152293.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:93471082 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:93471082 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:60551523 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:60551523 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99710561 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99710561 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:234593466 G>A maps to NM_005646.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:234593466 G>A maps to NM_005646.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:150460191 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:150460191 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150460191 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150460191 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:33448879 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:33448879 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19185866 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19185866 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:19185866 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:19185866 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:13561647 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:13561647 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:27825145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:27825145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:27825145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:27825145 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50384520 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50384520 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:37298964 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:37298964 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:37298964 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:37298964 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:34499178 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:34499178 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:179306822 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:179306822 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:120916425 C>T maps to NM_152715.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:120916425 C>T maps to NM_152715.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:64889184 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:64889184 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:62701010 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:62701010 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:62701010 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:62701010 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149749092 G>A maps to ENST00000451292 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:149749092 G>A maps to ENST00000451292 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:124184359 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:124184359 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:46620583 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:46620583 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:154479294 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:154479294 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:154479294 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:154479294 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:97862336 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:97862336 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:6716030 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:6716030 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:6716030 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:6716030 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53451106 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53451106 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:56679957 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:56679957 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:56679957 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:56679957 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:30704583 C>T maps to NM_031271.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:30704583 C>T maps to NM_031271.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:141678470 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:141678470 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:141678470 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:141678470 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:133479966 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:133479966 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:133483666 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:133483666 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:133479966 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:133479966 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:133483666 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:133483666 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:43577270 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:43577270 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:79357662 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:79357662 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:157159836 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:157159836 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:157158441 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:157158441 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:157159836 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:157159836 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29907370 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29907370 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:11485702 T>A maps to ENST00000423059 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:11485702 T>A maps to ENST00000423059 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:53263203 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:53263203 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:52257046 C>A maps to ENST00000494383 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:52257046 C>A maps to ENST00000494383 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:2560533 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:2560533 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:2560533 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:2560533 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:2616727 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:2616727 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:205237981 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:205237981 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:77809949 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:77809949 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:44402469 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:44402469 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:126135197 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:126135197 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:126137060 G>T maps to NM_052907.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:126137060 G>T maps to NM_052907.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:86970190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:86970190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:86970190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:86970190 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:5768340 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:5768340 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:72469852 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:72469852 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55889137 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55889137 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:15433704 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:15433704 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:15433704 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:15433704 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27263150 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27263150 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:27263150 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:27263150 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:32568361 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:32568361 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:56675565 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:56675565 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:56675565 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:56675565 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:16069290 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:16069290 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18720496 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18720496 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:112834954 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:112834954 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:68708240 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:68708240 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:68708240 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:68708240 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:88582583 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:88582583 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:117786555 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:117786555 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:103592752 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:103592752 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152226433 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152226433 T>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152226511 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152226511 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152226520 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:152226520 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:152226511 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:152226511 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:152226520 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:152226520 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:195605488 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:195605488 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:195605488 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:195605488 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55668985 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55668985 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:55668985 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:55668985 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:218713784 T>A maps to NM_022648.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:218713784 T>A maps to NM_022648.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:32017940 C>A maps to ENST00000375244 L3091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:32017940 C>A maps to ENST00000375244 L3091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:35741607 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:35741607 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:100084238 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:100084238 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:179063995 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:179063995 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:59763974 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:59763974 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:154155387 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:154155387 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:1418260 A>G maps to NM_000547.5 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:1418260 A>G maps to NM_000547.5 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:10941760 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:10941760 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:10941764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:10941764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:10920282 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:10920282 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:10941760 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:10941760 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:10941764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:10941764 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:30125267 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:30125267 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:30071587 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:30071587 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:25973378 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:25973378 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:25973378 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:25973378 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:72734211 C>T maps to NM_178125.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:72734211 C>T maps to NM_178125.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27521390 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27521390 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:51477086 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:51477086 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:189022143 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:189022143 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:230660101 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:230660101 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:29072957 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:29072957 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:29072957 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:29072957 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:38266181 A>T maps to NM_003306.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr13:38266181 A>T maps to NM_003306.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:73442629 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:73442629 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:73442629 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:73442629 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:31769447 A>G maps to NM_020856.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:31769447 A>G maps to NM_020856.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:176084057 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:176084057 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:100372859 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:100372859 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:39161448 G>T maps to ENST00000301819 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:39161448 G>T maps to ENST00000301819 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:166756186 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:166756186 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:166756186 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:166756186 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:46664499 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:46664499 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:51760222 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:51760222 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:51760222 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:51760222 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:38536326 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:38536326 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:46863506 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:46863506 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:46863506 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:46863506 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113286317 A>T maps to NM_153712.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:113286317 A>T maps to NM_153712.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179489966 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179489966 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179489966 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:179489966 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:54940620 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:54940620 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:49521709 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:49521709 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:6501468 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:6501468 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:6501468 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:6501468 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:57958296 T>G maps to NM_016261.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:57958296 T>G maps to NM_016261.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:138990583 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:138990583 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:4186204 C>T maps to NM_003342.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:4186204 C>T maps to NM_003342.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:90039432 G>A maps to NM_016021.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:90039432 G>A maps to NM_016021.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:74401443 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:74401443 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:42559877 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:42559877 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:42559877 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:42559877 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:170937266 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:170937266 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:170937266 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:170937266 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19404342 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19404342 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19413476 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19413476 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:19491399 G>C maps to ENST00000375267 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:19491399 G>C maps to ENST00000375267 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:136540315 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:136540315 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128917073 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128917073 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:70455390 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:70455390 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:70455390 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:70455390 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:70352548 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:70352548 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:162470959 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:162470959 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:43504189 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:43504189 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:43504189 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr21:43504189 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:26874948 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:26874948 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:17721042 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:17721042 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:17738540 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:17738540 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:35541201 C>A maps to ENST00000416672 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:35541201 C>A maps to ENST00000416672 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:11998303 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:11998303 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:11998303 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:11998303 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:48141412 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:48141412 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:48141412 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:48141412 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:126220180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:126220180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:126229652 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:126229652 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:126220180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:126220180 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:215812472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:215812472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:216257002 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:216257002 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:216465429 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:216465429 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:215812472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:215812472 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:215990576 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:215990576 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:216144147 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:216144147 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:216257002 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:216257002 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:216465429 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:216465429 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:113692338 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:113692338 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:11505372 G>T maps to NM_001080491.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:11505372 G>T maps to NM_001080491.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:8989485 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:8989485 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:6579802 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:6579802 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:78005901 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:78005901 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:78005901 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:78005901 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:86996124 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:86996124 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:86996124 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:86996124 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:62312632 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:62312632 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:122723320 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:122723320 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:38834965 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:38834965 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:38834965 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:38834965 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150048255 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:150048255 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:49842402 G>T maps to NM_198570.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:49842402 G>T maps to NM_198570.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61049512 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61049512 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:61049447 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:61049447 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:177046603 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:177046603 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:177046603 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:177046603 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:10086175 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr4:10086175 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128471545 C>T maps to NM_018383.4 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:128471545 C>T maps to NM_018383.4 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:74982503 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:74982503 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:74982503 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:74982503 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36577558 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:36577558 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:84360461 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:84360461 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:84360461 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:84360461 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:44417476 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:44417476 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:44417476 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr20:44417476 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:175432511 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:175432511 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:175432511 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:175432511 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:38430298 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:38430298 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:46326893 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:46326893 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:160164655 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:160164655 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:168549527 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:168549527 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:100455914 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr9:100455914 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:152373292 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:152373292 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:142089250 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:142089250 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:17232398 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:17232398 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:17232398 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:17232398 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:75265291 C>T maps to NM_019589.2 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr14:75265291 C>T maps to NM_019589.2 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:174047507 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:174047507 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:100357997 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:100357997 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:100357997 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:100357997 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:114070841 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:114070841 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:62519744 G>A maps to NM_024784.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:62519744 G>A maps to NM_024784.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:801197 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:801197 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:801197 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:801197 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:77191178 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:77191178 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:128940464 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chrX:128940464 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:135620883 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:135620883 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:135620883 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:135620883 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:77768222 C>T maps to NM_024721.4 I3022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:77768222 C>T maps to NM_024721.4 I3022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:178337439 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr5:178337439 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:39898381 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:39898381 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:29644963 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:29644963 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:52628090 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:52628090 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:52628090 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:52628090 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:136649680 G>A maps to NM_003413.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chrX:136649680 G>A maps to NM_003413.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75184558 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75184558 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75186181 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:75186181 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:21909430 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:21909430 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:53577534 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:53577534 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:53578891 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:53578891 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:44537212 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:44537212 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:44946973 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:44946973 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:5012589 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:5012589 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:5012589 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:5012589 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:32919718 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:32919718 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:32919718 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:32919718 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:24310355 C>G maps to NM_203282.2 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:24310355 C>G maps to NM_203282.2 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:22257839 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:22257839 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:22257839 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:22257839 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:116649816 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:116649816 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:116649816 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:116649816 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9529242 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9529242 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9529242 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9529242 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:133721119 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr12:133721119 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:56946312 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr15:56946312 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:15607769 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:15607769 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:28963356 C>T maps to NM_001010877.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr6:28963356 C>T maps to NM_001010877.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:64159551 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:64159551 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:64159551 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr10:64159551 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:62593890 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:62593890 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:56587943 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr18:56587943 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:2832299 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:2832299 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9730038 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9730038 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9730038 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:9730038 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:144731984 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr8:144731984 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:55993189 C>T maps to NM_033113.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:55993189 C>T maps to NM_033113.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:71632795 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:71632795 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:71632795 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:71632795 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:31073641 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr16:31073641 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:22375948 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:22375948 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:148767406 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:148767406 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:12502557 C>A maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:12502557 C>A maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:22604923 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr19:22604923 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29438582 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr22:29438582 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:50070955 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:50070955 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:102188082 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr3:102188082 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:71534923 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr1:71534923 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:136268957 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr2:136268957 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:3141884 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:3141884 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99662083 G>A maps to NM_145914.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr7:99662083 G>A maps to NM_145914.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:113628617 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr11:113628617 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:4012857 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01W-0928-08 chr17:4012857 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:53702153 G>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:53702153 G>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:73179337 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:73179337 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:1866665 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:1866665 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr18:56182184 G>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr18:56182184 G>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:41002087 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:41002087 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:25239924 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:25239924 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:44630733 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:44630733 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:7005639 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:7005639 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:119737437 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:119737437 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:10866619 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:10866619 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:116889311 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:116889311 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:57949761 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:57949761 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:19619493 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:19619493 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:91075712 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:91075712 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:17543063 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:17543063 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:77246967 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:77246967 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:141317174 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:141317174 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:54646695 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:54646695 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:14080572 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:14080572 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:21272521 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:21272521 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:90255181 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:90255181 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:47858247 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:47858247 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:38875966 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:38875966 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:111400449 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:111400449 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr21:37541814 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr21:37541814 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:46141741 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:46141741 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:69962796 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:69962796 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:104110935 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:104110935 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:146492916 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:146492916 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:18617754 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:18617754 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:9616222 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:9616222 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:237317148 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:237317148 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:150648455 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:150648455 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:53344207 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:53344207 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:11222181 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:11222181 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:161056032 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:161056032 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:13211507 C>T maps to NM_005583.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:13211507 C>T maps to NM_005583.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:102069262 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:102069262 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:247597625 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:247597625 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chrX:24523532 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chrX:24523532 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chrX:15443976 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chrX:15443976 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:50918037 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:50918037 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:142459537 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:142459537 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:9334781 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:9334781 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:117859694 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:117859694 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:155121196 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:155121196 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr20:48568711 C>T maps to ENST00000449816 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr20:48568711 C>T maps to ENST00000449816 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:75530897 G>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:75530897 G>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr13:50064942 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr13:50064942 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:19618002 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:19618002 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:84311438 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:84311438 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:214878839 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:214878839 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:88895613 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:88895613 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:33538239 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:33538239 C>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:51512347 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:51512347 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:41956079 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr4:41956079 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:77708817 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:77708817 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:29659713 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr12:29659713 A>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr11:68852673 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr11:68852673 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:59059141 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:59059141 C>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:49156586 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:49156586 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:132623901 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:132623901 A>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:23099193 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr16:23099193 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:22013813 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:22013813 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:49321795 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:49321795 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:559948 T>G did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:559948 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:2328265 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:2328265 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:67012368 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:67012368 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:67012368 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:67012368 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:16215758 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:16215758 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:6185747 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:6185747 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:6185747 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:6185747 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:114674663 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:114674663 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:64711461 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:64711461 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:131792869 G>A maps to NM_001115.2 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:131792869 G>A maps to NM_001115.2 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:45935870 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:45935870 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:45935870 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:45935870 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:38429610 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:38429610 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:36122950 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:36122950 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:36122950 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:36122950 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:110482188 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:110482188 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:24919054 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:24919054 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:24919054 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:24919054 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:1873703 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:1873703 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:2825191 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:2825191 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:239355229 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:239355229 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:239355229 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:239355229 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:176857322 G>T maps to ENST00000281881 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:176857322 G>T maps to ENST00000281881 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:28913762 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:28913762 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:1783290 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:1783290 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:79384942 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:79384942 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:70034721 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:70034721 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:70034721 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:70034721 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:160545762 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:160545762 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:72958447 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:72958447 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:72958447 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:72958447 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:20878090 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:20878090 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:20878090 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:20878090 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:55671127 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:55671127 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:23964270 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:23964270 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:23964270 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:23964270 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:157271176 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:157271176 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:157271176 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:157271176 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:113554385 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:113554385 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:113554385 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:113554385 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:96047894 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:96047894 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:180349113 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:180349113 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:115010537 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:115010537 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:68857203 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:68857203 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:62544478 G>C maps to NM_001786.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:62544478 G>C maps to NM_001786.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:196965132 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:196965132 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:196965132 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:196965132 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:125513879 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:125513879 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:430871 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:430871 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:7357506 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:7357506 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:66586480 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:66586480 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:141631427 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:141631427 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:141631427 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:141631427 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:100543524 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:100543524 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr13:100543524 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr13:100543524 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:100208349 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:100208349 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:100208349 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:100208349 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:75833581 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:75833581 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:105815123 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:105815123 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:109745530 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:109745530 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:160261034 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:160261034 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:46736905 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:46736905 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:46736905 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:46736905 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:68658166 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:68658166 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:68658166 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:68658166 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:89652085 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:89652085 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:125558757 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:125558757 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:125558757 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:125558757 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:2944625 G>T maps to NM_033225.5 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:2944625 G>T maps to NM_033225.5 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:113299490 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:113299490 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:113299490 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:113299490 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:70826586 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:70826586 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:70826586 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:70826586 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:68139131 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:68139131 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:47433265 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:47433265 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:39847319 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:39847319 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:39847319 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:39847319 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:58521970 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:58521970 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:58521970 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:58521970 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:155698985 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:155698985 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:155698985 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:155698985 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:124337910 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:124337910 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:124337910 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:124337910 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:7555868 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:7555868 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:82112484 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:82112484 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:172569197 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:172569197 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:83351927 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:83351927 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:133786073 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:133786073 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:113777080 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:113777080 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:197026634 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:197026634 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:38937447 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:38937447 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:38937447 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:38937447 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:19027098 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:19027098 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr9:19027098 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr9:19027098 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:9931117 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:9931117 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:39357094 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr13:39357094 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr13:39357094 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr13:39357094 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:46980950 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:46980950 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:74980511 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:74980511 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:74980511 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:74980511 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr21:34883583 A>G maps to NM_001136006.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr21:34883583 A>G maps to NM_001136006.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:56049804 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:56049804 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:134215101 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:134215101 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:74526921 G>A maps to NM_012201.5 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:74526921 G>A maps to NM_012201.5 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:123474361 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:123474361 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:123489403 G>T maps to ENST00000456860 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:123489403 G>T maps to ENST00000456860 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:47059643 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:47059643 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:38066034 G>A maps to NM_001165958.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:38066034 G>A maps to NM_001165958.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:9307017 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:9307017 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:43400349 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:43400349 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:65120246 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:65120246 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:89425350 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:89425350 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:89425350 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:89425350 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:26199715 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:26199715 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:26199715 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:26199715 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:29691111 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:29691111 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:29691111 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:29691111 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:112096891 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:112096891 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:112096891 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:112096891 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:41143263 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:41143263 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr21:41143263 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr21:41143263 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:71946218 C>T maps to NM_001567.3 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:71946218 C>T maps to NM_001567.3 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:7117439 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:7117439 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:7117439 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:7117439 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr15:90992934 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr15:90992934 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:75936793 G>T maps to NM_006633.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:75936793 G>T maps to NM_006633.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:2749784 C>A maps to NM_033267.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:2749784 C>A maps to NM_033267.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:20449143 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:20449143 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:20449143 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:20449143 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:24578216 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:24578216 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:24578216 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:24578216 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:27782765 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:27782765 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:94173014 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:94173014 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr14:94173014 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr14:94173014 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:43493620 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:43493620 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:43493620 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr18:43493620 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:72338983 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:72338983 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:126343404 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:126343404 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:35979504 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:35979504 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:35979504 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:35979504 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:50856479 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:50856479 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:38510460 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:38510460 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:55144062 C>T maps to ENST00000427581 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:55144062 C>T maps to ENST00000427581 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:70490550 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:70490550 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:70490550 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:70490550 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:5696661 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:5696661 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:133812254 C>T maps to NM_144648.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:133812254 C>T maps to NM_144648.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:84210040 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:84210040 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:52864148 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:52864148 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:52864148 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:52864148 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:33572577 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:33572577 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:39086483 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:39086483 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:69218331 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:69218331 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:69218331 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:69218331 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:154336620 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:154336620 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:154336620 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:154336620 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:71616089 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:71616089 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:71616089 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:71616089 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:195483793 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:195483793 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:10443184 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:10443184 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:10443184 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:10443184 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:23900896 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:23900896 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:16918146 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:16918146 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:198233233 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:198233233 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:198233233 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:198233233 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:42076224 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:42076224 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:42076224 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:42076224 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:23934428 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:23934428 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:23934428 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:23934428 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:117715714 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:117715714 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:117715714 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:117715714 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:51148975 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:51148975 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:51148975 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:51148975 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:163296024 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:163296024 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:163296024 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:163296024 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:101087498 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:101087498 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chrX:101087498 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chrX:101087498 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:50946203 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:50946203 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:50946203 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:50946203 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:44713243 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:44713243 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:31921383 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:31921383 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:31921383 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:31921383 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:54598412 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:54598412 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:6748514 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:6748514 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:34408747 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:34408747 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:122264135 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:122264135 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:91770428 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:91770428 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chrX:91770428 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chrX:91770428 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:56360377 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:56360377 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:56360377 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:56360377 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:140256556 C>A maps to NM_018903.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:140256556 C>A maps to NM_018903.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:140165843 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:140165843 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:140165843 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:140165843 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:183094702 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:183094702 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:656177 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:656177 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:54256563 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:54256563 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:7074754 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr12:7074754 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:8726637 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:8726637 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:8726637 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:8726637 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:88968091 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr4:88968091 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:88968091 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr4:88968091 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:160833113 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:160833113 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:67854238 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:67854238 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr14:67854238 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr14:67854238 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:132193284 C>A maps to NM_020911.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:132193284 C>A maps to NM_020911.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:152936127 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chrX:152936127 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:118383638 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:118383638 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:72400807 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr7:72400807 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:167339542 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:167339542 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:45121098 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr22:45121098 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:43241392 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:43241392 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:43257323 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:43257323 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:251769 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:251769 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:251769 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:251769 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:123301186 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:123301186 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:123301186 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:123301186 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr20:37163693 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr20:37163693 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr20:37163693 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr20:37163693 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:120336724 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:120336724 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:120336724 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:120336724 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:7734142 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:7734142 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:7734142 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:7734142 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr20:62708013 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr20:62708013 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:72939798 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr14:72939798 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:78359233 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:78359233 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:78359233 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr17:78359233 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:78674579 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:78674579 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:107066961 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr6:107066961 A>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:237608841 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:237608841 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:237608841 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:237608841 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:38938753 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:38938753 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:38991566 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:38991566 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:38938753 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:38938753 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:71395249 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:71395249 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr15:47873556 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr15:47873556 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr15:47873556 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr15:47873556 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:242274647 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:242274647 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:242274647 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:242274647 C>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr20:43150490 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr20:43150490 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:22364583 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:22364583 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:108681843 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:108681843 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:108681843 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:108681843 A>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:99122535 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:99122535 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr9:99122535 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr9:99122535 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:18270478 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:18270478 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:18270478 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr10:18270478 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:55733931 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:55733931 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:106878423 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:106878423 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:108336879 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:108336879 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:121425745 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:121425745 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:121425745 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr11:121425745 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:73832445 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:73832445 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:158606655 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:158606655 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:158606655 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:158606655 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:67071581 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:67071581 T>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:130060139 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:130060139 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:4327148 C>A maps to ENST00000314714 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:4327148 C>A maps to ENST00000314714 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:47225899 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:47225899 T>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:52936898 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr18:52936898 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:124156731 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:124156731 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:43767495 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:43767495 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr15:43548675 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr15:43548675 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr15:43548675 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr15:43548675 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:133894661 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:133894661 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:133894661 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:133894661 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:2794928 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:2794928 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:2794928 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:2794928 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:69056931 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:69056931 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:69056931 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr16:69056931 C>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:113723679 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:113723679 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:72355190 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr12:72355190 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:10942877 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:10942877 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr21:10942877 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr21:10942877 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:234835265 G>A maps to NM_024080.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:234835265 G>A maps to NM_024080.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:94818287 T>C maps to NM_014639.3 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:94818287 T>C maps to NM_014639.3 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:17738430 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:17738430 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:35453211 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:35453211 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:35453211 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr8:35453211 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:82815768 T>C maps to NM_004385.4 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:82815768 T>C maps to NM_004385.4 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:51470449 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:51470449 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:51470449 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:51470449 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:85594617 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:85594617 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:37506358 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:37506358 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:37506358 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:37506358 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:175437100 T>A maps to NM_003387.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:175437100 T>A maps to NM_003387.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:183508516 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:183508516 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:183508516 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:183508516 T>G did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:37354825 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:37354825 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr9:37354825 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr9:37354825 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:22191530 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr19:22191530 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:95847910 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:95847910 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:95847910 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr2:95847910 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:121488873 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:121488873 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:121488873 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr5:121488873 A>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:42956890 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:42956890 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:42956890 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:42956890 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:26694077 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:26694077 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:26694077 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr1:26694077 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:113955933 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr3:113955933 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:113955933 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01W-0928-08 chr3:113955933 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:226376668 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:226376668 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:226376668 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:226376668 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:23547388 C>G maps to NM_014977.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:23547388 C>G maps to NM_014977.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:100205475 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:100205475 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:125877378 C>A maps to ENST00000273450 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:125877378 C>A maps to ENST00000273450 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:19641801 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:19641801 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:41554285 A>T maps to ENST00000415018 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:41554285 A>T maps to ENST00000415018 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:114238790 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:114238790 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:114238790 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:114238790 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:29750961 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:29750961 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:62974283 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:62974283 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:62974283 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:62974283 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:123006937 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:123006937 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:123006937 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:123006937 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:155327011 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:155327011 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:26033088 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:26033088 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr18:31323435 T>A maps to NM_030632.1 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr18:31323435 T>A maps to NM_030632.1 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr16:347718 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr16:347718 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr21:11047704 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr21:11047704 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:96069880 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:96069880 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:96069880 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:96069880 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:64878676 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:64878676 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:64879031 G>A maps to NM_013265.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:64879031 G>A maps to NM_013265.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:32546494 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:32546494 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:8675650 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:8675650 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:8675650 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:8675650 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:67809251 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:67809251 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:67809251 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:67809251 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76826624 G>A maps to ENST00000360841 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76826624 G>A maps to ENST00000360841 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76826748 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76826748 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76831989 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:76831989 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:76831989 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:76831989 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:110489770 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:110489770 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:110489770 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:110489770 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:104968227 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:104968227 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:45296726 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:45296726 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:93170908 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:93170908 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:82976847 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:82976847 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:82976847 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:82976847 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:28605335 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:28605335 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:28605335 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:28605335 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:69993838 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:69993838 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:60308684 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:60308684 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:139865671 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:139865671 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:139865671 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:139865671 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr20:40054002 G>T maps to NM_032221.3 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr20:40054002 G>T maps to NM_032221.3 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:71522131 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:71522131 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:3085392 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:3085392 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:3085392 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:3085392 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:40837945 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:40837945 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:40837945 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:40837945 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:105833975 G>A maps to NM_000494.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:105833975 G>A maps to NM_000494.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:110831886 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:110831886 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr13:110827060 A>T maps to NM_001845.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr13:110827060 A>T maps to NM_001845.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr13:110831886 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr13:110831886 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:107408254 G>T maps to NM_033641.2 P1274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:107408254 G>T maps to NM_033641.2 P1274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:3651803 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:3651803 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:28782631 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:28782631 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:2975963 A>G maps to NM_033225.5 H2129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:2975963 A>G maps to NM_033225.5 H2129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:114388964 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:114388964 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:114388964 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:114388964 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:134305156 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:134305156 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:134305156 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:134305156 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:36521657 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:36521657 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr13:36521657 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr13:36521657 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:132179872 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:132179872 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:132179872 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:132179872 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr18:28908186 A>T maps to NM_001942.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr18:28908186 A>T maps to NM_001942.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:33128488 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:33128488 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr20:33128488 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr20:33128488 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:135183318 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:135183318 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:16942724 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:16942724 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:16942724 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:16942724 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:132445157 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:132445157 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:124632058 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:124632058 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:6146038 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:6146038 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:6146038 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:6146038 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:61646382 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:61646382 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:62274476 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:62274476 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:32883843 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:32883843 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr22:32883843 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr22:32883843 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:54497670 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:54497670 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:54497670 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:54497670 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:155530767 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:155530767 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:155530767 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:155530767 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:60602920 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:60602920 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:147014143 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:147014143 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:49196586 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:49196586 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:112015965 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:112015965 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:112020634 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:112020634 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:112015965 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:112015965 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:112020634 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:112020634 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:31178570 G>T maps to NM_024572.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:31178570 G>T maps to NM_024572.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:53373935 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:53373935 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:53373935 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:53373935 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:74046543 T>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:74046543 T>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:74046543 T>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:74046543 T>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:138530932 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:138530932 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:138530932 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:138530932 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:120181506 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:120181506 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:120181506 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:120181506 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:24446992 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:24446992 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:125813266 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:125813266 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:4499730 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:4499730 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:236760286 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:236760286 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:93184980 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:93184980 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:26107643 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:26107643 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:26107643 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:26107643 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:39330765 A>G maps to ENST00000221419 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:39330765 A>G maps to ENST00000221419 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:148690308 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:148690308 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:29973553 G>T maps to NM_014271.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:29973553 G>T maps to NM_014271.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:79577196 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:79577196 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:3651079 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:3651079 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:39767276 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:39767276 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:49935578 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:49935578 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:73045503 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:73045503 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:32573665 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:32573665 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:32573665 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:32573665 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr21:46047657 T>A maps to NM_198690.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr21:46047657 T>A maps to NM_198690.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:129099557 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:129099557 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:129099557 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:129099557 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:145544112 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:145544112 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:145544112 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:145544112 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:150941009 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:150941009 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:150941009 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:150941009 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:93170566 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:93170566 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:93170566 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:93170566 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:55179598 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:55179598 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:75070326 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:75070326 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:75070326 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:75070326 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:55479575 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:55479575 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:42116318 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:42116318 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr15:42116318 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr15:42116318 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:74772446 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:74772446 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:132641791 C>T maps to NM_015529.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:132641791 C>T maps to NM_015529.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:71519474 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:71519474 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr16:56692543 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr16:56692543 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr16:56692543 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr16:56692543 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:100518403 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:100518403 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:100518403 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:100518403 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr7:100663517 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr7:100663517 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr7:100663517 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr7:100663517 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:50962128 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:50962128 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:10363423 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:10363423 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:24418873 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:24418873 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:75394576 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:75394576 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:75394576 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:75394576 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:175436230 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:175436230 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:175436230 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr3:175436230 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:16891869 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:16891869 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:170523811 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:170523811 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:170523811 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:170523811 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:204971719 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:204971719 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:204971719 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:204971719 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:233839372 C>T maps to NM_019850.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:233839372 C>T maps to NM_019850.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:3010462 T>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:3010462 T>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:134070531 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:134070531 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:134070531 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:134070531 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:20404499 C>A maps to NM_001004063.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:20404499 C>A maps to NM_001004063.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:55563900 G>T maps to NM_001004735.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:55563900 G>T maps to NM_001004735.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:201814322 A>C maps to NM_006190.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:201814322 A>C maps to NM_006190.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:99663202 T>A maps to NM_001184880.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:99663202 T>A maps to NM_001184880.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:31049036 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:31049036 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:140261960 C>T maps to NM_018904.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:140261960 C>T maps to NM_018904.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117095403 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117095403 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117096529 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117096529 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117097785 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117097785 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117097808 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117097808 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117098129 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:117098129 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117095403 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117095403 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117097785 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117097785 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117097808 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117097808 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117098129 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:117098129 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:95395511 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:95395511 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:95395511 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:95395511 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr21:44189039 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr21:44189039 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr21:44189039 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr21:44189039 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:17500057 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:17500057 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:17500057 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:17500057 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:239186472 G>A maps to NM_022817.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:239186472 G>A maps to NM_022817.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:47303941 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:47303941 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:47303941 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:47303941 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:601719 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:601719 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:65110593 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:65110593 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:65110625 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr15:65110625 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr21:38445002 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr21:38445002 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:38511422 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr22:38511422 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:18846721 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:18846721 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:18846721 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:18846721 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:131936103 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:131936103 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:24861648 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:24861648 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:24861648 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:24861648 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:133248988 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:133248988 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:133249495 A>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr12:133249495 A>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:133248988 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr12:133248988 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:38166183 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr13:38166183 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:89183599 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:89183599 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:89183866 G>C maps to NM_152542.3 Y333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:89183866 G>C maps to NM_152542.3 Y333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:3342331 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:3342331 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:3342331 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:3342331 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:84663407 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:84663407 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:178885593 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:178885593 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:160235970 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:160235970 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:160235970 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:160235970 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:80388725 A>C maps to NM_006909.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:80388725 A>C maps to NM_006909.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:39306599 A>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:39306599 A>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:182617160 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:182617160 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:182617160 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:182617160 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:50044476 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr14:50044476 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:50044476 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr14:50044476 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:39305177 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:39305177 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:39305177 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:39305177 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:234235973 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:234235973 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:234235973 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:234235973 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:127818228 T>A maps to NM_173690.4 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:127818228 T>A maps to NM_173690.4 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:175292418 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:175292418 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:175292418 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:175292418 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:3514314 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:3514314 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:3514314 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:3514314 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:35922940 G>T maps to NM_052961.3 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:35922940 G>T maps to NM_052961.3 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:26372399 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:26372399 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:92918920 C>A maps to NM_152313.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:92918920 C>A maps to NM_152313.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:18916554 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:18916554 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:18923430 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:18923430 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:18923430 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:18923430 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:74911162 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:74911162 T>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:227954800 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:227954800 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:227954800 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:227954800 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:52826468 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:52826468 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:52826468 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:52826468 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:48764353 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:48764353 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:48764353 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:48764353 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:35759584 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr5:35759584 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:35759584 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr5:35759584 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:220350216 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:220350216 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:220350216 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:220350216 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr15:44891009 G>C maps to NM_025137.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr15:44891009 G>C maps to NM_025137.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr7:116778441 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr7:116778441 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:60551115 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr20:60551115 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:79286666 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:79286666 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:65155521 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr4:65155521 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:65155521 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr4:65155521 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:121039099 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr11:121039099 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:121039099 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr11:121039099 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:56702681 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:56702681 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:56702681 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:56702681 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:105360675 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:105360675 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr20:48700725 G>A maps to NM_199203.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr20:48700725 G>A maps to NM_199203.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:226034928 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr1:226034928 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:226034928 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr1:226034928 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:133734455 A>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:133734455 A>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:9592821 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr8:9592821 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:9592821 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr8:9592821 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:27076614 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:27076614 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:27076614 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:27076614 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:30113710 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr6:30113710 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:30113710 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:30113710 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:3448011 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr17:3448011 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:40815073 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr17:40815073 A>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:52273118 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr3:52273118 G>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:34802158 C>T maps to NM_017754.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr6:34802158 C>T maps to NM_017754.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:73055739 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:73055739 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:73055739 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:73055739 G>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:129045155 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chrX:129045155 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:129045155 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chrX:129045155 G>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:79840735 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr9:79840735 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:79840735 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr9:79840735 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:122665341 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:122665341 A>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:228750067 A>T maps to NM_178821.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr2:228750067 A>T maps to NM_178821.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:31598096 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr2:31598096 C>G did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:99502837 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr10:99502837 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:99502837 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr10:99502837 C>T did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:21991281 A>G maps to NM_003423.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:21991281 A>G maps to NM_003423.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:12474515 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:12474515 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:12474515 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:12474515 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:31038767 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:31038767 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:31038767 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:31038767 C>A did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:9580433 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01D-1040-01 chr19:9580433 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:9580433 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:9580433 T>C did not map to a codon.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:37383368 C>A maps to NM_001171979.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3774-01A-01W-0928-08 chr19:37383368 C>A maps to NM_001171979.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:121758573 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:121758573 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:95727812 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:95727812 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:44051609 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:44051609 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:148590237 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:148590237 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:148618712 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:148618712 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:20482753 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:20482753 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:20563722 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:20563722 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:135083317 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:135083317 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:136304590 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:136304590 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:5235319 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:5235319 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:129015675 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:129015675 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:43777792 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:43777792 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:45699487 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:45699487 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:7766995 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:7766995 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:123071265 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:123071265 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:131797819 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:131797819 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:67048135 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:67048135 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:26118421 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:26118421 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:116075542 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:116075542 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:130630178 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:130630178 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:33480107 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:33480107 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:49961518 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:49961518 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:104188804 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:104188804 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:110170266 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:110170266 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:4167248 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:4167248 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:17396644 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:17396644 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:69416102 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:69416102 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:46158964 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:46158964 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:2112985 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:2112985 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:43345188 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:43345188 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:130219414 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:130219414 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:3907715 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:3907715 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:161736077 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:161736077 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:160121796 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:160121796 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:117704335 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:117704335 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:11039276 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:11039276 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:88110133 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:88110133 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:215610627 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:215610627 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:23778190 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:23778190 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:60475256 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:60475256 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31604729 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31604729 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31606944 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31606944 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:1475704 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:1475704 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:581243 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:581243 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:26450522 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:26450522 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:180485397 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:180485397 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:112677972 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:112677972 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:91671272 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:91671272 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:8135175 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:8135175 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31893789 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31893789 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:33642889 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:33642889 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:32554965 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:32554965 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:11858846 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:11858846 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:77692218 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:77692218 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:49708978 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:49708978 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:13563668 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:13563668 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:140901188 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:140901188 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:2742671 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:2742671 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:181741170 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:181741170 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:40069129 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:40069129 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:27463730 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:27463730 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:46928545 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:46928545 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:121712337 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:121712337 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:3059248 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:3059248 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:40954446 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:40954446 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:70209030 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:70209030 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:42798489 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:42798489 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:167417199 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:167417199 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:21975056 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:21975056 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:95161195 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:95161195 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:61980996 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:61980996 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:7358970 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:7358970 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:143028445 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:143028445 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:71043102 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:71043102 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:36202031 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:36202031 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:23848445 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:23848445 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:58582578 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:58582578 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:58582600 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:58582600 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:2404387 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:2404387 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:146471329 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:146471329 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:32146699 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:32146699 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:70745760 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:70745760 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:110862108 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:110862108 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:10096330 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:10096330 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:48631727 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:48631727 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:30232740 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:30232740 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:148545962 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:148545962 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:194061746 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:194061746 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:1969971 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:1969971 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:201459267 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:201459267 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:23546601 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:23546601 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:105905220 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:105905220 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:37653070 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:37653070 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:41626229 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:41626229 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:16635316 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:16635316 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:95121342 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:95121342 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:162724679 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:162724679 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:35288959 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:35288959 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:182822416 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:182822416 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38134219 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38134219 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:124359697 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:124359697 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:7644080 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:7644080 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:11522838 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:11522838 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:225729528 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:225729528 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:117748607 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:117748607 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:463689 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:463689 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:463691 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:463691 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:53266921 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:53266921 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:28650879 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:28650879 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:32336057 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:32336057 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:100374152 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:100374152 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:130587684 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:130587684 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:132199648 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:132199648 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:66190032 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:66190032 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:93120051 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:93120051 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:222923142 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:222923142 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:150398229 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:150398229 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:40701598 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:40701598 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:28065776 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:28065776 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:10076082 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:10076082 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:128496759 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:128496759 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:28897158 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:28897158 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:4318974 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:4318974 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:47556844 C>A maps to ENST00000397748 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:47556844 C>A maps to ENST00000397748 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:27772782 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:27772782 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:35739149 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:35739149 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:136028892 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:136028892 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:13364900 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:13364900 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:133378256 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:133378256 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:32207497 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:32207497 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:154069949 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:154069949 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:24664452 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:24664452 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:50546235 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:50546235 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:149399201 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:149399201 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:18317439 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:18317439 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:118460327 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:118460327 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:113860509 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:113860509 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:38839119 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:38839119 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:37163426 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:37163426 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:37992303 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:37992303 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:104651235 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:104651235 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:68618814 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:68618814 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:42457566 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:42457566 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:46320170 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:46320170 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:160850237 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:160850237 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:39778053 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:39778053 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:196251342 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:196251342 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:113729526 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:113729526 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:16316676 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:16316676 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:200969135 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:200969135 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:51902456 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:51902456 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:129748787 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:129748787 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:112440581 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:112440581 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:32741686 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:32741686 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:22012990 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:22012990 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:124967082 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:124967082 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:55110785 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:55110785 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:54823729 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:54823729 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:55608520 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:55608520 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:99387650 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:99387650 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:100179642 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:100179642 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:33484614 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:33484614 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:2041573 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:2041573 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:26213295 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:26213295 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:165110955 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:165110955 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:45984975 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:45984975 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:136602110 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:136602110 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:116413288 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:116413288 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:3304105 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:3304105 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:37184705 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:37184705 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:46806703 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:46806703 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:8804134 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:8804134 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:108833178 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:108833178 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:24418846 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:24418846 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:59829846 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:59829846 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:121475883 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:121475883 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:108183759 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:108183759 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10429783 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10429783 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:109614010 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:109614010 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:57440554 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:57440554 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:192279182 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:192279182 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:101736057 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:101736057 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:152432945 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:152432945 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:55489205 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:55489205 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:120510024 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:120510024 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:205688811 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:205688811 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:102462214 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:102462214 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:125315399 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:125315399 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:73980582 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:73980582 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:79805011 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:79805011 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:110406663 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:110406663 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:102249584 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:102249584 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:226558082 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:226558082 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:125616666 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:125616666 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:127253621 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:127253621 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:647586 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:647586 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:122864365 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:122864365 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:100920841 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:100920841 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:133548004 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:133548004 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:111941720 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:111941720 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:8732355 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:8732355 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:81241088 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:81241088 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:204316371 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:204316371 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:43953680 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:43953680 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:43545986 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:43545986 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:57290972 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:57290972 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:140400359 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:140400359 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:127952041 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:127952041 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:70971109 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:70971109 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:46378442 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:46378442 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:27031583 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:27031583 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:1554850 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:1554850 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:29824279 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:29824279 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:43228104 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:43228104 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:43698282 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:43698282 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:43282762 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:43282762 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:46940780 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:46940780 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:45389061 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:45389061 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:158908178 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:158908178 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:135809820 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:135809820 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:133560364 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:133560364 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:5085977 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:5085977 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:50131117 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:50131117 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:73006898 T>C maps to ENST00000406236 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:73006898 T>C maps to ENST00000406236 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:22865271 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:22865271 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:5329712 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:5329712 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:47017305 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:47017305 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:237880448 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:237880448 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:123794211 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:123794211 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:78142561 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:78142561 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:18283677 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chrX:18283677 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38891958 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38891958 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:50648818 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:50648818 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:4555446 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:4555446 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:151108805 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:151108805 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:33069073 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr21:33069073 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:164750279 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:164750279 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:62985218 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:62985218 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:58015676 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:58015676 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:58017567 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:58017567 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:133985080 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:133985080 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:220503421 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:220503421 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:168110896 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:168110896 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:2103996 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:2103996 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:45750184 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:45750184 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:99204075 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:99204075 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:151043214 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:151043214 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:65261576 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:65261576 T>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:228856185 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:228856185 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168994768 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168994768 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:48374857 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:48374857 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31573081 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:31573081 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:131566420 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:131566420 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:133497483 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:133497483 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:44931947 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:44931947 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:2189210 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:2189210 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:102891256 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:102891256 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:94972079 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:94972079 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:12779559 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:12779559 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:69078951 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:69078951 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:46747538 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:46747538 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:170784269 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:170784269 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:170857123 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:170857123 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:179873206 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:179873206 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:6637759 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:6637759 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:20056588 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:20056588 A>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:3735909 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:3735909 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:30125109 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:30125109 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:50868036 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:50868036 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:3446924 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:3446924 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:130039874 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:130039874 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:71533329 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:71533329 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:179592220 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:179592220 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:179653992 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:179653992 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:190905528 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:190905528 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:53003521 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:53003521 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:215940152 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:215940152 A>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:5043223 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:5043223 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:8992193 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:8992193 T>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:144782617 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:144782617 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:42569455 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:42569455 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:27151320 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:27151320 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:127619754 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:127619754 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:241907843 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:241907843 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:241907868 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:241907868 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:134881194 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:134881194 C>G did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:64255018 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:64255018 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:57081644 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:57081644 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:53256 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:53256 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:3968179 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:3968179 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:8393935 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:8393935 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:73175248 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:73175248 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:50339600 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:50339600 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:117123856 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:117123856 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:54403762 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:54403762 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:26677770 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:26677770 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:27543283 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:27543283 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:26022409 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:26022409 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:11406062 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:11406062 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:1785722 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:1785722 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:48501155 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:48501155 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:6927171 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:6927171 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:22616780 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:22616780 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:92573375 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:92573375 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:103310434 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:103310434 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:62439147 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:62439147 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:122817516 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:122817516 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr14:60616734 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr14:60616734 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:45469010 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:45469010 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:13775602 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:13775602 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:37125517 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:37125517 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:62522347 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:62522347 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:114612844 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:114612844 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:3671998 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:3671998 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:94763660 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:94763660 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr13:115004506 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr13:115004506 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:126445890 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:126445890 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:121211890 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:121211890 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:32151528 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:32151528 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:68334687 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:68334687 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:23956632 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:23956632 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:46605758 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:46605758 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:169393728 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:169393728 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:50131628 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:50131628 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr14:73141104 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr14:73141104 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr22:43950646 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr22:43950646 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:23704827 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:23704827 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:23765081 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:23765081 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:43304462 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:43304462 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:488895 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:488895 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:154212958 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:154212958 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:14607604 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:14607604 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:108522153 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:108522153 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:109085398 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:109085398 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:78509110 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:78509110 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:191795369 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:191795369 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:104388396 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:104388396 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:167023551 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:167023551 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:5548020 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:5548020 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:106579178 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:106579178 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:43506179 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:43506179 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:54674519 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:54674519 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:26043767 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:26043767 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:183774847 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:183774847 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:129168600 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:129168600 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:99485981 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:99485981 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:81585391 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:81585391 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:121579072 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:121579072 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:33049815 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:33049815 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:10626570 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:10626570 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:53202417 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:53202417 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:54744671 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:54744671 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:46884102 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:46884102 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:44170803 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:44170803 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:44187664 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:44187664 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr14:24529672 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr14:24529672 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:130216902 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:130216902 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:4281093 T>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:4281093 T>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:65673792 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr3:65673792 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:56170726 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:56170726 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:10625863 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:10625863 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:11293059 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:11293059 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:113459420 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:113459420 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:10409440 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:10409440 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:1369046 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:1369046 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:55445115 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:55445115 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:143656971 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:143656971 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:76645436 T>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:76645436 T>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:229890248 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:229890248 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:27381506 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:27381506 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:15443915 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:15443915 C>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:151089944 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:151089944 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:76804235 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:76804235 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:231988073 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:231988073 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:117509962 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:117509962 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:61496895 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:61496895 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr13:49070518 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr13:49070518 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr13:25363413 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr13:25363413 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:11376156 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:11376156 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:5604571 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:5604571 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:52011776 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:52011776 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr22:30731791 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr22:30731791 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:19129863 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:19129863 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:46637422 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:46637422 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:129480837 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:129480837 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:40224045 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:40224045 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:246091366 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:246091366 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:147693632 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:147693632 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:118684132 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:118684132 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:30699488 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:30699488 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:134107494 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:134107494 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr22:29935170 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr22:29935170 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:11521372 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:11521372 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:2593028 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:2593028 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:5759288 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:5759288 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:72699179 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr15:72699179 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:186300622 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:186300622 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:23547193 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:23547193 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:5878981 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr11:5878981 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:41011893 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:41011893 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:46862280 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:46862280 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:179470525 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:179470525 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:63973763 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr8:63973763 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:216380486 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:216380486 A>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:128467451 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:128467451 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:78859457 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:78859457 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:112889568 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:112889568 T>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:32419834 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:32419834 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:44468912 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:44468912 A>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:46322524 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chrX:46322524 C>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:57828929 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr20:57828929 T>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:8862536 G>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:8862536 G>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:48173267 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:48173267 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:22066005 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:22066005 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr4:74007419 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr4:74007419 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:44594492 G>C maps to NM_016632.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:44594492 G>C maps to NM_016632.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:116931988 A>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:116931988 A>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:65871185 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:65871185 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:48655544 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:48655544 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:49220477 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:49220477 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:116268039 G>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:116268039 G>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:179998447 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:179998447 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:75899584 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:75899584 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr4:24531443 T>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr4:24531443 T>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:66759695 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:66759695 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr10:116590568 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr10:116590568 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:137777771 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:137777771 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:48148193 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:48148193 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:23407849 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:23407849 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:100125772 T>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:100125772 T>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:10394551 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:10394551 A>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:10588620 T>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:10588620 T>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr11:111428443 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr11:111428443 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:12583229 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:12583229 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:62851812 G>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:62851812 G>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:48465413 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:48465413 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr13:113678849 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr13:113678849 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr14:23887388 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr14:23887388 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr7:135322856 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr7:135322856 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:108372211 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:108372211 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:34443266 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:34443266 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:9787171 T>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:9787171 T>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:6535691 T>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:6535691 T>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:42666007 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:42666007 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr2:217363590 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr2:217363590 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:31351411 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:31351411 G>C did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:43850190 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:43850190 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:47108554 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:47108554 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr19:43920139 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr19:43920139 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr13:95227127 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr13:95227127 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:79351577 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:79351577 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr14:58878548 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr14:58878548 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:24816864 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr16:24816864 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:32040091 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr6:32040091 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:154144399 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:154144399 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:30354571 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:30354571 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:30530873 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr20:30530873 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr2:61622373 T>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr2:61622373 T>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:556492 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:556492 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr4:53545 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr4:53545 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:87150803 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:87150803 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:20554440 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:20554440 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:156907853 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:156907853 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:46605093 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:46605093 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:75532049 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:75532049 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:38424408 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:38424408 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:101762374 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:101762374 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:42368330 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:42368330 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:55488771 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:55488771 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2114368 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2114368 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2117214 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2117214 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2117396 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2117396 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:135751562 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:135751562 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr14:58811361 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr14:58811361 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:26079360 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:26079360 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:117075339 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:117075339 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:72874072 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:72874072 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:31605027 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:31605027 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:11900531 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:11900531 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:48879931 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:48879931 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:80404622 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:80404622 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2099075 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2099075 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr22:32545789 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr22:32545789 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:181705585 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:181705585 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:48680603 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:48680603 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:93113351 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:93113351 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:71252891 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:71252891 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:73501169 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:73501169 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:35832226 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:35832226 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:167404575 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:167404575 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:35208348 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:35208348 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:227452439 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:227452439 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:117279764 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:117279764 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:182423159 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:182423159 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:196757613 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:196757613 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:87025541 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:87025541 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:8687173 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:8687173 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:58585362 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:58585362 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:17185708 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:17185708 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:57583706 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:57583706 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:16943492 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:16943492 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:61123827 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:61123827 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr18:50451586 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr18:50451586 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:59893539 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:59893539 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:35333283 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:35333283 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:131992594 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:131992594 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:132041399 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:132041399 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:133923351 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:133923351 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:33418908 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:33418908 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:207141111 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:207141111 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:157513947 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:157513947 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:240458097 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:240458097 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:74862354 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:74862354 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:14550273 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:14550273 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:27220004 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:27220004 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:105859503 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:105859503 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142964559 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142964559 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142965071 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142965071 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142965073 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142965073 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142965158 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142965158 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:52220475 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:52220475 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:29974549 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:29974549 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:70955219 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:70955219 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:38411417 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:38411417 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:2649923 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:2649923 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:156641422 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:156641422 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:86568040 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:86568040 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:55281288 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:55281288 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:55354396 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:55354396 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:51582027 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:51582027 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:54782612 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:54782612 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:150444561 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:150444561 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:67399105 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:67399105 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:70257905 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:70257905 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:77748706 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:77748706 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:114537994 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:114537994 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:160737467 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:160737467 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:47703824 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:47703824 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:64572474 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:64572474 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:103343261 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:103343261 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:102595603 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:102595603 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr22:28146821 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr22:28146821 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:74690183 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:74690183 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:63568446 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:63568446 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:26432328 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:26432328 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:134023026 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:134023026 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:115791900 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:115791900 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:35806253 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:35806253 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:115380306 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:115380306 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:161967472 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:161967472 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:47776174 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:47776174 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:70048811 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:70048811 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:138453243 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:138453243 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:20769152 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:20769152 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:122843091 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:122843091 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:230492633 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:230492633 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:36297326 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:36297326 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:15679065 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:15679065 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:17818510 A>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chrX:17818510 A>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:109388338 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:109388338 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:79349938 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:79349938 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:113127722 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:113127722 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:89650745 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:89650745 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:34150154 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:34150154 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:23904262 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:23904262 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:9052541 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:9052541 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:48056007 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:48056007 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr18:61324049 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr18:61324049 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:64535327 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:64535327 C>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:52149453 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:52149453 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:84065339 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:84065339 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:62655774 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:62655774 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:484824 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:484824 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:27598578 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:27598578 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:108412103 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:108412103 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:108412105 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:108412105 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:22408180 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:22408180 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:118838651 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:118838651 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142919079 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142919079 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:179660115 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:179660115 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:20038677 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:20038677 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:20038684 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:20038684 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:202301180 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:202301180 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:13275911 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:13275911 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:73839351 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:73839351 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:61416020 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:61416020 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:53494102 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:53494102 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:100789191 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:100789191 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:67301282 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:67301282 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:141418749 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:141418749 T>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:62595128 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:62595128 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:40784457 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:40784457 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:67014736 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:67014736 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:109629403 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:109629403 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:76227083 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:76227083 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:180257415 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:180257415 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:100181939 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:100181939 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:71877714 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:71877714 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:125856585 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:125856585 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:73746727 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:73746727 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:33997298 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:33997298 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:36447305 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:36447305 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:47196679 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:47196679 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:7506664 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:7506664 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:1444623 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:1444623 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:106682473 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:106682473 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:63400253 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:63400253 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:108216782 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:108216782 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:71190062 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:71190062 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:52675163 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:52675163 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:102198972 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:102198972 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:91294986 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:91294986 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:76524980 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:76524980 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:5124651 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:5124651 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:2125595 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:2125595 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:6686320 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:6686320 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:48639071 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:48639071 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:18550932 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:18550932 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:5169842 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:5169842 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:16355356 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:16355356 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:178030837 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:178030837 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:88296877 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:88296877 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr13:111135122 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr13:111135122 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:107924026 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:107924026 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:31292313 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:31292313 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:25044387 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:25044387 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:143997361 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:143997361 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:66031002 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:66031002 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:19129929 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:19129929 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:94341404 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:94341404 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:117816922 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:117816922 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:93171701 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:93171701 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:55237954 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:55237954 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:129770990 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:129770990 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:45854878 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:45854878 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr4:5785246 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr4:5785246 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:820188 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:820188 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:135433375 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:135433375 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:128366946 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:128366946 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:45970357 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:45970357 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:49482621 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:49482621 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:180665624 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:180665624 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr21:34117806 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr21:34117806 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:44228396 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:44228396 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:170513815 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:170513815 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:45095156 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:45095156 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:99771298 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:99771298 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:132439993 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:132439993 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:24433368 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:24433368 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:35514083 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:35514083 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:26197520 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:26197520 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:8528410 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:8528410 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:33217259 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:33217259 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:39311448 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:39311448 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:86887186 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chrX:86887186 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:169688191 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:169688191 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:919872 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:919872 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:34653556 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:34653556 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:18423391 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:18423391 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:210518169 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:210518169 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:46494740 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:46494740 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:103559925 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:103559925 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118361002 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118361002 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:149904134 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:149904134 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:149907094 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:149907094 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:10216458 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:10216458 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:10450945 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:10450945 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:42456899 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:42456899 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:60747457 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:60747457 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:41048648 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:41048648 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:79910770 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:79910770 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:36334887 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:36334887 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:98254487 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:98254487 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:27272549 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:27272549 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:21743134 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:21743134 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:72293652 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:72293652 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:59064400 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:59064400 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:41985701 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:41985701 T>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:179312114 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:179312114 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:153572394 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:153572394 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:43520254 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:43520254 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:72667867 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:72667867 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:220368541 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:220368541 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:2861198 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:2861198 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:130834390 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:130834390 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:38900649 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:38900649 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr4:53729427 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr4:53729427 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:3247923 G>A maps to NM_002919.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:3247923 G>A maps to NM_002919.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:323739 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:323739 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:101020466 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:101020466 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:38967422 T>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:38967422 T>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:196210591 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:196210591 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:48090211 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:48090211 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr21:30378733 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr21:30378733 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:50861866 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:50861866 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:9077216 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:9077216 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:67881069 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:67881069 T>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:103008068 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:103008068 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:18923417 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:18923417 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:153631919 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:153631919 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:51675313 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:51675313 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:24365346 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:24365346 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:134477244 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:134477244 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:48048513 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:48048513 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:21852128 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:21852128 A>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:27009920 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:27009920 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:110022193 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:110022193 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:150460029 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:150460029 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:11675658 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:11675658 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:103380895 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:103380895 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:226055569 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:226055569 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:53037826 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:53037826 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:18215916 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:18215916 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:1306464 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr16:1306464 C>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr21:10916307 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr21:10916307 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118889464 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118889464 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:113220972 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:113220972 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:90794840 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:90794840 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:19511517 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:19511517 C>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:62783309 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr12:62783309 G>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:72868275 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:72868275 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:30889833 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:30889833 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:44416346 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:44416346 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:149173989 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr7:149173989 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:7568002 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:7568002 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:7714814 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:7714814 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:112150555 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:112150555 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:76205835 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:76205835 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:20487224 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:20487224 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:87772293 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:87772293 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:1598980 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:1598980 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:110563487 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:110563487 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:32878106 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:32878106 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:4889809 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:4889809 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:243788146 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:243788146 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118076812 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118076812 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:38514910 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:38514910 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:101472951 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:101472951 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:15870448 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:15870448 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161039488 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161039488 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:73057893 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:73057893 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:235377415 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:235377415 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:155317423 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:155317423 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:62559456 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:62559456 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:31019381 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:31019381 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:160144296 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:160144296 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:154300286 G>A maps to NM_020452.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:154300286 G>A maps to NM_020452.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:3556429 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:3556429 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:28844859 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:28844859 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:13489228 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:13489228 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:26248665 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:26248665 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:44093483 T>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:44093483 T>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:19644518 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:19644518 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr18:30991958 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr18:30991958 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:20150171 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:20150171 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:74855367 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:74855367 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:120906537 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:120906537 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:112579613 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:112579613 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:53753934 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:53753934 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:3776778 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:3776778 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:73502639 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:73502639 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:90581001 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:90581001 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:40947573 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:40947573 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:40947589 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:40947589 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:137626273 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:137626273 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:24498704 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:24498704 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:95158512 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:95158512 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:85956210 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:85956210 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:21198356 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:21198356 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:85530715 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:85530715 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:56841162 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:56841162 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:43990806 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:43990806 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:8618353 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:8618353 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:154520565 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:154520565 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:32163798 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:32163798 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:94057584 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:94057584 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:55933837 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:55933837 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:61972785 G>T maps to NM_022640.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:61972785 G>T maps to NM_022640.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:3076738 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:3076738 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:113697995 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:113697995 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:56669988 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:56669988 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:41471702 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:41471702 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:74636073 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:74636073 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:72014680 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:72014680 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:64332345 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:64332345 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:134130828 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:134130828 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:169173602 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:169173602 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:31525340 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:31525340 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:65878516 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:65878516 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:2199822 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:2199822 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr18:29104378 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr18:29104378 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:43936305 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:43936305 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:27308450 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:27308450 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:41568698 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:41568698 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:94067940 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:94067940 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:37864869 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:37864869 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:34143974 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:34143974 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:23716547 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:23716547 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:137846206 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:137846206 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:29693785 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:29693785 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:133602301 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:133602301 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:109171001 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:109171001 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:81041779 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:81041779 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:126505134 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:126505134 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:49999267 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:49999267 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:33400410 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:33400410 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:159277440 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:159277440 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161512660 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161512660 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:130567001 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:130567001 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:12627780 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:12627780 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:17445757 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr22:17445757 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:81539440 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:81539440 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:109085360 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:109085360 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:121740508 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:121740508 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:183932988 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:183932988 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:52731646 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:52731646 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:131038337 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:131038337 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:37792024 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:37792024 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:231774716 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:231774716 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:55145277 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:55145277 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:71000592 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:71000592 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:26801730 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:26801730 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:22192106 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:22192106 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:8305895 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:8305895 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:99472912 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:99472912 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:130416850 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:130416850 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:68619202 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:68619202 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:44432729 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:44432729 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:9442084 A>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:9442084 A>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:237300615 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:237300615 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:15688793 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:15688793 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:73765165 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:73765165 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:94120275 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:94120275 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:95518697 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:95518697 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:36888965 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:36888965 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:17831266 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:17831266 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:200973786 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:200973786 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:173710837 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:173710837 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:86880596 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:86880596 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:52886336 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:52886336 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:55147115 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:55147115 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:34652260 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:34652260 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:82407789 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:82407789 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:105502864 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:105502864 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:46477802 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:46477802 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:136709489 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:136709489 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:127335986 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:127335986 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:42854231 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:42854231 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:131113929 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:131113929 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:27964404 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:27964404 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:104747596 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:104747596 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:102650209 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:102650209 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:102480573 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:102480573 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:56022896 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:56022896 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:121463150 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:121463150 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:9077952 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:9077952 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:15448504 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:15448504 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:103505717 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:103505717 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:1034328 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:1034328 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:101087076 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:101087076 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:144096960 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:144096960 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:6585820 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:6585820 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:150698284 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:150698284 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:52303127 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:52303127 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:104208700 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:104208700 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:156849959 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:156849959 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:49425017 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:49425017 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:134049374 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:134049374 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:128703213 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:128703213 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:67414173 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:67414173 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:6912806 A>T maps to NM_003700.1 *309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:6912806 A>T maps to NM_003700.1 *309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:119116090 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:119116090 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:154919292 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:154919292 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:140712735 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:140712735 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:6273180 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:6273180 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:77378658 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:77378658 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:18936752 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:18936752 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118502600 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118502600 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:44001225 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:44001225 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:77594832 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:77594832 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:123481746 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:123481746 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:28843968 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:28843968 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:8709844 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:8709844 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:145001522 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:145001522 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:43967967 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:43967967 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:24806704 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:24806704 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:39246900 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:39246900 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:25292808 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:25292808 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:69013727 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:69013727 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:64795340 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:64795340 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:2836060 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:2836060 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:73577080 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:73577080 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:231945064 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:231945064 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:198713172 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:198713172 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:8389206 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:8389206 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161044215 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161044215 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161044389 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:161044389 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:55881111 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:55881111 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:4773289 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr20:4773289 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:155457828 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:155457828 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:103173934 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:103173934 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:63890417 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:63890417 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:201958701 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:201958701 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:210867516 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:210867516 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:210867593 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:210867593 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:99140512 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:99140512 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:237919579 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:237919579 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:134987333 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:134987333 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:130530633 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:130530633 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:128926926 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:128926926 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:62040516 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:62040516 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38766583 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38766583 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38798463 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38798463 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:50201262 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:50201262 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38311877 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38311877 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:131730012 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:131730012 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:10976903 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:10976903 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:1394810 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:1394810 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:103128622 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:103128622 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:28261864 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:28261864 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:96254926 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:96254926 T>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:172834886 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:172834886 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158641095 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158641095 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:131337473 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:131337473 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:54706729 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:54706729 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:149492765 C>T maps to ENST00000262089 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:149492765 C>T maps to ENST00000262089 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:27475203 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:27475203 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:75597419 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:75597419 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:47435886 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:47435886 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:152473323 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:152473323 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:71609795 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:71609795 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:70457851 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:70457851 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:98146860 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:98146860 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:81626934 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:81626934 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:150415096 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:150415096 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:231334785 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:231334785 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:99689363 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:99689363 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:113181800 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:113181800 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:34934858 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:34934858 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:157000686 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:157000686 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118247487 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118247487 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:33495434 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:33495434 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:126220015 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:126220015 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:8989493 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:8989493 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:77909508 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:77909508 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr18:61067250 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr18:61067250 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:54614734 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:54614734 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:27151250 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:27151250 G>C did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:128480479 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:128480479 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:31001157 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:31001157 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:183472280 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:183472280 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:128962911 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:128962911 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:53357493 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:53357493 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:20296722 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:20296722 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:84520343 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chrX:84520343 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:22063602 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:22063602 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:119027853 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:119027853 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:109679095 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:109679095 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:19450736 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:19450736 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:73952083 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:73952083 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:18153050 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:18153050 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:156997869 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:156997869 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:38913346 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:38913346 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:128956548 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:128956548 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:64748457 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:64748457 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:45743438 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:45743438 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:228389457 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:228389457 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:247063587 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:247063587 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:134253096 T>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:134253096 T>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:134254058 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:134254058 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:4882104 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:4882104 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:38711837 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:38711837 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:14797653 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:14797653 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:73944683 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:73944683 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:11353811 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:11353811 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:11353956 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:11353956 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:101095363 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:101095363 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:176984101 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:176984101 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:10452262 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:10452262 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr21:11021257 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr21:11021257 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:23637371 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:23637371 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:105973904 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:105973904 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:30447598 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:30447598 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:185143446 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:185143446 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:35504391 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:35504391 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:15623518 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:15623518 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:15623520 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:15623520 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:67287144 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:67287144 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:2760995 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:2760995 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:159162261 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:159162261 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:223939523 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:223939523 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:78163492 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:78163492 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:104904800 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:104904800 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:70206145 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:70206145 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:68588267 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:68588267 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:28544442 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:28544442 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:55734918 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:55734918 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:158326822 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:158326822 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:31323515 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:31323515 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:55857661 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:55857661 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:4423951 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:4423951 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:61978251 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:61978251 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:1334343 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:1334343 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:70739902 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:70739902 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:70647842 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:70647842 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:86308180 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:86308180 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:189862039 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:189862039 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:110862278 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:110862278 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:109048217 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:109048217 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:130008536 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:130008536 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:1414407 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:1414407 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:43678550 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:43678550 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:113277871 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:113277871 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:37679477 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:37679477 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:85404136 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:85404136 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:101200398 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:101200398 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:6697167 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:6697167 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:95439680 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:95439680 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:71730486 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:71730486 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:101386785 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:101386785 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:120612879 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:120612879 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:34817355 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:34817355 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:6240168 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:6240168 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:10680379 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:10680379 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:10691434 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:10691434 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:161569699 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:161569699 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:157718299 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:157718299 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:33035767 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:33035767 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:89392727 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:89392727 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:85987777 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:85987777 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:49210181 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:49210181 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:17443789 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:17443789 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:47428112 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:47428112 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:89909200 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:89909200 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:22737958 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:22737958 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:72618390 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:72618390 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:121769163 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:121769163 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:131977797 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:131977797 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:56374625 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:56374625 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:131025211 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:131025211 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:121386566 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:121386566 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:132730767 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:132730767 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:23296797 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:23296797 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:57602079 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:57602079 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:30538644 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:30538644 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:6383268 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:6383268 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:26415301 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:26415301 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:39880923 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:39880923 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:28377988 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:28377988 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:33074342 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:33074342 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:83561339 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:83561339 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:42829194 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:42829194 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:22198928 T>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:22198928 T>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:124266500 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:124266500 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:8275419 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:8275419 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:21187545 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:21187545 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:113742388 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:113742388 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:120606622 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:120606622 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:123149903 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:123149903 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:68649485 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:68649485 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:128260953 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:128260953 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:87723190 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:87723190 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:103599632 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:103599632 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:36693743 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:36693743 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:36694016 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:36694016 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:27689405 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:27689405 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:42460985 T>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:42460985 T>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:100139293 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:100139293 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:39719543 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:39719543 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:152733814 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:152733814 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:47981105 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:47981105 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:39595263 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:39595263 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:53004361 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:53004361 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:134338157 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:134338157 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:42157224 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:42157224 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:54872404 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:54872404 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:129714149 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:129714149 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:55178285 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:55178285 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:90986821 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:90986821 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:62861994 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:62861994 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:62903651 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:62903651 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:6994303 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:6994303 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160771712 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160771712 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:6594858 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:6594858 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:56160441 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:56160441 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:39096458 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:39096458 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:220800294 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:220800294 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:90428849 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:90428849 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:141760222 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:141760222 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:154861210 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:154861210 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:50581669 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:50581669 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:41903222 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:41903222 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:124632261 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:124632261 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:9015495 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:9015495 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:10408428 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:10408428 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:33567648 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:33567648 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:171258248 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:171258248 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:15784982 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:15784982 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:21074655 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:21074655 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:152500963 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:152500963 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:21191709 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:21191709 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:36962074 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:36962074 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:56443328 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:56443328 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:117697012 A>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:117697012 A>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:36338913 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:36338913 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:88679637 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:88679637 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:5291289 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:5291289 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:248167181 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:248167181 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:22332477 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:22332477 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:142749381 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:142749381 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:24856100 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:24856100 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:51535335 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:51535335 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:31855473 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:31855473 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:15225423 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:15225423 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:31847459 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:31847459 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:144110128 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:144110128 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:45312580 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:45312580 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:18691044 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:18691044 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:99950798 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:99950798 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:81157444 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:81157444 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:129288824 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:129288824 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:7606727 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:7606727 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:151400574 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:151400574 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:2200455 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:2200455 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:57146086 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:57146086 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:15993765 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:15993765 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:43382467 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:43382467 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:8633237 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:8633237 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:157396616 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:157396616 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:71065676 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:71065676 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:40743738 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:40743738 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:128877271 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:128877271 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:102718363 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:102718363 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:36207714 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:36207714 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:167943745 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:167943745 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:24644668 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:24644668 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:36120598 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:36120598 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:18237697 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:18237697 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:176012829 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:176012829 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:63802440 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:63802440 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:30477928 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:30477928 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:182550163 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:182550163 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:78335754 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:78335754 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:13742660 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr18:13742660 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:108913233 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:108913233 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:83636846 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:83636846 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:13947931 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:13947931 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:2834554 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:2834554 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:145153698 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:145153698 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160465762 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160465762 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:25849559 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:25849559 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:150847496 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:150847496 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:220494286 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:220494286 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:110709883 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:110709883 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:110716543 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:110716543 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:20648474 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:20648474 G>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:149582307 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:149582307 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:108439157 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:108439157 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:108589278 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:108589278 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:16205506 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:16205506 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:104129214 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:104129214 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:113148395 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:113148395 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:113251898 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:113251898 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:152725527 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:152725527 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:39812897 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr22:39812897 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:125534276 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:125534276 A>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:115117164 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:115117164 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:115120465 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:115120465 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:101396475 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:101396475 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:74872007 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:74872007 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:92327098 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:92327098 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:134034399 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:134034399 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:165697223 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:165697223 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:94797314 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:94797314 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:98921641 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:98921641 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:55666265 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:55666265 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:55666267 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:55666267 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:1308401 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr16:1308401 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr21:10942837 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr21:10942837 T>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr21:10971409 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr21:10971409 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:189026290 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:189026290 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:142625165 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:142625165 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:40817596 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:40817596 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:22848826 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:22848826 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:99949716 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:99949716 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48921114 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48921114 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:27664333 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:27664333 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrY:14850273 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrY:14850273 A>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:155127962 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chrX:155127962 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160393793 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160393793 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:98852816 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:98852816 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:6023480 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:6023480 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:100388762 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:100388762 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:36900798 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:36900798 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:40389767 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:40389767 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:56006545 A>C did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:56006545 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:35506651 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:35506651 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:128598330 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:128598330 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:8666047 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:8666047 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:7820841 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:7820841 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:100161344 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:100161344 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:5043656 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:5043656 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:118068675 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:118068675 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:213186784 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:213186784 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:69933827 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:69933827 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:29409424 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:29409424 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:72859046 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:72859046 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:113487066 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:113487066 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:193185341 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:193185341 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:32706529 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:32706529 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:96070171 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:96070171 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:180424110 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:180424110 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:105985208 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:105985208 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:169773438 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:169773438 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:247737773 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:247737773 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:20168806 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:20168806 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:97726797 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:97726797 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:40193437 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:40193437 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:181726318 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:181726318 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:121985605 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:121985605 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:44272473 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:44272473 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:42678002 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:42678002 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:54573584 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:54573584 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:26484572 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:26484572 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:21765019 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:21765019 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:20546820 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:20546820 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:117242772 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:117242772 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:40339155 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:40339155 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:26863484 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:26863484 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:42905437 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:42905437 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:42905450 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:42905450 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:3072686 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:3072686 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:124783217 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:124783217 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:10081550 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:10081550 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:109042257 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:109042257 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:207883740 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:207883740 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:49819666 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:49819666 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:49699033 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:49699033 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:122720769 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:122720769 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:34038006 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:34038006 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:34049031 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:34049031 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:36361517 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:36361517 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:10981974 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:10981974 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42818612 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42818612 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42827878 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42827878 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:137882758 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:137882758 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:24205197 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:24205197 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:151153985 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:151153985 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:142195204 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:142195204 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:69424474 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:69424474 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:31462516 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:31462516 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:118533727 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:118533727 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:38027130 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:38027130 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:169126309 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:169126309 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:7563903 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:7563903 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:158422363 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:158422363 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:74898991 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:74898991 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:12914909 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:12914909 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:10641522 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:10641522 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:14743589 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:14743589 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:75230973 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:75230973 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:72968241 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:72968241 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:61632768 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:61632768 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:17641792 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:17641792 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:117086431 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:117086431 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:12040324 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:12040324 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:8374358 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:8374358 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:150930993 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:150930993 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:92343782 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:92343782 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:137805524 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:137805524 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:102378841 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:102378841 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:106013202 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:106013202 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:171252250 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:171252250 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:49204840 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:49204840 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:120118702 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:120118702 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:27135313 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:27135313 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:46252305 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:46252305 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:47322140 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:47322140 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:158380532 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:158380532 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:55196431 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:55196431 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:4286470 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:4286470 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:14625539 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:14625539 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:2117863 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:2117863 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39823873 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39823873 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:131028028 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:131028028 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:171806688 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:171806688 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:23306248 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:23306248 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:25684823 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:25684823 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:48840351 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:48840351 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:54329520 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:54329520 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:18767432 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:18767432 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:26199485 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:26199485 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:38308719 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:38308719 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:185959284 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:185959284 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:185964274 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:185964274 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:186055632 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:186055632 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:82068948 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:82068948 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:148586521 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:148586521 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:118644930 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:118644930 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:140031638 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:140031638 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:113820006 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:113820006 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:100964567 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:100964567 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:153701263 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:153701263 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:156508833 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:156508833 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:12944170 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:12944170 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:3937322 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:3937322 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:215368230 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:215368230 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:202743724 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:202743724 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:27715462 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:27715462 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:29023329 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:29023329 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:245530036 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:245530036 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:31743889 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:31743889 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:39340603 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:39340603 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:31964724 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:31964724 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:129250738 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:129250738 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:43213815 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:43213815 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:71898270 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:71898270 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:62641290 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:62641290 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:141460199 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:141460199 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:24523587 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:24523587 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:32528798 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:32528798 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:151935195 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:151935195 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:54835716 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:54835716 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:10766173 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:10766173 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:103650053 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:103650053 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:161522877 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:161522877 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:13825652 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:13825652 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:71052428 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:71052428 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:107169846 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:107169846 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:132325032 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:132325032 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:33780308 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:33780308 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:17927573 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:17927573 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:149900972 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:149900972 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:74207312 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:74207312 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:1364225 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:1364225 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:65630742 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:65630742 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:74673798 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:74673798 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:10411132 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:10411132 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:101735599 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:101735599 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:72434488 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:72434488 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:16893658 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:16893658 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:21581992 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:21581992 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:45173406 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:45173406 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:73541596 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:73541596 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70387664 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70387664 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:115371928 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:115371928 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:115251097 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:115251097 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:102332725 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:102332725 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:102780299 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:102780299 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:99514146 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:99514146 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:22094594 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:22094594 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:22132529 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:22132529 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:597357 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:597357 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:33162840 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr20:33162840 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:47847824 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:47847824 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:81199371 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:81199371 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:137225062 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:137225062 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:64023115 T>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:64023115 T>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:118199150 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:118199150 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:65055390 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:65055390 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:7406038 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:7406038 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:72397318 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:72397318 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:82763324 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:82763324 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:18802185 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:18802185 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr22:22890448 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr22:22890448 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:139218121 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:139218121 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:43376392 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:43376392 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:71331543 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:71331543 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:209307270 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:209307270 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:80382858 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:80382858 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:241032263 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:241032263 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39002836 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39002836 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:237550706 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:237550706 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:237982599 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:237982599 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:237991773 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:237991773 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:128927571 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:128927571 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:38764762 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:38764762 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:4558195 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:4558195 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:101176555 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:101176555 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:158549109 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:158549109 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:224856463 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:224856463 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:73215351 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:73215351 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr22:25251479 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr22:25251479 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:3524527 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:3524527 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:160719948 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:160719948 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:100797997 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:100797997 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:95814397 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:95814397 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:18855480 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:18855480 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:130931073 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:130931073 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:62574601 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:62574601 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:96953168 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:96953168 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:108447943 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:108447943 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:206594683 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:206594683 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:48207046 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:48207046 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:48207143 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:48207143 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:23750112 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:23750112 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:16047116 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:16047116 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:70855424 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr14:70855424 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70679626 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:70679626 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:95539683 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:95539683 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:63084804 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:63084804 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:12924812 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:12924812 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:114150359 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr13:114150359 A>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:87025447 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:87025447 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:15584550 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:15584550 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:103220239 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:103220239 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:1860894 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:1860894 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:1957424 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:1957424 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:10935065 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:10935065 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:2204952 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:2204952 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:33943707 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:33943707 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:17735611 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:17735611 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:12422566 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:12422566 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:38767995 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:38767995 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:1976103 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:1976103 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:175431777 A>C maps to ENST00000409891 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:175431777 A>C maps to ENST00000409891 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:108618488 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:108618488 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:10106981 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chrX:10106981 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:147113579 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:147113579 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:44634919 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:44634919 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:52569545 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:52569545 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:215813271 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:215813271 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:48684386 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:48684386 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:67030037 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:67030037 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:183682967 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:183682967 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:35453852 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:35453852 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:32364580 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:32364580 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:104240540 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:104240540 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:158397768 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:158397768 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:127760249 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:127760249 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:33615810 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:33615810 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:7804682 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:7804682 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:100349489 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:100349489 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:19609423 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:19609423 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:116062393 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:116062393 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:47727215 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:47727215 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:67787273 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:67787273 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:77835388 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:77835388 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:61956228 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:61956228 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:90328845 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:90328845 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:169102723 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:169102723 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:201521558 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:201521558 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:63597758 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:63597758 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:39496196 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:39496196 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:36052347 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:36052347 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:47426323 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:47426323 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:6895153 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:6895153 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:18809060 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:18809060 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:101858905 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:101858905 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:123267081 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:123267081 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:96779363 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:96779363 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:116926830 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:116926830 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:119504878 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:119504878 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:203626575 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:203626575 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:79182688 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:79182688 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:33316610 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:33316610 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152969269 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152969269 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152773574 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152773574 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:60546675 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:60546675 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:102248145 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:102248145 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:30034901 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:30034901 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:111395741 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:111395741 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:31480615 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:31480615 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:614384 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:614384 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:56619964 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:56619964 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:31661282 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:31661282 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:3296561 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:3296561 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:58644974 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:58644974 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:105959222 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:105959222 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:241829663 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:241829663 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:24413505 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:24413505 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:43121131 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:43121131 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:121577440 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:121577440 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:65107423 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:65107423 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:81588570 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:81588570 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:81595046 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:81595046 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:81643696 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:81643696 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54501666 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54501666 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:159162527 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:159162527 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:3773057 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:3773057 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:179137145 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:179137145 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:110490842 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:110490842 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:55033348 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:55033348 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:159842719 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:159842719 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:208591506 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:208591506 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:109698924 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:109698924 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:54415861 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:54415861 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:59166737 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:59166737 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:68718740 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:68718740 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:46052492 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:46052492 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:56837409 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:56837409 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:101443407 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:101443407 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:55846673 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:55846673 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:146751896 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:146751896 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:175624015 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:175624015 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:78953309 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:78953309 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:101953695 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:101953695 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:6979954 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:6979954 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:27468188 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:27468188 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:87951772 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:87951772 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:32746536 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:32746536 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:24227952 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:24227952 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:246829231 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:246829231 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:103462788 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:103462788 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:121312757 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:121312757 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:121353626 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:121353626 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:101796744 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:101796744 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:109858928 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:109858928 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:189871539 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:189871539 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:227877073 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:227877073 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:107438409 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:107438409 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:10087340 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:10087340 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:47402745 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:47402745 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:47546264 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:47546264 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:76112015 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:76112015 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:130150670 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:130150670 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:36711248 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:36711248 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:36711439 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:36711439 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:211444257 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:211444257 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:2775079 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:2775079 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:2776117 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:2776117 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:125558485 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:125558485 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:126139093 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:126139093 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:101992211 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:101992211 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:4645848 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:4645848 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:113518774 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:113518774 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:77489230 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:77489230 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:69366570 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:69366570 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:75394861 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:75394861 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:143959283 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:143959283 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42523760 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42523760 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:4393075 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:4393075 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:58993031 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:58993031 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:155219890 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:155219890 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:124102987 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:124102987 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:35278555 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:35278555 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:115138581 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:115138581 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:37656979 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:37656979 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:189599709 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:189599709 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:21071570 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:21071570 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:196915772 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:196915772 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:98080316 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:98080316 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:169098041 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:169098041 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:99515236 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:99515236 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:115991634 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:115991634 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18002414 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18002414 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:117314470 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:117314470 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:29039176 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:29039176 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:28985941 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:28985941 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:56391557 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:56391557 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:95457503 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:95457503 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:95614095 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:95614095 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:103327090 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:103327090 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:44014218 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:44014218 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:137820498 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:137820498 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:20490839 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:20490839 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:5438166 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:5438166 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:21938026 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:21938026 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:89478447 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:89478447 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:97251131 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:97251131 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:26356868 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:26356868 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:59059926 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:59059926 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:175528023 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:175528023 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:175528025 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:175528025 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:190234232 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:190234232 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18891757 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18891757 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:92430620 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:92430620 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100190685 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100190685 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:137772602 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:137772602 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:159776120 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:159776120 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:192126017 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:192126017 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:102454355 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:102454355 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:110083280 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:110083280 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153589620 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153589620 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:28609550 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:28609550 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:240458367 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:240458367 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:109276256 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:109276256 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:14813199 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:14813199 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:135440052 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:135440052 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:131219566 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:131219566 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:94278920 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:94278920 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:101056345 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:101056345 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:130151416 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:130151416 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:72622412 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:72622412 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:74372871 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:74372871 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:101190364 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:101190364 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:42426509 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:42426509 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:1053126 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:1053126 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:19381272 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:19381272 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:18975280 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:18975280 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:28424001 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:28424001 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:150154427 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:150154427 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:83350390 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:83350390 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:46700537 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:46700537 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:148878160 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:148878160 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:100995264 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:100995264 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:33173526 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:33173526 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:111784039 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:111784039 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:70926486 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:70926486 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:118922014 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:118922014 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:42249583 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:42249583 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:185374929 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:185374929 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:18702610 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:18702610 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:67852194 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:67852194 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:148758825 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:148758825 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:113537311 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:113537311 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:155231203 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:155231203 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:28707882 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:28707882 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:98668953 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:98668953 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:15628733 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:15628733 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:15647805 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:15647805 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:211033608 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:211033608 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:215179451 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:215179451 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:196296186 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:196296186 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:36776446 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:36776446 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:142659391 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:142659391 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:19456049 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:19456049 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:86554800 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:86554800 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:113723452 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:113723452 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:1369126 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:1369126 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:45205396 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:45205396 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:132069745 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:132069745 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:55598245 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:55598245 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:186450615 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:186450615 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:160232066 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:160232066 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:38906947 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:38906947 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:39553376 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:39553376 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:52966952 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:52966952 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:31863899 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:31863899 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:31988756 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:31988756 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:201353729 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:201353729 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54868319 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54868319 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:107698408 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:107698408 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:910236 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:910236 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:152799928 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:152799928 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:65895900 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:65895900 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:28150620 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:28150620 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:47113256 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:47113256 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:24524176 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:24524176 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:1874439 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:1874439 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:109090909 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:109090909 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:43571249 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:43571249 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:21201535 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:21201535 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:161510314 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:161510314 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:39553131 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:39553131 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:165118953 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:165118953 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:119752159 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:119752159 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:3784984 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:3784984 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:54530405 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:54530405 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:138678977 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:138678977 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:127335689 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:127335689 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:90356445 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:90356445 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:141759639 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:141759639 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:74902063 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:74902063 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:22024168 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:22024168 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:127464434 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:127464434 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:102592106 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:102592106 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100843987 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100843987 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:71616095 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:71616095 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:60482740 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:60482740 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:66606032 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:66606032 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:149783174 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:149783174 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:11166993 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:11166993 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:236988601 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:236988601 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9009238 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9009238 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:10243789 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:10243789 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:50796466 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:50796466 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18027745 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18027745 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18057336 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:18057336 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:75399593 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:75399593 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:69961790 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:69961790 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:47873114 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:47873114 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:1914198 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:1914198 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:78152214 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:78152214 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:54902008 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:54902008 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:152483835 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:152483835 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:127076194 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:127076194 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:105350157 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:105350157 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:29672635 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:29672635 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:33364177 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:33364177 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:233757469 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:233757469 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42072648 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42072648 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:63776521 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:63776521 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:169707962 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:169707962 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:36322522 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:36322522 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:50385142 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:50385142 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:92929573 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:92929573 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:107880321 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:107880321 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:64435232 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:64435232 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152018680 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:152018680 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:132180298 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:132180298 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:163297241 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:163297241 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:71729392 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:71729392 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:5925611 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:5925611 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:167671758 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:167671758 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:183601371 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:183601371 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:44739897 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:44739897 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70775974 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70775974 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70784725 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70784725 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:7530610 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:7530610 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:67431943 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:67431943 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:58034375 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:58034375 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9203889 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9203889 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248100032 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248100032 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248186037 C>A maps to ENST00000355281 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248186037 C>A maps to ENST00000355281 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:55927836 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:55927836 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:26739100 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:26739100 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:4198809 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:4198809 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:17715218 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:17715218 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:73717767 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:73717767 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:34671894 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:34671894 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:25023799 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:25023799 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:25052074 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:25052074 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:52610551 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:52610551 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:91137921 C>A maps to NM_032967.2 S1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:91137921 C>A maps to NM_032967.2 S1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140257426 A>C maps to NM_031864.1 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140257426 A>C maps to NM_031864.1 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140228042 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140228042 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140871269 G>A maps to NM_032407.1 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140871269 G>A maps to NM_032407.1 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:71513626 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:71513626 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:183095701 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:183095701 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:31862585 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:31862585 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:654432 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:654432 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:149497144 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:149497144 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:13940701 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:13940701 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153095779 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153095779 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:73440126 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:73440126 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:38466961 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:38466961 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:59821709 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:59821709 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:3639072 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:3639072 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:3197667 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:3197667 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:111554096 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:111554096 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:47930058 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:47930058 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:88995853 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:88995853 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:51936892 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:51936892 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:26917278 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:26917278 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:113810345 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:113810345 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100849494 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100849494 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153036560 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153036560 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153040877 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:153040877 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:118351520 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:118351520 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:118236537 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:118236537 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:42199896 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:42199896 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:42199898 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:42199898 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:37492575 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:37492575 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:99140497 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:99140497 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:40206922 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:40206922 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:40209668 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:40209668 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:48222448 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:48222448 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:74527226 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:74527226 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:47305049 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:47305049 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:214185130 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:214185130 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:43228454 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:43228454 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:77255931 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:77255931 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:8340573 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:8340573 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:8465441 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:8465441 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:157366929 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:157366929 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:40743996 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:40743996 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:76251901 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:76251901 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:33740139 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:33740139 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:135960061 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:135960061 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:79384503 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:79384503 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:103181031 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:103181031 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:107082942 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:107082942 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:163042550 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:163042550 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:240986222 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:240986222 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:104671611 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:104671611 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:101299684 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:101299684 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:185056802 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:185056802 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:124755169 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:124755169 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:123005894 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:123005894 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:74655630 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:74655630 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:71655361 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:71655361 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:237580478 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:237580478 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:134988742 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:134988742 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:148664386 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:148664386 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:128925115 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:128925115 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:159603964 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:159603964 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:166165115 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:166165115 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:23223351 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:23223351 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:50252224 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:50252224 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:48057280 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:48057280 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:61653530 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:61653530 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:14412146 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:14412146 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:2831100 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:2831100 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154937910 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154937910 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:44841776 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:44841776 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:232629520 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:232629520 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:45235620 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:45235620 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:43223047 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:43223047 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:42399989 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:42399989 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:18280025 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:18280025 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:57191344 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:57191344 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:27425803 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:27425803 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:10953679 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:10953679 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:149580542 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:149580542 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70147909 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70147909 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:135115740 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:135115740 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:98923245 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:98923245 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:168999492 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:168999492 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:51449416 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:51449416 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:51621419 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:51621419 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:133715205 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:133715205 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:44047192 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:44047192 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:89911693 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:89911693 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:55648305 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:55648305 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:55657565 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:55657565 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:158647688 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:158647688 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100481570 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:100481570 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:48117895 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:48117895 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:130064464 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:130064464 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:68442797 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:68442797 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:191847321 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:191847321 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:89793754 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:89793754 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:102242329 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:102242329 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:13415673 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:13415673 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:74173959 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:74173959 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:23751184 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:23751184 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:52901670 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:52901670 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:133931799 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:133931799 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:11500225 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:11500225 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:100204633 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:100204633 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:102269666 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:102269666 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:98382517 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:98382517 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:154754315 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:154754315 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:117810410 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:117810410 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:32024797 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:32024797 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:186287786 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:186287786 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:10996049 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:10996049 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:138235801 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:138235801 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:119993597 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:119993597 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:89537744 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:89537744 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:189013139 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:189013139 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:230663564 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:230663564 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:33591143 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:33591143 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:142626675 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:142626675 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:79611986 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:79611986 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:47287846 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:47287846 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:91076936 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:91076936 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:179584211 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:179584211 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:34824241 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:34824241 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:96106090 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:96106090 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:101682690 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:101682690 T>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:6828389 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:6828389 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:17278278 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:17278278 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:6131423 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:6131423 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:110456312 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:110456312 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:122413046 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:122413046 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:228786323 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:228786323 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:6673926 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:6673926 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:10782086 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:10782086 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:17211894 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:17211894 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:17221489 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:17221489 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:167078553 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:167078553 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:114069084 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:114069084 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:129690961 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:129690961 G>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:128940159 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:128940159 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70470203 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:70470203 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58455523 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58455523 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:22257928 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:22257928 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:38246177 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:38246177 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58721322 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58721322 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:129339489 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:129339489 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:38306369 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:38306369 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:57803656 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:57803656 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:44104249 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:44104249 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:38287027 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:38287027 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:71632682 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:71632682 A>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:53746911 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:53746911 G>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:134421781 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chrX:134421781 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:146744699 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:146744699 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:75127340 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:75127340 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:136269204 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:136269204 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:56854606 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:56854606 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:215855764 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:215855764 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:2348615 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:2348615 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:67012549 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:67012549 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:87072908 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:87072908 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:20685728 G>T maps to NM_001163941.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:20685728 G>T maps to NM_001163941.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:179191280 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:179191280 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6393645 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6393645 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:48538981 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:48538981 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:20471394 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:20471394 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:148653786 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:148653786 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:52312925 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:52312925 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:42854981 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:42854981 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:39521275 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:39521275 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:33658453 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:33658453 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:136282719 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:136282719 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:129037058 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:129037058 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:73280704 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:73280704 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:18662190 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:18662190 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:75642251 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:75642251 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:41198797 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:41198797 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:167805892 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:167805892 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:50338950 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:50338950 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:37821623 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:37821623 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:247004093 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:247004093 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:151646945 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:151646945 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:43905698 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:43905698 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:112604603 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:112604603 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:74008304 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:74008304 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:74021309 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:74021309 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:37438555 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:37438555 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:77816556 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:77816556 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:220094861 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:220094861 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:5757051 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:5757051 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:101510308 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:101510308 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:45781890 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:45781890 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:69420347 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:69420347 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:39410220 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:39410220 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:39448531 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:39448531 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:121303999 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:121303999 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:11272833 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:11272833 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:156947958 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:156947958 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:23247945 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:23247945 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:27553767 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:27553767 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:74989621 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:74989621 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:53955771 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:53955771 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:177142507 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:177142507 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:124384102 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:124384102 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:112251468 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:112251468 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160091191 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160091191 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:203669879 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:203669879 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:138430116 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:138430116 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:55362864 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:55362864 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:77137081 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:77137081 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:33313628 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:33313628 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:52601781 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:52601781 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:173035134 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:173035134 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:140481322 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:140481322 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:32958908 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:32958908 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:105685407 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:105685407 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:105685409 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:105685409 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55813337 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55813337 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:79946452 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:79946452 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:50373875 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:50373875 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:50396413 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:50396413 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:118427678 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:118427678 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:33596521 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:33596521 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:102591217 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:102591217 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:88379939 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:88379939 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:97045290 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:97045290 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:76495978 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:76495978 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31505166 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31505166 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:54893249 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:54893249 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:30950215 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:30950215 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:1011722 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:1011722 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:172501592 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:172501592 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:31649700 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:31649700 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:24950142 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:24950142 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:34843462 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:34843462 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:71201990 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:71201990 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:98947241 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:98947241 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:159822591 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:159822591 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:159822597 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:159822597 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:131796142 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:131796142 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:41199778 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:41199778 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:35755490 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:35755490 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:53883742 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:53883742 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:48081121 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:48081121 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:108524479 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:108524479 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:57431681 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:57431681 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:72472975 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:72472975 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:49068814 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:49068814 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:48695177 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:48695177 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:201018108 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:201018108 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152729042 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152729042 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:7339848 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:7339848 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:7341317 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:7341317 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:114458638 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:114458638 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:3028039 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:3028039 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:40901117 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:40901117 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:104899698 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:104899698 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:116244099 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:116244099 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:32194617 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:32194617 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:57107101 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:57107101 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:106118014 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:106118014 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:99973370 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:99973370 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:62099828 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:62099828 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:74491063 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:74491063 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:9907173 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:9907173 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:100960516 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:100960516 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:21751825 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:21751825 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:61747992 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:61747992 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:22385528 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:22385528 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:135940280 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:135940280 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:55908876 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:55908876 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:113343709 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:113343709 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6191632 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6191632 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6194572 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6194572 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133448863 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133448863 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:57474531 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:57474531 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:16280592 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:16280592 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:11894512 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:11894512 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:137729350 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:137729350 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:123384731 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:123384731 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:32801155 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:32801155 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:34552968 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:34552968 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:76528696 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:76528696 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107002872 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107002872 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:70672839 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:70672839 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:139631585 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:139631585 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:139736918 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:139736918 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:139809176 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:139809176 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:109969262 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:109969262 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:110831468 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:110831468 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:107418539 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:107418539 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:238281043 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:238281043 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:19078932 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:19078932 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:19086858 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:19086858 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:27946051 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:27946051 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:30231193 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:30231193 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:68481710 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:68481710 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:9984413 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:9984413 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:36726280 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:36726280 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:5844727 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:5844727 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:21014050 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:21014050 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:113812607 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:113812607 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:114290751 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:114290751 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:58197951 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:58197951 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:11412059 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:11412059 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:3552108 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:3552108 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:101839883 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:101839883 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:36003981 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:36003981 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:134303770 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:134303770 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:72362136 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:72362136 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:27840720 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:27840720 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:86054045 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:86054045 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:86054053 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:86054053 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:88886240 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:88886240 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:50451549 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:50451549 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:155241432 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:155241432 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:71889206 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:71889206 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:162725666 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:162725666 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:108577362 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:108577362 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125778219 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125778219 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:134711001 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:134711001 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:169190182 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:169190182 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:117188455 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:117188455 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:958924 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:958924 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:72040302 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:72040302 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:37612439 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:37612439 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:96724771 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:96724771 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:231935827 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:231935827 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:83183881 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:83183881 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:84245909 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:84245909 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:36003432 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:36003432 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:21640826 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:21640826 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:21092770 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:21092770 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:196892569 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:196892569 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:38816407 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:38816407 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:11672668 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:11672668 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:34500873 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:34500873 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:34946080 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:34946080 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:169509879 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:169509879 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:51264526 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:51264526 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:66253942 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:66253942 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:109023602 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:109023602 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:32945753 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:32945753 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:27147679 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:27147679 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:56357949 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:56357949 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:77458227 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:77458227 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:121554258 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:121554258 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:139135619 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:139135619 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:57899557 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:57899557 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:22276208 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:22276208 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:36358068 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:36358068 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:36297281 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:36297281 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:37914835 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:37914835 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:14857694 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:14857694 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:111441349 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:111441349 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:38183907 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:38183907 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:91364012 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:91364012 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:13949252 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:13949252 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:637562 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:637562 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197019820 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197019820 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:61615529 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:61615529 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:23030551 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:23030551 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:184787669 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:184787669 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:66550909 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:66550909 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:177199315 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:177199315 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:95516201 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:95516201 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:124811671 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:124811671 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:14871430 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:14871430 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29463957 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29463957 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:8174680 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:8174680 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:5950824 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:5950824 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:123526815 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:123526815 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:125034044 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:125034044 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:108120973 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:108120973 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125318322 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125318322 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125351579 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125351579 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:155489049 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:155489049 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:123263527 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:123263527 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:154962196 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:154962196 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:171178106 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:171178106 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:159646435 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:159646435 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:89431851 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:89431851 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:94039016 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:94039016 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:116289619 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:116289619 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:12735609 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:12735609 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:70509543 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:70509543 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:161277763 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:161277763 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:26589642 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:26589642 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:69799689 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:69799689 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:11398930 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:11398930 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:56064923 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:56064923 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:27728446 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:27728446 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:930558 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:930558 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:135866463 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:135866463 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:74054834 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:74054834 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:33448151 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:33448151 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:46174713 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:46174713 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:4861914 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:4861914 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:62224330 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:62224330 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:235747243 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:235747243 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:84967769 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:84967769 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133375151 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133375151 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133381627 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133381627 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:155746288 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:155746288 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:45097209 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:45097209 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:110903093 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:110903093 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:123186602 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:123186602 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:131486605 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:131486605 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:25684793 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:25684793 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:11774134 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:11774134 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:158254164 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:158254164 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:158281335 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:158281335 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:102247724 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:102247724 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:120690669 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:120690669 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:66990858 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:66990858 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:14538197 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:14538197 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:48837567 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:48837567 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:146492786 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:146492786 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:89983717 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:89983717 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:89983719 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:89983719 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:106698650 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:106698650 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:156631633 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:156631633 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:45396548 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:45396548 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:43532663 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:43532663 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:27782673 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:27782673 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:30147247 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:30147247 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:43034553 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:43034553 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:53191883 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:53191883 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:46805353 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:46805353 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:114405567 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:114405567 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:183823315 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:183823315 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:71008232 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:71008232 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:52883301 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:52883301 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:18702948 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:18702948 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:42163753 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:42163753 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:113786675 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:113786675 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:143007286 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:143007286 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:77639377 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:77639377 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:15760626 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:15760626 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31405492 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31405492 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31424097 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31424097 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:3634498 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:3634498 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160851183 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160851183 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:42747042 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:42747042 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:39680364 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:39680364 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:196342229 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:196342229 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:36793535 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:36793535 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:109907301 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:109907301 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:85706145 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:85706145 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:114178638 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:114178638 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:27781093 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:27781093 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:42440253 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:42440253 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55247645 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55247645 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55297703 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55297703 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:55598003 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:55598003 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:52773821 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:52773821 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:129468347 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:129468347 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:129749050 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:129749050 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:60889318 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:60889318 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:31211924 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:31211924 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:8321963 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:8321963 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:25182151 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:25182151 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:16597297 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:16597297 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:40195139 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:40195139 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:111904015 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:111904015 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55107516 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55107516 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55107526 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55107526 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:90487826 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:90487826 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:36142566 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:36142566 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:165175279 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:165175279 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:135186256 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:135186256 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:160969700 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:160969700 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:82188469 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:82188469 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:141135742 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:141135742 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:76376782 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:76376782 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:40629570 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:40629570 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:130221421 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:130221421 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:35786961 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:35786961 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:21206556 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:21206556 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:179676193 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:179676193 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:165109674 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:165109674 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:165109811 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:165109811 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:220799159 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:220799159 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:66691208 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:66691208 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:119216675 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:119216675 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:38308322 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:38308322 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:27964148 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:27964148 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:151944974 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:151944974 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:122617797 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:122617797 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:89180256 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:89180256 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:102575211 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:102575211 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:30432892 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:30432892 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84772766 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84772766 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:64894232 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:64894232 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:11851179 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:11851179 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:11205169 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:11205169 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:125579452 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:125579452 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:1081269 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:1081269 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:135514872 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:135514872 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:10355229 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:10355229 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:30411460 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:30411460 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:192279443 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:192279443 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:62842716 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:62842716 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:30252379 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:30252379 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:78570161 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:78570161 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:16918196 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:16918196 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:134062553 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:134062553 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:35284695 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:35284695 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:115769576 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:115769576 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:21185788 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:21185788 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152496740 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152496740 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152506570 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152506570 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:97314010 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:97314010 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:45097678 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:45097678 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:45169763 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:45169763 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:47850137 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:47850137 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:23939128 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:23939128 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:52508631 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:52508631 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:63768064 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:63768064 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3600383 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3600383 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:57077622 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:57077622 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:57111433 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:57111433 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:56419432 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:56419432 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:7060809 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:7060809 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:132628998 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:132628998 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:65732255 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:65732255 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:153659053 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:153659053 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:34873895 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:34873895 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:52432652 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:52432652 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:115393012 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:115393012 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:52257205 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:52257205 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:84745401 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:84745401 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:124615349 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:124615349 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:206592784 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:206592784 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:50724467 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:50724467 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:152034205 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:152034205 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:163297418 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:163297418 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:163298126 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:163298126 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:101092838 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:101092838 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:228524066 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:228524066 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:103563925 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:103563925 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:183601574 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:183601574 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:78431261 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:78431261 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:50943525 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:50943525 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158435309 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158435309 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:248005245 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:248005245 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158724583 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158724583 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:103848448 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:103848448 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:77749368 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:77749368 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29650532 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29650532 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:152553524 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:152553524 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:17419873 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:17419873 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:39591522 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:39591522 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125616668 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:125616668 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:91715981 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:91715981 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:233313729 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:233313729 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:41300874 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:41300874 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:178592719 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:178592719 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:178862725 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:178862725 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:20704680 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:20704680 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:145015659 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:145015659 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:55161584 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:55161584 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:39881490 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:39881490 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:15230633 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:15230633 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:32057849 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:32057849 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:74085688 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:74085688 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:133909618 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:133909618 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:64421016 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:64421016 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:16216937 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:16216937 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:106512939 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:106512939 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:201253094 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:201253094 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:32945691 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:32945691 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:42437892 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:42437892 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:42037727 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:42037727 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:64028865 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:64028865 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:131951130 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:131951130 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:143478 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:143478 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6527484 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:6527484 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:131829849 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:131829849 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:132070104 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:132070104 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:118220660 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:118220660 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:84622680 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:84622680 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:84634095 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:84634095 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133248725 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:133248725 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:121248715 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:121248715 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:43159971 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:43159971 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:16270054 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:16270054 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:29001907 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:29001907 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:146086014 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:146086014 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:133553776 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:133553776 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:69015264 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:69015264 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:69033338 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:69033338 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50087277 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50087277 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43514021 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43514021 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43514658 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43514658 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43593537 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43593537 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43762925 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:43762925 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:14542012 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:14542012 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:231974287 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:231974287 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:71327996 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:71327996 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:71440155 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:71440155 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:136936160 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:136936160 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:128562490 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:128562490 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:158007148 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:158007148 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:52359490 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:52359490 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:52384651 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:52384651 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:546697 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:546697 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:156038318 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:156038318 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:55948681 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:55948681 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:36253961 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:36253961 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:112190880 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:112190880 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:114776578 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:114776578 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:114806651 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:114806651 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:179554590 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:179554590 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:114271262 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:114271262 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:103292094 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:103292094 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:73200238 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:73200238 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:163044499 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:163044499 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:72936674 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:72936674 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:66837752 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:66837752 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:41165979 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:41165979 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152295111 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152295111 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:51503799 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:51503799 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:19317380 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:19317380 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:25353695 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:25353695 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:68914232 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:68914232 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:84946552 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:84946552 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:60069869 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:60069869 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:32351501 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:32351501 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:33842357 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:33842357 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:33936742 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:33936742 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:134988008 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:134988008 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:234249027 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:234249027 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:35545323 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:35545323 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:15884754 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:15884754 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:27737309 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:27737309 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:78177195 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:78177195 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:41494215 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:41494215 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:17371152 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:17371152 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:177937179 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:177937179 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:9379901 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:9379901 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:61260282 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:61260282 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:61264780 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:61264780 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:70566337 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:70566337 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:73188227 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:73188227 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:155885361 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:155885361 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:14095344 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:14095344 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:148431893 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:148431893 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:51219504 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:51219504 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:46655361 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:46655361 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:41086465 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:41086465 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:41096801 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:41096801 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:38621510 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:38621510 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160460354 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160460354 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160461211 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:160461211 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:1081937 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:1081937 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:1093801 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:1093801 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:43247685 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:43247685 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:119014743 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:119014743 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:116569383 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:116569383 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:73111579 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:73111579 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:306077 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:306077 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:20636079 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:20636079 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:20658582 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:20658582 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:21383871 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:21383871 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:111887582 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:111887582 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:143237104 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:143237104 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:57857302 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:57857302 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:168999359 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:168999359 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:109762904 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:109762904 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:10280117 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:10280117 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84270502 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84270502 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:25200235 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:25200235 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:121554374 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:121554374 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:51351205 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:51351205 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:51705152 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:51705152 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:26404578 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:26404578 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:179312688 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:179312688 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:596760 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:596760 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:106937734 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:106937734 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:231036339 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:231036339 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:231135278 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:231135278 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:45993410 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:45993410 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:52938359 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:52938359 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:52948508 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:52948508 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:177116476 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:177116476 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:35628520 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:35628520 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:101871226 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:101871226 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:55656572 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158606041 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158606041 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158614874 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158614874 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158641787 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158641787 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158644087 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158644087 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158654894 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:158654894 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:36031098 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:36031098 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:64458825 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:64458825 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:54870664 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:54870664 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:48051814 G>C maps to ENST00000513569 L1L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:48051814 G>C maps to ENST00000513569 L1L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:48054860 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chrX:48054860 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:242434975 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:242434975 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:43703612 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:43703612 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:180934679 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:180934679 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:37406458 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:37406458 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:12188314 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:12188314 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:152605311 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:152605311 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:33560309 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:33560309 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55686463 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55686463 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:62554783 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:62554783 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:61391610 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:61391610 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:75915565 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:75915565 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:162276664 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:162276664 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:45139896 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:45139896 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:119427302 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:119427302 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:85457844 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:85457844 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:114832747 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:114832747 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:114839575 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:114839575 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:139653161 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:139653161 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:139717651 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:139717651 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:59620550 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:59620550 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:151753940 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:151753940 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:6703939 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:6703939 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:1294797 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:1294797 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:51518685 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:51518685 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:100229590 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:100229590 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:2381106 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:2381106 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:134145974 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:134145974 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:169635040 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:169635040 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:2426158 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:2426158 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:70368532 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:70368532 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:166976146 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:166976146 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:35704835 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:35704835 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:63014512 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:63014512 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:102896703 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:102896703 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:19498263 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:19498263 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:112380943 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:112380943 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:44402813 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:44402813 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:15433871 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:15433871 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:95614447 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:95614447 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:25775239 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:25775239 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:133769388 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:133769388 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:112834998 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:112834998 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:112849174 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:112849174 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:69098030 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:69098030 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:68691761 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:68691761 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:19737571 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:19737571 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152235768 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:152235768 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:74737435 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:74737435 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:76045133 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:76045133 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:175332816 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:175332816 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:175396978 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:175396978 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:72332703 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:72332703 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:10971219 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:10971219 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:17199436 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:17199436 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:42233434 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:42233434 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:72863766 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:72863766 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:12880964 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:12880964 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:55033002 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:55033002 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:5663627 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:5663627 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:45052207 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:45052207 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:5930876 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:5930876 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:122824230 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:122824230 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:77415138 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:77415138 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:142571145 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:142571145 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:141957388 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:141957388 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:130370057 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:130370057 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50249626 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50249626 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:39176801 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:39176801 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:46679822 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:46679822 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:21663114 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:21663114 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:91084441 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:91084441 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:34934960 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:34934960 T>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:157041330 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:157041330 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:10206972 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:10206972 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:193028606 G>T maps to ENST00000417752 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:193028606 G>T maps to ENST00000417752 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:20355579 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:20355579 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:20360573 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:20360573 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:17532127 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:17532127 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:61431316 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:61431316 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:7838115 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:7838115 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:43746588 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:43746588 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:77904244 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:77904244 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:37010341 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:37010341 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:2844139 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:2844139 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:54636783 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:54636783 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:61042086 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:61042086 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:70880762 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:70880762 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:55475023 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:55475023 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:109538479 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:109538479 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:167319851 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:167319851 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:84357952 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:84357952 A>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:31570316 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:31570316 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:56362927 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:56362927 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:21357749 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:21357749 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:88688816 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:88688816 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:73445057 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:73445057 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:57293201 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:57293201 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:57654226 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:57654226 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:15609642 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:15609642 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:53321171 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:53321171 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:180679232 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:180679232 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:148815165 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:148815165 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:9643420 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:9643420 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:38287052 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:38287052 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:56973747 C>A maps to ENST00000342634 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:56973747 C>A maps to ENST00000342634 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3363301 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3363301 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:2936785 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:2936785 G>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:185798285 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:185798285 T>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:22952647 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:22952647 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:238053708 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:238053708 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:187694717 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:187694717 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:187701942 G>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:187701942 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:67210777 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:67210777 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:215846872 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:215846872 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:67012629 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:67012629 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:148622032 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:148622032 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:111542183 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:111542183 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:20559543 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:20559543 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:179294748 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:179294748 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:236902903 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:236902903 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:155029329 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:155029329 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:33560989 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:33560989 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:72492162 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:72492162 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:7773219 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:7773219 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:116058953 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:116058953 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:148060051 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:148060051 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:100627996 T>C maps to NM_001025108.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:100627996 T>C maps to NM_001025108.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:109663776 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:109663776 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:129066147 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:129066147 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:8756971 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:8756971 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:74283395 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:74283395 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:5127542 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:5127542 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:85406316 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:85406316 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:203836193 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:203836193 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:213174122 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:213174122 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:114153291 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:114153291 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:92676116 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:92676116 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:197873877 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:197873877 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:102973213 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:102973213 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:22257941 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:22257941 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:40996620 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:40996620 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:6422206 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:6422206 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:39440104 C>T maps to NM_001006666.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:39440104 C>T maps to NM_001006666.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:33395002 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:33395002 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:43218489 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:43218489 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:6498239 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:6498239 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:32925162 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:32925162 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:11242517 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:11242517 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:135765051 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:135765051 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:135827283 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:135827283 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:35763342 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:35763342 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:69497902 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:69497902 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:37968012 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:37968012 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197108021 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197108021 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:294776 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:294776 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:138832141 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:138832141 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:193025092 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:193025092 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153664275 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153664275 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:80962870 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:80962870 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:171536078 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:171536078 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:102221496 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:102221496 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:32906374 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:32906374 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:66106349 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:66106349 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100608448 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100608448 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100617921 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100617921 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:56383242 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:56383242 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:111789749 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:111789749 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:111951113 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:111951113 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:57233709 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:57233709 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:60466895 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:60466895 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:111891100 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:111891100 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:58855018 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:58855018 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:111091509 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:111091509 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:7835308 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:7835308 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:11778994 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:11778994 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:40536032 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:40536032 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:38374078 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:38374078 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:139707072 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:139707072 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:40055904 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:40055904 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:18789650 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:18789650 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:54483031 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:54483031 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:15098689 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:15098689 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:3785656 C>T maps to ENST00000381771 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:3785656 C>T maps to ENST00000381771 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:7806268 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:7806268 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:42703267 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:42703267 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:74128144 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:74128144 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:107394312 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:107394312 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:52826312 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:52826312 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:100605697 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:100605697 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158298650 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158298650 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:149963468 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:149963468 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:149963873 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:149963873 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:24578541 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:24578541 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:202671361 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:202671361 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:68564997 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:68564997 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:87795418 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:87795418 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:146747203 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:146747203 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40120548 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40120548 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:86898238 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:86898238 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:11900188 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:11900188 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:73770666 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:73770666 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:1326087 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:1326087 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:47939928 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:47939928 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:32794837 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:32794837 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:205022455 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:205022455 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:121344836 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:121344836 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:121353607 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:121353607 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:139618607 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:139618607 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:139815034 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:139815034 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:107834720 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:107834720 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:130025218 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:130025218 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:148545952 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:148545952 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:211539732 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:211539732 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:43911573 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:43911573 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:113347553 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:113347553 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:113421304 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:113421304 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:70822903 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:70822903 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:122908952 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:122908952 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100093505 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100093505 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:67654412 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:67654412 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:80835154 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:80835154 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:16635173 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:16635173 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:150776739 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:150776739 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:111655819 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:111655819 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:36004219 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:36004219 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:74654232 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:74654232 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:176893886 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:176893886 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:31240958 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:31240958 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:6735417 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:6735417 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:9174081 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:9174081 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:137363414 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:137363414 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:107543851 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:107543851 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:83691442 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:83691442 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:124344715 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:124344715 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:38994557 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:38994557 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:132242072 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:132242072 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:83851930 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:83851930 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:116572640 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:116572640 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:116599677 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:116599677 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:28991429 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:28991429 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45412253 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45412253 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45412271 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45412271 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:137807114 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:137807114 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:109546710 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:109546710 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:32694554 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:32694554 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:36909838 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:36909838 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:46119819 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:46119819 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:132172455 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:132172455 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:101460488 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:101460488 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:66286286 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:66286286 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:100319143 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:100319143 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:220192221 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:220192221 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:65317138 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:65317138 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:212285356 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:212285356 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:45856278 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:45856278 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:128045981 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:128045981 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:572865 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:572865 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:45808415 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:45808415 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:159190557 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:159190557 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197036431 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197036431 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:126126819 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:126126819 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:134186195 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:134186195 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:15254804 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:15254804 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:103433152 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:103433152 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:10696586 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:10696586 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:24977089 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:24977089 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:119419209 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:119419209 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:119427808 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:119427808 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:32793038 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:32793038 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:176518923 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:176518923 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153595358 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153595358 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:29001282 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:29001282 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33149411 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33149411 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:114211083 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:114211083 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:143823054 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:143823054 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:66082843 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:66082843 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:46979657 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:46979657 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:887088 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:887088 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:173150974 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:173150974 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:34893158 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:34893158 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:9822935 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:9822935 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:78578100 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:78578100 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:3586736 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:3586736 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:48248738 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:48248738 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:37369783 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:37369783 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:136113844 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:136113844 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:35506985 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:35506985 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:123396936 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:123396936 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:51752134 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:51752134 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:43032599 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:43032599 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26417909 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26417909 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:152735899 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:152735899 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:83807848 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:83807848 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:43351087 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:43351087 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:26020599 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:26020599 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:100401838 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:100401838 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:231973146 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:231973146 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:90631766 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:90631766 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:6660036 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:6660036 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:47120769 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:47120769 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130413219 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130413219 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130415601 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:130415601 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:142653879 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:142653879 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:81552229 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:81552229 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:57138357 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:57138357 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:79674655 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:79674655 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:156813290 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:156813290 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:75954152 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:75954152 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:33065808 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:33065808 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:102105125 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:102105125 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:744376 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:744376 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:20189656 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:20189656 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:103587001 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:103587001 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26950452 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26950452 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:154685908 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:154685908 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:66975182 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:66975182 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:62407301 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:62407301 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:15725369 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:15725369 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:118239128 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:118239128 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:39709007 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:39709007 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:47289106 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:47289106 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:9994721 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:9994721 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:52967081 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:52967081 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:31859728 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:31859728 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:71293930 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:71293930 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153136158 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153136158 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:42163092 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:42163092 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:112462406 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:112462406 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:183101834 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:183101834 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:169547627 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:169547627 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:36982964 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:36982964 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:103871401 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:103871401 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:88446741 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:88446741 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:202284116 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:202284116 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:90433626 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:90433626 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:126156597 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:126156597 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:121402390 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:121402390 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:99766553 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:99766553 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:151604508 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:151604508 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:42373272 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:42373272 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:133881686 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:133881686 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:141253063 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:141253063 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:169999057 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:169999057 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:62855490 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:62855490 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:99861639 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:99861639 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:235937104 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:235937104 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:110849154 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:110849154 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:136705033 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:136705033 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:85412595 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:85412595 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:151127161 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:151127161 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:70342571 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:70342571 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:48655938 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:48655938 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:44102150 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:44102150 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:40431305 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:40431305 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:74719312 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:74719312 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158811865 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158811865 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158813621 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158813621 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:29637847 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:29637847 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:154018220 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:154018220 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:59828951 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:59828951 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:64879046 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:64879046 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:63574637 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:63574637 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:42338445 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:42338445 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:10305147 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:10305147 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:46902371 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:46902371 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:52676245 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:52676245 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:128327343 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:128327343 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:12666289 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:12666289 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:102769309 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:102769309 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:55274255 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:55274255 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:15492217 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:15492217 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:19923453 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:19923453 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:8347561 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:8347561 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:21176969 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:21176969 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:27352560 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:27352560 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:70532269 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:70532269 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:204923915 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:204923915 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:145656639 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:145656639 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:119072666 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:119072666 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:55447574 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:55447574 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:26093725 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:26093725 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:26101544 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:26101544 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:120430667 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:120430667 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:155718294 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:155718294 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57288443 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57288443 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:161202759 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:161202759 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:107984429 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:107984429 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:131781261 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:131781261 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:16885520 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:16885520 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:101620780 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:101620780 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:28277089 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:28277089 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:70774242 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:70774242 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153418615 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153418615 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153421720 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153421720 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:2452902 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:2452902 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:164815780 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:164815780 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:101182954 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:101182954 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:55141238 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:55141238 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:95507528 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:95507528 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:152682228 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:152682228 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:54960445 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:54960445 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:129752874 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:129752874 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:123624695 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:123624695 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:45959699 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:45959699 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:53965685 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:53965685 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:71876216 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:71876216 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:47722852 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:47722852 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:111632706 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:111632706 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:130827666 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:130827666 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:47869271 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:47869271 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:47927829 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:47927829 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:110401228 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:110401228 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:14581141 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:14581141 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:201291061 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:201291061 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:8698257 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:8698257 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:9365071 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:9365071 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:114864413 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:114864413 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153696085 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153696085 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153032305 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153032305 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:134381679 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:134381679 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:76806096 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:76806096 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:120932010 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:120932010 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:94245747 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:94245747 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:53814146 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:53814146 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:106882521 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:106882521 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:170699422 C>A maps to NM_006902.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:170699422 C>A maps to NM_006902.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:119229817 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:119229817 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:43373201 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:43373201 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:43376281 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:43376281 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:43674208 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:43674208 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:24615524 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:24615524 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:43591062 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:43591062 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:804727 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:804727 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:97278973 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:97278973 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:71318404 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:71318404 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:15699782 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:15699782 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40748748 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40748748 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40864945 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40864945 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:52252090 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:52252090 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:22196398 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:22196398 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:88272378 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:88272378 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:106362202 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:106362202 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:91503243 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:91503243 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:65357913 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:65357913 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:79314757 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:79314757 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:100019321 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:100019321 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:111751795 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:111751795 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:32586719 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:32586719 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:183891505 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:183891505 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:192127896 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:192127896 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:163138003 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:163138003 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:46808291 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:46808291 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:144459533 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:144459533 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:12876533 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:12876533 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:87345619 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:87345619 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:31521113 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:31521113 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:30777388 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:30777388 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:124757234 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:124757234 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:94485905 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:94485905 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:39926171 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:39926171 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:166912248 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:166912248 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:99131971 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:99131971 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:155297922 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:155297922 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237865242 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237865242 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33603234 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33603234 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33765572 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:33765572 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:34103249 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:34103249 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:73695960 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:73695960 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:38912392 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:38912392 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:50307382 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:50307382 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:84710910 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:84710910 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:97527634 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:97527634 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:43835801 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:43835801 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:158551400 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:158551400 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:95058669 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:95058669 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:224866330 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:224866330 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:26746976 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:26746976 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:85894217 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:85894217 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:155935752 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:155935752 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:84286758 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:84286758 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:96339116 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:96339116 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:164709071 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:164709071 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:164777167 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:164777167 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:56906175 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:56906175 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:63177394 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:63177394 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:95751120 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:95751120 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:99083415 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:99083415 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:79257313 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:79257313 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:108618619 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:108618619 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:115588725 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:115588725 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:110740250 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:110740250 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:40875514 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:40875514 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:1271110 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:1271110 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:106924209 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:106924209 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:121340895 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:121340895 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:109878786 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:109878786 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:214878631 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:214878631 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:140358263 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:140358263 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:144329226 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:144329226 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:35795728 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:35795728 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:44166524 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:44166524 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:44351209 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:44351209 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153047318 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153047318 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153063470 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153063470 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:52543152 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:52543152 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:33687162 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:33687162 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:47767975 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:47767975 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:39136040 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:39136040 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:149883285 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:149883285 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:70842254 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:70842254 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:110020638 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:110020638 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:99941665 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:99941665 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100531744 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100531744 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:234565707 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:234565707 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:67173329 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:67173329 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:45788014 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:45788014 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:102864702 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:102864702 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:122745443 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:122745443 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:2785689 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:2785689 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:119290114 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:119290114 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:156353203 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:156353203 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153524395 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153524395 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153524472 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:153524472 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:60601555 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:60601555 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:98192885 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:98192885 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:12263848 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:12263848 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:62729957 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:62729957 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:43808469 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:43808469 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:113567947 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:113567947 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:117800391 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:117800391 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:51397543 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:51397543 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:150444786 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:150444786 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:99849084 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:99849084 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:45395767 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:45395767 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:10908759 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:10908759 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:10919994 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:10919994 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:10942694 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr21:10942694 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:248039119 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:248039119 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100296847 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:100296847 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:81449855 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:81449855 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:54467056 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:54467056 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:22873412 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:22873412 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:19886633 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:19886633 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:157046906 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:157046906 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:118244005 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:118244005 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:42571301 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:42571301 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:54528768 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:54528768 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:91485503 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:91485503 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:33507864 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:33507864 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:33891882 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:33891882 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:215955618 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:215955618 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:216143890 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:216143890 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:216380496 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:216380496 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:31221209 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:31221209 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:154467158 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:154467158 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:100515036 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:100515036 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:62167001 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:62167001 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:22160990 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:22160990 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:61036366 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:61036366 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:117576742 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:117576742 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:53992224 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:53992224 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:68371993 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:68371993 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:96062228 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:96062228 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:13896332 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:13896332 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:111637935 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:111637935 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:21840350 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:21840350 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:17202973 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:17202973 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:72008595 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:72008595 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:142148039 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:142148039 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:31137435 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:31137435 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:57081615 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:57081615 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:84502437 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chrX:84502437 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:53950357 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:53950357 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:2373950 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:2373950 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:39008873 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:39008873 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:43769119 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:43769119 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:71465165 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:71465165 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:197951378 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:197951378 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:112111218 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:112111218 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:62139190 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:62139190 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:59147601 T>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:59147601 T>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:42254908 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:42254908 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr18:20951313 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr18:20951313 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:43495091 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:43495091 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:37210109 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:37210109 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:158326736 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:158326736 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:205496884 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:205496884 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:48687842 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:48687842 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:26510819 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:26510819 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:177683771 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:177683771 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:238267584 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:238267584 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr10:17171410 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr10:17171410 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:47957010 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:47957010 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:103091299 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:103091299 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:120599259 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:120599259 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr13:107862818 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr13:107862818 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr15:48748733 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr15:48748733 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:130062386 A>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:130062386 A>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:6556068 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:6556068 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:9862488 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:9862488 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:5593034 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:5593034 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:5593048 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:5593048 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:31619166 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:31619166 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr7:43351738 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr7:43351738 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr22:19422609 T>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr22:19422609 T>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr22:19422620 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr22:19422620 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:75108760 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:75108760 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr10:70987199 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr10:70987199 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:8822876 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:8822876 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:206944676 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:206944676 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr7:110526547 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr7:110526547 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:24655207 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:24655207 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:5077622 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:5077622 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:48424329 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:48424329 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:52886387 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:52886387 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:63276239 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:63276239 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:210570268 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:210570268 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:1248465 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:1248465 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:23875077 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:23875077 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:171376146 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:171376146 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:2065467 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:2065467 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:16068233 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:16068233 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:7229742 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:7229742 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:50733934 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:50733934 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr13:53623967 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr13:53623967 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:4673702 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:4673702 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:125647221 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:125647221 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:47319543 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:47319543 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:71692396 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:71692396 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:77660946 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:77660946 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:77660948 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:77660948 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:151196535 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:151196535 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr10:102057076 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr10:102057076 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:125301292 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:125301292 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:125301294 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:125301294 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:46687658 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:46687658 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:52724219 A>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:52724219 A>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:43585543 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:43585543 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:198672354 T>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:198672354 T>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr20:40738886 T>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr20:40738886 T>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:182569398 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:182569398 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:72943384 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:72943384 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:240933963 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:240933963 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:78349499 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:78349499 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:124735450 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:124735450 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:151798207 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:151798207 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:150337419 A>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:150337419 A>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chrX:134993298 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chrX:134993298 G>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr7:100454814 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr7:100454814 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:482624 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:482624 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:18827945 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:18827945 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:109893505 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:109893505 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:91025541 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:91025541 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:52547712 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:52547712 G>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:104118708 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:104118708 A>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:89962362 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:89962362 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:124163705 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:124163705 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:12926486 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:12926486 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:32544366 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:32544366 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:113193901 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:113193901 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:103269855 T>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:103269855 T>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:49340810 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:49340810 T>C did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:155650111 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:155650111 C>A did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:87447788 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr16:87447788 C>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:44496101 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:44496101 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:38029468 A>G did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:38029468 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:169783582 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:169783582 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:38913014 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:38913014 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:119976541 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:119976541 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr18:31263625 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr18:31263625 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:68031131 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:68031131 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr12:102558193 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr12:102558193 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr15:34434616 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr15:34434616 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:13769339 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:13769339 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr21:46057209 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr21:46057209 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:14744487 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:14744487 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:57346990 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:57346990 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:227171428 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:227171428 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:81601252 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:81601252 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:110494549 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:110494549 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr10:70525870 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr10:70525870 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:89430471 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:89430471 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:28512754 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:28512754 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:68720455 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:68720455 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:55897367 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:55897367 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:74350995 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:74350995 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:33143525 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:33143525 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:116994043 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:116994043 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:211459168 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:211459168 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:43276569 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:43276569 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:100188435 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:100188435 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:71146413 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:71146413 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:13769342 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:13769342 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:154519721 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:154519721 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:36958824 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:36958824 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:68929762 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:68929762 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:102584583 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:102584583 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:161488755 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:161488755 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:31070940 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:31070940 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:31167615 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:31167615 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:70443553 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:70443553 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:134241563 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:134241563 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:26499866 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:26499866 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:37208592 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:37208592 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr4:89393448 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr4:89393448 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:35677951 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:35677951 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:210686420 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:210686420 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:70923335 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:70923335 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:95878458 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:95878458 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:124048677 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:124048677 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:48823095 G>A maps to ENST00000419374 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:48823095 G>A maps to ENST00000419374 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr21:38997455 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr21:38997455 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142659419 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142659419 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:2829736 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:2829736 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:197403693 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:197403693 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr4:38690077 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr4:38690077 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:75622784 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:75622784 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:96432671 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:96432671 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:148342122 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:148342122 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:133886350 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:133886350 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:70655047 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:70655047 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:133637714 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:133637714 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:242159716 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:242159716 T>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr19:18239660 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr19:18239660 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr19:8998960 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr19:8998960 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr15:59564493 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr15:59564493 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr13:101844426 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr13:101844426 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:20959498 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:20959498 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:169337006 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:169337006 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:132082071 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:132082071 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:26689015 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:26689015 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:233152649 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:233152649 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:47599497 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr16:47599497 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:94341928 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:94341928 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:38803581 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:38803581 G>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:46939860 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:46939860 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:31921392 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:31921392 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:73659096 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:73659096 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:8846666 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:8846666 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:74477372 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:74477372 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156347349 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156347349 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:124764000 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:124764000 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:11355541 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:11355541 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr18:33611088 A>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr18:33611088 A>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:237666864 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:237666864 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr22:18073120 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr22:18073120 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:1244641 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:1244641 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:61296197 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:61296197 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:217975237 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:217975237 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:48058166 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chrX:48058166 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:149691269 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:149691269 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:85533695 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:85533695 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:168153121 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:168153121 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:4685708 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:4685708 A>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr15:81665101 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr15:81665101 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:103207490 C>T maps to NM_001198807.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:103207490 C>T maps to NM_001198807.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:77715823 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:77715823 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr21:19737630 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr21:19737630 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:218677213 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:218677213 C>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:14419789 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr5:14419789 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142574349 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142574349 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:48920944 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:48920944 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:24166724 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:24166724 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:100827082 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:100827082 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:55451630 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:55451630 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:148771459 T>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:148771459 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:215866253 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:215866253 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:215976247 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:215976247 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:119030877 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:119030877 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:44102556 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:44102556 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:179190910 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:179190910 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:15059113 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:15059113 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:77465554 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:77465554 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:84559959 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:84559959 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:943703 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:943703 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:78399860 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:78399860 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:147924846 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:147924846 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:12356494 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:12356494 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:178305771 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:178305771 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:241817406 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:241817406 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:5045923 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:5045923 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:104192003 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:104192003 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:109459670 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:109459670 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:92680670 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:92680670 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:37422838 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:37422838 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:37490273 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:37490273 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:33386949 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:33386949 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:93772008 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:93772008 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:109249474 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:109249474 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:7558816 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:7558816 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:50154323 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:50154323 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:15687018 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:15687018 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:19680368 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:19680368 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:30926059 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:30926059 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:31649503 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:31649503 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:37153741 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:37153741 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:41196040 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:41196040 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:40965100 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:40965100 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:140941315 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:140941315 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:81579631 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:81579631 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:159169441 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:159169441 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:12802847 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:12802847 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:3773206 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:3773206 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:30869283 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:30869283 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:3023560 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:3023560 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:104966936 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:104966936 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:121994652 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:121994652 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:105453049 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:105453049 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:105572072 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:105572072 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:14031828 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:14031828 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:110595236 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:110595236 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:159035631 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:159035631 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:540999 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:540999 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:43478085 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:43478085 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:112538751 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:112538751 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:149964082 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:149964082 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:137622830 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:137622830 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:59217105 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:59217105 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:25466681 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:25466681 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:56886972 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:56886972 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:34061601 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:34061601 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:42552876 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:42552876 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:233391498 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:233391498 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:76555336 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:76555336 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:76555338 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:76555338 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:40273553 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:40273553 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:189859866 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:189859866 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:111156435 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:111156435 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:68582655 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:68582655 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:61988472 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:61988472 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:18131616 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:18131616 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:67726512 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:67726512 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:36007661 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:36007661 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:72049684 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:72049684 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:90322341 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:90322341 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:114449825 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:114449825 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:61886044 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:61886044 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:124380531 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:124380531 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:20963676 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:20963676 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:68036930 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:68036930 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:32949604 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:32949604 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:57672278 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:57672278 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:107148345 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:107148345 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:132148041 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:132148041 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:41513147 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:41513147 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:89157042 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:89157042 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:222307543 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:222307543 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:56479038 A>T maps to NM_001005915.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:56479038 A>T maps to NM_001005915.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:64727070 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:64727070 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:74079891 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:74079891 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:184792549 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:184792549 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:190423728 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:190423728 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:5404730 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:5404730 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:48713015 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:48713015 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:137776489 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:137776489 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:17129688 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:17129688 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:28897158 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:28897158 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:171308805 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:171308805 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:89392960 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:89392960 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:49214304 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:49214304 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:37729896 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:37729896 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:37732275 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:37732275 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:27128270 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:27128270 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:130147291 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:130147291 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:74863359 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:74863359 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:33981819 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:33981819 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:38016147 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:38016147 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:121741978 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:121741978 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:34678732 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:34678732 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:133086983 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:133086983 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:24467099 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:24467099 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:24467376 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:24467376 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:176883576 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:176883576 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:119911989 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:119911989 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:40365548 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:40365548 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:158257520 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:158257520 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:176860329 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:176860329 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:110258522 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:110258522 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:72978357 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:72978357 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:73624437 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:73624437 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:18767184 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:18767184 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:73988937 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:73988937 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:96342621 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:96342621 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:28465958 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:28465958 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:100544123 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:100544123 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:29795819 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:29795819 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:29797815 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:29797815 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:26043725 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:26043725 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:204822743 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:204822743 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:57938863 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:57938863 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:52347217 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:52347217 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:173337486 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:173337486 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:31383837 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:31383837 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:102366763 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:102366763 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:6058530 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:6058530 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:42128461 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:42128461 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:163374207 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:163374207 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:88693989 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:88693989 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:6834952 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:6834952 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:55948681 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:55948681 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:55980228 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:55980228 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:154547493 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:154547493 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:118671180 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:118671180 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:44856677 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:44856677 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:73649768 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:73649768 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:39633212 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:39633212 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:39642596 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:39642596 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:145562166 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:145562166 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:67976567 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:67976567 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:145749478 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:145749478 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:40709160 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:40709160 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:235902103 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:235902103 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:39889967 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:39889967 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:47311392 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:47311392 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:160585753 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:160585753 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:63665607 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:63665607 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:54823835 G>A maps to ENST00000371389 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:54823835 G>A maps to ENST00000371389 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:168840364 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:168840364 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:6378708 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:6378708 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:99260595 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:99260595 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:21914612 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:21914612 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:1156350 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:1156350 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:1159474 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:1159474 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:113547036 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:113547036 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10249060 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10249060 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10263212 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10263212 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10552067 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10552067 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10355108 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:10355108 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:171458103 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:171458103 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:76462572 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:76462572 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:77211916 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:77211916 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:29957720 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:29957720 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:56370625 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:56370625 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:56392775 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:56392775 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:107820584 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:107820584 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:184022341 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:184022341 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:55872385 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:55872385 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:163378548 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:163378548 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:40568119 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:40568119 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:102569128 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:102569128 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:141324867 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:141324867 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:142546351 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:142546351 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:95761716 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:95761716 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:149245633 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:149245633 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:54343298 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:54343298 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:55131304 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:55131304 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:20387363 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:20387363 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:20395881 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:20395881 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:15135094 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:15135094 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:3845732 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:3845732 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:41864684 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:41864684 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:209197944 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:209197944 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:25156025 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr22:25156025 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:42284545 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:42284545 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:186919870 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:186919870 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:186919897 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:186919897 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:9424732 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:9424732 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:114874715 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:114874715 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:44538800 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:44538800 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:22335603 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:22335603 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:77746666 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:77746666 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:203453307 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:203453307 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:47295776 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:47295776 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:95953075 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:95953075 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:93617189 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:93617189 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:80943238 T>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:80943238 T>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:43770474 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:43770474 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:102989094 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:102989094 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:65340941 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:65340941 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:56169595 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:56169595 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:88971581 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:88971581 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:40877312 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:40877312 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:511243 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:511243 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:174245088 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:174245088 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:131348487 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:131348487 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:43694487 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:43694487 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:48386069 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:48386069 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:11508066 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:11508066 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:101008818 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:101008818 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:99140712 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:99140712 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:57247895 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:57247895 T>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:122990038 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:122990038 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:12145633 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:12145633 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:125299663 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:125299663 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:54827005 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:54827005 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:25823804 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:25823804 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:30389861 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:30389861 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:224862774 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:224862774 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr21:37423715 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr21:37423715 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:14167017 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:14167017 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:148410978 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:148410978 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:51960404 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:51960404 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:118606340 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:118606340 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:71250058 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:71250058 A>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:22675637 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:22675637 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:123844150 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:123844150 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:123978212 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:123978212 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:55912899 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:55912899 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:94877732 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:94877732 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:52679340 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:52679340 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:171482522 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:171482522 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:84652800 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:84652800 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:85431870 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:85431870 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:122635726 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:122635726 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:59560243 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:59560243 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:156838450 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:156838450 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:90446980 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:90446980 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65155502 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65155502 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65275150 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65275150 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:43545698 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:43545698 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:71634019 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:71634019 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:7999931 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:7999931 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:173174473 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:173174473 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:18044193 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:18044193 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:189026282 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:189026282 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:73457897 G>T maps to ENST00000377097 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:73457897 G>T maps to ENST00000377097 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:2114536 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:2114536 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:67855192 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:67855192 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:80718251 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:80718251 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:19755833 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr13:19755833 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:19505756 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:19505756 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:17740001 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:17740001 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:118905429 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:118905429 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:118922640 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:118922640 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:215955620 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:215955620 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:50757150 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:50757150 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrY:14928328 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrY:14928328 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:155128065 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:155128065 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:85593953 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:85593953 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:54358405 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:54358405 A>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:10066715 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chrX:10066715 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:87414504 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:87414504 A>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:38799567 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:38799567 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:138739810 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:138739810 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:3452492 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:3452492 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:28971176 T>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:28971176 T>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:30934398 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:30934398 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:59487 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:59487 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:22379628 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:22379628 G>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:238048889 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:238048889 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:982512 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:982512 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:45743382 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:45743382 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:78146363 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:78146363 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:91982015 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:91982015 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:241494530 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:241494530 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:6422340 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:6422340 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:41748685 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:41748685 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:31602154 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:31602154 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:92573633 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:92573633 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:45928509 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:45928509 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:129009783 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:129009783 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:159928476 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:159928476 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:6641715 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:6641715 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr22:37098676 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr22:37098676 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:95186490 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:95186490 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:71038445 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:71038445 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:205033424 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:205033424 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:70890295 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:70890295 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:55939118 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:55939118 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:100903981 A>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:100903981 A>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:91147758 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:91147758 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:10865777 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:10865777 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:41700442 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:41700442 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:12973174 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:12973174 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:109027176 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:109027176 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr18:29039788 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr18:29039788 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:41852074 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:41852074 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:44016898 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:44016898 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:55591905 C>T maps to NM_017729.3 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:55591905 C>T maps to NM_017729.3 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:67636994 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:67636994 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:133579024 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:133579024 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:46870827 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:46870827 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:175162375 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:175162375 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:147007155 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:147007155 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:65115562 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:65115562 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:140036331 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:140036331 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:13764647 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:13764647 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:119927726 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:119927726 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:28443943 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:28443943 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:54448628 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:54448628 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:153052786 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:153052786 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:1539500 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:1539500 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:95418916 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:95418916 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:3601087 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:3601087 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:187506320 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:187506320 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:5753319 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:5753319 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr13:113960769 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr13:113960769 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:71971672 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:71971672 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:75596380 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:75596380 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:105509130 T>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:105509130 T>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:46920262 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:46920262 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:70505614 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:70505614 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:126755908 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:126755908 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:88767656 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:88767656 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:109769928 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:109769928 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:102647007 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:102647007 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:55467348 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:55467348 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:108127030 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:108127030 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:158475832 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:158475832 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:24985430 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:24985430 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:124821201 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:124821201 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:15177201 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:15177201 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:135285514 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:135285514 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:24882640 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:24882640 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:55587135 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:55587135 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:55591056 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:55591056 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140165824 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140165824 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:17818029 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:17818029 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:47599959 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:47599959 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:41475704 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:41475704 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:49348608 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:49348608 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:39503774 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:39503774 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:23523133 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:23523133 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:43679766 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:43679766 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:159854886 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:159854886 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:27042373 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:27042373 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:33123194 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:33123194 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:65429627 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:65429627 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:7403234 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:7403234 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:21387668 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:21387668 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:74161668 A>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:74161668 A>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:38082377 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:38082377 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:25689776 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:25689776 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:17993110 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:17993110 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:21391851 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:21391851 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:217332864 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:217332864 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:246078978 T>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:246078978 T>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:130781700 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:130781700 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:144337425 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chrX:144337425 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:158609494 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:158609494 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:53224673 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr14:53224673 T>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:74179871 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:74179871 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:17208217 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:17208217 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:95541261 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:95541261 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:133918917 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:133918917 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:35714489 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:35714489 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:422753 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:422753 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:69097144 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:69097144 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:38572869 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:38572869 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:43733844 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr15:43733844 T>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:71510507 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:71510507 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:14479322 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:14479322 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr13:38266508 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr13:38266508 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:142572120 A>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:142572120 A>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:19513905 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:19513905 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:82815142 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:82815142 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:12406729 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:12406729 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:98914296 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:98914296 G>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:38176356 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:38176356 C>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:7606057 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:7606057 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:114069075 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:114069075 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:66992177 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:66992177 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:20767913 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:20767913 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:76209731 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:76209731 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:160197117 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:160197117 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:74035913 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:74035913 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:130342846 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:130342846 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:5239468 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:5239468 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:2899890 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:2899890 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:109854400 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:109854400 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:5149576 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:5149576 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:122602923 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:122602923 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:36093480 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:36093480 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:46717451 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:46717451 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:69009335 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:69009335 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:17939524 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:17939524 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:9839246 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:9839246 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:176914971 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:176914971 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:177030186 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:177030186 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:3909445 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:3909445 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:14614094 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:14614094 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:194162268 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:194162268 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:71170773 C>A maps to ENST00000454446 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:71170773 C>A maps to ENST00000454446 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:52549455 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:52549455 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:50209299 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:50209299 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:66113717 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:66113717 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:69949009 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:69949009 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:57076057 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:57076057 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:12819450 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:12819450 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:161337543 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:161337543 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:42679890 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:42679890 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:230907902 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:230907902 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:40949362 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:40949362 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:77244585 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:77244585 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:61592163 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:61592163 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:45067251 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:45067251 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:158326238 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:158326238 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:83531763 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:83531763 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr22:47108060 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr22:47108060 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:22217942 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:22217942 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:99827746 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:99827746 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:51287418 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:51287418 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:106888995 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:106888995 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:75865596 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:75865596 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:137702057 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:137702057 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:15018943 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:15018943 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:61196558 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:61196558 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:125530396 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:125530396 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:111655814 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:111655814 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:113599211 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:113599211 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr22:32179815 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr22:32179815 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:83195377 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:83195377 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:3814284 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:3814284 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:124383374 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:124383374 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:21627829 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:21627829 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:65864390 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:65864390 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:225796405 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:225796405 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:29203100 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:29203100 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:201980436 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:201980436 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:42522219 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:42522219 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:55591925 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:55591925 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:62175961 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:62175961 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:27657268 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:27657268 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:133833719 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:133833719 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:75538400 C>T maps to NM_024643.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:75538400 C>T maps to NM_024643.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:95483489 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:95483489 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:18148757 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:18148757 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:49175537 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:49175537 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:32793060 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:32793060 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:29588850 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:29588850 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:26805961 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:26805961 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:151818863 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:151818863 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:155143787 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:155143787 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:34897064 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:34897064 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:89478854 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:89478854 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:58009912 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:58009912 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:119912331 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:119912331 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:120745793 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:120745793 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:42165141 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:42165141 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:81374495 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:81374495 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:27782692 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:27782692 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:32975457 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:32975457 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:186143843 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:186143843 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:186392678 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:186392678 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:15753911 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:15753911 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:220315072 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:220315072 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:65678088 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:65678088 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:160501156 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:160501156 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:156810665 C>T maps to NM_014215.2 *1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:156810665 C>T maps to NM_014215.2 *1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:154586908 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:154586908 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:176638 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:176638 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:15702968 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:15702968 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:39913799 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:39913799 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:62995865 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:62995865 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:42796188 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:42796188 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:22697142 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:22697142 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:123145927 T>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:123145927 T>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:13211351 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:13211351 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:47371348 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:47371348 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:70462251 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:70462251 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:169995973 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:169995973 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:192564 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:192564 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:119611953 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:119611953 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:47504064 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:47504064 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:41281417 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:41281417 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:37038070 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:37038070 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:121444217 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:121444217 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:139071428 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:139071428 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:109874365 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:109874365 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:35769992 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:35769992 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:120382096 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:120382096 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:134022748 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:134022748 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:134055514 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:134055514 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:54901765 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:54901765 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:56125128 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:56125128 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:29639350 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:29639350 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:110435467 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chrX:110435467 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:206305414 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:206305414 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:47329120 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:47329120 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:17417242 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:17417242 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:20782724 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:20782724 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:95575564 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:95575564 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:125280831 T>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:125280831 T>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:64021839 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:64021839 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:161172986 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:161172986 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:118307816 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:118307816 T>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:26684621 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:26684621 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:145175887 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:145175887 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:50388346 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:50388346 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:31923084 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:31923084 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:18237314 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:18237314 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:118458669 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:118458669 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:151318884 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:151318884 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:45241247 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:45241247 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:107066957 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:107066957 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:9853987 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:9853987 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:108233862 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:108233862 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:169563825 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:169563825 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:179974755 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:179974755 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:134638414 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:134638414 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:116746210 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:116746210 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:22397982 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:22397982 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:75683501 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:75683501 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:92671491 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:92671491 T>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:50488029 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:50488029 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:18846502 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:18846502 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:44881426 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:44881426 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:65240237 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:65240237 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:94800705 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:94800705 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:104157099 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:104157099 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:40362174 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:40362174 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:36809701 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:36809701 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:210126111 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:210126111 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:61678783 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:61678783 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:61428569 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr17:61428569 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:150459922 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:150459922 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:98543345 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:98543345 G>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:3047195 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:3047195 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:72875087 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:72875087 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:184769582 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:184769582 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:1126339 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:1126339 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:1130581 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:1130581 A>C did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:37379307 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:37379307 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:7687784 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:7687784 G>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:72036449 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:72036449 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:176467987 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:176467987 A>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:57037371 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:57037371 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119029535 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119029535 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:27149636 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:27149636 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:132338228 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:132338228 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:89386531 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:89386531 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:78485718 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:78485718 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:5567584 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:5567584 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100244945 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100244945 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:5303903 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:5303903 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:77398296 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:77398296 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:43777547 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:43777547 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:43837706 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:43837706 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:64587608 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:64587608 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:7521031 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:7521031 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:24788448 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:24788448 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:111878264 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:111878264 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:67366086 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:67366086 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:75936566 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:75936566 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:50310438 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:50310438 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:76357714 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:76357714 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:16904837 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:16904837 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:109667789 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:109667789 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:241817580 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:241817580 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:241817590 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:241817590 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:39466624 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:39466624 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:19630929 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:19630929 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:74275210 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:74275210 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:101434149 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:101434149 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:125856648 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:125856648 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:233272932 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:233272932 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:202593400 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:202593400 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:110824110 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:110824110 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:113748488 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:113748488 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:61941080 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:61941080 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:54517824 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:54517824 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:54517844 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:54517844 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:101295475 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:101295475 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:101413922 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:101413922 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:419808 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:419808 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:80899155 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:80899155 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:130000092 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:130000092 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:68087703 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:68087703 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:143959610 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:143959610 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:69040403 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:69040403 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:119102196 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:119102196 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:16525581 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:16525581 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:74865419 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:74865419 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:23290986 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:23290986 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:52844125 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:52844125 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:35757083 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:35757083 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:4621895 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:4621895 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:140508732 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:140508732 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:78076129 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:78076129 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:62438717 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:62438717 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:119187756 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:119187756 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:160016543 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:160016543 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10413447 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10413447 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:152807403 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:152807403 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:152825151 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:152825151 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:114306063 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:114306063 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57037164 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57037164 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:81601412 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:81601412 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:42571226 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:42571226 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:35746839 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:35746839 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:142279074 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:142279074 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:41744067 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:41744067 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:99566080 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:99566080 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:69348552 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:69348552 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:31659340 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:31659340 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:58804728 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:58804728 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:889614 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:889614 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:112673090 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:112673090 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103420526 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103420526 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:45686181 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:45686181 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:74193517 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:74193517 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:56619363 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:56619363 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:40834483 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:40834483 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:179497458 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:179497458 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:182869052 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:182869052 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:75102181 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:75102181 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:2519923 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:2519923 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:20055048 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:20055048 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:46122236 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:46122236 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:200824635 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:200824635 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:74808758 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:74808758 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:165703311 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:165703311 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:40937516 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:40937516 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:42971888 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:42971888 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:120765986 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:120765986 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:30127184 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:30127184 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:53803959 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:53803959 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:48695520 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:48695520 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:1983717 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:1983717 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:18789698 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:18789698 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:12845175 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:12845175 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:110495760 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:110495760 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:104934645 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:104934645 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119149038 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119149038 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:54635430 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:54635430 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:97763934 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:97763934 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:57741599 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:57741599 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119034 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119034 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119140 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119140 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119230 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119230 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119550 C>G maps to NM_001080850.2 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119550 C>G maps to NM_001080850.2 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:150565159 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:150565159 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:32724509 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:32724509 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:55573253 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:55573253 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:34310984 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:34310984 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:56122989 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:56122989 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:158146771 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:158146771 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:167487603 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:167487603 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:44756740 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:44756740 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:60886358 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:60886358 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:115022718 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:115022718 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:110522909 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:110522909 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:91967260 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:91967260 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:95186574 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:95186574 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:25616604 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:25616604 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:60508195 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:60508195 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:130551823 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:130551823 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:115152131 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:115152131 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:15502018 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:15502018 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:56877750 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:56877750 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:620503 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:620503 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:50863530 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:50863530 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:51018041 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:51018041 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:59063359 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:59063359 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:42794337 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:42794337 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10030085 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10030085 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:14706195 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:14706195 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:10151727 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:10151727 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:7830239 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:7830239 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7295952 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7295952 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:21609322 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:21609322 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:21613539 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:21613539 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:17143190 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:17143190 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:41419235 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:41419235 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:74347061 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:74347061 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:51097336 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:51097336 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:103548295 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:103548295 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:71654492 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:71654492 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:105814995 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:105814995 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:70894643 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:70894643 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:56141374 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:56141374 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:177675174 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:177675174 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:110853875 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:110853875 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:107430275 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:107430275 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:189921587 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:189921587 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:47536541 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:47536541 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:47643887 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:47643887 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:120876392 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:120876392 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:129945770 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:129945770 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:8608443 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:8608443 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:207883748 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:207883748 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:197191609 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:197191609 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:3209247 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:3209247 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:49701584 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:49701584 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:75944502 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:75944502 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:34286002 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:34286002 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:113871357 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:113871357 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:104384793 T>A maps to ENST00000297577 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:104384793 T>A maps to ENST00000297577 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:57571959 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:57571959 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:48993370 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:48993370 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:118765376 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:118765376 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:99311208 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:99311208 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:15997121 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:15997121 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:47534476 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:47534476 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:20015206 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:20015206 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:90315015 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:90315015 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100680342 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100680342 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:155255944 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:155255944 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:126414280 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:126414280 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:65995142 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:65995142 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:59934548 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:59934548 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:14789810 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:14789810 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:137270094 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:137270094 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:137284474 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:137284474 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:50167175 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:50167175 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:46397830 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:46397830 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:154002885 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:154002885 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:11990114 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:11990114 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:13890988 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:13890988 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:196759991 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:196759991 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:100844367 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:100844367 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:131004652 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:131004652 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:109023180 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:109023180 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7867685 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7867685 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:109046776 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:109046776 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:117302209 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:117302209 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:28923406 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:28923406 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:32457820 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:32457820 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:118183684 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:118183684 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:45398545 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:45398545 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:57671873 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:57671873 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:96285424 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:96285424 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:74913999 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:74913999 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:83360667 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:83360667 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:120820375 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:120820375 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:120820463 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:120820463 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:78111830 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:78111830 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:45022657 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:45022657 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:42508130 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:42508130 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:111469591 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:111469591 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:132534821 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:132534821 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:143094630 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:143094630 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:110293209 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:110293209 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:11147724 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:11147724 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:45717764 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:45717764 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:133783724 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:133783724 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:51425435 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:51425435 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:53122713 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:53122713 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:73118705 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:73118705 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:73118752 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:73118752 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:73120511 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:73120511 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:150398826 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:150398826 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:114455050 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:114455050 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:24850198 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:24850198 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:29463876 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:29463876 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:99017618 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:99017618 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127782299 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127782299 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:55765773 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:55765773 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:17892000 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:17892000 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:125131772 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:125131772 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:102671009 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:102671009 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:34266981 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:34266981 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:240307674 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:240307674 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:240555899 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:240555899 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:42654377 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:42654377 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:108939442 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:108939442 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:114293953 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:114293953 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:131214382 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:131214382 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:37731136 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:37731136 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:12725091 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:12725091 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:52781493 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:52781493 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:180679406 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:180679406 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:27586133 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:27586133 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:34648933 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:34648933 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:158363923 G>A maps to ENST00000482640 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:158363923 G>A maps to ENST00000482640 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:134244035 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:134244035 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:96010234 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:96010234 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:155654098 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:155654098 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:2834838 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:2834838 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:19776222 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:19776222 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:36229172 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:36229172 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:58750104 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:58750104 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:20331192 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:20331192 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:135455293 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:135455293 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:46824576 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:46824576 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:133246449 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:133246449 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:87487603 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:87487603 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:120707555 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:120707555 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:7188114 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:7188114 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:114005343 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:114005343 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:30539655 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:30539655 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:108719258 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:108719258 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:25101351 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:25101351 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:73775079 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:73775079 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:15631041 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:15631041 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:26416384 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:26416384 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:26453224 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:26453224 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:1872290 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:1872290 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:5566772 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:5566772 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:141014297 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:141014297 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:240066123 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:240066123 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:18869187 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:18869187 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:156714212 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:156714212 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:50118313 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:50118313 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:50617249 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:50617249 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:50617271 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:50617271 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:28510944 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:28510944 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:210536153 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:210536153 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:27668978 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:27668978 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:40720185 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:40720185 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:35661071 G>T maps to NM_001003681.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:35661071 G>T maps to NM_001003681.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:179048120 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:179048120 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:245017936 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:245017936 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:63230946 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:63230946 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:95022601 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:95022601 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:1066896 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:1066896 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:79119869 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:79119869 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:1613986 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:1613986 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:110628657 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:110628657 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:137332382 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:137332382 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:62365225 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:62365225 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:15198740 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:15198740 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:1527662 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:1527662 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:66610873 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:66610873 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:32990274 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:32990274 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:42466540 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:42466540 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:30495337 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:30495337 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:40708233 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:40708233 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:5155204 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:5155204 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:61607428 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:61607428 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:62078083 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:62078083 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:7015829 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:7015829 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:136637453 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:136637453 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:35731875 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:35731875 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:35732110 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:35732110 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:15694694 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:15694694 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:27788409 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:27788409 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:36859597 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:36859597 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:168445426 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:168445426 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:202880398 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:202880398 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:20805969 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:20805969 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:86868837 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:86868837 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:241725668 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:241725668 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:160253516 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:160253516 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:117013442 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:117013442 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:62677092 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:62677092 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:41605589 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:41605589 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:42164411 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:42164411 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:55019475 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:55019475 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:169685926 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:169685926 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:54483819 T>A maps to ENST00000420619 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:54483819 T>A maps to ENST00000420619 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:189704524 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:189704524 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:18391146 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:18391146 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:71973991 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:71973991 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:55107415 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:55107415 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:156476919 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:156476919 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:100915783 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:100915783 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:1488650 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:1488650 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:39976175 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:39976175 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:170060865 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:170060865 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:48462736 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:48462736 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:40697714 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:40697714 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:47647671 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:47647671 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:2108766 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:2108766 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:152481990 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:152481990 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:75654117 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:75654117 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:44067476 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:44067476 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220799632 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220799632 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:51729158 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:51729158 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:13884562 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:13884562 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:6335039 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:6335039 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:70360842 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:70360842 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:3410312 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:3410312 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:21465050 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:21465050 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:8643647 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:8643647 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:151853436 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:151853436 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:21884229 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:21884229 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56230704 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56230704 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:44644778 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:44644778 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220935309 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220935309 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:132649475 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:132649475 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:13221527 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:13221527 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:71357403 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:71357403 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:84799293 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:84799293 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:59857957 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:59857957 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:59942818 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:59942818 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:38300629 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:38300629 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:93575768 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:93575768 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:9070226 G>C maps to NM_024690.2 S5740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:9070226 G>C maps to NM_024690.2 S5740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:108158798 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:108158798 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:10398692 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:10398692 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:10435283 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:10435283 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:10317484 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:10317484 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:123417087 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:123417087 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:16671656 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:16671656 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:109562598 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:109562598 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:171607702 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:171607702 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:3116306 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:3116306 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:89891255 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:89891255 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:50862709 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:50862709 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:20129112 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:20129112 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:15378563 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:15378563 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:134078732 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:134078732 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:54921837 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:54921837 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:24914294 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:24914294 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:24929406 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:24929406 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:46256776 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:46256776 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:46256798 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:46256798 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:47117101 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:47117101 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:94173118 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:94173118 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:219942154 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:219942154 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7321155 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7321155 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:55505857 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:55505857 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:247588912 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:247588912 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56572758 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56572758 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56223776 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56223776 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:43615930 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:43615930 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:10729164 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:10729164 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:14980809 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:14980809 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:120478061 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:120478061 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:100106319 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:100106319 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:69339716 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:69339716 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:74959987 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:74959987 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:34724314 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:34724314 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:93802940 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:93802940 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:87360082 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:87360082 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:153974176 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:153974176 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:102334863 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:102334863 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:102347900 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:102347900 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:41334055 G>T maps to NM_022567.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:41334055 G>T maps to NM_022567.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:28196863 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:28196863 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:131231634 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:131231634 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:53608427 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:53608427 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:107266504 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:107266504 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:9225411 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:9225411 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:59345541 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:59345541 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:32058304 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:32058304 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:41805606 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:41805606 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:51472679 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:51472679 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:226568666 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:226568666 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:44584861 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:44584861 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:223160400 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:223160400 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:70048652 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:70048652 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:134303794 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:134303794 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:95728687 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:95728687 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:14695562 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:14695562 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:120442040 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:120442040 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:160181326 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:160181326 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:22263445 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:22263445 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7138840 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7138840 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:36929363 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:36929363 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:73401818 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:73401818 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:73401827 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:73401827 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:67584461 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:67584461 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:3638833 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:3638833 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:8782713 C>G maps to NM_182734.1 S1145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:8782713 C>G maps to NM_182734.1 S1145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:40582699 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:40582699 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:198965950 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:198965950 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:145011085 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:145011085 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:6533258 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:6533258 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:161159687 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:161159687 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:132192228 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:132192228 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:50724536 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:50724536 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:190719863 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:190719863 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:118364834 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:118364834 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:46023906 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:46023906 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:46660383 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:46660383 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:79175509 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:79175509 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:81746847 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:81746847 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:135774400 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:135774400 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:212526427 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:212526427 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:47268178 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:47268178 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:68942926 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:68942926 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:69018601 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:69018601 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:54396516 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:54396516 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37494535 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37494535 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:102045134 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:102045134 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:36304009 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:36304009 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:37635388 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:37635388 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:142460512 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:142460512 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:73683771 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:73683771 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:43430572 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:43430572 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:43269756 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:43269756 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:88934346 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:88934346 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:40911204 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:40911204 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119509435 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119509435 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:32990723 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:32990723 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:154493665 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:154493665 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220335622 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220335622 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:20016989 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:20016989 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56374195 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56374195 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56380978 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56380978 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:28922319 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:28922319 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:150342353 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:150342353 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:131034599 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:131034599 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:80381787 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:80381787 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:114271500 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:114271500 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:49089624 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:49089624 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:79350088 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:79350088 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103234750 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103234750 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:72431596 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:72431596 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:72932425 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:72932425 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:241100014 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:241100014 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:25717431 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:25717431 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:95103983 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:95103983 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:95104729 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:95104729 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:104671486 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:104671486 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:40554005 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:40554005 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:14139277 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:14139277 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:158634606 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:158634606 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:124747091 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:124747091 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56510643 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56510643 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:93306071 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:93306071 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:81573445 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:81573445 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:63449498 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:63449498 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:10264018 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:10264018 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:41769590 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:41769590 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:34030867 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:34030867 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:5647924 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:5647924 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:234247424 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:234247424 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:51981347 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:51981347 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:238990302 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:238990302 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:18274795 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:18274795 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:4027035 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:4027035 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:151337870 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:151337870 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:151111779 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:151111779 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:101051735 T>C maps to ENST00000394085 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:101051735 T>C maps to ENST00000394085 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:77926983 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:77926983 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:19413016 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:19413016 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:32012688 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:32012688 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:37951669 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:37951669 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:67206942 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:67206942 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:77472166 G>C maps to NM_024776.2 S701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:77472166 G>C maps to NM_024776.2 S701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:26938470 G>C maps to NM_001174103.1 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:26938470 G>C maps to NM_001174103.1 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:2833709 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:2833709 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:430631 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:430631 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:18239032 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:18239032 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56355293 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56355293 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103703865 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103703865 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:56903834 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:56903834 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100458937 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100458937 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:38316295 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:38316295 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:107341477 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:107341477 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:85438605 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:85438605 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:45355469 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:45355469 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:125741823 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:125741823 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:24881342 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:24881342 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:48497447 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:48497447 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:20523993 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:20523993 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:143823208 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:143823208 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56567334 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56567334 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56567336 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:56567336 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:2707921 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:2707921 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:68398639 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:68398639 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:73450335 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:73450335 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:90749384 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:90749384 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:7595341 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:7595341 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:82719930 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:82719930 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:151640908 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:151640908 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:125216875 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:125216875 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:107005171 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:107005171 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:23893749 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:23893749 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:144337174 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:144337174 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:53468350 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:53468350 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55652825 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55652825 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:130653382 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:130653382 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:168920184 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:168920184 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37095029 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37095029 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:73123235 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:73123235 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:109318933 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:109318933 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:48382216 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:48382216 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:15224169 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:15224169 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:46357404 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:46357404 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:12112727 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:12112727 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:152501208 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:152501208 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72288198 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72288198 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:9651933 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:9651933 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:67400630 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:67400630 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:59543392 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:59543392 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:54885025 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:54885025 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841761 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841761 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841811 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841811 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:62228150 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:62228150 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:169632687 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:169632687 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:169632745 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:169632745 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:60600388 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:60600388 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:120466849 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:120466849 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:53797958 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:53797958 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:98525083 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:98525083 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:138858126 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:138858126 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:74315539 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:74315539 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:68725510 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:68725510 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:19755899 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:19755899 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:29724994 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:29724994 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:117840626 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:117840626 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:23057321 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:23057321 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:195609964 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:195609964 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:41243987 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:41243987 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:30134926 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:30134926 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:30140214 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:30140214 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55033062 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55033062 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:51448483 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:51448483 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:14369073 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:14369073 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:98529306 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:98529306 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:84412789 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:84412789 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:109968312 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:109968312 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:76124108 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:76124108 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:70455442 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:70455442 A>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:70346313 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:70346313 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:20359691 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:20359691 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:17750725 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:17750725 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:96106359 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:96106359 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:96141039 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:96141039 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:24891484 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:24891484 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:132623117 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:132623117 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:99936534 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:99936534 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:8990999 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:8990999 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:144758696 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:144758696 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:77913211 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:77913211 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6773090 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6773090 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:177605213 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:177605213 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:219288945 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:219288945 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:79929646 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:79929646 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:65253302 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chrX:65253302 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:215279358 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:215279358 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:61036303 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:61036303 A>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:55467192 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:55467192 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:118492816 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:118492816 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:109525212 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:109525212 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:158677334 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:158677334 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:167833148 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:167833148 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:78389539 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:78389539 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:89073829 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:89073829 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:113060966 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:113060966 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:122966660 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:122966660 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72008574 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72008574 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:77619808 G>T maps to NM_024721.4 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:77619808 G>T maps to NM_024721.4 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:28327343 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:28327343 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:286916 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:286916 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:44673752 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:44673752 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:22193723 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:22193723 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:3190662 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:3190662 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:53311417 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:53311417 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:52477489 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:52477489 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:71595768 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:71595768 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:88956812 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:88956812 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:102187771 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:102187771 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:2373437 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:2373437 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:109604845 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:109604845 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:6749395 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:6749395 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:236918312 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:236918312 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:39618683 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:39618683 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:77369511 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:77369511 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:112028520 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:112028520 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:58128015 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:58128015 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:109954584 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:109954584 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:115215952 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:115215952 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:112592100 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:112592100 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:73964752 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:73964752 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:55433218 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:55433218 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:26552644 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:26552644 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr9:32986119 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr9:32986119 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:32099696 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:32099696 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:160029779 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:160029779 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:47538076 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:47538076 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:25280380 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:25280380 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:73035218 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:73035218 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:1785453 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:1785453 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:70065786 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:70065786 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:116619164 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:116619164 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:111152147 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:111152147 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:20953577 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:20953577 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:9510204 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:9510204 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:3736274 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:3736274 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:32808262 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:32808262 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:65789362 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:65789362 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:117076672 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:117076672 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:65032450 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:65032450 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:21760846 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:21760846 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:202755503 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:202755503 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:96691533 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:96691533 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:17629313 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:17629313 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:34855234 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:34855234 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:418009 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:418009 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:8691693 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:8691693 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:189921587 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:189921587 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:27946556 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:27946556 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:73930653 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:73930653 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:28750104 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:28750104 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:43894043 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:43894043 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:149452812 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:149452812 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:113403034 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:113403034 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:20015300 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:20015300 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:95571629 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:95571629 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:468679 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:468679 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:42354806 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:42354806 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:13758947 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:13758947 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:11572591 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:11572591 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:32395763 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:32395763 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr21:38850431 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr21:38850431 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:31467365 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:31467365 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:42531614 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:42531614 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:66439242 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:66439242 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:23219337 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:23219337 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:66205319 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:66205319 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:10865431 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:10865431 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:206141343 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:206141343 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:45946326 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:45946326 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:153592802 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:153592802 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:147021995 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:147021995 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:49192920 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:49192920 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:79443998 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:79443998 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:4306190 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:4306190 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:49295497 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:49295497 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:66200202 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:66200202 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:161117161 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:161117161 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:27128288 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:27128288 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:27729530 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:27729530 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:42512402 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:42512402 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:57690572 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:57690572 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:24669280 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:24669280 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:37338050 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:37338050 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:13768216 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:13768216 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:114005388 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:114005388 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:110279824 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:110279824 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:186114800 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:186114800 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:155233053 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:155233053 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:237415898 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:237415898 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:91037915 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:91037915 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:68661643 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:68661643 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:52214505 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:52214505 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:7755253 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:7755253 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:23447670 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:23447670 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:58988419 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:58988419 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:108279758 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:108279758 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:44596042 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:44596042 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:21494656 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:21494656 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr9:139849762 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr9:139849762 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:136594072 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:136594072 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:141091945 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:141091945 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:141274655 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:141274655 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:141946238 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:141946238 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:57570764 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:57570764 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:57588638 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:57588638 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:75022417 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:75022417 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:26077524 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:26077524 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:63831785 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:63831785 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:238443295 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:238443295 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:93870593 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:93870593 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:79279666 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:79279666 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:10310341 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:10310341 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:128339426 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:128339426 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:16918547 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:16918547 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:196664342 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:196664342 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:881524 A>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:881524 A>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:21891584 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:21891584 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:102269749 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:102269749 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:56000695 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:56000695 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:108385303 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:108385303 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:103298605 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:103298605 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:43547761 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:43547761 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:77066697 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:77066697 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:125648691 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:125648691 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:55569380 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:55569380 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:165752637 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:165752637 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:20705158 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:20705158 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:55140636 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:55140636 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:92146466 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:92146466 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8787936 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8787936 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:130839340 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:130839340 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:50906869 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:50906869 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:43156944 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:43156944 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:58514032 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:58514032 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:23524676 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:23524676 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:43572055 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:43572055 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:64290115 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:64290115 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:18750449 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:18750449 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:51216442 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:51216442 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:170395402 T>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:170395402 T>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:170395420 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:170395420 A>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:80366446 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:80366446 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:34062077 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:34062077 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:167659256 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:167659256 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:43604703 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:43604703 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:111672847 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:111672847 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:86007204 T>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:86007204 T>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:87365603 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:87365603 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:48075452 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:48075452 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:71492502 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:71492502 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:54704988 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:54704988 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:16824144 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:16824144 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:148800605 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:148800605 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:27824156 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:27824156 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:102112088 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:102112088 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:173886420 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:173886420 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:29486794 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:29486794 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:73226175 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:73226175 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:36177274 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:36177274 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8195770 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8195770 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:92881598 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:92881598 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:76107464 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:76107464 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:85285941 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:85285941 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:143567218 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:143567218 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:20867939 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:20867939 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:25220716 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:25220716 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:51442833 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:51442833 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:51617133 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:51617133 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:51621670 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:51621670 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:118496507 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:118496507 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:144329224 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chrX:144329224 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:217856815 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:217856815 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:55656591 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:55656591 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:57095077 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:57095077 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:53045936 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:53045936 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:92977635 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:92977635 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:104092770 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:104092770 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:104109566 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:104109566 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:104160049 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:104160049 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:29779647 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:29779647 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:26685160 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:26685160 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:83790636 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr15:83790636 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:98443831 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:98443831 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:27258721 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:27258721 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:175049663 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:175049663 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:175375218 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:175375218 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:32029151 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:32029151 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:239257308 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:239257308 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:209936095 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:209936095 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:73513502 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:73513502 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:115576321 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:115576321 T>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:43570061 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:43570061 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:76201665 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr14:76201665 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:139598140 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:139598140 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:13271741 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:13271741 C>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:158922385 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:158922385 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:216538450 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:216538450 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:76802166 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:76802166 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:144768314 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:144768314 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:133033011 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:133033011 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:74999642 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:74999642 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:134896334 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:134896334 G>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:75907791 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:75907791 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:30958474 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:30958474 A>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:6024016 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:6024016 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:31589513 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:31589513 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:44049938 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:44049938 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:167045963 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:167045963 T>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:38109437 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:38109437 C>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:58718579 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:58718579 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:27602878 T>G did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:27602878 T>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:87225134 A>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:87225134 A>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:100613942 A>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:100613942 A>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:70188901 A>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:70188901 A>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr6:31612990 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr6:31612990 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr16:3652318 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr16:3652318 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:76508972 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:76508972 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:182873245 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:182873245 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:144124522 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:144124522 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:81978767 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:81978767 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:120198910 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:120198910 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr18:625071 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr18:625071 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:121295821 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:121295821 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:145620290 A>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:145620290 A>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr13:36379823 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr13:36379823 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:108544260 A>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:108544260 A>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:21920234 C>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:21920234 C>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:84864198 T>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:84864198 T>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:7083909 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:7083909 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr22:41488931 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr22:41488931 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr10:15838015 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr10:15838015 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr6:37417999 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr6:37417999 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:27566477 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:27566477 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:62257134 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:62257134 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:49951814 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr12:49951814 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:48504693 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr8:48504693 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr14:35593471 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr14:35593471 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:153138162 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:153138162 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr20:60887889 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr20:60887889 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:107566580 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:107566580 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:149902156 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:149902156 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:247599205 T>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:247599205 T>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:50170931 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:50170931 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:186412961 A>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:186412961 A>G did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:31862879 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:31862879 C>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr20:44048293 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr20:44048293 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr3:178918930 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr3:178918930 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:153698161 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:153698161 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr17:1580045 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr17:1580045 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr19:43348636 G>A maps to ENST00000449000 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr19:43348636 G>A maps to ENST00000449000 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr5:170336612 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr5:170336612 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:498686 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:498686 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr4:77631180 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr4:77631180 C>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr14:65236282 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr14:65236282 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:123184312 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chrX:123184312 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:48807742 T>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr2:48807742 T>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:151146181 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:151146181 G>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr21:43510598 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr21:43510598 G>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr4:85626530 A>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr4:85626530 A>T did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr4:64927 G>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr4:64927 G>C did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:148055158 A>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:148055158 A>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:144068194 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:144068194 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:138886594 A>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:138886594 A>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr1:11772263 T>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr1:11772263 T>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr9:99408069 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr9:99408069 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:60427999 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:60427999 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr12:107391863 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr12:107391863 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr19:41356097 C>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr19:41356097 C>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr17:57679846 A>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr17:57679846 A>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr8:48308832 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr8:48308832 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:27839379 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:27839379 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:91368770 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:91368770 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr9:78601189 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr9:78601189 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr17:9804297 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr17:9804297 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr1:232626557 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr1:232626557 C>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr6:118320456 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr6:118320456 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr5:112203237 A>C did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr5:112203237 A>C did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:111095481 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chrX:111095481 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:138921719 T>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:138921719 T>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr12:6076578 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr12:6076578 G>A did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr12:122361943 C>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr12:122361943 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:19612963 A>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:19612963 A>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr12:46298713 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr12:46298713 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:38721557 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:38721557 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:54410167 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:54410167 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:44806892 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:44806892 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:34059815 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:34059815 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chrX:32663038 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chrX:32663038 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:46295557 G>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:46295557 G>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr15:65779910 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr15:65779910 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr4:140058861 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr4:140058861 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:22696305 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:22696305 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:42007113 A>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:42007113 A>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:197634783 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:197634783 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:30671681 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:30671681 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr21:34804878 A>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr21:34804878 A>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:227920074 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:227920074 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:67519519 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:67519519 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr8:102705137 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr8:102705137 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chrX:100117348 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chrX:100117348 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:27656124 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:27656124 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:8785230 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:8785230 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:47244079 A>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr20:47244079 A>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:64795592 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr17:64795592 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:83764343 C>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:83764343 C>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:33441172 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:33441172 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr6:52400667 C>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr6:52400667 C>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:119993773 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:119993773 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:7684584 A>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:7684584 A>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:180651581 A>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:180651581 A>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr10:27420895 T>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr10:27420895 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:136288386 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:136288386 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:84561428 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:84561428 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:31144473 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:31144473 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:148715444 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:148715444 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:4832297 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:4832297 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:156562526 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:156562526 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:32084755 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:32084755 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:124206853 A>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:124206853 A>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:69949196 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:69949196 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171502148 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171502148 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171502151 T>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171502151 T>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:64671705 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:64671705 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:32546168 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:32546168 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:133118056 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:133118056 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:2952883 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:2952883 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:61564099 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:61564099 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:35823418 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:35823418 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:24493081 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:24493081 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:105653269 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:105653269 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:182430104 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:182430104 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:122159286 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:122159286 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:79041305 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:79041305 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:135107155 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:135107155 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chrX:1414240 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chrX:1414240 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:3565883 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:3565883 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:41596175 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:41596175 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:74104658 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:74104658 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:142565877 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:142565877 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:29255787 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:29255787 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:29268119 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:29268119 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:48501916 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:48501916 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:24180717 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:24180717 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:3531894 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:3531894 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:26569912 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:26569912 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:898003 T>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:898003 T>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:151229939 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:151229939 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:95327050 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:95327050 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:175326015 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:175326015 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:168054735 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:168054735 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:152870283 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:152870283 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:9927797 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:9927797 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:1073754 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:1073754 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:95027908 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:95027908 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:206651728 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:206651728 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:201842131 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:201842131 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:185350100 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:185350100 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:54805571 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:54805571 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:150649984 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:150649984 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:196311116 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:196311116 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:137751049 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:137751049 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:226516060 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:226516060 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:21009087 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:21009087 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:39622234 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:39622234 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:58830871 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:58830871 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:12317079 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:12317079 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:116406716 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:116406716 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:103347332 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:103347332 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:64894285 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:64894285 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:10533356 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:10533356 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:17264756 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:17264756 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr20:62868761 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr20:62868761 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:113126629 G>A maps to ENST00000316851 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:113126629 G>A maps to ENST00000316851 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:23598678 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:23598678 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:247597384 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:247597384 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:35793100 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:35793100 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:206418004 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:206418004 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:56138705 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:56138705 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:117094979 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:117094979 A>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:105160289 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:105160289 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:169411 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:169411 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:20357005 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:20357005 A>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:20357068 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:20357068 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:133201942 G>A maps to ENST00000320557 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:133201942 G>A maps to ENST00000320557 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:153529654 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:153529654 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:11560978 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:11560978 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:113795570 A>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:113795570 A>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:53728629 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:53728629 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:114271280 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:114271280 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:167653315 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:167653315 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:3262922 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:3262922 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:56484636 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:56484636 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:139300515 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:139300515 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:100911053 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:100911053 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:124955383 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:124955383 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:61486359 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:61486359 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:144459675 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:144459675 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:245927307 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:245927307 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:25154940 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:25154940 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:167663317 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:167663317 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:9055542 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:9055542 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:2224444 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:2224444 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:99783947 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:99783947 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:90676354 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr10:90676354 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:120012441 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:120012441 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:120012455 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:120012455 C>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:152763452 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:152763452 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:64464922 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:64464922 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:159147296 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:159147296 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:102915819 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr14:102915819 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr20:2375041 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr20:2375041 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:60599665 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:60599665 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:98383102 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:98383102 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:26646230 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:26646230 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:201334547 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:201334547 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:72343490 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:72343490 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:25983307 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:25983307 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:32859512 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:32859512 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:32859537 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:32859537 C>G did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:136629333 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:136629333 G>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:98804630 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr2:98804630 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr20:44187723 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr20:44187723 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:78149126 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:78149126 T>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:123976785 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:123976785 G>C did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:53995854 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:53995854 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:16267124 T>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:16267124 T>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:87774578 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:87774578 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:77354893 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:77354893 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:1866747 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:1866747 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr11:67258200 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr11:67258200 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:110971371 T>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:110971371 T>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:113362398 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:113362398 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:45740682 T>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:45740682 T>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:122690775 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:122690775 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:79389338 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:79389338 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:21680144 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:21680144 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:146279561 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:146279561 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:53707858 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:53707858 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:4872741 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:4872741 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr19:46914342 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr19:46914342 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:121825379 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:121825379 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:15808741 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:15808741 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:17167994 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:17167994 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:3165138 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:3165138 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:24544506 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:24544506 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:89703803 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:89703803 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:101200874 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:101200874 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:41565376 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:41565376 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:34772997 A>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:34772997 A>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:236381908 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:236381908 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:140262333 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:140262333 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:54161549 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:54161549 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:45931040 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:45931040 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:107356552 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:107356552 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:155252395 A>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:155252395 A>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:104136273 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:104136273 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:94362108 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:94362108 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr15:57924543 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr15:57924543 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:33433114 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:33433114 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:30746818 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chrX:30746818 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr19:17688728 T>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr19:17688728 T>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:101165833 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:101165833 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:167024895 A>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:167024895 A>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:91784626 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:91784626 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:70920097 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:70920097 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:33650240 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:33650240 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr21:35229204 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr21:35229204 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:5078537 A>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:5078537 A>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:215297864 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:215297864 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:6984006 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:6984006 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:55973070 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr4:55973070 T>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:189702312 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:189702312 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:96430379 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:96430379 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:56683330 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr16:56683330 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:55473431 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:55473431 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr11:76872170 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr11:76872170 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:2056639 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:2056639 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr18:55287961 T>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr18:55287961 T>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:30074166 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:30074166 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr19:36326454 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr19:36326454 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:129350614 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:129350614 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:107832164 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:107832164 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:37303179 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:37303179 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:159505882 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:159505882 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:35958140 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:35958140 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:242046704 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:242046704 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:102048830 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:102048830 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:4718903 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:4718903 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr11:20429589 T>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr11:20429589 T>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:169650877 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:169650877 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:102107728 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:102107728 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:122634182 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:122634182 G>C did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:21331752 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr12:21331752 A>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:98630573 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:98630573 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr14:78217553 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr14:78217553 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:234529355 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:234529355 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:150460567 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:150460567 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:1439875 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:1439875 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:49869565 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:49869565 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:28879521 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:28879521 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:39162729 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:39162729 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:78193850 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:78193850 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:67098949 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:67098949 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:67108482 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:67108482 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:66913616 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:66913616 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:74289035 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:74289035 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:48120766 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:48120766 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:74757235 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:74757235 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:8000403 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:8000403 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:7245163 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:7245163 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:32364574 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:32364574 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:104250466 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:104250466 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:39624317 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:39624317 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:28212481 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:28212481 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:79068700 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:79068700 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:18505001 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:18505001 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:49165905 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:49165905 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:131862071 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:131862071 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:131949308 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:131949308 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:50310415 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:50310415 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:84518074 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:84518074 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129053542 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129053542 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:49965550 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:49965550 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:5019783 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:5019783 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:56245987 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:56245987 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:53818454 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:53818454 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:134084612 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:134084612 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:114199555 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:114199555 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:92021500 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:92021500 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:74123892 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:74123892 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:69300317 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:69300317 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:75780197 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:75780197 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:47569109 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:47569109 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:155933031 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:155933031 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:133346040 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:133346040 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:52523777 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:52523777 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:69364219 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:69364219 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:38503678 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:38503678 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:56534705 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:56534705 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:107510241 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:107510241 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:41297022 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:41297022 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:13410786 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:13410786 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:50374863 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:50374863 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:33168481 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:33168481 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:101937110 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:101937110 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:82625778 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:82625778 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:88391733 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:88391733 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:60951810 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:60951810 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:40857054 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:40857054 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:7173949 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:7173949 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:55118513 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:55118513 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:184800746 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:184800746 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:140948479 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:140948479 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:2622161 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:2622161 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:81693535 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:81693535 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:62467263 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:62467263 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:62739043 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:62739043 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:91072930 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:91072930 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:41383313 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:41383313 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:111319116 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:111319116 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:14508122 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:14508122 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:25341438 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:25341438 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:83378631 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:83378631 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:51740262 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:51740262 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:49540075 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:49540075 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:49552163 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:49552163 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:126486091 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:126486091 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:33265065 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:33265065 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:42565480 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:42565480 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:73795259 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:73795259 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:54646690 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:54646690 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:99827756 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:99827756 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:147815473 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:147815473 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:33138072 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:33138072 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:71655415 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:71655415 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:71686991 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:71686991 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:105817970 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:105817970 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:46914421 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:46914421 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:86341088 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:86341088 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:189940031 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:189940031 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:31291086 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:31291086 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:19010789 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:19010789 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:31439055 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:31439055 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:1321466 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:1321466 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:87022229 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:87022229 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:97595799 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:97595799 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:34554531 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:34554531 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:113254142 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:113254142 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:23806088 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:23806088 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:23807012 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:23807012 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:15660109 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:15660109 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:39869017 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:39869017 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:44092437 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:44092437 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:162689026 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:162689026 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:47853132 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:47853132 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:196912040 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:196912040 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:28964991 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:28964991 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:158141057 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:158141057 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:36505881 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:36505881 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:117658621 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:117658621 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:37156732 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:37156732 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:77081977 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:77081977 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:22922538 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:22922538 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:41509064 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:41509064 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:56726474 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:56726474 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:133922955 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:133922955 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:29526450 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:29526450 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129103844 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129103844 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:87498630 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:87498630 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:14868464 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:14868464 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:92231523 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:92231523 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:34310771 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:34310771 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:146687286 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:146687286 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:147009951 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:147009951 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:147013827 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:147013827 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:32836650 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:32836650 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35642488 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35642488 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35642590 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35642590 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:39169403 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:39169403 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:29599391 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:29599391 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:151680306 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:151680306 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:151680311 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:151680311 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:150209770 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:150209770 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:102968323 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:102968323 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:217622576 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:217622576 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:25701419 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:25701419 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:112723598 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:112723598 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:117117029 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:117117029 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:123475935 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:123475935 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:165353426 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:165353426 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:120807083 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:120807083 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:146350652 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:146350652 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:108673765 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:108673765 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:2773256 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:2773256 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:7921090 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:7921090 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:45267395 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:45267395 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:65413571 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:65413571 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:186010016 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:186010016 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:113802830 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:113802830 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:102636285 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:102636285 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:104650925 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:104650925 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:190347103 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:190347103 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:76735001 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:76735001 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:62288472 A>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:62288472 A>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:19729829 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:19729829 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:182360444 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:182360444 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:15572989 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:15572989 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:31340631 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:31340631 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:156679712 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:156679712 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:5030065 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:5030065 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:133967123 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:133967123 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:87636699 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:87636699 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:35921599 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:35921599 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:97275365 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:97275365 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:118671457 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:118671457 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:28956801 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:28956801 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:10588363 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:10588363 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:52864795 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:52864795 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:112463223 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:112463223 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:37005410 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:37005410 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:55143904 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:55143904 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:100917091 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:100917091 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:62812575 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:62812575 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:58295381 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:58295381 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:140982940 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:140982940 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:54841648 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:54841648 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:67855586 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:67855586 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:168307844 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:168307844 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:89058857 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:89058857 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:89179850 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:89179850 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:158813936 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:158813936 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:43812324 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:43812324 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:125075706 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:125075706 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:48034054 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:48034054 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:56599111 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:56599111 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:63574524 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:63574524 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:44180485 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:44180485 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:18038983 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:18038983 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:171056645 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:171056645 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:101755487 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:101755487 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:101757238 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:101757238 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:78444945 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:78444945 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:35770461 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:35770461 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:46280080 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:46280080 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:123185619 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:123185619 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:84031924 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:84031924 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:42805423 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:42805423 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:24845162 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:24845162 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:7060131 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:7060131 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:50280812 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:50280812 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:9086125 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:9086125 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:150057783 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:150057783 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:228504378 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:228504378 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:97614180 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:97614180 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:128682711 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:128682711 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:103564335 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:103564335 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:55973839 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:55973839 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:56136350 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:56136350 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:71556091 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:71556091 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:31904713 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:31904713 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:103797630 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:103797630 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:69508373 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:69508373 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:30975988 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:30975988 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:197777815 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:197777815 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:54037539 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:54037539 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:18912308 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:18912308 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:77660919 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:77660919 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:8706496 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:8706496 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:22137126 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:22137126 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:59814631 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:59814631 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:44533834 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:44533834 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:153036343 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:153036343 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:152937711 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:152937711 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:24807065 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:24807065 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:53104313 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:53104313 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:131981332 A>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:131981332 A>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:23814336 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:23814336 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:42681573 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:42681573 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:22036611 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:22036611 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:113522034 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:113522034 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:299711 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:299711 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:70981355 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:70981355 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:47292667 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:47292667 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:35781996 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:35781996 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:97278771 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:97278771 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:474008 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:474008 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:141810475 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:141810475 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:198721615 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:198721615 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:9360754 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:9360754 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:29690614 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:29690614 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:33442287 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:33442287 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:15562826 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:15562826 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:155113881 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:155113881 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:103368702 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:103368702 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:43611988 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:43611988 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:3288090 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:3288090 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:77612554 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:77612554 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:48091538 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:48091538 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:49999586 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:49999586 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:55782219 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:55782219 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:66460255 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:66460255 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:151107030 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:151107030 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:51215165 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:51215165 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:57627913 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:57627913 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:1456685 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:1456685 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:2234640 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:2234640 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:18064051 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:18064051 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:205766954 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:205766954 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:75672459 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:75672459 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:152957094 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:152957094 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:20611880 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:20611880 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:48584868 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:48584868 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:88367606 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:88367606 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:96943764 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:96943764 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:25154910 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:25154910 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:39233755 A>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:39233755 A>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:231072859 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:231072859 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:231175800 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:231175800 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:228856145 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:228856145 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:158609273 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:158609273 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:155984895 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:155984895 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:48053754 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:48053754 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:66772770 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:66772770 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:33685898 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:33685898 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:40491442 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:40491442 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:8496462 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:8496462 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:202571689 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:202571689 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:99945017 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:99945017 A>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:71174561 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:71174561 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:150463062 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:150463062 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:38051222 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:38051222 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:52943024 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:52943024 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:117486713 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:117486713 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:36779321 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:36779321 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:134031947 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:134031947 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:362113 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:362113 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:122766628 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:122766628 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:52972376 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:52972376 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:2189501 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:2189501 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:32559445 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:32559445 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:155500379 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:155500379 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:30738537 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:30738537 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:77808394 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:77808394 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:126068335 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:126068335 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:12779931 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:12779931 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:68956381 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:68956381 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:74716531 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:74716531 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:62519026 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:62519026 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:2225040 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:2225040 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:123698789 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:123698789 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:100296270 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chrX:100296270 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:72981517 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:72981517 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:45825774 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:45825774 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:10114698 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:10114698 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:43314844 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:43314844 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:234675670 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:234675670 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:234557404 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:234557404 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:54342530 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:54342530 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:215847407 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:215847407 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:6153410 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:6153410 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:70885785 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:70885785 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:114649691 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:114649691 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:130165775 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:130165775 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:47588269 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:47588269 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:28555551 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:28555551 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:32380376 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:32380376 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:40438626 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:40438626 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:44946979 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:44946979 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:54074834 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:54074834 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:49856552 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:49856552 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:114296716 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:114296716 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:31040549 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:31040549 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:12432156 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:12432156 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:52403489 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:52403489 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:81571927 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:81571927 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:187704008 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:187704008 G>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr9:133989897 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr9:133989897 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:190593380 A>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:190593380 A>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr16:50357391 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr16:50357391 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr19:51767376 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr19:51767376 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr1:157801718 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr1:157801718 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr17:40950730 G>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr17:40950730 G>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr10:94834306 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr10:94834306 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr13:72249269 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr13:72249269 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:95593178 T>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:95593178 T>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr17:61903385 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr17:61903385 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chrX:132458608 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chrX:132458608 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr7:27219206 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr7:27219206 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:77639372 A>G did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:77639372 A>G did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr8:48504915 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr8:48504915 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:169622896 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:169622896 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr16:15835750 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr16:15835750 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:23858560 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:23858560 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:152512304 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:152512304 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:193360466 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:193360466 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr6:10697808 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr6:10697808 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr5:149283436 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr5:149283436 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:10930093 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:10930093 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr1:230486681 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr1:230486681 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:52159092 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:52159092 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:53217606 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:53217606 A>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr19:43698396 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr19:43698396 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:49737605 T>G did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr3:49737605 T>G did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr7:84697464 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr7:84697464 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr21:10970237 T>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr21:10970237 T>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:51448482 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:51448482 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr12:121154884 G>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr12:121154884 G>C did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr16:71513004 T>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr16:71513004 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:69869992 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:69869992 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:57221272 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:57221272 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:67188635 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:67188635 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:220078283 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:220078283 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:114168078 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:114168078 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:24799280 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:24799280 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:150817034 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:150817034 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47688627 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47688627 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:159036170 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:159036170 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:42891624 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:42891624 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:112223065 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:112223065 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:41574378 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:41574378 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:52281932 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:52281932 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:69300291 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:69300291 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:16309027 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:16309027 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:83360459 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:83360459 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:107397005 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:107397005 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:25276055 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:25276055 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:119504760 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:119504760 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:67515077 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:67515077 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:76903694 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:76903694 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:58201288 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:58201288 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:102994957 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:102994957 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:103174508 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:103174508 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:105974214 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:105974214 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:128191481 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:128191481 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:29226111 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:29226111 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:80404608 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:80404608 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:109649764 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:109649764 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:18794373 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:18794373 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:146617871 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:146617871 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:146648136 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:146648136 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:27362858 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:27362858 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:31122153 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:31122153 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:100858953 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:100858953 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:137627556 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:137627556 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47510314 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47510314 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:87025841 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:87025841 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:1510964 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:1510964 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:41463901 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:41463901 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:1367756 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:1367756 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:147259453 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:147259453 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:103387222 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:103387222 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:228159373 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:228159373 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:17298964 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:17298964 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:52774145 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:52774145 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:46521642 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:46521642 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:155011789 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:155011789 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:15736889 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:15736889 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:15739901 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:15739901 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:111742455 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:111742455 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:80671942 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:80671942 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:111904067 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:111904067 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:1485863 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:1485863 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:55655983 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:55655983 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:100829753 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:100829753 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:6523935 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:6523935 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:83810351 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:83810351 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:89703426 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:89703426 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:162879201 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:162879201 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:154681259 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:154681259 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:97771616 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:97771616 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:28970523 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:28970523 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:56497597 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:56497597 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:25720215 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:25720215 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:78472506 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:78472506 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:82512738 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:82512738 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:6078143 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:6078143 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:184041144 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:184041144 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:97200324 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:97200324 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:102861020 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:102861020 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:158528055 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:158528055 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:122728873 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:122728873 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:94782233 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:94782233 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:157766952 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:157766952 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:157772150 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:157772150 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:155505251 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:155505251 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:27939697 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:27939697 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:34324174 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:34324174 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:147007224 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:147007224 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:74671568 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:74671568 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:39450531 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:39450531 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:131216667 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:131216667 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:4317154 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:4317154 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:47163247 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:47163247 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:166615483 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:166615483 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:52993843 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:52993843 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:58711089 G>A maps to NM_080661.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:58711089 G>A maps to NM_080661.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:20325934 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:20325934 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:47681477 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:47681477 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:97246333 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:97246333 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:30537215 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:30537215 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:30537222 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:30537222 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:82969178 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:82969178 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:114274316 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:114274316 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:41008604 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:41008604 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:97191552 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:97191552 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:42845735 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:42845735 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:27782007 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:27782007 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:33095888 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:33095888 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:185959618 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:185959618 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:113802054 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:113802054 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:154587021 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:154587021 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:272869 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:272869 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:96048257 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:96048257 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:2757276 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:2757276 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:34818305 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:34818305 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:132038515 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:132038515 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:36349799 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:36349799 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:186461615 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:186461615 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:53294506 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:53294506 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:33777700 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:33777700 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:102987011 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:102987011 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:39917906 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:39917906 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:148009533 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:148009533 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:11913633 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:11913633 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:141747007 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:141747007 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:170097928 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:170097928 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:144803087 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:144803087 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:8486947 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:8486947 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:112776924 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:112776924 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:20456694 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:20456694 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:168325806 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:168325806 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:56350740 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:56350740 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:8993564 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:8993564 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:76564844 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:76564844 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:101710458 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:101710458 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:16935130 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:16935130 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:17839527 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:17839527 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:119070116 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chrX:119070116 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:160956048 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:160956048 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:26084383 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:26084383 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:45695894 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:45695894 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:6012904 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:6012904 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:142712223 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:142712223 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:50318348 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:50318348 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156844017 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156844017 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:228469980 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:228469980 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:248247109 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:248247109 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:176563603 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:176563603 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:140790302 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:140790302 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:133851587 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:133851587 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:45971883 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:45971883 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:111564642 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:111564642 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:209195471 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:209195471 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:96018748 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:96018748 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:161173127 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:161173127 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:118199643 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:118199643 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:132010487 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:132010487 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:130873058 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:130873058 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:94916566 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:94916566 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:101982169 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:101982169 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:170020821 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:170020821 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:6533789 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:6533789 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:23731777 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:23731777 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:8436734 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:8436734 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:109357153 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:109357153 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:73657186 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:73657186 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:163122242 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:163122242 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:79638955 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:79638955 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:11342264 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:11342264 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:21756019 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:21756019 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:45514520 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:45514520 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr21:48019475 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr21:48019475 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:71920694 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:71920694 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:65729185 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:65729185 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:125279716 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:125279716 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:159604239 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:159604239 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:6471154 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:6471154 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:185341887 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:185341887 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:224845214 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:224845214 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:41379222 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:41379222 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156177825 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156177825 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:85452050 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:85452050 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:118475786 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:118475786 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:168201115 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:168201115 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:2056632 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:2056632 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:172643063 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:172643063 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:55908977 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:55908977 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:72465898 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:72465898 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:67579480 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:67579480 A>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:29997471 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:29997471 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:72311625 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:72311625 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:141812826 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:141812826 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:100230990 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:100230990 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:35705475 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:35705475 T>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:122212559 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:122212559 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:20927238 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:20927238 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:175113396 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:175113396 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:20138182 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:20138182 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:140397022 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:140397022 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:92441644 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:92441644 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:110226573 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:110226573 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:112770551 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:112770551 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:100388345 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:100388345 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:94839459 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:94839459 C>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:219604892 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:219604892 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:99992547 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:99992547 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:69535445 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:69535445 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:70346636 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:70346636 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:19720039 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:19720039 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:48272942 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:48272942 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:55429137 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:55429137 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:96024895 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:96024895 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:6665593 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:6665593 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:31803457 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:31803457 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:72050618 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr12:72050618 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:81070970 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr10:81070970 T>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:44471653 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:44471653 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:57027785 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:57027785 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:57194507 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr7:57194507 A>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:52376969 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:52376969 T>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:34842537 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:34842537 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:67101832 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:67101832 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:131149080 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:131149080 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:29644618 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:29644618 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr5:37142325 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr5:37142325 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:77266148 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:77266148 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr3:134280397 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr3:134280397 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:110688013 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:110688013 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:10147635 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:10147635 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr5:177772041 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr5:177772041 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr13:110847347 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr13:110847347 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:39769037 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:39769037 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:954753 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:954753 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:955723 A>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:955723 A>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:124357583 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:124357583 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:57513262 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:57513262 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:220160762 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:220160762 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:56495859 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:56495859 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:236399749 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:236399749 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:40368939 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:40368939 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:72651865 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:72651865 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:48416321 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:48416321 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:45006836 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:45006836 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr6:33071550 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr6:33071550 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:120050057 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:120050057 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:120050081 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:120050081 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:120050375 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:120050375 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:38840081 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:38840081 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:153642429 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:153642429 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:3704342 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:3704342 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr6:149925942 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr6:149925942 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:32573723 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:32573723 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:38925114 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:38925114 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr6:129725162 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr6:129725162 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:25260723 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:25260723 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:46746052 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:46746052 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr3:65350770 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr3:65350770 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:73562087 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:73562087 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:60152821 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:60152821 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:20827067 T>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:20827067 T>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:84035345 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:84035345 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr3:52802732 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr3:52802732 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:33510590 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:33510590 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:154072648 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:154072648 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:20822934 A>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:20822934 A>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:93008616 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:93008616 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:66713136 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:66713136 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:95418994 T>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:95418994 T>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:79764732 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr10:79764732 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:70208127 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:70208127 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:202457642 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:202457642 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:228003649 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:228003649 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:43593409 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:43593409 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:220344518 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:220344518 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chrX:119246765 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chrX:119246765 C>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr18:40503401 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr18:40503401 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:11389676 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:11389676 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr20:62325859 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr20:62325859 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:167060856 T>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:167060856 T>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr7:80447809 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr7:80447809 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:38450581 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:38450581 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:14095018 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:14095018 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:22426538 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:22426538 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:121457111 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:121457111 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:4871100 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:4871100 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:16202692 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:16202692 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr20:13029531 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr20:13029531 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:21838697 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:21838697 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr20:58490677 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr20:58490677 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:64685265 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr14:64685265 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:55687000 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:55687000 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:152060022 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:152060022 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:51500951 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:51500951 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:98413482 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:98413482 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:10632267 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:10632267 T>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:123755143 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:123755143 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr9:74332811 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr9:74332811 G>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:189064970 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:189064970 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:2106188 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:2106188 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:43427042 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:43427042 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:4930709 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr19:4930709 T>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:160395220 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:160395220 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:21847811 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr8:21847811 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:57211522 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:57211522 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:215820144 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:215820144 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:48337899 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:48337899 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:67250406 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:67250406 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:179102624 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:179102624 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:5242136 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:5242136 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:64640244 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:64640244 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:78288878 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:78288878 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:100201249 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:100201249 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:4832324 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:4832324 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:140077569 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:140077569 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:41561685 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:41561685 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:54230858 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:54230858 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:98129588 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:98129588 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:33385891 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:33385891 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:115336759 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:115336759 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:42406369 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:42406369 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:123276739 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:123276739 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:62491862 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:62491862 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:119737395 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:119737395 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:47593015 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:47593015 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:42473540 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:42473540 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:58021690 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:58021690 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:11038783 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:11038783 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:31616639 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:31616639 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:127516262 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:127516262 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:80260010 A>T maps to NM_001114735.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:80260010 A>T maps to NM_001114735.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:136594377 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:136594377 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:61867806 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:61867806 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:111369270 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:111369270 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:46865168 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:46865168 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:13387595 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:13387595 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:51769220 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:51769220 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:170967187 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:170967187 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:182925009 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:182925009 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:206239198 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:206239198 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:28202989 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:28202989 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:61430746 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:61430746 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:129853459 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:129853459 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:58235359 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:58235359 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:40054016 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:40054016 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:54420818 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:54420818 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:159170716 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:159170716 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:122054167 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:122054167 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:14989402 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:14989402 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:54115228 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:54115228 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:16593222 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:16593222 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:111296693 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:111296693 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:66372805 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:66372805 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:21948229 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:21948229 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:17690178 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:17690178 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:13067988 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:13067988 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:50833509 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:50833509 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:53191486 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:53191486 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:122763322 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:122763322 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:74917166 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:74917166 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:81694617 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:81694617 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:21670370 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:21670370 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:74413829 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:74413829 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:103467448 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:103467448 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:121209991 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:121209991 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:139608944 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:139608944 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:238234069 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:238234069 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:61460172 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:61460172 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:4408564 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:4408564 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:37325395 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:37325395 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:113240829 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:113240829 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:57564491 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:57564491 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:49034430 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:49034430 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:99311199 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:99311199 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:85415498 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:85415498 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:172314472 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:172314472 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:30866586 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:30866586 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:44608666 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:44608666 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35071265 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35071265 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:118501006 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:118501006 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:7707807 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:7707807 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:21133527 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:21133527 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:13807618 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:13807618 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:37623694 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:37623694 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:113283210 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:113283210 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:100505378 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:100505378 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:28574413 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:28574413 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:28574417 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:28574417 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:30436162 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:30436162 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:96241396 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:96241396 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:86125861 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:86125861 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:19255839 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:19255839 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:5247047 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:5247047 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:34668257 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:34668257 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:73477879 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:73477879 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:119303312 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:119303312 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:140331210 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:140331210 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:93974450 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:93974450 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:15793839 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:15793839 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:212495100 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:212495100 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:53673323 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:53673323 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:133602294 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:133602294 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:82373576 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:82373576 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:93386361 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:93386361 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:43616394 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:43616394 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:71998478 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:71998478 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:129125677 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:129125677 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:13033739 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:13033739 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:92100104 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:92100104 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:45958667 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:45958667 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:32883841 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:32883841 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:142451730 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:142451730 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:50050828 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:50050828 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:159668054 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:159668054 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:109273272 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:109273272 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:4794843 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:4794843 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:66209191 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:66209191 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:90104006 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:90104006 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:153784364 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:153784364 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:120567337 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:120567337 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:48414557 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:48414557 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:92941767 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:92941767 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:150217053 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:150217053 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:151229541 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:151229541 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:52427624 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:52427624 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:25885783 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:25885783 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:110257468 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:110257468 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:124132463 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:124132463 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:239974837 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:239974837 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:18988711 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:18988711 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:242175998 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:242175998 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:45473081 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:45473081 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:43508706 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:43508706 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:92825064 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:92825064 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:72640156 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:72640156 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:40098420 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:40098420 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:46690529 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:46690529 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:148859240 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:148859240 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:22183715 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:22183715 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:209116369 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:209116369 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:39862922 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:39862922 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:118647348 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:118647348 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:133801913 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:133801913 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:155234298 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:155234298 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:76713529 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:76713529 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:100976359 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:100976359 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:61912272 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:61912272 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:105177173 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:105177173 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:77635772 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:77635772 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:237308222 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:237308222 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:15573152 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:15573152 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:15639325 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:15639325 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:31422266 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:31422266 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:31368547 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:31368547 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:46330174 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:46330174 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:93482980 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:93482980 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:26835476 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:26835476 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:42138619 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:42138619 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:75149447 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:75149447 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:123871905 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:123871905 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:39196901 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:39196901 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:142650847 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:142650847 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:1895157 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:1895157 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:8891839 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:8891839 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:170003436 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:170003436 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:51518934 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:51518934 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:10467406 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:10467406 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:38922677 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:38922677 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:153132494 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrX:153132494 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:112475990 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:112475990 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:209797142 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:209797142 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:30748668 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:30748668 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:156695247 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:156695247 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:65609841 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:65609841 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:38496730 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:38496730 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:54780052 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:54780052 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:62449562 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:62449562 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:11964654 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:11964654 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:53726385 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:53726385 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:65319379 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:65319379 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:150325381 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:150325381 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:78116159 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:78116159 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:91455582 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:91455582 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:136913249 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:136913249 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:160623732 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:160623732 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:152176039 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:152176039 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:47669837 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:47669837 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:878522 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:878522 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:32116846 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:32116846 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:141796296 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:141796296 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:18463457 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:18463457 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:109998813 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:109998813 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:2527972 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:2527972 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:13223518 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:13223518 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:60152490 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:60152490 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:60231727 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:60231727 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:56669609 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:56669609 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:151281381 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:151281381 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:64855013 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:64855013 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:11204845 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:11204845 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:30658021 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:30658021 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:124653605 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:124653605 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:9000075 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:9000075 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:113524455 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:113524455 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:46761017 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:46761017 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:1913922 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:1913922 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15608665 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15608665 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:41345096 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:41345096 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:102884220 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:102884220 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:21115343 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:21115343 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:127074762 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:127074762 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:7083434 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:7083434 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:56382139 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:56382139 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:123718649 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:123718649 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:88379262 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:88379262 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:28235700 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:28235700 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:183635158 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:183635158 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:203472584 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:203472584 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:163378430 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:163378430 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:176671932 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:176671932 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:145060701 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:145060701 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:14696037 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:14696037 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:14810540 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:14810540 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:144916338 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:144916338 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:54342865 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:54342865 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:149504256 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:149504256 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:22009633 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:22009633 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:41582587 C>A maps to NM_001164595.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:41582587 C>A maps to NM_001164595.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:56156500 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:56156500 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:71715482 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:71715482 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:601473 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:601473 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:81241364 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:81241364 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:110431255 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:110431255 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:144263856 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:144263856 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:18889138 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:18889138 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:161132762 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:161132762 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:7296315 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:7296315 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:630208 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:630208 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:72399020 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:72399020 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:38166352 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:38166352 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:19571470 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:19571470 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:76785702 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:76785702 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:11507027 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:11507027 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:64299224 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:64299224 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:179297098 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:179297098 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:23391798 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:23391798 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:95953924 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:95953924 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:150321585 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:150321585 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:142458357 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:142458357 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:43258443 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:43258443 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:15471115 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:15471115 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:71065962 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:71065962 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:158906614 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:158906614 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:37587073 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:37587073 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:29758783 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:29758783 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:56886195 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:56886195 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:114766431 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:114766431 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:53598098 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:53598098 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35627147 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35627147 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:31926269 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:31926269 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:79254329 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:79254329 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:85577736 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:85577736 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:71698254 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:71698254 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:29648170 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:29648170 A>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:141868789 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:141868789 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:67855320 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:67855320 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:237837534 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:237837534 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:18393371 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:18393371 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:78130560 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:78130560 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:13868724 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:13868724 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:210412802 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:210412802 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:210414898 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:210414898 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:74732123 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:74732123 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:38978476 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:38978476 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:28884515 G>T maps to NM_015503.2 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:28884515 G>T maps to NM_015503.2 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:440725 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:440725 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:110760109 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:110760109 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62948024 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62948024 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:92952922 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:92952922 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:92350326 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:92350326 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:75677101 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:75677101 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:19611845 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:19611845 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:28525390 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:28525390 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:67286440 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:67286440 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:133669844 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:133669844 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:168222381 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:168222381 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:203834118 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:203834118 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:51617387 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:51617387 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:101620894 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:101620894 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:108337045 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:108337045 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:231157279 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:231157279 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:35771596 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:35771596 A>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:220329125 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:220329125 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:234967453 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:234967453 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:158587786 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:158587786 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:2218841 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:2218841 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:125920469 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:125920469 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:203084620 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:203084620 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:113220675 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:113220675 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:58496353 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:58496353 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:152532771 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:152532771 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:35771597 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:35771597 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:117486968 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:117486968 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:43568647 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:43568647 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:156378517 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:156378517 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:98144285 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:98144285 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:135214205 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:135214205 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:123755942 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:123755942 A>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:35846182 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:35846182 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:10998191 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:10998191 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:18634326 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:18634326 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228602295 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228602295 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228602831 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228602831 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:73870435 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:73870435 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:55038381 C>A maps to ENST00000357530 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:55038381 C>A maps to ENST00000357530 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:72958721 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:72958721 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:81448603 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:81448603 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:81499002 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:81499002 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:94877668 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:94877668 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:89998932 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:89998932 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:37896960 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:37896960 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:109964249 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:109964249 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:61415908 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:61415908 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrY:15398479 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chrY:15398479 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:62161882 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:62161882 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:54614724 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:54614724 G>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:70853164 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:70853164 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:999727 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:999727 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:33282782 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:33282782 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:197145659 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:197145659 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:89074584 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:89074584 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:100000243 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:100000243 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:44804837 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:44804837 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:45498737 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:45498737 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:74580625 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:74580625 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:74592318 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:74592318 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:54074618 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:54074618 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:56669856 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:56669856 T>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:60182 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:60182 C>G did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:53579082 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:53579082 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:58239027 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:58239027 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:146686008 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:146686008 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:52876299 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:52876299 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:9225216 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:9225216 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:70301454 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:70301454 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:48563769 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:48563769 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:66890458 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:66890458 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:87056019 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:87056019 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:48201283 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:48201283 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:48172068 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:48172068 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:101557136 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:101557136 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:48745743 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:48745743 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:39994215 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:39994215 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:44099309 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:44099309 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:179190115 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:179190115 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150555800 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150555800 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:69375983 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:69375983 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:39442289 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:39442289 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:39550215 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:39550215 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:156936288 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:156936288 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:156940550 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:156940550 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:135083064 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:135083064 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:33641889 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:33641889 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:100649324 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:100649324 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:130275361 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:130275361 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:167778882 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:167778882 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:45742932 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:45742932 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7690790 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7690790 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7712951 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7712951 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7757840 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7757840 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7772957 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7772957 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7804828 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7804828 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:161567699 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:161567699 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:61413940 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:61413940 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:222843612 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:222843612 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:77805969 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:77805969 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:33046290 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:33046290 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:91729206 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:91729206 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:243788288 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:243788288 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:38457329 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:38457329 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:112592167 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:112592167 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:15749406 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:15749406 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:99109384 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:99109384 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156561834 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156561834 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:39477285 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:39477285 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:33387170 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:33387170 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:61915134 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:61915134 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:49790932 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:49790932 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:11204575 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:11204575 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156910315 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156910315 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:124413330 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:124413330 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:175976260 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:175976260 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:14631189 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:14631189 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:81474443 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:81474443 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:234184286 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:234184286 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:138864952 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:138864952 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:18102168 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:18102168 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:77243538 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:77243538 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:77286894 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:77286894 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:50241646 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:50241646 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:235616305 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:235616305 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:79058778 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:79058778 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66287000 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66287000 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:114424732 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:114424732 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:23541547 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:23541547 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:133166079 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:133166079 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:127834433 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:127834433 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:11403707 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:11403707 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:55777709 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:55777709 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:26238283 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:26238283 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:11904407 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:11904407 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:115536879 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:115536879 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:134754575 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:134754575 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:76250490 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:76250490 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:93483474 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:93483474 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:13387640 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:13387640 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:207195295 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:207195295 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:179352570 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:179352570 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57202733 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57202733 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:43748349 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:43748349 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:55111181 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:55111181 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:35467902 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:35467902 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:56728508 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:56728508 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:45949887 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:45949887 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:23967030 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:23967030 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:55408940 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:55408940 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:74040582 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:74040582 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:85051068 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:85051068 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:196236313 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:196236313 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41155229 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41155229 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41199691 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41199691 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:31736513 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:31736513 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:74587547 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:74587547 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:67287516 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:67287516 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2613956 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2613956 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2714980 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2714980 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:49067760 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:49067760 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:201009236 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:201009236 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:1974441 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:1974441 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:18629791 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:18629791 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:179151621 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:179151621 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:26526371 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:26526371 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:88951441 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:88951441 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33444389 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33444389 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:119961409 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:119961409 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:119978415 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:119978415 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:46506648 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:46506648 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158146805 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158146805 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:112063764 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:112063764 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:71060190 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:71060190 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:64606096 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:64606096 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:21883742 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:21883742 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:21883888 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:21883888 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:83781969 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:83781969 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:59217137 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:59217137 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:31960574 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:31960574 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:26957019 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:26957019 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:72667711 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:72667711 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:15812332 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:15812332 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:34901700 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:34901700 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:67007009 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:67007009 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:6185806 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:6185806 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:175666636 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:175666636 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:89944324 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:89944324 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:184103043 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:184103043 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233406046 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233406046 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:120204874 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:120204874 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:1511525 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:1511525 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:7893885 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:7893885 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:122763328 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:122763328 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10543798 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10543798 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10567779 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10567779 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10567876 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10567876 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:23848598 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:23848598 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150909241 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150909241 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:57996666 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:57996666 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:58631549 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:58631549 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:205033307 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:205033307 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:76513530 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:76513530 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:76592359 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:76592359 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:125282065 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:125282065 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:140160976 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:140160976 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:46083975 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:46083975 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:46085875 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:46085875 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:106898858 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:106898858 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:105836255 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:105836255 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:107824025 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:107824025 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:107924058 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:107924058 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:189915945 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:189915945 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:10081827 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:10081827 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:47541556 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:47541556 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:84185538 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:84185538 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:69006823 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:69006823 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:46737238 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:46737238 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:93896804 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:93896804 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:131300382 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:131300382 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:207780556 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:207780556 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3779918 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3779918 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:2830853 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:2830853 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:2830855 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:2830855 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:4645133 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:4645133 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34158384 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34158384 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34192016 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34192016 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:39764019 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:39764019 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:39783899 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:39783899 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:16893484 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:16893484 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:17089682 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:17089682 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:17171548 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:17171548 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:75043441 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:75043441 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:47395732 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:47395732 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:48982509 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:48982509 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:27852828 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:27852828 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:4393354 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:4393354 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57528723 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57528723 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:3964599 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:3964599 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:44100526 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:44100526 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:160251771 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:160251771 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:51057112 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:51057112 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:52765608 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:52765608 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:70363999 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:70363999 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:112298544 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:112298544 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:6477157 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:6477157 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:33047175 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:33047175 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:38126680 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:38126680 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:83252705 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:83252705 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:124390051 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:124390051 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:21654941 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:21654941 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:76506405 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:76506405 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:76506407 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:76506407 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:102966940 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:102966940 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:39178759 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:39178759 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:84867843 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:84867843 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:129231439 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:129231439 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:169472785 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:169472785 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:73220131 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:73220131 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27156066 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27156066 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:28736229 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:28736229 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:28910015 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:28910015 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:29054421 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:29054421 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:35396518 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:35396518 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:58959800 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:58959800 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:48624413 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:48624413 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:103039460 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:103039460 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:207569533 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:207569533 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:95258803 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:95258803 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:78473903 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:78473903 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:62338367 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:62338367 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:22285096 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:22285096 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:68058451 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:68058451 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:31850425 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:31850425 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:36384871 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:36384871 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:184040601 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:184040601 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:14762142 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:14762142 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:77705230 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:77705230 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:5397946 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:5397946 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:89498254 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:89498254 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97185204 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97185204 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:142566118 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:142566118 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:37866303 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:37866303 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:212568769 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:212568769 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:76587914 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:76587914 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:157067889 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:157067889 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:132937785 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:132937785 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:133833929 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:133833929 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:159239266 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:159239266 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:187201278 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:187201278 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:6267129 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:6267129 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:6318741 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:6318741 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:57420777 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:57420777 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:175535481 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:175535481 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6240127 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6240127 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15258119 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15258119 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:29247335 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:29247335 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:45540895 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:45540895 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15880185 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15880185 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:29527391 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:29527391 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:51864004 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:51864004 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:88930214 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:88930214 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:1643441 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:1643441 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:50979295 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:50979295 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:89811520 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:89811520 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:45623017 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:45623017 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150891245 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150891245 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:112922541 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:112922541 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:15935160 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:15935160 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:19184469 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:19184469 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:14922147 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:14922147 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:4554747 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:4554747 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:123239250 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:123239250 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:116034587 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:116034587 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:109275650 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:109275650 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:114299489 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:114299489 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:47570481 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:47570481 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:47427628 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:47427628 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:26505871 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:26505871 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:30819855 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:30819855 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:44192062 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:44192062 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:76979747 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:76979747 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:74021325 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:74021325 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:24629657 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:24629657 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:42465934 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:42465934 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:42718313 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:42718313 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59610632 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59610632 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:110390318 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:110390318 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:30747007 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:30747007 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:58483116 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:58483116 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:19776216 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:19776216 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:167764825 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:167764825 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:157407298 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:157407298 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:132889669 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:132889669 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:135443782 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:135443782 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:134940850 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:134940850 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:109446660 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:109446660 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:28493765 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:28493765 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123469443 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123469443 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:101878818 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:101878818 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:102511927 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:102511927 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:51752240 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:51752240 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:178415911 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:178415911 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:126544244 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:126544244 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:3629700 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:3629700 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:110260113 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:110260113 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:547499 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:547499 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:115337732 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:115337732 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:7866243 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:7866243 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:156515817 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:156515817 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:5290649 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:5290649 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:42159946 G>T maps to ENST00000393621 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:42159946 G>T maps to ENST00000393621 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41052495 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41052495 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:43447345 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:43447345 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:28375477 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:28375477 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:28413455 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:28413455 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:80679575 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:80679575 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:81340888 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:81340888 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:114500620 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:114500620 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:26157396 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:26157396 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:27775976 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:27775976 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:75108997 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:75108997 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:100995253 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:100995253 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:186390689 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:186390689 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:148842514 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:148842514 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:22183690 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:22183690 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:8306010 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:8306010 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158970047 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158970047 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:42232905 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:42232905 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:42249676 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:42249676 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:23390905 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:23390905 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:207010477 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:207010477 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:113819694 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:113819694 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:37524961 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:37524961 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:1460573 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:1460573 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:100950071 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:100950071 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:38352396 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:38352396 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:118866014 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:118866014 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:153744469 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:153744469 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:201827503 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:201827503 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:237415978 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:237415978 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:51937334 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:51937334 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:123150168 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:123150168 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:2747803 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:2747803 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:52223595 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:52223595 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:173352192 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:173352192 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15725834 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15725834 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:31435762 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:31435762 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:3632727 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:3632727 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:7658104 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:7658104 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:3199339 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:3199339 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:26596389 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:26596389 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:6051522 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:6051522 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:27066363 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:27066363 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:42132587 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:42132587 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:40327530 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:40327530 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:41303296 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:41303296 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:138650393 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:138650393 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:138670485 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:138670485 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:138671081 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:138671081 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:35739453 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:35739453 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:4830248 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:4830248 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:46288102 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:46288102 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:43890054 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:43890054 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:43896081 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:43896081 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:34972182 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:34972182 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:128697123 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:128697123 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:86570732 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:86570732 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:1903572 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:1903572 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:200530081 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:200530081 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:4906197 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:4906197 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55266611 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55266611 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:44569890 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:44569890 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:129761848 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:129761848 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:202880142 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:202880142 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51582062 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51582062 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51331125 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51331125 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:123103165 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:123103165 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:53166403 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:53166403 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:53091363 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:53091363 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:39726340 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:39726340 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:32253287 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:32253287 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:129663726 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:129663726 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:112522939 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:112522939 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:60887173 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:60887173 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:55433940 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:55433940 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:931759 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:931759 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:45500205 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:45500205 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:149983389 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:149983389 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:40800014 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:40800014 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:139639196 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:139639196 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:48935982 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:48935982 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:126777304 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:126777304 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55087625 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55087625 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55176536 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55176536 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:90534338 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:90534338 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:176778123 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:176778123 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:70409154 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:70409154 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:16757969 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:16757969 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150444682 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150444682 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:135178166 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:135178166 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:148346484 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:148346484 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:161085190 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:161085190 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:7087410 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:7087410 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2925419 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2925419 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:99762232 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:99762232 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:3712396 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:3712396 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:30901091 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:30901091 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2259100 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2259100 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2260695 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2260695 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:151283558 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:151283558 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:172944059 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:172944059 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:67537935 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:67537935 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:36641783 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:36641783 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:45959582 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:45959582 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:32800177 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:32800177 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:63672573 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:63672573 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:18233412 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:18233412 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:3784051 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:3784051 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:70948585 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:70948585 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:113744164 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:113744164 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:138708750 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:138708750 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:47669807 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:47669807 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:47669821 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:47669821 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:126783245 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:126783245 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:36865312 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:36865312 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:73008566 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:73008566 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56236012 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56236012 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158811873 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158811873 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:106199660 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:106199660 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:179322480 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:179322480 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:36921782 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:36921782 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:44814834 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:44814834 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:60565734 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:60565734 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:63526089 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:63526089 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:1081574 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:1081574 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:102008385 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:102008385 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:10369441 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:10369441 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:33574880 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:33574880 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:33578005 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:33578005 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:30421408 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:30421408 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:169502545 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:169502545 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:16681909 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:16681909 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:76565043 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:76565043 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:2088499 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:2088499 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:150042616 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:150042616 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:1855381 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:1855381 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:62854554 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:62854554 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:78445053 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:78445053 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:16918200 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:16918200 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:102884008 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:102884008 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:22790676 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:22790676 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:134063835 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:134063835 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:39689967 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:39689967 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:183821070 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:183821070 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:126136628 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:126136628 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2589994 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2589994 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:21178711 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:21178711 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:44902843 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:44902843 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:69693516 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:69693516 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:77193395 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:77193395 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:129754865 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:129754865 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233839310 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233839310 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:25791398 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:25791398 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:36995919 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:36995919 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:21493165 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:21493165 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:5456665 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:5456665 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:56544273 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:56544273 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15213358 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:15213358 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:89059880 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:89059880 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:110901995 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:110901995 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32780965 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32780965 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:24329305 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:24329305 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:115381983 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:115381983 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:107838572 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:107838572 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:52260316 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:52260316 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:50149447 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:50149447 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:152018790 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:152018790 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:6602675 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:6602675 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156834454 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156834454 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:110255551 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:110255551 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:37305005 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:37305005 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:135272443 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:135272443 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:62568982 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:62568982 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:113384831 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:113384831 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:48835351 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:48835351 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6865487 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6865487 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123893681 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123893681 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:57996358 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:57996358 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248247356 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248247356 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248247876 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248247876 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248616084 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248616084 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248084205 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248084205 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:102345920 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:102345920 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:22332695 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:22332695 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:5462855 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:5462855 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6008213 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6008213 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:148693385 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:148693385 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:21709213 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:21709213 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:32058768 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:32058768 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:17556724 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:17556724 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:6739803 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:6739803 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:51532095 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:51532095 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:162864321 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:162864321 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150780293 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:150780293 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:102546795 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:102546795 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:17843686 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:17843686 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:233120018 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:233120018 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:233353745 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:233353745 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:78547265 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:78547265 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:5570145 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:5570145 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:178562050 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:178562050 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:178592284 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:178592284 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:144915414 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:144915414 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:24551978 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:24551978 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32072175 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32072175 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:57344556 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:57344556 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:56763924 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:56763924 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:179576807 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:179576807 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:61018547 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:61018547 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:64410428 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:64410428 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:118485196 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:118485196 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:139745154 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:139745154 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:3656387 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:3656387 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:47930374 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:47930374 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3026605 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3026605 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:131467831 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:131467831 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:125267997 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:125267997 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:38524130 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:38524130 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:28825817 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:28825817 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:9459498 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:9459498 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:81914474 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:81914474 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:242383206 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:242383206 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:132109885 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:132109885 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:12024006 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:12024006 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:103041824 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:103041824 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:145912118 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:145912118 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:50727319 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:50727319 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:72153083 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:72153083 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:84537352 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:84537352 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:57887233 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:57887233 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:38172918 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:38172918 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:18807173 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:18807173 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:4937126 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:4937126 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:60712663 G>A maps to NM_177952.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:60712663 G>A maps to NM_177952.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:37531301 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:37531301 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:54976672 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:54976672 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:182826812 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:182826812 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:23509247 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:23509247 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:24197010 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:24197010 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:54394898 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:54394898 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:48731853 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:48731853 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:13628923 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:13628923 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:73686109 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:73686109 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:43448294 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:43448294 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:43520229 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:43520229 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:28114796 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:28114796 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:198608360 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:198608360 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:198668677 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:198668677 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:9090951 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:9090951 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55707829 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55707829 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:41306418 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:41306418 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:121637824 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:121637824 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:52252053 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:52252053 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:52387733 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:52387733 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:58385173 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:58385173 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:3146024 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:3146024 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66039814 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66039814 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:82705222 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:82705222 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:34687101 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:34687101 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:113546080 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:113546080 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:178111084 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:178111084 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:145648948 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:145648948 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:79385647 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:79385647 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:103234626 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:103234626 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:117244205 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:117244205 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:192545117 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:192545117 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:240969428 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:240969428 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:8132163 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:8132163 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:8160050 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:8160050 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:123900680 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:123900680 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:43386189 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:43386189 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:40695238 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:40695238 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:196201993 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:196201993 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:55609150 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:55609150 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:83403147 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:83403147 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:213434797 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:213434797 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:62305161 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:62305161 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:46541810 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:46541810 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:159560533 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:159560533 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:237663944 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:237663944 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:237890380 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:237890380 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:71912107 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:71912107 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:136577867 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:136577867 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:10013940 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:10013940 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:41502887 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:41502887 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123513123 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123513123 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:38664015 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:38664015 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:167284287 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:167284287 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:71354394 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:71354394 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:39555171 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:39555171 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:169588314 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:169588314 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:80433293 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:80433293 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:115815989 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:115815989 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:19707633 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:19707633 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:61223647 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:61223647 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:52890328 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:52890328 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:49135800 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:49135800 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:96339206 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:96339206 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:18250700 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:18250700 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:52002533 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:52002533 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:52130565 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:52130565 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:115321740 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:115321740 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:164751120 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:164751120 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:36171854 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:36171854 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:159921404 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:159921404 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:43262217 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:43262217 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:22387314 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:22387314 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:20031787 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:20031787 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:110756949 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:110756949 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:107314546 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:107314546 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:85464111 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:85464111 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:85488467 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:85488467 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:32427025 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:32427025 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:118147546 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:118147546 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:61451634 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:61451634 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:220502244 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:220502244 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:55691007 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:55691007 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:1394912 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:1394912 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:149584220 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:149584220 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:70145655 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:70145655 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:23245230 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:23245230 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:70527358 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:70527358 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:20512544 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:20512544 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150936138 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150936138 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:17865119 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:17865119 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2722723 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2722723 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2747477 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2747477 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2763595 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2763595 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:246091141 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:246091141 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:49831347 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:49831347 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:121799163 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:121799163 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:25155032 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:25155032 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:25213248 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:25213248 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:25213287 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:25213287 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:46198967 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:46198967 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:95018211 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:95018211 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:35759607 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:35759607 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:55903683 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:55903683 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:1165499 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:1165499 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158584890 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158584890 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158631213 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158631213 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:41066030 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:41066030 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:30724817 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:30724817 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:48206759 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:48206759 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:55020062 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:55020062 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:104118965 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:104118965 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:74476056 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:74476056 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:57248820 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:57248820 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:132824484 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:132824484 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:120941723 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:120941723 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:25326511 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:25326511 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:900022 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:900022 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:31573044 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:31573044 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:21840300 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:21840300 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:159128440 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:159128440 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:57406597 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:57406597 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:35836831 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:35836831 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:6639735 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:6639735 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:67400068 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:67400068 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:102529648 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:102529648 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151748774 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151748774 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:48230690 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:48230690 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:115857963 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:115857963 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:2290770 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:2290770 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:43527550 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:43527550 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:56723334 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:56723334 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151820640 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151820640 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:88472941 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:88472941 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:32526505 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:32526505 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56817008 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56817008 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98133621 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98133621 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98292781 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98292781 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:75315567 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:75315567 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:108985201 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:108985201 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:98448980 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:98448980 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:36231914 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:36231914 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:152058723 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:152058723 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:104228714 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:104228714 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:63170589 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:63170589 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:9316991 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:9316991 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:98940095 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:98940095 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:44453088 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:44453088 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:40444875 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:40444875 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:175372834 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:175372834 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:38554792 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:38554792 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:42601995 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:42601995 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:223991798 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:223991798 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:45472437 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:45472437 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:81609172 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:81609172 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:180319982 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:180319982 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179473883 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179473883 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179528864 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179528864 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:94701 C>A maps to ENST00000447903 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:94701 C>A maps to ENST00000447903 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:83669668 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:83669668 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:129592299 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:129592299 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:19455380 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:19455380 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:75131430 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:75131430 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:17728724 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:17728724 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:176305666 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:176305666 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:158971590 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:158971590 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:215853725 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:215853725 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:17205573 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:17205573 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:58283157 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:58283157 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:61448810 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:61448810 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:11955358 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:11955358 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:5033993 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:5033993 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:108116565 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:108116565 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:100587816 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:100587816 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:2845516 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:2845516 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:14947790 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:14947790 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:71130288 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:71130288 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10079224 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:10079224 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:44299680 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:44299680 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:151082055 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:151082055 T>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:44333263 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:44333263 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:2726121 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chrX:2726121 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:17294543 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:17294543 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:100333400 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:100333400 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:62384246 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:62384246 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:57440516 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:57440516 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:145161806 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:145161806 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:135602645 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:135602645 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:73464461 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:73464461 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:57290895 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:57290895 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:28327302 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:28327302 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:9495417 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:9495417 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3451955 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3451955 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:45004335 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:45004335 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:44802807 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:44802807 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:24270223 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:24270223 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:31906111 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:31906111 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:32340858 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:32340858 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:53625930 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:53625930 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:58087427 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:58087427 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:31166055 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:31166055 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:57199985 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:57199985 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:44764009 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:44764009 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27825850 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27825850 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:31048130 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:31048130 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:85341718 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:85341718 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:64839 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:64839 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:227826919 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:227826919 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:106060 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:106060 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:57988457 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:57988457 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:47879867 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:47879867 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:52566650 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:52566650 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:57220830 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:57220830 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:67082709 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:67082709 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:1044508 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:1044508 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:48141208 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:48141208 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:101594493 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:101594493 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:156775469 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:156775469 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:23562609 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:23562609 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:49511089 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:49511089 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:88016154 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:88016154 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:115226989 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:115226989 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:41545811 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:41545811 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:5939549 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:5939549 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:26678047 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:26678047 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:77512133 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:77512133 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:83358225 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:83358225 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:6432690 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:6432690 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:33386944 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:33386944 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:141036032 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:141036032 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:42398690 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:42398690 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:23321786 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:23321786 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:7080026 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:7080026 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:160099286 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:160099286 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:54059049 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:54059049 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:18238752 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:18238752 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:203378653 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:203378653 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:180376166 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:180376166 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:33141019 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:33141019 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:118424165 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:118424165 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:30035560 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:30035560 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:8131486 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:8131486 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:31660060 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:31660060 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:63664754 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:63664754 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:169673168 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:169673168 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:41149306 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:41149306 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:86250417 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:86250417 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:54418840 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:54418840 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:159163592 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:159163592 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:104934726 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:104934726 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:134331897 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:134331897 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:92963513 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:92963513 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:85626332 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:85626332 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:25583208 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:25583208 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:60511761 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:60511761 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:85972791 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:85972791 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:50805554 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:50805554 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:15808917 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:15808917 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:22303653 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:22303653 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:22303769 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:22303769 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:88515072 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:88515072 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:60036865 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:60036865 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:78056651 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:78056651 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:87666322 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:87666322 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:103348928 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:103348928 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:139696776 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:139696776 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:137619310 A>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:137619310 A>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:130020358 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:130020358 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:2777787 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:2777787 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:125530698 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:125530698 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:36775851 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:36775851 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:3087469 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:3087469 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:67679944 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:67679944 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:41450772 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:41450772 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:15661578 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:15661578 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:33290710 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:33290710 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:36383312 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:36383312 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:74124222 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:74124222 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:9171824 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:9171824 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:83183722 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:83183722 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:6697496 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:6697496 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:31379349 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:31379349 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:63098997 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:63098997 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:154172209 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:154172209 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:15524528 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:15524528 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:16921847 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:16921847 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:110884189 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:110884189 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:110901025 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:110901025 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:31864666 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:31864666 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:37917293 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:37917293 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:18556213 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:18556213 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:48829984 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:48829984 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:128044237 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:128044237 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:37608051 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:37608051 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:53671428 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:53671428 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:216741309 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:216741309 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:11142706 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:11142706 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:47529305 A>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:47529305 A>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:184767195 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:184767195 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:50060006 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:50060006 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:86602464 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:86602464 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:14851266 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:14851266 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:44281690 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:44281690 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:26534806 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:26534806 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:58010382 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:58010382 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:35884947 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:35884947 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:233594297 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:233594297 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:45008637 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:45008637 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:20329465 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:20329465 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:92345397 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:92345397 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:1106304 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:1106304 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:176867849 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:176867849 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:144764707 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:144764707 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:189448946 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:189448946 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:19373450 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:19373450 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:153214696 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:153214696 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:242194374 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:242194374 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:43702282 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:43702282 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:114134857 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:114134857 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:3225020 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:3225020 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:163150260 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:163150260 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:129222990 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:129222990 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:129236547 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:129236547 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:65622212 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:65622212 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:102626010 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:102626010 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:128032957 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:128032957 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:68632066 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:68632066 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:31336386 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:31336386 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:113829246 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:113829246 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:62078212 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:62078212 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:142641350 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:142641350 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:154523897 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:154523897 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:180907658 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:180907658 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:175223358 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:175223358 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:10397383 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:10397383 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:158063632 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:158063632 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:52841398 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:52841398 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:138415156 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:138415156 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:82437664 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:82437664 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:170053359 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:170053359 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:14108520 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:14108520 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:56171241 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:56171241 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:3779201 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:3779201 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:127411243 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:127411243 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:36210584 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:36210584 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:29638015 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:29638015 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:56356879 G>T maps to ENST00000340482 C184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:56356879 G>T maps to ENST00000340482 C184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:19077995 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:19077995 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:23866735 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:23866735 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:211155711 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:211155711 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:95082798 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:95082798 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:175184976 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:175184976 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:15696983 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:15696983 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:16908278 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:16908278 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:232327374 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:232327374 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:50583221 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:50583221 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:7065218 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:7065218 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26114990 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26114990 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:110901066 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:110901066 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:36326758 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:36326758 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:153660054 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:153660054 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:50733625 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:50733625 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:64416106 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:64416106 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:78709986 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:78709986 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:167630601 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:167630601 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:248247426 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:248247426 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:20502919 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:20502919 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:20295545 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:20295545 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:52861685 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:52861685 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:74803519 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:74803519 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:17657704 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:17657704 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:112900056 C>T maps to NM_007203.4 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:112900056 C>T maps to NM_007203.4 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:183605617 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:183605617 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:33073085 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:33073085 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:31829843 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:31829843 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:133895717 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:133895717 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:77661194 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:77661194 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26890571 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26890571 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:8770790 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:8770790 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:131951799 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:131951799 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr21:46703272 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr21:46703272 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:50902594 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:50902594 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:23826015 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:23826015 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:104220699 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:104220699 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:182850700 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:182850700 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:7064520 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:7064520 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:198703372 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:198703372 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:8748053 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:8748053 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:71066470 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:71066470 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:41400256 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:41400256 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:121694244 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:121694244 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:135907881 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:135907881 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:131976662 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:131976662 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:36278086 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:36278086 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:20563984 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:20563984 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:5927932 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:5927932 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:69036762 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:69036762 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:80363826 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:80363826 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:145634377 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:145634377 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:103202243 A>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:103202243 A>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:118469110 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:118469110 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:16475313 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:16475313 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:121286718 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:121286718 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:73108844 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:73108844 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:73108848 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:73108848 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:104302698 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:104302698 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr22:30776236 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr22:30776236 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:45091963 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:45091963 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:41820293 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:41820293 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:21762759 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:21762759 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:3624025 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:3624025 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:157994017 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:157994017 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:153835449 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:153835449 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:167319149 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:167319149 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:101133437 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:101133437 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:135171426 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:135171426 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:132237593 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:132237593 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:67763159 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:67763159 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:116728429 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:116728429 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:85488258 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:85488258 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:68404319 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:68404319 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:22273580 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:22273580 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:28544442 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:28544442 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:70706556 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:70706556 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:20530757 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:20530757 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:2161966 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:2161966 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:82713902 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:82713902 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:55371035 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:55371035 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:24048569 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:24048569 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:231150583 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:231150583 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:22657340 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:22657340 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:23760879 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:23760879 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:29811265 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:29811265 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:152489175 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:152489175 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:35271048 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:35271048 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:74868110 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:74868110 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:52928652 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:52928652 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:100230837 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:100230837 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:48359579 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:48359579 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:126068360 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:126068360 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:100349971 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrX:100349971 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:68812312 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:68812312 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:152230149 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:152230149 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:1950513 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:1950513 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:20000695 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:20000695 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr21:10935062 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr21:10935062 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:41196868 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:41196868 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:41197728 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:41197728 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:55032844 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:55032844 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:72732637 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:72732637 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:248039169 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:248039169 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:38225619 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:38225619 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:98490256 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:98490256 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:94527 G>A maps to ENST00000413237 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:94527 G>A maps to ENST00000413237 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:138043807 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:138043807 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:229783176 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:229783176 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:75264937 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:75264937 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrY:14888553 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chrY:14888553 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:39280316 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:39280316 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:112899486 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:112899486 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:100395401 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:100395401 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:25317108 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:25317108 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:40554958 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:40554958 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:64442297 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:64442297 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:44946726 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:44946726 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:9523935 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:9523935 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:52934611 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:52934611 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:71631176 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:71631176 G>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:40556271 T>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:40556271 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:125587111 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:125587111 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:4715541 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:4715541 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:39466549 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:39466549 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:67433998 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:67433998 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:38710957 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:38710957 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:203820378 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:203820378 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:16644280 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:16644280 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:70026199 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:70026199 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:160099208 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:160099208 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:28890181 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:28890181 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:62449029 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:62449029 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:32703580 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:32703580 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:76647210 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:76647210 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:35731032 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:35731032 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:3274967 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:3274967 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:58645572 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:58645572 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:113530509 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:113530509 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:165712879 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:165712879 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:39285356 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:39285356 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:49913231 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:49913231 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:135676392 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:135676392 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:111439233 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:111439233 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:42091698 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:42091698 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr22:29105849 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr22:29105849 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:93398117 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:93398117 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:160302204 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:160302204 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:3782012 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:3782012 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:53552174 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:53552174 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:9446339 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:9446339 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:955680 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:955680 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr10:22217403 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr10:22217403 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:162865052 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:162865052 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:40318861 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:40318861 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:67231869 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:67231869 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:93018657 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:93018657 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:190129790 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:190129790 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:150970048 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:150970048 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:152275135 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:152275135 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:154274740 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:154274740 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:54581211 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:54581211 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:157407024 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:157407024 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:93808580 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:93808580 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:120400768 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:120400768 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:29896308 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:29896308 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr21:44949576 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr21:44949576 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:8823087 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:8823087 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:113540279 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:113540279 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:33029994 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:33029994 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:75143156 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:75143156 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:22659630 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:22659630 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:123075810 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:123075810 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:52790037 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:52790037 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr15:68123099 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr15:68123099 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:6942710 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:6942710 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:40196514 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:40196514 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:41649022 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:41649022 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:110789172 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:110789172 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:46903193 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:46903193 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:160706477 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:160706477 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:20193767 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:20193767 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:119744939 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:119744939 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr22:50599507 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr22:50599507 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr22:26158987 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr22:26158987 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:102859472 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:102859472 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:233296006 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:233296006 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:186435329 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:186435329 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:22108522 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chrX:22108522 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:201437487 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:201437487 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:201437500 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:201437500 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:142430474 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:142430474 T>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:38122504 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:38122504 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:7662947 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:7662947 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:61924171 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:61924171 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:82092979 A>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:82092979 A>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:20491804 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:20491804 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:52412247 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:52412247 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:43938385 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:43938385 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:31511111 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:31511111 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:246927523 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:246927523 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:155771451 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:155771451 C>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:157817957 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:157817957 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:56629138 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:56629138 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:57192921 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:57192921 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr15:42154539 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr15:42154539 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:155979463 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:155979463 T>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:104155038 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:104155038 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:57640489 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:57640489 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:97362111 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:97362111 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:196022836 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:196022836 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:1944414 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:1944414 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:103718682 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:103718682 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:215953412 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr1:215953412 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:6134979 A>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:6134979 A>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:31567640 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:31567640 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:217021210 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:217021210 T>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:69184657 A>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:69184657 A>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:100364629 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:100364629 C>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:187368745 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:187368745 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:57653913 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:57653913 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:44653147 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:44653147 A>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr18:22932063 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr18:22932063 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:57828204 G>A did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:57828204 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:7715095 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:7715095 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:9006869 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:9006869 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:41107790 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:41107790 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:41131389 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:41131389 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:67189811 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:67189811 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:66981139 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:66981139 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:67003761 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:67003761 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:87190445 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:87190445 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:48256470 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:48256470 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:150923297 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:150923297 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:47340588 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:47340588 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76727690 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76727690 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:55077178 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:55077178 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:74035937 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:74035937 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:20548526 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:20548526 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:65480774 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:65480774 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:52314695 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:52314695 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:67412463 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:67412463 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:156915541 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:156915541 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:136303067 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:136303067 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:64756274 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:64756274 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154560547 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154560547 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:123044353 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:123044353 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:131964087 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:131964087 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:33585800 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:33585800 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:44152582 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:44152582 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:84515956 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:84515956 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:91714099 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:91714099 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117139858 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117139858 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:3749886 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:3749886 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:85382917 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:85382917 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:112033790 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:112033790 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:41542216 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:41542216 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:54517673 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:54517673 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:14798086 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:14798086 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:37441152 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:37441152 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:42022897 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:42022897 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:26781460 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:26781460 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156563888 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156563888 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:148800575 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:148800575 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:32096560 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:32096560 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:24941996 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:24941996 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:69015193 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:69015193 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161029314 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161029314 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156911842 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156911842 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:18948533 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:18948533 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:23244614 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:23244614 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:80806502 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:80806502 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:94919011 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:94919011 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:94417296 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:94417296 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:62577895 G>T maps to NM_020164.4 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:62577895 G>T maps to NM_020164.4 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:119943284 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:119943284 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:89574406 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:89574406 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:96761553 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:96761553 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:25946977 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:25946977 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:160061620 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:160061620 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:194180177 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:194180177 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160106830 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160106830 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160147257 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160147257 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28914821 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28914821 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:138432379 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:138432379 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:67472862 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:67472862 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:104053280 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:104053280 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154306938 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154306938 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154313296 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154313296 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154316290 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154316290 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:94118344 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:94118344 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:41762529 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:41762529 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:30724119 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:30724119 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:11029701 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:11029701 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:11058388 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:11058388 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:56536501 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:56536501 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156617924 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156617924 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:61871000 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:61871000 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:22616438 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:22616438 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:33945372 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:33945372 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:108011011 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:108011011 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:26391097 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:26391097 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21679748 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21679748 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:91662697 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:91662697 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:95884072 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:95884072 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23459212 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23459212 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:36909229 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:36909229 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:3546516 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:3546516 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56621646 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56621646 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:1231321 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:1231321 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:7743311 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:7743311 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:92696861 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:92696861 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:182873666 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:182873666 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:75114797 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:75114797 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:60990803 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:60990803 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:74867432 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:74867432 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:85059359 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:85059359 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:164435124 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:164435124 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:5961050 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:5961050 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37107687 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37107687 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37122496 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37122496 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:41037716 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:41037716 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:109480119 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:109480119 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:31736866 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:31736866 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:42971887 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:42971887 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:99755170 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:99755170 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:146277895 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:146277895 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:69688720 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:69688720 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150236031 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150236031 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150236103 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150236103 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:141010190 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:141010190 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:181707487 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:181707487 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:181731688 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:181731688 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:85932617 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:85932617 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159166862 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159166862 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:54117618 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:54117618 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:12811562 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:12811562 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:149636102 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:149636102 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:49899659 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:49899659 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:76889646 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:76889646 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32670141 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32670141 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:111291170 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:111291170 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:111317664 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:111317664 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52439480 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52439480 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:34416669 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:34416669 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:78079901 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:78079901 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145696533 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145696533 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28948896 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28948896 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28949219 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28949219 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158147091 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158147091 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:112648453 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:112648453 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:112066341 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:112066341 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160803826 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160803826 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72700975 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72700975 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:22416541 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:22416541 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:54606766 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:54606766 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:24535753 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:24535753 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:21882755 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:21882755 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:59174535 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:59174535 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:31316244 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:31316244 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:22360941 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:22360941 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43031141 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43031141 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:45024796 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:45024796 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:214782036 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:214782036 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:117246825 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:117246825 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:431183 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:431183 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:29548800 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:29548800 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:6980037 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:6980037 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:10145966 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:10145966 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:10151775 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:10151775 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:8618351 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:8618351 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:45923086 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:45923086 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:10542274 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:10542274 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:72006460 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:72006460 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:150661560 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:150661560 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:175843436 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:175843436 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23847726 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23847726 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:87671498 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:87671498 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:146829626 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:146829626 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:125555923 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:125555923 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:125671990 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:125671990 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7851201 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7851201 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:33138234 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:33138234 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:121237317 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:121237317 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32154450 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32154450 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:139614238 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:139614238 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:177771829 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:177771829 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117015370 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117015370 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117052425 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117052425 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117064343 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117064343 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117064505 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:117064505 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:10083743 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:10083743 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:70965126 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:70965126 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:71009652 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:71009652 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160260559 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160260559 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160261565 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160261565 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160261590 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160261590 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160267546 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160267546 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:101478326 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:101478326 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:1260005 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:1260005 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:122733080 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:122733080 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:113266448 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:113266448 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:68102871 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:68102871 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:23731241 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:23731241 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:19999169 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:19999169 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:225364087 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:225364087 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:36958279 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:36958279 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:84569409 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:84569409 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:22999275 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:22999275 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:51507852 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:51507852 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:15769377 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:15769377 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:15739434 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:15739434 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:109286888 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:109286888 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155671912 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155671912 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:16646699 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:16646699 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160188278 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160188278 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160252903 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160252903 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155018566 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155018566 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:19352392 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:19352392 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:32287164 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:32287164 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:42734389 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:42734389 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:137304499 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:137304499 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:125467171 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:125467171 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:140958641 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:140958641 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:415326 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:415326 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:79628817 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:79628817 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:124348439 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:124348439 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:21599448 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:21599448 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:13919218 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:13919218 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:196865349 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:196865349 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:11656325 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:11656325 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:56188233 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:56188233 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:230231493 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:230231493 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:45674638 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:45674638 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220250939 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220250939 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:225657958 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:225657958 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:169122950 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:169122950 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:51264673 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:51264673 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27121305 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27121305 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:113286088 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:113286088 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:56479106 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:56479106 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:45390186 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:45390186 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:304531 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:304531 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:44028892 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:44028892 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:120936036 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:120936036 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:19251620 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:19251620 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:131666016 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:131666016 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150485949 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150485949 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:12290834 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:12290834 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:62128791 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:62128791 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:34395179 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:34395179 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:40351498 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:40351498 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27592270 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:27592270 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:78118069 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:78118069 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:12908229 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:12908229 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:101439077 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:101439077 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:100380421 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:100380421 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:111482455 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:111482455 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:38186586 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:38186586 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:143092361 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:143092361 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:66270033 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:66270033 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:66361002 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:66361002 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:97439276 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:97439276 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:93968070 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:93968070 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:22924726 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:22924726 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:142564648 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:142564648 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:37868113 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:37868113 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157106151 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157106151 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:140242511 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:140242511 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:73053106 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:73053106 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:130710279 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:130710279 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:22999863 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:22999863 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:139190669 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:139190669 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:61043079 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:61043079 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:29268173 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:29268173 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:68934410 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:68934410 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:89118065 T>A maps to ENST00000330762 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:89118065 T>A maps to ENST00000330762 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:130861442 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:130861442 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:37581169 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:37581169 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:10089739 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:10089739 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:10106318 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:10106318 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29464984 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29464984 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29486518 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29486518 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:5609941 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:5609941 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:13039754 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:13039754 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:92592183 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:92592183 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:126402913 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:126402913 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:45929619 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:45929619 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:87380922 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:87380922 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161475930 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161475930 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157550197 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157550197 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157485554 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157485554 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157489646 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157489646 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157497307 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157497307 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159779071 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:159779071 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:32793150 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:32793150 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179341713 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179341713 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179343273 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179343273 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:28891525 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:28891525 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:33192153 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:33192153 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:240306057 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:240306057 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:50047433 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:50047433 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:50059884 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:50059884 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:171178117 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:171178117 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:203225262 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:203225262 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:79398894 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:79398894 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:49400635 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:49400635 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:32849247 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:32849247 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:37446173 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:37446173 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:78092445 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:78092445 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:1961208 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:1961208 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:27586186 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:27586186 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:9885022 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:9885022 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:89664365 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:89664365 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109069094 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109069094 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76979487 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76979487 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:134234321 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:134234321 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:58714479 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:58714479 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:42931460 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:42931460 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131036295 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131036295 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155784364 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155784364 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:113941368 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:113941368 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:46950455 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:46950455 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:122537221 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:122537221 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:105758305 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:105758305 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:102372662 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:102372662 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:102511943 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:102511943 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:148730430 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:148730430 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:56892616 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:56892616 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:39121976 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:39121976 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:134705030 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:134705030 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154247851 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154247851 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:106840768 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:106840768 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:48191839 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:48191839 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:31789501 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:31789501 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:28375743 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:28375743 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:80394974 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:80394974 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:210686404 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:210686404 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:191184536 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:191184536 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:75189007 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:75189007 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:25727535 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:25727535 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:31256268 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:31256268 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:121437059 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:121437059 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:27194525 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:27194525 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:54422170 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:54422170 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:26875202 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:26875202 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152195433 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152195433 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:26044074 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:26044074 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:145532732 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:145532732 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:31735727 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:31735727 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:70897651 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:70897651 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:25678951 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:25678951 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:21209646 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:21209646 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:112112721 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:112112721 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:102979109 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:102979109 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:70329021 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:70329021 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154437501 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154437501 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:79673046 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:79673046 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:128040029 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:128040029 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:77705769 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:77705769 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32672011 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32672011 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156532896 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156532896 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156542350 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156542350 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:182374252 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:182374252 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:37627015 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:37627015 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:3632950 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:3632950 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:31283127 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:31283127 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:73726950 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:73726950 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:7608422 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:7608422 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:7611544 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:7611544 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:7615249 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:7615249 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:4681162 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:4681162 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:35154268 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:35154268 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:87678712 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:87678712 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:39912310 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:39912310 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:40268989 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:40268989 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:170159925 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:170159925 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:78868233 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:78868233 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154705739 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154705739 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154821554 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154821554 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:44169215 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:44169215 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:61005992 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:61005992 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24905206 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24905206 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:43895517 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:43895517 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:22678519 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:22678519 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:123091738 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:123091738 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:138630048 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:138630048 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:29046015 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:29046015 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:21031414 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:21031414 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72348811 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72348811 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:137519857 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:137519857 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:200957523 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:200957523 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55246861 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55246861 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:27950602 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:27950602 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:39086438 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:39086438 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:52841488 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:52841488 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:53166490 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:53166490 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:52627068 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:52627068 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:112521397 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:112521397 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:50794878 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:50794878 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:45517810 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:45517810 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150939205 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150939205 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:73637987 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:73637987 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:203740073 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:203740073 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:36993452 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:36993452 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:36995373 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:36995373 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152648366 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152648366 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:65609715 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:65609715 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:95518124 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:95518124 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:104308386 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:104308386 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:54845141 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:54845141 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55177445 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55177445 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:41689959 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:41689959 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109297244 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109297244 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:83860645 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:83860645 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:91005604 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:91005604 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:70415709 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:70415709 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:148252935 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:148252935 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153233316 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153233316 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:99358715 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:99358715 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:99358717 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:99358717 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:197579411 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:197579411 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100179881 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100179881 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:141083284 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:141083284 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:141201752 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:141201752 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:141819844 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:141819844 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:170093516 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:170093516 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:50121435 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:50121435 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:65308246 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:65308246 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:149925137 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:149925137 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29599210 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29599210 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:30900802 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:30900802 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:39696922 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:39696922 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:39929401 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:39929401 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:21205437 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:21205437 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:161510237 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:161510237 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:75353800 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:75353800 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220835587 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220835587 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:85769160 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:85769160 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:5935210 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:5935210 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:47315173 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:47315173 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:63833069 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:63833069 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:90366262 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:90366262 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:37386719 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:37386719 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:36633030 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:36633030 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:141786543 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:141786543 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:74936389 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:74936389 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:151944944 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:151944944 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:223559350 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:223559350 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:17083968 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:17083968 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156707812 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156707812 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156708252 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156708252 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:131220326 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:131220326 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:55478602 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:55478602 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:55754427 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:55754427 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155584472 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155584472 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:95569287 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:95569287 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:49409759 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:49409759 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:29844965 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:29844965 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:3243044 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:3243044 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:153027360 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:153027360 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:8379069 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:8379069 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:50764900 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:50764900 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:108147321 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:108147321 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:10440521 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:10440521 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23851238 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23851238 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:33565715 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:33565715 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:33575776 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:33575776 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23892703 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:23892703 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:26168507 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:26168507 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:52553382 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:52553382 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:76602219 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:76602219 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:71202081 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:71202081 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:101742366 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:101742366 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:78334764 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:78334764 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:78334792 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:78334792 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:78522443 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:78522443 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:204058502 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:204058502 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:16908027 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:16908027 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:22849571 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:22849571 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:134090331 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:134090331 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:133486354 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:133486354 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:132980006 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:132980006 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:32246518 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:32246518 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:45209724 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:45209724 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:73454675 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:73454675 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:68215446 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:68215446 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:14150348 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:14150348 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:104157256 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:104157256 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:65735841 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:65735841 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:16337293 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:16337293 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15029133 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15029133 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15029135 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15029135 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:73865939 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:73865939 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:69760151 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:69760151 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161206232 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161206232 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161207732 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161207732 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:107866054 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:107866054 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:59498436 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:59498436 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:72717381 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:72717381 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:61389564 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:61389564 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131760929 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131760929 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:101581354 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:101581354 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:28141699 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:28141699 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:53602935 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:53602935 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:248166474 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:248166474 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:248247876 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:248247876 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:55889815 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:55889815 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:58110010 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:58110010 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:21728473 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:21728473 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29630179 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29630179 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:79801870 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:79801870 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:79804763 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:79804763 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:43545523 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:43545523 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:163483045 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:163483045 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:138454301 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:138454301 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:102237030 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:102237030 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:102249818 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:102249818 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:135202381 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:135202381 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:150773090 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:150773090 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:150842788 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:150842788 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:128728084 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:128728084 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24568755 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24568755 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:82390668 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:82390668 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:242793525 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:242793525 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:178705174 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:178705174 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:20704803 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:20704803 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:144857088 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:144857088 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:144859640 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:144859640 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:144922749 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:144922749 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:148711877 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:148711877 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156877326 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156877326 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:60974842 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:60974842 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:28792090 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:28792090 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151276173 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151276173 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151288003 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151288003 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:209214843 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:209214843 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:99972072 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:99972072 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57995234 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57995234 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:123497077 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:123497077 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:123497387 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:123497387 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:81204687 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:81204687 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:186880523 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:186880523 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:160885354 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:160885354 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:42046370 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:42046370 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:8705427 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:8705427 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:96022533 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:96022533 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:161135756 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:161135756 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:161152297 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:161152297 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:12026275 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:12026275 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:20500550 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:20500550 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:208269120 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:208269120 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:131831512 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:131831512 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:74336017 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:74336017 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:160224192 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:160224192 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:39647004 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:39647004 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:7619974 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:7619974 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151400942 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151400942 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:62533806 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:62533806 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:76254803 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:76254803 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:149214962 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:149214962 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:143767860 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:143767860 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:81108757 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:81108757 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161141049 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161141049 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:49137966 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:49137966 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:146077842 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:146077842 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:30093734 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:30093734 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:91527862 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:91527862 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:3301938 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:3301938 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:23526202 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:23526202 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:57156385 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:57156385 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:49034314 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:49034314 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:151372756 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:151372756 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:30103556 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:30103556 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:30132884 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:30132884 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:95944302 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:95944302 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:4056787 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:4056787 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:25140289 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:25140289 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:25160827 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:25160827 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150990600 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150990600 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43358274 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43358274 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43709504 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43709504 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151373710 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151373710 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:122326909 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:122326909 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:54148292 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:54148292 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:11591582 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:11591582 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:46945230 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:46945230 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:120684285 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:120684285 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:70980745 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:70980745 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40735633 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40735633 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40827859 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40827859 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40911123 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:40911123 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:108079763 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:108079763 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:52384672 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:52384672 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220369496 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220369496 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:34909162 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:34909162 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:85785639 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:85785639 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109347392 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109347392 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109388362 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109388362 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:36264926 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:36264926 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:131054657 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:131054657 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:28004655 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:28004655 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:145631244 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:145631244 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:178977174 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:178977174 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:79254790 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:79254790 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:183775501 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:183775501 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:163122258 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:163122258 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:49460110 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:49460110 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:49460376 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:49460376 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:38945286 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:38945286 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:123983338 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:123983338 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:105173351 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:105173351 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:96513587 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:96513587 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24619150 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:24619150 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:41823045 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:41823045 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:113325492 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:113325492 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:146015385 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:146015385 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:54705007 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:54705007 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:77524597 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:77524597 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:62294335 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:62294335 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:39025937 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:39025937 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237801646 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237801646 T>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153587691 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153587691 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:18266883 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:18266883 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26686460 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26686460 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:78134002 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:78134002 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:159439555 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:159439555 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:18265022 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:18265022 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:18265044 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:18265044 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:18338343 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:18338343 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:65303695 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:65303695 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:50251630 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:50251630 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:71379953 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:71379953 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151337181 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151337181 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:53922560 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:53922560 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:169586790 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:169586790 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:92064876 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:92064876 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151107998 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151107998 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151114956 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151114956 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:55878791 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:55878791 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:94963092 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:94963092 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:29885111 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:29885111 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:27190468 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:27190468 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:156186406 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:156186406 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:134495847 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:134495847 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:67763165 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:67763165 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:40834517 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:40834517 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:19705765 C>A maps to ENST00000379702 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chrX:19705765 C>A maps to ENST00000379702 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:51207308 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:51207308 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154940600 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154940600 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154940749 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154940749 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:52130576 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:52130576 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:65417543 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:65417543 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:46262237 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:46262237 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160589454 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160589454 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160607339 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160607339 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:48513038 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:48513038 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26817354 G>T maps to NM_001145975.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26817354 G>T maps to NM_001145975.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:135375852 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:135375852 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:119015203 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:119015203 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:92913677 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:92913677 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:48929292 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:48929292 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:66428293 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:66428293 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:58014270 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:58014270 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153751967 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153751967 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:10027615 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:10027615 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33951834 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33951834 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33984275 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33984275 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:85277885 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:85277885 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:110737418 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:110737418 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1218977 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1218977 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1442964 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1442964 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:103300811 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:103300811 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:101709338 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:101709338 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:20487972 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:20487972 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:20569278 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:20569278 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:168201501 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:168201501 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:168690746 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:168690746 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:217300021 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:217300021 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156247100 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:156247100 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:123127530 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:123127530 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:46195164 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:46195164 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:17836340 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:17836340 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:107854882 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:107854882 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:106899297 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:106899297 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:109856582 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:109856582 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26905630 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26905630 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:35692519 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:35692519 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:139307977 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:139307977 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158582585 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158582585 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158596574 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158596574 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131390082 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131390082 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:45774068 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:45774068 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:149509628 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:149509628 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:22439381 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:22439381 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:104151855 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:104151855 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:17747816 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:17747816 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:68449235 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:68449235 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:68449246 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:68449246 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:26949173 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:26949173 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220112046 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:220112046 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:23810609 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:23810609 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:35102634 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:35102634 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:46331249 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:46331249 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:149884757 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:149884757 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:113148098 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:113148098 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29811299 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29811299 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:10894541 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:10894541 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:152477331 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:152477331 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:152590216 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:152590216 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:152832733 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:152832733 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:64450415 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:64450415 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:158483009 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:158483009 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:40850300 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr18:40850300 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:9828799 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:9828799 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:8050982 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:8050982 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:8055902 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:8055902 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72290453 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72290453 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:36358762 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:36358762 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:13288666 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:13288666 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:119474218 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:119474218 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:85422592 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:85422592 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:139572282 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:139572282 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:67815464 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:67815464 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:179632354 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:179632354 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151748753 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151748753 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43910743 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:43910743 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:133485354 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:133485354 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:39885471 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:39885471 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155171153 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155171153 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151847243 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151847243 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:32513872 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:32513872 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:155565923 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:155565923 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:35720231 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:35720231 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:63004085 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:63004085 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:63031755 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:63031755 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:75441685 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:75441685 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:69381972 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:69381972 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:44238742 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:44238742 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:15241038 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:15241038 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:92021079 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:92021079 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:100331133 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:100331133 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151147040 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151147040 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:83359604 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:83359604 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:218713851 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:218713851 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:133320040 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:133320040 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:21945406 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:21945406 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:144345757 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:144345757 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:188925426 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:188925426 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:20067046 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:20067046 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:20069309 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:20069309 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:108568140 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:108568140 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:123824836 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:123824836 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:123957852 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:123957852 A>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72667413 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72667413 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:110131128 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:110131128 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:30157774 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:30157774 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:72733985 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:72733985 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:26384852 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:26384852 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:32915239 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:32915239 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:189065158 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:189065158 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:142499890 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:142499890 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:234835312 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:234835312 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:110236391 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:110236391 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:98596665 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:98596665 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31116702 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31116702 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31116965 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31116965 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:20773927 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:20773927 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:91044750 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:91044750 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179410891 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179410891 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179451810 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:179451810 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:22867640 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:22867640 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151530032 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:151530032 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154238972 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:154238972 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:109921557 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:109921557 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:35390016 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:35390016 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:73050587 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:73050587 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:35542044 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:35542044 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:43958575 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:43958575 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:216050949 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:216050949 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161131965 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:161131965 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:6970340 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:6970340 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:144759779 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:144759779 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160395210 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:160395210 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:108298000 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:108298000 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:118897307 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:118897307 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:77914969 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:77914969 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:12339552 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:12339552 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:38835000 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:38835000 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150044160 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150044160 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:98809315 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:98809315 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:203748903 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:203748903 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:203776156 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:203776156 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:1740616 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:1740616 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:1742119 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:1742119 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:9770210 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:9770210 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155650063 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155650063 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:20128601 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:20128601 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:145182047 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:145182047 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72004127 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72004127 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72004452 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:72004452 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:50713781 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:50713781 A>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:32397266 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:32397266 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:12462998 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:12462998 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:22817390 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:22817390 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:58111529 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:58111529 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:56006624 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:56006624 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:149191247 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:149191247 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:146062735 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:146062735 C>A did not map to a codon.
